Mirtazapine is a noradrenergic and specific serotonergic antidepressant (Na
SSA) which has predominantly been evaluated in the: treatment of major depr
ession. The drug had equivalent efficacy to tricyclic antidepressants and i
t was at least as effective as trazodone in the majority of available short
term trials in patients with moderate or severe depression, including thos
e with baseline anxiety symptoms or sleep disturbance and the elderly, A co
ntinuation study also showed that sustained remission rates were higher wit
h mirtazapine than with amitriptyline and that the drugs had similar effica
cy for the prevention of relapse. There is some evidence for a. faster onse
t of action with mirtazapine than with the selective serotonin (5-hydroxytr
yptamine: 5-HT) reuptake inhibitors (SSRIs), Mirtazapine was more effective
than the SSRI fluoxetine at weeks 3 and 4 of therapy and it was also more
effective than paroxetine and citalopram at weeks 1 and 2, respectively, in
short term assessments (6 or 8 weeks), preliminary data suggest that the d
rug may be effective as an augmentation or combination therapy in patients
with refractory depression.
Anticholinergic events and other events including tremor and dyspepsia are
less common with mirtazapine than with tricyclic antidepressants. There was
a greater tendency for SSRI-related adverse events with fluoxetine than wi
th mirtazapine, but, overall, mirtazapine hail a similar tolerability profi
le to the SSRIs, Increased appetite and bodyweight gain appear to be the on
ly events that are reported more often with mirtazapine than with comparato
r antidepressants. In vitro and in vivo data have suggested that mirtazapin
e is unlikely to affect the metabolism of drugs metabolised by cytochrome P
450 (CYP)2D6. although few formal drug interaction data are available.
Conclusions: Mirtazapine is effective and well tolerated for the treatment
of patients with moderate to severe major depression. Further research is r
equired to define the comparative efficacy of mirtazapine in specific patie
nt groups, including the elderly and those with severe depression. Clarific
ation of its efficacy as an augmentation therapy and in patients with refra
ctory depression and its role in improving the efficacy and reducing the ex
trapyramidal effects of antipsychotic drugs would also help to establish it
s clinical value, The low potential for interaction with drugs that are met
abolised by CYP2D6, including antipsychotics, tricyclic antidepressants and
some SSRIs, may also make mirtazapine an important option for the treatmen
t of major depression in patients who require polytherapy, Mirtazapine also
appears to be useful in patients with depression who present with anxiety
symptoms and sleep disturbance.