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

PSEUDOMONAS INFECTION ( 19 FDA reports)
ECZEMA ( 18 FDA reports)
SKIN ULCER ( 15 FDA reports)
SKIN HYPERPIGMENTATION ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
PRURITUS ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
RASH MACULO-PAPULAR ( 11 FDA reports)
CONTUSION ( 10 FDA reports)
DRY SKIN ( 10 FDA reports)
GANGRENE ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PITTING OEDEMA ( 10 FDA reports)
RASH PRURITIC ( 10 FDA reports)
SEPTAL PANNICULITIS ( 10 FDA reports)
TACHYCARDIA ( 10 FDA reports)
THROMBOPHLEBITIS ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
XEROSIS ( 10 FDA reports)
ARTHROPOD BITE ( 9 FDA reports)
DECUBITUS ULCER ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
DRY GANGRENE ( 8 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 8 FDA reports)
ATELECTASIS ( 7 FDA reports)
CHILLS ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 7 FDA reports)
LOBAR PNEUMONIA ( 7 FDA reports)
CYANOSIS ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
BEHCET'S SYNDROME ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
GLUCAGONOMA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ENTEROCOLITIS VIRAL ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
BITE ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NECROSIS ISCHAEMIC ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
SCAB ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC INDEX INCREASED ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use