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

ASTHENIA ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
KETOSIS ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
CHROMATURIA ( 2 FDA reports)
COMA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FALL ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SALIVARY GLAND ADENOMA ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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