Nomifensine

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(Redirected from Merital)

Nomifensine is a synthetic compound that was primarily used as an antidepressant in the 1970s and 1980s. It belongs to a class of medications known as dopamine reuptake inhibitors, which increase the levels of dopamine in the brain by preventing its reabsorption into neurons. This mechanism of action is similar to that of other antidepressants but with a unique focus on the dopamine system, distinguishing it from many other types of antidepressants that primarily target the serotonin system.

History[edit | edit source]

Nomifensine was developed in the 1970s and introduced for medical use under various brand names, including Merital. It was found to be effective in treating depression, with a relatively low incidence of traditional antidepressant side effects such as sedation, anticholinergic effects, and cardiovascular disturbances. However, its clinical use was short-lived. By the late 1980s, nomifensine was withdrawn from the market in many countries due to reports of rare but serious side effects, including hemolytic anemia, a condition where red blood cells are destroyed faster than they can be made.

Pharmacology[edit | edit source]

The pharmacological action of nomifensine is primarily based on its ability to inhibit the reuptake of dopamine, thereby increasing dopamine concentrations in the synaptic cleft and enhancing dopaminergic neurotransmission. This action is believed to contribute to its antidepressant and stimulant effects. Nomifensine also has minor effects on the reuptake of norepinephrine (noradrenaline) and very little effect on serotonin reuptake, making it distinct from many other antidepressants that act on serotonin pathways.

Clinical Use[edit | edit source]

Before its withdrawal, nomifensine was used to treat various types of depression, including atypical depression and depression resistant to other treatments. Its unique pharmacological profile made it a valuable option for patients who did not respond well to traditional antidepressants. Additionally, due to its stimulant properties, nomifensine was sometimes used to treat patients with depressive disorders accompanied by lethargy and fatigue.

Side Effects[edit | edit source]

While nomifensine was generally well-tolerated, it was associated with some side effects. Common adverse effects included insomnia, anxiety, and nausea. The most concerning side effect, however, was the risk of inducing hemolytic anemia, a serious and potentially life-threatening condition. This risk led to the reevaluation of nomifensine's safety profile and ultimately to its withdrawal from the market.

Current Status[edit | edit source]

As of the current knowledge cutoff in 2023, nomifensine is no longer available for clinical use. Its withdrawal from the market underscores the importance of post-marketing surveillance in the pharmaceutical industry and the need for ongoing evaluation of drug safety. Despite its removal, the study of nomifensine has contributed to a better understanding of the role of dopamine in depression and the potential for targeting different neurotransmitter systems in the treatment of mood disorders.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD