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

VOMITING ( 11 FDA reports)
HYPOTENSION ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
MELAENA ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
FALL ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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