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

PRURITUS ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PURPURA ( 5 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
RASH SCARLATINIFORM ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
DEHYDRATION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
PERSISTENT GENERALISED LYMPHADENOPATHY ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
POISONING ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
CHILLS ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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