The active substance of Ranloc Med is pantoprazole, which blocks the "pump" that produces stomach acid.
This way, the medicine reduces the amount of acid in the stomach.
Ranloc Med is used for short-term treatment of symptoms of gastroesophageal reflux disease (such as heartburn, acid reflux) in adults.
Reflux occurs when stomach acid flows back into the esophagus, which can lead to inflammation of the esophagus and cause pain. Other symptoms may also occur, such as painful burning in the chest that can spread to the throat (heartburn) and a sour taste in the mouth (acid reflux).
Symptoms related to reflux disease and heartburn may improve after the first day of taking pantoprazole, but this medicine is not intended for immediate relief of symptoms. To achieve complete relief of symptoms, it may be necessary to take the tablets for 2-3 consecutive days.
If after 2 weeks there is no improvement or you feel worse, you should contact your doctor.
Before starting to take pantoprazole, you should consult your doctor if:
You should not take this medicine without consulting your doctor for a period longer than 4 weeks. If the symptoms of reflux disease (heartburn or acid reflux) persist for more than 2 weeks, you should consult your doctor, who will decide whether long-term use of the medicine is necessary.
Long-term use of Ranloc Med may be associated with additional risks, such as:
You should immediately inform your doctorbefore or after taking this medicine if you notice the occurrence of the following symptoms, which may be signs of other, more serious diseases:
Your doctor may decide to perform additional tests.
If you are going to have a blood test, you should inform your doctor that you are taking this medicine.
Symptoms related to reflux disease and heartburn may improve after the first day of taking pantoprazole, but this medicine is not intended for immediate relief of symptoms.
You should not take it as a preventive measure.
If you have been suffering from recurring heartburn or indigestion for some time, you should remain under regular medical supervision.
Ranloc Med should not be used in children and adolescents under 18 years of age due to the lack of data on the safety of use of this medicine in this age group.
You should tell your doctor or pharmacist about all othermedicines you are currently taking or have recently taken, as well as any medicines you plan to take. Ranloc Med may reduce the effectiveness of some other medicines, especially those containing the following active substances:
You should not take Ranloc Med with other medicines that reduce the amount of stomach acid, such as other proton pump inhibitors (omeprazole, lansoprazole, or rabeprazole) or H2 antagonists (e.g., ranitidine, famotidine).
However, Ranloc Med can be taken with antacids (e.g., magaldrate, alginic acid, sodium bicarbonate, aluminum hydroxide, magnesium carbonate, or their combinations) if necessary.
You should not take this medicine if you are pregnant or breastfeeding.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, you should ask your doctor or pharmacist for advice before taking this medicine.
If you experience side effects such as dizziness or vision disturbances, you should not drive or operate machinery.
This medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially "sodium-free".
This medicine should always be taken in accordance with the information in this leaflet or as directed by your doctor or pharmacist. If you are unsure, you should ask your doctor or pharmacist.
You should take 1 tablet per day. Do not exceed the recommended daily dose of pantoprazole, which is 20 mg.
The medicine should be taken for at least 2-3 consecutive days. Treatment should be stopped after complete relief of symptoms. It is possible to experience relief of reflux and heartburn symptoms after just one day of taking pantoprazole, but this medicine is not intended for immediate relief of symptoms.
You should consult your doctor if, after taking this medicine continuously for 2 weeks, symptoms do not improve.
You should not take pantoprazole for more than 4 weeks without consulting your doctor.
The tablet should be taken before a meal, at the same time every day. The tablet should be swallowed whole, with water. Do not chew or crush it.
You should immediately consult your doctor or pharmacist if you have taken more than the recommended dose.
If possible, you should bring the medicine and the leaflet with you.
You should not take a double dose to make up for a missed dose. You should take the next scheduled dose the next day, at the usual time.
If you have any further questions about taking this medicine, you should ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
You should immediately inform your doctoror contact the nearest hospital emergency department if you experience any of the following serious side effects. At the same time, you should stop taking this medicine and bring this leaflet and/or the tablets with you.
Other side effects include:
very rare (may occur in less than 1 in 10,000 people):disturbances of orientation, decreased platelet count, which may cause increased tendency to bleeding and bruising, decreased white blood cell count, which may predispose to more frequent infections, concurrent, abnormal decrease in the number of red and white blood cells, as well as platelets (detected in blood tests).
Reporting side effects
If you experience any side effects, including those not listed in the leaflet, you should tell your doctor or pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products:
Jerozolimskie Avenue 181C, 02-222 Warsaw, tel.: 22 49-21-301, fax: 22 49-21-309.
Website: https://smz.ezdrowie.gov.pl.
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help to gather more information on the safety of this medicine.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and blister. The expiry date refers to the last day of the month.
There are no special storage requirements.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Core of the tablet: anhydrous sodium carbonate, mannitol (E 421), crospovidone type A, hydroxypropylcellulose, microcrystalline cellulose, calcium stearate
Coating of the tablet: hypromellose, propylene glycol, povidone K30, titanium dioxide (E 171), yellow iron oxide (E 172)
Enteric coating: methacrylic acid and ethyl acrylate copolymer (1:1), triethyl citrate, sodium lauryl sulfate, titanium dioxide (E 171), talc
Ranloc Med 20 mg gastro-resistant tablets are white, oval, biconvex, coated with a protective layer against stomach acid, smooth on both sides.
Cold-form blisters: blister packs consist of OPA/Aluminum/PVC/Aluminum.
Ranloc Med is available in blisters, placed in cardboard boxes, containing 7 or 14 gastro-resistant tablets. Not all pack sizes may be marketed.
Ranbaxy (Poland) Sp. z o.o.
Idzikowskiego 16
00-710 Warsaw
S.C. Terapia S.A.
Fabricii Street 124
Cluj Napoca, 400 632
Romania
Sun Pharmaceutical Industries Europe B.V.
Polarisavenue 87
2132 JH, Hoofddorp
Netherlands
Date of last revision of the leaflet:02.05.2023
The following lifestyle and dietary recommendations may also help alleviate heartburn or other acid-related symptoms:
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