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

ANAEMIA ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BONE OPERATION ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BILE DUCT PRESSURE INCREASED ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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