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

DIARRHOEA ( 67 FDA reports)
ANAEMIA ( 39 FDA reports)
NEUTROPHIL COUNT DECREASED ( 33 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 29 FDA reports)
BLOOD CREATININE INCREASED ( 28 FDA reports)
PLATELET COUNT DECREASED ( 26 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 21 FDA reports)
PLEURAL EFFUSION ( 19 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 18 FDA reports)
DYSPNOEA ( 18 FDA reports)
ASCITES ( 17 FDA reports)
ILEUS PARALYTIC ( 17 FDA reports)
PYREXIA ( 17 FDA reports)
NAUSEA ( 16 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
DEHYDRATION ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
HYPERURICAEMIA ( 13 FDA reports)
INTESTINAL OBSTRUCTION ( 12 FDA reports)
TUMOUR LYSIS SYNDROME ( 12 FDA reports)
VOMITING ( 12 FDA reports)
CONSTIPATION ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
ADMINISTRATION RELATED REACTION ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
BLOOD MAGNESIUM DECREASED ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
PERITONSILLITIS ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
RASH ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
COUGH ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
ILEUS ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MELAENA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SHOCK ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CALCIPHYLAXIS ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
DANDRUFF ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIVER CARCINOMA RUPTURED ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CANDIDA ENDOPHTHALMITIS ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PUTAMEN HAEMORRHAGE ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ASTEATOSIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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