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

DYSPNOEA ( 7 FDA reports)
ERYTHEMA ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 4 FDA reports)
HEPATOBILIARY DISEASE ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
RASH ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BUNION ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CRANIAL NERVE PARALYSIS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FALL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASS ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYURIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
UNWANTED PREGNANCY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARACENTESIS ABDOMEN ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)

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