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

NAUSEA ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
OVERDOSE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
DEATH ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
FALL ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use