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

RASH MACULO-PAPULAR ( 22 FDA reports)
PURPURA ( 22 FDA reports)
VAGINAL HAEMORRHAGE ( 21 FDA reports)
RASH ERYTHEMATOUS ( 21 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
RECTAL HAEMORRHAGE ( 20 FDA reports)
MELAENA ( 17 FDA reports)
ARTHRALGIA ( 16 FDA reports)
HAEMORRHAGE ( 14 FDA reports)
BLOOD BLISTER ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
FINGER HYPOPLASIA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
COLITIS ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)

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