Please choose an event type to view the corresponding MedsFacts report:

DIARRHOEA ( 6 FDA reports)
SPLENOMEGALY ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 5 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
HEADACHE ( 3 FDA reports)
URTICARIA ( 2 FDA reports)
COLITIS ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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