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

DEATH ( 19 FDA reports)
DYSPNOEA ( 17 FDA reports)
INFUSION RELATED REACTION ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
PYREXIA ( 17 FDA reports)
PNEUMONIA ( 16 FDA reports)
FEBRILE NEUTROPENIA ( 13 FDA reports)
RASH ( 13 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
DIARRHOEA ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
CHEST PAIN ( 9 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
VOMITING ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
CHILLS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
TREMOR ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CSF TEST ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS B DNA DECREASED ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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