URELEX HISED PLABOLYTE-M PLABOLYTE-M HYOCIT HYOCIT CALMIN-600 PERITONEAL DIALYSIS SOLN. PERITONEAL DIALYSIS SOLN. PERITONEAL DIALYSIS SOLN. PERITONEAL DIALYSIS SOLN. SEVOFLURANE STEREOFUNDIN ISO STERILYTE-M NUTRIFLEX PLUS NUTRIFLEX PLUS NUTRIFLLEX SPECIAL NUTRIFLLEX SPECIAL

Dose: 70 to 100 mg
Single Dose: 85 (85)
Frequency: 24 hourly
Route: IV
Instructions:

. It is of Synthetic origin and belongs to Sodium salt. It belongs to Electrolyte Supplement, Parenteral pharmacological group.The Molecular Weight of Sodium Acetate is 136.10. It is weakly alkaline drug, 2.00% solution of the drug is isotonic.

Sodium Acetate is contraindicated in conditions like Hypocalcaemia,Liver cirrhosis,Metabolic alkalosis,Edema.

The severe or irreversible adverse effects of Sodium Acetate, which give rise to further complications include Congestive conditions.The symptomatic adverse reactions produced by Sodium Acetate are more or less tolerable and if they become severe, they can be treated symptomatically, these include Flatulence, GI distention, Phlebitis, Hypokalemia, Hypernatremia, Overhydration, Metabolic alkalosis, Pulmonary edema, Hypoglycemia.

Sodium Acetate is primarily indicated in conditions like Acidosis, Electrolyte disorder, Hyponatraemia.

No data regarding the interactions of Sodium Acetate was found.

Drug should not be given to Pregnant Mothers.If prescribing authority justifies the benefits of the drug against the possible damages he/she should reevaluate them and consult the reference material and previous studies.

Inj Store in a well closed container.

Caution must be exercised in the administration of parenteral fluids, especially those containing sodium ions, to patients receiving corticosteroids or corticotropin. Solutions containing acetate ions should be used with caution as excess administration may result in metabolic alkalosis. Caution should be exercised in administering sodium-containing solutions to patients with severe renal function impairment, cirrhosis, cardiac failure, or other edematous or sodium-retaining states, as well as in patients with oliguria or anuria.