Does RIFAXIMIN Cause Intentional product use issue? 221 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 221 reports of Intentional product use issue have been filed in association with RIFAXIMIN (XIFAXAN). This represents 1.6% of all adverse event reports for RIFAXIMIN.
221
Reports of Intentional product use issue with RIFAXIMIN
1.6%
of all RIFAXIMIN reports
29
Deaths
115
Hospitalizations
How Dangerous Is Intentional product use issue From RIFAXIMIN?
Of the 221 reports, 29 (13.1%) resulted in death, 115 (52.0%) required hospitalization, and 3 (1.4%) 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 RIFAXIMIN. However, 221 reports have been filed with the FAERS database.
What Other Side Effects Does RIFAXIMIN Cause?
Death (3,687)
Hospitalisation (1,605)
Therapy interrupted (875)
Off label use (802)
Diarrhoea (709)
Ammonia increased (676)
Inability to afford medication (672)
Insurance issue (577)
Confusional state (530)
Hepatic cirrhosis (480)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which RIFAXIMIN Alternatives Have Lower Intentional product use issue Risk?
RIFAXIMIN vs RILMENIDINE
RIFAXIMIN vs RILONACEPT
RIFAXIMIN vs RILPIVIRINE
RIFAXIMIN vs RILUZOLE
RIFAXIMIN vs RIMABOTULINUMTOXINB