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

BONE DISORDER ( 164 FDA reports)
TOOTH EXTRACTION ( 149 FDA reports)
OSTEONECROSIS ( 147 FDA reports)
PAIN ( 146 FDA reports)
ANXIETY ( 137 FDA reports)
DYSPNOEA ( 101 FDA reports)
ANAEMIA ( 96 FDA reports)
OSTEOMYELITIS ( 94 FDA reports)
FATIGUE ( 90 FDA reports)
NAUSEA ( 88 FDA reports)
ERYTHEMA ( 86 FDA reports)
OSTEONECROSIS OF JAW ( 86 FDA reports)
BACK PAIN ( 82 FDA reports)
BONE DEBRIDEMENT ( 79 FDA reports)
IMPAIRED HEALING ( 77 FDA reports)
INJURY ( 74 FDA reports)
PNEUMONIA ( 74 FDA reports)
SWELLING ( 73 FDA reports)
NEUTROPENIA ( 69 FDA reports)
OEDEMA PERIPHERAL ( 69 FDA reports)
PYREXIA ( 69 FDA reports)
COUGH ( 67 FDA reports)
PARAESTHESIA ( 66 FDA reports)
PAIN IN JAW ( 65 FDA reports)
NEUROPATHY PERIPHERAL ( 64 FDA reports)
INFLAMMATION ( 60 FDA reports)
INFECTION ( 58 FDA reports)
SPINAL OSTEOARTHRITIS ( 58 FDA reports)
EMOTIONAL DISTRESS ( 57 FDA reports)
PAIN IN EXTREMITY ( 57 FDA reports)
ABDOMINAL PAIN ( 56 FDA reports)
LOOSE TOOTH ( 56 FDA reports)
OSTEOPENIA ( 56 FDA reports)
CHEST PAIN ( 55 FDA reports)
DIARRHOEA ( 55 FDA reports)
ARTHRALGIA ( 54 FDA reports)
TOOTH LOSS ( 54 FDA reports)
DEFORMITY ( 53 FDA reports)
DEPRESSION ( 53 FDA reports)
TOOTH DISORDER ( 52 FDA reports)
LEUKOPENIA ( 49 FDA reports)
THROMBOCYTOPENIA ( 49 FDA reports)
CONSTIPATION ( 48 FDA reports)
MULTIPLE MYELOMA ( 48 FDA reports)
DEBRIDEMENT ( 47 FDA reports)
HEADACHE ( 47 FDA reports)
PRIMARY SEQUESTRUM ( 47 FDA reports)
ORAL INFECTION ( 44 FDA reports)
TOOTHACHE ( 44 FDA reports)
CORONARY ARTERY DISEASE ( 43 FDA reports)
ANHEDONIA ( 42 FDA reports)
ASTHENIA ( 42 FDA reports)
BONE LESION ( 42 FDA reports)
BONE PAIN ( 42 FDA reports)
DENTAL CARIES ( 42 FDA reports)
ATELECTASIS ( 41 FDA reports)
SEQUESTRECTOMY ( 41 FDA reports)
DYSPHAGIA ( 40 FDA reports)
JAW DISORDER ( 40 FDA reports)
MUCOSAL INFLAMMATION ( 40 FDA reports)
PLEURAL EFFUSION ( 40 FDA reports)
DEATH ( 39 FDA reports)
ENDODONTIC PROCEDURE ( 39 FDA reports)
OEDEMA ( 39 FDA reports)
BONE FRAGMENTATION ( 37 FDA reports)
FEBRILE NEUTROPENIA ( 37 FDA reports)
RASH ( 37 FDA reports)
VOMITING ( 37 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 36 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 36 FDA reports)
GINGIVAL INFECTION ( 36 FDA reports)
INSOMNIA ( 36 FDA reports)
LYMPHADENOPATHY ( 36 FDA reports)
MASS ( 36 FDA reports)
METASTATIC NEOPLASM ( 36 FDA reports)
DECREASED INTEREST ( 35 FDA reports)
HYPOAESTHESIA ORAL ( 35 FDA reports)
HYPOPHAGIA ( 35 FDA reports)
HYPOTENSION ( 35 FDA reports)
PLATELET COUNT DECREASED ( 35 FDA reports)
RENAL FAILURE ( 35 FDA reports)
WEIGHT INCREASED ( 34 FDA reports)
BLOOD GLUCOSE INCREASED ( 33 FDA reports)
DEHYDRATION ( 33 FDA reports)
DRUG INEFFECTIVE ( 33 FDA reports)
HIATUS HERNIA ( 33 FDA reports)
HYPOAESTHESIA ( 33 FDA reports)
PERIODONTITIS ( 33 FDA reports)
TOOTH INFECTION ( 33 FDA reports)
WEIGHT DECREASED ( 33 FDA reports)
DIZZINESS ( 32 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 32 FDA reports)
MALAISE ( 32 FDA reports)
FISTULA ( 31 FDA reports)
MYALGIA ( 31 FDA reports)
NEOPLASM MALIGNANT ( 31 FDA reports)
ORAL SURGERY ( 31 FDA reports)
PERIODONTAL DISEASE ( 31 FDA reports)
CATARACT ( 30 FDA reports)
HAEMORRHOIDS ( 30 FDA reports)
JAW OPERATION ( 30 FDA reports)
METASTASES TO BONE ( 30 FDA reports)
CHEST DISCOMFORT ( 29 FDA reports)
FALL ( 29 FDA reports)
MUSCLE SPASMS ( 29 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 29 FDA reports)
OSTEOPOROSIS ( 29 FDA reports)
PLASMACYTOMA ( 29 FDA reports)
TOOTH REPAIR ( 29 FDA reports)
TUMOUR INVASION ( 29 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 29 FDA reports)
DECREASED APPETITE ( 28 FDA reports)
MUSCULAR WEAKNESS ( 28 FDA reports)
NODULE ( 28 FDA reports)
DENTAL CARE ( 27 FDA reports)
LIFE EXPECTANCY SHORTENED ( 27 FDA reports)
SWELLING FACE ( 27 FDA reports)
TOOTH ABSCESS ( 27 FDA reports)
ABSCESS ORAL ( 26 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 26 FDA reports)
CONFUSIONAL STATE ( 26 FDA reports)
FIBULA FRACTURE ( 26 FDA reports)
GAIT DISTURBANCE ( 26 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 26 FDA reports)
ORAL PAIN ( 26 FDA reports)
PROSTHESIS IMPLANTATION ( 26 FDA reports)
CEREBROVASCULAR ACCIDENT ( 25 FDA reports)
HAEMOGLOBIN DECREASED ( 25 FDA reports)
MYOCARDIAL INFARCTION ( 25 FDA reports)
SINUS DISORDER ( 25 FDA reports)
BREAST CANCER ( 24 FDA reports)
DIABETES MELLITUS ( 24 FDA reports)
METASTASES TO LIVER ( 24 FDA reports)
MUSCULOSKELETAL PAIN ( 24 FDA reports)
STOMATITIS ( 24 FDA reports)
BACTERIAL INFECTION ( 23 FDA reports)
DIVERTICULUM ( 23 FDA reports)
DRUG INTERACTION ( 23 FDA reports)
DYSPEPSIA ( 23 FDA reports)
HAEMOPTYSIS ( 23 FDA reports)
METASTASES TO LUNG ( 23 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 23 FDA reports)
SINUSITIS ( 23 FDA reports)
SKIN DISORDER ( 23 FDA reports)
URINARY TRACT INFECTION ( 23 FDA reports)
BONE DENSITY DECREASED ( 22 FDA reports)
BREAST CANCER METASTATIC ( 22 FDA reports)
CARDIOMEGALY ( 22 FDA reports)
CHILLS ( 22 FDA reports)
JOINT EFFUSION ( 22 FDA reports)
BLOOD CALCIUM DECREASED ( 21 FDA reports)
CATHETERISATION CARDIAC ( 21 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 21 FDA reports)
EXOSTOSIS ( 21 FDA reports)
HAEMATURIA ( 21 FDA reports)
HERPES VIRUS INFECTION ( 21 FDA reports)
HIP FRACTURE ( 21 FDA reports)
HYPOKALAEMIA ( 21 FDA reports)
HYPONATRAEMIA ( 21 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 21 FDA reports)
OSTEOARTHRITIS ( 21 FDA reports)
SUBCUTANEOUS ABSCESS ( 21 FDA reports)
TENDON DISORDER ( 21 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 20 FDA reports)
BONE TRIMMING ( 20 FDA reports)
BRONCHITIS ( 20 FDA reports)
CEREBRAL INFARCTION ( 20 FDA reports)
DENTAL OPERATION ( 20 FDA reports)
DISCOMFORT ( 20 FDA reports)
DISEASE PROGRESSION ( 20 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 20 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 20 FDA reports)
OSTEITIS ( 20 FDA reports)
PANCYTOPENIA ( 20 FDA reports)
POLLAKIURIA ( 20 FDA reports)
SINUS CONGESTION ( 20 FDA reports)
STEM CELL TRANSPLANT ( 20 FDA reports)
WOUND DRAINAGE ( 20 FDA reports)
ABDOMINAL DISCOMFORT ( 19 FDA reports)
ABDOMINAL DISTENSION ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 19 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 19 FDA reports)
DIPLOPIA ( 19 FDA reports)
DYSGEUSIA ( 19 FDA reports)
EXTRASKELETAL OSSIFICATION ( 19 FDA reports)
EYE HAEMORRHAGE ( 19 FDA reports)
FRACTURE ( 19 FDA reports)
ISCHAEMIA ( 19 FDA reports)
SPINAL DISORDER ( 19 FDA reports)
TONGUE DISORDER ( 19 FDA reports)
WOUND DEHISCENCE ( 19 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 18 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 18 FDA reports)
DYSPHONIA ( 18 FDA reports)
EAR PAIN ( 18 FDA reports)
FACIAL PAIN ( 18 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 18 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 18 FDA reports)
ORAL CAVITY FISTULA ( 18 FDA reports)
OSTEOMYELITIS CHRONIC ( 18 FDA reports)
RETCHING ( 18 FDA reports)
SPLENOMEGALY ( 18 FDA reports)
ABSCESS DRAINAGE ( 17 FDA reports)
ANGINA PECTORIS ( 17 FDA reports)
ARTHRITIS ( 17 FDA reports)
CHRONIC SINUSITIS ( 17 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 17 FDA reports)
COORDINATION ABNORMAL ( 17 FDA reports)
CRANIAL NERVE DISORDER ( 17 FDA reports)
CYST ( 17 FDA reports)
EMOTIONAL DISORDER ( 17 FDA reports)
EROSIVE OESOPHAGITIS ( 17 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 17 FDA reports)
GASTRITIS EROSIVE ( 17 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 17 FDA reports)
LUNG DISORDER ( 17 FDA reports)
MACROGLOSSIA ( 17 FDA reports)
MENINGIOMA ( 17 FDA reports)
MOUTH HAEMORRHAGE ( 17 FDA reports)
MUCOSAL EROSION ( 17 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 17 FDA reports)
NASAL MUCOSAL DISORDER ( 17 FDA reports)
ORAL DISCOMFORT ( 17 FDA reports)
OSTEORADIONECROSIS ( 17 FDA reports)
RENAL CYST ( 17 FDA reports)
SENSORY DISTURBANCE ( 17 FDA reports)
SINUS TACHYCARDIA ( 17 FDA reports)
TONGUE PARALYSIS ( 17 FDA reports)
TOOTH RESORPTION ( 17 FDA reports)
ASCITES ( 16 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
BONE MARROW FAILURE ( 16 FDA reports)
BREAST PAIN ( 16 FDA reports)
DENTAL FISTULA ( 16 FDA reports)
DIASTOLIC DYSFUNCTION ( 16 FDA reports)
GASTRITIS ( 16 FDA reports)
GROIN PAIN ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 16 FDA reports)
PAPILLOMA ( 16 FDA reports)
PATHOGEN RESISTANCE ( 16 FDA reports)
PRURITUS ( 16 FDA reports)
TONGUE DISCOLOURATION ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BIOPSY BONE ( 15 FDA reports)
CARDIOMYOPATHY ( 15 FDA reports)
CERVICOBRACHIAL SYNDROME ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
ECHOCARDIOGRAM ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
MAMMOGRAM ( 15 FDA reports)
MYOCARDIAL ISCHAEMIA ( 15 FDA reports)
NEOPLASM PROGRESSION ( 15 FDA reports)
PURULENT DISCHARGE ( 15 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 15 FDA reports)
SKIN DISCOLOURATION ( 15 FDA reports)
THROMBOSIS ( 15 FDA reports)
TRANSAMINASES INCREASED ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
X-RAY ABNORMAL ( 15 FDA reports)
ADRENAL INSUFFICIENCY ( 14 FDA reports)
ASPIRATION ( 14 FDA reports)
BLOOD AMYLASE INCREASED ( 14 FDA reports)
BONE MARROW TRANSPLANT ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 14 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 14 FDA reports)
DYSURIA ( 14 FDA reports)
EMPHYSEMA ( 14 FDA reports)
GINGIVAL SWELLING ( 14 FDA reports)
HIP ARTHROPLASTY ( 14 FDA reports)
HYDRONEPHROSIS ( 14 FDA reports)
HYPERMETROPIA ( 14 FDA reports)
NEPHROLITHIASIS ( 14 FDA reports)
PNEUMOCONIOSIS ( 14 FDA reports)
PRESBYOPIA ( 14 FDA reports)
PULMONARY HAEMORRHAGE ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
RASH PAPULAR ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SWOLLEN TONGUE ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
VENTRICULAR HYPERTROPHY ( 14 FDA reports)
BONE OPERATION ( 13 FDA reports)
CEREBRAL ATROPHY ( 13 FDA reports)
GAMMOPATHY ( 13 FDA reports)
GASTROENTERITIS ( 13 FDA reports)
LEUKOCYTOSIS ( 13 FDA reports)
NEOPLASM ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
RADICULAR PAIN ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
TRANSFUSION ( 13 FDA reports)
BACK DISORDER ( 12 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 12 FDA reports)
BONE DENSITY INCREASED ( 12 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 12 FDA reports)
GINGIVAL ERYTHEMA ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
ORAL HERPES ( 12 FDA reports)
OSTEOLYSIS ( 12 FDA reports)
PALLOR ( 12 FDA reports)
PULMONARY CONGESTION ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
SPINAL COLUMN STENOSIS ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
BREAST MASS ( 11 FDA reports)
CERVICAL DYSPLASIA ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
ERUCTATION ( 11 FDA reports)
FLATULENCE ( 11 FDA reports)
GINGIVAL PAIN ( 11 FDA reports)
HAEMANGIOMA ( 11 FDA reports)
HIP SURGERY ( 11 FDA reports)
HYPERCALCAEMIA ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LOCAL SWELLING ( 11 FDA reports)
MEDICAL DEVICE REMOVAL ( 11 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 11 FDA reports)
OROPHARYNGEAL BLISTERING ( 11 FDA reports)
OROPHARYNGEAL PAIN ( 11 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
TENDERNESS ( 11 FDA reports)
TORTICOLLIS ( 11 FDA reports)
TRACHEOBRONCHITIS ( 11 FDA reports)
UNRESPONSIVE TO STIMULI ( 11 FDA reports)
ABSCESS JAW ( 10 FDA reports)
AGRANULOCYTOSIS ( 10 FDA reports)
BACTERIAL TEST POSITIVE ( 10 FDA reports)
EJACULATION DISORDER ( 10 FDA reports)
ENTEROCOLITIS ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
GASTRIC HAEMORRHAGE ( 10 FDA reports)
GINGIVAL RECESSION ( 10 FDA reports)
GINGIVECTOMY ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HEPATIC LESION ( 10 FDA reports)
HEPATIC STEATOSIS ( 10 FDA reports)
HERPES ZOSTER ( 10 FDA reports)
HOSPITALISATION ( 10 FDA reports)
HYPERCAPNIA ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
INFARCTION ( 10 FDA reports)
JOINT CONTRACTURE ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
LYMPHOEDEMA ( 10 FDA reports)
MALNUTRITION ( 10 FDA reports)
MUSCLE ATROPHY ( 10 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
PHYSICAL DISABILITY ( 10 FDA reports)
POST PROCEDURAL FISTULA ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
RHINORRHOEA ( 10 FDA reports)
ROAD TRAFFIC ACCIDENT ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
STREPTOCOCCAL SEPSIS ( 10 FDA reports)
ATROPHY ( 9 FDA reports)
BLADDER OBSTRUCTION ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
DECUBITUS ULCER ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DENTAL TREATMENT ( 9 FDA reports)
DEVICE RELATED INFECTION ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
FISTULA DISCHARGE ( 9 FDA reports)
FLUID RETENTION ( 9 FDA reports)
FOREIGN BODY ( 9 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
HYPOCALCAEMIA ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
LACRIMATION INCREASED ( 9 FDA reports)
LEFT ATRIAL DILATATION ( 9 FDA reports)
LUNG NEOPLASM MALIGNANT ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
NIGHT SWEATS ( 9 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 9 FDA reports)
PERICARDIAL EFFUSION ( 9 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 9 FDA reports)
UTERINE DILATION AND CURETTAGE ( 9 FDA reports)
ADRENAL NEOPLASM ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 8 FDA reports)
BLADDER CANCER ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
BONE MARROW DISORDER ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 8 FDA reports)
CHEST X-RAY ABNORMAL ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RHINITIS ( 8 FDA reports)
SURGERY ( 8 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 8 FDA reports)
URETERAL STENT INSERTION ( 8 FDA reports)
VASCULAR CALCIFICATION ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CERUMEN IMPACTION ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
FOLLICULITIS ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
GINGIVAL OPERATION ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
MASTECTOMY ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
NAIL DYSTROPHY ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
ONYCHALGIA ( 7 FDA reports)
ONYCHOMYCOSIS ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RENAL ATROPHY ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
SCOLIOSIS ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANGER ( 6 FDA reports)
APPENDICECTOMY ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CARDIOTOXICITY ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
COLON POLYPECTOMY ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CORNEAL DYSTROPHY ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
EXPOSED BONE IN JAW ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
FOOT FRACTURE ( 6 FDA reports)
GOITRE ( 6 FDA reports)
GOUT ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
IMPLANT SITE DISCHARGE ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LYMPHADENECTOMY ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PANCREATIC PSEUDOCYST ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PERIODONTAL OPERATION ( 6 FDA reports)
POLYP ( 6 FDA reports)
POOR VENOUS ACCESS ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
BRAIN MASS ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
CYSTOCELE ( 5 FDA reports)
DENTURE WEARER ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
ESCHAR ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GLIOSIS ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MUSCLE INJURY ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
NAIL HYPERTROPHY ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
RECURRENT CANCER ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BONE SARCOMA ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOACUSIS ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PANCREATIC PSEUDOCYST DRAINAGE ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
RADIOTHERAPY ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
SCAR ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APLASIA ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BREAST OEDEMA ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
CRYING ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPOPITUITARISM ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHATIC OBSTRUCTION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIMORBIDITY ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RENAL CANCER METASTATIC ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINE POTASSIUM INCREASED ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAL POLYP ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APICAL GRANULOMA ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASPIRATION BIOPSY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE LESION EXCISION ( 2 FDA reports)
BREAST RECONSTRUCTION ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERMETABOLISM ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHASE REACTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CENTRAL VENOUS PRESSURE ABNORMAL ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEFICIENCY OF BILE SECRETION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUSCLE GRAFT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELOCYTE PRESENT ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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