Does DEVICE Cause Abdominal distension? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Abdominal distension have been filed in association with DEVICE. This represents 0.3% of all adverse event reports for DEVICE.
43
Reports of Abdominal distension with DEVICE
0.3%
of all DEVICE reports
2
Deaths
8
Hospitalizations
How Dangerous Is Abdominal distension From DEVICE?
Of the 43 reports, 2 (4.7%) resulted in death, 8 (18.6%) required hospitalization, and 1 (2.3%) were considered life-threatening.
Is Abdominal distension Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 43 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 Abdominal distension?
ADALIMUMAB (3,728)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,238)
LEVONORGESTREL (1,700)
METHOTREXATE (1,471)
TREPROSTINIL (1,437)
PREDNISONE (1,429)
SEMAGLUTIDE (1,424)
VEDOLIZUMAB (1,411)
INFLIXIMAB (1,328)
POLYETHYLENE GLYCOL 3350 (1,158)
Which DEVICE Alternatives Have Lower Abdominal distension Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN