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

DIARRHOEA ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
FALL ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
RASH ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL FAILURE NEONATAL ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RETCHING ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VOCAL CORD NEOPLASM ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIAL NERVE INFECTION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOSTHENURIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENIN-ANGIOTENSIN SYSTEM INHIBITION ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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