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19 Cards in this Set

  • Front
  • Back
Insulin - ordered by t-half
Lispro (rapid)
Aspart (rapid)
Regular (short)
NPH (intermediate)
Glargine (long)
Determi (long)
Sulfonylureas

MOA?
clinical use?
toxicities?
names?
close K+ channel in beta-cell membrane --> cell depolarizes --> insulin release via Ca++ influx

type II diabetes - stimulates insulin release
(not useful in type I b/c requires some islet cell fxn)

1st gen - disulfiram like effects
2nd gen - hypoglycemia

1st gen: Tolbutamide, Chlorpropamide
2nd gen: Glyburide, Glimepiride, Glipizide
Biguanides

MOA?
clinical use?
toxicities?
names?
exact MOA unknown
decrease gluconeogenesis,
increase glycolysis,
increase peripheral glucose uptake

oral. 1st line therapy in type 2 DM. can be used in pts w/o islet fxn (type 1)

most grave adverse effect - lactic acidosis
contraindicated in renal failure

Metformin
what is first line therapy in type 2 DM?
Metformin
what is contraindication for metformin?
renal failure

can cause grave lactic acidosis
Thiazolidinediones

-names?
-MOA?
-clinical use?
-toxicities?
Pioglitazone, Rosiglitazone

increase insulin sensitivity in peripheral tissue
binds to PPAR-gamma nuclear transcription regulator (adiponectin)

used as monotherapy in type 2 DM, or combined w/agents above

can cause weight gain, edema.
Hepatotoxicity, heart failure
alpha-glucosidase inhibitors

-names?
-MOA
-clinical use?
-toxicities?
acarbose, miglitol

inhibit intestinal brush border alpha-glucosidases
delayed sugar hydrolysis & glucose absorption, decreased postprandial hyperglycemia

monotherapy in type 2 DM, or in combination

can cause GI disturbances
Pramlinide?
mimetic;
decreases glucagon

used in type 2 DM

can cause hypoglycemia, nausea, diarrhea
Exenatide?
GLP-1 analog

increases insulin, decreases glucagon release

used in type 2 diabetes

can cause nausea, vomiting, pancreatitis
potassium perchlorate?
block iodine absorption by thyroid
(anion inhibitor)
iodide salts?
decrease synthesis & release of thyroid hormones
(anion inhibitor)
Methimazole? (other similar agent?)

MOA?
clinical use?
toxicity?
also, propylthiouracil

blocks peroxidase, inhibiting organification of iodide & coupling of thyroid hormone synthesis

propylthiouracil also blocks 5' deiodinase, decreasing peripheral conversion of T4 to T3

used for hyperthyroidism

can cause:
-skin rash, agranulocytosis (rare), aplastic anemia

propylthiouracil can cause hepatotoxicity
methimazole is a possible teratogen
Levothyroxine, triiodothyrine

MOA?
clinical use?
toxicity?
thyroxine replacement

used for hypothyroidism, myxedema

can cause tachycardia, heat intolerance, tremors, arrhythmia
GH?
used in GH deficiency and Turner syndrome
Octreotide?
somatostain

used to tx acromegaly, carcinoid, gastrinoma, glucagonoma
Oxytocin?
stimulates labor, uterine contractions, & milk-let down

controls uterine hemorrhage
ADH (desmopressin)?
used for central DI

also apparently can help in pts w/ von Willebrands / hemophilia too
Democlocycline?
ADH antagonist (member of tetracycline family - not used as antibiotic anymore)

used for siADH

can cause nephrogenic DI, photosensitivity, abnormaliteis of bone & teeth
Beclomethasone, triamcinolone, dexamethasone, hydrocortisone, prednisone?
Glucocorticoids

inhibits phospholipase A2 & expression of COX-2, decreasing produciton of leukotrienes & prostaglandins

used for addison's dz, inflammation, immune suppression, asthma

can cause iatrogenic cushing's syndrome, adrenocortical atrophy, peptic ulcers, diabetes, thin skin, easy brusing

adrenal insufficiency when drug stopped after chronic use