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

PYREXIA ( 86 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 80 FDA reports)
PNEUMONIA ( 76 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 72 FDA reports)
SEPSIS ( 66 FDA reports)
PLATELET COUNT DECREASED ( 62 FDA reports)
VOMITING ( 62 FDA reports)
ANAEMIA ( 61 FDA reports)
NAUSEA ( 57 FDA reports)
FEBRILE NEUTROPENIA ( 56 FDA reports)
CONDITION AGGRAVATED ( 52 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 47 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 47 FDA reports)
RENAL FAILURE ACUTE ( 46 FDA reports)
HYPERLIPIDAEMIA ( 45 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 45 FDA reports)
DIZZINESS ( 43 FDA reports)
THROMBOCYTOPENIA ( 41 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 40 FDA reports)
CALCULUS URINARY ( 40 FDA reports)
HIV WASTING SYNDROME ( 39 FDA reports)
BLOOD CREATININE INCREASED ( 38 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 38 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 38 FDA reports)
PLEURAL EFFUSION ( 38 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 38 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 37 FDA reports)
BLOOD UREA INCREASED ( 37 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 37 FDA reports)
SEPTIC SHOCK ( 37 FDA reports)
DIARRHOEA ( 35 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 32 FDA reports)
LIVER DISORDER ( 32 FDA reports)
PANCYTOPENIA ( 32 FDA reports)
RESPIRATORY FAILURE ( 32 FDA reports)
RENAL IMPAIRMENT ( 31 FDA reports)
NEUTROPHIL COUNT DECREASED ( 30 FDA reports)
HAEMOGLOBIN DECREASED ( 29 FDA reports)
HYPOALBUMINAEMIA ( 29 FDA reports)
HYPOCALCAEMIA ( 28 FDA reports)
INTERSTITIAL LUNG DISEASE ( 28 FDA reports)
ANOREXIA ( 26 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 26 FDA reports)
NEUTROPENIA ( 26 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 25 FDA reports)
RASH ( 25 FDA reports)
BLOOD BILIRUBIN INCREASED ( 24 FDA reports)
RENAL FAILURE ( 24 FDA reports)
HYPOKALAEMIA ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
INFECTION ( 23 FDA reports)
LEUKOPENIA ( 23 FDA reports)
HERPES ZOSTER ( 22 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 22 FDA reports)
INSOMNIA ( 21 FDA reports)
HYPERKALAEMIA ( 20 FDA reports)
HYPONATRAEMIA ( 20 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 20 FDA reports)
GASTRITIS ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
HYPOPROTEINAEMIA ( 19 FDA reports)
ELECTROLYTE IMBALANCE ( 18 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 17 FDA reports)
DISEASE PROGRESSION ( 17 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
TRANSAMINASES INCREASED ( 17 FDA reports)
AGRANULOCYTOSIS ( 16 FDA reports)
BLOOD URIC ACID INCREASED ( 16 FDA reports)
HEPATIC STEATOSIS ( 16 FDA reports)
MULTI-ORGAN FAILURE ( 16 FDA reports)
STOMATITIS ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
PULMONARY OEDEMA ( 15 FDA reports)
SHOCK ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 14 FDA reports)
DYSPNOEA ( 14 FDA reports)
GRAFT VERSUS HOST DISEASE ( 14 FDA reports)
NEUROPATHY PERIPHERAL ( 14 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
DEAFNESS ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
LYMPHOMA ( 13 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 13 FDA reports)
NEONATAL DISORDER ( 13 FDA reports)
PSEUDOMONAS INFECTION ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
BACTERIAL INFECTION ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
PROTEIN TOTAL INCREASED ( 12 FDA reports)
RENAL DISORDER ( 12 FDA reports)
VENTRICULAR FIBRILLATION ( 12 FDA reports)
BONE MARROW FAILURE ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
DYSPHAGIA ( 11 FDA reports)
FUNGAL DNA TEST POSITIVE ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
ASCITES ( 10 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BASOPHIL COUNT DECREASED ( 10 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
RASH MACULO-PAPULAR ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
WHEEZING ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
CANDIDA SEPSIS ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 9 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
WHITE BLOOD CELL DISORDER ( 9 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
CANDIDIASIS ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
MALAISE ( 8 FDA reports)
MULTIPLE MYELOMA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
RESTLESSNESS ( 8 FDA reports)
RETINAL HAEMORRHAGE ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
TREMOR ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CATHETER RELATED INFECTION ( 7 FDA reports)
DEATH ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HICCUPS ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
ILEUS ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
NEUROGENIC BLADDER ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ANURIA ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DUODENAL PERFORATION ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 6 FDA reports)
HAEMORRHAGIC DIATHESIS ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
ILLUSION ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
KAPOSI'S SARCOMA ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
OESOPHAGEAL CARCINOMA ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
SMALL INTESTINAL PERFORATION ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HEPATIC VEIN OCCLUSION ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NEUTROPENIC COLITIS ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FALL ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GALLBLADDER CANCER ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAIRY CELL LEUKAEMIA ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
SEPSIS NEONATAL ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 3 FDA reports)
APNOEA ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CORYNEBACTERIUM SEPSIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ENGRAFTMENT SYNDROME ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GLOSSOPTOSIS ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMOBILIA ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FOETAL HEART RATE INCREASED ( 2 FDA reports)
FOETAL MOVEMENTS DECREASED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PYOMETRA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
UMBILICAL CORD COMPRESSION ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID DECREASED ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL STAINING ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PITUITARY GLAND ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)

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