Metformin hydrochloride
Read the entire leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the leaflet
This medication contains metformin, a medication used to treat diabetes. It belongs to a group of medications called biguanides.
Insulin is a hormone produced by the pancreas that makes your body absorb 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. Metformin helps reduce 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 reduce the risk of complications associated with diabetes. Metformin is associated with maintaining body weight or a slight decrease in weight.
This medication 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 medications to treat diabetes (oral medications or insulin).
Children aged 10 and older, and adolescents can take this medication alone or with insulin.
Do not take Brotmin
If any of the above circumstances apply to you, consult your doctor before starting to take this medication.
Make sure to consult your doctor if
You should stop taking metformin for a certain period before and after the examination or surgical intervention. Your doctor will decide if you need any other treatment during this time. It is essential that you follow your doctor's instructions precisely.
Metformin can cause a very rare but very serious side effect called lactic acidosis, especially if your kidneys do not function 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 diseases).
If any of the above applies to you, consult your doctor for further instructions.
Consult your doctor immediately to indicate how to proceed if:
Stop taking this medication for a short period 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 medication and contact a doctor or the nearest hospital immediately if you experience any of the symptoms that produce lactic acidosis, 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 this medication during the procedure and for a period after it. Your doctor will decide when you should stop treatment with this medication and when to restart it.
Metformin alone does not cause hypoglycemia (a blood glucose concentration that is too low). However, if you take metformin with other diabetes medications 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 disturbances, or difficulty concentrating, it is usually helpful to eat or drink something that contains sugar.
During treatment with metformin, your doctor will regularly check your kidney function, at least once a year or more frequently if you are an elderly person and/or if your kidney function is deteriorating.
If you need to be administered a contrast medium containing iodine into your bloodstream, for example, in the context of an X-ray or examination, you should stop taking metformin before the injection or at the time of the injection. Your doctor will decide when you should stop treatment with this medication and when to restart it.
Inform your doctor if you are taking, have recently taken, or may need to take any other medication. You may need more frequent blood glucose and kidney function tests, or your doctor may need to adjust the dose of this medication. It is especially important to mention the following:
Avoid excessive alcohol consumption while taking metformin, as this can increase the risk of lactic acidosis (see "Warnings and precautions" section).
If you are pregnant, think you may be pregnant, or plan to become pregnant, consult your doctor to determine if you need to change your treatment or control your blood glucose levels.
This medication is not recommended if you are breastfeeding or plan to breastfeed your baby.
This medication alone does not cause hypoglycemia (a blood glucose concentration that is too low). This means it will not affect your ability to drive or use machines.
However, be especially careful if you take metformin with other diabetes medications that can cause hypoglycemia (such as sulfonylureas, insulin, meglitinides). The symptoms of hypoglycemia include weakness, dizziness, increased sweating, increased heart rate, vision disturbances, or difficulty concentrating. Do not drive or use machines if you start to feel these symptoms.
This medication contains less than 23 mg of sodium (1 mmol) per tablet, i.e., it is essentially "sodium-free".
Follow your doctor's instructions for taking this medication exactly. If in doubt, consult your doctor or pharmacist.
This medication cannot replace the benefits of a healthy lifestyle. Continue to follow any dietary advice your doctor has given you and exercise regularly.
The recommended dose is
Adultsusually start with 500 mg or 850 mg of this medication two or three times a day. The maximum daily dose is 3,000 mg divided into 3 doses.
If you have reduced kidney function, your doctor may prescribe a lower dose.
If insulin is also administered, your doctor will indicate how to start taking this medication.
Use in children and adolescents.
Children aged 10 and older, and adolescents usually start with 500 mg or 850 mg of this medication once a day. The maximum daily dose is 2,000 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 experience in this age group is limited.
Take this medication 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 this medication is too strong or too weak, consult your doctor or pharmacist.
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 decreased body temperature and heart rate. If you experience any of these symptoms, you should seek immediate medical attention, as lactic acidosis can lead to a coma. Stop taking this medication 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 medication and the amount ingested.
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 doubts about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone experiences them. The following side effects may occur:
Metformin can cause a very rare but very serious side effect called lactic acidosis (see "Warnings and precautions" section). If this happens to you, you should stop taking this medication and contact a doctor or the nearest hospital immediately, as lactic acidosis can lead to a coma.
Skin reactions such as skin redness (erythema), itching, or an itchy rash (urticaria).
Additional side effects in 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.
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medications: www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date shown on the label, after "CAD". The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medications should not be thrown down the drain or into the trash. Deposit the containers and medications you no longer need in the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the containers and medications you no longer need. This way, you will help protect the environment.
Each film-coated tablet contains 500 mg of metformin hydrochloride, equivalent to 390 mg of metformin base.
Each film-coated tablet contains 850 mg of metformin hydrochloride, equivalent to 662.9 mg of metformin base.
Each film-coated tablet contains 1,000 mg of metformin hydrochloride, equivalent to 780 mg of metformin base.
Film coating:
500 mg and 1,000 mg:poly(vinyl alcohol), titanium dioxide (E171), macrogol, talc
850 mg:yellow iron oxide (E172), poly(vinyl alcohol), titanium dioxide (E171), macrogol, talc.
Brotmin 500 mg film-coated tablets: oval, white, film-coated tablets, smooth on both sides, with dimensions of 16 mm x 8 mm.
Brotmin 850 mg film-coated tablets: oval, yellow, film-coated tablets, engraved with "MC" on one side and smooth on the other, with dimensions of 20.1 mm x 9.8 mm.
Brotmin 1,000 mg film-coated tablets: oval, white, film-coated tablets, with a score line on both sides, with dimensions of 21.2 mm x 10.2 mm. The tablet can be divided into equal doses.
500 mg tablets:
The tablets are presented in blisters of 9, 20, 21, 30, 40, 50, 56, 60, 84, 90, 100, 120, 200, 500, 600 or 1,000 tablets.
Only some pack sizes may be marketed.
850 mg and 1,000 mg tablets:
The tablets are presented in blisters of 8, 9, 10, 14, 20, 21, 30, 40, 50, 56, 60, 84, 90, 100, 120, 300, 600 or 1,000 tablets.
Only some pack sizes may be marketed.
Medochemie Iberia S.A.
Rua José Maria Nicolau, no 6 7°B,
1500-662, São Domingos de Benfica,
Lisboa, Portugal
Medochemie LTD
1-10 Constantinoupoleos street,
3011 Limassol,
Cyprus
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Medochemie Iberia S.A., Branch in Spain
Avenida de las Águilas, nº 2 B; 5th floor, office 6,
28044 Madrid
Spain
To obtain more information about this medication, please contact the local representative of the marketing authorization holder.
Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.