Tag: pharmacology lecture

  • 100+ Amazing Pharmacology Facts for Pharmacy, Medical and Nursing Students

    Pharmacology is a very important subject for every Medical, Pharmacy, and Nursing student. We have shared more than 100 Pharmacology Facts which will help every student to study and remember Pharmacology in a simple way. These pharmacology facts contains classification, mechanism of action, side effect, drug interaction of various drugs. Read the whole post and it will be so much helpful for everyone.

    100+ Pharmacology Facts for Pharmacy, Medical and Nursing Students

    Introduction

    1. The inhalational route is the route by which the rate of drug delivery can be controlled like i.v. infusion.
    2. Pharmacokinetics is also called ADME study as it deals with Absorption, Distribution, Metabolism, and Excretion of a drug.
    3. Bioavailability is the fraction of administered drug that reaches the systemic circulation in the unchanged form.
    4. Absorption and first-pass metabolism are two important determinants of bioavailability.
    5. AUC signifies the extent of absorption whereas Tmax. tells rate of absorption.
    6. Glucuronidation is the most common phase II metabolic reaction.
    7. The function of phase I reactions is to attach a functional group to the drug molecule whereas phase II reactions serve to attach a conjugate to the drug molecule.
    8. Glomerular filtration does not depend on lipid solubility.
    9. Lithium, KI, and rifampicin are secreted in saliva.
    10. Urine should be alkalinized for acidic drug poisoning whereas acidified for basic drug poisoning.
    11. Half-life is a secondary pharmacokinetic parameter derived from two primary parameters; Vd and CL.
    12. Inotropic receptors include GABAA, NM, NN, NMDA (receptors of glutamate), and 5-HT3 receptors.
    13. Insulin, growth hormone, prolactin, and cytokines act via enzymatic receptors.
    14. Drugs having steep DRC have a narrow therapeutic index (like barbiturates) than those having less steep curves (e.g.benzodiazepines).
    15. In phase 1 clinical trials, The drug is tested in healthy human volunteers and we cannot determine efficacy in this phase.
    16. Recently, Phase O trial has also been added and is known as microdose studies. This is added to expedite the marketing of the drug.
    17. Pharmacovigilance is the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other possible drug-related problems.
    18. An orphan drug is a pharmaceutical agent that has been developed specifically to treat a rare medical condition (affecting fewer than 200,000 people)

    Autonomic Nervous System

    1. Acetylcholine (ACh) is the principal neurotransmitter at the neuromuscular junction as well as at all preganglionic fibers.
    2. Saxitoxin (obtained from dinoflagellates) is a sodium channel blocker whereas α-bungarotoxin (a component of venom of banded krait) is an irreversible antagonist at NM receptors.
    3. Atropine is an antidote of choice for both organophosphate and carbamate poisoning.
    4. Latanoprost causes the growth of eyelashes as an adverse effect that can be utilized for the treatment of hypotrichosis.
    5. Apraclonidine can cause lid retraction whereas brimonidine is associated with anterior uveitis. Both of these can cause drowsiness.
    6. Tropicamide is the shortest-acting mydriatic.
    7. Onabotulinum toxin A has recently been approved to prevent headaches in adult patients with chronic migraines.
    8. Trospium has minimum CNS penetration among drugs used in overactive bladder.
    9. Solefancin is the longest-acting and oxybutynin is the shortest-acting drug among this group.
    10. The rate-limiting enzyme in catecholamine biosynthesis is tyrosine hydroxylase.
    11. Adrenaline is the drug of choice for anaphylactic shock.
    12. Dopamine is the drug of choice for a cardiogenic shock with oliguric renal failure.
    13. Mirabegron is a new drug approved for overactive bladder. It acts by stimulating b3 receptors.
    14. Ephedrine is the vasopressor of choice in pregnancy.
    15. Tamsulosin and silodosin have been found to cause intraoperative ‘floppy iris syndrome during cataract surgery.
    16. Contra-indications of nonselective β-blockers: A – Asthma, B – Block (AV), C – CHF, D – Diabetes.

    Autacoids

    1. Histamine is synthesized from histidine
    2. Histamine-induced fall in blood pressure is mediated by both H1 (early) as well as H2 (delayed and persistent) receptors.
    3. First-generation antihistamines are contraindicated in persons requiring constant attention.
    4. Tiprolisant is H3 inverse agonist used for Narcolepsy.
    5. Doxepin is a tricyclic antidepressant having the most potent H1 blocking action (800 times more potent than diphenhydramine).
    6. Terfenadine and Astemizole result in polymorphic ventricular tachycardia (Torsades de pointes) manifested as prolongation of QTc interval.
    7. Ergot derivatives can cause dry gangrene of hands and feet and coronary vasospasm.
    8. Sumatriptan is the drug of choice for aborting acute attacks of migraines.
    9. Frovatriptan is the longest acting and rizatriptan is the fastest acting 5HT1B/1D agonist.
    10. Both triptans and ergot alkaloids can cause coronary vasospasm and are contraindicated in ischemic heart disease.
    11. Triptans and ergotamine should not be administered within 24 hours of each other.
    12. Propanolol is the most commonly used drug for the prophylaxis of migraine attacks.
    13. Alprostadil is used to keep ductus arteriosus patent before surgery whereas NSAIDs like aspirin and indomethacin are used for the treatment of Patent ductus arteriosus.
    14. Misoprostol is the most specific drug whereas proton pump inhibitors are drugs of choice for the treatment of peptic ulcers due to chronic NSAID use.
    15. The use of misoprostol in pregnancy is associated with Moebius syndrome.
    16. The most potent agent known to cause an increase in capillary permeability is the platelet-activating factor.
    17. Paracetamol acts by inhibiting COX-3 in the brain
    18. Paracetamol (acetaminophen) has no anti-inflammatory activity and Nimesulide and nefopam do not act by decreasing PG synthesis
    19. Aspirin is the only irreversible inhibitor of the COX enzyme
    20. Aspirin is contraindicated in children (<12 yrs old) due to the increased risk of Reye’s syndrome.
    21. Piroxicam and tenoxicam are longest acting NSAIDs due to enterohepatic cycling.
    22. Rofecoxib and valdecoxib were withdrawn due to increased risk of thrombotic disorders like myocardial infarction.
    23. Hydroxychloroquine is the safest DMARD in pregnancy
    24. Colchicine is more effective and faster acting than NSAIDs

    Cardiovascular System

    1. Spironolactone is the only diuretic that decreases mortality in patients with CHF.
    2. Digoxin and digitoxin are the only inotropic drugs available that can be given orally.
    3. Digitalis is contra-indicated in Wolff-Parkinson-White (WPW) syndrome because it decreases the conduction through the AV node but not through the aberrant pathway.
    4. Digitalis can cause almost any cardiac arrhythmia except Mobitz type II heart block and atrial flutter.
    5. Nesiritide is a recombinant BNP
    6. ACE inhibitors and ARBs are indicated for all grades of CHF unless these are contraindicated.
    7. The combination of hydralazine and isosorbide dinitrate has also been shown to decrease mortality in patients with CHF
    8. The most widely used beta-blocker for CHF is carvedilol followed by metoprolol and bisoprolol.
    9. Moxonidine and rilmenidine are congeners of clonidine with longer half-lives. These drugs are selective for imidazoline receptors.
    10. Mecamylamine is a ganglion blocker used for smoking cessation.
    11. Phentolamine and tolazoline are drugs of choice for hypertensive emergencies in clonidine withdrawal and cheese reaction.
    12. Hydralazine is metabolized by acetylation and thus its effect is genetically determined due to the presence of slow and fast acetylation.
    13. Prolonged administration of sodium nitroprusside can result in accumulation of cyanide leading to toxicity particularly in patients with renal disease.
    14. Clevidipine is an ultrashort acting DHP, recently approved for hypertensive emergencies
    15. Bradykinin is involved in the causation of dry cough and angioedema due to ACE inhibitors.
    16. Verapamil can cause constipation and ankle edema.
    17. Ranolazine has no effect on heart rate and blood pressure
    18. Pentazocine and pethidine should not be used for myocardial infarction since these agents cause tachycardia and can worsen the symptoms.
    19. Lignocaine is the drug of choice for digitals-induced ventricular arrhythmias
    20. Amiodarone is the longest acting whereas adenosine is the shortest acting anti-arrhythmic drug
    21. Vernakalant is a multi-ion channel blocker recommended for converting recent-onset atrial fibrillation to normal sinus rhythm.
    22. Lomitapide acts by inhibiting microsomal triglyceride transfer protein (MTP). This protein is necessary for VLDL assembly and secretion in the liver.

    Kidney

    1. Ethacrynic acid is a highly ototoxic diuretic.
    2. Amiloride is the drug of choice for lithium-induced diabetes insipidus.
    3. Aldosterone antagonists act from the interstitial site of the tubular cell whereas all other diuretics act from the luminal side.
    4. Thiazides are used for the treatment of patients with recurrent Ca++ stones in the kidney.
    5. Furosemide possesses vasodilatory action which is responsible for the quick relief in LVF and pulmonary edema.
    6. Acetazolamide, dorzolamide, and brinzolamide are non-competitive but reversible inhibitors of carbonic anhydrase

    Endocrinology

    1. Nafarelin and buserelin can be administered by nasal route.
    2. Oxidation, organification, and coupling reactions are catalyzed by the thyroid peroxidase enzyme.
    3. Propylthiouracil is the drug of choice for hyperthyroidism in the first trimester of pregnancy and in lactation. For all other patients, methimazole is preferred.
    4. Lispro, Glulisine, and Aspart, all contain the letter ‘s’, which means short-acting.
    5. Insulin degludec is longest acting insulin and unlike insulin glargine, it can be mixed with other insulins too.
    6. Sulfonylureas (except glyburide) and meglitinides (nateglinide and repaglinide) are safe in renal failure.
    7. Metformin is the drug of choice for type 2 diabetes mellitus.
    8. Metformin is the only oral agent that has been demonstrated to reduce macrovascular events in type 2 DM.
    9. Dexamethasone suppression test is used to test the intactness of HPA axis function and diagnosis of Cushing’s syndrome.
    10. Progesterone is added to hormone replacement to decrease the risk of endometrial carcinoma.
    11. Ospemifene is a new SERM indicated for dyspareunia due to menopause

    Central Nervous System

    1. Barbiturates are absolutely contraindicated in acute intermittent porphyria
    2. Tasimelteon is a melatonin receptor agonist (like ramelteon) indicated for the treatment of non24 hour sleep-wake disorder in totally blind.
    3. Tolcapone inhibits COMT in the periphery as well as the brain whereas entacapone acts only in the periphery.
    4. Pramipexole and ropinirole are long-acting and do not cause gangrene. These are now the first-choice drugs for Parkinsonism.
    5. Pramipexole and Ropinirole are used for the treatment of restless leg syndrome
    6. Rotigotine is a dopamine agonist that can be administered through a transdermal patch but was discontinued due to crystal formation on the patches.
    7. Rivastigmine is approved for the treatment of dementia due to Alzheimer’s disease as well as due to Parkinsonism’s.
    8. Penicillamine and trientine can worsen neurological symptoms in Wilson’s disease, therefore are not recommended for initial neurological therapy.
    9. Benzodiazepines (preferably lorazepam) are the drug of choice for status epilepticus.
    10. Eslicarbazepine is a Na+ channel blocker (like carbamazepine) indicated for adjunctive treatment of focal seizures.
    11. Carbamazepine is the drug of choice for partial seizures and trigeminal neuralgia.
    12. Zonisamide and topiramate can cause renal stones.
    13. Clozapine-induced convulsions are dose-dependent adverse effects whereas agranulocytosis is independent of dose.
    14. Prazosin decreases nightmares and improves the quality of sleep in post-traumatic stress disorder.
    15. Mirtazapine is also known as nor-adrenergic and specific serotonergic anti-depressant (NSSA).
    16. Bupropion is used for smoking cessation.
    17. Naltrexone is an opioid antagonist that can be used to reduce alcohol craving.
    18. Fentanyl is responsible for post-operative muscle rigidity whereas succinylcholine causes postoperative muscle pain and fasciculations.
    19. Pethidine is used to reduce shivering after anesthesia

    Anesthesia

    1. Adrenaline is added to LA to make them long-acting whereas sodium bicarbonate makes them fast-acting.
    2. Dantrolene is the drug of choice for the treatment of malignant hyperthermia and is also useful in neurolept malignant syndrome.
    3. Rapacuronium has been withdrawn due to reports of severe bronchoconstriction
    4. Sevoflurane, Trilene, and methoxyflurane should not be used in closed circuit
    5. Enflurane is contra-indicated in epilepsy as it can raise intracranial tension and produce tonic-clonic seizures.
    6. Isoflurane is an inhalational agent of choice for producing controlled hypotension.
    7. Xenon can be considered as an ideal inhalational anesthetic

    Hematology

    1. The antidote to acute iron poisoning is desferrioxamine (i.m.) whereas, for chronic iron overload, deferiprone (oral) is preferred.
    2. Vitamin B12 is absorbed in the terminal ileum whereas iron is absorbed in the duodenum.
    3. Aspirin inhibits thromboxane synthesis but does not inhibit the enzyme thromboxane synthetase
    4. Vitamin K is involved in the activation of various clotting factors (like II, VII, IX, and X) as well as anti-clotting proteins (like protein C and S)
    5. Warfarin may lead to dermal vascular necrosis and hypercoagulation as early appearing (3-10 days after initiation of therapy) adverse effects.
    6. Rivaroxaban and Apixaban are new oral anticoagulants that act by direct inhibition of factor Xa
    7. Reteplase and tenecteplase are known as bolus fibrinolytic

    Respiratory System

    1. Potassium iodide acts directly (by irritating bronchial glands) as well as indirectly (by gastric irritation) to increase bronchial secretions.
    2. The only drugs effective for the treatment of an acute attack of bronchial asthma are bronchodilators
    3. Umeclidinium (anticholinergic) plus vilanterol (Laba) combination is recently approved for maintenance treatment of COPD.
    4. Anticholinergic drugs are bronchodilators of choice in patients of bronchial asthma on β blocker therapy.
    5. Theophylline is a potent vasodilator and can cause hypotension which leads to reflex tachycardia.
    6. Children clear theophylline faster than adults (require high dose) whereas clearance of theophylline is slower in elderly, premature infants, and neonates (require less dose).
    7. Ketotifen has antihistaminic action apart from mast cell stabilizing property.

    Gastrointestinal Tract

    1. The major role of antacids in peptic ulcers is to provide prompt relief from ulcer pain.
    2. Recent studies have suggested an increase in the risk of hip fracture in patients taking PPI in long term.
    3. Antihistamines (H2 blockers) are more effective for reducing basal (nocturnal) acid secretion (histamine-mediated) than stimulated acid secretion (stimulated by gastrin, ACh, as well as histamine).
    4. Sucralfate should not be given with antacids as it polymerizes only in an acidic medium.
    5. A combination of doxylamine (antihistaminic) with pyridoxine (Vit B6) in high dose is the safest antiemetic drug in pregnancy
    6. Domperidone decreases l-dopa induced vomiting without interfering with its efficacy
    7. Atropine is added to lopermide to decrease its addictive potential.

    Chemotherapy

    1. Ampicillin should be avoided in patients with viral illness particularly EBV because it can cause a rash in these patients.
    2. Nafcillin can cause neutropenia
    3. Ceftriaxone and cefoperazone are secreted in the bile.
    4. Cefazolin is the drug of choice for surgical prophylaxis.
    5. Cefotetan, cefmetazole, and cefoxitin are active against anaerobes like Bacteroides fragilis.
    6. Aztreonam is the only beta-lactam antibiotic that can be used in patients having severe allergies to penicillins or cephalosporins.
    7. Cycloserine has potential neurotoxic effects (tremors and seizures). It also causes neuropsychiatric symptoms.
    8. Chloramphenicol may lead to grey baby syndrome and bone marrow suppression.
    9. All tetracyclines are excreted primarily in the urine except doxycycline. Doxycycline is excreted in the feces and thus can be used in the presence of renal failure.
    10. Sulfisoxazole is the most soluble sulfonamide. Thus it has a minimum risk of causing crystalluria
    11. Cotrimoxazole is the drug of choice for pneumocystosis and nocardiosis.
    12. Gatifloxacin has recently been withdrawn from India due to its dysglycemic effects.
    13. Isoniazid is metabolized by ACETYLATION which is genetically controlled. Slow acetylators are predisposed to toxicity, particularly peripheral neuritis.
    14. Rifampicin is secreted in bile, so does not require dose adjustment in renal failure.
    15. Ethambutol and streptomycin are NOT hepatotoxic
    16. Rifaximin is a rifampicin derivative indicated for Traveller’s diarrhea (E.coli) and hepatic encephalopathy.
    17. Dapsone is the drug of choice for the treatment of dermatitis herpetiformis.
    18. Fluconazole is antifungal DOC for prophylaxis whereas voriconazole is DOC for treatment of febrile neutropenia
    19. Acyclovir is the drug of choice for H. Simplex encephalitis
    20. Nelfinavir is the only protease inhibitor for which ritonavir boosting is not recommended.
    21. Prolonged use of high doses of chloroquine can result in blindness due to retinal damage (Bull’s eye maculopathy).
    22. Mefloquine is effective as a single dose treatment of malaria
    23. Artemisinins are the fastest-acting drugs against malaria.
    24. Liposomal amphotericin B is the treatment of choice for visceral leishmaniasis.
    25. Miltefosine and sitamaquine can be administered orally for kala-azar.
    26. Albendazole is the drug of choice for the treatment of all nematode infestations including cutaneous larva migrans (creeping eruption), visceral larva migrans (toxocariasis), and neurocysticercosis except Enterobius (mebendazole), wuchereria and brugia (DEC), onchocerca and Strongyloides (ivermectin), and dracunculus (Metronidazole).
    27. Pertuzumab is a monoclonal antibody against her-2/neu. It is used in combination with trastuzumab (bind to a different region of the her-2 receptor) for metastatic breast carcinoma.
    28. Abiraterone acts by inhibiting 17-a hydroxylase and is indicated in refractory prostate cancer
    29. Lenalidomide is approved for the treatment of mantle cell lymphoma and multiple myeloma

    Conclusion

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  • Antianginal Drugs Free Pharmacology Notes – 2021

    Antianginal drugs are used to treat Angina Pectoris (chest pain) which is a symptom of ischemic heart disease. Due to anigina pectoris heart do no get the required amount of oxygen and nutrients and fails to work to properly. In this Note, we will learn about the Classification, Mechanism of Action, Adverse Effects, Advantages and Drug Interection of antianginal drugs.

    Antianginal Drugs Free Pharmacology Notes - 2021
    Antianginal Drugs Free Pharmacology Notes – 2021

    What is Angina Pectoris ?

    Anginal pectoris disease affect the coronary arteries which supply oxygenated blood from left
    ventricle to heart tissues. In angina pectoris the lumen of artery become restricted and it becomes less efficient in supplying the blood and oxygen to heart called as ischemia.

    The following two types of angina are mainly seen:
    1) Classic Angina (Angina of Exercise): This angina pain occurs w hen the demand of oxygen exceeds the s upply of oxygen, most commonly due to diminished coronary flow.
    2) Vasospastic (Prinzmetal’s or Variant) Angina: This angina pain occurs at rest and is characterised by reversible coronary vasospasm , which in turn reduces the supply of oxygen

    Some individuals however show mixed angina, characterised by both exercise induced and resting attacks of angina.

    Symptoms of Angina Pectoris includes:

    • Weakness
    • Heartburn
    • Cramping
    • Indigestion
    • Sweating
    • Nausea
    • Shortness of breath

    Classification of Antianginal Drugs

    The antianginal drugs are are classified between the following types:

    • Nitrates:
      • Short acting: Glyceryl trinitrate (GTN)
      • Long acting: Isosorbide dinitrate, Isosorbide mononitrate ,Erythrityl tetranitrate, Pentaerythrityl tetranitrate
    • β Blockers: Metoprolol, Atenolol, Bisoprolol, Celiprolol
    • Cytoprotective Drugs: Trimetazidine, Ranolazine.
    • Potassium Channel Opener: Nicorandil, Pinacidil, Cromakalim,Minoxidil, Diazoxide
    • Calcium Channel Blockers:
      • Verapamil, Diltiazem
      • Dihydropyridine —Nifedipine, Amlodipine, Nitrendipine,Nimodipine

    Antianginal Drugs – Nitrates

    Organic nitrites and nitrates are simple nitric and nitrous acid esters of glycerol having different
    volatilities (e.g., isosorbide dinitrate and isosorbide mononitrate are solids at room temperature, nitroglycerine is moderately volatile, and amyl nitrite is highly volatile). These compounds are used in angina pectoris. They rapidly reduce the myocardial oxygen demand, followed by rapid relief of symptoms. They are effective in classic as well as in variant angina pectoris.

    Mechanism of Action

    Nitrates inhibit coronary vasoconstriction or spasm as a result of which perfusion of the myocardium increases, thus, relieving vasospastic angina. Nitrates also cause venodilation, resulting in decreased preload and myocardial oxygen consumption. Due to this action, nitrates are effectively used in classic angina

    Mechanism of Action of Nitrates
    Mechanism of Action of Nitrates

    Therapeutic Uses

    Therapeutic uses of Nitrates are given below:

    • Angina pectoris
    • Acute coronary syndromes
    • Myocardial infarction (MI)
    • CHF and acute LVF
    • Biliary colic
    • Esophageal spasm
    • Cynaide poisoning

    Adverse Effect

    The most common toxic effects of nitrates are the responses evoked by vasodilation.

    • These include tachycardia (from the baroreceptor reflex)
    • Orthostatic hypotension (a direct extension of the venodilator effect), and
    • Throbbing headache from meningeal artery vasodilatation.

    Drug Interection

    Nitrates + Sildenafil can lead to severe hypotension, myocardial infarction and death.

    Antianginal Drugs – Calcium Channel Blockers

    Calcium channel blockers invariably block L-type Ca2+ channel, and decrease heart rate, contracitility and conduction velocity. They also reduce left-ventricular filling pressure, which reduces workload and overall oxygen demand of the heart.

    Mechanism of Action

    Calcium channel blockers act by blocking the voltage -sensitive calcium channels. They act on the inner side of the membrane and bind to the channels in depolarized membrane .
    As a result of drug binding , the channels open rarely after depolarization. A marked decrease in trans membrane Ca2+ion current relaxes the smooth muscles.

    Therapeutic Action

    Calcium channel blockers are used for the treatment of stable as well as variant angina. In variant angina, they cause relaxation of coronary artery spasm , thus increasing the cardiac oxygen supply; while in stable angina, they cause relaxation of peripheral arterioles, resulting in decreased after load and cardiac oxygen demand. Verapamil and Diltiazem moderately reduce oxygen demand by suppressing the heart rate and contractility.

    Adverse Effects

    Calcium channel blockers give rise to cardiovascular adverse effects. Blood pressure reduces due to dilation of peripheral arterioles , resulting in induced reflex tachycardia. This reaction mainly occurs with nifedipine and rarely with verapamil and diltiazem. Due to their suppressant effects on the heart, verapamil and diltiazem should be used carefully in patients taking β-blockers and suffering from bradycardia, heart failure, or AV block.

    Antianginal Drugs – β Blockers

    β blockers are the drugs that block the action of cathecholamines through β receptors. Some β Blockers drugs are Timolol, metoprolol, atenolol, and propranolol.

    Mechanism of Action

    The β-adrenergic antagonists decrease the oxygen demand by reducing the heart rate. They oppose sympathetic stimulation , which increases heart rate, contraction force, and oxygen rate.

    Therapeutic Effect

    The β-adrenergic antagonists in combination with nitrates are used for the treatment of angina pectoris. Persistent angina can be trea ted using drugs from two or more classes, i.e., β adrenergic blockers combined with long -acting nitrates or calcium channel blockers.
    The β-adrenergic antagonists due to their antihypertensive action are ideal for patients having hypertension and coronary artery disease. They are the drugs of choice for the prophylaxis of chronic angina

    Adverse Effects

    The adverse effects of β-adrenergic antagonists are hypotension, bradycardia, insomnia (inability to sleep), bizarre dreams, diminished sex drive, impotence, and depression.

    Antianginal Drugs – Potassium Channel Openers

    The potassium channel openers which were used earlier for the treatment of severe hypertension and hypertensive eme rgencies are minoxidil and diazoxide; but use of these agents has been reduced after synthesis of some novel potassium channel openers, like nicorandil, pinacidil, and cromakalim.

    Mechanism of Action

    • These drug opens the ATP – sensitive K channels
    • Opening of this leads to hyper polarization
    • Followed by closing of calcium channels
    • Less intracellular calcium — muscle relaxation

    Therapeutic Uses

    Potassium channel openers are used in patients who have undergone optimal management with other d rugs, but still remain symptomatic, often while they await surgery or angioplasty.

    Adverse Effects

    Common adverse effects o f potassium channel openers are flushing, palpitation, weakness, headache, mouth ulcers, nausea, and vomiting.

    Newer Antianginal Drugs

    Some new antianginal drugs are discussed below:

    Ranolazine: This drug reduces the number of angina episodes per week and increases exercise tolerance. These benefits were however moderate and smaller in women than in men.

    Trimetazidine: It is an anti -ischemic (anti-anginal) metabolic agent. It improves myocardial glucose utilization by inhibiting fatty acid metabolism.

    Dipyridamole: It is a powerful coronary dilator; increases total coronary flow by preventing uptake and degradation of adenosine.

    Conclusion

    If you also want to submit your notes to help students you can contact us for submitting your notes. To contact us click here. If you find this post ”Antianginal Drugs Free Pharmacology Notes – 2021“ helpful then share it with your friends also.

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  • Scope of Pharmacology with Free PDF Note – 2021

    What is the scope of Pharmacology? Why should we read Pharmacology? Why Pharmacology is an important subject for the medicos? Are you also searching for the answer to these questions? Then you are in right place, here your search for the answers comes to an end. In this post “Scope of Pharmacology,” we are going to discuss the History, Present, and the Future Scopes of Pharmacology Subject.

    You will get the latest details about this course on our website MyPharmaGuide. We at MyPharmaGuide share all kind of latest information related to the Medical world and Pharmacy world. You will get all kind of PDF Books and Notes here. Moreover, we share Question Papers, Articles related to Medical and Pharmacy world.

    Scope of pharmacology
    Scope of pharmacology

    What is the Scope of Pharmacology ?

    The science of Pharmacology has interfaces with Anatomy and Physiology, Organic and Inorganic Chemistry, Microbiology and Pathophysiology. Pharmacology is related to action and uses of drugs. In the development of new drugs, pharmacology has the greatest contribution. It has two main components: pharmacodynamics and pharmacokinetics. Pharmacodynamics deals with what the drug does to the human/animal body. It involves the study of the action of drugs on receptors, its mechanism of action, indications for clinical use, contraindications and adverse reactions caused by drugs. Pharmacokinetics deals with what the body does towards drugs. It has four main components: Absorption, Distribution, Metabolism and Excretion (ADME). Out of these four components, absorption, distribution and excretion are dependent on transport through membranes without any chemical change in the entity. In metabolism, there is a chemical change in the moiety because of the action of enzymes in the body. Cytochrome enzymes in the liver are the main metabolising enzymes in the liver. A drug may have n number of metabolites. Every metabolite can have different activities in the body. Thus, what we observe as action(s) of drugs is the net effect of main drug moiety and its metabolites. Several factors can alter the ADME of drugs. It is the main reason why we get different kinds of actions for the same drug in different individuals.

    Clinical pharmacology and therapeutics primarily deal with the actions of the drug in human beings. It incorporates indications, therapeutic uses, contra-indications, posology, bioavailability, prescription writing and drug nomenclature. The science of clinical toxicology is an extension of clinical pharmacology. Forensic toxicology addresses to medico-legal aspects of the use of drugs. Pharmacovigilance is gaining vital importance in the last few decades. It involves the study of adverse reactions of drugs and their safety. Based on observations on pharmacovigilance, some drugs have been withdrawn from the market due to severe adverse reactions.

    History of Pharmacology

    Here in this part we will discuss about the scientist who contributes in the field of Pharmacology and made this subject more useful.

    • Galen is known as the Father of Pharmacy. His most popular medicinal invention was Theriac.
    • Mahadeva Lal Schroff is known as the Father of Indian Pharmacy because of his contribution to Pharmacy education in India. He introduced a 3-year Pharmacy course at Banaras Hindu University.
    • William Procter is known as the Father of American Pharmacy.
    • Hippocrates is considered the Father of medicine because of his books on Modern Medicine.
    • Oswald Schmiedeberg is known as the Father of Pharmacology. He is the founder of Modern Pharmacology.
    • Sir Ram Nath Chopra is considered the Father of Indian Pharmacology.
    • Sir James Black is known as the Father of Modern Pharmacology. He developed the drug Propranolol.
    • Dr. Frederick Banting and his medical student Charles Best discovered insulin in the year 1921.
    • German biochemist Paul Ehrlich Ehrlich coined the term chemotherapy and Magic Bullet concept.

    Download the full note on Scope of Pharmacology and Introduction of Pharmacology from below.

    Conclusion

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  • Pharmacology PDF Notes For Pharmacy Students Download – 2020

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    Pharmacology PDF Notes For Pharmacy Students Download - 2020
    Pharmacology PDF Notes For Pharmacy Students Download – 2020

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