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Alogliptin/Metformin

    DEA Class; Rx

    Common Brand Names; Kazano

    • Antidiabetics, Biguanides/Dipeptyl Peptidase-IV Inhibitors

    Oral combination of a biguanide (metformin) and a dipeptidy-peptidase-4 (DPP-4) inhibitor (alogliptin)
    Used in adults for the treatment of type 2 diabetes mellitus
    Per boxed warning the risk of lactic acidosis due to metformin requires care in prescribing and monitoring

    Indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus

    Starting dose based on patient’s current regimen

    For the treatment of type 2 diabetes mellitus in combination with diet and exercise.

    Renal impairment (ie, eGFR <30 ml/min/1.73 m²); renal impairment may also result from medical conditions (eg, shock, acute MI, septicemia)

    Acute or chronic metabolic acidosis, including diabetic ketoacidosis; diabetic ketoacidosis should be treated with insulin

    Hypersensitivity to alogliptin or metformin, including anaphylaxis, angioedema, or severe cutaneous adverse reactions including Stevens-Johnson syndrome

    • Upper respiratory tract infection (8%)
    • Nasopharyngitis (6.8%)
    • Hypoglycemia (1.8-6.3%)
    • Diarrhea (5.5%)
    • Hypertension (5.5%)
    • Headache (5.3%)
    • Back pain (4.3%)
    • Urinary tract infection (4.2%)
    • Hypersensitivity (0.6%)
    • Pancreatitis (0.2%)
    • Severe and disabling arthralgia
    • Anaphylaxis, angioedema, rash, urticaria
    • Severe cutaneous adverse reactions, including Stevens-Johnson syndrome
    • Hepatic enzyme elevations
    • Fulminant hepatic failure
    • Bullous pemphigoid
    • Rhabdomyolysis
    • Constipation
    • Nausea
    • Ileus
    • Adverse Effects
    • Renal and urinary disorders: Tubulointerstitial nephritis

    Lactic acidosis (see Black Box Warnings)

    Pancreatitis reported

    Caution with sensitivity to another DPP-4 inhibitor or metformin; discontinue if serious hypersensitivity reaction suspected (see Contraindications)

    Fatal and nonfatal hepatic failure reported; type 2 DM is also known to cause fatty liver disease and liver enzyme elevation; monitor carefully and interrupt alogliptin treatment if LFTs elevated, do not restart alogliptin without another explanation for the liver test abnormalities

    Insulin and insulin secretagogues (eg, sulfonylureas) are known to cause hypoglycemia; therefore, a lower dose of insulin of insulin secretagogue may be needed to minimize hypoglycemia risk

    Coadministration with drugs that may affect renal function or metformin elimination

    Temporarily withhold metformin for any surgical procedures that restrict fluid/food intake

    Hypoxic conditions (eg, shock, acute CHF, acute MI) associated with lactic acidosis (see Black Box Warnings)

    Alcohol potentiates metformin’s effect on lactate metabolism; avoid excessive alcohol intake

    Metformin may decrease vitamin B12 levels

    Hypoglycemia may occur with metformin if calorie intake is deficient

    Severe and disabling arthralgia reported in patients taking DPP-4 inhibitors; consider as a possible cause for severe joint pain and discontinue drug if appropriate

    Limited available data in pregnant women are not sufficient to inform a drug-associated risk for major birth defects and miscarriage

    There is no information regarding presence of metformin or alogliptin in human milk, effects on breastfed infant, or effects on milk production

    Adults

    Alogliptin 25 mg/day PO and metformin 2000 mg/day PO.

    Geriatric

    Alogliptin 25 mg/day PO and metformin 2000 mg/day PO.

    Adolescents

    Safety and efficacy have not been established.

    Children

    Safety and efficacy have not been established.

    Infants

    Not indicated.

    Neonates

    Not indicated.

    Alogliptin/metformin

    tablet

    • 12.5mg/500mg
    • 12.5mg/1000mg