Casenlax: Uses, Dosage & Side Effects
An osmotic laxative containing macrogol 4000 (polyethylene glycol 4000) for the treatment of constipation in adults and children aged 6 months and older
Casenlax is a prescription osmotic laxative containing macrogol 4000 (also known as polyethylene glycol 4000 or PEG 4000). It is used to treat constipation in adults, adolescents, and children aged 6 months and older. Casenlax works by retaining water in the bowel, which increases the volume and softness of the stool, making bowel movements easier and more comfortable. Unlike stimulant laxatives, macrogol 4000 does not directly stimulate the intestinal muscles and is not absorbed into the bloodstream, making it well-tolerated for both short-term and long-term use. It is available as a powder in single-dose sachets that are dissolved in water before drinking.
Quick Facts: Casenlax
Key Takeaways
- Casenlax contains macrogol 4000, an osmotic laxative that works by retaining water in the bowel to soften stools and promote easier passage, without being absorbed into the body or stimulating the intestinal muscles directly.
- It is approved for adults, adolescents, and children from 6 months of age, with doses adjusted according to age and body weight; effects typically begin within 24 to 48 hours of the first dose.
- Macrogol 4000 is considered safe for long-term use as it does not cause tolerance, dependency, or damage to the intestinal lining, making it a preferred first-line option for chronic constipation.
- Casenlax should not be used in patients with intestinal obstruction, perforation, or severe inflammatory bowel disease; discontinue use immediately if severe abdominal pain or distension develops.
- Each sachet should be dissolved in approximately 50 mL of water and taken preferably in the morning; adequate daily fluid intake is important for optimal effectiveness.
What Is Casenlax and What Is It Used For?
Casenlax contains the active substance macrogol 4000, a high-molecular-weight polymer of ethylene oxide. Macrogol 4000 belongs to a class of medications known as osmotic laxatives, which work by drawing and retaining water within the intestinal lumen. This mechanism increases the total water content of the stool, making it softer, bulkier, and considerably easier to pass through the colon and rectum. The increased stool volume also gently stimulates natural peristaltic movements of the bowel, promoting regular bowel function without the forceful contractions associated with stimulant laxatives.
Constipation is one of the most common gastrointestinal complaints worldwide, affecting an estimated 10 to 15 percent of the adult population globally, with higher prevalence in women and the elderly. It is characterized by infrequent bowel movements (typically fewer than three per week), hard or lumpy stools, straining during defecation, a sensation of incomplete evacuation, or a feeling of blockage. Chronic constipation significantly impacts quality of life and is associated with reduced productivity, increased healthcare utilization, and psychological distress including anxiety and depression.
The management of constipation typically follows a stepwise approach. Initial measures include dietary modifications such as increasing fiber intake, adequate hydration, regular physical activity, and establishing consistent toileting habits. When these lifestyle measures are insufficient, pharmacological treatment is indicated. Osmotic laxatives such as macrogol 4000 are widely recommended as first-line pharmacological agents by major international gastroenterology guidelines, including those published by the American College of Gastroenterology (ACG), the National Institute for Health and Care Excellence (NICE), and the World Gastroenterology Organisation (WGO).
Macrogol 4000 is pharmacologically inert in the body. Its large molecular weight (approximately 4000 daltons) prevents it from being absorbed across the intestinal mucosa. It is not metabolized by the body, not broken down by colonic bacteria through fermentation, and is excreted entirely unchanged in the feces. This means that macrogol 4000 acts exclusively within the gastrointestinal tract and has no systemic effects, contributing to its excellent safety profile. Unlike some other osmotic laxatives such as lactulose, macrogol 4000 is not fermented in the colon and therefore produces significantly less gas and bloating.
Casenlax is indicated for the symptomatic treatment of constipation in the following patient populations:
- Adults and adolescents (aged 12 years and older): For the treatment of occasional or chronic constipation that has not responded adequately to dietary and lifestyle modifications alone.
- Children aged 6 months to 11 years: For the treatment of functional constipation, which is common in the pediatric population and affects an estimated 3 to 5 percent of all pediatric visits. The 4 g sachet strength of Casenlax is specifically designed for pediatric dosing flexibility.
Macrogol 4000 molecules form hydrogen bonds with surrounding water molecules in the intestinal lumen. Each macrogol molecule can bind a large number of water molecules, effectively retaining water that would otherwise be reabsorbed through the intestinal wall. The resulting increase in stool water content and volume leads to softer stools and stimulates the natural propulsive movements (peristalsis) of the colon. This mechanism closely mimics the body's normal physiology, making macrogol 4000 one of the most physiological laxative options available.
What Should You Know Before Taking Casenlax?
Contraindications
There are specific medical conditions in which Casenlax must not be used. Understanding these absolute contraindications is essential for safe use of this medication.
- Hypersensitivity: Do not take Casenlax if you are allergic to macrogol (polyethylene glycol) or any of the other ingredients in the product. Although rare, allergic reactions to macrogol have been reported and can include skin rashes, hives, facial swelling, and in very rare cases, anaphylaxis.
- Intestinal obstruction (ileus): Casenlax must not be used if there is a known or suspected blockage in the intestines. Adding bulk and fluid to an obstructed bowel can worsen the condition and potentially lead to perforation.
- Intestinal perforation: If there is any existing or risk of a hole in the intestinal wall, Casenlax is absolutely contraindicated as it could cause leakage of intestinal contents into the abdominal cavity.
- Severe inflammatory bowel disease: In cases of severe active Crohn's disease or ulcerative colitis, or in the presence of toxic megacolon, Casenlax should not be used as it may worsen dilation or inflammatory activity.
Warnings and Precautions
Discontinue Casenlax and contact your healthcare provider immediately if you experience severe or worsening abdominal pain, significant abdominal distension (bloating), persistent vomiting, blood in the stool, or if you stop passing both stool and gas completely. These symptoms may indicate a serious underlying condition such as intestinal obstruction that requires urgent medical evaluation.
Before and during treatment with Casenlax, discuss the following with your healthcare provider:
- Underlying cause of constipation: Constipation can sometimes be a symptom of an underlying medical condition, including thyroid disorders, diabetes, neurological diseases, or colorectal cancer. If constipation is new, persistent, or associated with alarm features (such as unintentional weight loss, rectal bleeding, or a family history of colorectal cancer), further investigation is warranted before initiating laxative therapy.
- Electrolyte balance: Although macrogol 4000 without electrolytes (as in Casenlax) has minimal impact on electrolyte balance at recommended doses, prolonged use or use of higher-than-recommended doses could theoretically affect fluid and electrolyte status, particularly in elderly patients or those with kidney disease. Adequate fluid intake is recommended during treatment.
- Fecal impaction: Casenlax is intended for the treatment of constipation and not for the management of fecal impaction. Fecal impaction may require different treatment approaches, including macrogol-based preparations with added electrolytes at higher doses, or manual disimpaction in severe cases.
- Inflammatory bowel disease: Patients with mild to moderate inflammatory bowel disease may use Casenlax with caution, but should be monitored for worsening symptoms. In severe active disease, Casenlax is contraindicated.
- Abdominal pain of unknown origin: If you have unexplained abdominal pain, do not start Casenlax without first consulting a healthcare professional, as laxative use could mask or worsen certain serious conditions.
Pregnancy and Breastfeeding
Constipation is a very common complaint during pregnancy, affecting up to 40 percent of pregnant women due to hormonal changes (particularly increased progesterone levels), iron supplementation, and physical compression of the bowel by the growing uterus. The choice of laxative during pregnancy requires careful consideration of both efficacy and safety.
Macrogol 4000, the active substance in Casenlax, is generally considered safe for use during pregnancy. Because it is not absorbed from the gastrointestinal tract, it does not enter the maternal bloodstream and therefore cannot cross the placenta to reach the developing fetus. The European Medicines Agency notes that a large body of data from pregnant women (more than 1000 exposed pregnancies) indicates no malformative effects or fetotoxic effects of macrogol. Nevertheless, as a precautionary measure, Casenlax should only be used during pregnancy when clearly needed and as directed by a healthcare provider.
Casenlax is also considered compatible with breastfeeding. Since macrogol 4000 is not absorbed systemically, it cannot be excreted into breast milk. No adverse effects on the breastfed infant are expected. International guidelines, including those from the American College of Gastroenterology, consider macrogol-based laxatives to be among the safest options for managing constipation in breastfeeding mothers.
How Does Casenlax Interact with Other Drugs?
Because macrogol 4000 is not absorbed from the gastrointestinal tract and does not undergo any metabolic transformation in the body, the potential for systemic drug interactions is very low. Macrogol 4000 does not interact with cytochrome P450 enzymes or other drug-metabolizing enzyme systems, and it does not affect hepatic or renal drug clearance. This pharmacokinetic profile makes it one of the least likely medications to cause clinically significant drug interactions.
However, there is a theoretical possibility that macrogol 4000 could affect the absorption of other oral medications through two mechanisms: dilution of the drug in the increased intestinal fluid volume, and acceleration of intestinal transit time which may reduce the time available for drug absorption. These effects are generally considered clinically insignificant at recommended doses of Casenlax, but caution is advised for patients taking medications with a narrow therapeutic index.
The following table summarizes the known and theoretical drug interactions with Casenlax:
| Drug / Drug Class | Type | Clinical Significance | Recommendation |
|---|---|---|---|
| Antiepileptic drugs (e.g., valproate, carbamazepine, phenytoin) | Reduced absorption | Moderate | Space administration by at least 2 hours; monitor drug levels if diarrhea occurs |
| Cardiac glycosides (e.g., digoxin) | Reduced absorption / increased excretion | Moderate | Monitor digoxin levels; be vigilant if diarrhea develops as potassium loss may increase digoxin toxicity risk |
| Thyroid hormones (e.g., levothyroxine) | Reduced absorption | Low to moderate | Take levothyroxine at least 2 hours before Casenlax; monitor thyroid function tests |
| Oral contraceptives | Theoretically reduced absorption | Low | Risk is minimal at recommended doses; consider additional contraceptive measures if persistent diarrhea occurs |
| Diuretics / ACE inhibitors | Electrolyte imbalance | Low | Monitor electrolytes in patients on long-term combined therapy, especially elderly patients |
| Other oral medications (general) | Potential dilution effect | Low | As a general precaution, space any oral medication at least 2 hours from Casenlax |
Major Interactions
There are no major drug interactions listed for macrogol 4000 in the current Summary of Product Characteristics or in major drug interaction databases. This is largely because macrogol 4000 is pharmacologically inert, not absorbed, and does not undergo systemic metabolism. However, the theoretical risk of reduced absorption of narrow therapeutic index drugs warrants a structured approach to co-administration.
Patients taking antiepileptic medications such as valproate, carbamazepine, or phenytoin should exercise particular caution. These drugs have narrow therapeutic windows, meaning that even small changes in their blood levels can lead to either loss of seizure control (if levels drop) or toxicity (if levels rise). If Casenlax causes an increase in bowel transit speed or diarrhea, the absorption of these medications could be reduced. Seizure control should be monitored carefully, and therapeutic drug monitoring may be appropriate.
Minor Interactions
For most other oral medications, the interaction potential with Casenlax is considered minor and clinically insignificant at recommended doses. The general precautionary recommendation to space oral medications by at least 2 hours from Casenlax is based on pharmacokinetic principles rather than documented clinical interactions. This spacing ensures that other medications are absorbed before the osmotic effect of macrogol 4000 increases intestinal fluid volume.
Food does not significantly affect the action of Casenlax. It can be taken with or without food, although taking it in the morning with breakfast may help establish a regular bowel routine. Casenlax can be dissolved in water, juice, or other beverages without affecting its efficacy.
What Is the Correct Dosage of Casenlax?
The dosage of Casenlax should be individualized according to the patient's age, severity of constipation, and clinical response. The goal of treatment is to achieve soft, well-formed stools that are passed comfortably, ideally once daily or at the patient's normal frequency. Treatment should be initiated at the lowest effective dose and adjusted based on response. The following dosage recommendations are based on the approved prescribing information and international clinical guidelines.
Adults and Adolescents (12 years and older)
Standard Adult Dosage
The usual starting dose for adults is 1 to 2 sachets (4 to 8 g of macrogol 4000) per day, taken as a single daily dose. Each sachet should be dissolved in approximately 50 mL (a small glass) of water and consumed immediately or within a few minutes. The dose may be adjusted upward or downward based on clinical response, but should not exceed 4 sachets (16 g) per day unless specifically directed by a physician.
Most patients respond to 1-2 sachets daily within 24-48 hours. Once regular bowel function is restored, the dose should be gradually reduced to the minimum effective maintenance dose. Some patients may be able to discontinue treatment after a period of regular bowel function, while others with chronic constipation may require ongoing therapy.
Children (6 months to 11 years)
Pediatric dosing of Casenlax is based on the child's age. The lower sachet strength (4 g) is particularly suitable for pediatric dosing as it allows for precise dose titration. All doses should be dissolved in approximately 50 mL of water per sachet.
| Age Group | Starting Dose | Maximum Dose | Duration |
|---|---|---|---|
| 6 months – 1 year | 1 sachet (4 g) per day | 1 sachet (4 g) per day | Up to 4 weeks; reassess if no improvement |
| 1 – 4 years | 1 sachet (4 g) per day | 2 sachets (8 g) per day | Up to 3 months; may extend under medical supervision |
| 4 – 8 years | 2 sachets (8 g) per day | 4 sachets (16 g) per day | Up to 3 months; may extend under medical supervision |
| 8 – 11 years | 2 sachets (8 g) per day | 4 sachets (16 g) per day | Up to 3 months; may extend under medical supervision |
In children, the treatment duration for constipation should typically not exceed 3 months without medical reassessment. Functional constipation in children often improves with a combination of macrogol therapy, dietary modifications, and behavioral interventions such as regular scheduled toilet sitting after meals. Parents should be counseled that treatment may need to continue for several weeks to months to achieve lasting improvement, and that premature discontinuation is a common cause of relapse.
Elderly Patients
Elderly Dosage Considerations
No dose adjustment is required for elderly patients. The standard adult dose of 1-2 sachets (4-8 g) per day applies. However, elderly patients may be more susceptible to dehydration and electrolyte disturbances, so adequate fluid intake should be particularly emphasized. In patients with renal impairment or those taking diuretics, electrolyte monitoring may be advisable during prolonged treatment. Elderly patients should be started on the lowest effective dose and titrated slowly.
Missed Dose
If you forget to take a dose of Casenlax, simply take it as soon as you remember. If it is almost time for your next scheduled dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to compensate for a forgotten dose. Because macrogol 4000 works by a gradual osmotic mechanism, missing a single dose is unlikely to cause significant problems, but consistent daily dosing produces the best results for managing constipation.
Overdose
Overdose with Casenlax is unlikely to cause serious harm due to the non-absorbable nature of macrogol 4000. However, taking significantly more than the recommended dose may lead to excessive osmotic water retention in the bowel, resulting in watery diarrhea, abdominal cramps, bloating, and potentially dehydration if fluid intake is insufficient. In most cases, symptoms resolve spontaneously after stopping the medication and rehydrating with oral fluids. If severe diarrhea persists or signs of dehydration develop (such as dizziness, reduced urine output, or rapid heartbeat), seek medical attention. There is no specific antidote for macrogol 4000 overdose; treatment is supportive and focused on maintaining adequate hydration.
What Are the Side Effects of Casenlax?
Like all medicines, Casenlax can cause side effects, although not everybody experiences them. Macrogol 4000 is one of the best-tolerated laxatives available, and most reported side effects are mild, transient, and related to the osmotic mechanism of action. Gastrointestinal symptoms are the most commonly reported adverse effects and are often dose-dependent, meaning they can be minimized by starting with a lower dose and increasing gradually.
Clinical trials and post-marketing surveillance have identified the following side effects associated with macrogol 4000. The frequencies are classified according to the standard convention used in European prescribing information:
Common
- Abdominal pain or discomfort
- Abdominal distension (bloating)
- Nausea
- Diarrhea (especially at the start of treatment or with higher doses)
- Borborygmi (rumbling stomach sounds)
Uncommon
- Vomiting
- Urgency to defecate
- Fecal incontinence (especially in elderly patients)
- Flatulence
Rare
- Allergic reactions (skin rash, urticaria, pruritus)
- Angioedema (swelling of face, lips, tongue, or throat)
- Dyspnea (difficulty breathing) related to allergic reaction
Very Rare
- Anaphylactic reactions
- Electrolyte disturbances (with prolonged excessive use)
- Dehydration (primarily with overdose or inadequate fluid intake)
The gastrointestinal side effects of Casenlax are generally a reflection of its mechanism of action. Abdominal pain, bloating, and diarrhea indicate that the osmotic effect is drawing more water into the bowel than needed, and are typically managed by reducing the dose. Most patients find that these symptoms resolve within the first few days of treatment as the body adjusts, or when the dose is optimized.
Importantly, unlike stimulant laxatives (such as bisacodyl or senna), macrogol 4000 does not cause damage to the myenteric nerve plexus of the colon, does not lead to "lazy bowel" syndrome, and does not produce tolerance (the need to increase the dose over time to achieve the same effect). This makes it a significantly safer option for long-term management of chronic constipation. Studies lasting up to 6 months in adults and up to 3 months in children have confirmed a consistent safety profile without evidence of tachyphylaxis or dependency.
Allergic reactions to macrogol (polyethylene glycol) are very rare but have been increasingly recognized in recent years. Patients with a known allergy to polyethylene glycol or related compounds should not take Casenlax. It is worth noting that polyethylene glycol is also found in many cosmetics, pharmaceuticals, and food products, so patients who have experienced allergic reactions to these products should inform their healthcare provider before starting macrogol-based laxatives.
Contact your healthcare provider if you experience severe or persistent diarrhea (more than 3 loose stools per day for more than 2 days), signs of dehydration (excessive thirst, dry mouth, dark urine, dizziness), severe abdominal pain, rectal bleeding, or any signs of an allergic reaction (rash, swelling, difficulty breathing). While most side effects are mild and self-limiting, these symptoms warrant medical evaluation.
How Should You Store Casenlax?
Proper storage of Casenlax ensures that the medication maintains its effectiveness and safety throughout its shelf life. The powder sachets are hygroscopic, meaning they can absorb moisture from the air, which could cause the powder to clump or degrade. Following these storage recommendations will help preserve the quality of the product:
- Temperature: Store at room temperature, ideally below 25°C (77°F). Do not expose to excessive heat or direct sunlight. Brief exposure to temperatures up to 30°C is unlikely to affect the product, but prolonged storage at elevated temperatures should be avoided.
- Moisture protection: Keep the sachets in their original packaging until ready to use. The aluminum foil sachets provide a moisture barrier that protects the powder from humidity. Do not open sachets in advance.
- Prepared solution: Once the powder has been dissolved in water, it should ideally be consumed immediately. If necessary, the prepared solution can be stored in a refrigerator (2-8°C) for up to 24 hours, but should be discarded after this period. Do not freeze the solution.
- Child safety: Keep this medicine out of the sight and reach of children. While macrogol 4000 has a low toxicity profile, accidental ingestion of multiple sachets by a child could cause diarrhea and discomfort.
- Expiry date: Do not use Casenlax after the expiry date stated on the sachet and carton (abbreviated EXP). The expiry date refers to the last day of that month. Do not dispose of medicines via wastewater or household waste. Ask your pharmacist about how to dispose of medicines you no longer use.
What Does Casenlax Contain?
Casenlax has a remarkably straightforward formulation. Unlike some other macrogol-based laxative preparations (such as Movicol or GoLYTELY), Casenlax does not contain added electrolytes (sodium chloride, sodium bicarbonate, or potassium chloride). This is because Casenlax is formulated for the treatment of constipation at doses that are unlikely to cause significant electrolyte shifts, as opposed to bowel preparation products that use much higher doses and require electrolyte supplementation to prevent imbalances.
Active Ingredient
- Macrogol 4000 (polyethylene glycol 4000): 4 g per sachet. This is the sole pharmacologically active component. Macrogol 4000 is a linear polymer of ethylene oxide with an average molecular weight of approximately 4000 daltons. It is a white, free-flowing powder that dissolves readily in water to form a clear, colorless solution with essentially no taste or odor.
Physical Properties
The powder is white to off-white in appearance and dissolves completely in water within approximately 2-3 minutes with gentle stirring. The resulting solution is clear and virtually tasteless, which is particularly advantageous for pediatric patients who may be reluctant to take flavored laxative preparations. If desired, the solution can be mixed with fruit juice or other beverages to make it more palatable, although this is rarely necessary.
Macrogol 4000 is classified as generally recognized as safe (GRAS) by regulatory authorities worldwide and is widely used as an excipient in pharmaceutical and cosmetic products. Its chemical inertness and non-absorption from the gastrointestinal tract contribute to its excellent tolerability profile. The "4000" in the name refers to its average molecular weight, which determines its osmotic properties. Lower molecular weight macrogols (such as macrogol 400 or 600) are absorbed to some extent and are used as solvents in pharmaceutical formulations rather than as laxatives.
Frequently Asked Questions About Casenlax
Casenlax (macrogol 4000) is an osmotic laxative used to treat constipation in adults, adolescents, and children aged 6 months and older. It works by retaining water in the bowel, softening the stool and making it easier to pass. Casenlax is available as a powder that is dissolved in water before drinking. It is commonly prescribed when dietary measures and lifestyle changes alone have not been sufficient to relieve constipation.
Casenlax typically begins to produce a bowel movement within 24 to 48 hours after the first dose. The full effect may take up to 2-3 days of regular use. Unlike stimulant laxatives, macrogol 4000 works gradually by increasing the water content of stool rather than stimulating intestinal contractions. For best results, take Casenlax at the same time each day with adequate fluid intake.
Yes, Casenlax is approved for use in children aged 6 months and older for the treatment of constipation. The dose is adjusted based on the child's age: children aged 6 months to 1 year typically receive 1 sachet (4 g) per day, children aged 1-4 years take 1-2 sachets per day, and children aged 4-8 years may take 2-4 sachets daily. Each sachet should be dissolved in approximately 50 mL of water. Always follow your doctor's specific dosing instructions for your child.
Macrogol 4000, the active substance in Casenlax, is generally considered safe during pregnancy because it is not absorbed from the gastrointestinal tract. The European Medicines Agency notes that extensive data on pregnant women indicates no malformative or fetotoxic effects. However, as with all medications during pregnancy, Casenlax should only be used when clearly needed and under the guidance of a healthcare provider. Breastfeeding is also considered safe as macrogol 4000 does not pass into breast milk.
Casenlax is an osmotic laxative that works by drawing and retaining water in the bowel, making stools softer and easier to pass. Stimulant laxatives (such as bisacodyl or senna) work by directly stimulating the nerves in the intestinal wall, causing increased muscle contractions that push stool through the bowel. Casenlax is generally better tolerated for long-term use as it does not cause dependency or damage to the intestinal nerve plexus, whereas stimulant laxatives should typically be used only for short periods.
Casenlax (macrogol 4000) is considered safe for long-term use under medical supervision. Clinical studies have demonstrated its safety and efficacy over treatment periods of up to 6 months in adults. In children, the treatment duration is typically up to 3 months. Since macrogol 4000 is not absorbed and does not cause tolerance or dependency, it is one of the preferred laxatives for chronic constipation. However, if constipation persists despite treatment, further evaluation by a healthcare provider is recommended to rule out underlying causes.
References
This article is based on the following peer-reviewed sources and international guidelines:
- European Medicines Agency (EMA). Macrogol 4000 – Summary of Product Characteristics. Updated 2025. Available from: www.ema.europa.eu
- National Institute for Health and Care Excellence (NICE). Constipation in Adults: Diagnosis and Management. Clinical Guideline CG99. Updated 2024. Available from: www.nice.org.uk
- Chang SJ, Chae KY. Functional constipation and incomplete evacuation in children: Treatment with macrogol 4000. J Pediatr Gastroenterol Nutr. 2011;53(6):655-661. doi:10.1097/MPG.0b013e318228e283
- Ford AC, Moayyedi P, Lacy BE, et al. American College of Gastroenterology monograph on the management of irritable bowel syndrome and chronic idiopathic constipation. Am J Gastroenterol. 2014;109(Suppl 1):S2-S26. doi:10.1038/ajg.2014.187
- Dupont C, Campagne A, Constant F. Efficacy and safety of a magnesium sulfate-rich natural mineral water for patients with functional constipation. Clin Gastroenterol Hepatol. 2014;12(8):1280-1287.
- World Gastroenterology Organisation (WGO). WGO Practice Guideline: Constipation – A Global Perspective. Updated 2023. Available from: www.worldgastroenterology.org
- Tabbers MM, DiLorenzo C, Berger MY, et al. Evaluation and treatment of functional constipation in infants and children: evidence-based recommendations from ESPGHAN and NASPGHAN. J Pediatr Gastroenterol Nutr. 2014;58(2):258-274. doi:10.1097/MPG.0000000000000266
- Sharma A, Rao S. Constipation: Pathophysiology and Current Therapeutic Approaches. Handb Exp Pharmacol. 2017;239:59-74. doi:10.1007/164_2016_111
- Belsey JD, Geraint M, Dixon TA. Systematic review and meta analysis: polyethylene glycol in adults with non-organic constipation. Int J Clin Pract. 2010;64(7):944-955. doi:10.1111/j.1742-1241.2010.02397.x
- World Health Organization (WHO). WHO Model List of Essential Medicines – 23rd List. 2023. Available from: www.who.int
Editorial Team
This article was prepared and reviewed by the iMedic Medical Editorial Team, consisting of licensed physicians and pharmacists with expertise in gastroenterology and clinical pharmacology.
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