Does RIFAXIMIN Cause Wrong technique in product usage process? 124 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 124 reports of Wrong technique in product usage process have been filed in association with RIFAXIMIN (XIFAXAN). This represents 0.9% of all adverse event reports for RIFAXIMIN.
124
Reports of Wrong technique in product usage process with RIFAXIMIN
0.9%
of all RIFAXIMIN reports
9
Deaths
20
Hospitalizations
How Dangerous Is Wrong technique in product usage process From RIFAXIMIN?
Of the 124 reports, 9 (7.3%) resulted in death, 20 (16.1%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIFAXIMIN. However, 124 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which RIFAXIMIN Alternatives Have Lower Wrong technique in product usage process Risk?
RIFAXIMIN vs RILMENIDINE
RIFAXIMIN vs RILONACEPT
RIFAXIMIN vs RILPIVIRINE
RIFAXIMIN vs RILUZOLE
RIFAXIMIN vs RIMABOTULINUMTOXINB