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| 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 |
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