Drug safety surveillance within a strategy for the management of non-chemotherapy drug-induced neutropenia.
José Luis Revuelta-HerreroRaquel García-SánchezJavier Anguita-VelascoAna de Lorenzo-PintoCristina Ortega-NavarroMaría Sanjurjo-SáezPublished in: International journal of clinical pharmacy (2019)
Background Severe non-chemotherapy drug-induced neutropenia is a rare idiosyncratic drug reaction that is considered potentially fatal. Objective To report, in terms of drug safety surveillance, the results of an institutional strategy for NCDIN. Method An observational and prospective study including all adult patients who received filgrastim for the treatment of NCDIN from June 2015 to December 2017 was carried out by hematologists and clinical pharmacists. Results 13 patients with severe NCDIN were included in the study. The median age was 51 (range 24-80) years old and 46.2% were male. Seven patients had one or more negative prognostic factors (age > 65 years, renal impairment, autoimmune diseases and/or a neutrophil count at diagnosis < 0.1 × 109 cells/L). A single drug was identified as causative in 3 patients, while in 10 cases, 2-3 drugs were considered as potentially causative. The most frequent drugs were metamizole, piperacillin/tazobactam, dexketoprofen and linezolid, among others. Seven patients developed NCDIN during their hospital stay while 6 were admitted to the emergency department. Patients were using a median of 11 drugs (IQR 8-15) at the time of diagnosis. No deaths were recorded. Conclusion Metamizole and piperacillin/tazobactam are the most common drugs linked to non-chemotherapy drug-induced neutropenia in our cohort.
Keyphrases
- drug induced
- liver injury
- prognostic factors
- end stage renal disease
- emergency department
- ejection fraction
- newly diagnosed
- chronic kidney disease
- adverse drug
- peritoneal dialysis
- healthcare
- primary care
- radiation therapy
- signaling pathway
- young adults
- electronic health record
- general practice
- chemotherapy induced
- cell cycle arrest
- locally advanced
- replacement therapy