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

RENAL FAILURE ( 715 FDA reports)
PAIN ( 568 FDA reports)
INJURY ( 478 FDA reports)
ANXIETY ( 476 FDA reports)
UNEVALUABLE EVENT ( 440 FDA reports)
RENAL IMPAIRMENT ( 425 FDA reports)
FEAR ( 401 FDA reports)
EMOTIONAL DISTRESS ( 381 FDA reports)
MULTI-ORGAN FAILURE ( 370 FDA reports)
RENAL INJURY ( 361 FDA reports)
STRESS ( 325 FDA reports)
SEPSIS ( 287 FDA reports)
PYREXIA ( 274 FDA reports)
RESPIRATORY FAILURE ( 270 FDA reports)
ANHEDONIA ( 267 FDA reports)
DEATH ( 253 FDA reports)
RENAL FAILURE ACUTE ( 220 FDA reports)
PNEUMONIA ( 218 FDA reports)
HYPOTENSION ( 192 FDA reports)
PLEURAL EFFUSION ( 189 FDA reports)
ANAEMIA ( 177 FDA reports)
PLATELET COUNT DECREASED ( 155 FDA reports)
DEPRESSION ( 149 FDA reports)
DYSPNOEA ( 149 FDA reports)
ASCITES ( 147 FDA reports)
THROMBOCYTOPENIA ( 140 FDA reports)
BLOOD BILIRUBIN INCREASED ( 130 FDA reports)
HAEMOGLOBIN DECREASED ( 125 FDA reports)
DIARRHOEA ( 118 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 115 FDA reports)
CARDIAC ARREST ( 109 FDA reports)
BLOOD POTASSIUM DECREASED ( 100 FDA reports)
PULMONARY OEDEMA ( 97 FDA reports)
SEPTIC SHOCK ( 97 FDA reports)
VOMITING ( 97 FDA reports)
CEREBROVASCULAR ACCIDENT ( 92 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 90 FDA reports)
OEDEMA PERIPHERAL ( 89 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 88 FDA reports)
HEPATITIS C ( 88 FDA reports)
HEPATIC FAILURE ( 85 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 84 FDA reports)
NAUSEA ( 83 FDA reports)
BLOOD PRESSURE DECREASED ( 82 FDA reports)
CARDIAC FAILURE ( 82 FDA reports)
LOSS OF CONSCIOUSNESS ( 82 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 78 FDA reports)
ERYTHEMA ( 77 FDA reports)
PANCYTOPENIA ( 76 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 73 FDA reports)
RASH ( 73 FDA reports)
FEBRILE NEUTROPENIA ( 72 FDA reports)
INFECTION ( 71 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 70 FDA reports)
CONVULSION ( 69 FDA reports)
HYPOKALAEMIA ( 69 FDA reports)
HYPERTENSION ( 68 FDA reports)
MYOCARDIAL INFARCTION ( 68 FDA reports)
CELLULITIS ( 67 FDA reports)
ASTHENIA ( 65 FDA reports)
ABDOMINAL DISTENSION ( 64 FDA reports)
BLOOD CREATININE INCREASED ( 64 FDA reports)
FATIGUE ( 63 FDA reports)
NEUTROPENIA ( 63 FDA reports)
ABDOMINAL PAIN ( 62 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 62 FDA reports)
CONDITION AGGRAVATED ( 62 FDA reports)
SHOCK ( 62 FDA reports)
CARDIO-RESPIRATORY ARREST ( 61 FDA reports)
LIVER DISORDER ( 59 FDA reports)
BLOOD UREA INCREASED ( 58 FDA reports)
OEDEMA ( 58 FDA reports)
ATRIAL FIBRILLATION ( 55 FDA reports)
DEHYDRATION ( 55 FDA reports)
HYPOALBUMINAEMIA ( 55 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 54 FDA reports)
RESPIRATORY DISTRESS ( 54 FDA reports)
TREMOR ( 52 FDA reports)
HYPOXIA ( 51 FDA reports)
BRADYCARDIA ( 50 FDA reports)
DISEASE PROGRESSION ( 50 FDA reports)
HYPONATRAEMIA ( 50 FDA reports)
HYPERKALAEMIA ( 48 FDA reports)
MALAISE ( 47 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 47 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 46 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 46 FDA reports)
FALL ( 46 FDA reports)
DIABETES MELLITUS ( 45 FDA reports)
STEVENS-JOHNSON SYNDROME ( 45 FDA reports)
TACHYCARDIA ( 44 FDA reports)
BONE MARROW FAILURE ( 43 FDA reports)
HAEMATOCRIT DECREASED ( 43 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 43 FDA reports)
CHILLS ( 41 FDA reports)
INTERSTITIAL LUNG DISEASE ( 41 FDA reports)
OXYGEN SATURATION DECREASED ( 40 FDA reports)
URINARY TRACT INFECTION ( 40 FDA reports)
DIALYSIS ( 39 FDA reports)
GENERALISED OEDEMA ( 39 FDA reports)
RENAL DISORDER ( 39 FDA reports)
STAPHYLOCOCCAL INFECTION ( 39 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 38 FDA reports)
HAEMORRHAGE ( 38 FDA reports)
HYPERGLYCAEMIA ( 38 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 38 FDA reports)
RENAL FAILURE CHRONIC ( 38 FDA reports)
STENOTROPHOMONAS INFECTION ( 38 FDA reports)
ANAPHYLACTIC SHOCK ( 37 FDA reports)
CEREBRAL HAEMORRHAGE ( 37 FDA reports)
DIZZINESS ( 37 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 37 FDA reports)
PNEUMOTHORAX ( 37 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 36 FDA reports)
CONFUSIONAL STATE ( 36 FDA reports)
HEADACHE ( 36 FDA reports)
CARDIOGENIC SHOCK ( 35 FDA reports)
COUGH ( 34 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 34 FDA reports)
POST PROCEDURAL COMPLICATION ( 34 FDA reports)
PULMONARY EMBOLISM ( 34 FDA reports)
COAGULOPATHY ( 33 FDA reports)
DECREASED APPETITE ( 33 FDA reports)
DRUG ERUPTION ( 33 FDA reports)
ENCEPHALOPATHY ( 33 FDA reports)
HEPATIC ENCEPHALOPATHY ( 33 FDA reports)
HYPERSENSITIVITY ( 33 FDA reports)
JAUNDICE ( 33 FDA reports)
MALNUTRITION ( 33 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 33 FDA reports)
CARDIAC DISORDER ( 32 FDA reports)
CHOLESTASIS ( 32 FDA reports)
DRUG INEFFECTIVE ( 32 FDA reports)
SCAR ( 32 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 31 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 31 FDA reports)
INFUSION RELATED REACTION ( 31 FDA reports)
NEUTROPHIL COUNT DECREASED ( 31 FDA reports)
OLIGURIA ( 31 FDA reports)
ACUTE RESPIRATORY FAILURE ( 30 FDA reports)
ARRHYTHMIA ( 30 FDA reports)
BACTERIAL SEPSIS ( 30 FDA reports)
HYPERHIDROSIS ( 30 FDA reports)
LEUKOPENIA ( 30 FDA reports)
PNEUMONIA ASPIRATION ( 30 FDA reports)
PRURITUS ( 30 FDA reports)
WEIGHT INCREASED ( 30 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 29 FDA reports)
CONSTIPATION ( 29 FDA reports)
FUNGAL INFECTION ( 29 FDA reports)
HAEMODIALYSIS ( 29 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 29 FDA reports)
MOBILITY DECREASED ( 29 FDA reports)
UNRESPONSIVE TO STIMULI ( 29 FDA reports)
COMA ( 28 FDA reports)
HEPATITIS B ( 28 FDA reports)
ILEUS ( 28 FDA reports)
LEUKOCYTOSIS ( 28 FDA reports)
HYPERNATRAEMIA ( 27 FDA reports)
MENTAL STATUS CHANGES ( 27 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 27 FDA reports)
PANCREATITIS ( 27 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 27 FDA reports)
BLOOD ALBUMIN DECREASED ( 26 FDA reports)
CHEST PAIN ( 26 FDA reports)
DEEP VEIN THROMBOSIS ( 26 FDA reports)
DEFORMITY ( 26 FDA reports)
DRUG INTERACTION ( 26 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 26 FDA reports)
METABOLIC ACIDOSIS ( 26 FDA reports)
NERVOUSNESS ( 26 FDA reports)
SOMNOLENCE ( 26 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 26 FDA reports)
TUMOUR LYSIS SYNDROME ( 26 FDA reports)
CHEST DISCOMFORT ( 25 FDA reports)
EPISTAXIS ( 25 FDA reports)
FLUID OVERLOAD ( 25 FDA reports)
HYPERBILIRUBINAEMIA ( 25 FDA reports)
MUSCULAR WEAKNESS ( 25 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 25 FDA reports)
SKIN TIGHTNESS ( 25 FDA reports)
VENTRICULAR TACHYCARDIA ( 25 FDA reports)
ATELECTASIS ( 24 FDA reports)
BLOOD CULTURE POSITIVE ( 24 FDA reports)
BRAIN OEDEMA ( 24 FDA reports)
BRONCHOSPASM ( 24 FDA reports)
DERMATITIS EXFOLIATIVE ( 24 FDA reports)
ASPIRATION ( 23 FDA reports)
BACK PAIN ( 23 FDA reports)
CARDIOVASCULAR DISORDER ( 23 FDA reports)
GRAFT VERSUS HOST DISEASE ( 23 FDA reports)
LUNG DISORDER ( 23 FDA reports)
PERICARDIAL EFFUSION ( 23 FDA reports)
RENAL TUBULAR NECROSIS ( 23 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 22 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 22 FDA reports)
DYSPHAGIA ( 22 FDA reports)
FEAR OF DEATH ( 22 FDA reports)
FEELING ABNORMAL ( 22 FDA reports)
FIBROSIS ( 22 FDA reports)
HAEMOPTYSIS ( 22 FDA reports)
HYPOAESTHESIA ( 22 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 22 FDA reports)
LUNG INFILTRATION ( 22 FDA reports)
ORGAN FAILURE ( 22 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 22 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 22 FDA reports)
SKIN EXFOLIATION ( 22 FDA reports)
ANAPHYLACTIC REACTION ( 21 FDA reports)
DRY SKIN ( 21 FDA reports)
HALLUCINATION ( 21 FDA reports)
JOINT STIFFNESS ( 21 FDA reports)
MELAENA ( 21 FDA reports)
NEUROPATHY PERIPHERAL ( 21 FDA reports)
PULMONARY HAEMORRHAGE ( 21 FDA reports)
PULMONARY HYPERTENSION ( 21 FDA reports)
RESPIRATORY ARREST ( 21 FDA reports)
SKIN DISCOLOURATION ( 21 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 21 FDA reports)
ASPERGILLOSIS ( 20 FDA reports)
BACTERIAL INFECTION ( 20 FDA reports)
BRAIN CONTUSION ( 20 FDA reports)
BURSITIS ( 20 FDA reports)
CIRCULATORY COLLAPSE ( 20 FDA reports)
DISABILITY ( 20 FDA reports)
ENTEROCOCCAL INFECTION ( 20 FDA reports)
HEPATIC CIRRHOSIS ( 20 FDA reports)
INTESTINAL OBSTRUCTION ( 20 FDA reports)
MUCOSAL INFLAMMATION ( 20 FDA reports)
SKIN HYPERTROPHY ( 20 FDA reports)
SKIN INDURATION ( 20 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 20 FDA reports)
URINE OUTPUT DECREASED ( 20 FDA reports)
VENTRICULAR FIBRILLATION ( 20 FDA reports)
HAEMATEMESIS ( 19 FDA reports)
HAEMODYNAMIC INSTABILITY ( 19 FDA reports)
HEPATOMEGALY ( 19 FDA reports)
HYPOPROTEINAEMIA ( 19 FDA reports)
MYOCARDIAL ISCHAEMIA ( 19 FDA reports)
NEUROBLASTOMA RECURRENT ( 19 FDA reports)
VIRAL INFECTION ( 19 FDA reports)
ACIDOSIS ( 18 FDA reports)
BLISTER ( 18 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 18 FDA reports)
COLITIS ISCHAEMIC ( 18 FDA reports)
DRUG TOXICITY ( 18 FDA reports)
GANGRENE ( 18 FDA reports)
MINERAL METABOLISM DISORDER ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 18 FDA reports)
BLOOD GLUCOSE INCREASED ( 17 FDA reports)
CARDIOMEGALY ( 17 FDA reports)
CHOLANGITIS ( 17 FDA reports)
DYSPHONIA ( 17 FDA reports)
GAIT DISTURBANCE ( 17 FDA reports)
LIVER CARCINOMA RUPTURED ( 17 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 17 FDA reports)
PERITONITIS ( 17 FDA reports)
PSEUDOMONAS INFECTION ( 17 FDA reports)
SPLENOMEGALY ( 17 FDA reports)
URTICARIA ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
ACUTE PULMONARY OEDEMA ( 16 FDA reports)
AGITATION ( 16 FDA reports)
ANURIA ( 16 FDA reports)
BACTERAEMIA ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
CANDIDIASIS ( 16 FDA reports)
CEREBRAL INFARCTION ( 16 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 16 FDA reports)
ELECTROLYTE IMBALANCE ( 16 FDA reports)
HEPATOTOXICITY ( 16 FDA reports)
LIVER TRANSPLANT REJECTION ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 16 FDA reports)
PROTHROMBIN TIME PROLONGED ( 16 FDA reports)
PULMONARY CONGESTION ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
ANOREXIA ( 15 FDA reports)
BLOOD AMYLASE INCREASED ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
DEVICE RELATED INFECTION ( 15 FDA reports)
ESCHERICHIA INFECTION ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
HAEMATOMA ( 15 FDA reports)
HEPATITIS C POSITIVE ( 15 FDA reports)
HYPERTHERMIA ( 15 FDA reports)
NEPHROPATHY TOXIC ( 15 FDA reports)
NO THERAPEUTIC RESPONSE ( 15 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
PROTEIN TOTAL DECREASED ( 15 FDA reports)
TACHYPNOEA ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
COLITIS ( 14 FDA reports)
CORONARY ARTERY DISEASE ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
EATING DISORDER ( 14 FDA reports)
EMOTIONAL DISORDER ( 14 FDA reports)
GASTRIC ULCER ( 14 FDA reports)
HAEMATURIA ( 14 FDA reports)
HEART RATE INCREASED ( 14 FDA reports)
HEPATIC VEIN OCCLUSION ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
MENTAL DISORDER ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
PSYCHIATRIC SYMPTOM ( 14 FDA reports)
STOMATITIS ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
VISUAL IMPAIRMENT ( 14 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 13 FDA reports)
CATHETER RELATED INFECTION ( 13 FDA reports)
DYSARTHRIA ( 13 FDA reports)
ENCEPHALITIS ( 13 FDA reports)
HEPATIC ENZYME INCREASED ( 13 FDA reports)
HEPATITIS C VIRUS ( 13 FDA reports)
HYPERURICAEMIA ( 13 FDA reports)
HYPOGLYCAEMIA ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
LYMPHOMA ( 13 FDA reports)
PAIN OF SKIN ( 13 FDA reports)
RESPIRATORY DEPRESSION ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
SKIN FIBROSIS ( 13 FDA reports)
SKIN HYPERPIGMENTATION ( 13 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 13 FDA reports)
THERAPY NON-RESPONDER ( 13 FDA reports)
TRANSAMINASES INCREASED ( 13 FDA reports)
URINARY RETENTION ( 13 FDA reports)
VENTRICULAR HYPOKINESIA ( 13 FDA reports)
AGRANULOCYTOSIS ( 12 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 12 FDA reports)
ANGINA PECTORIS ( 12 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 12 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 12 FDA reports)
CYST ( 12 FDA reports)
HAEMOLYSIS ( 12 FDA reports)
HYPOTHERMIA ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 12 FDA reports)
METABOLIC DISORDER ( 12 FDA reports)
NERVOUS SYSTEM DISORDER ( 12 FDA reports)
ORAL DISORDER ( 12 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
SKIN PLAQUE ( 12 FDA reports)
STENOTROPHOMONAS SEPSIS ( 12 FDA reports)
VENA CAVA THROMBOSIS ( 12 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 11 FDA reports)
ALOPECIA ( 11 FDA reports)
BLINDNESS ( 11 FDA reports)
BLOOD CALCIUM DECREASED ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 11 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 11 FDA reports)
BONE PAIN ( 11 FDA reports)
CAECITIS ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
CLOSTRIDIAL INFECTION ( 11 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 11 FDA reports)
COMA HEPATIC ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
DYSURIA ( 11 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
OVARIAN CANCER ( 11 FDA reports)
PERITONITIS BACTERIAL ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 10 FDA reports)
BACTERIA URINE IDENTIFIED ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
CYTOLYTIC HEPATITIS ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
FLUID RETENTION ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HEARING IMPAIRED ( 10 FDA reports)
HYPOVOLAEMIA ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 10 FDA reports)
JOINT CONTRACTURE ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
NEPHROTIC SYNDROME ( 10 FDA reports)
NYSTAGMUS ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
PNEUMONITIS CHEMICAL ( 10 FDA reports)
PROCEDURAL COMPLICATION ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
RENAL CYST ( 10 FDA reports)
RESPIRATORY TRACT INFECTION ( 10 FDA reports)
RIGHT VENTRICULAR FAILURE ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
SWELLING ( 10 FDA reports)
TORSADE DE POINTES ( 10 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 10 FDA reports)
VENOOCCLUSIVE DISEASE ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
CARDIOPULMONARY FAILURE ( 9 FDA reports)
CASTLEMAN'S DISEASE ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DELIRIUM ( 9 FDA reports)
EYE INFECTION VIRAL ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
GRAND MAL CONVULSION ( 9 FDA reports)
HEPATIC CONGESTION ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
IRON DEFICIENCY ANAEMIA ( 9 FDA reports)
LIVEDO RETICULARIS ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
MYOPATHY ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
PERIPHERAL ISCHAEMIA ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
PULMONARY INFARCTION ( 9 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TRAUMATIC LUNG INJURY ( 9 FDA reports)
TUBERCULOSIS ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
ASTHMA ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
ENDOCARDITIS BACTERIAL ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPOCOAGULABLE STATE ( 8 FDA reports)
HYPOTHYROIDISM ( 8 FDA reports)
INCONTINENCE ( 8 FDA reports)
JEJUNAL PERFORATION ( 8 FDA reports)
LABORATORY TEST ABNORMAL ( 8 FDA reports)
LARGE INTESTINE PERFORATION ( 8 FDA reports)
LIP EROSION ( 8 FDA reports)
MOUTH ULCERATION ( 8 FDA reports)
NEPHROLITHIASIS ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
PETECHIAE ( 8 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 8 FDA reports)
POSTOPERATIVE ILEUS ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
SYSTEMIC MYCOSIS ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
TRANSFUSION ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
ASCITES INFECTION ( 7 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 7 FDA reports)
BONE DISORDER ( 7 FDA reports)
CACHEXIA ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DEVICE RELATED SEPSIS ( 7 FDA reports)
DRUG-INDUCED LIVER INJURY ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
ENGRAFTMENT SYNDROME ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 7 FDA reports)
INTESTINAL ISCHAEMIA ( 7 FDA reports)
KIDNEY ENLARGEMENT ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 7 FDA reports)
MECHANICAL VENTILATION ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NEONATAL DISORDER ( 7 FDA reports)
NEUROLOGICAL SYMPTOM ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
NEUTROPENIC COLITIS ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
PSYCHOLOGICAL TRAUMA ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
SKIN TURGOR DECREASED ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
SPUTUM PURULENT ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
TOOTH DISORDER ( 7 FDA reports)
TOOTH EXTRACTION ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
ABDOMINAL ABSCESS ( 6 FDA reports)
ABDOMINAL SEPSIS ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
EXANTHEM ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
MENINGISM ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RALES ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RECTAL CANCER STAGE 0 ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
SEPTIC EMBOLUS ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SKIN NECROSIS ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
SURGICAL PROCEDURE REPEATED ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
THERMAL BURN ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABDOMINAL INFECTION ( 5 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
AORTIC STENOSIS ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASBESTOSIS ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BILE DUCT OBSTRUCTION ( 5 FDA reports)
BLINDNESS UNILATERAL ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
BREAKTHROUGH PAIN ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CHEST TUBE INSERTION ( 5 FDA reports)
CHOLECYSTECTOMY ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
CYSTITIS HAEMORRHAGIC ( 5 FDA reports)
CYTOKINE RELEASE SYNDROME ( 5 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 5 FDA reports)
DENTURE WEARER ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DUODENAL PERFORATION ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ENCEPHALITIS HERPES ( 5 FDA reports)
ENTEROCOCCAL SEPSIS ( 5 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC FIBROSIS ( 5 FDA reports)
HEPATIC HAEMATOMA ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYDROTHORAX ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LASER THERAPY ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
PLEURAL DECORTICATION ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PROSTATE CANCER METASTATIC ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PSEUDOMONAL SEPSIS ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SERRATIA SEPSIS ( 5 FDA reports)
SHOCK HAEMORRHAGIC ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SOPOR ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
SPLENIC ABSCESS ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
TOOTH LOSS ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
ZYGOMYCOSIS ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ACUTE PRERENAL FAILURE ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
AXONAL NEUROPATHY ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BILIARY SEPSIS ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS TEST ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
ENCEPHALOMALACIA ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATIC SIDEROSIS ( 4 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 4 FDA reports)
HEPATITIS B VIRUS ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEUROBLASTOMA ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RENAL TRANSPLANT ( 4 FDA reports)
RENAL VEIN OCCLUSION ( 4 FDA reports)
RETINAL INFARCTION ( 4 FDA reports)
RIGHT ATRIAL DILATATION ( 4 FDA reports)
SEPSIS NEONATAL ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
THORACOSTOMY ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TRICHOSPORON INFECTION ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CHOLANGITIS SCLEROSING ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 3 FDA reports)
CYTOTOXIC OEDEMA ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GOUT ( 3 FDA reports)
GRAFT DYSFUNCTION ( 3 FDA reports)
GRAFT LOSS ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HEPATIC VEIN THROMBOSIS ( 3 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HIV TEST POSITIVE ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
ISOLATED ADRENOCORTICOTROPIC HORMONE DEFICIENCY ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
MYELOCYTE PRESENT ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 3 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SHUNT STENOSIS ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
SPLENIC INFECTION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THORACIC HAEMORRHAGE ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
ULCER ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER IRRIGATION ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONGENITAL BLADDER ANOMALY ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIVERTICULAR FISTULA ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSTROPHIA MYOTONICA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAPTOGLOBIN ABNORMAL ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATITIS POST TRANSFUSION ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCISION SITE CELLULITIS ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERNAL HERNIA ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MASS ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
OVARIAN EPITHELIAL CANCER ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLATELET COUNT NORMAL ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URATE NEPHROPATHY ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VIRAL MUTATION IDENTIFIED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WOUND INFECTION FUNGAL ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALLOIMMUNISATION ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMA URAEMIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
END-TIDAL CO2 DECREASED ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAMILIAL HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISORDER ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS INFECTION ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNISATION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KABUKI MAKE-UP SYNDROME ( 1 FDA reports)
KERNICTERUS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
METASTASES TO ABDOMINAL WALL ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA NEONATAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMINOGEN ACTIVATOR INHIBITOR INCREASED ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA RECURRENT ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID ATROPHY ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TISSUE ANOXIA ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYMPANOMETRY ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND SKULL ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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