Purpose: Studies have documented potential drug-drug interactions (pDDI's) occurring in cancer patients mainly with solid malignancies, either in the ambulatory or hospital settings. While hematopoietic stem cell transplant (HSCT) patients during their bone marrow transplantation unit (BMTU) stay have rather complex medical regimens combining chemotherapy, anti-infectious agents, immunosuppressive agents and supportivecare drugs, studies on potential DDI's are lacking. Our objective was to evaluate the prevalence and the density of pharmacokinetic and pharmacodynamic potential DDI's, and the evolution of the renal function in hematopoietic stem cell transplant (HSCT) adult recipients during their BMTU stay. Method: retrospective study in 31 adult patients consecutively admitted to the BMTU. Results: Prevalence of pharmacokinetic interactions was 10-time lower than the pharmacodynamic interactions. The contra-indications were rare, and only of pharmacokinetic origin. The main drugs involved in pharmacokinetic DDI's were ciclosporine, methotrexate, esomeprazole, tramadol and vincristine. The median number of potential nephrotoxicity-related DDI's per patient was 7 and the median number of days during which nephrotoxicity-related DDI's potentially occurred was 77 days per patient. The decrease in glomerular filtration rate (GFR) throughout the BMTU stay (mean decrease of 13 ml/min) was correlated with the number of days of potential nephrotoxic drug interactions. Conclusions: Potential DDI's in HCST patients in BMTU were quite common. The DDI's from pharmacokinetic origin were less frequent, but of higher grade, than those of pharmacodynamic origin. The decrease in GFR suggests that the density of potential nephrotoxic drug interactions may be an issue to be considered in these patients.