Does DEVICE Cause Irritable bowel syndrome? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Irritable bowel syndrome have been filed in association with DEVICE. This represents 0.2% of all adverse event reports for DEVICE.
20
Reports of Irritable bowel syndrome with DEVICE
0.2%
of all DEVICE reports
6
Deaths
12
Hospitalizations
How Dangerous Is Irritable bowel syndrome From DEVICE?
Of the 20 reports, 6 (30.0%) resulted in death, 12 (60.0%) required hospitalization, and 7 (35.0%) were considered life-threatening.
Is Irritable bowel syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
What Other Drugs Cause Irritable bowel syndrome?
METHOTREXATE (4,155)
ABATACEPT (4,069)
ADALIMUMAB (3,915)
LEFLUNOMIDE (3,897)
TOCILIZUMAB (3,854)
CERTOLIZUMAB PEGOL (3,740)
GOLIMUMAB (3,684)
ETANERCEPT (3,419)
RITUXIMAB (3,393)
ACETAMINOPHEN (3,337)
Which DEVICE Alternatives Have Lower Irritable bowel syndrome Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN