Pharm 6 Flashcards

2
Q

MOA of thiazolindinediones

A

Stimulate PPAR-gamma receptor to regulate CHO and lipid metabolism

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3
Q

SE of Thiazolindinediones

A

Weight gain, edema, hepatotoxicity (3A4), worsens CHF –> HF, fracture, bladder cancer

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4
Q

Hyperglycemic agent that increases cAMP and results in glycogenolysis, gluconeogenesis, reverses hypoglycemia, also used to reverse severe beta-blocker overdose and smooth muscle relaxation

A

Glucagon

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5
Q

Available bisphosphonates

A

Alendronate, etidronate, risedronate, pamidronate, tiludronate, and zoledronic acid

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6
Q

MOA of Bisphosphonates

A

Inhibits osteoclast bone resorption

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7
Q

Uses of bisphosphonates

A

Osteoporosis, Paget’s disease, and osteolytic bone lesions, and hypercalcemia from malignancy

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8
Q

Major SE of bisphosphonates

A

Chemical esophagitis

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9
Q

Bisphosphonates that cannot be used on continuous basis because it caused osteomalacia

A

Etidronate

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10
Q

Used for prevention of postmenopausal osteoporosis in women

A

Calcium reguators Bisphosphonates: alendronate, risedronate, ibandronate, Estrogen (HRT-Hormone replacement therapy)

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11
Q

Used especially in postmenopausal women, dosage should be 1500 mg

A

Calcium

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12
Q

Vitamin given with calcium to ensure proper absorption

A

Vitamin D

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13
Q

Disease caused by excess ergot alkaloids

A

St. Anthony’s Fire

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14
Q

Endogenous substances commonly interpreted as histamine, serotonin, prostaglandins, and vasoactive peptides

A

Autocoids

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15
Q

Syndrome of hypersecretion of gastric acid and pepsin usually caused by gastrinoma; it is associated with severe peptic ulceration and diarrhea

A

Zollinger-Ellison Syndrome

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16
Q

Generation of antihistamine that has the most CNS effects

A

First generation due to being more lipid-soluble

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17
Q

Major indication for H1 receptor antagonist

A

Use in IgE mediated allergic reaction

18
Q

Antihistamine that can be used for anxiety and insomnia and is not addictive

A

hydroxyzine (Atarax)

19
Q

H1 antagonist used in motion sickness

A

Dimenhydrinate, meclizine, and other 1st generation

20
Q

Most common side effect of 1st generation antihistamines

A

Sedation

21
Q

Lethal arrhythmias resulting from concurrent therapy with azole fungals (metabolized by CYP 3A4) and these antihistamines which inhibit the 3A4 iso-enzyme.

A

Terfenadine and astemizole (have been removed from the market)

22
Q

Clinical use for H2 blockers

A

Acid reflux disease, duodenal ulcer and peptic ulcer disease

23
Q

Receptors for serotonin (5HT-1) are located

A

Mostly in the brain, and they mediate synaptic inhibition via increased K+ conductance

24
Q

Triptan available in parenteral and nasal formulation

A

Sumatriptan

25
Q

H1 blocker that is also a serotonin antagonist

A

Cyproheptadine

26
Q

5HT2 antagonist mediate synaptic excitation in the CNS and smooth muscle contraction

A

Ketanserin, cyproheptadine, and ergot alkaloids (partial agonist of alpha and serotonin receptors)

27
Q

5ht-3 antagonist that has been MOST associated with QRS and QTc prolongation and should not be used in patients with heart disease

A

Dolasetron

28
Q

Drug used in ergot alkaloids overdose, ischemia and gangrene

A

Nitroprusside

29
Q

Reason ergot alkaloids are contraindicated in pregnancy

A

Uterine contractions

30
Q

SE of ergot alkaloids

A

Hallucinations resembling psychosis

31
Q

Peptide causing increased capillary permeability and edema

A

Bradykinin and histamine