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Pharmacology and Toxicology is a subject that imposes a great responsibility on the veterinary and medical practitioner in their day to day clinical practice. Conceptualizing the concepts and making them at ease to the budding vets is the need of the hour.
The central dogma of revisiting the concepts lies well with the practices of the objective type questions to help individuals in attaining a great success in their academic and professional pursuit.
This book contains 11 chapters encompassing the multiple-choice questions, true false and fill in the blanks vis a vis matching to consolidate the scientific acumen of the students in brightening their future. The main highlight of this book is the vast coverage of new chapters related to drug discovery, multi drug resistance (MDR) and clinical pharmacology and Veterinary therapeutics.
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Pharmacology and Toxicology is a subject that imposes a great responsibility on the veterinary and medical practitioner in their day to day clinical practice. Conceptualizing the concepts and making them at ease to the budding vets is the need of the hour. The central dogma of revisiting the concepts lies well with the practices of the objective type questions to help individuals in attaining a great success in their academic and professional pursuit. This book will provide a comprehensive detailing of the subject and build their analytical approach to mitigate the academic challenges in the competitive exams viz.
Pharmacology and Toxicology is a subject that imposes a great responsibility on the veterinary and medical practitioner in their day to day clinical practice. Conceptualizing the concepts and making them at ease to the budding vets is the need of the hour. The central dogma of revisiting the concepts lies well with the practices of the objective type questions to help individuals in attaining a great success in their academic and professional pursuit. This book will provide a comprehensive detailing of the subject and build their analytical approach to mitigate the academic challenges in the competitive exams viz.
1 Source and Nature of Drugs and Pharmacokinetics
Amit Shukla, Soumen Choudhury, Atul Prakash
Q1. The exit of drug from C.S.F. irrespective of its entry is by
Passive diffusion
Filtration
Facilitated diffusion
All of the above
Q2. The number of half-lives required to reach 99% of steady state concentration is
3.3
4.4
5.5
6.6
Q3. The receptor concept was first introduced by
J.N. Langley in 1878
Simonis in 1964
Paul Ehrlich in 1926
Walksman in 1826
Q1. The exit of drug from C.S.F. irrespective of its entry is by
Passive diffusion
Filtration
Facilitated diffusion
All of the above
Q2. The number of half-lives required to reach 99% of steady state concentration is
3.3
4.4
5.5
6.6
Q3. The receptor concept was first introduced by
J.N. Langley in 1878
Simonis in 1964
Paul Ehrlich in 1926
Walksman in 1826
2 Mechanism and Problem of Drug Resistance
Amit Shukla, Soumen Choudhury, Atul Prakash
Q1. Resistance in tetracycline is due to mutational changes in
Tet A gene
Kat G
Par C par E
Inh A
Q2. Single step mutation can be seen in
Erythromycin
Tetracycline
Chloramphenicol
Rifampicin
Q3. Multistep mutation is observed in
Streptomycin
Rifampicin
Both A and C
Tetracycline
Q1. Resistance in tetracycline is due to mutational changes in
Tet A gene
Kat G
Par C par E
Inh A
Q2. Single step mutation can be seen in
Erythromycin
Tetracycline
Chloramphenicol
Rifampicin
Q3. Multistep mutation is observed in
Streptomycin
Rifampicin
Both A and C
Tetracycline
3 Chemotherapy
Amit Shukla, Soumen Choudhury, Atul Prakash
Q1. The nitrogen atom of amino group in basic structure of sulfonamide is designated as
N1
N2
N3
N4
Q2. Trimethoprim produces synergistic action by interfering the synthesis of
Dihydrofolic acid from tetrahydrofolic acid
Tetrahydrofolic acid from dihydrofolic acid
mRNA from DNA
tRNA from DNA
Q3. An ophthalmic sulfonamide is
Sulfaguinidine
Sulfadimidine
Sulfadimethoxine
Sodium sulfacetamide
Q1. The nitrogen atom of amino group in basic structure of sulfonamide is designated as
N1
N2
N3
N4
Q2. Trimethoprim produces synergistic action by interfering the synthesis of
Dihydrofolic acid from tetrahydrofolic acid
Tetrahydrofolic acid from dihydrofolic acid
mRNA from DNA
tRNA from DNA
Q3. An ophthalmic sulfonamide is
Sulfaguinidine
Sulfadimidine
Sulfadimethoxine
Sodium sulfacetamide
4 Toxicopathology
Sakshi Tiwari, Amit Shukla
Q1. Glucuronide conjugation occurs in the compounds with following functional groups:
Hydroxyl
Carboxyl
Amino
All above
Q2. Which of the following is not a chelating agent:
Dimercaprol
Penicillamine
Dimethyl sulfoxide
Ca-EDTA
Q3. Most appropriate treatment of acute organophosphate toxicity:
Atropine alone
2-PAM alone
Atropine + 2-PAM
Sod. Thiosulphate alone
Q1. Glucuronide conjugation occurs in the compounds with following functional groups:
Hydroxyl
Carboxyl
Amino
All above
Q2. Which of the following is not a chelating agent:
Dimercaprol
Penicillamine
Dimethyl sulfoxide
Ca-EDTA
Q3. Most appropriate treatment of acute organophosphate toxicity:
Atropine alone
2-PAM alone
Atropine + 2-PAM
Sod. Thiosulphate alone
5 Practice Set-1
Amit Shukla, Soumen Choudhury, Atul Prakash
Q1. Penicillins disrupt the formation of following peptide bond during its antibacterial action on bacteria:
D-alanine-D-aspartate
D-alanine- D-glutamate
D-Glycine-D-alanine
D-alanine-D-alanine
Q2. In E.coli, topoisomerase IV, the target enzyme of the quinolones is encoded by the genes
parC and parE
gyrA and gyrB
par C and gyr A
parE and gyrB
Q3. Streptomycin interferes in protein synthesis by inhibiting the start codon
AUG
AAU
UUA
AGUa
Q1. Penicillins disrupt the formation of following peptide bond during its antibacterial action on bacteria:
D-alanine-D-aspartate
D-alanine- D-glutamate
D-Glycine-D-alanine
D-alanine-D-alanine
Q2. In E.coli, topoisomerase IV, the target enzyme of the quinolones is encoded by the genes
parC and parE
gyrA and gyrB
par C and gyr A
parE and gyrB
Q3. Streptomycin interferes in protein synthesis by inhibiting the start codon
AUG
AAU
UUA
AGUa
6 Practice Set-2
Soumen Choudhury, Amit Shukla, Atul Prakash
Q1. The exit of drug from C.S.F. irrespective of its entry is by:
Passive diffusion
Filtration
Facilitated diffusion
All of the above.
Q2. The number of half-lives required to reach 99% of steady state concentration is:
3.3
4.4
5.5
6.6
Q3. The receptor concept was first introduced by:
J.N. Langely in 1878
Simonis in 1964
Paul Ehrlich in 1926
Wakcsman in 1826
Q1. The exit of drug from C.S.F. irrespective of its entry is by:
Passive diffusion
Filtration
Facilitated diffusion
All of the above.
Q2. The number of half-lives required to reach 99% of steady state concentration is:
3.3
4.4
5.5
6.6
Q3. The receptor concept was first introduced by:
J.N. Langely in 1878
Simonis in 1964
Paul Ehrlich in 1926
Wakcsman in 1826
7 Toxicity of Important Agrochemicals and Their Detoxification..
Atul Prakash, Amit Shukla, Soumen Choudhury, Sakshi Tiwari
Q1. Alpha naphthyl thiourea is less toxic
In an empty stomach
With oily food
Full stomach
Not affected
Q2. A rodenticide that blocks tricarboxylic acid cycle by competitive inhibition of the enzyme aconitase
Fluoroacetamide
Pindone
Chloralose
All the above
Q3. ANTU is less toxic in an empty stomach a) In an empty stomach it will irritate the stomach wall resulting in vomiting and throwing away the poison and hence no toxicity.
Absorb only with fatty materials
Immediate absorption and detoxification
All the above
None of the above
Q2. A rodenticide that blocks tricarboxylic acid cycle by competitive inhibition of the enzyme aconitase
Fluoroacetamide
Pindone
Chloralose
All the above
Q3. ANTU is less toxic in an empty stomach a) In an empty stomach it will irritate the stomach wall resulting in vomiting and throwing away the poison and hence no toxicity.
Absorb only with fatty materials
Immediate absorption and detoxification
All the above
None of the above
8 Drugs Acting on Different Body Systems
Atul Prakash, Amit Shukla, Soumen Choudhury
Q1. Halothane is metabolized in to
Trifluoracetic acid
Inorganic chloride
Bromine
All the above
Q2. Psychomotor stimulants causes
Excitement
Relieve fatigue
Increase motor activity
All the above
Q3. Repeated administration of barbiturate causes
Tolerance
Drug dependence
Toxicity
All the above
9 Practice Set-3
Amit Shukla, Soumen Choudhury, Sakshi Tiwari
PART-A
1. Indicate True/False for the following
Super infection phenomenon is common with antibiotics that are given as depot preparation.______
A combination of penicillin and chlortetracycline leads to antagonism of antimicrobial activity.______
Bactericidal drugs act most effectively on toxins librated by organism.
Most of the laboratory sensitivity tests are conducted at a pH of 4-5.______
Super infection phenomenon is common with antibiotics that are given as depot preparation.______
A combination of penicillin and chlortetracycline leads to antagonism of antimicrobial activity.______
Bactericidal drugs act most effectively on toxins librated by organism.
Most of the laboratory sensitivity tests are conducted at a pH of 4-5.______
10 Veterinary Therapeutics and Drug Discovery
Soumen Choudhury, Amit Shukla, Atul Prakash
Q1. Which of the following is semisynthetic product:
Chlortetracycline
Chloramphenicol
Tetracycline
Oxytetracycline
Q2. Natural source of amphotericin B is:
Streptomyces aureofaciencs
Streptomyces nodosus
Streptomyces erythreus
Streptomyces venezuelse
Q3. Following is /are mitotic inhibitor
Paclitaxel
Griseofulvin
Vinblastine
All of the above
Q1. Which of the following is semisynthetic product:
Chlortetracycline
Chloramphenicol
Tetracycline
Oxytetracycline
Q2. Natural source of amphotericin B is:
Streptomyces aureofaciencs
Streptomyces nodosus
Streptomyces erythreus
Streptomyces venezuelse
Q3. Following is /are mitotic inhibitor
Paclitaxel
Griseofulvin
Vinblastine
All of the above
11 Practice Set-4
Soumen Choudhury, Amit Shukla, Atul Prakash
PART-A
Q1. Elimination of drug is studied under?
Pharmacokinetics
Pharmacometrics
Toxicodynamics
Toxicoelimination
Q2. Serpentine receptor is characterized by
7 Transmembrane loop
Petals of lilly like structure
Zinc fingers
JAK STAT
Q3. Status epilepsy is treated best with lorazepm/diazepam
Per rectal
Intravenous
Intramuscular
Oral