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

PYREXIA ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
RENAL FAILURE CHRONIC ( 10 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RASH ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INJURY ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MANIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
URINARY BLADDER SARCOMA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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