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

DEAFNESS NEUROSENSORY ( 7 FDA reports)
DIZZINESS ( 4 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COMA ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
FALL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)

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