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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 Presyncope? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Presyncope have been filed in association with KETOTIFEN (Eye Itch Relief). This represents 0.1% of all adverse event reports for KETOTIFEN.

6
Reports of Presyncope with KETOTIFEN
0.1%
of all KETOTIFEN reports
0
Deaths
3
Hospitalizations

How Dangerous Is Presyncope From KETOTIFEN?

Of the 6 reports, 3 (50.0%) required hospitalization.

Is Presyncope Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOTIFEN. However, 6 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 Presyncope?

TREPROSTINIL (585) BISOPROLOL (485) LEVONORGESTREL (429) ADALIMUMAB (420) AMBRISENTAN (407) ASPIRIN (370) TAMSULOSIN (361) FUROSEMIDE (348) SERTRALINE (337) ETANERCEPT (334)

Which KETOTIFEN Alternatives Have Lower Presyncope Risk?

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

Related Pages

KETOTIFEN Full Profile All Presyncope Reports All Drugs Causing Presyncope KETOTIFEN Demographics