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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 OXYQUINOLINE Cause Intentional product use issue? 52 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Intentional product use issue have been filed in association with OXYQUINOLINE (TRIMO SAN). This represents 42.6% of all adverse event reports for OXYQUINOLINE.

52
Reports of Intentional product use issue with OXYQUINOLINE
42.6%
of all OXYQUINOLINE reports
48
Deaths
52
Hospitalizations

How Dangerous Is Intentional product use issue From OXYQUINOLINE?

Of the 52 reports, 48 (92.3%) resulted in death, 52 (100.0%) required hospitalization, and 47 (90.4%) were considered life-threatening.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OXYQUINOLINE. However, 52 reports have been filed with the FAERS database.

What Other Side Effects Does OXYQUINOLINE Cause?

Drug ineffective (96) Pain (81) Joint swelling (70) Pulmonary embolism (62) Rheumatoid arthritis (59) Drug intolerance (57) Stomatitis (56)