SODIUM BICARBONATE
Clinical safety rating: safe
Animal studies have demonstrated safety
Sodium bicarbonate dissociates to provide bicarbonate ion, which buffers excess hydrogen ions in the blood, increasing pH and reversing acidosis.
| Metabolism | Sodium bicarbonate is not metabolized; it dissociates to bicarbonate and sodium. Bicarbonate is rapidly converted to carbon dioxide by carbonic anhydrase in erythrocytes and renal tubules, and CO2 is excreted via lungs. |
| Excretion | Renal: >99% as bicarbonate; minimal biliary/fecal elimination |
| Half-life | 5-6 hours in normal renal function; prolonged in renal impairment (up to 15-20 hours) |
| Protein binding | <1% (not significantly protein bound) |
| Volume of Distribution | 0.3-0.4 L/kg (distributes primarily in extracellular fluid) |
| Bioavailability | Oral: ~100% (but rapid conversion to CO2 in stomach may reduce effective systemic absorption) |
| Onset of Action | Intravenous: immediate (within 1-2 minutes); Oral: 15-30 minutes |
| Duration of Action | Intravenous: 1-2 hours (buffer effect); Oral: 30-60 minutes (systemic effect); depends on acid-base status and renal function |
For metabolic acidosis: 50-150 mEq intravenously over 4-8 hours, dose adjusted based on base deficit or serum bicarbonate. For cardiac arrest: 1 mEq/kg intravenously initially, then 0.5 mEq/kg every 10 minutes. For urinary alkalinization: 325-2000 mg orally every 6 hours, titrate to urine pH 7-8.
| Dosage form | SOLUTION |
| Renal impairment | No specific dose adjustment required; monitor sodium and fluid status. In severe renal impairment (GFR <10 mL/min), use with caution due to risk of volume overload and metabolic alkalosis. Not removed by hemodialysis. |
| Liver impairment | No dosage adjustment necessary for hepatic impairment. Use with caution in severe hepatic impairment due to potential for fluid overload and electrolyte disturbances. |
| Pediatric use | Metabolic acidosis: 1-2 mEq/kg intravenously over 1-2 hours, repeat based on blood gas. Cardiac arrest: 1 mEq/kg intravenously initially, may repeat 0.5 mEq/kg every 10 minutes. Urinary alkalinization: 1-2 mEq/kg orally every 6 hours, adjust to urine pH. |
| Geriatric use | Use with caution due to increased risk of fluid overload and electrolyte imbalances. Start at lower end of dosing range and titrate based on response and renal function. Monitor serum sodium, bicarbonate, and renal function frequently. |
| 1st trimester | Consult provider |
| 2nd trimester | Consult provider |
| 3rd trimester | Consult provider |
Clinical note
Can decrease the levels of many drugs by increasing urinary pH Can cause metabolic alkalosis and fluid overload.
| Breastfeeding | Sodium bicarbonate is excreted into breast milk in small amounts. M/P ratio is not established. Considered compatible with breastfeeding, but monitor infant for metabolic alkalosis risk. |
| Teratogenic Risk | Sodium bicarbonate is generally considered low risk. No evidence of teratogenicity. Use during pregnancy is acceptable if clinically indicated. |
| Fetal Monitoring |
■ FDA Black Box Warning
In cardiac arrest, routine use is not recommended; may cause paradoxical intracellular acidosis, hyperosmolality, and decreased tissue oxygen delivery.
| Common Effects | hyperkalemia |
| Serious Effects |
["Metabolic alkalosis","Respiratory alkalosis","Hypocalcemia (unless used to treat cardiac arrest)","Severe pulmonary edema or hypertension","Patients losing chloride from vomiting or gastrointestinal suction"]
| Precautions | ["Risk of metabolic alkalosis with excessive use","Fluid overload due to sodium content, especially in heart failure, renal impairment, or cirrhosis","Hypocalcemia and reduced ionized calcium leading to tetany","Extravasation risk; intravenous administration should be via central line for concentrated solutions","Monitor serum electrolytes, pH, and calcium during therapy"] |
Loading safety data…
| Monitor serum electrolytes, bicarbonate, and acid-base status. Watch for fluid overload, hypernatremia, and hypocalcemia in mother; assess fetal heart rate during administration. |
| Fertility Effects | No known adverse effects on fertility. Does not significantly impact reproductive function. |