What are the ingredients in Dulcolax kids soft chews? How do you take Dulcolax kids soft chews? What are the warnings for using Dulcolax kids soft chews?

Ingredients in Dulcolax Kids Soft Chews

Dulcolax kids soft chews contain the following ingredients: corn syrup, FD&C red no. 40, glycerin, hydrogenated coconut oil, lecithin (soy), natural flavor, sucrose, and water. Each chew also contains 500 mg of magnesium and 2 mg of sodium.

Dosage and Usage of Dulcolax Kids Soft Chews

Dulcolax kids soft chews are recommended to be taken with a full glass (8 oz) of liquid. The dosage varies by age:

• Adults and children 12 years and over: 2 to 4 chews
• Children 6 to under 12 years: 1 to 2 chews
• Children 4 to under 6 years: 1 chew (single dose or divided doses)
• Children under 4 years: ask a doctor

The chews can be taken as a single daily dose or in divided doses, but do not exceed the maximum recommended daily dose in a 24-hour period.

Warnings and Precautions for Dulcolax Kids Soft Chews

Before using Dulcolax kids soft chews, consult with a doctor or pharmacist if you are taking any prescription drugs, as the product may interact with certain medications. Stop use and ask a doctor if you experience rectal bleeding, fail to have a bowel movement after using the product, or need to use a laxative for more than 1 week.

Additionally, pregnant or breastfeeding women should consult a health professional before using Dulcolax kids soft chews. Individuals with kidney disease or a magnesium-restricted diet should also ask a doctor before use.

If you notice a sudden change in bowel habits that lasts over 2 weeks, or experience stomach pain, nausea, or vomiting, stop using the product and consult a doctor. Keep Dulcolax kids soft chews out of the reach of children, and in case of overdose, seek medical help or contact a Poison Control Center immediately.

Benefits of Dulcolax Kids Soft Chews

Dulcolax kids soft chews are a laxative product designed to provide relief for constipation in children. The soft chew format may be more appealing and easier to administer to children compared to other laxative formulations. The product contains magnesium, which can help draw water into the intestines and stimulate bowel movements.

Comparing Dulcolax Kids Soft Chews to Other Laxatives

Dulcolax kids soft chews are a saline laxative, which work by drawing water into the intestines to soften stool and stimulate bowel movements. This is different from other laxative types, such as stimulant laxatives or osmotic laxatives, which work through different mechanisms.

When choosing a laxative for a child, it’s important to consult with a healthcare provider to determine the most appropriate product based on the child’s age, symptoms, and medical history.

Storing and Handling Dulcolax Kids Soft Chews

Dulcolax kids soft chews should be stored at room temperature between 68째F and 77째F (20째C and 25째C). The product should be kept out of reach of children, and in case of overdose, immediate medical attention should be sought.

Frequently Asked Questions about Dulcolax Kids Soft Chews

What is the recommended dosage of Dulcolax kids soft chews for children?

The recommended dosage of Dulcolax kids soft chews varies by age: adults and children 12 years and over should take 2 to 4 chews, children 6 to under 12 years should take 1 to 2 chews, and children 4 to under 6 years should take 1 chew (single dose or divided doses).

Are Dulcolax kids soft chews safe for pregnant or breastfeeding women?

Pregnant or breastfeeding women should consult a health professional before using Dulcolax kids soft chews, as the safety and efficacy of the product in these populations has not been fully established.

Can Dulcolax kids soft chews interact with other medications?

Yes, Dulcolax kids soft chews may interact with certain prescription drugs. It’s important to consult a doctor or pharmacist before using the product if you are taking any other medications.

What should I do if I experience side effects from Dulcolax kids soft chews?

If you experience side effects such as rectal bleeding, failure to have a bowel movement, sudden changes in bowel habits, stomach pain, nausea, or vomiting, stop using the product and consult a doctor immediately.

Dulcolax Saline Laxative, 1200 mg, Kids, Soft Chews, Watermelon (15 each) Delivery or Pickup Near Me

Dulcolax Saline Laxative, 1200 mg, Kids, Soft Chews, Watermelon (15 each) Delivery or Pickup Near Me – Instacart

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15 each

15 each

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About

Details

In Each Chew: Other Information: Each chew contains; Magnesium 500 mg, sodium 2 mg. Store at room temperature 20 degrees – 25 degrees C (68 degrees – 77 degrees F).

Ingredients

Corn Syrup, Fd&c Red No. 40, Glycerin, Nydrogenated Coconut Oil, Lecithin (soy), Natural Flavor, Sucrose, Water

Directions

drink a full glass (8 oz) of liquid with each dose dose may be taken as a single daily dose or in divided doses do not exceed the maximum recommended daily dose in a 24 hour period adults and children 12 years of age and over take 2 to 4 chews children 6 to under 12 years of age take 1 to 2 chews children 4 to under 6 years of age take 1 chew (single dose or in divided doses) children under 4 years of age ask a doctor

Warnings

Ask a doctor or pharmacist before use if you are taking a prescription drug. This product may interact with certain prescription drugs. Stop use and ask a doctor if – you have rectal bleeding or fail to have a bowel movement after using this product. These could be signs of a serious condition. you need to use a laxative for more than 1 week if pregnant or breast-feeding, ask a health professional before use. Ask a doctor before use if you have kidney disease – a magnesium-restricted diet stomach pain, nausea or vomiting – noticed a sudden change in bowel habits that lasts over 2 weeks. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

About

Details

In Each Chew: Other Information: Each chew contains; Magnesium 500 mg, sodium 2 mg. Store at room temperature 20 degrees – 25 degrees C (68 degrees – 77 degrees F).

Ingredients

Corn Syrup, Fd&c Red No. 40, Glycerin, Nydrogenated Coconut Oil, Lecithin (soy), Natural Flavor, Sucrose, Water

Directions

drink a full glass (8 oz) of liquid with each dose dose may be taken as a single daily dose or in divided doses do not exceed the maximum recommended daily dose in a 24 hour period adults and children 12 years of age and over take 2 to 4 chews children 6 to under 12 years of age take 1 to 2 chews children 4 to under 6 years of age take 1 chew (single dose or in divided doses) children under 4 years of age ask a doctor

Warnings

Ask a doctor or pharmacist before use if you are taking a prescription drug. This product may interact with certain prescription drugs. Stop use and ask a doctor if – you have rectal bleeding or fail to have a bowel movement after using this product. These could be signs of a serious condition. you need to use a laxative for more than 1 week if pregnant or breast-feeding, ask a health professional before use. Ask a doctor before use if you have kidney disease – a magnesium-restricted diet stomach pain, nausea or vomiting – noticed a sudden change in bowel habits that lasts over 2 weeks. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

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Dulcolax Suppositories For Children – 5mg – 5 Suppositories

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• How to Use

• Delivery & Return

Dulcolax Suppositories For Children 5mg is packed full of Bisacodyl, which actively works as a proven and safe compound, without side effects, that relieves those suffering from constipation. The active ingredients is mixed with a safe wax-like substance which firm at room temperature and melt inside of the body once inserted in the rectum.

Bisacodyl 5mg

Caution before using Dulcolax Suppositories:

• Should not be used with anal fissures or ulcerative procitis with mucosal damage are present.
• If you suffer from any of the following intestinal problems, ileus, intestinal obstruction, acute appendicitis, acute inflammatory bowel disease or any other surgical abdominal condition.
• If you are suffering from severe dehydration.
• Do not exceed dosage.

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This product is typically dispatched within 1-2 working days from date of order

Please note that we do not operate at the weekends. Orders placed after 2pm Friday will not get processed until the following Monday morning.

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Our standard delivery charge is £2.90.
We use a tracked 48 Hour service for our standard delivery.

Important Information About Shipping to Third-Party Logistics Providers 
Please note that Medicine Marketplace cannot be held liable or responsible for any claims of missing or damaged goods that may occur during the shipping to third-party logistics providers, including Amazon’s third-party re-labeller’s.

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Standard Delivery

Our standard delivery charge is £3.90. We aim to deliver orders within 3-5 working days to the shipping address provided by you in your order if the shipping address is in the UK.  For orders being delivered outside mainland UK, this will be longer and we cannot give a guaranteed delivery time due to the differences between carriers. Delivery timescales are estimates only. If you do not receive your order within 14 days of us confirming your order has been sent you must notify us and we will investigate the non-delivery provided.

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£5.99 – Next working day (excluding Saturdays & Sundays) on orders placed before 4pm. Orders placed after 4pm will be delivered on the 2nd working day after the order is placed.

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Private prescription medicines are sent by Royal Mail Special Delivery free of charge (all private prescription items have a minimum order value of £5.00).
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If you’re not completely satisfied with your order, you can return it within 28 days. We cannot accept the return of prescription medicines.

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Catalog :: Medicines :: Digestive system :: Laxatives :: Dulcolax® 5mg №30 tab.

Dosage form, dosage

Enteric coated tablets 5 mg

Pharmacotherapeutic group

Digestive tract and metabolism. Drugs for the treatment of constipation. Contact laxatives. Bisacodyl.

ATX code A06AB02

Indications for use

• symptomatic treatment of constipation

Checklist before use

Contraindications

• hypersensitivity to bisacodyl or other components of the drug
• severe dehydration
• acute inflammatory bowel disease, ulcerative colitis, Crohn’s disease
• severe abdominal pain of indeterminate location, including severe pain accompanied by nausea and vomiting, which may indicate a serious illness
• occlusive and subocclusive syndromes
• persons with hereditary fructose intolerance, Lapp-lactase enzyme deficiency, glucose-galactose malabsorption
• children under 6 years of age

9000 3 Necessary precautions for use

Drug therapy for constipation should be be accompanied by the following hygiene and dietary measures:

• diet rich in fiber and fluids
• adherence to recommendations for physical activity and rules for the normalization of bowel movements.

Long-term use (more than 10 days) is not recommended as it may cause:

• severe functional bowel disorder, melanosis, fluid and electrolyte imbalance and hypokalemia.
• drug dependence with regular need for laxatives, the need to increase the dosage and severe constipation upon withdrawal. Addiction varies among patients and can occur without the knowledge of the physician.

In patients suffering from fluid loss, where dehydration can be dangerous (renal failure, elderly patients), the use of the drug should be suspended and resumed only under medical supervision. Loss of fluids can cause dehydration, signs of which may include thirst and oliguria.

The simultaneous use of the drug with drugs that cause bidirectional ventricular tachycardia is not recommended

Patients may experience rectorrhagia (look for blood in the stool), which is usually mild and self-limiting. If you have rectorrhagia, you should contact your doctor.

Cases of dizziness and fainting have been reported, presumably related to defecation.

In children, stimulant laxatives should only be used in exceptional cases, as the risk of impaired defecation reflex function must be taken into account.

Simultaneous use with other laxatives may increase the gastrointestinal side effects of Dulcolax®.

The drug is not recommended for persons with hereditary fructose or galactose intolerance, Lapp-lactase or sucrase-isomaltase deficiency, glucose and/or galactose malabsorption.

The drug Dulcolax® contains castor oil, which can cause gastrointestinal disturbances (mild laxative effect, diarrhoea).

Interactions with other drugs

Undesirable combinations 05

• antiarrhythmics : amiodarone, bretylium, disopyramide, quinidine, sotalol
• not antiarrhythmics preparations : astemizole, bepridil, erythromycin IV, halofantrine, pentamidine, sultropide, terfenadine, vincamine

Non-stimulant laxatives should be used.

Combinations requiring precautions for use

Medicines containing digitalis:

Hypokalemia increases the toxic effect of medicines containing digitalis. The level of potassium in the blood should be monitored and, if necessary, an ECG should be performed. Non-stimulant laxatives should be used.

Other potassium-lowering drugs:

Hypokalemic diuretics (singly or in combination), amphotericin B (intravenously), corticosteroids (glucocorticoids and mineralocorticoids: systemic route of administration), tetracosactide. Increased risk of hypokalemia (additive effect). Monitoring and, if necessary, correction of the level of potassium in the blood is required. Non-stimulant laxatives should be used.

Co-administration of with upper GI deacidifiers, such as alkaline preparations, antacids, proton pump inhibitors, or milk, may reduce the resistance of the tablet shell and lead to dyspepsia and stomach irritation.

Special warnings

Pregnancy

The drug is not recommended during pregnancy, as the available clinical and preclinical data are insufficient.

Lactation

According to data, neither bisacodyl nor its glucuronides pass into the breast milk of lactating women, so Dulcolax ^® can be used during lactation.

Fertility

Human fertility studies have not been conducted.

Features of the effect of the drug on the ability to drive vehicles or potentially dangerous mechanisms

Studies have not been conducted. However, patients should be aware of the possibility of dizziness and/or fainting due to the parasympathetic vascular response to constipation-related abdominal pain.

Directions for use

Dosage regimen

Adults: maximum dose 1-2 tablets (5-10 mg) per day.

Children

Children aged 6 to 12 years 1 tablet (5 mg) 1 time per day for 2 to 10 days.

In children under 12 years of age with chronic or prolonged constipation, the use of the drug is possible only on prescription!

Method and route of administration

Treatment is recommended to start with the lowest dose. Dosage may be adjusted to the maximum recommended daily dose until regular stools are obtained. Exceeding the maximum daily dosage is unacceptable.

Tablets are recommended to be taken at night (effect after 10 hours) for stools the next morning, or in the morning on an empty stomach (effect after 5 hours). The tablets should be swallowed whole with a sufficient amount of liquid.

It is not recommended to take tablets along with products that lower the acidity of the upper gastrointestinal tract, such as milk, antacids or proton pump inhibitors, in order to prevent premature dissolution of the shell of the tablet

Measures, which must be taken in case of an overdose of 9000

Symptoms: diarrhea, dehydration, abdominal cramps, impaired potassium and other electrolyte metabolism.

Chronic overdose of Dulcolax ^® may cause diarrhea, abdominal pain, hypokalemia, which may be associated with muscle weakness.

Cases of renal tubular lesions, metabolic alkalosis, secondary aldosteronism, and urolithiasis have also been described in association with chronic abuse of laxatives.

Treatment: symptomatic. It may be necessary to restore water and electrolyte imbalance, which is especially important for elderly patients and children. It may be useful to take antispasmodics.

Description of adverse reactions that occur with the standard use of the drug and measures to be taken in this case (if necessary)

Adverse events are listed below by system organ class and frequency according to the following classification: very often (≥ 1/10), common (≥ 1/100 to <1/10), uncommon (≥1/1000 to <1/100), rare (≥1/10,000 to <1/1000 ), very rare (<1/10,000), frequency unknown (adverse reactions, the frequency of which is unknown, since it cannot be estimated from the available data).

Common ( ≥ 1/100 to <1/10)

• diarrhea, nausea, abdominal pain and cramps

Uncommon ( ≥1/1000 to <1/100)

• rectorrhagia (blood in the stool), anorectal discomfort (burning and anorectal pain), vomiting
• dizziness*

Rare ( ≥1/10,000 to <1/1000)

• anaphylactic reactions, angioedema
• generalized pruritus

900 21 dehydration

• syncope*
• colitis, including ischemic colitis

*available information suggests that dizziness and syncope are suspected to be associated with a parasympathetic vascular reaction in abdominal cramps and defecation

Frequency unknown (adverse reactions, the frequency of which is unknown, as it cannot be estimated from the available data)

• hypokalemia

Composition of the medicinal product mg,

excipients: lactose monohydrate, dried corn starch, soluble starch, glycerin 85 %, magnesium stearate,

shell composition: magnesium stearate, sucrose, talc, acacia (powder), titanium dioxide (E 171), copolymer of methacrylic acid and methyl methacrylate (1 : 1) (Eudragit L 100), copolymer of methacrylic acid and methyl methacrylate (1: 2) (Eudragit S 100), castor oil, macrogol 6000, yellow iron oxide (E 172), white wax, carnauba wax, shellac, purified water, anhydrous ethanol, acetone.

Description of appearance, odor, taste

Round, biconvex tablets, sugar/enteric-coated beige-yellow color with a smooth shiny surface. Tablet diameter is from 5.8 mm to 6.2 mm, thickness is from 3.2 mm to 3.8 mm.

Release form and packaging

10 tablets are placed in blisters made of PVC film and aluminum foil.

3 blister packs, together with instructions for medical use in Kazakh and Russian, are put into a cardboard pack.

Shelf life

3 years.

Do not use after the expiration date.

Storage conditions

Store below 25°C.

Keep out of reach of children!

Pharmacy conditions

Without prescription

Producer information

Delpharm Reims, Reims, France

10 rueColonel Charbon neaux, 51100 Reims, France

phone: +330326888110

Active ingredient

Bisacodyl

Dosage form

oral tablets

Need

9002 1

Laxatives

Thermolabile mode

No

Dispensing conditions

OTC

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Available Shipping Methods

• Courier “to the door”

Dulcolax pico 30 ml drops

Instructions for medical use

Dulcolax® Pico

Trade name

Dulcolax Pico

International generic name

Sodium picosulfate

Dosage form

Oral drops 7 . 5 mg/ml 15 ml, 30 ml

Composition

100 ml contains

active substance – sodium picosulfate monohydrate 7.5 mg,

excipients: sodium benzoate, liquid sorbitol (not crystallized), sodium citrate dihydrate, citric acid monohydrate, purified water.

Description

Clear, colorless to yellow or light yellow-brown, slightly viscous solution with almost imperceptible odor

Pharmacotherapeutic group

Laxatives. Contact laxatives.

Sodium picosulfate.

ATC code A06AB08

Pharmacological properties

Pharmacokinetics

Absorption. After ingestion, sodium picosulfate reaches the large intestine without being absorbed from the gastrointestinal tract and thus without being exposed to the hepatic circulation.

Biotransformation. Sodium picosulfate is converted to the active compound of the drug bis-(p-hydroxyphenyl)-pyridyl-2-methane in the distal segment of the intestine by cleavage by intestinal bacteria.

Elimination. After conversion, only a small amount of bis-(p-hydroxyphenyl)-pyridyl-2-methane is absorbed and combined in the intestinal wall and liver to form inactive bis-(p-hydroxyphenyl)-pyridyl-2-methane glucuronide. After ingestion of 10 mg sodium picosulfate, 10.4% of the total dose is excreted as bis-(p-hydroxyphenyl)-pyridyl-2-methane glucuronide in the urine after 48 hours. In general, urinary excretion decreases when higher doses of sodium picosulfate are taken.

The time of development of the laxative effect of the drug is determined by the rate of release of the active metabolite and is 6-12 hours. There is no direct or inverse relationship between the laxative effect of the active metabolite and its serum concentration.

Pharmacodynamics

Sodium picosulfate, the active ingredient in Dulcolax Pico, is a locally acting laxative from the triarylmethane group. After bacterial digestion in the colon, it stimulates its mucous membrane, reduces the absorption of electrolytes and water, and enhances intestinal motility.

The active form of the drug, formed by hydrolysis under the influence of intestinal microorganisms, directly excites the nervous structures of the intestinal wall, as a result of which the passage of intestinal contents is accelerated.

As a colonic laxative, sodium picosulfate specifically stimulates the natural bowel movement in the lower gastrointestinal tract. Thus, sodium picosulfate is ineffective in altering digestion or absorption of calories or essential nutrients in the small intestine.

Indications for use

– constipation and conditions requiring assistance in bowel movements (atonic constipation, stool regulation (hemorrhoids, proctitis, anal fissures), preparation for surgery, instrumental and x-ray studies).

Route of administration and doses

It is recommended to start taking the drug with the minimum sufficient dose. To obtain the desired effect, the dose may be increased to the maximum recommended dose. Do not exceed the maximum recommended dose.

The drug is recommended to be taken at night, before going to bed, to ensure bowel movements the next morning.

1 ml contains 7.5 mg (=15 drops)

Adults: 10-20 drops (5-10 mg) per day

Children over 10 years old: 10-20 drops (5-10 mg) per day

Children aged 4-10 years: 5-10 drops (2.5-5 mg) per day

Children under 4 years of age: the recommended dose is 0.25 mg per kg of body weight per day sodium picosulfate).

Side effects

Side effects are defined as follows:

Very common ≥ 1/10

Common ≥ 1/100 – < 1/10

Uncommon ≥ 1/1,000 – < 1/100 900 05

Rare ≥ 1 /10,000 – < 1/1,000

Very rare < 1/10,000

Unknown frequency cannot be estimated from available data

Immune system disorders:

Unknown:

– hypersensitivity

Nervous system disorders:

Uncommon:

– dizziness and defecation))

Gastrointestinal disorders:

Very common

Diarrhea

Common

Abdominal pain

Abdominal cramps

Abdominal discomfort

5

Uncommon:

– nausea, vomiting

Dermatological disorders:

Unknown:

– skin reactions such as angioedema, drug dermatitis, rash, itching

Contraindications

– ileus or intestinal obstruction

– severe febrile conditions with severe abdominal pain (eg appendicitis) associated with possible nausea and vomiting

– acute inflammatory bowel disease

– severe dehydration

– hypersensitivity to sodium picosulfate or other components of the drug

– hereditary intolerance to fructose and galactose (see “Special instructions”)

Drug interactions

Glucocorticosteroids, diuretics increase the risk of developing electrolyte disturbances with increasing doses. This may increase the sensitivity to cardiac glycosides.

Broad-spectrum antibiotics reduce the laxative effect.

Precautions

As with any laxative, DULCOLAX PIKO should not be taken daily or for long periods without determining the cause of constipation. This can lead to a violation of the water and electrolyte balance, as well as cause hypokalemia.

Cases of dizziness and/or fainting have been observed in patients taking Dulcolax Pico, which may be associated with straining during bowel movements or with a parasympathetic reaction to abdominal pain associated with constipation, and not necessarily with the use of sodium picosulfate.

Not recommended for use in children without first consulting a doctor.

1 ml drops contains 0.45 g of sorbitol, which is equal to 0.6 g of sorbitol per maximum recommended daily dosage for the treatment of adults and children over 10 years of age. Patients with hereditary fructose intolerance should not take this medicine.

Fertility, pregnancy and lactation

Adequate and well-controlled studies of the effects of the drug on the body of pregnant women have not been conducted. However, many years of experience with the use of the drug during pregnancy did not reveal any cases of unwanted or side effects.

However, Dulcolax Pico, like all other medicines, should be used during pregnancy with caution and under medical supervision. If necessary, the use of the drug should evaluate the potential benefit of therapy for the mother and the possible risk to the fetus.

According to clinical data, neither sodium picosulfate nor its glucuronides pass into the breast milk of lactating women, so Dulcolax Pico can be used during breastfeeding.

Studies of the effect of the drug on human fertility have not been conducted.

Features of the effect of the drug on the ability to drive a vehicle or potentially dangerous mechanisms

The effect of the drug on the ability to drive a vehicle or potentially dangerous mechanisms has not been studied. However, patients should be aware that adverse events such as dizziness and/or fainting may occur due to a parasympathetic vascular response (eg, abdominal cramps). In the event of abdominal cramps, patients should avoid potentially hazardous activities, including driving vehicles or using various mechanisms.

Overdose

Symptoms: diarrhea, abdominal pain, dehydration, clinically significant loss of fluid, potassium and other electrolytes.

In chronic overdose, ischemia of the colonic mucosa, chronic diarrhea, abdominal pain, hypokalemia, secondary hyperaldosteronism, and urolithiasis may develop.

Chronic laxative abuse may result in renal tubular damage, metabolic alkalosis, and muscle weakness associated with hypokalemia.

Treatment: induction of vomiting or gastric lavage, infusion therapy and correction of water and electrolyte imbalance, antispasmodics.

Presentation and packaging

15 ml or 30 ml in a plastic bottle sealed with a dropper stopper and a screw cap.