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EPIGLOTTITIS ( 8 FDA reports)
COUGH ( 8 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
LARYNGITIS ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
AGITATION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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