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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 administered? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Recalled product administered have been filed in association with SODIUM (Sodium Chloride). This represents 0.2% of all adverse event reports for SODIUM.

40
Reports of Recalled product administered with SODIUM
0.2%
of all SODIUM reports
2
Deaths
0
Hospitalizations

How Dangerous Is Recalled product administered From SODIUM?

Of the 40 reports, 2 (5.0%) resulted in death, and 4 (10.0%) 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 SODIUM. However, 40 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 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 SODIUM Alternatives Have Lower Recalled product administered 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 administered Reports All Drugs Causing Recalled product administered SODIUM Demographics