Pharmacology and Toxicology drugs

 Chapter 4: Drugs Acting on Central Nervous System-I 

General Anaesthetics 

Introduction 

Stages of Anaesthesia 

Classification of General Anaesthetics

Inhalational

Gas:-

Nitrous oxide 

Volatile liquids:-

Ether Halothane

Isoflurane

Desflurane

Sevoflurane

Intravenous Fast acting drugs

Thiopentone sod. , Methohexitone sod. , Propofol , Etomidate ,Benzodiazepines, Midazolam, Diazepam, Lorazepam

Dissociative anaesthesia

Ketamine

Opioid analgesia

Fentanyl

  Analgesic, Antipyretic and Non-Steroidal Anti-Inflammatory Drugs 

Introduction 

Classification 

A. Nonselective COX inhibitors (traditional NSAIDs)

1. Salicylates: Aspirin.

2. Propionic acid derivatives: Ibuprofen, Naproxen, Ketoprofen, Flurbiprofen.

3. Fenamate: Mephenamic acid.

4. Enolic acid derivatives: Piroxicam,

Tenoxicam.

5. Acetic acid derivatives: Ketorolac, Indolmethacin, Nabumetone.

6. Pyrazolone derivatives: Phenylbutazone, Oxyphenbutazone.

B. Preferential COX-2 inhibitors

Nimesulide, Diclofenac, Aceclofenac,

Meloxicam, Etodolac.

C. Selective COX-2 (Cyclooxygenase-2) inhibitors

Celecoxib, Etoricoxib, Parecoxib.

D. Analgesic-antipyretics with poor

antiinflammatory action

1. Paraaminophenol derivative: Paracetamol (Acetaminophen).

2. Pyrazolone derivatives: Metamizol (Dipyrone), Propiphenazone.

3. Benzoxazocine derivative: Nefopam.

Narcotic Analgesics 

Introduction 

Classification 

1) Morphine Analogues: These compounds are closely related to morphine structure and are even synthesised from it. They may be agonists [e.g., morphine, dimorphine (heroin), and codeine], partial agonists (e.g., nalorphine and levorphan), or antagonists (e.g., naloxone). 

2) Synthetic Derivatives with Structures Unrelated to Morphine 

i) Phenylpiperidine Series: Pethidine and Fentanyl. 

ii) Methad one Series: Methadone and Dextropropoxyphene. 

iii) Benzomorphan Series: Pentazocine and Cyclazocine. 

iv) Semisynthetic Thebaine Derivatives: Etorphine and Buprenorphine. 

Anti-Rheumatic Remedies 

Introduction NSAIDS

1) Disease Modifying Anti-Rheumatic Drugs (DMARD) Biologic DMARDS

a) Nonbiological drugs:

i) Immuno suppressants:

Methotrexate, Azathioprine , Cyclosporine 

ii) Other immuno modulators:

Sulfasalazine, Hydroxychloro quine/chloroquine, Leflunomide, Tofacitinib

b) Biological agents:

i) TNF α-inhibitors:

Etanercept, Infliximab, Adalimumab

ii) Other biologicals:

Anakinra,Abatacept,Rituximab

 2) Adjuvant drugs:

Prednisolone and other glucocorticoids

Anti-Gout Remedies 

Introduction 

Classification

Anti-gout drugs can be classified as follows: 

1) Based on Mechanism of Action 

i) Inhibit Uric Acid Synthesis: Allopurinol. 

ii) Increase Uric Acid Excretion: Probenecid and Sulphinpyrazone. 

iii) Inhibit Neutrophil Migration into Joint: Colchicine. 

iv) Inhibit Inflammation and Pain: NSAIDS. 

2) Based on Clinical Use 

i) Drugs Used in Acute Gout: Colchicine, NSAIDS, and Prednisolone. 

ii) Drugs Used in Chronic Gout: Allopurinol, Probenecid, and Sulphinpyrazone.

 

Chapter 5: Drugs Acting on Central Nervous System-II 

Sedatives and Hypnotics 

Introduction 

Classification 

1) Urea Derivatives 

i) Diureides: Barbiturates. 

a) Long Acting Barbiturates: Phenobarbitone and Mephobarbitone. 

b) Short Acting Barbiturates: Butobarbitone, Secobarbitone, and Pentobarbitone.

c) Ultra Short Acting: Thiopentone and Hexobarbitone. 

 ii) Related Ureides: Glutethimide. 

2) Benzodiazepines

i) Hypnotics: Diazepam, Clonazepam, Flurazepam, and Nitrazepam. 

ii) Antianxiety Drugs: Chlordiazepoxide, and Lorazepam.  Diazepam, 

iii) Anticonvulsants: Diazepam, Clonazepam, and Oxazepam 

3) Newer Non-Benzodiazepines Hypnotics: Zopiclone and Zolpidem. 

4) Miscellaneous: Chloral hydrates, Triclofos, and Paraldehyde.

 Psychopharmacological Agents

 Introduction 

Classification 

Psychopharmacological agents are classified based on their clinical use and behavioural changes they induce: 

1) Anti-Anxiety Agents (Anxiolytics): These drugs diminish pathological anxiety, tension, apprehension, and agitation without affecting other behaviours. 

2) Antipsychotic Agents (Neuroleptics): These drugs are used for treating schizophrenia and other forms of psychoses.  

3) Antidepressants: These drugs are used  in endogenous depression. These sanup 

4) Antimanic Agents: These drugs are used for  prophylaxis in bipolar depressions and for manic phase of the disease.  

5) Hallucinogens (Psychotomimetics and Psychodysleptics): These drugs induce schizoid symptoms including hallucinations.

Anticonvulsants 

Introduction 

Classification

1) Hydantoin Derivatives: Phenytoin, Methatoin, and Ethotoin. 

2) Barbiturate & Deoxybarbiturate: 

Phenobarbitone, and Primidone. 

3) Succinimides: Ethosuximide and Methsuximide. 

4) GABA Transaminase Inhibitors: Sodium valproate and Vigabatrin 

5) Iminostilbenes: Carbamazepine and Oxcarbazepine. 

6) GABA Agonist: Gabapentin Clonazepam, Lorazepam, 

7) Benzodiazepines: Clobazam, and Diazepam. 

8) Phenyltriazine: Lamotrigine.

 

Analeptics 

Introduction 

Respiratory stimulant, CNS stimulant

Classification 

Analeptics are classified as follows: 

1) Based on their Prior Influence on the Definite Domain of the CNS

i) Drugs that Influence the Brain Cortex: 

Coffeinum-natrii benzoas. 

ii) Drugs that Influence the Medulla Oblongata: 

Cordiaminum, Aethimizolum, Camphora, Sulfocamphocainum. 

iii) Drugs that Influence the Medulla Spinalis: 

Strychnine nitrate

2) Based on Their Type of Action

i) Analeptics of Direct Action: Coffeinum-natrii benzoas, Aethimizolum.

ii) Analeptics of Reflexive Action: hydrochloridum, Cytitonum. Lobelini 

iii) Analeptics of Mixed Action: Cordiaminum, Corbogenun, Sulfocamphocainum, Camphora.

Centrally Acting Muscle Relaxants

 Introduction 

Classification 

The centrally acting muscle relaxants may be grouped as: 

1) Barbiturates: Phenobarbitone. or Glycerol Ethers: Carisoprodol, 

2) Mephenesin Congeners Mephenesin, Methocarbamol, Chormezanone, and Chlorzoxazone. 

3) Benzodiazepines: Diazepam. Meprobamate, 

4) GABA Derivative: Baclofen.

Anti-Parkinsorism Agents 

Introduction 

Classification 

I. Drugs affecting brain dopaminergics ystem

(a) Dopamine precursor : Levodopa (l-dopa)

(b) Peripheral decarboxylase inhibitors :

Carbidopa, Benserazide.

(c) Dopaminergic agonists: Bromocriptine,

Ropinirole, Pramipexole

(d) MAO-B inhibitor: Selegiline, Rasagiline

(e) COMT inhibitors: Entacapone, Tolcapone

(f) Glutamate (NMDA receptor) antagonist (Dopamine facilitator): Amantadine.

II. Drugs affecting brain cholinergic system

(a) Central anticholinergics: Trihexyphenidyl (Benzhexol), Procyclidine, Biperiden.

(b) Antihistaminics : Orphenadrine,

Promethazine

Local Anaesthetics 

Introduction 

Classification

1) Injectable anaesthetic

i) Low potency, short duration

Procaine,Chloroprocaine

ii) Intermediate potency and duration

Lidocaine (Lignocaine), 

Prilocaine

iii) High potency, long duration

Tetracaine (Amethocaine), 

Bupivacaine, Ropivacaine, 

Dibucaine (Cinchocaine)

2) Surface anaesthetic

i) Soluble 

Benoxinate, Cocaine, Lidocaine, Tetracaine

ii) Insoluble

 Benzocaine

 Butylaminobenzoate (Butamben)

 Oxethazaine

 Exercise

 Chapter 6: Drugs Acting on Autonomic Nervous System-I 

Drugs Acting on Autonomic Nervous System 

Introduction 

Cholinergic Transmission 

Cholinergic Receptors 

Cholinergic Drugs 

Introduction

Actions of cholinergic drugs (or parasympathomimetic drugs) are similar to that of acetylcholine. They exert their actions by directly binding to the cholinergic receptors (cholinergic agonists) or by increasing the availability of acetylcholine at these sites by indirect acting agents.

 Classification 

Cholinergic drugs can be classified into: 

1) Direct Acting Agents (Cholinergic Agonists): These drugs produce actions similar to ACh by directly interacting with cholinergic receptors: 

i) Choline Esters: Acetylcholine, Methacholine, Carbachol, and Bethanechol. 

ii) Cholinergic Alkaloids: Muscarine, Pilocarpine, Arecholine, and Oxotremorine.

2) Indirect Acting Agents (Anticholinesterase): These drugs produce actions similar to ACh by increasing the availability of ACh at the sites: 

i) Reversible 

a) Carbamates 

Tertiary Amines: These can blood brain barrier. For example, Physostigmine. 

Quaternary Amines: These cannot cross blood brain barrier. For example, Distigmine, Pyridostigmine. cross Neostigmine, and 

b) Acridine: Tacrine. 

ii) Irreversible 

a) Organophosphorus Compounds: Disopropyl Parathion, Tabun, Soman, Echothiophate, and TEPP. fluorophosphate,  Sarin, 

b) Carbamates: They are used as insecticides. 

For example, Carbaryl and Propoxur.

Anticholinergic Drugs 

Introduction

 Classification 

Anticholinergic drugs are classified into two classes: 

1) Anti-Muscarinic Agents: These act by inhibiting the actions of ACh by blocking the acetylcholine receptors. muscarinic 

2) Anti-Nicotinic, Agents: These act by inhibiting the actions of ACh at nicotinic acetylcholine receptors. 

i) Ganglionic Blockers (NN Blockers): These interfere with nicotinic ACh receptors and block impulse transmission at the sympathetic ganglia. 

ii) Neuromuscular Blockers (NM Blockers): These block the transmission of ACh at the motor end plate.


anti-muscarinic

The anticholinergic drugs that block the action of ACh on muscarinic receptors are called as anti-muscarinic agents, muscarinic receptor antagonist, or atropinic Anti-Muscarinic Agents agents.

 Anti-muscarinic agents can be classified as follows: 

1) Natural Scopolamine (hyoscine) 

2) Semi-Synthetic Agents

Ipratropium, Homatropine, Propantheline, Tiotropium bromide, and Hyoscine butyl bromide. Classification Occurring Agents: Atropine pue 

3) Synthetic Agents

Pirenzepine, Isopropamide, Oxyphenonium, Dicyclomine, Trihexyphenidyl, and Tropicamide

Ganglionic blockers

Classification

1) Quarternary Ammonium Compounds:

Hexamethonium and Pentolinium.

2) Secondary or Tertiary Amines: Mecamylamine and Pempidine.

3) Monosulphonium Compounds: Trimethaphan camsilate.

4) Persistent Depolarising Blockers: Nicotine (large dose) and Anticholinesterases (large dose)

 Chapter 7: Drugs Acting on Autonomic Nervous System-II

 Introduction 

Adrenergic Transmission Adrenergic Receptors  

Adrenergic System 

Adrenergic Drugs

Introduction

Adrenergic agonists Or sympathomimetic agents

Classification 

1) Direct-Acting Sympathomimetic Agents: They stimulate the adrenergic receptors directly, e-g., Epinephrine or Norepinephrine. 

2) Indirect-Acting Sympathomimetic Agents

They act by stimulating the release of nor-epinephrine from the terminal nerve endings, e.g., Amphetamine. 

3) Mixed-Acting Sympathomimetic Agents

They act both directly (stimulating adrenergic receptor sites) and indirectly (stimulating release of nor-epinephrine from the terminal nerve endings), e.g., Ephedrine.

Adrenergic Receptor Blockers Introduction 

Antiadrenergic agent or Adrenoceptor antagonist

A) Classification of α-adrenoceptor blockers

 1) Non-Selective: Phenoxybenzamine, Ergotamine, Dihydroergotamine, Tolazoline, Phentolamine, and Chlorpromazine.

2) α1-Selective: Prazosin, Terazosin, Doxazosin, and Tamsulosin.

3) α2-Selective: Yohimbine.

B) Classification of β-adrenoceptor blockers

 1) Cardioselective β1 Blockers:

Metoprolol, Acebutolol, Esmolol, Atenolol, and Binoprolol. Amongst them, Acebutolol also exerts an intrinsic sympathomimetic activity.


2) Non-Selective β1, and β2 Blockers

i) Selective β-Blockers: Timolol and Nadolol.

ii) β-Blockers Membrane Stabilising Activity: Propranolol

iii) B-Blockers with Membrane Stabilising and Intrinsic Sympathomimetic Activity:

Oxprenolol and Pindolol. 

iv) Miscellaneous: Sotalol.

3) Selective B2 Blockers: Butoxamine and ICI 118551. 

4) α+β-Blockers: Labetalol, Carvedilol and Celiprolol.

Neuron Blockers 

Introduction 

Example

Guanethidine ,Reserpine

 Neuromuscular Blockers 

Introduction

 Classification 

The classification of muscle relaxants is based on their mode of action, duration of action, and site of action, which is as follows: 

1) Drugs Acting Peripherally at the Neuromuscular Junction

These drugs are further categorised in the following sub-classes: Competitive Blockers or Non-Depolarising Blockers: They may be: 

a) Long ,  Acting (60-120 Minutes):Doxacurium Pancuronium, Pipecuronium and Vecuronium.

b) Intermediate Acting (20-50 Minutes): Atracurium and Rocuronium. 

c) Short Acting (10-20 Minutes): Mivacurium.

ii) Depolarising Blockers: Succinyl choline. 

iii) Inhibition Botulinus toxins type A and B-Bungarotoxin. of Release of Acetylcholine: 

2) Drugs Acting Centrally: Diazepam, Baclofen, and Mephenesin. 

3) Drugs Acting Directly on Muscle: Dantrolene.

Myasthenia Gravis 

Myasthenia Gravis cause by a breakdown in communication between nerves & muscles

Drugs Used

Following drugs are used in the treatment of Myasthenia Gravis: 

1) Modulation of Neuromuscular Transmission

The Neuromuscular transmission is modulated by administration of anticholinesterases (cholinesterase inhibitors) such as pyridostigmine bromide (Mestinon) and neostigmine bromide (Prostigmin). 

2) Immunomodulation: Modulation of the immune system is brought about by: 

i) Plasma Exchange: 

It helps to remove abnormal antibodies.


ii) Intravenous Immune Globulin (IVIG): 

It brings about down-regulation of antibodies directed against AChR. 

iii) Immunoabsorption: This procedure helps to remove anti-AChR ABs.

iv) Immunosuppression: Corticosteroids (e.g., prednisone) and other immunosuppressant like azathioprine, cyclosporin, mycophenolate mofetil, and tacrolimus can be used to suppress the immune system thus suppressing the production of abnormal antibodies.


Drugs like aminoglycoside antibiotics, d-tubocurarine (d- TC) and other neuromuscular blockers, B-blockers, ether, phenytoin, etc., should not be used as they aggravate myasthenia and are hence contraindicated.

Drugs Acting on Eye - Mydriatics

 Introduction

 1) Tropicamide, 2) Phenylephrine


 Glaucoma 

Introduction 

Drugs Used

Acute Congestive (Narrow-Angle) Glaucoma 

Osmotic Agents 

1) Mannitol (20%) i.v. 2) Glycerol (50%) oral 

Carbonic Anhydrase Inhibitors Acetazolamide, i.v., oral 

β-Blockers Timolol (0.5%), topical 

Miotics Pilocarpine (2%), topical

 Prostaglandins Latanoprost (0.005%), topical

Chronic Simple (Wide-Angle) Glaucoma β-Blockers

 1) Timolol (0.25%) 2) Betaxolol (0.25%) 3) Carteolol (1%), topical

 Prostaglandins Latanoprost (0.005%), topical 

Carbonic Anhydrase Inhibitors

1) Dorzolamide (2%), topical 

2) Brinzolamide, topical 

3) Acetazolamide, oral 

α-Adrenergic Agonists 

1) Dipivefrine (0.1%), topical 

2) Apraclonidine (1%), topical 

Miotics 

Pilocarpine (0.5%), topical

 Exercise 

Chapter 8: Drugs Acting on Respiratory System  

Introduction

1) Respiratory Stimulants 

Doxapram

Prethcamide

Naloxone (Narcan)

Yohimbine

Strychnine, Picrotoxin, and Pentylenetetrazol (PTZ)

2) Expectorants (Mucokinetics)

(a) Bronchial secretion enhancers: Sodium or Potassium citrate, Potassium iodide, Guaiphenesin (Glyceryl guaiacolate), balsum of Tolu, Vasaka, Ammonium chloride.

(b) Mucolytics: Bromhexine, Ambroxol, Acetyl cysteine, Carbocisteine

3. Antitussives (Cough centre suppressants)

(a) Opioids: Codeine, Ethylmorphine,

Pholcodeine.

(b) Nonopioids

Noscapine, Dextromethorphan, Chlophedianol.

(c) Antihistamines: Chlorpheniramine, Diphenhydramine, Promethazine.

(d) Peripherally acting: Prenoxdiazine.

4. Adjuvant antitussives Bronchodilators: Salbutamol, Terbutalin.

4) Bronchodilators

1) Sympathomimetic Agents (B2 Agonists)

i) Short Acting: Salbutamol and Terbutaline. 

ii) Longer Acting: Formoterol, Pirbuterol, and Ibuterol. Salmeterol, Fenoterol, 

2) Xanthine Derivatives: Theophylline and Aminophylline. 

3) Anti-Cholinergic Agents: Ipratropium bromide and Atropine.  

5) Nasal Decongestants 

1) Nasal Preparations: Ephedrine hydrochloride 0.5%, Phenylephrine 1-2%, Xylometazoline 0.05%-0.1%," Oxymetazoline 0.025%, Naphazoline 0.05%-0.1%. 

2) Oral Preparations: Phenyl propanolamine 25, 50mg tablets, Pseudoephedrine 30mg tablet or 30mg/5ml syrup.

Chapter 9: Autocoids

 Autocoids 

Introduction 

Classification 

Histamine 

Introduction 

Along with histamine, betazole (histalog) and impromidine act as histamine agonists: 

1) Betazole: The activity of betazole is ten times greater at H2-receptors than at H₁-receptors.

2) Impromidine: Impromidine is an agent used for investigations with about 10,000 H₂ to H, activity ratio.

3) Methimepip: Methimepip is a histamine agonist acting specifically against H3 receptors.

Antihistamines (Histamine Antagonists)

Histamine antagonists are the drugs or agents that antagonise the action of histamine. Following are the three types of histamine receptor antagonists:

 1) H₁-Antagonists: These are classical antihistamines blocking the physiological effects of histamine and used in allergic disorders.

H1-antagonists can be classified as 

A) First Generation H₁-Antagonists: They cross blood-brain barrier readily and produce drowsiness.


i) Ethanolamines (e.g., Diphenhydramine hydrochloride, dimenhydrinate).

ii) Ethylenediamines (e.g., Pyrilamine maleate,tripelennamine hydrochloride).

iii) Alkylamines (e.g., Chlorpheniramine maleate,

brompheniramine maleate).

iv) Piperazines (e.g., Cyclizine hydrochloride, meclizine hydrochloride).

v) Piperidines 

(e.g.,Cyproheptadine hydrochloride).

vi) Phenothiazines (e.g., Promethazine hydrochloride). 

vii) Tricylic Dibenzoxepins (e.g., Doxepin hydrochloride).

A) Second Generation H₁-Antagonists: They do not cross blood-brain barrier readily thus produce less drowsiness.

i) Alkylamines (e.g., Acrivastine).


ii) Piperazines (e.g., Cetirizine hydrochloride).

iii) Phthalazinones (e.g., Azelastine hydrochloride).

iv) Piperidines (e.g., Terfenadine, astemizole, loratadine, fexofenadine).

2) H2-Antagonists: Cimetidine, Ranitidine and Famotidine are H₂-antagonists reducing gastric HCI secretion and used in peptic ulcer diseases.

3) H3-Antagonists: Thioperamide an H-antagonist regulates histamine release from histaminergic neurons of CNS by presynaptic auto-regulatory mechanism. It is not recommended to be used therapeutically.

Serotonin

 Introduction 

Physiological Role

 Prostaglandins 

Introduction 

Pharmacological Actions

Chapter 10: Cardiovascular Drugs

 Introduction Cardiotonics 

Antiarrhythmic Agents 

Introduction 

Classification

Class  Basic Mechanism

I Sodium Channel Blocker 

Reduce phase 0 slope and peak of action potential.

IA Moderate

Moderate reduction in phase 0 slope: increase APD; increase ERP

Quinidine, Procainamide

IB Weak 

Small reduction in phase 0 slope: reduce APD; decrease ERP.

Lidocaine, Phenytoin

IC Strong 

Pronounced reduction in phase 0 slope: no effect on APD orERP

Flecainide, Propafenone

II Beta-Blocker:-

Block sympathetic activity; reduce rate and conduction.

 Propranolol, Metoprolol

III Potassium- Channel Blocker:-

Delay re-polarisation (phase 3) and thereby increase action potential duration and effective refractory period.

 Amiodaron, Bretylium 

IV Calcium-Channel Blocker:-

Block L-type calcium-channels; most effective at SA and AV nodes; reduce rate and conduction.

Verapamil, Diltiazem, Nifedipine

Antianginal Agents 

Introduction

Classification 

1) Vasodilator Drugs 

i) Organic Nitrites and Nitrates: a) Amyl nitrite, b) Isosorbide dinitrate, c) Isosorbide mononitrate, and d) Nitro-glycerine. 

i) Calcium Channel Blockers: a) Amlodipine, b) Nifedipine, c) Diltiazem, and d) Verapamil. 

ii) Potassium Channel Opener: Nicorandil.

2) β-Adrenoceptor Antagonists (β-Blockers) i) Atenolol, ii) Metoprolol, iii) Nadolol, and iv) Propranolol. 

3) Metabolic Modifiers i) Ranolazine, and ii) Ranolazine

Antihypertensive Agents 

Introduction 

Classification

1) Diuretics 

i) Thiazides: Hydrochlorothiazide, Chlorthalidone, and Indapamide. 

ii) Loop Diuretics: Furosemide, Bumetanide, and Torsemide. 

iii) K* Sparing Diuretics: Amiloride, and Triamterene Spironolactone,. 

2) Angiotensin Converting Enzyme Inhibitors: Captopril, Enalapril, Lisinopril, Ramipril, Perindopril, Fosinopril, Trandolapril, Quinapril, and Benazepril. 

3) Angiotensin II Receptor Antagonists: 

Telmisartan ,Losartan, Candesartan, Valsartan, Eprosartan, and Irbesartan.  

4) Ganglion Blockers: Trimethaphan. 

5) Adrenergic Drugs 

i) Centrally Acting Drugs:

Methyldopa, Guanabenz, and Guanfacine, Clonidine, 

ii) Adrenergic Neuron Blockers: Guanithidine and Reserpine. 

iii) Sympatholytics (Adrenergic Receptor Blockers) : 

a) α Blockers

Prazosin, Terazosin, Doxazosin, Phenoxybenzamine, and Phentolamine.

 b) β Blockers: Propranolol, Atenolol, Esmolol, and Metoprolol. 

c) α & β Blockers: Labetalol, Carvedilol. 

6) Ca++ Channel Blockers: Verapamil, Nifedipine, Nicardipine, Nimodipine, Amlodipine, and Felodipine. 

7) Vasodilators 

i) Arteriolar Dilators: Hydralazine, Minoxidil, and Diazoxide. 

ii) Arteriolar and Venular Dilators: Sodium nitroprusside.

Peripheral Vasodilators 

Introduction 

Mechanism of Action 

Drugs Used in Atherosclerosis

Introduction 

The build-up of fats, cholesterol and other substances in and on the artery walls.

Classification 

The anti- hyperlipidemic drugs are divided into: 

1) HMG-CoA Reductase Inhibitors (Statins): Lovastatin, Simvastatin, Pravastatin, and Atorvastatin. 

2) Bile Acid Sequestrants (Resins): Cholestyramine and Colestipol. 

3) Fibric Acid Derivatives (Fibrates): Clofibrate, Gemfibrozil, Bezafibrate, and Fenofibrate. 

4) Triglyceride Synthesis and Lipolysis Inhibitors: Nicotinic acid. 

5) Others: Probucol and Omega-3 fatty acids.


 Chapter 11: Drugs Acting on Blood and Blood-Forming Organs

 Drugs Acting on Blood and Blood Forming Organs Introduction Blood Forming Organs 

Haematinics

 Introduction Hematinics are substances that are essential to the proper formation of the components of blood.

 Iron ,Folic Acid ,Vitamin B12 (Cyanocobalamin)

 Coagulants 

Introduction 

Classification 

Vitamin K 

i) K1 (from plants, fat-soluble) Phytonadione(Phytomenadione) (Phylloquinone).  

ii) K3 Menadione(synthetic

a) Fat-soluble  Menadione Acetomenaphthone. 

b) Water-soluble - Menadione sodium bisulfite, Menadione sodium diphosphate.  

 (2) Miscellaneous

i) Fibrinogen (human), 

ii) Antihaemophilic factor, 

iii) Desmopressin, iv) Adrenochrome monosemicarbazone, v) Rutin, Ethamsylate.

Anticoagulants 

Introduction 

Classification

These drugs are used to decrease the coagulability of blood. They can be classified as follow: 

1) Injectable Anticoagulants: Lepirudin, Heparin, Ancrod

2) Oral Anticoagulants 

i) Coumarin Derivatives: Bishydroxy coumarin (dicumarol), Warfarin sodium, Acenocoumarin, Ethylbiscoumacetate. 

ii) Indandione Derivative: Phenindione.

Haemostatics 

Introduction 

Classification

Local Agents (Styptics) :

Astringents, Adrenaline ,Thrombin, Fibrin glue Gelatin, Calcium alginate, Oxidised cellulose, Russell's viper venom

Systemic Agents :

Vitamin ,Fibrinogen ,Antihaemophilic factor, Adrenochrome, Adrenochrome monosemicarbazone, Ethamsylate, Desmopressin ,Tranexamic acid, Epsilon amino-caproic acid

 Blood Substitutes 

Introduction 

Requisites for Blood Substitutes 

Classification of Blood Substitutes 

Plasma Expanders 

Introduction

Classification

1) Human albumin, 2) Dextran, 3) Polyvinylpyrrolidone, 4) Hetastarch, 5) Degraded gelatine polymer.


 Chapter 12: Drugs Affecting Renal Function

 Diuretics 

Introduction 

Classification On the basis of their intensity, diuretics can be categorised 

1) High Efficacy Diuretics (Inhibitors of N+-K+- 2Cl- Co-transport)

i) Sulphamoyl Derivatives:

Bumetanide ,Furosemide

ii) Phenoxyacetic Acid Derivatives:

Ethacrynic acid.

iii) Organomercurials: Mersalyl. 

2) Medium Efficacy Diuretics (Inhibitors of Na*- Cl Symporter

i) Benzothiadiazines (Thiazides): Chlorothiazide, Hydrochlorothiazide, Hydroflumethiazide, Clopamide. Benzthiazide, 

ii) Thiazide like Diuretics (Related Heterocyclics): Chlorthalidone, Xipamide, Indapamide.  Metolazone, 

3) Weak or Adjunctive Diuretics

 i) Carbonic Anhydrase Inhibitors: Acetazolamide. 

ii) Potassium Sparing Diuretics

a) Aldosterone Antagonists: Spironolactone.

 b) Directly Acting Diuretics (Inhibitors of Renal Epithelial Na* Channel): Triamterene, Amiloride.

iii) Osmotic Diuretics: Mannitol, Isosorbide, Glycerol. 

iv) Xanthines: Theophylline.

Antidiuretics 

Introduction 

Classification

1) Antidiuretic Hormone (ADH, Vasopressin), e.g., Desmopressin, Lypressin, Terlipressin. 

2) Thiazide diuretics, e.g., Amiloride. 

3) Miscellaneous, e.g., Indomethacin, Chlorpropamide, Carbamazepine.

Chapter 13: Hermones and Hormone Antagonists 

Hormones and Hormone Antagonists Introduciion

Classification 

1) Pituitary 

i) Anterior Pituitary

 a) Growth Hormone (GH), Prolactin (Prl), 

b) Adrenocorticotropic Hormone (ACTH,Corticotropin), 

c) Thyroid Stimulating Hormone (TSH, Thyrotropin), 

d) Gonadotropins Follicle Stimulating Hormone (FSH) and Luteinizing Hormone (LH).  

ii) Posterior Pituitary 

a) Oxytocin,

b) Antidiuretic Hormone (ADH, Vasopressin). 

2) Thyroid: Thyroxine (T4), Triiodothyronine (T3), Calcitonin. 

3) Parathyroid: Parathormone (PTH). 

4) Pancreas: Insulin, Glucagon.

5) Adrenals 

i) Cortex 

a) Glucocorticoids (hydrocortisone),

b) Mineralocorticoids (aldosterone),

c) Sex steroids (dehydroepiandrosterone).

ii) Medulla: Adrenaline, Noradrenaline 

6) Gonads

i) Androgens (testosterone), ii) Estrogens (estradiol), iii) Progestins (progesterone).

Hormone Antagonists

 Hypoglycaemic Agents 

Introduction 

Classification

A. Enhance Insulin secretion

1. Sulfonylureas (KATP Channel blockers)

First generation: Tolbutamide

Second generation: Glibenclamide (Glyburide),Glipizide, Gliclazide, Glimepiride

2. Meglitinide/phenylalanine analogues

Repaglinide, Nateglinide

3. Glucagon-like peptide-1 (GLP-1) receptor agonists (Injectable drugs)

Exenatide, Liraglutide

4. Dipeptidyl peptidase-4 (DPP-4) inhibitors

Sitagliptin, Vildagliptin, Saxagliptin, Alogliptin,

Linagliptin

B. Overcome Insulin resistance

1. Biguanide (AMPK activator)

Metformin

2. Thiazolidinediones (PPARγ activator)

Pioglitazone

C. Miscellaneous antidiabetic drugs

1. α-Glucosidase inhibitors

Acarbose, Miglitol, Voglibose

2. Amylin analogue

Pramlintide

3. Dopamine-D2 receptor agonist

Bromocriptin

4. Sodium-glucose cotransport-2 (SGLT-2) inhibitor

Dapagliflozin 


Anti-Thyroid Drugs

Introduction

Classification

1. Inhibit hormone synthesis (Antithyroid drugs)

Propylthiouracil, Methimazole, Carbimazole.

2. Inhibit iodide trapping (Ionic inhibitors)

Thiocyanates (–SCN), Perchlorates (–ClO4),

Nitrates (–NO3).

3. Inhibit hormone release

Iodine, Iodides of Na and K, Organic iodide.

4. Destroy thyroid tissue:

Radioactive iodine (131I, 125I, 123I).

Sex Hormones 

Androgens

Androgens are classified in two classes:

 1) Naturally Occurring Androgens 

i) Testosterone, 

ii) Dihydrotestosterone, 

iii) Dehydroepiandrosterone, and 

iv) Androsterone.

2) Synthetic Androgens 

i) Methyl testosterone, 

ii) Fluoxymesterone, 

iii) Testosterone undecanoate, 

iv) Mesterolone.

 Estrogens

Estrogens are classified as given below: 

1) Natural Estrogens 

i) Estradiol (the most common type in women of child bearing age), 

ii) Estrone (the only estrogen body makes after menopause), and 

iii) Estriol (the main estrogen during pregnancy). 

2) Synthetic Estrogens 

i) Steroidal a) Ethinylestradiol, b) Mestranol, and c) Tibolone. 

ii) Nonsteroidal a) Diethylstilbestrol (stilbestrol), b) Hexestrol, and c) Dienestrol.

Progesterone

1) Natural Progestin: Progesterone. 

2) Synthetic Progestins 

i) Progesterone Derivatives 

a) Older Compounds •Medroxyprogesterone androgenic acetate (weak ),

•Megestrol acetate,  

•Dydrogesterone,

• Hydroxyprogesterone caproate (long acting injection). 

b) Newer Compound: Nomegestrol acetate. 

ii) 19-Nortestosterone Derivatives 

(a) Older Compounds 

 Norethindrone (Norethisterone),

Norethynodrel, Ethynodiol diacetate, Lynestrenol (Ethinylestrenol), Allylestrenol, Norgestrel (Gonane), Levonorgestrel.

b) Newer Compounds (Gonanes)

Desogestrel,

Norgestimate,

Gestodene.

Oral Contraceptives 

COMBINED PILLS

1.Norgestrel 0.3mg Ethinylestradiol30 µg 

2. Norgestrel 0.5 mg Ethinylestradiol 50 µg

3. Levonorgestrel 0.25 mg Ethinylestradiol 50 µg

4. Levonorgestrel 0.15 mg Ethinylestradiol 30 µg

5. Levonorgestrel 0.1 mg Ethinylestradiol 20 µg

6. Desogestrel 0.15 mg Ethinylestradiol 30 µg

7. Desogestrel 0.15 mg Ethinylestradiol 20 µg

POSTCOITAL PILL

1. Levonorgestrel 0.25 mg Ethinylestradiol 50 µg 

2. Levonorgestrel 0.75 mg ,1.5 mg

MINI PILLS

1. Norethindrone 0.35 mg

2. Norgestrel 75 µg

Corticosteroids 

Introduction 

Classification

Two types of corticosteroids are given below: 

1) Glucocorticoids: They control carbohydrate, fat and protein metabolism. They are showing anti-inflammatory action by inhibiting the phospholipid release, reducing the eosinophil action and a number of other mechanisms.

a) Short acting Hydrocortisone (Cortisol)

b) Intermediate acting Prednisolone, Methyl prednisolone, Triamcinolone, Deflazacort

c) Long acting Dexamethasone, Betamethasone

2) Mineralocorticoids: They regulate the electrolyte and water levels by stimulating the sodium retention in the kidney.

Example

Desoxycorticosterone acetate (DOCA), Fludrocortisone, Aldosterone


Chapter 14: Drugs Acting On Digestive System 

Drugs Acting on Digestive System

 Introduction 

Carminatives 

 Bitters 

Introduction 

Classification 

Antisecretory Agents 

Antacids 

Drugs Used in Peptic Ulcer 

1. Reduction of gastric acid secretion

(a) H2 antihistamines: Cimetidine,

Ranitidine, Famotidine, Roxatidine

(b) Proton pump inhibitors: Omeprazole, Pantoprazole, Esomeprazole, Lansoprazole, Rabeprazole, Dexrabeprazole

(c) Anticholinergic drugs: Pirenzepine, Propantheline, Oxyphenonium

(d) Prostaglandin analogue: Misoprostol

2. Neutralization of gastric acid (Antacids)

(a) Systemic: Sodium bicarbonate,

Sod. citrate

(b) Non systemic: Magnesium hydroxide,

Mag. trisilicate, Aluminium hydroxide

gel, Magaldrate, Calcium carbonate

3. Ulcer protectives: Sucralfate, Colloidal bismuth subcitrate (CBS)

4. Anti-H. pylori drugs: Amoxicillin,

Clarithromycin, Metronidazole, Tinidazole, Tetracycline

Ulcer Protectives 

Laxatives (Purgatives) 

Introduction 

Classification

1. Bulk forming:

Dietary fibre: Bran, Psyllium (Plantago)

Ispaghula, Methylcellulose

2. Stool softener:

Docusates (DOSS), Liquid paraffin

3. Stimulant purgatives:

(a) Diphenylmethanes

Phenolphthalein, Bisacodyl, Sodium

picosulfate

(b) Anthraquinones (Emodins)

Senna, Cascara sagrada

(c) 5-HT4 agonist

Prucalopride

(d) Fixed oil

Castor oil

4. Osmotic purgatives:

Magnesium salts: sulfate, hydroxide

Sodium salts: sulfate, phosphate

Sod. pot. tartrate

Lactulose

 Antidiarrhoeals

 Introduction 

Classification 

1 ) Anti - Motility Agents : Morphine ,Codeine , Loperamide , and Bismuth subsalicylate . 

2 ) Cannabinoid Receptor Agonists: Tetrahydrocannabinol and Cyclohexylphenols .  

3 ) Adsorbents : Kaolin , Pectin , Chalk , Charcoal , Methyl Cellulose , and Activated attapulgite . 

4 ) Antispasmodic Agents : Dicyclomine , Mebeverine and Propantheline .

Emetics 

Introduction

 Mechanism of Action 

Anti-Emetics 

Introduction 

Classification 

1. Anticholinergics: Hyoscine, Dicyclomine

2. H1 antihistaminics: Promethazine,

Diphenhydramine,

Dimenhydrinate,

Doxylamine,

Meclozine (Meclizine),

Cinnarizine.

3. Neuroleptics(D2 blockers): Chlorpromazine,

 Triflupromazine,

Prochlorperazine,

Haloperidol,

4. Prokinetic drugs: Metoclopramide,

Domperidone, Cisapride, Mosapride, Itopride

5. 5-HT3 antagonists: Ondansetron,

Granisetron,

Palonosetron,

Ramosetron

6. NK1 receptor antagonists: Aprepitant,

 Fosaprepitant

7. Adjuvant antiemetics Dexamethasone,Benzodiazepines,

Dronabinol, Nabilone

 Chapter 15: Chemotherapy of Microbial Diseases - I

  Introduction 

Classification of Antimicrobial Agents 

Classification

1) Based on the Chemical Structure 

i) Antibiotics

a) β-Lactam Antibiotics:

Cephalosporins, Carbapenems , 

Penicillins, Monobactams,

b) Aminoglycosides: Streptomycin, Gentamycin, Framycetin, Neomycin, 

c) Macrolide Antibiotics:

Roxithromycin,

Azithromycin,

Erythromycin, Clarithromycin,

d) Tetracyclines: Doxycycline, Minocycline, Oxytetracycline,etc. 

e) Nitrobenzene Derivatives:

Chloramphenicol, etc. 

f) Polypeptide Antibiotics: Polymyxin-B, Colistin, Bacitracin, Tyrothricin, etc.

g) Polyene Antibiotics: Nystatin. Hamycin, Amphotericin-B, etc. 

h) Miscellaneous Agents:

Rifampicin, Lincomycin, Vancomycin, Fusidic acid, Cycloserine, Viomycin, Griseofulvin, etc. 

ii) Chemotherapeutic Agents Other than Antibiotics 

a) Sulphonamides and Related Agents:

Sulfadiazine, Sulfamethoxazole, Sulfones (Dapsone) Para aminosalicylic acid (PAS),etc. 

b) Diaminopyrimidines: Pyrimethamine.

c) Quinolones and Fluoroquinolones: 

Nalidixic acid, Norfloxacin, Ciprofloxacin,ofloxacin, etc. 

d) Nitrofuran Derivatives: Nitrofurantoin,

Furazolidone, etc. 

e) Nitroimidazoles: Metronidazole, Tinidazole etc.

f) Imidazole Derivatives: Miconazole,

Clotrimazole, Ketoconazole, Fluconazole,etc.

g) Nicotinic Acid Derivatives: Isoniazid, Pyrazinamide, Ethionamide, etc. 

h) Miscellaneous Agents: Ethambutol,

Thiacetazone, Clofazimine, etc.


2) Based on the Mechanism of Action 

i) Inhibit Cell Wall Synthesis: Penicillins, Cephalosporins, Cycloserine, Vancomycin,

Bacitracin.

ii) Cause Leakage from Cell Membranes: Polypeptides Polymyxins, Colistin, Bacitracin. Polyenes-Amphotericin B, Nystatin, Hamycin.

iii) Inhibit Protein Synthesis: Tetracyclines,Chloramphenicol, Erythromycin, Clindamycin, Linezolid. iv) Cause Misreading of m-RNA Code and Affect Permeability: Aminoglycosides - Streptomycin,

Gentamicin, etc. 

v) Inhibit DNA Gyrase: Fluoroquinolones

Ciprofloxacin and others.

vi) Interfere with DNA Function: Rifampin, Metronidazole.

vii) Interfere with DNA Synthesis: Acyclovir, Zidovudine.

viii) Interfere with Intermediary Metabolism: Sulphonamides, Sulphones, PAS, Trimethoprim, Pyrimethamine, Ethambutol.

3) Based on their Range of Action

i) Broad Spectrum Antibiotics: Those effective against Gram +ve, Gram -ve, rickettsia and chlamydia. For example, Tetracycline,

Chloramphenicol etc. 

ii) Relative Broad Spectrum Antibiotics: Those effective against gram +ve and gram-ve bacteria. For example, Ampicillin group, Cephalosporins, Rifamycins, etc.

iii) Narrow Spectrum Antibiotics

a) Those effective only against gram +ve bacteria, e.g., Penicillin, Erythromycin

group, Vancomycin.

b) Those effective only against gram -ve

bacteria, e.g., Streptomycin and other aminoglycoside antibiotics, Colistin, Polymyxin-B.

c) Antifungal Antibiotics: Hamycin, Nystatin, Griseofulvin etc.

d) Anticancer Antibiotics: Actinomycin Bicomycin, Mitomycin, Mithramycin etc.

4) Based on Types of Organisms Against which Primarily Active 

i) Antibacterial: Penicillins, Aminoglycosides, Erythromycin, etc.

ii) Antifungal: Griseofulvin, Amphotericin-B, Ketoconazole, etc.

iii) Antiviral: Acyclovir, Amantadine, Zidovudine,etc.

iv) Antiprotozoal:

Chloroquine, Pyrimethamine,

Metronidazole, Diloxanide, etc. 

v) Anthelmintic: Mebendazole,

Pyrantel, Niclosamide, Diethylcarbamazine, etc.

5) Based on the Type of Action

Table 15.1: Primarily bacteriostatic

Sulphonamides

Erythromycin Ethambutol

Tetracyclines Chloramphenicol

Clindamycin Linezolid

Table 15.2: Primarily Bactericidal

Penicillins

Cephalosporins

Aminoglycosides

Vancomycin Nalidixic Acid

Polypeptides

Rifampin Isoniazid

Ciprofloxacin

Metronidazole Pyrazinamide Cotrimoxazole

6) Based on the Source of Antibiotic i) Fungi: Penicillin, Griseofulvin, Cephalosporin.

ii) Bacteria: Polymyxin B, Tyrothricin. Colistin, Aztreonam, Bacitracin.

iii) Actinomycetes: Aminoglycosides, Macrolides, Tetracyclines, Polyenes, Chloramphenicol.

Sulphonamides

Classification

 1) Short acting (4-8 hours): Sulfadiazine, etc.ction

2) Intermediate acting(8-12 hours):

Sulfamethoxazole, Sulfamoxole, etc

3) Long acting (~7 day) 

Sulfamethopyrazine,

Sulfadoxine,

4) Special Purpose Sulphonamides: Sulfacetamide, Sulfasalazine , Mafenide, Silver sulfadiazine, etc.

Penicillin

Classification

1. Acid-resistant alternative to penicillin G

Phenoxymethyl penicillin (Penicillin V).

2. Penicillinase-resistant penicillins

Methicillin, Cloxacillin, Dicloxacillin.

3. Extended spectrum penicillins

(a) Aminopenicillins: Ampicillin,

Bacampicillin, Amoxicillin.

(b) Carboxypenicillins: Carbenicillin.

(c) Ureidopenicillins: Piperacillin,

Mezlocillin.

β-lactamase inhibitors Clavulanic acid

 Sulbactam, Tazobactam

Cephalosporins 

First generation cephalosporins

Parenteral: Cefazolin 

Oral:Cephalexin, Cefadroxil

Second generation cephalosporins

Parenteral 

Cefuroxime 

Cefoxitin* 

Oral

Cefuroxime axetil ,Cefaclor, 

Cefprozil

Third generation cephalosporins

Parenteral          

Cefotaxime         

Ceftizoxime       

Ceftriaxone       

Ceftazidime       

Cefoperazone     

Oral 

Cefixime 

Cefpodoxime proxetil

Cefdinir

Ceftibuten

Ceftamet pivoxil

Fourth generation cephalosporins

Parenteral

Cefepime

Cefpirome

Fifth generation cephalosporins

Parenteral

Ceftaroline fosamil

Ceftobiprole medocaril

Tetracyclines 

Chloramphenicol

Classification Aminoglycosides Quinolones Macrolides 

Urinary Antiseptics 

Introduction 

Nitrofurantoin, 

Methenamine (Hexamine), 

Phenazopyridine

Chapter 16: Chemotherapy of Microbial Diseases - II 

Anti-Tubercular 

Introduction 

Classification

First line drugs

1. Isoniazid (H) 4. Ethambutol (E)

2. Rifampin (R) 5. Streptomycin (S)

3. Pyrazinamide (Z)

• Second line drugs

• Ethionamide (Eto) Fluoroquinolones

• Prothionamide (Pto) • Ofloxacin (Ofx)

• Cycloserine (Cs) • Levofloxacin (Lvx/Lfx)

• Terizidone (Trd) • Moxifloxacin (Mfx)

• Para-aminosalicylic acid (PAS) • Ciprofloxacin (Cfx)

 Injectable drugs

• Rifabutin • Kanamycin (Km)

• Thiacetazone (Thz) • Amikacin (Am)

• Capreomycin (Cm)

Anti-Fungal 

Agents Introduction

Classification 

1. Antibiotics

A. Polyenes: Amphotericin B (AMB),

Nystatin, Hamycin

B. Echinocandins:Caspofungin, Micafungin,

Anidulafungin

C. Heterocyclic benzofuran: Griseofulvin

2. Antimetabolite: Flucytosine (5-FC)

3. Azoles

A. Imidazoles

Topical: Clotrimazole, Econazole,

Miconazole, Oxiconazole

Systemic: Ketoconazole

B. Triazoles: Fluconazole,

(systemic) Itraconazole,

Voriconazole,

Posaconazole

4. Allylamine: Terbinafine

5. Other topical agents:

Tolnaftate, Undecylenic acid, Benzoic acid,

Quiniodochlor, Ciclopirox olamine, Butenafine,

Sod. thiosulfate.

Individual Drugs 

Anti-Viral 

Drugs Introduction 

Classification 

1. Anti-Herpes virus

Idoxuridine, Trifluridine, Acyclovir,

Valacyclovir, Famciclovir, Ganciclovir,

Valganciclovir, Cidofovir, Foscarnet,

Fomivirsen

2. Anti-Influenza virus

Amantadine, Rimantadine, Oseltamivir,

Zanamivir

3. Anti-Hepatitis virus/Nonselective antiviral drugs

Primarily for hepatitis B: Lamivudine,

Adefovir dipivoxil, Tenofovir

Primarily for hepatitis C: Ribavirin,

Interferon α

4. Anti-Retrovirus

(a) Nucleoside reverse transcriptase inhibitors (NRTIs): Zidovudine (AZT),Didanosine, Stavudine,

Lamivudine, Abacavir, Emtricitabine,

Tenofovir (Nt RTI)

(b) Nonnucleoside reverse transcriptase inhibitors (NNRTIs): Nevirapine, Efavirenz, Delavirdine

(c) Protease inhibitors: Ritonavir,

Atazanavir, Indinavir, Nelfinavir,

Saquinavir, Amprenavir, Lopinavir

(d) Entry (Fusion) inhibitor: Enfuvirtide

(e) CCR5 receptor inhibitor: Maraviroc

(f) Integrase inhibitor: Raltegravir

Anti-Leprotic Drugs 

Introduction 

Classification 

1. Sulfone: Dapsone (DDS)

2. Phenazine derivative: Clofazimine

3. Antitubercular drugs: Rifampin,

Ethionamide

4. Other antibiotics Ofloxacin,

Moxifloxacin,

Minocycline,

Clarithromycin


Chemotherapy of Protozoal Diseases- 

Anti- Malarial 

Drugs Introduction 

Classification

 1. 4-Aminoquinolines Chloroquine (CQ)

Amodiaquine (AQ)

Piperaquine

2. Quinoline-methanol Mefloquine

3. Cinchona alkaloid Quinine, Quinidine

4. Biguanide Proguanil

(Chloroguanide)

5. Diaminopyrimidine Pyrimethamine

6. 8-Aminoquinoline Primaquine

Tafenoquine

7. Sulfonamides Sulfadoxine

and sulfone Sulfamethopyrazine Dapsone

8. Antibiotics Tetracycline

Doxycycline

Clindamycin

9. Sesquiterpine Artesunate

lactones Artemether

Arteether

Arterolane

10. Amino alcohols Halofantrine

Lumefantrine

11. Naphthyridine Pyronaridine

12. Naphthoquinone Atovaquone

* WHO: World Malaria Report, Dec. 2011 

Anthelmintic Drugs 

Introduction 

Classification 

1. ROUNDWORM Mebendazole, Albendazole, Piperazine, Levamisole

Ascaris lumbricoides Pyrantel Ivermectin

2. HOOKWORM

Ancylostoma Pyrantel, Mebendazole, Levamisole

duodenale Albendazole

Necator americanus Mebendazole, Albendazole Pyrantel

3. PIN WORM Pyrantel, Mebendazole, Piperazine

Enterobius (Oxyuris) Albendazole

vermicularis

4. THREAD WORM

Strongyloides stercoralis Ivermectin Albendazole

5. WHIPWORM

Trichuris trichiura Mebendazole Albendazole

6. Trichinella spiralis Albendazole Mebendazole

7. FILARIA Diethyl carbamazine, Albendazole

Wuchereria bancrofti, Ivermectin

Brugia malayi

8. GUINEAWORM Metronidazole Mebendazole

Dracunculus medinensis

9. TAPEWORMS

Taenia saginata Praziquantel, Niclosamide Albendazole

Taenia solium Praziquantel Niclosamide, Albendazole

Hymenolepis nana Praziquantel Niclosamide, Nitazoxanide

Neurocysticercosis Albendazole Praziquantel

10. HYDATID DISEASE

Echinococcus granulosus, Albendazole Mebendazole

E. multilocularis AlbendazoleIndividual Drugs 

Chemotherapy of Cancer 

Introduction 

Classification

A. Cytotoxic drugs

1. Alkylating agents Mechlorethamine

Nitrogen mustards (Mustine HCl)

Cyclophosphamide,

Ifosfamide,

Chlorambucil,

Melphalan

Ethylenimine Thio-TEPA

Alkyl sulfonate Busulfan

Nitrosoureas Carmustine (BCNU),

Lomustine (CCNU)

Triazine Dacarbazine (DTIC),

Temozolomide

Methylhydrazine Procarbazine

2. Platinum Cisplatin,

coordination Carboplatin,

complexes Oxaliplatin

3. Antimetabolites

Folate Methotrexate (Mtx)

antagonist Pemetrexed

Purine 6-Mercaptopurine (6-MP),

antagonist 6-Thioguanine (6-TG),

Azathioprine, Fludarabine

Pyrimidine 5-Fluorouracil (5-FU),

antagonist Capecitabine, Cytarabine

(cytosine arabinoside)

4. Microtubule Vincristine (Oncovin),

damaging Vinblastine, Vinorelbine

agents Paclitaxel, Docetaxel

Estramustine

5. Topoisomerase-2 Etoposide

inhibitors

6. Topoisomerase-1 Topotecan,

inhibitors Irinotecan

7. Antibiotics Actinomycin D

(Dactinomycin),

Doxorubicin,

Daunorubicin

(Rubidomycin),

Epirubicin,

Mitoxantrone,

Bleomycins,

Mitomycin C

8. Miscellaneous Hydroxyurea,

L-Asparaginase,

Tretinoin,

Arsenic trioxide

B. Targeted drugs

1. Tyrosine protein- Imatinib,

kinase inhibitors Nilotinib

2. EGF receptor Gefitinib, Erlotinib

inhibitors Cetuximab

3. Angiogenesis Bevacizumab

inhibitors Sunitinib

4. Proteasome Bortezomib

inhibitor

5. Unarmed Rituximab,

monoclonal Trastuzumab

antibody

C. Hormonal drugs

1. Glucocorticoids Prednisolone and

others

2. Estrogens Fosfestrol,

Ethinylestradiol

3. Selective estrogen Tamoxifen,

receptor modulators Toremifene

4. Selective estrogen Fulvestrant

receptor down

regulators

5. Aromatase Letrozole,

inhibitors Anastrozole,

Exemestane

6. Antiandrogen Flutamide,

Bicalutamide

7. 5-α reductase Finasteride,

inhibitor Dutasteride

8. GnRH analogues Nafarelin, Leuprorelin

Triptorelin

9. Progestins Hydroxyprogesterone

acetate, 

 Exercise

 Chapter 17: Disinfectants and Antiseptics 

Disinfectants and Antiseptics Introduction 

Classification 

1. Phenol derivatives:  Phenol, Cresol,

Hexylresorcinol, Chloroxylenol,

Hexachlorophene.

2. Oxidizing agents:  Pot. permangnate,

Hydrogen peroxide, Benzoyl peroxide.

3. Halogens:  Iodine, Iodophores, Chlorine,

Chlorophores.

4. Biguanide: Chlorhexidine.

5. Quaternary ammonium (Cationic): Cetrimide, Benzalkonium chloride, Dequalinium chloride.

6. Soaps: of Sod. and Pot.

7. Alcohols: Ethanol, Isopropanol.

8. Aldehydes: Formaldehyde, Glutaraldehyde.

9. Acids: Boric acid, Acetic acid.

10. Metallic salts: Silver nitrate, Silver

sulfadiazine, Mild silver protein, Zinc

sulfate, Calamine, Zinc oxide.

11. Dyes:Gentian violet, Acriflavine, Proflavine.

12. Furan derivative: Nitrofurazone

Exercise Solved

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