A. Tacrolimus

B. Tramadol

C. Levocetrizine

A. Ibuprofen (Motrin)

C. Aceteminophen

D. Ketoroloc

A. Stropine

B. Morphine

C. Propanolol

B. Myocardial infarction

C. Epilepsy

D. Wernickes ecephalo pathy

A. Vecuronium

B. Atracurium

C. Rocuronium

A. Bio-experiment

B. Biodegradable

D. Bio-statement

A. Gelatin foam

C. Trannic acid

D. Adrenaline

A. Diclofenac sodium

C. Ibuprofen

D. Aspirin

A. Fosinopril

C. Quinapril

D. Benzopril

A. Carbamazepine

B. Phenobarbitone

C. Ethosuxamide

A. Ephederine

B. Propranolone

D. Morphine

A. Phenobarbitone

C. Meprobamate

D. Pentobarbitone

A. Local anesthetic property

B. Antibiotic action

C. Local anesthetic and antiseptic action

A. Pharmacological action of the drug

B. Antigen antibody reaction

C. previous exposure to the drug

B. Hunter John

C. Harpes David

D. Harvey william

B. It is the proportion (fraction) of unchanged drug that reaches the systemic circulation

C. Biovailability of an orally administered drug can be calculated by comparing the area under cure (o-a) after oral and intravenous (IV) administration

D. Biovailability can be determined from plasma concentration or urinary excretion data

A. Epinephrine

B. Sodium nitrate

C. Isosorbide dinitrate

A. Phenobarbitone

C. Sodium valporate

D. Ethosuximide

B. Used in asthma

C. Na level decrease

D. Increase quality of life

A. Age < 5 years

B. History of epilepsy

D. Raised intracranial tension

A. Rapid biotransformation

B. Ability to enter and leave brain tissue every rapidly

C. Rapid accumulation in body fat

A. Spinal cord

B. Hypothalamus

C. Corpus callosum

A. Causes pain when injected subcutaneously

B. Causes arteriolar dialation

C. Is released following injury and in certain allergic responses

A. Hydroxyzine

B. Diphenhydramine

C. Promethazine

A. Amphetamine

C. Phenylephrine

D. Nor epinephrine

A. Pyrazamide

B. Rifampicin

C. Isoniazide

A. Procaine

B. Cyclopropane

C. Etomidate

A. They inhibit ALA synthase

C. They induce heme oxygenase

D. They inhibit heme oxygenase

B. Aspirin

C. Sulidec

D. Ketoprofen

A. Atropine

B. Chlorpromazine

D. Adrenalin

A. More breaks down causes more toxicity

B. Mandibular infiltration is more effective than nerve block in mandibular molar teeth

C. Is amide which is metabolized in liver

A. Decreased salivation

B. Decreased sweating

D. Mydriasis

A. 20 to 30% N20

C. 5 to 20% N20

D. 30 to 50% N20

A. Nifedipine

B. Erythromycin

C. Cyclosporin

D. Aspirin

A. Nifedipine

B. a-Methldopa

D. Hydralazine

B. Enflurane

C. Halothane

D. Isoflurane

B. Phenochyromocytoma

C. Secondary shock

D. Migraine

A. IgE

C. IgG

D. IgM

A. Drug dependence

B. Carcinoma forming tendency

C. Intolerance to a drug

A. Lignocaine

C. Procaine

D. Benzacaine

A. Pentazocine

B. ASA

D. Propoxyphene

A. Phenobarbitone

B. Phenytoin sodium

C. Carbamazepine

A. Nifedipine

B. Sodium Nitro prusside

C. Hydrallazine

A. The oldest member of a class of drugs

B. The proto type member of a class of drugs

C. A drug that is stored in body tissues and is then gradually released in the direction

A. Ethylene glycol

B. Tetracycline

C. Ethambutol

A. Readily croses placental barrier

B. Causes pulmonary hypertension of newborn

C. It delay onset of labour

B. Succinylcholine

C. Hydrocortisone

D. All of the above

A. Mg Causes constipation, Al causes diarrhoea

C. Mg act as buffering agent and Al antagonize its action

D. Both increase gastric motility

A. Alveolar exchage

B. Pulmonary ventilation

C. solubility of anaesthetic in tissue

A. Respiratory arrest

B. Excitation

C. Surgical anesthesia