Abstract

PurposeTizanidine, an alpha-adrenergic substance with antinociceptive and antihypertensive effects, is extensively metabolized via cytochrome P450 (CYP) 1A2. Therefore, coadministration with potent CYP1A2 inhibitors, such as ciprofloxacin, is contraindicated. However, both drugs are broadly utilized in various countries. Their concomitant use bears an inherent high risk for clinically significant symptoms, especially in multimorbid patients experiencing polypharmacy. This study aims to investigate the impact of coadministration of tizanidine and ciprofloxacin using real-world pharmacovigilance data and to raise awareness of this potentially underestimated safety issue.MethodsWe conducted a retrospective study including Individual Case Safety Reports (ICSR) registered until March 1, 2017, in the World Health Organization (WHO) global database. Demographic data, drug administration information, the course of the adverse drug reaction (ADR), its severity, and outcomes were analyzed for cases reporting ciprofloxacin comedication.ResultsIn 91 (2.0%) of the identified 4192 worldwide ICSR on tizanidine, coadministration of ciprofloxacin was reported. Most of the patients were female (n = 59, 64.8%) with a median age of 54 years (range 13–85 years). The countries contributing most reports were the USA (n = 54, 59.3%) and Switzerland (n = 16, 17.6%). ADRs reported most often affected the nervous system and the cardiac function, especially with large tizanidine doses or drugs with CNS and cardiovascular depressant effects. In two cases, a fatal outcome was reported.ConclusionDespite the existing formal contraindication, the concomitant use of tizanidine and ciprofloxacin can be observed in real-world clinical practice. Reactions mainly affected the central nervous and the cardiovascular system resulting in potentially severe adverse effects. The concomitant use of tizanidine and ciprofloxacin should absolutely be avoided.

Highlights

  • Tizanidine is an alpha-adrenergic substance reducing spasticity [1, 2]

  • Other reported comedications were analyzed for cytochrome P450 (CYP) interactions and classified based on their effects as central nervous system or cardiovascular depressants according to the labelling in the respective summary of product characteristics (SmPC)

  • All reported terms and Worldwide, 4192 Individual Case Safety Reports (ICSR) on tizanidine were identified in the World Health Organization (WHO) database in the study period

Read more

Summary

Introduction

Tizanidine is an alpha-adrenergic substance reducing spasticity [1, 2]. It is indicated for the treatment of painful muscle spasms, especially caused by multiple sclerosis, brain, or spinal. Tizanidine has a low oral bioavailability with a high first-pass effect, considerable interindividual variability, and a narrow therapeutic range [2, 4]. It is extensively metabolized via cytochrome P450 (CYP) 1A2 in the liver before it reaches the systemic circulation [2]. Coadministration with CYP1A2 inhibitors is not recommended and a formal contraindication exists for patients treated with strong CYP1A2 inhibitors, such as the fluoroquinolone antibiotic ciprofloxacin [5]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call