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

HYPOTENSION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SYNCOPE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DEATH ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
BASILAR MIGRAINE ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
HEPATIC VEIN DILATATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
CERVICOGENIC HEADACHE ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
COUGH ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERITONEAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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