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

PNEUMONIA ( 18 FDA reports)
HODGKIN'S DISEASE ( 13 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 11 FDA reports)
DYSPNOEA ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
DIARRHOEA ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
FALL ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NOCARDIA TEST POSITIVE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RETCHING ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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