miglitol contraindications priligy
Commonly reported side effects of miglitol include: abdominal pain, diarrhea, gastrointestinal signs and symptoms, and flatulence. To help you remember, take it at the same times each day.Tell your doctor if your condition does not get better or if it gets worse (your Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Miglitol decreases plasma concentrations of several drugs, including glyburide and metformin. In the colon, bacteria will digest the complex carbohydrates, causing GI side-effects flatulence (78%) and diarrhea (14%). Pooled data from controlled studies suggest a dose-response for both HbA1c and one-hour postprandial plasma glucose throughout the recommended dosage range. Miglitol is fairly well absorbed by the body, as opposed to acarbose. Miglitol requires 1-deoxynojirimycin as a precursor which can be obtained via three different routes: extraction from plants such as the mulberry tree, fermentation using various bacterial strains, and a complete chemical synthesis.In 207 patients with type 2 diabetes who used insulin and took miglitol or placebo, Another multicenter, double-blind, randomized, and placebo-controlled study to determine the effect of miglitol treatment involved 192 patients who had been receiving sulfonylureas for at least 6 months prior to the trial and the results were recorded after 8, 14, and 20 weeks from the start of the study (Miglitol has similar side effects as acarbose, such as diarrhea, flatulence, and abdominal pain (Post hoc analysis of the STOP-NIDDM trial database suggests that treatment of patients who have IGT with acarbose is associated with a reduction in the risk of cardiovascular disease and hypertension.Pharmacokinetic studies showed that patients with renal impairment (creatinine clearance <25 mL/min/1.73mAcarbose can reduce plasma concentrations of digoxin by impairing its absorption [An 82-year-old man with type 2 diabetes, taking digoxin and voglibose 0.9 mg/day, had digoxin serum concentrations in the target range [A 69-year-old woman with diabetes mellitus and heart failure repeatedly had unusual subtherapeutic plasma digoxin concentrations [In a randomized, crossover study in healthy men, acarbose 100–200 mg reduced the AUC and CIn one study there was no interaction of voglibose with digoxin [In eight healthy subjects taking acarbose 100 mg tds, colestyramine 12 g/day for 6 days improved the reduction in postprandial insulin concentration; the serum insulin concentration rebounded to 31% above baseline when both drugs were withdrawn [In a placebo-controlled study in six patients with type 2 diabetes, acarbose 300 mg/day for 7 days had no significant effect on the pharmacokinetics of a single dose of glibenclamide 5 mg [In a double-blind, crossover study in 12 healthy men, voglibose 5 mg tds for 8 days had no significant effect on the pharmacokinetics of a single dose of glibenclamide 1.75 mg [In 24 healthy volunteers thioctic acid 600 mg orally had no significant effect on the actions of acarbose 50 mg and acarbose did not alter the pharmacokinetics of thioctic acid [Acarbose may increase the availability of warfarin [In a double-blind, randomized, crossover study in 12 healthy volunteers, cefalexin 500 mg increased the CThe combination of metformin with other drugs that can lower the blood glucose concentration can result in severe hypoglycemia.A 79-year-old woman was admitted to hospital stuporose and unresponsive [The combination of metformin, which itself does not cause hypoglycemia, with an ACE inhibitor, nitrofurantoin, and an NSAID, which all have glucose-lowering effects, and poor food intake may have led to hypoglycemia in this case.Iodinated contrast media can induce acute renal insufficiency in patients taking metformin [take a blood sample for creatinine baseline estimation before giving a contrast medium;withdraw metformin 48 hours before the investigation;if the urine output is normal for 48 hours after the radiological procedure the patient can resume metformin;when it is discovered after a procedure that the preinvestigation creatinine was raised (since the procedure may be carried out before the creatinine is known), the patient’s physician should be contacted and the creatinine must be measured again within 48 hours.In January 1998 the FDA approved a package insert stating: “Glucophage (metformin) should be discontinued at the time of or prior to the procedure and withheld for 48 hours subsequent to the procedure and reinstituted only after renal function has been re-evaluated and found to be normal” [Drug interactions can precipitate metformin-induced lactic acidosis, as has been reported after the addition of indometacin [A 57-year-old woman, who had taken metformin 500 mg bd for 15 years, took indometacin 50 mg qds for 2 months.
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.In contrast to sulfonylureas, miglitol does not enhance insulin secretion; the antihyperglycemic action of miglitol results from a reversible inhibition of membrane-bound intestinal alpha-glucosidases which hydrolyze oligosaccharides and disaccharides to glucose and other monosaccharides in the brush border of the small intestine. Patient w/ diabetic ketoacidosis, inflammatory bowel disease, colonic ulceration, partial intestinal obstruction or predisposition to this condition, chronic intestinal diseases associated w/ marked disorders of digestion or absorption and co-existing conditions … She developed oliguria and acidosis (pH 6.82, serum lactate 21 mmol/l, creatinine 480 μmol/l). Miglitol is a desoxynojirimycin derivative, and is chemically known as 3,4,5-piperidinetriol, 1-(2-hydroxyethyl)-2-(hydroxymethyl)-, [2R-(2α,3β,4α, 5β)]-. Proper dietary management alone may be effective in controlling the blood glucose and symptoms of hyperglycemia. DESCRIPTION. These studies revealed no evidence of fetal malformations attributable to miglitol. Severe hypoglycemia may require the use of either intravenous glucose infusion or glucagon injection.Acarbose was the first AGI with now > 25 years in clinical use, and has the most data on mode of action, therapeutic benefits, and cardiovascular outcome trials. In patients taking miglitol, oral glucose (dextrose) should be used instead of sucrose (cane sugar) in the treatment of mild-to-moderate hypoglycemia since the hydrolysis of sucrose to glucose and fructose is inhibited by miglitol. Measurement of glycosylated hemoglobin levels is recommended for the monitoring of long-term glycemic control.Several studies investigated the possible interaction between miglitol and glyburide. Although the levels of miglitol reached in human milk are exceedingly low, it is recommended that miglitol tablets not be administered to a nursing woman.Safety and effectiveness of miglitol tablets in pediatric patients have not been established.Of the total number of subjects in clinical studies of miglitol tablets in the United States, patients valid for safety analyses included 24% over 65, and 3% over 75. In U.S. placebo-controlled trials, the incidences of abdominal pain, diarrhea, and flatulence were 11.7%, 28.7%, and 41.5% respectively in 962 patients treated with miglitol tablets, 25 mg to 100 mg 3 times daily, whereas the corresponding incidences were 4.7%, 10.0%, and 12.0% in 603 placebo-treated patients. Miglitol is soluble in water and has a pKa of 5.9. Hypersensitivity to miglitol. Sucrose, whose hydrolysis to glucose and fructose is inhibited by miglitol tablets, is unsuitable for the rapid correction of hypoglycemia. It is a pseudo tetrasaccharide and has a 10Miglitol by contrast is synthesized by biotechnological and chemical procedures. Dosage adjustment to correct the increased plasma concentrations is not feasible because miglitol acts locally. Contraindications. Miglitol, also an alpha-glucosidase inhibitor, may impair the oral absorption of digoxin and lead to subtherapeutic serum digoxin concentrations in some patients. In rabbits, doses of 10, 45, and 200 mg/kg corresponding to levels of approximately 0.5, 3, and 10 times the human exposure were examined. Select one or more newsletters to continue. Miglitol decreases plasma concentrations of several drugs, including glyburide and metformin. Properly discard this product when it is expired or no longer needed. Miglitol is a deoxynojirimycin derivative that inhibits disaccharide-hydrolysing enzymes in the small intestine.
The elimination half-life of miglitol from plasma is approximately 2 hours.Because miglitol is excreted primarily by the kidneys, accumulation of miglitol is expected in patients with renal impairment.
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