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

PYREXIA ( 201 FDA reports)
INTERSTITIAL LUNG DISEASE ( 132 FDA reports)
PNEUMONIA ( 122 FDA reports)
PLATELET COUNT DECREASED ( 113 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 112 FDA reports)
MALAISE ( 110 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 106 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 104 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 103 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 101 FDA reports)
RENAL IMPAIRMENT ( 95 FDA reports)
RASH ( 89 FDA reports)
VOMITING ( 88 FDA reports)
DIARRHOEA ( 87 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 85 FDA reports)
ANAEMIA ( 84 FDA reports)
BLOOD CREATININE INCREASED ( 79 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 79 FDA reports)
NAUSEA ( 79 FDA reports)
LIVER DISORDER ( 64 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 63 FDA reports)
HAEMOGLOBIN DECREASED ( 62 FDA reports)
SEPSIS ( 62 FDA reports)
HEADACHE ( 61 FDA reports)
DIZZINESS ( 59 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 58 FDA reports)
DECREASED APPETITE ( 58 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 58 FDA reports)
BLOOD PRESSURE DECREASED ( 54 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 54 FDA reports)
CONDITION AGGRAVATED ( 53 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 52 FDA reports)
BLOOD UREA INCREASED ( 52 FDA reports)
HERPES ZOSTER ( 52 FDA reports)
HYPOGLYCAEMIA ( 51 FDA reports)
BRONCHITIS ( 50 FDA reports)
CEREBRAL INFARCTION ( 50 FDA reports)
NEUTROPHIL COUNT DECREASED ( 50 FDA reports)
PANCYTOPENIA ( 50 FDA reports)
RENAL FAILURE ACUTE ( 50 FDA reports)
ARTHRALGIA ( 49 FDA reports)
DRUG INTERACTION ( 47 FDA reports)
COUGH ( 46 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 45 FDA reports)
GAIT DISTURBANCE ( 43 FDA reports)
DYSPNOEA ( 42 FDA reports)
NASOPHARYNGITIS ( 42 FDA reports)
BLOOD BILIRUBIN INCREASED ( 41 FDA reports)
FEBRILE NEUTROPENIA ( 41 FDA reports)
DYSARTHRIA ( 39 FDA reports)
OEDEMA PERIPHERAL ( 38 FDA reports)
RESPIRATORY FAILURE ( 38 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 38 FDA reports)
ENCEPHALOPATHY ( 37 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 37 FDA reports)
SHOCK ( 37 FDA reports)
DELIRIUM ( 36 FDA reports)
STOMATITIS ( 36 FDA reports)
DEHYDRATION ( 35 FDA reports)
LOSS OF CONSCIOUSNESS ( 35 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 35 FDA reports)
CARDIAC FAILURE ( 34 FDA reports)
FEMUR FRACTURE ( 34 FDA reports)
HAEMATOCRIT DECREASED ( 34 FDA reports)
THROMBOCYTOPENIA ( 34 FDA reports)
HYPERTENSION ( 33 FDA reports)
CONSTIPATION ( 32 FDA reports)
CONVULSION ( 32 FDA reports)
FALL ( 32 FDA reports)
GASTROENTERITIS ( 32 FDA reports)
RENAL DISORDER ( 32 FDA reports)
RHEUMATOID ARTHRITIS ( 31 FDA reports)
HYPERKALAEMIA ( 30 FDA reports)
PAIN ( 30 FDA reports)
SKIN ULCER ( 29 FDA reports)
SOMNOLENCE ( 29 FDA reports)
URINARY TRACT INFECTION ( 29 FDA reports)
BACK PAIN ( 28 FDA reports)
HALLUCINATION ( 28 FDA reports)
HYPONATRAEMIA ( 28 FDA reports)
MUSCULAR WEAKNESS ( 27 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 27 FDA reports)
PAIN IN EXTREMITY ( 27 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 26 FDA reports)
DRUG INEFFECTIVE ( 26 FDA reports)
OSTEOMYELITIS ( 26 FDA reports)
PLEURAL EFFUSION ( 26 FDA reports)
SPEECH DISORDER ( 26 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
BLOOD PRESSURE INCREASED ( 25 FDA reports)
CEREBRAL HAEMORRHAGE ( 25 FDA reports)
GASTRIC ULCER ( 25 FDA reports)
HYPOAESTHESIA ( 25 FDA reports)
INFUSION RELATED REACTION ( 25 FDA reports)
ANOREXIA ( 24 FDA reports)
DEATH ( 24 FDA reports)
ENTEROCOLITIS ( 24 FDA reports)
INSOMNIA ( 24 FDA reports)
MELAENA ( 24 FDA reports)
OROPHARYNGEAL PAIN ( 24 FDA reports)
PERITONITIS ( 24 FDA reports)
PHARYNGITIS ( 24 FDA reports)
RALES ( 24 FDA reports)
ARRHYTHMIA ( 23 FDA reports)
BLOOD POTASSIUM DECREASED ( 23 FDA reports)
ILEUS ( 23 FDA reports)
PROTEIN URINE PRESENT ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
BLISTER ( 22 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 22 FDA reports)
PULMONARY OEDEMA ( 22 FDA reports)
VASCULITIS ( 22 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
HAEMODIALYSIS ( 21 FDA reports)
NERVOUS SYSTEM DISORDER ( 21 FDA reports)
NEUTROPHIL COUNT INCREASED ( 21 FDA reports)
ASTHENIA ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 20 FDA reports)
OSTEONECROSIS ( 20 FDA reports)
RETINAL HAEMORRHAGE ( 20 FDA reports)
INFECTION ( 19 FDA reports)
INFLUENZA ( 19 FDA reports)
LYMPHADENITIS ( 19 FDA reports)
OEDEMA ( 19 FDA reports)
PRURITUS ( 19 FDA reports)
STEVENS-JOHNSON SYNDROME ( 19 FDA reports)
URTICARIA ( 19 FDA reports)
AGRANULOCYTOSIS ( 18 FDA reports)
BLOOD POTASSIUM INCREASED ( 18 FDA reports)
BRADYCARDIA ( 18 FDA reports)
ERYTHEMA ( 18 FDA reports)
FATIGUE ( 18 FDA reports)
HAEMATOCHEZIA ( 18 FDA reports)
MYALGIA ( 18 FDA reports)
RESTLESSNESS ( 18 FDA reports)
BLOOD ALBUMIN DECREASED ( 17 FDA reports)
DRUG ERUPTION ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
HYPERURICAEMIA ( 17 FDA reports)
HYPOPHAGIA ( 17 FDA reports)
LARGE INTESTINE PERFORATION ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
OVERDOSE ( 17 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 16 FDA reports)
ANAPHYLACTIC SHOCK ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 16 FDA reports)
CATARACT ( 16 FDA reports)
CHEST PAIN ( 16 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
HYPOKALAEMIA ( 16 FDA reports)
LARGE INTESTINE CARCINOMA ( 16 FDA reports)
NEPHROTIC SYNDROME ( 16 FDA reports)
RENAL FAILURE CHRONIC ( 16 FDA reports)
SPINAL COMPRESSION FRACTURE ( 16 FDA reports)
ASTHMA ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
CALCULUS URINARY ( 15 FDA reports)
DEEP VEIN THROMBOSIS ( 15 FDA reports)
GASTRIC CANCER ( 15 FDA reports)
HEMIPLEGIA ( 15 FDA reports)
HYPOCALCAEMIA ( 15 FDA reports)
PULMONARY TUBERCULOSIS ( 15 FDA reports)
SEPTIC SHOCK ( 15 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
ABNORMAL BEHAVIOUR ( 14 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 14 FDA reports)
DISEASE PROGRESSION ( 14 FDA reports)
DYSLALIA ( 14 FDA reports)
FIBRIN D DIMER INCREASED ( 14 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPOTHYROIDISM ( 14 FDA reports)
LUMBAR SPINAL STENOSIS ( 14 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 14 FDA reports)
NEOPLASM MALIGNANT ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
TINNITUS ( 14 FDA reports)
ABDOMINAL DISTENSION ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 13 FDA reports)
ANGINA PECTORIS ( 13 FDA reports)
ASCITES ( 13 FDA reports)
BONE DISORDER ( 13 FDA reports)
BONE MARROW FAILURE ( 13 FDA reports)
CELLULITIS ( 13 FDA reports)
CHILLS ( 13 FDA reports)
DIALYSIS ( 13 FDA reports)
DRUG LEVEL INCREASED ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
HYPOXIA ( 13 FDA reports)
LUNG DISORDER ( 13 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 13 FDA reports)
NEUROSIS ( 13 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 13 FDA reports)
URINE OUTPUT DECREASED ( 13 FDA reports)
ABASIA ( 12 FDA reports)
ABSCESS NECK ( 12 FDA reports)
AGITATION ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
DEVICE RELATED INFECTION ( 12 FDA reports)
DISORIENTATION ( 12 FDA reports)
INTESTINAL ISCHAEMIA ( 12 FDA reports)
LIVER ABSCESS ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
OSTEOMALACIA ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 12 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
SHOCK HAEMORRHAGIC ( 12 FDA reports)
THROMBOSIS ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
VIRAL INFECTION ( 12 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 12 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 11 FDA reports)
ALOPECIA ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
DYSKINESIA ( 11 FDA reports)
ENTERITIS INFECTIOUS ( 11 FDA reports)
FEELING HOT ( 11 FDA reports)
GLOSSITIS ( 11 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 11 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 11 FDA reports)
NEUROPATHY PERIPHERAL ( 11 FDA reports)
OLIGURIA ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
PRODUCTIVE COUGH ( 11 FDA reports)
PROTEIN TOTAL DECREASED ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
VISUAL FIELD DEFECT ( 11 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 10 FDA reports)
AFFECT LABILITY ( 10 FDA reports)
AMYLOIDOSIS ( 10 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
BLOOD CHLORIDE DECREASED ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
DEAFNESS BILATERAL ( 10 FDA reports)
DYSPEPSIA ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
HEART RATE DECREASED ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
INTESTINAL OBSTRUCTION ( 10 FDA reports)
JUVENILE ARTHRITIS ( 10 FDA reports)
LUNG NEOPLASM MALIGNANT ( 10 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
MENTAL DISORDER ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
PERTUSSIS ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
TEMPERATURE INTOLERANCE ( 10 FDA reports)
VARICELLA ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
ANURIA ( 9 FDA reports)
BLEPHARITIS ( 9 FDA reports)
CANDIDIASIS ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CHOLECYSTITIS ( 9 FDA reports)
COMA ( 9 FDA reports)
COMPRESSION FRACTURE ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
GENERALISED OEDEMA ( 9 FDA reports)
GRANULOCYTOPENIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
MOVEMENT DISORDER ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
OPTIC NEURITIS ( 9 FDA reports)
ORAL CANDIDIASIS ( 9 FDA reports)
PLEURISY ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
TREMOR ( 9 FDA reports)
URINARY RETENTION ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
AMMONIA INCREASED ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
COORDINATION ABNORMAL ( 8 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 8 FDA reports)
DERMAL CYST ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
FANCONI SYNDROME ACQUIRED ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERCOAGULATION ( 8 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 8 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
ORAL INTAKE REDUCED ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 8 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
PYELONEPHRITIS ( 8 FDA reports)
REFLUX OESOPHAGITIS ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
SURGERY ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
VITRECTOMY ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DELUSION ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
HALLUCINATION, VISUAL ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 7 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
LACUNAR INFARCTION ( 7 FDA reports)
LYMPH NODE TUBERCULOSIS ( 7 FDA reports)
MONOPLEGIA ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PAPILLOEDEMA ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PYODERMA GANGRENOSUM ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
TUMOUR EMBOLISM ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ABSCESS ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANGIOSARCOMA ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BLOOD CALCIUM INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DERMATITIS ALLERGIC ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPOAESTHESIA ORAL ( 6 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
MYOSITIS ( 6 FDA reports)
NEOPLASM PROGRESSION ( 6 FDA reports)
OESOPHAGEAL POLYP ( 6 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PERIODONTITIS ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
SPUTUM RETENTION ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SWELLING ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ACNE ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 5 FDA reports)
B-CELL LYMPHOMA ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 5 FDA reports)
BRAIN ABSCESS ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CEREBRAL DISORDER ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CLONIC CONVULSION ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
ENTEROCOCCAL INFECTION ( 5 FDA reports)
EPIDERMOLYSIS BULLOSA ( 5 FDA reports)
ESCHERICHIA INFECTION ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
HYPERAMMONAEMIA ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
MEASLES ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MYELITIS TRANSVERSE ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
MYRINGITIS ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NEUROMYELITIS OPTICA ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PANNICULITIS ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PNEUMOMEDIASTINUM ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POLYARTERITIS NODOSA ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RENAL TUBULAR ACIDOSIS ( 5 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
TENDERNESS ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
TOOTH INFECTION ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
TUBERCULOUS PLEURISY ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 4 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD INSULIN INCREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BRAIN STEM ISCHAEMIA ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CASTLEMAN'S DISEASE ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHRONIC SINUSITIS ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENCEPHALITIS VIRAL ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FANCONI SYNDROME ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GASTRIC MUCOSAL LESION ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYDROPNEUMOTHORAX ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERPHOSPHATASAEMIA ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INJURY ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTERVERTEBRAL DISCITIS ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PRIMARY CEREBELLAR DEGENERATION ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SCAB ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
TACHYPHYLAXIS ( 4 FDA reports)
THIRST ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 4 FDA reports)
URETERIC DILATATION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR FLUTTER ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
VOLUME BLOOD DECREASED ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACETONAEMIC VOMITING ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ATLANTOAXIAL INSTABILITY ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GALLBLADDER PERFORATION ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HAEMOSTASIS ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOZINCAEMIA ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LARYNGEAL GRANULOMA ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MEGAKARYOCYTES INCREASED ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEONATAL ASPHYXIA ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
OESOPHAGEAL FISTULA ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PITUITARY CYST ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TERMINAL DRIBBLING ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TOLOSA-HUNT SYNDROME ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
AIRWAY BURNS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTI FACTOR IX ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATROPHY OF TONGUE PAPILLAE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 2 FDA reports)
COARCTATION OF THE AORTA ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ECZEMA VESICULAR ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
FACIAL SPASM ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTRACARDIAC MASS ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIPOGRANULOMA ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MELANOSIS ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEOPLASM OF ORBIT ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPORTAL OEDEMA ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROTEIN TOTAL ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY HAEMATOMA ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL CYST INFECTION ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SLEEP-RELATED EATING DISORDER ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URACHAL ABSCESS ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC OPERATION ( 2 FDA reports)
URINE NITROGEN ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B DNA INCREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
ILEAL ULCER PERFORATION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRAUTERINE INFECTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINEA MANUUM ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URACHAL ABNORMALITY ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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