Does POTASSIUM Cause Incorrect product administration duration? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product administration duration have been filed in association with POTASSIUM (POTASSIUM CITRATE). This represents 0.1% of all adverse event reports for POTASSIUM.
7
Reports of Incorrect product administration duration with POTASSIUM
0.1%
of all POTASSIUM reports
0
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From POTASSIUM?
Of the 7 reports, 5 (71.4%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POTASSIUM. However, 7 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which POTASSIUM Alternatives Have Lower Incorrect product administration duration Risk?
POTASSIUM vs POTASSIUM, DIBASIC
POTASSIUM vs POTASSIUM IODIDE
POTASSIUM vs POTASSIUM, MONOBASIC
POTASSIUM vs POTASSIUM\SODIUM FLUORIDE
POTASSIUM vs POVIDONE-IODINE