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

DIZZINESS ( 5 FDA reports)
HYPOTENSION ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use