NSAIDS And other CNS Drugs

A. Olanzee
B. Clozae
C. Risperidone
D. Thioridazone

A. Flumazenil
B. Furazolidone
C. Naloxone
D. Naltrexone

A. Bromocriptine
B. Lysergic acid diethylamide (LSD)
C. Ketanserin
D. Methysergide

A. Produce distortion in sleep more than other sedatives
B. More safe than other sedatives when take in larger amounts
C. After metabolism of other drugs in liver
D. All have metabolically active substrates

A. Ach is transmitter at both pre & post synaptic junction
B. It causes dilatation of skeletal muscles
C. Post ganglionic fibres are longer than pre ganglionic fibres
D. Noradrenalin is the neurotransmitter at post ganglionic junction

A. They depress ALA synthase
B. They inhibit ALA synthase
C. They induce heme oxygenase
D. They inhibit heme oxygenase

A. The analgesic and anti-inflammatory effects identical to that of Non-selective NSAID
B. They do not offer the cardio protective effect
C. Safe in patients with renal insufficiency
D. Fewer incidence of gastrointestinal side effect

A. Atracurium
B. Vecuronium
C. Rocuronium
D. Doxacurium

A. Diarrhea
B. Lacrimation
C. Mydriasis
D. Excessive speech

A. Mu receptor antagonist
B. Kappa receptor antagonist
C. Mu receptor partial agnoist
D. Kappa receptor partial agonist