Package Leaflet: Information for the User
Metformin Pensa 850 mg film-coated tablets EFG
metformin hydrochloride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Metformin Pensa is a medicine used to treat diabetes. It belongs to a group of medicines called biguanides (a class of oral antidiabetics).
Insulin is a hormone produced by the pancreas that makes your body take in glucose (sugar) from the blood. Your body uses glucose to produce energy or stores it for future use.
If you have diabetes, your pancreas does not produce enough insulin or your body cannot use the insulin it produces properly. This causes high blood glucose levels. This medicine helps to lower your blood glucose to as normal a level as possible.
If you are an adult with overweight, taking metformin for a long time also helps to reduce the risk of complications associated with diabetes. Metformin is associated with maintaining body weight or a slight decrease in body weight.
Metformin is used to treat patients with type 2 diabetes (also called "non-insulin-dependent diabetes") when diet and exercise alone are not enough to control their blood glucose levels. It is especially used in patients with overweight.
Adults can take metformin alone or with other medicines to treat diabetes (oral medicines or insulin). Children aged 10 years and older, and adolescents can take metformin alone or with insulin.
Do not take Metformin Pensa
If any of the above applies to you, consult your doctor before starting to take this medicine.
Make sure to consult your doctor if
You should stop taking metformin for a certain period of time before and after the examination or surgery. Your doctor will decide if you need any other treatment during this time. It is important that you follow your doctor's instructions precisely.
Warnings and precautions
Risk of lactic acidosis.
Metformin can cause a very rare but very serious side effect called lactic acidosis, especially if your kidneys are not working properly. The risk of developing lactic acidosis is also increased with uncontrolled diabetes, severe infections, prolonged fasting or alcohol consumption, dehydration (see more information below), liver problems, and any medical disorder in which a part of the body has a reduced oxygen supply (such as acute and severe heart disease). If any of the above applies to you, consult your doctor for further instructions.
Consult your doctor immediately to be told how to proceed if:
Stop taking this medicine for a short period of time if you have a disorder that may be associated with dehydration(significant loss of body fluids), such as severe vomiting, diarrhea, fever, heat exposure, or if you drink less fluid than usual. Consult your doctor for further instructions.
Stop taking this medicine and contact a doctor or the nearest hospital immediately if you experience any of the symptoms that lactic acidosis produces,as this disorder can lead to a coma.
The symptoms of lactic acidosis include:
Lactic acidosis is a medical emergency and should be treated in a hospital.
If you need to undergo major surgery, you should stop taking metformin during the procedure and for a period of time after it. Your doctor will decide when you should stop taking metformin and when you can restart it.
Metformin alone does not cause hypoglycemia (a blood glucose concentration that is too low). However, if you take metformin with other diabetes medicines that can cause hypoglycemia (such as sulfonylureas, insulin, meglitinides), there is a risk of hypoglycemia. If you experience symptoms of hypoglycemia, such as weakness, dizziness, increased sweating, increased heart rate, vision disorders, or difficulty concentrating, it is usually helpful to eat or drink something that contains sugar.
During treatment with metformin, your doctor will check your kidney function regularly, at least once a year or more frequently if you are an elderly person and/or if your kidney function is deteriorating.
Other medicines and Metformin Pensa
If you need to be given an injection of a contrast medium that contains iodine into your bloodstream, for example, in the context of an X-ray or a scan, you should stop taking metformin before the injection or at the time of the injection. Your doctor will decide when you should stop taking metformin and when you can restart it.
Tell your doctor if you are taking, have recently taken, or might take any other medicines. You may need more frequent blood glucose and kidney function tests, or your doctor may need to adjust the dose of metformin. It is especially important to mention the following:
Taking Metformin Pensa with alcohol
Avoid excessive alcohol consumption while taking metformin, as this can increase the risk of lactic acidosis (see section "Warnings and precautions").
Pregnancy and breastfeeding
Diabetic women who are pregnant or plan to become pregnant should not receive treatment with metformin. Instead, insulin should be used to keep blood glucose levels as close to normal as possible. Tell your doctor if you are pregnant or plan to become pregnant so that your treatment can be changed to insulin.
This medicine should not be used during breastfeeding. If you are pregnant or breastfeeding, or think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines
This medicine does not cause hypoglycemia (a blood glucose concentration that is too low) on its own. This means it will not affect your ability to drive or use machines.
However, be careful if you take metformin with other diabetes medicines that can cause hypoglycemia (such as sulfonylureas, insulin, meglitinides). The symptoms of hypoglycemia include weakness, dizziness, increased sweating, increased heart rate, vision disorders, or difficulty concentrating. Do not drive or use machines if you start to feel these symptoms.
Follow exactly the administration instructions of this medicine given by your doctor. In case of doubt, consult your doctor or pharmacist.
Metformin cannot replace the benefits of a healthy lifestyle. Continue to follow any dietary advice your doctor has given you and exercise regularly.
Recommended dose
Children aged 10 years and older and adolescents usually start with 500 mg or 850 mg of metformin once a day. The maximum daily dose is 2000 mg divided into 2 or 3 doses. Treatment of children between 10 and 12 years is only recommended under specific advice from your doctor, as clinical experience in this patient group is limited.
Adults usually start with 500 mg or 850 mg of metformin, two or three times a day. The maximum daily dose is 3000 mg divided into 3 doses.
If you have reduced kidney function, your doctor may prescribe a lower dose.
If you are also given insulin, your doctor will tell you how to start taking metformin.
Monitoring
How to take Metformin Pensa
Take metformin with meals or after meals.
This will prevent you from experiencing side effects that affect your digestion. Do not chew or crush the tablets. Swallow each tablet with a glass of water.
If, after some time, you think the effect of metformin is too strong or too weak, consult your doctor or pharmacist.
If you take more Metformin Pensa than you should
If you have taken more metformin than you should, you may experience lactic acidosis. The symptoms of lactic acidosis are non-specific, such as vomiting, stomach pain (abdominal pain) with cramps, a general feeling of discomfort with intense fatigue, and difficulty breathing. Additional symptoms may include a decrease in body temperature and heart rate. If you experience any of these symptoms, seek medical attention immediately, as lactic acidosis can lead to a coma. Stop taking this medicine immediately and contact your doctor or the nearest hospital as soon as possible.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service. Phone: 91 562 04 20, indicating the medicine and the amount taken.
If you forget to take Metformin Pensa
Do not take a double dose to make up for forgotten doses. Take the next dose at the usual time. If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. The following side effects may occur:
Metformin can cause a very rare but very serious side effect called lactic acidosis (see section "Warnings and precautions"), if this happens to you, you must stop taking this medicine and contact a doctor or the nearest hospital immediately,as lactic acidosis can lead to a coma.
Very common side effects (affecting more than 1 in 10 people):
Common side effects (affecting less than 1 in 10 people):
Very rare side effects (affecting less than 1 in 10,000 people):
Children and adolescents
Limited data in children and adolescents showed that the side effects were similar in nature and severity to those observed in adults.
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children. If a child is being treated with metformin, it is recommended that parents and caregivers supervise how this medicine is used.
No special storage conditions are required.
Do not use this medicine after the expiry date which is stated on the carton, after "EXP". The expiry date is the last day of the month shown.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Tablet core
Povidone, magnesium stearate.
Tablet coating
Hypromellose, macrogol.
Appearance of the Product and Package Contents
Metformina Galenicum is presented in the form of film-coated tablets, white-yellow in color, oval, biconvex with a notch between M and B on one side and a notch on the other side. The notch is only for fractionation and to facilitate swallowing, but not for dividing into equal doses.
The dimensions of the tablets are: 17.9 x 10.0 mm ± 0.3 mm
Blister pack (transparent PVC/PVDC/Aluminum) with 50 and 60 tablets.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Galenicum Health, S.L.
Avda. Diagonal, 123, 11th floor
08005 Barcelona
Spain
Manufacturer
SAG MANUFACTURING S.L.U
National Highway I, Km 36
San Agustin de Guadalix 28750
Madrid, Spain
or
Galenicum Health, S.L.U.
Sant Gabriel, 50,
Esplugues de Llobregat
08950 Barcelona
Spain
Date of the last revision of this prospectus: March 2025
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.