Does KETOTIFEN Cause Condition aggravated? 83 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Condition aggravated have been filed in association with KETOTIFEN (Eye Itch Relief). This represents 1.6% of all adverse event reports for KETOTIFEN.
83
Reports of Condition aggravated with KETOTIFEN
1.6%
of all KETOTIFEN reports
1
Deaths
10
Hospitalizations
How Dangerous Is Condition aggravated From KETOTIFEN?
Of the 83 reports, 1 (1.2%) resulted in death, 10 (12.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOTIFEN. However, 83 reports have been filed with the FAERS database.
What Other Side Effects Does KETOTIFEN Cause?
Treatment failure (3,038)
Drug ineffective (798)
Eye irritation (455)
Eye pain (208)
Ocular hyperaemia (166)
Eye pruritus (164)
Hypersensitivity (102)
Vision blurred (87)
Eye swelling (72)
Product quality issue (55)
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 KETOTIFEN Alternatives Have Lower Condition aggravated Risk?
KETOTIFEN vs KLONOPIN
KETOTIFEN vs L-ASPARAGINASE
KETOTIFEN vs LABETALOL
KETOTIFEN vs LABETALOL\LABETALOL
KETOTIFEN vs LACIDIPINE