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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does KETOTIFEN Cause Treatment failure? 3,038 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 3,038 reports of Treatment failure have been filed in association with KETOTIFEN (Eye Itch Relief). This represents 58.3% of all adverse event reports for KETOTIFEN.

3,038
Reports of Treatment failure with KETOTIFEN
58.3%
of all KETOTIFEN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Treatment failure From KETOTIFEN?

Of the 3,038 reports, 1 (0.0%) required hospitalization.

Is Treatment failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOTIFEN. However, 3,038 reports have been filed with the FAERS database.

What Other Side Effects Does KETOTIFEN Cause?

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) Product quality issue (55)

What Other Drugs Cause Treatment failure?

METHOTREXATE (14,672) ETANERCEPT (11,893) ADALIMUMAB (9,990) ABATACEPT (9,301) RITUXIMAB (9,217) TOCILIZUMAB (9,097) HYDROXYCHLOROQUINE (8,786) LEFLUNOMIDE (8,686) INFLIXIMAB (8,535) SULFASALAZINE (7,423)

Which KETOTIFEN Alternatives Have Lower Treatment failure Risk?

KETOTIFEN vs KLONOPIN KETOTIFEN vs L-ASPARAGINASE KETOTIFEN vs LABETALOL KETOTIFEN vs LABETALOL\LABETALOL KETOTIFEN vs LACIDIPINE

Related Pages

KETOTIFEN Full Profile All Treatment failure Reports All Drugs Causing Treatment failure KETOTIFEN Demographics