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

PYREXIA ( 37 FDA reports)
HEPATIC ENCEPHALOPATHY ( 33 FDA reports)
PLATELET COUNT DECREASED ( 31 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 27 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 25 FDA reports)
ANAEMIA ( 22 FDA reports)
RENAL IMPAIRMENT ( 21 FDA reports)
HEPATIC FAILURE ( 17 FDA reports)
RASH ( 17 FDA reports)
DIARRHOEA ( 16 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 16 FDA reports)
SEPSIS ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
HEPATIC CIRRHOSIS ( 14 FDA reports)
LIPASE INCREASED ( 14 FDA reports)
INFECTIOUS PERITONITIS ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ILEUS PARALYTIC ( 12 FDA reports)
MALAISE ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
LIVER CARCINOMA RUPTURED ( 10 FDA reports)
ASCITES ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
RETROPERITONEAL ABSCESS ( 8 FDA reports)
CHOLANGITIS ( 7 FDA reports)
HYPERAMMONAEMIA ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPERLACTACIDAEMIA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD CHLORIDE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
ILEUS ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
PERIHEPATIC ABSCESS ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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