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

PAIN ( 240 FDA reports)
NAUSEA ( 232 FDA reports)
DYSPNOEA ( 221 FDA reports)
ANXIETY ( 211 FDA reports)
BACK PAIN ( 210 FDA reports)
BONE DISORDER ( 204 FDA reports)
OSTEONECROSIS OF JAW ( 186 FDA reports)
PLEURAL EFFUSION ( 182 FDA reports)
VOMITING ( 181 FDA reports)
FATIGUE ( 178 FDA reports)
ANAEMIA ( 175 FDA reports)
DIARRHOEA ( 160 FDA reports)
ASTHENIA ( 149 FDA reports)
TOOTH EXTRACTION ( 148 FDA reports)
INJURY ( 147 FDA reports)
DEPRESSION ( 143 FDA reports)
IMPAIRED HEALING ( 142 FDA reports)
PYREXIA ( 137 FDA reports)
OSTEOMYELITIS ( 134 FDA reports)
ARTHRALGIA ( 133 FDA reports)
CHEST PAIN ( 133 FDA reports)
HEADACHE ( 127 FDA reports)
HYPERTENSION ( 122 FDA reports)
SWELLING ( 121 FDA reports)
OEDEMA PERIPHERAL ( 115 FDA reports)
OSTEONECROSIS ( 115 FDA reports)
DEEP VEIN THROMBOSIS ( 114 FDA reports)
DENTAL CARIES ( 114 FDA reports)
SPINAL OSTEOARTHRITIS ( 113 FDA reports)
DEHYDRATION ( 111 FDA reports)
OSTEOARTHRITIS ( 111 FDA reports)
PAIN IN JAW ( 108 FDA reports)
PNEUMONIA ( 108 FDA reports)
NEUROPATHY PERIPHERAL ( 106 FDA reports)
COUGH ( 104 FDA reports)
HYPOTENSION ( 104 FDA reports)
ABDOMINAL PAIN ( 101 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 101 FDA reports)
MENTAL STATUS CHANGES ( 100 FDA reports)
PAIN IN EXTREMITY ( 100 FDA reports)
BONE DEBRIDEMENT ( 99 FDA reports)
HYPOAESTHESIA ( 99 FDA reports)
CONSTIPATION ( 97 FDA reports)
TOOTH DISORDER ( 97 FDA reports)
HIATUS HERNIA ( 94 FDA reports)
BRONCHITIS ( 92 FDA reports)
CONFUSIONAL STATE ( 90 FDA reports)
DIZZINESS ( 90 FDA reports)
PRIMARY SEQUESTRUM ( 89 FDA reports)
PANCYTOPENIA ( 85 FDA reports)
RENAL FAILURE ACUTE ( 85 FDA reports)
ERYTHEMA ( 84 FDA reports)
HAEMOGLOBIN DECREASED ( 83 FDA reports)
LYMPHADENOPATHY ( 83 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 81 FDA reports)
INFECTION ( 81 FDA reports)
CHILLS ( 79 FDA reports)
BONE DENSITY DECREASED ( 78 FDA reports)
PLATELET COUNT DECREASED ( 78 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 76 FDA reports)
PRURITUS ( 76 FDA reports)
ATELECTASIS ( 75 FDA reports)
FALL ( 73 FDA reports)
FISTULA ( 73 FDA reports)
OSTEOPENIA ( 73 FDA reports)
TREMOR ( 73 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 71 FDA reports)
PARAESTHESIA ( 70 FDA reports)
THROMBOCYTOPENIA ( 70 FDA reports)
INSOMNIA ( 69 FDA reports)
RIB FRACTURE ( 69 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 68 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 68 FDA reports)
PULMONARY EMBOLISM ( 68 FDA reports)
RASH ( 68 FDA reports)
WEIGHT DECREASED ( 68 FDA reports)
RECTAL HAEMORRHAGE ( 67 FDA reports)
CELLULITIS ( 66 FDA reports)
ENDODONTIC PROCEDURE ( 66 FDA reports)
METASTASES TO BONE ( 66 FDA reports)
PURULENT DISCHARGE ( 66 FDA reports)
SINUSITIS ( 66 FDA reports)
DIVERTICULUM ( 65 FDA reports)
DYSPNOEA EXERTIONAL ( 65 FDA reports)
URINARY TRACT INFECTION ( 65 FDA reports)
HAEMORRHOIDS ( 64 FDA reports)
NEUTROPENIA ( 64 FDA reports)
BLOOD CREATININE INCREASED ( 63 FDA reports)
HAEMATOCRIT DECREASED ( 63 FDA reports)
LUNG NEOPLASM ( 63 FDA reports)
GINGIVAL BLEEDING ( 62 FDA reports)
EXOSTOSIS ( 61 FDA reports)
HYPERCALCAEMIA ( 61 FDA reports)
METASTASES TO LIVER ( 61 FDA reports)
MOUTH ULCERATION ( 61 FDA reports)
TOOTH ABSCESS ( 61 FDA reports)
NECK PAIN ( 60 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 60 FDA reports)
CARPAL TUNNEL SYNDROME ( 59 FDA reports)
RHINITIS ( 59 FDA reports)
TOOTHACHE ( 59 FDA reports)
INFLAMMATION ( 58 FDA reports)
RESPIRATORY FAILURE ( 58 FDA reports)
DECREASED APPETITE ( 57 FDA reports)
OSTEOPOROSIS ( 57 FDA reports)
ANHEDONIA ( 56 FDA reports)
TOOTH LOSS ( 56 FDA reports)
RENAL FAILURE ( 55 FDA reports)
DIVERTICULUM INTESTINAL ( 54 FDA reports)
SEQUESTRECTOMY ( 54 FDA reports)
BONE PAIN ( 53 FDA reports)
GAIT DISTURBANCE ( 53 FDA reports)
MUSCULAR WEAKNESS ( 53 FDA reports)
NEOPLASM MALIGNANT ( 53 FDA reports)
SYNCOPE ( 53 FDA reports)
DYSURIA ( 52 FDA reports)
JAW DISORDER ( 52 FDA reports)
HYPOXIA ( 51 FDA reports)
DEATH ( 50 FDA reports)
LOOSE TOOTH ( 49 FDA reports)
SWELLING FACE ( 49 FDA reports)
BLOOD UREA INCREASED ( 48 FDA reports)
DIABETES MELLITUS ( 48 FDA reports)
HOT FLUSH ( 48 FDA reports)
MUSCLE SPASMS ( 48 FDA reports)
NEPHROLITHIASIS ( 48 FDA reports)
ORAL PAIN ( 48 FDA reports)
EMOTIONAL DISTRESS ( 47 FDA reports)
MITRAL VALVE INCOMPETENCE ( 47 FDA reports)
SEPSIS ( 47 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 47 FDA reports)
CATARACT ( 46 FDA reports)
DYSPHAGIA ( 46 FDA reports)
JAW OPERATION ( 46 FDA reports)
STOMATITIS ( 46 FDA reports)
CARDIOMEGALY ( 45 FDA reports)
BONE LESION ( 44 FDA reports)
HAEMATOCHEZIA ( 44 FDA reports)
TACHYCARDIA ( 44 FDA reports)
TENDERNESS ( 44 FDA reports)
METASTASES TO SPINE ( 43 FDA reports)
URINARY INCONTINENCE ( 43 FDA reports)
GINGIVAL INFECTION ( 42 FDA reports)
HYPOAESTHESIA ORAL ( 42 FDA reports)
CHEST DISCOMFORT ( 41 FDA reports)
GINGIVAL PAIN ( 41 FDA reports)
MASTICATION DISORDER ( 41 FDA reports)
MUCOSAL INFLAMMATION ( 41 FDA reports)
PERIODONTAL DISEASE ( 41 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 40 FDA reports)
ATRIAL FIBRILLATION ( 40 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 40 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 40 FDA reports)
LEUKOPENIA ( 40 FDA reports)
PLEURITIC PAIN ( 40 FDA reports)
RENAL CYST ( 40 FDA reports)
WEIGHT INCREASED ( 40 FDA reports)
CONTUSION ( 39 FDA reports)
DENTAL OPERATION ( 39 FDA reports)
HYPERLIPIDAEMIA ( 39 FDA reports)
MALAISE ( 39 FDA reports)
BURSITIS ( 38 FDA reports)
CEREBROVASCULAR ACCIDENT ( 38 FDA reports)
DECREASED INTEREST ( 38 FDA reports)
FEBRILE NEUTROPENIA ( 38 FDA reports)
HYPERSENSITIVITY ( 38 FDA reports)
OSTEOSCLEROSIS ( 38 FDA reports)
VERTIGO ( 38 FDA reports)
ALOPECIA ( 37 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 37 FDA reports)
BLOOD CALCIUM DECREASED ( 37 FDA reports)
CARDIAC ARREST ( 37 FDA reports)
DEBRIDEMENT ( 37 FDA reports)
HAEMATURIA ( 37 FDA reports)
HYPOKALAEMIA ( 37 FDA reports)
OSTEOLYSIS ( 37 FDA reports)
ARTHRITIS ( 36 FDA reports)
BLOOD GLUCOSE INCREASED ( 36 FDA reports)
GINGIVITIS ( 36 FDA reports)
LOSS OF CONSCIOUSNESS ( 36 FDA reports)
PULMONARY HYPERTENSION ( 36 FDA reports)
WHEEZING ( 36 FDA reports)
FLUSHING ( 35 FDA reports)
HYPOPHAGIA ( 34 FDA reports)
LARYNGOSPASM ( 34 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 34 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 34 FDA reports)
CARDIOMYOPATHY ( 33 FDA reports)
DYSPHONIA ( 33 FDA reports)
MULTIPLE MYELOMA ( 33 FDA reports)
TOOTH IMPACTED ( 33 FDA reports)
TOOTH INFECTION ( 33 FDA reports)
ULCER ( 33 FDA reports)
VISUAL IMPAIRMENT ( 33 FDA reports)
HEPATIC CYST ( 32 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 32 FDA reports)
OPEN WOUND ( 32 FDA reports)
RADICULOPATHY ( 32 FDA reports)
ROTATOR CUFF SYNDROME ( 32 FDA reports)
COLITIS ( 31 FDA reports)
CONVULSION ( 31 FDA reports)
DEFORMITY ( 31 FDA reports)
DYSGEUSIA ( 31 FDA reports)
EXPOSED BONE IN JAW ( 31 FDA reports)
IRON DEFICIENCY ANAEMIA ( 31 FDA reports)
NOCTURIA ( 31 FDA reports)
ORAL DISORDER ( 31 FDA reports)
RESPIRATORY DISTRESS ( 31 FDA reports)
SOFT TISSUE DISORDER ( 31 FDA reports)
SURGERY ( 31 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 31 FDA reports)
COMA ( 30 FDA reports)
GINGIVAL SWELLING ( 30 FDA reports)
LYMPHOEDEMA ( 30 FDA reports)
MASTECTOMY ( 30 FDA reports)
SINUS DISORDER ( 30 FDA reports)
SLEEP APNOEA SYNDROME ( 30 FDA reports)
BLOOD PRESSURE INCREASED ( 29 FDA reports)
CERVICAL SPINAL STENOSIS ( 29 FDA reports)
COORDINATION ABNORMAL ( 29 FDA reports)
DENTURE WEARER ( 29 FDA reports)
HERPES ZOSTER ( 29 FDA reports)
HYPERHIDROSIS ( 29 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 29 FDA reports)
LUMBAR SPINAL STENOSIS ( 29 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 29 FDA reports)
STRESS FRACTURE ( 29 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 29 FDA reports)
CHOLELITHIASIS ( 28 FDA reports)
COMPRESSION FRACTURE ( 28 FDA reports)
EAR PAIN ( 28 FDA reports)
HIP FRACTURE ( 28 FDA reports)
LUNG DISORDER ( 28 FDA reports)
MYOCARDIAL INFARCTION ( 28 FDA reports)
ONYCHOMYCOSIS ( 28 FDA reports)
POLYURIA ( 28 FDA reports)
TENDONITIS ( 28 FDA reports)
BONE NEOPLASM MALIGNANT ( 27 FDA reports)
CYST ( 27 FDA reports)
FAECES DISCOLOURED ( 27 FDA reports)
FEMUR FRACTURE ( 27 FDA reports)
GINGIVAL ULCERATION ( 27 FDA reports)
HAEMOPTYSIS ( 27 FDA reports)
HAEMORRHAGE ( 27 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 27 FDA reports)
LUNG NEOPLASM MALIGNANT ( 27 FDA reports)
ABDOMINAL PAIN UPPER ( 26 FDA reports)
ARTERIOSCLEROSIS ( 26 FDA reports)
DEAFNESS NEUROSENSORY ( 26 FDA reports)
FLUID RETENTION ( 26 FDA reports)
HEPATIC STEATOSIS ( 26 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 26 FDA reports)
METASTASES TO LUNG ( 26 FDA reports)
SINUS TACHYCARDIA ( 26 FDA reports)
BACTERIAL INFECTION ( 25 FDA reports)
DRY EYE ( 25 FDA reports)
INCISIONAL DRAINAGE ( 25 FDA reports)
NASAL CONGESTION ( 25 FDA reports)
ORAL SURGERY ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
SOMNOLENCE ( 25 FDA reports)
AGRANULOCYTOSIS ( 24 FDA reports)
AMNESIA ( 24 FDA reports)
ANAPHYLACTIC REACTION ( 24 FDA reports)
CARDIAC MURMUR ( 24 FDA reports)
DEAFNESS ( 24 FDA reports)
FOREIGN BODY ( 24 FDA reports)
GLAUCOMA ( 24 FDA reports)
HYDRONEPHROSIS ( 24 FDA reports)
LOBAR PNEUMONIA ( 24 FDA reports)
NEOPLASM ( 24 FDA reports)
OVARIAN CANCER ( 24 FDA reports)
PERIODONTITIS ( 24 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 24 FDA reports)
TELANGIECTASIA ( 24 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 23 FDA reports)
BALANCE DISORDER ( 23 FDA reports)
BONE OPERATION ( 23 FDA reports)
DISEASE PROGRESSION ( 23 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 23 FDA reports)
HYPERPARATHYROIDISM ( 23 FDA reports)
METASTATIC NEOPLASM ( 23 FDA reports)
MUSCLE TWITCHING ( 23 FDA reports)
OROPHARYNGEAL PAIN ( 23 FDA reports)
OXYGEN SATURATION DECREASED ( 23 FDA reports)
PHARYNGEAL OEDEMA ( 23 FDA reports)
PRODUCTIVE COUGH ( 23 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 23 FDA reports)
SYNOVIAL CYST ( 23 FDA reports)
VISION BLURRED ( 23 FDA reports)
BONE MARROW FAILURE ( 22 FDA reports)
CYANOSIS ( 22 FDA reports)
FOOT FRACTURE ( 22 FDA reports)
GASTROENTERITIS ( 22 FDA reports)
HEART RATE INCREASED ( 22 FDA reports)
HEART RATE IRREGULAR ( 22 FDA reports)
INFUSION RELATED REACTION ( 22 FDA reports)
LUNG INFILTRATION ( 22 FDA reports)
MALNUTRITION ( 22 FDA reports)
MUSCULOSKELETAL PAIN ( 22 FDA reports)
ORAL DISCOMFORT ( 22 FDA reports)
PULPITIS DENTAL ( 22 FDA reports)
SENSITIVITY OF TEETH ( 22 FDA reports)
ABSCESS DRAINAGE ( 21 FDA reports)
ACTINOMYCOSIS ( 21 FDA reports)
AORTIC VALVE INCOMPETENCE ( 21 FDA reports)
ASPIRATION PLEURAL CAVITY ( 21 FDA reports)
ASTHMA ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 21 FDA reports)
BLOOD PRESSURE DECREASED ( 21 FDA reports)
CATHETER REMOVAL ( 21 FDA reports)
CEREBRAL ISCHAEMIA ( 21 FDA reports)
COAGULOPATHY ( 21 FDA reports)
EMPHYSEMA ( 21 FDA reports)
MEMORY IMPAIRMENT ( 21 FDA reports)
SPEECH DISORDER ( 21 FDA reports)
SPONDYLOLISTHESIS ( 21 FDA reports)
STAPHYLOCOCCAL INFECTION ( 21 FDA reports)
STOMATOCYTES PRESENT ( 21 FDA reports)
ANGINA PECTORIS ( 20 FDA reports)
ARTHROPATHY ( 20 FDA reports)
DYSARTHRIA ( 20 FDA reports)
HEART VALVE INCOMPETENCE ( 20 FDA reports)
HEPATIC LESION ( 20 FDA reports)
LIBIDO DECREASED ( 20 FDA reports)
NEUTROPHIL COUNT DECREASED ( 20 FDA reports)
OCULAR HYPERAEMIA ( 20 FDA reports)
PARAESTHESIA ORAL ( 20 FDA reports)
SCOLIOSIS ( 20 FDA reports)
SPINAL COLUMN STENOSIS ( 20 FDA reports)
TYPE 2 DIABETES MELLITUS ( 20 FDA reports)
ABDOMINAL DISTENSION ( 19 FDA reports)
ABSCESS JAW ( 19 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
CONJUNCTIVITIS ( 19 FDA reports)
DYSPHEMIA ( 19 FDA reports)
ENTEROCOCCAL INFECTION ( 19 FDA reports)
FIBROSIS ( 19 FDA reports)
HILAR LYMPHADENOPATHY ( 19 FDA reports)
ILEUS ( 19 FDA reports)
INTESTINAL ISCHAEMIA ( 19 FDA reports)
MASS ( 19 FDA reports)
MOBILITY DECREASED ( 19 FDA reports)
NIGHT SWEATS ( 19 FDA reports)
OEDEMA MUCOSAL ( 19 FDA reports)
RADICULAR PAIN ( 19 FDA reports)
RESTLESS LEGS SYNDROME ( 19 FDA reports)
RHONCHI ( 19 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 19 FDA reports)
SCAR ( 19 FDA reports)
SLEEP DISORDER ( 19 FDA reports)
SPINAL HAEMANGIOMA ( 19 FDA reports)
STRESS ( 19 FDA reports)
TENOSYNOVITIS ( 19 FDA reports)
THROAT TIGHTNESS ( 19 FDA reports)
URTICARIA ( 19 FDA reports)
VERTEBROPLASTY ( 19 FDA reports)
WOUND TREATMENT ( 19 FDA reports)
ALVEOLAR OSTEITIS ( 18 FDA reports)
ANEURYSM ( 18 FDA reports)
ASCITES ( 18 FDA reports)
CANDIDIASIS ( 18 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 18 FDA reports)
CHOKING ( 18 FDA reports)
DISORIENTATION ( 18 FDA reports)
EYE PRURITUS ( 18 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 18 FDA reports)
HEPATIC FAILURE ( 18 FDA reports)
HYPOCALCAEMIA ( 18 FDA reports)
JAW FRACTURE ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 18 FDA reports)
ORAL CAVITY FISTULA ( 18 FDA reports)
ORTHOSTATIC HYPOTENSION ( 18 FDA reports)
OSTEITIS ( 18 FDA reports)
PERICARDIAL EFFUSION ( 18 FDA reports)
PERIODONTAL OPERATION ( 18 FDA reports)
PNEUMOTHORAX ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
TACHYPNOEA ( 18 FDA reports)
TENDON INJURY ( 18 FDA reports)
THROMBOSIS ( 18 FDA reports)
TONGUE INJURY ( 18 FDA reports)
ACCIDENT AT WORK ( 17 FDA reports)
ANDROGENS ABNORMAL ( 17 FDA reports)
AORTIC ANEURYSM ( 17 FDA reports)
DENTAL CARE ( 17 FDA reports)
DEVICE OCCLUSION ( 17 FDA reports)
DISCOMFORT ( 17 FDA reports)
EPICONDYLITIS ( 17 FDA reports)
EPISTAXIS ( 17 FDA reports)
EYELID PTOSIS ( 17 FDA reports)
FUNGAL INFECTION ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HYPOTHYROIDISM ( 17 FDA reports)
JOINT INJURY ( 17 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 17 FDA reports)
OSTEOMALACIA ( 17 FDA reports)
OSTEOSARCOMA METASTATIC ( 17 FDA reports)
PARKINSON'S DISEASE ( 17 FDA reports)
PELVIC FRACTURE ( 17 FDA reports)
PHYSICAL DISABILITY ( 17 FDA reports)
PLEURAL FIBROSIS ( 17 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 17 FDA reports)
SYNOVITIS ( 17 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
BONE FRAGMENTATION ( 16 FDA reports)
CARDIO-RESPIRATORY ARREST ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
ENCEPHALOPATHY ( 16 FDA reports)
ENDOTRACHEAL INTUBATION ( 16 FDA reports)
HAEMANGIOMA ( 16 FDA reports)
HEMIPARESIS ( 16 FDA reports)
HUMERUS FRACTURE ( 16 FDA reports)
HYPERKERATOSIS ( 16 FDA reports)
INTERSTITIAL LUNG DISEASE ( 16 FDA reports)
MIGRAINE ( 16 FDA reports)
NASAL ULCER ( 16 FDA reports)
OESOPHAGITIS ( 16 FDA reports)
POLYP ( 16 FDA reports)
POSTNASAL DRIP ( 16 FDA reports)
SEASONAL ALLERGY ( 16 FDA reports)
THYROID NEOPLASM ( 16 FDA reports)
ABDOMINAL HERNIA ( 15 FDA reports)
ABSCESS ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
BONE EROSION ( 15 FDA reports)
BONE LOSS ( 15 FDA reports)
CAROTID ARTERY DISEASE ( 15 FDA reports)
CERVICAL DYSPLASIA ( 15 FDA reports)
CHRONIC SINUSITIS ( 15 FDA reports)
DEPRESSED MOOD ( 15 FDA reports)
FEELING HOT ( 15 FDA reports)
GASTRITIS ( 15 FDA reports)
HEPATIC CANCER METASTATIC ( 15 FDA reports)
HYPOALBUMINAEMIA ( 15 FDA reports)
HYPOPHOSPHATAEMIA ( 15 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 15 FDA reports)
ONYCHALGIA ( 15 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 15 FDA reports)
PHLEBITIS ( 15 FDA reports)
PLANTAR FASCIITIS ( 15 FDA reports)
RADIATION INJURY ( 15 FDA reports)
RETINAL MELANOMA ( 15 FDA reports)
ROSACEA ( 15 FDA reports)
URINE ODOUR ABNORMAL ( 15 FDA reports)
ADENOMA BENIGN ( 14 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 14 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 14 FDA reports)
ARTHROSCOPY ( 14 FDA reports)
BENIGN COLONIC NEOPLASM ( 14 FDA reports)
BLADDER CANCER RECURRENT ( 14 FDA reports)
BRAIN CANCER METASTATIC ( 14 FDA reports)
BRONCHIECTASIS ( 14 FDA reports)
CALCULUS URETERIC ( 14 FDA reports)
CAROTID ARTERY STENOSIS ( 14 FDA reports)
CLAUSTROPHOBIA ( 14 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
FACET JOINT SYNDROME ( 14 FDA reports)
GINGIVAL ERYTHEMA ( 14 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 14 FDA reports)
JUGULAR VEIN THROMBOSIS ( 14 FDA reports)
LIGAMENT RUPTURE ( 14 FDA reports)
MELAENA ( 14 FDA reports)
OBESITY ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
POLYARTHRITIS ( 14 FDA reports)
POOR QUALITY SLEEP ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
RENAL TUBULAR NECROSIS ( 14 FDA reports)
SEBORRHOEIC KERATOSIS ( 14 FDA reports)
SINUS BRADYCARDIA ( 14 FDA reports)
SINUS CONGESTION ( 14 FDA reports)
UROSEPSIS ( 14 FDA reports)
UTERINE LEIOMYOMA ( 14 FDA reports)
ANGIOEDEMA ( 13 FDA reports)
BONE SCAN ABNORMAL ( 13 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
CATHETER PLACEMENT ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 13 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 13 FDA reports)
CEREBRAL ATROPHY ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
DENTAL DISCOMFORT ( 13 FDA reports)
DERMATITIS ACNEIFORM ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
FAECAL INCONTINENCE ( 13 FDA reports)
GINGIVAL ABSCESS ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
HERNIA REPAIR ( 13 FDA reports)
HISTOPLASMOSIS ( 13 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 13 FDA reports)
METASTASES TO LYMPH NODES ( 13 FDA reports)
MOUTH HAEMORRHAGE ( 13 FDA reports)
OEDEMA ( 13 FDA reports)
PAIN OF SKIN ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PEPTIC ULCER ( 13 FDA reports)
PERIARTHRITIS ( 13 FDA reports)
PULMONARY MASS ( 13 FDA reports)
PULMONARY OEDEMA ( 13 FDA reports)
RALES ( 13 FDA reports)
SCLERODERMA ( 13 FDA reports)
SPINAL FRACTURE ( 13 FDA reports)
TENDON DISORDER ( 13 FDA reports)
TONGUE BITING ( 13 FDA reports)
VITREOUS FLOATERS ( 13 FDA reports)
ATROPHY ( 12 FDA reports)
BONE SWELLING ( 12 FDA reports)
BREAST CANCER ( 12 FDA reports)
DISABILITY ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
GENERALISED OEDEMA ( 12 FDA reports)
HALLUCINATION ( 12 FDA reports)
HODGKIN'S DISEASE ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
HYPOMAGNESAEMIA ( 12 FDA reports)
JOINT DISLOCATION ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LEUKOCYTOSIS ( 12 FDA reports)
LUNG HYPERINFLATION ( 12 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
ORAL CANDIDIASIS ( 12 FDA reports)
PLATELET COUNT INCREASED ( 12 FDA reports)
POOR PERIPHERAL CIRCULATION ( 12 FDA reports)
PULMONARY FIBROSIS ( 12 FDA reports)
PURULENCE ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
RENAL FAILURE CHRONIC ( 12 FDA reports)
RETCHING ( 12 FDA reports)
SKIN INDURATION ( 12 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 12 FDA reports)
TOOTH INJURY ( 12 FDA reports)
UTERINE CANCER ( 12 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
ACIDOSIS ( 11 FDA reports)
ADNEXA UTERI CYST ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 11 FDA reports)
AGITATION ( 11 FDA reports)
BILIARY DYSKINESIA ( 11 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 11 FDA reports)
BREATH ODOUR ( 11 FDA reports)
CARDIAC FAILURE CHRONIC ( 11 FDA reports)
CATHETER RELATED INFECTION ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
DIVERTICULITIS ( 11 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
HYPERCHOLESTEROLAEMIA ( 11 FDA reports)
HYPERGLYCAEMIA ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
LARYNGITIS ( 11 FDA reports)
MASS EXCISION ( 11 FDA reports)
MITRAL VALVE PROLAPSE ( 11 FDA reports)
OESOPHAGEAL DISORDER ( 11 FDA reports)
ORAL INFECTION ( 11 FDA reports)
PNEUMONIA ASPIRATION ( 11 FDA reports)
PNEUMONITIS ( 11 FDA reports)
POST PROCEDURAL COMPLICATION ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
RADICULITIS ( 11 FDA reports)
SENSORY LOSS ( 11 FDA reports)
SKIN DISCOLOURATION ( 11 FDA reports)
SPLENOMEGALY ( 11 FDA reports)
SUBDURAL HAEMATOMA ( 11 FDA reports)
THYROID CYST ( 11 FDA reports)
URINARY TRACT OBSTRUCTION ( 11 FDA reports)
VASCULITIS ( 11 FDA reports)
WHEELCHAIR USER ( 11 FDA reports)
WOUND DEBRIDEMENT ( 11 FDA reports)
ABDOMINAL DISCOMFORT ( 10 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 10 FDA reports)
AGGRESSION ( 10 FDA reports)
APHONIA ( 10 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BONE TRIMMING ( 10 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 10 FDA reports)
BREATH SOUNDS ABNORMAL ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 10 FDA reports)
CALCINOSIS ( 10 FDA reports)
CARDIAC DISORDER ( 10 FDA reports)
CARDIAC SEPTAL DEFECT ( 10 FDA reports)
CYST ASPIRATION ( 10 FDA reports)
DECUBITUS ULCER ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
DYSKINESIA ( 10 FDA reports)
EJECTION FRACTION DECREASED ( 10 FDA reports)
ENTERITIS ( 10 FDA reports)
ENTHESOPATHY ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
FACIAL PALSY ( 10 FDA reports)
FEMALE STERILISATION ( 10 FDA reports)
FURUNCLE ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HYPERAEMIA ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 10 FDA reports)
INGROWING NAIL ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
LIGAMENT SPRAIN ( 10 FDA reports)
MAXILLOFACIAL OPERATION ( 10 FDA reports)
METASTASES TO THE MEDIASTINUM ( 10 FDA reports)
MYOPIA ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
PALLOR ( 10 FDA reports)
PERIODONTAL INFECTION ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
PHOTOPHOBIA ( 10 FDA reports)
PLASMACYTOMA ( 10 FDA reports)
POOR PERSONAL HYGIENE ( 10 FDA reports)
PROSTHESIS IMPLANTATION ( 10 FDA reports)
PROTEIN TOTAL INCREASED ( 10 FDA reports)
PULSE ABSENT ( 10 FDA reports)
RADICULAR SYNDROME ( 10 FDA reports)
RESPIRATORY ARREST ( 10 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 10 FDA reports)
SEPSIS SYNDROME ( 10 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 10 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 10 FDA reports)
THORACOTOMY ( 10 FDA reports)
TONGUE PARALYSIS ( 10 FDA reports)
TUMOUR INVASION ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 10 FDA reports)
VOCAL CORD PARALYSIS ( 10 FDA reports)
VOCAL CORD THICKENING ( 10 FDA reports)
WOUND DEHISCENCE ( 10 FDA reports)
WOUND INFECTION ( 10 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
BREAST MASS ( 9 FDA reports)
BRUXISM ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CATHETER RELATED COMPLICATION ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
COMMINUTED FRACTURE ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DENTAL PLAQUE ( 9 FDA reports)
DENTAL TREATMENT ( 9 FDA reports)
DEVICE RELATED SEPSIS ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
EMOTIONAL DISORDER ( 9 FDA reports)
FACIAL NEURALGIA ( 9 FDA reports)
FIBULA FRACTURE ( 9 FDA reports)
GINGIVAL OEDEMA ( 9 FDA reports)
HEPATOSPLENOMEGALY ( 9 FDA reports)
HYPERCHLORAEMIA ( 9 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
LYMPHADENECTOMY ( 9 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MECHANICAL VENTILATION ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MOOD SWINGS ( 9 FDA reports)
MORTON'S NEUROMA ( 9 FDA reports)
NEURALGIA ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
PULMONARY CONGESTION ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RECTAL FISSURE ( 9 FDA reports)
REFLUX OESOPHAGITIS ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
RIGHT ATRIAL DILATATION ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
SEPTIC SHOCK ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SPLENIC INFARCTION ( 9 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 9 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 9 FDA reports)
SYNCOPE VASOVAGAL ( 9 FDA reports)
TOOTH FRACTURE ( 9 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 9 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
APTYALISM ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 8 FDA reports)
ASTERIXIS ( 8 FDA reports)
AXILLARY MASS ( 8 FDA reports)
BACTERIAL TEST POSITIVE ( 8 FDA reports)
BIOPSY BONE ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 8 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 8 FDA reports)
BONE NEOPLASM ( 8 FDA reports)
BREAST CANCER IN SITU ( 8 FDA reports)
BREAST CANCER METASTATIC ( 8 FDA reports)
BREAST LUMP REMOVAL ( 8 FDA reports)
BRONCHOPNEUMONIA ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CARDIAC ENZYMES INCREASED ( 8 FDA reports)
CARDIOTOXICITY ( 8 FDA reports)
CERVICOBRACHIAL SYNDROME ( 8 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 8 FDA reports)
COR PULMONALE CHRONIC ( 8 FDA reports)
CRANIAL NERVE DISORDER ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
EFFUSION ( 8 FDA reports)
EPIDURAL LIPOMATOSIS ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 8 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 8 FDA reports)
GASTRODUODENITIS ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
HAEMATOMA ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
HYPOACUSIS ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
ILEUS PARALYTIC ( 8 FDA reports)
INGUINAL HERNIA ( 8 FDA reports)
JOINT SWELLING ( 8 FDA reports)
LIPOMA ( 8 FDA reports)
LOWER LIMB FRACTURE ( 8 FDA reports)
LUNG OPERATION ( 8 FDA reports)
MACROGLOSSIA ( 8 FDA reports)
MALOCCLUSION ( 8 FDA reports)
MANDIBULECTOMY ( 8 FDA reports)
MENISCUS REMOVAL ( 8 FDA reports)
MUCOSAL EROSION ( 8 FDA reports)
MUCOSAL ULCERATION ( 8 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 8 FDA reports)
NASAL MUCOSAL DISORDER ( 8 FDA reports)
NERVE INJURY ( 8 FDA reports)
NODULE ( 8 FDA reports)
ODYNOPHAGIA ( 8 FDA reports)
OSTEITIS DEFORMANS ( 8 FDA reports)
OSTEOMYELITIS CHRONIC ( 8 FDA reports)
OSTEORADIONECROSIS ( 8 FDA reports)
OVARIAN CYST ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
POOR DENTAL CONDITION ( 8 FDA reports)
RADIATION OESOPHAGITIS ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SKIN PAPILLOMA ( 8 FDA reports)
SPINAL CORD DISORDER ( 8 FDA reports)
SPLENIC CYST ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
THROMBOCYTOSIS ( 8 FDA reports)
THROMBOPHLEBITIS ( 8 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 8 FDA reports)
TOOTH RESORPTION ( 8 FDA reports)
TROPONIN INCREASED ( 8 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 8 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
UTERINE ENLARGEMENT ( 8 FDA reports)
VASCULAR OPERATION ( 8 FDA reports)
VENA CAVA FILTER INSERTION ( 8 FDA reports)
VIITH NERVE PARALYSIS ( 8 FDA reports)
VITREOUS DETACHMENT ( 8 FDA reports)
WEGENER'S GRANULOMATOSIS ( 8 FDA reports)
AORTIC DISORDER ( 7 FDA reports)
APHASIA ( 7 FDA reports)
APNOEA ( 7 FDA reports)
ATROPHIC VULVOVAGINITIS ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
CARDIAC VALVE DISEASE ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CERUMEN IMPACTION ( 7 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
CLUSTER HEADACHE ( 7 FDA reports)
COLLAPSE OF LUNG ( 7 FDA reports)
DEAFNESS BILATERAL ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DIZZINESS POSTURAL ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
GINGIVAL EROSION ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HORDEOLUM ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 7 FDA reports)
LIP BLISTER ( 7 FDA reports)
LIP ULCERATION ( 7 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
LUNG CONSOLIDATION ( 7 FDA reports)
MACROCYTOSIS ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MENIERE'S DISEASE ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
NASAL DISORDER ( 7 FDA reports)
NASAL POLYPS ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 7 FDA reports)
NEUROENDOCRINE TUMOUR ( 7 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 7 FDA reports)
OOPHORECTOMY BILATERAL ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 7 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 7 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
REFLUX LARYNGITIS ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
ROTATOR CUFF REPAIR ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 7 FDA reports)
SKIN LESION EXCISION ( 7 FDA reports)
SMEAR CERVIX ABNORMAL ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
ABASIA ( 6 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 6 FDA reports)
ARTIFICIAL MENOPAUSE ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BONE MARROW OEDEMA ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRAIN HYPOXIA ( 6 FDA reports)
BREAST ENLARGEMENT ( 6 FDA reports)
CARCINOID SYNDROME ( 6 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CAROTID BRUIT ( 6 FDA reports)
CHONDROMALACIA ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 6 FDA reports)
DEPENDENCE ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 6 FDA reports)
DRUG ABUSER ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 6 FDA reports)
FISTULA DISCHARGE ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GOITRE ( 6 FDA reports)
GRANULOCYTOPENIA ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HOMICIDAL IDEATION ( 6 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
JOINT CONTRACTURE ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MEDICAL DEVICE REMOVAL ( 6 FDA reports)
METASTASES TO THORAX ( 6 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
ORAL HERPES ( 6 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 6 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
POSTURING ( 6 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
SIALOADENITIS ( 6 FDA reports)
SPIROMETRY ABNORMAL ( 6 FDA reports)
SPUTUM ABNORMAL ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
SWOLLEN TEAR DUCT ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
THEFT ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
URINE FLOW DECREASED ( 6 FDA reports)
VENOUS OCCLUSION ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ACNE ( 5 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 5 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACTERIAL TEST NEGATIVE ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
BREAST CYST ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CLOSED FRACTURE MANIPULATION ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
DENTAL FISTULA ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
EXTRAVASATION ( 5 FDA reports)
EXTREMITY CONTRACTURE ( 5 FDA reports)
FASCIITIS ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
LOCALISED INFECTION ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
OTITIS MEDIA ( 5 FDA reports)
PANCOAST'S TUMOUR ( 5 FDA reports)
PERINEPHRIC ABSCESS ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RED BLOOD CELLS URINE ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN FIBROSIS ( 5 FDA reports)
SKIN GRAFT ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SPONDYLITIC MYELOPATHY ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URINE ANALYSIS ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VAGINITIS BACTERIAL ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
WHITE BLOOD CELL COUNT ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANGER ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 4 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MYELOMA RECURRENCE ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OSTEOMYELITIS DRAINAGE ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERICARDIAL CYST ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
POIKILOCYTOSIS ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PROSTATE CANCER RECURRENT ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
TOOTH DEPOSIT ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
UTERINE FIBROSIS ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WOUND DRAINAGE ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ARTERIAL CATHETERISATION ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
COLLATERAL CIRCULATION ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EMBOLISM VENOUS ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LIGAMENT INJURY ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NASAL SEPTUM PERFORATION ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PLASTIC SURGERY TO THE FACE ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL NAUSEA ( 3 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 3 FDA reports)
POSTPARTUM DEPRESSION ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SOFT TISSUE INFLAMMATION ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
AORTIC BRUIT ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DENTAL FLUORIDE THERAPY ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FEAR ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GUM NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MEDIASTINOSCOPY ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
UTERINE ATROPHY ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRONTAL SINUS OPERATIONS ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL ANAESTHESIA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISCOMFORT ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STARING ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use