Sodium Salicylate - leitarniðurstöður

Bandaríkin - enska - NLM (National Library of Medicine)

aquaprime liquid sodium salicylate- sodium salicylate liquid

blendpack, inc. - sodium salicylate (unii: wiq1h85syp) (salicylic acid - unii:o414pz4lpz) - for use in the drinking water of poultry and swine as an aid in reducing pain, fever and inflammation calf label claim indications for use, calves: supportive treatment of pyrexia in acute respiratory disease, in combination with appropriate (e.g., anti-infective) therapy if necessary. contraindications, calves: do not use sodium salicylate in neonates or calves less than 2 weeks of age dosage, calves: 40 mg sodium salicylate per kg body weight once daily, for 1-3 days. administer orally in drinking water or milk (replacer). recommended withdrawal period for all food animals following use at “usual dosages”: meat 24 hours.

Belgía - enska - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sodium salicyl 80 % wsp 800 mg/g or. sol. (pwdr.) jar

dopharma (research) n.v. - sodium salicylate 800 mg/g - eq. salicylic acid 690 mg/g - powder for oral solution - 800 mg/g - sodium salicylate 800 mg/g - sodium salicylate - cattle; pig

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

ionolyte sodium chloride, sodium acetate trihydrate, potassium chloride, magnesium chloride, injection for intravenous infusion 1000 ml freeflex bag

fresenius kabi australia pty ltd - potassium chloride, quantity: 0.3 g/l; magnesium chloride hexahydrate, quantity: 0.3 g/l; sodium chloride, quantity: 6.02 g/l; sodium acetate trihydrate, quantity: 4.63 g/l - injection, intravenous infusion - excipient ingredients: sodium hydroxide; water for injections; hydrochloric acid - ionolyte is indicated for:,- mild metabolic acidosis,- as a source of water and electrolytes

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

ionolyte sodium chloride, sodium acetate trihydrate, potassium chloride, magnesium chloride, injection for intravenous infusion 500 ml freeflex bag

Bandaríkin - enska - NLM (National Library of Medicine)

sodium phenylacetate and sodium benzoate injection, solution, concentrate

trigen laboratories, 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, 10%/10% 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. pregnancy category c. animal reproduction studies have not been conducted with sodium phenylacetate and sodium benzoate injection, 10%/10%. it is not known whether sodium phenylacetate and sodium benzoate injection, 10%/10% can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. thus, sodium phenylacetate and sodium benzoate injection, 10%/10% should be given to a pregnant woman only if clearly needed. it is not known whether sodium phenylacetate, sodium benzoate, or their

Bandaríkin - enska - NLM (National Library of Medicine)

sodium phenylacetate and sodium benzoate injection, solution, concentrate

ailex pharmaceuticals, 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, 10%/10% 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. pregnancy category c. animal reproduction studies have not been conducted with sodium phenylacetate and sodium benzoate injection, 10%/10%. it is not known whether sodium phenylacetate and sodium benzoate injection, 10%/10% can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. thus, sodium phenylacetate and sodium benzoate injection, 10%/10% should be given to a pregnant woman only if clearly needed. it is not known whether sodium phenylacetate, sodium benzoate, or their conjugation p

Írland - enska - HPRA (Health Products Regulatory Authority)

sodium salicyl 800 mg/g, powder for oral solution for cattle (calves) and pigs

dopharma research b.v. - sodium salicylate ph. eur. (equivalent to salicylic acid as sodium salt) - powder for oral solution - 800 mg/ml - sodium salicylate - bovine, porcine - n.s.a.i.d

Ísrael - enska - Ministry of Health

sodium chloride 0.9 % intravenous infusion bp

teva medical marketing ltd. - sodium chloride - solution for infusion - sodium chloride 0.9 %w/v - sodium chloride - sodium chloride - treatment of isotonic extracellular dehydration. treatment of sodium depletion. vehicle or diluent of compatible drugs for parenteral administration.

Ísrael - enska - Ministry of Health

sodium chloride 0.9 % intravenous infusion bp

Ástralía - enska - APVMA (Australian Pesticides and Veterinary Medicines Authority)

butasyl injection phenylbutazone 186 mg/ml and sodium salicylate 50 mg/ml