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

THROMBOCYTOPENIA ( 18 FDA reports)
PNEUMONIA ( 17 FDA reports)
NEUTROPENIA ( 15 FDA reports)
DIARRHOEA ( 11 FDA reports)
CONSTIPATION ( 9 FDA reports)
GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
CANDIDIASIS ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
INFECTION ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
VANISHING BILE DUCT SYNDROME ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUCORMYCOSIS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PRODUCT PACKAGING ISSUE ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BURKITT'S LEUKAEMIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL NECROSIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SIALOCELE ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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