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

MEDICATION ERROR ( 6 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FALL ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
RASH ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERMEDIATE UVEITIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POISONING ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILLARY DEFORMITY ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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