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

LIVER DISORDER ( 5 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
CRYING ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
ERYTHEMA ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
RASH ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)

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