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

INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
BACK PAIN ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FLAVOBACTERIUM TEST POSITIVE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
FALL ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)

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