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Abepride (Glimepiride)

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Abepride is a medicine used to treat type 2 diabetes. Type 2 diabetes is a condition where the body doesn't make enough insulin, or the insulin that it makes doesn't work properly. This can cause high blood sugar levels (hyperglycaemia).

Other names for this medication:
Adglin, Betaglim, Biopride, Cgryl, Dezacor, Diamin, Enselin, Estimet, Gamaryl, Gemer, Glimcheck, Glimetis, Glimivir, Glimlok, Glimpax, Glimstar, Glipril, Gliri, Glycinova, Glymon, Glyree, Glytab, Gride, Karmelitus, Meprji, Stator, Swimet, Vedator, Zogli

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Also known as: Glimepiride


Generic Abepride is the medication of high quality, which is taken in treatment of type 2 diabetes. The target of this perfect remedy is struggle against type 2 diabetes. Abepride is also known as Glimepiride, Diapride, Amyline, Euglim. Generic Abepride is acting by stimulating the pancreas to produce more insulin. It is sulfonylureas. Generic name of Generic Abepride is Glimepiride. Brand name of Generic Abepride is Abepride.


Take Generic Abepride tablets orally with breakfast or the first big meal of the day. Do not crush or chew it. Take Generic Abepride at the same time once a day with water. If you want to achieve most effective results do not stop taking Generic Abepride suddenly.


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An Abepride overdose can cause life-threatening hypoglycemia.

Symptoms of severe hypoglycemia include extreme weakness, confusion, tremors, sweating, fast heart rate, trouble speaking, nausea, vomiting, rapid breathing, fainting, and seizure (convulsions).


Store at room temperature below 30 degrees C (86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Abepride are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


You should not use Abepride if you are allergic to glimepiride, sulphonamides, or if you have:

an allergy to sulfa drugs; or diabetic ketoacidosis (call your doctor for treatment).

To make sure Abepride is safe for you, tell your doctor if you have ever had:

heart disease; liver or kidney disease; or an enzyme deficiency called glucose-6-phosphate dehydrogenase deficiency (G6PD).

Abepride may increase your risk of serious heart problems, but not treating your diabetes can also damage your heart and other organs. Talk to your doctor about the risks and benefits of this medicine.

Follow your doctor's instructions about using Abepride if you are pregnant or you become pregnant. Controlling diabetes is very important during pregnancy, and having high blood sugar may cause complications in both the mother and the baby. However, you may need to stop taking Abepride for a short time just before your due date.

Medications similar to glimepiride have caused severe hypoglycemia in newborn babies whose mothers used the medicine near the time of delivery. If you take glimepiride during pregnancy, stop taking this medicine at least 2 weeks before your due date.

If you breastfeed while taking glimepiride, call your doctor if your baby shows signs of hypoglycemia (extreme drowsiness, feeding problems, mottled skin, blue lips, feeling cold or jittery, or having a seizure).

Abepride is not approved for use by anyone younger than 18 years old.

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Pathogenesis of a genotype C strain of bovine parainfluenza virus type 3 infection in albino guinea pigs. Yeast endocytic adaptor AP-2 binds the stress sensor Mid2 and functions in polarized cell responses. Moreover, OVNIp enables automated exploitation of de novo sequences generated from unassigned MS/MS spectra leading to higher sequence coverage and enhancing confidence in the identified proteins. We used the pharmacological model of isolated rabbit carotid arteries with intact or mechanically removed endothelium. The positive SMO signalling is not downregulated in BCCs because of the mutational inactivation of PTC. To prospectively assess the performance of noninvasive electrocardiographic mapping (ECM) in the pre-/periprocedural localization of OTVT origin to guide acarbose tab 50mg ablation and to compare the accuracy of ECM with that of published ECG algorithms. Soft-tissue infections traditionally have been viewed as carrying a lower risk of death than other types of infection such as pneumonia, blood stream, and intra-abdominal. In this Review, we discuss the evidence for these interacting pathways and describe how the capacity of KIT, and other receptors, to influence FcepsilonRI-dependent mast-cell-mediator release might be a function of the relative abilities of these receptors to activate these alternative pathways.

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