Mirtazapine, commonly known by its trade names Remeron, Avanza, and Zispin, is a tetracyclic antidepressant that was first developed in the 1980s. Mirtazapine is primarily used in the treatment of
major depressive disorder (MDD), but it has also shown efficacy in treating
anxiety disorders,
obsessive-compulsive disorder (OCD), and
post-traumatic stress disorder (PTSD). The drug is known for its sedative properties and is often prescribed as an alternative to other antidepressants for patients who suffer from
insomnia. Initially developed by the Dutch pharmaceutical company
Organon, mirtazapine received FDA approval for the treatment of
depression in 1996. Research into its efficacy and mechanisms is ongoing, with numerous clinical studies investigating its wider applications and long-term effects.
Mirtazapine works by modulating neurotransmitters in the brain, specifically norepinephrine and serotonin. Unlike selective serotonin reuptake inhibitors (SSRIs) that primarily affect serotonin levels, mirtazapine has a dual mechanism of action. It functions as an antagonist at central presynaptic
alpha-2 adrenergic inhibitory autoreceptors and heteroreceptors, leading to an increase in the release of norepinephrine and serotonin. Additionally, mirtazapine antagonizes
serotonin type 2 (5-HT2) and type 3 (5-HT3) receptors, which may contribute to its anxiolytic and antiemetic properties. The drug also has antihistaminergic effects, which are responsible for its sedative actions. This complex mechanism makes mirtazapine a unique option among antidepressants, offering benefits for patients who may not respond well to SSRIs or serotonin-norepinephrine reuptake inhibitors (SNRIs).
Mirtazapine is typically administered orally in tablet form, with dosages ranging from 15 mg to 45 mg per day. The drug is usually taken once daily, preferably before bedtime due to its sedative effects. It's important to follow the doctor's instructions regarding dosage and timing to achieve the best therapeutic outcomes. Mirtazapine is known for its relatively rapid onset of action compared to other antidepressants, with some patients reporting an improvement in sleep and appetite within the first week of treatment. However, it may take several weeks to experience the full antidepressant effects. For this reason, it is crucial to continue taking the medication as prescribed, even if immediate improvements are not evident. Gradual dose adjustments may be necessary based on the patient’s response and tolerability.
Like all medications, mirtazapine comes with potential side effects. Common side effects include
drowsiness,
increased appetite,
weight gain, and
dry mouth. These are generally mild and often diminish with continued use. However, some patients may experience more severe side effects such as
dizziness,
confusion, or abnormal thinking. In rare cases, mirtazapine can cause
agranulocytosis, a potentially life-threatening condition characterized by a severe reduction in white blood cells. Therefore, regular blood tests may be recommended during the initial months of treatment. Mirtazapine is contraindicated in individuals with a known hypersensitivity to the drug or any of its components. It should be used with caution in patients with a history of
seizures,
hepatic or renal impairment, and
bipolar disorder. Abrupt discontinuation of mirtazapine can lead to withdrawal symptoms such as
nausea,
headache, and
irritability, so it is advisable to taper the dose gradually under medical supervision.
Mirtazapine can interact with various other medications, potentially altering its effectiveness and increasing the risk of adverse reactions. Concomitant use of mirtazapine with monoamine oxidase inhibitors (MAOIs) is contraindicated due to the risk of a hypertensive crisis. A washout period of at least 14 days is recommended when switching between mirtazapine and an MAOI. The drug can also interact with other central nervous system depressants, such as benzodiazepines, opioids, and alcohol, leading to
enhanced sedation and
respiratory depression. Furthermore, mirtazapine may potentiate the effects of antihypertensive medications, necessitating close monitoring of blood pressure. Caution is advised when mirtazapine is combined with serotonergic drugs like SSRIs, SNRIs, or triptans, as this can increase the risk of
serotonin syndrome, a potentially life-threatening condition characterized by symptoms such as
agitation,
hallucinations, and autonomic instability. Patients should always inform their healthcare provider of all medications they are taking, including over-the-counter drugs and supplements, to prevent harmful interactions and ensure safe and effective treatment with mirtazapine.
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