Metformin hydrochloride
This medicine is intended for adult patients only.
Metformin hydrochloride, the active substance of Meladine SR, prolonged-release tablets, belongs to a group of medicines called biguanides, used to treat type 2 diabetes (non-insulin-dependent).
Meladine SR is used in combination with diet and physical exercise to reduce the risk of developing type 2 diabetes in adults with overweight, when diet and exercise alone have not been sufficient to control blood glucose levels (sugar) for 3 to 6 months. There is a high risk of developing type 2 diabetes if the patient has additional risk factors, such as high blood pressure, age over 40, abnormal blood lipid levels, or diabetes during pregnancy.
This medicine is particularly effective if the patient is under 45 years old, has significant overweight, high blood glucose levels after meals, or developed diabetes during pregnancy.
Meladine SR is used in patients with type 2 diabetes, when diet and physical exercise alone have not been sufficient to achieve normal blood glucose levels. Insulin is a hormone that allows the body to take up glucose from the blood, which it uses to produce energy or stores for later use. In patients with type 2 diabetes, the pancreas does not produce enough insulin or the body is unable to use the insulin produced properly. This leads to an excessive increase in blood glucose levels, which can cause a range of serious and long-term disorders, making it important to continue taking the medicine even if there are no obvious symptoms. Meladine SR increases the body's sensitivity to insulin and helps the body use glucose properly.
Taking Meladine SR is associated with maintaining a stable body weight or moderate weight loss.
Meladine SR has been specially developed to release the active substance slowly from the tablet into the body, which distinguishes it from many other types of metformin tablets.
Meladine SR may cause a very rare but very serious side effect called lactic acidosis, especially if the patient has kidney function disorders. The risk of lactic acidosis also increases in case of uncontrolled diabetes, severe infection, prolonged fasting, or alcohol consumption, dehydration (see more information below), liver function disorders, and any conditions in which a part of the body is not sufficiently supplied with oxygen (e.g., acute severe heart disease).
If any of the above circumstances apply to you, you should consult your doctor for more detailed instructions.
condition that may be associated with dehydration(significant fluid loss from the body), such as severe vomiting, diarrhea, fever, exposure to high temperatures, or if you drink less fluids than usual. You should consult your doctor for more detailed instructions.
as this condition can lead to a coma.
Symptoms of lactic acidosis include:
Lactic acidosis is a life-threatening condition that requires immediate hospital treatment.
If you are to undergo a major surgical procedure, you should not take Meladine SR during the procedure and for some time after it. Your doctor will decide when you should stop and restart treatment with Meladine SR.
During treatment with Meladine SR, your doctor will monitor your kidney function at least once a year or more often if you are elderly and/or have worsening kidney function.
In patients over 75 years old, treatment with Meladine SR should not be initiated to reduce the risk of developing type 2 diabetes.
It may happen that the tablet coating is visible in the stool. You should not be concerned, as this is normal when taking this type of tablet.
You should follow the dietary recommendations given by your doctor and ensure that you eat carbohydrates regularly throughout the day.
You should not stop taking this medicine without consulting your doctor.
If you are to receive an intravenous iodine-containing contrast agent, for example, for an X-ray examination or computed tomography, you should stop taking Meladine SR before or at the latest at the time of administration.
Your doctor will decide when you should stop and restart treatment with Meladine SR.
You should tell your doctor about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take. You may need more frequent monitoring of blood glucose levels and kidney function or modification of the Meladine SR dose by your doctor. It is particularly important to inform your doctor about the following medicines:
You should avoid consuming excessive amounts of alcohol while taking Meladine SR, as this may increase the risk of lactic acidosis (see "Warnings and precautions").
If you are pregnant, think you may be pregnant, or plan to have a baby, you should consult your doctor, as changes in treatment or blood glucose monitoring may be necessary.
This medicine is not recommended for breastfeeding women or those planning to breastfeed.
Meladine SR, when used alone, does not cause hypoglycemia (symptoms of low blood glucose levels, such as fainting, disorientation, and increased sweating) and therefore does not affect your ability to drive or use machines.
You should be particularly careful if you are taking Meladine SR with other antidiabetic medicines that can cause hypoglycemia (such as sulfonylureas, insulin, and meglitinides). Symptoms of hypoglycemia include weakness, dizziness, increased sweating, rapid heartbeat, vision disturbances, or difficulty concentrating. If you experience such symptoms, you should not drive or use machines.
Your doctor may recommend taking Meladine SR alone or in combination with other oral antidiabetic medicines or insulin.
This medicine should always be taken exactly as prescribed by your doctor.
If you are unsure, you should consult your doctor or pharmacist. You should swallow the tablets whole, with a glass of water. The tablets should not be chewed.
Recommended dosage
Treatment usually starts with a dose of 500 mg of Meladine SR once a day.
After about two weeks of taking the medicine, your doctor may adjust the dose based on your blood glucose levels. The maximum dose of Meladine SR is 2000 mg per day.
If you have kidney function disorders, your doctor may prescribe a lower dose.
Usually, you should take the tablets once a day with your evening meal.
In some cases, your doctor may recommend taking the tablets twice a day.
The tablets should always be taken with a meal.
If you accidentally take extra tablets, you should not be concerned, but if you experience unusual symptoms, you should contact your doctor. In case of significant overdose, lactic acidosis is more likely to occur. Unusual symptoms of lactic acidosis include vomiting, abdominal pain with muscle cramps, general feeling of being unwell with severe fatigue, and breathing difficulties. Other symptoms include decreased body temperature and slowed heart rate. If you experience such symptoms, you should seek immediate hospital treatment, as lactic acidosis can lead to a coma. You should stop taking Meladine SR and contact your doctor or the nearest hospital immediately.
As soon as you remember, you should take the missed dose with any meal.
You should not take a double dose to make up for the missed dose.
Like all medicines, Meladine SR can cause side effects, although not everybody gets them.
The following side effects may occur:
Meladine SR may very rarely cause (may affect up to 1 in 10,000 people) a very serious side effect called lactic acidosis (see "Warnings and precautions"). If this happens to you, you should stop taking Meladine SR and contact your doctor or the nearest hospital immediately, as lactic acidosis can lead to a coma.
Other possible side effects are listed below by frequency of occurrence:
Common (may affect up to 1 in 10 people):
Very rare (may affect up to 1 in 10,000 people):
If you experience any side effects, including those not listed in this leaflet, you should tell your doctor or pharmacist. 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
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.
The medicine should be stored out of sight and reach of children.
There are no special storage instructions for this medicine.
Do not swallow the desiccant.
Do not take this medicine after the expiry date stated on the label of the bottle after: EXP. The expiry date refers to the last day of the month stated.
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.
Each prolonged-release tablet contains 750 mg or 1000 mg of the active substance – metformin hydrochloride.
The other ingredients are: microcrystalline cellulose, hypromellose, anhydrous colloidal silica, and magnesium stearate.
Meladine SR 750 mg are white to almost white, biconvex, oblong, uncoated tablets with dimensions of 19.2 mm x 9.3 mm, with the inscription "FN2" on one side and smooth on the other.
Meladine SR 1000 mg are white to almost white, biconvex, oblong, uncoated tablets with dimensions of 22.2 mm x 11.0 mm, with the inscription "FN3" on one side and smooth on the other.
Meladine SR is packaged in HDPE bottles containing 30 prolonged-release tablets.
Not all pack sizes may be marketed.
Accord Healthcare Polska Sp. z o.o.
Taśmowa 7
02-677 Warsaw
Tel: +48 22 577 28 00
Accord Healthcare Polska Sp. z o.o.
Lutomierska 50
95-200 Pabianice
Accord Healthcare B.V.
Winthontlaan 200
3526 KV Utrecht | |
Netherlands |
Member State | Medicinal product name |
Finland | Metformin Accord 750 mg depottabletti Metformin Accord 1000 mg depottabletti |
Poland | Meladine SR |
Romania | Metformin Accord 750 mg comprimate cu eliberare prelungită Metformin Accord 1000 mg comprimate cu eliberare prelungită |
United Kingdom (Northern Ireland) | Metformin SR 500 mg prolonged release tablets Metformin SR 1000 mg prolonged release tablets |
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