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

DYSPNOEA ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
LETHARGY ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FALL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SWELLING ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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