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

FALL ( 1647 FDA reports)
ARTHRALGIA ( 1463 FDA reports)
FEMUR FRACTURE ( 1314 FDA reports)
NAUSEA ( 1237 FDA reports)
PAIN ( 1222 FDA reports)
PAIN IN EXTREMITY ( 1097 FDA reports)
ANXIETY ( 974 FDA reports)
BACK PAIN ( 972 FDA reports)
DIARRHOEA ( 972 FDA reports)
FATIGUE ( 901 FDA reports)
DYSPNOEA ( 862 FDA reports)
HEADACHE ( 855 FDA reports)
DEPRESSION ( 851 FDA reports)
DIZZINESS ( 829 FDA reports)
OSTEONECROSIS ( 829 FDA reports)
VOMITING ( 825 FDA reports)
OEDEMA PERIPHERAL ( 776 FDA reports)
HYPERTENSION ( 768 FDA reports)
ASTHENIA ( 764 FDA reports)
ANAEMIA ( 756 FDA reports)
OSTEONECROSIS OF JAW ( 745 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 709 FDA reports)
CHEST PAIN ( 705 FDA reports)
OSTEOARTHRITIS ( 695 FDA reports)
OSTEOMYELITIS ( 642 FDA reports)
TOOTH DISORDER ( 627 FDA reports)
IMPAIRED HEALING ( 625 FDA reports)
DRUG INEFFECTIVE ( 615 FDA reports)
MYALGIA ( 599 FDA reports)
PYREXIA ( 598 FDA reports)
WEIGHT DECREASED ( 589 FDA reports)
URINARY TRACT INFECTION ( 557 FDA reports)
CONSTIPATION ( 551 FDA reports)
LOW TURNOVER OSTEOPATHY ( 546 FDA reports)
MALAISE ( 536 FDA reports)
GAIT DISTURBANCE ( 531 FDA reports)
COUGH ( 521 FDA reports)
INSOMNIA ( 516 FDA reports)
PNEUMONIA ( 510 FDA reports)
OSTEOPOROSIS ( 506 FDA reports)
ABDOMINAL PAIN ( 498 FDA reports)
JAW DISORDER ( 493 FDA reports)
BONE DISORDER ( 482 FDA reports)
BONE PAIN ( 470 FDA reports)
DENTAL CARIES ( 465 FDA reports)
RASH ( 457 FDA reports)
MUSCLE SPASMS ( 427 FDA reports)
PAIN IN JAW ( 426 FDA reports)
STRESS FRACTURE ( 422 FDA reports)
MUSCULAR WEAKNESS ( 409 FDA reports)
DEHYDRATION ( 407 FDA reports)
MUSCULOSKELETAL PAIN ( 391 FDA reports)
DYSPEPSIA ( 382 FDA reports)
HYPOAESTHESIA ( 377 FDA reports)
ABDOMINAL PAIN UPPER ( 374 FDA reports)
CELLULITIS ( 369 FDA reports)
ARTHRITIS ( 359 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 356 FDA reports)
BONE DENSITY DECREASED ( 354 FDA reports)
WEIGHT INCREASED ( 354 FDA reports)
DYSPHAGIA ( 349 FDA reports)
EXOSTOSIS ( 349 FDA reports)
ATRIAL FIBRILLATION ( 346 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 346 FDA reports)
ARTHROPATHY ( 341 FDA reports)
OSTEOPENIA ( 339 FDA reports)
BRONCHITIS ( 336 FDA reports)
PARAESTHESIA ( 336 FDA reports)
HYPOTENSION ( 334 FDA reports)
NECK PAIN ( 332 FDA reports)
SINUSITIS ( 328 FDA reports)
CONDITION AGGRAVATED ( 325 FDA reports)
HYPERLIPIDAEMIA ( 322 FDA reports)
TOOTH FRACTURE ( 320 FDA reports)
CONTUSION ( 317 FDA reports)
ABDOMINAL DISCOMFORT ( 315 FDA reports)
PRURITUS ( 305 FDA reports)
CATARACT ( 302 FDA reports)
FEELING ABNORMAL ( 302 FDA reports)
INFECTION ( 296 FDA reports)
CHILLS ( 289 FDA reports)
SPINAL OSTEOARTHRITIS ( 289 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 287 FDA reports)
ADVERSE DRUG REACTION ( 286 FDA reports)
INJURY ( 283 FDA reports)
PALPITATIONS ( 264 FDA reports)
BURSITIS ( 262 FDA reports)
ALOPECIA ( 261 FDA reports)
RENAL FAILURE ( 261 FDA reports)
TOOTH ABSCESS ( 258 FDA reports)
DRUG HYPERSENSITIVITY ( 257 FDA reports)
TREMOR ( 256 FDA reports)
BLOOD PRESSURE INCREASED ( 254 FDA reports)
TOOTH EXTRACTION ( 253 FDA reports)
JOINT SWELLING ( 252 FDA reports)
MYOCARDIAL INFARCTION ( 251 FDA reports)
ORAL INFECTION ( 250 FDA reports)
VISION BLURRED ( 250 FDA reports)
RENAL FAILURE ACUTE ( 249 FDA reports)
DECREASED APPETITE ( 248 FDA reports)
ERYTHEMA ( 248 FDA reports)
PLEURAL EFFUSION ( 245 FDA reports)
HAEMOGLOBIN DECREASED ( 244 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 243 FDA reports)
ASTHMA ( 241 FDA reports)
FOOT FRACTURE ( 241 FDA reports)
HYPOKALAEMIA ( 241 FDA reports)
DIVERTICULUM ( 239 FDA reports)
HAEMORRHOIDS ( 237 FDA reports)
RHEUMATOID ARTHRITIS ( 235 FDA reports)
SOMNOLENCE ( 229 FDA reports)
RIB FRACTURE ( 227 FDA reports)
TOOTHACHE ( 227 FDA reports)
CONFUSIONAL STATE ( 226 FDA reports)
ROTATOR CUFF SYNDROME ( 226 FDA reports)
HYPERHIDROSIS ( 225 FDA reports)
HERPES ZOSTER ( 224 FDA reports)
CEREBROVASCULAR ACCIDENT ( 221 FDA reports)
DEVICE FAILURE ( 220 FDA reports)
HYPERSENSITIVITY ( 217 FDA reports)
LOSS OF CONSCIOUSNESS ( 217 FDA reports)
TOOTH INFECTION ( 208 FDA reports)
BLOOD GLUCOSE INCREASED ( 207 FDA reports)
TOOTH LOSS ( 207 FDA reports)
PATHOLOGICAL FRACTURE ( 206 FDA reports)
VERTIGO ( 205 FDA reports)
DEEP VEIN THROMBOSIS ( 202 FDA reports)
ORAL DISORDER ( 200 FDA reports)
SWELLING ( 199 FDA reports)
CARDIAC DISORDER ( 197 FDA reports)
DRY MOUTH ( 197 FDA reports)
DYSGEUSIA ( 197 FDA reports)
HIATUS HERNIA ( 196 FDA reports)
HYPONATRAEMIA ( 196 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 196 FDA reports)
ADVERSE EVENT ( 195 FDA reports)
GASTROINTESTINAL DISORDER ( 195 FDA reports)
INFLUENZA LIKE ILLNESS ( 195 FDA reports)
VITAMIN D DEFICIENCY ( 194 FDA reports)
FRACTURE NONUNION ( 193 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 193 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 191 FDA reports)
SEPSIS ( 191 FDA reports)
CONVULSION ( 189 FDA reports)
DEATH ( 188 FDA reports)
EMOTIONAL DISTRESS ( 188 FDA reports)
MOUTH ULCERATION ( 188 FDA reports)
HIP FRACTURE ( 183 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 183 FDA reports)
CORONARY ARTERY DISEASE ( 181 FDA reports)
DIABETES MELLITUS ( 181 FDA reports)
GASTRITIS ( 180 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 179 FDA reports)
CHEST DISCOMFORT ( 179 FDA reports)
ORAL TORUS ( 179 FDA reports)
NEPHROLITHIASIS ( 178 FDA reports)
FRACTURE ( 177 FDA reports)
GINGIVAL DISORDER ( 176 FDA reports)
LOOSE TOOTH ( 176 FDA reports)
RESPIRATORY FAILURE ( 173 FDA reports)
SYNCOPE ( 173 FDA reports)
URTICARIA ( 173 FDA reports)
ANAEMIA POSTOPERATIVE ( 172 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 171 FDA reports)
PULMONARY EMBOLISM ( 171 FDA reports)
HYPOTHYROIDISM ( 170 FDA reports)
MEMORY IMPAIRMENT ( 170 FDA reports)
ABDOMINAL DISTENSION ( 169 FDA reports)
ABSCESS ( 168 FDA reports)
HOT FLUSH ( 167 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 167 FDA reports)
HEART RATE INCREASED ( 162 FDA reports)
LYMPHADENOPATHY ( 162 FDA reports)
NASOPHARYNGITIS ( 162 FDA reports)
PURULENT DISCHARGE ( 162 FDA reports)
ANHEDONIA ( 160 FDA reports)
BREAST CANCER ( 160 FDA reports)
DRUG INTERACTION ( 159 FDA reports)
TENDONITIS ( 158 FDA reports)
BALANCE DISORDER ( 156 FDA reports)
HYPERCHOLESTEROLAEMIA ( 154 FDA reports)
RADIUS FRACTURE ( 154 FDA reports)
ROAD TRAFFIC ACCIDENT ( 154 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 153 FDA reports)
SPINAL FRACTURE ( 153 FDA reports)
CHOLELITHIASIS ( 152 FDA reports)
INTERSTITIAL LUNG DISEASE ( 152 FDA reports)
GINGIVAL BLEEDING ( 150 FDA reports)
DIVERTICULITIS ( 149 FDA reports)
SCOLIOSIS ( 149 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 148 FDA reports)
HAEMATURIA ( 147 FDA reports)
OROPHARYNGEAL PAIN ( 146 FDA reports)
SLEEP DISORDER ( 146 FDA reports)
TACHYCARDIA ( 146 FDA reports)
MOBILITY DECREASED ( 145 FDA reports)
STOMATITIS ( 145 FDA reports)
THROMBOCYTOPENIA ( 145 FDA reports)
BLOOD PRESSURE DECREASED ( 144 FDA reports)
FRACTURE DISPLACEMENT ( 144 FDA reports)
NEUROPATHY PERIPHERAL ( 144 FDA reports)
ANGINA PECTORIS ( 143 FDA reports)
FISTULA ( 143 FDA reports)
GASTRIC DISORDER ( 142 FDA reports)
RECTAL HAEMORRHAGE ( 142 FDA reports)
DRUG INTOLERANCE ( 141 FDA reports)
DYSPHONIA ( 141 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 141 FDA reports)
STAPHYLOCOCCAL INFECTION ( 140 FDA reports)
RESORPTION BONE INCREASED ( 139 FDA reports)
RENAL CYST ( 138 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 138 FDA reports)
ABASIA ( 137 FDA reports)
FIBROMYALGIA ( 136 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 135 FDA reports)
CARPAL TUNNEL SYNDROME ( 135 FDA reports)
COLONIC POLYP ( 135 FDA reports)
GINGIVAL SWELLING ( 135 FDA reports)
FLUID RETENTION ( 134 FDA reports)
POLLAKIURIA ( 134 FDA reports)
PRIMARY SEQUESTRUM ( 133 FDA reports)
JAW FRACTURE ( 132 FDA reports)
MIGRAINE ( 132 FDA reports)
VISUAL IMPAIRMENT ( 132 FDA reports)
EYE PAIN ( 130 FDA reports)
MUSCLE STRAIN ( 130 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 130 FDA reports)
PERIODONTAL DISEASE ( 128 FDA reports)
SKIN DISORDER ( 128 FDA reports)
SPINAL COMPRESSION FRACTURE ( 128 FDA reports)
SWELLING FACE ( 127 FDA reports)
THROMBOSIS ( 127 FDA reports)
EMPHYSEMA ( 126 FDA reports)
GALLBLADDER DISORDER ( 126 FDA reports)
NIGHT SWEATS ( 126 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 125 FDA reports)
HAEMATOMA ( 125 FDA reports)
OVERDOSE ( 125 FDA reports)
PERIODONTITIS ( 125 FDA reports)
SPINAL COLUMN STENOSIS ( 125 FDA reports)
GINGIVITIS ( 124 FDA reports)
INFLAMMATION ( 124 FDA reports)
FUNGAL INFECTION ( 123 FDA reports)
TINNITUS ( 123 FDA reports)
ATELECTASIS ( 122 FDA reports)
OSTEITIS ( 122 FDA reports)
GINGIVAL PAIN ( 121 FDA reports)
HAEMATOCRIT DECREASED ( 121 FDA reports)
PULMONARY HYPERTENSION ( 121 FDA reports)
SENSITIVITY OF TEETH ( 121 FDA reports)
BASAL CELL CARCINOMA ( 120 FDA reports)
CARDIOMEGALY ( 119 FDA reports)
ORAL PAIN ( 118 FDA reports)
AMNESIA ( 117 FDA reports)
ANOREXIA ( 116 FDA reports)
BONE LOSS ( 115 FDA reports)
PANCREATITIS ( 115 FDA reports)
FLATULENCE ( 114 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 113 FDA reports)
UPPER LIMB FRACTURE ( 113 FDA reports)
URINARY INCONTINENCE ( 111 FDA reports)
ANKLE FRACTURE ( 110 FDA reports)
BURNING SENSATION ( 110 FDA reports)
CYST ( 110 FDA reports)
HYPOPHAGIA ( 110 FDA reports)
LIMB INJURY ( 110 FDA reports)
MASTICATION DISORDER ( 110 FDA reports)
PLATELET COUNT DECREASED ( 110 FDA reports)
WRIST FRACTURE ( 109 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 108 FDA reports)
INFLUENZA ( 108 FDA reports)
ATROPHIC VULVOVAGINITIS ( 107 FDA reports)
FRACTURE DELAYED UNION ( 107 FDA reports)
GASTRIC ULCER ( 107 FDA reports)
HAEMORRHAGE ( 107 FDA reports)
MITRAL VALVE INCOMPETENCE ( 107 FDA reports)
STRESS ( 107 FDA reports)
CARDIAC FAILURE ( 106 FDA reports)
ARRHYTHMIA ( 104 FDA reports)
NERVOUSNESS ( 104 FDA reports)
SPONDYLOLISTHESIS ( 104 FDA reports)
VISUAL ACUITY REDUCED ( 104 FDA reports)
LIGAMENT SPRAIN ( 103 FDA reports)
LUMBAR RADICULOPATHY ( 103 FDA reports)
RENAL DISORDER ( 103 FDA reports)
VIRAL INFECTION ( 103 FDA reports)
BUNION ( 102 FDA reports)
DYSURIA ( 102 FDA reports)
FISTULA DISCHARGE ( 102 FDA reports)
INJECTION SITE PAIN ( 102 FDA reports)
LEUKOCYTOSIS ( 102 FDA reports)
NEOPLASM MALIGNANT ( 102 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 102 FDA reports)
RENAL FAILURE CHRONIC ( 102 FDA reports)
SINUS DISORDER ( 102 FDA reports)
EAR PAIN ( 101 FDA reports)
OEDEMA ( 101 FDA reports)
LUNG DISORDER ( 100 FDA reports)
DISABILITY ( 99 FDA reports)
FLUSHING ( 99 FDA reports)
OESOPHAGITIS ( 99 FDA reports)
HEART RATE IRREGULAR ( 98 FDA reports)
INJECTION SITE HAEMORRHAGE ( 98 FDA reports)
COMPRESSION FRACTURE ( 97 FDA reports)
JOINT DISLOCATION ( 97 FDA reports)
JOINT INJURY ( 97 FDA reports)
ABSCESS JAW ( 96 FDA reports)
HYPERGLYCAEMIA ( 96 FDA reports)
PANCYTOPENIA ( 96 FDA reports)
SKIN LESION ( 96 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 95 FDA reports)
FACIAL PAIN ( 95 FDA reports)
GASTROENTERITIS ( 94 FDA reports)
GLAUCOMA ( 94 FDA reports)
MENISCUS LESION ( 94 FDA reports)
SPEECH DISORDER ( 94 FDA reports)
SPINAL DISORDER ( 94 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 93 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 93 FDA reports)
DEFORMITY ( 92 FDA reports)
DRY EYE ( 92 FDA reports)
GROIN PAIN ( 92 FDA reports)
INJECTION SITE ERYTHEMA ( 92 FDA reports)
NEUTROPENIA ( 92 FDA reports)
HEAD INJURY ( 91 FDA reports)
MITRAL VALVE PROLAPSE ( 91 FDA reports)
POST PROCEDURAL COMPLICATION ( 91 FDA reports)
BRUXISM ( 90 FDA reports)
DYSLIPIDAEMIA ( 90 FDA reports)
EPISTAXIS ( 90 FDA reports)
HAEMATOCHEZIA ( 90 FDA reports)
NEURALGIA ( 90 FDA reports)
GOITRE ( 89 FDA reports)
HUMERUS FRACTURE ( 89 FDA reports)
SLEEP APNOEA SYNDROME ( 89 FDA reports)
BLOOD CREATININE INCREASED ( 88 FDA reports)
CARDIAC MURMUR ( 88 FDA reports)
DIVERTICULUM INTESTINAL ( 88 FDA reports)
RHINITIS ALLERGIC ( 88 FDA reports)
CYSTITIS ( 87 FDA reports)
ORAL CAVITY FISTULA ( 87 FDA reports)
PULMONARY FIBROSIS ( 87 FDA reports)
WHEEZING ( 87 FDA reports)
ECZEMA ( 86 FDA reports)
RESPIRATORY DISORDER ( 86 FDA reports)
INCORRECT DOSE ADMINISTERED ( 85 FDA reports)
LUNG NEOPLASM ( 85 FDA reports)
MALNUTRITION ( 85 FDA reports)
RHINORRHOEA ( 85 FDA reports)
SEASONAL ALLERGY ( 85 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 85 FDA reports)
URINARY RETENTION ( 85 FDA reports)
WOUND DEHISCENCE ( 85 FDA reports)
BREAST MASS ( 84 FDA reports)
ENDODONTIC PROCEDURE ( 84 FDA reports)
GINGIVAL RECESSION ( 84 FDA reports)
IRON DEFICIENCY ANAEMIA ( 84 FDA reports)
TREATMENT NONCOMPLIANCE ( 84 FDA reports)
ARTERIOSCLEROSIS ( 83 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 83 FDA reports)
TYPE 2 DIABETES MELLITUS ( 83 FDA reports)
FEELING HOT ( 82 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 81 FDA reports)
FEAR ( 81 FDA reports)
GLOSSODYNIA ( 81 FDA reports)
HAND FRACTURE ( 81 FDA reports)
LIVER DISORDER ( 81 FDA reports)
MULTIPLE MYELOMA ( 81 FDA reports)
SKELETAL INJURY ( 81 FDA reports)
BLOOD UREA INCREASED ( 80 FDA reports)
HYPOAESTHESIA ORAL ( 80 FDA reports)
SCIATICA ( 80 FDA reports)
NASAL CONGESTION ( 79 FDA reports)
PANIC ATTACK ( 79 FDA reports)
THYROID DISORDER ( 79 FDA reports)
FOOT DEFORMITY ( 78 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 78 FDA reports)
SINUS CONGESTION ( 78 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 77 FDA reports)
SKIN ULCER ( 77 FDA reports)
TIBIA FRACTURE ( 77 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 76 FDA reports)
BODY HEIGHT DECREASED ( 75 FDA reports)
CHRONIC SINUSITIS ( 75 FDA reports)
DENTAL FISTULA ( 75 FDA reports)
HALLUCINATION ( 75 FDA reports)
JOINT STIFFNESS ( 75 FDA reports)
ACTINOMYCOSIS ( 74 FDA reports)
BREAST CANCER FEMALE ( 74 FDA reports)
HYPERKERATOSIS ( 74 FDA reports)
INFUSION RELATED REACTION ( 74 FDA reports)
LUMBAR SPINAL STENOSIS ( 74 FDA reports)
PERICARDIAL EFFUSION ( 74 FDA reports)
RENAL IMPAIRMENT ( 74 FDA reports)
RESTLESS LEGS SYNDROME ( 74 FDA reports)
BACK INJURY ( 73 FDA reports)
BREAST DISORDER ( 73 FDA reports)
CANDIDIASIS ( 73 FDA reports)
HYPOGLYCAEMIA ( 73 FDA reports)
INCREASED TENDENCY TO BRUISE ( 73 FDA reports)
EATING DISORDER ( 72 FDA reports)
IRRITABLE BOWEL SYNDROME ( 72 FDA reports)
JAUNDICE ( 72 FDA reports)
JOINT EFFUSION ( 72 FDA reports)
PLANTAR FASCIITIS ( 72 FDA reports)
SEBORRHOEIC KERATOSIS ( 72 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 71 FDA reports)
BLOOD POTASSIUM DECREASED ( 71 FDA reports)
BRADYCARDIA ( 71 FDA reports)
BREAST CYST ( 71 FDA reports)
CERVICOBRACHIAL SYNDROME ( 71 FDA reports)
DISCOMFORT ( 71 FDA reports)
DYSPNOEA EXERTIONAL ( 71 FDA reports)
FEMORAL NECK FRACTURE ( 71 FDA reports)
SINUS TACHYCARDIA ( 71 FDA reports)
BLADDER DISORDER ( 70 FDA reports)
HAEMORRHAGIC ANAEMIA ( 70 FDA reports)
LETHARGY ( 70 FDA reports)
ORAL CANDIDIASIS ( 70 FDA reports)
SCAR ( 70 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 70 FDA reports)
THROAT IRRITATION ( 70 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 69 FDA reports)
DYSSTASIA ( 69 FDA reports)
HAEMATEMESIS ( 69 FDA reports)
LUNG INFILTRATION ( 69 FDA reports)
RADICULOPATHY ( 69 FDA reports)
UTERINE DISORDER ( 69 FDA reports)
DISORIENTATION ( 68 FDA reports)
EXCORIATION ( 68 FDA reports)
FIBULA FRACTURE ( 68 FDA reports)
AGITATION ( 67 FDA reports)
DIPLOPIA ( 67 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 67 FDA reports)
MOVEMENT DISORDER ( 67 FDA reports)
PELVIC FRACTURE ( 67 FDA reports)
PEPTIC ULCER ( 67 FDA reports)
ABDOMINAL PAIN LOWER ( 66 FDA reports)
CAROTID ARTERY STENOSIS ( 66 FDA reports)
HEPATIC ENZYME INCREASED ( 66 FDA reports)
METASTATIC NEOPLASM ( 66 FDA reports)
OVARIAN CYST ( 66 FDA reports)
INTESTINAL OBSTRUCTION ( 65 FDA reports)
LUNG NEOPLASM MALIGNANT ( 65 FDA reports)
THYROID NEOPLASM ( 65 FDA reports)
BONE LESION ( 64 FDA reports)
CARDIAC ARREST ( 64 FDA reports)
CEREBRAL ISCHAEMIA ( 64 FDA reports)
DERMATITIS ( 64 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 64 FDA reports)
MASS ( 64 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 64 FDA reports)
APHASIA ( 63 FDA reports)
BLOOD POTASSIUM INCREASED ( 63 FDA reports)
BONE MARROW OEDEMA ( 63 FDA reports)
COGNITIVE DISORDER ( 63 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 63 FDA reports)
PARAESTHESIA ORAL ( 63 FDA reports)
PRODUCTIVE COUGH ( 63 FDA reports)
RECTOCELE ( 63 FDA reports)
ANGIOPATHY ( 62 FDA reports)
COLITIS ( 62 FDA reports)
DEVICE BREAKAGE ( 62 FDA reports)
DISTURBANCE IN ATTENTION ( 62 FDA reports)
ECCHYMOSIS ( 62 FDA reports)
HYPOXIA ( 62 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 62 FDA reports)
TENDERNESS ( 62 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 62 FDA reports)
AORTIC ANEURYSM ( 61 FDA reports)
APPENDIX DISORDER ( 61 FDA reports)
CHOLESTASIS ( 61 FDA reports)
DYSARTHRIA ( 61 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 61 FDA reports)
IMPAIRED WORK ABILITY ( 61 FDA reports)
TRISMUS ( 61 FDA reports)
BLOOD CALCIUM DECREASED ( 60 FDA reports)
BONE FRAGMENTATION ( 60 FDA reports)
DRUG EFFECT DECREASED ( 60 FDA reports)
PULMONARY CONGESTION ( 60 FDA reports)
TONGUE DISCOLOURATION ( 60 FDA reports)
VARICOSE VEIN ( 60 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 59 FDA reports)
CALCIUM DEFICIENCY ( 59 FDA reports)
METASTASES TO BONE ( 59 FDA reports)
PROCEDURAL PAIN ( 59 FDA reports)
RASH ERYTHEMATOUS ( 59 FDA reports)
UNEVALUABLE EVENT ( 59 FDA reports)
VAGINAL INFECTION ( 59 FDA reports)
VULVOVAGINAL DRYNESS ( 59 FDA reports)
CERUMEN IMPACTION ( 58 FDA reports)
DRUG DOSE OMISSION ( 58 FDA reports)
DRY SKIN ( 58 FDA reports)
SUBDURAL HAEMATOMA ( 58 FDA reports)
SYNOVIAL CYST ( 58 FDA reports)
TOOTH DEPOSIT ( 58 FDA reports)
AORTIC VALVE INCOMPETENCE ( 57 FDA reports)
ASCITES ( 57 FDA reports)
CYSTOCELE ( 57 FDA reports)
EYE DISORDER ( 57 FDA reports)
HYPOVOLAEMIA ( 57 FDA reports)
LOWER LIMB FRACTURE ( 57 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 57 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 57 FDA reports)
TRANSAMINASES INCREASED ( 57 FDA reports)
UTERINE LEIOMYOMA ( 57 FDA reports)
HALLUCINATION, AUDITORY ( 56 FDA reports)
LEUKOPENIA ( 56 FDA reports)
MENTAL STATUS CHANGES ( 56 FDA reports)
METASTASES TO LIVER ( 56 FDA reports)
OCULAR HYPERAEMIA ( 56 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 56 FDA reports)
RESPIRATORY DISTRESS ( 56 FDA reports)
SEPTIC SHOCK ( 56 FDA reports)
AGRANULOCYTOSIS ( 55 FDA reports)
CHOLECYSTITIS ( 55 FDA reports)
INGROWING NAIL ( 55 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 55 FDA reports)
LYMPHOMA ( 55 FDA reports)
MULTI-ORGAN FAILURE ( 55 FDA reports)
PHARYNGITIS ( 55 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 55 FDA reports)
BLOOD GLUCOSE DECREASED ( 54 FDA reports)
COMMINUTED FRACTURE ( 54 FDA reports)
DEAFNESS ( 54 FDA reports)
OSTEOMYELITIS CHRONIC ( 54 FDA reports)
SUICIDAL IDEATION ( 54 FDA reports)
TRIGGER FINGER ( 54 FDA reports)
WALKING AID USER ( 54 FDA reports)
DEVICE RELATED INFECTION ( 53 FDA reports)
ILL-DEFINED DISORDER ( 53 FDA reports)
KNEE ARTHROPLASTY ( 53 FDA reports)
PRESYNCOPE ( 53 FDA reports)
PRODUCT QUALITY ISSUE ( 53 FDA reports)
SKIN EXFOLIATION ( 53 FDA reports)
SQUAMOUS CELL CARCINOMA ( 53 FDA reports)
STRESS URINARY INCONTINENCE ( 53 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 53 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 52 FDA reports)
EAR INFECTION ( 52 FDA reports)
ECONOMIC PROBLEM ( 52 FDA reports)
HEPATIC STEATOSIS ( 52 FDA reports)
HEPATITIS ( 52 FDA reports)
OTITIS EXTERNA ( 52 FDA reports)
OTITIS MEDIA ( 52 FDA reports)
PELVIC PAIN ( 52 FDA reports)
RESTLESSNESS ( 52 FDA reports)
ABNORMAL DREAMS ( 51 FDA reports)
BLOOD BILIRUBIN INCREASED ( 51 FDA reports)
DEMENTIA ( 51 FDA reports)
DYSKINESIA ( 51 FDA reports)
MAJOR DEPRESSION ( 51 FDA reports)
MEDICATION ERROR ( 51 FDA reports)
MULTIPLE FRACTURES ( 51 FDA reports)
SOFT TISSUE DISORDER ( 51 FDA reports)
SURGERY ( 51 FDA reports)
TENDON DISORDER ( 51 FDA reports)
BLISTER ( 50 FDA reports)
BONE GRAFT ( 50 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 50 FDA reports)
GINGIVAL INFECTION ( 50 FDA reports)
IRRITABILITY ( 50 FDA reports)
JOINT SPRAIN ( 50 FDA reports)
KIDNEY INFECTION ( 50 FDA reports)
OPEN WOUND ( 50 FDA reports)
PERITONITIS ( 50 FDA reports)
RASH PRURITIC ( 50 FDA reports)
STOMACH DISCOMFORT ( 50 FDA reports)
TENDON RUPTURE ( 50 FDA reports)
BACK DISORDER ( 49 FDA reports)
CEREBRAL ATROPHY ( 49 FDA reports)
NERVE INJURY ( 49 FDA reports)
OXYGEN SATURATION DECREASED ( 49 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 49 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 49 FDA reports)
ULNA FRACTURE ( 49 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 49 FDA reports)
BLOOD ALBUMIN DECREASED ( 48 FDA reports)
GLOSSITIS ( 48 FDA reports)
HAEMOPTYSIS ( 48 FDA reports)
HYPOCALCAEMIA ( 48 FDA reports)
NOCTURIA ( 48 FDA reports)
OBESITY ( 48 FDA reports)
PULMONARY OEDEMA ( 48 FDA reports)
SKIN LACERATION ( 48 FDA reports)
SKIN PAPILLOMA ( 48 FDA reports)
AZOTAEMIA ( 47 FDA reports)
BLINDNESS ( 47 FDA reports)
CALCINOSIS ( 47 FDA reports)
CONCUSSION ( 47 FDA reports)
EYE IRRITATION ( 47 FDA reports)
LARYNGITIS ( 47 FDA reports)
LIMB ASYMMETRY ( 47 FDA reports)
LOBAR PNEUMONIA ( 47 FDA reports)
LOCAL SWELLING ( 47 FDA reports)
MICTURITION URGENCY ( 47 FDA reports)
RETCHING ( 47 FDA reports)
ULCER ( 47 FDA reports)
CARDIO-RESPIRATORY ARREST ( 46 FDA reports)
CATARACT OPERATION ( 46 FDA reports)
DECREASED INTEREST ( 46 FDA reports)
DEPRESSED MOOD ( 46 FDA reports)
DYSTHYMIC DISORDER ( 46 FDA reports)
EYE HAEMORRHAGE ( 46 FDA reports)
HYPERKALAEMIA ( 46 FDA reports)
MELANOCYTIC NAEVUS ( 46 FDA reports)
MYOCARDIAL ISCHAEMIA ( 46 FDA reports)
PHOTOPHOBIA ( 46 FDA reports)
PURULENCE ( 46 FDA reports)
RHABDOMYOLYSIS ( 46 FDA reports)
WEIGHT BEARING DIFFICULTY ( 46 FDA reports)
AGEUSIA ( 45 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 45 FDA reports)
COLITIS ISCHAEMIC ( 45 FDA reports)
COMA ( 45 FDA reports)
DRUG TOXICITY ( 45 FDA reports)
DYSPAREUNIA ( 45 FDA reports)
GINGIVAL ABSCESS ( 45 FDA reports)
HAEMANGIOMA ( 45 FDA reports)
HYPOKINESIA ( 45 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 45 FDA reports)
MIDDLE INSOMNIA ( 45 FDA reports)
MUSCLE INJURY ( 45 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 45 FDA reports)
PSORIASIS ( 45 FDA reports)
RASH GENERALISED ( 45 FDA reports)
SKIN CANCER ( 45 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 45 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 45 FDA reports)
ATYPICAL FEMUR FRACTURE ( 44 FDA reports)
CAROTID BRUIT ( 44 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 44 FDA reports)
DISEASE PROGRESSION ( 44 FDA reports)
DRUG ADMINISTRATION ERROR ( 44 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 44 FDA reports)
KYPHOSIS ( 44 FDA reports)
ORTHOSTATIC HYPOTENSION ( 44 FDA reports)
PRURITUS GENERALISED ( 44 FDA reports)
RAYNAUD'S PHENOMENON ( 44 FDA reports)
RHINITIS ( 44 FDA reports)
SENSORY DISTURBANCE ( 44 FDA reports)
VASCULITIS ( 44 FDA reports)
ACUTE RESPIRATORY FAILURE ( 43 FDA reports)
AUTOIMMUNE THYROIDITIS ( 43 FDA reports)
CEREBRAL INFARCTION ( 43 FDA reports)
HIP ARTHROPLASTY ( 43 FDA reports)
LIPOMA ( 43 FDA reports)
MEDICAL DEVICE COMPLICATION ( 43 FDA reports)
MENOPAUSE ( 43 FDA reports)
MUSCLE CRAMP ( 43 FDA reports)
NAIL DISORDER ( 43 FDA reports)
PANCREATITIS ACUTE ( 43 FDA reports)
ADRENAL INSUFFICIENCY ( 42 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 42 FDA reports)
ARTHROPOD BITE ( 42 FDA reports)
BACTERIAL INFECTION ( 42 FDA reports)
CONJUNCTIVITIS ( 42 FDA reports)
CROHN'S DISEASE ( 42 FDA reports)
CYTOLYTIC HEPATITIS ( 42 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 42 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 42 FDA reports)
ERUCTATION ( 42 FDA reports)
HEARING IMPAIRED ( 42 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 42 FDA reports)
MYELODYSPLASTIC SYNDROME ( 42 FDA reports)
ANGER ( 41 FDA reports)
DIFFICULTY IN WALKING ( 41 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 41 FDA reports)
EDENTULOUS ( 41 FDA reports)
EYE SWELLING ( 41 FDA reports)
GASTROENTERITIS VIRAL ( 41 FDA reports)
HEPATIC CYST ( 41 FDA reports)
HYPERPARATHYROIDISM ( 41 FDA reports)
INGUINAL HERNIA ( 41 FDA reports)
MELAENA ( 41 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 41 FDA reports)
TRIGEMINAL NEURALGIA ( 41 FDA reports)
VISUAL DISTURBANCE ( 41 FDA reports)
ABSCESS ORAL ( 40 FDA reports)
ACUTE SINUSITIS ( 40 FDA reports)
BLOOD SODIUM DECREASED ( 40 FDA reports)
EAR DISORDER ( 40 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 40 FDA reports)
FRACTURE MALUNION ( 40 FDA reports)
HEPATIC CIRRHOSIS ( 40 FDA reports)
HYPERCALCAEMIA ( 40 FDA reports)
LARGE INTESTINE PERFORATION ( 40 FDA reports)
LYMPHOEDEMA ( 40 FDA reports)
PNEUMONIA ASPIRATION ( 40 FDA reports)
BODY TEMPERATURE INCREASED ( 39 FDA reports)
CARDIOMYOPATHY ( 39 FDA reports)
CEREBRAL HAEMORRHAGE ( 39 FDA reports)
DELIRIUM ( 39 FDA reports)
DENTAL PLAQUE ( 39 FDA reports)
LIBIDO DECREASED ( 39 FDA reports)
MENTAL DISORDER ( 39 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 39 FDA reports)
PYELONEPHRITIS ( 39 FDA reports)
SYNOVITIS ( 39 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 39 FDA reports)
ACNE ( 38 FDA reports)
BACTERAEMIA ( 38 FDA reports)
BONE EROSION ( 38 FDA reports)
EJECTION FRACTION DECREASED ( 38 FDA reports)
HEPATIC LESION ( 38 FDA reports)
HYPERTHYROIDISM ( 38 FDA reports)
HYPOALBUMINAEMIA ( 38 FDA reports)
LACERATION ( 38 FDA reports)
MUCOSAL INFLAMMATION ( 38 FDA reports)
VITAMIN B12 DEFICIENCY ( 38 FDA reports)
WOUND DRAINAGE ( 38 FDA reports)
BARRETT'S OESOPHAGUS ( 37 FDA reports)
DIABETIC RETINOPATHY ( 37 FDA reports)
FLUID OVERLOAD ( 37 FDA reports)
HEMIPARESIS ( 37 FDA reports)
HERNIA ( 37 FDA reports)
ILEUS ( 37 FDA reports)
MULTIPLE INJURIES ( 37 FDA reports)
NO THERAPEUTIC RESPONSE ( 37 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 37 FDA reports)
OEDEMA MOUTH ( 37 FDA reports)
OESOPHAGEAL PAIN ( 37 FDA reports)
PHYSICAL DISABILITY ( 37 FDA reports)
SEROMA ( 37 FDA reports)
THERMAL BURN ( 37 FDA reports)
AORTIC STENOSIS ( 36 FDA reports)
BONE DENSITY INCREASED ( 36 FDA reports)
FEBRILE NEUTROPENIA ( 36 FDA reports)
GASTRIC CANCER ( 36 FDA reports)
GRAND MAL CONVULSION ( 36 FDA reports)
HEART RATE DECREASED ( 36 FDA reports)
HEPATIC FAILURE ( 36 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 36 FDA reports)
LOCALISED INFECTION ( 36 FDA reports)
MACULAR DEGENERATION ( 36 FDA reports)
MUSCLE TWITCHING ( 36 FDA reports)
OSTEOSCLEROSIS ( 36 FDA reports)
RENAL PAIN ( 36 FDA reports)
RESPIRATORY TRACT CONGESTION ( 36 FDA reports)
SHOCK ( 36 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 36 FDA reports)
ABDOMINAL TENDERNESS ( 35 FDA reports)
ANGIOEDEMA ( 35 FDA reports)
AUTOIMMUNE DISORDER ( 35 FDA reports)
COLON CANCER ( 35 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 35 FDA reports)
FAECAL INCONTINENCE ( 35 FDA reports)
GINGIVAL ULCERATION ( 35 FDA reports)
JOINT INSTABILITY ( 35 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 35 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 35 FDA reports)
MOOD SWINGS ( 35 FDA reports)
MUSCULOSKELETAL DISORDER ( 35 FDA reports)
NIGHTMARE ( 35 FDA reports)
OFF LABEL USE ( 35 FDA reports)
PALLOR ( 35 FDA reports)
PNEUMONIA BACTERIAL ( 35 FDA reports)
RETINAL DETACHMENT ( 35 FDA reports)
SKIN DISCOLOURATION ( 35 FDA reports)
THROAT TIGHTNESS ( 35 FDA reports)
APPENDICITIS ( 34 FDA reports)
CAROTID ARTERY DISEASE ( 34 FDA reports)
DIABETIC NEUROPATHY ( 34 FDA reports)
DUODENAL ULCER ( 34 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 34 FDA reports)
LUNG HYPERINFLATION ( 34 FDA reports)
MALIGNANT MELANOMA ( 34 FDA reports)
METASTASES TO SPINE ( 34 FDA reports)
MULTIPLE SCLEROSIS ( 34 FDA reports)
NEURITIS ( 34 FDA reports)
PLEURISY ( 34 FDA reports)
PLEURITIC PAIN ( 34 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 34 FDA reports)
SACROILIITIS ( 34 FDA reports)
SENSATION OF HEAVINESS ( 34 FDA reports)
SINUS BRADYCARDIA ( 34 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 34 FDA reports)
ANOSMIA ( 33 FDA reports)
ATRIAL FLUTTER ( 33 FDA reports)
ATROPHY ( 33 FDA reports)
CRYING ( 33 FDA reports)
DEVICE DISLOCATION ( 33 FDA reports)
EXPOSED BONE IN JAW ( 33 FDA reports)
FACE OEDEMA ( 33 FDA reports)
FAECES DISCOLOURED ( 33 FDA reports)
FLANK PAIN ( 33 FDA reports)
HEPATITIS B ( 33 FDA reports)
ODYNOPHAGIA ( 33 FDA reports)
OESOPHAGEAL DISORDER ( 33 FDA reports)
PERIODONTAL INFECTION ( 33 FDA reports)
PNEUMOTHORAX ( 33 FDA reports)
SEQUESTRECTOMY ( 33 FDA reports)
BIPOLAR DISORDER ( 32 FDA reports)
BREAST RECONSTRUCTION ( 32 FDA reports)
ELECTROLYTE IMBALANCE ( 32 FDA reports)
FEELING COLD ( 32 FDA reports)
GOUT ( 32 FDA reports)
HYPERTONIC BLADDER ( 32 FDA reports)
JOINT CREPITATION ( 32 FDA reports)
LIGAMENT RUPTURE ( 32 FDA reports)
LIMB DISCOMFORT ( 32 FDA reports)
MENIERE'S DISEASE ( 32 FDA reports)
MUSCLE DISORDER ( 32 FDA reports)
NASAL SEPTUM DEVIATION ( 32 FDA reports)
NEPHROPATHY ( 32 FDA reports)
OESOPHAGEAL STENOSIS ( 32 FDA reports)
OSTEOGENESIS IMPERFECTA ( 32 FDA reports)
PERICARDITIS ( 32 FDA reports)
PERONEAL NERVE PALSY ( 32 FDA reports)
SPLENIC GRANULOMA ( 32 FDA reports)
STEM CELL TRANSPLANT ( 32 FDA reports)
SUTURE RELATED COMPLICATION ( 32 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 32 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 32 FDA reports)
VAGINAL HAEMORRHAGE ( 32 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 31 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 31 FDA reports)
BREAST CANCER IN SITU ( 31 FDA reports)
DISEASE RECURRENCE ( 31 FDA reports)
FACE INJURY ( 31 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 31 FDA reports)
INTENTIONAL DRUG MISUSE ( 31 FDA reports)
LICHENOID KERATOSIS ( 31 FDA reports)
LUNG INFECTION ( 31 FDA reports)
OSTEOLYSIS ( 31 FDA reports)
PARKINSON'S DISEASE ( 31 FDA reports)
SJOGREN'S SYNDROME ( 31 FDA reports)
THINKING ABNORMAL ( 31 FDA reports)
VENOUS INSUFFICIENCY ( 31 FDA reports)
VITAMIN D DECREASED ( 31 FDA reports)
VITREOUS FLOATERS ( 31 FDA reports)
WOUND ( 31 FDA reports)
ABSCESS DRAINAGE ( 30 FDA reports)
ALVEOLAR OSTEITIS ( 30 FDA reports)
BLOOD CALCIUM INCREASED ( 30 FDA reports)
BONE NEOPLASM MALIGNANT ( 30 FDA reports)
CHOKING ( 30 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 30 FDA reports)
LACUNAR INFARCTION ( 30 FDA reports)
MUSCLE ATROPHY ( 30 FDA reports)
NERVOUS SYSTEM DISORDER ( 30 FDA reports)
OSTEOMALACIA ( 30 FDA reports)
PARATHYROID DISORDER ( 30 FDA reports)
PERNICIOUS ANAEMIA ( 30 FDA reports)
PHOTOPSIA ( 30 FDA reports)
ACROCHORDON ( 29 FDA reports)
APHONIA ( 29 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 29 FDA reports)
BLOOD BLISTER ( 29 FDA reports)
BLOOD DISORDER ( 29 FDA reports)
BONE MARROW FAILURE ( 29 FDA reports)
BREAST PAIN ( 29 FDA reports)
CEREBROVASCULAR DISORDER ( 29 FDA reports)
CHONDROPATHY ( 29 FDA reports)
COLITIS ULCERATIVE ( 29 FDA reports)
DERMATITIS CONTACT ( 29 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 29 FDA reports)
HERPES SIMPLEX ( 29 FDA reports)
INCONTINENCE ( 29 FDA reports)
INJECTION SITE REACTION ( 29 FDA reports)
ISCHAEMIA ( 29 FDA reports)
MASTOIDITIS ( 29 FDA reports)
METASTASES TO LUNG ( 29 FDA reports)
NODULE ( 29 FDA reports)
NON-CARDIAC CHEST PAIN ( 29 FDA reports)
ONYCHOMYCOSIS ( 29 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 29 FDA reports)
PETECHIAE ( 29 FDA reports)
PNEUMONITIS ( 29 FDA reports)
POOR QUALITY SLEEP ( 29 FDA reports)
POST PROCEDURAL INFECTION ( 29 FDA reports)
SARCOIDOSIS ( 29 FDA reports)
SUICIDE ATTEMPT ( 29 FDA reports)
TENOSYNOVITIS ( 29 FDA reports)
APICAL GRANULOMA ( 28 FDA reports)
APPETITE DISORDER ( 28 FDA reports)
AREFLEXIA ( 28 FDA reports)
BONE DEBRIDEMENT ( 28 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 28 FDA reports)
CHROMATURIA ( 28 FDA reports)
COAGULOPATHY ( 28 FDA reports)
CORONARY ARTERY OCCLUSION ( 28 FDA reports)
DENTAL NECROSIS ( 28 FDA reports)
DRUG ABUSE ( 28 FDA reports)
EMOTIONAL DISORDER ( 28 FDA reports)
ENTEROCOCCAL INFECTION ( 28 FDA reports)
FACIAL BONES FRACTURE ( 28 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 28 FDA reports)
HOSPITALISATION ( 28 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 28 FDA reports)
LACRIMATION INCREASED ( 28 FDA reports)
LYMPHADENITIS ( 28 FDA reports)
MALOCCLUSION ( 28 FDA reports)
OCCULT BLOOD POSITIVE ( 28 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 28 FDA reports)
OROPHARYNGEAL BLISTERING ( 28 FDA reports)
PLATELET COUNT INCREASED ( 28 FDA reports)
POLYMYALGIA RHEUMATICA ( 28 FDA reports)
POLYP ( 28 FDA reports)
POSTURE ABNORMAL ( 28 FDA reports)
SINUS POLYP ( 28 FDA reports)
TOOTH IMPACTED ( 28 FDA reports)
WALKING DISABILITY ( 28 FDA reports)
ANXIETY DISORDER ( 27 FDA reports)
BEDRIDDEN ( 27 FDA reports)
DERMAL CYST ( 27 FDA reports)
DIASTOLIC DYSFUNCTION ( 27 FDA reports)
EPILEPSY ( 27 FDA reports)
INJECTION SITE PRURITUS ( 27 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
METABOLIC ACIDOSIS ( 27 FDA reports)
NECROSIS ( 27 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 27 FDA reports)
PSYCHOTIC DISORDER ( 27 FDA reports)
RASH MACULAR ( 27 FDA reports)
RASH PAPULAR ( 27 FDA reports)
STREPTOCOCCAL INFECTION ( 27 FDA reports)
VIITH NERVE PARALYSIS ( 27 FDA reports)
ADHESION ( 26 FDA reports)
AGGRESSION ( 26 FDA reports)
APHTHOUS STOMATITIS ( 26 FDA reports)
ARTHRITIS BACTERIAL ( 26 FDA reports)
ATRIAL TACHYCARDIA ( 26 FDA reports)
BLEPHAROSPASM ( 26 FDA reports)
DRUG ERUPTION ( 26 FDA reports)
EPICONDYLITIS ( 26 FDA reports)
ESSENTIAL HYPERTENSION ( 26 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 26 FDA reports)
FEMORAL ARTERY OCCLUSION ( 26 FDA reports)
GASTROINTESTINAL PAIN ( 26 FDA reports)
HYPOACUSIS ( 26 FDA reports)
HYPOAESTHESIA FACIAL ( 26 FDA reports)
MALIGNANT HYPERTENSION ( 26 FDA reports)
OSTEOMA ( 26 FDA reports)
OSTEORADIONECROSIS ( 26 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 26 FDA reports)
PROTHROMBIN TIME PROLONGED ( 26 FDA reports)
PULMONARY GRANULOMA ( 26 FDA reports)
PULPITIS DENTAL ( 26 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 26 FDA reports)
TONSILLAR DISORDER ( 26 FDA reports)
TOOTH INJURY ( 26 FDA reports)
VENTRICULAR TACHYCARDIA ( 26 FDA reports)
WOUND INFECTION ( 26 FDA reports)
ANAPHYLACTIC REACTION ( 25 FDA reports)
BLOOD URINE PRESENT ( 25 FDA reports)
BREATH ODOUR ( 25 FDA reports)
BRONCHOSPASM ( 25 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 25 FDA reports)
FIBROUS HISTIOCYTOMA ( 25 FDA reports)
FOOD POISONING ( 25 FDA reports)
GENERALISED ANXIETY DISORDER ( 25 FDA reports)
GRANULOMA ( 25 FDA reports)
HYPOGONADISM ( 25 FDA reports)
ISCHAEMIC STROKE ( 25 FDA reports)
LIP DISORDER ( 25 FDA reports)
MYOPATHY ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
PARANOIA ( 25 FDA reports)
PHARYNGEAL OEDEMA ( 25 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 25 FDA reports)
PROCTALGIA ( 25 FDA reports)
PULMONARY TUBERCULOSIS ( 25 FDA reports)
SIALOADENITIS ( 25 FDA reports)
SUBCUTANEOUS NODULE ( 25 FDA reports)
TONGUE ULCERATION ( 25 FDA reports)
URINARY TRACT DISORDER ( 25 FDA reports)
VASCULAR CALCIFICATION ( 25 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 25 FDA reports)
ACUTE PRERENAL FAILURE ( 24 FDA reports)
CARDIAC VALVE DISEASE ( 24 FDA reports)
CAROTID ARTERY OCCLUSION ( 24 FDA reports)
CHOLECYSTECTOMY ( 24 FDA reports)
CLOSTRIDIAL INFECTION ( 24 FDA reports)
DECREASED ACTIVITY ( 24 FDA reports)
EROSIVE OESOPHAGITIS ( 24 FDA reports)
GENERALISED OEDEMA ( 24 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 24 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 24 FDA reports)
HERPES VIRUS INFECTION ( 24 FDA reports)
IMMOBILE ( 24 FDA reports)
LEFT ATRIAL DILATATION ( 24 FDA reports)
MYOSITIS ( 24 FDA reports)
NECK INJURY ( 24 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 24 FDA reports)
ORAL FIBROMA ( 24 FDA reports)
ORAL INTAKE REDUCED ( 24 FDA reports)
PROSTATE CANCER ( 24 FDA reports)
SKIN INDURATION ( 24 FDA reports)
TOOTH DISCOLOURATION ( 24 FDA reports)
VENTRICULAR HYPOKINESIA ( 24 FDA reports)
ABDOMINAL ADHESIONS ( 23 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 23 FDA reports)
ANIMAL BITE ( 23 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 23 FDA reports)
BREAST DISCHARGE ( 23 FDA reports)
CERVICAL SPINAL STENOSIS ( 23 FDA reports)
CLAVICLE FRACTURE ( 23 FDA reports)
COLON ADENOMA ( 23 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 23 FDA reports)
DUODENITIS ( 23 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 23 FDA reports)
EXERCISE TOLERANCE DECREASED ( 23 FDA reports)
FEELING JITTERY ( 23 FDA reports)
FRACTURED COCCYX ( 23 FDA reports)
HYPOPHOSPHATAEMIA ( 23 FDA reports)
IATROGENIC INJURY ( 23 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 23 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 23 FDA reports)
JAW CYST ( 23 FDA reports)
JAW OPERATION ( 23 FDA reports)
LIP SWELLING ( 23 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 23 FDA reports)
MUSCLE TIGHTNESS ( 23 FDA reports)
NEUROPATHY ( 23 FDA reports)
ORAL HERPES ( 23 FDA reports)
OROANTRAL FISTULA ( 23 FDA reports)
PARALYSIS ( 23 FDA reports)
PHLEBITIS ( 23 FDA reports)
POLYURIA ( 23 FDA reports)
PUBIS FRACTURE ( 23 FDA reports)
QUALITY OF LIFE DECREASED ( 23 FDA reports)
SINUS HEADACHE ( 23 FDA reports)
TREATMENT FAILURE ( 23 FDA reports)
UVEITIS ( 23 FDA reports)
WEIGHT FLUCTUATION ( 23 FDA reports)
BLADDER CANCER ( 22 FDA reports)
BLINDNESS UNILATERAL ( 22 FDA reports)
BLOOD CHLORIDE DECREASED ( 22 FDA reports)
BONE MARROW DISORDER ( 22 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 22 FDA reports)
CIRCULATORY COLLAPSE ( 22 FDA reports)
CUBITAL TUNNEL SYNDROME ( 22 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 22 FDA reports)
EYELID OEDEMA ( 22 FDA reports)
EYELID PTOSIS ( 22 FDA reports)
FIBROSIS ( 22 FDA reports)
HAEMANGIOMA OF LIVER ( 22 FDA reports)
INTRACRANIAL ANEURYSM ( 22 FDA reports)
MENOPAUSAL SYMPTOMS ( 22 FDA reports)
NEUROMA ( 22 FDA reports)
OOPHORECTOMY ( 22 FDA reports)
OSTEOPOROTIC FRACTURE ( 22 FDA reports)
PATELLA FRACTURE ( 22 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 22 FDA reports)
PROTEINURIA ( 22 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 22 FDA reports)
RETINAL HAEMORRHAGE ( 22 FDA reports)
SWOLLEN TONGUE ( 22 FDA reports)
TUBERCULOSIS ( 22 FDA reports)
VEIN DISORDER ( 22 FDA reports)
WHEELCHAIR USER ( 22 FDA reports)
WITHDRAWAL SYNDROME ( 22 FDA reports)
APHAGIA ( 21 FDA reports)
BONE ATROPHY ( 21 FDA reports)
CARTILAGE INJURY ( 21 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 21 FDA reports)
CYANOSIS ( 21 FDA reports)
DENTURE WEARER ( 21 FDA reports)
DILATATION ATRIAL ( 21 FDA reports)
DRUG PRESCRIBING ERROR ( 21 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 21 FDA reports)
HEMIPLEGIA ( 21 FDA reports)
HODGKIN'S DISEASE ( 21 FDA reports)
LABORATORY TEST ABNORMAL ( 21 FDA reports)
LYMPHOPENIA ( 21 FDA reports)
MASTECTOMY ( 21 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 21 FDA reports)
NEUROGENIC BLADDER ( 21 FDA reports)
ORAL MUCOSA ATROPHY ( 21 FDA reports)
OSTEITIS DEFORMANS ( 21 FDA reports)
OVARIAN ENLARGEMENT ( 21 FDA reports)
RESPIRATORY ARREST ( 21 FDA reports)
SINUS OPERATION ( 21 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 21 FDA reports)
SPINAL CORD COMPRESSION ( 21 FDA reports)
TENOSYNOVITIS STENOSANS ( 21 FDA reports)
VITREOUS DETACHMENT ( 21 FDA reports)
ABNORMAL BEHAVIOUR ( 20 FDA reports)
ABORTION SPONTANEOUS ( 20 FDA reports)
ACCIDENTAL OVERDOSE ( 20 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 20 FDA reports)
ANAPHYLACTIC SHOCK ( 20 FDA reports)
APPENDICECTOMY ( 20 FDA reports)
BREAST CALCIFICATIONS ( 20 FDA reports)
BREAST CANCER RECURRENT ( 20 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 20 FDA reports)
CARDIOVASCULAR DISORDER ( 20 FDA reports)
DEBRIDEMENT ( 20 FDA reports)
DERMATITIS ALLERGIC ( 20 FDA reports)
ECZEMA ASTEATOTIC ( 20 FDA reports)
FACIAL PALSY ( 20 FDA reports)
GASTRITIS EROSIVE ( 20 FDA reports)
HYDRONEPHROSIS ( 20 FDA reports)
ICHTHYOSIS ( 20 FDA reports)
IMPAIRED DRIVING ABILITY ( 20 FDA reports)
INCREASED APPETITE ( 20 FDA reports)
INJECTION SITE HAEMATOMA ( 20 FDA reports)
INJECTION SITE SWELLING ( 20 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 20 FDA reports)
MUCOSAL ULCERATION ( 20 FDA reports)
ORAL SURGERY ( 20 FDA reports)
ORTHODONTIC APPLIANCE USER ( 20 FDA reports)
OTITIS MEDIA ACUTE ( 20 FDA reports)
PERIARTHRITIS ( 20 FDA reports)
PROTEIN TOTAL DECREASED ( 20 FDA reports)
PSORIATIC ARTHROPATHY ( 20 FDA reports)
RADICULITIS LUMBOSACRAL ( 20 FDA reports)
SCAB ( 20 FDA reports)
SCLERITIS ( 20 FDA reports)
SHOULDER PAIN ( 20 FDA reports)
SPLENIC ARTERY ANEURYSM ( 20 FDA reports)
SUBCUTANEOUS ABSCESS ( 20 FDA reports)
TARDIVE DYSKINESIA ( 20 FDA reports)
TENDON INJURY ( 20 FDA reports)
THIRST ( 20 FDA reports)
UNRESPONSIVE TO STIMULI ( 20 FDA reports)
VERTEBROPLASTY ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK ( 19 FDA reports)
BLOOD IRON INCREASED ( 19 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 19 FDA reports)
CYSTITIS INTERSTITIAL ( 19 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 19 FDA reports)
DEAFNESS NEUROSENSORY ( 19 FDA reports)
DEAFNESS UNILATERAL ( 19 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 19 FDA reports)
FINGER DEFORMITY ( 19 FDA reports)
HEPATITIS CHOLESTATIC ( 19 FDA reports)
HILAR LYMPHADENOPATHY ( 19 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 19 FDA reports)
HYPOVITAMINOSIS ( 19 FDA reports)
INCOHERENT ( 19 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 19 FDA reports)
LICHEN PLANUS ( 19 FDA reports)
LIPASE INCREASED ( 19 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 19 FDA reports)
MENORRHAGIA ( 19 FDA reports)
MENSTRUAL DISORDER ( 19 FDA reports)
MENTAL IMPAIRMENT ( 19 FDA reports)
MOUTH HAEMORRHAGE ( 19 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 19 FDA reports)
PHOTOSENSITIVITY REACTION ( 19 FDA reports)
POST PROCEDURAL FISTULA ( 19 FDA reports)
RECTAL ABSCESS ( 19 FDA reports)
RECTAL FISSURE ( 19 FDA reports)
SALIVARY HYPERSECRETION ( 19 FDA reports)
SKIN BURNING SENSATION ( 19 FDA reports)
SPINAL DECOMPRESSION ( 19 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 19 FDA reports)
UROSEPSIS ( 19 FDA reports)
VENTRICULAR HYPERTROPHY ( 19 FDA reports)
ABSCESS LIMB ( 18 FDA reports)
ADENOCARCINOMA ( 18 FDA reports)
ALVEOLITIS ( 18 FDA reports)
ANGINA UNSTABLE ( 18 FDA reports)
ANOGENITAL WARTS ( 18 FDA reports)
BLOOD AMYLASE INCREASED ( 18 FDA reports)
CATARACT NUCLEAR ( 18 FDA reports)
CHEST X-RAY ABNORMAL ( 18 FDA reports)
CLAUSTROPHOBIA ( 18 FDA reports)
COLD SWEAT ( 18 FDA reports)
COSTOCHONDRITIS ( 18 FDA reports)
CYST ASPIRATION ( 18 FDA reports)
DECUBITUS ULCER ( 18 FDA reports)
DILATATION VENTRICULAR ( 18 FDA reports)
DISSEMINATED TUBERCULOSIS ( 18 FDA reports)
ENTEROBACTER INFECTION ( 18 FDA reports)
ERYTHEMA OF EYELID ( 18 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 18 FDA reports)
HYPOMAGNESAEMIA ( 18 FDA reports)
HYSTERECTOMY ( 18 FDA reports)
JOINT CONTRACTURE ( 18 FDA reports)
KLEBSIELLA INFECTION ( 18 FDA reports)
MAXILLOFACIAL OPERATION ( 18 FDA reports)
NERVE COMPRESSION ( 18 FDA reports)
NEUTROPHIL COUNT INCREASED ( 18 FDA reports)
PERIODONTAL OPERATION ( 18 FDA reports)
PNEUMONIA VIRAL ( 18 FDA reports)
PULMONARY MASS ( 18 FDA reports)
PURPURA ( 18 FDA reports)
RADICULAR SYNDROME ( 18 FDA reports)
RECTAL POLYP ( 18 FDA reports)
RENAL TUBULAR DISORDER ( 18 FDA reports)
SERUM FERRITIN INCREASED ( 18 FDA reports)
SKIN INFECTION ( 18 FDA reports)
SPONDYLITIS ( 18 FDA reports)
TRAUMATIC FRACTURE ( 18 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 18 FDA reports)
URINE ANALYSIS ABNORMAL ( 18 FDA reports)
WOUND SECRETION ( 18 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 17 FDA reports)
ANGIOFIBROMA ( 17 FDA reports)
B-CELL LYMPHOMA ( 17 FDA reports)
BRONCHIECTASIS ( 17 FDA reports)
BRONCHITIS CHRONIC ( 17 FDA reports)
BRONCHOPNEUMONIA ( 17 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 17 FDA reports)
COORDINATION ABNORMAL ( 17 FDA reports)
DEVICE MALFUNCTION ( 17 FDA reports)
DIALYSIS ( 17 FDA reports)
DRUG DEPENDENCE ( 17 FDA reports)
ENCEPHALOPATHY ( 17 FDA reports)
GANGRENE ( 17 FDA reports)
GASTRIC HAEMORRHAGE ( 17 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 17 FDA reports)
HIP SURGERY ( 17 FDA reports)
HYDROCEPHALUS ( 17 FDA reports)
HYPERAESTHESIA ( 17 FDA reports)
HYPOPARATHYROIDISM ( 17 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 17 FDA reports)
LIPOPROTEIN (A) INCREASED ( 17 FDA reports)
LIVER INJURY ( 17 FDA reports)
MYELOPATHY ( 17 FDA reports)
OESOPHAGEAL SPASM ( 17 FDA reports)
OESOPHAGEAL ULCER ( 17 FDA reports)
PAINFUL RESPIRATION ( 17 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 17 FDA reports)
PSYCHIATRIC SYMPTOM ( 17 FDA reports)
PYOGENIC GRANULOMA ( 17 FDA reports)
RENAL TUBULAR NECROSIS ( 17 FDA reports)
RETINOPATHY ( 17 FDA reports)
SKIN NEOPLASM EXCISION ( 17 FDA reports)
SKIN TIGHTNESS ( 17 FDA reports)
SPINAL LAMINECTOMY ( 17 FDA reports)
SPUTUM DISCOLOURED ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 17 FDA reports)
TENDON PAIN ( 17 FDA reports)
TENSION ( 17 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 17 FDA reports)
THROMBOCYTOSIS ( 17 FDA reports)
TINEA PEDIS ( 17 FDA reports)
TONGUE COATED ( 17 FDA reports)
TONGUE DISORDER ( 17 FDA reports)
TOOTH EROSION ( 17 FDA reports)
TOOTH REPAIR ( 17 FDA reports)
ABDOMINAL MASS ( 16 FDA reports)
ACCIDENT ( 16 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 16 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 16 FDA reports)
BLOOD IRON DECREASED ( 16 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 16 FDA reports)
CACHEXIA ( 16 FDA reports)
CARDIAC PACEMAKER INSERTION ( 16 FDA reports)
COLITIS MICROSCOPIC ( 16 FDA reports)
CONDUCTIVE DEAFNESS ( 16 FDA reports)
DRUG DISPENSING ERROR ( 16 FDA reports)
ESCHAR ( 16 FDA reports)
FORMICATION ( 16 FDA reports)
FUNGAL SKIN INFECTION ( 16 FDA reports)
HAEMARTHROSIS ( 16 FDA reports)
HAEMORRHAGIC STROKE ( 16 FDA reports)
HELICOBACTER INFECTION ( 16 FDA reports)
HEPATOMEGALY ( 16 FDA reports)
HYPERSOMNIA ( 16 FDA reports)
HYPERTENSIVE HEART DISEASE ( 16 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 16 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 16 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 16 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 16 FDA reports)
LARGE INTESTINAL ULCER ( 16 FDA reports)
LIMB DEFORMITY ( 16 FDA reports)
METASTASES TO THE MEDIASTINUM ( 16 FDA reports)
MOOD ALTERED ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 16 FDA reports)
PATHOLOGICAL GAMBLING ( 16 FDA reports)
PERSONALITY CHANGE ( 16 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 16 FDA reports)
PSEUDOMONAS INFECTION ( 16 FDA reports)
RADIOTHERAPY ( 16 FDA reports)
RALES ( 16 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 16 FDA reports)
RETINOPATHY HYPERTENSIVE ( 16 FDA reports)
STRESS SYMPTOMS ( 16 FDA reports)
SUDDEN DEATH ( 16 FDA reports)
TENSION HEADACHE ( 16 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 16 FDA reports)
VISUAL FIELD DEFECT ( 16 FDA reports)
WOUND HAEMORRHAGE ( 16 FDA reports)
ACIDOSIS ( 15 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 15 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 15 FDA reports)
AMENORRHOEA ( 15 FDA reports)
ANURIA ( 15 FDA reports)
APATHY ( 15 FDA reports)
BLEPHARITIS ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 15 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 15 FDA reports)
CULTURE URINE POSITIVE ( 15 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 15 FDA reports)
DIVERTICULAR PERFORATION ( 15 FDA reports)
ERECTILE DYSFUNCTION ( 15 FDA reports)
EYE DISCHARGE ( 15 FDA reports)
EYE INFECTION ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
FOREARM FRACTURE ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 15 FDA reports)
HYPERTENSIVE CRISIS ( 15 FDA reports)
HYPOVENTILATION ( 15 FDA reports)
INTESTINAL POLYP ( 15 FDA reports)
JOINT ARTHROPLASTY ( 15 FDA reports)
LABYRINTHITIS ( 15 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 15 FDA reports)
MAMMOGRAM ABNORMAL ( 15 FDA reports)
METASTASES TO LYMPH NODES ( 15 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 15 FDA reports)
NEOPLASM ( 15 FDA reports)
NEPHROGENIC ANAEMIA ( 15 FDA reports)
NEPHROSCLEROSIS ( 15 FDA reports)
NEUTROPHIL COUNT DECREASED ( 15 FDA reports)
NODULE ON EXTREMITY ( 15 FDA reports)
OSTEOARTHROPATHY ( 15 FDA reports)
PARONYCHIA ( 15 FDA reports)
PLASMACYTOSIS ( 15 FDA reports)
PROCTITIS ( 15 FDA reports)
ROSACEA ( 15 FDA reports)
SINUSITIS FUNGAL ( 15 FDA reports)
SKIN ATROPHY ( 15 FDA reports)
SNORING ( 15 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 15 FDA reports)
SPLEEN DISORDER ( 15 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 15 FDA reports)
STEVENS-JOHNSON SYNDROME ( 15 FDA reports)
ULCER HAEMORRHAGE ( 15 FDA reports)
VAGINAL DISORDER ( 15 FDA reports)
VENTRICULAR FIBRILLATION ( 15 FDA reports)
VESTIBULAR DISORDER ( 15 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 14 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 14 FDA reports)
ASBESTOSIS ( 14 FDA reports)
ATAXIA ( 14 FDA reports)
AUTOIMMUNE HEPATITIS ( 14 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 14 FDA reports)
BIOPSY LYMPH GLAND ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 14 FDA reports)
BONE GIANT CELL TUMOUR ( 14 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 14 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 14 FDA reports)
BREAST CANCER METASTATIC ( 14 FDA reports)
BREAST TENDERNESS ( 14 FDA reports)
BUNION OPERATION ( 14 FDA reports)
C-TELOPEPTIDE ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 14 FDA reports)
DUPUYTREN'S CONTRACTURE ( 14 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 14 FDA reports)
ESCHERICHIA SEPSIS ( 14 FDA reports)
EYE PRURITUS ( 14 FDA reports)
FASCIITIS ( 14 FDA reports)
GALLBLADDER POLYP ( 14 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 14 FDA reports)
GINGIVAL GRAFT ( 14 FDA reports)
HAIR TEXTURE ABNORMAL ( 14 FDA reports)
HALLUCINATION, VISUAL ( 14 FDA reports)
HEART RATE ABNORMAL ( 14 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 14 FDA reports)
LYMPHADENECTOMY ( 14 FDA reports)
MEASLES ( 14 FDA reports)
MORTON'S NEUROMA ( 14 FDA reports)
MOTOR DYSFUNCTION ( 14 FDA reports)
MUMPS ( 14 FDA reports)
MUSCLE HYPERTROPHY ( 14 FDA reports)
MUSCLE SPASTICITY ( 14 FDA reports)
ONYCHOPHAGIA ( 14 FDA reports)
OSTEOMYELITIS ACUTE ( 14 FDA reports)
OVARIAN CANCER ( 14 FDA reports)
PALATAL DISORDER ( 14 FDA reports)
PAPULE ( 14 FDA reports)
PERIPHERAL COLDNESS ( 14 FDA reports)
PERIPHERAL ISCHAEMIA ( 14 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 14 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 14 FDA reports)
PROCEDURAL COMPLICATION ( 14 FDA reports)
PROSTATOMEGALY ( 14 FDA reports)
PYURIA ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 14 FDA reports)
SCHIZOPHRENIA ( 14 FDA reports)
SEDATION ( 14 FDA reports)
SHOULDER ARTHROPLASTY ( 14 FDA reports)
SKIN NECROSIS ( 14 FDA reports)
SNEEZING ( 14 FDA reports)
SPONDYLOARTHROPATHY ( 14 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 14 FDA reports)
THERAPY NON-RESPONDER ( 14 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
TRACHEITIS ( 14 FDA reports)
URINE OUTPUT DECREASED ( 14 FDA reports)
UTERINE HAEMORRHAGE ( 14 FDA reports)
VAGINAL DISCHARGE ( 14 FDA reports)
VARICELLA ( 14 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 14 FDA reports)
VITREOUS HAEMORRHAGE ( 14 FDA reports)
ABDOMINAL WALL ABSCESS ( 13 FDA reports)
ACETABULUM FRACTURE ( 13 FDA reports)
ACTINIC KERATOSIS ( 13 FDA reports)
ANGIONEUROTIC OEDEMA ( 13 FDA reports)
ARTHRITIS INFECTIVE ( 13 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 13 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 13 FDA reports)
BONE METABOLISM DISORDER ( 13 FDA reports)
BOWEN'S DISEASE ( 13 FDA reports)
CARDIAC FLUTTER ( 13 FDA reports)
CARDIOGENIC SHOCK ( 13 FDA reports)
CATHETER RELATED INFECTION ( 13 FDA reports)
CERVICAL CORD COMPRESSION ( 13 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 13 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
CORONARY ARTERY STENOSIS ( 13 FDA reports)
CREPITATIONS ( 13 FDA reports)
DEMYELINATION ( 13 FDA reports)
DENTAL CARE ( 13 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 13 FDA reports)
DIZZINESS POSTURAL ( 13 FDA reports)
DRUG LEVEL INCREASED ( 13 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 13 FDA reports)
EYE INFLAMMATION ( 13 FDA reports)
FOREIGN BODY ( 13 FDA reports)
GASTRIC POLYPS ( 13 FDA reports)
GASTROINTESTINAL PERFORATION ( 13 FDA reports)
HEAD DISCOMFORT ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
LACTIC ACIDOSIS ( 13 FDA reports)
LOSS OF CONTROL OF LEGS ( 13 FDA reports)
MAMMOPLASTY ( 13 FDA reports)
MEDICAL DEVICE REMOVAL ( 13 FDA reports)
METABOLIC DISORDER ( 13 FDA reports)
MITRAL VALVE DISEASE ( 13 FDA reports)
MOUTH INJURY ( 13 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 13 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 13 FDA reports)
OEDEMA MUCOSAL ( 13 FDA reports)
OPEN REDUCTION OF FRACTURE ( 13 FDA reports)
OPTIC NEURITIS ( 13 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 13 FDA reports)
PANCREATIC CARCINOMA ( 13 FDA reports)
PARTIAL SEIZURES ( 13 FDA reports)
PELVIC PROLAPSE ( 13 FDA reports)
PERICARDIAL CALCIFICATION ( 13 FDA reports)
POST HERPETIC NEURALGIA ( 13 FDA reports)
RETINAL VASCULAR DISORDER ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
SKIN HYPERTROPHY ( 13 FDA reports)
SOFT TISSUE INFLAMMATION ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
VASCULAR SKIN DISORDER ( 13 FDA reports)
VENOUS THROMBOSIS ( 13 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 12 FDA reports)
ADENOMA BENIGN ( 12 FDA reports)
ADRENAL ADENOMA ( 12 FDA reports)
ANAL ABSCESS ( 12 FDA reports)
ANAL HAEMORRHAGE ( 12 FDA reports)
AORTIC DISORDER ( 12 FDA reports)
BACTERIAL SEPSIS ( 12 FDA reports)
BIOPSY BREAST ABNORMAL ( 12 FDA reports)
BLOOD PRESSURE ( 12 FDA reports)
BONE OPERATION ( 12 FDA reports)
BONE SWELLING ( 12 FDA reports)
BREAST PROSTHESIS REMOVAL ( 12 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
BUTTERFLY RASH ( 12 FDA reports)
CAPILLARY DISORDER ( 12 FDA reports)
CARDIAC ENZYMES INCREASED ( 12 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 12 FDA reports)
CHEST WALL OPERATION ( 12 FDA reports)
CHOLECYSTITIS CHRONIC ( 12 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
CUTIS LAXA ( 12 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 12 FDA reports)
DERMATITIS EXFOLIATIVE ( 12 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 12 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 12 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 12 FDA reports)
EPIGASTRIC DISCOMFORT ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
EYELID CYST ( 12 FDA reports)
FOOD ALLERGY ( 12 FDA reports)
FRACTURED SACRUM ( 12 FDA reports)
GASTRIC ULCER PERFORATION ( 12 FDA reports)
GASTRITIS ATROPHIC ( 12 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 12 FDA reports)
GYNAECOMASTIA ( 12 FDA reports)
HAEMOPHILUS INFECTION ( 12 FDA reports)
HELICOBACTER TEST POSITIVE ( 12 FDA reports)
HIP DEFORMITY ( 12 FDA reports)
HUNGER ( 12 FDA reports)
HYPERCALCIURIA ( 12 FDA reports)
IMMUNODEFICIENCY ( 12 FDA reports)
INJECTION SITE IRRITATION ( 12 FDA reports)
INTERVERTEBRAL DISCITIS ( 12 FDA reports)
IRITIS ( 12 FDA reports)
IRON DEFICIENCY ( 12 FDA reports)
JOINT HYPEREXTENSION ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
LACTOSE INTOLERANCE ( 12 FDA reports)
LARYNGEAL OEDEMA ( 12 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 12 FDA reports)
LUNG ADENOCARCINOMA ( 12 FDA reports)
MALABSORPTION ( 12 FDA reports)
MENINGITIS ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
METASTASES TO MENINGES ( 12 FDA reports)
NEPHROTIC SYNDROME ( 12 FDA reports)
OVARIAN DISORDER ( 12 FDA reports)
PERIORBITAL HAEMATOMA ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
PLASTIC SURGERY ( 12 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 12 FDA reports)
POLYDIPSIA ( 12 FDA reports)
POLYNEUROPATHY ( 12 FDA reports)
POSTOPERATIVE ADHESION ( 12 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 12 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 12 FDA reports)
RADIATION INJURY ( 12 FDA reports)
RENAL ARTERY STENOSIS ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
RIGHT VENTRICULAR FAILURE ( 12 FDA reports)
SKIN FISSURES ( 12 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 12 FDA reports)
STENT PLACEMENT ( 12 FDA reports)
TRAUMATIC ULCER ( 12 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 12 FDA reports)
URINE ODOUR ABNORMAL ( 12 FDA reports)
VASCULAR INSUFFICIENCY ( 12 FDA reports)
VENOUS OCCLUSION ( 12 FDA reports)
VERTIGO POSITIONAL ( 12 FDA reports)
ABDOMINAL HERNIA ( 11 FDA reports)
ABSCESS NECK ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 11 FDA reports)
ANGIOLIPOMA ( 11 FDA reports)
APLASIA PURE RED CELL ( 11 FDA reports)
APPLICATION SITE ERYTHEMA ( 11 FDA reports)
ASPIRATION ( 11 FDA reports)
BENIGN BONE NEOPLASM ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 11 FDA reports)
BLOOD TEST ABNORMAL ( 11 FDA reports)
BONE CYST ( 11 FDA reports)
BONE FORMATION INCREASED ( 11 FDA reports)
BONE SARCOMA ( 11 FDA reports)
BRAIN NEOPLASM ( 11 FDA reports)
BUNDLE BRANCH BLOCK ( 11 FDA reports)
BUTTOCK PAIN ( 11 FDA reports)
CANDIDURIA ( 11 FDA reports)
CERVIX CARCINOMA ( 11 FDA reports)
CHOLECYSTITIS ACUTE ( 11 FDA reports)
COELIAC DISEASE ( 11 FDA reports)
CONNECTIVE TISSUE DISORDER ( 11 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 11 FDA reports)
DELUSION ( 11 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 11 FDA reports)
DEVICE COMPONENT ISSUE ( 11 FDA reports)
DIABETIC COMA ( 11 FDA reports)
DROOLING ( 11 FDA reports)
EAR DISCOMFORT ( 11 FDA reports)
EMBOLISM ( 11 FDA reports)
ENTEROCOLITIS ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
ERYTHEMA NODOSUM ( 11 FDA reports)
EYE INJURY ( 11 FDA reports)
FRUSTRATION ( 11 FDA reports)
FURUNCLE ( 11 FDA reports)
GALLBLADDER OPERATION ( 11 FDA reports)
GENERAL SYMPTOM ( 11 FDA reports)
GINGIVAL BLISTER ( 11 FDA reports)
GRAVITATIONAL OEDEMA ( 11 FDA reports)
HAIR GROWTH ABNORMAL ( 11 FDA reports)
HAND DEFORMITY ( 11 FDA reports)
HEPATITIS A ( 11 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 11 FDA reports)
HYPOCHLORAEMIA ( 11 FDA reports)
HYPOTONIC URINARY BLADDER ( 11 FDA reports)
IMMUNOSUPPRESSION ( 11 FDA reports)
INJECTION SITE DISCOLOURATION ( 11 FDA reports)
INJECTION SITE MASS ( 11 FDA reports)
INJECTION SITE NODULE ( 11 FDA reports)
INTESTINAL RESECTION ( 11 FDA reports)
LUPUS NEPHRITIS ( 11 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 11 FDA reports)
MACROCYTOSIS ( 11 FDA reports)
MACULAR OEDEMA ( 11 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 11 FDA reports)
MITRAL VALVE CALCIFICATION ( 11 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 11 FDA reports)
MUSCLE HAEMORRHAGE ( 11 FDA reports)
MYOCLONUS ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NASAL POLYPS ( 11 FDA reports)
NECK MASS ( 11 FDA reports)
NEOPLASM PROGRESSION ( 11 FDA reports)
NEPHRITIS INTERSTITIAL ( 11 FDA reports)
ORAL FUNGAL INFECTION ( 11 FDA reports)
ORTHOPEDIC PROCEDURE ( 11 FDA reports)
PNEUMONIA CHLAMYDIAL ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PROCEDURAL HYPOTENSION ( 11 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 11 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 11 FDA reports)
REFLUX OESOPHAGITIS ( 11 FDA reports)
RENAL ATROPHY ( 11 FDA reports)
RESPIRATORY TRACT INFECTION ( 11 FDA reports)
RETINAL DISORDER ( 11 FDA reports)
SALPINGO-OOPHORECTOMY ( 11 FDA reports)
SENSATION OF FOREIGN BODY ( 11 FDA reports)
SINOBRONCHITIS ( 11 FDA reports)
SKIN NODULE ( 11 FDA reports)
SKIN ODOUR ABNORMAL ( 11 FDA reports)
SPINAL CORD DISORDER ( 11 FDA reports)
SUBMANDIBULAR MASS ( 11 FDA reports)
SYNOVIAL RUPTURE ( 11 FDA reports)
THROMBOPHLEBITIS ( 11 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 11 FDA reports)
UMBILICAL HERNIA ( 11 FDA reports)
URINE ABNORMALITY ( 11 FDA reports)
VENA CAVA THROMBOSIS ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
ABDOMINAL RIGIDITY ( 10 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
AKINESIA ( 10 FDA reports)
ALCOHOLISM ( 10 FDA reports)
ALVEOLITIS ALLERGIC ( 10 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 10 FDA reports)
AORTIC VALVE SCLEROSIS ( 10 FDA reports)
ARTICULAR CALCIFICATION ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 10 FDA reports)
BASEDOW'S DISEASE ( 10 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 10 FDA reports)
BIPOLAR I DISORDER ( 10 FDA reports)
BLADDER PAIN ( 10 FDA reports)
BLOOD CULTURE POSITIVE ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 10 FDA reports)
BURNS SECOND DEGREE ( 10 FDA reports)
CLUBBING ( 10 FDA reports)
CLUMSINESS ( 10 FDA reports)
COLLAGEN DISORDER ( 10 FDA reports)
COLONIC OBSTRUCTION ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 10 FDA reports)
CUTANEOUS VASCULITIS ( 10 FDA reports)
DERMATITIS PSORIASIFORM ( 10 FDA reports)
DIABETIC NEPHROPATHY ( 10 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 10 FDA reports)
DYSAESTHESIA ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 10 FDA reports)
FAILURE OF IMPLANT ( 10 FDA reports)
FAILURE TO THRIVE ( 10 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 10 FDA reports)
FLUID INTAKE REDUCED ( 10 FDA reports)
GASTROINTESTINAL NECROSIS ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 10 FDA reports)
GRIP STRENGTH DECREASED ( 10 FDA reports)
HAEMOLYTIC ANAEMIA ( 10 FDA reports)
HEART DISEASE CONGENITAL ( 10 FDA reports)
HEPATITIS C ( 10 FDA reports)
HEPATOCELLULAR DAMAGE ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INJECTION SITE ABSCESS ( 10 FDA reports)
INJECTION SITE RASH ( 10 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 10 FDA reports)
JOINT ABSCESS ( 10 FDA reports)
LATEX ALLERGY ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 10 FDA reports)
MONOCLONAL GAMMOPATHY ( 10 FDA reports)
MUSCLE CONTRACTURE ( 10 FDA reports)
MUSCLE RIGIDITY ( 10 FDA reports)
MUSCLE RUPTURE ( 10 FDA reports)
NASAL ULCER ( 10 FDA reports)
NEUROSIS ( 10 FDA reports)
NOSE DEFORMITY ( 10 FDA reports)
OCCIPITAL NEURALGIA ( 10 FDA reports)
ODONTOGENIC CYST ( 10 FDA reports)
OESOPHAGEAL CARCINOMA ( 10 FDA reports)
OESOPHAGEAL RUPTURE ( 10 FDA reports)
OPTIC NERVE INJURY ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PARANASAL SINUS DISCOMFORT ( 10 FDA reports)
PAROTID DUCT OBSTRUCTION ( 10 FDA reports)
PEAU D'ORANGE ( 10 FDA reports)
PERSECUTORY DELUSION ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
POLYARTHRITIS ( 10 FDA reports)
POLYP COLORECTAL ( 10 FDA reports)
POOR VENOUS ACCESS ( 10 FDA reports)
PREGNANCY ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
RENAL INJURY ( 10 FDA reports)
RETINAL VEIN OCCLUSION ( 10 FDA reports)
SCARLET FEVER ( 10 FDA reports)
SEPSIS SYNDROME ( 10 FDA reports)
SHOCK HAEMORRHAGIC ( 10 FDA reports)
SICK SINUS SYNDROME ( 10 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 10 FDA reports)
STATUS ASTHMATICUS ( 10 FDA reports)
STREPTOCOCCAL SEPSIS ( 10 FDA reports)
STRESS CARDIOMYOPATHY ( 10 FDA reports)
STRESS ULCER ( 10 FDA reports)
THROMBOCYTHAEMIA ( 10 FDA reports)
TRANSFUSION ( 10 FDA reports)
TUBERCULOUS PLEURISY ( 10 FDA reports)
TUMOUR EXCISION ( 10 FDA reports)
ULCERATIVE KERATITIS ( 10 FDA reports)
UNDERDOSE ( 10 FDA reports)
URETHRAL INTRINSIC SPHINCTER DEFICIENCY ( 10 FDA reports)
URGE INCONTINENCE ( 10 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 10 FDA reports)
URINE OUTPUT INCREASED ( 10 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VAGINAL POLYP ( 10 FDA reports)
VAGINAL PROLAPSE ( 10 FDA reports)
VOCAL CORD DISORDER ( 10 FDA reports)
ABDOMINAL ABSCESS ( 9 FDA reports)
ABSCESS SOFT TISSUE ( 9 FDA reports)
ACUTE STRESS DISORDER ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANAL INFLAMMATION ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
AORTIC CALCIFICATION ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 9 FDA reports)
BLOODY DISCHARGE ( 9 FDA reports)
BONE DENSITY ABNORMAL ( 9 FDA reports)
BRAIN MASS ( 9 FDA reports)
BREAST MICROCALCIFICATION ( 9 FDA reports)
BREAST OPERATION ( 9 FDA reports)
CAESAREAN SECTION ( 9 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CHEST WALL PAIN ( 9 FDA reports)
CHOKING SENSATION ( 9 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 9 FDA reports)
CINCHONISM ( 9 FDA reports)
DENTAL DISCOMFORT ( 9 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 9 FDA reports)
DRY THROAT ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 9 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 9 FDA reports)
EMBOLISM ARTERIAL ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
EXPIRED DRUG ADMINISTERED ( 9 FDA reports)
FEELING DRUNK ( 9 FDA reports)
FISTULA REPAIR ( 9 FDA reports)
FOOT OPERATION ( 9 FDA reports)
GASTROINTESTINAL INFECTION ( 9 FDA reports)
GINGIVAL OEDEMA ( 9 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 9 FDA reports)
GUILLAIN-BARRE SYNDROME ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HEPATIC MASS ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HEPATITIS FULMINANT ( 9 FDA reports)
HORDEOLUM ( 9 FDA reports)
HYPERTHERMIA ( 9 FDA reports)
HYPOTONIA ( 9 FDA reports)
IMMUNE SYSTEM DISORDER ( 9 FDA reports)
INCISION SITE INFECTION ( 9 FDA reports)
INCISIONAL HERNIA ( 9 FDA reports)
INFECTIOUS PERITONITIS ( 9 FDA reports)
INJECTION SITE BURNING ( 9 FDA reports)
INTENTIONAL SELF-INJURY ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
INTESTINAL PERFORATION ( 9 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 9 FDA reports)
IVTH NERVE PARALYSIS ( 9 FDA reports)
LUPUS-LIKE SYNDROME ( 9 FDA reports)
MENINGIOMA ( 9 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
MONOPLEGIA ( 9 FDA reports)
MYASTHENIA GRAVIS ( 9 FDA reports)
NASAL DISCOMFORT ( 9 FDA reports)
NEPHROCALCINOSIS ( 9 FDA reports)
NEURECTOMY ( 9 FDA reports)
NEURODEGENERATIVE DISORDER ( 9 FDA reports)
NO ADVERSE EVENT ( 9 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 9 FDA reports)
OPTIC NERVE DISORDER ( 9 FDA reports)
ORGANISING PNEUMONIA ( 9 FDA reports)
ORTHOPNOEA ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
OVARIAN MASS ( 9 FDA reports)
PARATHYROID TUMOUR BENIGN ( 9 FDA reports)
PATHOGEN RESISTANCE ( 9 FDA reports)
PHLEBOLITH ( 9 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 9 FDA reports)
POOR PERIPHERAL CIRCULATION ( 9 FDA reports)
POSTMENOPAUSE ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RADICULITIS ( 9 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 9 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
RETINAL EXUDATES ( 9 FDA reports)
ROTATOR CUFF REPAIR ( 9 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SKIN FIBROSIS ( 9 FDA reports)
SKIN MASS ( 9 FDA reports)
SLUGGISHNESS ( 9 FDA reports)
SOPOR ( 9 FDA reports)
SPONDYLOSIS ( 9 FDA reports)
STEROID THERAPY ( 9 FDA reports)
TRENDELENBURG'S SYMPTOM ( 9 FDA reports)
TUNNEL VISION ( 9 FDA reports)
URETHRAL CARUNCLE ( 9 FDA reports)
URINE PHOSPHATE INCREASED ( 9 FDA reports)
UTERINE POLYP ( 9 FDA reports)
ABDOMINAL SEPSIS ( 8 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ABSCESS OF SALIVARY GLAND ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
AKATHISIA ( 8 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 8 FDA reports)
ANEURYSM ( 8 FDA reports)
ANORGASMIA ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BACTERIAL TEST POSITIVE ( 8 FDA reports)
BENIGN NEOPLASM OF SKIN ( 8 FDA reports)
BILE DUCT OBSTRUCTION ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BITE ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 8 FDA reports)
BLOOD CALCIUM ABNORMAL ( 8 FDA reports)
BLOOD CREATINE INCREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 8 FDA reports)
BRAIN ABSCESS ( 8 FDA reports)
BREAST CANCER STAGE I ( 8 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 8 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 8 FDA reports)
BRONCHITIS ACUTE ( 8 FDA reports)
CAECUM OPERATION ( 8 FDA reports)
CARDIAC ANEURYSM ( 8 FDA reports)
CATHETER SITE PAIN ( 8 FDA reports)
CATHETERISATION CARDIAC ( 8 FDA reports)
CEREBRAL DISORDER ( 8 FDA reports)
CHOLANGITIS ( 8 FDA reports)
CHOLECYSTITIS INFECTIVE ( 8 FDA reports)
COLLAPSE OF LUNG ( 8 FDA reports)
CRANIOCEREBRAL INJURY ( 8 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 8 FDA reports)
DERMATOMYOSITIS ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
FACIAL NERVE DISORDER ( 8 FDA reports)
FIBRIN D DIMER INCREASED ( 8 FDA reports)
FLAT AFFECT ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FOOD INTOLERANCE ( 8 FDA reports)
FOREIGN BODY IN EYE ( 8 FDA reports)
GAIT DEVIATION ( 8 FDA reports)
GENERALISED ERYTHEMA ( 8 FDA reports)
HAEMORRHAGIC DIATHESIS ( 8 FDA reports)
HAEMORRHAGIC DISORDER ( 8 FDA reports)
HAIR COLOUR CHANGES ( 8 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
HYPERTRICHOSIS ( 8 FDA reports)
HYPOTRICHOSIS ( 8 FDA reports)
IMPAIRED FASTING GLUCOSE ( 8 FDA reports)
INCISION SITE CELLULITIS ( 8 FDA reports)
INCISION SITE HAEMORRHAGE ( 8 FDA reports)
INFECTED DERMAL CYST ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
JAUNDICE CHOLESTATIC ( 8 FDA reports)
JOINT DISLOCATION REDUCTION ( 8 FDA reports)
JOINT LOCK ( 8 FDA reports)
LACRIMATION DECREASED ( 8 FDA reports)
LIP PAIN ( 8 FDA reports)
LOCALISED OEDEMA ( 8 FDA reports)
LYME DISEASE ( 8 FDA reports)
LYMPHOCELE ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
MUCOUS STOOLS ( 8 FDA reports)
MYCOTIC ALLERGY ( 8 FDA reports)
NAIL OPERATION ( 8 FDA reports)
NASAL OEDEMA ( 8 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
OPERATIVE HAEMORRHAGE ( 8 FDA reports)
PANCREATIC NECROSIS ( 8 FDA reports)
PARAPROTEINAEMIA ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PEMPHIGOID ( 8 FDA reports)
PERFORATED ULCER ( 8 FDA reports)
PHOBIA ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PORPHYRIA NON-ACUTE ( 8 FDA reports)
POST PROCEDURAL DISCOMFORT ( 8 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
PROCEDURAL NAUSEA ( 8 FDA reports)
PROCEDURAL VOMITING ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
SACRALISATION ( 8 FDA reports)
SCRATCH ( 8 FDA reports)
SKIN HYPERPIGMENTATION ( 8 FDA reports)
SLEEP PARALYSIS ( 8 FDA reports)
SLEEP TALKING ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
SPONDYLOLYSIS ( 8 FDA reports)
STOMATITIS NECROTISING ( 8 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 8 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 8 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
TEMPORAL ARTERITIS ( 8 FDA reports)
TERMINAL INSOMNIA ( 8 FDA reports)
THYROID MASS ( 8 FDA reports)
THYROIDITIS ( 8 FDA reports)
TONGUE GEOGRAPHIC ( 8 FDA reports)
TUMOUR MARKER INCREASED ( 8 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 8 FDA reports)
URETHRAL STENOSIS ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
URTICARIA THERMAL ( 8 FDA reports)
UTERINE DILATION AND CURETTAGE ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 7 FDA reports)
ACTINOMYCES TEST POSITIVE ( 7 FDA reports)
ADENOIDAL DISORDER ( 7 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 7 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 7 FDA reports)
AORTIC VALVE STENOSIS ( 7 FDA reports)
APPENDICITIS PERFORATED ( 7 FDA reports)
ARTERIAL DISORDER ( 7 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD MAGNESIUM DECREASED ( 7 FDA reports)
BONE DEFORMITY ( 7 FDA reports)
BONE FISSURE ( 7 FDA reports)
BONE NEOPLASM ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BREATH SOUNDS ABNORMAL ( 7 FDA reports)
BULLOUS IMPETIGO ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIOPULMONARY FAILURE ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
CONTRAST MEDIA ALLERGY ( 7 FDA reports)
CORONARY ANGIOPLASTY ( 7 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
CYST REMOVAL ( 7 FDA reports)
CYSTITIS HAEMORRHAGIC ( 7 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 7 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 7 FDA reports)
DEVICE INTOLERANCE ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
ENDOPHTHALMITIS ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
EUSTACHIAN TUBE DISORDER ( 7 FDA reports)
FAECALOMA ( 7 FDA reports)
FASCIAL INFECTION ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
GASTRIC PERFORATION ( 7 FDA reports)
GASTRIC PH DECREASED ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
GINGIVITIS ULCERATIVE ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
HAEMOSIDEROSIS ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 7 FDA reports)
HERNIA OBSTRUCTIVE ( 7 FDA reports)
HYPERCAPNIA ( 7 FDA reports)
HYPERPLASIA ( 7 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 7 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
INFUSION SITE CELLULITIS ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INJECTION SITE WARMTH ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
KNEE OPERATION ( 7 FDA reports)
LIVER SCAN ABNORMAL ( 7 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 7 FDA reports)
MANIA ( 7 FDA reports)
MEAN CELL VOLUME DECREASED ( 7 FDA reports)
MERALGIA PARAESTHETICA ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OESOPHAGEAL OEDEMA ( 7 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 7 FDA reports)
ORAL DISCHARGE ( 7 FDA reports)
ORAL PRURITUS ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PAROTID GLAND ENLARGEMENT ( 7 FDA reports)
PERIPROSTHETIC FRACTURE ( 7 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 7 FDA reports)
POOR PERSONAL HYGIENE ( 7 FDA reports)
POST PROCEDURAL DRAINAGE ( 7 FDA reports)
POST PROCEDURAL SWELLING ( 7 FDA reports)
POSTNASAL DRIP ( 7 FDA reports)
PREMATURE AGEING ( 7 FDA reports)
PROCEDURAL HEADACHE ( 7 FDA reports)
PULSE ABSENT ( 7 FDA reports)
REFLUX LARYNGITIS ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 7 FDA reports)
RETINAL VEIN THROMBOSIS ( 7 FDA reports)
SENILE DEMENTIA ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SKIN CYST EXCISION ( 7 FDA reports)
SKIN WRINKLING ( 7 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 7 FDA reports)
SOFT TISSUE NECROSIS ( 7 FDA reports)
SPLENIC RUPTURE ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
SUICIDAL BEHAVIOUR ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
THYROID CANCER ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
TRAUMATIC LIVER INJURY ( 7 FDA reports)
URINARY BLADDER POLYP ( 7 FDA reports)
VAGINITIS BACTERIAL ( 7 FDA reports)
VASOMOTOR RHINITIS ( 7 FDA reports)
WEIGHT LOSS POOR ( 7 FDA reports)
WHITE BLOOD CELL DISORDER ( 7 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 6 FDA reports)
ACCIDENTAL NEEDLE STICK ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ALLERGY TO ANIMAL ( 6 FDA reports)
ALLERGY TO CHEMICALS ( 6 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 6 FDA reports)
ANAL FISTULA ( 6 FDA reports)
ANGIOMYOLIPOMA ( 6 FDA reports)
ANGIOSARCOMA ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
APPLICATION SITE PAIN ( 6 FDA reports)
APPLICATION SITE PRURITUS ( 6 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
BIFASCICULAR BLOCK ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLADDER DIVERTICULUM ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BONE CALLUS EXCESSIVE ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
CALCIFICATION OF MUSCLE ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 6 FDA reports)
CELL DEATH ( 6 FDA reports)
CEREBRAL THROMBOSIS ( 6 FDA reports)
CERVICAL DYSPLASIA ( 6 FDA reports)
CHONDROCALCINOSIS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
COITAL BLEEDING ( 6 FDA reports)
COLON POLYPECTOMY ( 6 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 6 FDA reports)
CORNEAL DEPOSITS ( 6 FDA reports)
CYST RUPTURE ( 6 FDA reports)
CYSTITIS KLEBSIELLA ( 6 FDA reports)
DENTAL IMPLANTATION ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DISLOCATION OF VERTEBRA ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
ENDOCRINE NEOPLASM MALIGNANT ( 6 FDA reports)
ENEMA ADMINISTRATION ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EYE ALLERGY ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
EYE PENETRATION ( 6 FDA reports)
EYELID DISORDER ( 6 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 6 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GINGIVECTOMY ( 6 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 6 FDA reports)
GOUTY ARTHRITIS ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
HELICOBACTER GASTRITIS ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HOSTILITY ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
IMPAIRED SELF-CARE ( 6 FDA reports)
INNER EAR DISORDER ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
IODINE ALLERGY ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
JOINT WARMTH ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LABILE HYPERTENSION ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LIGAMENT DISORDER ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
LIVEDO RETICULARIS ( 6 FDA reports)
LUNG CONSOLIDATION ( 6 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 6 FDA reports)
MASS EXCISION ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 6 FDA reports)
MELANOSIS COLI ( 6 FDA reports)
MENINGITIS VIRAL ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MYODESOPSIA ( 6 FDA reports)
NECROSIS ISCHAEMIC ( 6 FDA reports)
NEUROENDOCRINE CARCINOMA ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 6 FDA reports)
OSTEOMYELITIS BACTERIAL ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PAPILLOEDEMA ( 6 FDA reports)
PEMPHIGUS ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PERITONEAL TUBERCULOSIS ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
POST PROCEDURAL URINE LEAK ( 6 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PSYCHOSOMATIC DISEASE ( 6 FDA reports)
PUBIC RAMI FRACTURE ( 6 FDA reports)
PYODERMA ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
RHEUMATOID NODULE ( 6 FDA reports)
SALIVARY GLAND DISORDER ( 6 FDA reports)
SALIVARY GLAND MASS ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SENILE OSTEOPOROSIS ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SKIN GRAFT FAILURE ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
SPIDER NAEVUS ( 6 FDA reports)
SPIDER VEIN ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
TETANY ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 6 FDA reports)
THYROIDECTOMY ( 6 FDA reports)
THYROIDITIS SUBACUTE ( 6 FDA reports)
TOBACCO ABUSE ( 6 FDA reports)
TOOTH CROWDING ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TRICHORRHEXIS ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
TUMOUR LYSIS SYNDROME ( 6 FDA reports)
TYPE 1 DIABETES MELLITUS ( 6 FDA reports)
URETERIC STENOSIS ( 6 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 6 FDA reports)
URINE FLOW DECREASED ( 6 FDA reports)
UTERINE PROLAPSE ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VENTRICULAR DYSFUNCTION ( 6 FDA reports)
VULVAL DISORDER ( 6 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACUTE ABDOMEN ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ADJUSTMENT DISORDER ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ALLERGY TO ARTHROPOD STING ( 5 FDA reports)
ANASTOMOTIC COMPLICATION ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
AORTIC VALVE DISEASE ( 5 FDA reports)
APPLICATION SITE RASH ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
AURA ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 5 FDA reports)
BACTERIAL DISEASE CARRIER ( 5 FDA reports)
BENIGN NEOPLASM ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BILIARY CIRRHOSIS ( 5 FDA reports)
BLADDER PROLAPSE ( 5 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BODY TINEA ( 5 FDA reports)
BONE FORMATION DECREASED ( 5 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 5 FDA reports)
BRACHIAL PLEXOPATHY ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BREAST ATROPHY ( 5 FDA reports)
BREAST DISCOMFORT ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
CARBON DIOXIDE INCREASED ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CEREBELLAR HAEMATOMA ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CHANGE OF BOWEL HABIT ( 5 FDA reports)
CHOREA ( 5 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
CLONUS ( 5 FDA reports)
COCCYDYNIA ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
COMPLICATED FRACTURE ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DEVICE ISSUE ( 5 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
EAR NEOPLASM MALIGNANT ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 5 FDA reports)
ENDOMETRIAL CANCER ( 5 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 5 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ENTEROSTOMY ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
EYE NAEVUS ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEAR OF DEATH ( 5 FDA reports)
FIBROMATOSIS ( 5 FDA reports)
FUNGAL OESOPHAGITIS ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC MUCOSAL LESION ( 5 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GAZE PALSY ( 5 FDA reports)
GENITAL HERPES ( 5 FDA reports)
GLIOBLASTOMA ( 5 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 5 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERTROPHY BREAST ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
HYPOPNOEA ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
ILIAC ARTERY STENOSIS ( 5 FDA reports)
ILLUSION ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
LEIOMYOMA ( 5 FDA reports)
LEUKOARAIOSIS ( 5 FDA reports)
LIMB CRUSHING INJURY ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LOCALISED OSTEOARTHRITIS ( 5 FDA reports)
LUDWIG ANGINA ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MASTOID DISORDER ( 5 FDA reports)
MEDICAL DEVICE PAIN ( 5 FDA reports)
MEDICAL DEVICE SITE REACTION ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
METAPLASIA ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
METATARSALGIA ( 5 FDA reports)
METATARSUS PRIMUS VARUS ( 5 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NEUTROPHIL COUNT ( 5 FDA reports)
NOCTURNAL DYSPNOEA ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
OBSTRUCTION ( 5 FDA reports)
OESOPHAGITIS ULCERATIVE ( 5 FDA reports)
ONYCHALGIA ( 5 FDA reports)
OPHTHALMOPLEGIA ( 5 FDA reports)
ORAL PAPILLOMA ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PAPILLOMA ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERICARDITIS LUPUS ( 5 FDA reports)
PERIPHERAL EMBOLISM ( 5 FDA reports)
PERSONALITY DISORDER ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PITUITARY TUMOUR BENIGN ( 5 FDA reports)
PLANTAR FASCIAL FIBROMATOSIS ( 5 FDA reports)
PLEURAL INFECTION BACTERIAL ( 5 FDA reports)
PO2 DECREASED ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 5 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RENAL CANCER ( 5 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 5 FDA reports)
RESUSCITATION ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RHEUMATOID FACTOR INCREASED ( 5 FDA reports)
SALIVARY GLAND PAIN ( 5 FDA reports)
SCAPULA FRACTURE ( 5 FDA reports)
SELF-INDUCED VOMITING ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SEROTONIN SYNDROME ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SKIN DEGENERATIVE DISORDER ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SMEAR CERVIX ABNORMAL ( 5 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 5 FDA reports)
SOFT TISSUE MASS ( 5 FDA reports)
SOMATISATION DISORDER ( 5 FDA reports)
SPINAL COLUMN INJURY ( 5 FDA reports)
STASIS DERMATITIS ( 5 FDA reports)
STERNAL FRACTURE ( 5 FDA reports)
STITCH ABSCESS ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
THYMOMA ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
URINE CALCIUM DECREASED ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
VASCULAR OCCLUSION ( 5 FDA reports)
VESTIBULAR NEURONITIS ( 5 FDA reports)
VITAMIN D INCREASED ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ADENOMYOSIS ( 4 FDA reports)
AGORAPHOBIA ( 4 FDA reports)
ALLERGY TO VACCINE ( 4 FDA reports)
AMYOTROPHY ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIAL BRUIT ( 4 FDA reports)
ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BENIGN BREAST NEOPLASM ( 4 FDA reports)
BILIARY CYST ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BINGE EATING ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLOOD CHLORIDE INCREASED ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BONE SCAN ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
CALCIUM METABOLISM DISORDER ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CELLULITIS STREPTOCOCCAL ( 4 FDA reports)
CEREBROVASCULAR SPASM ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHLAMYDIA TEST POSITIVE ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
COLON CANCER STAGE IV ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYSTOPEXY ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 4 FDA reports)
DUODENITIS HAEMORRHAGIC ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENCHONDROMA ( 4 FDA reports)
ENTEROBACTER TEST POSITIVE ( 4 FDA reports)
EOSINOPHIL COUNT DECREASED ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 4 FDA reports)
EPIDURAL FIBROSIS ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 4 FDA reports)
EXTRADURAL ABSCESS ( 4 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 4 FDA reports)
FACIAL NEURALGIA ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
FRACTURED ISCHIUM ( 4 FDA reports)
GASTRIC CANCER STAGE IV ( 4 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 4 FDA reports)
GINGIVAL INJURY ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
HAEMOGLOBIN ABNORMAL ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEPATIC ARTERY OCCLUSION ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HOMICIDAL IDEATION ( 4 FDA reports)
HOUSE DUST ALLERGY ( 4 FDA reports)
HUMAN BITE ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPERPROTEINAEMIA ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
ILIUM FRACTURE ( 4 FDA reports)
IMPLANT SITE INFECTION ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCISION SITE ERYTHEMA ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE ANAESTHESIA ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTESTINAL PROLAPSE ( 4 FDA reports)
INTESTINAL STOMA ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KIDNEY ENLARGEMENT ( 4 FDA reports)
KNEE DEFORMITY ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LISTERIA SEPSIS ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LYMPHORRHOEA ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MURPHY'S SIGN POSITIVE ( 4 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYELOCYTOSIS ( 4 FDA reports)
MYELOMALACIA ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NASAL MUCOSAL HYPERTROPHY ( 4 FDA reports)
NASAL OBSTRUCTION ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NODAL OSTEOARTHRITIS ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OVARIAN EPITHELIAL CANCER ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERIOSTITIS ( 4 FDA reports)
PHARYNGEAL CYST ( 4 FDA reports)
PHLEBITIS SUPERFICIAL ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POST PROCEDURAL DISCHARGE ( 4 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 4 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PULMONARY HILUM MASS ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RADIATION OESOPHAGITIS ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RESPIRATORY PARALYSIS ( 4 FDA reports)
RETINAL ISCHAEMIA ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
RHONCHI ( 4 FDA reports)
SARCOMA ( 4 FDA reports)
SCAN ABDOMEN ABNORMAL ( 4 FDA reports)
SCIATIC NERVE NEUROPATHY ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
TENDON SHEATH INCISION ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
THYROXINE DECREASED ( 4 FDA reports)
TIC ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 4 FDA reports)
TRAUMATIC OCCLUSION ( 4 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 4 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 4 FDA reports)
VAGINAL BURNING SENSATION ( 4 FDA reports)
VAGINAL LESION ( 4 FDA reports)
VAGINAL ODOUR ( 4 FDA reports)
VARICOSE VEIN OPERATION ( 4 FDA reports)
VASCULAR PURPURA ( 4 FDA reports)
VEIN PAIN ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VERTIGO CNS ORIGIN ( 4 FDA reports)
VIRAL TITRE INCREASED ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
WRIST SURGERY ( 4 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALLERGIC COUGH ( 3 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ATLANTOAXIAL INSTABILITY ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
AVERSION ( 3 FDA reports)
BACTERIAL TOXAEMIA ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BILIRUBIN URINE ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 3 FDA reports)
BLADDER DISCOMFORT ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD GASTRIN INCREASED ( 3 FDA reports)
BONE FISTULA ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BRAIN OPERATION ( 3 FDA reports)
BREAST CANCER STAGE II ( 3 FDA reports)
BREAST DISORDER FEMALE ( 3 FDA reports)
BREAST HYPERPLASIA ( 3 FDA reports)
BRONCHITIS HAEMOPHILUS ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 3 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 3 FDA reports)
CARDIAC SEPTAL DEFECT ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CELLULITIS GANGRENOUS ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CHALAZION ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHOREOATHETOSIS ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL DYSTROPHY ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DENTAL PROSTHESIS USER ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIAPHRAGMATIC HERNIA ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRY SOCKET ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EPIDURITIS ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EYELID MARGIN CRUSTING ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEMORAL HERNIA REPAIR ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 3 FDA reports)
GENITAL PRURITUS FEMALE ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GINGIVAL DISCOLOURATION ( 3 FDA reports)
GINGIVAL EROSION ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GREENSTICK FRACTURE ( 3 FDA reports)
GUN SHOT WOUND ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HEART VALVE CALCIFICATION ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HORMONE THERAPY ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPEROXALURIA ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOTONIA NEONATAL ( 3 FDA reports)
IMPLANT SITE ABSCESS ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTESTINAL ANASTOMOSIS ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
JOINT DESTRUCTION ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGEAL GRANULOMA ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LIMB OPERATION ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG CREPITATION ( 3 FDA reports)
LUNG CYST ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MASTOID ABSCESS ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 3 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 3 FDA reports)
MENINGITIS TUBERCULOUS ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MITRAL VALVE DISEASE MIXED ( 3 FDA reports)
MIXED HYPERLIPIDAEMIA ( 3 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MYOCARDIAL RUPTURE ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEURILEMMOMA BENIGN ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL MASS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
ORTHOSIS USER ( 3 FDA reports)
OVARIAN ATROPHY ( 3 FDA reports)
PACEMAKER COMPLICATION ( 3 FDA reports)
PACHYMENINGITIS ( 3 FDA reports)
PANCOAST'S TUMOUR ( 3 FDA reports)
PANCREAS INFECTION ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PANNICULITIS LOBULAR ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PH URINE INCREASED ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POSTICTAL PARALYSIS ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PROSTHESIS IMPLANTATION ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSEUDOENDOPHTHALMITIS ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PTERYGIUM ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RADICULAR PAIN ( 3 FDA reports)
RADICULITIS CERVICAL ( 3 FDA reports)
READING DISORDER ( 3 FDA reports)
RECTAL LESION ( 3 FDA reports)
RED BLOOD CELL ABNORMALITY ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RHINITIS SEASONAL ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
SALIVARY GLAND CANCER ( 3 FDA reports)
SCLERAL DISORDER ( 3 FDA reports)
SECONDARY SEQUESTRUM ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SERONEGATIVE ARTHRITIS ( 3 FDA reports)
SERUM FERRITIN DECREASED ( 3 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SLEEP-RELATED EATING DISORDER ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SPINAL FUSION ACQUIRED ( 3 FDA reports)
SPINAL MENINGEAL CYST ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SYNOVECTOMY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
TINEL'S SIGN ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH DECALCIFICATION ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRACHEAL INJURY ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 3 FDA reports)
TYMPANOSCLEROSIS ( 3 FDA reports)
ULNOCARPAL ABUTMENT SYNDROME ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINOMA ( 3 FDA reports)
UTERINE ATROPHY ( 3 FDA reports)
UTEROVAGINAL PROLAPSE ( 3 FDA reports)
VAGINAL PAIN ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR HEADACHE ( 3 FDA reports)
VASOCONSTRICTION ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VITREOUS DEGENERATION ( 3 FDA reports)
VOLUME BLOOD DECREASED ( 3 FDA reports)
VON WILLEBRAND'S DISEASE ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
WHITE BLOOD CELLS URINE ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND HAEMATOMA ( 3 FDA reports)
ABDOMINAL BRUIT ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACINETOBACTER BACTERAEMIA ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACQUIRED CLAW TOE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTINIC ELASTOSIS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALCOHOL DETOXIFICATION ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANKLE DEFORMITY ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC DISSECTION RUPTURE ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE OEDEMA ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ARTICULAR DISC DISORDER ( 2 FDA reports)
ASPERGILLOMA ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACK CRUSHING ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BAROTITIS MEDIA ( 2 FDA reports)
BAROTRAUMA ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY LUNG ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 2 FDA reports)
BONE RESORPTION TEST ABNORMAL ( 2 FDA reports)
BORRELIA INFECTION ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST INDURATION ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
BURSA INJURY ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CEMENTO OSSEOUS DYSPLASIA ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLEMENT FACTOR DECREASED ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 2 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 2 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 2 FDA reports)
CONGENITAL OSTEODYSTROPHY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONSTRICTED AFFECT ( 2 FDA reports)
CONUS MEDULLARIS SYNDROME ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMATOSIS ( 2 FDA reports)
DEVICE CONNECTION ISSUE ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOCRINE TEST ABNORMAL ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
EPISCLERAL HYPERAEMIA ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ERYTHROPLASIA ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EYE DEGENERATIVE DISORDER ( 2 FDA reports)
EYE LUXATION ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FACIAL SPASM ( 2 FDA reports)
FACTOR XI DEFICIENCY ( 2 FDA reports)
FALLOPIAN TUBE DISORDER ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GALLBLADDER NECROSIS ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRINOMA ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GINGIVAL OPERATION ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLIOMA ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMATOTYMPANUM ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HIV TEST FALSE POSITIVE ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERVITAMINOSIS D ( 2 FDA reports)
HYPNAGOGIC HALLUCINATION ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
IMMOBILISATION PROLONGED ( 2 FDA reports)
IMPLANT TISSUE NECROSIS ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSTILLATION SITE IRRITATION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC NEPHROPATHY ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL ERYTHEMA ( 2 FDA reports)
LARYNGITIS BACTERIAL ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LEUKODERMA ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 2 FDA reports)
MEDIASTINOSCOPY ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
METASTASES TO EYE ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
N-TELOPEPTIDE URINE INCREASED ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECK DEFORMITY ( 2 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NEOPLASM OF APPENDIX ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
OSTECTOMY ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL NERVE INJURY ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONITIS LUPUS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PH URINE DECREASED ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLATELET COUNT ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST-TRAUMATIC PAIN ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY ATRESIA ( 2 FDA reports)
PULMONARY SARCOIDOSIS ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADIOISOTOPE SCAN ABNORMAL ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RECTOCELE REPAIR ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL SALT-WASTING SYNDROME ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
REVISION OF INTERNAL FIXATION ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RIB DEFORMITY ( 2 FDA reports)
RIB HYPOPLASIA ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOULDER DEFORMITY ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS TARSI SYNDROME ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENIC CALCIFICATION ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STIFF PERSON SYNDROME ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCAL ABSCESS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
THROMBOANGIITIS OBLITERANS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME ( 2 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 2 FDA reports)
UNEQUAL LIMB LENGTH ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETHRAL SYNDROME ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINARY TRACT OPERATION ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE DILATION AND EVACUATION ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL STRICTURE ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 2 FDA reports)
VIITH NERVE INJURY ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VOLVULUS OF SMALL BOWEL ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
VULVOVAGINITIS ( 2 FDA reports)
WAARDENBURG SYNDROME ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
YAWNING ( 2 FDA reports)
YELLOW NAIL SYNDROME ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACNE CONGLOBATA ( 1 FDA reports)
ACROCHORDON EXCISION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAL CANCER STAGE II ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTERIOR CHAMBER DISORDER ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ATRIAL RUPTURE ( 1 FDA reports)
AUDITORY MEATUS EXTERNAL EROSION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF CHOROID ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT CANCER STAGE III ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY BREAST NORMAL ( 1 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD LEAD INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST FIBROSIS ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CAPNOCYTOPHAGIA INFECTION ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARTILAGE DEVELOPMENT DISORDER ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS PASTEURELLA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHOLESTEATOMA REMOVAL ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORIORETINAL ATROPHY ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL RUBELLA INFECTION ( 1 FDA reports)
CONGENITAL VARICELLA INFECTION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTRALATERAL BREAST CANCER ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORTISOL FREE URINE INCREASED ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEAFNESS TRAUMATIC ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE EXTRUSION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLECTOMY ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCRINE NEOPLASM ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER CANCER STAGE IV ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
HAEMODYNAMIC REBOUND ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 1 FDA reports)
HOMEOPATHY ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPOCALCIURIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
IDIOPATHIC CAPILLARITIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNISATION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE PRURITUS ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PARAESTHESIA ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSPIRATORY CAPACITY ABNORMAL ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSCOPY ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOW TENSION GLAUCOMA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBOSACRAL PLEXUS INJURY ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS HAEMOPHILUS ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGENIA ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MILIA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE OEDEMA ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME UNCLASSIFIABLE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUMB CHIN SYNDROME ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL NEOPLASM BENIGN ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSTEOCALCIN INCREASED ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN ADHESION ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN THRESHOLD DECREASED ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE III ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANTOTHENIC ACID DEFICIENCY ( 1 FDA reports)
PARAPHARYNGEAL ABSCESS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIODONTAL DESTRUCTION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PICA ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY ENLARGEMENT ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADIOISOTOPE SCAN ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL BURR CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING POLYCHONDRITIS ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RICKETTSIOSIS ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALT CRAVING ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEBACEOUS HYPERPLASIA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN TUBERCULOSIS ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL FLUID RED BLOOD CELLS POSITIVE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA MANUUM ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE PIGMENTATION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULIN TEST ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
UTERINE CARCINOMA IN SITU ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE INVERSION ( 1 FDA reports)
UTERINE MALPOSITION ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN C DECREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOGRANULOMA ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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