A. Paracetamol

C. Verapamil

D. Salbutamol

A. Td50

B. Md50

D. Ld50

A. Affinity

B. Purity of Enzyme

C. Physiological role

A. Poorly suited for oral administration

B. High membrane penetrability

D. The effect is more pronounced in venous

A. Decrease action of prothrombin III

C. Known to cause idiopathic thrombocytosis

D. Mixture of sulphated polypeptide

B. cAMP

C. cGMP

D. PGI2

A. Ciprofloxacin

C. Diphenhydramine

D. Carbamezapine

A. Adrenal steroids

B. H1 histamine receptor antagonist

C. Anticholinergic

A. Shock

C. Anaphylaxis

D. Asthma

B. Toxicity effect

C. Drug on Drug effect

D. Side effect

B. White blood cells

C. Serum

D. Haemoglobin

A. Are more common than first order kinetics

B. Show a plot of drug concentration versus time that is linear

D. Decrease in concentration exponentially with time

B. Cerebral blood flow

C. Partial pressure of GA

D. Blood solubility

B. Half life

C. Clearance

D. Rate of administration

A. Atosiban

B. Ritodrine

D. Isoxsuprine

B. Use in head injury patient

C. Use of agonist with mixed agonist-antagonist

D. use in impaired pulmonary function

A. Carcinogens

C. All of the above

D. Allergens

A. Is healthy

C. None of the above

D. With severe systemic disease

A. Nitrous oxide

B. Ethyl Ether

C. Thiopental

A. Barbiturates

C. Metronidazole

D. Tetracycline

B. 24

C. 48

D. 12

B. Very active against sensitive gram positive cocci

C. Destroyed by gastric acid

D. Used for treatment of meningococcal meningitis

A. Phenylbutazone

C. Ibuprofen

D. Aspirin

A. Doxycycline

C. Penicillin

D. Streptomycin

A. Salbutamol

C. Atropine

D. Adrenaline

A. Fentanyl

C. Thiopentone

D. Propofol

A. Misopristol

B. Nedocromil

C. Zileuton

B. Penicillamine

C. DMSA

D. BAL

A. Increasing A-V conduction

B. Increasing cardiac conduction velocity

C. Increasing spontaneous pacemaker activity

A. PDE inhibitor

B. Androgen receptor blocker

C. Alpha blocker

A. Cleaning surgical instruments

B. Dinisfect water in wells

D. Gargling

A. Niclosamide

B. Pyrantel

C. Metronidazole

B. Medulla

C. Cortex

D. Limbic system

B. Aseptic precautions are required

C. Bioavailability is 100%

D. It is useful in emergencies

B. Lignocaine

C. Benzocaine

D. Tetracaine

A. Hydolysis

B. Oxidation

D. Reduction

A. Lignocaine

B. None of the above

D. Procaine

A. Blocks arrhythmia

B. Increases perfusion to heart

C. Slows SA node conductivity

A. Bone

C. Kidney

D. Liver

A. Propanidid

B. Fentany droperodol

C. Theiopentone sodium

B. Crohns disease (treatment)

C. To reduce the number of draining enterocutaneous fistula(s) in patients with fistulizing crohns disease

D. Rheumatoid arthritis (treatment)

A. cholera

C. Amoebiasis

D. Malaria

A. Counter irritant

B. Mummifying agent

C. Anticoagulant

A. Increase excretion of OCPs

B. Obstruction of fallopian tubes

D. Decreased absorption of OCPs

A. Tremors

B. Hypotension

C. Obesity

B. Drug toxicty

C. Drugs Lethal effect

D. Drug potency

A. It is the drug of choice for status epilepticus

C. Carbamazepine is an enzyme inhibitor

D. Can cause megaloblastic anemia

A. Streptomycin

B. Procaine

C. Insulin

A. Proplofol

B. Ether

D. Isoflurane

B. Misoprostal

C. Pantoprazole

D. Ranitidine