Does SUCRALFATE Cause Product prescribing issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product prescribing issue have been filed in association with SUCRALFATE (Sucralfate). This represents 0.3% of all adverse event reports for SUCRALFATE.
5
Reports of Product prescribing issue with SUCRALFATE
0.3%
of all SUCRALFATE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product prescribing issue From SUCRALFATE?
Of the 5 reports, 2 (40.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUCRALFATE. However, 5 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which SUCRALFATE Alternatives Have Lower Product prescribing issue Risk?
SUCRALFATE vs SUCROFERRIC OXYHYDROXIDE
SUCRALFATE vs SUCROSE
SUCRALFATE vs SUFENTANIL
SUCRALFATE vs SUGAMMADEX
SUCRALFATE vs SULBACTAM