c agents, ace inhibitors, angiotensin ii receptor blocking agents, disopyramide, fibrates, fluoxetine, monoamine oxidase inhibitors, pentoxifylline, pramlintide, propoxyphene, salicylates, somatostatin analogs (e.g., octreotide), sulfonamide antibiotics, nonsteroidal anti-inflammatory agents, chloramphenicol, probenecid, coumarins, voriconazole, h2 receptor antagonists, and quinolones. when these medications are administered to a patient receiving glipizide extended-release tablets, monitor the patient closely for hypoglycemia. when these medications are discontinued from a patient receiving glipizide extended-release tablets, monitor the patient closely for worsening glycemic control. the following are examples of medication that may reduce the glucose-lowering effect of glipizide extended-release tablets, leading to worsening glycemic control: atypical antipsychotics (e.g., olanzapine and clozapine), corticosteroids, danazol, diuretics, estrogens, glucagon, isoniazid, niacin, oral contraceptives, phenothiazines, progestogens (e.g., in oral contraceptives), protease inhibitors, somatropin, sympathomimetic agents (e.g., albuterol, epinephrine, terbutaline), thyroid hormones, phenytoin, nicotinic acid, and calcium channel blocking drugs. when such drugs are administered to patients receiving glipizide extended-release tablets, monitor the patients closely for worsening glycemic control. when these medications are discontinued from patients receiving glipizide extended-release tablets, monitor the patient closely for hypoglycemia. alcohol, beta-blockers, clonidine, and reserpine may lead to either potentiation or weakening of the glucose-lowering effect. increased frequency of monitoring may be required when glipizide extended-release tablets is coadministered with these drugs. the signs of hypoglycemia may be reduced or absent in patients taking sympatholytic drugs such as beta-blockers, clonidine, guanethidine, and reserpine. increased frequency of monitoring may be required when glipizide extended-release tablets is coadministered with these drugs. 7.2 miconazole monitor patients closely for hypoglycemia when glipizide extended-release tablets are coadministered with miconazole. a potential interaction between oral miconazole and oral hypoglycemic agents leading to severe hypoglycemia has been reported [see clinical pharmacology ( 12.3 )] . 7.3 fluconazole monitor patients closely for hypoglycemia when glipizide extended-release tablets are coadministered with fluconazole. concomitant treatment with fluconazole increases plasma concentrations of glipizide, which may lead to hypoglycemia [see clinical pharmacology ( 12.3 )] . 7.4 colesevelam glipizide extended-release tablets should be administered at least 4 hours prior to the administration of colesevelam. colesevelam can reduce the maximum plasma concentration and total exposure of glipizide when the two are coadministered [see clinical pharmacology ( 12.3 )] .

oglycemia. a lower dose of glipizide extended-release tablets may be required to minimize the risk of hypoglycemia when combining it with other anti-diabetic medications. educate patients to recognize and manage hypoglycemia. when initiating and increasing glipizide extended-release tablets in patients who may be predisposed to hypoglycemia (e.g., the elderly, patients with renal impairment, patients on other anti-diabetic medications) start at 2.5 mg. debilitated or malnourished patients, and those with adrenal, pituitary, or hepatic impairment are particularly susceptible to the hypoglycemic action of anti-diabetic medications. hypoglycemia is also more likely to occur when caloric intake is deficient, after severe or prolonged exercise, or when alcohol is ingested. the patient's ability to concentrate and react may be impaired as a result of hypoglycemia. early warning symptoms of hypoglycemia may be different or less pronounced in patients with autonomic neuropathy, the elderly, and in patients who are taking beta-adrenergic blocking medications or other sympatholytic agents. these situations may result in severe hypoglycemia before the patient is aware of the hypoglycemia. these impairments may present a risk in situations where these abilities are especially important, such as driving or operating other machinery. severe hypoglycemia can lead to unconsciousness or convulsions and may result in temporary or permanent impairment of brain function or death. 5.2 hemolytic anemia treatment of patients with glucose 6-phosphate dehydrogenase (g6pd) deficiency with sulfonylurea agents, including glipizide extended-release tablets, can lead to hemolytic anemia. avoid use of glipizide extended-release tablets in patients with g6pd deficiency. in post marketing reports, hemolytic anemia has also been reported in patients who did not have known g6pd deficiency. 5.3 increased risk of cardiovascular mortality with sulfonylureas the administration of oral hypoglycemic drugs has been reported to be associated with increased cardiovascular mortality as compared to treatment with diet alone or diet plus insulin. this warning is based on the study conducted by the university group diabetes program (ugdp), a long-term prospective clinical trial designed to evaluate the effectiveness of glucose-lowering drugs in preventing or delaying vascular complications in patients with type 2 diabetes mellitus. the study involved 823 patients who were randomly assigned to one of four treatment groups. ugdp reported that patients treated for 5 to 8 years with diet plus a fixed dose of tolbutamide (1.5 grams per day) had a rate of cardiovascular mortality approximately 2½ times that of patients treated with diet alone. a significant increase in total mortality was not observed, but the use of tolbutamide was discontinued based on the increase in cardiovascular mortality, thus limiting the opportunity for the study to show an increase in overall mortality. despite controversy regarding the interpretation of these results, the findings of the ugdp study provide an adequate basis for this warning. the patient should be informed of the potential risks and advantages of glipizide and of alternative modes of therapy. although only one drug in the sulfonylurea class (tolbutamide) was included in this study, it is prudent from a safety standpoint to consider that this warning may also apply to other oral hypoglycemic drugs in this class, in view of their close similarities in mode of action and chemical structure. 5.4 macrovascular outcomes there have been no clinical studies establishing conclusive evidence of macrovascular risk reduction with glipizide extended-release tablets or any other anti-diabetic drug. 5.5 gastrointestinal obstruction there have been reports of obstructive symptoms in patients with known strictures in association with the ingestion of another drug with this non-dissolvable extended release formulation. avoid use of glipizide extended-release tablets in patients with preexisting severe gastrointestinal narrowing (pathologic or iatrogenic).

ay be switched to glipizide extended-release tablets once daily at the nearest equivalent total daily dose. 2.2 use with other glucose lowering agents when adding glipizide extended-release tablets to other anti-diabetic drugs, initiate glipizide extended-release tablets at 5 mg once daily. start patients at increased risk for hypoglycemia at a lower dose. when colesevelam is coadministered with glipizide er, maximum plasma concentration and total exposure to glipizide is reduced. therefore, glipizide extended-release tablets should be administered at least 4 hours prior to colesevelam.

t recommended dosages. in these trials, approximately 180 patients were treated with glipizide extended-release tablets for at least 6 months. table 1 summarizes the incidence of adverse reactions, other than hypoglycemia, that were reported in pooled double-blind, placebo-controlled trials in ≥3% of glipizide extended-release tablet-treated patients and more commonly than in patients who received placebo. table 1: incidence (%) of adverse reactions reported in ≥3% of patients treated in placebo-controlled clinical trials and more commonly in patients treated with glipizide extended-release tablets (excluding hypoglycemia) glipizide extended-release tablets (%) placebo (%) (n=278) (n=69) adverse effect dizziness 6.8 5.8 diarrhea 5.4 0.0 nervousness 3.6 2.9 tremor 3.6 0.0 flatulence 3.2 1.4 hypoglycemia of the 580 patients that received glipizide extended-release tablets in clinical trials, 3.4% had hypoglycemia documented by a blood-glucose measurement <60 mg/dl and/or symptoms believed to be associated with hypoglycemia and 2.6% of patients discontinued for this reason. hypoglycemia was not reported for any placebo patients. gastrointestinal reactions in clinical trials, the incidence of gastrointestinal (gi) side effects (nausea, vomiting, constipation, dyspepsia), occurred in less than 3% of glipizide extended-release tablet-treated patients and were more common in glipizide extended-release tablet-treated patients than those receiving placebo. dermatologic reactions in clinical trials, allergic skin reactions, i.e., urticaria occurred in less than 1.5% of treated patients and were more common in glipizide extended-release tablet-treated patients than those receiving placebo. these may be transient and may disappear despite continued use of glipizide xl; if skin reactions persist, the drug should be discontinued. laboratory tests: mild to moderate elevations of alt, ldh, alkaline phosphatase, bun and creatinine have been noted. the relationship of these abnormalities to glipizide is uncertain. 6.2 postmarketing experience the following adverse reactions have been identified during post approval use of glipizide extended-release tablets. because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. abdominal pain cholestatic and hepatocellular forms of liver injury accompanied by jaundice leukopenia, agranulocytosis, thrombocytopenia, hemolytic anemia [see warnings and precautions ( 5.2 )] , aplastic anemia, pancytopenia hepatic porphyria and disulfiram-like reactions hyponatremia and the syndrome of inappropriate antidiuretic hormone (siadh) secretion rash there have been reports of gastrointestinal irritation and gastrointestinal bleeding with use of another drug with this non-dissolvable extended release formulation.

c agents, ace inhibitors, angiotensin ii receptor blocking agents, disopyramide, fibrates, fluoxetine, monoamine oxidase inhibitors, pentoxifylline, pramlintide, propoxyphene, salicylates, somatostatin analogs (e.g., octreotide), sulfonamide antibiotics, nonsteroidal anti-inflammatory agents, chloramphenicol, probenecid, coumarins, voriconazole, h2 receptor antagonists, and quinolones. when these medications are administered to a patient receiving glipizide extended-release tablets, monitor the patient closely for hypoglycemia. when these medications are discontinued from a patient receiving glipizide extended-release tablets, monitor the patient closely for worsening glycemic control. the following are examples of medication that may reduce the glucose-lowering effect of glipizide extended-release tablets, leading to worsening glycemic control: atypical antipsychotics (e.g., olanzapine and clozapine), corticosteroids, danazol, diuretics, estrogens, glucagon, isoniazid, niacin, oral contraceptives, phenothiazines, progestogens (e.g., in oral contraceptives), protease inhibitors, somatropin, sympathomimetic agents (e.g., albuterol, epinephrine, terbutaline), thyroid hormones, phenytoin, nicotinic acid, and calcium channel blocking drugs. when such drugs are administered to patients receiving glipizide extended-release tablets, monitor the patients closely for worsening glycemic control. when these medications are discontinued from patients receiving glipizide extended-release tablets, monitor the patient closely for hypoglycemia. alcohol, beta-blockers, clonidine, and reserpine may lead to either potentiation or weakening of the glucose-lowering effect. increased frequency of monitoring may be required when glipizide extended-release tablets is coadministered with these drugs. the signs of hypoglycemia may be reduced or absent in patients taking sympatholytic drugs such as beta-blockers, clonidine, guanethidine, and reserpine. increased frequency of monitoring may be required when glipizide extended-release tablets is coadministered with these drugs. 7.2 miconazole monitor patients closely for hypoglycemia when glipizide extended-release tablets are coadministered with miconazole. a potential interaction between oral miconazole and oral hypoglycemic agents leading to severe hypoglycemia has been reported [see clinical pharmacology ( 12.3 )] . 7.3 fluconazole monitor patients closely for hypoglycemia when glipizide extended-release tablets are coadministered with fluconazole. concomitant treatment with fluconazole increases plasma concentrations of glipizide, which may lead to hypoglycemia [see clinical pharmacology ( 12.3 )] . 7.4 colesevelam glipizide extended-release tablets should be administered at least 4 hours prior to the administration of colesevelam. colesevelam can reduce the maximum plasma concentration and total exposure of glipizide when the two are coadministered [see clinical pharmacology ( 12.3 )] .

ollowing administration of glipizide to pregnant rats and rabbits during organogenesis at doses 833 times and 8 times the human dose based on body surface area, respectively. however, increased pup mortality was observed in rats administered glipizide from gestation day 15 throughout lactation at doses 2 times the maximum human dose based on body surface area (see data). the estimated background risk of major birth defects is 6 to 10% in women with pre-gestational diabetes with a hba1c >7 and has been reported to be as high as 20 to 25% in women with hba1c >10. the estimated background risk of miscarriage for the indicated population is unknown. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk poorly-controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, miscarriage, preterm delivery, stillbirth, and delivery complications. poorly controlled diabetes increases the fetal risk for major birth defects, stillbirth, and macrosomia related morbidity. fetal/neonatal adverse reactions neonates of women with gestational diabetes who are treated with sulfonylureas during pregnancy may be at increased risk for neonatal intensive care admission and may develop respiratory distress, hypoglycemia, birth injury, and be large for gestational age. prolonged severe hypoglycemia, lasting 4 to 10 days, has been reported in neonates born to mothers receiving a sulfonylurea at the time of delivery and has been reported with the use of agents with a prolonged half-life. observe newborns for symptoms of hypoglycemia and respiratory distress and manage accordingly. dose adjustments during pregnancy and the postpartum period due to reports of prolonged severe hypoglycemia in neonates born to mothers receiving a sulfonylurea at the time of delivery, glipizide extended-release tablets should be discontinued at least two weeks before expected delivery (see fetal/neonatal adverse reactions). data animal data in teratology studies in rats and rabbits, pregnant animals received daily oral doses of glipizide during the period of organogenesis at doses up to 2000 mg/kg/day and 10 mg/kg/day (approximately 833 and 8 times the human dose based on body surface area), respectively. there were no adverse effects on embryo-fetal development at any of the doses tested. in a peri- and postnatal study in pregnant rats, there was a reduced number of pups born alive following administration of glipizide from gestation day 15 throughout lactation through weaning at doses ≥5 mg/kg/day (about 2 times the recommended maximum human dose based on body surface area). 8.2 lactation risk summary breastfed infants of lactating women using glipizide extended-release tablets should be monitored for symptoms of hypoglycemia (see clinical considerations) . although glipizide was undetectable in human milk in one small clinical lactation study; this result is not conclusive because of the limitations of the assay used in the study. there are no data on the effects of glipizide on milk production. the developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for glipizide extended-release tablets and any potential adverse effects on the breastfed child from glipizide extended-release tablets or from the underlying maternal condition. clinical considerations monitoring for adverse reactions monitor breastfed infants for signs of hypoglycemia (e.g., jitters, cyanosis, apnea, hypothermia, excessive sleepiness, poor feeding, seizures). 8.4 pediatric use safety and effectiveness in children have not been established. 8.5 geriatric use there were no overall differences in effectiveness or safety between younger and older patients, but greater sensitivity of some individuals cannot be ruled out. elderly patients are particularly susceptible to the hypoglycemic action of anti-diabetic agents. hypoglycemia may be difficult to recognize in these patients. therefore, dosing should be conservative to avoid hypoglycemia [see dosage and administration ( 2.1 ), warnings and precautions ( 5.1 ) and clinical pharmacology ( 12.3 )]. 8.6 hepatic impairment there is no information regarding the effects of hepatic impairment on the disposition of glipizide. however, since glipizide is highly protein bound and hepatic biotransformation is the predominant route of elimination, the pharmacokinetics and/or pharmacodynamics of glipizide may be altered in patients with hepatic impairment. if hypoglycemia occurs in such patients, it may be prolonged and appropriate management should be instituted [see dosage and administration ( 2.1 ), warnings and precautions ( 5.1 ) and clinical pharmacology ( 12.3 )].

d in rats administered glipizide from gestation day 15 throughout lactation at doses 2 times the maximum human dose based on body surface area (see data). the estimated background risk of major birth defects is 6 to 10% in women with pre-gestational diabetes with a hba1c >7 and has been reported to be as high as 20 to 25% in women with hba1c >10. the estimated background risk of miscarriage for the indicated population is unknown. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk poorly-controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, miscarriage, preterm delivery, stillbirth, and delivery complications. poorly controlled diabetes increases the fetal risk for major birth defects, stillbirth, and macrosomia related morbidity. fetal/neonatal adverse reactions neonates of women with gestational diabetes who are treated with sulfonylureas during pregnancy may be at increased risk for neonatal intensive care admission and may develop respiratory distress, hypoglycemia, birth injury, and be large for gestational age. prolonged severe hypoglycemia, lasting 4 to 10 days, has been reported in neonates born to mothers receiving a sulfonylurea at the time of delivery and has been reported with the use of agents with a prolonged half-life. observe newborns for symptoms of hypoglycemia and respiratory distress and manage accordingly. dose adjustments during pregnancy and the postpartum period due to reports of prolonged severe hypoglycemia in neonates born to mothers receiving a sulfonylurea at the time of delivery, glipizide extended-release tablets should be discontinued at least two weeks before expected delivery (see fetal/neonatal adverse reactions). data animal data in teratology studies in rats and rabbits, pregnant animals received daily oral doses of glipizide during the period of organogenesis at doses up to 2000 mg/kg/day and 10 mg/kg/day (approximately 833 and 8 times the human dose based on body surface area), respectively. there were no adverse effects on embryo-fetal development at any of the doses tested. in a peri- and postnatal study in pregnant rats, there was a reduced number of pups born alive following administration of glipizide from gestation day 15 throughout lactation through weaning at doses ≥5 mg/kg/day (about 2 times the recommended maximum human dose based on body surface area).

lease tablets in subjects with type 2 diabete mellitus, once daily administration produced reductions in hemoglobin a1c, fasting plasma glucose and postprandial glucose. the relationship between dose and reduction in hemoglobin a1c was not established, however subjects treated with 20 mg had a greater reduction in fasting plasma glucose compared to subjects treated with 5 mg. 12.3 pharmacokinetics absorption the absolute bioavailability of glipizide was 100% after single oral doses in patients with type 2 diabetes mellitus. beginning 2 to 3 hours after administration of glipizide extended-release tablets, plasma drug concentrations gradually rise reaching maximum concentrations within 6 to 12 hours after dosing. with subsequent once daily dosing of glipizide extended-release tablets, plasma glipizide concentrations are maintained throughout the 24 hour dosing interval with less peak to trough fluctuation than that observed with twice daily dosing of immediate release glipizide. the mean relative bioavailability of glipizide in 21 males with type 2 diabetes mellitus after administration of 20 mg glipizide extended-release tablets, compared to immediate release glipizide (10 mg given twice daily), was 90% at steady-state. steady-state plasma concentrations were achieved by at least the fifth day of dosing with glipizide extended-release tablets in 21 males with type 2 diabetes mellitus and patients younger than 65 years. no accumulation of drug was observed in patients with type 2 diabetes mellitus during chronic dosing with glipizide extended-release tablets. administration of glipizide extended-release tablets with food has no effect on the 2 to 3 hour lag time in drug absorption. in a single dose, food effect study in 21 healthy male subjects, the administration of glipizide extended-release tablets immediately before a high fat breakfast resulted in a 40% increase in the glipizide mean c max value, which was significant, but the effect on the auc was not significant. there was no change in glucose response between the fed and fasting state. markedly reduced gi retention times of the glipizide extended-release tablets over prolonged periods (e.g., short bowel syndrome) may influence the pharmacokinetic profile of the drug and potentially result in lower plasma concentrations. in a multiple dose study in 26 males with type 2 diabetes mellitus, the pharmacokinetics of glipizide were linear with glipizide extended-release tablets in that the plasma drug concentrations increased proportionately with dose. in a single dose study in 24 healthy subjects, four 5 mg, two 10 mg, and one 20 mg glipizide extended-release tablets were bioequivalent. in a separate single dose study in 36 healthy subjects, four 2.5-mg glipizide extended-release tablets were bioequivalent to one 10 mg glipizide extended-release tablets. distribution the mean volume of distribution was approximately 10 liters after single intravenous doses in patients with type 2 diabetes mellitus. glipizide is 98 to 99% bound to serum proteins, primarily to albumin. metabolism the major metabolites of glipizide are products of aromatic hydroxylation and have no hypoglycemic activity. a minor metabolite, an acetylamino-ethyl benzene derivative, which accounts for less than 2% of a dose, is reported to have 1/10 to 1/3 as much hypoglycemic activity as the parent compound. elimination glipizide is eliminated primarily by hepatic biotransformation: less than 10% of a dose is excreted as unchanged drug in urine and feces; approximately 90% of a dose is excreted as biotransformation products in urine (80%) and feces (10%). the mean total body clearance of glipizide was approximately 3 liters per hour after single intravenous doses in patients with type 2 diabetes mellitus. the mean terminal elimination half-life of glipizide ranged from 2 to 5 hours after single or multiple doses in patients with type 2 diabetes mellitus. specific populations pediatric: studies characterizing the pharmacokinetics of glipizide in pediatric patients have not been performed. geriatric: there were no differences in the pharmacokinetics of glipizide after single dose administration to older diabetic subjects compared to younger healthy subjects [see use in specific populations ( 8.5 )]. renal impairment: the pharmacokinetics of glipizide has not been evaluated in patients with varying degree of renal impairment. limited data indicates that glipizide biotransformation products may remain in circulation for a longer time in subjects with renal impairment than that seen in subjects with normal renal function. hepatic impairment: the pharmacokinetics of glipizide has not been evaluated in patients with hepatic impairment. drug-drug interactions miconazole a potential interaction between oral miconazole and oral glipizide leading to severe hypoglycemia has been reported. whether this interaction also occurs with the intravenous, topical, or vaginal preparations of miconazole is not known [see drug interactions ( 7.2 )]. fluconazole concomitant treatment with fluconazole increases plasma concentrations of glipizide. the effect of concomitant administration of diflucan® (fluconazole) and glipizide has been demonstrated in a placebo controlled crossover study in healthy volunteers. all subjects received glipizide alone and following treatment with 100 mg of diflucan® as a single daily oral dose for 7 days. the mean percentage increase in the glipizide auc after fluconazole administration was 56.9% (range: 35 to 81%) [see drug interactions ( 7.3 )]. colesevelam colesevelam can reduce the maximum plasma concentration and total exposure of glipizide when the two are coadministered. in studies assessing the effect of colesevelam on the pharmacokinetics of glipizide er in healthy volunteers, reductions in glipizide auc 0-∞ and c max of 12% and 13%, respectively were observed when colesevelam was coadministered with glipizide er. when glipizide er was administered 4 hours prior to colesevelam, there was no significant change in glipizide auc 0-∞ or c max , -4% and 0%, respectively [see drug interactions ( 7.4 )].

th type 2 diabetes mellitus and patients younger than 65 years. no accumulation of drug was observed in patients with type 2 diabetes mellitus during chronic dosing with glipizide extended-release tablets. administration of glipizide extended-release tablets with food has no effect on the 2 to 3 hour lag time in drug absorption. in a single dose, food effect study in 21 healthy male subjects, the administration of glipizide extended-release tablets immediately before a high fat breakfast resulted in a 40% increase in the glipizide mean c max value, which was significant, but the effect on the auc was not significant. there was no change in glucose response between the fed and fasting state. markedly reduced gi retention times of the glipizide extended-release tablets over prolonged periods (e.g., short bowel syndrome) may influence the pharmacokinetic profile of the drug and potentially result in lower plasma concentrations. in a multiple dose study in 26 males with type 2 diabetes mellitus, the pharmacokinetics of glipizide were linear with glipizide extended-release tablets in that the plasma drug concentrations increased proportionately with dose. in a single dose study in 24 healthy subjects, four 5 mg, two 10 mg, and one 20 mg glipizide extended-release tablets were bioequivalent. in a separate single dose study in 36 healthy subjects, four 2.5-mg glipizide extended-release tablets were bioequivalent to one 10 mg glipizide extended-release tablets. distribution the mean volume of distribution was approximately 10 liters after single intravenous doses in patients with type 2 diabetes mellitus. glipizide is 98 to 99% bound to serum proteins, primarily to albumin. metabolism the major metabolites of glipizide are products of aromatic hydroxylation and have no hypoglycemic activity. a minor metabolite, an acetylamino-ethyl benzene derivative, which accounts for less than 2% of a dose, is reported to have 1/10 to 1/3 as much hypoglycemic activity as the parent compound. elimination glipizide is eliminated primarily by hepatic biotransformation: less than 10% of a dose is excreted as unchanged drug in urine and feces; approximately 90% of a dose is excreted as biotransformation products in urine (80%) and feces (10%). the mean total body clearance of glipizide was approximately 3 liters per hour after single intravenous doses in patients with type 2 diabetes mellitus. the mean terminal elimination half-life of glipizide ranged from 2 to 5 hours after single or multiple doses in patients with type 2 diabetes mellitus. specific populations pediatric: studies characterizing the pharmacokinetics of glipizide in pediatric patients have not been performed. geriatric: there were no differences in the pharmacokinetics of glipizide after single dose administration to older diabetic subjects compared to younger healthy subjects [see use in specific populations ( 8.5 )]. renal impairment: the pharmacokinetics of glipizide has not been evaluated in patients with varying degree of renal impairment. limited data indicates that glipizide biotransformation products may remain in circulation for a longer time in subjects with renal impairment than that seen in subjects with normal renal function. hepatic impairment: the pharmacokinetics of glipizide has not been evaluated in patients with hepatic impairment. drug-drug interactions miconazole a potential interaction between oral miconazole and oral glipizide leading to severe hypoglycemia has been reported. whether this interaction also occurs with the intravenous, topical, or vaginal preparations of miconazole is not known [see drug interactions ( 7.2 )]. fluconazole concomitant treatment with fluconazole increases plasma concentrations of glipizide. the effect of concomitant administration of diflucan® (fluconazole) and glipizide has been demonstrated in a placebo controlled crossover study in healthy volunteers. all subjects received glipizide alone and following treatment with 100 mg of diflucan® as a single daily oral dose for 7 days. the mean percentage increase in the glipizide auc after fluconazole administration was 56.9% (range: 35 to 81%) [see drug interactions ( 7.3 )]. colesevelam colesevelam can reduce the maximum plasma concentration and total exposure of glipizide when the two are coadministered. in studies assessing the effect of colesevelam on the pharmacokinetics of glipizide er in healthy volunteers, reductions in glipizide auc 0-∞ and c max of 12% and 13%, respectively were observed when colesevelam was coadministered with glipizide er. when glipizide er was administered 4 hours prior to colesevelam, there was no significant change in glipizide auc 0-∞ or c max , -4% and 0%, respectively [see drug interactions ( 7.4 )].

ductive potential to inform their prescriber of a known or suspected pregnancy [ see use in specific populations ( 8.1 ) ]. lactation advise breastfeeding women taking glipizide extended-release tablets to monitor breastfed infants for signs of hypoglycemia (e.g., jitters, cyanosis, hypothermia, excessive sleepiness, poor feeding, seizures) [ see use in specific populations ( 8.2 ) ]. this product's label may have been updated. for full prescribing information, please contact par pharmaceutical at 1-800-828-9393 or visit www.parpharm.com .