Generic AmarylGlimepiride 2mg | |||||||||||||||||||||
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Generic Amaryl (Glimepiride 2mg)
Amaryl
Glimepiride
Sugar diabetes of type 2.
Glimepiride stimulates secretion and release of insulin by pancreatic cells, the drug deflates sugar level not increasing insulin level.
Glimepiride should be administrated to adults orally: the starting dose is 1—2 mg once daily during breakfast, for elderly patients the starting dose should be 1 mg/daily, a supporting dose will be 1—4 mg once daily; if the dose of 2 mg/daily has proven to be inefficient it may by increased by 2 mg/daily more with an interval of 1—2 weeks under control of plasma glucose, the maximal dose should be 8 mg/daily.
Hypersensitivity, sugar diabetes of type 1, acute aggravation of sugar diabetes, on the verge of diabetic coma condition of a patient or coma condition, hyperosmolar coma. Liver and kidneys failure, major burns, trauma, greater surgeries, bowel obstruction, retention of gastric emptying, the states accompanied with food malabsorption, progression of hypoglycemia (infectious diseases), leucopenia, pregnancy, lactation period.
Glimepiride should be taken with caution in cases of fever syndrome, alcoholism, adrenal insufficiency, and sugar diabetes of type 2 of sliding course or unsteady one, thyroid gland diseases.
The drug should be administered individually under a strict medical control, if there is a need of combined use of medications you should necessarily see you doctor for advice!
In overdosing side effects are significantly enhanced.
Manifestations of hunger, nausea, vomiting, apathy, drowsiness, depression, sleep disorders, acute weakness, anxiety, impairment in ability to concentrate attention, speech disorder and vision disorder, sense shock, dizziness, convulsions, shallow breath, bradycardia, rise of arterial tension, tachycardia, impairment of consciousness, coma.
Glimepiride is counterindicated in pregnancy and lactation. In case of oncoming of pregnancy the patient should be transferred to insulin therapy as soon as possible. During the treatment breastfeeding should be stopped.
During the treatment it is not recommended to carry out activities which require alertness and rapidity of psychomotor action.
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