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

SOMNOLENCE ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
URETHRAL REPAIR ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DEATH ( 1 FDA reports)
COLITIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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