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

ASTHMA ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
THIRST ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
INFECTION ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
INJURY ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MALAISE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
COMA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ABSCESS ( 1 FDA reports)

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