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

VOMITING ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)

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