SODIUM BICARBONATE 5 GR (325 MG)- sodium bicarbonate tablet United States - English - NLM (National Library of Medicine)

sodium bicarbonate 5 gr (325 mg)- sodium bicarbonate tablet

citragen pharmaceuticals inc. - sodium bicarbonate (unii: 8mdf5v39qo) (sodium cation - unii:lyr4m0nh37) - sodium bicarbonate 325 mg - antacid relieves: acid indigestion heartburn sour stomach upset stomach associated with these symptoms

SODIUM BICARBONATE 10 GR (650 MG)- sodium bicarbonate tablet United States - English - NLM (National Library of Medicine)

sodium bicarbonate 10 gr (650 mg)- sodium bicarbonate tablet

citragen pharmaceuticals inc. - sodium bicarbonate (unii: 8mdf5v39qo) (sodium cation - unii:lyr4m0nh37) - sodium bicarbonate 650 mg - antacid relieves: - acid indigestion - heartburn - sour stomach - upset stomach associated with these symptoms

SODIUM BICARBONATE - sodium bicarbonate tablet, orally disintegrating United States - English - NLM (National Library of Medicine)

sodium bicarbonate - sodium bicarbonate tablet, orally disintegrating

rising pharmaceuticals, inc. - sodium bicarbonate (unii: 8mdf5v39qo) (bicarbonate ion - unii:hn1zra3q20) - sodium bicarbonate 650 mg - relieves • acid indigestion • heartburn • sour stomach • upset stomach associated with these symptoms

SODIUM BICARBONATE- sodium bicarbonate tablet, orally disintegrating United States - English - NLM (National Library of Medicine)

sodium bicarbonate- sodium bicarbonate tablet, orally disintegrating

aphena pharma solutions - tennessee, llc - sodium bicarbonate (unii: 8mdf5v39qo) (bicarbonate ion - unii:hn1zra3q20) - sodium bicarbonate 650 mg - relieves • acid indigestion • heartburn • sour stomach • upset stomach associated with these symptoms

Gaviscon Extra Oral Suspension Sodium alginate 500 mg Sodium bicarbonate 213 mg Calcium carbonate 325 mg Ireland - English - HPRA (Health Products Regulatory Authority)

gaviscon extra oral suspension sodium alginate 500 mg sodium bicarbonate 213 mg calcium carbonate 325 mg

reckitt benckiser ireland ltd - sodium alginate; sodium bicarbonate; calcium carbonate - oral suspension - 500 mg+213 mg+325 milligram(s) - other drugs for peptic ulcer and gastro-oesophageal reflux disease (gord); alginic acid

SODIUM BICARBONATE injection, solution United States - English - NLM (National Library of Medicine)

sodium bicarbonate injection, solution

mckesson corporation dba sky packaging - sodium bicarbonate (unii: 8mdf5v39qo) (bicarbonate ion - unii:hn1zra3q20, sodium cation - unii:lyr4m0nh37) - sodium bicarbonate 84 mg in 1 ml - sodium bicarbonate injection, usp is indicated in the treatment of metabolic acidosis which may occur in severe renal disease, uncontrolled diabetes, circulatory insufficiency due to shock or severe dehydration, extracorporeal circulation of blood, cardiac arrest and severe primary lactic acidosis. sodium bicarbonate is further indicated in the treatment of certain drug intoxications, including barbiturates (where dissociation of the barbiturate-protein complex is desired), in poisoning by salicylates or methyl alcohol and in hemolytic reactions requiring alkalinization of the urine to diminish nephrotoxicity of blood pigments. sodium bicarbonate also is indicated in severe diarrhea which is often accompanied by a significant loss of bicarbonate. treatment of metabolic acidosis should, if possible, be superimposed on measures designed to control the basic cause of the acidosis ― e.g., insulin in uncomplicated diabetes, blood volume restoration in shock. but since an appreciable time interval may elapse before

SODIUM BICARBONATE injection, solution United States - English - NLM (National Library of Medicine)

sodium bicarbonate injection, solution

phebra pty ltd - sodium bicarbonate (unii: 8mdf5v39qo) (bicarbonate ion - unii:hn1zra3q20) - sodium bicarbonate 84 mg in 1 ml - sodium bicarbonate injection is indicated as an alkalinising agent in the treatment of metabolic acidosis which may occur in many conditions including diabetes, starvation, hepatitis, cardiac arrest, shock, severe dehydration, renal insufficiency, severe diarrhoea, addison's disease or administration of acidifying salts (e.g. excessive sodium chloride, calcium chloride, ammonium chloride). sodium bicarbonate injection is also used to increase urinary ph in order to increase the solubility of certain weak acids (e.g. cystine, sulphonamides, uric acid) and in the treatment of certain intoxications (e.g. methanol, phenobarbitone, salicylates, lithium) to decrease renal absorption of the drug or to correct acidosis. sodium bicarbonate injection is contraindicated in patients with renal failure, respiratory or metabolic alkalosis, hypoventilation or chloride depletion, hypernatraemia, hypertension, oedema, congestive heart failure, eclampsia, aldosteronism, a history of urinary calculi and consistent potassium dep

Phebra SODIUM BICARBONATE 8.4% w/v 840 mg/10 mL injection BP vial Australia - English - Department of Health (Therapeutic Goods Administration)

phebra sodium bicarbonate 8.4% w/v 840 mg/10 ml injection bp vial

phebra pty ltd - sodium bicarbonate, quantity: 84 mg/ml - injection, solution - excipient ingredients: disodium edetate; water for injections - sodium bicarbonate injection is indicated as an alkalinising agent in the treatment of metabolic acidosis which may occur in many conditions including diabetes, starvation, hepatitis, cardiac arrest, shock, severe dehydration, renal insufficiency, severe diarrhoea, addison's disease or administration of acidifying salts (e.g. excessive sodium chloride, calcium chloride, ammonium chloride). sodium bicarbonate injection is also used to increase urinary ph in order to increase the solubility of certain weak acids (e.g. cystine, sulphonamides, uric acid) and in the treatment of certain intoxications (e.g. methanol, phenobarbitone, salicylates, lithium) to decrease renal absorption of the drug or to correct acidosis.

Phebra SODIUM BICARBONATE 8.4% w/v 8.4 g/100 mL injection BP vial Australia - English - Department of Health (Therapeutic Goods Administration)

phebra sodium bicarbonate 8.4% w/v 8.4 g/100 ml injection bp vial

phebra pty ltd - sodium bicarbonate, quantity: 84 mg/ml - injection, solution - excipient ingredients: disodium edetate; water for injections - sodium bicarbonate injection is indicated as an alkalinising agent in the treatment of metabolic acidosis which may occur in many conditions including diabetes, starvation, hepatitis, cardiac arrest, shock, severe dehydration, renal insufficiency, severe diarrhoea, addison's disease or administration of acidifying salts (e.g. excessive sodium chloride, calcium chloride, ammonium chloride). sodium bicarbonate injection is also used to increase urinary ph in order to increase the solubility of certain weak acids (e.g. cystine, sulphonamides, uric acid) and in the treatment of certain intoxications (e.g. methanol, phenobarbitone, salicylates, lithium) to decrease renal absorption of the drug or to correct acidosis.

SODIUM PHENYLACETATE AND SODIUM BENZOATE injection, solution, concentrate United States - English - NLM (National Library of Medicine)

sodium phenylacetate and sodium benzoate injection, solution, concentrate

mylan institutional llc - sodium phenylacetate (unii: 48n6u1781g) (phenylacetic acid - unii:er5i1w795a), sodium benzoate (unii: oj245fe5eu) (benzoic acid - unii:8skn0b0mim) - sodium phenylacetate 100 mg in 1 ml - sodium phenylacetate and sodium benzoate injection is indicated as adjunctive therapy in pediatric and adult patients for the treatment of acute hyperammonemia and associated encephalopathy in patients with deficiencies in enzymes of the urea cycle. during acute hyperammonemic episodes, arginine supplementation, caloric supplementation, dietary protein restriction, hemodialysis, and other ammonia lowering therapies should be considered [see warnings and precautions (5) ]. none. available data with sodium phenylacetate and sodium benzoate injection use in pregnant women are insufficient to identify a drug-associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes. animal reproduction studies have not been conducted with sodium phenylacetate and sodium benzoate injection. the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. g