Saxagliptin (Onglyza) is a DPP-IV inhibitor that is used to treat patients with diabetes mellitus type 2.
It increases the half-life of endogenous incretins and causes glucose-dependent insulin secretion.
Saxagliptin (Onglyza) Uses:
-
Diabetes mellitus, type 2:
- It is used as adjunctive therapy to diet and exercise for improving glycemic control in adults with type 2 diabetes mellitus as monotherapy or in combination therapy.
Saxagliptin (Onglyza) Dose in Adults
Saxagliptin (Onglyza) Dose in the treatment of type 2 Diabetes mellitus:
- Oral: 2.5 to 5 mg OD
Concomitant use with strong CYP3A4/5 inhibitors
-
- 5 mg OD
-
Concomitant use with insulin or insulin secretagogues:
- lowering the dosage of insulin or insulin secretagogues may be necessary (eg, sulfonylureas).
Use in Children:
Not indicated.
Pregnancy Risk Category: B
- Poorly controlled diabetes can lead to adverse maternal and fetal outcomes. Preeclampsia and diabetic ketoacidosis are all possible.
- Preventing these negative outcomes is possible by keeping maternal blood glucose and HbA levels as close as possible to their target levels before conception and throughout pregnancy.
- For the treatment of diabetes during pregnancy, agents other than saxagliptin should be considered.
Use of Saxagliptin during lactation
- It is unknown whether breast milk contains saxagliptin.
- According to the manufacturer, there are some things you should consider when considering breastfeeding during therapy.
- The risk of infant exposure
- Breastfeeding is good for the infant
- The mother reaps the benefits of the treatment
Dose in Kidney Disease:
- eGFR >=45mL/minute/1.73m 2Osage adjustment is not required.
- eGFR = 45 mL/minute/1.73 25 mg OD.
- ESRD requires hemodialysis5 mg OD after dialysis
- Peritoneal dialysisThere were no dosage adjustments in the labeling of the manufacturer (has not been tested).
Dose in Liver disease:
- Mild to severe impairment: Dosage adjustment not necessary.
Less Common Side Effects of Saxagliptin (Onglyza):
-
Cardiovascular:
- Peripheral Edema
-
Central Nervous System:
- Headache
-
Endocrine & Metabolic:
- Hypoglycemia
-
Genitourinary:
- Urinary Tract Infection
-
Hematologic & Oncologic:
- Lymphocytopenia
- Thrombocytopenia
-
Hypersensitivity:
- Hypersensitivity Reaction
Contraindications to Saxagliptin (Onglyza):
Canadian labeling: Additional contraindications:
- Hypersensitivity, including anaphylaxis and angioedema, & exfoliative conditions of the skin (to saxagliptin)
- Hypersensitivity to DPP-4 Inhibitors
- Diabetic ketoacidosis
- Precoma/Diabetic coma
- Type 1 diabetes mellitus
Warnings and precautions
-
Arthralgia
- DPP-IV inhibitor can cause severe and debilitating arthralgia. It may appear within a few days to years after treatment began.
- The symptoms may disappear if therapy is stopped. If DPPIV inhibitor therapy are resumed, symptoms may recur.
-
Bullous pemphigoid
- Bullous pemphigoid can occur when DPP-4 inhibitor is used.
- Topical or systemic immunosuppressive therapy may need to be administered. It may also resolve with discontinuation DPP-4 inhibitor therapy.
- Report any blisters or erosions to your doctor immediately. If you suspect bullous pemphigoid, discontinue treatment and consult a dermatologist.
-
Hematologic:
- There was a noticeable drop in lymphocyte count (dose-related).
- The clinical significance of this finding is not known. Patients with persistent or unusual infections should monitor their lymphocyte count.
-
Hypersensitivity reactions
- Anaphylaxis, exfoliative dermatologic reactions, and angioedema have all been reported as hypersensitivity reactions. If you experience severe symptoms, discontinue use.
- These events usually occur within the first three month of starting therapy.
- They may also occur after the initial dose. If you have experienced angioedema from the use of DPP-IV inhibitors, be cautious.
-
Pancreatitis
- Acute pancreatitis may occur. You should monitor for symptoms and signs of pancreatitis.
- If there are suspicions, the drug should immediately be stopped. Patients with a history or risk factors for pancreatitis should be treated with caution.
-
Bariatric surgery
- Absorption altered:
- The gastric bypass and Sleeve Gastrectomy Surgery can cause anatomical and transit changes that may affect absorption.
- Exposure to Glucagon-like peptide-1 and its therapeutic efficacy
- You should monitor your symptoms for pancreatitis.
- Gastric bypass and Sleeve Gastrectomy may increase endogenous glucagon-like Peptide-1 secretion.
- Absorption altered:
-
Heart Failure:
- In a multi-center, randomized, double-blind placebo-controlled trial, heart failure (HF), which required hospitalization, was reported in type 2 diabetes patients who had a history of or are at high risk for cardiovascular events. Patients with preexisting renal impairment or heart failure were at higher risk.
- In an ambulatory setting with lower baseline cardiovascular risk factors, a population-based retrospective study did not show an increase in the risk of patients taking saxagliptin relative to other agents (eg sitagliptin or pioglitazone),
- Therapy should be closely monitored for signs and symptoms of heart disease. If the condition worsens, therapy should be stopped immediately.
- According to the AHA's scientific statement, saxagliptin may be an agent that can exacerbate the underlying myocardial dysfunction (magnitude major).
- The ADA recommends that patients with HF should not use saxagliptin.
-
Renal impairment
- Patients with end-stage renal disease (ESRD) and moderate to severe renal impairment (eGFR 45 mL/min/1.73 m) should exercise caution. It could be essential to modify the dosage.
Saxagliptin: Drug Interaction
Alpha-Lipoic Acid |
May strengthen an anti-diabetic agent's hypoglycemic impact. |
Androgens |
Can make blood glucose lowering medications more effective at lowering blood sugar. Danazol is an exception. |
Angiotensin-Converting Enzyme Inhibitors |
Dipeptidyl Peptidase-IV Inhibitors may make angiotensin-converting enzyme inhibitors more harmful or toxic. Particularly, there may be a higher incidence of angioedema. |
Aprepitant |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). |
Clofazimine |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). |
CYP3A4 Inducers (Strong) |
May lower the level of SAXagliptin in the serum. |
CYP3A4 Inhibitors (Moderate) |
May lower the level of SAXagliptin in the serum. |
Direct Acting Antiviral Agents (HCV) |
|
Duvelisib |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). |
Erdafitinib |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). |
Erdafitinib |
May strengthen an anti-diabetic agent's hypoglycemic impact. |
Fosaprepitant |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). |
Fosnetupitant |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). |
Hyperglycemia-Associated Agents |
May increase the hypoglycemic effects of an anti-diabetic drug. |
Hypoglycemia-Associated Agents |
May reduce an anti-diabetic agent's therapeutic efficacy. |
Larotrectinib |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Lumacaftor |
May decrease the serum concentration of P-glycoprotein/ABCB1 Substrates. Lumacaftor may increase the serum concentration of P-glycoprotein/ABCB1 Substrates. |
Maitake |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. |
Monoamine Oxidase Inhibitors |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. |
Netupitant |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Palbociclib |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Pegvisomant |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. |
P-glycoprotein/ABCB1 Inducers |
May decrease the serum concentration of Pglycoprotein/ABCB1 Substrates. P-glycoprotein inducers may also further limit the distribution of p-glycoprotein substrates to specific cells/tissues/organs where p-glycoprotein is present in large amounts (e.g., brain, T-lymphocytes, testes, etc.). |
P-glycoprotein/ABCB1 Inhibitors |
May increase the serum concentration of Pglycoprotein/ABCB1 Substrates. P-glycoprotein inhibitors may also enhance the distribution of pglycoprotein substrates to specific cells/tissues/organs where p-glycoprotein is present in large amounts (e.g., brain, T-lymphocytes, testes, etc.). |
Prothionamide |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. |
Quinolones |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. Quinolones may diminish the therapeutic effect of Blood Glucose Lowering Agents. Specifically, if an agent is being used to treat diabetes, loss of blood sugar control may occur with quinolone use. |
Ranolazine |
May increase the serum concentration of P-glycoprotein/ABCB1 Substrates. |
Ritodrine |
May diminish the therapeutic effect of Antidiabetic Agents. |
Salicylates |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. |
Selective Serotonin Reuptake Inhibitors |
May enhance the hypoglycemic effect of Blood Glucose Lowering Agents. |
Simeprevir |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Thiazide and Thiazide-Like Diuretics |
May diminish the therapeutic effect of Antidiabetic Agents. |
Risk Factor D (Consider therapy modification) |
|
CYP3A4 Inhibitors (Strong |
May increase the serum concentration of SAXagliptin. Management: Saxagliptin U.S. product labeling recommends limiting saxagliptin adult dose to 2.5 mg/day when used with a strong CYP3A4 inhibitor. Monitor for increased saxagliptin levels/effects. A similar recommendation is not made in the Canadian product labeling. |
Insulins |
Dipeptidyl Peptidase-IV Inhibitors may improve insulin's ability to lower blood sugar. When starting treatment with a dipeptidyl peptidase-IV inhibitor, take into account lowering the insulin dosage and keep an eye out for hypoglycemia in the patients. |
MiFEPRIStone |
May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors). Management: During and two weeks after mifepristone treatment, reduce doses of CYP3A4 substrates and keep an eye out for elevated amounts or toxicity. Fentanyl, pimozide, quinidine, sirolimus, and tacrolimus should all be avoided. Cyclosporine should also be avoided. |
Stiripentol |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Management: Use of stiripentol with CYP3A4 substrates that are considered to have a narrow therapeutic index should be avoided due to the increased risk for adverse effects and toxicity. Any CYP3A4 substrate used with stiripentol requires closer monitoring. |
Sulfonylureas |
Dipeptidyl Peptidase-IV Inhibitors may enhance the hypoglycemic effect of Sulfonylureas. Management: Consider a decrease in sulfonylurea dose when initiating therapy with a dipeptidyl peptidase-IV inhibitor and monitor patients for hypoglycemia. |
Risk Factor X (Avoid combination) |
|
Conivaptan |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Fusidic Acid (Systemic) |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Idelalisib |
May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). |
Monitoring parameters:
- Plasma glucose
- HbA
- Renal function
- lymphocyte count
- Signs/symptoms of heart failure and/or pancreatitis.
How to administer Saxagliptin?
Oral: May administer without relation to a meal. Should be swallowed as a whole; do not split or cut tablets.
Mechanism of action of Saxagliptin (Onglyza):
- The dipeptidyl-peptidase IV (DPP IV) enzyme is inhibited by saxagliptin, which prolongs the active incretin levels.
- Glucose homeostasis is regulated by incretin hormones such glucose-dependent insulinotropic peptide (GIP) and glucagon-like protein-1 (GLP-1).
- They boost the production and release of insulin from pancreatic beta cells while lowering glucagon secretion from pancreatic alpha cells.
- A decrease in glucagon secretion leads to a decrease of liver glucose production.
- Normal physiological circumstances see the liver release incretin hormones throughout a day.
- These levels increase after meals. The DPP-IV enzyme causes rapid inactivation.
Duration: 24 hours
Protein binding: Negligible
Metabolism: Occurs in the liver via CYP3A4/5 to 5-hydroxy saxagliptin (active; ~50% potency of the parent compound)
Half-life elimination: Saxagliptin: 2.5 hours; 5-hydroxy saxagliptin: 3.1 hours
Time to peak, plasma: Saxagliptin: 2 hours; 5-hydroxy saxagliptin: 4 hours
Excretion:
- Urine (75%, 24% of the total dose as saxagliptin, 36% of the total dose as 5-hydroxy saxagliptin)
- Feces
International Brand Names of Saxagliptin:
- Formigliptin
- Glipitrose
- Glyza
- Ongliza
- Onglyza
- Sixtin
Saxagliptin Brand Names in Pakistan:
No Brands Available in Pakistan.