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NEPHROGENIC SYSTEMIC FIBROSIS ( 9 FDA reports)
PNEUMONIA ( 6 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INFECTIVE TENOSYNOVITIS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PAIN ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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