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MALAISE ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
STOMATITIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
INSOMNIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
RASH ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
ANGER ( 1 FDA reports)
DEATH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
AGITATION ( 1 FDA reports)

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