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

PYREXIA ( 23 FDA reports)
DYSPNOEA ( 13 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
VOMITING ( 11 FDA reports)
HEPATITIS ( 8 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HYPERCAPNIA ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 6 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
COMA ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
AGITATION ( 1 FDA reports)
ANTI-HBC ANTIBODY NEGATIVE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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