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Adride (Glimepiride)
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Adride

Adride is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes. It may also be used with other diabetes medications. Adride belongs to the class of drugs known as sulfonylureas. It lowers blood sugar by causing the release of your body's natural insulin.

Other names for this medication:
Accuglim, Adride, Aroglim, Capril, Conpride, Daoryl, Diagraph, Diapex, Diazero, Duopi, Emperide, Forme, Gleam, Glifix, Glimecure, Glimefide, Glimepiride, Glimerit, Glimetrol, Glimfit, Glimiperide, Glimiriv, Glimpid, Glimpil, Glimser, Glinidd, Gluconorm, Glucut, Insurol, Isryl, Keogli, Merid, Metapride, Obimet, Prichek, Vipride, Voglibite, Volpost, Zorep, Zoryl, Zulip

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Also known as: Glimepiride

Description

Adride (glimepiride) is an oral diabetes medicine that helps control blood sugar levels.

Adride is used together with diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus. This medicine is not for treating type 1 diabetes.

Insulin or other diabetes medicines are sometimes used in combination with Adride if needed.

Dosage

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

Overdose

If you overdose Generic Adride and you don't feel good you should visit your doctor or health care provider immediately.

Storage

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 Adride 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.

Contraindications

You should not use Adride 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 Adride 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).

Adride 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 Adride 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 Adride 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).

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

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To assess the reliability of computed tomography (CT) cholangiography in evaluating the anatomy of the intrahepatic biliary ducts. A series of thermal images were recorded by an infrared thermal imaging camera during the downpack procedure. Behavioural interventions are recommended as first-line therapy for the management of urinary incontinence. CNTFR-deficient mice show profound neuronal deficits at birth, leading to a lethal phenotype. Studies on emotional processing report that schizophrenic patients present a specific pattern of emotional responding that usually includes deficits in emotional expressiveness, increased feelings of unpleasant emotion but decreased feelings of pleasant emotion, and increased physiological reactivity. We have previously shown that HCV infection modulates phosphorylation of Akt, a downstream target of IRS-1. A single-blinded randomized controlled trial, with outcome assessments at baseline, postintervention (6 wk), and follow-up (18 wk). cDTA reveals that Sc and Sp transcripts that encode orthologous proteins have similar synthesis rates, whereas decay rates are fivefold lower in Sp, resulting in similar mRNA concentrations despite the larger Sp cell volume. Recent knowledge of the endocrine background of malignant disease.

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The aim of this study was to assess the role of aortic elasticity parameters to predict AA growth rates in patients with AA dilation (AAD). Disruptions of TIR1, TIR3, or TIR4 prevent anaerobic growth, indicating that each protein is essential for anaerobic adaptation. Data regarding the clinical relevance of pulmonary infarction (PI) in patients with pulmonary embolism (PE) are lacking. It is likely that these effects are related to work, both through neuroendocrine stress mechanisms associated with certain job characteristics and through job-determined adverse health-related behaviour. Arterial hypertension, serious public health problem in black Africa. The mechanisms mediating the effect of n-3 fatty acids on triglyceride (TG) biosynthesis in rats. Electrophoretic mobility of lymphocytes from healthy individuals and cancer patients was analyzed by means of a fully automated cell electrophoresis apparatus (Parmoquant). Inhibition of growth hormone signaling by the fasting-induced hormone FGF21.

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