Sitagil Tablet 100mg

PRESENTATION

Sitagil 25: Each tablet contains Sitagliptin Phosphate Monohydrate INN equivalent to Sitagliptin 25 mg.

Sitagil 50: Each tablet contains Sitagliptin Phosphate Monohydrate INN equivalent to Sitagliptin 50 mg.

Sitagil 100: Each tablet contains Sitagliptin Phosphate Monohydrate INN equivalent to Sitagliptin 100 mg

DESCRIPTION

Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor, which exerts its action by slowing the inactivation of incretin

hormones. Incretin hormones, including glucagon-like peptide-1(GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), are

released by the intestine throughout the day and levels are increased in response to a meal. These hormones are rapidly

inactivated by the enzyme, DPP-4. The incretins are part of an endogenous system involved in the physiologic regulation of glucose

homeostasis. When blood glucose concentrations are normal or elevated, GLP-1 and GIP increase insulin synthesis and release from

pancreatic beta cells by intracellular signaling pathways involving cyclic AMP. GLP-1 also lowers glucagon secretion from

pancreatic alpha cells, leading to reduced hepatic glucose production.

INDICATIONS

Sitagil is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Sitagil is indicated as monotherapy and also indicated for use in combination with metformin, sulfonylurea or thiazolidinediones

when diet and exercise plus the single agent does not result in adequate glycemic control.

DOSAGE & ADMINISTRATION

- The recommended dose of Sitagliptin is 100 mg once daily. Sitagliptin can be taken with or without food.

- For patients with mild renal insufficiency ( creatinine clearance [CrCl]>50ml/min), no dosage adjustment is required.

- For patients with moderate renal insufficiency ( CrCl.>30 to <50 ml/min women), the dose of Sitagliptin is 50 mg once daily.

- For patients with severe renal insufficiency (CrCl<30 ml/min) or with end-stage renal disease (ESRD) requiring hemodialysis or

peritoneal dialysis, the dose of Sitagliptin is 25 mg once daily.

Pediatric Use:

Safety and effectiveness of Sitagliptin in pediatric patients under 18 years of age have not been established.

Geriatric Use:

No overall differences in safety or effectiveness were observed between subjects over 65 years. The drug is excreted by the

kidney. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection in the

elderly.

SIDE EFFECTS

Adverse reactions like upper respiratory tract infection, nasopharyngitis, and headache can occur. Hypoglycemia occurs in patients

treated with the combination of Sitagliptin and sulfonylurea, with or without Metformin.

PRECAUTIONS

- Dosage adjustment is recommended in patients with moderate or severe renal insufficiency and in patients with ESRD.

- When used with a sulfonylurea a lower dose of sulfonylurea may be required to reduce the risk of hypoglycemia.

USE IN PREGNANCY & LACTATION

Pregnanacy: Safety in pregnant women has not been established. Sitagliptin should be used during pregnancy only if the potential

benefit justifies the potential risk of the fetus.

Nursing mothers: It is not known whether Sitagliptin is secreted in human milk, it should not be administered to a breast feeding

woman.

DRUG INTERACTION

There was a slight increase in the area under the curve and mean peak drug concentration of Digoxin with the co-administration of

100 mg Sitagliptin for 10 days.

OVER DOSE

In the event of an overdose, it is reasonable to employ the usual supportivemeasures as dictated by the patient’s clinical status.

Sitagliptin is modestly dialyzable. Prolonged hemodialysis may be considered if clinically appropriate.

COMMERCIAL PACK

Sitagil 25: Each box contains 3 Alu-Alu blister strips of 10 tablets.

Sitagil 50: Each box contains 2 Alu-Alu blister strips of 10 tablets.

Sitagil 100: Each box contains 3 Alu-Alu blister strips of 10 tablets