Sodium chloride | Sodium chloride-SOLOpharm Politvist injection solution 0.9% 10 ml ampoules plastic 10 pcs.
Special Price
$13.58
Regular Price
$22.00
In stock
SKU
BID608261
Release form
Injection 0.9%
Injection 0.9%
Release form
Injection 0.9%
Pharmacological action of
Drug for rehydration and detoxification for parenteral administration
Indications
Plasmoisotonic fluid replacement, hypochloremic alkalosis, hyponatremia with dehydration, intoxication, dissolution and dilution of parenteral drugs (as a base solution).
Contraindications
Hypernatremia, hyperchloremia, hypokalemia, extracellular hyperhydration, intracellular dehydration, circulatory disorders associated with the risk of developing cerebral edema and lungs, cerebral edema, pulmonary edema, decompensated cardiac hypertension, which can cause hypertension and sodium retardation such as: primary and secondary aldosteronism, caused, for example, by arterial hypertension, congestive heart failure by value liver disease (including cirrhosis), kidney disease (including arterial stenosis and nephrosclerosis), preeclampsia, concomitant administration of glucocorticosteroids in high doses, contraindications to the drugs added to the solution.
Use during pregnancy and lactation
Data on the use of the drug during pregnancy and during breast-feeding are insufficient.
It is possible to use during pregnancy and during breastfeeding in cases where the expected benefit to the mother outweighs the possible risk of complications.
Special instructions
During any infusion, it is necessary to monitor the patient's condition, the clinical biological indicators, it is especially important to evaluate blood plasma electrolytes.
In the body of children, because of the immaturity of renal function, sodium excretion may slow down. Therefore, in such patients, repeated infusions should be carried out only after determining the concentration of sodium in the blood plasma.
If hypersensitivity reactions or infusion reactions occur, the infusion should be stopped immediately and the necessary therapeutic measures indicated.
Depending on the volume and rate of infusion against the background of intravenous administration of the drug, there is a risk of developing hypervolemia and (or) overload with dissolved substances and disturbances in the balance of electrolytes.
In patients with renal failure, the drug should be used with extreme caution or not at all. The use of the drug in such patients can lead to sodium retention.
Use only a clear solution, with no visible inclusions and if the packaging is not damaged. Enter immediately after connecting to the infusion system. The solution should be administered using sterile equipment in compliance with aseptic and antiseptic rules. In order to avoid air entering the infusion system, it should be filled with a solution, releasing the residual air from the container completely.
As with all parenteral solutions, the compatibility of the added substances with the solution should be determined before dissolution. Drugs known as incompatible with it should not be used with 0.9% sodium chloride solution.
The doctor must determine the compatibility of the added drug with a 0.9% sodium chloride solution by checking for possible discoloration and / or the appearance of a precipitate, insoluble complexes or crystals. Before adding, it is necessary to determine whether the added substance is soluble and stable in water at a pH level, as in the sodium chloride solution of 0.9%.
When adding the drug, it is necessary to determine the isotonicity of the resulting solution before administration. Before adding drugs to the solution, they must be thoroughly mixed in compliance with aseptic rules. The prepared solution should be introduced immediately after preparation, do not store! Every unused dose should be disposed of.
Composition
Sodium chloride 9 g,
water for injection up to 1 l.
Side effects
If used correctly, undesirable effects are unlikely.
Adverse reactions recorded during post-marketing use are grouped by system and organ according to the MedDRA Dictionary and are listed below in decreasing order of severity, without indicating frequency of occurrence.
From the circulatory system: acidosis, hyperhydration, hypokalemia.
On the part of the immune system: hypersensitivity reactions or infusion reactions, including hypotension, pyrexia, tremor, chills, urticaria, rash, itching.
General disorders and disorders at the injection site: reactions at the injection site, such as erythema, hemorrhage / hematoma, burning sensation, urticaria at the injection site thrombosis or phlebitis at the injection site.
Other: fever, infection at the injection site (in violation of antiseptic rules).
When using the drug as a base solution (solvent) for other drugs, the probability of side effects is determined by the properties of these drugs.
In this case, if adverse reactions occur, you should suspend the administration of the solution, evaluate the patient's condition, take adequate measures and save the remaining solution for analysis, if necessary.
Drug Interactions
Compatible with colloidal hemodynamic blood substitutes (mutual enhancement of effect).
When mixed with other medicines, compatibility is visually monitored.
Overdose
Symptoms: nausea, vomiting, diarrhea, spastic abdominal pain, thirst, decreased salivation and lacrimation, increased sweating, fever, tachycardia, increased blood pressure, renal failure, peripheral edema, pulmonary edema, respiratory arrest, headache, dizziness, anxiety, irritability, weakness, muscle cramps and stiffness, generalized convulsions, coma and death.
Excessive administration of 0.9% sodium chloride solution can cause hypernatremia. Excessive intake of chloride in the body can lead to hyperchloremic acidosis.
If a 0.9% sodium chloride solution is used as a base solution for diluting and transporting other drugs, symptoms and complaints of excessive administration are most often associated with the properties of the drugs added to the solution.
In case of unintentional excessive administration of the solution, treatment should be discontinued and the patient's condition evaluated.
Treatment: symptomatic.
Deystvuyuschee substances
Sodium chloride
Dosage
solution for u ektsy
Appointment by
Pregnant by doctor's appointment, Children by doctor's appointment, Adults, Lactating mothers prewrod49k13d appointment ca, Prescription Nursing Mothers, Nursing Moms, Adult Prescription
Grotex Ltd. LLC, Russia
Injection 0.9%
Pharmacological action of
Drug for rehydration and detoxification for parenteral administration
Indications
Plasmoisotonic fluid replacement, hypochloremic alkalosis, hyponatremia with dehydration, intoxication, dissolution and dilution of parenteral drugs (as a base solution).
Contraindications
Hypernatremia, hyperchloremia, hypokalemia, extracellular hyperhydration, intracellular dehydration, circulatory disorders associated with the risk of developing cerebral edema and lungs, cerebral edema, pulmonary edema, decompensated cardiac hypertension, which can cause hypertension and sodium retardation such as: primary and secondary aldosteronism, caused, for example, by arterial hypertension, congestive heart failure by value liver disease (including cirrhosis), kidney disease (including arterial stenosis and nephrosclerosis), preeclampsia, concomitant administration of glucocorticosteroids in high doses, contraindications to the drugs added to the solution.
Use during pregnancy and lactation
Data on the use of the drug during pregnancy and during breast-feeding are insufficient.
It is possible to use during pregnancy and during breastfeeding in cases where the expected benefit to the mother outweighs the possible risk of complications.
Special instructions
During any infusion, it is necessary to monitor the patient's condition, the clinical biological indicators, it is especially important to evaluate blood plasma electrolytes.
In the body of children, because of the immaturity of renal function, sodium excretion may slow down. Therefore, in such patients, repeated infusions should be carried out only after determining the concentration of sodium in the blood plasma.
If hypersensitivity reactions or infusion reactions occur, the infusion should be stopped immediately and the necessary therapeutic measures indicated.
Depending on the volume and rate of infusion against the background of intravenous administration of the drug, there is a risk of developing hypervolemia and (or) overload with dissolved substances and disturbances in the balance of electrolytes.
In patients with renal failure, the drug should be used with extreme caution or not at all. The use of the drug in such patients can lead to sodium retention.
Use only a clear solution, with no visible inclusions and if the packaging is not damaged. Enter immediately after connecting to the infusion system. The solution should be administered using sterile equipment in compliance with aseptic and antiseptic rules. In order to avoid air entering the infusion system, it should be filled with a solution, releasing the residual air from the container completely.
As with all parenteral solutions, the compatibility of the added substances with the solution should be determined before dissolution. Drugs known as incompatible with it should not be used with 0.9% sodium chloride solution.
The doctor must determine the compatibility of the added drug with a 0.9% sodium chloride solution by checking for possible discoloration and / or the appearance of a precipitate, insoluble complexes or crystals. Before adding, it is necessary to determine whether the added substance is soluble and stable in water at a pH level, as in the sodium chloride solution of 0.9%.
When adding the drug, it is necessary to determine the isotonicity of the resulting solution before administration. Before adding drugs to the solution, they must be thoroughly mixed in compliance with aseptic rules. The prepared solution should be introduced immediately after preparation, do not store! Every unused dose should be disposed of.
Composition
Sodium chloride 9 g,
water for injection up to 1 l.
Side effects
If used correctly, undesirable effects are unlikely.
Adverse reactions recorded during post-marketing use are grouped by system and organ according to the MedDRA Dictionary and are listed below in decreasing order of severity, without indicating frequency of occurrence.
From the circulatory system: acidosis, hyperhydration, hypokalemia.
On the part of the immune system: hypersensitivity reactions or infusion reactions, including hypotension, pyrexia, tremor, chills, urticaria, rash, itching.
General disorders and disorders at the injection site: reactions at the injection site, such as erythema, hemorrhage / hematoma, burning sensation, urticaria at the injection site thrombosis or phlebitis at the injection site.
Other: fever, infection at the injection site (in violation of antiseptic rules).
When using the drug as a base solution (solvent) for other drugs, the probability of side effects is determined by the properties of these drugs.
In this case, if adverse reactions occur, you should suspend the administration of the solution, evaluate the patient's condition, take adequate measures and save the remaining solution for analysis, if necessary.
Drug Interactions
Compatible with colloidal hemodynamic blood substitutes (mutual enhancement of effect).
When mixed with other medicines, compatibility is visually monitored.
Overdose
Symptoms: nausea, vomiting, diarrhea, spastic abdominal pain, thirst, decreased salivation and lacrimation, increased sweating, fever, tachycardia, increased blood pressure, renal failure, peripheral edema, pulmonary edema, respiratory arrest, headache, dizziness, anxiety, irritability, weakness, muscle cramps and stiffness, generalized convulsions, coma and death.
Excessive administration of 0.9% sodium chloride solution can cause hypernatremia. Excessive intake of chloride in the body can lead to hyperchloremic acidosis.
If a 0.9% sodium chloride solution is used as a base solution for diluting and transporting other drugs, symptoms and complaints of excessive administration are most often associated with the properties of the drugs added to the solution.
In case of unintentional excessive administration of the solution, treatment should be discontinued and the patient's condition evaluated.
Treatment: symptomatic.
Deystvuyuschee substances
Sodium chloride
Dosage
solution for u ektsy
Appointment by
Pregnant by doctor's appointment, Children by doctor's appointment, Adults, Lactating mothers prewrod49k13d appointment ca, Prescription Nursing Mothers, Nursing Moms, Adult Prescription
Grotex Ltd. LLC, Russia
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