Pharmacology of Valsartan

Introduction/Overview Valsartan represents a cornerstone agent in the management of cardiovascular and renal disorders mediated by the renin-angiotensin-aldosterone system (RAAS). As a selective angiotensin II receptor blocker (ARB), it exerts its therapeutic effects by antagonizing the actions of angiotensin II at the AT1 receptor subtype. The clinical introduction of valsartan provided a significant therapeutic alternative … Read more

Pharmacology of Telmisartan

Introduction/Overview Telmisartan is an orally active antihypertensive agent belonging to the class of angiotensin II receptor blockers. As a cornerstone in the management of hypertension and related cardiovascular disorders, its pharmacological profile is characterized by potent and selective antagonism of the angiotensin II type 1 receptor. The clinical relevance of telmisartan extends beyond blood pressure … Read more

Pharmacology of Acetazolamide

Introduction/Overview Acetazolamide represents a cornerstone therapeutic agent within the class of carbonic anhydrase inhibitors, distinguished by its unique mechanism of action and diverse clinical applications. First introduced in the 1950s, it remains a critical drug in the management of several conditions, ranging from ophthalmic disorders to neurological and respiratory ailments. Its primary action, the inhibition … Read more

Pharmacology of Dextromethorphan

Introduction/Overview Dextromethorphan, the d-isomer of the codeine analog levorphanol, is a centrally acting antitussive agent devoid of analgesic or addictive properties at therapeutic doses. First approved for medical use in the 1950s, it has become one of the most widely used over-the-counter medications globally for the symptomatic relief of non-productive cough. Its clinical relevance extends … Read more

Pharmacology of Acetylcysteine

Introduction/Overview Acetylcysteine, also known as N-acetylcysteine (NAC), is a multifunctional pharmacological agent with a broad spectrum of clinical applications rooted in its unique biochemical properties. Originally developed as a mucolytic agent, its therapeutic utility has expanded significantly following the discovery of its efficacy as an antidote for acetaminophen (paracetamol) poisoning. The drug serves as a … Read more

Pharmacology of Fluticasone

Introduction/Overview Fluticasone represents a cornerstone synthetic glucocorticoid medication extensively utilized in the management of chronic inflammatory respiratory and dermatological conditions. As a potent anti-inflammatory agent, its development marked a significant advancement in topical and inhaled corticosteroid therapy, primarily due to its favorable pharmacokinetic profile which enhances therapeutic index. The clinical relevance of fluticasone is substantial, … Read more

Pharmacology of Budesonide

Introduction/Overview Budesonide represents a cornerstone agent within the class of synthetic glucocorticoids, distinguished by its high topical potency and extensive first-pass metabolism. As a non-halogenated corticosteroid, it is formulated for targeted delivery to mucosal surfaces, primarily in the respiratory and gastrointestinal tracts, thereby maximizing therapeutic effect at the site of disease while minimizing systemic exposure. … Read more

Pharmacology of Terbutaline

Introduction/Overview Terbutaline represents a cornerstone agent within the therapeutic arsenal for obstructive pulmonary diseases. As a selective beta2-adrenergic receptor agonist, its primary clinical utility lies in the relief of bronchospasm. The drug’s pharmacological profile, characterized by its ability to relax smooth muscle in the airways, vasculature, and uterus, underpins its use in both respiratory and … Read more

Pharmacology of Salmeterol

Introduction/Overview Salmeterol xinafoate represents a cornerstone in the maintenance therapy of obstructive airway diseases, specifically asthma and chronic obstructive pulmonary disease (COPD). As a long-acting beta2-adrenoceptor agonist (LABA), it provides sustained bronchodilation, contrasting sharply with the rapid onset and short duration of its predecessor, salbutamol. The clinical introduction of salmeterol marked a significant advancement, enabling … Read more

Pharmacology of Misoprostol

Introduction/Overview Misoprostol is a synthetic prostaglandin E1 (PGE1) analog with a diverse and critical profile of therapeutic applications. Initially developed for the prevention of gastric mucosal injury associated with nonsteroidal anti-inflammatory drug (NSAID) therapy, its pharmacological actions on smooth muscle and the uterine cervix have led to its widespread use in obstetrics and gynecology. The … Read more