Product image of Kayexalate Calcium (Calcium Polystyrene Sulfonate) supplied by GNH India

Kayexalate Calcium

Active Ingredient:
Calcium Polystyrene Sulfonate
Origin:
EU

Kayexalate Calcium (Calcium Polystyrene Sulfonate)

Calcium Polystyrene Sulfonate, the active ingredient in Kayexalate Calcium, is a cation exchange resin presented as an oral powder for oral and rectal use. It is employed to treat hyperkalemia by reducing elevated serum potassium levels in adult patients. It is indicated for acute or chronic potassium excess when conventional measures are insufficient.

GNH India supplies Kayexalate Calcium as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution.

Manufacturer / TM Owner

Sanofi Belgium

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Indications & Clinical Uses

Kayexalate Calcium is employed in the management of conditions characterized by elevated potassium levels.

  • Hyperkalemia: lowers serum potassium concentrations in patients with acute or chronic elevation.
  • Acute hyperkalemia: provides rapid potassium removal when urgent reduction is clinically required.
  • Chronic hyperkalemia: assists in maintaining potassium balance in patients with persistent excess.
  • Renal failure-associated hyperkalemia: helps control potassium levels when renal excretion is impaired.
  • Cardiac risk due to hyperkalemia: reduces the likelihood of arrhythmias by decreasing serum potassium.

How It Works

  • Calcium Polystyrene Sulfonate is a cation exchange resin that remains in the gastrointestinal lumen. Its polymer matrix contains calcium ions that exchange with potassium ions present in the intestinal contents. The bound potassium is not absorbed and is eliminated in the feces, thereby decreasing the amount of potassium reabsorbed into the bloodstream and lowering serum potassium levels.

Side Effects

Kayexalate Calcium may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Constipation: reduced bowel movements leading to hard stools.
  • Nausea: feeling of sickness or urge to vomit.
  • Vomiting: expulsion of stomach contents.
  • Abdominal discomfort: cramping or pain in the stomach area.
  • Diarrhea: loose, watery stools.
  • Taste alteration: metallic or unpleasant taste.
  • Flatulence: increased gas production.

Serious or Rare Side Effects

  • Intestinal necrosis or perforation: severe damage to the bowel wall that may require surgery.
  • Severe electrolyte disturbances: significant drops in calcium or rises in calcium levels.
  • Allergic reactions: rash, itching, swelling, or anaphylactic response.

Precautions & Warnings

Before prescribing Kayexalate Calcium, clinicians should consider several safety precautions to minimize risks.

  • Assess baseline serum potassium: confirm hyperkalemia, determine severity, and document values.
  • Monitor calcium levels: regularly check serum calcium to detect hypocalcemia or hypercalcemia.
  • Use cautiously in patients with bowel disorders: constipation, ulcerative colitis, or recent surgery increase risk of intestinal injury.
  • Avoid in severe hypocalcemia: the resin may further lower calcium and exacerbate symptoms.
  • Adjust use in renal impairment: reduced kidney function may alter potassium handling; monitor closely.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Kayexalate Calcium can affect the absorption or action of several concomitant medicines.

Major Interactions (Avoid)

  • Oral potassium supplements: simultaneous use may reduce the effectiveness of potassium supplementation.
  • Antacids containing aluminum or magnesium: can bind the resin and diminish potassium removal.
  • Calcium‑containing medications: may compete for exchange sites, lowering resin efficacy.
  • Iron supplements: binding may reduce iron absorption, avoid co‑administration.

Moderate Interactions (Monitor Closely)

  • Levothyroxine: resin may decrease its absorption; separate administration by at least 4 hours.
  • Digoxin: monitor serum digoxin levels as binding may alter its bioavailability.
  • ACE inhibitors or ARBs: combined effect on potassium; monitor serum potassium closely.
  • Loop diuretics: may increase potassium loss; monitor potassium levels.

Frequently Asked Questions

Kayexalate Calcium is prescribed to lower elevated serum potassium levels in patients with hyperkalemia. It is used when potassium concentrations are dangerously high, such as in acute episodes, chronic kidney disease, or other conditions where potassium excretion is impaired.

Calcium Polystyrene Sulfonate is a cation exchange resin that stays within the gastrointestinal tract. Its calcium ions exchange with potassium ions in the intestinal contents, binding potassium so it is eliminated in the feces, which reduces the amount of potassium re‑absorbed into the bloodstream.

The dose of Kayexalate Calcium is individualized by the prescribing clinician. Factors such as the patient’s current serum potassium level, the rate of potassium rise, renal function, and overall clinical status guide the amount and frequency of administration.

Safety data for Calcium Polystyrene Sulfonate in pregnancy and lactation are limited. The product should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified health professional.

To place an order, submit an enquiry on the Kayexalate Calcium product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

The most common alternative is sodium polystyrene sulfonate, which exchanges sodium for potassium. Calcium Polystyrene Sulfonate exchanges calcium instead of sodium, potentially offering a lower sodium load for patients who need to limit sodium intake, while providing a similar potassium‑binding effect.

Store Kayexalate Calcium at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Kayexalate Calcium is supplied as an oral powder that can be mixed with water or another suitable liquid and ingested. It may also be administered rectally as an enema, depending on the clinical situation and prescriber’s instructions.

Serious adverse events include intestinal necrosis or perforation, severe electrolyte disturbances such as marked hypocalcemia or hypercalcemia, and allergic reactions that can progress to anaphylaxis. Prompt medical attention is required if any of these symptoms occur.

Kayexalate Calcium should be avoided in patients with severe hypocalcemia, known bowel obstruction, recent gastrointestinal surgery, or active inflammatory bowel disease, as the resin may worsen these conditions. It is also contraindicated in individuals with known hypersensitivity to the product.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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