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

RASH ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
VOMITING ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)

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