Does POTASSIUM Cause Recalled product administered? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Recalled product administered have been filed in association with POTASSIUM (POTASSIUM CITRATE). This represents 0.4% of all adverse event reports for POTASSIUM.
52
Reports of Recalled product administered with POTASSIUM
0.4%
of all POTASSIUM reports
10
Deaths
8
Hospitalizations
How Dangerous Is Recalled product administered From POTASSIUM?
Of the 52 reports, 10 (19.2%) resulted in death, 8 (15.4%) required hospitalization, and 2 (3.8%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POTASSIUM. However, 52 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which POTASSIUM Alternatives Have Lower Recalled product administered Risk?
POTASSIUM vs POTASSIUM, DIBASIC
POTASSIUM vs POTASSIUM IODIDE
POTASSIUM vs POTASSIUM, MONOBASIC
POTASSIUM vs POTASSIUM\SODIUM FLUORIDE
POTASSIUM vs POVIDONE-IODINE