Angelo Louise J, Lee Kelly C
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, CA, USA.
J Pharm Pract. 2013 Oct;26(5):514-7. doi: 10.1177/0897190013489573. Epub 2013 Jun 13.
Venlafaxine is a serotonin norepinephrine reuptake inhibitor that is used for mood, anxiety, and pain disorders. We report a case of dose-related paresthesias in association with venlafaxine use in a patient with major depressive disorder.
A young male patient with major depression started treatment with venlafaxine XR at 37.5 mg/d, and the dose was titrated to 75 mg/d with no significant adverse effects. Upon increasing the dose to 150 mg/d, the patient reported tingling, numbness, and itching in his upper extremities. The dose was reduced to 75 mg/d, at which time, the symptoms disappeared. Since the patient still had target symptoms of depression, the patient was willing to try increasing the dose back to 150 mg/d. Upon rechallenge, the tingling, numbness, and itching reappeared. The dose of venlafaxine was decreased back to 75 mg/d. Per the Naranjo scale, the probability score for the above adverse drug reaction is 5 (probable). We discuss the published evidence of paresthesias associated with antidepressants and clinical implications for recognizing paresthesias during venlafaxine treatment that may be useful for clinicians.
Clinicians need to be aware of the possible emergence of paresthesias with venlafaxine treatment, especially at doses of ≥ 150 mg/day. Patients who receive venlafaxine for pain disorders should be closely monitored for worsening of pain symptoms and may require adjustment of their doses.
文拉法辛是一种5-羟色胺去甲肾上腺素再摄取抑制剂,用于治疗情绪、焦虑和疼痛障碍。我们报告一例在重度抑郁症患者中使用文拉法辛出现与剂量相关的感觉异常的病例。
一名患有重度抑郁症的年轻男性患者开始使用文拉法辛缓释片治疗,起始剂量为37.5毫克/天,剂量滴定至75毫克/天,未出现明显不良反应。当剂量增加至150毫克/天时,患者报告上肢有刺痛、麻木和瘙痒感。剂量减至75毫克/天时,症状消失。由于患者仍有抑郁症的目标症状,患者愿意尝试将剂量增加回150毫克/天。再次给药后,刺痛、麻木和瘙痒再次出现。文拉法辛剂量再次减至75毫克/天。根据纳伦霍量表,上述药物不良反应的概率评分为5分(很可能)。我们讨论了已发表的与抗抑郁药相关的感觉异常的证据以及在文拉法辛治疗期间识别感觉异常的临床意义,这可能对临床医生有用。
临床医生需要意识到文拉法辛治疗可能出现感觉异常,尤其是在剂量≥150毫克/天的情况下。接受文拉法辛治疗疼痛障碍的患者应密切监测疼痛症状是否恶化,可能需要调整剂量。