Picosalax - Product Information
|Ingredients:||sodium picosulfate, magnesium oxide-light, citric acid (forming magnesium citrate in solution), potassium bicarbonate, saccharin sodium, orange flavour|
Name of the Medicine
Sodium picosulfate. Molecular formula C18H13NNa2O8S2, MW 481.4, CAS: 10040-45-6 Magnesium oxide - light. Molecular formula: MgO, MW: 40.3, CAS: 1309-48-4
Citric acid. Molecular formula: C6H8O7, MW: 192.1, CAS: 77-92-9
Life-threatening dehydration and/or electrolyte disturbances may occur in ‘at risk’ groups (see ‘Contraindications’ and ‘Precautions’).
White crystalline powder.
Active ingredients: sodium picosulfate 10.0mg with magnesium citrate formed in solution from magnesium oxide 3.5g and citric acid 12.0g.
Inactive: potassium bicarbonate (equivalent to 5mmol (195mg) potassium), saccharin sodium, orange flavour (containing lactose).
The active components of PICOSALAX are sodium picosulfate, which stimulates bowel movements following metabolism by colonic bacteria, and magnesium citrate which acts as an osmotic laxative by increasing intestinal osmotic pressure thereby promoting retention of fluid within the bowel. The combined action of these components results in evacuation of the bowel contents.
Sodium picosulfate itself is pharmacologically inactive but is metabolised to an active metabolite, desacetylbisacodyl (bis(p-hydroxyphenyl)pyridyl-2-methane), which influences the chemoreceptors in the mucosa to increase intestinal motility. Desacetylbisacodyl is the same active metabolite formed following ingestion of bisacodyl, is insoluble in water and is minimally absorbed from the gastro-intestinal tract.
For clearance of the bowel prior to examination by radiography, endoscopy or surgery.
PICOSALAX is contraindicated in patients with congestive heart failure, known or suspected gastrointestinal obstruction or perforation, gastric retention, gastro-intestinal ulceration, toxic colitis, toxic megacolon, ileus, those with a stoma, nausea and vomiting, acute surgical abdominal conditions such as acute appendicitis, severe dehydration, rhabdomyolysis, hypermagnesemia, active inflammatory bowel disease or hypersensitivity to any of the ingredients.
In patients with severely reduced renal function, accumulation of magnesium in plasma may occur. Another preparation should be used in such cases.
PICOSALAX should not be used in patients with undiagnosed abdominal symptoms.
Use with caution in patients with recent gastro-intestinal surgery, renal impairment, heart disease or inflammatory bowel disease. Those patients with kidney disease or impaired renal function should be monitored, as should those with pre-existing electrolyte disturbances. Diabetics may need adjustment of their medication and careful monitoring of their blood glucose.
Patients using diuretics or other medications (such as corticosteroids, lithium) that may affect water and/or electrolyte balance should also be monitored (See INTERACTIONS WITH OTHER MEDICINES).
In all patients, adequate fluid intake should be maintained. An insufficient or excessive oral intake of water and electrolytes could create clinically significant deficiencies, particularly in less fit patients. In this regard, children, the elderly, debilitated individuals and patients at risk of hypokalaemia may need particular attention. Prompt corrective action should be taken to restore fluid/electrolyte balance in patients with signs or symptoms of hypokalemia or hyponatraemia. Drinking only water to replace the fluid losses may lead to electrolyte imbalance. The period of bowel cleansing should not exceed 24 hours because longer preparation may increase the risk of water and electrolyte imbalance (See DOSAGE AND ADMINISTRATION).
PICOSALAX may modify the absorption of regularly prescribed oral medication and should be used with caution e.g. there have been isolated reports of seizures in patients on anti-epileptics, with previously controlled epilepsy.
This medicine contains 5mmol (or 195mg) potassium per sachet. This should be taken into consideration by patients with reduced kidney function or patients on a controlled potassium diet.
PICOSALAX contains lactose as a component of the flavour (approximately 5mg per sachet). Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.
PICOSALAX is not intended for use as a routine laxative.
Use in children
PICOSALAX should not be used in children under 9 years of age.
Use in pregnancy
Whilst animal reproduction studies with sodium picosulfate have revealed no evidence of a harmful action on the fetus, clinical experience of the use of PICOSALAX during pregnancy is limited and caution should be observed, particularly during the first trimester.
Use in lactation
Neither sodium picosulfate nor magnesium citrate has been shown to be excreted in breast milk. As there is no experience with the use of PICOSALAX in nursing mothers, the product should only be used if clearly indicated.
Interactions With Other Medicines
As a purgative, PICOSALAX increases gastrointestinal transit rate. The absorption of other orally administered medicines (e.g. anti-epileptics, contraceptives, anti-diabetics, antibiotics) may therefore be modified during the treatment period.
Broad spectrum antibiotics may decrease the effect of PICOSALAX by interfering with the colonic bacteria needed to break down sodium picosulfate to form its active substance.
Medicines with the potential to chelate with magnesium (e.g. tetracyclines and fluoroquinolone antibiotics, iron, digoxin, chlorpromazine and penicillamine) should be taken at least 2 hours before and not less than 6 hours after administration of PICOSALAX.
Care should be taken with patients already receiving drugs which may be associated with hypokalaemia (such as diuretics or corticosteroids or drugs where hypokalaemia is a particular risk i.e. cardiac glycosides).
Caution is also advised when PICOSALAX is used in patients on NSAIDs or drugs known to induce SIADH (Syndrome of Inappropriate Antidiuretic Hormone secretion) e.g. tricyclic antidepressants, selective serotonin re-uptake inhibitors, antipsychotic drugs and carbamazepine as these drugs may increase the risk of water retention and/or electrolyte imbalance.
The efficacy of PICOSALAX is lowered by bulk-forming laxatives.
The most frequent adverse reactions seen in clinical trials are nausea, headache and vomiting.
|Common (≥1/100 to
(≥1/1000 to <1/100)
estimated from the
|Headache||Epilepsy, grand mal
pain, aphthoid ileal
*Isolated cases of mild reversible aphthoid ileal ulcers have been reported.
The frequencies of the adverse effects are based on post-marketing experience.
Diarrhoea and faecal incontinence are the primary clinical effect of PICOSALAX. Isolated cases of severe diarrhoea have been reported post-marketing.
Hyponatraemia has been reported with or without associated convulsions. In epileptic patients, there have been isolated reports of seizure/grand mal convulsion without associated hyponatraemia.
There have been isolated reports of anaphylactic reaction.
Dosage and Administration
Instructions for timing of dose and dietary and fluid restrictions vary greatly between centres and may over-ride the recommendations given below. Clinical studies with PICOSALAX have shown the following regimens to be effective.
Adults (including the elderly) and Children Aged 9 Years of age and Older
(if the procedure is scheduled for the afternoon, it is recommended that the Split-Dose regimen be used):
Split-Dose Regimen (evening-before and day of the procedure)
The first PICOSALAX sachet is taken the night before the procedure, and the second is taken the next day, in the morning prior to the procedure.
On the day before the procedure – 1 sachet:
- The first reconstituted sachet is taken in the evening (e.g., 5:00 to 9:00pm),
followed by at least five 250mL drinks of clear liquids, spread over several hours
On the day of the procedure – 1 sachet:
- The second reconstituted sachet is taken in the morning (5-9 hours before the procedure), followed by at least three 250mL drinks of clear liquids, spread over several hours
- Clear liquids may be consumed until 2 hours before the time of the procedure.
Day-Before Regimen (evening-before the procedure only)
The first PICOSALAX sachet is taken in the afternoon or early evening and the second is taken approximately 6 hours later, the night before the procedure.
On the day before the procedure – 2 sachets:
- The first reconstituted sachet is taken in the afternoon or early evening (e.g., 4:00 to 6:00PM), followed by at least five 250mL drinks of clear liquids, spread over several hours
- The second reconstituted sachet is taken in the late evening (e.g., 10:00pm to 12:00am), followed by at least three 250mL drinks of clear liquids, spread over several hours
- Clear liquids may be consumed until 2 hours before the time of the procedure.
Directions for Reconstitution
Immediately before use, mix the contents of one sachet in approximately 150mL (2/3rd of a cup) of water. Stir for 2-3 minutes, the solution should now become an off-white, cloudy liquid with a faint odour of orange. If it becomes warm wait until it cools sufficiently to drink. Drink the solution. Do not prepare the solution in advance.
Patients should be warned to expect frequent, loose bowel movements. To avoid dehydration it is recommended to drink a sufficient amount of clear liquids whilst the effects of PICOSALAX persist. Apart from the liquid intake together with the treatment regimen (PICOSALAX + additional liquids), a normal, thirst-driven intake of clear liquids is recommended. Clear liquids may include water, clear soup, fruit juice without pulp, soft drinks, tea and/or coffee without milk (including soy and cream). Patients should be advised NOT to drink just water alone but to also drink a balanced electrolyte solution; drinking only water to replace fluid losses may lead to electrolyte imbalance, particularly hypokalemia or hyponatraemia and possibly seizures (See PRECAUTIONS). Patients should be instructed to consume only clear fluids (no solid food or milk) on the day before the procedure up until 2 hours before the time of the procedure.
Overdosage would lead to profuse diarrhoea with dehydration and fluid/electrolyte imbalance. Treatment is by general supportive measures and correction of fluid and electrolyte imbalance.
Presentation and Storage Conditions
2 sachets each containing 16.1g of powder for oral solution. Store below 300C.
Name and Address of the Sponsor
Ferring Pharmaceuticals Pty Ltd
Suite 2, Level 1, Building 1
20 Bridge Street
Pymble NSW 2073
Poisons Schedule of the Medicine
Schedule 3 (Pharmacist Only Medicine)
Date of First Inclusion in the Australian Register of Therapeutic Goods (artg)
15 May 2007
Date of Most Recent Amendment
12 December 2014