PROURSAN 400 mg Фильм-Coated Таблетки
Рассмотрение рецепта онлайн
Врач рассмотрит ваш случай и примет решение о назначении рецепта, если это медицински оправдано.
Поговорите с врачом об этом лекарстве
Обсудите симптомы и возможные дальнейшие шаги на онлайн-консультации.
Инструкция по применению PROURSAN
Содержание инструкции
Proursan 400 mg film-coated tablets
Ursodeoxycholic acid
Read this leaflet carefully before you start taking this medicine as it contains important information for you.
- Keep this leaflet. You may need to read it again.
- If you have any questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not pass it on to others, even if their symptoms are the same as yours, as it could be harmful.
- If you get any side effects, even those not listed in this leaflet, tell your doctor or pharmacist. See section 4.
Contents of this leaflet
- 1. What Proursan is and what it is used for
- 2. What you need to know before you take Proursan
- 3. How to take Proursan
- 4. Possible side effects
- 5. How to store Proursan
- 6. Contents of the pack and other information
1. What is Proursan and what is it used for
Ursodeoxycholic acid, the active ingredient of Proursan, is a natural bile acid. It is present in
small quantities in human bile.
Proursan is used:
- to dissolve gallstones caused by excess cholesterol in the gallbladder, if the gallstones are not visible with a simple X-ray (X-ray visible gallstones do not dissolve) and do not measure more than 15 mm in diameter. The gallbladder must still be functioning despite the gallstone(s).
- for the treatment of symptoms of primary biliary cholangitis (PBC, a chronic disease of the bile ducts that can progress to cirrhosis of the liver) in patients without decompensated cirrhosis of the liver (a widespread and chronic liver disease, in which poor liver function due to the disease can no longer be corrected),
- for the treatment of liver disease (hepatopathy) related to a disease called cystic fibrosis in children between 6 and 18 years of age.
2. What you need to know before taking Proursan
Do not take Proursan if
- you are allergic to bile acids (such as ursodesoxycholic acid) or to any of the other ingredients of this medicine (listed in section 6),
- you have an acute inflammation of the gallbladder (cholecystitis) and bile ducts,
- you have a blockage of the common bile duct or cystic duct (obstruction of the bile ducts),
- you have frequent cramp-like pains in the upper abdomen (biliary colic),
- your doctor has told you that you have calcified gallstones,
- you have a problem with gallbladder contraction,
- you are a child suffering from biliary atresia and have poor bile flow, even after surgery.
Warnings and precautions
Talk to your doctor or pharmacist before taking Proursan.
For the first 3 months of treatment, your doctor must regularly check liver function,
every 4 weeks. Subsequently, the checks must be repeated every 3 months.
If the medicine is being used to dissolve gallstones, your doctor should prescribe you an examination
to scan your gallbladder after the first 6-10 months of treatment.
If you are taking Proursan to dissolve gallstones, tell your doctor if you are taking
medicines that contain estrogenic hormones, as these medicines stimulate the formation of
gallstones.
When used in the treatment of PBC, in rare cases symptoms may worsen at the beginning of
treatment. If this occurs, contact your doctor to evaluate a reduction of the initial dose.
Immediately inform your doctor if you have diarrhea, as this may require a reduction
of the dose or discontinuation of treatment.
Children and adolescents
Proursan is not suitable for children under 6 years of age due to the tablet dosage.
Other medicines and Proursan
Tell your doctor or pharmacist if you are taking, have recently taken or might take
any other medicines,
as the effect of these medicines may be altered:
A reduction in effectsof Proursan is possible when taken simultaneously with the following
medicines:
- cholestyramine, colestipol (used to lower blood fat levels) or antacids containing aluminum hydroxide or smectite (aluminum oxide) (used to bind stomach acid): If you absolutely need to use a medicine containing any of these substances, you should take it at least two hours before or after Proursan.
A reduction in effectsof the following medicines is possible when taken
simultaneously with Proursan:
- ciprofloxacin and dapsone (antibiotics), nitrendipine (used to treat high blood pressure) and other medicines metabolized in a similar way. Your doctor may need to adjust the dose of these medicines. A change in effectsof the following medicines is possible when taken simultaneously with Proursan:
- cyclosporine (to reduce the activity of the immune system). If you are being treated with cyclosporine, your doctor should check its amount in your blood. If necessary, your doctor will adjust the dose.
- rosuvastatin (for high cholesterol and related diseases).
If you are taking Proursan to dissolve gallstones, tell your doctor if you are taking
medicines that contain estrogenic hormones or agents that reduce blood cholesterol levels, such as
clofibrate. These medicines stimulate the formation of gallstones, which is an effect contrary to
that of treatment with Proursan.
Pregnancy, breastfeeding and fertility
If you are pregnant, suspect you may be pregnant or are planning to become pregnant, or if you are
breastfeeding, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
No data are available regarding the use of ursodesoxycholic acid in pregnant women,
or are limited. Studies conducted in animals have shown reproductive toxicity. Proursan
should not be used during pregnancy unless strictly necessary.
Women of childbearing potential
If you are a woman, you should consult your doctor even if you are not pregnant.
Women of childbearing potential should only be treated if they are using reliable contraceptive methods: the
use of non-hormonal or low-estrogen oral contraceptives is recommended.
However, if you are taking Proursan to dissolve gallstones, you should use effective non-hormonal
contraceptives, as hormonal oral contraceptives may promote the formation of gallstones.
The doctor should rule out the possibility of pregnancy before starting treatment.
Breastfeeding
According to some documented cases of breastfeeding women, levels of ursodesoxycholic acid in
breast milk are very low and adverse reactions in breastfed infants are unlikely.
Fertility
Animal studies have not shown an influence of ursodesoxycholic acid on fertility.
No data are available on the effects on fertility in humans after treatment with ursodesoxycholic acid.
Driving and using machines
No effects on the ability to drive and operate machines have been observed.
Proursan contains sodium (sodium starch glycolate A)
This medicine contains less than 1 mmol of sodium (23 mg) per tablet, i.e. it is essentially
“sodium-free”.
3. How to take Proursan
Take this medicine following exactly the instructions of your doctor or pharmacist. If you have any doubts, ask your doctor or pharmacist.
To dissolve cholesterol stones
Dosage
The recommended dose is approximately 10 mg of ursodeoxycholic acid per kg of body weight (b.w.) per day, as follows:
If you weigh less than 47 kg or are unable to swallow Proursan, other formulations containing ursodeoxycholic acid may be available to you.
Method of administration
Swallow the tablets whole with water or other liquid. Take the tablets in the evening before bedtime. Take the medicine regularly.
Duration of treatment
| 47-50 kg | 1 tablet |
| 51-70 kg | 1 and a half tablets |
| 71-90 kg | 2 tablets |
| 91-110 kg | 2 and a half tablets |
| over 110 kg | 3 tablets |
It usually takes 6-24 months to dissolve the gallstones. If after 12 months there has been no reduction in the size of the gallstones, therapy should be discontinued.
Every 6 months the doctor must check if the treatment is working. On each of these check-up examinations, it must be checked whether the stones have hardened compared to the previous examination, due to an accumulation of calcium. In such a case, the doctor will interrupt the treatment.
For the treatment of primary biliary cholangitis (chronic inflammatory disease of the bile ducts)
Dosage
The daily dose of these film-coated tablets depends on body weight and varies from 1 and a half to 4 tablets.
| Body weight (kg) | Proursan 400 mg film-coated tablets | |||
| first 3 months | afterwards | |||
| morning | midday | evening | evening (1 per day) | |
| 47-50 | half | half | half | 1 and a half |
| 51-62 | half | half | 1 | 2 |
| 63-78 | half | half | 1 and a half | 2 and a half |
| 79-93 | half | 1 | 1 and a half | 3 |
| 94-109 | 1 | 1 | 1 and a half | 3 and a half |
| over 110 | 1 | 1 | 2 | 4 |
If you weigh less than 47 kg or are unable to swallow Proursan, other pharmaceutical forms containing ursodeoxycholic acid (suspension) are available.
Method of administration
Swallow the tablets whole (do not chew) with water or other liquid.
During the first 3 months of treatment, you must take Proursan in the morning, at midday and in the evening.
When liver function values improve, you can take the total daily dose once a day, in the evening. Take the medicine regularly.
Duration of treatment
Treatment with Proursan can be continued indefinitely in case of primary biliary cholangitis
Note
If you suffer from primary biliary cholangitis, symptoms may worsen at the beginning of treatment. For example, you may experience an increase in itching, although this happens only in rare cases. If this occurs, treatment may be continued with a reduced daily dose of Proursan. The doctor will then increase your daily dose every week, until you reach the required dose again.
Use in children and adolescents (6-18 years) for the treatment of liver disease (hepatopathy) related to cystic fibrosis
Dosage
The recommended dose is approximately 20 mg per kg per day divided into 2-3 doses. If necessary, the doctor may further increase the dose to 30 mg per kg of body weight per day.
| Body weight [kg] | Daily dose (mg/kg b.w.) | Proursan 400 mg film-coated tablets | ||
| morning | midday | evening | ||
| 20-24 | 17-20 | half |
| half |
| 25-29 | 21-24 | half | half | half |
If you feel that the effect of Proursan is too strong or too weak, consult your doctor or pharmacist.
If you take more Proursan than you should
In case of overdose, diarrhea may occur. Immediately inform your doctor if you have persistent diarrhea. If you suffer from diarrhea, make sure to drink enough fluids to restore electrolyte balance.
If you forget to take Proursan
Do not take a double dose to make up for a missed dose, but continue treatment with the prescribed dose.
If you stop taking Proursan
Always consult your doctor before deciding to stop treatment with Proursan or to discontinue it prematurely.
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Common side effects(may affect up to 1 in 10 people):
- soft or loose stools or diarrhoea. Very rare side effects (may affect up to 1 in 10,000 people):
- during treatment of primary biliary cholangitis: severe pain in the upper right side of the abdomen, severe worsening of hepatic cirrhosis, which improves partially after discontinuation of treatment,
- hardening of bile stones,
- urticaria.
Reporting of side effects
If you get any side effects, even those not listed in this leaflet, please tell your doctor or pharmacist. You can also report side effects directly through the national reporting system at: https://www.aifa.gov.it/content/segnalazioni-
reazioni-avverse
By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store Proursan
Keep this medicine out of the sight and reach of children.
| 30-39 | 15-20 | half | half | half |
| 40-49 | 20-25 | half | half | one and a half |
| 50-59 | 20-24 | half | 1 | one and a half |
| 60-69 | 20-23 | 1 | 1 | or 1 and a half |
| 70-79 | 20-23 | 1 | one and a half | one and a half |
| 80-89 | 20-23 | one and a half | one and a half | c 1 and a half |
| 90-99 | 20-22 | one and a half | one and a half | 2 |
| 100-109 | 20-22 | one and a half | 2 | a 2 |
| >110 | ≤22 | 2 | 2 | 2 |
This medicine does not require any particular storage conditions.
Do not use this medicine after the expiry date which is stated on the package and blister after
“Expiry”. The expiry date refers to the last day of that month.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to
dispose of medicines you no longer use. This will help protect the environment.
6. Contents of the pack and other information
What Proursan contains
- The active ingredient is ursodeoxycholic acid. Each film-coated tablet contains 400 mg of ursodeoxycholic acid.
- The other ingredients are: tablet core: corn starch, pregelatinized corn starch, sodium starch glycolate A, anhydrous colloidal silica, magnesium stearate, tablet coating: white Opadry 03B28796: hypromellose 6, titanium dioxide, macrogol 400.
Description of Proursan and contents of the pack
Proursan is constituted by film-coated tablets, almost white in colour, round, biconvex, with
a scoring line on both sides, with an average diameter of approximately 12 mm. The tablet can be divided into
equal doses.
Proursan is available in packs of 20, 40, 50, 60, 80 or 100 film-coated tablets.
Not all pack sizes may be marketed.
Marketing Authorisation Holder and Manufacturer
PRO.MED.CS Praha a.s., Telčská 377/1, Michle, 140 00 Prague 4, Czech Republic
This medicinal product is authorised in the Member States of the European Economic Area with the
following denominations:
Italy Proursan
Hungary Proursan 400mg filmtabletta
France Proursan 400mg comprimé pelliculé
Proursan 500 mg film-coated tablets
Ursodesoxycholic acid
equivalent medicine
Read this leaflet carefully before you start taking this medicine as it contains important
information for you.
- Keep this leaflet. You may need to read it again.
- If you have any questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not pass it on to others, even if their symptoms are the same as yours, as it could be harmful.
- If you get any side effects, even those not listed in this leaflet, tell your doctor or pharmacist. See section 4.
Contents of this leaflet
- 1. What Proursan is and what it is used for
- 2. What you need to know before you take Proursan
- 3. How to take Proursan
- 4. Possible side effects
- 5. How to store Proursan
- 6. Contents of the pack and other information
1. What is Proursan and what is it used for
Ursodeoxycholic acid, the active ingredient of Proursan, is a natural bile acid. It is present in
small quantities in human bile.
Proursan is used:
- to dissolve gallstones caused by excess cholesterol in the gallbladder, if the gallstones are not visible with a simple X-ray (X-ray visible gallstones do not dissolve) and do not measure more than 15 mm in diameter. The gallbladder must still be functioning despite the gallstone(s).
- for the treatment of symptoms of primary biliary cholangitis (PBC, a chronic disease of the bile ducts that can progress to cirrhosis of the liver) in patients without decompensated cirrhosis of the liver (a widespread and chronic liver disease, in which poor liver function due to the disease can no longer be corrected),
- for the treatment of liver disease (hepatopathy) related to a disease called cystic fibrosis in children between 6 and 18 years of age.
2. What you need to know before taking Proursan
Do not take Proursan if
- you are allergic to bile acids (such as ursodesoxycholic acid) or to any of the other ingredients of this medicine (listed in section 6),
- you have an acute inflammation of the gallbladder (cholecystitis) and bile ducts,
- you have a blockage of the common bile duct or cystic duct (obstruction of the bile ducts),
- you have frequent cramp-like pains in the upper abdomen (biliary colic),
- your doctor has told you that you have calcified gallstones,
- you have a problem with the contraction of the gallbladder,
- you are a child suffering from biliary atresia and have poor bile flow, even after surgery.
Consult your doctor if you have any of the diseases or conditions listed above, or if you have had them in the
past.
Warnings and precautions
Consult your doctor or pharmacist before taking Proursan.
For the first 3 months of treatment, your doctor must regularly check liver function,
every 4 weeks. Subsequently, the checks must be repeated every 3 months.
If the medicine is used to dissolve gallstones, your doctor must prescribe you an examination
to scan your gallbladder after the first 6-10 months of treatment.
If you are taking Proursan to dissolve gallstones, tell your doctor if you are taking
medicines that contain estrogenic hormones, as these medicines stimulate the formation of
gallstones.
When used in the treatment of PBC, in rare cases symptoms may worsen at the beginning of
treatment. If this occurs, consult your doctor to assess a reduction in the initial dose.
Immediately inform your doctor if you have diarrhea, as this may require a reduction
in the dose or discontinuation of treatment.
Children and adolescents
Proursan is not suitable for children under 6 years of age due to the dosage form.
Other medicines and Proursan
Tell your doctor or pharmacist if you are taking, have recently taken or might take
any other medicines,
because the effect of these medicines may be altered (interactions):
A reduction in effectsof Proursan is possible when taken simultaneously with the following
medicines:
- cholestyramine, colestipol (used to lower blood fat levels) or antacids containing aluminum hydroxide or smectite (aluminum oxide) (used to bind stomach acid): If you absolutely need to use a medicine containing any of these substances, you must take it at least two hours before or after Proursan.
A reduction in effectsof the following medicines is possible when taken
simultaneously with Proursan:
- ciprofloxacin and dapsone (antibiotics), nitrendipine (used to treat high blood pressure) and other medicines metabolized in a similar way. Your doctor may need to adjust the dose of these medicines. A change in effectsof the following medicines is possible when taken with the following medicines simultaneously with Proursan:
- cyclosporine (to reduce the activity of the immune system). If you are being treated with cyclosporine, your doctor must check its amount in your blood. If necessary, your doctor will adjust the dose.
- rosuvastatin (for high cholesterol and related diseases).
If you are taking Proursan to dissolve gallstones, tell your doctor if you are taking
medicines that contain estrogenic hormones or agents that reduce blood cholesterol, such as
clofibrate. These medicines stimulate the formation of gallstones, which is an effect contrary to
that of treatment with Proursan.
Pregnancy, breastfeeding and fertility
If you are pregnant, suspect you may be pregnant or are planning to become pregnant, or if you are breastfeeding,
ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
There are no data available regarding the use of ursodesoxycholic acid in pregnant women,
or they are limited. Studies conducted in animals have shown reproductive toxicity. Proursan
should not be used during pregnancy unless strictly necessary.
Women of childbearing potential
If you are a woman, you should consult your doctor even if you are not pregnant.
Women of childbearing potential should only be treated if they are using reliable contraceptive methods: the use of
non-hormonal or low-estrogen oral contraceptives is recommended.
However, if you are taking Proursan to dissolve gallstones, you should use effective non-hormonal contraceptives, as
oral hormonal contraceptives may promote the formation of gallstones.
The doctor must rule out the possibility of pregnancy before starting treatment.
Breastfeeding
According to some documented cases of breastfeeding women, levels of ursodesoxycholic acid in
breast milk are very low and adverse reactions in breastfed infants are unlikely.
to be expected.
Fertility
Animal studies have not shown an influence of ursodesoxycholic acid on fertility.
There are no data on the effects on fertility in humans after treatment with ursodesoxycholic acid.
Driving and operating machinery
No effects on the ability to drive and operate machinery have been observed.
Proursan contains sodium (sodium starch glycolate A)
This medicine contains less than 1 mmol of sodium (23 mg) per film-coated tablet, i.e.
it is essentially “sodium-free”.
3. How to take Proursan
Take this medicine following exactly the instructions of your doctor or pharmacist. If you
have any doubts, ask your doctor or pharmacist.
To dissolve cholesterol stones
Dosage
The recommended dose is approximately 10 mg of ursodeoxycholic acid per kg of body weight (b.w.) per
day, as follows:
If you weigh less than 47 kg or are unable to swallow Proursan, other formulations containing ursodeoxycholic acid may be available to you.
Method of administration
Swallow the tablets whole with a glass of water or other liquid. Take the tablets in the evening
before bedtime. Take the medicine regularly.
| n 47-60 kg | 1 tablet |
| 61-80 kg | 1 and a half tablets |
| e 81-100 kg | 2 tablets |
| over 100 kg | 2 and a half tablets |
Duration of treatment
It usually takes 6-24 months to dissolve the gallstones. If after 12 months there has been no
reduction in the size of the gallstones, therapy should be discontinued.
Every 6 months the doctor must check if the treatment is working. On each of
these check-ups, it should be checked if the stones have hardened compared to
the previous examination, due to an accumulation of calcium. In this case the doctor will stop the
treatment.
For the treatment of primary biliary cholangitis (chronic inflammatory disease of the bile
ducts)
Dosage
The daily dose of these film-coated tablets depends on body weight and varies from 1
and a half tablets to 3 and a half tablets.
| Body weight (kg) | F Proursan 500 mg film-coated tablets | |||
| First 3 months | Subsequently | |||
| morning | midday | l evening | evening (once a day) | |
| 47-62 | half | half | half | 1 and a half |
| 63-78 | half | half | and 1 | 2 |
| 79-93 | half | 1 | 1 | 2 and a half |
| 94-109 | 1 | 1 | d 1 | 3 |
| over 110 | 1 | 1 | 1 and a half | 3 and a half |
If you weigh less than 47 kg or are unable to swallow Proursan, another formulation containing ursodeoxycholic acid may be available to you.
Method of administration
Swallow the tablets whole (do not chew), with a glass of water or other liquid.
During the first 3 months of treatment, you must take Proursan in the morning, at midday and in the evening.
When liver function values improve, you can take the total daily dose once a
day, in the evening.
Take the medicine regularly.
Duration of treatment
Treatment with Proursan can be continued indefinitely in case of primary biliary
cholangitis
Note
If you suffer from primary biliary cholangitis, symptoms may worsen at the beginning of treatment. For
example, you may experience an increase in itching, although this happens only in rare cases. If this occurs, treatment may be continued with a reduced daily dose of Proursan. The doctor
will then increase your daily dose every week, until you reach the required dose again.
Use in children and adolescents (6-18 years) for the treatment of liver disease
(hepatopathy) related to cystic fibrosis
Dosage
The recommended dose is approximately 20 mg per kg per day divided into 2-3 doses. ,
If necessary, the doctor may further increase the dose to 30 mg per kg of body weight
per day.
| Body weight (kg) | Proursan 500 mg film-coated tablets | ||
| morning | midday | evening | |
| 20-29 | half | half | |
| 30-39 | half | half | half |
| 40-49 | half | half | 1 |
| 50-59 | half | 1 | 1 |
| 60-69 | 1 | 1 | 1 |
| 70-79 | 1 | 1 | 1 and a half |
| 80-89 | 1 | 1 and a half | 1 and a half |
| 90-99 | 1 and a half | 1 and a half | 1 and a half |
| 100-109 | 1 and a half | 1 and a half | 2 |
| over 110 | 1 and a half | 2 | 2 |
If you feel that the effect of Proursan is too strong or too weak, consult your doctor or
pharmacist.
If you take more Proursan than you should
In case of overdose, diarrhea may occur. Inform your doctor immediately if you have persistent diarrhea. If you suffer from diarrhea, make sure to drink enough fluids to restore
electrolyte balance.
If you forget to take Proursan
Do not take a double dose to make up for a missed dose, but continue treatment
with the prescribed dose.
If you stop taking Proursan
Always consult your doctor before deciding to stop taking Proursan or to
discontinue it prematurely.
If you have any doubts about the use of this medicine, ask your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Common side effects(may affect up to 1 in 10 people):
- soft or loose stools or diarrhoea. Very rare side effects (may affect up to 1 in 10,000 people):
- during treatment of primary biliary cholangitis: severe pain in the upper right side of the abdomen, severe worsening of hepatic cirrhosis, which improves partially after stopping treatment,
- hardening of bile stones,
- urticaria.
Reporting of side effects
If you get any side effects, even those not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly through the national reporting system at: https://www.aifa.gov.it/content/segnalazioni-reazioni-
avverse.
By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store Proursan
Keep this medicine out of the sight and reach of children.
This medicine does not require any particular storage conditions.
Do not use this medicine after the expiry date which is stated on the package and on the blister after
“Exp.”. The expiry date refers to the last day of that month.
Do not dispose of any medicine in waste water or household waste. Ask your pharmacist how to
dispose of medicines you no longer use. This will help protect the environment.
6. Package contents and other information
What Proursan contains
The active ingredient is ursodeoxycholic acid. Each film-coated tablet
contains 500 mg of ursodeoxycholic acid.
The other ingredients are:
- tablet core: corn starch, pregelatinized corn starch, sodium starch glycolate A, anhydrous colloidal silica, magnesium stearate,
- tablet coating: White Opadry 03B28796: hypromellose 6, titanium dioxide (E171), macrogol 400.
Description of Proursan and package contents
Proursan is constituted by film-coated tablets of almost white color, oval shaped with an
incision line on both sides, 17 mm in length and 9 mm
in width. The tablet can be divided into equal doses.
Proursan is available in packs of 20, 40, 50, 60, 80 or 100 film-coated
tablets. Not all pack sizes may be
marketed.
Marketing authorisation holder and manufacturer
PRO.MED.CS Praha a.s., Telčská 377/1, Michle, 140 00 Prague 4, Czech Republic
This medicinal product is authorised in the Member States of the European Economic
Area under the following denominations:
Italy Proursan
Hungary Proursan 500mg filmtabletta
Bulgaria Proursan 500mg филмирани таблетки
Croatia Ursosan 500mg filmom obložene tablete
Denmark Proursan
France Proursan 500mg comprimé pelliculé
Не уверены, подходит ли вам это лекарство?
Обсудите симптомы и варианты лечения с врачом онлайн.
Уже начали прием и появились вопросы?
Обсудите свое состояние и дальнейшие шаги с врачом онлайн.
- Страна регистрации
- Форма выпускаFilm-coated tablet, 400 MG
- Код АТХA05AA02
- Действующее вещество
- Отпускается по рецептуДа
- Производитель
- Информация на этой странице носит справочный характер и не является медицинской консультацией. Перед началом приема лекарства обязательно проконсультируйтесь с врачом.
- Аналоги PROURSANФорма выпуска: Hard capsule, 250 MGДействующее вещество: урсодезоксихолевая кислотаПроизводитель: ABC FARMACEUTICI S.P.A.Отпускается по рецептуФорма выпуска: Hard capsule, 300 MGДействующее вещество: урсодезоксихолевая кислотаПроизводитель: AUROBINDO PHARMA (ITALIA) S.R.L.Отпускается по рецептуФорма выпуска: Hard capsule, 300 MGДействующее вещество: урсодезоксихолевая кислотаПроизводитель: DOC GENERICI SRLОтпускается по рецепту
Аналоги PROURSAN в других странах
Лекарства с тем же действующим веществом, доступные в других странах.
Аналог PROURSAN в Испания
Аналог PROURSAN в Польша
Аналог PROURSAN в Украина
Врачи онлайн по PROURSAN
Обсудите применение PROURSAN и возможные следующие шаги — по оценке врача.
Получите рецепт на PROURSAN онлайн
Заполните форму за 2 минуты
Расскажите о симптомах, истории болезни и нужном препарате.
Выберите врача или мы назначим
Выберите специалиста или мы подберём ближайшего доступного врача.
Врач рассматривает ваш случай
Обычно в течение 30 минут. Может задать уточняющие вопросы в чате.
Получите в любой аптеке
Электронный рецепт отправляется на вашу почту — действителен по всей Польше.
Часто задаваемые вопросы
PROURSAN требует рецепта в Италия. Вы можете уточнить у врача онлайн, подходит ли это лекарство для вашей ситуации.
Действующее вещество PROURSAN — урсодезоксихолевая кислота. Эта информация помогает определить лекарства с тем же составом под другими торговыми названиями.
PROURSAN производится компанией PRO.MED.CS Praha a.s.. Упаковка и торговое название могут отличаться в зависимости от дистрибьютора.
Врачи, включая Семейные врачи, Психиатры, Дерматологи, Кардиологи, Эндокринологи, Гастроэнтерологи, Пульмонологи, Нефрологи, Ревматологи, Гематологи, Инфекционисты, Аллергологи, Гериатры, Педиатры, Онкологи, могут оценить целесообразность применения PROURSAN с учетом вашей ситуации и местных правил. Вы можете записаться на онлайн-консультацию, чтобы обсудить возможные варианты.
Польша имеет хорошо развитую систему здравоохранения в крупных городах, таких как Варшава, Краков, Вроцлав и Гданьск. Аптеки широко доступны и работают в соответствии с действующим законодательством, обеспечивая доступ к рецептурным препаратам.
Вы можете купить PROURSAN в Варшаве, Кракове, Вроцлаве или Гданьске в любой аптеке при наличии действующего рецепта.
Чтобы получить рецепт, вы можете воспользоваться Oladoctor:
Другие лекарства с тем же действующим веществом (урсодезоксихолевая кислота) включают AKIDO URSODESOSSIKOLIKO ABK, AKIDO URSODESOSSIKOLIKO AUROBINDO, AKIDO URSODESOSSIKOLIKO DOK JENERIKI. Они могут отличаться торговым названием или формой выпуска, но содержат одинаковый терапевтический компонент. Перед изменением лечения рекомендуется проконсультироваться с врачом.
