What the label lists and what reports show
Sodium acetate side effects
Sodium acetate's FDA label lists its adverse reactions in its own words. FAERS holds 275 reports naming it through July 30, 2026; the reaction reported most often, leaving out the conditions it is used for, product-use terms and outcomes, is pyrexia (19 reports).
- Generic listed
- In shortage
Check it at the source: the sodium acetate FDA label on DailyMed (effective March 26, 2026, Hospira, Inc.); the FDA FAERS public dashboard.
What does the label list?
From the label: adverse reactionsSodium overload can occur with intravenous infusion of excessive amounts of sodium-containing solutions. See WARNINGS and PRECAUTIONS .
Source: FDA drug label, Hospira, Inc., effective March 26, 2026 (SPL set ce9a7469-c4ba-4f60-8f7a-47ef0974316e), via openFDA; the full label on DailyMed
What do FAERS reports show?
275 reports list sodium acetate among the medicines taken, each a report of something that happened, not proof the medicine caused it; 56 are coded as a death and 126 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Of the 20 reactions below, none is named by the same term (in US spelling) in the label's adverse reactions, warnings or patient leaflet; a reaction the label does not name may still be there under another word, and a report does not show that the medicine caused it.
The 25 most reported reactions
Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026; reactions as MedDRA preferred terms
What next?
- Sodium acetate: the full record
- label, generics, price, shortages, recalls
- Report a side effect to the FDA
- MedWatch
- Side effects hub
- the most reported medicines and reactions