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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 Recalled product? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Recalled product have been filed in association with SODIUM (Sodium Chloride). This represents 0.0% of all adverse event reports for SODIUM.

5
Reports of Recalled product with SODIUM
0.0%
of all SODIUM reports
0
Deaths
1
Hospitalizations

How Dangerous Is Recalled product From SODIUM?

Of the 5 reports, 1 (20.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Recalled product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SODIUM. However, 5 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 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 SODIUM Alternatives Have Lower Recalled product 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 Recalled product Reports All Drugs Causing Recalled product SODIUM Demographics