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

MYOCARDIAL INFARCTION ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
FALL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
PAIN ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)

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