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

PANOPHTHALMITIS ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
DEATH ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
CHILLS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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