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COMPOUND MACROGOL is a brand name for Sodium. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: For the treatment of chronic constipation. Compound Macrogol Oral Powder Sugar Free is also effective in resolving faecal impaction, defined as refractory constipation with faecal loading of the rectum and/or colon. Compound Macrogol Oral Powder Sugar Free is indicated in adults, adolescents and the elderly.
Verbatim from this product's MHRA label. Tap a section to expand.
Compound Macrogol Oral Powder Sugar Free is for oral use.
Posology Chronic Constipation:
A course of treatment for chronic constipation with Compound Macrogol Oral Powder Sugar Free does not normally exceed 2 weeks, although this can be repeated if required. As for all laxatives, prolonged use is not usually recommended.
Extended use may be necessary in the care of patients with severe chronic or resistant constipation, secondary to multiple sclerosis or Parkinson's Disease, or induced by regular constipating medication in particular opioids and antimuscarinics.
Adults, adolescents and the elderly: 1-3 sachets daily in divided doses, according to individual response. For extended use, the dose can be adjusted down to 1 or 2 sachets daily.
Children below 12 years old:
Not recommended.
Faecal Impaction:
A course of treatment for faecal impaction with Compound Macrogol Oral Powder Sugar Free does not normally exceed 3 days. Adults, adolescents and the elderly: 8 sachets daily, all of which should be consumed within a 6 hour period.
Children below 12 years old:
Not recommended.
Patients with impaired cardiovascular function:
For the treatment of faecal impaction the dose should be divided so that no more than 2 sachets are taken in any one hour.
Patients with renal insufficiency:
No dosage change is necessary for the treatment of constipation or faecal impaction. Method of administration Each sachet should be dissolved in 125ml water. For use in faecal impaction, 8 sachets may be dissolved in 1 litre of water.
8. g. oedema, shortness of breath, increasing fatigue, dehydration, cardiac failure) Compound Macrogol Oral Powder Sugar Free should be stopped immediately and electrolytes measured and any abnormality should be treated appropriately.
5). This medicinal product contains 187mg of sodium per sachet, equivalent to approximately 9% of the WHO recommended maximum daily intake of 2g sodium for an adult. When used to treat chronic constipation the maximum daily dose of this product is equivalent to approximately 28% of the WHO recommended maximum daily intake for sodium.
Compound Macrogol Oral Powder Sugar Free is considered high in sodium. This should be particularly taken into account for those on a low salt diet. 5. 5 Interaction with other medicinal products and other forms of interaction Macrogol 3350 raises the solubility of medicinal products that are soluble in alcohol and mainly insoluble in water.
4). g. anti-epileptics. Therefore, other medicines should not be taken orally for one hour before and for one hour after taking Compound Macrogol Oral Powder Sugar Free. Compound Macrogol Oral Powder Sugar Free may result in a potential interactive effect if used with starch-based food thickeners.
The macrogol ingredient counteracts the thickening effect of starch, effectively liquefying preparations that need to remain thick for people with swallowing problems. 6 Fertility, pregnancy and lactation Pregnancy There are limited amount of data from the use of Compound Macrogol Oral Powder Sugar Free in pregnant women.
3). Clinically, no effects during pregnancy are anticipated, since systemic exposure to macrogol 3350 is negligible. Compound Macrogol Oral Powder Sugar Free can be used during pregnancy. Breast-feeding No effects on the breastfed newborn/infant are anticipated since the systemic exposure of the breast-feeding woman to macrogol 3350 is negligible.
The fluid content of Compound Macrogol Oral Powder Sugar Free when re- constituted with water does not replace regular fluid intake and adequate fluid intake must be maintained. The faecal impaction diagnosis should be confirmed by appropriate physical or radiological examination of the rectum and abdomen.
8. g. oedema, shortness of breath, increasing fatigue, dehydration, cardiac failure) Compound Macrogol Oral Powder Sugar Free should be stopped immediately and electrolytes measured and any abnormality should be treated appropriately.
5). This medicinal product contains 187mg of sodium per sachet, equivalent to approximately 9% of the WHO recommended maximum daily intake of 2g sodium for an adult. When used to treat chronic constipation the maximum daily dose of this product is equivalent to approximately 28% of the WHO recommended maximum daily intake for sodium.
Compound Macrogol Oral Powder Sugar Free is considered high in sodium. This should be particularly taken into account for those on a low salt diet. 5.
g. ulcerative colitis, Crohn’s disease and toxic megacolon). 1.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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Compound Macrogol Oral Powder Sugar Free can be used during breast- feeding. Fertility There are no data on the effects of Compound Macrogol Oral Powder Sugar Free on fertility in humans. 3). 7 Effects on ability to drive and use machines Compound Macrogol Oral Powder Sugar Free has no influence on the ability to drive and use machines.
8 Undesirable effects Reactions related to the gastrointestinal tract occur most commonly. These reactions may occur as a consequence of expansion of the contents of the gastrointestinal tract, and an increase in motility due to the pharmacologic effects of Compound Macrogol Oral Powder Sugar Free.
Mild diarrhoea usually responds to dose reduction. The frequency of the adverse effects is not known as it cannot be estimated from the available data. System Organ Class Adverse Event Immune system disorders Allergic reactions, including anaphylaxis, angioedema, dyspnoea, rash, urticaria, and pruritus.
Skin and subcutaneous tissue disorders Erythema Metabolism and nutrition disorders Electrolyte disturbances, particularly hyperkalaemia and hypokalaemia. Nervous system disorders Headache Gastrointestinal disorders Abdominal pain, diarrhoea, vomiting, nausea, dyspepsia, abdominal distension, borborygmi, flatulence, anorectal discomfort.
General disorders and administration site conditions Peripheral oedema Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product.
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