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

FALL ( 6 FDA reports)
CHEST PAIN ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BREAST INJURY ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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