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Published on: May 20, 2020
Mirtazapine-induced arthralgia
Anneke Passier1, Eugène van Puijenbroek
1Netherlands Pharmacovigilance Centre Lareb, Goudsbloemvallei 7, 5327 MH 's-Hertogenbosch, the Netherlands. A.Passier@Lareb.nl
Aim:
With this article, we intend to corroborate the assumed association between mirtazapine and arthralgia by presentation of eight case reports, and we describe a possible mechanism of action.
Methods And Results:
The Netherlands Pharmacovigilance Centre Lareb received eight case reports on arthralgia associated with use of mirtazapine. These case reports are presented in short. We also present worldwide data on this association.
Conclusions:
The Lareb reports support the association between mirtazapine and arthralgia. A comparison is made between mirtazapine, mianserin and nefazodone, as these antidepressants show similarities in their mode of action and are all associated with arthralgia. We suggest that this adverse drug reaction may be induced by enhanced 5HT1-mediated neurotransmission.
Insights
Mirtazapine use is linked to arthralgia (joint pain), supported by eight case reports. This adverse drug reaction may stem from enhanced serotonin 5HT1 neurotransmission.
Area of Science:
- Pharmacovigilance
- Clinical Case Studies
- Neuropharmacology
Background:
- Mirtazapine is a widely prescribed antidepressant.
- Arthralgia is a potential adverse drug reaction.
- Previous data suggested a possible link between mirtazapine and arthralgia.
Observation:
- The Netherlands Pharmacovigilance Centre Lareb collected eight case reports of arthralgia in patients using mirtazapine.
- Worldwide data on this association was also reviewed.
Findings:
- The case reports provide evidence supporting a link between mirtazapine and arthralgia.
- Mianserin and nefazodone, which share similarities with mirtazapine, are also associated with arthralgia.
Implications:
- The findings suggest that arthralgia is a plausible adverse drug reaction associated with mirtazapine.
- Enhanced 5HT1-mediated neurotransmission is proposed as a potential mechanism for mirtazapine-induced arthralgia.
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