The classification scheme given below focuses on each compound's main
psychotropic effects which in some cases classifies it differently from
what might be considered its primary pharmacological effect (i.e., based
on therapeutic use). For example, pseudoephedrine is a popular decongestant
that has mild stimulatory properties. Pseudoephedrine's decongestant
effect might be considered its primary effect, while its stimulatory effect
would be considered a secondary side-effect. However, from a psychopharmacological
perspective, pseudoephedrine's stimulatory effect is its primary effect
and its decongestant action is a secondary (although therapeutically more
useful) effect. Therefore, pseudoephedrine is classified below as a mild
stimulant like caffeine and nicotine.
| Drug Class |
Primary Effects/Approved Medicinal Uses |
Examples |
| Opiates/Opioids/Narcotic Analgesics |
analgesia, cough suppression, antidiarrhea, suppression of opiate withdrawal,
sedation; currently used therapeutically for the first four effects |
opium, morphine, codeine, heroin (diacetyl morphine), fentanyl,
methadone, meperidine, L-alpha-acetylmethadol (LAAM) |
| Narcotic/Opiate Antagonists |
block the effects of narcotics; used to treat opiate overdose |
naloxone, naltrexone |
| Psychomotor Stimulants |
stimulate psychological and sensory-motor functioning; used therapeutically
to treat ADHD and narcolepsy, sometimes as an appetite suppressant, occasionally
antifatigue, formerly for asthma and for sinsus decongestion |
amphetamine, methamphetamine, cocaine, methylphenidate |
| Other Stimulants |
similar to psychomotor stimulants but with much less efficacy; various
therapeutic effects including caffeine compounded with aspirin in some
OTC pain relievers, ephedrine in OTC asthma medicines, pseudoephedrine
in OTC sinus decongestants and OTC appetite suppressants |
caffeine, nicotine, ephedrine, pseudoephedrine |
| Barbiturates |
general decrease in CNS arousal/excitability level; used therapeutically
for anesthetic, anticonvulsant, sedative, and hypnotic effects |
thiopental, secobarbital, pentobarbital, phenobarbital |
| Minor Tranquilizers |
general decrease in CNS arousal/excitability level, but low dose are
somewhat selective for anxiety and much less sedative than barbiturates;
used therapeutically as anxiolytics, benzodiazepines also as anesthetics
and anticonvulsants |
includes two subclasses: benzodiazepines (e.g.,. diazepam, chlordiazepoxide,
flunitrazepam [Rohypnol]) and muscle relaxants (e.g., meprobamate) |
| Major Tranquilizers (antipsychotics/neuroleptics) |
general sedation at high doses, with selective antipsychotic activity
at lower doses; used therapeutically to treat schizophrenia and other major
psychotic disorders |
haloperidol, pimozide, flupenthixol, chlorpromazine, spiroperidol,
clozapine |
| Antidepressants |
no perceptible CNS effects in normals, but effectively alleviate depression
in many depressives; used therapeutically to treat depression |
includes three subclasses: monoamine oxidase inhibitors (e.g.,
pargyline), tricyclic antidepressants (e.g., amitriptyline, desmethylimipramine),
and selective serotonin reuptake inhibitors (SSRIs: e.g., sertaline) |
| Antimanic |
dampens extreme mood swings in some people; used to treat manic-depressive
(bipolar) disorders |
lithium |
| Alcohol |
general decrease in CNS arousal/excitability level; no current therapeutic
uses, but formerly used as an anesthetic and a sedative |
ethyl alcohol (other alcohols have similar actions but are associated
with very toxic effects, e.g., methanol) |
| Volatile Anesthetics |
general decrease in CNS arousal/excitability level; used therapeutically
for anesthesia |
nitrous oxide, halothane, ether |
| Volatile Solvents |
produce feelings of intoxication, can produce hallucinations at high
doses; no therapeutics uses (all can cause marked brain damage in moderately
low concentrations |
toluene, benzene, naphtha |
| Psychogenics |
produce altered states of consciousness; hallucinogenics produce hallucinations
sometimes reported as "mystic" experiences; cannabinoids usually
produce increased feelings of "well being" and "mellow" intoxication; the
"pleasantness" of the states produced by both classes probably depends
partially on expectancies; no approved therapeutic uses, but cannabinoids
are being increasingly used for their antinausea, anxiolytic, and appetite-stimulating
effects in severely ill patients (e.g., AIDS) |
includes two subclasses: hallucinogenics (e.g., lysergic acid
diethylaminde [LSD], mescaline, psilocybin) and cannabinoids (e.g.,
marijuana, hashish). |
| Stimulatory Hallucinogenics (cf. former psychotomimetics) |
produce a mixture of psychomotor stimulant and hallucinogenic effects,
depending on dose and other factors; no therapeutic uses, except phencyclidine
as a veterinary anesthetic |
MDMA (ecstasy), phencyclidine (PCP), ketamine (?) |
Abbreviations: ADHD, attention deficit
hyperactivity disorder; AIDS, acquired immune deficiency syndrome;
CNS,
central nervous system; OTC, over-the-counter (nonprescription)
medicines.
| Schedule |
Abuse
Liability
|
Approved
Medical Use
|
Availability
|
Examples |
| Schedule I |
High
|
No
|
investigational
use only
|
-
marijuana, THC
-
LSD, mescaline, peyote
-
heroin
|
| Schedule II |
High
|
Yes
|
written
prescription
with no refills |
-
amphetamine, methamphetamine, cocaine
-
codeine, levorphanol, meperidine
methadone, morphine, opium
-
amobarbital, pentobarbital, secobarbital
-
phencyclidine
|
| Schedule III |
Moderately High
|
Yes
|
written or
telephone
prescription
with refills |
-
Tylenol with codeine, paregoric
-
chlorphentermine
-
anabolic steroids
|
| Schedule IV |
Moderate
|
Yes
|
written or
telephone
prescription
with refills |
-
chloral hydrate
-
chlordiazepoxide, diazepam, flunitrazepam
-
meprobamate
-
methohexital, phenobarbital
|
| Schedule V |
Low
|
Yes
|
prescription
not necessary |
-
Robitussin A-C (contains less than 100 mg codeine per 100 ml)
|
Note: Drugs are continually being reclassified.
The above listing (except for Schedule V) is from the information contained
on the DEA's license application/renewal form (DEA-225) dated April 1988.