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

ANAEMIA ( 2235 FDA reports)
APLASIA PURE RED CELL ( 1465 FDA reports)
PAIN ( 1412 FDA reports)
FATIGUE ( 1165 FDA reports)
HAEMOGLOBIN DECREASED ( 1151 FDA reports)
DYSPNOEA ( 1102 FDA reports)
ANXIETY ( 978 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 963 FDA reports)
PYREXIA ( 890 FDA reports)
ASTHENIA ( 889 FDA reports)
DIARRHOEA ( 888 FDA reports)
NAUSEA ( 856 FDA reports)
OEDEMA PERIPHERAL ( 772 FDA reports)
VOMITING ( 766 FDA reports)
OSTEONECROSIS OF JAW ( 704 FDA reports)
PNEUMONIA ( 704 FDA reports)
DRUG INEFFECTIVE ( 680 FDA reports)
THROMBOCYTOPENIA ( 660 FDA reports)
PLEURAL EFFUSION ( 657 FDA reports)
BONE DISORDER ( 656 FDA reports)
BACK PAIN ( 651 FDA reports)
DEATH ( 617 FDA reports)
ARTHRALGIA ( 596 FDA reports)
DEHYDRATION ( 575 FDA reports)
HYPERTENSION ( 569 FDA reports)
WEIGHT DECREASED ( 558 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 554 FDA reports)
INFECTION ( 552 FDA reports)
PANCYTOPENIA ( 552 FDA reports)
INJURY ( 547 FDA reports)
PAIN IN EXTREMITY ( 536 FDA reports)
HYPOTENSION ( 533 FDA reports)
FALL ( 531 FDA reports)
ABDOMINAL PAIN ( 522 FDA reports)
RENAL FAILURE ( 521 FDA reports)
HYPOAESTHESIA ( 504 FDA reports)
OSTEOMYELITIS ( 504 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 489 FDA reports)
TOOTH EXTRACTION ( 477 FDA reports)
NEUROPATHY PERIPHERAL ( 471 FDA reports)
DIZZINESS ( 470 FDA reports)
URINARY TRACT INFECTION ( 457 FDA reports)
CONSTIPATION ( 447 FDA reports)
RENAL FAILURE ACUTE ( 437 FDA reports)
HEADACHE ( 431 FDA reports)
OSTEONECROSIS ( 430 FDA reports)
NEUTROPENIA ( 425 FDA reports)
CHEST PAIN ( 421 FDA reports)
EMOTIONAL DISTRESS ( 418 FDA reports)
PAIN IN JAW ( 409 FDA reports)
OSTEOARTHRITIS ( 397 FDA reports)
DEEP VEIN THROMBOSIS ( 396 FDA reports)
ATELECTASIS ( 394 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 393 FDA reports)
ERYTHEMA ( 387 FDA reports)
DEPRESSION ( 377 FDA reports)
SEPSIS ( 370 FDA reports)
COUGH ( 367 FDA reports)
DEFORMITY ( 358 FDA reports)
SPINAL OSTEOARTHRITIS ( 356 FDA reports)
IMPAIRED HEALING ( 353 FDA reports)
RASH ( 353 FDA reports)
DECREASED APPETITE ( 350 FDA reports)
PRURITUS ( 349 FDA reports)
PARAESTHESIA ( 345 FDA reports)
CONFUSIONAL STATE ( 344 FDA reports)
BLOOD CREATININE INCREASED ( 343 FDA reports)
MULTIPLE MYELOMA ( 343 FDA reports)
GAIT DISTURBANCE ( 341 FDA reports)
MALAISE ( 341 FDA reports)
ANHEDONIA ( 325 FDA reports)
MUSCULAR WEAKNESS ( 323 FDA reports)
MYELODYSPLASTIC SYNDROME ( 315 FDA reports)
CELLULITIS ( 306 FDA reports)
BRONCHITIS ( 301 FDA reports)
SWELLING ( 296 FDA reports)
RECTAL HAEMORRHAGE ( 294 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 292 FDA reports)
BONE PAIN ( 280 FDA reports)
DYSPHAGIA ( 280 FDA reports)
ATRIAL FIBRILLATION ( 279 FDA reports)
SYNCOPE ( 278 FDA reports)
METASTASES TO BONE ( 276 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 274 FDA reports)
MUSCULOSKELETAL PAIN ( 272 FDA reports)
RESPIRATORY FAILURE ( 270 FDA reports)
PLATELET COUNT DECREASED ( 267 FDA reports)
BONE LESION ( 266 FDA reports)
HAEMORRHOIDS ( 261 FDA reports)
LYMPHADENOPATHY ( 261 FDA reports)
RENAL FAILURE CHRONIC ( 260 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 257 FDA reports)
OSTEOPENIA ( 255 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 255 FDA reports)
MYOCARDIAL INFARCTION ( 250 FDA reports)
CHILLS ( 247 FDA reports)
OEDEMA ( 244 FDA reports)
LEUKOPENIA ( 240 FDA reports)
DENTAL CARIES ( 236 FDA reports)
TOOTHACHE ( 233 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 230 FDA reports)
PULMONARY EMBOLISM ( 230 FDA reports)
DISEASE PROGRESSION ( 229 FDA reports)
HYPOKALAEMIA ( 228 FDA reports)
BLOOD GLUCOSE INCREASED ( 227 FDA reports)
CARDIOMEGALY ( 225 FDA reports)
BONE MARROW FAILURE ( 222 FDA reports)
HAEMATURIA ( 222 FDA reports)
DECREASED INTEREST ( 221 FDA reports)
HYPOPHAGIA ( 219 FDA reports)
OSTEOPOROSIS ( 219 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 218 FDA reports)
INSOMNIA ( 218 FDA reports)
VISION BLURRED ( 215 FDA reports)
HIATUS HERNIA ( 213 FDA reports)
CONVULSION ( 212 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 211 FDA reports)
MENTAL STATUS CHANGES ( 211 FDA reports)
MYALGIA ( 211 FDA reports)
CONTUSION ( 209 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 209 FDA reports)
CEREBROVASCULAR ACCIDENT ( 207 FDA reports)
SINUSITIS ( 207 FDA reports)
GASTRITIS ( 205 FDA reports)
SCAR ( 203 FDA reports)
EPISTAXIS ( 200 FDA reports)
HAEMORRHAGE ( 199 FDA reports)
EXOSTOSIS ( 196 FDA reports)
HYPERKALAEMIA ( 195 FDA reports)
SKIN HYPERTROPHY ( 193 FDA reports)
BLOOD PRESSURE INCREASED ( 191 FDA reports)
CONDITION AGGRAVATED ( 186 FDA reports)
COLONIC POLYP ( 183 FDA reports)
HAEMATOCRIT DECREASED ( 183 FDA reports)
CATARACT ( 182 FDA reports)
MITRAL VALVE INCOMPETENCE ( 181 FDA reports)
NEOPLASM MALIGNANT ( 181 FDA reports)
CHOLELITHIASIS ( 178 FDA reports)
MOBILITY DECREASED ( 178 FDA reports)
SKIN INDURATION ( 177 FDA reports)
CORONARY ARTERY DISEASE ( 173 FDA reports)
MUCOSAL INFLAMMATION ( 173 FDA reports)
LOSS OF CONSCIOUSNESS ( 172 FDA reports)
TACHYCARDIA ( 172 FDA reports)
WEIGHT INCREASED ( 172 FDA reports)
DYSPNOEA EXERTIONAL ( 169 FDA reports)
PRIMARY SEQUESTRUM ( 169 FDA reports)
MUSCLE SPASMS ( 167 FDA reports)
NECK PAIN ( 167 FDA reports)
TOOTH LOSS ( 167 FDA reports)
PULMONARY OEDEMA ( 165 FDA reports)
LOOSE TOOTH ( 164 FDA reports)
HYPERSENSITIVITY ( 163 FDA reports)
THROMBOSIS ( 161 FDA reports)
CARDIAC ARREST ( 160 FDA reports)
INFLAMMATION ( 160 FDA reports)
DIVERTICULUM ( 156 FDA reports)
ORAL PAIN ( 156 FDA reports)
RENAL IMPAIRMENT ( 156 FDA reports)
LUNG NEOPLASM ( 155 FDA reports)
STAPHYLOCOCCAL INFECTION ( 155 FDA reports)
CARDIOMYOPATHY ( 153 FDA reports)
DISABILITY ( 153 FDA reports)
HYPOXIA ( 152 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 152 FDA reports)
OSTEOLYSIS ( 152 FDA reports)
SKIN TIGHTNESS ( 151 FDA reports)
SWELLING FACE ( 151 FDA reports)
SOMNOLENCE ( 150 FDA reports)
TOOTH DISORDER ( 149 FDA reports)
ARTERIOSCLEROSIS ( 148 FDA reports)
PHYSICAL DISABILITY ( 148 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 148 FDA reports)
HERPES ZOSTER ( 147 FDA reports)
ABDOMINAL PAIN UPPER ( 146 FDA reports)
LUNG INFILTRATION ( 144 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 144 FDA reports)
PATHOLOGICAL FRACTURE ( 144 FDA reports)
RIB FRACTURE ( 142 FDA reports)
HOSPITALISATION ( 141 FDA reports)
ASCITES ( 140 FDA reports)
EMPHYSEMA ( 140 FDA reports)
HYPONATRAEMIA ( 140 FDA reports)
REFRACTORY ANAEMIA ( 140 FDA reports)
BLOOD UREA INCREASED ( 138 FDA reports)
MASTICATION DISORDER ( 138 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 136 FDA reports)
HYPERHIDROSIS ( 135 FDA reports)
SKIN LESION ( 135 FDA reports)
OROPHARYNGEAL PAIN ( 134 FDA reports)
BONE DEBRIDEMENT ( 133 FDA reports)
CHEST DISCOMFORT ( 133 FDA reports)
FEBRILE NEUTROPENIA ( 133 FDA reports)
LEUKOCYTOSIS ( 133 FDA reports)
CYSTITIS ( 132 FDA reports)
HEPATIC ENZYME INCREASED ( 132 FDA reports)
LETHARGY ( 132 FDA reports)
BLOOD CALCIUM DECREASED ( 131 FDA reports)
GASTRITIS EROSIVE ( 131 FDA reports)
RENAL CYST ( 131 FDA reports)
HYPERCHOLESTEROLAEMIA ( 130 FDA reports)
TOOTH FRACTURE ( 130 FDA reports)
ARTHRITIS ( 129 FDA reports)
SKIN EXFOLIATION ( 128 FDA reports)
GINGIVAL INFECTION ( 126 FDA reports)
HYPOCALCAEMIA ( 126 FDA reports)
INJECTION SITE PAIN ( 126 FDA reports)
OSTEOSCLEROSIS ( 126 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 125 FDA reports)
FEELING ABNORMAL ( 124 FDA reports)
LUNG DISORDER ( 124 FDA reports)
MALNUTRITION ( 124 FDA reports)
PERICARDIAL EFFUSION ( 124 FDA reports)
JAW DISORDER ( 123 FDA reports)
PALPITATIONS ( 123 FDA reports)
STOMATITIS ( 123 FDA reports)
ABSCESS JAW ( 122 FDA reports)
SCOLIOSIS ( 122 FDA reports)
BURSITIS ( 121 FDA reports)
DIVERTICULUM INTESTINAL ( 120 FDA reports)
HYPERLIPIDAEMIA ( 119 FDA reports)
TOOTH ABSCESS ( 118 FDA reports)
METASTASES TO LIVER ( 117 FDA reports)
ORAL DISORDER ( 117 FDA reports)
SKIN ULCER ( 117 FDA reports)
VARICOSE VEIN ( 116 FDA reports)
JOINT CONTRACTURE ( 115 FDA reports)
NEPHROLITHIASIS ( 115 FDA reports)
SKIN DISCOLOURATION ( 115 FDA reports)
FIBROSIS ( 114 FDA reports)
METASTASES TO SPINE ( 114 FDA reports)
RADICULOPATHY ( 114 FDA reports)
ARRHYTHMIA ( 113 FDA reports)
INTERSTITIAL LUNG DISEASE ( 113 FDA reports)
EXPOSED BONE IN JAW ( 112 FDA reports)
GINGIVAL PAIN ( 112 FDA reports)
JAW FRACTURE ( 112 FDA reports)
OESOPHAGITIS ( 112 FDA reports)
BALANCE DISORDER ( 111 FDA reports)
PULMONARY FIBROSIS ( 111 FDA reports)
RESPIRATORY DISTRESS ( 111 FDA reports)
SINUS TACHYCARDIA ( 111 FDA reports)
BLOOD ALBUMIN DECREASED ( 110 FDA reports)
CARDIAC DISORDER ( 110 FDA reports)
LUMBAR SPINAL STENOSIS ( 110 FDA reports)
MUSCLE TWITCHING ( 110 FDA reports)
RIGHT VENTRICULAR FAILURE ( 110 FDA reports)
TREMOR ( 110 FDA reports)
URINARY INCONTINENCE ( 110 FDA reports)
URTICARIA ( 110 FDA reports)
AZOTAEMIA ( 109 FDA reports)
CARDIAC FAILURE ( 109 FDA reports)
DRY SKIN ( 109 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 108 FDA reports)
JOINT STIFFNESS ( 108 FDA reports)
LIFE EXPECTANCY SHORTENED ( 108 FDA reports)
MULTI-ORGAN FAILURE ( 108 FDA reports)
HOT FLUSH ( 107 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 107 FDA reports)
PULMONARY HYPERTENSION ( 107 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 106 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 105 FDA reports)
DECUBITUS ULCER ( 105 FDA reports)
DIABETES MELLITUS ( 105 FDA reports)
DYSPEPSIA ( 105 FDA reports)
LEFT VENTRICULAR FAILURE ( 105 FDA reports)
MEMORY IMPAIRMENT ( 105 FDA reports)
METASTASES TO LUNG ( 105 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 105 FDA reports)
SINUS DISORDER ( 105 FDA reports)
COMPRESSION FRACTURE ( 104 FDA reports)
OSTEITIS ( 103 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 102 FDA reports)
FLUID OVERLOAD ( 102 FDA reports)
HYPERGLYCAEMIA ( 102 FDA reports)
ANGINA PECTORIS ( 101 FDA reports)
HYPOGLYCAEMIA ( 101 FDA reports)
MASS ( 101 FDA reports)
SKIN HYPERPIGMENTATION ( 101 FDA reports)
SYNOVIAL CYST ( 101 FDA reports)
VISUAL ACUITY REDUCED ( 101 FDA reports)
BLOOD PRESSURE DECREASED ( 100 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 100 FDA reports)
HYPOPNOEA ( 100 FDA reports)
SKIN DISORDER ( 100 FDA reports)
SPINAL COLUMN STENOSIS ( 100 FDA reports)
HAEMATOMA ( 99 FDA reports)
SPINAL COMPRESSION FRACTURE ( 99 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 98 FDA reports)
ANAL FISSURE ( 98 FDA reports)
DYSURIA ( 98 FDA reports)
NEURALGIA ( 98 FDA reports)
SEPTIC SHOCK ( 98 FDA reports)
VAGINAL ABSCESS ( 98 FDA reports)
DEBRIDEMENT ( 97 FDA reports)
HEPATIC LESION ( 97 FDA reports)
OVERDOSE ( 97 FDA reports)
BONE DENSITY DECREASED ( 96 FDA reports)
PERIODONTAL DISEASE ( 96 FDA reports)
POLLAKIURIA ( 96 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 96 FDA reports)
CEREBRAL ATROPHY ( 95 FDA reports)
SLEEP APNOEA SYNDROME ( 95 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 94 FDA reports)
CANDIDIASIS ( 94 FDA reports)
DISCOMFORT ( 94 FDA reports)
DYSARTHRIA ( 94 FDA reports)
JAW OPERATION ( 94 FDA reports)
BRADYCARDIA ( 93 FDA reports)
SKIN FIBROSIS ( 93 FDA reports)
ABASIA ( 92 FDA reports)
ACTINOMYCOSIS ( 92 FDA reports)
ALOPECIA ( 92 FDA reports)
HEART RATE INCREASED ( 92 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 92 FDA reports)
SPLENOMEGALY ( 92 FDA reports)
SURGERY ( 92 FDA reports)
COAGULOPATHY ( 91 FDA reports)
HAEMATOCHEZIA ( 91 FDA reports)
HIP FRACTURE ( 91 FDA reports)
METABOLIC ACIDOSIS ( 91 FDA reports)
PROTHROMBIN TIME PROLONGED ( 91 FDA reports)
PROTEINURIA ( 90 FDA reports)
RASH GENERALISED ( 90 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 89 FDA reports)
HAEMODIALYSIS ( 89 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 89 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 89 FDA reports)
VERTIGO ( 89 FDA reports)
ABDOMINAL DISTENSION ( 88 FDA reports)
BACTERAEMIA ( 87 FDA reports)
ROTATOR CUFF SYNDROME ( 87 FDA reports)
TOOTH INFECTION ( 87 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 86 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 86 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 86 FDA reports)
ABSCESS ( 85 FDA reports)
ASTHMA ( 85 FDA reports)
ENDODONTIC PROCEDURE ( 85 FDA reports)
ONYCHOMYCOSIS ( 85 FDA reports)
PERITONITIS ( 85 FDA reports)
PERITONITIS BACTERIAL ( 85 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 84 FDA reports)
BREAST CANCER METASTATIC ( 84 FDA reports)
DEAFNESS ( 84 FDA reports)
DRY MOUTH ( 84 FDA reports)
HAEMOPTYSIS ( 84 FDA reports)
HEPATIC FAILURE ( 84 FDA reports)
HYDRONEPHROSIS ( 84 FDA reports)
SERUM FERRITIN INCREASED ( 83 FDA reports)
ANOREXIA ( 82 FDA reports)
CYST ( 82 FDA reports)
JOINT SWELLING ( 82 FDA reports)
STEM CELL TRANSPLANT ( 82 FDA reports)
COLITIS ( 81 FDA reports)
HEPATIC STEATOSIS ( 81 FDA reports)
PRODUCTIVE COUGH ( 81 FDA reports)
RENAL DISORDER ( 81 FDA reports)
BLOOD POTASSIUM DECREASED ( 80 FDA reports)
HYPERKERATOSIS ( 80 FDA reports)
HYPERCALCAEMIA ( 79 FDA reports)
NIGHT SWEATS ( 79 FDA reports)
CHOLECYSTITIS ( 78 FDA reports)
IRON DEFICIENCY ( 78 FDA reports)
GLAUCOMA ( 77 FDA reports)
HALLUCINATION ( 77 FDA reports)
HYPOMAGNESAEMIA ( 77 FDA reports)
TENDONITIS ( 77 FDA reports)
FLUID RETENTION ( 76 FDA reports)
GINGIVAL BLEEDING ( 76 FDA reports)
WOUND DEHISCENCE ( 76 FDA reports)
CARDIAC MURMUR ( 75 FDA reports)
WHEEZING ( 75 FDA reports)
BLOOD POTASSIUM INCREASED ( 74 FDA reports)
ARTHROPATHY ( 73 FDA reports)
BONE MARROW DEPRESSION ( 73 FDA reports)
CARPAL TUNNEL SYNDROME ( 73 FDA reports)
DIALYSIS ( 73 FDA reports)
EAR PAIN ( 73 FDA reports)
FISTULA ( 73 FDA reports)
GENERALISED OEDEMA ( 73 FDA reports)
HYPOTHYROIDISM ( 73 FDA reports)
MOUTH ULCERATION ( 73 FDA reports)
RASH ERYTHEMATOUS ( 73 FDA reports)
CEREBRAL ISCHAEMIA ( 72 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 72 FDA reports)
HAEMOLYSIS ( 72 FDA reports)
KYPHOSIS ( 72 FDA reports)
VIRAL INFECTION ( 71 FDA reports)
BONE EROSION ( 70 FDA reports)
ENTEROCOCCAL INFECTION ( 70 FDA reports)
GOITRE ( 70 FDA reports)
GOUT ( 70 FDA reports)
SEQUESTRECTOMY ( 70 FDA reports)
FLANK PAIN ( 69 FDA reports)
GINGIVITIS ( 69 FDA reports)
GROIN PAIN ( 69 FDA reports)
UNRESPONSIVE TO STIMULI ( 69 FDA reports)
EOSINOPHILIA ( 67 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 67 FDA reports)
METASTATIC NEOPLASM ( 67 FDA reports)
PLASMACYTOSIS ( 67 FDA reports)
WALKING AID USER ( 67 FDA reports)
DRUG INTERACTION ( 66 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 66 FDA reports)
CERVICAL SPINAL STENOSIS ( 65 FDA reports)
DERMATITIS ( 65 FDA reports)
EXTREMITY CONTRACTURE ( 65 FDA reports)
GALLBLADDER DISORDER ( 65 FDA reports)
OBESITY ( 65 FDA reports)
PURULENCE ( 65 FDA reports)
RASH PRURITIC ( 65 FDA reports)
SKIN PLAQUE ( 65 FDA reports)
TREATMENT NONCOMPLIANCE ( 65 FDA reports)
DRUG HYPERSENSITIVITY ( 64 FDA reports)
PULMONARY CONGESTION ( 64 FDA reports)
BLOOD SODIUM DECREASED ( 63 FDA reports)
LYMPHOEDEMA ( 63 FDA reports)
PULMONARY MASS ( 63 FDA reports)
VISUAL IMPAIRMENT ( 63 FDA reports)
BURNING SENSATION ( 62 FDA reports)
FAECAL INCONTINENCE ( 62 FDA reports)
FULL BLOOD COUNT DECREASED ( 62 FDA reports)
GINGIVAL DISORDER ( 62 FDA reports)
PNEUMONIA ASPIRATION ( 62 FDA reports)
RETICULOCYTE COUNT DECREASED ( 62 FDA reports)
SCIATICA ( 62 FDA reports)
BONE FRAGMENTATION ( 61 FDA reports)
CEREBRAL INFARCTION ( 61 FDA reports)
DENTAL OPERATION ( 61 FDA reports)
LUNG NEOPLASM MALIGNANT ( 61 FDA reports)
PLASMACYTOMA ( 61 FDA reports)
BACTERIAL INFECTION ( 60 FDA reports)
CATARACT OPERATION ( 60 FDA reports)
FLUSHING ( 60 FDA reports)
HYPOVOLAEMIA ( 60 FDA reports)
RENAL TRANSPLANT ( 60 FDA reports)
RESPIRATORY ARREST ( 60 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 60 FDA reports)
TRANSFUSION ( 60 FDA reports)
AORTIC ANEURYSM ( 59 FDA reports)
BONE LOSS ( 59 FDA reports)
CARDIOVASCULAR DISORDER ( 59 FDA reports)
DIPLOPIA ( 59 FDA reports)
LOCAL SWELLING ( 59 FDA reports)
MITRAL VALVE PROLAPSE ( 59 FDA reports)
TENDERNESS ( 59 FDA reports)
TINNITUS ( 59 FDA reports)
APLASTIC ANAEMIA ( 58 FDA reports)
DENTAL FISTULA ( 58 FDA reports)
EJECTION FRACTION DECREASED ( 58 FDA reports)
PLATELET COUNT INCREASED ( 58 FDA reports)
WOUND DRAINAGE ( 58 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 57 FDA reports)
PURULENT DISCHARGE ( 57 FDA reports)
RASH MACULO-PAPULAR ( 57 FDA reports)
SPONDYLOLISTHESIS ( 57 FDA reports)
AMNESIA ( 56 FDA reports)
AORTIC VALVE INCOMPETENCE ( 56 FDA reports)
BONE NEOPLASM MALIGNANT ( 56 FDA reports)
DEVICE RELATED INFECTION ( 56 FDA reports)
DYSPHONIA ( 56 FDA reports)
FACIAL PAIN ( 56 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 56 FDA reports)
THERAPY NON-RESPONDER ( 56 FDA reports)
DIABETIC RETINOPATHY ( 55 FDA reports)
EATING DISORDER ( 55 FDA reports)
HAEMATEMESIS ( 55 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 55 FDA reports)
NO THERAPEUTIC RESPONSE ( 55 FDA reports)
PERONEAL NERVE PALSY ( 55 FDA reports)
VITREOUS FLOATERS ( 55 FDA reports)
CAROTID BRUIT ( 54 FDA reports)
DERMAL CYST ( 54 FDA reports)
HEPATIC CYST ( 54 FDA reports)
JOINT EFFUSION ( 54 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 54 FDA reports)
TRISMUS ( 54 FDA reports)
ULCER ( 54 FDA reports)
FEELING HOT ( 53 FDA reports)
INFLUENZA LIKE ILLNESS ( 53 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 53 FDA reports)
NEUTROPHIL COUNT DECREASED ( 53 FDA reports)
ORAL SURGERY ( 53 FDA reports)
RHABDOMYOLYSIS ( 53 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 53 FDA reports)
AGRANULOCYTOSIS ( 52 FDA reports)
VAGINAL HAEMORRHAGE ( 52 FDA reports)
ABSCESS ORAL ( 51 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 51 FDA reports)
BREATH ODOUR ( 51 FDA reports)
HERNIA ( 51 FDA reports)
ILEUS ( 51 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 51 FDA reports)
LIMB INJURY ( 51 FDA reports)
ORAL INFECTION ( 51 FDA reports)
PAIN OF SKIN ( 51 FDA reports)
RENAL TUBULAR NECROSIS ( 51 FDA reports)
ABSCESS DRAINAGE ( 50 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 50 FDA reports)
ECZEMA ( 50 FDA reports)
HAEMOGLOBIN INCREASED ( 50 FDA reports)
INFLUENZA ( 50 FDA reports)
MYELOMA RECURRENCE ( 50 FDA reports)
ORTHOSTATIC HYPOTENSION ( 50 FDA reports)
RENAL ATROPHY ( 50 FDA reports)
RETCHING ( 50 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 50 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 49 FDA reports)
CARDIO-RESPIRATORY ARREST ( 49 FDA reports)
ELECTROLYTE IMBALANCE ( 49 FDA reports)
GASTROENTERITIS ( 49 FDA reports)
HEART RATE IRREGULAR ( 49 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 49 FDA reports)
PNEUMOTHORAX ( 49 FDA reports)
ACUTE CORONARY SYNDROME ( 48 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 48 FDA reports)
DISORIENTATION ( 48 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 48 FDA reports)
ORAL CAVITY FISTULA ( 48 FDA reports)
PERIODONTITIS ( 48 FDA reports)
PERIORBITAL OEDEMA ( 48 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 48 FDA reports)
UTERINE LEIOMYOMA ( 48 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 48 FDA reports)
AGITATION ( 47 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 47 FDA reports)
BLINDNESS ( 47 FDA reports)
BONE MARROW OEDEMA ( 47 FDA reports)
CALCIPHYLAXIS ( 47 FDA reports)
DYSGEUSIA ( 47 FDA reports)
EYE SWELLING ( 47 FDA reports)
FAILURE TO THRIVE ( 47 FDA reports)
GRANULOMA ( 47 FDA reports)
LOBAR PNEUMONIA ( 47 FDA reports)
LOCALISED INFECTION ( 47 FDA reports)
MUSCLE STRAIN ( 47 FDA reports)
NERVOUSNESS ( 47 FDA reports)
RESPIRATORY DISORDER ( 47 FDA reports)
SEDATION ( 47 FDA reports)
VIITH NERVE PARALYSIS ( 47 FDA reports)
ASPIRATION PLEURAL CAVITY ( 46 FDA reports)
BLOOD IRON DECREASED ( 46 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 46 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 46 FDA reports)
DEPRESSED MOOD ( 46 FDA reports)
DRUG TOXICITY ( 46 FDA reports)
ENCEPHALOPATHY ( 46 FDA reports)
HEPATOMEGALY ( 46 FDA reports)
MENTAL DISORDER ( 46 FDA reports)
NEURITIS ( 46 FDA reports)
PALLOR ( 46 FDA reports)
RASH MACULAR ( 46 FDA reports)
WHEELCHAIR USER ( 46 FDA reports)
BODY TEMPERATURE INCREASED ( 45 FDA reports)
EXCORIATION ( 45 FDA reports)
GINGIVAL SWELLING ( 45 FDA reports)
IRON DEFICIENCY ANAEMIA ( 45 FDA reports)
MUSCLE CONTRACTURE ( 45 FDA reports)
OCCULT BLOOD POSITIVE ( 45 FDA reports)
POST PROCEDURAL COMPLICATION ( 45 FDA reports)
RADICULAR PAIN ( 45 FDA reports)
THROMBOPHLEBITIS ( 45 FDA reports)
VENOUS OCCLUSION ( 45 FDA reports)
ABDOMINAL DISCOMFORT ( 44 FDA reports)
BASAL CELL CARCINOMA ( 44 FDA reports)
CATHETER PLACEMENT ( 44 FDA reports)
CHRONIC SINUSITIS ( 44 FDA reports)
COMA ( 44 FDA reports)
FACE OEDEMA ( 44 FDA reports)
FIBROMYALGIA ( 44 FDA reports)
JAUNDICE ( 44 FDA reports)
LIGAMENT SPRAIN ( 44 FDA reports)
LIVER DISORDER ( 44 FDA reports)
LUNG CONSOLIDATION ( 44 FDA reports)
NASOPHARYNGITIS ( 44 FDA reports)
PARAPLEGIA ( 44 FDA reports)
RADIOTHERAPY ( 44 FDA reports)
TRANSPLANT REJECTION ( 44 FDA reports)
ANAPHYLACTIC REACTION ( 43 FDA reports)
BLISTER ( 43 FDA reports)
DRY EYE ( 43 FDA reports)
ECCHYMOSIS ( 43 FDA reports)
EDENTULOUS ( 43 FDA reports)
FEELING COLD ( 43 FDA reports)
MELAENA ( 43 FDA reports)
OTITIS MEDIA ( 43 FDA reports)
SKIN ATROPHY ( 43 FDA reports)
SLEEP DISORDER ( 43 FDA reports)
TENDON DISORDER ( 43 FDA reports)
UNEVALUABLE EVENT ( 43 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 42 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 42 FDA reports)
CACHEXIA ( 42 FDA reports)
CERUMEN IMPACTION ( 42 FDA reports)
HAEMOGLOBIN ABNORMAL ( 42 FDA reports)
HYPOAESTHESIA ORAL ( 42 FDA reports)
OCULAR HYPERAEMIA ( 42 FDA reports)
ORAL CANDIDIASIS ( 42 FDA reports)
OXYGEN SATURATION DECREASED ( 42 FDA reports)
PLEURAL FIBROSIS ( 42 FDA reports)
PRURITUS GENERALISED ( 42 FDA reports)
SARCOIDOSIS ( 42 FDA reports)
TYPE 2 DIABETES MELLITUS ( 42 FDA reports)
VENOUS THROMBOSIS ( 42 FDA reports)
CATHETER RELATED INFECTION ( 41 FDA reports)
DIASTOLIC DYSFUNCTION ( 41 FDA reports)
GINGIVAL ERYTHEMA ( 41 FDA reports)
HAEMANGIOMA ( 41 FDA reports)
HYPOACUSIS ( 41 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 41 FDA reports)
RHINORRHOEA ( 41 FDA reports)
STRESS ( 41 FDA reports)
CYANOSIS ( 40 FDA reports)
DENTURE WEARER ( 40 FDA reports)
FEMUR FRACTURE ( 40 FDA reports)
FIBULA FRACTURE ( 40 FDA reports)
GINGIVAL RECESSION ( 40 FDA reports)
HORDEOLUM ( 40 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 40 FDA reports)
JOINT SPRAIN ( 40 FDA reports)
LYMPHOMA ( 40 FDA reports)
NODULE ( 40 FDA reports)
PHLEBITIS ( 40 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 39 FDA reports)
ANGINA UNSTABLE ( 39 FDA reports)
ATRIAL FLUTTER ( 39 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 39 FDA reports)
CARDIOGENIC SHOCK ( 39 FDA reports)
FEMORAL NECK FRACTURE ( 39 FDA reports)
INCONTINENCE ( 39 FDA reports)
JOINT INJURY ( 39 FDA reports)
JUGULAR VEIN THROMBOSIS ( 39 FDA reports)
PARALYSIS ( 39 FDA reports)
PLEURITIC PAIN ( 39 FDA reports)
SEBORRHOEIC KERATOSIS ( 39 FDA reports)
SINUS BRADYCARDIA ( 39 FDA reports)
SUBDURAL HAEMATOMA ( 39 FDA reports)
VENTRICULAR TACHYCARDIA ( 39 FDA reports)
ANGIOEDEMA ( 38 FDA reports)
BLOOD BILIRUBIN INCREASED ( 38 FDA reports)
BONE MARROW TRANSPLANT ( 38 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 38 FDA reports)
DIVERTICULITIS ( 38 FDA reports)
FOOT DEFORMITY ( 38 FDA reports)
HAEMOLYTIC ANAEMIA ( 38 FDA reports)
HEPATITIS ( 38 FDA reports)
HYPERMETROPIA ( 38 FDA reports)
HYPERTENSIVE CRISIS ( 38 FDA reports)
INCREASED TENDENCY TO BRUISE ( 38 FDA reports)
INTESTINAL ISCHAEMIA ( 38 FDA reports)
NEPHROGENIC ANAEMIA ( 38 FDA reports)
NEPHROPATHY ( 38 FDA reports)
ORAL INTAKE REDUCED ( 38 FDA reports)
PELVIC PAIN ( 38 FDA reports)
PURPURA ( 38 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 38 FDA reports)
URINARY RETENTION ( 38 FDA reports)
BLOOD GLUCOSE DECREASED ( 37 FDA reports)
CIRCULATORY COLLAPSE ( 37 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 37 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 37 FDA reports)
DRUG ERUPTION ( 37 FDA reports)
FACET JOINT SYNDROME ( 37 FDA reports)
HEMIPLEGIA ( 37 FDA reports)
LUMBAR RADICULOPATHY ( 37 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 37 FDA reports)
OVARIAN CYST ( 37 FDA reports)
PIGMENTATION DISORDER ( 37 FDA reports)
RESTLESSNESS ( 37 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 37 FDA reports)
SENSITIVITY OF TEETH ( 37 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 37 FDA reports)
STRESS FRACTURE ( 37 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 37 FDA reports)
URINE OUTPUT DECREASED ( 37 FDA reports)
VITAMIN B12 DEFICIENCY ( 37 FDA reports)
APHASIA ( 36 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 36 FDA reports)
BLEPHARITIS ( 36 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 36 FDA reports)
BLOOD COUNT ABNORMAL ( 36 FDA reports)
FUNGAL INFECTION ( 36 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 36 FDA reports)
ISCHAEMIA ( 36 FDA reports)
MYOCARDIAL ISCHAEMIA ( 36 FDA reports)
NEUTROPHIL COUNT INCREASED ( 36 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 36 FDA reports)
PELVIC FRACTURE ( 36 FDA reports)
POLYP ( 36 FDA reports)
PYELONEPHRITIS ( 36 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 35 FDA reports)
ANGIOPATHY ( 35 FDA reports)
DYSKINESIA ( 35 FDA reports)
EAR INFECTION ( 35 FDA reports)
FAECALOMA ( 35 FDA reports)
HILAR LYMPHADENOPATHY ( 35 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 35 FDA reports)
MOUTH HAEMORRHAGE ( 35 FDA reports)
MYOCLONUS ( 35 FDA reports)
NEPHROTIC SYNDROME ( 35 FDA reports)
NOCTURIA ( 35 FDA reports)
PANCREATITIS ( 35 FDA reports)
PROSTATE CANCER ( 35 FDA reports)
REFLUX OESOPHAGITIS ( 35 FDA reports)
RHEUMATOID ARTHRITIS ( 35 FDA reports)
RHINITIS ALLERGIC ( 35 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 35 FDA reports)
VERTEBROPLASTY ( 35 FDA reports)
AORTIC CALCIFICATION ( 34 FDA reports)
CARDIAC TAMPONADE ( 34 FDA reports)
EYELID OEDEMA ( 34 FDA reports)
FACIAL PALSY ( 34 FDA reports)
FAECES DISCOLOURED ( 34 FDA reports)
GASTRIC ULCER ( 34 FDA reports)
HYPERPARATHYROIDISM ( 34 FDA reports)
INGROWING NAIL ( 34 FDA reports)
LIMB DISCOMFORT ( 34 FDA reports)
MUSCLE TIGHTNESS ( 34 FDA reports)
NECK INJURY ( 34 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 34 FDA reports)
PERICARDITIS ( 34 FDA reports)
PROSTATOMEGALY ( 34 FDA reports)
SPINAL DISORDER ( 34 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 33 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 33 FDA reports)
DERMATITIS CONTACT ( 33 FDA reports)
HYPOALBUMINAEMIA ( 33 FDA reports)
HYSTERECTOMY ( 33 FDA reports)
PLANTAR FASCIITIS ( 33 FDA reports)
POLYURIA ( 33 FDA reports)
PRESYNCOPE ( 33 FDA reports)
SHOCK ( 33 FDA reports)
SHUNT OCCLUSION ( 33 FDA reports)
SPINAL COLUMN INJURY ( 33 FDA reports)
SUICIDAL IDEATION ( 33 FDA reports)
ASTIGMATISM ( 32 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 32 FDA reports)
BREAST CANCER ( 32 FDA reports)
ESCHERICHIA INFECTION ( 32 FDA reports)
GASTRIC HAEMORRHAGE ( 32 FDA reports)
HEPATIC CIRRHOSIS ( 32 FDA reports)
MICTURITION URGENCY ( 32 FDA reports)
NEOPLASM PROGRESSION ( 32 FDA reports)
OPEN WOUND ( 32 FDA reports)
ORTHOPNOEA ( 32 FDA reports)
PROTEIN TOTAL DECREASED ( 32 FDA reports)
PROTEIN URINE PRESENT ( 32 FDA reports)
PSEUDOMONAS INFECTION ( 32 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 32 FDA reports)
RETICULOCYTE COUNT INCREASED ( 32 FDA reports)
SPINAL CORD COMPRESSION ( 32 FDA reports)
APHAGIA ( 31 FDA reports)
ATAXIA ( 31 FDA reports)
DELIRIUM ( 31 FDA reports)
DERMATITIS EXFOLIATIVE ( 31 FDA reports)
DIABETIC NEUROPATHY ( 31 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 31 FDA reports)
INGUINAL HERNIA ( 31 FDA reports)
MASS EXCISION ( 31 FDA reports)
MEDICATION ERROR ( 31 FDA reports)
MENINGIOMA ( 31 FDA reports)
MYOPATHY ( 31 FDA reports)
PARAESTHESIA ORAL ( 31 FDA reports)
PHOTOPSIA ( 31 FDA reports)
SKIN BURNING SENSATION ( 31 FDA reports)
TOXIC SKIN ERUPTION ( 31 FDA reports)
TRANSFUSION REACTION ( 31 FDA reports)
ABDOMINAL PAIN LOWER ( 30 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 30 FDA reports)
ATRIAL TACHYCARDIA ( 30 FDA reports)
BONE NEOPLASM ( 30 FDA reports)
BRONCHIECTASIS ( 30 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 30 FDA reports)
CAROTID ARTERY STENOSIS ( 30 FDA reports)
COLON CANCER ( 30 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 30 FDA reports)
FISTULA DISCHARGE ( 30 FDA reports)
FRACTURED SACRUM ( 30 FDA reports)
LEUKOENCEPHALOPATHY ( 30 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 30 FDA reports)
MASTECTOMY ( 30 FDA reports)
MEAN CELL VOLUME INCREASED ( 30 FDA reports)
METASTASIS ( 30 FDA reports)
ONYCHOCLASIS ( 30 FDA reports)
OVERWEIGHT ( 30 FDA reports)
RESPIRATORY TRACT CONGESTION ( 30 FDA reports)
SPINAL FUSION SURGERY ( 30 FDA reports)
SWOLLEN TONGUE ( 30 FDA reports)
THROMBOCYTOSIS ( 30 FDA reports)
VULVOVAGINAL DRYNESS ( 30 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 29 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 29 FDA reports)
LACERATION ( 29 FDA reports)
LUNG INFECTION ( 29 FDA reports)
MYOSITIS ( 29 FDA reports)
NEUROGENIC BLADDER ( 29 FDA reports)
OCULAR HYPERTENSION ( 29 FDA reports)
PUBIS FRACTURE ( 29 FDA reports)
RENAL INJURY ( 29 FDA reports)
SENSORY LOSS ( 29 FDA reports)
SKIN LACERATION ( 29 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 29 FDA reports)
TONGUE ULCERATION ( 29 FDA reports)
VARICELLA ( 29 FDA reports)
WOUND INFECTION ( 29 FDA reports)
BLADDER CANCER ( 28 FDA reports)
CERVIX CARCINOMA ( 28 FDA reports)
CHOLECYSTECTOMY ( 28 FDA reports)
CLOSTRIDIAL INFECTION ( 28 FDA reports)
CONJUNCTIVITIS ( 28 FDA reports)
DEMENTIA ( 28 FDA reports)
DIABETIC KETOACIDOSIS ( 28 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 28 FDA reports)
HEAD INJURY ( 28 FDA reports)
HEARING IMPAIRED ( 28 FDA reports)
LEG AMPUTATION ( 28 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 28 FDA reports)
MALIGNANT MELANOMA ( 28 FDA reports)
OTITIS EXTERNA ( 28 FDA reports)
PNEUMONITIS ( 28 FDA reports)
RASH PAPULAR ( 28 FDA reports)
SEPSIS SYNDROME ( 28 FDA reports)
SOFT TISSUE DISORDER ( 28 FDA reports)
SPEECH DISORDER ( 28 FDA reports)
VESICAL FISTULA ( 28 FDA reports)
WOUND DEBRIDEMENT ( 28 FDA reports)
ANURIA ( 27 FDA reports)
BONE SCAN ABNORMAL ( 27 FDA reports)
BOWEN'S DISEASE ( 27 FDA reports)
BREAST MASS ( 27 FDA reports)
BREAST RECONSTRUCTION ( 27 FDA reports)
CARDIAC VALVE DISEASE ( 27 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 27 FDA reports)
DRUG INTOLERANCE ( 27 FDA reports)
EMOTIONAL DISORDER ( 27 FDA reports)
ENDOCARDITIS ( 27 FDA reports)
EPICONDYLITIS ( 27 FDA reports)
GASTROINTESTINAL PAIN ( 27 FDA reports)
HEMIPARESIS ( 27 FDA reports)
HIP ARTHROPLASTY ( 27 FDA reports)
INFUSION RELATED REACTION ( 27 FDA reports)
LYMPHOPENIA ( 27 FDA reports)
MIGRAINE ( 27 FDA reports)
PEAU D'ORANGE ( 27 FDA reports)
PULMONARY GRANULOMA ( 27 FDA reports)
RENAL PAIN ( 27 FDA reports)
RETINAL HAEMORRHAGE ( 27 FDA reports)
SENSORY DISTURBANCE ( 27 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 27 FDA reports)
TACHYPNOEA ( 27 FDA reports)
TONGUE INJURY ( 27 FDA reports)
TRANSPLANT FAILURE ( 27 FDA reports)
ABNORMAL SENSATION IN EYE ( 26 FDA reports)
ACIDOSIS ( 26 FDA reports)
ASEPTIC NECROSIS BONE ( 26 FDA reports)
CAROTID ARTERY DISEASE ( 26 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 26 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 26 FDA reports)
GLOSSODYNIA ( 26 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 26 FDA reports)
INCORRECT DOSE ADMINISTERED ( 26 FDA reports)
KIDNEY INFECTION ( 26 FDA reports)
MARROW HYPERPLASIA ( 26 FDA reports)
MEDICAL DEVICE COMPLICATION ( 26 FDA reports)
NASAL CONGESTION ( 26 FDA reports)
OEDEMA MOUTH ( 26 FDA reports)
OEDEMA MUCOSAL ( 26 FDA reports)
OSTEOMYELITIS ACUTE ( 26 FDA reports)
ROAD TRAFFIC ACCIDENT ( 26 FDA reports)
SOFT TISSUE INFECTION ( 26 FDA reports)
VASODILATATION ( 26 FDA reports)
VENTRICULAR FIBRILLATION ( 26 FDA reports)
ASPIRATION ( 25 FDA reports)
BRAIN OEDEMA ( 25 FDA reports)
BRONCHOPNEUMONIA ( 25 FDA reports)
DECREASED ACTIVITY ( 25 FDA reports)
DILATATION VENTRICULAR ( 25 FDA reports)
DISEASE RECURRENCE ( 25 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 25 FDA reports)
ESSENTIAL HYPERTENSION ( 25 FDA reports)
EYE NAEVUS ( 25 FDA reports)
IMPLANT SITE INFECTION ( 25 FDA reports)
INTESTINAL PERFORATION ( 25 FDA reports)
LACRIMATION INCREASED ( 25 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 25 FDA reports)
MOOD SWINGS ( 25 FDA reports)
ODYNOPHAGIA ( 25 FDA reports)
OPTIC NERVE CUPPING ( 25 FDA reports)
PETECHIAE ( 25 FDA reports)
PLEURISY ( 25 FDA reports)
RADIATION ASSOCIATED PAIN ( 25 FDA reports)
RESPIRATORY TRACT INFECTION ( 25 FDA reports)
THYROID DISORDER ( 25 FDA reports)
VITAMIN D DEFICIENCY ( 25 FDA reports)
ABDOMINAL HERNIA ( 24 FDA reports)
ACCIDENTAL OVERDOSE ( 24 FDA reports)
ACUTE SINUSITIS ( 24 FDA reports)
ANAEMIA MACROCYTIC ( 24 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 24 FDA reports)
BREAST CANCER RECURRENT ( 24 FDA reports)
CEREBRAL HAEMORRHAGE ( 24 FDA reports)
CERVICAL DYSPLASIA ( 24 FDA reports)
ECONOMIC PROBLEM ( 24 FDA reports)
EMBOLISM ( 24 FDA reports)
FOLLICULITIS ( 24 FDA reports)
GASTROENTERITIS VIRAL ( 24 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 24 FDA reports)
HEPATIC ENCEPHALOPATHY ( 24 FDA reports)
IMPAIRED WORK ABILITY ( 24 FDA reports)
INCISIONAL DRAINAGE ( 24 FDA reports)
MECHANICAL VENTILATION ( 24 FDA reports)
MENISCUS LESION ( 24 FDA reports)
METABOLIC ENCEPHALOPATHY ( 24 FDA reports)
METASTASES TO LYMPH NODES ( 24 FDA reports)
NASAL DISORDER ( 24 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 24 FDA reports)
OSTEOMYELITIS CHRONIC ( 24 FDA reports)
OSTEORADIONECROSIS ( 24 FDA reports)
RALES ( 24 FDA reports)
SQUAMOUS CELL CARCINOMA ( 24 FDA reports)
VASCULITIS ( 24 FDA reports)
ACUTE PRERENAL FAILURE ( 23 FDA reports)
AGGRESSION ( 23 FDA reports)
AORTIC STENOSIS ( 23 FDA reports)
BEDRIDDEN ( 23 FDA reports)
BILIARY DILATATION ( 23 FDA reports)
CALCULUS URETERIC ( 23 FDA reports)
CERVICITIS ( 23 FDA reports)
CHEST TUBE INSERTION ( 23 FDA reports)
DENTAL DISCOMFORT ( 23 FDA reports)
DERMOID CYST ( 23 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 23 FDA reports)
DRUG RESISTANCE ( 23 FDA reports)
EXFOLIATIVE RASH ( 23 FDA reports)
FRACTURE ( 23 FDA reports)
HYPERPHOSPHATAEMIA ( 23 FDA reports)
HYPOKINESIA ( 23 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 23 FDA reports)
MOTOR DYSFUNCTION ( 23 FDA reports)
MULTIPLE INJURIES ( 23 FDA reports)
OESOPHAGITIS ULCERATIVE ( 23 FDA reports)
OLIGURIA ( 23 FDA reports)
ORAL DISCOMFORT ( 23 FDA reports)
PSORIASIS ( 23 FDA reports)
RENAL CANCER ( 23 FDA reports)
RIGHT ATRIAL DILATATION ( 23 FDA reports)
SIALOADENITIS ( 23 FDA reports)
SINUS CONGESTION ( 23 FDA reports)
SPINAL FRACTURE ( 23 FDA reports)
TRACHEAL DEVIATION ( 23 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 23 FDA reports)
UROSEPSIS ( 23 FDA reports)
VISUAL FIELD DEFECT ( 23 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 22 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 22 FDA reports)
ARTERIOVENOUS FISTULA ( 22 FDA reports)
BLOOD URINE PRESENT ( 22 FDA reports)
BONE TRIMMING ( 22 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 22 FDA reports)
CATHETER RELATED COMPLICATION ( 22 FDA reports)
CEREBROVASCULAR DISORDER ( 22 FDA reports)
COLONOSCOPY ABNORMAL ( 22 FDA reports)
DENTAL CARE ( 22 FDA reports)
DRUG EFFECT DECREASED ( 22 FDA reports)
FOOT FRACTURE ( 22 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 22 FDA reports)
HODGKIN'S DISEASE ( 22 FDA reports)
HYDROCEPHALUS ( 22 FDA reports)
INJECTION SITE HAEMORRHAGE ( 22 FDA reports)
INJECTION SITE REACTION ( 22 FDA reports)
LIVEDO RETICULARIS ( 22 FDA reports)
MUCOSAL ULCERATION ( 22 FDA reports)
MUSCULOSKELETAL DISORDER ( 22 FDA reports)
OFF LABEL USE ( 22 FDA reports)
OROANTRAL FISTULA ( 22 FDA reports)
PARAPROTEINAEMIA ( 22 FDA reports)
RESPIRATORY DEPRESSION ( 22 FDA reports)
RETICULOCYTOPENIA ( 22 FDA reports)
SKIN PAPILLOMA ( 22 FDA reports)
SPLENIC INFARCTION ( 22 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 22 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 22 FDA reports)
TOE AMPUTATION ( 22 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 22 FDA reports)
URINARY HESITATION ( 22 FDA reports)
ACNE ( 21 FDA reports)
ACUTE PULMONARY OEDEMA ( 21 FDA reports)
AFFECTIVE DISORDER ( 21 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 21 FDA reports)
BONE MARROW DISORDER ( 21 FDA reports)
BREAST OPERATION ( 21 FDA reports)
BREAST PAIN ( 21 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 21 FDA reports)
CAESAREAN SECTION ( 21 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 21 FDA reports)
CORONARY ARTERY BYPASS ( 21 FDA reports)
DYSPLASIA ( 21 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 21 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 21 FDA reports)
GASTRIC POLYPS ( 21 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 21 FDA reports)
GRAND MAL CONVULSION ( 21 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 21 FDA reports)
INTRAOCULAR LENS IMPLANT ( 21 FDA reports)
ISCHAEMIC STROKE ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MENTAL IMPAIRMENT ( 21 FDA reports)
METABOLIC DISORDER ( 21 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 21 FDA reports)
NEPHROSCLEROSIS ( 21 FDA reports)
NEUROPATHY ( 21 FDA reports)
OROPHARYNGEAL BLISTERING ( 21 FDA reports)
PATELLA FRACTURE ( 21 FDA reports)
PERFORMANCE STATUS DECREASED ( 21 FDA reports)
PERNICIOUS ANAEMIA ( 21 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 21 FDA reports)
RADIATION INJURY ( 21 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 21 FDA reports)
SKIN SWELLING ( 21 FDA reports)
STILLBIRTH ( 21 FDA reports)
THYROID NEOPLASM ( 21 FDA reports)
TONGUE PARALYSIS ( 21 FDA reports)
TRACHEOBRONCHITIS ( 21 FDA reports)
UTERINE HAEMORRHAGE ( 21 FDA reports)
VENOUS INSUFFICIENCY ( 21 FDA reports)
VENTRICULAR HYPOKINESIA ( 21 FDA reports)
ANISOCYTOSIS ( 20 FDA reports)
BACK DISORDER ( 20 FDA reports)
BLOOD BICARBONATE DECREASED ( 20 FDA reports)
BLOOD CULTURE POSITIVE ( 20 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 20 FDA reports)
BRONCHITIS CHRONIC ( 20 FDA reports)
COGNITIVE DISORDER ( 20 FDA reports)
DRUG ABUSE ( 20 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 20 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
GANGRENE ( 20 FDA reports)
GASTRITIS HAEMORRHAGIC ( 20 FDA reports)
GASTROINTESTINAL DISORDER ( 20 FDA reports)
HYPERTENSIVE HEART DISEASE ( 20 FDA reports)
INTESTINAL OBSTRUCTION ( 20 FDA reports)
LIP SWELLING ( 20 FDA reports)
LOCALISED OEDEMA ( 20 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 20 FDA reports)
NERVOUS SYSTEM DISORDER ( 20 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 20 FDA reports)
PATHOGEN RESISTANCE ( 20 FDA reports)
PEPTIC ULCER ( 20 FDA reports)
PROSTHESIS IMPLANTATION ( 20 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 20 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 20 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 20 FDA reports)
THROMBOSIS IN DEVICE ( 20 FDA reports)
TIBIA FRACTURE ( 20 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 20 FDA reports)
VOCAL CORD PARALYSIS ( 20 FDA reports)
WOUND COMPLICATION ( 20 FDA reports)
ABSCESS NECK ( 19 FDA reports)
ACTINIC KERATOSIS ( 19 FDA reports)
ADENOCARCINOMA ( 19 FDA reports)
ANAL INFLAMMATION ( 19 FDA reports)
BRONCHOSPASM ( 19 FDA reports)
CATHETERISATION CARDIAC ( 19 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 19 FDA reports)
COLLAPSE OF LUNG ( 19 FDA reports)
COLON ADENOMA ( 19 FDA reports)
DRUG ADMINISTRATION ERROR ( 19 FDA reports)
ENDOTRACHEAL INTUBATION ( 19 FDA reports)
ERECTILE DYSFUNCTION ( 19 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 19 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 19 FDA reports)
HEPATITIS CHOLESTATIC ( 19 FDA reports)
HERPES SIMPLEX ( 19 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 19 FDA reports)
HYPOVENTILATION ( 19 FDA reports)
ICHTHYOSIS ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
MEDICAL DEVICE REMOVAL ( 19 FDA reports)
MUCOSAL EROSION ( 19 FDA reports)
NASAL SEPTUM DEVIATION ( 19 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 19 FDA reports)
PHARYNGITIS ( 19 FDA reports)
PRESBYOPIA ( 19 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 19 FDA reports)
SKIN NECROSIS ( 19 FDA reports)
SKIN NEOPLASM EXCISION ( 19 FDA reports)
SKIN REACTION ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 19 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 18 FDA reports)
ACUTE STRESS DISORDER ( 18 FDA reports)
AGEUSIA ( 18 FDA reports)
AXILLARY MASS ( 18 FDA reports)
BACTERIAL TEST POSITIVE ( 18 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 18 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 18 FDA reports)
CHOLESTASIS ( 18 FDA reports)
COOMBS TEST POSITIVE ( 18 FDA reports)
DELUSION ( 18 FDA reports)
DUODENITIS ( 18 FDA reports)
DYSSTASIA ( 18 FDA reports)
DYSTONIA ( 18 FDA reports)
EAR CONGESTION ( 18 FDA reports)
EPILEPSY ( 18 FDA reports)
EYE MOVEMENT DISORDER ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
FEAR ( 18 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 18 FDA reports)
INJECTION SITE SWELLING ( 18 FDA reports)
IRON OVERLOAD ( 18 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 18 FDA reports)
LIBIDO DECREASED ( 18 FDA reports)
MUSCLE DISORDER ( 18 FDA reports)
PARANASAL SINUS DISCOMFORT ( 18 FDA reports)
PARVOVIRUS INFECTION ( 18 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 18 FDA reports)
PHYSIOTHERAPY ( 18 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 18 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 18 FDA reports)
RHINITIS SEASONAL ( 18 FDA reports)
SALIVARY GLAND DISORDER ( 18 FDA reports)
SEBORRHOEIC DERMATITIS ( 18 FDA reports)
THORACOTOMY ( 18 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 18 FDA reports)
URINE ANALYSIS ABNORMAL ( 18 FDA reports)
VENOUS THROMBOSIS LIMB ( 18 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 18 FDA reports)
ACUTE RESPIRATORY FAILURE ( 17 FDA reports)
APHTHOUS STOMATITIS ( 17 FDA reports)
BIOPSY BONE ( 17 FDA reports)
BLADDER DISORDER ( 17 FDA reports)
BLOOD CHLORIDE INCREASED ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 17 FDA reports)
BLOOD IRON INCREASED ( 17 FDA reports)
BLOOD URIC ACID INCREASED ( 17 FDA reports)
BONE SWELLING ( 17 FDA reports)
CHONDROMALACIA ( 17 FDA reports)
CYSTITIS HAEMORRHAGIC ( 17 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 17 FDA reports)
EFFUSION ( 17 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 17 FDA reports)
FEBRILE BONE MARROW APLASIA ( 17 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 17 FDA reports)
GINGIVAL EROSION ( 17 FDA reports)
GYNAECOMASTIA ( 17 FDA reports)
HAEMORRHAGIC DIATHESIS ( 17 FDA reports)
HYPERSOMNIA ( 17 FDA reports)
HYPERTHYROIDISM ( 17 FDA reports)
INJECTION SITE HAEMATOMA ( 17 FDA reports)
INJECTION SITE IRRITATION ( 17 FDA reports)
INTERMITTENT CLAUDICATION ( 17 FDA reports)
JOINT DISLOCATION ( 17 FDA reports)
MALIGNANT HYPERTENSION ( 17 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 17 FDA reports)
METASTASES TO THORAX ( 17 FDA reports)
OESOPHAGEAL DISORDER ( 17 FDA reports)
PANCREATIC CARCINOMA ( 17 FDA reports)
PELVIC HAEMATOMA ( 17 FDA reports)
PERIARTHRITIS ( 17 FDA reports)
PERIPHERAL ISCHAEMIA ( 17 FDA reports)
PITTING OEDEMA ( 17 FDA reports)
PULMONARY HAEMORRHAGE ( 17 FDA reports)
RADIUS FRACTURE ( 17 FDA reports)
RENAL CELL CARCINOMA ( 17 FDA reports)
RESPIRATORY RATE INCREASED ( 17 FDA reports)
RESUSCITATION ( 17 FDA reports)
SENSATION OF HEAVINESS ( 17 FDA reports)
SINUS ARRHYTHMIA ( 17 FDA reports)
SOFT TISSUE INFLAMMATION ( 17 FDA reports)
STENT PLACEMENT ( 17 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
URETERIC OBSTRUCTION ( 17 FDA reports)
URETHRAL OBSTRUCTION ( 17 FDA reports)
X-RAY ABNORMAL ( 17 FDA reports)
AORTIC VALVE DISEASE ( 16 FDA reports)
ATROPHIC VULVOVAGINITIS ( 16 FDA reports)
BLOOD MAGNESIUM DECREASED ( 16 FDA reports)
BODY HEIGHT DECREASED ( 16 FDA reports)
BONE DEFORMITY ( 16 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 16 FDA reports)
CARDIAC FAILURE CHRONIC ( 16 FDA reports)
CRANIAL NERVE DISORDER ( 16 FDA reports)
DEVICE FAILURE ( 16 FDA reports)
ECZEMA ASTEATOTIC ( 16 FDA reports)
ESCHERICHIA SEPSIS ( 16 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 16 FDA reports)
FIBROUS HISTIOCYTOMA ( 16 FDA reports)
GALLBLADDER OPERATION ( 16 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 16 FDA reports)
HAEMODYNAMIC INSTABILITY ( 16 FDA reports)
HAIR GROWTH ABNORMAL ( 16 FDA reports)
HYPERAESTHESIA ( 16 FDA reports)
HYPOTONIA ( 16 FDA reports)
LARGE INTESTINE PERFORATION ( 16 FDA reports)
LIGAMENT DISORDER ( 16 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 16 FDA reports)
MICROCYTIC ANAEMIA ( 16 FDA reports)
NAIL DYSTROPHY ( 16 FDA reports)
NASAL POLYPS ( 16 FDA reports)
NECROSIS ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
ONYCHALGIA ( 16 FDA reports)
OPEN REDUCTION OF FRACTURE ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
ORAL MUCOSA ATROPHY ( 16 FDA reports)
ORTHODONTIC APPLIANCE USER ( 16 FDA reports)
PELVIC DISCOMFORT ( 16 FDA reports)
PERIOSTITIS ( 16 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 16 FDA reports)
POLYCYTHAEMIA ( 16 FDA reports)
PROSTATE CANCER METASTATIC ( 16 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
PULMONARY HILUM MASS ( 16 FDA reports)
RASH PUSTULAR ( 16 FDA reports)
RED BLOOD CELL ABNORMALITY ( 16 FDA reports)
ROTATOR CUFF REPAIR ( 16 FDA reports)
SERRATIA BACTERAEMIA ( 16 FDA reports)
SINUS OPERATION ( 16 FDA reports)
SPLENIC RUPTURE ( 16 FDA reports)
STRESS URINARY INCONTINENCE ( 16 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 16 FDA reports)
SUBCUTANEOUS ABSCESS ( 16 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 16 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 16 FDA reports)
TOOTH REPAIR ( 16 FDA reports)
TUMOUR LYSIS SYNDROME ( 16 FDA reports)
VENTRICULAR HYPERTROPHY ( 16 FDA reports)
WRIST FRACTURE ( 16 FDA reports)
ABDOMINAL ABSCESS ( 15 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
ACUTE ABDOMEN ( 15 FDA reports)
ADRENAL MASS ( 15 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 15 FDA reports)
APLASIA ( 15 FDA reports)
AURICULAR SWELLING ( 15 FDA reports)
BIOPSY BLADDER ABNORMAL ( 15 FDA reports)
BIOPSY SKIN ABNORMAL ( 15 FDA reports)
BLADDER CYST ( 15 FDA reports)
BLOOD CHLORIDE DECREASED ( 15 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 15 FDA reports)
BODY DYSMORPHIC DISORDER ( 15 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 15 FDA reports)
CATHETER SITE HAEMORRHAGE ( 15 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 15 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 15 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
COSTOCHONDRITIS ( 15 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 15 FDA reports)
CUBITAL TUNNEL SYNDROME ( 15 FDA reports)
CUSHINGOID ( 15 FDA reports)
CYSTITIS KLEBSIELLA ( 15 FDA reports)
CYSTOCELE ( 15 FDA reports)
DEAFNESS NEUROSENSORY ( 15 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 15 FDA reports)
DERMATITIS ALLERGIC ( 15 FDA reports)
DRUG DOSE OMISSION ( 15 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 15 FDA reports)
FAT NECROSIS ( 15 FDA reports)
FOLATE DEFICIENCY ( 15 FDA reports)
GINGIVAL ULCERATION ( 15 FDA reports)
GRAFT VERSUS HOST DISEASE ( 15 FDA reports)
HALLUCINATION, AUDITORY ( 15 FDA reports)
HALLUCINATION, VISUAL ( 15 FDA reports)
HISTOPLASMOSIS ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
KNEE ARTHROPLASTY ( 15 FDA reports)
MACROGLOSSIA ( 15 FDA reports)
NASAL MUCOSAL DISORDER ( 15 FDA reports)
NEOPLASM ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER ( 15 FDA reports)
ORAL HERPES ( 15 FDA reports)
PANCREATIC DISORDER ( 15 FDA reports)
PARONYCHIA ( 15 FDA reports)
PELVIC PROLAPSE ( 15 FDA reports)
PHOTOSENSITIVITY REACTION ( 15 FDA reports)
PLEURODESIS ( 15 FDA reports)
POLYARTHRITIS ( 15 FDA reports)
POLYNEUROPATHY ( 15 FDA reports)
PROSTATITIS ( 15 FDA reports)
RADICULITIS LUMBOSACRAL ( 15 FDA reports)
RESORPTION BONE INCREASED ( 15 FDA reports)
RESTLESS LEGS SYNDROME ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
SPINAL CORPECTOMY ( 15 FDA reports)
TONGUE COATED ( 15 FDA reports)
TONGUE DISCOLOURATION ( 15 FDA reports)
TOOTH RESORPTION ( 15 FDA reports)
TUMOUR MARKER INCREASED ( 15 FDA reports)
URETHRAL CARUNCLE ( 15 FDA reports)
VENA CAVA THROMBOSIS ( 15 FDA reports)
WOUND SECRETION ( 15 FDA reports)
ADENOMA BENIGN ( 14 FDA reports)
ADVERSE DRUG REACTION ( 14 FDA reports)
APPENDICITIS ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
BLOOD CREATINE INCREASED ( 14 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 14 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 14 FDA reports)
BLOOD PRESSURE ABNORMAL ( 14 FDA reports)
BRAIN CANCER METASTATIC ( 14 FDA reports)
BREAST CANCER FEMALE ( 14 FDA reports)
BREAST DISCHARGE ( 14 FDA reports)
CARCINOID SYNDROME ( 14 FDA reports)
CARDIOPULMONARY FAILURE ( 14 FDA reports)
CAROTID BODY TUMOUR ( 14 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 14 FDA reports)
CYST RUPTURE ( 14 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 14 FDA reports)
ECHOCARDIOGRAM ( 14 FDA reports)
EMPYEMA ( 14 FDA reports)
ENCEPHALITIS ( 14 FDA reports)
ENCEPHALOMALACIA ( 14 FDA reports)
ENTHESOPATHY ( 14 FDA reports)
FLUID REPLACEMENT ( 14 FDA reports)
GASTROENTERITIS RADIATION ( 14 FDA reports)
GENITAL HERPES ( 14 FDA reports)
GRAFT DYSFUNCTION ( 14 FDA reports)
GRANULOCYTOPENIA ( 14 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 14 FDA reports)
HEPATIC CANCER METASTATIC ( 14 FDA reports)
HEPATIC NEOPLASM ( 14 FDA reports)
HYPOAESTHESIA FACIAL ( 14 FDA reports)
INGUINAL HERNIA REPAIR ( 14 FDA reports)
INJECTION SITE BRUISING ( 14 FDA reports)
IRRITABLE BOWEL SYNDROME ( 14 FDA reports)
KLEBSIELLA INFECTION ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
LARYNGITIS ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
METAPLASIA ( 14 FDA reports)
METASTASES TO NASAL SINUSES ( 14 FDA reports)
OBSTRUCTIVE UROPATHY ( 14 FDA reports)
PANCREATIC ATROPHY ( 14 FDA reports)
PANCREATIC CALCIFICATION ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
PAROTID GLAND ENLARGEMENT ( 14 FDA reports)
POST HERPETIC NEURALGIA ( 14 FDA reports)
PREMATURE BABY ( 14 FDA reports)
QUADRIPARESIS ( 14 FDA reports)
QUALITY OF LIFE DECREASED ( 14 FDA reports)
RECTAL ULCER ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 14 FDA reports)
SICK SINUS SYNDROME ( 14 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 14 FDA reports)
SKIN CYST EXCISION ( 14 FDA reports)
SKIN FRAGILITY ( 14 FDA reports)
SKIN WARM ( 14 FDA reports)
SPINAL DECOMPRESSION ( 14 FDA reports)
SPINAL HAEMANGIOMA ( 14 FDA reports)
SPLEEN DISORDER ( 14 FDA reports)
SPONDYLOARTHROPATHY ( 14 FDA reports)
STOMATITIS NECROTISING ( 14 FDA reports)
TACHYARRHYTHMIA ( 14 FDA reports)
TENOSYNOVITIS ( 14 FDA reports)
TROPONIN INCREASED ( 14 FDA reports)
VARICES OESOPHAGEAL ( 14 FDA reports)
VENA CAVA FILTER INSERTION ( 14 FDA reports)
VITAMIN B12 INCREASED ( 14 FDA reports)
ABDOMINAL MASS ( 13 FDA reports)
ACROCHORDON ( 13 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 13 FDA reports)
BENCE JONES PROTEINURIA ( 13 FDA reports)
BIOPSY ( 13 FDA reports)
BLINDNESS UNILATERAL ( 13 FDA reports)
BREATH SOUNDS ABNORMAL ( 13 FDA reports)
CHOLANGITIS ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
DENTAL NECROSIS ( 13 FDA reports)
DENTAL TREATMENT ( 13 FDA reports)
DIURETIC THERAPY ( 13 FDA reports)
DYSLIPIDAEMIA ( 13 FDA reports)
ENTEROCOLITIS ( 13 FDA reports)
GAMMOPATHY ( 13 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
HYPOGEUSIA ( 13 FDA reports)
IMMUNOGLOBULINS DECREASED ( 13 FDA reports)
INTESTINAL RESECTION ( 13 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 13 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 13 FDA reports)
LYMPHADENECTOMY ( 13 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 13 FDA reports)
MACROCYTOSIS ( 13 FDA reports)
MAMMOGRAM ( 13 FDA reports)
MASTOIDITIS ( 13 FDA reports)
MENORRHAGIA ( 13 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 13 FDA reports)
MUCOSAL HAEMORRHAGE ( 13 FDA reports)
MUSCLE ATROPHY ( 13 FDA reports)
MYELOFIBROSIS ( 13 FDA reports)
NAIL HYPERTROPHY ( 13 FDA reports)
NEPHROPATHY TOXIC ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NODAL OSTEOARTHRITIS ( 13 FDA reports)
OPTIC NEURITIS ( 13 FDA reports)
OVARIAN CYST RUPTURED ( 13 FDA reports)
PERITONEAL DIALYSIS ( 13 FDA reports)
PHARYNGEAL OEDEMA ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
PORTAL HYPERTENSION ( 13 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 13 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 13 FDA reports)
POSTURE ABNORMAL ( 13 FDA reports)
PROCEDURAL COMPLICATION ( 13 FDA reports)
RADICAL HYSTERECTOMY ( 13 FDA reports)
RENAL MASS ( 13 FDA reports)
SCAPULA FRACTURE ( 13 FDA reports)
SINUS POLYP ( 13 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 13 FDA reports)
SPONDYLOLYSIS ( 13 FDA reports)
SUDDEN DEATH ( 13 FDA reports)
TEMPERATURE INTOLERANCE ( 13 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 13 FDA reports)
TOOTH DISCOLOURATION ( 13 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 13 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 13 FDA reports)
VISUAL DISTURBANCE ( 13 FDA reports)
ACCIDENT ( 12 FDA reports)
ACETABULUM FRACTURE ( 12 FDA reports)
ACUTE PHASE REACTION ( 12 FDA reports)
ADNEXA UTERI MASS ( 12 FDA reports)
ALLERGIC COUGH ( 12 FDA reports)
ALOPECIA AREATA ( 12 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 12 FDA reports)
AORTIC BRUIT ( 12 FDA reports)
AORTIC DILATATION ( 12 FDA reports)
AORTIC VALVE STENOSIS ( 12 FDA reports)
APPENDICITIS PERFORATED ( 12 FDA reports)
BACTERIAL TEST NEGATIVE ( 12 FDA reports)
BIOPSY BREAST ABNORMAL ( 12 FDA reports)
BIOPSY LYMPH GLAND ( 12 FDA reports)
BONE OPERATION ( 12 FDA reports)
BREAST PROSTHESIS REMOVAL ( 12 FDA reports)
BREAST PROSTHESIS USER ( 12 FDA reports)
CARDIAC VALVE SCLEROSIS ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 12 FDA reports)
COLITIS ISCHAEMIC ( 12 FDA reports)
COLON CANCER METASTATIC ( 12 FDA reports)
DERMATITIS BULLOUS ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
ENDOMETRIAL ATROPHY ( 12 FDA reports)
ERYTHEMA OF EYELID ( 12 FDA reports)
EXTRASKELETAL OSSIFICATION ( 12 FDA reports)
FOREIGN BODY ( 12 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 12 FDA reports)
FURUNCLE ( 12 FDA reports)
GRAFT LOSS ( 12 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 12 FDA reports)
HAEMOCHROMATOSIS ( 12 FDA reports)
HEART RATE DECREASED ( 12 FDA reports)
HICCUPS ( 12 FDA reports)
IMMUNOSUPPRESSION ( 12 FDA reports)
INFECTIOUS PERITONITIS ( 12 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 12 FDA reports)
INJECTION SITE ERYTHEMA ( 12 FDA reports)
INJECTION SITE PRURITUS ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 12 FDA reports)
INTRACARDIAC THROMBUS ( 12 FDA reports)
IRRITABILITY ( 12 FDA reports)
LIPIDS INCREASED ( 12 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 12 FDA reports)
MICROCYTOSIS ( 12 FDA reports)
NECROTISING FASCIITIS ( 12 FDA reports)
NEUTROPENIC SEPSIS ( 12 FDA reports)
ORAL FUNGAL INFECTION ( 12 FDA reports)
ORAL SOFT TISSUE DISORDER ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PARATHYROIDECTOMY ( 12 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 12 FDA reports)
PARVOVIRUS B19 TEST ( 12 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 12 FDA reports)
PLATELET COUNT ABNORMAL ( 12 FDA reports)
PRODUCT QUALITY ISSUE ( 12 FDA reports)
RADICULITIS BRACHIAL ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
RHINITIS ( 12 FDA reports)
SINUS CANCER METASTATIC ( 12 FDA reports)
STASIS DERMATITIS ( 12 FDA reports)
STATUS EPILEPTICUS ( 12 FDA reports)
TEETH BRITTLE ( 12 FDA reports)
TENDON RUPTURE ( 12 FDA reports)
THYMOMA ( 12 FDA reports)
THYROIDITIS ( 12 FDA reports)
TOOTH EROSION ( 12 FDA reports)
TOOTH IMPACTED ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
WALKING DISABILITY ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 11 FDA reports)
ABSCESS LIMB ( 11 FDA reports)
ACUTE LEUKAEMIA ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
ALVEOLOPLASTY ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 11 FDA reports)
ANKLE FRACTURE ( 11 FDA reports)
ANTIBODY TEST POSITIVE ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
AXILLARY VEIN THROMBOSIS ( 11 FDA reports)
BACK INJURY ( 11 FDA reports)
BARRETT'S OESOPHAGUS ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 11 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BUNDLE BRANCH BLOCK ( 11 FDA reports)
CANDIDURIA ( 11 FDA reports)
CHONDROCALCINOSIS ( 11 FDA reports)
COLONOSCOPY ( 11 FDA reports)
CSF PROTEIN INCREASED ( 11 FDA reports)
CYST DRAINAGE ( 11 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
EJECTION FRACTION ABNORMAL ( 11 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 11 FDA reports)
FACIAL BONES FRACTURE ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 11 FDA reports)
GASTROINTESTINAL INFECTION ( 11 FDA reports)
GINGIVAL ABSCESS ( 11 FDA reports)
HAEMATOTOXICITY ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
HYPERCAPNIA ( 11 FDA reports)
HYPERCHLORAEMIA ( 11 FDA reports)
HYPERTHERMIA ( 11 FDA reports)
HYPOPROTEINAEMIA ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INFARCTION ( 11 FDA reports)
INGUINAL MASS ( 11 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 11 FDA reports)
LEUKAEMIA ( 11 FDA reports)
LYMPHOCELE ( 11 FDA reports)
MALABSORPTION ( 11 FDA reports)
MELANOCYTIC NAEVUS ( 11 FDA reports)
MERALGIA PARAESTHETICA ( 11 FDA reports)
MOUTH CYST ( 11 FDA reports)
MUSCLE FIBROSIS ( 11 FDA reports)
NAIL DISCOLOURATION ( 11 FDA reports)
NERVE INJURY ( 11 FDA reports)
NEUROENDOCRINE TUMOUR ( 11 FDA reports)
NEUROSENSORY HYPOACUSIS ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 11 FDA reports)
OESOPHAGEAL ULCER ( 11 FDA reports)
OOPHORECTOMY ( 11 FDA reports)
ORTHOPEDIC PROCEDURE ( 11 FDA reports)
OSTEOMALACIA ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 11 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 11 FDA reports)
PREMATURE LABOUR ( 11 FDA reports)
PULPITIS DENTAL ( 11 FDA reports)
PULSE PRESSURE DECREASED ( 11 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 11 FDA reports)
RENAL STONE REMOVAL ( 11 FDA reports)
RENAL TUBULAR ACIDOSIS ( 11 FDA reports)
SEPTIC EMBOLUS ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SPINAL LAMINECTOMY ( 11 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 11 FDA reports)
SYNCOPE VASOVAGAL ( 11 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 11 FDA reports)
THORACOSTOMY ( 11 FDA reports)
THROMBOCYTHAEMIA ( 11 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 11 FDA reports)
UTERINE MASS ( 11 FDA reports)
UTEROVAGINAL PROLAPSE ( 11 FDA reports)
VITREOUS DETACHMENT ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 10 FDA reports)
AORTIC VALVE CALCIFICATION ( 10 FDA reports)
ARTERIOVENOUS MALFORMATION ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 10 FDA reports)
BLOOD IRON ABNORMAL ( 10 FDA reports)
BLOOD LACTIC ACID INCREASED ( 10 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 10 FDA reports)
BODY TEMPERATURE DECREASED ( 10 FDA reports)
BONE ABSCESS ( 10 FDA reports)
BRACHIAL PLEXOPATHY ( 10 FDA reports)
BREAST NEOPLASM ( 10 FDA reports)
CARDIAC SEPTAL DEFECT ( 10 FDA reports)
CARDIOTOXICITY ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 10 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 10 FDA reports)
CRYOGLOBULINAEMIA ( 10 FDA reports)
CULTURE URINE POSITIVE ( 10 FDA reports)
DENTAL PROSTHESIS USER ( 10 FDA reports)
DEVICE OCCLUSION ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
DUODENAL ULCER ( 10 FDA reports)
ENDOSCOPY ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
ESCHERICHIA BACTERAEMIA ( 10 FDA reports)
EYE DISCHARGE ( 10 FDA reports)
EYE DISORDER ( 10 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 10 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 10 FDA reports)
GINGIVAL HYPERTROPHY ( 10 FDA reports)
HEAD DISCOMFORT ( 10 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 10 FDA reports)
HERNIA REPAIR ( 10 FDA reports)
HIP SURGERY ( 10 FDA reports)
HYDROCELE ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
HYPOTHERMIA ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
INJECTION SITE RASH ( 10 FDA reports)
LOWER EXTREMITY MASS ( 10 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
MASTITIS ( 10 FDA reports)
MITRAL VALVE DISEASE ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 10 FDA reports)
NECK MASS ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA ( 10 FDA reports)
NEUROGENIC BOWEL ( 10 FDA reports)
NON-CARDIAC CHEST PAIN ( 10 FDA reports)
OCULAR ICTERUS ( 10 FDA reports)
ORAL DISCHARGE ( 10 FDA reports)
OVARIAN MASS ( 10 FDA reports)
PENILE INFECTION ( 10 FDA reports)
PERIPHERAL EMBOLISM ( 10 FDA reports)
PILONIDAL CYST ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 10 FDA reports)
PNEUMONIA VIRAL ( 10 FDA reports)
POLYMYALGIA RHEUMATICA ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
PREMATURE DELIVERY ( 10 FDA reports)
PYELOCALIECTASIS ( 10 FDA reports)
RENAL TUBULAR DISORDER ( 10 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
TESTICULAR PAIN ( 10 FDA reports)
THROAT IRRITATION ( 10 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 10 FDA reports)
UMBILICAL HERNIA ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 10 FDA reports)
URINE COLOUR ABNORMAL ( 10 FDA reports)
VASCULAR CALCIFICATION ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 10 FDA reports)
WOUND ( 10 FDA reports)
ADRENAL DISORDER ( 9 FDA reports)
ALKALOSIS ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
ANAPHYLACTOID REACTION ( 9 FDA reports)
AREFLEXIA ( 9 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
BLOOD FOLATE INCREASED ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
BONE MARROW TOXICITY ( 9 FDA reports)
BREAST CALCIFICATIONS ( 9 FDA reports)
BREAST CYST ( 9 FDA reports)
BREAST TENDERNESS ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CARBON DIOXIDE INCREASED ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CARDIAC OUTPUT DECREASED ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
DILATATION ATRIAL ( 9 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
ENDOCARDIAL FIBROSIS ( 9 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
EXPIRED DRUG ADMINISTERED ( 9 FDA reports)
FACE INJURY ( 9 FDA reports)
FEMORAL ARTERY OCCLUSION ( 9 FDA reports)
FIBROADENOMA OF BREAST ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 9 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 9 FDA reports)
GLIOSIS ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEAT EXHAUSTION ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
HEPATORENAL SYNDROME ( 9 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 9 FDA reports)
HYPERCOAGULATION ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 9 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
LOWER LIMB FRACTURE ( 9 FDA reports)
LUPUS NEPHRITIS ( 9 FDA reports)
MACULAR OEDEMA ( 9 FDA reports)
METASTASES TO KIDNEY ( 9 FDA reports)
METASTASES TO PANCREAS ( 9 FDA reports)
MITRAL VALVE STENOSIS ( 9 FDA reports)
MULTIPLE SCLEROSIS ( 9 FDA reports)
MYOCARDIAL FIBROSIS ( 9 FDA reports)
MYOSCLEROSIS ( 9 FDA reports)
NAIL DISORDER ( 9 FDA reports)
NASAL ODOUR ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NERVE BLOCK ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 9 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 9 FDA reports)
PANCREATIC CYST ( 9 FDA reports)
PANCREATIC DUCT DILATATION ( 9 FDA reports)
PERIPHERAL COLDNESS ( 9 FDA reports)
PROTEUS INFECTION ( 9 FDA reports)
PULMONARY ARTERY DILATATION ( 9 FDA reports)
PULSE ABSENT ( 9 FDA reports)
RADICAL MASTECTOMY ( 9 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
RHEUMATIC FEVER ( 9 FDA reports)
SALIVARY GLAND PAIN ( 9 FDA reports)
SIGMOIDITIS ( 9 FDA reports)
SINUS HEADACHE ( 9 FDA reports)
SJOGREN'S SYNDROME ( 9 FDA reports)
SKIN IRRITATION ( 9 FDA reports)
SPLENIC LESION ( 9 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 9 FDA reports)
STEVENS-JOHNSON SYNDROME ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 9 FDA reports)
THROAT TIGHTNESS ( 9 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
TUBERCULOSIS ( 9 FDA reports)
URAEMIC ENCEPHALOPATHY ( 9 FDA reports)
URETHRAL STENOSIS ( 9 FDA reports)
URTICARIA GENERALISED ( 9 FDA reports)
UTERINE CANCER ( 9 FDA reports)
VASCULAR OPERATION ( 9 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACNE CYSTIC ( 8 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
ALVEOLAR OSTEITIS ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANASTOMOTIC COMPLICATION ( 8 FDA reports)
APPENDICECTOMY ( 8 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 8 FDA reports)
BILE DUCT OBSTRUCTION ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BONE FISTULA ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CARDIAC FAILURE ACUTE ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 8 FDA reports)
CERVICAL MYELOPATHY ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
CLAUSTROPHOBIA ( 8 FDA reports)
CLONUS ( 8 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
EPIDURAL LIPOMATOSIS ( 8 FDA reports)
EYE ALLERGY ( 8 FDA reports)
EYE HAEMORRHAGE ( 8 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 8 FDA reports)
FISTULA REPAIR ( 8 FDA reports)
GENERALISED ERYTHEMA ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HEART VALVE INCOMPETENCE ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HEPATOSPLENOMEGALY ( 8 FDA reports)
HOMOCYSTINAEMIA ( 8 FDA reports)
HYPERPHAGIA ( 8 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 8 FDA reports)
IMMUNOGLOBULINS INCREASED ( 8 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 8 FDA reports)
LACUNAR INFARCTION ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LUDWIG ANGINA ( 8 FDA reports)
LUNG OPERATION ( 8 FDA reports)
LYMPHOCYTIC INFILTRATION ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
METASTASES TO ABDOMINAL WALL ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 8 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 8 FDA reports)
NEPHRECTOMY ( 8 FDA reports)
NEURODERMATITIS ( 8 FDA reports)
OBSTRUCTION ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
OXYGEN SUPPLEMENTATION ( 8 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PELVIC ADHESIONS ( 8 FDA reports)
PERIODONTAL OPERATION ( 8 FDA reports)
PERIORBITAL HAEMATOMA ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
PLEURAL DISORDER ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
POIKILOCYTOSIS ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POOR PERSONAL HYGIENE ( 8 FDA reports)
PORTAL VEIN THROMBOSIS ( 8 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 8 FDA reports)
RADICULAR CYST ( 8 FDA reports)
RENAL ARTERY STENOSIS ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
RESPIRATION ABNORMAL ( 8 FDA reports)
RETROPERITONEAL HAEMATOMA ( 8 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 8 FDA reports)
SEROSITIS ( 8 FDA reports)
SERUM SICKNESS ( 8 FDA reports)
SKIN EROSION ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SKIN TURGOR DECREASED ( 8 FDA reports)
SPINAL CORD DISORDER ( 8 FDA reports)
SPLENIC ABSCESS ( 8 FDA reports)
SPLENIC CALCIFICATION ( 8 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 8 FDA reports)
SUPERINFECTION ( 8 FDA reports)
SYRINGOMYELIA ( 8 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 8 FDA reports)
TESTIS CANCER ( 8 FDA reports)
TONGUE NEOPLASM ( 8 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 8 FDA reports)
TUBERCULIN TEST POSITIVE ( 8 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 8 FDA reports)
VASCULAR COMPRESSION ( 8 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 8 FDA reports)
XEROSIS ( 8 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ACANTHOLYSIS ( 7 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
AORTIC VALVE REPLACEMENT ( 7 FDA reports)
APATHY ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 7 FDA reports)
ASPHYXIA ( 7 FDA reports)
AUTOIMMUNE DISORDER ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
BRAIN OPERATION ( 7 FDA reports)
BRONCHOPLEURAL FISTULA ( 7 FDA reports)
CATHETER REMOVAL ( 7 FDA reports)
CENTRAL LINE INFECTION ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
COAGULATION TIME PROLONGED ( 7 FDA reports)
COLECTOMY ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
CONDUCTION DISORDER ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
CYSTITIS NONINFECTIVE ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 7 FDA reports)
DYSTROPHIC CALCIFICATION ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
EAR TUBE INSERTION ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENTEROVESICAL FISTULA ( 7 FDA reports)
EPIGASTRIC DISCOMFORT ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
ERYTHEMA INFECTIOSUM ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
ESCHERICHIA TEST POSITIVE ( 7 FDA reports)
EXTRADURAL HAEMATOMA ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
FRACTURE DISPLACEMENT ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 7 FDA reports)
GASTROINTESTINAL PERFORATION ( 7 FDA reports)
GESTATIONAL DIABETES ( 7 FDA reports)
GRAFT INFECTION ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HAEMORRHAGE URINARY TRACT ( 7 FDA reports)
HAEMORRHAGIC ANAEMIA ( 7 FDA reports)
HAND FRACTURE ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HEPATIC MASS ( 7 FDA reports)
HIGH FREQUENCY ABLATION ( 7 FDA reports)
HOSPICE CARE ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYDROPNEUMOTHORAX ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
IMMOBILE ( 7 FDA reports)
IMMUNODEFICIENCY ( 7 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 7 FDA reports)
INCOHERENT ( 7 FDA reports)
INCORRECT STORAGE OF DRUG ( 7 FDA reports)
INFERTILITY ( 7 FDA reports)
INJECTION SITE MASS ( 7 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 7 FDA reports)
INTRA-UTERINE DEATH ( 7 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 7 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 7 FDA reports)
LABILE BLOOD PRESSURE ( 7 FDA reports)
LABORATORY TEST INTERFERENCE ( 7 FDA reports)
LIGAMENT INJURY ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
LIPODYSTROPHY ACQUIRED ( 7 FDA reports)
LUNG HYPERINFLATION ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
MAXILLOFACIAL OPERATION ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MEAN CELL VOLUME DECREASED ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
METASTATIC CARCINOID TUMOUR ( 7 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 7 FDA reports)
MONOCLONAL GAMMOPATHY ( 7 FDA reports)
MONOPLEGIA ( 7 FDA reports)
NERVE ROOT LESION ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 7 FDA reports)
ONYCHOLYSIS ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 7 FDA reports)
PAPILLOEDEMA ( 7 FDA reports)
PARAPARESIS ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PARTIAL SEIZURES ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PERICARDIAL DRAINAGE ( 7 FDA reports)
PLATELET TRANSFUSION ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
POLYCYSTIC OVARIES ( 7 FDA reports)
PREGNANCY ( 7 FDA reports)
PROTEIN TOTAL INCREASED ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PULMONARY VASCULAR DISORDER ( 7 FDA reports)
RADIATION SKIN INJURY ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
RECTAL POLYP ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RESIDUAL URINE VOLUME ( 7 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
SEROMA ( 7 FDA reports)
SERUM FERRITIN DECREASED ( 7 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SLUGGISHNESS ( 7 FDA reports)
SPINAL DEFORMITY ( 7 FDA reports)
SPONDYLITIS ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
TERMINAL STATE ( 7 FDA reports)
THERAPY CESSATION ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
THIRST ( 7 FDA reports)
TOBACCO ABUSE ( 7 FDA reports)
TRANSPLANT ( 7 FDA reports)
TREATMENT FAILURE ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
UTERINE PROLAPSE ( 7 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ABDOMINAL SYMPTOM ( 6 FDA reports)
ADHESION ( 6 FDA reports)
ADJUSTMENT DISORDER ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
APHONIA ( 6 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLADDER NECK OPERATION ( 6 FDA reports)
BLEEDING TIME PROLONGED ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOODY DISCHARGE ( 6 FDA reports)
BURNS SECOND DEGREE ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
CARDIAC HYPERTROPHY ( 6 FDA reports)
CATHETER SITE ERYTHEMA ( 6 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CHRONIC TONSILLITIS ( 6 FDA reports)
CITROBACTER INFECTION ( 6 FDA reports)
COLLATERAL CIRCULATION ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 6 FDA reports)
CORNEAL DYSTROPHY ( 6 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 6 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 6 FDA reports)
DERMATITIS DIAPER ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
ENDOMETRIAL CANCER ( 6 FDA reports)
ENEMA ADMINISTRATION ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 6 FDA reports)
ESSENTIAL TREMOR ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FUNGAL OESOPHAGITIS ( 6 FDA reports)
GALLBLADDER POLYP ( 6 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 6 FDA reports)
GESTATIONAL HYPERTENSION ( 6 FDA reports)
GRAM STAIN ( 6 FDA reports)
HAEMATOMA INFECTION ( 6 FDA reports)
HAEMORRHAGIC STROKE ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HELICOBACTER GASTRITIS ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HUMERUS FRACTURE ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INTESTINAL POLYP ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LENS DISORDER ( 6 FDA reports)
LESION EXCISION ( 6 FDA reports)
LEUKAEMOID REACTION ( 6 FDA reports)
LEUKOCYTURIA ( 6 FDA reports)
LICHENIFICATION ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 6 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
MACULAR DEGENERATION ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MANDIBULECTOMY ( 6 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
MENTAL RETARDATION ( 6 FDA reports)
METASTASES TO CHEST WALL ( 6 FDA reports)
METASTASES TO MENINGES ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
MIDDLE EAR EFFUSION ( 6 FDA reports)
MITRAL VALVE CALCIFICATION ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEPHRITIS ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
NEUTROPHILIA ( 6 FDA reports)
OESOPHAGEAL STENOSIS ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PERITONSILLAR ABSCESS ( 6 FDA reports)
PINGUECULA ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
POOR VENOUS ACCESS ( 6 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
PYOTHORAX ( 6 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 6 FDA reports)
RETINAL EXUDATES ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SECONDARY SEQUESTRUM ( 6 FDA reports)
SHOULDER PAIN ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
SUPRANUCLEAR PALSY ( 6 FDA reports)
SWOLLEN TEAR DUCT ( 6 FDA reports)
T-CELL LYMPHOMA ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
THYROIDECTOMY ( 6 FDA reports)
TONSILLITIS ( 6 FDA reports)
TYPE 1 DIABETES MELLITUS ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 6 FDA reports)
URETHRAL FISTULA ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
UTERINE ATONY ( 6 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
APNOEA ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACTERIA STOOL IDENTIFIED ( 5 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BACTEROIDES TEST POSITIVE ( 5 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
BIOPSY BONE ABNORMAL ( 5 FDA reports)
BLADDER NEOPLASM ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BREAST CELLULITIS ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CELLULITIS ORBITAL ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
CLOSED FRACTURE MANIPULATION ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
DERMATITIS PSORIASIFORM ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DEVICE INTERACTION ( 5 FDA reports)
DIABETIC FOOT INFECTION ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
EMBOLISM ARTERIAL ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ERYTHROPENIA ( 5 FDA reports)
EXOMPHALOS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FOETAL DEATH ( 5 FDA reports)
FUNGAL PERITONITIS ( 5 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL CARCINOMA ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
HAEMATOSPERMIA ( 5 FDA reports)
HAEMOSIDEROSIS ( 5 FDA reports)
HEPATIC FIBROSIS ( 5 FDA reports)
HEPATOBLASTOMA ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HERPES OESOPHAGITIS ( 5 FDA reports)
HYDROMYELIA ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERPYREXIA ( 5 FDA reports)
HYPERVOLAEMIA ( 5 FDA reports)
HYPOPLASTIC ANAEMIA ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INJECTION SITE INDURATION ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
JOINT SURGERY ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LEUKAEMIA PLASMACYTIC ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
MELANOSIS COLI ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METASTASES TO PLEURA ( 5 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MIXED DEAFNESS ( 5 FDA reports)
MYRINGOTOMY ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
OSTEOMYELITIS BACTERIAL ( 5 FDA reports)
OTITIS MEDIA ACUTE ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PARATHYROID TUMOUR BENIGN ( 5 FDA reports)
PELVIC VENOUS THROMBOSIS ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PENILE PAIN ( 5 FDA reports)
PERICARDIAL EXCISION ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 5 FDA reports)
PERITONEAL INFECTION ( 5 FDA reports)
PO2 DECREASED ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
RENAL GRAFT LOSS ( 5 FDA reports)
RENAL HAEMATOMA ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY TRACT OEDEMA ( 5 FDA reports)
RETINAL DETACHMENT ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SHUNT THROMBOSIS ( 5 FDA reports)
SKIN INFECTION ( 5 FDA reports)
SKIN INFLAMMATION ( 5 FDA reports)
SKIN MASS ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SOFT TISSUE MASS ( 5 FDA reports)
SPIDER VEIN ( 5 FDA reports)
SPONDYLITIC MYELOPATHY ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
SYRINGE ISSUE ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
URETHRAL DILATATION ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
URINARY TRACT OPERATION ( 5 FDA reports)
URINOMA ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VAGINAL OPERATION ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 5 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ABSCESS SOFT TISSUE ( 4 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
AMAUROSIS ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANGIODYSPLASIA ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANIMAL SCRATCH ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ASPIRATION BONE MARROW ( 4 FDA reports)
ATRIAL THROMBOSIS ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BACTEROIDES INFECTION ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BIOPSY BONE MARROW ( 4 FDA reports)
BIOPSY KIDNEY ( 4 FDA reports)
BK VIRUS INFECTION ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD OESTROGEN INCREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 4 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 4 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 4 FDA reports)
BRADYPHRENIA ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 4 FDA reports)
BUDD-CHIARI SYNDROME ( 4 FDA reports)
BUNION ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CARBON DIOXIDE DECREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CAROTID ARTERY OCCLUSION ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CATHETER SITE SWELLING ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CRYING ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DEVICE RELATED SEPSIS ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 4 FDA reports)
DIABETIC ULCER ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DUODENAL ULCER PERFORATION ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
ERYTHROID SERIES ABNORMAL ( 4 FDA reports)
ERYTHROMELALGIA ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
FABRY'S DISEASE ( 4 FDA reports)
FACIAL ASYMMETRY ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 4 FDA reports)
HEAT RASH ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
INCISIONAL HERNIA ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFUSION SITE EXTRAVASATION ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTESTINAL PROLAPSE ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
IRON METABOLISM DISORDER ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LIPIDS ABNORMAL ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOW TURNOVER OSTEOPATHY ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MESENTERITIS ( 4 FDA reports)
MESOTHELIOMA ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
MONOCYTOSIS ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
MYELOID MATURATION ARREST ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NEEDLE ISSUE ( 4 FDA reports)
NEPHRITIC SYNDROME ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
ORBITAL OEDEMA ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
OSTEITIS DEFORMANS ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
PARATHYROID DISORDER ( 4 FDA reports)
PERINEURIAL CYST ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PERITONITIS SCLEROSING ( 4 FDA reports)
PERIVASCULAR DERMATITIS ( 4 FDA reports)
PHLEBOTHROMBOSIS ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PLEURISY VIRAL ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POLYP COLORECTAL ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PORPHYRIA NON-ACUTE ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RECTOCELE ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
REGURGITATION ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RETICULOCYTOSIS ( 4 FDA reports)
SCAB ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
STERNAL FRACTURE ( 4 FDA reports)
SUBMANDIBULAR MASS ( 4 FDA reports)
SUPRAPUBIC PAIN ( 4 FDA reports)
TETANY ( 4 FDA reports)
TOOTH DEPOSIT ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
ULTRAFILTRATION FAILURE ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
VENOUS STENOSIS ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
AIR EMBOLISM ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALLOIMMUNISATION ( 3 FDA reports)
ANGIOGRAM ABNORMAL ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APHERESIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 3 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
CARBON DIOXIDE ABNORMAL ( 3 FDA reports)
CARCINOID TUMOUR PULMONARY ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CAROTID ENDARTERECTOMY ( 3 FDA reports)
CAT SCRATCH DISEASE ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CATHETER SITE EROSION ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
CLONAL EVOLUTION ( 3 FDA reports)
COLPORRHAPHY ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FRONTAL SINUS OPERATION ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GINGIVAL OPERATION ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART AND LUNG TRANSPLANT ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC VEIN THROMBOSIS ( 3 FDA reports)
HEPATITIS B ANTIBODY ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOGLOBULINAEMIA ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INDWELLING CATHETER MANAGEMENT ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE VESICLES ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MALIGNANT RENAL HYPERTENSION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MEGAKARYOCYTES INCREASED ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
MESOTHELIOMA MALIGNANT ( 3 FDA reports)
METASTASES TO BONE MARROW ( 3 FDA reports)
METASTASES TO SKIN ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MYOCARDIAC ABSCESS ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OSTEOARTHROPATHY ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
PAGET-SCHROETTER SYNDROME ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PANEL-REACTIVE ANTIBODY ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARAKERATOSIS ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 3 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYHYDRAMNIOS ( 3 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PROTEIN S DEFICIENCY ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PSORIATIC ARTHROPATHY ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RETROPERITONEAL ABSCESS ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SHUNT STENOSIS ( 3 FDA reports)
SIDEROBLASTIC ANAEMIA ( 3 FDA reports)
SINUSITIS FUNGAL ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN ULCER HAEMORRHAGE ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SNORING ( 3 FDA reports)
SODIUM RETENTION ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STENT REMOVAL ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYNOVECTOMY ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
VAGINOPLASTY ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANGIOSCLEROSIS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 2 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC VALVE DISEASE MIXED ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AZOOSPERMIA ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD FOLATE ABNORMAL ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD UREA ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN STEM THROMBOSIS ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CEREBRAL VASOCONSTRICTION ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION TIME ( 2 FDA reports)
COLON INJURY ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONGENITAL PNEUMONIA ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COPPER DEFICIENCY ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE ISSUE ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA INFECTED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRINOMA ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS B DNA INCREASED ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERNAL INJURY ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL STOMA SITE BLEEDING ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
JEALOUS DELUSION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
KYPHOSCOLIOSIS ( 2 FDA reports)
LARYNGITIS BACTERIAL ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LOCAL ANAESTHESIA ( 2 FDA reports)
LOCAL REACTION ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPH NODE CANCER METASTATIC ( 2 FDA reports)
LYMPHANGIECTASIA ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
LYMPHOMA TRANSFORMATION ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MOANING ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEPHROANGIOSCLEROSIS ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
NUCLEATED RED CELLS ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORAL MUCOSAL PETECHIAE ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANMYELOPATHY ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PAROXYSMAL CHOREOATHETOSIS ( 2 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERICARDITIS URAEMIC ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHOSPHENES ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADICAL PROSTATECTOMY ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL HYPERTENSION ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL LYMPHOCELE ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALMONELLA BACTERAEMIA ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEPTIC PHLEBITIS ( 2 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN GRAFT INFECTION ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC HAEMATOMA ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STARING ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TRANSFERRIN DECREASED ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TREPONEMA TEST POSITIVE ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC FISTULA ( 2 FDA reports)
URETHRAL NEOPLASM ( 2 FDA reports)
URINARY FISTULA ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINE COPPER INCREASED ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
UROGENITAL FISTULA ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VALVULOPLASTY CARDIAC ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VITAMIN B12 ABNORMAL ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOLUME BLOOD INCREASED ( 2 FDA reports)
WART EXCISION ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL X-RAY ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADRENAL GLAND INJURY ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOVULVAR FISTULA ( 1 FDA reports)
ANTHRAX ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY NEGATIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE DESQUAMATION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY THYROID GLAND ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER LESION EXCISION ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD THROMBOPLASTIN ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL CYST ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX CARCINOMA RECURRENT ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER STAGE 0 ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EHLERS-DANLOS SYNDROME ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL MORPHOLOGY ABNORMAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROPLASIA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERESIS ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRONTAL SINUS OPERATIONS ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INHIBITING ANTIBODIES ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL FISTULA REPAIR ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL CANCER STAGE IV ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB PROSTHESIS USER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYSINURIC PROTEIN INTOLERANCE ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT RECURRENT ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO OESOPHAGUS ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEOPLASM OF APPENDIX ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA METASTATIC ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROMUSCULAR BLOCKING THERAPY ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTRALISING ANTIBODIES NEGATIVE ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULAR VASCULITIS ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOMA CUTIS ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERINEAL INDURATION ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLASMA CELLS DECREASED ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT DOSAGE FORM ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGRESSIVE BULBAR PALSY ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ACANTHOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CANCER RECURRENT ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETROPERITONEAL OEDEMA ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL PIGMENTATION ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPINOCEREBELLAR ATAXIA ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
THALASSAEMIA ALPHA ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THROMBOSIS PROPHYLAXIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROID PAIN ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOSTOMY INFECTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URACHAL ABNORMALITY ( 1 FDA reports)
URAEMIC ACIDOSIS ( 1 FDA reports)
URETERIC REPAIR ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORDECTOMY ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVAL CELLULITIS ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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