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The most important serious adverse events associated with SUTENT® (sunitinib) treatment of solid tumour patients were pulmonary embolism, thrombocytopenia, tumour haemorrhage, febrile neutropenia, and hypertension.
The most very common adverse events of any grade included: fatigue; gastrointestinal disorders, such as diarrhoea, nausea, stomatitis, dyspepsia and vomiting; skin discolouration; rash; hand-foot syndrome (palmar-plantar erythrodysaesthesia; dry skin; hair colour changes; mucosal inflammation; asthenia, dysgeusia, anorexia and hypertension. Fatigue, hypertension and neutropenia were the most common adverse events of Grade 3 maximum severity; and increased lipase was the most frequently occurring adverse event of Grade 4 maximum severity in patients with solid tumours.a
The treatment-emergent, all causality frequency of adverse events reported in patients who received SUTENT® (sunitinib) in single-medicine studies in advanced RCC, GIST and pNET and from post-marketing experience are listed below, by system organ class, frequency category and grade of severity.
Frequencies are defined as: very common (1/10), common (1/100 to < 1/10), uncommon (1/1 000 to < 1/100), rare (1/10 000 to < 1/1000), very rare (< 1/10 000).
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