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

RENAL FAILURE ACUTE ( 19 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 16 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
BILE DUCT OBSTRUCTION ( 10 FDA reports)
CHOLANGITIS ACUTE ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
DYSPHONIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
BRADYCARDIA ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
VIRAL TEST POSITIVE ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
DEVICE DISLOCATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BIOPSY PROSTATE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
RADICAL PROSTATECTOMY ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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