General Pharma:
Ø Sources of drugs
Ø Active principles: alkaloids,
glycosides
Ø Difference between fixed and
volatile oils
Ø Drug administration: Oral route ,
Parenteral , IV, IM, Intradermal ,trans
Ø Pharmacokinetics; absorption,
distribution, plasma protein binding
Ø Biotransformation ( all very important):
mixed function oxidase
Ø Enzyme induction & inhibition
all v imp
Ø Excretion
Ø Bio availability
Ø Half life
Ø Mechanism of drug action
Ø Affinity & intrinsic activity
Ø Graded and Quantal dose response
curve and what info they give v imp
Ø Synergism
Ø Antagonism (important)
Ø Tolerance
Ø Anaphylaxis
Ø Cumulation
Ø Pharmacogenetics (important)
Ø Allergy , types & treatment
Ø Hypersensitivity reactions
Ø Adverse drug reactions
Ø Drug dependence (features only)
Ø Definition from bioassay
Ø Drug interactions (very important for MCQ’s)
Mini Katzung:
Ø Definitions
Ø Permeation
Ø 1st and zero order kinetics
Ø Spare receptors
Ø Therapeutic index and window
Ø Signaling mechanisms
Ø Up and down regulation of
receptors
Ø Volume of distribution
Ø Clearance
Ø Maintenance and loading dose
Ø Orphan drug
Lippincott:
Study following topics from Lippincott:
Ø Volume of distribution (very important)
Ø Bio availability
Ø 1st and zero order kinetics
Ø p450 system
Ø Elimination
Ø Clearance
Ø Kinetics of IV infusion
Ø Steady state concentration
Ø Dose-response relationships
Ø Quantal dose relationships
Chemotherapy: (Katzung)
Very important
section and most difficult to retain
Beta lactams (Very important)
Ø Classification
Ø Mechanism of action
Ø Classification cell wall
synthesis inhibitors.
Ø Penicillin’s. MOA and mechanism
of resistance.
Ø Ampicillin. Amoxicillin
Ø Toxicity
Ø Cephalosporin’s
Ø Toxicity
Ø Tazobactam
Ø Vancomycin
Ø Moa of protein synthesis
inhibitors.
Ø Chloramphenicol. (Moa+ Uses+
Toxicity- important)
Ø Tetracyclines.
Ø Antibacterial spectrum
Ø Uses. Toxicity.
Ø Macrolides.
Ø Spectrum.
Ø Erythromycin.
Ø Toxicity.
Ø Clindamycin.
Ø Aminoglycosides v imp
Ø Pharmacokimetics
Ø Sulfonamides. (Mechanism of action +Uses + Toxicity- very
important)
Ø Trimethoprim-sulfamethoxazole aka
cotrimoxazole.
Ø Fluoroquinolones
Ø Antimycobacterial {1st
line drugs}+{2nd line drugs} ( most important)
Ø Isoniazid (Moa+ Toxicity)
Ø Rifampin. (moa+ Toxicity)
Ø Ethambutol. (Moa + Toxicity)
Ø Pyrizinamide. (Moa + Toxicity)
Ø Regimens (very important)
Ø Dapsone
Anti fungal: (important)
Ø Classification
Ø Amphotericin. (Moa+ Use+ Toxicity)
Ø Flucytosine. Moa.
Ø Azoles. (Moa+ Uses+ toxicity).
Ø Griseofulvin.
Ø Terbinafine important
Ø Topical drugs
Anti viral:
Ø Classification imp
Ø Acyclovir
Ø Anti-HIV /antiretroviral (Types +
Names+ Prototypes)
Ø Abacavir
Ø Zidovudine
Ø Amantadine
Ø Drugs used in hepatitis
Ø Interferons (very important)
Miscellaneous:
Ø Metronidazole (moa+ uses +
toxicity-important)
Ø Nalidixic acid
Anti protozoal:
Ø Drugs amebiasis table
Ø Antimalarial (1st line
+ 2nd line + 3rd line+ For resistance+ For travelling all
very imp)
Ø Anthelmintics read only
Ø Albendazole
Ø Mebendazole
Ø
ll Classification Tables are Important.
Ø
(MINI KATZUNG )
·
ANS:
Ø Chapter 6: Cholinergic/Adrenergic
Transmission, Cholinoceptors.
Ø Chapter 7: Tissue and Organ
Effects, Table 7-3
Ø Chapter 8: Pharmacokinetics of
Muscuranic Antagonists, its Effects, Contraindications, Cholinesterase
Regenerators, Trimethaphan
Ø Chapter 9: M.O.A, Effects on CNS,
Eye, Vascular System and Heart, Table 9-1, Clinical Uses in CVS, bronchi and
genitourinary tract.
Ø Chapter 10: Pharmacokinetics, effects,
table 10-2.
·
CVS:
Ø Chapter 11: Table 11-1,
Sympathoplegics, fig 11-1, Angiotensin antagonists and rennin inhibitor, fig
11-3.
Ø Chapter 12: fig12-1, Nitrates,
effects of Calcium channel blocking drugs, table 12-1, newer drugs.
Ø Chapter 13: fig 13-1, 2, Cardiac
effects of cardiac glycosides, digitalis toxicity, phosphodiesterase
inhibitors.
Ø Chapter 14: Torsades de pointes +
table 14-1 + group 3 antiarrhythmics,fig + fig 14-4,6.
·
Diuretics:
Ø Chapter 15: Study Whole chapter.
·
Autacoids:
Ø Chapter 16: table 16-1 +
Histamine receptors and effects + serotonin clinical uses + hyperpyrexic
syndromes + ergots alkaloids
Ø Chapter 18: Prostaglandins:
Synthesis + MOA+ Fig 18-1+ Clinical Uses.
·
Respiratory
System:
Ø Chapter 20: Study whole chapter.
·
GIT:
Ø Chapter 59: PPI, Colloidal
bismuth, Drugs promoting GIT motility, Drugs for IBS, Drugs for IBD, Ant
diarrheal drugs.
·
CNS:
Ø Chapter 21: fig 21-1, table21-1.
Ø Chap 22: Benzodiazepines,
Barbiturates, Pharmacodynamics, Toxicity, Buspirone, Ramelton side effects.
Ø Chapter 23: Acute and chronic
effects of ethanol, tolerance
Ø Chapter 24: phenytoin,
carbamazepine, M.O.A, toxicity, benzodiazepines +
lamotrigine+phenytoin+valproic acid from table 24-1
Ø Chapter 25: Stages of Anesthesia,
fig 25-1, minimum alveolar anesthetic conc., effects of inhaled anesthetics,
ketamine, and etomidate.
Ø Chapter 26: Route of
Administration, M.O.A, fig26-1, toxicity.
Ø Chapter 28: levadopa, MAOI,
amantadine.
Ø Chapter 29:M.O.A, toxicity,
Lithium
Ø Chapter 30: TCAs, SSRIs,
SNRIs.clinical uses, toxicity of TCAs and SSRI, serotonin syndrome.
Ø Chapter 31: M.O.A of morphine,
acute effects, clinical uses, management of acute pulmonary edema, toxicity,
naloxone.
·
BLOOD:
Ø Chapter 33: IRON
Ø Chapter 34: heparin, table34-1,
warfarin, and aspirin.
Ø Chapter 35: drugs treatment strategies,
familial hypertriglyceridemia, and niacin
Ø Chapter 36: aspirin uses, moa,
toxicity, interactions, Acetaminophen toxicity, DMARDs, leflunomide,
allopurinol
·
ENDOCRINE
:
Ø Chapter 37:fig37-1, mecasermine,
prolactin, Endogenous gonadotropin Production.
Ø Chapter 38: synthesis and
transport of thyroid hormones, MOA, fig 38-1, table38-1, effects of TH,
antithyroid drugs-thiamine.
Ø Chapter 39: M.O.A, organ and
tissue effect, fig 39-1, clinical uses, synthesis inhibitors.
Ø Chapter 40: Hormonal contraceptives,
fig 40-1, 2, clomiphene.
Ø Chapter 41: Insulin effects,
preparation, Noninsulin ant diabetic drugs-Insulin secretagogues, alpha-glucoside
inhibitors, exenatide, Type 1&2 Diabetes.
Ø Chapter 42: Bisphosphonates.
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