Glimepiride
Glibetic contains the active substance glimepiride, which, when taken orally, lowers the blood sugar (glucose) level. The medicine belongs to the group of sulfonylurea derivatives.
Glibetic is indicated for the treatment of type 2 diabetes (non-insulin-dependent) when diet, physical exercise, and weight loss are not sufficiently effective. The medicine can be used in combination with metformin or insulin.
Before starting treatment with Glibetic, you should discuss it with your doctor or pharmacist.
During treatment with Glibetic, regular blood sugar tests are necessary. Your doctor may also recommend blood tests to monitor your blood cell count and liver function.
The patient should follow the treatment plan prescribed by the doctor in order to achieve proper blood sugar control. This means that, in addition to taking the tablets regularly, the patient should follow a diet, exercise, and, if necessary, lose weight. You should also take care to have regular blood sugar tests (and possibly urine tests) as recommended by your doctor.
During the first few weeks of treatment, the risk of low blood sugar (hypoglycemia) may be increased, so the patient should be under close medical supervision.
Low blood sugar may occur if:
If such a risk exists, you should inform your doctor so that they can adjust the glimepiride dose or change the entire treatment plan if necessary.
If the patient experiences low blood sugar (hypoglycemia), the following symptoms may occur:
headache, feeling of hunger, exhaustion, nausea, vomiting, fatigue, drowsiness, sleep disturbances, anxiety, aggression, decreased concentration, attention, and reaction time, depression, disorientation, speech and vision disorders, difficulty speaking or understanding speech (aphasia), tremors, weakness, sensory organ disorders, dizziness, helplessness.
The following symptoms may also occur: sweating, sticky skin, anxiety, rapid heartbeat, high blood pressure, feeling of irregular or forceful heartbeat (palpitations), sudden chest pain that may radiate (angina pectoris), and arrhythmias.
If blood sugar levels continue to decrease, severe disorientation (delirium), seizures, loss of self-control, shallow breathing, and slowed heart rate may occur, and the patient may lose consciousness. The clinical picture of severe low blood sugar may resemble a stroke.
In most cases, the symptoms of low blood sugar disappear very quickly if the patient consumes sugar, e.g., sugar cubes, sweet juice, sweetened tea (artificial sweeteners are ineffective).
Symptoms of low blood sugar may not occur, be less severe, or develop slowly. The patient may not be aware that their blood sugar level has decreased. This can happen in elderly patients, those taking certain medications (e.g., central nervous system depressants or beta-adrenergic blockers), or those with certain endocrine disorders (e.g., thyroid, pituitary, or adrenal cortex disorders).
In stressful situations (e.g., accidents, emergency surgery, infections with fever), temporary replacement with insulin may be indicated.
Symptoms of high blood sugar (hyperglycemia - may occur if Glibetic does not sufficiently lower blood sugar levels, if the patient does not follow the doctor's recommendations, or if a particularly stressful situation occurs) may include: increased thirst, frequent urination, dry mouth, dry and itchy skin, fungal or skin infections, decreased patient activity.
In such cases, you should contact your doctor immediately.
You should inform your doctor if you have a deficiency of glucose-6-phosphate dehydrogenase (a rare hereditary disease). In this case, the doctor may decide to change the medicine.
Use in patients with liver and/or kidney disorders
There is no data on the use of Glibetic in patients with severe liver dysfunction and in patients undergoing dialysis. In patients with severe kidney or liver dysfunction, a change to insulin is recommended.
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.
Taking Glibetic with certain medicines may cause both increased and decreased effects of glimepiride's blood sugar-lowering action. The effect of other medicines may also be disrupted if taken with Glibetic. Therefore, other medicines should only be taken with the doctor's consent (or prescription).
The blood sugar-lowering effect of Glibetic may be increased, and symptoms of low blood sugar may occur if any of the following medicines are taken:
The blood sugar-lowering effect of Glibetic may be decreased, and symptoms of high blood sugar may occur if any of the following medicines are taken:
Medicines used to treat stomach and duodenal ulcers (H receptor antagonists) or medicines that lower blood pressure (beta-adrenergic blockers, clonidine, and reserpine) may increase or decrease the effect of glimepiride's blood sugar-lowering action.
Medicines that act on the central nervous system (beta-adrenergic blockers, clonidine, guanethidine, or reserpine) may mask or completely eliminate the symptoms of low blood sugar.
Glibetic may increase or decrease the effect of medicines that prevent blood clotting (coumarin derivatives).
The medicine should be taken directly before or during breakfast, or another main meal. The tablets should be swallowed whole, washed down with water.
Alcohol may increase or decrease the effect of Glibetic in an unpredictable way.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, you should consult your doctor or pharmacist before taking this medicine.
Pregnancy
Glibetic is contraindicated during pregnancy. During pregnancy, insulin should be used. Women planning to become pregnant should inform their doctor.
Breastfeeding
Glibetic is contraindicated in breastfeeding women.
Due to hypoglycemia or hyperglycemia, or as a result of vision, concentration, and reaction disturbances, the patient's ability to drive and operate machines may be impaired. It should be considered whether, in these circumstances, it is possible to drive or operate machines.
If you have been diagnosed with intolerance to some sugars, you should contact your doctor before taking the medicine.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means the medicine is considered "sodium-free".
This medicine should always be taken according to the doctor's recommendations. In case of doubts, you should consult a doctor. The doses of the medicine may be different for different patients.
Changes in external factors, diet, physical exercise, stress may require changes in the medicine's dosage. Oral anti-diabetic medicines or insulin are not effective if the patient does not follow the prescribed diet.
The dosage is determined by the doctor based on the results of blood glucose and urine tests. Usually, a single daily dose of glimepiride is sufficient. It is recommended to take the medicine shortly before or during breakfast, or (if breakfast is skipped) shortly before or during the first main meal.
The tablets should be swallowed whole, washed down with a small amount of water.
Initially, glimepiride is administered in a dose of 1 mg per day. If this dose provides good glycemic control, it should be taken as a maintenance dose.
In the absence of satisfactory glycemic control, the doctor may gradually increase the dose based on the results of glycemic control, at 1-2 week intervals, up to a daily dose of 2 mg, 3 mg, or 4 mg of glimepiride.
Only in exceptional cases does a dose of glimepiride greater than 4 mg per day provide better therapeutic results.
The maximum recommended daily dose is 6 mg of glimepiride.
In patients who have not achieved satisfactory efficacy with the maximum daily dose of metformin, the doctor may use combination therapy with glimepiride. While maintaining the metformin dose, treatment with Glibetic should be started with a low dose, which, depending on the efficacy of glucose control, can be increased up to the maximum daily dose. Combination therapy should be started under close medical supervision.
In patients who have not achieved satisfactory efficacy with the maximum daily dose of Glibetic, the doctor may, if necessary, start concurrent treatment with insulin.
While maintaining the Glibetic dose, insulin treatment should be started with a low dose, which can be gradually increased depending on the efficacy of glucose control. Combination therapy should be started under close medical supervision.
During treatment, if blood sugar control improves and insulin sensitivity increases, the need for glimepiride may decrease. Therefore, to avoid hypoglycemia, it should be considered to reduce the dose or completely discontinue the medicine. The doctor will also consider changing the dosage in case of changes in the patient's weight or lifestyle, as well as the occurrence of other factors that increase the risk of hypo- or hyperglycemia.
It is possible to change the treatment by replacing other oral anti-diabetic medicines with Glibetic. The recommended initial dose of Glibetic is 1 mg per day.
Depending on the response to treatment, the doctor may gradually increase the dose of Glibetic, according to the above recommendations.
In exceptional cases, in patients with type 2 diabetes treated with insulin, a change in treatment to Glibetic may be indicated.
The change in treatment should be carried out under close medical supervision.
See section 2. Warnings and precautions.
If you feel that the effect of the medicine is too strong or too weak, you should consult your doctor.
Do not change the dosage of the medicine yourself.
In case of taking a higher dose of the medicine than recommended, you should immediately contact your doctor, who will provide appropriate treatment.
Taking too much of the medicine can cause hypoglycemia lasting from 12 to 72 hours (symptoms - see Warnings and precautions). Symptoms may not occur until 24 hours after taking the excessive amount of medicine. In case of significant overdose, gastric lavage can be performed and activated charcoal administered. In a conscious patient with symptoms of hypoglycemia, vomiting should be induced, water or lemonade with activated charcoal, sodium sulfate (as a laxative), and carbohydrates (sugar) should be administered orally.
In case of missing a dose, it should be taken as soon as possible. Do not take a double dose to make up for the missed dose.
In case of any further doubts related to the use of this medicine, you should consult your doctor.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following frequency classification of side effects has been adopted:
Very common (occurs in more than 1 in 10 patients): not reported.
Common (occurs in less than 1 in 10 patients): not reported.
Uncommon (occurs in less than 1 in 100 patients): not reported.
Rare (occurs in less than 1 in 1,000 patients): changes in blood count (usually reversible after discontinuation of the medicine), hypoglycemia (i.e., low blood sugar, which usually occurs suddenly and can be dangerous - see also sections 2 and 3).
Very rare (occurs in less than 1 in 10,000 patients): allergic vasculitis; hypersensitivity reactions (usually mild, can also be severe with respiratory, blood pressure, and shock disorders); nausea, vomiting, and diarrhea; pressure or discomfort in the abdominal cavity, abdominal pain; liver function disorders (e.g., including cholestasis or jaundice), hepatitis that can lead to liver failure, decreased sodium levels in the serum.
Frequency not known (cannot be estimated from the available data): transient vision disturbances, which usually occur at the beginning of treatment; increased liver enzyme activity; cross-hypersensitivity to sulfonylurea derivatives, sulfonamides, or related substances; symptoms of skin allergy, such as itching, rash, and urticaria, hypersensitivity to light.
If you experience any side effects, including any side effects not listed in the leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: +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 the medicine.
Do not store above 25°C. Store in the original packaging to protect from light and moisture.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the specified month.
The inscription on the packaging after the abbreviation EXP means the expiry date, and after the abbreviation Lot/LOT means the batch number.
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.
Glibetic 1 mg, tablets: tablet is oblong, pink, with a score line on both sides.
Glibetic 2 mg, tablets: tablet is oblong, green, with a score line on both sides.
Glibetic 3 mg, tablets: tablet is oblong, cream, with a score line on both sides.
Glibetic 4 mg, tablets: tablet is oblong, blue, with a score line on both sides.
The packaging contains 30 tablets.
PHARMACEUTICAL WORKS POLPHARMA S.A.
Pelplińska 19, 83-200 Starogard Gdański
phone: +48 22 364 61 01
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