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

INTERSTITIAL LUNG DISEASE ( 29 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 26 FDA reports)
RENAL IMPAIRMENT ( 23 FDA reports)
DECREASED APPETITE ( 21 FDA reports)
ANAEMIA ( 19 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 17 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
CEREBRAL INFARCTION ( 15 FDA reports)
DIARRHOEA ( 15 FDA reports)
PYREXIA ( 15 FDA reports)
HYPERKALAEMIA ( 14 FDA reports)
MELAENA ( 14 FDA reports)
HYPERTENSION ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
RASH ( 11 FDA reports)
DEHYDRATION ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
FALL ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
OVARIAN NEOPLASM ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ASCITES ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEPENDENCE ON RESPIRATOR ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
GRAFT LOSS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)

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