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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does POTASSIUM Cause Recalled product? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Recalled product have been filed in association with POTASSIUM (POTASSIUM CITRATE). This represents 0.1% of all adverse event reports for POTASSIUM.

17
Reports of Recalled product with POTASSIUM
0.1%
of all POTASSIUM reports
5
Deaths
3
Hospitalizations

How Dangerous Is Recalled product From POTASSIUM?

Of the 17 reports, 5 (29.4%) resulted in death, 3 (17.6%) required hospitalization.

Is Recalled product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for POTASSIUM. However, 17 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?

PARATHYROID HORMONE (900) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80) CALCITRIOL (68) CALCIUM (66) REMDESIVIR (36) LEVOTHYROXINE\LIOTHYRONINE (34) TESTOSTERONE (32) VALSARTAN (32) CHLORHEXIDINE (28) ALCOHOL (26)

Which POTASSIUM Alternatives Have Lower Recalled product Risk?

POTASSIUM vs POTASSIUM, DIBASIC POTASSIUM vs POTASSIUM IODIDE POTASSIUM vs POTASSIUM, MONOBASIC POTASSIUM vs POTASSIUM\SODIUM FLUORIDE POTASSIUM vs POVIDONE-IODINE

Related Pages

POTASSIUM Full Profile All Recalled product Reports All Drugs Causing Recalled product POTASSIUM Demographics