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

HYPOGLYCAEMIA ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
RENAL FAILURE ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
SEDATION ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
AKINESIA ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GINGIVAL PAIN ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DEATH ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ADMINISTRATION SITE REACTION ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)

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