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BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
PLEURAL EFFUSION ( 16 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
BLOOD UREA INCREASED ( 14 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 13 FDA reports)
BLOOD URIC ACID INCREASED ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
FEBRILE NEUTROPENIA ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 13 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
PROTEIN TOTAL INCREASED ( 12 FDA reports)
FUNGAL DNA TEST POSITIVE ( 11 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
BASOPHIL COUNT DECREASED ( 10 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
MULTIPLE MYELOMA ( 7 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
RASH ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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