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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 SODIUM Cause Product dose omission issue? 67 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Product dose omission issue have been filed in association with SODIUM (Sodium Chloride). This represents 0.3% of all adverse event reports for SODIUM.

67
Reports of Product dose omission issue with SODIUM
0.3%
of all SODIUM reports
23
Deaths
32
Hospitalizations

How Dangerous Is Product dose omission issue From SODIUM?

Of the 67 reports, 23 (34.3%) resulted in death, 32 (47.8%) required hospitalization, and 21 (31.3%) 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 SODIUM. However, 67 reports have been filed with the FAERS database.

What Other Side Effects Does SODIUM Cause?

Paraesthesia (5,812) Nausea (4,170) Dizziness (3,270) Feeling hot (2,964) Pallor (2,745) Hyperhidrosis (2,444) Asthenia (1,699) Myelosuppression (1,696) Drug ineffective (1,370) Thirst (1,343)

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 SODIUM Alternatives Have Lower Product dose omission issue Risk?

SODIUM vs SODIUM BICARBONATE SODIUM vs SODIUM BICARBONATE\SODIUM SODIUM vs SODIUM BORATE SODIUM vs SODIUM, DIBASIC\SODIUM, MONOBASIC SODIUM vs SODIUM FERRIC COMPLEX

Related Pages

SODIUM Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue SODIUM Demographics