Liver Toxicity From Solifenacin.

نویسندگان

  • Umair Masood
  • Anuj Sharma
  • Divey Manocha
چکیده

To the Editor: An 84-year-old woman with a history of end-stage renal disease presented to the hospital with abdominal pain and bilious vomiting. On admission, she was found to have significant elevation in serum aminotransferases (AST 5 367 U/L and ALT 5 639 U/L,) and marginal elevation in alkaline phosphatase level (171 U/L). Basic metabolic panel was at her baseline. A thorough investigation to rule out various causes of acute liver injury was found to be negative (Table 1). On further investigation, it was found that patient was recently started on solifenacin (5 mg PO daily) 2 weeks before presentation. On discontinuation of the drug, patient’s liver function tests significantly improved over the course of next 2 days with eventual normalization on follow-up after 2 weeks of discharge. Solifenacin is a drug commonly used to control symptoms of an overactive bladder. Common side effects include dry mouth, constipation, and blurred vision due to its anticholinergic properties. Although it is metabolized in the liver, liver toxicity is not a known side effect of the drug. The temporal association of the liver injury with respect to the initiation of solifenacin and resolution of liver function tests after its discontinuation implicate the drug as the causative agent for the liver injury in our patient. In addition, negative extensive workup performed to rule out other causes of liver injury further solidifies this conclusion. As solifenacin is mostly excreted by the kidneys, it is possible that the drug may have reached toxic levels in our patient due to her end-stage renal disease. Our patient had a hepatocellular pattern of liver injury illustrated by significant elevation in aminotranferases compared with alkaline phosphatase and a Roussel Uclaf Causality Assessment Method (RUCAM) ratio of 12.5. Further investigation would need to be performed to determine the mechanism of liver injury induced by solifenacin. Because of clinical improvement, a liver biopsy was not indicated and not performed in this case. Nonetheless, our case identifies solifenacin as a potential cause of liver toxicity making it important for clinicians to recognize this side effect to perhaps prevent serious outcomes such as fulminant hepatic failure. Umair Masood, MD Anuj Sharma, MD Divey Manocha, MD Department of Medicine, State University of New York Upstate Medical University Syracuse, NY

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Open-label study of the safety and pharmacokinetics of solifenacin in subjects with hepatic impairment.

Determining the pharmacokinetics and safety of solifenacin succinate, a once-daily, oral antimuscarinic agent indicated for treatment of overactive bladder, in subjects with hepatic impairment. In this open-label study, 16 subjects (eight with moderate hepatic impairment [defined as a Child-Pugh score of 7 - 9], eight healthy) received a single oral 10 mg solifenacin dose. Blood and urine were ...

متن کامل

A semiphysiological population model for prediction of the pharmacokinetics of drugs under liver and renal disease conditions.

The application of model-based drug development in special populations becomes increasingly important for clinical trial optimization, mostly by providing a rationale for dose selection and thereby aiding risk-benefit assessment. In this article, a semiphysiological approach is presented, enabling the extrapolation of the pharmacokinetics from healthy subjects to patients with different disease...

متن کامل

Microsoft Word - 89773423-file00

The application of model-based drug development in special populations becomes increasingly important for clinical trial optimization, mostly by providing rationale for dose selection and thereby aiding risk-benefit assessment. In this paper, a semi-physiological approach is presented enabling the extrapolation of the pharmacokinetics from healthy subjects to patients with different disease con...

متن کامل

Solifenacin in Multiple Sclerosis Patients with Overactive Bladder: A Prospective Study

Objective. To assess the efficacy and the effect on Qol of solifenacin for the treatment of OAB in MS patients. Patients and Methods. Thirty MS patients suffering from OAB were treated with solifenacin 5/10 mg for 8 weeks. The first 4 weeks patients received solifenacin 5 mg. At week 4 patients could request a dose increase to 10 mg. The efficacy was evaluated at 8 weeks. Results. After 4 weeks...

متن کامل

Clinical Study Solifenacin inMultiple Sclerosis Patients with Overactive Bladder: A Prospective Study

Objective. To assess the efficacy and the effect on Qol of solifenacin for the treatment of OAB in MS patients. Patients and Methods. Thirty MS patients suffering from OAB were treated with solifenacin 5/10 mg for 8 weeks. The first 4 weeks patients received solifenacin 5 mg. At week 4 patients could request a dose increase to 10 mg. The efficacy was evaluated at 8 weeks. Results. After 4 weeks...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • American journal of therapeutics

دوره 24 4  شماره 

صفحات  -

تاریخ انتشار 2017