05 Endocrine and Diabetes Medications
Review major endocrine and diabetes medications by drug class, principal action, common indication, and important safety considerations.
therapy
replaces or supplements pancreatic . People with type 1 diabetes require it. In type 2 diabetes, it may be added when other treatment does not adequately control blood glucose or in certain clinical situations.
is commonly grouped by how quickly it works and whether it provides meal-time coverage, called bolus or prandial coverage, or background coverage, called basal coverage. All can cause . Some products are available in different concentrations, so the exact product matters. Timing varies by product and formulation; a class label is not a dosing instruction.
Rapid-acting: lispro (Humalog), aspart (NovoLog), and glulisine (Apidra) work quickly and provide meal-time or bolus coverage.
Short-acting: regular human (Humulin R, Novolin R) is used for meal-time coverage and is the classic used intravenously in some acute-care settings.
Intermediate-acting: NPH, also called isophane (Humulin N, Novolin N), provides intermediate basal coverage and has a noticeable peak.
Long-acting basal: glargine (Lantus, Basaglar, Toujeo) provides background coverage and generally has little or no pronounced peak.
Ultra-long-acting basal: degludec (Tresiba) provides extended background coverage.
Inhaled rapid-acting: human delivered by inhalation (Afrezza) provides meal-time coverage; it is not a substitute for basal when basal coverage is needed.
A useful timing association is lispro, aspart, and glulisine as rapid-acting; regular as short-acting; NPH as intermediate-acting; and glargine and degludec as basal insulins.
Glucose-lowering medicines
Oral and other glucose-lowering medicines primarily treat type 2 diabetes; they do not replace in type 1 diabetes. The classes act in different ways, and some of their risks or benefits depend on a patient's other conditions. Brand examples are familiar U.S. examples; availability and marketed brands can change, and combination products may contain more than one generic drug.
Medicines that affect release or sensitivity
Biguanide: (Glucophage) lowers liver glucose production and improves sensitivity. Gastrointestinal effects are common; usually does not cause by itself.
Sulfonylureas: glipizide (Glucotrol), glimepiride (Amaryl), and glyburide (DiaBeta) stimulate pancreatic release. They can cause and weight gain.
Meglitinides: repaglinide (Prandin) and nateglinide (Starlix) stimulate release for a short time around meals. is possible.
Thiazolidinedione (TZD): pioglitazone (Actos) improves sensitivity. It can cause fluid retention and worsen heart failure.
Medicines that act through incretins or the intestine
DPP-4 inhibitors: sitagliptin (Januvia), linagliptin (Tradjenta), and saxagliptin (Onglyza) increase incretin hormone activity, supporting glucose-dependent release. This class is often tested as generally weight-neutral.
GLP-1 receptor agonists: oral semaglutide (Rybelsus) increases glucose-dependent release and slows gastric emptying; nausea and other gastrointestinal effects may occur. Injectable examples include dulaglutide (Trulicity), liraglutide (Victoza), and exenatide (Byetta, Bydureon). This class is not .
Alpha-glucosidase inhibitor: acarbose (Precose) slows carbohydrate digestion and absorption in the intestine and can cause gastrointestinal effects.
Medicines that promote urinary glucose loss
SGLT2 inhibitors: empagliflozin (Jardiance), dapagliflozin (Farxiga), and canagliflozin (Invokana) promote urinary glucose excretion. Testable risks include genital yeast infections and, rarely, ketoacidosis.
Pramlintide (Symlin) is an injectable amylin analogue used with mealtime in selected patients; it is not a substitute for . The main class contrasts are that decreases hepatic glucose output, sulfonylureas increase secretion and can cause , SGLT2 inhibitors increase glucose loss in urine, and GLP-1 medicines act through incretin pathways.
Thyroid medications
Thyroid medicines may replace hormone or reduce its production, depending on whether thyroid hormone is low or excessive.
(Synthroid, Levoxyl, Tirosint) is synthetic T4 and the first-line replacement for hypothyroidism. It is a replacement hormone, not an antithyroid drug. Calcium and iron can interfere with its absorption, so they are commonly separated from it.
Liothyronine (Cytomel) is synthetic T3 used for thyroid-hormone replacement; it is used less commonly than .
(Tapazole) is a thionamide antithyroid drug that reduces thyroid-hormone production. It is commonly used for hyperthyroidism, including Graves disease. Fever or sore throat while taking warrants prompt clinical evaluation because of the risk of low white blood cell counts.
Propylthiouracil (PTU) is a thionamide antithyroid drug. It reduces thyroid-hormone production and also reduces peripheral T4-to-T3 conversion. It is often preferred over during the first trimester of pregnancy; serious liver injury is an important risk.
The central distinction is that treats low thyroid hormone, while and PTU treat excess thyroid hormone.
and adrenal replacement
include glucocorticoids, which have anti-inflammatory and immunosuppressive effects, and drugs with mineralocorticoid activity, which affects salt and fluid balance. Common systemic glucocorticoids include prednisone (Deltasone), prednisolone (Orapred), methylprednisolone (Medrol), dexamethasone (Decadron), and (Cortef). They are used for many inflammatory and immune conditions; also replaces cortisol in adrenal insufficiency.
Long-term or high-dose systemic corticosteroid use can suppress the body's own cortisol production and may raise blood glucose. Prolonged therapy should not be stopped abruptly without medical direction; a gradual dose reduction may be required.
For primary adrenal insufficiency, commonly replaces cortisol, while fludrocortisone (Florinef) replaces aldosterone when needed. Stress or illness may require clinician-directed adjustment of replacement therapy.
Other endocrine therapies
Several other endocrine medicines are associated with specific hormone-related conditions or emergencies.
(DDAVP) is a vasopressin analogue, or antidiuretic hormone, used for central diabetes insipidus. It reduces excessive urine production; monitor for water retention and low sodium. It treats central diabetes insipidus by acting like antidiuretic hormone, and diabetes insipidus is distinct from diabetes mellitus.
Cabergoline (Dostinex) and bromocriptine (Parlodel) are dopamine agonists used for hyperprolactinemia, often from a prolactin-secreting pituitary tumor. They reduce prolactin secretion; bromocriptine also has other uses.
Octreotide (Sandostatin) is a somatostatin analogue used for acromegaly and for symptoms from certain hormone-secreting tumors. In appropriate cases, it suppresses growth-hormone secretion.
(Gvoke, Baqsimi, Zegalogue) is a hyperglycemic hormone used for emergency treatment of severe when a person cannot safely take oral glucose.