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

HYPERHIDROSIS ( 5 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
VOMITING ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
PAIN ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)

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