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

HYPOTENSION ( 18 FDA reports)
DYSPNOEA ( 15 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 12 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
COAGULOPATHY ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
EPISTAXIS ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
MELAENA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CARDIORENAL SYNDROME ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
RASH ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SWELLING ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
COMA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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