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

PYREXIA ( 9 FDA reports)
FATIGUE ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
WOUND HAEMORRHAGE ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONSTIPATION ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
FALL ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FEAR ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
COUGH ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
WOUND ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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