Nateglinide tablets should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.In the rabbit, embryonic development was adversely affected and the incidence of gall bladder agenesis or small gallbladder was increased at a dose of 500 mg/kg (approximately 27 times the human therapeutic exposure of 120 mg three times daily, based on body surface area). The weight, the diameter and the hardness of the obtained tablet were 416.1 mg, 10 mmpsi, about 60 N, respectively. For information about enrolling in MedicAlert, call 1-888-633-4298 (US) or 1-800-668-1507 (Canada).HOW TO USE THIS INFORMATION: This is a summary and does NOT have all possible information about this product. Exercise Tell your doctor right away if you have symptoms of high or low blood sugar. If you have any questions, consult your doctor or pharmacist.Take this medication by mouth 1-30 minutes before each main meal, usually 3 times daily, or as directed by your doctor. Button close - press enter or select to This copyrighted material has been downloaded from a licensed data provider.The above information is intended to supplement, not substitute for, the expertise and judgment of your health care professional. (See also Side Effects section.)
Consult your pharmacist or local waste disposal company.Your condition can cause complications in a medical emergency.

Increased hunger increase the response to nateglinide and may require the dose of nateglinide to
FDA Prescribing Information. Consult your doctor because increased stress may require a change in your treatment plan, medications, or blood sugar testing.During pregnancy, this medication should be used only when clearly needed. Consult your doctor before breast-feeding.Drug interactions may change how your medications work or increase your risk for serious side effects. This is very important in order to determine the correct dose. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction:This is not a complete list of possible side effects. Similarly, Nateglinide had no influence on the serum protein binding of propranolol, glyburide, nicardipine, warfarin, phenytoin, acetylsalicylic acid, and tolbutamide in vitro. Ketoacidosis. It works by stimulating the body to produce more insulin. A study for a 78 year old man who takes Eliquis, Lopressor, Lipitor, Lozol, Altace, Norvasc - 24 minutes ago; A study for a 50 year old woman who takes Dexamethasone Intensol - 25 minutes ago; A study for a 59 year old man who takes Toprol-xl - 27 minutes ago However, prudent evaluation of individual cases is warranted in the clinical setting.The effect of coadministered drugs on the pharmacokinetics of Nateglinide and the effect of Nateglinide on pharmacokinetics of coadministered drugs are shown in Tables 3 and 4. Dispense in a tight container (USP).Instruct patients to take Nateglinide tablets 1 to 30 minutes before meals. dependent) is caused by: INGREDIENTS AND APPEARANCE. Hypoglycemic symptoms without loss of consciousness or neurological findings should be treated with oral glucose and adjustments in dosage and/or meal patterns. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Nateglinide is used alone or with other medications to control high blood sugar along with a proper diet and exercise program. In clinical trials, the mean weight increases with Nateglinide tablets 60 mg (3 times daily) and Nateglinide tablets 120 mg (3 times daily) compared to placebo were 1.0 kg and 1.6 kg respectively.Increases in Uric Acid: There were increases in mean uric acid levels for patients treated with Nateglinide tablets alone, Nateglinide tablets in combination with metformin, metformin alone, and glyburide alone.