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

EXTRAPYRAMIDAL DISORDER ( 12 FDA reports)
EMBOLISM VENOUS ( 10 FDA reports)
STOMATITIS ( 10 FDA reports)
ANAEMIA ( 7 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
DEATH ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ELECTROLYTE DEPLETION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
ILEUS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)

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