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

ANGIONEUROTIC OEDEMA ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
HYPOTENSION ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use