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

RENAL FAILURE ACUTE ( 11 FDA reports)
EMBOLISM ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
VENOUS THROMBOSIS ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
VENOUS THROMBOSIS LIMB ( 7 FDA reports)
SPLENIC INFARCTION ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
INTESTINAL GANGRENE ( 7 FDA reports)
DEHYDRATION ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYDROCEPHALUS ( 6 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
TACHYCARDIA ( 4 FDA reports)
DYSPNOEA ( 3 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
GOITRE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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