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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 BEPOTASTINE BESILATE Cause Condition aggravated? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with BEPOTASTINE BESILATE (Bepotastine Besilate Ophthalmic Solution 1.5%). This represents 3.5% of all adverse event reports for BEPOTASTINE BESILATE.

5
Reports of Condition aggravated with BEPOTASTINE BESILATE
3.5%
of all BEPOTASTINE BESILATE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From BEPOTASTINE BESILATE?

Of the 5 reports.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BEPOTASTINE BESILATE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does BEPOTASTINE BESILATE Cause?

Treatment failure (24) Drug ineffective (17) Eye irritation (17) Dysgeusia (11) Vision blurred (8) Headache (7) Eye pruritus (6) Off label use (6) Lacrimation increased (5) Ocular hyperaemia (5)

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 BEPOTASTINE BESILATE Alternatives Have Lower Condition aggravated Risk?

BEPOTASTINE BESILATE vs BERACTANT BEPOTASTINE BESILATE vs BERAPROST BEPOTASTINE BESILATE vs BEROTRALSTAT BEPOTASTINE BESILATE vs BESIFLOXACIN BEPOTASTINE BESILATE vs BETA CAROTENE

Related Pages

BEPOTASTINE BESILATE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated BEPOTASTINE BESILATE Demographics