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

PHOTOSENSITIVITY REACTION ( 5 FDA reports)
ANAEMIA ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
BACK PAIN ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
RASH ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)

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