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

PYREXIA ( 7 FDA reports)
DIARRHOEA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)

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