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

PYREXIA ( 28 FDA reports)
INTERSTITIAL LUNG DISEASE ( 26 FDA reports)
FEBRILE NEUTROPENIA ( 25 FDA reports)
MALAISE ( 22 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 17 FDA reports)
BRONCHITIS ( 16 FDA reports)
COUGH ( 16 FDA reports)
DYSPNOEA ( 16 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
OROPHARYNGEAL PAIN ( 16 FDA reports)
RALES ( 16 FDA reports)
ORTHOSTATIC HYPOTENSION ( 13 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
ARTHRALGIA ( 12 FDA reports)
RHEUMATOID ARTHRITIS ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
LEUKOPENIA ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
MULTIPLE MYELOMA ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
SHOCK HAEMORRHAGIC ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMORRHAGIC DIATHESIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHILLS ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RASH ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBRIN DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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