Cardiovascular Drugs: A Comprehensive Overview, Lecture notes of Cardiology

A concise overview of cardiovascular drugs, covering anti-hypertensive agents, drugs used in heart failure, anti-angina drugs, drugs used in dyslipidemia, and drugs for arrhythmias. It details the mechanisms of action, administration routes, effects, side effects, and contraindications of various drugs, including ace inhibitors, arbs, calcium channel blockers, sympatholytic agents, vasodilators, and diuretics. The document also discusses drugs used in angina pectoris and dyslipidemia, offering a structured approach to understanding cardiovascular pharmacology. It is a useful resource for medical students and healthcare professionals seeking a quick reference on cardiovascular medications. The document also includes information on drug dosages and potential toxicities, making it a valuable tool for clinical practice.

Typology: Lecture notes

2025/2026

Available from 10/22/2025

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CARDIOVASCULAR DRUGS
1.ANTI-HYPERTENSIVE AGENTS
2. DRUGS USED IN HEART FAILURE
3. ANTI-ANGINA DRUGS
4. DRUGS USED IN DYSLIPIDEMIA
5. DRUGS FOR ARRHYTHMIAS
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1

CARDIOVASCULAR DRUGS

1.ANTI-HYPERTENSIVE AGENTS

  1. DRUGS USED IN HEART FAILURE
  2. ANTI-ANGINA DRUGS
  3. DRUGS USED IN DYSLIPIDEMIA
  4. DRUGS FOR ARRHYTHMIAS

a) Angiotensin Converting Enzyme (ACE)

inhibitors

e.g. Enalapril, captopril, lisinopril,

ramipril.

Mxn : inhibit conversion of angiotensin I

to angiotensin II.

Adm : all administered per oral.

Effects:

i) reduce peripheral vascular resistance

ii) reduce circulating blood volume.

S/E: hypotension, acute renal failure,

hyperkalemia, dry cough, allergic skin

rashes.

C/I: Renal failure; pregnancy

10/22/2025 compiled by PMM 4

c) Calcium channel blockers

E.g. amlodipine, nifedipine, felodipine,

verapamil, diltiazem.

Adm: per oral.

Mxn: inhibit influx of calcium into

arterial smooth muscle cells hence

reducing contraction.

Effect: reduce peripheral vascular

resistance.

S/E: hypotension, palpitation,

perspiration, dizziness, headache, GIT

disturbance.

C/I: cardiogenic shock, hypotension,

pregnancy (except nifedipine)

d)Sympatholytic agents

Mxn: generally they reduce symphathetic

effects on arteries and the heart.

Effects: reduce peripheral vascular resistance,

reduced cardiac conractility, heart rate &

cardiac output.

 Centrally acting e.g. Methyldopa

S/E : sedation, depression, nightmares,

hemolytic anaemia, vertigo.

 Beta-blockers e.g. propranolol, metoprolol,

esmolol, atenolol

S/E: bradycardia, bronchospasm, heart failure,

hypoglycemia, GIT disturbance.

f) Diuretics

Mxn : reduce the circulating blood volume by

inducing diuresis.

  • Classified according to predominant point of

action on the nephron.

 Carbonic anhydrase inhibitors

Mxn: inhibit carbonic anhydrase in the PCT,

blocking reabsorption of NaHCO 3

. E.g.

acetazolamide.

Uses : (rarely used in hypertension)

  • Glaucoma, metabolic alkalosis.

S/E : renal stone formation, hypokalemia,

paresthesias, metabolic acidosis.

C/I : hepatic cirrhosis

Loop diuretics

E.g. furosemide, torsemide, bumetanide,

ethacrynic acid.

Mxn : inhibit NaCL re-absorption in the thick

ascending limb of loop of henle.

Uses : hypertension, hyperkalemia, acute

renal failure, heart failure, edema &

ascites.

S/E : hypokalemia, hyperuricemia,

ototoxicity, nephrotoxicity, dehydraton,

hypomagnesemia.

C/I: allergy to sulphonamides, anuria, early

in pregnancy.

Potassium sparing diuretics

E.g. spironolactone, triamterene, amiloride.

Mxn : antagonise the effects of aldosterone

at late DCT & collecting tubules.

Uses : (usually combined with other

diuretics to prevent hypokalemia)

  • hyperaldosteronism, hypokalemia.

S/E : hyperkalemia, metabolic acidosis,

gynecomastia, acute renal failure, kidney

stones.

C/I : chronic renal insufficiency.

10/22/2025 compiled by PMM 11

Osmotic diuretics

E.g. Mannitol

Mxn : promote water diuresis by

osmosis.

Adm : I.V infusion.

Use: (rarely used in hypertension)

To reduce intracranial pressure

Glaucoma (to reduce intraocular

pressure)

S/E : dehydration, hyperkalemia,

hypernatremia.

10/22/2025 compiled by PMM 13

b) Vasodilators

Generally vasodilators reduce the

workload of the heart by reducing both

the preload & afterload.

Arterial vasodilators reduce afterload

i.e peripheral vascular resistance

Venodilators reduce the preload i.e. the

venous return.

Venodilators & arterial dilators reduce

both preload and afterload.

NB : a general side effect is postural

hypotension.

c) Beta blockers( beta-receptor

antagonists)

Effects:

Slow down the heart rate

Decrease the force of contraction

Prevent remodeling such as

hypertrophy of ventricular walls.

NB : Usually combined with diuretics or

ACE inhibitors.

Uses

Heart failure in atrial fibrillation

Usually added to diuretics, ACE

inhibitors, & beta-blockers.

Dose: 0.125-0.25mg OD. (PO).

Toxicity

Sinus bradycardia

Sino-atrial arrest

Hyperkalemia

Heart block

NB : it has a narrow therapeutic index

hence requires ECG & electrolyte

monitoring.

3. DRUGS USED IN ANGINA

PECTORIS

Angina is a vice-like chest pain caused

by accumulation of metabolites

resulting from myocardial ischemia.

a) Nitrates : Nitroglycerine is the

prototype drug. Its derivatives include:

  • Isosorbide dinitrate (sublingual; per oral)
  • Isosorbide mononitrate (sublingual; per

oral)

  • Amyl nitrate (inhalant)

Mxn: converted to nitric oxide which

induces smooth muscle relaxation &

4. DRUGS USED IN DYSLIPIDEMIA

Low density (LDL) & very low density

lipoproteins (VLDL) are rich in

cholesterol and triglycerides –

associated with cardiac diseases &

atherosclerosis.

High density lipoproteins (HDL)

facilitate transport of cholesterol &

triglycerides for metabolism in the liver

hence they have a beneficial role.

NB: Drugs used either lower the levels

of VLDL & LDL or increase the levels of

HDL.

a).HMG-CoA reductase inhibitors (“statins”)

  • E.g. simvastatin, lovastatin, fluvastatin,

rosuvastatin.

Mxn: inhibit HMG-CoA reductase which

catalyses the initial steps in cholesterol

synthesis.

Effect : reduces LDL, small increase in HDL.

Adm: per oral with evening meal.

S/E: Rhabdomyolysis, myopathy,

hypersensitivity reactions.

C/I: pregnancy & lactation, hypersensitivity,

impaired liver or renal function, children

less than 18 years.