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Pramlintide

    DEA Class; Rx

    Common Brand Names; Symlin, SymlinPen 120, SymlinPen 60

    • Antidiabetics, Amylinomimetics

    Synthetic injectable amylin analog
    Used primarily as an adjunct to insulin in adults with type 1 and type 2 diabetes mellitus; improves glycemic control and causes modest (0.5 to 2 kg) weight loss
    Slows gastric emptying, suppresses postprandial glucagon secretion

    Indicated for the treatment of type 1 diabetes mellitus in patients who use mealtime insulin and who have failed to achieve desired glucose control despite optimal insulin therapy.

    For the treatment of type 2 diabetes mellitus in patients who use mealtime insulin and who have failed to achieve desired glucose control despite optimal insulin therapy.

    Hypersensitivity

    Gastroparesis

    Hypoglycemia unawareness

    Nausea

    Headache

    Vomiting

    Anorexia

    Severe hypoglycemia

    Inflicted injury

    1-10%

    Dizziness

    Fatigue

    Abdominal pain

    Pharyngitis

    Cough

    Arthralgia

    Allergic reaction

    Injection site reactions

    Risk of severe insulin-induced hypoglycemia; pramlintide alone does not cause hypoglycemia; however, since it is indicated to be coadministered with mealtime insulin therapy, and in this setting there is an increased risk of severe hypoglycemia

    Do not mix with insulin – administer the two separately

    Slows gastric emptying, which may delay the absorption of concomitantly administered oral medications; administer the concomitant oral medication at least 1 hr prior or 2 hr after pramlintide

    Slows gastric emptying; not recommended if taking other medications that alter gastrointestinal motility

    Never share pen between patients even if needle is changed

    Erythema, edema, or pruritus at site of injection reported; may be related to other factors, such as irritants in a skin cleansing agent or improper injection technique

    Available data from a small number of reports in manufacturer’s safety database on use in pregnant women are not sufficient to determine a drug-associated risk for major birth defects, miscarriage, or other adverse maternal or fetal outcomes

    There is no data on presence in human milk, effects on breastfed infant, or on milk production

    Specific maximum dosage information is not available. Individualize dosage based on careful monitoring of blood glucose and other clinical parameters in all patient populations.

    Pramlintide Acetate

    injectable solution

    • 0.6mg/mL

    pen-injector

    • 15mcg/dose
    • 30mcg/dose
    • 45mcg/dose
    • 60mcg/dose
    • 120mcg/dose