Serum concentration as a predictor of tigecycline-induced hypofibrinogenemia in critically ill patients: A retrospective cohort study
Author:
Publisher
Elsevier BV
Subject
Infectious Diseases,Microbiology (medical),General Medicine
Reference23 articles.
1. Tigecycline-associated hypofibrinogenemia in a real-world setting;Campany-Herrero;Int J Clin Pharm,2020
2. Tigecycline 300 cSSSI Study Group, Tigecycline 305 cSSSI Study Group. The efficacy and safety of tigecycline in the treatment of skin and skin-structure infections: results of 2 double-blind phase 3 comparison studies with vancomycin-aztreonam;Ellis-Grosse;Clin Infect Dis,2005
3. Best practice in therapeutic drug monitoring;Gross;Br J Clin Pharmacol,2001
4. Clinical characteristics and risk factors of tigecycline-associated hypofibrinogenaemia in critically ill patients;Hu;Eur J Clin Pharmacol,2020
5. Adverse event profile of tigecycline: data mining of the public version of the U.S. Food and Drug Administration adverse event reporting system;Kadoyama;Biol Pharm Bull,2012
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1. Mid‐dosing interval concentration is important for polymyxin B exposure and acute kidney injury in critically ill patients;CPT: Pharmacometrics & Systems Pharmacology;2023-09-17
2. Comparison of bleeding risk and hypofibrinogenemia-associated risk factors between tigecycline with cefoperazone/sulbactam therapy and other tigecycline-based combination therapies;Frontiers in Pharmacology;2023-06-07
3. Pharmacokinetic/Pharmacodynamic Target Attainment of Tigecycline in Patients with Hepatic Impairment in a Real-World Setting;Therapeutic Drug Monitoring;2023-06-02
4. Tigecycline;Reactions Weekly;2022-10-08
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