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PARKINSON'S DISEASE ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
SOMNOLENCE ( 4 FDA reports)
NODULE ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RASH ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
INDURATION ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
FALL ( 3 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
VIRUS STOOL TEST POSITIVE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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