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LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
VOMITING ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
ANGER ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COMA ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
AURA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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