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Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml is a Product of the Generic Polyethylene Glycol 3350 + Electrolytes

Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml belongs to the generic category of Polyethylene Glycol 3350 + Electrolytes. This medicine should be used according to a doctor's advice. We have provided detailed information about the uses, dosage, effectiveness, side effects, precautions, drug interactions, storage conditions, and other important details of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml. Our goal is to present essential medicine information in one place for patients, caregivers, and healthcare professionals. To better understand Polyethylene Glycol 3350 + Electrolytes and ensure the safe use of this medicine, please read the information below carefully and consult a healthcare professional when necessary.

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Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

Ziska Pharmaceuticals Ltd. · Oral Solution

Generic

Polyethylene Glycol 3350 + Electrolytes

Strength(13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml
Unit Price
160

/ 100 ml bottle

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Description of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml may be available as a prescription or over-the-counter medicine, depending on local regulations and medical recommendations. It is used for the treatment and management of specific conditions or symptoms. The way this medicine is used may vary depending on the patient's condition and the advice of a healthcare provider. Detailed information about the approved uses, therapeutic applications, and other relevant details of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml is provided below to help users gain a clear understanding of this medicine.

What Is Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml Indications and Uses?

For use in adults and children over 12 years of age for effective relief from constipation and treatment of chronic constipation. Also effective in resolving fecal impaction, defined as refractory constipation with fecal loading of the rectum and colon.


Pharmacology (Source, Chemical and Physical Composition) Of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

Macrogol, also known as polyethylene glycol exerts an osmotic action in the gut, which induces a laxative effect. Macrogol increases stool volume, which triggers colon motility via neuromuscular pathways. The physiological consequence is an improved propulsive colonic transportation of the soften stools and a facilitation of the defecation. Electrolytes combined with Macrogol are exchanged across the intestinal barrier (mucosa) with serum electrolytes and excreted without net gain or loss of sodium, potassium and water. Macrogol is unchanged along the gut. It is virtually unabsorbed from the gastrointestinal tract.


Dosage And Administration of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

For adults and children aged 12 years and above: (Powder for Suspension)

Constipation: The dose is 1 sachet daily. This may be increased to 2-3 sachets daily, if required. 
Fecal Impaction: 8 sachets daily, consumed within 6 hours. A course of treatment for fecal impaction does not normally exceed 3 days. 
Patients with renal insufficiency: No dosage change is necessary for treatment of either constipation or fecal impaction.
Direction of use: Each sachet should be dissolved in 125 ml water. For fecal impaction 8 sachets may be dissolved in 1 litre of water. Store the solution refrigerated and discard any solution not used within 6 hours. 

For adults and children aged 12 years and above: (Oral Solution) 

Constipation: 25 ml of Polyethylene Glycol 3350 and electrolytes oral solution added to 100 ml of water once daily (to make a total volume of 125 ml). This may be increased to 2-3 doses of 25 ml daily (each 25 ml dose added to 100 ml of water), if required according to individual response.
Fecal Impaction: 8 doses of 25 ml daily (each 25 ml dose added to 100 ml of water). A course of treatment for fecal impaction does not normally exceed 3 days.
Direction of use: 25 ml of oral solution added to 100 ml of water (to make a total volume of 125 ml). Any unused diluted solution should be discarded within 24 hours.


Drug Interactions of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

There is a possibility that the absorption of other medicinal products could be transiently reduced during use with this preparation. There have been isolated reports of decreased efficacy with some concomitantly administered medicinal products, e.g. anti-epileptics.


Side Effects of Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

Generally well tolerated. However side effects like allergic reactions, electrolyte disturbances particularly hyperkalaemia and hypokalaemia, abdominal pain, diarrhea, headache, peripheral edema may appear.


Use During Pregnancy and Lactation

Clinically, no effects during pregnancy are anticipated, since systemic exposure to Macrogol (3350) is negligible. This oral solution can be used during pregnancy. No effects on the breastfed newborn/infant are anticipated since the systemic exposure of the breast-feeding woman to Macrogol (3350) is negligible. This oral solution can be used during breastfeeding.


Precautions And Warnings for Movifast (13.125 gm+350.7 mg+178.5 mg+46.6 mg)/25 ml

Patients with impaired cardiovascular function: For the treatment of fecal impaction the dose should be divided so that no more than two sachets are taken in any one hour. If patients develop any symptoms indicating shifts of fluid/electrolytes (e.g. edema, shortness of breath, increasing fatigue, dehydration, cardiac failure) Movilax should be stopped immediately and any abnormality should be treated appropriately. Prolonged use with all laxatives is undesirable and may lead to dependence.


Therapeutic Class

Osmotic purgatives


Storage Conditions of It

Store below 30° C and in a place protected from light. Do not refrigerate.

Data Source: Data source of Indications and Usages, Pharmacology, Dosage & Administration, Drug Interactions, Side Effects, Use during Pregnancy & Lactation, Precautions & Warnings, Use in Special Populations, Therapeutic Class, and Storage Conditions is the concerned medicine company or respective organization.

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The information provided on All Samadhan is intended for general informational purposes only and is prepared based on our best practices. It is not a substitute for professional medical advice, diagnosis, or treatment. While we strive to keep the information accurate and up to date, we do not guarantee its completeness or accuracy. The absence of specific information or warnings about any medicine or service should not be considered as an assurance or endorsement by All Samadhan. All Samadhan shall not be held responsible for any consequences arising from the use of this information. We strongly recommend consulting a qualified healthcare professional or physician for any medical concerns, questions, or clarifications.All Samadhan is a digital healthcare software platform operated by MS Genius Experts. We provide technology solutions for pharmacies and healthcare providers; we are not a direct seller or dispenser of prescription medicines

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