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

ATAXIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
ANAEMIA ( 5 FDA reports)
BRADYKINESIA ( 5 FDA reports)
PERICARDITIS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
VOMITING ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)

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