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

CEREBRAL HAEMORRHAGE ( 9 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INJURY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TETANY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
VENIPUNCTURE SITE THROMBOSIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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