Micrazyme capsules 25000 units 100 pcs

Pharmacotherapeutic group

A digestive enzyme agent.

TAC code: A09AA02.

Pharmacological properties

Mikrazym® is pancreatin pellets in capsules. Composition of the product includes natural enzymes from animal pancreas – protease, lipase and amylase, providing digestion of proteins, fats and carbohydrates of food.

After taking Mikrazima® the capsule dissolves quickly in the stomach, releasing enteric-coated pancreatin pellets. Due to their small size pellets are quickly and evenly mixed with food and at the same time with the food lump easily penetrate into the duodenum and then into the small intestine where pancreatic enzymes are released and become active, promoting fast and complete digestion of proteins, fats and carbohydrates of food.

The rapid mixing of pancreatin pellets with the stomach contents, their uniform distribution in it, simultaneous passage with the chyme and also preservation of enzymes before their work in the intestine (due to the presence of an enteric-soluble shell of pellets) ensure higher digestive activity and maximum approximation of the drug to the natural process of digestion. The enzymatic activity of Mikrazim® is maximum 30 minutes after oral administration, which ensures rapid onset of the effect.

After interaction with the substrates, protease, lipase and amylase in the lower intestine lose activity and are excreted together with the intestinal contents.

Mikrazym® is not absorbed from the gastrointestinal tract and acts only in the intestinal lumen.

Indications

Substitution therapy in external pancreatic secretory insufficiency: chronic pancreatitis, pancreatectomy, condition after radiation, dyspepsia, cystic fibrosis; flatulence, diarrhea of non-infectious genesis.

Digestive disorders (condition after resection of the stomach and small intestine): to improve digestion in persons with normal gastrointestinal tract function in case of poor nutrition (consumption of fatty foods, large amounts of food, irregular meals) and with disorders of chewing function, sedentary lifestyle, prolonged immobilization. Remheld’s syndrome (gastrocardia syndrome).

Preparing for radiological examination and ultrasound of the abdominal cavity.

Active ingredient

Composition

metacrylic acid and ethylacrylate copolymer [1:1] (as a 30% dispersion, additionally containing polysorbate-80, sodium lauryl sulfate) -25.3 mg/63.2 mg, triethylcitrate-5.1 mg/12.6 mg, simethicone emulsion 30%, dry weight (32.6%) – 0.1 mg/0.3 mg including: dimethicone -27.8%; silicon colloid precipitated -1.3%; silicon colloid suspended -0.9%; methylcellulose -2.5%; sorbic acid -0.1%, water -67.4%, talc -12.6 mg/31.6 mg.

Capsule shell composition:

How to take, the dosage

The dose of the drug is adjusted individually depending on age, severity of symptoms, and dietary composition. The dose is adjusted using the registered drugs Micrasym® 10,000 units and Micrasym® 25,000 units.

The capsules are taken orally with plenty of non-alkaline liquid (water, fruit juices). If a single dose of the drug is more than 1 capsule, half of the total number of capsules should be taken immediately before a meal, and the other half with a meal. If the single dose is 1 capsule, it should be taken with a meal.

If swallowing is difficult (e.g., in children or the elderly), the capsule may be opened and the drug taken directly in pellets, previously mixed with liquid or liquid foods (pH< 5.0) that do not require chewing (apple puree, yogurt). Grinding or chewing the pellets or adding them to foods with a pH higher than 5.5 will destroy their gastric juice-protective shell. Any mixture of pellets with food or liquid should be taken immediately after preparation.

The allowable dose for children under 1.5 years of age is 50,000 IU/day; over 1.5 years of age, 100,000 IU/day.

The duration of pancreatin can vary from a few days (digestive disorders) to several months or years (long-term replacement therapy).

Pancreatine replacement therapy for various types of exocrine pancreatic insufficiency.

The dose is chosen individually and depends on the severity of external pancreatic secretory insufficiency, the individual eating habits, and the age of the patient.

Steatorrhea (more than 15 g of fat in stools per day).

If there is diarrhea, weight loss, and no effect of diet therapy, 25,000 IU of lipase is prescribed with each meal. If necessary and if well tolerated, the dose is increased to 30,000 to 35,000 IU of lipase per meal. Further dose increases, in most cases, do not improve treatment outcomes and require reassessment of the diagnosis, reduction in dietary fat content and/or additional prescribing of proton pump inhibitors.

In mild steatorrhea that is not accompanied by diarrhea and weight loss, 10,000 IU to 25,000 IU of lipase per administration is indicated.

Mucoviscidosis.

The initial estimated dose for children under 4 years of age is 1,000 IU of lipase per kilogram of body weight at each meal; for children over 4 years of age, 500 IU of lipase per kilogram of body weight at each meal. The dose should be selected individually, depending on the severity of the disease, severity of steatorrhea and nutritional status. The maintenance dose for most patients should not exceed 10,000 IU of lipase per kilogram of body weight per day.

Interaction

Special Instructions

Children and adults receiving pancreatin therapy at high doses for a long time should be monitored by a specialist.

The main causes of ineffectiveness of enzyme therapy are: inactivation of enzymes in the duodenum as a result of acidification of its contents; concomitant diseases of the small intestine (worm infestations, dysbiosis); non-compliance with the recommended regimen by patients; use of enzymes that have lost their activity.

Contraindications

Side effects

Overdose

Symptoms: increased uric acid in the urine (hyperuricuria) and blood (hyperuricemia). In children – constipation.

Treatment: withdrawal of the drug, symptomatic therapy.

Pregnancy use

Similarities