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

DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
NAUSEA ( 7 FDA reports)
ANAEMIA ( 5 FDA reports)
ACNE ( 4 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
INFECTION ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
VOMITING ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)

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