Does SUCRALFATE Cause Product dose omission? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission have been filed in association with SUCRALFATE (Sucralfate). This represents 0.4% of all adverse event reports for SUCRALFATE.
7
Reports of Product dose omission with SUCRALFATE
0.4%
of all SUCRALFATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From SUCRALFATE?
Of the 7 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUCRALFATE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does SUCRALFATE Cause?
Drug ineffective (313)
Off label use (300)
Nausea (275)
Constipation (222)
Headache (215)
Abdominal pain (196)
Pain (195)
Weight decreased (191)
Pyrexia (188)
Malaise (171)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which SUCRALFATE Alternatives Have Lower Product dose omission Risk?
SUCRALFATE vs SUCROFERRIC OXYHYDROXIDE
SUCRALFATE vs SUCROSE
SUCRALFATE vs SUFENTANIL
SUCRALFATE vs SUGAMMADEX
SUCRALFATE vs SULBACTAM