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IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
ASTHMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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