|
|
| Depressants
In medicine, a drug or
other agent that slows the activity of
vital organs of the body. Depressants
acting on the central nervous system include
general anesthetics, opiates, alcohol,
and hypnotics. Tranquilizing drugs (ataractics)
act primarily on the lower levels of the
brain, relieving tension without reducing
mental sharpness.
Chloral
Hydrate
| Classification |
Depressants |
| CSA |
Schedule
IV |
| Trade
or Other Names |
Noctec;
Somnos; Felsules |
| Medical
Uses |
Hypnotic |
| Physical
Dependence |
Moderate |
| Tolerance |
Yes |
| Duration |
5-8(hours) |
| Usual
Method |
Oral |
| Possible
Effects |
Slurred
speech; Disorientation; Drunken behavior
without odor of alcohol |
| Overdose |
Shallow
respiration; Clammy skin; Dilated
pupils; Weak and rapid pulse; Coma;
Possible death |
| Withdrawal |
Anxiety;
Insomnia; Tremors; Delirium; Convulsions;
Possible death |
Barbiturates
| Classification |
Depressants |
| CSA |
Schedule
II, III, IV |
| Trade
or Other Names |
Amytal;
Florinal; Nembutal; Seconal; Tuinal;
Phenobarbital; Pentobarbital |
| Medical
Uses |
Anesthetic;
Anti-convulsant; Sedative; Hypnotic;
Veterinary euthanasia agent |
| Physical
Dependence |
Moderate |
| Tolerance |
Yes |
| Duration |
5-8(hours) |
| Usual
Method |
Oral;
Injected |
| Possible
Effects |
Slurred
speech; Disorientation; Drunken behavior
without odor of alcohol |
| Overdose |
Shallow
respiration; Clammy skin; Dilated
pupils; Weak and rapid pulse; Coma;
Possible death |
| Withdrawal |
Anxiety;
Insomnia; Tremors; Delirium; Convulsions;
Possible death |
Benzodiazepines
| Classification |
Depressants |
| CSA |
Schedule
IV |
| Trade
or Other Names |
Ativan;
Dalmane; Diazepam; Librium; Xanax;
Serax; Valium; Tranxene; Verstran;
Versed; Halcion; Paxpam; Restoril |
| Medical
Uses |
Anti-anxiety;
Sedative; Anti-convulsant; Hypnotic
Physical Dependence Low |
| Physical
Dependence |
Low |
| Tolerance |
Yes |
| Duration |
4-8(hours) |
| Usual
Method |
Oral;
Injected |
| Possible
Effects |
Slurred
speech; Disorientation; Drunken behavior
without odor of alcohol |
| Overdose |
Shallow
respiration; Clammy skin; Dilated
pupils; Weak and rapid pulse; Coma;
Possible death |
| Withdrawal |
Anxiety;
Insomnia; Tremors; Delirium; Convulsions;
Possible death |
Glutethimide
| Classification |
Depressants |
| CSA |
Schedule
II |
| Trade
or Other Names |
Doriden |
| Medical
Uses |
Sedative;
Hypnotic |
| Physical
Dependence |
High |
| Tolerance |
Yes |
| Duration |
4-8(hours) |
| Usual
Method |
Oral |
| Possible
Effects |
Slurred
speech; Disorientation; Drunken behavior
without odor of alcohol |
| Overdose |
Shallow
respiration; Clammy skin; Dilated
pupils; Weak and rapid pulse; Coma;
Possible death |
| Withdrawal |
Anxiety;
Insomnia; Tremors; Delirium; Convulsions;
Possible death |
|
|
Narcotics The narcotic
analgesics act primarily on the CNS. The
perception of and emotional response to
pain is modified when the narcotic analgesics
bind with stereospecific receptors in
the CNS. Five major groups of opioid receptors
are known: mu, kappa, sigma, delta and
epsilon. Narcotic analgesic activity occurs
at the mu, kappa and sigma receptors.
Opioid agonists such as morphine and others
exert their activity mainly at the mu
receptor. Mixed agonist-antagonists such
as butorphanol, nalbuphine and pentazocine
act primarily at the kappa receptors (thought
to mediate analgesic effects) and sigma
receptors (may produce subjective and
psychotomimetic effects).
As well as
analgesia, opioid agonist activity in
the CNS causes suppression of the cough
reflex, change in mood such as euphoria
or dysphoria, mental clouding and EEG
changes. Nausea and vomiting, probably
caused by stimulation of the chemoreceptor
trigger zone, can also occur. Peripheral
vasodilation, reduced peripheral resistance
and the inhibition of baroreceptors can
result in orthostatic hypotension and
fainting. The inhibition of peristalsis
can lead to constipation while increased
bladder sphincter tone may cause urinary
retention.
Large
doses may elicit excitation or seizures.
Morphine and its congeners cause miosis.
In therapeutic doses they increase accommodation
and sensitivity to light reflex and decrease
intraocular pressure in both normal patients
and those with glaucoma.
|
| Stimulants
Any drug that
excites any bodily function, but more
specifically those that stimulate the
brain and central nervous system. Stimulants
induce alertness, elevated mood, wakefulness,
increased speech and motor activity and
decrease appetite. Their therapeutic use
is limited, but their mood-elevating effects
make some of them potent drugs of abuse.
The major stimulant drugs are amphetamines
and related compounds, methylxanthines
(methylated purines), cocaine, and nicotine.
Amphetamines
achieve their effect by increasing the
amount and activity of the neurotransmitter
norepinephrine (noradrenaline) within
the brain. They facilitate the release
of norepinephrine by nerve cells and interfere
with the cells' reuptake and breakdown
of the chemical, thereby increasing its
availability within the brain. The most
commonly used amphetamines are methamphetamine
(Methedrine), amphetamine sulfate (Benzedrine),
and dextroamphetamine sulfate (Dexedrine).
Amphetamines were first used in the 1930s
to treat narcolepsy and subsequently became
prescribed for obesity and fatigue.
Their heavy
or prolonged use causes irritability,
restlessness, hyperactivity, anxiety,
excessive speech, and rapid mood swings.
Still higher doses or chronic use can
cause agitation, tremor, confusion, and,
in the most serious cases, a state resembling
paranoid schizophrenia. Moreover, letdown
effects of deep depression and physical
exhaustion may occur after only a single
dose of moderate strength wears off. With
repeated use, tolerance develops, so that
a user needs to take larger doses, but
the accompanying dependence is not strong
enough to be termed a physical addiction.
Amphetamines are widely abused, in some
cases by workers or students seeking enhanced
physical energy and mental acuity to fulfill
demanding tasks.
Certain drugs related to
the amphetamines have the same mode of
action but are somewhat milder stimulants.
Among them are phenmetrazine (Preludin)
and methylphenidate (Ritalin). The latter
drug is widely used to slow down
hyperactive children and improve their
ability to concentrate.
The methylxanthines are
even milder stimulants. Unlike the amphetamines
and methylphenidate, which are synthetically
manufactured, these compounds occur naturally
in various plants and have been used by
humans for many centuries. The most important
of them are caffeine, theophylline, and
theobromine. The strongest is caffeine,
which is the active ingredient of coffee,
tea, cola beverages, and maté.
Theobromine is the active ingredient in
cocoa. Caffeine constricts blood vessels
of the brain; for this reason it is often
a component of headache remedies. Theophylline
is used in the treatment of severe asthma
because of its capacity for relaxing the
bronchioles in the lungs.
Cocaine is one of the strongest
and shortest-acting stimulants and has
a high potential for abuse owing to its
euphoric and habit-forming effects. Nicotine,
the active ingredient in cigarettes and
other tobacco products, may also be regarded
as a stimulant. |
| Hallucinogins
Hallucinogenic
drugs are substances that distort the
perception of objective reality. The most
well-known hallucinogens include phencyclidine,
otherwise known as PCP, angel dust, or
loveboat; lysergic acid diethylamide,
commonly known as LSD or acid; mescaline
and peyote; and psilocybin, or "magic"
mushrooms. Under the influence of hallucinogens,
the senses of direction, distance, and
time become disoriented.
These drugs
can produce unpredictable, erratic, and
violent behavior in users that sometimes
leads to serious injuries and death. The
effect of hallucinogens can last for 12
hours.
LSD produces
tolerance, so that users who take the
drug repeatedly must take higher and higher
doses in order to achieve the same state
of intoxication. This is extremely dangerous,
given the unpredictability of the drug,
and can result in increased risk of convulsions,
coma, heart and lung failure, and even
death.
Mescaline
& Peyote | Amphetamine Variants
| Phencyclidine & Analogs
LSD
| Classification |
Hallucinogen |
| CSA |
Schedule
I |
| Trade
or Other Names |
Acid;
Microdot |
| Medical
Uses |
None |
| Physical
Dependence |
None |
| Psychological
Dependence |
Moderate |
| Tolerance |
Yes |
| Duration |
8-12(hours) |
| Usual
Method |
Oral |
| Possible
Effects |
Illusions
and hallucinations; Altered perception
of time and distance |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Longer;
more intense "trip" episodes;
Psychosis; Possible death
Withdrawal Unknown |
Mescaline
& Peyote
| Classification |
Hallucinogen |
| CSA |
Schedule
I |
| Trade
or Other Names |
Mescal;
Buttons; Cactus |
| Medical
Uses |
None |
| Physical
Dependence |
None |
| Psychological
Dependence |
Moderate |
| Tolerance |
Yes |
| Duration |
8-12(hours) |
| Usual
Method |
Oral |
| Possible
Effects |
Illusions
and hallucinations; Altered perception
of time and distance |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Longer;
more intense "trip" episodes;
Psychosis; Possible death
Withdrawal Unknown |
Amphetamine Variants
| Classification |
Hallucinogen |
| CSA |
Schedule
I |
| Trade
or Other Names |
2,5-DMA;
STP; MDA; MDMA; Ecstacy; DOM; DOB |
| Medical
Uses |
None |
| Physical
Dependence |
None |
| Psychological
Dependence |
Moderate |
| Tolerance |
Yes |
| Duration |
Variable(hours) |
| Usual
Method |
Oral;
Injected |
| Possible
Effects |
Illusions
and hallucinations; Altered perception
of time and distance |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Longer;
more intense "trip" episodes;
Psychosis; Possible death
Withdrawal Unknown |
Phencyclidine
& Analogs
| Classification |
Hallucinogen |
| CSA |
Schedule
I, II |
| Trade
or Other Names |
PCE;
PCPy; TCP; PCP; Hog; Loveboat;Angel
Dust |
| Medical
Uses |
None |
| Physical
Dependence |
None |
| Psychological
Dependence |
High |
| Tolerance |
Yes |
| Duration |
Days(hours) |
| Usual
Method |
Oral;
Smoked |
| Possible
Effects |
Illusions
and hallucinations; Altered perception
of time and distance |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Longer;
more intense "trip" episodes;
Psychosis; Possible death
Withdrawal Unknown |
|
| Anabolic
Steriods
Anabolic Steroid
abuse has become a national concern. These
drugs are used illicitly by weight lifters,
body builders, long distant runners, cyclists,
and others who claim that the drugs give
them a competitive advantage and/or improve
their physical appearance. Once viewed
as a problem associated only with professional
athletes, recent reports estimate that
5 to 12 percent of male high school students
and 1 percent of female students have
used anabolic steroids by the time they
were seniors.
Concerns over
a growing illicit market and prevalence
of abuse combined with the possibility
of harmful long-term effects of steroid
use, led Congress to place anabolic steroids
into Schedule III of the Controlled Substance
Act (CSA).
The CSA defines
anabolic steroids as any drug or hormonal
substance chemically and pharmacologically
related to testosterone (other than estrogens,
progestins, and corticosteroids), that
promotes muscle growth. Most illicit anabolic
steroids are sold at gyms, competitions
and through mail order operations.
For the most
part, these substances are smuggled into
the United States. Those commonly encountered
on the illicit market include: boldenone
(Equipose), ethylestrenol (Maxibolin),
fluoxymesterone (Halotestin), methandriol,
methandrostenolone (Dianabol), Depo-Testosterone
Android - 25 (mehyltestosterone), nandrolone
(Durabolin, Deca-Durabolin), oxandrolone
(Anavar), oxymetholone (Anadrol), stanozolol
(Winstrol), testosterone and trenbolone
(Finajet). In addition, a number of bogus
or counterfeit products are sold as anabolic
steroids.
A limited number of anabolic
steroids have been approved for medical
and veterinary use. The primary legitimate
use of these drugs in humans is for the
replacement of inadequate levels of testosterone
resulting from a reduction or absence
of functioning testes. In veterinary practice,
anabolic steroids are used to promote
feed efficiency and to improve weight
gain, vigor, and hair coat. They are also
used in veterinary practice to treat anemia
and counteract tissue breakdown during
illness and trauma.
When used in combination
with exercise training and high protein
diet, anabolic steroids can promote increased
size and strength of muscles, improve
endurance and decrease recovery time between
workouts. They are taken orally or by
intramuscular injection. Users concerned
about drug tolerance often take steroids
on a schedule called a cycle. A cycle
is a period of between six and 14 weeks
of steroid use followed by a period of
abstinence or reduction in use.
Additionally, users tend
to "stack" the drugs, using
multiple drugs concurrently. Although
the benefits of these practices are unsubstantiated,
most users feel that cycling and stacking
enhance the efficiency of the drugs and
limit their side effects.
Another mode of steroid
use is "pyramiding." Users slowly
escalate steroid use (increasing the number
of drugs used at one time and/or the dose
and frequency of one or more steroids)
reaching a peak amount at mid-cycle and
gradually tapering the dose toward the
end of the cycle. The escalation of steroid
use can vary with different types of training.
Body builders and weight lifters tend
to escalate their dose to a much higher
level than do long distance runners or
swimmers. |
| Cannabis
Plant genus belonging to
the family Cannabaceae of the nettle order
(Urticales). The genus comprises one species,
hemp (q.v.; C. sativa), a stout, aromatic,
erect annual herb that originated in Central
Asia and is now cultivated widely in the
North Temperate Zone. A tall, canelike
variety is raised for the production of
hemp fibre, while the female plant of
a short, branchier variety is prized as
the more abundant source of marijuana.
Marijuana
| Classification |
Cannabis |
| CSA |
Schedule
I |
| Trade
or Other Names |
Pot;
Acapulco Gold; Grass; Reefer; Sinsemilla;
Thai sticks |
| Medical
Uses |
None |
| Physical
Dependence |
Unknown |
| Psychological
Dependence |
Moderate |
| Tolerance |
Yes |
| Duration |
2-4(hours) |
| Usual
Method |
Smoked;
Oral |
| Possible
Effects |
Euphoria;
Relaxed inhibitions; Increased appetite;
Disorientation |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Occasional
reports of insomnia; Hyperactivity;
Decreased appetite |
Tetrahydrocanabinol
| Classification |
Cannabis |
| CSA |
Schedule
I, II |
| Trade
or Other Names |
THC;
Marinol |
| Medical
Uses |
Anti-nauseant |
| Physical
Dependence |
Unknown |
| Tolerance |
Yes |
| Duration |
2-4(hours) |
| Usual
Method |
Smoked;
Oral |
| Possible
Effects |
Euphoria;
Relaxed inhibitions; Increased appetite;
Disorientation |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Occasional
reports of insomnia; Hyperactivity;
Decreased appetite |
Hashish
& Hashish Oil
| Classification |
Cannabis |
| CSA |
Schedule
I |
| Trade
or Other Names |
Hash;
Hash oil |
| Medical
Uses |
Anti-nauseant |
| Physical
Dependence |
Unknown |
| Tolerance |
Yes |
| Duration |
2-4(hours) |
| Usual
Method |
Smoked;
Oral |
| Possible
Effects |
Euphoria;
Relaxed inhibitions; Increased appetite;
Disorientation |
| Overdose |
Fatigue;
Paranoia; Possible psychosis |
| Withdrawal |
Occasional
reports of insomnia; Hyperactivity;
Decreased appetite |
|
|
|