General Drug Information Flashcards

1
Q

Minimum standards for drug identification

A
  • Use of an analytical scheme based on validated methods

* competence of analyst

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2
Q

What are the three analytical categories

A

A, B, C

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3
Q

If category A test is performed then______

A

Then atleast one other technique from category A,B, or C shall be used

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4
Q

When category A technique is not used then_____

A

Then atleast 3 different validated methods shall be employed (2/3 should be From category B)

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5
Q

Improve quality of the forensic examination of seized drugs

A

SWGDRUG

scientific working group for the analysis of seized drugs

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6
Q

Drug Chemistry

A

Any substance:

  • that causes dependency in humans
  • intended for use in the diagnosis,cure,mitigation,treatment, or prevention of disease
  • that alters the mind,sense,mood, or thought
  • losted in US pharmacopeia, homeopathic pharmacopeia, national formulary
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7
Q

Natural Classification

A

Alkaloids
Caffeine
Cannabis

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8
Q

Semisynthetic Classification

A

Heroin
Hormones
Steroids

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9
Q

Synthetic Classification

A

Benzodiazepines

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10
Q

Physiologic Classification

A
Analgesic
Depressants
Dissociative Anesthetics
Hallucinogens
Narcotics
Stimulants
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11
Q

Analgesic

A

Pain relief (aspirin,ibuprofen, morphine)

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12
Q

Depressant

A

Suppresses nervous system response (barbiturates, Valium)

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13
Q

Dissociative Anesthetics

A

Removes you from reality (ketamine,PCP)

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14
Q

Hallucinogens

A

Out of body experience (LSD, Psulocybin)

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15
Q

Narcotics

A

Induce sleep (heroin, morphine,codeine)

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16
Q

Stimulants

A

(Amphetamine, cocaine,nicotine)

17
Q

Common forms of drugs

A
Powders
Plant matter
Pills
Precursor 
Paraphernalia
18
Q

Toxicology

A

The study of how natural or man made poisons cause undesirable effects in living organisms

19
Q

Toxic

A

Poisonous or deadly effects

20
Q

Toxicant

A

Chemical that can injure or kill humans, animals, or plants; a poison

21
Q

Pharmokinetics

A

Relationship b/w dosage regimen and profile of drug concentration in blood over time

22
Q

Pharmacodynamics

A

Relationships b/w drug concentration time profile and therapeutic and toxic effects

23
Q

Pharmokinetics and Pharmacodynamics:

A

Aspects of

  • absorption
  • distribution
  • excretion
  • metabolism
  • compartmental modeling
24
Q

Toxicokinetics

A

Subdivision of pharmacokinetics concerned with impact of toxins on normal body-drug interactions

25
Routes of absorption
``` Oral Inhalation Intravenous Intramuscular Rectal Oral mucosa Intrathecal Dermal Ocular Intranasally ```
26
Solubility
Maximum concentration of a substance that may be completely dissolved in a given solvent at a given temp and pressure
27
Solubility
``` Polar (delta > 50) Semi-polar (delta = 20-50) Non polar (delta = 1-20) ```
28
Solubility and Distribution of Stomach and Intestines
``` Stomach = pH of 2 Intestine = pH of 8 ```
29
Agonist
Drug that binds to receptors and thereby alters the proportion of receptors in the active conformation resulting in biological response
30
Chemical Antagonism
Chemical interaction b/w drug and either a chemical or another drug leading to a reduced or nil response
31
Physiologic Antagonism
Occurs when two drugs acting in different receptors and pathways exert opposing actions in same physiologic system
32
Pharmacokinetic Antagonism
Result of one drug suppressing the effect of a second drug by reducing its absorption, altering its distribution, or increasing its rate of elimination
33
Pharmacological Antagonism
Occurs when antagonist inhibits the effect of a full or partial agonist by acting on the same pathway but not necessarily on the same receptor
34
Volume of distribution
Indicates where a drug is to be found primarily in the blood or in another bodily site
35
Sites of elimination
Kidney | Liver
36
Major excretory organs
Liver Kidney Other organs also have lesser roles in drug elimination
37
Drug clearance
Volume of blood in a defined region of the body that is cleared of a drug in a unit of time