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PMS-SITAGLIPTIN is a brand name for Sitagliptin, supplied as a tablet. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Monotherapy: pms-SITAGLIPTIN (sitagliptin) is indicated for use as an adjunct to diet and exercise to improve glycemic control in adult patients with type 2 diabetes mellitus for whom metformin is inappropriate due to contraindications or intolerance. Add-on combination: pms-SITAGLIPTIN is indicated in adult…
Verbatim from this product's HC label. Tap a section to expand.
and 10 CLINICAL PHARMACOLOGY). 2 CONTRAINDICATIONS Patients with a history of a hypersensitive reaction to pms-SITAGLIPTIN or to any ingredient in the formulation, including any non-medicinal ingredient or component of the container (see 7 WARNINGS AND PRECAUTIONS and 8 ADVERSE REACTIONS).
For a complete listing, see the
). For a complete listing, see the 6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING section). , Sulfonylurea) When pms-SITAGLIPTIN is used in combination with metformin and a sulfonylurea or with insulin (with or without metformin), a lower dose of the insulin secretagogue or insulin may be considered to reduce the risk of hypoglycemia (see 7 WARNINGS AND PRECAUTIONS and 8 ADVERSE REACTIONS).
2 Recommended Dose and Dosage Adjustment The recommended dose of pms-SITAGLIPTIN is 100 mg once daily as monotherapy or as combination therapy with metformin, with metformin and a sulfonylurea, with insulin (with or without metformin), or with pioglitazone (with or without metformin).
Renal Impairment:
Sitaglitin is renally excreted. Renal function must be assessed prior to initiation of pms-SITAGLIPTIN and periodically thereafter because, there is a dosage adjustment based upon renal function (see 7 WARNINGS AND PRECAUTIONS, Monitoring and Laboratory Tests).
73 m2) or with end-stage renal disease (ESRD) including those requiring hemodialysis or peritoneal dialysis, the dose of pms-SITAGLIPTIN is 25 mg once daily. pms-SITAGLIPTIN may be administered without regard to the timing of dialysis.
73 m2, the dose of pms-SITAGLIPTIN is 50 mg once daily. 73 m2. 73 m2). When considering the use of sitagliptin in combination with another anti-diabetic product, its conditions for use in patients with renal impairment should be followed.
Hepatic Impairment:
No dosage adjustment of pms-SITAGLIPTIN is necessary in patients with mild or moderate hepatic impairment. Sitagliptin has not been studied in patients with severe hepatic impairment and is not recommended for use in this population.
, 4 DOSAGE AND ADMINISTRATION and 10 CLINICAL PHARMACOLOGY). 2 CONTRAINDICATIONS Patients with a history of a hypersensitive reaction to pms-SITAGLIPTIN or to any ingredient in the formulation, including any non-medicinal ingredient or component of the container (see 7 WARNINGS AND PRECAUTIONS and
Patients with a history of a hypersensitive reaction to pms-SITAGLIPTIN or to any ingredient in the formulation, including any non-medicinal ingredient or component of the container (see 7 WARNINGS AND PRECAUTIONS and 8 ADVERSE REACTIONS).
For a complete listing, see the 6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING section).
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
Other brands of Sitagliptin in Canada.
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Brand names are compiled from public regulatory records for active-ingredient mapping only. Drugvu is not affiliated with any manufacturer. This is not medical advice.
Pediatrics (<18 years of age):
Health Canada has not authorized an indication for pediatric use.
Geriatrics (≥65 years of age):
No dosage adjustment is necessary for geriatric patients. However, because sitagliptin is substantially excreted by the kidney, and because aging can be associated with reduced renal function, renal function should be assessed more frequently in elderly patients (see 7 WARNINGS AND PRECAUTIONS, Special Populations).
4 Administration pms-SITAGLIPTIN can be taken with or without food. 5 Missed Dose If a dose of pms-SITAGLIPTIN is missed, it should be taken as soon as the patient remembers. A double dose of pms-SITAGLIPTIN should not be taken on the same day.
, remove unabsorbed material from the gastrointestinal tract, employ clinical monitoring (including obtaining an electrocardiogram), and institute supportive therapy if required. Sitagliptin is modestly dialyzable. 5% of the dose was removed over a 3- to 4-hour hemodialysis session.
Prolonged hemodialysis may be considered if clinically appropriate. It is not known if sitagliptin is dialyzable by peritoneal dialysis. For management of a suspected drug overdose, contact your regional poison control centre. 6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING Table 1 – Dosage Forms, Strengths, Composition and Packaging.
Route of Administration Dosage Form / Strength / Composition Non-Medicinal Ingredients Oral Film-coated Tablet 25 mg §, 50 mg§§ and 100 mg§§§ sitagliptin Anhydrous Dibasic Calcium Phosphate, Croscarmellose Sodium, Magnesium Stearate, Microcrystalline Cellulose Povidone, Sodium Stearyl Fumarate.
5 mg of sitagliptin phosphate monohydrate The pms-SITAGLIPTIN 25 mg film-coated tablets are: Pink color, circular, biconvex, film-coated tablets debossed with "M 25" on one side and plain on the other side.
The pms-SITAGLIPTIN 50 mg film-coated tablets are:
Light beige color, circular, biconvex, film-coated tablets debossed with "M 26" on one side and plain on the other side.
The pms-SITAGLIPTIN 100 mg film-coated tablets are:
Beige color, circular, biconvex, film-coated tablets debossed with "M 27" on one side and plain on the other side. pms-SITAGLIPTIN 25 mg, 50 mg and 100 mg film-coated tablets are supplied in a blister pack of 30 (3 blister pms-SITAGLIPTIN (sitagliptin) Page 7 of 56 strips of 10 tablets) and in bottles of 30, 90 and 1000 tablets.
pms-SITAGLIPTIN (sitagliptin) Page 8 of 56 7 WARNINGS AND PRECAUTIONS General pms-SITAGLIPTIN should not be used in patients with type 1 diabetes or for the treatment of diabetic ketoacidosis. Driving and Operating Machinery Patients should be warned about driving or operating a vehicle or potentially dangerous machinery under conditions where a risk of hypoglycemia is present.
When pms-SITAGLIPTIN is used in combination with metformin and a sulfonylurea, or in combination with insulin (with or without metformin), patients should be advised to take precautions to avoid hypoglycemia while driving or operating a vehicle or potentially dangerous machinery.
Endocrine and Metabolism Hypoglycemia:
When sitagliptin was used in combination with metformin and a sulfonylurea, or with a stable dose of insulin (with or […]
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