Duspatalin 200 mg 30 pcs. extended release capsules

Duspatalin relieves pain caused by spasms of the intestinal muscles. Helps speed up the treatment of irritable bowel syndrome, and also significantly reduces the risk of relapse. Having a pronounced antispasmodic effect, Duspatalin does not cause hypotension of the smooth muscles of the gastrointestinal tract.

general characteristics

Duspatalin is produced in Holland. You can purchase the drug in the form of tablets of 135 g and capsules of 200 mg. The capsule form contains a larger amount of the main active ingredient compared to tablets. Due to this, you can achieve a long-lasting effect from taking the drug. Therefore, on the packaging of capsules there is the word “retard”, which means “slow down” in English.

The capsules are covered with a dense gelatin-based shell; each capsule contains white granules. Markings on capsules: “245”, “S”, “7”. You can purchase packages containing 10, 20, 30, 50, 60 and 90 capsules.

The tablets are round in shape and white in color. They can be purchased in the same quantities as capsules, and also in packs of 15, 40, 100 and 120 pieces.

Regardless of the release form, the main active ingredient remains the same - mebeverine. However, the auxiliary components in capsules and tablets are different. Their comparative characteristics are presented in the table.

Effect of taking

Taking Duspatalin allows you to relieve spasm from the smooth muscles of the digestive organs. This occurs by eliminating tension, which provokes pain. Since the intestines contain the most smooth muscles, the drug has the most pronounced effect on it. Elimination of hypertonicity occurs without affecting the peristalsis of the organ. Therefore, feces pass through the intestines without any slowdown. That is, Duspatalin has a targeted effect on the smooth muscles of the intestine, eliminating pain. At the same time, the sphincter of Oddi relaxes, which normalizes the flow of bile and provides an analgesic effect for biliary colic.

If the activity of intestinal smooth muscles is increased, then taking Duspatalin will bring it back to normal. However, the peristalsis of the organ will not be completely stopped, that is, its reflex hypotension will not occur.

After passing the drug through the organs of the digestive system, it enters the intestines, from where it is transported through the bloodstream to the liver. There, certain biochemical reactions are triggered, and the medicinal substance breaks down into metabolites. In this form, it is excreted from the body in urine. The main active substance is not released from the capsule as quickly as from tablets, so the therapeutic effect is extended for 16 hours. Moreover, for this it will be enough to take the drug once.

Duspatalin: what kind of medicine is it?

Duspatalin is an antispasmodic agent, the effect of which is mainly directed on the smooth muscles of the intestine. At the same time, there will be no effect on the normal functioning of the digestive organ, so the drug does not cause relaxation of the gastrointestinal tract tissues. In addition, Duspatalin has an anesthetic effect on the gastrointestinal tract.

The drug is taken for pain associated with intestinal dysfunction. Duspatalin acts symptomatically. That is, it does not treat the disease that caused the intestinal spasm, but only relieves the symptom - relaxes the smooth muscles where it is necessary, without affecting healthy areas of the intestine. This pain is especially typical during sudden attacks of diarrhea, when intestinal spasms and cramps interfere with a normal lifestyle. At the same time, Duspatalin can stop frequent and loose stools, reducing chaotic intestinal activity, which accelerates the process of movement of feces along its entire length.

When should Duspatalin be used?

Indications for taking the drug:

• Spasm-type pain localized in the epigastric region.
• Intestinal and biliary colic.
• Irritable bowel syndrome.
• Disturbances in the functioning of the gallbladder.
• Underwent surgery for resection of the gallbladder.
• Spasms of the smooth muscles of the digestive system against the background of pathologies of other organs (pain due to pancreatitis or cholecystitis).
• Pain caused by a functional disorder of the digestive system.
• Pain, discomfort and spasm in the intestines of a different etiology.

Which is better: Duspatalin or Drotaverine

Drotaverine, like Duspatalin, is an antispasmodic that affects smooth muscles. On the shelves, Drotaverine is often hidden under the trade name No-shpa. This drug is prescribed for certain types of pain caused by cholecystitis, cholangitis, pyelitis and cystitis. But, unlike Duspatalin, Drotaverine dilates blood vessels. Its spectrum of action is not limited to the smooth muscles of the gastrointestinal tract.

No-spa is prescribed to pregnant women with a threat of premature birth, if there is increased uterine tone. In addition, I use the drug during labor if delivery is prevented by spasm of the uterine pharynx.

A contraindication for taking Drotaverine is lactase deficiency, so in such patients it is better to relieve spasms of the intestines and other gastrointestinal organs with products that do not contain lactose among the auxiliary elements.

Contraindications for Duspatalin include, in addition to childhood and intolerance to the components, pregnancy. The same cannot be said about Drotaverine: it is prescribed to pregnant women, however, despite the stated safety, expectant mothers must coordinate the use of any medications with their local obstetrician-gynecologist.

Instructions for use

Duspatalin in tablet form

The drug is not crushed before oral administration, washed down with plain water. You should take the medicine 30 minutes before meals.

It is permissible to take three tablets per day: in the morning, at lunchtime and in the evening. You should stop taking the drug after you feel better, that is, as soon as the pain stops.

The drug should not be discontinued abruptly. You must adhere to the following scheme:

• The first 7 days of withdrawal: take the drug 1 tablet in the morning and at lunch, and drink 1/2 tablet in the evening.
• From days 7 to 14, drink a whole tablet in the morning and evening.
• From days 14 to 21, take a whole tablet in the morning, and 1/2 of the drug in the evening.
• From days 21 to 28, take the drug 1 tablet in the morning.

According to this scheme, leading domestic clinicians who treat diseases of the digestive system suggest discontinuing the drug.

Depending on the specific case, the withdrawal regimen may be reviewed by the treating doctor. So, if after reducing the dose of the drug, the patient feels well, then it is possible to reduce the withdrawal regimen to 14 days. If the patient feels unsatisfactory when the dose is reduced by 1 tablet, then it should be reduced by 1/2 tablet. The patient's well-being should be monitored for at least 2 days.

Most experts recommend reducing the dosage by 1/2 tablet. If there is a need for faster withdrawal of the drug, then after 2 days you can again reduce the dosage by 1/2 tablet. Provided that the patient’s well-being does not deteriorate, this regimen should be continued until the end of the week (counting from the first day of dose reduction). If the patient begins to feel worse, then they switch to the classic scheme of stopping the drug. If the trend is positive, you can continue. That is, at the beginning of each subsequent week you will need to reduce the dose by 1/2 tablet, and after 2 days by another 1/2 tablet.

Abrupt withdrawal of the drug is unacceptable.

Duspatalin capsules

Do not chew the capsules, swallow them whole with plain water. The drug is taken 20 minutes before meals, 2 times a day.

The course of treatment is determined by the complete disappearance of pain and spasms. After this, you can begin to gradually reduce the dosage of the drug. Just like tablets, capsules should not be abandoned abruptly. The dosage should be reduced gradually. Drug withdrawal regimen:

1. For the first 7-14 days, you need to take 1 capsule in the morning.
2. After 7-14 days, you must stop taking the medicine.

To decide how long before you should stop taking the capsules - 7 or 14 days in advance, you need to take a two-day break after taking 1 capsule per day for a week. If during this time your health does not worsen, then you can completely refuse further treatment. Provided that the patient begins to feel worse, the course of therapy is extended for another 7 days, continuing to take 1 capsule in the morning. Then the drug is abandoned altogether.

Overdose

If a person takes too large a dose of the drug, this will lead to increased nervous excitability. To neutralize the effect of the drug, you should rinse your stomach and take activated charcoal orally. In the future, the patient is indicated for symptomatic treatment.

Concomitant use with other drugs

Duspatalin can be taken simultaneously with other medications.

It should be noted that Duspatalin can cause dizziness, so during the therapeutic course it is highly advisable to abandon activities that require increased concentration.

Duspatalin 200 mg 30 pcs. extended release capsules

pharmachologic effect

Antispasmodic, myotropic.

Composition and release form Duspatalin 200 mg 30 pcs. extended release capsules

Long-acting capsules - 1 capsule:

• Active ingredients: mebeverine hydrochloride - 200 mg;
• Excipients: magnesium stearate - 13.1 mg; methacrylic acid copolymer - 10.4 mg; talc - 4.9 mg; hypromellose - 0.1 mg; copolymer of methacrylic and ethacrylic acids - 15.2 mg; glycerol triacetate - 2.9 mg;
• Hard gelatin capsule: gelatin - 74.2 mg; titanium dioxide (E171) - 1.8 mg.

There are 15 pcs in a blister; There are 2 or 3 blisters in a cardboard pack.

Description of the dosage form

Hard gelatin capsules No. 1, opaque, white with markings: “245” on the capsule body, “S” and “7” on the capsule cap. The contents of the capsules are white or almost white granules.

Directions for use and doses

Orally, 20 minutes before meals, without chewing and with water, 200 mg 2 times a day (morning and evening).

Pharmacodynamics

Antispasmodic myotropic action, has a direct effect on the smooth muscles of the gastrointestinal tract (mainly the large intestine). Eliminates spasm without affecting normal intestinal motility. Does not have anticholinergic effects.

Pharmacokinetics

When taken orally, it undergoes presystemic hydrolysis and is not detected in plasma. Metabolized in the liver to veratric acid and mebeverine alcohol. It is excreted mainly by the kidneys in the form of metabolites, in small quantities with bile. Mebeverine capsules have sustained release properties. Even after repeated administration, no significant accumulation is observed.

Indications for use Duspatalin 200 mg 30 pcs. extended release capsules

In adults:

• spasm of the gastrointestinal tract (including those caused by organic disease);
• intestinal and biliary colic;
• irritable bowel syndrome.

For children over 12 years of age:

• functional gastrointestinal disorders accompanied by abdominal pain.

Contraindications

Hypersensitivity to any component of the drug.

Application of Duspatalin 200 mg 30 pcs. extended-release capsules during pregnancy and lactation

In animal experiments, no teratogenic effect was detected. When prescribing the drug during pregnancy, it is necessary to balance the benefits for the mother and the potential risk for the fetus. In therapeutic doses, mebeverine does not pass into breast milk, so it can be used during breastfeeding.

special instructions

During the treatment period, care should be taken when driving vehicles and while engaging in potentially hazardous activities that require increased concentration and speed of psychomotor reactions.

Overdose

Symptoms: increased excitability of the central nervous system (theoretically).

Treatment: gastric lavage, symptomatic therapy. A specific antidote is unknown.

Side effects Duspatalin 200 mg 30 pcs. extended release capsules

Rarely - dizziness, extremely rarely - urticaria, Quincke's edema, facial edema and exanthema.

Treatment of children with Duspatalin

Duspatalin is contraindicated for those under 12 years of age.

If the child is already 12 years old, the doctor may prescribe him Duspatalin to eliminate spasms and pain in the intestines and other organs of the digestive system.

Doctors recommend taking the drug for children with the following disorders:

• Heaviness and pain in the abdomen.
• Intestinal colic.
• Abdominal pain due to overeating.
• Abdominal pain caused by nervous tension.
• Irritable bowel syndrome in a child.
• Pain due to dietary errors. So, if a teenager suffers from abdominal pain due to a functional digestive disorder (the child ate a lot of baked goods, fast food or drank a lot of carbonated water), then he should immediately take a Duspatalin capsule. Another capsule is taken in the evening. The next day, treatment can be stopped, provided that your health has stabilized. If the child continues to feel unwell, the drug can be continued. When treatment is delayed for more than 7 days, the drug will need to be discontinued gradually, according to the scheme recommended for an adult.

So, only a doctor can prescribe courses of Duspatalin to a child. As a rule, this treatment regimen is rarely practiced. It is indicated for disturbances in the outflow of bile. Until the child's condition stabilizes, he will need to take two capsules of the drug per day. The withdrawal of the drug lasts for 10 days, during which time the child receives 1 capsule per day. Then they stop taking the medicine altogether.

Taking Duspatalin during pregnancy

Antispasmodics are prescribed during pregnancy with increased uterine tone. For this purpose, women are prescribed No-shpa. However, when a spasm passes to the smooth muscles of the intestines, it is better to use Duspatalin. With uterine hypertonicity, this drug will be ineffective.

Duspatalin should also be used during pregnancy if spasm of the sphincter of Oddi is observed. This leads to impaired bile flow and abdominal pain.

Studies have been conducted regarding the effects of Duspatalin on the fetus. During the experiments, it was possible to establish that the drug does not have a negative effect on the child in the womb. Therefore, if a doctor recommends taking a drug during pregnancy, then the benefits of its use outweigh all possible risks. Self-prescription of Duspatalin is unacceptable; consultation with a specialist is mandatory.

During pregnancy, you can only take capsules; tablets are strictly contraindicated during this period. You should not combine Duspatalin with other antispasmodics, for example, Papaverine or No-shpa.

The dose for pregnant women per day is 2 capsules. One of them is taken in the morning, and the second in the evening. The course of treatment continues until there is a noticeable improvement in well-being. The drug is discontinued gradually; for this purpose, drink 1 capsule per day for 14 days. After 14 days, the drug is completely stopped.

Duspatalin is often prescribed to women who, even before conceiving a child, suffered from spasms of the sphincter of Oddi. Often this condition accompanies chronic inflammation of the pancreas or occurs after surgery for resection of the gallbladder.

If a woman experiences a spasm of the smooth muscles of the intestine due to emotional stress, or as a result of errors in the diet, then you can take the medicine once. The cancellation scheme is not practiced in this case.

Duspatalin

Duspatalin (active ingredient mebeverine) is an antispasmodic drug used in gastroenterological practice for various types of pain, spastic phenomena and discomfort in the intestines. The drug has a direct myotropic effect on the smooth muscle framework of the gastrointestinal tract (primarily the large intestine). The pharmacological effect of duspatalin is based on the blockade of sodium channels in the membrane of muscle cells (as a result of which the penetration of sodium and calcium ions into them is impaired), inhibition of membrane depolarization processes, which ultimately prevents muscle contractions. Against this background, the smooth muscles of the digestive tract relax and spasms are eliminated. As for normal intestinal motility, the drug does not have any effect on it, which, of course, is its undeniable advantage. Duspatalin does not have an anticholinergic effect.

Duspatalin is available only in dosage forms for internal use: tablets and capsules, which should be taken whole along with a sufficient amount of liquid. The standard schedule for taking duspatalin: 1 capsule/tablet three times a day (in capsules - twice a day) 20 minutes before meals.

There are no restrictions on the duration of taking the drug. If for certain reasons a scheduled dose of the drug was missed, you should not “act out” by taking several single doses at a time. In this case, it is recommended to continue taking duspatalin as usual.

The drug has virtually no contraindications. This statement is also true regarding its use during pregnancy and breastfeeding, however, in this case, doctors make a reservation that it is always necessary to balance the expected benefits of taking the drug for the mother and the potential risks of unexpected side effects for the fetus. In any case, the final decision should be made by a specialist. As for lactation (breastfeeding), the use of duspatalin during this period does not entail any threat, because the drug is not able to pass into breast milk. Cases of duspatalin overdose have not been described in the medical literature to date, but in such cases it is theoretically possible to increase the reactivity of the central nervous system. In these situations, intestinal lavage and therapeutic correction of overdose symptoms are indicated.

Taking Duspatalin for pancreatitis

Duspatalin is an effective means of eliminating pain due to pancreatitis. This process is always accompanied by a violation of the outflow of pancreatic juice and spasm of the sphincter of Oddi. This problem can be solved by taking Duspatalin.

Due to inflammation of the pancreas, the excretory ducts become spasmodic, and juice is released in large quantities. As a result, the iron begins to digest itself with its own enzymes. To prevent this situation, it is necessary to expand the excretory ducts, relieving the spasm from them. It is Duspatalin that copes with this problem better than other antispasmodics.

The drug is prescribed for minor exacerbation of pancreatitis, which improves the patient’s well-being. For treatment, capsules are used, taking 1 capsule twice a day (morning and evening).

Treatment should continue until the patient's condition has stabilized. Then the drug is gradually withdrawn.

Duspatalin can also be used to prevent exacerbation of inflammation of the pancreas, provided that the disease is chronic. To do this, take 1 capsule 2 times a day for 14 days, and then take one capsule a day for another 7 days. In the future, the use of the drug is completely abandoned.

Is it possible to take Duspatalin for pancreatitis?

Pancreatitis is a disease of the pancreas in which the process of releasing enzymes into the duodenum, intended for the breakdown of fats and carbohydrates, is disrupted. Without coming into contact with food, and remaining in the body or ducts of the pancreas, enzymes begin to destroy the organ that produces them. Which leads to severe pain, in addition to the dangerous consequences of the release of decay products through the bloodstream into other organs.

The cause of impaired enzyme release may be dysfunction of the sphincter responsible for their release into the duodenum. Duspatalin, by relaxing the muscles of the tight sphincter, can facilitate the process of emptying the pancreas, which will improve the functioning of the gastrointestinal tract. In addition, the drug has an analgesic effect, which is very helpful for acute pain in the left hypochondrium.

Side effects of the drug

Side effects when taking the drug occur extremely rarely. A study was conducted involving 8 antispasmodics that are used to treat irritable bowel syndrome. During the experiment, it was possible to establish that Duspatalin, of all drugs, produces fewer side effects.

However, some patients may experience the following problems:

• Dizziness;
• Skin rashes;
• Quincke's edema and facial swelling;
• Allergy in the form of exanthema;
• Skin itching;
• Headache;
• Diarrhea or constipation;
• Nausea.

Analogs

Russian pharmaceutical companies produce analogues and synonyms of the drug Duspatalin. Synonymous drugs contain mebeverine, while analogues have different components, but a similar therapeutic effect.

Drugs synonymous with Duspatalin:

• Niaspam in capsules.
• Sparex in capsules.
• Mebeverine in tablet form.

Duspatalin analogues:

• Trigan in the form of tablets and in the form of injections for intramuscular administration.
• Trimedat tablets.
• Spascuprel in tablets.
• Dibazol tablets.
• Buscopan tablets.
• Bendazole tablets.
• Dicetel in tablets.
• No-spa in tablets.
• Drotaverine tablets.
• Papaverine tablets.

Inexpensive analogues of Duspatalin

Duspatalin analog drugs for the treatment of irritable bowel syndrome at a lower price: Sparex, Trigan and Niaspam.

If we consider inexpensive antispasmodics, then these include: Drotaverine, No-shpa, Papaverine, Dicetel.

Reviews

Patients who received Duspatalin leave more positive reviews about it. They indicate that the drug allows you to quickly cope with intestinal and stomach colic, eliminate functional digestive disorders, and abdominal pain after overeating.

Patients with irritable bowel syndrome note that Duspatalin makes it possible to get rid of pain, regulate bowel movements, and reduce bloating. Patients receiving antibacterial treatment often suffer from dysbiosis, which causes severe abdominal pain. Duspatalin copes well with this problem. The pain begins to subside within half an hour after the first dose of the drug. Moreover, the capsules have a prolonged action.

Duspatalin has positive reviews from patients suffering from inflammation of the pancreas and gallbladder. The drug quickly relieves spasm, which leads to normalization of the patient's condition. Even with exacerbation of pancreatitis and cholecystitis, pain can be completely managed within 2-3 days. Patients with chronic pathologies take Duspatalin for preventive purposes and note its high effectiveness in preventing the development of relapses.

Negative reviews about Duspatalin are extremely rare. They boil down to the fact that the drug did not eliminate pain during exacerbation of inflammation of the pancreas or gall bladder. However, you should not expect a lightning-fast solution to the problem, since pain relief should take 2-3 days, not several hours. Therefore, such reviews can be considered not entirely justified.

Some people become disillusioned with the drug and take it inappropriately. Patients often indicate that Duspatalin did not help cope with gastritis or stomach ulcers. But this medicine is not intended to treat these diseases. Duspatalin is an antispasmodic and its main effect is to reduce pain.

Reviews from experts

Practicing gynecologists note that Duspatalin allows you to get rid of intestinal colic in pregnant women, regardless of the nature of their occurrence.

Therapists and gastroenterologists indicate that Duspatalin can be successfully used in the treatment of irritable bowel syndrome, pancreatitis, cholecystitis, as well as to get rid of negative symptoms that arise from functional digestive disorders.

Doctors indicate that Duspatalin cannot be used as a monocomponent for pancreatitis. The drug should be part of a complex therapy regimen. Otherwise, it will not be possible to achieve recovery.

Duspatalin in the treatment of functional diseases of the intestine and biliary tract

P

The first international classification of functional diseases of the gastrointestinal tract was presented at the XIII Gastroenterological Congress in 1988 in Rome.
It was then that the term irritable bowel syndrome was first officially approved and clinical criteria for its diagnosis were given. Irritable bowel syndrome (IBS) code K 58. according to the International Classification of Diseases (ICD X) - disorders of the motor and secretory function of the intestines, characterized by the presence of pain or abdominal discomfort for 12, not necessarily consecutive weeks over the last 12 months in combination with two of the following three signs: stop after defecation;
associated with changes in stool frequency; associated with changes in the shape of feces . This includes: IBS with diarrhea (code K 58.0), IBS without diarrhea (code K 58.9) and IBS with constipation (code K 59.0). Despite the heterogeneity of IBS, previous acute intestinal infections with the development of intestinal dysbiosis play a significant role in its occurrence.

And the greatest interest, especially in surgical clinics, is in conditions after cholecystectomy, accompanied by a violation of the functional state of the biliary tract. Over the past decades, the incidence of calculous cholecystitis has acquired a steady upward trend. Cholecystectomy has become the most common operation after appendectomy. More than 110 thousand operations are performed per year in Russia. According to various authors, 20–40% of patients who have undergone cholecystectomy still have complaints related to pain and dyspeptic disorders, which are usually regarded as postcholecystectomy syndrome: code K 91.5. according to the International Classification of Diseases (ICD X).

It should be noted that postcholecystectomy syndrome

is a collective concept that unites various pathological conditions and associated clinical manifestations observed in patients after removal of the gallbladder. Most authors who have studied this problem consider the term used to be not entirely successful. The term postcholecystectomy syndrome is currently used to designate dysfunction of the sphincter of Oddi (SDO) that develops after surgery, caused by a violation of the tone of the sphincter of the common bile duct, pancreatic duct or common sphincter, preventing the normal outflow of bile and pancreatic secretions into the duodenum in the obligatory absence of organic obstacles. In this regard, correct interpretation of pathophysiological disorders in the functioning of the sphincter apparatus of the biliary tract is important for making a diagnosis.

Despite intensive research and the search for new pharmacological groups of drugs for the treatment of irritable bowel syndrome and dysfunctional diseases of the biliary tract, the leading role in the treatment of abdominal pain in these diseases belongs to myotropic antispasmodics

. Numerous clinical studies have proven the effectiveness and good tolerability of myotropic antispasmodics for functional diseases of the intestine and biliary tract. However, the pharmacological group of myotropic antispasmodics is heterogeneous, and when choosing a drug, its mechanism of action should be taken into account, since abdominal pain is very often combined with other clinical symptoms, primarily flatulence, constipation and diarrhea.

Duspatalin (mebeverine hydrochloride) turned out to be the drug of choice in the treatment of these functional disorders.

. The main clinical advantage of Duspatalin is that it is indicated for patients with abdominal pain of functional origin, which is accompanied by both constipation and diarrhea, since the drug has a normalizing effect on intestinal function.

Mebeverine is a drug with an antispastic effect that has affinity for muscle tissue. It is used for the symptomatic treatment of abdominal pain, distress and discomfort associated with irritable bowel syndrome and sphincter of Oddi dysfunction. Mebeverine is also used to relieve spasms in various parts of the gastrointestinal tract due to its organic lesions.

The drug was first registered in 1965. Since then, it has been prescribed to (on average) 6.5 million patients per year worldwide. Mebeverine is currently sold in 74 countries under the trade names Colafac®, Duspatal®, Duspatalin®, Colospa®, Colotal® or Rudakol®.

It is widely recognized that double-blind, placebo-controlled clinical trials are absolutely essential when evaluating treatments for IBS and sphincter of Oddi dysfunction, given the high response rates to placebo (Cann, 1989). Over the past thirty-odd years, the effects of mebeverine have been studied in several double-blind, placebo-controlled clinical trials, including Connell (1965), Tasman-Jones (1973), Berthelot & Centonze (1981) and Prout (1983). The drug was also evaluated in comparison with standard drugs such as alverine citrate (Tudor, 1986), fenoverine (Salandre & Mignon, 1989) and dicycloverine (Grillage et al., 1990).

Mebeverine was statistically more effective than placebo in relieving abdominal pain and bowel dysfunction. Mebeverine has also proven effective in comparison with other antispastic agents.

Data on the safety and tolerability of the drug were obtained from clinical studies involving more than 3,500 patients taking mebeverine. The drug was always well tolerated by patients, even when using doses exceeding therapeutic ones. Most authors reported literally no side effects with treatment. The autonomic nervous system is not involved in the mechanism of action of mebeverine, therefore the drug in therapeutic doses does not have typical anticholinergic side effects. This makes it possible to use the drug in patients with concomitant diseases such as prostatic hypertrophy, urinary retention or glaucoma.

The most common drug in Russia is Duspatalin.

. A special feature of the drug is that smooth muscle contractions are not completely suppressed by mebeverine, which indicates the preservation of normal peristalsis after suppression of hypermotility. Indeed, there is no known dose of mebeverine that completely inhibits peristaltic movements, i.e. would cause hypotension.

Experimental studies show that mebeverine has two effects. First, the drug has an antispastic effect, reducing the permeability of smooth muscle cells to Na+. Secondly, it indirectly reduces the outflow of K+ and, accordingly, does not cause hypotension.

Contraction of smooth muscles of the gastrointestinal tract occurs when acetylcholine stimulates muscarinic receptors on the surface of the muscle cell. This causes sodium channels in the membrane to open, allowing Na+ to enter the cell. The resulting depolarization of the cell, in turn, promotes the opening of calcium channels and the entry of Ca2+ into the cell. The increased intracellular Ca2+ level leads to phosphorylation of myosin and, accordingly, to muscle contraction.

At therapeutic doses, mebeverine has a direct blocking effect on sodium channels, which limits the influx of Na+ and prevents the sequence of events leading to muscle spasm.

In addition to muscarinic receptors, smooth muscle cells in the wall of the gastrointestinal tract also have α1-adrenergic receptors associated with Ca2+ stores. This depot, located on the cell membrane, constantly restores the level of Ca2+ from the extracellular environment. Stimulation of the receptor by norepinephrine leads to the mobilization of Ca2+ from this depot into the intracellular space - a process that causes the opening of the channel for K+, which leads to hyperpolarization and decreased tone.

Mebeverine blocks the filling of the depot with extracellular Ca2+. Thus, if the a1-adrenergic receptor is activated in the presence of the drug, the depot is emptied, but cannot be filled again. Accordingly, the outflow of K+ is short-lived and permanent relaxation or hypotension does not occur.

Research into the effectiveness of Duspatalin in the treatment of functional bowel disorders has been conducted almost since its entry into the market. Data on the most authoritative studies are shown in Table 1.

The general conclusion of many authors after the study can be briefly summarized as follows: “The results obtained with mebeverine treatment are statistically significantly superior to the results obtained with placebo (p < 0.05)” (Tasman-Jones, 1973) or “In only 30 days, mebeverine resulted in to almost complete remission of abdominal pain and flatulence" (Secco et al., 1983). The results are presented in Figure 1.

Rice. 1. Evaluation of the effectiveness of mebeverine in the treatment of irritable bowel syndrome compared with placebo

The high effectiveness of mebeverine in the treatment of irritable bowel syndrome and sphincter of Oddia dysfunction has been noted in a number of other studies; the effectiveness of the drug in reducing pain and flatulence is presented in Figure 2.

Rice. 2. Efficacy of mebeverine in the treatment of IBS and sphincter of Oddi dysfunction

All research data on the effectiveness of mebeverine and comparing its effectiveness with placebo are statistically reliable, which proves
the need to choose Duspatalin for the treatment of spastic conditions and functional disorders of the gastrointestinal tract
.

A very important positive property of the drug is its low toxicity. Safety and tolerability data were obtained from clinical studies involving more than 3,500 patients treated with mebeverine.

In all studies, mebeverine was well tolerated by patients. Hematological and biochemical parameters remained unchanged throughout the course of treatment. Since the drug's introduction in 1965, no serious side effects have been reported. In an analysis of studies of drugs commonly used in the treatment of IBS and DSO, mebeverine ranked first in the absence of side effects (Poynard et al., 1994).

In most clinical studies of mebeverine, there was no mention of competitive symptoms occurring. This gives the drug a significant advantage over standard anticholinergic drugs, which, to obtain a therapeutic effect, must be prescribed in doses that act not only on the target organ, but also on other parts of the body.

Tasman-Jones (1973) noted that “the absence of anticholinergic properties is clearly an advantage; not only because the patient does not have unpleasant side effects, such as dry mouth, visual disturbances and constipation, but also because mebeverine is not contraindicated in patients with glaucoma and prostatic hypertrophy.”

Studies that used higher than standard doses also do not report a significant increase in side effects. Available data from the use of mebeverine at doses of 800 mg, 810 mg or 600 mg per day confirm that there were no clinically significant changes in safety parameters (Kastein, 1988; Van Outryve et al., 1996). Most patients tolerated these doses without experiencing noticeable side effects.

Thus, given the numerous studies on the use of mebeverine, some researchers suggest monotherapy with Duspatalin for such serious conditions as sphincter of Oddi dysfunction after cholecystectomy

(Ilchenko A.A., 2002). It was shown that after 2 weeks of Duspatalin therapy in patients who underwent cholecystectomy and have dysfunctional disorders of the sphincter apparatus of the biliary tract, there was a positive trend in pain relief, as well as normalization of both laboratory and ultrasound parameters.

The results obtained allow us to recommend Duspatalin to patients with various types of sphincter of Oddi dysfunction, both as monotherapy and in combination with other drugs. If necessary, it can be combined with antibacterial, enzyme preparations, as well as prokinetics. The undoubted advantage of the drug is the fact that it has a direct, almost selective antispastic effect on the smooth muscle tissue of the gastrointestinal tract. The exception is patients with organic lesions: choledocholithiasis; not eliminated or newly emerged stenosis of the large duodenal papilla and the distal part of the common bile duct.

A significant improvement in the condition is observed when treating irritable bowel syndrome with Duspatalin (Minushkin O.N., 2001), expressed in the disappearance or reduction of pain in patients by the 7th day of therapy. By day 14, pain was completely relieved in 60% of patients and significantly decreased in intensity and duration in 26.6% of patients. Abdominal bloating disappeared by day 7 of treatment. After 2 weeks, a clear trend toward normalization of stool frequency and consistency during diarrhea was noted. Heaviness in the right hypochondrium and discomfort in the epigastrium, noted in 16 patients, disappeared in 90% of patients.

After 2 weeks of treatment with Duspatalin, colon motility normalized in 50% of patients, and a tendency toward a decrease in increased motor activity appeared. In patients with diarrhea, the passage time through the gastrointestinal tract increased. The time of the carbolene test before treatment was 17.5 hours, after 2 weeks of treatment – ​​28.0 hours.

Thus, Duspatalin is a highly effective drug

in the treatment of irritable bowel syndrome and sphincter of Oddi dysfunction.

conclusions

1. The drug Duspatalin effectively relieves symptoms associated with impaired motor function of the intestines and biliary tract.

2. Duspatalin can be actively used to influence the main symptoms of functional disorders of the gastrointestinal tract, pain and spasm, flatulence, as a violation of the tone of the intestinal wall, and disturbances in the frequency and consistency of stool.
Literature:
1. Grigoriev P.Ya. Recommendations (protocols) for the diagnosis and treatment of patients with diseases of the digestive system. Practicing physician today. Gastroenterology series. 2002, No. 1, p. 3 – 34.

2. Dadvani S.A., Vetshev P.S., Shuludko A.M., “Cholelithiasis,” M., 2000, pp. 114–115.

3. Ilchenko A.A. Dysfunctional disorders of the biliary tract // Consilium medicum. (Appendix. Gastroenterology.) 2002. No. 1. pp. 20–23.

4. Kolesnikov L.L. Human sphincter apparatus. St. Petersburg, 2000. P. 99.

5. Minushkin O.N., Elizavetina G.A., Ardatskaya M.D. Treatment of functional disorders of the intestines and biliary system, occurring with abdominal pain and flatulence // Klin. Pharmacol. and ter. 2002. No. 1. P. 1–3.

6. Nozdrachev A.D., Bazhenov Yu.I., Barannikova I.A., Batuev A.S. – Beginnings of Physiology – St. Petersburg, Lan.2001.

7. Evans P., Bak., Kellow J. Mebeverine alters small bowel motility in irritable bowel syndrome // Aliment. Pharmacol. Ther. 1996. No. 10. R. 773.

What to choose: Duspatalin or Trimedat?

Trimedat and Duspatalin have a similar therapeutic effect, since both of these drugs relieve muscle spasm. The difference is that Trimedat has a wider spectrum of action compared to Duspatalin, so it is used to treat severe pathologies of the digestive system. If the patient has chronic pancreatitis or cholecystitis, or an exacerbation of the disease occurs, then Duspatalin can be taken.

In any case, the doctor must prescribe this or that drug, based on the individual characteristics of the patient’s body. Trimedat is more suitable for some patients, and Duspatalin for others.

What to choose: Duspatalin or Dicetel?

Dicetel has a less pronounced effect compared to Duspatalin. The drug will not completely relieve spasm from the ducts of the pancreas and gallbladder, which occurs against the background of inflammation of these organs. In addition, taking Dicetel is associated with a greater risk of developing allergic reactions than taking Duspatalin.

However, if a person has a digestive disorder caused by an irrational approach to nutrition, Dicetel can be used. In this case, the drug will cope well with the task of pain relief.

Is it possible to take Duspatalin for gastritis?

Gastritis is an inflammation of the gastric mucosa, which can be caused by various reasons. If the disease is of bacterial or fungal etiology, therapy is prescribed with narrowly targeted antibiotics or antifungal agents that affect the type of pathogenic microorganisms. Duspatalin can be used as an antispasmodic if the disease is accompanied by pain that occurs due to increased tone of the stomach muscles. Taking Duspatalin will not affect the treatment of diagnosed gastritis.