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

FEBRILE NEUTROPENIA ( 154 FDA reports)
PNEUMONIA ( 135 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 67 FDA reports)
SEPSIS ( 66 FDA reports)
PYREXIA ( 60 FDA reports)
NAUSEA ( 57 FDA reports)
THROMBOCYTOPENIA ( 51 FDA reports)
HYPOTENSION ( 50 FDA reports)
NEUTROPENIA ( 48 FDA reports)
HAEMOGLOBIN DECREASED ( 46 FDA reports)
PLATELET COUNT DECREASED ( 46 FDA reports)
FATIGUE ( 44 FDA reports)
DIARRHOEA ( 40 FDA reports)
DYSPNOEA ( 36 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 35 FDA reports)
PANCYTOPENIA ( 34 FDA reports)
ANAEMIA ( 31 FDA reports)
DEATH ( 31 FDA reports)
RENAL FAILURE ( 31 FDA reports)
ASTHENIA ( 28 FDA reports)
BLOOD UREA INCREASED ( 28 FDA reports)
BLOOD CREATININE INCREASED ( 26 FDA reports)
HYPOXIA ( 25 FDA reports)
INFECTION ( 25 FDA reports)
MULTI-ORGAN FAILURE ( 25 FDA reports)
PAIN ( 25 FDA reports)
PLEURAL EFFUSION ( 25 FDA reports)
NEUTROPHIL COUNT DECREASED ( 24 FDA reports)
ABDOMINAL PAIN ( 23 FDA reports)
DEHYDRATION ( 23 FDA reports)
DISEASE PROGRESSION ( 23 FDA reports)
RESPIRATORY FAILURE ( 22 FDA reports)
MYELODYSPLASTIC SYNDROME ( 21 FDA reports)
HEPATIC FAILURE ( 20 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 20 FDA reports)
RENAL FAILURE ACUTE ( 20 FDA reports)
RASH ( 19 FDA reports)
ATRIAL FIBRILLATION ( 18 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
BLOOD SODIUM DECREASED ( 17 FDA reports)
CARDIAC FAILURE ( 17 FDA reports)
CELLULITIS ( 17 FDA reports)
COUGH ( 17 FDA reports)
CONSTIPATION ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
HAEMORRHAGE ( 16 FDA reports)
CHILLS ( 15 FDA reports)
VOMITING ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
PULMONARY HAEMORRHAGE ( 14 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
FALL ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
RESPIRATORY DISTRESS ( 13 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 12 FDA reports)
LUNG DISORDER ( 12 FDA reports)
NO THERAPEUTIC RESPONSE ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BACTERAEMIA ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
ABORTION INDUCED ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
CEREBRAL HAEMORRHAGE ( 10 FDA reports)
COLITIS ( 10 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
FIRST TRIMESTER PREGNANCY ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
MYOCARDIAL ISCHAEMIA ( 10 FDA reports)
PULMONARY FIBROSIS ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BONE MARROW FAILURE ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
SUDDEN DEATH ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ANAL ABSCESS ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
MALAISE ( 8 FDA reports)
MOUTH HAEMORRHAGE ( 8 FDA reports)
ORGAN FAILURE ( 8 FDA reports)
PNEUMONIA FUNGAL ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
ASCITES ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
THROMBOCYTOSIS ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABSCESS ( 6 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ARTERIAL THROMBOSIS ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CAECITIS ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
HAEMATOTOXICITY ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
LEFT VENTRICULAR FAILURE ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PHLEBITIS ( 6 FDA reports)
PRESYNCOPE ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
SURGERY ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
TREMOR ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
APLASIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEUKAEMIA CUTIS ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MYCOPLASMA TEST POSITIVE ( 3 FDA reports)
MYOCARDITIS BACTERIAL ( 3 FDA reports)
NECROTISING GASTRITIS ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROTHROMBIN TIME ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
BARTHOLIN'S CYST ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEPTOSPIROSIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RALES ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
VASCULAR ANOMALY ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIPOSARCOMA METASTATIC ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHILIC PANNICULITIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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