Section Contents:
- Antiarrhythmic Drugs.
- Adrenoceptor agonists.
- Antiplatelets.
- Benzodiazepine antagonist.
- Anaesthetic Agents
- Angina Drugs
- Antithrombotic Drugs
- Fibrinolytics.
- Antihypertensive medication.
- Antidiabetic Drugs.
- Muscle Relaxants.
- Antidepressants.
- Antipsychotics
- Antiepileptics
- Antivirals
- …
Antiarrhythmic Drugs
Lignocaine (Lidocaine)
Classification: amide-type local anaesthetic and Class 1B antiarrhythmic (Shortens Repolarisation) (Kundra & Vinayagam, 2020); (Rossiter, 2022, p. 140).

Amiodarone
Classification: Class 3 antiarrhythmic (Șorodoc et al., 2024); (Rossiter, 2022, p. 142).


Sotalol / Sotalol Hydrochloride
Classification: Class 3 antiarrhythmic, which possesses Class 2 activity (non-selective β-Blocker and K channel blocker) (Rossiter, 2022, p. 143); (Rizkallah & Refaat, 2023).


Adenosine
Classification: Endogenous purine nucleoside autacoid that signals through four G protein-coupled adenosine receptor subtypes: A1, A2A, A2B, and A3 (Borea et al., 2018).



Digoxin
Classification: Cardiac glycoside (Patocka et al., 2020).


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Magnesium Sulphate 50%
Classification: Electrolyte with anticonvulsant, calcium-antagonistic, and NMDA-blocking properties (Marín et al., 2025); (Soleimanpour et al., 2022); (Mathew & Panonnummal, 2021).


Metoprolol tartrate
Classification: cardioselective β1-adrenergic receptor blocker (Hamadeh et al., 2014); (Vinereanu et al., 2020).

Esmolol
Classification: ultra-short-acting, cardioselective β1-adrenergic receptor blocker (Wiest & Haney, 2012); (Rossiter, 2022, p. 164).

Vaughan-Williams Classification of anti-arrhythmic agents
The Vaughan-Williams classification groups anti-arrhythmic agents into 4 according to the predominant electrophysiologic mechanism of action. This classification framework contains limitations (Lei et al., 2018). Class I sodium-channel blockers, Class II beta-blockers, Class III action-potential prolonging drugs, and Class IV calcium-channel blockers. Class I is subdivided into Ia, Ib, and Ic according to effects on action potential duration and sodium-channel (Janse, 1994).
| Class | Mechanism | Example |
|---|---|---|
| Class 1 IA: Prolongs repolarization. IB: Shortens repolarization. IC: No effect on repolarization. | Na channel Blockers | 1-A: Procainamide, Quinidine. 1-B: Lignocaine. 1-C: Flecainide, Propafenone. |
| Class IV | Ca Channel Blockers (Non-dihydropyridine) | Verapamil Diltiazem |
| Class III | K Channel Blockers | Amiodarone Sotalol |
| Class II | β Blockers | Metoprolol Esmolol Propranolol |
____________________________________________________________________________________________________________________________________________________________
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Adrenoceptor agonists
Dobutamine
Classification: β1-Adrenergic receptor agonist; synthetic catecholamine (Farmakis et al., 2019).

(β1 > β2 > α)
| DoButamine | Dopamine | |
|---|---|---|
| Naturality | Synthetic | Natural |
| Receptor affinity | β1 > β2 > α | D1 > β1 > α |
| Vasopressor | No | Yes |
| Noradrenaline secretion | No | Yes |
Dopamine
Classification: kuningi.

(D1 > β1 > α).
Stimulation of NA secretion
| Dose | Receptor | Organ | Effects | Indications |
| 2-5 mcg/kg/min | D1![]() | – Renal vasculature. – Mesenteric vascular bed | – Renal vasodilation – ↑renal blood flow – ↑GFR – ↑Na excretion | – Congestive Cardiac failure. – Acute Renal Failure |
| 5-10 mcg/kg/min | β1![]() | – Heart | – ↑ Cardiac contractility(inotropy). – ↑ Heart Rate (chronotropy) | – Congestive Cardiac failure. – Cardiogenic shock. – Septic Shock. |
| 10-20 mcg/kg/min | α1 | – Vascular smooth mm | – Peripheral vasoconstriction. – ↑ BP. | – Acute symptomatic hypotension (Adjunct to fluid resuscitation) |
Adrenaline / Epinephrine
Classification: endogenous catecholamine, sympathomimetic agonist, and non-selective adrenergic receptor agonist (Baker & Summers, 2024); (Motiejunaite et al., 2021); (Xu et al., 2023),(Rossiter, 2022, p. 144).


Receptor affinity β1 = β2; α1 = α2
Isoproterenol
Classification: catecholamine; sympathomimetic nonselective β-adrenergic receptor agonist (Bader Eddin et al., 2025).

(β1 = β2 >>α)
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Phenylephrine
Classification: sympathomimetic α1-adrenergic receptor agonist (Thiele et al., 2011).

________________________________________________________
…
Antiplatelets
Aspirin / ASA (Acetylsalicylic acid)
Classification: platelet aggregation inhibitor; antithrombotic agent; non-steroidal anti-inflammatory drug (Sun et al., 2025), .

…
Clopidogrel
Classification: antiplatelet drug, P2Y12 receptor inhibitor (Thomas et al., 2023).

…
________________________________________________________
Atropine
Classification: Anticholinergic: muscarinic receptor antagonist (Huang et al., 2023).

…
Bevacizumab (Avastin)
Classification: anti-VEGF recombinant humanised IgG1 monoclonal antibody (Russo et al., 2017).

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Charcoal, Activated (Activated Carbon)

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Diazepam
Classification: long-acting benzodiazepine (Vitukade, 2024); (Dessai et al., 2024). Anxiolytic, anticonvulsant, sedative, hypnotic, and muscle relaxant (Vitukade, 2024).

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Lorazepam
Classification: benzodiazepine (Rundio, 2012). Anxiolytic, anticonvulsant, sedative, hypnotic, and CNS depressant (Rundio, 2012); (Ameer & Greenblatt, 1981).

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Benzodiazepine antagonist
Flumazenil
Classification: competitive benzodiazepine antagonist (Kloeck, 2023, p. 22), (Whitwam & Amrein, 1995), (Rossiter, 2022, p. 457).

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Anaesthetic Agents
Etomidate
Classification: imidazole derivative, non-barbiturate sedative-hypnotic (Zheng et al., 2025), steroidogenesis enzyme inhibitor (Pence et al., 2022).

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Ketamine
Classification: dissociative anaesthetic, NMDA receptor antagonist (Zanos et al., 2018).

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Propofol
Classification: short-acting sedative-hypnotic (Sahinovic et al., 2018), 2,6-diisopropylphenol (Larijani et al., 1989).

Thiopental Sodium
Classification: ultra-short-acting thiobarbiturate (barbituric acid derivative) general anaesthetic (Čižmáriková et al., 2023), (Russo & Bressolle, 1998).

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Furosemide
Classification: Loop diuretic (Xue et al., 2025), (Boles Ponto & Schoenwald, 1990). BCS (Biopharmaceutics Classification System) Class IV (Pham et al., 2023).



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Glucose 50%

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ANGINA
Verapamil / Verapamil hydrochloride
Classification: phenylalkylamine calcium channel blocker (Popović et al., 2020); nondihydropyridine CCB (Eisenberg et al., 2004), Class IV antiarrhythmic drug (Thipe et al., 2023).


Diltiazem
Classification: benzothiazepine calcium channel blocker (Özkaya & Yazganoğlu, 2014); nondihydropyridine CCB (Lee, 2023). Class 4 antiarrhythmic drug (Özkaya & Yazganoğlu, 2014).

| Dihydropyridine CCB | Non-Dihydropyridine CCB | |
| Examples | Amlodipine Felodipine Nifedipine | Verapamil Diltiazem |
| MOA | Blocking active (opened) voltage-gated L-Type Calcium channels. | Blocking closed voltage-gated L-Type Calcium channels. |
| Areas of effects | Vascular smooth muscles – Peripheral arteries | Cardiac conduction system – SA node – AV node |
| Maximum Effects | Vasodilatation – Reduced Blood pressure | – Slow down rate of cardiac contractility. – Slow down rate of cardiac conduction. |
| Effect on Inotropy (contraction strength) | Nil | Reduces |
| Effect on Chronotropy (heart rate / contraction rate) | Nil | Reduces |
| Effect on dromotropy (impulse conduction velocity) | Nil | Reduces |
| Indications | – Hypertension – Angina pectoris – Raynaud’s phenomenon (Nifedipine) – Cerebrovascular events (nimodipine) | – Angina – PSVT – Atrial Fibrillation. – Atrial flutter – Hypertension. |
ANTITHROMBOTICS
Enoxaparin
Classification: unfractionated heparin (UFH) derivative (Hao et al., 2019); Low molecular weight heparin (LMWH) (Imbalzano et al., 2024);

Unfractionated Heparin (UFH)
Classification: unfractionated heparin (UFH).

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Antithrombotic Drugs
Warfarin
Classification: hydroxycoumarin anticoagulant (Hunt & Levi, 2018); Vitamin K antagonist (VKA) (Liu et al., 2022).

Antihaemorrhagic
Antifibrinolytic
Tranexamic Acid
Classification: synthetic lysine-derived analogue antifibrinolytic (Cai et al., 2020).


Vitamin K
Vitamin K1 / Phytomenadione / Phylloquinone (Konakion Injectable)
Classification: fat-soluble (Pawaria et al., 2023) antihemorrhagic vitamin (Simes et al., 2020).


Protamine sulfate (PS)
Classification: unfractionated heparin (UFH) reversal antidote (Levy et al., 2023); cationic arginine-rich polypeptide (protein) (Li, 2019).

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Hypertension
HCT (Hydrochlorothiazide)
Classification: thiazide-type diuretic (benzothiadiazine ring) (Ernst & Fravel, 2022); antihypertensive diuretic (Mendes et al., 2016); Biopharmaceutics Classification System (BCS) Class IV (Mendes et al., 2016).


Indapamide
Classification: thiazide-like diuretic (Ernst & Fravel, 2022); antihypertensive diuretic (Caruso et al., 1983).

Amlodipine
Classification: Dihydropyridine Calcium Channel Blocker (CCB) (Jambhale & Afifa, 2025).

Felodipine
Classification: vascular-selective (Navadiya & Tiwari, 2015) Dihydropyridine Calcium Channel Blocker (CCB) (McDonagh et al., 2025); BCS Class II [low solubility and high permeability] (Fuhr et al., 2022).

Nifedipine
Classification: 1,4-Dihydropyridine Calcium Channel Blocker (Triggle, 2003); L-type calcium channel blocker (Devi Sri et al., 2025).

Captopril
Classification: ACE inhibitor (Kendall et al., 1982). First orally active ACE inhibitor (Heel et al., 1980).


Enalapril / Enalapril maleate
Classification: ACE inhibitor (Seifi et al., 2024); nonsulfhydryl, orally active prodrug (Thind, 1990).


Lisinopril
Classification: ACE inhibitor (Lancaster & Todd, 1988); nonsulfhydryl, orally active prodrug (Thind, 1990).

Candesartan / Candesartan cilexetil
Classification: angiotensin II type 1 receptor antagonist (Michel et al., 2013).

Irbesartan
Classification: angiotensin II type 1 receptor antagonist (Michel et al., 2013).

Losartan / Losartan potassium
Classification: angiotensin II type 1 receptor antagonist (Michel et al., 2013).

Valsartan
Classification: angiotensin II type 1 receptor antagonist (Siddiqui, 2011).

Telmisartan
Classification: angiotensin II type 1 receptor antagonist (Chen et al., 2025).

Amiloride-Hydrochlorothiazide (Combo)
Classification: K-sparring diuretic.
[Adco-Retic]

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Diabetes
Metformin
Classification: biguanide (Singh et al., 2025).

Glibenclamide
Classification: 2nd generation sulfonylurea (Kurland et al., 2013).


Gliclazide
Classification: 2nd Generation Sulfonylurea (Mapa et al., 2020).

Glipizide
Classification: 2nd Generation Sulfonylurea (Lebovitz, 1985).

Glimepiride
Classification: Sulfonylurea (Azhar et al., 2025).

Dapagliflozin
Classification: Sodium-glucose cotransporter-2 (SGLT-2) inhibitor (Plosker, 2012).


Empagliflozin
Classification: Sodium-glucose cotransporter-2 (SGLT-2) inhibitor (Forycka et al., 2022).


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Insulin: Short-Acting Human insulin

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Thyroid Hormones
Levothyroxine Sodium
Classification: synthetic T4 thyroid hormone replacement (Schiavo et al., 2021).

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Naloxone
Classification: competitive opioid receptor antagonist (Saari et al., 2024).

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Oxytocin
Classification: peptide hormone receptor; uterotonic or oxytocic agent (Hermesch et al., 2024).

ANTIEPILEPTICSzantsimedics.org
Phenobarbital Sodium
Classification: Barbiturate (Laxmi, 2017).

Primidone
Classification: phenobarbital metabolite (Johannessen & Johannessen Landmark, 2020).

Phenytoin
Classification: antiseizure hydantoin derivative (Patocka et al., 2020).

Clobazam
Classification: 1,5-benzodiazepine (Sankar, 2012); (Rossiter, 2022, p. 485).

Clonazepam
Classification: 1,4-benzodiazepine (Teli et al., 2023); (Ruiz Ramirez et al., 2025); (Rossiter, 2022, p. 484).


Diazepam
Classification: 1,4-benzodiazepine (Teli et al., 2023); (Rossiter, 2022, p. 485).

Lorazepam
Classification: 1,4-benzodiazepine (Teli et al., 2023); (Rossiter, 2022, p. 485).

Midazolam
Classification: 1,4-benzodiazepine (Teli et al., 2023); (Rossiter, 2022, p. 485).

Carbamazepine
Classification: tricyclic iminostilbene derivative (Rossiter, 2022, p. 486); BCS Class II (García et al., 2021).

Valproic Acid
Classification: antiepileptic drug (AED) or antiseizure (Safdar & Ismail, 2023); Mood stabilising (Diederich et al., 2010) fatty acid (Rossiter, 2022, p. 488);

Antipsychotic Drugs
1st generation (Typical) antipsychotics
Chlorpromazine
Classification: 1st generation antipsychotic (D2 receptor antagonist) (Leucht & Davis, 2022); phenothiazine derivative (Rossiter, 2022, p. 505), (Saha et al., 2016)

Flupentixol
Classification: 1st generation antipsychotic (D2 receptor antagonist); thioxanthene derivative (Rossiter, 2022, p. 505).

Zuclopenthixol
Classification: 1st generation antipsychotic (D2 receptor antagonist); thioxanthene derivative (Rossiter, 2022, p. 505).

Haloperidol
Classification: 1st generation antipsychotic (D2 receptor antagonist); butyrophenone neuroleptic (Rossiter, 2022, p. 505).

Clozapine
Classification: 2nd generation antipsychotics (5HT2A/2C + D2 receptor antagonist) (Solmi et al., 2017); (Rossiter, 2022, p. 509).

Clotiapine
Classification: 2nd generation antipsychotics (5HT2A/2C + D2 receptor antagonist); (Rossiter, 2022, p. 509).

Risperidone
Classification: 2nd generation antipsychotics (5HT2A/2C + D2 receptor antagonist) (Solmi et al., 2017); (Rossiter, 2022, p. 509).

Olanzapine
Classification: 2nd generation antipsychotics (5HT2A/2C + D2 receptor antagonist) (Solmi et al., 2017); (Rossiter, 2022, p. 509)..

Quetiapine
Classification: 2nd generation antipsychotics (5HT2A/2C + D2 receptor antagonist) (Solmi et al., 2017); (Rossiter, 2022, p. 509)..

Atypical antipsychotics / 3rd Gen
Aripiprazole
Classification: Third-generation antipsychotic (Stelmach et al., 2023).
Lithium carbonate
Classification: Mood stabiliser (Nucci et al., 2026); inorganic lithium salt (Lyons & Gossell-Williams, 2024).


Mineral Supplement
Calcium Chloride

Potassium chloride 15%

Sodium Bicarbonate 8.4%

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Corticosteroids
Hydrocortisone
Classification: Natural glucocorticoid (Yang & Yu, 2021), corticosteroid (Kowalska & Szeleszczuk, 2024).

Methylprednisolone
Classification: synthetic glucocorticoid corticosteroid (Zhou et al., 2025).

Prednisone
Classification: synthetic glucocorticoid corticosteroid (Offor et al., 2025).

Betamethasone
Classification: synthetic glucocorticoid corticosteroid (Kochova et al., 2023).

Rivaroxaban (Xarelto)
Classification: selective, direct factor Xa inhibitor (Kreutz, 2012).

Sodium Polystyrene Sulfonate (Kayexalate)
Classification: cation-exchange resin (Varriale & Ngai, 2014); potassium-chelating agent (Labriola & Jadoul, 2020)

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Muscle Relaxation
Suxamethonium Chloride (Succinylcholine chloride)
Classification: depolarizing neuromuscular blocking agent (NMBA) (Alvarellos et al., 2015).

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Atracurium besylate
Classification: benzylisoquinoline non-depolarising neuromuscular blocking agent (NMBA) (Clark-Price, 2022).

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Rocuronium
Classification: aminosteroid, nondepolarizing neuromuscular blocking agent (Bevan, 1994).


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Fibrinolytics
Alteplase
Classification: fibrinolytic thrombolytic (Rashedi et al., 2024); Recombinant tPA thrombolytic (Morrow & Mutch, 2022).


Tenecteplase
Classification: fibrinolytic thrombolytic; genetically engineered tissue plasminogen activator (tPA) (Tanswell et al., 2002).

Reteplase
Classification: fibrinolytic thrombolytic; recombinant plasminogen activator, a mutant of alteplase (Nishanth et al., 2019).
Streptokinase
Classification: fibrinolytic thrombolytic; plasminogen activator (Rashedi et al., 2024); bacterial / microbial plasminogen activator (Adivitiya & Khasa, 2017).

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Antidepressants
Citalopram
Classification: selective serotonin reuptake inhibitor (SSRI) (Edinoff et al., 2021).

Ecitalopram
Classification: selective serotonin reuptake inhibitor (SSRI) (Edinoff et al., 2021)

Fluoxetine
Classification: selective serotonin reuptake inhibitor (SSRI) (Edinoff et al., 2021)

Fluvoxamine
Classification: selective serotonin reuptake inhibitor (SSRI) (Edinoff et al., 2021).

Paroxetine
Classification: selective serotonin reuptake inhibitor (SSRI) (Edinoff et al., 2021).


Sertraline
Classification: selective serotonin reuptake inhibitor (SSRI) (Edinoff et al., 2021).

Amitriptyline hydrochloride
Classification: TCA antidepressant (Jørgensen et al., 2021).

Clomipramine
Classification: TCA antidepressant (Jørgensen et al., 2021).

Imipramine hydrochloride
Classification: TCA antidepressant (Jørgensen et al., 2021).

Trimipramine
Classification: TCA antidepressant (Jørgensen et al., 2021).

Dosulepin
Classification: TCA antidepressant(Jørgensen et al., 2021).

| . | Tricyclic Antidepressants (TCA) | Selective Serotonin Reuptake Inhibitors (SSRI) |
|---|---|---|
| MOA | Inhibit the re-uptake of both NA and 5-HT at presynaptic terminal membrane. This results in increased levels of NA and 5-HT in the synaptic cleft. | Only Inhibit the re-uptake of 5-HT at presynaptic terminal membrane |
| Example | – Amitriptyline hydrochloride – Clomipramine hydrochloride – Imipramine hydrochloride – Trimipramine – Dosulepin | – Citalopram – Imipramine hydrochloride – Escitalopram – Trimipramine – Dosulepin |
5-HT = 5-Hydroxytrptamine (Serotonin); NA = Noradrenaline
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Antimalarials
Mefloquine
Classification: quinoline-based (Mereddy & Ronayne, 2018) chemoprophylaxis (Jong & Nothdurft, 2001).

Atovaquone/Proguanil
Classification: fixed dose combination (McKeage & Scott, 2003); Chemoprophylaxis (Jong & Nothdurft, 2001); Atovaquone is a naphthoquinone (Baggish & Hill, 2002) and Proguanil is a biguanide derivative (LakshmanaRao, 2017).

Doxycycline
Classification: Tetracycline antibiotic (Holmes & Charles, 2009); Chemoprophylaxis (Jong & Nothdurft, 2001).

Artemether/Lumefantrine
Classification: artemisinin-based combination therapy (ACT) (Makanga & Krudsood, 2009). Artemether is an artemisinin derivative (Patel et al., 2012) and Lumefantrine is a aryl-amino alcohol.

Artesunate
Classification: artemisinin derivative (Kouakou et al., 2019).

Vaccines
Hepatitis A inactivated vaccine



Hepatitis B vaccine


ANTIVIRALS
Oseltamivir (Tamiflu)
Classification: neuraminidase (sialidase) inhibitor.

Zanamivir (Relenza)
Classification: neuraminidase (sialidase) inhibitor.

Acyclovir
Classification: Nucleoside analogue.


Famciclovir
Classification: Nucleoside analogue.

Ganciclovir
Classification: Nucleoside analogue.

Valaciclovir
Classification: Nucleoside analogue.

Intravenous fluids
Sodium chloride 0.9%

Hypertonic Saline

| Abbreviation | Latin | English |
|---|---|---|
| a.c. | ante cibum | Before Food. |
| b.d. | bis die | Twice daily. |
| o.d. | omni die | Every day. |
| o.m. | omni mane | Every morning. |
| o.n. | omni nocte | Every night. |
| p.c. | post cibum | After food |
| p.r.n. | pro re nata | When required. |
| q.d.s | quater die sumendus | To be taken 4 times daily. |
| q.i.d. | quater in die | 4 times daily. |
| stat | statim | Immediately. |
| t.d.s | ter die sumendus | To be taken 3 times daily. |
| t.i.d. | ter in die | 3 times daily. |
…
| REFENCES |
|---|
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