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PANCREATITIS ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
HEPATITIS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
INFECTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FALL ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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