Drugs list Flashcards

1
Q

Acetazolamide

A

Carbonic anhydrase inhibitor

Leads to accumulation of H2CO3 and thus H+ and HCO3-, lowers pH - altitude sickness

Increased excretion of HCO3- and Cl- (CA needed for reabsorption) - weak diuretic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Adenosine

A

Anti-dysrhythmic

Supraventricular tachycardia

Adenosine causes transient heart block in the atrioventricular (AV) node. A1 receptor - inhibits adenylyl cyclase, reducing cAMP - cell hyperpolarization by increasing K+ efflux via inward rectifier K+ channels - subsequently inhibiting Ca2+ current

Class V

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Adrenaline

A

Nonselective agonist of all adrenergic receptors, α1, α2, β1, β2, and β3.

Increases heart rate; contractility; conduction across AV node
Increases respiratory rate; bronchodilation
Stimulates glycogenolysis
Systemic Vasoconstriction and vasodilation
Triggers lipolysis
Muscle contraction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Amiloride

A

Potassium sparing diuretic

Directly blocking the epithelial sodium channel (ENaC) Inhibits sodium reabsorption in the late distal convoluted tubules, connecting tubules, and collecting ducts in the nephron. Promotes the loss of sodium and water from the body, and reduces potassium excretion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Amiodarone

A

Anti-dysrhythmic

VT, AF

Prolongs repolarization phase

Blocker of voltage gated potassium (KCNH2) and voltage gated calcium channels (CACNA2D2).

Amiodarone slows conduction rate and prolongs the refractory period of the SA and AV nodes, ventricles, bundles of His, and the Purkinje fibres without exhibiting any effects on the conduction rate

Class III

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Amphetamines

A

Inhibit reuptake of monoamines
( dopamine, noradrenaline and serotonin)

Stimulates CNS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Aspirin

A

Anti-inflammatory and anti-hypertensive

Suppress the production of prostaglandins and thromboxanes is due to its irreversible inactivation of the cyclooxygenase (COX) enzyme required for prostaglandin sythesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Atenolol

A

Selective beta 1 adrenergic antagonist

Beta blocker reduces heart excitability, arrhythmia, angina, tachycardia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Atropine

A

M2 cholinergic antagonist

Used to treat bradycardia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Propanolol

A

Non-selective beta adrenergic antagonist

Beta blocker reduces heart excitability, arrhythmia, angina, tachycardia

Also blocks beta 2 so should not be given to asthmatic patients

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Bendroflumethiazide

A

Thiazide diuretic

Inhibits NCC (sodium chloride symporter) in distal tubule

More sodium remains in the urine (in the lumen), draws more water to lumen, increasing the volume of urine produced.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Botulinum toxin

A

Toxin cleaves SNARE proteins

Acetylcholine vesicles can’t bind to the intracellular cell membrane, vesicles of neurotransmitter not released.

This stops nerve signaling, leading to paralysis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Digoxin

A

Cardiac glycoside

Inhibition of the Na+/K+ ATPase.

Increase in intracellular sodium levels, resulting in decreased activity of the sodium-calcium exchanger,

Increase in the intracellular calcium concentration that is available to the contractile proteins.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Ouabain

A

Cardiac glycoside

Inhibition of the Na+/K+ ATPase.

Increase in intracellular sodium levels, resulting in decreased activity of the sodium-calcium exchanger,

Increase in the intracellular calcium concentration that is available to the contractile proteins.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Dobutamine

A

Dobutamine is predominantly a β1-adrenergic agonist (sympathomimetic)

Used in heart failure to increase CO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Furosemide

A

Loop diuretic

Inhibits the NKCC2 in the TALH

Reduces Na+ reabsorption, more water in interstitium, increased urine excretion

17
Q

Insulin

A

Widespread actions to promote anabolism and reduces raised plasma glucose

Used in type I diabetes and extreme cases of type II

18
Q

Isoprenaline

A

Beta adrenergic agonist

Can be used to treat bradycardia

19
Q

Lidocaine

A

Blocks VGNC

Influx of sodium is interrupted, an action potential cannot arise and signal conduction is inhibited (i.e in nociceptors)

Local anaesthetic

20
Q

Mannitol

A

Osmotic diuretic

Injected intravenously, and then freely filtered at the kidney, where it raises the osmotic pressure of the urine and draws additional water into it.

Rare use in the treatment of life-threatening cerebral oedema.

21
Q

Neostigmine

A

Acetylcholinesterase inhibitor

More ACh in cleft - enhances cholinergic transmission

22
Q

Omeprazole

A

Inhibits proton pump H+/K+ATPase on parietal cells

Reduce stomach acid, used to treat peptic ulcers

23
Q

Penicillin

A

Antibiotic

Interfere with bacterial cell wall formation and remodelling

24
Q

Ranitidine

A

Histamine (H2-receptor) antagonists

Block the amplifying effect of the mast (ECL) cells on parietal cell stimulation, and so substantially reduce acid secretion

Used to treat peptic ulcers

25
Q

Salbutamol

A

Beta 2 adrenergic agonist

Promotes smooth muscle relaxation of the brochioles

Used to treat asthmatic attacks

26
Q

Spironolactone

A

Potassium sparing diuretic

Aldosterone receptor (mineralocorticoid) antagonist

27
Q

Suxamethonium

A

Depolarising NMJ blocking drug

Generates an action potential, AChE cannot remove the drug so the membrane cannot repolarise.

Maintained depolarisation means that the voltage gated sodium channels are inactivated.

28
Q

Tetrodotoxin

A

Blocks voltage gated Na+ channels

Prevents excitability of neurone

29
Q

Tubocurarine

A

Antagonist for the nicotinic acetylcholine receptor (nAChr)

Blocks the receptor site from ACh.

30
Q

Vercuronium

A

Competes for the nAChr receptors at the motor end plate, thereby exerting its muscle-relaxing properties

31
Q

Verapamil

A

Block voltage-dependent calcium channels.

Class-IV antiarrhythmic agent.

Verapamil is also a Kv voltage gated potassium channel blocker.