Does SODIUM, MONOBASIC Cause Condition aggravated? 126 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 126 reports of Condition aggravated have been filed in association with SODIUM, MONOBASIC. This represents 55.8% of all adverse event reports for SODIUM, MONOBASIC.
126
Reports of Condition aggravated with SODIUM, MONOBASIC
55.8%
of all SODIUM, MONOBASIC reports
125
Deaths
92
Hospitalizations
How Dangerous Is Condition aggravated From SODIUM, MONOBASIC?
Of the 126 reports, 125 (99.2%) resulted in death, 92 (73.0%) required hospitalization, and 89 (70.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM, MONOBASIC. However, 126 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM, MONOBASIC Cause?
Hyponatraemia (185)
Stress (183)
General physical health deterioration (182)
Multiple organ dysfunction syndrome (182)
Sepsis (180)
Vomiting (178)
Appendicitis (177)
Ascites (177)
Appendicolith (176)
Abdominal distension (174)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which SODIUM, MONOBASIC Alternatives Have Lower Condition aggravated Risk?
SODIUM, MONOBASIC vs SODIUM MONOFLUOROPHOSPHATE
SODIUM, MONOBASIC vs SODIUM NITROPRUSSIDE
SODIUM, MONOBASIC vs SODIUM OXYBATE
SODIUM, MONOBASIC vs SODIUM PHENYLBUTYRATE
SODIUM, MONOBASIC vs SODIUM PHENYLBUTYRATE\TAURURSODIOL