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

LIGAMENT RUPTURE ( 5 FDA reports)
SEPSIS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
DEATH ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
ILEUS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
LEUKODERMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
COMA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)

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