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

PLATELET COUNT DECREASED ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
CARDIAC MALPOSITION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NASAL OBSTRUCTION ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RHINOVIRUS INFECTION ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BREATH SOUNDS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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