Package Leaflet: Information for the User
Metormina Tevagen 1,000 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 and other information
Metformina Tevagen contains metformin, a medicine used to treat diabetes. It belongs to a group of medicines called biguanides.
Insulin is a hormone produced by the pancreas that makes your body take 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 leads to 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 from 10 years old and adolescents can take metformin alone or with insulin.
Do not take Metformina Tevagen
If any of the above circumstances apply 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 before and after the examination or surgery. Your doctor will decide if you need any other treatment during this time. It is essential 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. Stop taking this medicine 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 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.
Consult your doctor quickly to indicate how to proceed if:
If you need to undergo major surgery, you should stop taking metformin during the procedure and for a period after it. Your doctor will decide when you should stop taking metformin and when you can restart it.
Metformina Tevagen 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 disturbances, 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 worsening.
Other medicines and Metformina Tevagen
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 examination, 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 Metformina Tevagen 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
If you are pregnant, think you may be pregnant, or are planning to have a baby, talk to your doctor, as your treatment may need to be changed or your blood glucose levels monitored.
This medicine is not recommended if you are breastfeeding or planning to breastfeed your baby.
Driving and using machines
Metformin 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 medicines 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.
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 from 10 years old 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 old 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, 2 or 3 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 Metformina Tevagen
Take metformin with meals or after meals. This will prevent you from suffering from 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 Metformina Tevagen than you should
If you have taken more metformin than you should, you may suffer from 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, you should seek medical attention immediatelyas lactic acidosis can lead to a coma. Stop taking Metformina Tevagen 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 ingested.
If you forget to take Metformina Tevagen
Do not take a double dose to make up for forgotten doses. Take the next dose at the usual time.
If you have any further questions on 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 should stop taking this medicine and contact a doctor or the nearest hospital immediately, as lactic acidosis can lead to a coma.
Common side effects (may affect up to 1 in 10 people):
Very rare side effects (may affect up to 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, even if it is possible side effects not listed in this leaflet. You can also report them 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.
Composition of Metformina Tevagen
Each Metformina Tevagen 1,000 mg film-coated tablet contains 1,000 mg of metformin hydrochloride, equivalent to 780 mg of metformin base.
Core: povidone, anhydrous colloidal silica, magnesium stearate (E470b).
Coating: hypromellose, titanium dioxide (E171), and macrogol (E1521).
Appearance of the Product and Container Content
Metformina Tevagen 1,000 mg film-coated tablets are white or almost white, oval, marked on one side with "9" on the left and "3" on the right of the score line, and on the other side marked with "72" on the left and "14" on the right of the score line, with approximate dimensions of 19 mm x 9 mm.
The score line is only for fracturing and facilitating swallowing, but not for dividing into equal doses.
The tablets are supplied in blister packs of 20, 28, 30, 40, 50, 56, 60, 80, 84, 90, 100, 105, 120, and 180 tablets, and in HDPE bottles with a polypropylene cap and desiccant of 60, 100, 180, and 210 tablets.
Only some pack sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Teva B.V.
Swensweg 5,
2031GA Haarlem,
Netherlands
Manufacturer
TEVA CZECH Industries s.r.o.
Ostravská 305/29 747 70 OPAVA-KOMÁROV
Czech Republic
Or
Teva Pharmaceutical Works Private Limited Company
Pallagi ut 13 4042 Debrecen
Hungary
For further information about this medicinal product, please contact the local representative of the marketing authorization holder:
Teva Pharma, S.L.U.
Anabel Segura 11, Edificio Albatros B, 1st floor
28108 Alcobendas Madrid
Spain
Date of the Last Revision of this Leaflet: 03/2025
Detailed information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/