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PMS-Sodium Polystyrene Sulfonate: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
1 g, 250 mg
Active ingredient:

Patient Medication Information: uses, side effects, how to take - PMS-Sodium Polystyrene Sulfonate

ABOUT THIS MEDICATION

What the medication is used for:

pms-SODIUM POLYSTYRENE SULFONATE is used to remove high amounts of potassium from the blood.

What it does:

pms-SODIUM POLYSTYRENE SULFONATE attaches to the extra potassium in the body, particularly in the large intestine, so it can be removed from the body in the stool.

When it should not be used:

Do not take pms-SODIUM POLYSTYRENE SULFONATE if:

  • You have a bowel obstruction (blocked

    intestine).

  • You have low levels of potassium in your blood.
  • If you are allergic to sodium polystyrene

    sulfonate

Do not use pms-SODIUM POLYSTYRENE SULFONATE in newborn babies who have slowed movements in their gut (caused by other medications or following surgery).

Do not give pms-SODIUM POLYSTYRENE SULFONATE by mouth to newborn babies. pms-SODIUM POLYSTYRENE SULFONATE should only be given rectally to newborns.

What the medicinal ingredient is:

Sodium polystyrene sulfonate

What the non-medicinal ingredients are:

Powder for suspension: None

Oral suspension: Sorbitol, methylparaben, propylparaben

What dosage forms it comes in:

  • Powder for suspension (for oral or rectal use)

    • Oral suspension (for oral use)

WARNINGS AND PRECAUTIONS

BEFORE you use pms-SODIUM

POLYSTYRENE SULFONATE, talk to your doctor, nurse or pharmacist if you have or have had any medical conditions, especially the following:

  • Heart problems
  • High blood pressure
  • Problems with your bowel or constipation
  • Severe burns
  • Low blood volume, which can occur with dehydration or bleeding
  • Electrolyte imbalance. pms-SODIUM

    POLYSTYRENE SULFONATE therapy can worsen these imbalances. Your doctor may want to check the levels of the electrolytes in your blood more frequently during treatment.

  • Kidney problems
  • Edema (swelling of the face, hands or feet with fluid)
  • You require low salt diet.
  • You are pregnant or intend to become pregnant.

  • You are breastfeeding. It is not known if pms-SODIUM POLYSTYRENE SULFONATE passes into breast milk.

When taken by mouth, avoid taking pms-SODIUM POLYSTYRENE SULFONATE at the same time as other orally administered medications (see “PROPER USE OF THIS MEDICATION”).

Magnesium containing laxatives should not be used with pms-SODIUM POLYSTYRENE

SULFONATE.

INTERACTIONS WITH THIS MEDICATION

As with most medicines, interactions with other drugs are possible. Tell your doctor, nurse or pharmacist about all the medicines you take, including drugs prescribed by other doctors, vitamins, minerals, natural supplements or alternative medicines (non-prescription drugs or over the counter drugs).

When taken by mouth, pms-SODIUM

POLYSTYRENE SULFONATE may interfere with how other oral medicines are absorbed (see “PROPER USE OF THIS MEDICATION”).

IMPORTANT: PLEASE READ

The following may interact with pms-SODIUM POLYSTYRENE SULFONATE:

  • Digoxin, a medicine used for heart problems.
  • Laxatives such as magnesium

    hydroxide or aluminum carbonate

  • Thyroxine, a medicine for hypothyroidism
  • Lithium, a medicine which can be used to treat

    bipolar disorder.

  • Antacids containing aluminum or magnesium
  • Sorbitol (a ‘sugar free’ sweetener used to

    sweeten food).

  • Immunosuppressant drugs

I

PROPER USE OF THIS MEDICATION

NTERACTIONS WITH THIS MEDICATION Usual dose:

pms-SODIUM POLYSTYRENE SULFONATE Powder for Suspension can be given by mouth or in the rectum.

pms-SODIUM POLYSTYRENE SULFONATE Oral Suspension is given only by mouth.

The amount of pms-SODIUM POLYSTYRENE SULFONATE you need to take will depend upon the amount of potassium in your blood.

Once the mixture of pms-SODIUM

POLYSTYRENE SULFONATE Powder for Suspension has been prepared, it should be used straight away. If it needs to be stored, it should be stored for no longer than 24 hours. Do not heat pms-SODIUM POLYSTYRENE SULFONATE.

Your doctor will decide exactly how much pms-SODIUM POLYSTYRENE SULFONATE you need to take. The usual doses are:

ORAL DOSING

When taken by mouth, pms-SODIUM

POLYSTYRENE SULFONATE should be taken at least 3 hours before or 3 hours after other oral medications. For patients with gastroparesis (a condition preventing your stomach from emptying properly), a 6-hour separation should be considered. Consult your health care provider for

recommendations (see “WARNINGS AND PRECAUTIONS” and “INTERACTIONS WITH THIS MEDICATION”).

  • pms-SODIUM POLYSTYRENE SULFONATE

    Powder for Suspension is usually given by mouth mixed in a small amount of water. It can

    also be mixed with food or sweetened liquid. Do NOT mix pms-SODIUM POLYSTYRENE SULFONATE with orange juice or fruit juice which contains potassium.

    • pms-SODIUM POLYSTYRENE SULFONATE

      Oral Suspension does not require any preparation before use. Shake the bottle well before drinking.

Be careful not to inhale pms-SODIUM

POLYSTYRENE SULFONATE Powder for Suspension accidentally. Breathing in the powder may cause coughing and shortness of breath.

Your doctor will regularly check the potassium, calcium and magnesium levels in your blood. The doctor may change the dose or stop the pms-SODIUM POLYSTYRENE SULFONATE depending on what the results of these blood tests are.

Adults, including the elderly:

  • pms-SODIUM POLYSTYRENE SULFONATE

    Powder for Suspension: 15 grams (about 4 level teaspoons) one to four times daily as indicated above.

  • pms-SODIUM POLYSTYRENE SULFONATE

    Oral Suspension: 15 grams (60 mL) one to four times daily as indicated above.

Children:

You should follow the dosing recommended by your doctor.

For children, pms-SODIUM POLYSTYRENE SULFONATE is preferably given with a drink (NOT a fruit juice because of the high potassium content) or a little jam or honey.

Newborn babies (neonates)

pms-SODIUM POLYSTYRENE SULFONATE should not be given by mouth.

RECTAL DOSING

Rectal dosing only applies to pms-SODIUM POLYSTYRENE SULFONATE Powder for Suspension. The enema is usually given by a doctor or nurse.

Adults:

IMPORTANT: PLEASE READ as possible. Afterwards, the colon needs to be washed out to remove pms-SODIUM POLYSTYRENE SULFONATE.

Children and newborn babies (neonates):

Overdose:

Taking too much pms-SODIUM

POLYSTYRENE SULFONATE may reduce your potassium in your blood below the normal level. If you take too much of this medication, you may feel irritable, confused, have muscle weakness, have diminished reflexes or paralysis.

If you think you have taken too much pms-SODIUM POLYSTYRENE SULFONATE, contact your healthcare professional, hospital emergency department or regional Poison Control Centre immediately, even if there are no symptoms.

Missed Dose:

Do not take a double dose to make up for the dose you have missed. If it is almost time for the dose, skip the dose you missed and take the next dose when you are meant to.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Side effects may include:

  • Nausea and vomiting
  • Diarrhea
  • Loss of appetite

If any of these affects you severely, tell your doctor, nurse or pharmacist.

SERIOUS SIDE EFFECTS, AND WHAT TO DO
ABOUT THEM
Symptom / effectTalk with your doctor or pharmacistStop taking drug and call your doctor or pharmacist
Only if severeIn all cases

Constipation

(bloating and swelling of the abdomen)

x

Abdominal pain

(pain in your stomach and rectum)

x
Stomach irritation and bleeding (vomit that looks like coffee grounds)x

Rectal bleeding

(black bloody or tarry stools)

x

Allergic reaction

(rash; itching; swelling of the face, tongue and throat; severe dizziness and trouble breathing)

x

High level of sodium

(swelling)

x
Low level of potassium (muscle cramps, feeling tired, confused, having muscle weakness or change in the heart rate)x
Low level of calcium (feeling nervous or unable to relax, having fits, or muscle cramps)x

Fecal Impaction

(leaking liquid stool, stomach pain, feeling the need to push, nausea, vomiting, loss of appetite)

x

Bowel obstruction

(cramping, severe stomach pain, vomiting, bloating,

x
IMPORTANT: PLEASE READ

constipation,

inability to pass gas)

Bowel perforation

(severe stomach pain, chills, fever, nausea vomiting)

x

This is not a complete list of side effects. For any unexpected effects while taking pms-SODIUM POLYSTYRENE SULFONATE, contact your doctor or pharmacist.

HOW TO STORE IT

Store at room temperature (15°C to 30°C). Keep out of reach and sight of children.

Reporting Side Effects

You can report any suspected side effects associated with the use of health products to Health Canada by:

  • Visiting the Web page on Adverse Reaction

    Reporting (https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting.html) for information on how to report online, by mail or by fax; or

  • Calling toll-free at 1-866-234-2345.

NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

If you want more information about pms-SODIUM POLYSTYRENE SULFONATE:

  • Talk to your healthcare professional
  • Find the full Prescribing Information that is prepared for healthcare professionals and includes this Consumer Information by visiting the Health Canada website (https://health-products.canada.ca/dpd-bdpp/index-eng.jsp); the manufacturer’s website (www.pharmascience.com); or by calling 1-888-550-6060.

    Pharmascience Inc.

    Montreal, Quebec

    H4P 2T4

Last revised: July 09, 2020

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02501864

Revision date stated in the text: July 9, 2020

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for PMS-Sodium Polystyrene Sulfonate

Rx or OTC
Prescription (Rx)?
DIN 02501864, 02501872
Schedule(s) PRESCRIPTION
Active ingredient(s) Sodium polystyrene sulfonate
Dosage form(s) Powder For Suspension, Suspension
Route(s) of administration Oral, Rectal
Drug class (WHO ATC)
  1. V Various drug classes
    1. V03 All other therapeutic products
      1. V03A All other therapeutic products
        1. V03AE Drugs for treatment of hyperkalemia and hyperphosphatemia
          1. V03AE01 Polystyrene sulphonate
Company PHARMASCIENCE INC
Current status Approved
Current status date July 9, 2020
Strengths and forms
DIN Strength Dosage form(s) Current status
02501864 1 G Powder For Suspension Approved July 9, 2020
02501872 250 MG Suspension Approved July 9, 2020

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.