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

KIDNEY TRANSPLANT REJECTION ( 637 FDA reports)
BLOOD CREATININE INCREASED ( 384 FDA reports)
PYREXIA ( 313 FDA reports)
DIARRHOEA ( 294 FDA reports)
DRUG INEFFECTIVE ( 293 FDA reports)
HAEMOGLOBIN DECREASED ( 260 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 248 FDA reports)
ANAEMIA ( 236 FDA reports)
RENAL FAILURE ACUTE ( 231 FDA reports)
PNEUMONIA ( 216 FDA reports)
DEATH ( 202 FDA reports)
VOMITING ( 183 FDA reports)
DYSPNOEA ( 182 FDA reports)
RENAL TUBULAR NECROSIS ( 180 FDA reports)
RENAL IMPAIRMENT ( 179 FDA reports)
HAEMATOCRIT DECREASED ( 175 FDA reports)
DEHYDRATION ( 174 FDA reports)
CONDITION AGGRAVATED ( 171 FDA reports)
OEDEMA PERIPHERAL ( 164 FDA reports)
TRANSPLANT REJECTION ( 160 FDA reports)
NAUSEA ( 159 FDA reports)
RENAL FAILURE ( 158 FDA reports)
HAEMODIALYSIS ( 156 FDA reports)
ASTHENIA ( 146 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 145 FDA reports)
DRUG INTERACTION ( 137 FDA reports)
THROMBOCYTOPENIA ( 126 FDA reports)
HYPERTENSION ( 117 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 114 FDA reports)
HYPOTENSION ( 109 FDA reports)
PNEUMONITIS ( 109 FDA reports)
WEIGHT DECREASED ( 109 FDA reports)
DRUG TOXICITY ( 106 FDA reports)
BLOOD GLUCOSE INCREASED ( 104 FDA reports)
PLATELET COUNT DECREASED ( 102 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 100 FDA reports)
PLEURAL EFFUSION ( 99 FDA reports)
BLOOD UREA INCREASED ( 97 FDA reports)
LIVER TRANSPLANT REJECTION ( 97 FDA reports)
LEUKOPENIA ( 96 FDA reports)
SEPSIS ( 96 FDA reports)
DIALYSIS ( 92 FDA reports)
MULTI-ORGAN FAILURE ( 92 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 89 FDA reports)
DIABETES MELLITUS ( 88 FDA reports)
PROTEINURIA ( 88 FDA reports)
LYMPHOCELE ( 87 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 85 FDA reports)
CONVULSION ( 83 FDA reports)
URINARY TRACT INFECTION ( 82 FDA reports)
PAIN ( 81 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 78 FDA reports)
RESPIRATORY FAILURE ( 77 FDA reports)
DEEP VEIN THROMBOSIS ( 76 FDA reports)
INFECTION ( 76 FDA reports)
INTERSTITIAL LUNG DISEASE ( 76 FDA reports)
MYOCARDIAL INFARCTION ( 76 FDA reports)
FATIGUE ( 75 FDA reports)
RASH ( 75 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 74 FDA reports)
OEDEMA ( 74 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 73 FDA reports)
CARDIAC ARREST ( 73 FDA reports)
ABDOMINAL PAIN ( 71 FDA reports)
ATRIAL FIBRILLATION ( 71 FDA reports)
COUGH ( 71 FDA reports)
IMMUNOSUPPRESSION ( 71 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 71 FDA reports)
ARTHRALGIA ( 68 FDA reports)
POST PROCEDURAL COMPLICATION ( 65 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 64 FDA reports)
GRAFT DYSFUNCTION ( 64 FDA reports)
CHEST PAIN ( 63 FDA reports)
MALAISE ( 63 FDA reports)
DISEASE RECURRENCE ( 62 FDA reports)
IMPAIRED HEALING ( 62 FDA reports)
PULMONARY OEDEMA ( 62 FDA reports)
CEREBROVASCULAR ACCIDENT ( 61 FDA reports)
HYPERLIPIDAEMIA ( 61 FDA reports)
PAIN IN EXTREMITY ( 61 FDA reports)
CARDIAC FAILURE ( 59 FDA reports)
TREMOR ( 58 FDA reports)
DISEASE PROGRESSION ( 57 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 56 FDA reports)
HEADACHE ( 56 FDA reports)
NEPHROPATHY TOXIC ( 56 FDA reports)
PERICARDIAL EFFUSION ( 56 FDA reports)
BLOOD CREATINE INCREASED ( 54 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 54 FDA reports)
CHOLESTASIS ( 54 FDA reports)
DRUG LEVEL INCREASED ( 54 FDA reports)
CHILLS ( 53 FDA reports)
FLUID OVERLOAD ( 53 FDA reports)
LUNG DISORDER ( 53 FDA reports)
RENAL FAILURE CHRONIC ( 53 FDA reports)
STAPHYLOCOCCAL INFECTION ( 53 FDA reports)
LUNG INFILTRATION ( 52 FDA reports)
HYDRONEPHROSIS ( 51 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 50 FDA reports)
ATELECTASIS ( 48 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 48 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 48 FDA reports)
CELLULITIS ( 48 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 47 FDA reports)
PANCYTOPENIA ( 47 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 46 FDA reports)
ASCITES ( 46 FDA reports)
HYPOXIA ( 46 FDA reports)
HAEMATURIA ( 45 FDA reports)
TRANSPLANT FAILURE ( 45 FDA reports)
CARDIOMEGALY ( 44 FDA reports)
MYOPATHY ( 43 FDA reports)
NEPHROTIC SYNDROME ( 43 FDA reports)
BACK PAIN ( 42 FDA reports)
DECREASED APPETITE ( 42 FDA reports)
BLOOD BILIRUBIN INCREASED ( 41 FDA reports)
LYMPHADENOPATHY ( 41 FDA reports)
PULMONARY EMBOLISM ( 41 FDA reports)
ABDOMINAL PAIN UPPER ( 40 FDA reports)
EPISTAXIS ( 40 FDA reports)
HYPERGLYCAEMIA ( 40 FDA reports)
MUSCULAR WEAKNESS ( 40 FDA reports)
MYALGIA ( 40 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 39 FDA reports)
WEIGHT INCREASED ( 39 FDA reports)
CANDIDIASIS ( 38 FDA reports)
CONFUSIONAL STATE ( 38 FDA reports)
BLOOD POTASSIUM INCREASED ( 37 FDA reports)
HEART TRANSPLANT REJECTION ( 37 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 36 FDA reports)
DEPRESSION ( 36 FDA reports)
DIZZINESS ( 36 FDA reports)
GASTRITIS ( 36 FDA reports)
OSTEONECROSIS ( 36 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 35 FDA reports)
HEPATIC FAILURE ( 35 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 35 FDA reports)
BLOOD PRESSURE INCREASED ( 34 FDA reports)
HAEMOPTYSIS ( 34 FDA reports)
HYPERKALAEMIA ( 34 FDA reports)
OVERDOSE ( 34 FDA reports)
SEPTIC SHOCK ( 34 FDA reports)
ANXIETY ( 33 FDA reports)
BACTERIAL INFECTION ( 33 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 33 FDA reports)
FALL ( 33 FDA reports)
PSEUDOMONAS INFECTION ( 33 FDA reports)
CACHEXIA ( 32 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 32 FDA reports)
INFLAMMATION ( 32 FDA reports)
NEUTROPENIA ( 32 FDA reports)
GRAFT VERSUS HOST DISEASE ( 31 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 31 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 31 FDA reports)
PHARYNGITIS ( 31 FDA reports)
PRURITUS ( 31 FDA reports)
PULMONARY CONGESTION ( 31 FDA reports)
STOMATITIS ( 31 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 31 FDA reports)
MITRAL VALVE INCOMPETENCE ( 30 FDA reports)
ANURIA ( 29 FDA reports)
BODY TEMPERATURE INCREASED ( 29 FDA reports)
BRONCHOPNEUMONIA ( 29 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 29 FDA reports)
MOUTH ULCERATION ( 29 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 29 FDA reports)
RENAL DISORDER ( 29 FDA reports)
APHTHOUS STOMATITIS ( 28 FDA reports)
BACTERAEMIA ( 28 FDA reports)
BLOOD SODIUM DECREASED ( 28 FDA reports)
COLITIS ( 28 FDA reports)
ERYTHEMA ( 28 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 28 FDA reports)
HYPOKALAEMIA ( 28 FDA reports)
MOBILITY DECREASED ( 28 FDA reports)
NEPHRITIS INTERSTITIAL ( 28 FDA reports)
TREATMENT NONCOMPLIANCE ( 28 FDA reports)
BLOOD BICARBONATE DECREASED ( 27 FDA reports)
BRONCHITIS ( 27 FDA reports)
HEPATIC ENZYME INCREASED ( 27 FDA reports)
JAUNDICE ( 27 FDA reports)
LETHARGY ( 27 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
METABOLIC ACIDOSIS ( 27 FDA reports)
ABDOMINAL DISTENSION ( 26 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 26 FDA reports)
ENTEROCOCCAL INFECTION ( 26 FDA reports)
FEBRILE NEUTROPENIA ( 26 FDA reports)
INSOMNIA ( 26 FDA reports)
OXYGEN SATURATION DECREASED ( 26 FDA reports)
TACHYCARDIA ( 26 FDA reports)
WOUND INFECTION ( 26 FDA reports)
ABDOMINAL PAIN LOWER ( 25 FDA reports)
BASAL CELL CARCINOMA ( 25 FDA reports)
BK VIRUS INFECTION ( 25 FDA reports)
HYPONATRAEMIA ( 25 FDA reports)
HYPOVOLAEMIA ( 25 FDA reports)
KLEBSIELLA INFECTION ( 25 FDA reports)
OFF LABEL USE ( 25 FDA reports)
RENAL TRANSPLANT ( 25 FDA reports)
ACNE ( 24 FDA reports)
AMNESIA ( 24 FDA reports)
BALANCE DISORDER ( 24 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 24 FDA reports)
GAIT DISTURBANCE ( 24 FDA reports)
GASTROENTERITIS ( 24 FDA reports)
HIV INFECTION ( 24 FDA reports)
DYSURIA ( 23 FDA reports)
EJECTION FRACTION DECREASED ( 23 FDA reports)
HAEMORRHAGE ( 23 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 23 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 23 FDA reports)
LIVER DISORDER ( 23 FDA reports)
LOSS OF CONSCIOUSNESS ( 23 FDA reports)
PARAESTHESIA ( 23 FDA reports)
PROSTATE CANCER ( 23 FDA reports)
PULMONARY HAEMORRHAGE ( 23 FDA reports)
SINUSITIS ( 23 FDA reports)
SKIN HYPERTROPHY ( 23 FDA reports)
SKIN INDURATION ( 23 FDA reports)
SKIN ULCER ( 23 FDA reports)
THROMBOSIS ( 23 FDA reports)
BLOOD CHLORIDE INCREASED ( 22 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 22 FDA reports)
DYSARTHRIA ( 22 FDA reports)
DYSPNOEA EXERTIONAL ( 22 FDA reports)
HAEMATOMA ( 22 FDA reports)
HAEMOLYSIS ( 22 FDA reports)
HEPATIC ENCEPHALOPATHY ( 22 FDA reports)
HEPATITIS ( 22 FDA reports)
KIDNEY FIBROSIS ( 22 FDA reports)
PULMONARY FIBROSIS ( 22 FDA reports)
PYELONEPHRITIS ( 22 FDA reports)
RASH PRURITIC ( 22 FDA reports)
RENAL TUBULAR DISORDER ( 22 FDA reports)
RHABDOMYOLYSIS ( 22 FDA reports)
SEROMA ( 22 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 22 FDA reports)
THERAPY NON-RESPONDER ( 22 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 22 FDA reports)
URETERIC STENOSIS ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
ANOREXIA ( 21 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 21 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 21 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 21 FDA reports)
DYSPHAGIA ( 21 FDA reports)
HYPERHIDROSIS ( 21 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 21 FDA reports)
MALNUTRITION ( 21 FDA reports)
NEPHROPATHY ( 21 FDA reports)
NEPHROSCLEROSIS ( 21 FDA reports)
RENAL TUBULAR ATROPHY ( 21 FDA reports)
RESPIRATORY DISTRESS ( 21 FDA reports)
SHOCK ( 21 FDA reports)
SOMNOLENCE ( 21 FDA reports)
VENTRICULAR HYPERTROPHY ( 21 FDA reports)
WOUND DEHISCENCE ( 21 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 20 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 20 FDA reports)
COMA ( 20 FDA reports)
ESCHERICHIA INFECTION ( 20 FDA reports)
FEELING ABNORMAL ( 20 FDA reports)
GRAFT COMPLICATION ( 20 FDA reports)
JOINT SWELLING ( 20 FDA reports)
LABORATORY TEST ABNORMAL ( 20 FDA reports)
MUCOSAL INFLAMMATION ( 20 FDA reports)
NECROSIS ( 20 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 20 FDA reports)
SCAR ( 20 FDA reports)
ACUTE HEPATIC FAILURE ( 19 FDA reports)
AZOTAEMIA ( 19 FDA reports)
CARDIO-RESPIRATORY ARREST ( 19 FDA reports)
COAGULOPATHY ( 19 FDA reports)
DRUG LEVEL DECREASED ( 19 FDA reports)
GASTROINTESTINAL DISORDER ( 19 FDA reports)
HEPATIC STEATOSIS ( 19 FDA reports)
INFLUENZA ( 19 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 19 FDA reports)
PULMONARY HYPERTENSION ( 19 FDA reports)
URINE OUTPUT DECREASED ( 19 FDA reports)
ABORTION SPONTANEOUS ( 18 FDA reports)
ACUTE PULMONARY OEDEMA ( 18 FDA reports)
ASPERGILLOSIS ( 18 FDA reports)
BLOOD POTASSIUM DECREASED ( 18 FDA reports)
BONE PAIN ( 18 FDA reports)
CATHETER RELATED INFECTION ( 18 FDA reports)
CHOLANGITIS ( 18 FDA reports)
CLOSTRIDIAL INFECTION ( 18 FDA reports)
CYTOLYTIC HEPATITIS ( 18 FDA reports)
DEFORMITY ( 18 FDA reports)
DRY SKIN ( 18 FDA reports)
FUNGAL INFECTION ( 18 FDA reports)
HEART RATE INCREASED ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 18 FDA reports)
LUNG CONSOLIDATION ( 18 FDA reports)
SPUTUM CULTURE POSITIVE ( 18 FDA reports)
SQUAMOUS CELL CARCINOMA ( 18 FDA reports)
CLOSTRIDIUM COLITIS ( 17 FDA reports)
CONSTIPATION ( 17 FDA reports)
EMOTIONAL DISTRESS ( 17 FDA reports)
FIBROSIS ( 17 FDA reports)
HEPATIC ARTERY STENOSIS ( 17 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
ILEUS ( 17 FDA reports)
LIVER TRANSPLANT ( 17 FDA reports)
LYMPHOEDEMA ( 17 FDA reports)
MYOCARDIAL ISCHAEMIA ( 17 FDA reports)
NASOPHARYNGITIS ( 17 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 17 FDA reports)
OLIGURIA ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
PROTHROMBIN TIME PROLONGED ( 17 FDA reports)
RESPIRATORY DISORDER ( 17 FDA reports)
RESPIRATORY RATE INCREASED ( 17 FDA reports)
BLOOD CALCIUM DECREASED ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 16 FDA reports)
CHEST X-RAY ABNORMAL ( 16 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 16 FDA reports)
COORDINATION ABNORMAL ( 16 FDA reports)
DIABETIC FOOT ( 16 FDA reports)
DIVERTICULITIS ( 16 FDA reports)
HEPATIC NECROSIS ( 16 FDA reports)
HYPOAESTHESIA ( 16 FDA reports)
HYPOCALCAEMIA ( 16 FDA reports)
MEDICATION ERROR ( 16 FDA reports)
ORAL INTAKE REDUCED ( 16 FDA reports)
OSTEOARTHRITIS ( 16 FDA reports)
PCO2 DECREASED ( 16 FDA reports)
PERINEPHRIC COLLECTION ( 16 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 16 FDA reports)
PULMONARY TOXICITY ( 16 FDA reports)
RASH GENERALISED ( 16 FDA reports)
RENAL CYST ( 16 FDA reports)
SEBACEOUS CARCINOMA ( 16 FDA reports)
ACUTE CORONARY SYNDROME ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
CARDIAC MURMUR ( 15 FDA reports)
CEREBRAL ISCHAEMIA ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
CULTURE URINE POSITIVE ( 15 FDA reports)
CYSTITIS ( 15 FDA reports)
DRUG INTOLERANCE ( 15 FDA reports)
FLUID RETENTION ( 15 FDA reports)
HYPOMAGNESAEMIA ( 15 FDA reports)
INFLUENZA LIKE ILLNESS ( 15 FDA reports)
INTRACARDIAC THROMBUS ( 15 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 15 FDA reports)
MENTAL STATUS CHANGES ( 15 FDA reports)
MUSCLE ATROPHY ( 15 FDA reports)
OCULAR ICTERUS ( 15 FDA reports)
PERITONEAL DIALYSIS ( 15 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 15 FDA reports)
TOE AMPUTATION ( 15 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 15 FDA reports)
VENOUS THROMBOSIS ( 15 FDA reports)
VENTRICULAR FIBRILLATION ( 15 FDA reports)
ABDOMINAL HERNIA ( 14 FDA reports)
ACCIDENTAL OVERDOSE ( 14 FDA reports)
ACIDOSIS ( 14 FDA reports)
ACUTE ABDOMEN ( 14 FDA reports)
ANGIONEUROTIC OEDEMA ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 14 FDA reports)
BLOOD CHLORIDE DECREASED ( 14 FDA reports)
BODY TEMPERATURE DECREASED ( 14 FDA reports)
DRUG EFFECT DECREASED ( 14 FDA reports)
DRUG HYPERSENSITIVITY ( 14 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 14 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 14 FDA reports)
GASTRIC ULCER ( 14 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 14 FDA reports)
GENERALISED OEDEMA ( 14 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 14 FDA reports)
HAEMATEMESIS ( 14 FDA reports)
HAND FRACTURE ( 14 FDA reports)
HERNIA ( 14 FDA reports)
HERPES SIMPLEX ( 14 FDA reports)
HYPOPHOSPHATAEMIA ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 14 FDA reports)
MALIGNANT TUMOUR EXCISION ( 14 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 14 FDA reports)
NEPHROLITHIASIS ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
PERIRENAL HAEMATOMA ( 14 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 14 FDA reports)
PREMATURE BABY ( 14 FDA reports)
SKIN CANCER ( 14 FDA reports)
SKIN DISCOLOURATION ( 14 FDA reports)
TUBERCULOSIS ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
URINARY FISTULA ( 14 FDA reports)
URINE COLOUR ABNORMAL ( 14 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ARTERIOSCLEROSIS ( 13 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 13 FDA reports)
BLOOD CULTURE POSITIVE ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
ENDOCARDITIS ( 13 FDA reports)
GRAFT LOSS ( 13 FDA reports)
HERPES VIRUS INFECTION ( 13 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 13 FDA reports)
IRON DEFICIENCY ANAEMIA ( 13 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 13 FDA reports)
JOINT STIFFNESS ( 13 FDA reports)
LEG AMPUTATION ( 13 FDA reports)
LOBAR PNEUMONIA ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
METRORRHAGIA ( 13 FDA reports)
MICROANGIOPATHY ( 13 FDA reports)
NEUROPATHY PERIPHERAL ( 13 FDA reports)
POST PROCEDURAL HAEMATOMA ( 13 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 13 FDA reports)
UROSEPSIS ( 13 FDA reports)
URTICARIA ( 13 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 13 FDA reports)
ANGINA UNSTABLE ( 12 FDA reports)
DRUG RESISTANCE ( 12 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
GLOMERULONEPHRITIS ( 12 FDA reports)
GOITRE ( 12 FDA reports)
GOUT ( 12 FDA reports)
GRAND MAL CONVULSION ( 12 FDA reports)
HAEMATOCHEZIA ( 12 FDA reports)
HAEMORRHOIDS ( 12 FDA reports)
HIP FRACTURE ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
ILEUS PARALYTIC ( 12 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 12 FDA reports)
NEPHROGENIC ANAEMIA ( 12 FDA reports)
ODYNOPHAGIA ( 12 FDA reports)
ORAL CANDIDIASIS ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
PRODUCTIVE COUGH ( 12 FDA reports)
RASH MACULAR ( 12 FDA reports)
RENAL HAEMATOMA ( 12 FDA reports)
SALMONELLOSIS ( 12 FDA reports)
SCRATCH ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
SPLENOMEGALY ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
URETERIC OBSTRUCTION ( 12 FDA reports)
URINARY RETENTION ( 12 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 12 FDA reports)
VASCULAR GRAFT COMPLICATION ( 12 FDA reports)
ALOPECIA ( 11 FDA reports)
ALVEOLITIS ALLERGIC ( 11 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 11 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 11 FDA reports)
BRONCHIECTASIS ( 11 FDA reports)
CARDIAC FAILURE ACUTE ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 11 FDA reports)
CREPITATIONS ( 11 FDA reports)
DISCOMFORT ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
DRUG DOSE OMISSION ( 11 FDA reports)
GANGRENE ( 11 FDA reports)
GRANULOMA ( 11 FDA reports)
HAEMOPHILUS INFECTION ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
JOINT CONTRACTURE ( 11 FDA reports)
MELAENA ( 11 FDA reports)
METASTASIS ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
OESOPHAGEAL ULCER ( 11 FDA reports)
OVARIAN CYST ( 11 FDA reports)
PERICARDITIS ( 11 FDA reports)
PO2 DECREASED ( 11 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 11 FDA reports)
PROTEIN TOTAL DECREASED ( 11 FDA reports)
PYELONEPHRITIS ACUTE ( 11 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
RENAL HAEMORRHAGE ( 11 FDA reports)
RETROPERITONEAL HAEMATOMA ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
SKIN FIBROSIS ( 11 FDA reports)
SKIN TIGHTNESS ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
URINARY INCONTINENCE ( 11 FDA reports)
VARICOSE VEIN ( 11 FDA reports)
WOUND COMPLICATION ( 11 FDA reports)
WOUND SECRETION ( 11 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 10 FDA reports)
BRADYCARDIA ( 10 FDA reports)
COLON CANCER ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
GASTROINTESTINAL PAIN ( 10 FDA reports)
HEPATITIS ACUTE ( 10 FDA reports)
HEPATITIS C ( 10 FDA reports)
HUMERUS FRACTURE ( 10 FDA reports)
IGA NEPHROPATHY ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INJURY ( 10 FDA reports)
INTESTINAL PROLAPSE ( 10 FDA reports)
LARYNGITIS BACTERIAL ( 10 FDA reports)
LARYNGITIS FUNGAL ( 10 FDA reports)
LOCALISED INFECTION ( 10 FDA reports)
MENSTRUATION IRREGULAR ( 10 FDA reports)
NEUROTOXICITY ( 10 FDA reports)
PLATELET COUNT INCREASED ( 10 FDA reports)
PROTEIN URINE PRESENT ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
TOOTH DISORDER ( 10 FDA reports)
UTERINE CANCER ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
ABSCESS ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
AORTIC CALCIFICATION ( 9 FDA reports)
ARTHRITIS ( 9 FDA reports)
BLADDER MASS ( 9 FDA reports)
BLOOD SODIUM INCREASED ( 9 FDA reports)
BONE MARROW DEPRESSION ( 9 FDA reports)
CATARACT ( 9 FDA reports)
CIRCULATORY COLLAPSE ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
DYSPEPSIA ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 9 FDA reports)
HAEMORRHAGIC INFARCTION ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
HEPATIC FIBROSIS ( 9 FDA reports)
HIATUS HERNIA ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
INCREASED TENDENCY TO BRUISE ( 9 FDA reports)
INTESTINAL DILATATION ( 9 FDA reports)
LEFT VENTRICULAR FAILURE ( 9 FDA reports)
MALIGNANT MELANOMA ( 9 FDA reports)
MASS ( 9 FDA reports)
METASTASES TO LIVER ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 9 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 9 FDA reports)
RENAL INFARCT ( 9 FDA reports)
SKIN DISORDER ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 9 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 9 FDA reports)
TROPONIN INCREASED ( 9 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 9 FDA reports)
URINARY TRACT OBSTRUCTION ( 9 FDA reports)
URINOMA ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
APHAGIA ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
ASTHMA ( 8 FDA reports)
BILE DUCT OBSTRUCTION ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 8 FDA reports)
BLOOD GLUCOSE DECREASED ( 8 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 8 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CARDIAC TAMPONADE ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
CITROBACTER INFECTION ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
EMBOLIC STROKE ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
FACIAL PALSY ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GLOMERULOSCLEROSIS ( 8 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HYPERVOLAEMIA ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
INFANTILE SPASMS ( 8 FDA reports)
INTUBATION ( 8 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
LYMPHOPENIA ( 8 FDA reports)
MYOSITIS ( 8 FDA reports)
OESOPHAGITIS ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 8 FDA reports)
POSTOPERATIVE INFECTION ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 8 FDA reports)
SINUS HEADACHE ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 8 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 8 FDA reports)
ACINETOBACTER INFECTION ( 7 FDA reports)
ADENOVIRUS INFECTION ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ALVEOLAR PROTEINOSIS ( 7 FDA reports)
AORTIC DILATATION ( 7 FDA reports)
ATRIAL FLUTTER ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BLADDER CANCER ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
BRONCHIAL CARCINOMA ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CENTRAL LINE INFECTION ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 7 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
CYST ( 7 FDA reports)
DECUBITUS ULCER ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
DRUG LEVEL FLUCTUATING ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
DRY GANGRENE ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
ELECTROLYTE IMBALANCE ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
FLANK PAIN ( 7 FDA reports)
GASTRITIS EROSIVE ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HIP ARTHROPLASTY ( 7 FDA reports)
HOSPITALISATION ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPOCHROMIC ANAEMIA ( 7 FDA reports)
KAPOSI'S SARCOMA ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYCOPLASMA INFECTION ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
NEPHROCALCINOSIS ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 7 FDA reports)
PROCTOCOLITIS ( 7 FDA reports)
PROSTATE CANCER METASTATIC ( 7 FDA reports)
PURULENCE ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RENAL ABSCESS ( 7 FDA reports)
RENAL LYMPHOCELE ( 7 FDA reports)
RENAL VESSEL DISORDER ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
RETICULOCYTE COUNT DECREASED ( 7 FDA reports)
SCAB ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
SWELLING ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
TUBEROUS SCLEROSIS ( 7 FDA reports)
VASCULAR CALCIFICATION ( 7 FDA reports)
VENOOCCLUSIVE DISEASE ( 7 FDA reports)
VENTRICULAR DYSFUNCTION ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
WOUND EVISCERATION ( 7 FDA reports)
ACTINIC KERATOSIS ( 6 FDA reports)
AEROMONA INFECTION ( 6 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ANGIOPATHY ( 6 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
AORTIC VALVE STENOSIS ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ASPIRATION ( 6 FDA reports)
AZOOSPERMIA ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLEEDING TIME PROLONGED ( 6 FDA reports)
BLOOD BICARBONATE INCREASED ( 6 FDA reports)
BLOOD CREATININE DECREASED ( 6 FDA reports)
BLOOD PH DECREASED ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BRAIN ABSCESS ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CALCIPHYLAXIS ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CHOKING SENSATION ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
COLITIS ULCERATIVE ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
ENTEROBACTER BACTERAEMIA ( 6 FDA reports)
ENTEROBACTER INFECTION ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
IMPAIRED SELF-CARE ( 6 FDA reports)
IMPLANT SITE INFECTION ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 6 FDA reports)
METASTATIC NEOPLASM ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
NEOPLASM PROGRESSION ( 6 FDA reports)
NEPHRECTOMY ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 6 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 6 FDA reports)
OESOPHAGEAL CARCINOMA ( 6 FDA reports)
PANCREAS TRANSPLANT ( 6 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PERINEPHRIC EFFUSION ( 6 FDA reports)
PHLEBITIS ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PNEUMOCOCCAL SEPSIS ( 6 FDA reports)
PNEUMONIA ASPERGILLUS ( 6 FDA reports)
PNEUMONIA LEGIONELLA ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
PYELOCALIECTASIS ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SKIN ODOUR ABNORMAL ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SUBDURAL HAEMATOMA ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ABDOMINAL HAEMATOMA ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
ALOPECIA EFFLUVIUM ( 5 FDA reports)
ANASTOMOTIC COMPLICATION ( 5 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 5 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLADDER DISTENSION ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BONE DISORDER ( 5 FDA reports)
BONE MARROW TOXICITY ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 5 FDA reports)
DIARRHOEA INFECTIOUS ( 5 FDA reports)
DIFFICULTY IN WALKING ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESCHAR ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEAR ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
HEPATIC CANCER METASTATIC ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LARYNGEAL CANCER ( 5 FDA reports)
LARYNGEAL STENOSIS ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
LUNG TRANSPLANT REJECTION ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MARROW HYPERPLASIA ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MICROTIA ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 5 FDA reports)
OBSTRUCTIVE UROPATHY ( 5 FDA reports)
OESOPHAGITIS ULCERATIVE ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
PAIN OF SKIN ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PNEUMATOSIS ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
PULMONARY GRANULOMA ( 5 FDA reports)
PULMONARY TUBERCULOSIS ( 5 FDA reports)
RALES ( 5 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 5 FDA reports)
RENAL GRAFT LOSS ( 5 FDA reports)
RENAL ISCHAEMIA ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SCOLIOSIS ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SOFT TISSUE INFECTION ( 5 FDA reports)
SPLENIC LESION ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STARING ( 5 FDA reports)
STRESS ( 5 FDA reports)
SURGERY ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
ULCER ( 5 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VENOUS STENOSIS ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
VOLVULUS ( 5 FDA reports)
WOUND ABSCESS ( 5 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ACID FAST BACILLI INFECTION ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANASTOMOTIC STENOSIS ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ARTERIAL HAEMORRHAGE ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BACTERIAL PYELONEPHRITIS ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BONE CALLUS EXCESSIVE ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
COLON ADENOMA ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 4 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CULTURE WOUND POSITIVE ( 4 FDA reports)
CYCLIC VOMITING SYNDROME ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 4 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETIC GANGRENE ( 4 FDA reports)
DIASTOLIC HYPERTENSION ( 4 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
EROSIVE OESOPHAGITIS ( 4 FDA reports)
ERYTHROID SERIES ABNORMAL ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GALLBLADDER OEDEMA ( 4 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
GENITAL CANDIDIASIS ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
ILIAC VEIN OCCLUSION ( 4 FDA reports)
INCISION SITE HAEMATOMA ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KIDNEY ENLARGEMENT ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIP DISORDER ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MARFAN'S SYNDROME ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MEDIASTINAL DISORDER ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MYELOMA RECURRENCE ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROPATHIC ARTHROPATHY ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PAPILLARY THYROID CANCER ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERINEPHRIC ABSCESS ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PH BODY FLUID DECREASED ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA HAEMOPHILUS ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
POLYOMAVIRUS INTERSTITIAL NEPHRITIS ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 4 FDA reports)
RENAL NECROSIS ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
TRANSPLANT ABSCESS ( 4 FDA reports)
TROPONIN T INCREASED ( 4 FDA reports)
URETERIC FISTULA ( 4 FDA reports)
URINARY TRACT DISORDER ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
VESICAL FISTULA ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ALCOHOL USE ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD FOLATE ABNORMAL ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 3 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
BONE MARROW OEDEMA ( 3 FDA reports)
BONE OPERATION ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INFECTED LYMPHOCELE ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INTRAOCULAR LENS IMPLANT ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LEGIONELLA INFECTION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
LYMPHANGIOSARCOMA ( 3 FDA reports)
MACROCEPHALY ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OVARIAN ADENOMA ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PARVOVIRUS INFECTION ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PLASMAPHERESIS ( 3 FDA reports)
PLEURAL CALCIFICATION ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
PROCALCITONIN INCREASED ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 3 FDA reports)
RENAL CORTICAL NECROSIS ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL VEIN OCCLUSION ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SODIUM RETENTION ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URINARY ANASTOMOTIC LEAK ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VASCULITIS GASTROINTESTINAL ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
X-RAY LIMB ABNORMAL ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADENOIDITIS ( 2 FDA reports)
ALPHA GLOBULIN INCREASED ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 2 FDA reports)
ASPERMIA ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL FOOD POISONING ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILE DUCT CANCER RECURRENT ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY LUNG ABNORMAL ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FISTULA REPAIR ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HERNIAL EVENTRATION ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLAMMATION LOCALISED ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIGAMENT PAIN ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO PITUITARY GLAND ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUROMUSCULAR BLOCKING THERAPY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OVARIAN DYSGERMINOMA STAGE UNSPECIFIED ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANEL-REACTIVE ANTIBODY INCREASED ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PH BODY FLUID INCREASED ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PLACENTAL CHORIOANGIOMA ( 2 FDA reports)
PLACENTAL HYPERTROPHY ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEURAL NEOPLASM ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRODUCT CONTAINER ISSUE ( 2 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 2 FDA reports)
PROSTATECTOMY ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULMONARY VASCULITIS ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL INFILTRATES ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SKIN CANCER METASTATIC ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPERMATOZOA ABNORMAL ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPLENIC VARICES ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL DILATATION ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VIRAL DIARRHOEA ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WOUND ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABDOMINAL X-RAY ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS STERILE ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMPUTATION REVISION ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL CANCER STAGE IV ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGINA BULLOSA HAEMORRHAGICA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM RENAL ABNORMAL ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE COMPLICATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY BLOOD VESSEL ABNORMAL ( 1 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 1 FDA reports)
BIOPSY HEART ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS PHARYNGEAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS VIRAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CROSSMATCH COMPATIBLE ( 1 FDA reports)
CROSSMATCH INCOMPATIBLE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF PROTEIN ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
DECREASED INSULIN REQUIREMENT ( 1 FDA reports)
DELAYED ENGRAFTMENT ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENZYME LEVEL INCREASED ( 1 FDA reports)
EPIDIDYMAL CYST ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTRINSIC ILIAC VEIN COMPRESSION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PROSTHESIS INSERTION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS HERPES ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITALIA EXTERNAL PAINFUL ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS POST TRANSFUSION ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
KIDNEY ANASTOMOSIS ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIGAMENT OPERATION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MANIA ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MISCARRIAGE OF PARTNER ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NEPHROURETERECTOMY ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORCHITIS NONINFECTIVE ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN ADHESION ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURA CARCINOMA ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTATOVESICULITIS ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL LIPOMATOSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELECTIVE IGG SUBCLASS DEFICIENCY ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPERMATOGENESIS ABNORMAL ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN ARTERY ANEURYSM ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPRAVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVIAL SARCOMA RECURRENT ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR CANCER METASTATIC ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TESTICULAR NECROSIS ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URAEMIC GASTROPATHY ( 1 FDA reports)
URETERIC REIMPLANTATION ( 1 FDA reports)
URETERIC REPAIR ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO DECREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)