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

PYREXIA ( 130 FDA reports)
INTERSTITIAL LUNG DISEASE ( 116 FDA reports)
PLATELET COUNT DECREASED ( 109 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 90 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 86 FDA reports)
PNEUMONIA ( 85 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 84 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 76 FDA reports)
ANAEMIA ( 76 FDA reports)
HAEMOGLOBIN DECREASED ( 72 FDA reports)
RENAL FAILURE ACUTE ( 71 FDA reports)
RHABDOMYOLYSIS ( 70 FDA reports)
MALAISE ( 69 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 67 FDA reports)
DIZZINESS ( 67 FDA reports)
DIARRHOEA ( 64 FDA reports)
NAUSEA ( 62 FDA reports)
RENAL IMPAIRMENT ( 62 FDA reports)
BLOOD CREATININE INCREASED ( 60 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 60 FDA reports)
LIVER DISORDER ( 59 FDA reports)
CEREBRAL INFARCTION ( 55 FDA reports)
DECREASED APPETITE ( 55 FDA reports)
PANCYTOPENIA ( 55 FDA reports)
VOMITING ( 54 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 53 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 53 FDA reports)
HYPOGLYCAEMIA ( 53 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 52 FDA reports)
OEDEMA PERIPHERAL ( 50 FDA reports)
RESPIRATORY FAILURE ( 50 FDA reports)
DYSPNOEA ( 49 FDA reports)
CARDIAC FAILURE ( 48 FDA reports)
BLOOD UREA INCREASED ( 46 FDA reports)
HYPERTENSION ( 43 FDA reports)
PLEURAL EFFUSION ( 43 FDA reports)
RENAL FAILURE ( 43 FDA reports)
HYPERKALAEMIA ( 42 FDA reports)
ANOREXIA ( 41 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 41 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 40 FDA reports)
RASH ( 39 FDA reports)
BLOOD PRESSURE DECREASED ( 38 FDA reports)
HAEMATOCRIT DECREASED ( 38 FDA reports)
LOSS OF CONSCIOUSNESS ( 38 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 37 FDA reports)
SEPSIS ( 37 FDA reports)
CONDITION AGGRAVATED ( 36 FDA reports)
BRADYCARDIA ( 35 FDA reports)
BLOOD GLUCOSE INCREASED ( 33 FDA reports)
DRUG INTERACTION ( 33 FDA reports)
HYPONATRAEMIA ( 33 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 33 FDA reports)
ABDOMINAL PAIN ( 32 FDA reports)
CONVULSION ( 31 FDA reports)
DEHYDRATION ( 30 FDA reports)
ENCEPHALOPATHY ( 30 FDA reports)
ERYTHEMA ( 30 FDA reports)
SHOCK ( 30 FDA reports)
BLOOD PRESSURE INCREASED ( 28 FDA reports)
DELIRIUM ( 28 FDA reports)
OVERDOSE ( 28 FDA reports)
TREMOR ( 28 FDA reports)
ASTHENIA ( 27 FDA reports)
GAIT DISTURBANCE ( 27 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 26 FDA reports)
RENAL DISORDER ( 26 FDA reports)
THROMBOCYTOPENIA ( 26 FDA reports)
DEATH ( 24 FDA reports)
HYPOTENSION ( 24 FDA reports)
ATRIAL FIBRILLATION ( 23 FDA reports)
CARDIO-RESPIRATORY ARREST ( 23 FDA reports)
CHEST PAIN ( 23 FDA reports)
JAUNDICE ( 23 FDA reports)
NEUTROPHIL COUNT DECREASED ( 23 FDA reports)
BONE MARROW FAILURE ( 22 FDA reports)
CONSTIPATION ( 22 FDA reports)
DIALYSIS ( 22 FDA reports)
DYSARTHRIA ( 22 FDA reports)
PAIN IN EXTREMITY ( 22 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 22 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
GASTRIC CANCER ( 21 FDA reports)
SOMNOLENCE ( 21 FDA reports)
DRUG ERUPTION ( 20 FDA reports)
FALL ( 20 FDA reports)
INSOMNIA ( 20 FDA reports)
MELAENA ( 20 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
HEADACHE ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 19 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 19 FDA reports)
STOMATITIS ( 19 FDA reports)
BLOOD BILIRUBIN INCREASED ( 18 FDA reports)
COUGH ( 18 FDA reports)
ERYTHEMA MULTIFORME ( 18 FDA reports)
HALLUCINATION ( 18 FDA reports)
HYPOKALAEMIA ( 18 FDA reports)
NASOPHARYNGITIS ( 18 FDA reports)
BLOOD POTASSIUM INCREASED ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
DISEASE PROGRESSION ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
HYPOAESTHESIA ( 17 FDA reports)
MYALGIA ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
STEVENS-JOHNSON SYNDROME ( 17 FDA reports)
BLOOD URIC ACID INCREASED ( 16 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 16 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 16 FDA reports)
MUSCULAR WEAKNESS ( 16 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 16 FDA reports)
URINE OUTPUT DECREASED ( 16 FDA reports)
GASTRIC ULCER ( 15 FDA reports)
GENERALISED OEDEMA ( 15 FDA reports)
INTENTIONAL OVERDOSE ( 15 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 15 FDA reports)
WEIGHT INCREASED ( 15 FDA reports)
ANURIA ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
ASCITES ( 14 FDA reports)
CEREBRAL HAEMORRHAGE ( 14 FDA reports)
DEMENTIA ( 14 FDA reports)
HEPATIC ENZYME INCREASED ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
ILEUS ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
SPEECH DISORDER ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 13 FDA reports)
HAEMORRHAGE ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
PAIN ( 13 FDA reports)
PNEUMONIA ASPIRATION ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 12 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
ANGIOEDEMA ( 12 FDA reports)
BLOOD SODIUM DECREASED ( 12 FDA reports)
DRUG LEVEL INCREASED ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
EOSINOPHIL COUNT INCREASED ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 12 FDA reports)
INTESTINAL OBSTRUCTION ( 12 FDA reports)
LEUKOPENIA ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 11 FDA reports)
BLOOD AMYLASE INCREASED ( 11 FDA reports)
DIABETIC NEPHROPATHY ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
HAEMOLYTIC ANAEMIA ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
SUICIDE ATTEMPT ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
ACUTE LEUKAEMIA ( 10 FDA reports)
BLISTER ( 10 FDA reports)
BONE DISORDER ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
FEMUR FRACTURE ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
MYOCLONUS ( 10 FDA reports)
QUADRIPLEGIA ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
CHILLS ( 9 FDA reports)
COMA ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 9 FDA reports)
DIFFICULTY IN WALKING ( 9 FDA reports)
DYSSTASIA ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
HYPOAESTHESIA ORAL ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PSYCHIATRIC SYMPTOM ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SPONDYLITIS ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ABASIA ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 8 FDA reports)
DUODENAL ULCER PERFORATION ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HEMIPLEGIA ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
OSTEOMYELITIS ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BLOOD CHLORIDE DECREASED ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
CHEST X-RAY ABNORMAL ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
CLONIC CONVULSION ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPOGLYCAEMIC COMA ( 7 FDA reports)
INFLAMMATION ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
NEPHRITIS INTERSTITIAL ( 7 FDA reports)
NEPHROPATHY ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
PURPURA ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
THIRST ( 7 FDA reports)
TOOTH EXTRACTION ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
VITREOUS HAEMORRHAGE ( 7 FDA reports)
ALOPECIA ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BLEEDING TIME PROLONGED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BONE TRIMMING ( 6 FDA reports)
COLON POLYPECTOMY ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LIP EROSION ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OSTEITIS ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PENILE ULCERATION ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
SCROTAL ULCER ( 6 FDA reports)
SEQUESTRECTOMY ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
SWELLING ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
AGITATION ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSLALIA ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 5 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
GRIP STRENGTH DECREASED ( 5 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INJURY ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 5 FDA reports)
POLYNEUROPATHY ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
RADIATION PNEUMONITIS ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
SURGERY ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BILOMA ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROLYTE DEPLETION ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
GASTRIC LAVAGE ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GLOMERULOSCLEROSIS ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TENSION ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COMPRESSION FRACTURE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONVULSIONS LOCAL ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPHAEMA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
ILEAL ULCER PERFORATION ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
PACING THRESHOLD DECREASED ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
RETROPERITONEAL ABSCESS ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TETANY ( 3 FDA reports)
TONIC CONVULSION ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AMNIOTIC CAVITY DISORDER ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
APATHY ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD KETONE BODY PRESENT ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CERVICAL ROOT PAIN ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDOSCOPY SMALL INTESTINE ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS NORMAL ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 2 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOCUTANEOUS RASH ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEPHROURETERECTOMY ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURAL INFECTION BACTERIAL ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL IMPAIRMENT NEONATAL ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETERECTOMY ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY PROSTATE ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BETA-D-GLUCAN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYSTITIS-LIKE SYMPTOM ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE EROSION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAPAN COMA SCALE ABNORMAL ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONSILLITIS ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY AIR LEAKAGE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SHOPLIFTING ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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