Endocrine Pharm EC Flashcards

1
Q

Lispro, Aspart, Glulisine (MOA, Use, Tox)

A

Rapid-acting insulin (Increase K uptake, increase glycogen and TG, increase protein synthesis)

Type 1 and 2 DM, Gestational diabetes, Life-threatening hyperkalemia

Hypoglycemia, hypersensitivity (very rare)

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2
Q

Regular (MOA, Use, Tox)

A

Short-acting insulin (Increase K uptake, increase glycogen and TG, increase protein synthesis)

Type 1 and 2 DM, Gestational diabetes, Life-threatening hyperkalemia

Hypoglycemia, hypersensitivity (very rare)

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3
Q

NPH (MOA, Use, Tox)

A

Intermediate-acting insulin (Increase K uptake, increase glycogen and TG, increase protein synthesis)

Type 1 and 2 DM, Gestational diabetes, Life-threatening hyperkalemia

Hypoglycemia, hypersensitivity (very rare)

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4
Q

Glargine, Detemir (MOA, Use, Tox)

A

Long-acting insulin (Increase K uptake, increase glycogen and TG, increase protein synthesis)

Type 1 and 2 DM, Gestational diabetes, Life-threatening hyperkalemia

Hypoglycemia, hypersensitivity (very rare)

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5
Q

Metformin (MOA, Use, Tox)

A

Biguanide (acts on liver)
Decrease gluconeogenesis
Increase glycolysis and peripheral glucose uptake

First line for T2 DM

GI upset
LACTIC ACIDOSIS (contraindicated in renal failure)
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6
Q

Glyburide, Glimepiride, Glipizide (MOA, Use, Tox)

A

Second generation sulfonylureas
Close K channel in beta-cell, depolarization, Ca influx, endogenous insulin release

T2 DM (requires some islet function, useless in T1)

Hypoglycemia

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7
Q

Tolbutamide, Chlorpropamide (MOA, Use, Tox)

A

First generation sulfonylureas
Close K channel in beta-cell, depolarization, Ca influx, endogenous insulin release

T2 DM (requires some islet function, useless in T1)

Disulfiram-like reaction

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8
Q

Pioglitazone, Rosiglitazone (MOA, Use, Tox)

A

Increase insulin sensitivity in peripheral tissue
Bind PPAR-gamma nuclear transcription regulator

T2 DM (often in combo)

Weight gain, edema, hepatotoxicity, heart failure

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9
Q

Acarbose, Miglitol (MOA, Use, Tox)

A

Inhibit brush border alpha-glucosidases
Delay sugar hydrolysis and glucose absorption which DECREASES POST-PRANDIAL HYPERGLYCEMIA

T2 DM (often in combo)

GI disturbance

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10
Q

Exenatide, Liraglutide (MOA, Use, Tox)

A

GLP-1 analogs
Increase insulin, decrease glucagon resistance

T2 DM

N/V, Pancreatitis

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11
Q

Pramlintide (MOA, Use, Tox)

A

Amylin analog - Decrease glucagon

T1&2 DM

Hypoglycemia, Nausea, Diarrhea

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12
Q

Linagliptin, Saxagliptin, Sitagliptin (MOA, Use, Tox)

A

DPP-4 inhibitors
Increase insulin, decrease glucagon release

T2 DM

UTIs and URIs

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13
Q

Propylthiouracil, Methimazole (MOA, Use, Tox)

A

Block peroxidase, inhibiting organification of iodide and coupling of thyroid hormone synthesis
PTU also blocks 5’-deiodinase (decrease peripheral activation to T3)

Hyperthyroidism

Skin rash, Agranulocytosis (rare), Aplastic anemia, Hepatotoxicity (PTU), Teratogen (Methimazole)

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14
Q

Levothyroxine, Triiodothyronine (MOA, Use, Tox)

A

Thyroxine replacement

Hypothyroidism, myxedema

Tachycardia, heat intolerance, tremors, arrhythmias

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15
Q

Growth hormone (clinical use)

A

GH deficiency

Turner syndrome

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16
Q

Octreotide (clinical use)

A

Somatostatin

Acromegaly
Carcinoid
Gastrinoma
Glucagonoma
Esophageal varices
17
Q

Oxytocin (clinical use)

A

Simulates labor/uterine contractions
Stimulates milk letdown
Controls uterine hemorrhage

18
Q

Desmopressin [ADH] (clinical use)

A

Pituitary (central) DI

19
Q

Demeclocycline (MOA, Use, Tox)

A

ADH antagonist (tetracycline family)

SIADH

Nephrogenic DI, Photosensitivity, Bone/Teeth abnormalities

20
Q

Hydrocortisone, Prednisone, Triamcinolone, Dexamethasone, Beclomethasone (MOA, Use, Tox)

A

Glucocorticoids
Decrease production of leukotrienes and prostaglandins by INHIBITING PHOSPHOLIPASE A2 and EXPRESSION OF COX2

Addison’s, inflammation, immunosuppression, asthma

Iatrogenic Cushing’s, adrenal insufficiency when drop stopped abruptly after chronic use