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

DEATH ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
NEUTROPENIA ( 13 FDA reports)
THROMBOCYTOPENIA ( 13 FDA reports)
FEBRILE NEUTROPENIA ( 12 FDA reports)
VOMITING ( 12 FDA reports)
FATIGUE ( 10 FDA reports)
FALL ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
ASTHMA ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 6 FDA reports)
ARTHRITIS BACTERIAL ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
INFECTION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SWELLING ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
BACTERAEMIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 3 FDA reports)
ANAL STENOSIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COUGH ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL HAEMATOMA ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENTEROBACTER SEPSIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
RASH ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOROIDAL HAEMORRHAGE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRONKHITE-CANADA SYNDROME ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHYSICAL TESTICLE EXAMINATION ABNORMAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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