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

DYSPNOEA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)

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