Does TIMOLOL Cause Condition aggravated? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Condition aggravated have been filed in association with TIMOLOL (Timoptic). This represents 1.2% of all adverse event reports for TIMOLOL.
91
Reports of Condition aggravated with TIMOLOL
1.2%
of all TIMOLOL reports
12
Deaths
5
Hospitalizations
How Dangerous Is Condition aggravated From TIMOLOL?
Of the 91 reports, 12 (13.2%) resulted in death, 5 (5.5%) required hospitalization, and 14 (15.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 91 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which TIMOLOL Alternatives Have Lower Condition aggravated Risk?
TIMOLOL vs TIMOLOL\TRAVOPROST
TIMOLOL vs TINIDAZOLE
TIMOLOL vs TINZAPARIN
TIMOLOL vs TIOCONAZOLE
TIMOLOL vs TIOPRONIN