Generic: Potassium Chloride + Sodium Acetate + Sodium Chloride
Type: Infusion
Pack Size: 500ml
Not Available
Potassium Chloride + Sodium Acetate + Sodium Chloride is indicated as a source of water and electrolytes.
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Cholera saline comprises a variety of electrolytes that are commonly depleted in a variety of situations, such as diarrhea, vomiting, excessive perspiration, and so on. As a result, this saline is used to replenish and restore the body's normal electrolyte balance in cases of cholera, as well as diarrhea, vomiting, and fluid loss.
Each 100 ml solution contains-
Possible reactions that may occur due to the Cholera Saline solution or the administration technique include:
Additional symptoms that may arise include:
Although reactions at the injection site are rare, they can occasionally occur within 5 to 7 days following administration. Symptoms may include erythema (redness), swelling, soreness, tenderness, and induration (hardening or thickening of the tissue).
Cholera saline is a solution containing electrolytes that are often depleted in conditions such as diarrhea, vomiting, and excessive sweating. It is used to restore the body's electrolyte balance and replenish fluids in cases of cholera, as well as in diarrhea, vomiting, and fluid loss.
The pyrogen-free sterile injection solution of Cholera saline contains Sodium Chloride, Potassium Chloride, and Sodium Acetate (as Trihydrate) dissolved in Water. It is a sterile solution used for medical purposes.
The adult dose of Cholera Saline for intravenous administration varies based on individual patient requirements. The volume and rate of infusion will be determined by the patient's needs and the physician's judgment, taking into account factors such as age, weight, and clinical condition.
The recommended flow rate is up to 100 drops per minute per 70 kg body weight. However, the specific dosage and infusion rate should be determined by the healthcare provider based on the patient's specific circumstances.
It is important to follow the guidance and instructions provided by the healthcare professional regarding the volume, rate, and duration of infusion for Cholera Saline.
The volume and rate of infusion of Cholera Saline will be determined by the patient's requirements and the physician's judgment. Factors such as age, weight, and clinical condition of the patient will be taken into consideration.
Here is a step-by-step administration procedure for Cholera Saline:
Lithium: Concurrent use of Potassium Chloride in Sodium Chloride Injection may increase renal sodium and lithium clearance, potentially resulting in decreased lithium concentrations. It is important to monitor serum lithium concentrations during concomitant use.
Other Products that Cause Hyperkalemia: The administration of Potassium Chloride in Sodium Chloride Injection in patients who are concurrently or recently treated with products known to cause hyperkalemia increases the risk of severe and potentially fatal hyperkalemia. Avoid using Potassium Chloride in Sodium Chloride Injection in patients receiving such products, including potassium-sparing diuretics, angiotensin-converting enzyme inhibitors (ACE inhibitors), angiotensin receptor blockers (ARBs), and certain immunosuppressants (cyclosporine and tacrolimus). If use cannot be avoided, close monitoring of serum potassium concentrations is advised.
Other Products that Affect Fluid and/or Electrolyte Balance: Concomitant use of Potassium Chloride in Sodium Chloride Injection with medications associated with sodium and fluid retention, such as corticosteroids or corticotropin, may increase the risk of hypernatremia and volume overload. Avoid using Potassium Chloride in Sodium Chloride Injection in patients receiving such products. If use cannot be avoided, monitor serum electrolytes, fluid balance, and acid-base balance.
Other Drugs that Increase the Risk of Hyponatremia: Potassium Chloride in Sodium Chloride Injection should be used with caution in patients receiving medications known to cause hyponatremia, such as diuretics and certain antiepileptic and psychotropic medications. These drugs can increase the risk of developing hyponatremia. If use cannot be avoided, monitor serum sodium concentrations closely.
In cases of acute respiratory or active infection, it is advisable to defer the administration of saline. Additionally, if a patient is receiving corticosteroids or other immunosuppressive drugs, it is recommended to avoid giving saline as it may potentially impair their immune response. It is important to consider these factors and consult with a healthcare professional for appropriate management in such situations.
There are no adequate and well-controlled studies on the use of Potassium Chloride in Sodium Chloride Injection, USP in pregnant or lactating women and animal reproduction studies have not been conducted with this drug. Therefore, it is also not known whether Potassium Chloride in Sodium Chloride Injection, or USP can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Potassium Chloride in Sodium Chloride Injection, USP should be given to a pregnant woman only if the potential benefit justifies the potential risk to the fetus.
It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Potassium Chloride in Sodium Chloride Injection, USP is administered to a nursing mother.
Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.
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