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

ANAEMIA ( 11 FDA reports)
PNEUMONIA ( 7 FDA reports)
HYPERTENSION ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
ORAL INTAKE REDUCED ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
COMA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
AGEUSIA ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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