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Part 3 study guide for graduate level pharmacology exams. Tailored to Tennessee but applicable to any university

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This is the third part of my pharmacology study guides. This earned me an "A" on my exam. Contains good general information for all graduate level pharmacology students. Originally made as a study guide but can be used as a note template, or as a foundation for more information. It was made using the CDC, ANA, AHA, ACC, ADA, and Davis' Drug Guide.

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Warfarin Pharmacokinetics/Active Ingredient - Oral vitamin K antagonist; warfarin sodium inhibits vitamin K-dependent clotting
factors II, VII, IX, X and proteins C/S; delayed onset 3–5 days; half-life ~36–42 hours; CYP450 metabolism
Warfarin Starting Dose - 2–5 mg PO daily; lower doses in elderly, liver disease, malnutrition, or high bleeding risk
Warfarin Indications - Atrial fibrillation stroke prevention, DVT/PE treatment, mechanical heart valves
Warfarin vs Antiplatelets - Warfarin prevents fibrin clot formation through coagulation pathways; antiplatelets inhibit platelet
aggregation and are used for arterial disease (MI, stroke, CAD, PCI)
Warfarin Contraindications - Pregnancy, active bleeding, severe liver disease, inability to monitor INR, hemorrhagic disorders
Warfarin Patient Teaching - Maintain consistent vitamin K intake; avoid NSAIDs unless prescribed; report bleeding; use soft
toothbrush/electric razor; notify provider before starting new medications
Warfarin Antidote - Vitamin K (phytonadione); severe bleeding may require PCC or FFP
INR Monitoring After Starting Warfarin - Draw INR within 2–3 days after initiation and adjust until therapeutic
Target INR for Atrial Fibrillation/DVT/PE - 2.0–3.0
Target INR for Mechanical Mitral Valve - 2.5–3.5
Target INR for Mechanical Aortic Valve - 2.0–3.0 depending on risk factors

Major Antiplatelet Drugs - Aspirin (COX inhibitor ↓ thromboxane A2), clopidogrel/prasugrel/ticagrelor (P2Y12 receptor inhibitors),
dipyridamole (PDE inhibitor), abciximab/eptifibatide (GP IIb/IIIa inhibitors)​
Aspirin Pharmacokinetics - Irreversibly inhibits platelet COX-1, preventing thromboxane A2 formation; effect lasts 7–10 days for
platelet lifespan​
Clopidogrel Pharmacokinetics - Prodrug activated by CYP450 enzymes; irreversibly blocks P2Y12 receptors; decreased
effectiveness with CYP2C19 inhibitors​
Ticagrelor Pharmacokinetics - Reversible P2Y12 inhibitor with rapid onset; does not require hepatic activation​
Heparin Pharmacokinetics - Parenteral anticoagulant that activates antithrombin III, inhibiting thrombin and factor Xa; rapid onset;
monitored by aPTT​
Heparin Contraindications - Active bleeding, severe thrombocytopenia, history of heparin-induced thrombocytopenia (HIT),
hypersensitivity​
Heparin Pregnancy Category - Category B; preferred anticoagulant in pregnancy because it does not cross the placenta​
Low Molecular Weight Heparin (LMWH) - Enoxaparin; primarily inhibits factor Xa; predictable anticoagulant response with less
monitoring than unfractionated heparin​
LMWH Contraindications - Active bleeding, severe renal impairment, history of HIT, thrombocytopenia, hypersensitivity​
CHADS₂ Score - Stroke risk assessment for atrial fibrillation: CHF = 1 point, HTN = 1 point, Age ≥75 = 1 point, Diabetes = 1 point,
Stroke/TIA history = 2 points​
PCI Anticoagulants - Unfractionated heparin, bivalirudin, or low molecular weight heparin; combined with antiplatelet therapy
(aspirin + P2Y12 inhibitor)​
Missed Anticoagulant Dose Education - Take dose when remembered unless close to next dose; do not double dose; contact
provider for repeated missed doses​
Iron Supplement Education - Take on empty stomach with vitamin C for improved absorption; avoid calcium, antacids, and dairy
around dosing; dark stools are expected; constipation is common​
Average Daily Iron Intake - Adult men/postmenopausal women: 8 mg/day; premenopausal women: 18 mg/day​
Iron Contraindications - Hemochromatosis, hemosiderosis, anemia not caused by iron deficiency, hypersensitivity​
Iron Toxicity Signs - Severe abdominal pain, vomiting, diarrhea, GI bleeding, metabolic acidosis, shock, organ failure​
Adult Iron Deficiency Anemia Dose - Ferrous sulfate providing approximately 100–200 mg elemental iron/day in divided doses​
Folic Acid Contraindications - Hypersensitivity; avoid treating undiagnosed vitamin B12 deficiency because neurologic damage
may worsen​
Folic Acid Pregnancy Dose - 400–800 mcg daily for prevention of neural tube defects; higher doses for high-risk patients​
Vitamin B12 Deficiency Treatment - Cyanocobalamin IM injections or high-dose oral therapy depending on cause and absorption
ability​
Vitamin B12 Therapy Not Needed - Normal B12 levels and no evidence of deficiency; avoid unnecessary supplementation

Hematopoietic Growth Factors - Erythropoietin stimulates RBC production; filgrastim/pegfilgrastim stimulate neutrophil production​
Hematopoietic Growth Factor Administration - Usually subcutaneous; monitor CBC, hemoglobin, neutrophil response, and
adverse effects​
Hematopoietic Growth Factor Contraindications - Hypersensitivity; uncontrolled hypertension with erythropoietin; caution with
malignancy due to possible tumor stimulation​
Live Vaccine Contraindications - Pregnancy, immunocompromised patients, severe immune suppression, recent
immunosuppressive therapy​
MMR Vaccine Schedule - Two doses; first dose at 12–15 months, second dose at 4–6 years; adults without immunity receive 2
doses separated by ≥28 days​
Influenza Vaccine Recommendation - Annual vaccination recommended for everyone ≥6 months of age​
Influenza Vaccine Contraindications - Severe allergic reaction to previous influenza vaccine or vaccine component; delay with
moderate/severe acute illness​

, Flu Vaccine Education - Influenza vaccine cannot cause influenza; mild fever, soreness, and fatigue are immune responses, not
infection

Cyclosporine Indications - Immunosuppressant used for prevention of organ transplant rejection and treatment of autoimmune
disorders such as rheumatoid arthritis and psoriasis​
Cyclosporine Mechanism of Action - Calcineurin inhibitor that decreases T-cell activation and inhibits IL-2 production​
Cyclosporine Major Side Effects - Nephrotoxicity, hypertension, hyperkalemia, tremor, hirsutism, gingival hyperplasia, increased
infection risk​
Cyclosporine Monitoring - Renal function, blood pressure, electrolytes, liver function, drug levels, signs of infection​
TSH Indicating Levothyroxine Treatment - Elevated TSH with decreased free T4 indicates primary hypothyroidism requiring
treatment​
Levothyroxine Mechanism of Action - Synthetic T4 hormone converted to active T3; replaces deficient thyroid hormone and
regulates metabolism​
Levothyroxine Initial Dose - Healthy adults: approximately 1.6 mcg/kg/day; elderly or cardiac patients start low (12.5–50 mcg/day)
and titrate slowly​
Levothyroxine Administration - Take on empty stomach 30–60 minutes before breakfast; separate calcium, iron, and antacids by
at least 4 hours​
Levothyroxine Monitoring - Check TSH 6–8 weeks after initiation or dose changes; monitor every 6–12 months once stable​
Levothyroxine Contraindications - Untreated adrenal insufficiency, thyrotoxicosis, acute MI, hypersensitivity​
Levothyroxine Overdose Symptoms - Tachycardia, palpitations, anxiety, tremor, insomnia, weight loss, heat intolerance​
Hyperthyroidism Treatment - Antithyroid medications (methimazole, propylthiouracil), radioactive iodine therapy, or surgery
depending on cause and severity​
Methimazole Mechanism of Action - Inhibits thyroid peroxidase, decreasing thyroid hormone synthesis​
Propylthiouracil (PTU) Mechanism of Action - Inhibits thyroid peroxidase and blocks peripheral conversion of T4 to T3​
Methimazole Preferred Use - First-line for most patients with hyperthyroidism because of longer duration and fewer adverse
effects than PTU​
PTU Preferred Use - First trimester pregnancy and thyroid storm due to inhibition of peripheral T4 to T3 conversion​
Antithyroid Drug Major Adverse Effects - Agranulocytosis, hepatotoxicity, rash, arthralgia, GI upset​
Antithyroid Drug Patient Education - Report fever, sore throat, or infection symptoms immediately due to risk of agranulocytosis​
HIV Treatment Goal - Suppress viral replication to undetectable levels, increase CD4 count, prevent disease progression, and
reduce transmission risk​
Initiation of Antiretroviral Therapy (ART) - Begin treatment as soon as possible after HIV diagnosis regardless of CD4 count​
Six HIV Medication Classes - Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse
transcriptase inhibitors (NNRTIs), protease inhibitors (PIs), integrase strand transfer inhibitors (INSTIs), entry inhibitors, capsid
inhibitors​
NRTI Mechanism - Block reverse transcriptase by acting as false nucleoside substrates, stopping viral DNA synthesis​
NNRTI Mechanism - Directly inhibit reverse transcriptase enzyme activity​
Protease Inhibitor Mechanism - Block viral protease, preventing maturation of infectious HIV particles​
Integrase Inhibitor Mechanism - Prevent integration of viral DNA into host DNA​
Entry/Fusion Inhibitor Mechanism - Prevent HIV attachment or fusion with host cells​
Capsid Inhibitor Mechanism - Disrupt HIV capsid formation and viral replication​
HIV Post-Exposure Prophylaxis (PEP) - Three-drug ART regimen started within 72 hours of exposure and continued for 28 days​
HIV Pre-Exposure Prophylaxis (PrEP) - Preventive antiretroviral medication for HIV-negative individuals at high risk of exposure;
requires adherence and routine HIV testing​
Common Causes of HIV Medication Resistance - Poor adherence, missed doses, incorrect dosing, drug interactions, incomplete
viral suppression, viral mutations​
Pancreatitis Treatment - Supportive care with IV fluids, pain control, bowel rest, nutritional support, and treatment of underlying
cause​
Pancreatitis Medication Considerations - Opioids may be used for pain but can cause sedation, constipation, and respiratory
depression; monitor hydration and complications​
Pancreatic Enzyme Education - Take enzymes with every meal and snack; swallow capsules whole; dose depends on fat content;
improves digestion and nutrient absorption​
Insulin Pharmacodynamics - Binds insulin receptors causing increased glucose uptake into muscle/adipose tissue, decreased
hepatic glucose production, and increased glycogen synthesis​
Basal Insulin - Long-acting insulin providing continuous background glucose control; examples: glargine, detemir, degludec​
Bolus Insulin - Rapid- or short-acting insulin used for mealtime glucose control and correction doses; examples: lispro, aspart,
glulisine, regular insulin​
Rapid-Acting Insulin Peak/Duration - Lispro, aspart, glulisine: onset ~15 minutes; peak 1–2 hours; duration 3–5 hours​
Short-Acting Insulin Peak/Duration - Regular insulin: onset 30–60 minutes; peak 2–4 hours; duration 5–8 hours​
Intermediate-Acting Insulin Peak/Duration - NPH: onset 1–2 hours; peak 4–12 hours; duration 12–18 hours​
Long-Acting Insulin Peak/Duration - Glargine/detemir: minimal peak; duration approximately 24 hours; degludec duration >42

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