Does SUCRALFATE Cause Haemoglobin decreased? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Haemoglobin decreased have been filed in association with SUCRALFATE (Sucralfate). This represents 0.7% of all adverse event reports for SUCRALFATE.
13
Reports of Haemoglobin decreased with SUCRALFATE
0.7%
of all SUCRALFATE reports
3
Deaths
7
Hospitalizations
How Dangerous Is Haemoglobin decreased From SUCRALFATE?
Of the 13 reports, 3 (23.1%) resulted in death, 7 (53.8%) required hospitalization, and 2 (15.4%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUCRALFATE. However, 13 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which SUCRALFATE Alternatives Have Lower Haemoglobin decreased Risk?
SUCRALFATE vs SUCROFERRIC OXYHYDROXIDE
SUCRALFATE vs SUCROSE
SUCRALFATE vs SUFENTANIL
SUCRALFATE vs SUGAMMADEX
SUCRALFATE vs SULBACTAM