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

NAUSEA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOCRIT NORMAL ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
ANTERIOR CHAMBER FLARE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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