(Cisapride)
Gasprid is a medicine in the form of tablets for oral administration, containing 5 mg or 10 mg of cisapride. The preparation is used exclusively in adults for the treatment of acute and severe symptomatic exacerbation of chronic idiopathic or occurring in the course of diabetes, delayed gastric emptying, when other treatment methods are ineffective.
Gasprid stimulates the motility of the gastrointestinal tract, increases the tension of the lower esophageal sphincter, accelerates gastric and duodenal emptying, and the passage of food through the intestines.
or certain antihistamines (such as: astemizole and terfenadine).
Before starting to take Gasprid, discuss it with your doctor or pharmacist:
If any of the above situations apply to the patient (and in case of doubt), before taking Gasprid, consult a doctor, pharmacist, or nurse.
Tell your doctor about all the medicines you are taking now or have taken recently, as well as any medicines you plan to take..
Taking oral anticoagulants (e.g. acenocoumarol) at the same time may lead to an increase in the effect of the anticoagulant and the risk of bleeding. Remember to adjust the dose of the oral anticoagulant during treatment and up to 8 days after the end of cisapride treatment.
A temporary increase in the sedative effect of diazepam may occur, caused by increased absorption rate.
Do not take Gasprid with grapefruit juice or alcohol.
The medicine should be taken at least 15 minutes before a meal and before bedtime.
During cisapride treatment, it is not recommended to consume grapefruit juice repeatedly.
The tablet should be swallowed whole, do not divide or crush it.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor or pharmacist before taking this medicine.
Pregnancy
The medicine may be used during pregnancy only in cases where, in the doctor's opinion, the benefit to the mother outweighs the potential risk to the fetus.
In studies of a large group of people, cisapride did not increase the incidence of fetal malformations. Nevertheless, when using Gasprid during pregnancy, especially in the first trimester, consider the expected benefits of using the medicine in relation to the potential risk.
Breastfeeding
Although the penetration of cisapride into breast milk is minimal, breastfeeding is not recommended during Gasprid treatment.
In the elderly, there is no need to change the dosage of the medicine.
In patients with liver or kidney failure, it is recommended to reduce the daily dose by half.
The medicine does not affect the ability to drive or operate machines. It does not cause sedation or drowsiness. However, Gasprid may accelerate the absorption of substances that act depressingly on the central nervous system, such as barbiturates or alcohol. Therefore, if Gasprid is taken at the same time as these substances, caution should be exercised.
If you have been diagnosed with an intolerance to some sugars, consult your doctor before taking the medicine.
Gasprid contains less than 1 mmol (23 mg) of sodium per tablet, which means the medicine is considered "sodium-free".
Always take this medicine exactly as your doctor has told you. If you are not sure, ask your doctor or pharmacist.
Gasprid is intended only for adults.
Treatment with Gasprid should be started in a hospital setting and strictly monitored by a specialist doctor experienced in the treatment of acute and severe symptomatic exacerbation of chronic idiopathic or occurring in the course of diabetes, delayed gastric emptying (gastroparesis).
Method of administration
Gasprid should be taken 15 minutes before a meal and preferably before bedtime, (when a fourth dose of the medicine is necessary), with a liquid.
Recommended dose
The recommended dose of Gasprid is 10 mg three to four times a day. Do not take more than 40 mg per day.
Do not take Gasprid with grapefruit juice.
Gasprid should only be used for short-term treatment.
Do not divide or crush the tablets.
Symptoms
Symptoms that may occur as a result of an overdose are: abdominal cramps and frequent bowel movements.
Arrhythmias may also occur.
Treatment
In case of an overdose, hospitalization is necessary. Activated charcoal administration, clinical observation of the patient, and ECG monitoring are recommended. Particular attention should be paid to the ECG record of heart function, with particular emphasis on QT interval prolongation or bradycardia, and electrolyte imbalance (especially hypokalemia and hypomagnesemia).
Take it as soon as possible, unless it is time for the next dose.
Do not take a double dose to make up for a missed dose.
If you have any doubts about taking the medicine, consult your doctor or pharmacist.
Like all medicines, Gasprid can cause side effects, although not everybody gets them.
There have been reports of serious arrhythmias, even life-threatening, in some cases. In most cases, these effects occurred in patients who were taking other medicines and (or) had a history of heart disease or factors that increase the risk of arrhythmias
Frequency of side effects:
The following side effects have been observed:
Gastrointestinal disorders:
Transient abdominal cramps, rumbling in the abdomen, and diarrhea.
General disorders:
Cases of hypersensitivity, including rash, urticaria, and itching, mild and transient headaches or dizziness. There have also been reports of dose-dependent frequent urination.
Nervous system disorders:
Single cases of seizures and other symptoms such as: muscle stiffness, facial rigidity, slowed movement, restlessness, involuntary muscle contractions.
Reproductive system and breast disorders:
Transient cases of gynecomastia (breast tissue enlargement) and galactorrhea, sometimes with elevated prolactin levels.
Liver and biliary disorders:
Reports of transient liver function disorders, with or without jaundice.
Respiratory, thoracic, and mediastinal disorders:
Bronchospasm.
If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Post-Marketing Surveillance of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Store in a temperature below 25°C.
Keep the medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the blister and carton after: Expiry date (EXP). The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Tablets.
1 blister pack of 30 tablets (30 tablets) in a cardboard box.
Tablets.
2 blisters of 15 tablets (30 tablets) in a cardboard box.
Teva Pharmaceuticals Polska Sp. z o.o.
ul. Emilii Plater 53
00-113 Warsaw
tel.: (22) 345 93 00
Teva Operations Poland Sp. z o.o.
ul. Mogilska 80
31-546 Krakow
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