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

PYREXIA ( 329 FDA reports)
PAIN ( 282 FDA reports)
DIARRHOEA ( 260 FDA reports)
SEPSIS ( 257 FDA reports)
PNEUMONIA ( 249 FDA reports)
OSTEONECROSIS ( 245 FDA reports)
BONE DISORDER ( 236 FDA reports)
OSTEONECROSIS OF JAW ( 236 FDA reports)
ANXIETY ( 227 FDA reports)
FEBRILE NEUTROPENIA ( 214 FDA reports)
ANAEMIA ( 197 FDA reports)
MULTIPLE MYELOMA ( 193 FDA reports)
PANCYTOPENIA ( 182 FDA reports)
DYSPNOEA ( 179 FDA reports)
TOOTH EXTRACTION ( 177 FDA reports)
INJURY ( 170 FDA reports)
FATIGUE ( 167 FDA reports)
INFECTION ( 165 FDA reports)
NEUROPATHY PERIPHERAL ( 164 FDA reports)
PAIN IN JAW ( 157 FDA reports)
RENAL FAILURE ( 157 FDA reports)
OSTEOMYELITIS ( 153 FDA reports)
OSTEOPENIA ( 148 FDA reports)
RENAL FAILURE ACUTE ( 145 FDA reports)
NAUSEA ( 144 FDA reports)
ASTHENIA ( 143 FDA reports)
NEUTROPENIA ( 143 FDA reports)
BACK PAIN ( 141 FDA reports)
HERPES ZOSTER ( 140 FDA reports)
CONSTIPATION ( 138 FDA reports)
THROMBOCYTOPENIA ( 133 FDA reports)
BRONCHITIS ( 130 FDA reports)
PAIN IN EXTREMITY ( 128 FDA reports)
FALL ( 121 FDA reports)
ARTHRALGIA ( 120 FDA reports)
CHEST PAIN ( 120 FDA reports)
VOMITING ( 118 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 114 FDA reports)
OEDEMA PERIPHERAL ( 111 FDA reports)
MUCOSAL INFLAMMATION ( 108 FDA reports)
IMPAIRED HEALING ( 106 FDA reports)
STOMATITIS ( 106 FDA reports)
ANHEDONIA ( 105 FDA reports)
CARDIOMEGALY ( 103 FDA reports)
CARDIAC FAILURE ( 102 FDA reports)
DEFORMITY ( 101 FDA reports)
DECREASED APPETITE ( 100 FDA reports)
HYPERTENSION ( 99 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 97 FDA reports)
RESPIRATORY FAILURE ( 97 FDA reports)
BLOOD CREATININE INCREASED ( 95 FDA reports)
SWELLING ( 95 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 93 FDA reports)
COUGH ( 93 FDA reports)
HYPOAESTHESIA ( 92 FDA reports)
CATARACT ( 91 FDA reports)
DEPRESSION ( 91 FDA reports)
MUCOUS MEMBRANE DISORDER ( 91 FDA reports)
OSTEOARTHRITIS ( 89 FDA reports)
BONE LESION ( 88 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 88 FDA reports)
EMOTIONAL DISTRESS ( 87 FDA reports)
PLATELET COUNT DECREASED ( 87 FDA reports)
URINARY TRACT INFECTION ( 87 FDA reports)
ATELECTASIS ( 86 FDA reports)
LEUKOPENIA ( 83 FDA reports)
INTERSTITIAL LUNG DISEASE ( 81 FDA reports)
DEATH ( 79 FDA reports)
HYPOKALAEMIA ( 77 FDA reports)
SPINAL OSTEOARTHRITIS ( 77 FDA reports)
BONE PAIN ( 76 FDA reports)
PLEURAL EFFUSION ( 76 FDA reports)
SEPTIC SHOCK ( 75 FDA reports)
ACTINOMYCOSIS ( 74 FDA reports)
DEHYDRATION ( 74 FDA reports)
HAEMOGLOBIN DECREASED ( 74 FDA reports)
RASH ( 73 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 73 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 72 FDA reports)
INSOMNIA ( 72 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 72 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 72 FDA reports)
ABDOMINAL PAIN ( 71 FDA reports)
COMPRESSION FRACTURE ( 71 FDA reports)
PARAESTHESIA ( 71 FDA reports)
EXOSTOSIS ( 70 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 69 FDA reports)
RENAL IMPAIRMENT ( 69 FDA reports)
STEM CELL TRANSPLANT ( 69 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 67 FDA reports)
ATRIAL FIBRILLATION ( 66 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 66 FDA reports)
ERYTHEMA ( 66 FDA reports)
SEQUESTRECTOMY ( 66 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 66 FDA reports)
GRAFT VERSUS HOST DISEASE ( 65 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 64 FDA reports)
CORONARY ARTERY DISEASE ( 64 FDA reports)
MALAISE ( 64 FDA reports)
WEIGHT DECREASED ( 64 FDA reports)
CONFUSIONAL STATE ( 63 FDA reports)
RECTAL HAEMORRHAGE ( 63 FDA reports)
DIZZINESS ( 61 FDA reports)
SINUSITIS ( 61 FDA reports)
DISEASE PROGRESSION ( 60 FDA reports)
PURULENT DISCHARGE ( 60 FDA reports)
ANOREXIA ( 59 FDA reports)
CHILLS ( 59 FDA reports)
MULTI-ORGAN FAILURE ( 58 FDA reports)
OROPHARYNGEAL PAIN ( 58 FDA reports)
OSTEOPOROSIS ( 58 FDA reports)
BONE DEBRIDEMENT ( 57 FDA reports)
NEOPLASM MALIGNANT ( 57 FDA reports)
TOOTHACHE ( 56 FDA reports)
ORAL PAIN ( 55 FDA reports)
WEIGHT INCREASED ( 55 FDA reports)
LOOSE TOOTH ( 54 FDA reports)
DENTAL CARIES ( 53 FDA reports)
DYSPHAGIA ( 53 FDA reports)
JAW DISORDER ( 53 FDA reports)
PRIMARY SEQUESTRUM ( 53 FDA reports)
BONE MARROW FAILURE ( 52 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 51 FDA reports)
DEEP VEIN THROMBOSIS ( 51 FDA reports)
EPISTAXIS ( 51 FDA reports)
HYPONATRAEMIA ( 51 FDA reports)
HYPOPHAGIA ( 51 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 50 FDA reports)
LIVER DISORDER ( 50 FDA reports)
MUSCLE SPASMS ( 50 FDA reports)
RIB FRACTURE ( 50 FDA reports)
OSTEOLYSIS ( 49 FDA reports)
TENDONITIS ( 49 FDA reports)
CONVULSION ( 48 FDA reports)
FISTULA ( 48 FDA reports)
HYPERLIPIDAEMIA ( 48 FDA reports)
NASAL CONGESTION ( 48 FDA reports)
TOOTH INFECTION ( 48 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 47 FDA reports)
MITRAL VALVE INCOMPETENCE ( 47 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 47 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 46 FDA reports)
EMPHYSEMA ( 46 FDA reports)
GINGIVAL BLEEDING ( 46 FDA reports)
PHYSICAL DISABILITY ( 46 FDA reports)
PROTEINURIA ( 46 FDA reports)
SLEEP APNOEA SYNDROME ( 46 FDA reports)
SPINAL COMPRESSION FRACTURE ( 46 FDA reports)
ABSCESS JAW ( 45 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 45 FDA reports)
DENTURE WEARER ( 45 FDA reports)
DIABETES MELLITUS ( 45 FDA reports)
HEADACHE ( 45 FDA reports)
MYALGIA ( 45 FDA reports)
PRODUCTIVE COUGH ( 45 FDA reports)
BLOOD BILIRUBIN INCREASED ( 44 FDA reports)
HYPOTENSION ( 44 FDA reports)
OEDEMA ( 44 FDA reports)
RENAL DISORDER ( 44 FDA reports)
MUSCULOSKELETAL PAIN ( 43 FDA reports)
PULMONARY OEDEMA ( 43 FDA reports)
SPINAL COLUMN STENOSIS ( 43 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 43 FDA reports)
BURSITIS ( 42 FDA reports)
DIVERTICULUM ( 42 FDA reports)
GAIT DISTURBANCE ( 42 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 42 FDA reports)
NEUTROPHIL COUNT DECREASED ( 42 FDA reports)
ABDOMINAL PAIN UPPER ( 41 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 41 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 41 FDA reports)
METASTASES TO BONE ( 41 FDA reports)
MYELODYSPLASTIC SYNDROME ( 41 FDA reports)
STAPHYLOCOCCAL INFECTION ( 41 FDA reports)
TACHYCARDIA ( 41 FDA reports)
DRUG TOXICITY ( 40 FDA reports)
HIATUS HERNIA ( 40 FDA reports)
LUMBAR SPINAL STENOSIS ( 40 FDA reports)
PULMONARY FIBROSIS ( 40 FDA reports)
PULMONARY HYPERTENSION ( 40 FDA reports)
TOOTH DISORDER ( 40 FDA reports)
LUNG INFILTRATION ( 39 FDA reports)
TENDERNESS ( 39 FDA reports)
ARTERIOSCLEROSIS ( 38 FDA reports)
DISABILITY ( 38 FDA reports)
DYSPNOEA EXERTIONAL ( 38 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 38 FDA reports)
RENAL FAILURE CHRONIC ( 38 FDA reports)
BACTERIAL INFECTION ( 37 FDA reports)
BURNING SENSATION ( 37 FDA reports)
HAEMATURIA ( 37 FDA reports)
HYPERCALCAEMIA ( 37 FDA reports)
LUNG DISORDER ( 37 FDA reports)
SWELLING FACE ( 37 FDA reports)
ASEPTIC NECROSIS BONE ( 36 FDA reports)
CYSTITIS HAEMORRHAGIC ( 36 FDA reports)
HAEMATOCHEZIA ( 36 FDA reports)
OSTEITIS ( 36 FDA reports)
PLANTAR FASCIITIS ( 36 FDA reports)
TOOTH LOSS ( 36 FDA reports)
DEBRIDEMENT ( 35 FDA reports)
GINGIVAL SWELLING ( 35 FDA reports)
HAEMORRHOIDS ( 35 FDA reports)
HEPATIC FAILURE ( 35 FDA reports)
HYPOXIA ( 35 FDA reports)
RADICULOPATHY ( 35 FDA reports)
SINUS DISORDER ( 35 FDA reports)
AMNESIA ( 34 FDA reports)
ASTHMA ( 34 FDA reports)
FUNGAL INFECTION ( 34 FDA reports)
NOCTURIA ( 34 FDA reports)
PRURITUS ( 34 FDA reports)
SPONDYLOLISTHESIS ( 34 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 33 FDA reports)
DIVERTICULUM INTESTINAL ( 33 FDA reports)
DYSURIA ( 33 FDA reports)
EXPOSED BONE IN JAW ( 33 FDA reports)
HYPERHIDROSIS ( 33 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 33 FDA reports)
NEPHROLITHIASIS ( 33 FDA reports)
OXYGEN SATURATION DECREASED ( 33 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 32 FDA reports)
CARDIOMYOPATHY ( 32 FDA reports)
CELLULITIS ( 32 FDA reports)
GINGIVAL INFECTION ( 32 FDA reports)
JAUNDICE ( 32 FDA reports)
NECK PAIN ( 32 FDA reports)
POST HERPETIC NEURALGIA ( 32 FDA reports)
ROTATOR CUFF SYNDROME ( 32 FDA reports)
CONTUSION ( 31 FDA reports)
HAEMORRHAGE ( 31 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 31 FDA reports)
METASTASES TO SPINE ( 31 FDA reports)
MOUTH HAEMORRHAGE ( 31 FDA reports)
MYOCARDIAL INFARCTION ( 31 FDA reports)
PLASMACYTOSIS ( 31 FDA reports)
SINUS TACHYCARDIA ( 31 FDA reports)
VERTEBROPLASTY ( 31 FDA reports)
ANGINA PECTORIS ( 30 FDA reports)
BLOOD GLUCOSE INCREASED ( 30 FDA reports)
BLOOD UREA INCREASED ( 30 FDA reports)
BREAST PAIN ( 30 FDA reports)
DISCOMFORT ( 30 FDA reports)
GLAUCOMA ( 30 FDA reports)
HYPERGLYCAEMIA ( 30 FDA reports)
INFLAMMATION ( 30 FDA reports)
LUNG NEOPLASM ( 30 FDA reports)
LYMPHADENOPATHY ( 30 FDA reports)
NEURALGIA ( 30 FDA reports)
NIGHT SWEATS ( 30 FDA reports)
TOOTH FRACTURE ( 30 FDA reports)
VISION BLURRED ( 30 FDA reports)
DISORIENTATION ( 29 FDA reports)
DYSPEPSIA ( 29 FDA reports)
EATING DISORDER ( 29 FDA reports)
INFLUENZA ( 29 FDA reports)
JAW OPERATION ( 29 FDA reports)
LIFE EXPECTANCY SHORTENED ( 29 FDA reports)
RENAL CYST ( 29 FDA reports)
RESTLESS LEGS SYNDROME ( 29 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 29 FDA reports)
TOXIC SKIN ERUPTION ( 29 FDA reports)
ABSCESS DRAINAGE ( 28 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 28 FDA reports)
BLOOD CALCIUM DECREASED ( 28 FDA reports)
CHEST DISCOMFORT ( 28 FDA reports)
LOSS OF CONSCIOUSNESS ( 28 FDA reports)
MUSCULAR WEAKNESS ( 28 FDA reports)
SCAR ( 28 FDA reports)
SYSTEMIC CANDIDA ( 28 FDA reports)
URINARY RETENTION ( 28 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 27 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 27 FDA reports)
CEREBRAL HAEMORRHAGE ( 27 FDA reports)
CONDITION AGGRAVATED ( 27 FDA reports)
HYPOTHYROIDISM ( 27 FDA reports)
MYOCARDIAL ISCHAEMIA ( 27 FDA reports)
OESOPHAGITIS ( 27 FDA reports)
ORAL DISORDER ( 27 FDA reports)
ORAL SURGERY ( 27 FDA reports)
PULMONARY EMBOLISM ( 27 FDA reports)
UROSEPSIS ( 27 FDA reports)
BASAL CELL CARCINOMA ( 26 FDA reports)
DECREASED INTEREST ( 26 FDA reports)
DENTAL OPERATION ( 26 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 26 FDA reports)
HYPERCHOLESTEROLAEMIA ( 26 FDA reports)
INGUINAL HERNIA ( 26 FDA reports)
MIGRAINE ( 26 FDA reports)
PATHOLOGICAL FRACTURE ( 26 FDA reports)
RESPIRATORY DISTRESS ( 26 FDA reports)
SCIATICA ( 26 FDA reports)
SQUAMOUS CELL CARCINOMA ( 26 FDA reports)
SYNCOPE ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 25 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 25 FDA reports)
RHABDOMYOLYSIS ( 25 FDA reports)
SINUS CONGESTION ( 25 FDA reports)
WHEEZING ( 25 FDA reports)
BLOOD PRESSURE INCREASED ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
COLONIC POLYP ( 24 FDA reports)
GASTROENTERITIS ( 24 FDA reports)
IMMUNODEFICIENCY ( 24 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 24 FDA reports)
LUNG CONSOLIDATION ( 24 FDA reports)
MENTAL STATUS CHANGES ( 24 FDA reports)
PERIODONTITIS ( 24 FDA reports)
SEBORRHOEIC KERATOSIS ( 24 FDA reports)
SPONDYLITIS ( 24 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 24 FDA reports)
URINARY INCONTINENCE ( 24 FDA reports)
VISUAL ACUITY REDUCED ( 24 FDA reports)
ARRHYTHMIA ( 23 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 23 FDA reports)
CARPAL TUNNEL SYNDROME ( 23 FDA reports)
EYELID PTOSIS ( 23 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 23 FDA reports)
HYPOCALCAEMIA ( 23 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 23 FDA reports)
PLASMACYTOMA ( 23 FDA reports)
PULMONARY HAEMORRHAGE ( 23 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 23 FDA reports)
VERTIGO ( 23 FDA reports)
ABDOMINAL DISTENSION ( 22 FDA reports)
ASCITES ( 22 FDA reports)
CATHETERISATION CARDIAC ( 22 FDA reports)
GINGIVAL DISORDER ( 22 FDA reports)
GRANULOMA ( 22 FDA reports)
GROIN PAIN ( 22 FDA reports)
PALPITATIONS ( 22 FDA reports)
POLLAKIURIA ( 22 FDA reports)
X-RAY ABNORMAL ( 22 FDA reports)
ABDOMINAL DISCOMFORT ( 21 FDA reports)
ABSCESS ( 21 FDA reports)
ACUTE SINUSITIS ( 21 FDA reports)
ASPERGILLOSIS ( 21 FDA reports)
BENIGN COLONIC NEOPLASM ( 21 FDA reports)
BLADDER CANCER RECURRENT ( 21 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 21 FDA reports)
ENCEPHALOPATHY ( 21 FDA reports)
ENGRAFTMENT SYNDROME ( 21 FDA reports)
HAEMATOCRIT DECREASED ( 21 FDA reports)
HAEMOPTYSIS ( 21 FDA reports)
HIP FRACTURE ( 21 FDA reports)
HYPOGLYCAEMIA ( 21 FDA reports)
INTESTINAL OBSTRUCTION ( 21 FDA reports)
PSORIASIS ( 21 FDA reports)
SPEECH DISORDER ( 21 FDA reports)
VENTRICULAR DYSFUNCTION ( 21 FDA reports)
ALOPECIA ( 20 FDA reports)
AORTIC CALCIFICATION ( 20 FDA reports)
BRONCHOPNEUMONIA ( 20 FDA reports)
CARDIAC FAILURE ACUTE ( 20 FDA reports)
DELIRIUM ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
MYOCLONUS ( 20 FDA reports)
ORAL HERPES ( 20 FDA reports)
PALLOR ( 20 FDA reports)
POOR PERSONAL HYGIENE ( 20 FDA reports)
SCOLIOSIS ( 20 FDA reports)
TOOTH ABSCESS ( 20 FDA reports)
UPPER LIMB FRACTURE ( 20 FDA reports)
WALKING AID USER ( 20 FDA reports)
ALVEOLOPLASTY ( 19 FDA reports)
ARTHRITIS ( 19 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 19 FDA reports)
BONE MARROW TRANSPLANT ( 19 FDA reports)
CARDIAC ARREST ( 19 FDA reports)
COLITIS ( 19 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
FEMUR FRACTURE ( 19 FDA reports)
GASTRITIS ( 19 FDA reports)
GASTROINTESTINAL TOXICITY ( 19 FDA reports)
HEPATIC VEIN OCCLUSION ( 19 FDA reports)
HYPERKALAEMIA ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
MASS ( 19 FDA reports)
ONYCHOMYCOSIS ( 19 FDA reports)
PLEURAL FIBROSIS ( 19 FDA reports)
POLYNEUROPATHY ( 19 FDA reports)
RADIUS FRACTURE ( 19 FDA reports)
RESPIRATORY ARREST ( 19 FDA reports)
RHINORRHOEA ( 19 FDA reports)
SHOCK ( 19 FDA reports)
SOFT TISSUE INFLAMMATION ( 19 FDA reports)
BONE FRAGMENTATION ( 18 FDA reports)
BREAST MASS ( 18 FDA reports)
CATARACT OPERATION ( 18 FDA reports)
CIRCULATORY COLLAPSE ( 18 FDA reports)
DENTAL FISTULA ( 18 FDA reports)
DEPRESSED MOOD ( 18 FDA reports)
EXCORIATION ( 18 FDA reports)
GENERALISED OEDEMA ( 18 FDA reports)
GINGIVAL ULCERATION ( 18 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 18 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 18 FDA reports)
HEPATITIS B ( 18 FDA reports)
HYPERMETROPIA ( 18 FDA reports)
HYPERPARATHYROIDISM ( 18 FDA reports)
HYPERSENSITIVITY ( 18 FDA reports)
HYPOMAGNESAEMIA ( 18 FDA reports)
JOINT SWELLING ( 18 FDA reports)
MONOCLONAL GAMMOPATHY ( 18 FDA reports)
MOUTH ULCERATION ( 18 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 18 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 18 FDA reports)
PATHOGEN RESISTANCE ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
WOUND DEBRIDEMENT ( 18 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 17 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 17 FDA reports)
AORTIC STENOSIS ( 17 FDA reports)
ARTHROPATHY ( 17 FDA reports)
BODY TEMPERATURE INCREASED ( 17 FDA reports)
BONE OPERATION ( 17 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 17 FDA reports)
DYSARTHRIA ( 17 FDA reports)
ENCEPHALITIS VIRAL ( 17 FDA reports)
ENTEROCOLITIS ( 17 FDA reports)
FACIAL PAIN ( 17 FDA reports)
FISTULA REPAIR ( 17 FDA reports)
HEPATOTOXICITY ( 17 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 17 FDA reports)
IRON DEFICIENCY ANAEMIA ( 17 FDA reports)
LUMBAR RADICULOPATHY ( 17 FDA reports)
METABOLIC ACIDOSIS ( 17 FDA reports)
OESOPHAGEAL DISORDER ( 17 FDA reports)
PARAPROTEINAEMIA ( 17 FDA reports)
PEPTIC ULCER ( 17 FDA reports)
PERICARDIAL EFFUSION ( 17 FDA reports)
PLEURISY ( 17 FDA reports)
PURULENCE ( 17 FDA reports)
RADIOTHERAPY ( 17 FDA reports)
SKIN EXFOLIATION ( 17 FDA reports)
SPINAL FRACTURE ( 17 FDA reports)
SYNOVIAL CYST ( 17 FDA reports)
TONGUE DISCOLOURATION ( 17 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 17 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 16 FDA reports)
BLOOD ALBUMIN DECREASED ( 16 FDA reports)
BONE EROSION ( 16 FDA reports)
CARDIAC DISORDER ( 16 FDA reports)
EMPYEMA ( 16 FDA reports)
FAILURE TO THRIVE ( 16 FDA reports)
FOLLICULITIS ( 16 FDA reports)
LIGHT CHAIN ANALYSIS ( 16 FDA reports)
LIPOMA ( 16 FDA reports)
MYOSITIS ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
OEDEMA MUCOSAL ( 16 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 16 FDA reports)
PELVIC FRACTURE ( 16 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 16 FDA reports)
PRESYNCOPE ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
RALES ( 16 FDA reports)
RHONCHI ( 16 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 16 FDA reports)
THYROID NEOPLASM ( 16 FDA reports)
WOUND DRAINAGE ( 16 FDA reports)
ANISOCYTOSIS ( 15 FDA reports)
AZOTAEMIA ( 15 FDA reports)
BONE SARCOMA ( 15 FDA reports)
BRAIN OEDEMA ( 15 FDA reports)
BRONCHIECTASIS ( 15 FDA reports)
CERVICAL DYSPLASIA ( 15 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 15 FDA reports)
DIASTOLIC DYSFUNCTION ( 15 FDA reports)
ECHOCARDIOGRAM ( 15 FDA reports)
FOOT FRACTURE ( 15 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 15 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 15 FDA reports)
HAEMOPHILUS INFECTION ( 15 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 15 FDA reports)
HEART RATE INCREASED ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
HYPERTROPHY ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
LETHARGY ( 15 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
MAMMOGRAM ( 15 FDA reports)
METASTATIC NEOPLASM ( 15 FDA reports)
OESOPHAGEAL PAIN ( 15 FDA reports)
OESOPHAGEAL STENOSIS ( 15 FDA reports)
PARATHYROID TUMOUR BENIGN ( 15 FDA reports)
PLEURITIC PAIN ( 15 FDA reports)
PNEUMOTHORAX ( 15 FDA reports)
PROSTATE CANCER ( 15 FDA reports)
PROTEIN URINE ABSENT ( 15 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 15 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 15 FDA reports)
SKELETAL SURVEY ABNORMAL ( 15 FDA reports)
ACTINIC KERATOSIS ( 14 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 14 FDA reports)
APLASIA ( 14 FDA reports)
BREAST TENDERNESS ( 14 FDA reports)
COMA ( 14 FDA reports)
CYST ( 14 FDA reports)
DEVICE MALFUNCTION ( 14 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 14 FDA reports)
DYSAESTHESIA ( 14 FDA reports)
FOOT DEFORMITY ( 14 FDA reports)
GINGIVITIS ( 14 FDA reports)
GLOMERULOSCLEROSIS ( 14 FDA reports)
GOUT ( 14 FDA reports)
JOINT SPRAIN ( 14 FDA reports)
LIMB CRUSHING INJURY ( 14 FDA reports)
MELAENA ( 14 FDA reports)
MYELOMA RECURRENCE ( 14 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 14 FDA reports)
MYOPATHY ( 14 FDA reports)
OSTEOMYELITIS CHRONIC ( 14 FDA reports)
OSTEOTOMY ( 14 FDA reports)
PERIPHERAL COLDNESS ( 14 FDA reports)
POOR QUALITY SLEEP ( 14 FDA reports)
PULMONARY CONGESTION ( 14 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SPINAL HAEMANGIOMA ( 14 FDA reports)
SPINAL MYELOGRAM ( 14 FDA reports)
SYNOVIAL DISORDER ( 14 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 14 FDA reports)
URINE ODOUR ABNORMAL ( 14 FDA reports)
ACIDOSIS ( 13 FDA reports)
AGRANULOCYTOSIS ( 13 FDA reports)
APHASIA ( 13 FDA reports)
BONE NEOPLASM MALIGNANT ( 13 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 13 FDA reports)
CARDIO-RESPIRATORY ARREST ( 13 FDA reports)
CHOLECYSTITIS ( 13 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 13 FDA reports)
ENCEPHALITIS HERPES ( 13 FDA reports)
ESSENTIAL HYPERTENSION ( 13 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
FIBROSIS ( 13 FDA reports)
GINGIVAL ERYTHEMA ( 13 FDA reports)
GINGIVAL PAIN ( 13 FDA reports)
GLOMERULONEPHRITIS ( 13 FDA reports)
GOITRE ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
HISTOLOGY ABNORMAL ( 13 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 13 FDA reports)
ILEUS PARALYTIC ( 13 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 13 FDA reports)
NODULE ( 13 FDA reports)
OESOPHAGEAL SPASM ( 13 FDA reports)
OPERATIVE HAEMORRHAGE ( 13 FDA reports)
OVERDOSE ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
PULPITIS DENTAL ( 13 FDA reports)
RENAL TUBULAR NECROSIS ( 13 FDA reports)
SENSATION OF FOREIGN BODY ( 13 FDA reports)
STREPTOCOCCAL SEPSIS ( 13 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 13 FDA reports)
TRISMUS ( 13 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 13 FDA reports)
VAGINAL HAEMORRHAGE ( 13 FDA reports)
VARICELLA ( 13 FDA reports)
VENA CAVA THROMBOSIS ( 13 FDA reports)
VENOOCCLUSIVE DISEASE ( 13 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 13 FDA reports)
AORTIC VALVE INCOMPETENCE ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD URINE PRESENT ( 12 FDA reports)
CANDIDIASIS ( 12 FDA reports)
DECUBITUS ULCER ( 12 FDA reports)
DENTAL PROSTHESIS USER ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
EXPLORATORY OPERATION ( 12 FDA reports)
FACET JOINT SYNDROME ( 12 FDA reports)
GENERAL ANAESTHESIA ( 12 FDA reports)
HAEMODIALYSIS ( 12 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 12 FDA reports)
HEPATOMEGALY ( 12 FDA reports)
HOT FLUSH ( 12 FDA reports)
MACULAR HOLE ( 12 FDA reports)
NASAL OPERATION ( 12 FDA reports)
NERVOUS SYSTEM DISORDER ( 12 FDA reports)
NERVOUSNESS ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 12 FDA reports)
OEDEMA MOUTH ( 12 FDA reports)
ORAL INFECTION ( 12 FDA reports)
PETECHIAE ( 12 FDA reports)
PNEUMONIA ASPIRATION ( 12 FDA reports)
POST PROCEDURAL HAEMATOMA ( 12 FDA reports)
PRESBYOPIA ( 12 FDA reports)
RASH PRURITIC ( 12 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 12 FDA reports)
ROSACEA ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 12 FDA reports)
TONGUE DISORDER ( 12 FDA reports)
TONSILLAR DISORDER ( 12 FDA reports)
TREMOR ( 12 FDA reports)
UTERINE CANCER ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ADENOVIRUS INFECTION ( 11 FDA reports)
ANGIOPATHY ( 11 FDA reports)
AORTIC VALVE CALCIFICATION ( 11 FDA reports)
BLOOD AMYLASE INCREASED ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 11 FDA reports)
BREAST LUMP REMOVAL ( 11 FDA reports)
CARDIAC VALVE DISEASE ( 11 FDA reports)
CAROTID ARTERY STENOSIS ( 11 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 11 FDA reports)
CHOLESTASIS ( 11 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 11 FDA reports)
CYSTITIS NONINFECTIVE ( 11 FDA reports)
DRY MOUTH ( 11 FDA reports)
DRY SKIN ( 11 FDA reports)
DYSKINESIA ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
FACE OEDEMA ( 11 FDA reports)
GASTRIC ULCER ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HYPERTHERMIA ( 11 FDA reports)
IRITIS ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LUNG INFECTION ( 11 FDA reports)
MALNUTRITION ( 11 FDA reports)
OPEN WOUND ( 11 FDA reports)
ORAL DISCHARGE ( 11 FDA reports)
ORTHOSTATIC HYPOTENSION ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 11 FDA reports)
PAROTITIS ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
PROSTATIC CALCIFICATION ( 11 FDA reports)
RASH MACULO-PAPULAR ( 11 FDA reports)
RENAL TUBULAR DISORDER ( 11 FDA reports)
RESPIRATORY ACIDOSIS ( 11 FDA reports)
RETINITIS ( 11 FDA reports)
SPINAL DISORDER ( 11 FDA reports)
SUDDEN CARDIAC DEATH ( 11 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
SURGERY ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
URINE OUTPUT DECREASED ( 11 FDA reports)
VASCULITIS ( 11 FDA reports)
VIRAL INFECTION ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ACUTE PULMONARY OEDEMA ( 10 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
ANURIA ( 10 FDA reports)
BIOPSY BONE ABNORMAL ( 10 FDA reports)
BLEPHARITIS ( 10 FDA reports)
BONE MARROW DEPRESSION ( 10 FDA reports)
BONE MARROW DISORDER ( 10 FDA reports)
BREAST CANCER ( 10 FDA reports)
CHEST X-RAY ABNORMAL ( 10 FDA reports)
CHORIORETINAL DISORDER ( 10 FDA reports)
DEMENTIA ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DENTAL TREATMENT ( 10 FDA reports)
DYSGEUSIA ( 10 FDA reports)
EARLY SATIETY ( 10 FDA reports)
ENDODONTIC PROCEDURE ( 10 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 10 FDA reports)
EYE MOVEMENT DISORDER ( 10 FDA reports)
GASTRODUODENITIS ( 10 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
HYPERKERATOSIS ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
ILEUS ( 10 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 10 FDA reports)
INFARCTION ( 10 FDA reports)
ISCHAEMIA ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
MITRAL VALVE CALCIFICATION ( 10 FDA reports)
MYELITIS TRANSVERSE ( 10 FDA reports)
NEOPLASM ( 10 FDA reports)
NERVE INJURY ( 10 FDA reports)
PAROTID GLAND ENLARGEMENT ( 10 FDA reports)
PERINEURIAL CYST ( 10 FDA reports)
PERIORBITAL HAEMATOMA ( 10 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 10 FDA reports)
PLASTIC SURGERY ( 10 FDA reports)
PNEUMONIA FUNGAL ( 10 FDA reports)
POLYP ( 10 FDA reports)
POST LAMINECTOMY SYNDROME ( 10 FDA reports)
PROTEIN TOTAL DECREASED ( 10 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
SENSITIVITY OF TEETH ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
SPUTUM PURULENT ( 10 FDA reports)
SUBDURAL HAEMATOMA ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
THORACOTOMY ( 10 FDA reports)
THYROIDECTOMY ( 10 FDA reports)
TOOTH DEPOSIT ( 10 FDA reports)
ULCER ( 10 FDA reports)
ACUTE LEUKAEMIA ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
CEREBRAL ATROPHY ( 9 FDA reports)
CHORIORETINOPATHY ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
COLLAPSE OF LUNG ( 9 FDA reports)
CYTOLYTIC HEPATITIS ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
DUPUYTREN'S CONTRACTURE ( 9 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 9 FDA reports)
ENGRAFT FAILURE ( 9 FDA reports)
EYELID OEDEMA ( 9 FDA reports)
FUNGAEMIA ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
GYNAECOMASTIA ( 9 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPOVOLAEMIA ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
INGROWING NAIL ( 9 FDA reports)
INTRAOCULAR LENS IMPLANT ( 9 FDA reports)
LUNG HYPERINFLATION ( 9 FDA reports)
MENINGIOMA ( 9 FDA reports)
MYELITIS ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
OPEN REDUCTION OF FRACTURE ( 9 FDA reports)
PELVIC HAEMATOMA ( 9 FDA reports)
PERIODONTAL DISEASE ( 9 FDA reports)
PHARYNGEAL OEDEMA ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 9 FDA reports)
RETINAL DISORDER ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 9 FDA reports)
TUMOUR NECROSIS ( 9 FDA reports)
ANGINA UNSTABLE ( 8 FDA reports)
AORTIC DILATATION ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
APLASTIC ANAEMIA ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
BACTERIAL TEST POSITIVE ( 8 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 8 FDA reports)
BLOOD POTASSIUM DECREASED ( 8 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 8 FDA reports)
BRAIN STEM HAEMORRHAGE ( 8 FDA reports)
BREAST DISCHARGE ( 8 FDA reports)
BREATH ODOUR ( 8 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
BUNION ( 8 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 8 FDA reports)
CHROMATURIA ( 8 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
CYST REMOVAL ( 8 FDA reports)
DEMYELINATION ( 8 FDA reports)
DEVICE RELATED INFECTION ( 8 FDA reports)
EJECTION FRACTION DECREASED ( 8 FDA reports)
ENTEROCOCCAL INFECTION ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
FIBROMA ( 8 FDA reports)
GALLBLADDER DISORDER ( 8 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HEART RATE IRREGULAR ( 8 FDA reports)
HEPATIC CYST ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
INTERVERTEBRAL DISCITIS ( 8 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 8 FDA reports)
JOINT CONTRACTURE ( 8 FDA reports)
LARGE INTESTINAL ULCER ( 8 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 8 FDA reports)
LYMPHOCYTIC INFILTRATION ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
MUSCLE HAEMORRHAGE ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
NEURITIS ( 8 FDA reports)
ORAL CAVITY FISTULA ( 8 FDA reports)
OVERWEIGHT ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
PROCEDURAL PAIN ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
RENAL OSTEODYSTROPHY ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SERUM FERRITIN INCREASED ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
SPLENIC GRANULOMA ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
TOOTH REPAIR ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
ADNEXA UTERI MASS ( 7 FDA reports)
ANGIOMYOLIPOMA ( 7 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 7 FDA reports)
ANXIETY DISORDER ( 7 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BETA GLOBULIN INCREASED ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BLINDNESS ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 7 FDA reports)
BRAIN NEOPLASM ( 7 FDA reports)
BRAIN OPERATION ( 7 FDA reports)
CATHETER PLACEMENT ( 7 FDA reports)
CATHETER REMOVAL ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
CUBITAL TUNNEL SYNDROME ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
EAR INFECTION ( 7 FDA reports)
ELECTROLYTE IMBALANCE ( 7 FDA reports)
EYE PAIN ( 7 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
GINGIVAL RECESSION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 7 FDA reports)
HAEMATOTOXICITY ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERAMYLASAEMIA ( 7 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
JOINT EFFUSION ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LOCAL SWELLING ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MALIGNANT MELANOMA ( 7 FDA reports)
MECHANICAL VENTILATION ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MYELOFIBROSIS ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 7 FDA reports)
OLIGURIA ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
OVARIAN MASS ( 7 FDA reports)
PNEUMONITIS ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
RED BLOOD CELL ABNORMALITY ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 7 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SEPSIS SYNDROME ( 7 FDA reports)
SKIN EROSION ( 7 FDA reports)
SNORING ( 7 FDA reports)
SUBRETINAL FIBROSIS ( 7 FDA reports)
TENDON INJURY ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
TOOTH IMPACTED ( 7 FDA reports)
TOXIC ENCEPHALOPATHY ( 7 FDA reports)
VENTRICULAR ARRHYTHMIA ( 7 FDA reports)
VENTRICULAR FIBRILLATION ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 6 FDA reports)
BEDRIDDEN ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 6 FDA reports)
BONE SCAN ABNORMAL ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
CANDIDA SEPSIS ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 6 FDA reports)
CORNEAL DYSTROPHY ( 6 FDA reports)
CORONARY ANGIOPLASTY ( 6 FDA reports)
DENTAL CARE ( 6 FDA reports)
DIABETES INSIPIDUS ( 6 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GRIP STRENGTH DECREASED ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HELICOBACTER GASTRITIS ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
JOINT SURGERY ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
LENS DISORDER ( 6 FDA reports)
MENISCUS LESION ( 6 FDA reports)
NEOPLASM PROGRESSION ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 6 FDA reports)
ODONTOGENIC CYST ( 6 FDA reports)
ORAL SOFT TISSUE DISORDER ( 6 FDA reports)
ORTHOPNOEA ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 6 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 6 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
PROSTATOMEGALY ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
RHABDOMYOSARCOMA ( 6 FDA reports)
SKIN HYPERPIGMENTATION ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
STENT PLACEMENT ( 6 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
THYROID MASS ( 6 FDA reports)
TIBIA FRACTURE ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
TUMOUR EXCISION ( 6 FDA reports)
TUMOUR LYSIS SYNDROME ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 5 FDA reports)
ALVEOLITIS ( 5 FDA reports)
ANGER ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CALCULUS URETHRAL ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DENTAL PLAQUE ( 5 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DYSPHEMIA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
ENTEROCOCCAL SEPSIS ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
FLASHBACK ( 5 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 5 FDA reports)
HALITOSIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HAPTOGLOBIN DECREASED ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
HUMERUS FRACTURE ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
LEFT ATRIAL DILATATION ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LITHOTRIPSY ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MASTOIDITIS ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MUSCLE INJURY ( 5 FDA reports)
MYELOCYTOSIS ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 5 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PAPILLOMA ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PIGMENTATION DISORDER ( 5 FDA reports)
PNEUMOCONIOSIS ( 5 FDA reports)
PNEUMONIA ASPERGILLUS ( 5 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RECURRENT CANCER ( 5 FDA reports)
REFRACTORY ANAEMIA ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
SCAN BONE MARROW ABNORMAL ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SOFT TISSUE INFECTION ( 5 FDA reports)
SOFT TISSUE MASS ( 5 FDA reports)
SPINAL LAMINECTOMY ( 5 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 5 FDA reports)
TENDON DISORDER ( 5 FDA reports)
TENDON SHEATH INCISION ( 5 FDA reports)
TENOLYSIS ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
TUMOUR INVASION ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
URETERAL STENT INSERTION ( 5 FDA reports)
URINE ABNORMALITY ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
VIITH NERVE PARALYSIS ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANTITHROMBIN III DECREASED ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHONDROMALACIA ( 4 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 4 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DRY SOCKET ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
DYSPLASTIC NAEVUS ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
LESION EXCISION ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PNEUMOMEDIASTINUM ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
POVERTY OF SPEECH ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
PULMONARY VEIN OCCLUSION ( 4 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
STARING ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
SYSTEMIC MYCOSIS ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
WOUND TREATMENT ( 4 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAL STENOSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BONE FORMATION INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CHORIORETINAL ATROPHY ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CRYING ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DERMAL CYST ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENDOCERVICAL CURETTAGE ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FUSARIUM INFECTION ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MEDULLOBLASTOMA ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUROBLASTOMA RECURRENT ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
ORAL NEOPLASM ( 3 FDA reports)
OSTEOMYELITIS DRAINAGE ( 3 FDA reports)
OSTEOPETROSIS ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PUTAMEN HAEMORRHAGE ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPONDYLOARTHROPATHY ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TONIC CONVULSION ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
AMOEBIC COLITIS ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
APICAL GRANULOMA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BETA 2 MICROGLOBULIN DECREASED ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHROMOSOMAL DELETION ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
COOMBS TEST NEGATIVE ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYTOKINE STORM ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ENCEPHALITIS FUNGAL ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUID INTAKE RESTRICTION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERAL NUTRITION DISORDER ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPAPLASTIN DECREASED ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS B VIRUS ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
HEPATOBLASTOMA ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
IIIRD NERVE PARESIS ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JAW LESION EXCISION ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG CYST BENIGN ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGIOMA MALIGNANT ( 2 FDA reports)
MENINGIOMA SURGERY ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA TOXOPLASMAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PROSTATECTOMY ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
REYE'S SYNDROME ( 2 FDA reports)
RHABDOMYOMA ( 2 FDA reports)
SALIVARY GLAND PAIN ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THIRST ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS MANAGEMENT ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA RECURRENT ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
ECCENTRIC FIXATION ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ERYTHROBLAST MORPHOLOGY ABNORMAL ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FASCIOLIASIS ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTATIC OCULAR MELANOMA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCINTIGRAPHY ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPHEROCYTIC ANAEMIA ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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