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

GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
ANAEMIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
ENDOTOXIC SHOCK ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
THIRST ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
PHAGOCYTOSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ASCITES ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
STRESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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