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Linagliptin

    DEA Class; Rx

    Common Brand Names; Tradjenta

    • Antidiabetics, Dipeptyl Peptidase-IV Inhibitors

    Oral DPP-4 inhibitor given once daily; reduces breakdown of GLP-1 which increases insulin secretion
    Used in adults with type 2 diabetes mellitus; mean A1C reduction 0.7%
    Used as monotherapy or in combination with other medications, with the exception of GLP-1 agonists

    Indicated for adults with type 2 diabetes mellitus along with diet and exercise to lower blood sugar; may be used as monotherapy or in combination with other common antidiabetic medications including metformin, sulfonylurea, pioglitazone, or insulin

    Hypersensitivity (eg, anaphylaxis, angioedema, exfoliative skin conditions, urticaria, or bronchial hyperreactivity)

    Type 1 diabetes mellitus

    Diabetic ketoacidosis

    Nasopharyngitis (4.3%)

    Hyperlipidemia (2.8%; with pioglitazone)

    Cough (2.4%; with metformin and sulfonylurea)

    Hypertriglyceridemia (2.4%; with sulfonylurea)

    Weight gain (2.3%; with pioglitazone)

    Hypoglycemia

    • 7.6% overall incidence
    • 22.9% incidence compared with placebo plus metformin and a sulfonylurea
    • Incidence similar to placebo with monotherapy or combined with metformin or pioglitazone

    Acute pancreatitis, including fatal pancreatitis

    Hypersensitivity reactions including anaphylaxis, angioedema, and exfoliative skin conditions

    Severe and disabling arthralgia

    Bullous pemphigoid

    Rash

    Mouth ulceration, stomatitis

    Rhabdomyolysis

    Heart failure

    Hypoglycemia with concomitant use of insulin and insulin secretagogues

    Use in combination with an insulin secretagogue (eg, sulfonylurea) was associated with a higher rate of hypoglycemia compared with placebo in a clinical trial; a lower dose of insulin secretagogue or insulin may be required to reduce risk of hypoglycemia when used in combination with this drug

    Rifampin decreased linagliptin exposure suggesting that the levels may be reduced when administered in combination with a strong P-gp or CYP 3A4 inducer; alternative treatment is strongly recommended when linagliptin is to be administered with P-gp or CYP 3A4 inducers

    Serious hypersensitivity reactions reported including anaphylaxis, angioedema, and exfoliative skin conditions

    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

    Heart failure has been observed with two other members of the DPP-4 inhibitor class; consider risks and benefits of empagliflozin in patients with risk factors for heart failure; monitor for signs and symptoms; if heart failure develops, manage accordingly to standard of care and consider interrupting treatment

    Bullous pemphigoid reported with DPP-4 inhibitor use, which required hospitalization; in reported cases, patients recovered with topical or systemic immunosuppressive treatment and discontinuation of DPP-4 inhibitor; patients should report development blisters/erosions; discontinue DPP-4 therapy and consult a dermatologist if bullous pemphigoid suspected

    There have been no clinical studies establishing conclusive evidence of macrovascular risk reduction with therapy

    The limited data in pregnant women are not sufficient to inform of drug-associated risk for major birth defects and miscarriage; there are risks to the mother and fetus associated with poorly controlled diabetes in pregnancy

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

    Adults

    5 mg/day PO.

    Geriatric

    5 mg/day PO.

    Adolescents

    Safety and efficacy have not been established.

    Children

    Safety and efficacy have not been established.

    Infants

    Not indicated.

    Linagliptin

    tablet

    • 5mg