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

COMPLETED SUICIDE ( 6 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
TREMOR ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)

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