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

PYREXIA ( 18 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 16 FDA reports)
STEVENS-JOHNSON SYNDROME ( 15 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
PNEUMOTHORAX ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
HEPATITIS B ( 11 FDA reports)
CONVULSION ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
LEUKOPENIA ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
DIARRHOEA ( 7 FDA reports)
ILEUS ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
BLISTER ( 6 FDA reports)
CYST ( 6 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ASCITES ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTROPLEURAL FISTULA ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OVARIAN CANCER RECURRENT ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FEAR ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
ILEAL STENOSIS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SURGERY ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THIRST ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DURAL ABSCESS ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PARANEOPLASTIC ENCEPHALOMYELITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURAL FISTULA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR METAL TEST ABNORMAL ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RALES ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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