| Definition Antianxiety
drugs are medicines that calm and relax people with
excessive anxiety, nervousness, or tension, or for
short-term control of social phobia disorder or specific
phobia disorder.
Purpose
Antianxiety agents, or anxiolytics, may be used to
treat mild transient bouts of anxiety as well as more
pronounced episodes of social phobia and specific
phobia. Clinically significant anxiety is marked by
several symptoms. The patient experiences marked or
persistent fear of one or more social or performance
situations in which he or she is exposed to unfamiliar
people or possible scrutiny by others, and may react in
a humiliating or embarrassing way. The exposure to the
feared situation produces an anxiety attack. Fear of
these episodes of anxiety leads to avoidance behavior,
which impairs normal social functioning, including
working or attending classes. The patient is aware that
these fears are unjustified.
Antianxiety
DrugsBrand Name (Generic Name)Possible Common Side Effects Include:
Atarax (hydroxyzine
hydrochloride)Drowsiness,
dry mouth Ativan
(lorazepam)Dizziness, excessive calm, weakness BuSpar, Buspirone (buspirone hydrochloride)Dry mouth, dizziness, headache, fatigue, nausea Centrax
(pazepam)Decreased coordination, dizziness, drowsiness, fatigue, weakness Librium,
Libritabs (chlordiazepoxide)Constipation,
drowsiness, nausea, swelling Miltown,
Equanil (meprobamate)Diarrhea,
bruising, fever, headache, nausea, rash, slurred
speech Serax
(oxazepam)Dizziness,
fainting, headache, liver problems, decreased
coordination, nausea, swelling, vertigo Stelazine
(trifluoperazine hydrochloride)Abnormal
glucose in urine, allergic reactions, blurred
vision, constipation, eye spasms, fluid retention
and swelling Tranxene,
Tranxene-SD (clorazepate dipotassium)Drowsiness Valium (diazepam)Decreased
coordination, drowsiness, light-headedness
Description
In psychiatric practice, treatment of anxiety has
largely turned from traditional antianxiety agents,
anxiolytics, to antidepressant therapies. In current
use, the benzodiazepines, the best known class of
anxiolytics, have been largely supplanted by selective
serotonin reuptake inhibitors (SSRIs). Among the
preferred SSRIs for generalized anxiety disorder are
paroxetine (Paxil), escitalopram (Lexapro), and
venlafaxine (Effexor), which also has norepinephrine.
Other SSRIs are fluoxetine (Prozac) and sertraline
(Zoloft). Venlafaxine and Paroxetine have been shown
particularly effective in relieving symptoms of social
anxiety.
However, traditional anxiolytics remain useful for
patients who need a rapid onset of action, or whose
frequency of exposure to anxiety provoking stimuli is
low enough to eliminate the need for continued
treatment. While SSRIs may require three to five weeks
to show any effects, and must be taken continuously,
benzodiazepines may produce a response within 30
minutes, and may be dosed on an as-needed basis.
The intermediate action benzodiazepines, alprazolam (Xanax),
and lorazepam (Ativan) are the appropriate choice for
treatment of mild anxiety and social phobia. Diazepam
(Valium) is still widely used for anxiety, but its
active metabolite, desmethyldiazepam, which has a long
half-life, may make this a poorer choice than other
drugs in its class. There is considerable variation
between individuals in metabolism of benzodiazepines, so
patient response may not be predictable. As a class,
benzodiazepines are used not only as anxiolytics, but
also as sedatives, muscle relaxants, and in treatment of
epilepsy and alcoholism. The distinctions between these
uses are largely determined by onset and duration of
action, and route of administration.
Buspirone (BuSpar), which is not chemically related
to other classes of central nervous system drugs, is
also a traditional anxiolytic, although it is now
considered either a third line or adjunctive agent for
use after trials of SSRIs and benzodiazepines. It is
appropriate for use in patients who have either failed
trials of other treatments, or who should not receive
benzodiazepines because of a history of substance abuse
problems. Buspirone, in common with antidepressants,
requires a two to three week period before there is
clinical evidence of improvement, and must be
continuously dosed to maintain its effects.
Benzodiazepines are controlled drugs under federal
law. The number of U.S. drug-abuse related trips to
emergency departments involving benzodiazepine
medications exceeded 100,000 in 2002. Buspirone is not a
controlled substance and has no established abuse
potential.
Recommended dosage
Benzodiazepines should be administered 30 to 60
minutes before exposure to the anticipated stress.
Dosage should be individualized to minimize sedation.
The normal dose of alprazolam is 0.25-0.5 mg. The usual
dose of lorazepam is 2-3 mg. Doses may be repeated if
necessary.
Buspirone is initially dosed at 5 mg three times a
day. Patients should increase the dosage 5 mg/day, at
intervals of two to three days, as needed and should not
exceed 60 mg/day. Two to three weeks may be required
before a satisfactory response is seen.
Precautions
Benzodiazepines should not be used in patients with
psychosis, acute narrow angle glaucoma, or liver
disease. The drugs can act as respiratory depressants
and should be avoided in patients with respiratory
conditions. Benzodiazepines are potentially addictive
and should not be administered to patients with
substance abuse disorders. Because benzodiazepines are
sedative, they should be avoided in patients who must
remain alert. Their use for periods over four months has
not been documented. These drugs should not be used
during the second and third trimester of pregnancy,
although use during the first trimester appears to be
safe. They should not be taken while breastfeeding.
Physicians and pharmacists should be consulted about use
in children.
Buspirone is metabolized by the liver and excreted by
the kidney, and should be used with care in patients
with hepatic or renal disease. The drug is classified as
schedule B during pregnancy, but should not be taken
during breastfeeding. Its use in children under the age
of 18 years has not been studied.
In 2004, the FDA cautioned revealed that certain
SSRIs could lead to increased risk of suicide in
children and adolescents who took them for depression.
Parents should check with physicians to receive more
information on SSRIs when they are prescribed for teens
and children with anxiety.
Side effects
The most common side effects of benzodiazepines are
secondary to their CNS effects and include sedation and
sleepiness; depression; lethargy; apathy; fatigue;
hypoactivity; lightheadedness; memory impairment;
disorientation; anterograde amnesia; restlessness;
confusion; crying or sobbing; delirium; headache;
slurred speech; aphonia; dysarthria; stupor; seizures;
coma; syncope; rigidity; tremor; dystonia; vertigo;
dizziness; euphoria; nervousness; irritability;
difficulty in concentration; agitation; inability to
perform complex mental functions; akathisia; hemiparesis;
hypotonia; unsteadiness; ataxia; incoordination;
weakness; vivid dreams; psychomotor retardation;
"glassy-eyed" appearance; extrapyramidal symptoms;
paradoxical reactions. Other reactions include changes
in heart rate and blood pressure, changes in bowel
function, severe skin rash and changes in genitourinary
function. Other adverse effects have been reported.
Buspirone has a low incidence of side effects.
Dizziness and drowsiness are the most commonly reported
adverse effects. Other CNS effects include dream
disturbances; depersonalization, dysphoria, noise
intolerance, euphoria, akathisia, fearfulness, loss of
interest, disassociative reaction, hallucinations,
suicidal ideation, seizures; feelings of claustrophobia,
cold intolerance, stupor and slurred speech, psychosis.
Rarely, heart problems, including congestive heart
failure and myocardial infarction, have been reported.
Other adverse effects have been reported.
Interactions
The metabolism of alprazolam may be increased by:
cimetidine, oral contraceptives, disulfiram, fluoxetine,
isoniazid, ketoconazole, metoprolol, propoxyphene,
propranolol and valproic acid. The absorption of all
benzodiazepines is inhibited by concomitant use of
antacids. Benzodiazepines may increase blood levels of
digoxin, and reduce the efficacy of levodopa. Other drug
interactions have been reported.
Buspirone levels will be increased by concomitant use
of erythromycin, itraconazole, and nefazadone. Doses
should be adjusted based on clinical response. Use of
buspirone at the same time as mono-amine oxidase
inhibitors (MAOIs, phenelzine, tranycypromine) may cause
severe blood pressure elevations. Use of buspirone with
MAOIs should be avoided.
Key Terms
- Anxiety
- Worry or tension in response to real or
imagined stress, danger, or dreaded situations.
Physical reactions, such as fast pulse,
sweating, trembling, fatigue, and weakness may
accompany anxiety.
- Epilepsy
- A brain disorder with symptoms that include
seizures.
- Panic disorder
- An disorder in which people have sudden and
intense attacks of anxiety in certain
situations. Symptoms such as shortness of
breath, sweating, dizziness, chest pain, and
extreme fear often accompany the attacks.
- Phobia
- An intense, abnormal, or illogical fear of
something specific, such as heights or open
spaces.
- Pregnancy category B
- Animal studies indicate no fetal risk, but
no human studies; or adverse effects in animals,
but not in well-controlled human studies.
- Pregnancy category C
- No adequate human or animal studies; or
adverse fetal effects in animal studies, but no
available human data.
- Seizure
- A sudden attack, spasm, or convulsion.
For Your Information
Resources
Periodicals
- "Abuse of Anti-anxiety Drugs Up, Study of ER
Visits Shows." Drug Week (September 17, 2004): 225.
- Finn, Robert. "Venlafaxine and Paroxetine Both
Relieve Social Anxiety." Clinical Psychiatry News
(September 2004): 41.
- Sherman, Carl. "GAD Patients Often Require
Combined Therapy." Clinical Psychiatry News (August
2004): 12-14.
Gale Encyclopedia of Medicine, Published December, 2002
by the Gale Group The Essay Author is Samuel D. Uretsky,
PharmD. |