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Mirtazapine

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Mirtazapine is an antidepressant introduced by Organon International in 1996 used for the treatment of mild to severe depression. Although Mirtazapine has a tetracyclic chemical structure it is classified as a noradrenergic and specific serotonergic antidepressant (NaSSA). Mirtazapine may be used in preference to an SSRI due to the fact that it causes fewer sexual dsyfunction problems. Due to its unique pharmacologic profile, mirtazapine is virtually devoid of anticholinergic, adrenolytic, and serotonin-related side effects[#endnote_Burrows].

Trade Names

Mirtazapine is marketed under the tradenames Remeron® in the U.S. and Finland, Avanza® in Australia, Zispin® in the UK & Ireland, Norset® in France, Remergon® in Belgium, Remergil® in Germany and Mirtabene® in Austria).

Indications

Mirtazapine is primarily used to treat the symptoms of depression. It can also be used to treat panic disorder[#endnote_Baldwin], generalized anxiety disorder[#endnote_Goodnick], obsessive-compulsive disorder (OCD)[#endnote_Koran] and post traumatic stress disorder (PTSD)[#endnote_Baldwin].

Mechanism of action

It is thought to work by blocking presynaptic alpha-2 adrenergic receptors that normally inhibit the release of the neurotransmitters norepinephrine (noradrenaline) and serotonin, thereby increasing active levels in the synapse. Mirtazapine also blocks post-synaptic 5-HT2 and 5-HT3 receptors—an action which is thought to enhance serotonergic neurotransmission while causing a low incidence of side effects.

Side effects

The side effects that do occur are thought to be primarily related to the blockage of histamine receptors, which decreases with higher dosages.

Side effects occurring commonly:

Side effects occurring rarely:

Side effects to tell your doctor about and stop taking mirtazapine immediately

Interestingly, its side effect profile can be used for benefit in certain clinical situations. The drowsiness, increased appetite, and weight gain it causes are useful in patients with depressive disorders with prominent sleep and appetite disturbances. In addition, it is quite useful in inpatient situations in which patients suffer from nausea since it also antagonizes the 5-HT3 receptor, the target of the popular anti-emetic ondansetron (Zofran®).

Dosage

The usual starting dose for mirtazapine is 15 mg once daily, usually at bedtime (Due to the sedative nature and disturbed visual perception). Doses may be increased every 1-2 weeks up to a maximum dose of 45 mg daily. It may be taken with or without food. Dissolving tablets can even be taken without water.

Pregnancy and Lactation

Drug-Drug Interactions

Due to the sedative effects of Mirtazapine, alcohol should not be taken. Excessive sedation may result when it is used with other sedating drugs, such as benzodiazepines. Mirtazapine should not be used within 14 days of the use of a monoamine oxidase inhibitor because of the possibility that a hypertensive emergency will be triggered.

References

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Monoamine oxidase inhibitors (MAOI):

Reversible Inhibitor of Monoamine oxidase A (RIMA):

Dopamine Reuptake Inhibitor (DARI):

Norepinephrine-dopamine reuptake inhibitors:

Norepinephrine Reuptake Inhibitor (NRI) or (NARI):

Serotonin-Norepinephrine Reuptake Inhibitor (SNRI):

Selective Serotonin Reuptake Inhibitor (SSRI):

Selective Serotonin Reuptake Enhancer (SSRE):

Tricyclic antidepressants (TCA):

Tetracyclic antidepressants:

Noradrenergic and Specific Serotonergic Antidepressant (NaSSA):

 


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