Lipid Pharm Flashcards

1
Q

Statins (MOA/AE/Tests)

A

*FIRST line therapy

MOA: inhibit HMG CoA reductase = increase LDL R exp. = decrease LDLC (and decrease TGs)

AE:
-Hepatotoxicity
-SKM toxicity (mmmr)

*should get baseline LFTs (ALT/AST) and CK

Increased SKM tox with:
1. Increased statin dose
2. Drug-drug interactions
3. Low thyroid hormone levels
4. Low vitamin D levels

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2
Q

Ezetimibe (MOA/AE)

A

MOA: inhibits NPC1L, increase LDL R exp. = decrease LDLC

AE: minimal

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3
Q

Cholestyramine, Colestipol, Colesevelam (MOA/AE)

A

BA Sequestrants

MOA: increase LDL R exp. = decrease LDLC

AE: very safe bc not absorbed systemically
-GI (bloat/constipation/nausea/flatulence)
-Can affect GI abs. of other drugs/fat sol vits

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4
Q

Alirocumab, Evolocumab (MOA/AE)

A

PCSK-9 Inhibitors (monoclonal antibody, SC inj)

MOA: increase LDL R exp. = decrease LDLC

AE:
-Inject site rxn
-Allergic rxn

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5
Q

Niacin (MOA/AE)

A

MOA: activate gpcr on adipose, decrease TG synthesis = decrease VLDL and LDLC

AE: FIDHHHH
-Flushing, itching, dyspepsia, headache
-Hepatotoxicity
-Hyperglycemia
-Hyperuricemia

*Increased risk of SKM toxicity with statins

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6
Q

Fenofibrate, Gemfibrozil (MOA/AE)

A

FIBrates

MOA: activate PPARα, decrease VLDL, may increase LDLC (increase fatty acid ox. also)

AE:
-GI (dyspepsia, abd. pain, diarrhea, constipation)
-Increase gallstone formation
-Increase risk of SKM tox with statins (esp. gem)

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7
Q

Highest LDL-C Lowering

A

Statins, PCSK9 inhibitors

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8
Q

Highest TG Lowering

A

Fibrates, Niacin, Statins

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9
Q

Highest HDL-C Raising

A

Niacin

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10
Q

Used for: Hyperthyroidism

A

Anti-thyroid drugs (Meth and PTU)

MOA: inhibit thyroid peroxidase, decrease levels of TH

AE:
-Rash
-Hepatotoxicity
-Agranulocytosis

Meth preferred; PTU = black box warning for
hepatotoxicity (reserved for intolerance to methimazole or 1st trimester pregnancy)

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