PHARMACOLOGY💊 Flashcards

1
Q

any chemical substance used in the diagnosis, tx & prevention of diseases

A

Drug

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2
Q

Most convenient route of administration

A

Oral PO

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3
Q

Most rapid

A

Inhalation

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4
Q

Emergency , rapid onset

A

IV

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5
Q

Most important site of absorption

A

Small Intestine

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6
Q

Duodenum

A

10 inches

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7
Q

Jejunum

A

8 feet

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8
Q

Ileum

A

12 feet

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9
Q

Gastric emptying

A

4 hrs

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10
Q

Most important factor that governs absorption

A

Lipid Solubility

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11
Q

Henderson Hasselbalch Equation

A

Weak Acids- acidic- non-ionized
Weak Bases- basic - Non- Ionized
Weak Acid- basic - Ionized
Weak Bases -acidic - Ionized

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12
Q

All Local Anesthetics are

A

BASES

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13
Q

Safe BP control for pregnancy

A

Methyldopa

Hydralazine

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14
Q

Zero Order Kinetics Drugs TAPE

A
  1. Theophylline
  2. Aspirin
  3. Phenytoin
  4. Ethanol
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15
Q

Lipid soluble to water soluble

A

Metabolism

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16
Q

reduction & oxidation

A

Phase 1

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17
Q
Conjugation (transferase)
glycine conj.
glucuronidation
acetylation
sultation
A

Phase 2

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18
Q

Major organ for metabolism

A

Liver

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19
Q

Largest family of reductase & oxidases of drug metabolism

A

Cytochrome p450 phase 1

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20
Q

Highest Hepatic 1st Pass

A

Oral Route

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21
Q

Higher Plasma Concentration

A

Faster Elimination = Linear Kinetics

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22
Q

Most drug follw this

A

1st Order Kinetics

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23
Q

Time required to reduce the amount of drug in the body by one half

A

Half- life (t 1/2)

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24
Q

regulatory proteins

A

Receptors

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25
Examples of receptors
Transporters LA (NaK channels) Enzymes
26
drugs that binds to & activates a receptor or stabilizes the receptor in its active state
Agonist
27
drugs that binds to & activates the receptos to the Maximum Extent
Full Agonist
28
drug that binds to activates the receptor to a LESSER EXTENT even when dose is increased
Partial Agonist
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drug that has a higher affinity for the inactive receptor therefore reducing the receptor's constitutive activity - NO physiologic activation will be observed
Inverse Agonist
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route of administration is placed in the space beneath the tongue & upon dissolutionof thd dosage form, becomes absorbed through thr sublingual veins into the systemic circulation
Sublingual Administration - this route bypasses the hepatic circulation
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administered using a suppositorty. This route is ideal for a px who is unconscious or vomiting intractably
Rectal Administration
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Parenteral ainjection bypass the GIT
IV, Subcutaneous, IM, Intradermal & Intrathecal routes
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SYMPA
``` Fight/ Flight Pupil : Mydriasis Heart : ⬆️ HR Bronchioles: Bronchodilation GIT: ⬇️ Urinary Bladder : Detrussor - relax Sphincter- contract Peripheral B. V (nasal mucoas, GI/splanchnic, skin) : Constriction ```
34
PARA
``` Rest / Digest MIOSIS ⬇️HR Bronchoconstriction ⬆️ GIT Detrusor & Sphincter: Contract Peripheral B.V (nasal mucosa, GI/ splanchnic, skin) : Dilation ```
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cranio-sacral , 37910
Parasympathetic
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Thoraco- lumbar
Sympathetic
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(+) inotropy
⬆️ depth of contraction
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(+) chronotropy
⬆️ HR
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⬆️ Dromotropy
Faster conduction velocity
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2 drugs compete w/ each other
Antagonism
41
Pharmacologic antagonism
trip tp jerusalem
42
Chemical Antagonism
A=B
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Physiologic Antagonism
``` A= ⬆️ HR B= ⬇️HR ```
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bawal | calcium , aluminum, magnesium
Tetracycline | Why: Chemical antagonism
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Cholinergic agonist
Chol Pilocarpine STIGMINE
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Cholinergic Agonist
Parasympathetic
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Cholinergic Antagonist
Sympathetic
48
Adrenergic Agonist
Sympathetic
49
ADR Antagonist
Parasympathetic
50
Indications of the Cholinergic Agonists
1. Glaucoma 2. Ileus 3. Dry Mouth 4. M.G 5. Tachycardia
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absent peristalsis
Ileus
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DOC Glaucoma
Pilocarpine Metacholine Carbachol Physostigmine
53
DOC Ileus
Betanochol | Neostigmine
54
Dry mouth
Pilocarpine
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Tachycardia
supraventricular Edrophonium
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Myasthenia Gravis
Pyridostigmine (tx*) | Edrophonium
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Autoimmune Disease skeletal. attach nicotinic receptors Ach in skeletal muscle skeletal muscle weakness
M.G
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Diagnosis of M.G
Edrophonium
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A lot of adverse effects
Pilocarpine
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Indications of Cholinergic Antagonists
1. Opthalmic 2. Respiratory (asthma) 3. GIT / Genitourinary
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Cholinergic Antagonist
TROP
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Ophthalmic
``` Atropine (longest acting) Scopolamine (hyoscine) Homatropine Cyclopentolate Tropicamide (shortest acting) ```
63
CUR, Succinylcholine
Neuromuscular blocker | nicotinic receptors
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Respiratory Asthma
Ipratropium | Tiotropium
65
GIT/Gastrointestinal
Atropine | Scopolamine (hyoscine)
66
binds the nm receptor & promotes depolarization, but the long duration of receptor activation causes the receptor to be desensitized eventually incapable of mediating muscle contraction
Depolarizing Blocker
67
Depolarizing blocker
Succinylcholine (suxamethonium)
68
directly antagonizes the Nm receptor to promote paralysis
Non- depolarizing blockers
69
Adrenergic Agonist
``` Nasal congestion Asthma Cardiogenic shock Anaphylactic shock Hypertension ```
70
Alpha 1 selective agonist
Phenylephine | Phenylpropanolamine
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Non- selective Alpha Agonist
Oxymetazoline
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Cardiogenic shock DOC
Dobutamine
73
Asthma | beta 2- selective agonist (bronchodilation)
Salbutamol - short actiing immediate onset | Formoterol, Salmeterol - long acting
74
Cardiogenic shock beta 1 selective agonist (bronchodilation)
Dobutamine
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Non- selecta beta agonist
NE
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Alpha 2 agonists: Hypertension
* Clonidine | * Methyldopa (for hypertensive pregnant women)
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PHE, PHE , PHE
Non- selective Alpha antagonist Phenoxybenzamine Phentolamine Pheochromocytoma
78
benign Tumor of adrenal gland excessive produce of Ep & NE | Tx. Cntrol BP prior surgery
Phenoxybenzamine Phentolamine Pheochromocytoma
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Alpha 1 selective antagonist
Azosin
80
Olol
Beta blockers
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olo
beta blocker
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Vaughn-Williams Classification of Antiarrhythmic Drugs
Na B K Ca