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MUCORMYCOSIS ( 5 FDA reports)
GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
ZYGOMYCOSIS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
LUNG DISORDER ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
ASCITES ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NASAL NECROSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
PAIN ( 1 FDA reports)
PELVIC KIDNEY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
ACRODERMATITIS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RENAL AGENESIS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
UTEROVAGINAL PROLAPSE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)

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