Endocrine Drugs Flashcards

(36 cards)

1
Q

This is a drug for hypothyroidism that is used for hypothyroid crisis. It is 3 to 4 times more active than Levothyroxine (T4)

A

Liothyronine (T3)

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2
Q

This is a drug for hypothyroidism that is a combination of synthetic T4 and T3 in a ratio of 4:1

A

Liotrix

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3
Q

This is a drug for hypothyroidism that contains T4 but without T3

A

Levothyroxine

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4
Q

This is a drug for hyperthyroidism that inhibits thyroid peroxidase and condensation/coupling.
SE: Pruritic maculopapular rash

A

Thioamides/ Thionamides
Propylthiouracil, Methimazole, Carbimazole

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5
Q

This is a thioamide that also inhibits peripheral conversion of T4 to T3. It has a short DOA, less potent, and is indicated for pregnant women and for thyroid storm
AE: Hepatitis

A

PTU/ propylthiouracil

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6
Q

A thioamide that has longer DOA, 10x more potent, used as maintenance treatment but should not be used by pregnant women as it is teratogenic and can cause cutis aplasia. It is the first like drug of choice for hyperthyroidism
AE: Cholestatic jaundice

A

MMI/ methimazole

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7
Q

This is a drug for hyperthyroidism that inhibits iodide uptake through competitive inhibition of Na/I symporter
SE: Aplastic anemia

A

Anionic inhibitors or inorganic anions
Potassium perchlorate, thiocyanate

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8
Q

This is a drug for hyperthyroidism that exerts Wolff-Chaikoff effects (negative feedback). It is not for long term use
AE: Iodism
CI: Pregnancy

A

Iodides
Lugol’s solution, KIss (potassium iodide saturated solution)

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9
Q

This is a drug for hyperthyroidism that inhibits the release of thyroid hormone and inhibits peripheral conversion of T4 to T3. It can be indicated for thyroid storm

A

Radiocontrast dyes

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10
Q

This is a drug for hyperthyroidism that inhibits peripheral iodination of T4 to T3. It can be used for thyroid storm

A

Propranolol

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11
Q

This is a drug for hyperthyroidism that interferes with peripheral conversion of T3 to T4. It is an adjunct treatment for thyroid storm

A

Prednisone
Dexamethasone

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12
Q

This is a drug for hyperthyroidism that emits a high dose beta radiation for cellular and DNA damage. It is the most commonly used hyperthyroid treatment in the US
Precaution: Stop thioamides 1 week before this
CI: Pregnancy

A

Radioactive iodine (I-131)

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13
Q

This is a type of insulin based on therapeutic use where it is used to control post-prandial hyperglycemia and are usually short acting
SE: Hypoglycemia, lipodystrophy

A

Prandial insulin

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14
Q

This is a type of insulin based on therapeutic use where it provides control of blood sugar throughout the day and are long acting
SE: Hypoglycemia, lipodystrophy

A

Basal insulin

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15
Q

This is a type of insulin based on duration that is in monomer form and should be given right before or after meals

A

Ultra rapid acting insulin
Insulin Lispro (Humalog)
Insulin Aspart (Novolog/ Novorapid)
Insulin Glulisine (Apidra)

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16
Q

This is a type of insulin based on duration that is hexamer in form and is given 30 minutes before the meal. This is the only insulin that is given IV

A

Short acting
Regular insulin
Humulin, Actrapid or Novolin
Velosulin

17
Q

This is a type of insulin based on duration that is given twice a day to control blood sugar throughout the day

A

Intermediate acting
Isophane insulin (Neutral Protamine Hagedorn/ NPH insulin)
Lente

18
Q

This is a type of insulin based on duration that is given once daily to control blood sugar throughout the day

This insulin is soluble and ‘peakless’

A

Long acting
Ultralente
Insulin Glargine/ Lantus
Insulin Detemir/Levemir
Insulin Degludec

Insulin Glargine/Lantus

19
Q

They are oral hypoglycemic agents that promote insulin release from the beta cells of the pancreas by blocking the ATP-sensitive K channels which lead to insulin exocytosis
SE: Hypoglycemia, weight gain

A

Insulin secretagogues
Sulfonylurea and meglitinides

20
Q

An insulin secretagogue that cannot control post-prandial hyperglycemia

A

Sulfonylurea
1st gen: Chlorpropamide, Tolbutamide, Acetohexamide, Tolazamide
2nd gen: Glibenclamide, Glipizide, Gliclazide, Glimepiride

21
Q

A first generation secretagogue that has the longest half life but has the most side effects

A

Chlorpropamide

22
Q

A first generation secretagogue that has the fastest onset but is the most cardiotoxic. It is the safest 1st generation sulfonylurea for the elderly

23
Q

A first generation secretagogue that is converted to an active metabolite (hydrohexamide)

A

Acetohexamide

24
Q

They are the second generation secretagogues that are more potent than the first generation but have less side effects

A

Glibenclamide, Glipizide, Gliclazide, Glimepiride

25
An insulin secretagogue that acts on the liver to decrease hepatic glucose production and on the muscle and tissue to increase peripheral tissue response to insulin
Biguanides Phenformin, Metformin
26
A biguanide that is the only drug that is indicated for pre-diabetes. It is also the first line for type-2 DM, especially those who are newly diagnosed with it and has no contraindications SE: Diarrhea, lactic acidosis CI: Renal failure, hepatic failure, CHF
Metformin
27
They are oral hypoglycemic agents that inhibits the alpha-glucosidase located in the intestinal bush border AE: Flatulence, abdominal pain, diarrhea CI: Intestinal bowel disease
Alpha-glucosidase inhibitors Acarbose, Miglitol
28
They are oral hypoglycemic agents that decreases insulin resistance. It is an agonist for peroxisome proliferator-activated receptor (PPAR) to increase insulin sensitivity AE: Edema, weight gain, HTN CI: Heart failure One of the drugs in this class has an AE of bladder cancer One of the drugs in this class has an AE of HF
Thiazolidinediones Pioglitazone, Rosiglitazone Pioglitazone Rosiglitazone
29
They are oral hypoglycemic agents that decrease glucagon secretion and increases peripheral tissue response. The analog of the drug is co-secreted with insulin following food intake One of the drugs has an AE of weight loss and hypoglycemia
Amylin analogue Pramlintide
30
They are oral hypoglycemic agents that stimulate insulin release, reduce food intake by enhancing satiety, decrease glucagon secretion, and promote beta cell proliferation. The hormone named after this drug is the hormone produced after eating
Incretin mimetics Glucagon-like peptide agonist (GLP-1), Dipeptidyl peptidase IV inhibitor (DPP-4)
31
They are incretin mimetics that exert activity by activating the GLP-1 receptor. It is direct acting and can be given SC
GLP-1 (Glucagon-like peptide) agonist Exenatide, Liraglutide
32
They are incretin mimetics used to prevent the deactivation of GLP-1 and is taken orally. It is indirect acting
DPP-4 (Dipeptidyl peptidase IV) inhibitor
33
They are oral hypoglycemic agents that is responsible for reabsorbing filtered glucose in the kidney, thereby having decreased reabsorption AE: UTI, frequent urination
SGLT2 (Sodium glucose transporter-2 inhibitor)
34
Oral hypoglycemic agents that cause weight loss
GLP-1 agonists SGLT2 inhibitors Amylin analogue
35
Oral hypoglycemic agents used to control post-prandial glucose elevation
Alpha-glucosidase inhibitors GLP-1 agonists DPP-4 inhibitors Amylin analogue
36
Oral hypoglycemic agents that can cause weight loss and control post-prandial glucose elevation
GLP-1 agonist Amylin analogue