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

CHEST PAIN ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
VOMITING ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)

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