Mood Disorders and Suicide 211
laypeople raised concerns about whether SSRI use was associated with increased
suicide rates. Studies comparing SSRIs to other antidepressants did, in fact, fi nd a
greater risk for suicidal thoughts and suicide attempts in children and adolescents
taking such medications (Martinez et al., 2005); these fi ndings led to a “black box”
warning label, indicating that the medications may increase the risk of suicide in
children who take them and that the children should be closely monitored for sui-
cidal thoughts or behavior or for an increase in depressive symptoms. Since the
warning label was mandated, additional research suggests that the benefi ts of SSRI
antidepressants for youngsters outweigh any risk of suicide, although people taking
them should continue to be carefully monitored (Bridge et al., 2007). Although stud-
ies of adults did not fi nd an increased suicide risk with SSRIs generally (Fergusson
et al., 2005; Gunnell, Saperia, & Ashby, 2005), they did fi nd an increased suicide
risk with the SSRI paroxetine (Paxil) (Aursnes et al., 2005). Moreover, studies of
SSRI use by adults revealed an increased risk of nonlethal self-harming behavior-
(Martinez et al., 2005; Tihonen et al., 2006).
Medications for depression are continually being developed. Researchers seek
to minimize the side effects of existing medications and to create new drugs for
people who do not get suffi cient relief from existing ones. For instance, some newer
antidepressants, such as venlafaxine (Effexor) and duloxetine (Cymbalta), affect
neurons that respond both to serotonin and norepinephrine; such medications are
sometimes referred to as serotonin/norepinephrine reuptake inhibitors (SNRIs).
Some other new antidepressants that affect noradrenaline (the alternative term for
norepinephrine) and serotonin are referred to as noradrenergic and specifi c seroton-
ergic antidepressants (NaSSAs, where Na stands for “noradrenergic”). The antide-
pressantmirtazapine (Remeron) is a NaSSa.
Clinicians may also prescribe any of the antidepressants discussed above for
dysthymia. The decision regarding which antidepressant to prescribe for any de-
pressive disorder is not yet based entirely on science—it is not presently possible
to predict which antidepressant will be the most effective with the least side effects
for a given individual (assuming that medication is the preferred treatment). Being
able to predict side effects is important because they often lead patients to stop the
medication. In fact, a majority of patients who receive medication for depression
stop taking the medication before it has had a chance to be maximally effective
either within the fi rst few weeks, before it can take full effect, or during an extended
period of better mood (Aikens, Nease, & Klinkman, 2008; National Committee for
Quality Assurance, 2007).
Some people with depression who do not want to
take prescription medication have successfully used an
extract from a flowering plant called St. John’s wort
(Hypericum perforatum). Results of meta- analytic stud-
ies comparing St. John’s wort to prescription antidepres-
sants and placebos indicate that the herbal medication
can help those with mild to moderate depression, and
sometimes—but less commonly—even those with severe
depression (Linde, Berner, & Krison, 2008; Linde et al.,
2005). Patients taking St. John’s wort report fewer side
effects than do patients taking prescription medications
(Linde, Berner, & Kriston, 2008); the most common side
effect is dry mouth or dizziness.
Another medication for which a prescription is not
necessary is ademetionine,orS-adenosyl-L-methionine
(SAMe), which was found to be as effective as the TCA
imiprimine and superior to a placebo (Agency for Health
Care Policy and Research, 2002; Pancheri, Scapicchio, &
Dell Chiaie, 2002). SAMe has been reported to reduce
depression more quickly than other antidepressants—in
about a week.
St. John’s wort, shown here as the plant and in capsule form, may lessen mild to moderate
depression but may not be as effective as antidepressant medication for those with
severe MDD (Linde et al., 2005).
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