It includes a wide array of symptoms from mild flushing and itching to lethal anaphylaxis. The pathogenic mechanisms by which the reactions occur are still unclear, although

they seem to vary SC79 widely among agents. The exact prevalence of these reactions is difficult to evaluate, and such a problems is hindering the establishment of treatments. Previously, pharmacoepidemiological studies have been conducted to confirm that adverse events have accompanied the use of cisplatin, carboplatin, and oxaliplatin [6, 7]. More than a million case reports on adverse events (AERs) submitted to the US Food and Drug Administration (FDA) database Quisinostat nmr were used, and a statistically significant association with an adverse event was detected as a signal, by applying standardized official pharmacovigilance methods [8–14]. This database relies on reports of spontaneous adverse events to the FDA generated

by health professionals, consumers, and manufacturers, and the system is referred ACY-738 to as the Adverse Event Reporting System (AERS). These platinum agents have been proven to cause nausea, vomiting, acute renal failure, neutropenia, thrombocytopenia, and peripheral sensory neuropathy [6]. In terms of susceptibility, their rank-order was consistent with clinical observations, suggesting the usefulness of the AERS database and the data mining method used [6]. The National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.0 was applied to evaluate the susceptibility to hypersensitivity reactions, and carboplatin

and oxaliplatin were proved to cause mild, GPX6 severe, or lethal reactions [7]. However, the same analytical method failed to detect signals for cisplatin-associated reactions [7]. In the present study, AERs submitted to the FDA were analyzed to detect signals for HSRs caused by paclitaxel, docetaxel, procarbazine, asparaginase, teniposide, and etoposide, in order to more clarify the critical factors to reproduce the clinical observations on HSRs. Additionally, agents thought to be associated with HSRs were also analyzed, including doxorubicin, 6-mercaptopurine, 5-fluorouracil, cyclophosphamide and cytarabine. Methods Data sources Input data for this study were taken from the public release of the FDA’s AERS database, which covers the period from the first quarter of 2004 through the end of 2009. The data structure of AERS is in compliance with international safety reporting guidance, ICH E2B, consisting of 7 data sets; patient demographic and administrative information (DEMO), drug/biologic information (DRUG), adverse events (REAC), patient outcomes (OUTC), report sources (RPSR), drug therapy start and end dates (THER), and indications for use/diagnosis (INDI). The adverse events in REAC are coded using preferred terms (PTs) in the Medical Dictionary for Regulatory Activities (MedDRA) terminology.