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

NEPHROGENIC SYSTEMIC FIBROSIS ( 33 FDA reports)
GANGRENE ( 27 FDA reports)
LEG AMPUTATION ( 21 FDA reports)
ANXIETY ( 18 FDA reports)
TREMOR ( 15 FDA reports)
TOE AMPUTATION ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
SLEEP DISORDER ( 15 FDA reports)
PULMONARY HYPERTENSION ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
BLOOD DISORDER ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
CELLULITIS ( 15 FDA reports)
PAIN ( 15 FDA reports)
COUGH ( 15 FDA reports)
OSTEOMYELITIS ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
MULTIPLE INJURIES ( 15 FDA reports)
MENTAL STATUS CHANGES ( 15 FDA reports)
INFECTION ( 15 FDA reports)
IMPAIRED HEALING ( 15 FDA reports)
ABASIA ( 12 FDA reports)
HEMIPARESIS ( 12 FDA reports)
MENTAL DISORDER ( 12 FDA reports)
FOOT AMPUTATION ( 12 FDA reports)
DISEASE COMPLICATION ( 12 FDA reports)
PERONEAL NERVE PALSY ( 12 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 12 FDA reports)
PROCEDURAL PAIN ( 12 FDA reports)
RADICULOPATHY ( 12 FDA reports)
SCIATICA ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 12 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
GOUT ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
SINUS ARRHYTHMIA ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
NAUSEA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)

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