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PRODUCT QUALITY ISSUE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
ASTHENIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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