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

AORTIC STENOSIS ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
IRON DEFICIENCY ANAEMIA ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
CARDIAC STRESS TEST ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
EXERCISE TOLERANCE DECREASED ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
PAIN ( 4 FDA reports)
CONTUSION ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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