A 57-year-old man developed leukopenia, thrombocytopenia, anaemia, skin rash, alopecia, nail changes and peripheral neuropathy during treatment with paclitaxel [nab-paclitaxel] and gemcitabine [routes not stated] while he was enrolled in metastatic pancreatic adenocarcinoma clinical trial.The man had been diagnosed with metastatic pancreatic cancer. He started receiving first line chemotherapy with paclitaxel at a dose of 125 mg/m 2 and gemcitabine at a dose of 1,000 mg/m 2 , both administered on days 1, 8, 15, 29, 36 and 43 of a 56 day cycle with subsequent cycles on days 1, 8, 15 of a 28 day cycle. He developed grade 3 leukopenia during cycle 2. Paclitaxel dose was reduced to 100 mg/m 2 and gemcitabine dose was reduced to 800 mg/m 2 . He received treatment with granulocyte colony-stimulating factor, but he again developed grade 3 leukopenia. Therefore, dose was further reduced to 75 mg/m 2 for paclitaxel and 600 mg/m 2 for gemcitabine. He also developed grade 1 thrombocytopenia, grade 2 anaemia, alopecia, skin rash, peripheral neuropathy and nail changes.The man had received a total of 12 cycles of chemotherapy. Later, he started second line chemotherapy as his pancreatic adenocarcinoma progressed. Subsequently, he developed peritoneal carcinomatosis and consecutive intestinal obstruction. At the end of September 2013, he died [Outcomes not stated].