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STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
PERITONITIS SCLEROSING ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
FUNGAL PERITONITIS ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
ABASIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
COMA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)

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