Does KETOTIFEN Cause Therapy non-responder? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Therapy non-responder have been filed in association with KETOTIFEN (Eye Itch Relief). This represents 0.2% of all adverse event reports for KETOTIFEN.
12
Reports of Therapy non-responder with KETOTIFEN
0.2%
of all KETOTIFEN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Therapy non-responder From KETOTIFEN?
Of the 12 reports, 1 (8.3%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Therapy non-responder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOTIFEN. However, 12 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)
Condition aggravated (83)
Eye swelling (72)
What Other Drugs Cause Therapy non-responder?
ETANERCEPT (3,472)
APREMILAST (3,360)
METHOTREXATE (2,965)
RITUXIMAB (2,731)
ADALIMUMAB (2,595)
PREDNISONE (2,563)
TREPROSTINIL (2,289)
INFLIXIMAB (2,122)
TOCILIZUMAB (1,775)
HYDROXYCHLOROQUINE (1,699)
Which KETOTIFEN Alternatives Have Lower Therapy non-responder Risk?
KETOTIFEN vs KLONOPIN
KETOTIFEN vs L-ASPARAGINASE
KETOTIFEN vs LABETALOL
KETOTIFEN vs LABETALOL\LABETALOL
KETOTIFEN vs LACIDIPINE