Does POTASSIUM Cause Product dose omission issue? 82 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 82 reports of Product dose omission issue have been filed in association with POTASSIUM (POTASSIUM CITRATE). This represents 0.7% of all adverse event reports for POTASSIUM.
82
Reports of Product dose omission issue with POTASSIUM
0.7%
of all POTASSIUM reports
24
Deaths
47
Hospitalizations
How Dangerous Is Product dose omission issue From POTASSIUM?
Of the 82 reports, 24 (29.3%) resulted in death, 47 (57.3%) required hospitalization, and 20 (24.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POTASSIUM. However, 82 reports have been filed with the FAERS database.
What Other Side Effects Does POTASSIUM Cause?
Drug ineffective (1,115)
Hyperkalaemia (944)
Off label use (789)
Nausea (747)
Dyspnoea (711)
Diarrhoea (690)
Malaise (678)
Abdominal pain (636)
Acute kidney injury (614)
Vomiting (588)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which POTASSIUM Alternatives Have Lower Product dose omission issue Risk?
POTASSIUM vs POTASSIUM, DIBASIC
POTASSIUM vs POTASSIUM IODIDE
POTASSIUM vs POTASSIUM, MONOBASIC
POTASSIUM vs POTASSIUM\SODIUM FLUORIDE
POTASSIUM vs POVIDONE-IODINE