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

PNEUMONIA ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
PYREXIA ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
VOMITING ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
DEATH ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)

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