Glipizide description, usages, side effects, indications, overdosage, supplying and lots more!

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Glipizide

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

GLIPIZIDE DESCRIPTION



Glipizide




CLINICAL PHARMACOLOGY

Mechanism of Action:

Pharmacokinetics


Other Effects:



PHARMACOKINETICS




INDICATIONS & USAGE







GLIPIZIDE CONTRAINDICATIONS





WARNINGS

SPECIAL WARNING ON INCREASED RISK OF CARDIOVASCULAR MORTALITY:
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 Diabetics 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 non-insulin-dependent diabetes. The study involved 823 patients who were randomly assigned to one of four treatment groups. (Diabetes, 19, supp. 2:747-830, 1970).
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 2times 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.


PRECAUTIONS

General
Renal and Hepatic Disease:

Hypoglycemia:
Loss of Control of Blood Glucose


LABORATORY TESTS



INFORMATION FOR PATIENTS




DRUG INTERACTIONS





CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY



PREGNANCY

Teratogenic Effects:



Nonteratogenic Effects:


NURSING MOTHERS



PEDIATRIC USE



GERIATRIC USE



GLIPIZIDE ADVERSE REACTIONS


Hypoglycemia:PRECAUTIONSOVERDOSAGE
Gastrointestinal:
Dermatologic:
Hematologic:
Metabolic:
Endocrine Reactions:
Miscellaneous:
Laboratory Tests:

OVERDOSAGE




DOSAGE & ADMINISTRATION




Initial Dose:
Titration:
Maintenance:
PRECAUTIONS
Patients Receiving Insulin:





Patients Receiving Other Oral Hypoglycemic Agents:

HOW SUPPLIED




STORAGE AND HANDLING





PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Glipizide

Glipizide

Glipizide TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-537(NDC:0591-0461)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GLIPIZIDE GLIPIZIDE 10 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
ANHYDROUS LACTOSE
cellulose, microcrystalline
STARCH, CORN
STEARIC ACID

Product Characteristics

Color Size Imprint Code Shape
white 10 mm WATSON;461 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-537-28 300 in 1 CANISTER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074223 2011-09-26


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Be sure to consult your doctor before taking any medication!
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