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

RESPIRATORY FAILURE ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
ASCITES ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELOCYTE PRESENT ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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