PATIENT INFORMATION LEAFLET
Glimepiride Kern Pharma 2 mg Tablets
Read this leaflet carefully before you start taking this medicine because it contains important information for you.
Glimepirida belongs to a group of medications known as oral antidiabetics, which reduce blood glucose to normal levels in adult patients with diabetes (type 2 diabetes).
This medication is prescribed to treat adult diabetes (type 2 diabetes) when diet, physical exercise, and weight reduction alone are not sufficient.
Do not take Glimepirida Kern Pharma
Warnings and precautions
Consult your doctor or pharmacist before starting to take your medicine:
Hypoglycemia may occur in patients who lack an enzyme called glucose-6-phosphate dehydrogenase, leading to hemolytic anemia.
Important information about hypoglycemia (low blood sugar)
If you are taking glimepiride, you may experience hypoglycemia (low blood sugar). Please see below for more information about hypoglycemia, its symptoms, and treatment.
Factors that may increase the risk of hypoglycemia:
Symptoms of hypoglycemia:
If your blood sugar levels continue to drop, you may experience significant confusion (delirium), seizures, loss of self-control, shallow breathing, and a slower heart rate, and you may become unconscious. The clinical picture of severe hypoglycemia resembles a stroke.
Treatment of hypoglycemia
In most cases, hypoglycemia symptoms disappear quickly when you consume sugar, such as sugar cubes, sweet juices, or sweet tea.
Therefore, you should always carry something sweet with you (e.g., sugar cubes). Remember that artificial sweeteners are not effective. Please consult your doctor or seek hospital attention if you do not recover or if symptoms recur.
Blood tests
Your blood sugar and urine levels should be regularly monitored. Your doctor may request blood tests to check your blood cell count and liver function.
Use of other medicines
Inform your doctor or pharmacist if you are using or have recently used any other medication, including those purchased without a prescription, as it may be necessary to interrupt treatment or adjust the dose of one or more of them.
If you take glimepiride with the following compounds, hypoglycemia (low blood sugar) may occur:
If you take glimepiride with the following compounds, hypoglycemia (low blood sugar) may occur:
If you take glimepiride with the following compounds, both hypoglycemia and hyperglycemia may occur:
Glimepiride may increase or decrease the effects of the following medications:
Taking Glimepirida Kern Pharma with food and drinks
Consuming alcohol may unpredictably increase or decrease the hypoglycemic effect of this medication.
Glimepiride should be taken shortly before or during a meal.
Pregnancy and lactation
If you are pregnant or breastfeeding, or if you think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before taking this medication.
Pregnancy
Glimepiride should not be taken during pregnancy. Consult your doctor if you are pregnant, think you may be pregnant, or are planning to become pregnant.
Lactation
Glimepiride may pass into breast milk. Glimepiride should not be used during lactation.
Driving and operating machinery:
Consult your doctor or pharmacist before using any medication.
Your ability to concentrate and react may be impaired due to symptoms caused by hypoglycemia or hyperglycemia, such as visual disturbances.
This may be hazardous in situations where these skills are essential (e.g., driving or operating machinery). Therefore, consult your doctor if it is recommended to drive or operate machinery.
Important information about some components of Glimepirida Kern Pharma
This medication contains lactose. If your doctor has indicated that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow exactly the administration instructions of this medication indicated by your doctor. Consult your doctor or pharmacist if you have doubts.
Remember to take your medication.
The basis of satisfactory diabetes treatment lies in a good diet, regular physical activity, and regular blood and urine controls. The negative effects resulting from not maintaining the diet cannot be compensated with tablets or insulin.
Dosage is based on the results of the metabolic examination (blood and urine glucose determinations).
The initial dose is 1 mg of glimepiride per day orally. In case of good regulation, the same dose can be used as maintenance treatment.
If regulation is not satisfactory, your doctor will indicate a gradual increase in dose up to 2, 3, or 4 mg of glimepiride per day.
Only in exceptional cases, it is recommended to take more than 4 mg of glimepiride per day, with the maximum recommended dose being 6 mg of glimepiride per day.
If you experience a hypoglycemic reaction after taking a single dose of 1 mg of glimepiride, inform your doctor as you may be regulated solely with diet.
During treatment with glimepiride, it is possible that the dose you need may decrease. Therefore, your doctor may need to adjust the daily dose according to your needs and even discontinue treatment.
If you are being treated with metformin and do not achieve adequate metabolic control, your doctor may complement the treatment with glimepiride. Your doctor will indicate the necessary dose of Glimepiride Kern Pharma to be used in conjunction with metformin.
Your doctor will decide if you need to complement Glimepiride Kern Pharma treatment with insulin. In that case, they will indicate the dose of insulin you will need to take in conjunction with glimepiride tablets.
If you estimate that the action of glimepiride is too strong or too weak, inform your doctor or pharmacist.
Glimepiride tablets should be taken without chewing, accompanied by a small amount of liquid.
Normally, a daily dose of glimepiride is sufficient. It is recommended that you take this dose a little before or during a generous breakfast, or if you do not take this, a little before or during the first meal.
Your doctor will indicate the duration of your treatment with Glimepiride Kern Pharma. Do not discontinue treatment before, as your blood sugar level may become unbalanced again.
Use in children
Glimepiride Kern Pharma has not been studied in children.
Older adults
No specific studies have been conducted in older adults.
Since biological functions may be decreased, your doctor will adjust the dose with greater caution and close monitoring will be necessary.
If you take more Glimepiride Kern Pharma than you should
You may cause an excessive reduction in blood sugar (see "Warnings and precautions") that may last from 12 to 72 hours and even recur after initial recovery. Symptoms may appear even 24 hours after ingestion. If this occurs, visit your doctor or the nearest hospital emergency service, bringing this leaflet with you.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
If you forgot to take Glimepiride Kern Pharma
Do not take a double dose to compensate for the missed doses.
If you interrupt treatment with Glimepiride Kern Pharma
If you interrupt or discontinue treatment, be aware that the desired effect of reducing blood sugar will not be achieved or that the disease will worsen again. Continue taking glimepiride until your doctor tells you to stop.
If you have any other doubts about the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
Consult your doctor immediately if you experience any of the following symptoms:
Some patients have experienced the following side effects while taking glimepiride:
Rare side effects(affect up to 1 in 1,000 people)
These changes usually disappear when treatment with glimepiride is stopped.
Very rare side effects(affect up to 1 in 10,000 people)
Other side effects include:
Reporting side effects:
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this prospectus. You can also report them directly through the Spanish System of Pharmacovigilance of Medicines for Human Use http://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
No special storage conditions are required.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after “CAD”. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at the SIGRE collection point of the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Glimepiride Kern Pharma
Appearance of the product and contents of the packaging
Glimepiride Kern Pharma is presented in the form of oblong tablets, green in color, and scored on both faces. Each package contains 30 or 120 tablets (standard package), or 500 tablets (clinical package).
Other presentations
Glimepiride Kern Pharma 4 mg tablets EFG. Standard packages of 30 or 120 tablets, or clinical package of 500 tablets.
Holder of the marketing authorization
Kern Pharma, S.L.
Venus, 72 – Pol. Ind. Colón II
08228 Terrassa - Barcelona
Spain
Responsible for manufacturing
Edmond Pharma S.R.L.
Strada Statale dei Giovi No. 131
20037 Paderno Dugnano
Milan (Italy)
or
Kern Pharma, S.L.
Venus, 72 - Pol. Ind. Colón II
08228 Terrassa - Barcelona
Spain
Last review date of this leaflet: June 2015
The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/.
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