SODIUM BICARBONATE

Brand names: SODIUM BICARBONATE, Sodium Bicarbonate, Anti-Empacho, Sodium Bicarbonate 5 gr, Sodium Bicarbonate 10 GR (650 MG), BM Sodium bicarbonate (Nat Bicarb), After Bite Advanced, Sodium Bicarbonate 10 gr, EcoDent Ultimate Essential Mouthcare Spicy-Cool Cinnamon, D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO, De La Cruz Desempacho, Sodium Bicarbonate 10 gr (650 mg), Humco Sodium Bicarbonate, Sodium Bicarbonate Antacid, Insect sting relief pad 01, Medis Sodium Bicarbonate, DE LA CRUZ SODIUM BICARBONATE ANTACID, Sodium Bicarbonate 10 gr. (650 mg), AHHH Bite Relief, Bestmade Natural Products Sodium Bicarbonate (Nat Bicarb), DR. SANA BICARBONATO DE SODIO 4 Fl oz and 6 Floz, After Bite Kids, sodium bicarbonate, Insect sting relief latex 01, ADRIAN BICARBONATO SODIUM BICARBONATE USP-4 oz, 8 oz and 16 oz, Arm and Hammer Baking Soda, Sanar Baking Soda 8oz 100% pure, Rapidol Sodium Bicarbonate, Sodium Bicarbonate 5 gr (325 mg), Itch Eraser Sensitive, EcoDent Ultimate Essential Mouthcare Sparkling Clean Mint, After Bite X Tech

Boxed warning

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Warnings

PRECAUTIONS General Do not use unless solution is clear and the container or seal is intact. Discard unused portion. The potentially large loads of sodium given with bicarbonate require that caution be exercised in the use of sodium bicarbonate in patients with congestive heart failure or other edematous or sodium-retaining states, as well as in patients with oliguria or anuria. See table in HOW SUPPLIED section for amount of sodium present in the solution. Caution must be exercised in the administration of parenteral fluids, especially those containing sodium ions, to patients receiving corticosteroids or corticotropin. Potassium depletion may predispose to metabolic alkalosis and coexistent hypocalcemia may be associated with carpopedal spasm as the plasma pH rises. These dangers can be minimized if such electrolyte imbalances are appropriately treated prior to or concomitantly with bicarbonate infusion. Laboratory Tests The aim of all bicarbonate therapy is to produce a substantial correction of the low total CO 2 content and blood pH, but the risks of overdosage and alkalosis should be avoided. Hence, repeated fractional doses and periodic monitoring by appropriate laboratory tests are recommended to minimize the possibility of overdosage. Drug Interactions Additives may be incompatible; norepinephrine and dobutamine are incompatible with sodium bicarbonate solution. The addition of sodium bicarbonate to parenteral solutions containing calcium should be avoided, except where compatibility has been previously established. Precipitation or haze may result from sodium bicarbonate-calcium admixtures. NOTE: Do not use the injection if it contains precipitate. Additives may be incompatible. Consult with pharmacist, if available. When introducing additives, consult with pharmacist, if available. When introducing additives, use aseptic technique, mix thoroughly and do not store. Pregnancy: Teratogenic Effects. Animal reproduction studies have not been conducted with sodium bicarbonate. It is also not known whether sodium bicarbonate can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Sodium bicarbonate should be given to a pregnant woman only if clearly needed. Pediatric Rapid injection (10 mL/min) of hypertonic sodium bicarbonate injection solutions into neonates and children under two years of age may produce hypernatremia, a decrease in cerebrospinal fluid pressure and possible intracranial hemorrhage. The rate of administration in such patients should therefore be limited to no more than 8 mEq/kg/day. A 4.2% solution may be preferred for such slow administration. In emergencies such as cardiac arrest, the risk of rapid infusion must be weighed against the potential for fatality due to acidosis. Geriatric Clinical studies of sodium bicarbonate injection did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function and of concomitant disease or other drug therapy.

Contraindications

CONTRAINDICATIONS Sodium Bicarbonate Injection, USP is contraindicated in patients who are losing chloride by vomiting or from continuous gastrointestinal suction, and in patients receiving diuretics known to produce a hypochloremic alkalosis.

Overdose

OVERDOSAGE Should alkalosis result, the bicarbonate should be stopped and the patient managed according to the degree of alkalosis present. 0.9% sodium chloride injection intravenous may be given; potassium chloride also may be indicated if there is hypokalemia. Severe alkalosis may be accompanied by hyperirritability or tetany and these symptoms may be controlled by calcium gluconate. An acidifying agent such as ammonium chloride may also be indicated in severe alkalosis. See WARNINGS and PRECAUTIONS.

Drug interactions

Drug Interactions Additives may be incompatible; norepinephrine and dobutamine are incompatible with sodium bicarbonate solution. The addition of sodium bicarbonate to parenteral solutions containing calcium should be avoided, except where compatibility has been previously established. Precipitation or haze may result from sodium bicarbonate-calcium admixtures. NOTE: Do not use the injection if it contains precipitate. Additives may be incompatible. Consult with pharmacist, if available. When introducing additives, consult with pharmacist, if available. When introducing additives, use aseptic technique, mix thoroughly and do not store.

Uses

CONTRAINDICATIONS Sodium bicarbonate injection is contraindicated in patients who are losing chloride by vomiting or from continuous gastrointestinal suction, and in patients receiving diuretics known to produce a hypochloremic alkalosis.

Dosage forms & strengths

INJECTION, SOLUTION POWDER CRYSTAL LIQUID TABLET INJECTION TABLET, SOLUBLE CLOTH GEL CREAM LOTION
SODIUM BICARBONATE 84 mg/mL SODIUM BICARBONATE 1 kg/kg SODIUM BICARBONATE 2.6 g/2.6g SODIUM BICARBONATE 525 mg/15mL SODIUM BICARBONATE 325 mg/1 SODIUM BICARBONATE 650 mg/1 SODIUM BICARBONATE 6 [hp_X]/60mg SODIUM BICARBONATE .7 g/14g SODIUM BICARBONATE 648 mg/1 SODIUM BICARBONATE 42 mg/mL SODIUM BICARBONATE 25 mg/mL SODIUM BICARBONATE 315 mg/g SODIUM BICARBONATE 1000 mg/g SODIUM BICARBONATE .05 g/1 SODIUM BICARBONATE 5 g/25g SODIUM BICARBONATE 6 [hp_X]/6[hp_X] SODIUM BICARBONATE 1.04 g/20g SODIUM BICARBONATE 12.6 mg/mL SODIUM BICARBONATE 5 g/100g SODIUM BICARBONATE 1 g/g SODIUM BICARBONATE 25 kg/25kg SODIUM BICARBONATE 2.616 g/2.616g SODIUM BICARBONATE 616 mg/g SODIUM BICARBONATE 75 mg/mL SODIUM BICARBONATE 50 mg/1000mL

Directions do not use the maximum dosage for more than 2 weeks tablets may be swallowed whole or dissolved in water prior to use adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hours adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours

Ingredients

Active:

Active ingredient (in each tablet) Sodium Bicarbonate 10 gr. (650 mg)

Inactive:

Inactive ingredients microcrystalline cellulose, stearic acid

All identified pills

Side effects

OVERDOSAGE Should alkalosis result, the bicarbonate should be stopped and the patient managed according to the degree of alkalosis present. 0.9% sodium chloride injection intravenous may be given; potassium chloride also may be indicated if there is hypokalemia. Severe alkalosis may be accompanied by hyperirritability or tetany and these symptoms may be controlled by calcium gluconate. An acidifying agent such as ammonium chloride may also be indicated in severe alkalosis. See WARNINGS and PRECAUTIONS .

Official source

DailyMed