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

HIP FRACTURE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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