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ASCITES ( 9 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 8 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
DIARRHOEA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
PSEUDOCYST ( 4 FDA reports)
SHOCK ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
BACK PAIN ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
COMA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)

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