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

PLATELET COUNT DECREASED ( 22 FDA reports)
ANAEMIA ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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