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

FEMUR FRACTURE ( 4593 FDA reports)
FALL ( 2879 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2222 FDA reports)
OSTEOARTHRITIS ( 1728 FDA reports)
ARTHRALGIA ( 1680 FDA reports)
HYPERTENSION ( 1357 FDA reports)
PAIN IN EXTREMITY ( 1351 FDA reports)
STRESS FRACTURE ( 1293 FDA reports)
ANXIETY ( 1255 FDA reports)
BACK PAIN ( 1082 FDA reports)
DEPRESSION ( 1066 FDA reports)
HYPERLIPIDAEMIA ( 1048 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1045 FDA reports)
BONE DISORDER ( 1035 FDA reports)
TOOTH DISORDER ( 1022 FDA reports)
FATIGUE ( 968 FDA reports)
NAUSEA ( 941 FDA reports)
PAIN ( 908 FDA reports)
ANAEMIA ( 902 FDA reports)
OSTEOPOROSIS ( 850 FDA reports)
URINARY TRACT INFECTION ( 838 FDA reports)
OEDEMA PERIPHERAL ( 813 FDA reports)
DIARRHOEA ( 790 FDA reports)
FOOT FRACTURE ( 784 FDA reports)
VITAMIN D DEFICIENCY ( 781 FDA reports)
ARTHROPATHY ( 780 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 756 FDA reports)
IMPAIRED HEALING ( 742 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 736 FDA reports)
PNEUMONIA ( 735 FDA reports)
CATARACT ( 723 FDA reports)
BURSITIS ( 717 FDA reports)
DYSPNOEA ( 717 FDA reports)
HEADACHE ( 714 FDA reports)
ARTHRITIS ( 713 FDA reports)
DIZZINESS ( 702 FDA reports)
SPINAL OSTEOARTHRITIS ( 698 FDA reports)
INSOMNIA ( 686 FDA reports)
OSTEONECROSIS OF JAW ( 679 FDA reports)
PYREXIA ( 651 FDA reports)
ASTHENIA ( 646 FDA reports)
GAIT DISTURBANCE ( 643 FDA reports)
CHEST PAIN ( 626 FDA reports)
CONSTIPATION ( 611 FDA reports)
CONTUSION ( 603 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 603 FDA reports)
DRUG INEFFECTIVE ( 601 FDA reports)
HAEMORRHOIDS ( 590 FDA reports)
BRONCHITIS ( 576 FDA reports)
FRACTURE NONUNION ( 557 FDA reports)
ADVERSE DRUG REACTION ( 541 FDA reports)
VOMITING ( 533 FDA reports)
MUSCLE SPASMS ( 525 FDA reports)
DIVERTICULUM ( 521 FDA reports)
HYPERCHOLESTEROLAEMIA ( 513 FDA reports)
RIB FRACTURE ( 510 FDA reports)
COUGH ( 506 FDA reports)
FRACTURE ( 500 FDA reports)
DENTAL CARIES ( 493 FDA reports)
DRUG HYPERSENSITIVITY ( 486 FDA reports)
ROTATOR CUFF SYNDROME ( 485 FDA reports)
ANAEMIA POSTOPERATIVE ( 484 FDA reports)
ASTHMA ( 475 FDA reports)
DEVICE FAILURE ( 471 FDA reports)
OSTEOPENIA ( 455 FDA reports)
MALAISE ( 454 FDA reports)
MYALGIA ( 445 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 443 FDA reports)
RASH ( 432 FDA reports)
CELLULITIS ( 423 FDA reports)
ADVERSE EVENT ( 421 FDA reports)
ABDOMINAL PAIN ( 398 FDA reports)
HERPES ZOSTER ( 398 FDA reports)
HIATUS HERNIA ( 395 FDA reports)
WEIGHT DECREASED ( 393 FDA reports)
HYPOTHYROIDISM ( 389 FDA reports)
RHEUMATOID ARTHRITIS ( 388 FDA reports)
SCOLIOSIS ( 387 FDA reports)
WEIGHT INCREASED ( 387 FDA reports)
HAEMORRHAGIC ANAEMIA ( 386 FDA reports)
EXOSTOSIS ( 385 FDA reports)
HYPOAESTHESIA ( 377 FDA reports)
SCIATICA ( 367 FDA reports)
CARPAL TUNNEL SYNDROME ( 344 FDA reports)
SPINAL COLUMN STENOSIS ( 342 FDA reports)
CORONARY ARTERY DISEASE ( 339 FDA reports)
PARAESTHESIA ( 339 FDA reports)
MUSCULAR WEAKNESS ( 338 FDA reports)
GASTRITIS ( 333 FDA reports)
ROAD TRAFFIC ACCIDENT ( 330 FDA reports)
FOOT DEFORMITY ( 329 FDA reports)
HYPOTENSION ( 326 FDA reports)
DEHYDRATION ( 324 FDA reports)
SINUSITIS ( 323 FDA reports)
BONE DENSITY DECREASED ( 319 FDA reports)
INFECTION ( 318 FDA reports)
DECREASED APPETITE ( 317 FDA reports)
HYPOKALAEMIA ( 317 FDA reports)
MUSCULOSKELETAL PAIN ( 315 FDA reports)
SYNCOPE ( 312 FDA reports)
RHINITIS ALLERGIC ( 309 FDA reports)
OSTEOMYELITIS ( 308 FDA reports)
UTERINE DISORDER ( 305 FDA reports)
MUSCLE STRAIN ( 304 FDA reports)
COLONIC POLYP ( 303 FDA reports)
HYPONATRAEMIA ( 302 FDA reports)
BLOOD PRESSURE INCREASED ( 301 FDA reports)
NEUROPATHY PERIPHERAL ( 298 FDA reports)
PRURITUS ( 298 FDA reports)
OSTEONECROSIS ( 296 FDA reports)
HIP FRACTURE ( 294 FDA reports)
URINARY INCONTINENCE ( 294 FDA reports)
TOOTH FRACTURE ( 289 FDA reports)
DEEP VEIN THROMBOSIS ( 289 FDA reports)
DYSPEPSIA ( 288 FDA reports)
PALPITATIONS ( 284 FDA reports)
DYSPHAGIA ( 279 FDA reports)
LUNG NEOPLASM ( 276 FDA reports)
LIGAMENT SPRAIN ( 273 FDA reports)
MYOCARDIAL INFARCTION ( 273 FDA reports)
ATRIAL FIBRILLATION ( 268 FDA reports)
HYPERSENSITIVITY ( 268 FDA reports)
GALLBLADDER DISORDER ( 264 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 262 FDA reports)
JOINT SWELLING ( 261 FDA reports)
HAEMOGLOBIN DECREASED ( 259 FDA reports)
NECK PAIN ( 257 FDA reports)
GASTROINTESTINAL DISORDER ( 253 FDA reports)
TENDONITIS ( 251 FDA reports)
SPINAL DISORDER ( 248 FDA reports)
CARDIAC MURMUR ( 247 FDA reports)
RENAL FAILURE ACUTE ( 247 FDA reports)
SEPSIS ( 245 FDA reports)
OVERDOSE ( 244 FDA reports)
JOINT EFFUSION ( 243 FDA reports)
WRIST FRACTURE ( 243 FDA reports)
RENAL FAILURE ( 241 FDA reports)
APPENDIX DISORDER ( 237 FDA reports)
MENISCUS LESION ( 236 FDA reports)
ANKLE FRACTURE ( 234 FDA reports)
CEREBROVASCULAR ACCIDENT ( 233 FDA reports)
CARDIAC DISORDER ( 231 FDA reports)
INTERSTITIAL LUNG DISEASE ( 231 FDA reports)
LUMBAR RADICULOPATHY ( 231 FDA reports)
SPONDYLOLISTHESIS ( 229 FDA reports)
PULMONARY EMBOLISM ( 228 FDA reports)
LUMBAR SPINAL STENOSIS ( 227 FDA reports)
SLEEP DISORDER ( 226 FDA reports)
GINGIVAL DISORDER ( 225 FDA reports)
SPINAL COMPRESSION FRACTURE ( 224 FDA reports)
POLLAKIURIA ( 223 FDA reports)
BALANCE DISORDER ( 222 FDA reports)
CALCIUM DEFICIENCY ( 222 FDA reports)
FRACTURE DELAYED UNION ( 220 FDA reports)
ORAL DISORDER ( 220 FDA reports)
TONSILLAR DISORDER ( 220 FDA reports)
RENAL CYST ( 219 FDA reports)
DIABETES MELLITUS ( 218 FDA reports)
BASAL CELL CARCINOMA ( 216 FDA reports)
CONDITION AGGRAVATED ( 216 FDA reports)
TINNITUS ( 216 FDA reports)
CONFUSIONAL STATE ( 212 FDA reports)
LEUKOCYTOSIS ( 212 FDA reports)
DYSLIPIDAEMIA ( 211 FDA reports)
IRRITABLE BOWEL SYNDROME ( 211 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 210 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 210 FDA reports)
NEPHROLITHIASIS ( 210 FDA reports)
ABDOMINAL PAIN UPPER ( 208 FDA reports)
SKIN LESION ( 208 FDA reports)
VERTIGO ( 208 FDA reports)
STRESS ( 206 FDA reports)
DRY MOUTH ( 206 FDA reports)
OEDEMA ( 206 FDA reports)
BREAST CANCER ( 205 FDA reports)
ERYTHEMA ( 205 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 205 FDA reports)
CYST ( 201 FDA reports)
HAEMATOMA ( 201 FDA reports)
HAND FRACTURE ( 201 FDA reports)
RADICULOPATHY ( 200 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 199 FDA reports)
MEMORY IMPAIRMENT ( 198 FDA reports)
SINUS DISORDER ( 198 FDA reports)
TACHYCARDIA ( 195 FDA reports)
BONE PAIN ( 194 FDA reports)
TIBIA FRACTURE ( 193 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 192 FDA reports)
MIGRAINE ( 191 FDA reports)
CONVULSION ( 190 FDA reports)
HOT FLUSH ( 190 FDA reports)
ALOPECIA ( 188 FDA reports)
MULTIPLE FRACTURES ( 188 FDA reports)
ORAL INFECTION ( 188 FDA reports)
BREAST DISORDER ( 187 FDA reports)
DRUG INTERACTION ( 187 FDA reports)
RESPIRATORY FAILURE ( 187 FDA reports)
LACERATION ( 186 FDA reports)
ABDOMINAL DISCOMFORT ( 185 FDA reports)
CERUMEN IMPACTION ( 185 FDA reports)
DYSPHONIA ( 181 FDA reports)
RADIUS FRACTURE ( 181 FDA reports)
RESTLESS LEGS SYNDROME ( 181 FDA reports)
ATROPHIC VULVOVAGINITIS ( 180 FDA reports)
JAW DISORDER ( 180 FDA reports)
JOINT DISLOCATION ( 179 FDA reports)
DYSURIA ( 177 FDA reports)
FIBROMYALGIA ( 175 FDA reports)
IRON DEFICIENCY ANAEMIA ( 174 FDA reports)
JOINT INJURY ( 174 FDA reports)
HAEMATURIA ( 173 FDA reports)
PLEURAL EFFUSION ( 173 FDA reports)
CHOLELITHIASIS ( 172 FDA reports)
INJURY ( 172 FDA reports)
PULMONARY FIBROSIS ( 172 FDA reports)
TOOTH EXTRACTION ( 172 FDA reports)
EMOTIONAL DISTRESS ( 171 FDA reports)
SLEEP APNOEA SYNDROME ( 170 FDA reports)
STAPHYLOCOCCAL INFECTION ( 170 FDA reports)
RECTAL HAEMORRHAGE ( 169 FDA reports)
URINARY RETENTION ( 166 FDA reports)
CYSTITIS ( 165 FDA reports)
NASOPHARYNGITIS ( 163 FDA reports)
SYNOVIAL CYST ( 163 FDA reports)
VISION BLURRED ( 163 FDA reports)
STRESS URINARY INCONTINENCE ( 160 FDA reports)
CARDIOMEGALY ( 160 FDA reports)
EXCORIATION ( 160 FDA reports)
FIBULA FRACTURE ( 160 FDA reports)
ATELECTASIS ( 159 FDA reports)
GLAUCOMA ( 156 FDA reports)
ESSENTIAL HYPERTENSION ( 155 FDA reports)
INCREASED TENDENCY TO BRUISE ( 154 FDA reports)
INJECTION SITE PAIN ( 154 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 154 FDA reports)
TYPE 2 DIABETES MELLITUS ( 153 FDA reports)
URTICARIA ( 153 FDA reports)
OROPHARYNGEAL PAIN ( 152 FDA reports)
BACK DISORDER ( 151 FDA reports)
CHEST DISCOMFORT ( 151 FDA reports)
DIVERTICULUM INTESTINAL ( 150 FDA reports)
LIMB INJURY ( 150 FDA reports)
EYE DISORDER ( 149 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 149 FDA reports)
LOSS OF CONSCIOUSNESS ( 149 FDA reports)
BLOOD GLUCOSE INCREASED ( 147 FDA reports)
DYSPNOEA EXERTIONAL ( 146 FDA reports)
THROMBOSIS ( 146 FDA reports)
GINGIVAL BLEEDING ( 145 FDA reports)
BUNION ( 144 FDA reports)
DEATH ( 144 FDA reports)
LIMB ASYMMETRY ( 144 FDA reports)
MITRAL VALVE INCOMPETENCE ( 144 FDA reports)
PATHOLOGICAL FRACTURE ( 143 FDA reports)
PLATELET COUNT DECREASED ( 143 FDA reports)
TOOTH ABSCESS ( 143 FDA reports)
RENAL FAILURE CHRONIC ( 142 FDA reports)
VARICOSE VEIN ( 141 FDA reports)
STOMATITIS ( 140 FDA reports)
DIVERTICULITIS ( 140 FDA reports)
LUNG DISORDER ( 140 FDA reports)
MITRAL VALVE PROLAPSE ( 139 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 139 FDA reports)
COLON ADENOMA ( 138 FDA reports)
BODY HEIGHT DECREASED ( 137 FDA reports)
CYSTOCELE ( 137 FDA reports)
LYMPHADENOPATHY ( 137 FDA reports)
CARDIAC FAILURE ( 136 FDA reports)
NOCTURIA ( 136 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 136 FDA reports)
PUBIS FRACTURE ( 135 FDA reports)
ECZEMA ( 134 FDA reports)
KYPHOSIS ( 134 FDA reports)
PAIN IN JAW ( 134 FDA reports)
ABDOMINAL DISTENSION ( 133 FDA reports)
BLOOD CREATININE INCREASED ( 133 FDA reports)
CAROTID ARTERY STENOSIS ( 133 FDA reports)
DRUG INTOLERANCE ( 133 FDA reports)
PERIODONTAL DISEASE ( 133 FDA reports)
BONE LOSS ( 132 FDA reports)
GROIN PAIN ( 132 FDA reports)
THROMBOCYTOPENIA ( 132 FDA reports)
TRIGGER FINGER ( 131 FDA reports)
UPPER LIMB FRACTURE ( 131 FDA reports)
BRADYCARDIA ( 131 FDA reports)
OESOPHAGITIS ( 131 FDA reports)
EMPHYSEMA ( 130 FDA reports)
EPISTAXIS ( 130 FDA reports)
TOOTHACHE ( 130 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 129 FDA reports)
ABSCESS ( 128 FDA reports)
BLADDER DISORDER ( 127 FDA reports)
COMPRESSION FRACTURE ( 127 FDA reports)
HEPATIC STEATOSIS ( 127 FDA reports)
FUNGAL INFECTION ( 126 FDA reports)
RENAL IMPAIRMENT ( 126 FDA reports)
TREMOR ( 126 FDA reports)
CHILLS ( 125 FDA reports)
HYPERGLYCAEMIA ( 125 FDA reports)
OSTEOGENESIS IMPERFECTA ( 125 FDA reports)
AMNESIA ( 124 FDA reports)
PLANTAR FASCIITIS ( 124 FDA reports)
SOMNOLENCE ( 124 FDA reports)
VISUAL IMPAIRMENT ( 124 FDA reports)
OBESITY ( 122 FDA reports)
PANIC ATTACK ( 122 FDA reports)
OFF LABEL USE ( 121 FDA reports)
NEURALGIA ( 120 FDA reports)
ARRHYTHMIA ( 119 FDA reports)
GASTRIC ULCER ( 119 FDA reports)
SPINAL FRACTURE ( 118 FDA reports)
TENDON DISORDER ( 118 FDA reports)
HEAD INJURY ( 117 FDA reports)
HYPERHIDROSIS ( 117 FDA reports)
ACUTE SINUSITIS ( 116 FDA reports)
ANGINA PECTORIS ( 116 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 116 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 116 FDA reports)
SKIN DISORDER ( 116 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 116 FDA reports)
TOOTH INFECTION ( 115 FDA reports)
ECCHYMOSIS ( 115 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 115 FDA reports)
ARTERIOSCLEROSIS ( 114 FDA reports)
DEAFNESS ( 114 FDA reports)
MICTURITION URGENCY ( 114 FDA reports)
TREATMENT NONCOMPLIANCE ( 114 FDA reports)
LIVER DISORDER ( 113 FDA reports)
SEBORRHOEIC KERATOSIS ( 113 FDA reports)
VITAMIN B12 DEFICIENCY ( 112 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 111 FDA reports)
FEELING ABNORMAL ( 111 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 111 FDA reports)
HYPERCALCAEMIA ( 111 FDA reports)
PANCYTOPENIA ( 111 FDA reports)
HAEMATOCHEZIA ( 110 FDA reports)
HYPOXIA ( 110 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 110 FDA reports)
HYPERTONIC BLADDER ( 107 FDA reports)
MOBILITY DECREASED ( 107 FDA reports)
PULMONARY HYPERTENSION ( 107 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 106 FDA reports)
NIGHT SWEATS ( 106 FDA reports)
EAR PAIN ( 105 FDA reports)
SKIN ULCER ( 105 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 104 FDA reports)
GOITRE ( 103 FDA reports)
MASS ( 103 FDA reports)
ONYCHOMYCOSIS ( 103 FDA reports)
INCORRECT DOSE ADMINISTERED ( 102 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 102 FDA reports)
DRY SKIN ( 101 FDA reports)
APHTHOUS STOMATITIS ( 100 FDA reports)
FEAR OF DISEASE ( 100 FDA reports)
PERIODONTITIS ( 100 FDA reports)
PEPTIC ULCER ( 99 FDA reports)
BREAST CALCIFICATIONS ( 98 FDA reports)
COLITIS ( 97 FDA reports)
GINGIVITIS ( 97 FDA reports)
HAEMORRHAGE ( 97 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 96 FDA reports)
PRESYNCOPE ( 96 FDA reports)
FLATULENCE ( 95 FDA reports)
GOUT ( 95 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 95 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 94 FDA reports)
BLOOD PRESSURE DECREASED ( 94 FDA reports)
HYPERPARATHYROIDISM ( 94 FDA reports)
POOR QUALITY SLEEP ( 94 FDA reports)
ANHEDONIA ( 93 FDA reports)
NEUTROPENIA ( 93 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 93 FDA reports)
SWELLING ( 92 FDA reports)
ANXIETY DISORDER ( 92 FDA reports)
BLOOD UREA INCREASED ( 92 FDA reports)
HAEMATOCRIT DECREASED ( 92 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 92 FDA reports)
ORAL TORUS ( 92 FDA reports)
FLUSHING ( 91 FDA reports)
LOWER LIMB FRACTURE ( 91 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 91 FDA reports)
INJECTION SITE ERYTHEMA ( 90 FDA reports)
OVARIAN CYST ( 90 FDA reports)
THYROID DISORDER ( 90 FDA reports)
GASTROENTERITIS ( 89 FDA reports)
PELVIC FRACTURE ( 89 FDA reports)
PSORIASIS ( 89 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 88 FDA reports)
RENAL DISORDER ( 88 FDA reports)
ROSACEA ( 88 FDA reports)
SENSITIVITY OF TEETH ( 88 FDA reports)
WHEEZING ( 88 FDA reports)
VENOUS INSUFFICIENCY ( 87 FDA reports)
TOOTH LOSS ( 85 FDA reports)
ACTINIC KERATOSIS ( 85 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 85 FDA reports)
MAJOR DEPRESSION ( 85 FDA reports)
GASTRIC POLYPS ( 84 FDA reports)
PANCREATITIS ( 84 FDA reports)
SEPTIC SHOCK ( 84 FDA reports)
HYPOAESTHESIA ORAL ( 82 FDA reports)
INFLAMMATION ( 82 FDA reports)
MENTAL DISORDER ( 82 FDA reports)
SKIN CANCER ( 82 FDA reports)
VISUAL ACUITY REDUCED ( 82 FDA reports)
ULCER ( 81 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 81 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 81 FDA reports)
DRY EYE ( 81 FDA reports)
FEMORAL NECK FRACTURE ( 81 FDA reports)
HEPATIC ENZYME INCREASED ( 81 FDA reports)
SINUS TACHYCARDIA ( 81 FDA reports)
ADENOIDAL DISORDER ( 80 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 80 FDA reports)
BLINDNESS ( 80 FDA reports)
BLOOD POTASSIUM DECREASED ( 80 FDA reports)
CARDIAC ARREST ( 80 FDA reports)
LARYNGITIS ( 80 FDA reports)
URGE INCONTINENCE ( 80 FDA reports)
ULNA FRACTURE ( 79 FDA reports)
QUALITY OF LIFE DECREASED ( 79 FDA reports)
SEASONAL ALLERGY ( 79 FDA reports)
DEMENTIA ( 78 FDA reports)
HEART RATE INCREASED ( 78 FDA reports)
HYPERKALAEMIA ( 78 FDA reports)
NASAL CONGESTION ( 78 FDA reports)
RECTOCELE ( 78 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 77 FDA reports)
BREAST CYST ( 77 FDA reports)
BREAST MASS ( 77 FDA reports)
FLANK PAIN ( 77 FDA reports)
INFLUENZA ( 77 FDA reports)
MOUTH ULCERATION ( 77 FDA reports)
SJOGREN'S SYNDROME ( 77 FDA reports)
THYROID NEOPLASM ( 77 FDA reports)
DERMAL CYST ( 76 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 76 FDA reports)
PATELLA FRACTURE ( 76 FDA reports)
SCAR ( 76 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 74 FDA reports)
OSTEITIS ( 74 FDA reports)
PERIARTHRITIS ( 74 FDA reports)
SURGERY ( 74 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 74 FDA reports)
SYNOVITIS ( 73 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 73 FDA reports)
BRONCHITIS CHRONIC ( 73 FDA reports)
EPICONDYLITIS ( 73 FDA reports)
LIMB DISCOMFORT ( 73 FDA reports)
METASTASES TO BONE ( 73 FDA reports)
PRODUCTIVE COUGH ( 73 FDA reports)
CEREBRAL INFARCTION ( 72 FDA reports)
DYSGEUSIA ( 72 FDA reports)
FISTULA DISCHARGE ( 72 FDA reports)
MULTIPLE INJURIES ( 72 FDA reports)
ORAL CAVITY FISTULA ( 72 FDA reports)
DERMATITIS CONTACT ( 71 FDA reports)
HYPOGLYCAEMIA ( 71 FDA reports)
NASAL SEPTUM DEVIATION ( 71 FDA reports)
TENOSYNOVITIS ( 71 FDA reports)
SUICIDAL IDEATION ( 70 FDA reports)
UTERINE LEIOMYOMA ( 70 FDA reports)
CHRONIC SINUSITIS ( 70 FDA reports)
HEART RATE IRREGULAR ( 70 FDA reports)
MUSCULOSKELETAL DISORDER ( 70 FDA reports)
PHARYNGITIS ( 70 FDA reports)
ATROPHY ( 69 FDA reports)
HUMERUS FRACTURE ( 69 FDA reports)
INGROWING NAIL ( 69 FDA reports)
RECTAL POLYP ( 69 FDA reports)
VIRAL INFECTION ( 69 FDA reports)
VITAMIN D DECREASED ( 69 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 68 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 68 FDA reports)
CERVICOBRACHIAL SYNDROME ( 67 FDA reports)
DERMATITIS ( 67 FDA reports)
HERNIA ( 67 FDA reports)
JOINT STIFFNESS ( 67 FDA reports)
LIPOMA ( 67 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 67 FDA reports)
RHABDOMYOLYSIS ( 67 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 67 FDA reports)
CAROTID BRUIT ( 66 FDA reports)
GASTROENTERITIS VIRAL ( 66 FDA reports)
HYPERKERATOSIS ( 66 FDA reports)
HYPOACUSIS ( 66 FDA reports)
SACROILIITIS ( 66 FDA reports)
ABASIA ( 65 FDA reports)
BONE CYST ( 65 FDA reports)
HYPOCALCAEMIA ( 65 FDA reports)
MUSCLE INJURY ( 65 FDA reports)
MYOCARDIAL ISCHAEMIA ( 65 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 65 FDA reports)
DRUG ADMINISTRATION ERROR ( 64 FDA reports)
GASTRIC DISORDER ( 64 FDA reports)
HEPATIC CYST ( 64 FDA reports)
NODULE ( 64 FDA reports)
PERONEAL NERVE PALSY ( 64 FDA reports)
POLYARTHRITIS ( 64 FDA reports)
RESPIRATORY TRACT INFECTION ( 64 FDA reports)
SINUS BRADYCARDIA ( 64 FDA reports)
SKIN DISCOLOURATION ( 64 FDA reports)
COGNITIVE DISORDER ( 63 FDA reports)
FISTULA ( 63 FDA reports)
HALLUCINATION ( 63 FDA reports)
RESPIRATORY DISORDER ( 63 FDA reports)
BLOOD DISORDER ( 62 FDA reports)
BURNING SENSATION ( 62 FDA reports)
CARDIOVASCULAR DISORDER ( 62 FDA reports)
GINGIVAL PAIN ( 62 FDA reports)
JOINT CREPITATION ( 62 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 61 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 61 FDA reports)
MACULAR DEGENERATION ( 61 FDA reports)
MUSCLE ATROPHY ( 61 FDA reports)
OVARIAN DISORDER ( 61 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 61 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 61 FDA reports)
ACNE ( 60 FDA reports)
BARRETT'S OESOPHAGUS ( 60 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 60 FDA reports)
DIASTOLIC DYSFUNCTION ( 60 FDA reports)
HAEMATEMESIS ( 60 FDA reports)
LICHENOID KERATOSIS ( 60 FDA reports)
MEDICAL DEVICE COMPLICATION ( 60 FDA reports)
MENTAL STATUS CHANGES ( 60 FDA reports)
OTITIS MEDIA ( 60 FDA reports)
OXYGEN SATURATION DECREASED ( 60 FDA reports)
PANCREATITIS ACUTE ( 60 FDA reports)
PULMONARY OEDEMA ( 60 FDA reports)
SKELETAL INJURY ( 60 FDA reports)
COLITIS ISCHAEMIC ( 59 FDA reports)
HEPATITIS ( 59 FDA reports)
HORMONE LEVEL ABNORMAL ( 59 FDA reports)
INCISIONAL HERNIA ( 59 FDA reports)
INJECTION SITE PRURITUS ( 59 FDA reports)
LUNG INFILTRATION ( 59 FDA reports)
OTITIS EXTERNA ( 59 FDA reports)
PRODUCT QUALITY ISSUE ( 59 FDA reports)
ACROCHORDON ( 58 FDA reports)
BACK INJURY ( 58 FDA reports)
BLOOD CALCIUM INCREASED ( 58 FDA reports)
DEVICE BREAKAGE ( 58 FDA reports)
DRUG ERUPTION ( 58 FDA reports)
HYPOMAGNESAEMIA ( 58 FDA reports)
LETHARGY ( 58 FDA reports)
MELANOCYTIC NAEVUS ( 58 FDA reports)
NEPHROPATHY ( 58 FDA reports)
NERVE COMPRESSION ( 58 FDA reports)
OESOPHAGEAL ULCER ( 58 FDA reports)
PELVIC PAIN ( 58 FDA reports)
PYELONEPHRITIS ( 58 FDA reports)
CERVICAL SPINAL STENOSIS ( 57 FDA reports)
ISCHAEMIA ( 57 FDA reports)
JAW FRACTURE ( 57 FDA reports)
LEUKOPENIA ( 57 FDA reports)
RETINAL TEAR ( 57 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 56 FDA reports)
DRUG EFFECT DECREASED ( 56 FDA reports)
EAR INFECTION ( 56 FDA reports)
NERVOUSNESS ( 56 FDA reports)
OESTROGEN DEFICIENCY ( 56 FDA reports)
ORAL PAIN ( 56 FDA reports)
SPONDYLITIS ( 56 FDA reports)
VASCULAR CALCIFICATION ( 55 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 55 FDA reports)
FACET JOINT SYNDROME ( 55 FDA reports)
FAECAL INCONTINENCE ( 55 FDA reports)
INJECTION SITE HAEMORRHAGE ( 55 FDA reports)
RETINAL DETACHMENT ( 55 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 54 FDA reports)
FRACTURE DISPLACEMENT ( 54 FDA reports)
HAEMANGIOMA ( 54 FDA reports)
MULTI-ORGAN FAILURE ( 54 FDA reports)
OESOPHAGEAL STENOSIS ( 54 FDA reports)
ORTHOSTATIC HYPOTENSION ( 54 FDA reports)
PERICARDIAL EFFUSION ( 54 FDA reports)
SKIN PAPILLOMA ( 54 FDA reports)
AORTIC STENOSIS ( 53 FDA reports)
CANDIDIASIS ( 53 FDA reports)
DEAFNESS NEUROSENSORY ( 53 FDA reports)
DYSARTHRIA ( 53 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 53 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 53 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 53 FDA reports)
INGUINAL HERNIA ( 53 FDA reports)
INTERMITTENT CLAUDICATION ( 53 FDA reports)
INTESTINAL OBSTRUCTION ( 53 FDA reports)
JAUNDICE ( 53 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 53 FDA reports)
MALIGNANT MELANOMA ( 53 FDA reports)
MELAENA ( 53 FDA reports)
SINUS CONGESTION ( 53 FDA reports)
SWELLING FACE ( 53 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 52 FDA reports)
AZOTAEMIA ( 52 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 52 FDA reports)
DELIRIUM ( 52 FDA reports)
INFLUENZA LIKE ILLNESS ( 52 FDA reports)
PRURITUS GENERALISED ( 52 FDA reports)
CHOLECYSTITIS ( 51 FDA reports)
CONCUSSION ( 51 FDA reports)
CONJUNCTIVITIS ( 51 FDA reports)
LOOSE TOOTH ( 51 FDA reports)
MULTIPLE MYELOMA ( 51 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 51 FDA reports)
VAGINAL DISCHARGE ( 51 FDA reports)
TENDON RUPTURE ( 50 FDA reports)
BLISTER ( 50 FDA reports)
BRONCHOPNEUMONIA ( 50 FDA reports)
CARDIAC VALVE DISEASE ( 50 FDA reports)
CARDIOMYOPATHY ( 50 FDA reports)
CAROTID ARTERY OCCLUSION ( 50 FDA reports)
EATING DISORDER ( 50 FDA reports)
FLUID RETENTION ( 50 FDA reports)
GINGIVAL RECESSION ( 50 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 50 FDA reports)
PURULENT DISCHARGE ( 50 FDA reports)
SEROMA ( 50 FDA reports)
CEREBRAL ATROPHY ( 49 FDA reports)
DRUG DOSE OMISSION ( 49 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 49 FDA reports)
ORAL HERPES ( 49 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 49 FDA reports)
SQUAMOUS CELL CARCINOMA ( 49 FDA reports)
VIITH NERVE PARALYSIS ( 49 FDA reports)
WOUND INFECTION ( 48 FDA reports)
BACTERIAL INFECTION ( 48 FDA reports)
CROHN'S DISEASE ( 48 FDA reports)
ENDOMETRIOSIS ( 48 FDA reports)
FRACTURED SACRUM ( 48 FDA reports)
LABORATORY TEST ABNORMAL ( 48 FDA reports)
METATARSALGIA ( 48 FDA reports)
MYOSITIS ( 48 FDA reports)
OCCULT BLOOD POSITIVE ( 48 FDA reports)
PNEUMONIA ASPIRATION ( 48 FDA reports)
ABSCESS ORAL ( 47 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 47 FDA reports)
BLOOD BILIRUBIN INCREASED ( 47 FDA reports)
CARDIO-RESPIRATORY ARREST ( 47 FDA reports)
CEREBRAL HAEMORRHAGE ( 47 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 47 FDA reports)
MERALGIA PARAESTHETICA ( 47 FDA reports)
PNEUMOTHORAX ( 47 FDA reports)
CALCULUS URETERIC ( 46 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 46 FDA reports)
POST PROCEDURAL COMPLICATION ( 46 FDA reports)
POST PROCEDURAL INFECTION ( 46 FDA reports)
RHINORRHOEA ( 46 FDA reports)
TENSION HEADACHE ( 46 FDA reports)
ABDOMINAL PAIN LOWER ( 45 FDA reports)
AORTIC VALVE INCOMPETENCE ( 45 FDA reports)
DIPLOPIA ( 45 FDA reports)
FEAR ( 45 FDA reports)
HEARING IMPAIRED ( 45 FDA reports)
HYPERTHYROIDISM ( 45 FDA reports)
JOINT INSTABILITY ( 45 FDA reports)
LOCALISED INFECTION ( 45 FDA reports)
LYMPHOMA ( 45 FDA reports)
MYOPATHY ( 45 FDA reports)
NEURITIS ( 45 FDA reports)
POLYMYALGIA RHEUMATICA ( 45 FDA reports)
SPEECH DISORDER ( 45 FDA reports)
ACCIDENTAL EXPOSURE ( 44 FDA reports)
BLOOD CALCIUM DECREASED ( 44 FDA reports)
BREAST CANCER IN SITU ( 44 FDA reports)
CHONDROCALCINOSIS ( 44 FDA reports)
PROTEINURIA ( 44 FDA reports)
VASCULITIS ( 44 FDA reports)
BENIGN NEOPLASM ( 43 FDA reports)
DIABETIC RETINOPATHY ( 43 FDA reports)
DYSSTASIA ( 43 FDA reports)
EAR DISORDER ( 43 FDA reports)
ESCHERICHIA INFECTION ( 43 FDA reports)
EXPOSED BONE IN JAW ( 43 FDA reports)
GASTRITIS EROSIVE ( 43 FDA reports)
LARYNGEAL OEDEMA ( 43 FDA reports)
RESPIRATORY DISTRESS ( 43 FDA reports)
ANGIOPATHY ( 42 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 42 FDA reports)
EYE PAIN ( 42 FDA reports)
HAEMOPTYSIS ( 42 FDA reports)
HYPERTENSIVE HEART DISEASE ( 42 FDA reports)
INJECTION SITE IRRITATION ( 42 FDA reports)
LIMB DEFORMITY ( 42 FDA reports)
LIPIDS INCREASED ( 42 FDA reports)
MALNUTRITION ( 42 FDA reports)
ORAL CANDIDIASIS ( 42 FDA reports)
RADICULAR PAIN ( 42 FDA reports)
ATYPICAL FEMUR FRACTURE ( 41 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 41 FDA reports)
CHONDROPATHY ( 41 FDA reports)
CHROMATURIA ( 41 FDA reports)
DEVICE RELATED INFECTION ( 41 FDA reports)
DISORIENTATION ( 41 FDA reports)
HELICOBACTER GASTRITIS ( 41 FDA reports)
HYPOALBUMINAEMIA ( 41 FDA reports)
KNEE ARTHROPLASTY ( 41 FDA reports)
MAMMOGRAM ABNORMAL ( 41 FDA reports)
PLEURISY ( 41 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 41 FDA reports)
RADICULITIS LUMBOSACRAL ( 41 FDA reports)
SINUS HEADACHE ( 41 FDA reports)
SKIN EXFOLIATION ( 41 FDA reports)
STASIS DERMATITIS ( 41 FDA reports)
VENTRICULAR TACHYCARDIA ( 41 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 40 FDA reports)
ACUTE RESPIRATORY FAILURE ( 40 FDA reports)
BODY TEMPERATURE INCREASED ( 40 FDA reports)
CEREBRAL ISCHAEMIA ( 40 FDA reports)
FACE INJURY ( 40 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 40 FDA reports)
KYPHOSCOLIOSIS ( 40 FDA reports)
LEFT ATRIAL DILATATION ( 40 FDA reports)
POST PROCEDURAL CONSTIPATION ( 40 FDA reports)
RHINITIS ( 40 FDA reports)
ARTHROPOD BITE ( 39 FDA reports)
BLOOD SODIUM DECREASED ( 39 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 39 FDA reports)
BONE METABOLISM DISORDER ( 39 FDA reports)
DYSTHYMIC DISORDER ( 39 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 39 FDA reports)
HAIR TEXTURE ABNORMAL ( 39 FDA reports)
HYDRONEPHROSIS ( 39 FDA reports)
INJECTION SITE SWELLING ( 39 FDA reports)
LABYRINTHITIS ( 39 FDA reports)
MEDICATION ERROR ( 39 FDA reports)
NECROSIS ( 39 FDA reports)
PAIN OF SKIN ( 39 FDA reports)
POLYP COLORECTAL ( 39 FDA reports)
TENOSYNOVITIS STENOSANS ( 39 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 39 FDA reports)
TUBERCULOSIS ( 39 FDA reports)
VAGINAL INFECTION ( 38 FDA reports)
VULVOVAGINAL DRYNESS ( 38 FDA reports)
ASCITES ( 38 FDA reports)
ATAXIA ( 38 FDA reports)
BLOOD ALBUMIN DECREASED ( 38 FDA reports)
CAROTID ARTERY DISEASE ( 38 FDA reports)
ELECTROLYTE IMBALANCE ( 38 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 38 FDA reports)
INCONTINENCE ( 38 FDA reports)
LIGAMENT RUPTURE ( 38 FDA reports)
OSTEOSCLEROSIS ( 38 FDA reports)
PARKINSON'S DISEASE ( 38 FDA reports)
AGITATION ( 37 FDA reports)
ALCOHOL ABUSE ( 37 FDA reports)
ANOREXIA ( 37 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 37 FDA reports)
BONE MARROW FAILURE ( 37 FDA reports)
BRUXISM ( 37 FDA reports)
CIRCULATORY COLLAPSE ( 37 FDA reports)
COAGULOPATHY ( 37 FDA reports)
DEAFNESS BILATERAL ( 37 FDA reports)
ECONOMIC PROBLEM ( 37 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 37 FDA reports)
HYPOVOLAEMIA ( 37 FDA reports)
LIGAMENT DISORDER ( 37 FDA reports)
MENOPAUSE ( 37 FDA reports)
METABOLIC ACIDOSIS ( 37 FDA reports)
MIXED INCONTINENCE ( 37 FDA reports)
MONARTHRITIS ( 37 FDA reports)
NEOPLASM MALIGNANT ( 37 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 37 FDA reports)
RENAL ARTERY STENOSIS ( 37 FDA reports)
SNORING ( 37 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 37 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
TEMPERATURE INTOLERANCE ( 36 FDA reports)
ADENOMA BENIGN ( 36 FDA reports)
COSTOCHONDRITIS ( 36 FDA reports)
DISCOMFORT ( 36 FDA reports)
DRUG ABUSE ( 36 FDA reports)
FEBRILE NEUTROPENIA ( 36 FDA reports)
GRIEF REACTION ( 36 FDA reports)
INJECTION SITE BURNING ( 36 FDA reports)
LOBAR PNEUMONIA ( 36 FDA reports)
MYELODYSPLASTIC SYNDROME ( 36 FDA reports)
POLYP ( 36 FDA reports)
SHOCK ( 36 FDA reports)
AGGRESSION ( 35 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 35 FDA reports)
ARTHRITIS BACTERIAL ( 35 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 35 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 35 FDA reports)
FALLOPIAN TUBE DISORDER ( 35 FDA reports)
FOREIGN BODY ( 35 FDA reports)
HYPOPHAGIA ( 35 FDA reports)
PHLEBITIS ( 35 FDA reports)
PHLEBOLITH ( 35 FDA reports)
PNEUMONIA BACTERIAL ( 35 FDA reports)
POLYNEUROPATHY ( 35 FDA reports)
PSORIATIC ARTHROPATHY ( 35 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 35 FDA reports)
SICK SINUS SYNDROME ( 35 FDA reports)
SMEAR CERVIX ABNORMAL ( 35 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 35 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 34 FDA reports)
VAGINAL HAEMORRHAGE ( 34 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 34 FDA reports)
BENIGN NEOPLASM OF SKIN ( 34 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 34 FDA reports)
BLOOD POTASSIUM INCREASED ( 34 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 34 FDA reports)
CONNECTIVE TISSUE DISORDER ( 34 FDA reports)
CORNEAL ABRASION ( 34 FDA reports)
DEVICE DISLOCATION ( 34 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 34 FDA reports)
DYSKINESIA ( 34 FDA reports)
DYSPAREUNIA ( 34 FDA reports)
FEELING JITTERY ( 34 FDA reports)
FRACTURED COCCYX ( 34 FDA reports)
GINGIVAL SWELLING ( 34 FDA reports)
GRANULOMA ( 34 FDA reports)
HEART RATE DECREASED ( 34 FDA reports)
HYSTERECTOMY ( 34 FDA reports)
IMMUNE SYSTEM DISORDER ( 34 FDA reports)
IMMUNOSUPPRESSION ( 34 FDA reports)
INCISION SITE CELLULITIS ( 34 FDA reports)
LUNG INFECTION ( 34 FDA reports)
NERVE INJURY ( 34 FDA reports)
NEUTROPHIL COUNT DECREASED ( 34 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 34 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 34 FDA reports)
PULMONARY GRANULOMA ( 34 FDA reports)
RAYNAUD'S PHENOMENON ( 34 FDA reports)
BRONCHIECTASIS ( 33 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 33 FDA reports)
ENCEPHALOPATHY ( 33 FDA reports)
EPILEPSY ( 33 FDA reports)
EYE INFECTION ( 33 FDA reports)
EYELID PTOSIS ( 33 FDA reports)
FURUNCLE ( 33 FDA reports)
GLOSSODYNIA ( 33 FDA reports)
LUNG NEOPLASM MALIGNANT ( 33 FDA reports)
MUSCLE RUPTURE ( 33 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 33 FDA reports)
SEDATION ( 33 FDA reports)
SENSORY DISTURBANCE ( 33 FDA reports)
UNEVALUABLE EVENT ( 33 FDA reports)
UROSEPSIS ( 33 FDA reports)
VAGINAL DISORDER ( 33 FDA reports)
VITREOUS DETACHMENT ( 33 FDA reports)
AFFECTIVE DISORDER ( 32 FDA reports)
BLOOD URINE PRESENT ( 32 FDA reports)
DECUBITUS ULCER ( 32 FDA reports)
FACIAL PAIN ( 32 FDA reports)
FIBROADENOMA OF BREAST ( 32 FDA reports)
FRACTURE MALUNION ( 32 FDA reports)
JOINT CONTRACTURE ( 32 FDA reports)
LACUNAR INFARCTION ( 32 FDA reports)
MALABSORPTION ( 32 FDA reports)
MOVEMENT DISORDER ( 32 FDA reports)
NEUROGENIC BLADDER ( 32 FDA reports)
PERIORBITAL HAEMATOMA ( 32 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 32 FDA reports)
RASH GENERALISED ( 32 FDA reports)
SOFT TISSUE INFECTION ( 32 FDA reports)
BLADDER PROLAPSE ( 31 FDA reports)
BLEPHARITIS ( 31 FDA reports)
BREAST PAIN ( 31 FDA reports)
COMPLETED SUICIDE ( 31 FDA reports)
DIZZINESS POSTURAL ( 31 FDA reports)
DUODENITIS ( 31 FDA reports)
ENTEROCOLITIS ( 31 FDA reports)
FACE OEDEMA ( 31 FDA reports)
HIP ARTHROPLASTY ( 31 FDA reports)
HYPERSOMNIA ( 31 FDA reports)
MALIGNANT HYPERTENSION ( 31 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 31 FDA reports)
OESOPHAGEAL DISORDER ( 31 FDA reports)
PROCEDURAL PAIN ( 31 FDA reports)
RASH ERYTHEMATOUS ( 31 FDA reports)
RASH PRURITIC ( 31 FDA reports)
SKIN INFECTION ( 31 FDA reports)
STERNAL FRACTURE ( 31 FDA reports)
TONGUE DISCOLOURATION ( 31 FDA reports)
TOOTH DISCOLOURATION ( 31 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 31 FDA reports)
VISUAL FIELD DEFECT ( 31 FDA reports)
WOUND ( 30 FDA reports)
ILL-DEFINED DISORDER ( 30 FDA reports)
JOINT SPRAIN ( 30 FDA reports)
LIP SWELLING ( 30 FDA reports)
LOCAL SWELLING ( 30 FDA reports)
NO THERAPEUTIC RESPONSE ( 30 FDA reports)
PROTEIN TOTAL DECREASED ( 30 FDA reports)
SEROTONIN SYNDROME ( 30 FDA reports)
ABDOMINAL TENDERNESS ( 29 FDA reports)
ADRENAL INSUFFICIENCY ( 29 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 29 FDA reports)
CEREBROVASCULAR DISORDER ( 29 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 29 FDA reports)
FACIAL BONES FRACTURE ( 29 FDA reports)
FAECES DISCOLOURED ( 29 FDA reports)
FOOD ALLERGY ( 29 FDA reports)
HELICOBACTER INFECTION ( 29 FDA reports)
HYPOPARATHYROIDISM ( 29 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 29 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 29 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 29 FDA reports)
MACROCYTOSIS ( 29 FDA reports)
MITRAL VALVE CALCIFICATION ( 29 FDA reports)
NEPHROTIC SYNDROME ( 29 FDA reports)
OPEN WOUND ( 29 FDA reports)
OPTIC NEURITIS ( 29 FDA reports)
RETINAL DISORDER ( 29 FDA reports)
SKIN INDURATION ( 29 FDA reports)
SPINAL CORD COMPRESSION ( 29 FDA reports)
SPLENOMEGALY ( 29 FDA reports)
TENDERNESS ( 29 FDA reports)
TINEA PEDIS ( 29 FDA reports)
TREATMENT FAILURE ( 29 FDA reports)
URETHRAL CARUNCLE ( 29 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 29 FDA reports)
THROAT IRRITATION ( 28 FDA reports)
UTERINE POLYP ( 28 FDA reports)
VERTIGO POSITIONAL ( 28 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 28 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 28 FDA reports)
BONE FRAGMENTATION ( 28 FDA reports)
CHEILITIS ( 28 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 28 FDA reports)
DENTAL FISTULA ( 28 FDA reports)
DUODENAL ULCER ( 28 FDA reports)
ERECTILE DYSFUNCTION ( 28 FDA reports)
FUNGAL SKIN INFECTION ( 28 FDA reports)
HEPATIC FAILURE ( 28 FDA reports)
HIP DEFORMITY ( 28 FDA reports)
IRRITABILITY ( 28 FDA reports)
MYOPIA ( 28 FDA reports)
ORGANISING PNEUMONIA ( 28 FDA reports)
PLEURAL FIBROSIS ( 28 FDA reports)
PNEUMONITIS ( 28 FDA reports)
POST LAMINECTOMY SYNDROME ( 28 FDA reports)
PRESBYOPIA ( 28 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 28 FDA reports)
ABSCESS JAW ( 27 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 27 FDA reports)
CARTILAGE INJURY ( 27 FDA reports)
CLAVICLE FRACTURE ( 27 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 27 FDA reports)
DISEASE PROGRESSION ( 27 FDA reports)
ENTHESOPATHY ( 27 FDA reports)
FEELING HOT ( 27 FDA reports)
HAEMARTHROSIS ( 27 FDA reports)
INTESTINAL POLYP ( 27 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 27 FDA reports)
MENTAL IMPAIRMENT ( 27 FDA reports)
METASTATIC NEOPLASM ( 27 FDA reports)
OSTEOMALACIA ( 27 FDA reports)
OTITIS MEDIA ACUTE ( 27 FDA reports)
PHYSICAL DISABILITY ( 27 FDA reports)
PROCTALGIA ( 27 FDA reports)
PROSTATE CANCER ( 27 FDA reports)
PULPITIS DENTAL ( 27 FDA reports)
RECTAL FISSURE ( 27 FDA reports)
STEROID THERAPY ( 27 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 27 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 27 FDA reports)
UTERINE PROLAPSE ( 27 FDA reports)
VEIN DISORDER ( 27 FDA reports)
URINE OUTPUT DECREASED ( 26 FDA reports)
ALVEOLITIS ( 26 FDA reports)
AORTIC CALCIFICATION ( 26 FDA reports)
AORTIC VALVE DISEASE ( 26 FDA reports)
AREFLEXIA ( 26 FDA reports)
BONE LESION ( 26 FDA reports)
BREAST CANCER FEMALE ( 26 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 26 FDA reports)
HALLUCINATION, AUDITORY ( 26 FDA reports)
HYPOKINESIA ( 26 FDA reports)
NERVOUS SYSTEM DISORDER ( 26 FDA reports)
PELVIC PROLAPSE ( 26 FDA reports)
PROCEDURAL HAEMORRHAGE ( 26 FDA reports)
RASH MACULAR ( 26 FDA reports)
ANGER ( 25 FDA reports)
BIPOLAR DISORDER ( 25 FDA reports)
CATARACT OPERATION ( 25 FDA reports)
CHOLECYSTECTOMY ( 25 FDA reports)
CLOSTRIDIAL INFECTION ( 25 FDA reports)
CRANIOCEREBRAL INJURY ( 25 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 25 FDA reports)
DEVICE MALFUNCTION ( 25 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 25 FDA reports)
EAR PRURITUS ( 25 FDA reports)
ENTEROCOCCAL INFECTION ( 25 FDA reports)
EOSINOPHILIA ( 25 FDA reports)
EPIGASTRIC DISCOMFORT ( 25 FDA reports)
EROSIVE OESOPHAGITIS ( 25 FDA reports)
FEELING COLD ( 25 FDA reports)
HELICOBACTER TEST POSITIVE ( 25 FDA reports)
IMPAIRED FASTING GLUCOSE ( 25 FDA reports)
INFUSION RELATED REACTION ( 25 FDA reports)
MITRAL VALVE STENOSIS ( 25 FDA reports)
MUSCLE CONTRACTURE ( 25 FDA reports)
MUSCLE DISORDER ( 25 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 25 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 25 FDA reports)
RETINAL DEGENERATION ( 25 FDA reports)
SARCOIDOSIS ( 25 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 25 FDA reports)
TONSILLITIS ( 25 FDA reports)
SUBCUTANEOUS ABSCESS ( 24 FDA reports)
UMBILICAL HERNIA ( 24 FDA reports)
UNRESPONSIVE TO STIMULI ( 24 FDA reports)
ABDOMINAL HERNIA ( 24 FDA reports)
BREAST ENLARGEMENT ( 24 FDA reports)
BRONCHOSPASM ( 24 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 24 FDA reports)
CERVICAL DYSPLASIA ( 24 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 24 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
CORONARY ARTERY OCCLUSION ( 24 FDA reports)
CYSTITIS INTERSTITIAL ( 24 FDA reports)
DEFORMITY ( 24 FDA reports)
DENTAL CARE ( 24 FDA reports)
DENTAL DISCOMFORT ( 24 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 24 FDA reports)
EXERCISE LACK OF ( 24 FDA reports)
FAECALOMA ( 24 FDA reports)
GINGIVAL INFECTION ( 24 FDA reports)
HEMIPARESIS ( 24 FDA reports)
HERPES SIMPLEX ( 24 FDA reports)
HOSPITALISATION ( 24 FDA reports)
ILEUS ( 24 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 24 FDA reports)
INJECTION SITE REACTION ( 24 FDA reports)
PANIC DISORDER ( 24 FDA reports)
PARATHYROID DISORDER ( 24 FDA reports)
PERNICIOUS ANAEMIA ( 24 FDA reports)
PSEUDOMONAS INFECTION ( 24 FDA reports)
SALIVARY HYPERSECRETION ( 24 FDA reports)
SENSATION OF HEAVINESS ( 24 FDA reports)
SOFT TISSUE DISORDER ( 24 FDA reports)
ABSCESS LIMB ( 23 FDA reports)
APHASIA ( 23 FDA reports)
BLOOD GLUCOSE DECREASED ( 23 FDA reports)
BONE OPERATION ( 23 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 23 FDA reports)
CATARACT NUCLEAR ( 23 FDA reports)
CHEST X-RAY ABNORMAL ( 23 FDA reports)
CYANOSIS ( 23 FDA reports)
DENTAL NECROSIS ( 23 FDA reports)
DIFFICULTY IN WALKING ( 23 FDA reports)
EJECTION FRACTION DECREASED ( 23 FDA reports)
EMOTIONAL DISORDER ( 23 FDA reports)
EYE IRRITATION ( 23 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 23 FDA reports)
GENERALISED ANXIETY DISORDER ( 23 FDA reports)
GRAND MAL CONVULSION ( 23 FDA reports)
HAEMORRHAGIC DIATHESIS ( 23 FDA reports)
HALLUCINATION, VISUAL ( 23 FDA reports)
IMMOBILE ( 23 FDA reports)
INCISION SITE HAEMATOMA ( 23 FDA reports)
INTRACRANIAL ANEURYSM ( 23 FDA reports)
LEIOMYOMA ( 23 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 23 FDA reports)
MENOPAUSAL SYMPTOMS ( 23 FDA reports)
NAIL DISORDER ( 23 FDA reports)
NECK MASS ( 23 FDA reports)
NEPHROSCLEROSIS ( 23 FDA reports)
ORAL DISCOMFORT ( 23 FDA reports)
OSTEOMA ( 23 FDA reports)
PERICARDITIS ( 23 FDA reports)
PHARYNGEAL OEDEMA ( 23 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 23 FDA reports)
PHOTOSENSITIVITY REACTION ( 23 FDA reports)
POSTURE ABNORMAL ( 23 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 23 FDA reports)
RADICULITIS ( 23 FDA reports)
SPINAL CORD INJURY ( 23 FDA reports)
STEVENS-JOHNSON SYNDROME ( 23 FDA reports)
SWOLLEN TONGUE ( 23 FDA reports)
THROAT TIGHTNESS ( 23 FDA reports)
TOOTH DEPOSIT ( 23 FDA reports)
TRANSAMINASES INCREASED ( 23 FDA reports)
TRISMUS ( 23 FDA reports)
WALKING AID USER ( 23 FDA reports)
SPLENIC ARTERY ANEURYSM ( 22 FDA reports)
TERMINAL INSOMNIA ( 22 FDA reports)
TRAUMATIC HAEMATOMA ( 22 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 22 FDA reports)
VOCAL CORD DISORDER ( 22 FDA reports)
WALKING DISABILITY ( 22 FDA reports)
WEIGHT LOSS POOR ( 22 FDA reports)
WOUND DEHISCENCE ( 22 FDA reports)
WOUND HAEMORRHAGE ( 22 FDA reports)
WRONG DRUG ADMINISTERED ( 22 FDA reports)
ACETABULUM FRACTURE ( 22 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 22 FDA reports)
AORTIC ANEURYSM ( 22 FDA reports)
ATRIAL FLUTTER ( 22 FDA reports)
BRAIN OEDEMA ( 22 FDA reports)
BREAST CANCER STAGE I ( 22 FDA reports)
CARBUNCLE ( 22 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 22 FDA reports)
COLITIS MICROSCOPIC ( 22 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 22 FDA reports)
CUTIS LAXA ( 22 FDA reports)
DIABETIC NEUROPATHY ( 22 FDA reports)
DISTURBANCE IN ATTENTION ( 22 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
HEPATOMEGALY ( 22 FDA reports)
HYPERCAPNIA ( 22 FDA reports)
INJECTION SITE HAEMATOMA ( 22 FDA reports)
LYMPHOEDEMA ( 22 FDA reports)
NEOPLASM SKIN ( 22 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 22 FDA reports)
OEDEMA MOUTH ( 22 FDA reports)
PELVIC ADHESIONS ( 22 FDA reports)
PERIPHERAL COLDNESS ( 22 FDA reports)
RASH PAPULAR ( 22 FDA reports)
RESPIRATORY TRACT CONGESTION ( 22 FDA reports)
RHONCHI ( 22 FDA reports)
SCOTOMA ( 22 FDA reports)
SPINAL COLUMN INJURY ( 22 FDA reports)
ADRENAL DISORDER ( 21 FDA reports)
ANAL PRURITUS ( 21 FDA reports)
AORTIC DISORDER ( 21 FDA reports)
BONE NEOPLASM MALIGNANT ( 21 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 21 FDA reports)
DILATATION ATRIAL ( 21 FDA reports)
ESCHERICHIA TEST POSITIVE ( 21 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 21 FDA reports)
HYPOPHOSPHATAEMIA ( 21 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 21 FDA reports)
INJECTION SITE NODULE ( 21 FDA reports)
LABILE HYPERTENSION ( 21 FDA reports)
LIGAMENT INJURY ( 21 FDA reports)
MEDICAL DEVICE PAIN ( 21 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 21 FDA reports)
PROTEIN URINE PRESENT ( 21 FDA reports)
PULMONARY MASS ( 21 FDA reports)
PULMONARY TUBERCULOSIS ( 21 FDA reports)
THYROID CANCER ( 21 FDA reports)
TONSILLECTOMY ( 21 FDA reports)
SUBDURAL HAEMATOMA ( 20 FDA reports)
TYPE 1 DIABETES MELLITUS ( 20 FDA reports)
VITILIGO ( 20 FDA reports)
ACCIDENT ( 20 FDA reports)
AGRANULOCYTOSIS ( 20 FDA reports)
APPENDICITIS ( 20 FDA reports)
BASEDOW'S DISEASE ( 20 FDA reports)
BLOOD IRON DECREASED ( 20 FDA reports)
BLOOD PRESSURE ( 20 FDA reports)
BREAST DISORDER FEMALE ( 20 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 20 FDA reports)
CEREBRAL CALCIFICATION ( 20 FDA reports)
COORDINATION ABNORMAL ( 20 FDA reports)
CORNEAL DYSTROPHY ( 20 FDA reports)
CRYING ( 20 FDA reports)
ENTERITIS ( 20 FDA reports)
ERYTHEMA MULTIFORME ( 20 FDA reports)
EXERCISE TOLERANCE DECREASED ( 20 FDA reports)
FAMILY STRESS ( 20 FDA reports)
HERPES VIRUS INFECTION ( 20 FDA reports)
HYPERURICAEMIA ( 20 FDA reports)
KNEE DEFORMITY ( 20 FDA reports)
METASTASES TO LIVER ( 20 FDA reports)
PELVIC MASS ( 20 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 20 FDA reports)
PERIPROSTHETIC FRACTURE ( 20 FDA reports)
PERITONITIS ( 20 FDA reports)
PROCEDURAL COMPLICATION ( 20 FDA reports)
PULMONARY CONGESTION ( 20 FDA reports)
RASH PUSTULAR ( 20 FDA reports)
RECTAL ABSCESS ( 20 FDA reports)
RENAL CELL CARCINOMA ( 20 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 20 FDA reports)
RHEUMATOID FACTOR INCREASED ( 20 FDA reports)
SEBORRHOEIC DERMATITIS ( 20 FDA reports)
SENSATION OF FOREIGN BODY ( 20 FDA reports)
ABSCESS DRAINAGE ( 19 FDA reports)
ACTINOMYCOSIS ( 19 FDA reports)
AUTOIMMUNE DISORDER ( 19 FDA reports)
BREAST TENDERNESS ( 19 FDA reports)
CENTRAL OBESITY ( 19 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 19 FDA reports)
CUSHING'S SYNDROME ( 19 FDA reports)
DRUG LEVEL INCREASED ( 19 FDA reports)
DRUG TOXICITY ( 19 FDA reports)
DUPUYTREN'S CONTRACTURE ( 19 FDA reports)
HAEMORRHAGIC DISORDER ( 19 FDA reports)
HEPATITIS A ( 19 FDA reports)
IMPAIRED SELF-CARE ( 19 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 19 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 19 FDA reports)
LOCALISED OEDEMA ( 19 FDA reports)
MASTICATION DISORDER ( 19 FDA reports)
NASAL POLYPS ( 19 FDA reports)
OESOPHAGEAL IRRITATION ( 19 FDA reports)
OSTEOPOROTIC FRACTURE ( 19 FDA reports)
PLASTIC SURGERY ( 19 FDA reports)
POLYURIA ( 19 FDA reports)
PULMONARY INFARCTION ( 19 FDA reports)
PURPURA ( 19 FDA reports)
PURULENCE ( 19 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 19 FDA reports)
RENAL HYPERTROPHY ( 19 FDA reports)
RENAL MASS ( 19 FDA reports)
RESPIRATORY ARREST ( 19 FDA reports)
STITCH ABSCESS ( 19 FDA reports)
THROMBOPHLEBITIS ( 19 FDA reports)
TONGUE DISORDER ( 19 FDA reports)
URINARY TRACT OBSTRUCTION ( 19 FDA reports)
UVEITIS ( 19 FDA reports)
TACHYARRHYTHMIA ( 18 FDA reports)
THERAPY NON-RESPONDER ( 18 FDA reports)
THERMAL BURN ( 18 FDA reports)
TINEA INFECTION ( 18 FDA reports)
TOOTH IMPACTED ( 18 FDA reports)
YELLOW SKIN ( 18 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 18 FDA reports)
ANAL FISTULA ( 18 FDA reports)
ANGIOEDEMA ( 18 FDA reports)
ANOSMIA ( 18 FDA reports)
APLASTIC ANAEMIA ( 18 FDA reports)
APPENDICECTOMY ( 18 FDA reports)
ASPIRATION ( 18 FDA reports)
BENIGN BREAST NEOPLASM ( 18 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 18 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 18 FDA reports)
BLINDNESS UNILATERAL ( 18 FDA reports)
BREAST FIBROSIS ( 18 FDA reports)
BREAST RECONSTRUCTION ( 18 FDA reports)
CHANGE OF BOWEL HABIT ( 18 FDA reports)
CHEST WALL OPERATION ( 18 FDA reports)
CHOKING ( 18 FDA reports)
COELIAC DISEASE ( 18 FDA reports)
CUBITAL TUNNEL SYNDROME ( 18 FDA reports)
DEAFNESS TRAUMATIC ( 18 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 18 FDA reports)
DENTAL IMPLANTATION ( 18 FDA reports)
DENTAL PLAQUE ( 18 FDA reports)
DYSPLASTIC NAEVUS ( 18 FDA reports)
FIBRIN D DIMER INCREASED ( 18 FDA reports)
HAEMODIALYSIS ( 18 FDA reports)
IMMUNODEFICIENCY ( 18 FDA reports)
INCISION SITE ABSCESS ( 18 FDA reports)
INTESTINAL PERFORATION ( 18 FDA reports)
JOINT ARTHROPLASTY ( 18 FDA reports)
LENS DISLOCATION ( 18 FDA reports)
MULTIPLE SCLEROSIS ( 18 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 18 FDA reports)
MUSCLE TWITCHING ( 18 FDA reports)
NAIL DYSTROPHY ( 18 FDA reports)
NON-CARDIAC CHEST PAIN ( 18 FDA reports)
ODYNOPHAGIA ( 18 FDA reports)
PALLOR ( 18 FDA reports)
PARATHYROID TUMOUR BENIGN ( 18 FDA reports)
POOR PERIPHERAL CIRCULATION ( 18 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 18 FDA reports)
REPETITIVE STRAIN INJURY ( 18 FDA reports)
SCAPULA FRACTURE ( 18 FDA reports)
SKIN CANDIDA ( 18 FDA reports)
ALLERGIC SINUSITIS ( 17 FDA reports)
AORTIC VALVE STENOSIS ( 17 FDA reports)
AUTOIMMUNE HEPATITIS ( 17 FDA reports)
BACTERIAL TEST POSITIVE ( 17 FDA reports)
BONE GRAFT ( 17 FDA reports)
CATARACT SUBCAPSULAR ( 17 FDA reports)
CHOLECYSTITIS CHRONIC ( 17 FDA reports)
COCCYDYNIA ( 17 FDA reports)
COMA ( 17 FDA reports)
CORONARY ARTERY STENOSIS ( 17 FDA reports)
DEPRESSED MOOD ( 17 FDA reports)
DRUG DEPENDENCE ( 17 FDA reports)
DYSTONIA ( 17 FDA reports)
EMBOLISM ( 17 FDA reports)
EYE SWELLING ( 17 FDA reports)
FIBROSIS ( 17 FDA reports)
FOREARM FRACTURE ( 17 FDA reports)
GENERALISED OEDEMA ( 17 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 17 FDA reports)
HEPATIC CIRRHOSIS ( 17 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 17 FDA reports)
INCISIONAL DRAINAGE ( 17 FDA reports)
INJECTION SITE EXTRAVASATION ( 17 FDA reports)
INJECTION SITE RASH ( 17 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 17 FDA reports)
LOOSE BODY IN JOINT ( 17 FDA reports)
LUPUS-LIKE SYNDROME ( 17 FDA reports)
LYMPHOPENIA ( 17 FDA reports)
MACULAR HOLE ( 17 FDA reports)
MENSTRUAL DISORDER ( 17 FDA reports)
METABOLIC SYNDROME ( 17 FDA reports)
MITRAL VALVE DISEASE MIXED ( 17 FDA reports)
MOTOR DYSFUNCTION ( 17 FDA reports)
MULTIPLE ALLERGIES ( 17 FDA reports)
MUSCLE TIGHTNESS ( 17 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 17 FDA reports)
OCULAR HYPERAEMIA ( 17 FDA reports)
OVERWEIGHT ( 17 FDA reports)
PEMPHIGOID ( 17 FDA reports)
PERINEURIAL CYST ( 17 FDA reports)
PIRIFORMIS SYNDROME ( 17 FDA reports)
POLYDIPSIA ( 17 FDA reports)
POOR PERSONAL HYGIENE ( 17 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 17 FDA reports)
PYURIA ( 17 FDA reports)
SKIN FISSURES ( 17 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 17 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 17 FDA reports)
TERMINAL STATE ( 17 FDA reports)
URETHRAL INTRINSIC SPHINCTER DEFICIENCY ( 17 FDA reports)
UTERINE CERVIX ATROPHY ( 17 FDA reports)
WOUND DRAINAGE ( 17 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 16 FDA reports)
SUDDEN DEATH ( 16 FDA reports)
TOBACCO ABUSE ( 16 FDA reports)
TOXIC SKIN ERUPTION ( 16 FDA reports)
UTERINE CERVICAL EROSION ( 16 FDA reports)
VENTRICULAR FIBRILLATION ( 16 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 16 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
APPENDICITIS PERFORATED ( 16 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 16 FDA reports)
BLOOD SODIUM INCREASED ( 16 FDA reports)
BONE DEFORMITY ( 16 FDA reports)
BREAST DISCOMFORT ( 16 FDA reports)
DEPENDENCE ( 16 FDA reports)
DISABILITY ( 16 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 16 FDA reports)
EUSTACHIAN TUBE DISORDER ( 16 FDA reports)
EXTERNAL EAR DISORDER ( 16 FDA reports)
EYELID OEDEMA ( 16 FDA reports)
FEMALE STERILISATION ( 16 FDA reports)
FIBROUS HISTIOCYTOMA ( 16 FDA reports)
FINGER DEFORMITY ( 16 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 16 FDA reports)
GENITAL DISCHARGE ( 16 FDA reports)
GLOSSITIS ( 16 FDA reports)
HYPERTENSIVE CRISIS ( 16 FDA reports)
HYPERTROPHY ( 16 FDA reports)
INCISION SITE INFECTION ( 16 FDA reports)
INCREASED APPETITE ( 16 FDA reports)
INNER EAR DISORDER ( 16 FDA reports)
LIP ULCERATION ( 16 FDA reports)
LIPOMA OF BREAST ( 16 FDA reports)
MENORRHAGIA ( 16 FDA reports)
MOUTH HAEMORRHAGE ( 16 FDA reports)
MUCOSAL ATROPHY ( 16 FDA reports)
MUCOSAL INFLAMMATION ( 16 FDA reports)
NASAL DISORDER ( 16 FDA reports)
NEOPLASM ( 16 FDA reports)
NEPHROGENIC ANAEMIA ( 16 FDA reports)
NEUTROPHIL COUNT INCREASED ( 16 FDA reports)
PARKINSONISM ( 16 FDA reports)
PLATELET COUNT INCREASED ( 16 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
RETINOPATHY HYPERTENSIVE ( 16 FDA reports)
RIGHT VENTRICULAR FAILURE ( 16 FDA reports)
SECRETION DISCHARGE ( 16 FDA reports)
SINUS OPERATION ( 16 FDA reports)
SKIN BURNING SENSATION ( 16 FDA reports)
ABNORMAL DREAMS ( 15 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 15 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 15 FDA reports)
ADRENAL MASS ( 15 FDA reports)
ARACHNOIDITIS ( 15 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 15 FDA reports)
BLADDER CANCER ( 15 FDA reports)
BONE INFARCTION ( 15 FDA reports)
BURNS SECOND DEGREE ( 15 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 15 FDA reports)
CEREBRAL DISORDER ( 15 FDA reports)
CERVICAL POLYP ( 15 FDA reports)
COMMINUTED FRACTURE ( 15 FDA reports)
CYSTITIS NONINFECTIVE ( 15 FDA reports)
DENTAL PROSTHESIS USER ( 15 FDA reports)
DEPRESSIVE SYMPTOM ( 15 FDA reports)
DERMATOMYOSITIS ( 15 FDA reports)
DISEASE RECURRENCE ( 15 FDA reports)
DRUG TOLERANCE ( 15 FDA reports)
DUODENAL ULCER PERFORATION ( 15 FDA reports)
DYSAESTHESIA ( 15 FDA reports)
ENDOMETRIAL CANCER ( 15 FDA reports)
ERYSIPELAS ( 15 FDA reports)
EXTRASYSTOLES ( 15 FDA reports)
GASTRIC DILATATION ( 15 FDA reports)
HAEMATOMA EVACUATION ( 15 FDA reports)
HAEMATOMA INFECTION ( 15 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 15 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 15 FDA reports)
JAW CYST ( 15 FDA reports)
LEFT VENTRICULAR FAILURE ( 15 FDA reports)
MACULAR OEDEMA ( 15 FDA reports)
MALIGNANT MELANOMA STAGE II ( 15 FDA reports)
MENINGITIS ( 15 FDA reports)
MORTON'S NEUROMA ( 15 FDA reports)
MYELOPATHY ( 15 FDA reports)
OCCIPITAL NEURALGIA ( 15 FDA reports)
OPTIC ATROPHY ( 15 FDA reports)
PLASMACYTOMA ( 15 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 15 FDA reports)
POSTMENOPAUSE ( 15 FDA reports)
RADIOTHERAPY ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
SLUGGISHNESS ( 15 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 15 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 15 FDA reports)
TRAUMATIC BRAIN INJURY ( 15 FDA reports)
URINE ANALYSIS ABNORMAL ( 15 FDA reports)
URINE ODOUR ABNORMAL ( 15 FDA reports)
VOLVULUS ( 15 FDA reports)
TONGUE ULCERATION ( 14 FDA reports)
TRACHEOBRONCHITIS ( 14 FDA reports)
TRICHOMONIASIS ( 14 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VAGINITIS BACTERIAL ( 14 FDA reports)
VISUAL DISTURBANCE ( 14 FDA reports)
VITRECTOMY ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
ABNORMAL BEHAVIOUR ( 14 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 14 FDA reports)
ALLERGIC OEDEMA ( 14 FDA reports)
ALVEOLAR OSTEITIS ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 14 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 14 FDA reports)
APPLICATION SITE ERYTHEMA ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLADDER SPASM ( 14 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 14 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 14 FDA reports)
BREAST NEOPLASM ( 14 FDA reports)
CHOLECYSTITIS ACUTE ( 14 FDA reports)
COLON CANCER ( 14 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 14 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 14 FDA reports)
ENDOMETRIAL DISORDER ( 14 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 14 FDA reports)
GASTROINTESTINAL PAIN ( 14 FDA reports)
HAEMANGIOMA OF LIVER ( 14 FDA reports)
HEPATITIS ACUTE ( 14 FDA reports)
INFUSION SITE CELLULITIS ( 14 FDA reports)
INJECTION SITE WARMTH ( 14 FDA reports)
INTESTINAL ISCHAEMIA ( 14 FDA reports)
ISCHAEMIC STROKE ( 14 FDA reports)
KIDNEY INFECTION ( 14 FDA reports)
LENTIGO ( 14 FDA reports)
LICHEN SCLEROSUS ( 14 FDA reports)
LUNG CONSOLIDATION ( 14 FDA reports)
LYMPHOCYTOSIS ( 14 FDA reports)
MELANOSIS COLI ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
MOOD SWINGS ( 14 FDA reports)
NASAL DISCOMFORT ( 14 FDA reports)
NON-SMALL CELL LUNG CANCER ( 14 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 14 FDA reports)
OESOPHAGEAL SPASM ( 14 FDA reports)
OROANTRAL FISTULA ( 14 FDA reports)
PANCREATIC CYST ( 14 FDA reports)
PANCREATIC DUCT DILATATION ( 14 FDA reports)
PARANASAL CYST ( 14 FDA reports)
PAROTITIS ( 14 FDA reports)
PHOTOPSIA ( 14 FDA reports)
POST HERPETIC NEURALGIA ( 14 FDA reports)
PYELONEPHRITIS ACUTE ( 14 FDA reports)
RADICULAR SYNDROME ( 14 FDA reports)
RENAL TUBULAR NECROSIS ( 14 FDA reports)
RESORPTION BONE INCREASED ( 14 FDA reports)
RHEUMATOID VASCULITIS ( 14 FDA reports)
RHINITIS SEASONAL ( 14 FDA reports)
SEXUAL ABUSE ( 14 FDA reports)
SKIN HYPERTROPHY ( 14 FDA reports)
ADENOTONSILLECTOMY ( 13 FDA reports)
ADHESION ( 13 FDA reports)
AGEUSIA ( 13 FDA reports)
ANGINA UNSTABLE ( 13 FDA reports)
APATHY ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
BLOOD BLISTER ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 13 FDA reports)
BLOOD PRESSURE ABNORMAL ( 13 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 13 FDA reports)
BRAIN MASS ( 13 FDA reports)
BREATH SOUNDS ABNORMAL ( 13 FDA reports)
CHEST INJURY ( 13 FDA reports)
CLAUSTROPHOBIA ( 13 FDA reports)
DEVICE COMPONENT ISSUE ( 13 FDA reports)
DIVERTICULAR PERFORATION ( 13 FDA reports)
EAR HAEMORRHAGE ( 13 FDA reports)
EDENTULOUS ( 13 FDA reports)
EMPYEMA ( 13 FDA reports)
ENDODONTIC PROCEDURE ( 13 FDA reports)
EYE INJURY ( 13 FDA reports)
FOLATE DEFICIENCY ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
GOUTY ARTHRITIS ( 13 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 13 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
IATROGENIC INJURY ( 13 FDA reports)
INFECTIOUS PERITONITIS ( 13 FDA reports)
INFUSION SITE EXTRAVASATION ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
LARGE INTESTINAL ULCER ( 13 FDA reports)
LARGE INTESTINE PERFORATION ( 13 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 13 FDA reports)
MASTOID DISORDER ( 13 FDA reports)
MEAN CELL VOLUME INCREASED ( 13 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 13 FDA reports)
MIGRAINE WITH AURA ( 13 FDA reports)
NAIL INFECTION ( 13 FDA reports)
NASAL SEPTUM DISORDER ( 13 FDA reports)
NEPHROPATHY TOXIC ( 13 FDA reports)
NERVE ROOT LESION ( 13 FDA reports)
NEURODEGENERATIVE DISORDER ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NEUTROPENIC SEPSIS ( 13 FDA reports)
NIGHTMARE ( 13 FDA reports)
NODAL OSTEOARTHRITIS ( 13 FDA reports)
OESOPHAGEAL CARCINOMA ( 13 FDA reports)
OOPHORECTOMY ( 13 FDA reports)
ORAL FUNGAL INFECTION ( 13 FDA reports)
OSTEITIS DEFORMANS ( 13 FDA reports)
OSTEOMYELITIS CHRONIC ( 13 FDA reports)
PALATAL DISORDER ( 13 FDA reports)
PAPILLOEDEMA ( 13 FDA reports)
PAPILLOMA ( 13 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 13 FDA reports)
PERIOSTITIS ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
RETINAL ISCHAEMIA ( 13 FDA reports)
SEBORRHOEA ( 13 FDA reports)
SERONEGATIVE ARTHRITIS ( 13 FDA reports)
SKIN MASS ( 13 FDA reports)
SKIN TIGHTNESS ( 13 FDA reports)
SPINAL DEFORMITY ( 13 FDA reports)
SPONDYLITIC MYELOPATHY ( 13 FDA reports)
THROMBOCYTOSIS ( 13 FDA reports)
TRANSFUSION ( 13 FDA reports)
TRIGEMINAL NEURALGIA ( 13 FDA reports)
URETERAL DISORDER ( 13 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
VULVAL DISORDER ( 13 FDA reports)
SPUTUM DISCOLOURED ( 12 FDA reports)
STOMACH MASS ( 12 FDA reports)
TENDINOUS CONTRACTURE ( 12 FDA reports)
TENDON INJURY ( 12 FDA reports)
THIRST ( 12 FDA reports)
THYROID CYST ( 12 FDA reports)
URETHRITIS NONINFECTIVE ( 12 FDA reports)
URINARY TRACT DISORDER ( 12 FDA reports)
VULVOVAGINITIS ( 12 FDA reports)
WHIPLASH INJURY ( 12 FDA reports)
WITHDRAWAL BLEED ( 12 FDA reports)
WOUND SECRETION ( 12 FDA reports)
ACUTE PULMONARY OEDEMA ( 12 FDA reports)
ARTHROSCOPY ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 12 FDA reports)
AUTOIMMUNE THYROIDITIS ( 12 FDA reports)
AVULSION FRACTURE ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BACTERIAL DISEASE CARRIER ( 12 FDA reports)
BILIARY COLIC ( 12 FDA reports)
BLOOD CHOLESTEROL ( 12 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 12 FDA reports)
BREAST HYPERPLASIA ( 12 FDA reports)
CAPSULAR CONTRACTURE ASSOCIATED WITH BREAST IMPLANT ( 12 FDA reports)
CARDIAC FAILURE CHRONIC ( 12 FDA reports)
CARDIAC HYPERTROPHY ( 12 FDA reports)
CARDITIS ( 12 FDA reports)
CASTLEMAN'S DISEASE ( 12 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 12 FDA reports)
COCCIDIOIDOMYCOSIS ( 12 FDA reports)
CORONARY ARTERY BYPASS ( 12 FDA reports)
DEAFNESS UNILATERAL ( 12 FDA reports)
DECREASED ACTIVITY ( 12 FDA reports)
DENTAL PULP DISORDER ( 12 FDA reports)
DERMATITIS ALLERGIC ( 12 FDA reports)
DETRUSOR SPHINCTER DYSSYNERGIA ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
DISLOCATION OF VERTEBRA ( 12 FDA reports)
DISSEMINATED TUBERCULOSIS ( 12 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 12 FDA reports)
ECZEMA EYELIDS ( 12 FDA reports)
ENTEROCELE ( 12 FDA reports)
EYE HAEMORRHAGE ( 12 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 12 FDA reports)
FOOT OPERATION ( 12 FDA reports)
HAEMORRHAGIC STROKE ( 12 FDA reports)
HEPATIC CANCER METASTATIC ( 12 FDA reports)
HYPOCOAGULABLE STATE ( 12 FDA reports)
HYPOTHERMIA ( 12 FDA reports)
INJECTION SITE URTICARIA ( 12 FDA reports)
IRON DEFICIENCY ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 12 FDA reports)
LIBIDO DECREASED ( 12 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 12 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 12 FDA reports)
METASTASES TO SPINE ( 12 FDA reports)
MIXED HYPERLIPIDAEMIA ( 12 FDA reports)
MYELITIS TRANSVERSE ( 12 FDA reports)
MYOCLONUS ( 12 FDA reports)
NASAL OBSTRUCTION ( 12 FDA reports)
NEUROPATHIC ARTHROPATHY ( 12 FDA reports)
NEUROPATHIC ULCER ( 12 FDA reports)
NIGHT BLINDNESS ( 12 FDA reports)
ONYCHALGIA ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
ORAL INTAKE REDUCED ( 12 FDA reports)
OSTEOCHONDROMA ( 12 FDA reports)
OSTEOPETROSIS ( 12 FDA reports)
OVARIAN NEOPLASM ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PHOTOPHOBIA ( 12 FDA reports)
PLAGUE ( 12 FDA reports)
PROCEDURAL HYPERTENSION ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 12 FDA reports)
PULMONARY SARCOIDOSIS ( 12 FDA reports)
RECTAL DISCHARGE ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
RENAL OSTEODYSTROPHY ( 12 FDA reports)
RESTLESSNESS ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SALMONELLOSIS ( 12 FDA reports)
SKIN REACTION ( 12 FDA reports)
SKULL FRACTURE ( 12 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 12 FDA reports)
SOMNAMBULISM ( 12 FDA reports)
SPINAL DECOMPRESSION ( 12 FDA reports)
SPINAL LAMINECTOMY ( 12 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ADENOCARCINOMA ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
ANAL INJURY ( 11 FDA reports)
ANGIOMYOLIPOMA ( 11 FDA reports)
APPLICATION SITE PAIN ( 11 FDA reports)
ATRIAL SEPTAL DEFECT ( 11 FDA reports)
BLEPHAROSPASM ( 11 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
CACHEXIA ( 11 FDA reports)
CALCULUS BLADDER ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 11 FDA reports)
CARDIOGENIC SHOCK ( 11 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 11 FDA reports)
CERVICAL MYELOPATHY ( 11 FDA reports)
CHOLESTASIS ( 11 FDA reports)
CONDUCTIVE DEAFNESS ( 11 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 11 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 11 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
EOSINOPHIL COUNT INCREASED ( 11 FDA reports)
EYE INFLAMMATION ( 11 FDA reports)
FAECES HARD ( 11 FDA reports)
GINGIVAL ABSCESS ( 11 FDA reports)
GINGIVAL ULCERATION ( 11 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 11 FDA reports)
HEPATOTOXICITY ( 11 FDA reports)
HICCUPS ( 11 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 FDA reports)
HODGKIN'S DISEASE ( 11 FDA reports)
HYPERPLASIA ( 11 FDA reports)
HYPOVOLAEMIC SHOCK ( 11 FDA reports)
ILEUS PARALYTIC ( 11 FDA reports)
INCISION SITE PAIN ( 11 FDA reports)
INFUSION SITE ERYTHEMA ( 11 FDA reports)
INJECTION SITE BRUISING ( 11 FDA reports)
INJECTION SITE STINGING ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LEUKAEMIA ( 11 FDA reports)
LEUKOPLAKIA ORAL ( 11 FDA reports)
LIVEDO RETICULARIS ( 11 FDA reports)
LUNG HYPERINFLATION ( 11 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 11 FDA reports)
METASTASES TO LUNG ( 11 FDA reports)
METASTASES TO LYMPH NODES ( 11 FDA reports)
METRORRHAGIA ( 11 FDA reports)
MIDDLE INSOMNIA ( 11 FDA reports)
MORGANELLA INFECTION ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
OCULAR HYPERTENSION ( 11 FDA reports)
ORAL DISCHARGE ( 11 FDA reports)
PLEURAL DISORDER ( 11 FDA reports)
PNEUMONIA LEGIONELLA ( 11 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 11 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 11 FDA reports)
PYODERMA ( 11 FDA reports)
PYOGENIC GRANULOMA ( 11 FDA reports)
RALES ( 11 FDA reports)
REFLEXES ABNORMAL ( 11 FDA reports)
REFLUX OESOPHAGITIS ( 11 FDA reports)
RETINAL VEIN OCCLUSION ( 11 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 11 FDA reports)
SALIVARY GLAND ADENOMA ( 11 FDA reports)
SKIN ATROPHY ( 11 FDA reports)
SKIN LACERATION ( 11 FDA reports)
STOMACH DISCOMFORT ( 11 FDA reports)
SUDDEN HEARING LOSS ( 11 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 11 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 11 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 11 FDA reports)
VENOUS THROMBOSIS ( 11 FDA reports)
WOUND COMPLICATION ( 11 FDA reports)
SPUTUM INCREASED ( 10 FDA reports)
TACHYPNOEA ( 10 FDA reports)
TARDIVE DYSKINESIA ( 10 FDA reports)
TUBERCULOUS PLEURISY ( 10 FDA reports)
UNDERDOSE ( 10 FDA reports)
URETHRAL STENOSIS ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
UTEROVAGINAL PROLAPSE ( 10 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
ABDOMINAL INFECTION ( 10 FDA reports)
ABNORMAL WEIGHT GAIN ( 10 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 10 FDA reports)
ANEURYSM ( 10 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 10 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 10 FDA reports)
BENIGN RENAL NEOPLASM ( 10 FDA reports)
BIPOLAR I DISORDER ( 10 FDA reports)
BLOOD IRON INCREASED ( 10 FDA reports)
BLOOD MAGNESIUM DECREASED ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 10 FDA reports)
BONE ABSCESS ( 10 FDA reports)
BONE MARROW TRANSPLANT ( 10 FDA reports)
BREAST CANCER METASTATIC ( 10 FDA reports)
BREAST NECROSIS ( 10 FDA reports)
CARCINOID TUMOUR ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
CHRONIC TONSILLITIS ( 10 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 10 FDA reports)
CYSTITIS ESCHERICHIA ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
DEMYELINATION ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
DRUG PRESCRIBING ERROR ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
EYE PRURITUS ( 10 FDA reports)
FACIAL PALSY ( 10 FDA reports)
FANCONI SYNDROME ACQUIRED ( 10 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
GYNAECOMASTIA ( 10 FDA reports)
HEMIPLEGIA ( 10 FDA reports)
HYPERCALCIURIA ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
IMPLANT SITE ABSCESS ( 10 FDA reports)
INTERVERTEBRAL DISC INJURY ( 10 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 10 FDA reports)
INTRAOCULAR LENS IMPLANT ( 10 FDA reports)
JOINT SURGERY ( 10 FDA reports)
MENSTRUATION IRREGULAR ( 10 FDA reports)
MITRAL VALVE DISEASE ( 10 FDA reports)
MONOPLEGIA ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MYRINGITIS ( 10 FDA reports)
NECROTISING FASCIITIS ( 10 FDA reports)
NEUROMA ( 10 FDA reports)
NEUROMYOPATHY ( 10 FDA reports)
OESOPHAGEAL PAIN ( 10 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 10 FDA reports)
OLIGURIA ( 10 FDA reports)
OSTEITIS CONDENSANS ( 10 FDA reports)
OSTEOMYELITIS ACUTE ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
PLATELET DISORDER ( 10 FDA reports)
POST PROCEDURAL HAEMATOMA ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
RENAL COLIC ( 10 FDA reports)
RENAL INJURY ( 10 FDA reports)
RETCHING ( 10 FDA reports)
SALPINGO-OOPHORECTOMY ( 10 FDA reports)
SECONDARY SEQUESTRUM ( 10 FDA reports)
SENSORY LOSS ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SIALOADENITIS ( 10 FDA reports)
SINUS ARREST ( 10 FDA reports)
SINUS ARRHYTHMIA ( 10 FDA reports)
SKIN FIBROSIS ( 10 FDA reports)
ABDOMINAL ABSCESS ( 9 FDA reports)
ACCIDENT AT WORK ( 9 FDA reports)
ACUTE HEPATIC FAILURE ( 9 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 9 FDA reports)
ANAL ABSCESS ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANIMAL BITE ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
APALLIC SYNDROME ( 9 FDA reports)
APHONIA ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 9 FDA reports)
BILE DUCT STENOSIS ( 9 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BIOPSY ( 9 FDA reports)
BLEPHARAL PIGMENTATION ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 9 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 9 FDA reports)
BORDERLINE GLAUCOMA ( 9 FDA reports)
BREAKTHROUGH PAIN ( 9 FDA reports)
CALCULUS URINARY ( 9 FDA reports)
CEREBRAL HAEMATOMA ( 9 FDA reports)
CERVICAL CORD COMPRESSION ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
COLD SWEAT ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
DIABETIC FOOT ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
DYSMENORRHOEA ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
ENTEROCOLITIS BACTERIAL ( 9 FDA reports)
ERYTHRASMA ( 9 FDA reports)
ESSENTIAL TREMOR ( 9 FDA reports)
EYELASH THICKENING ( 9 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 9 FDA reports)
FIBROMA ( 9 FDA reports)
FISTULA REPAIR ( 9 FDA reports)
GASTRIC CANCER ( 9 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
GENITAL HERPES ( 9 FDA reports)
GLIOSIS ( 9 FDA reports)
GRAM STAIN POSITIVE ( 9 FDA reports)
GRANULOCYTOPENIA ( 9 FDA reports)
HAIR GROWTH ABNORMAL ( 9 FDA reports)
HIP SURGERY ( 9 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 9 FDA reports)
HYPERCHROMIC ANAEMIA ( 9 FDA reports)
HYPERVENTILATION ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
IMPAIRED WORK ABILITY ( 9 FDA reports)
INADEQUATE ANALGESIA ( 9 FDA reports)
INJECTION RELATED REACTION ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
IRIS HYPERPIGMENTATION ( 9 FDA reports)
JAW OPERATION ( 9 FDA reports)
KERATITIS ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LEUKOENCEPHALOPATHY ( 9 FDA reports)
LIPASE DECREASED ( 9 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 9 FDA reports)
MANIA ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
MYOCARDITIS ( 9 FDA reports)
NAIL AVULSION ( 9 FDA reports)
NAIL OPERATION ( 9 FDA reports)
NASAL DRYNESS ( 9 FDA reports)
NECK INJURY ( 9 FDA reports)
NEURODERMATITIS ( 9 FDA reports)
NEUROLOGICAL SYMPTOM ( 9 FDA reports)
ORAL FIBROMA ( 9 FDA reports)
OTORRHOEA ( 9 FDA reports)
PANCREATIC CARCINOMA ( 9 FDA reports)
PAROSMIA ( 9 FDA reports)
PERINEAL CYST ( 9 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 9 FDA reports)
PHYSICAL ASSAULT ( 9 FDA reports)
PYODERMA GANGRENOSUM ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
SMALL INTESTINE ULCER ( 9 FDA reports)
SNEEZING ( 9 FDA reports)
SPLEEN DISORDER ( 9 FDA reports)
SPUTUM PURULENT ( 9 FDA reports)
SUICIDE ATTEMPT ( 9 FDA reports)
SURGICAL FAILURE ( 9 FDA reports)
TARSAL TUNNEL SYNDROME ( 9 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 9 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
TRAUMATIC ARTHRITIS ( 9 FDA reports)
TRAUMATIC FRACTURE ( 9 FDA reports)
TROPONIN I INCREASED ( 9 FDA reports)
UPPER EXTREMITY MASS ( 9 FDA reports)
UTERINE CERVIX STENOSIS ( 9 FDA reports)
VAGINAL INFLAMMATION ( 9 FDA reports)
VITAMIN D INCREASED ( 9 FDA reports)
VULVOVAGINAL DISCOMFORT ( 9 FDA reports)
WEGENER'S GRANULOMATOSIS ( 9 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
STREPTOCOCCAL INFECTION ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
THELITIS ( 8 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
TOXIC ENCEPHALOPATHY ( 8 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
VULVOVAGINAL PRURITUS ( 8 FDA reports)
WEIGHT BEARING DIFFICULTY ( 8 FDA reports)
WEIGHT FLUCTUATION ( 8 FDA reports)
ABDOMINAL ADHESIONS ( 8 FDA reports)
ADNEXA UTERI CYST ( 8 FDA reports)
AGORAPHOBIA ( 8 FDA reports)
ALLERGY TO VACCINE ( 8 FDA reports)
ANGIODYSPLASIA ( 8 FDA reports)
ANTIBODY TEST POSITIVE ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 8 FDA reports)
APLASIA PURE RED CELL ( 8 FDA reports)
ATROPHODERMA OF PASINI AND PIERINI ( 8 FDA reports)
AUTOMATIC BLADDER ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BEDRIDDEN ( 8 FDA reports)
BICYTOPENIA ( 8 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
BIOPSY LIP ( 8 FDA reports)
BLADDER IRRITATION ( 8 FDA reports)
BLADDER OPERATION ( 8 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
BODY TEMPERATURE DECREASED ( 8 FDA reports)
BONE FORMATION DECREASED ( 8 FDA reports)
BONE MARROW OEDEMA ( 8 FDA reports)
BONE SCAN ABNORMAL ( 8 FDA reports)
BRADYARRHYTHMIA ( 8 FDA reports)
BREAST HAEMATOMA ( 8 FDA reports)
BURSA DISORDER ( 8 FDA reports)
BUTTERFLY RASH ( 8 FDA reports)
CALCINOSIS ( 8 FDA reports)
CARDIAC ANEURYSM ( 8 FDA reports)
CARDIAC FLUTTER ( 8 FDA reports)
CELLULITIS ORBITAL ( 8 FDA reports)
CERVIX CARCINOMA ( 8 FDA reports)
CREPITATIONS ( 8 FDA reports)
DRUG EFFECT INCREASED ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 8 FDA reports)
EYELID DISORDER ( 8 FDA reports)
FAT EMBOLISM ( 8 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 8 FDA reports)
FIBROMATOSIS ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FOREIGN BODY REACTION ( 8 FDA reports)
FRACTURED ISCHIUM ( 8 FDA reports)
GASTRITIS HAEMORRHAGIC ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 8 FDA reports)
GRANULOCYTE COUNT DECREASED ( 8 FDA reports)
HAEMATOCRIT ABNORMAL ( 8 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 8 FDA reports)
HEART VALVE INCOMPETENCE ( 8 FDA reports)
HEPATIC LESION ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HUNGER ( 8 FDA reports)
HYPERADRENALISM ( 8 FDA reports)
HYPOPROTEINAEMIA ( 8 FDA reports)
INCISION SITE HAEMORRHAGE ( 8 FDA reports)
INFECTED CYST ( 8 FDA reports)
INJECTION SITE INDURATION ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
INTESTINAL DILATATION ( 8 FDA reports)
KERATOACANTHOMA ( 8 FDA reports)
LACRIMATION DECREASED ( 8 FDA reports)
LIP DISORDER ( 8 FDA reports)
LIP INJURY ( 8 FDA reports)
LIP NEOPLASM ( 8 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 8 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 8 FDA reports)
OCCULT BLOOD ( 8 FDA reports)
OESOPHAGITIS ULCERATIVE ( 8 FDA reports)
OPEN ANGLE GLAUCOMA ( 8 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PANCREATIC MASS ( 8 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 8 FDA reports)
PENIS DISORDER ( 8 FDA reports)
PERITONSILLAR ABSCESS ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
PITUITARY TUMOUR BENIGN ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
POSTOPERATIVE FEVER ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
PRURITUS ALLERGIC ( 8 FDA reports)
PULMONARY TOXICITY ( 8 FDA reports)
RASH MORBILLIFORM ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RENAL PAIN ( 8 FDA reports)
RESPIRATION ABNORMAL ( 8 FDA reports)
RESPIRATORY ACIDOSIS ( 8 FDA reports)
RETINAL HAEMORRHAGE ( 8 FDA reports)
RETINAL TOXICITY ( 8 FDA reports)
SALIVARY GLAND MASS ( 8 FDA reports)
SCOLIOSIS RADIATION ( 8 FDA reports)
SENSORY LEVEL ABNORMAL ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SOFT TISSUE INJURY ( 8 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ABDOMINOPLASTY ( 7 FDA reports)
ACQUIRED CLAW TOE ( 7 FDA reports)
ACUTE ABDOMEN ( 7 FDA reports)
ADJUSTMENT DISORDER ( 7 FDA reports)
ADRENAL SUPPRESSION ( 7 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 7 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 7 FDA reports)
AMAUROSIS ( 7 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 7 FDA reports)
ANGIOKERATOMA ( 7 FDA reports)
ANOGENITAL WARTS ( 7 FDA reports)
ANTICOAGULANT THERAPY ( 7 FDA reports)
ANURIA ( 7 FDA reports)
AORTIC DILATATION ( 7 FDA reports)
AORTIC VALVE CALCIFICATION ( 7 FDA reports)
APPLICATION SITE PRURITUS ( 7 FDA reports)
ARTERIAL HAEMORRHAGE ( 7 FDA reports)
ARTHRODESIS ( 7 FDA reports)
ARTHROPOD STING ( 7 FDA reports)
ASTHMATIC CRISIS ( 7 FDA reports)
ASTIGMATISM ( 7 FDA reports)
ATHEROSCLEROSIS ( 7 FDA reports)
AURICULOTEMPORAL SYNDROME ( 7 FDA reports)
BLEEDING VARICOSE VEIN ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 7 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 7 FDA reports)
BUNION OPERATION ( 7 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 7 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 7 FDA reports)
CAROTID ARTERY ANEURYSM ( 7 FDA reports)
CATHETER SITE PAIN ( 7 FDA reports)
CEREBRAL PALSY ( 7 FDA reports)
CHEMICAL POISONING ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 7 FDA reports)
CITROBACTER INFECTION ( 7 FDA reports)
CORNEAL DISORDER ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 7 FDA reports)
DERMATITIS BULLOUS ( 7 FDA reports)
DEVICE MATERIAL ISSUE ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DRY GANGRENE ( 7 FDA reports)
DYSHIDROSIS ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 7 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 7 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 7 FDA reports)
EROSIVE DUODENITIS ( 7 FDA reports)
EXTREMITY CONTRACTURE ( 7 FDA reports)
EYE ALLERGY ( 7 FDA reports)
EYE OPERATION ( 7 FDA reports)
FAECALITH ( 7 FDA reports)
FAT TISSUE INCREASED ( 7 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 7 FDA reports)
FRUSTRATION ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
GRAVITATIONAL OEDEMA ( 7 FDA reports)
HAEMOPHILUS INFECTION ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HALLUCINATIONS, MIXED ( 7 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 7 FDA reports)
HYPERPHAGIA ( 7 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
HYPOVITAMINOSIS ( 7 FDA reports)
INCREASED BRONCHIAL SECRETION ( 7 FDA reports)
INJECTION SITE MASS ( 7 FDA reports)
INSULIN RESISTANCE ( 7 FDA reports)
IODINE ALLERGY ( 7 FDA reports)
JOINT HYPEREXTENSION ( 7 FDA reports)
JOINT LOCK ( 7 FDA reports)
JUDGEMENT IMPAIRED ( 7 FDA reports)
JUVENILE ARTHRITIS ( 7 FDA reports)
KIDNEY MALROTATION ( 7 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 7 FDA reports)
LATEX ALLERGY ( 7 FDA reports)
LICHEN MYXOEDEMATOSUS ( 7 FDA reports)
LIPOSUCTION ( 7 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 7 FDA reports)
LYME DISEASE ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
MADAROSIS ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MEDICAL DEVICE REMOVAL ( 7 FDA reports)
METABOLIC ALKALOSIS ( 7 FDA reports)
METAL POISONING ( 7 FDA reports)
MONOCYTOSIS ( 7 FDA reports)
MUSCLE ENZYME INCREASED ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NERVE ROOT COMPRESSION ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
OBSESSIVE THOUGHTS ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OESOPHAGEAL INJURY ( 7 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 7 FDA reports)
ONYCHOCLASIS ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
ORAL MUCOSAL BLISTERING ( 7 FDA reports)
OVARIAN MASS ( 7 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 7 FDA reports)
PAPULE ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PAROTID ABSCESS ( 7 FDA reports)
PHARYNGEAL ABSCESS ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
POST CONCUSSION SYNDROME ( 7 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 7 FDA reports)
POSTOPERATIVE ABSCESS ( 7 FDA reports)
POSTOPERATIVE ILEUS ( 7 FDA reports)
PREMATURE AGEING ( 7 FDA reports)
PROCEDURAL HYPOTENSION ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
PYOTHORAX ( 7 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
REFLUX GASTRITIS ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 7 FDA reports)
RHEUMATOID NODULE ( 7 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 7 FDA reports)
SCAB ( 7 FDA reports)
SEQUESTRECTOMY ( 7 FDA reports)
SHOULDER ARTHROPLASTY ( 7 FDA reports)
SINUS POLYP ( 7 FDA reports)
SOFT TISSUE INFLAMMATION ( 7 FDA reports)
SOFT TISSUE MASS ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
SYMPHYSIOLYSIS ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 7 FDA reports)
THINKING ABNORMAL ( 7 FDA reports)
TOXIC NEUROPATHY ( 7 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 7 FDA reports)
TRAUMATIC OCCLUSION ( 7 FDA reports)
URETHRAL DILATATION ( 7 FDA reports)
VAGINAL LEUKOPLAKIA ( 7 FDA reports)
VAGINAL ULCERATION ( 7 FDA reports)
VASCULAR STENOSIS ( 7 FDA reports)
VASODILATATION ( 7 FDA reports)
VENTRICULAR ARRHYTHMIA ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 7 FDA reports)
VULVA CYST ( 7 FDA reports)
WART EXCISION ( 7 FDA reports)
STRESS ULCER ( 6 FDA reports)
SUTURE RELATED COMPLICATION ( 6 FDA reports)
SYSTEMIC CANDIDA ( 6 FDA reports)
TERATOGENICITY ( 6 FDA reports)
TETANY ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
TRANSAMINASES ABNORMAL ( 6 FDA reports)
TRANSPLANT REJECTION ( 6 FDA reports)
ULNAR NERVE PALSY ( 6 FDA reports)
URETERIC OBSTRUCTION ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
URTICARIA CHRONIC ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VENTRICULAR DYSFUNCTION ( 6 FDA reports)
VERTIGO CNS ORIGIN ( 6 FDA reports)
VIRAL LABYRINTHITIS ( 6 FDA reports)
VOCAL CORD NEOPLASM ( 6 FDA reports)
ABSCESS SOFT TISSUE ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 6 FDA reports)
ADENOIDECTOMY ( 6 FDA reports)
ADNEXA UTERI MASS ( 6 FDA reports)
ALOPECIA EFFLUVIUM ( 6 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 6 FDA reports)
ANGINA BULLOSA HAEMORRHAGICA ( 6 FDA reports)
ANORECTAL DISORDER ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
APNOEA ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 6 FDA reports)
APPLICATION SITE VESICLES ( 6 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
BENIGN OVARIAN TUMOUR ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD CHLORIDE DECREASED ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BOWEN'S DISEASE ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 6 FDA reports)
BREAST DISCHARGE ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CARDIAC VALVE SCLEROSIS ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 6 FDA reports)
CEREBELLAR HAEMORRHAGE ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
CHEST WALL MASS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CLEFT LIP AND PALATE ( 6 FDA reports)
CLOSTRIDIUM COLITIS ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CORONARY ARTERY EMBOLISM ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
CUTANEOUS VASCULITIS ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
CYSTOID MACULAR OEDEMA ( 6 FDA reports)
CYSTOPEXY ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
ENURESIS ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
EYE DISCHARGE ( 6 FDA reports)
EYELID RETRACTION ( 6 FDA reports)
EYELID TUMOUR ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 6 FDA reports)
FELTY'S SYNDROME ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 6 FDA reports)
GINGIVAL HYPERPLASIA ( 6 FDA reports)
GINGIVAL INJURY ( 6 FDA reports)
GLOMERULONEPHRITIS ( 6 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMOLYSIS ( 6 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 6 FDA reports)
HAIR COLOUR CHANGES ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HERNIA OBSTRUCTIVE ( 6 FDA reports)
HYDROURETER ( 6 FDA reports)
HYPERAMYLASAEMIA ( 6 FDA reports)
HYPERPHOSPHATAEMIA ( 6 FDA reports)
HYPERTRICHOSIS ( 6 FDA reports)
HYPOCHLORAEMIA ( 6 FDA reports)
HYPOPHOSPHATASIA ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
HYPOTONIA ( 6 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
IMPACTED FRACTURE ( 6 FDA reports)
IMPLANT SITE REACTION ( 6 FDA reports)
INCISION SITE ERYTHEMA ( 6 FDA reports)
INITIAL INSOMNIA ( 6 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 6 FDA reports)
INTESTINAL STENOSIS ( 6 FDA reports)
INTRACRANIAL HAEMATOMA ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
KNEE IMPINGEMENT SYNDROME ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LIMB CRUSHING INJURY ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
MALIGNANT MELANOMA IN SITU ( 6 FDA reports)
MASTOCYTOSIS ( 6 FDA reports)
MILK-ALKALI SYNDROME ( 6 FDA reports)
MOUTH INJURY ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
MUSCULAR DYSTROPHY ( 6 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 6 FDA reports)
NEPHRITIS ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
OPTIC DISC DRUSEN ( 6 FDA reports)
OPTIC NERVE CUPPING ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
OROPHARYNGEAL PLAQUE ( 6 FDA reports)
OSTEOARTHROPATHY ( 6 FDA reports)
OSTEORADIONECROSIS ( 6 FDA reports)
PALATAL OEDEMA ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PCO2 DECREASED ( 6 FDA reports)
PERINEAL PAIN ( 6 FDA reports)
PERIORBITAL CELLULITIS ( 6 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 6 FDA reports)
PORPHYRIA NON-ACUTE ( 6 FDA reports)
POST-TUSSIVE VOMITING ( 6 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 6 FDA reports)
POSTOPERATIVE INFECTION ( 6 FDA reports)
PRIMARY HYPOTHYROIDISM ( 6 FDA reports)
PSEUDOPOLYP ( 6 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 6 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
RHEUMATIC FEVER ( 6 FDA reports)
RHEUMATOID LUNG ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SEBACEOUS GLAND DISORDER ( 6 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SPIGELIAN HERNIA ( 6 FDA reports)
SPINAL CLAUDICATION ( 6 FDA reports)
SPINAL PAIN ( 6 FDA reports)
ABDOMINAL WALL DISORDER ( 5 FDA reports)
ABORTION INDUCED ( 5 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACARODERMATITIS ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
ACTINOMYCES TEST POSITIVE ( 5 FDA reports)
ALBUMIN URINE PRESENT ( 5 FDA reports)
ALLERGIC COUGH ( 5 FDA reports)
ALLERGY TO ARTHROPOD STING ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANASTOMOTIC STENOSIS ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANIMAL SCRATCH ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APPETITE DISORDER ( 5 FDA reports)
ARTERIAL DISORDER ( 5 FDA reports)
ARTHRITIS VIRAL ( 5 FDA reports)
ARTHROFIBROSIS ( 5 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 5 FDA reports)
BACTERIAL PYELONEPHRITIS ( 5 FDA reports)
BEHCET'S SYNDROME ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BLADDER MASS ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BODY TINEA ( 5 FDA reports)
BONE MARROW TOXICITY ( 5 FDA reports)
BRAIN CONTUSION ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BREAST INFECTION ( 5 FDA reports)
BRONCHIOLITIS ( 5 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 5 FDA reports)
CANDIDA TEST POSITIVE ( 5 FDA reports)
CARBON DIOXIDE INCREASED ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CELL MARKER INCREASED ( 5 FDA reports)
CEREBELLAR HAEMATOMA ( 5 FDA reports)
CHONDROMALACIA ( 5 FDA reports)
CHONDROSARCOMA ( 5 FDA reports)
CHORIORETINAL ATROPHY ( 5 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 5 FDA reports)
CLUSTER HEADACHE ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
COLON INJURY ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DENTURE WEARER ( 5 FDA reports)
DEVICE CONNECTION ISSUE ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
DUODENAL STENOSIS ( 5 FDA reports)
EAR NEOPLASM ( 5 FDA reports)
ELBOW OPERATION ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
EXTRADURAL ABSCESS ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FACTOR VIII DEFICIENCY ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
FINGER AMPUTATION ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
FUNGAEMIA ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC INFECTION ( 5 FDA reports)
GASTRIC PERFORATION ( 5 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 5 FDA reports)
GASTROINTESTINAL CARCINOMA ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
GRIP STRENGTH DECREASED ( 5 FDA reports)
GROIN ABSCESS ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HALO VISION ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEMIANOPIA ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HOMOCYSTINAEMIA ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPERAMMONAEMIA ( 5 FDA reports)
HYPOGONADISM ( 5 FDA reports)
HYPOLIPIDAEMIA ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 5 FDA reports)
IMPLANT SITE INFECTION ( 5 FDA reports)
INADEQUATE DIET ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INTESTINAL MASS ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 5 FDA reports)
IVTH NERVE PARALYSIS ( 5 FDA reports)
KERATOSIS PILARIS ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LIP BLISTER ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
MEDIASTINITIS ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 5 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 5 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MIDDLE EAR EFFUSION ( 5 FDA reports)
MITRAL VALVE REPLACEMENT ( 5 FDA reports)
MONONEURITIS ( 5 FDA reports)
MUSCLE FATIGUE ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 5 FDA reports)
MYELOFIBROSIS ( 5 FDA reports)
MYELOMALACIA ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 5 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 5 FDA reports)
ORAL PUSTULE ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
OTITIS MEDIA CHRONIC ( 5 FDA reports)
OXYGEN SATURATION ABNORMAL ( 5 FDA reports)
PANCREATIC ATROPHY ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PANCREATIC NEOPLASM ( 5 FDA reports)
PARASPINAL ABSCESS ( 5 FDA reports)
PERICORONITIS ( 5 FDA reports)
PERIPHERAL EMBOLISM ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
POOR VENOUS ACCESS ( 5 FDA reports)
PROTEIN TOTAL ABNORMAL ( 5 FDA reports)
PRURITUS GENITAL ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
REFRACTORY ANAEMIA ( 5 FDA reports)
RENAL CANCER ( 5 FDA reports)
RETINAL VEIN THROMBOSIS ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RHINITIS PERENNIAL ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SINOBRONCHITIS ( 5 FDA reports)
SKIN GRAFT FAILURE ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 5 FDA reports)
SPERMATOCELE ( 5 FDA reports)
SPIDER NAEVUS ( 5 FDA reports)
SPINAL CORD DISORDER ( 5 FDA reports)
SPINAL OPERATION ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
SYRINGOMYELIA ( 5 FDA reports)
TALIPES ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
THYROXINE FREE INCREASED ( 5 FDA reports)
TOOTH CROWDING ( 5 FDA reports)
UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
VASCULITIC RASH ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VENOUS THROMBOSIS LIMB ( 5 FDA reports)
VERTEBROPLASTY ( 5 FDA reports)
VESTIBULAR DISORDER ( 5 FDA reports)
VIRAL PHARYNGITIS ( 5 FDA reports)
VITAMIN D ABNORMAL ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
X-RAY ABNORMAL ( 5 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 4 FDA reports)
TENDON CALCIFICATION ( 4 FDA reports)
THORACIC OUTLET SYNDROME ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THYROIDITIS SUBACUTE ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TRACHEITIS ( 4 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 4 FDA reports)
TRICUSPID VALVE PROLAPSE ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TYMPANOSCLEROSIS ( 4 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE CALCIUM INCREASED ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
UTERINE SPASM ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VENOUS INJURY ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
VOGT-KOYANAGI-HARADA SYNDROME ( 4 FDA reports)
VULVAL HAEMATOMA ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABDOMINAL INJURY ( 4 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACCIDENTAL NEEDLE STICK ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 4 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
ALVEOLITIS FIBROSING ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANORECTAL DISCOMFORT ( 4 FDA reports)
ANTIBODY TEST ABNORMAL ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APPLICATION SITE HAEMATOMA ( 4 FDA reports)
APTYALISM ( 4 FDA reports)
ARACHNOID CYST ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
AXILLARY MASS ( 4 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 4 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 4 FDA reports)
BONE DENSITY ABNORMAL ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BREAST ABSCESS ( 4 FDA reports)
BREAST PROSTHESIS REMOVAL ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
CALCIUM IONISED ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CATHETERISATION CARDIAC ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHOLESTEATOMA ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
CONGENITAL KNEE DEFORMITY ( 4 FDA reports)
COR PULMONALE ACUTE ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYST REMOVAL ( 4 FDA reports)
CYSTITIS KLEBSIELLA ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 4 FDA reports)
DENTAL TREATMENT ( 4 FDA reports)
DERMOID CYST ( 4 FDA reports)
DEVICE DAMAGE ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DIABETIC VASCULAR DISORDER ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DYSLOGIA ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ELECTROLYTE DEPLETION ( 4 FDA reports)
ENDOTOXIC SHOCK ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EYELID INJURY ( 4 FDA reports)
FALLOPIAN TUBE CYST ( 4 FDA reports)
FEBRILE CONVULSION ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
GASTROENTERITIS SALMONELLA ( 4 FDA reports)
GASTROINTESTINAL NEOPLASM ( 4 FDA reports)
GROWTH OF EYELASHES ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEMICEPHALALGIA ( 4 FDA reports)
HEPATIC CALCIFICATION ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HORMONE THERAPY ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPOSMIA ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
ILEAL STENOSIS ( 4 FDA reports)
IMPLANT SITE PAIN ( 4 FDA reports)
INFECTED VARICOSE VEIN ( 4 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 4 FDA reports)
INFECTIVE SPONDYLITIS ( 4 FDA reports)
INFECTIVE TENOSYNOVITIS ( 4 FDA reports)
INHALATION THERAPY ( 4 FDA reports)
INJECTION SITE CELLULITIS ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
IRIDOCELE ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
JOINT LAXITY ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LARYNGEAL NEOPLASM ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LIPOHYPERTROPHY ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LOSS OF CONTROL OF LEGS ( 4 FDA reports)
LOSS OF LIBIDO ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
LUMBAR SPINE FLATTENING ( 4 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 4 FDA reports)
LYMPHANGITIS ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
LYMPHORRHOEA ( 4 FDA reports)
MACULAR FIBROSIS ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MENISCAL DEGENERATION ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 4 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 4 FDA reports)
MYCOTIC ALLERGY ( 4 FDA reports)
NEISSERIA TEST POSITIVE ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESOPHAGEAL PERFORATION ( 4 FDA reports)
OESOPHAGEAL RUPTURE ( 4 FDA reports)
OSTEOCHONDROSIS ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PILONIDAL CYST ( 4 FDA reports)
PINEAL GLAND CYST ( 4 FDA reports)
PLANTAR FASCIAL FIBROMATOSIS ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POST PROCEDURAL SWELLING ( 4 FDA reports)
POST-TRAUMATIC EPILEPSY ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
PRE-EXISTING DISEASE ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PROCEDURAL NAUSEA ( 4 FDA reports)
PROCTOCOLITIS ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
PRODUCT FORMULATION ISSUE ( 4 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 4 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
PYOMYOSITIS ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
RADICULITIS CERVICAL ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RECTAL NEOPLASM ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
RENAL CYST HAEMORRHAGE ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RETINITIS PIGMENTOSA ( 4 FDA reports)
SALPINGITIS ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SCLERAL DISCOLOURATION ( 4 FDA reports)
SHUNT MALFUNCTION ( 4 FDA reports)
SIALOMETAPLASIA ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN MACERATION ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SPIDER VEIN ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ACCIDENT AT HOME ( 3 FDA reports)
ACOUSTIC NEUROMA ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 3 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APPLICATION SITE INFLAMMATION ( 3 FDA reports)
APPLICATION SITE WARMTH ( 3 FDA reports)
ARTERIAL BRUIT ( 3 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ASPERGILLOMA ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BLADDER CANCER RECURRENT ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BONE GIANT CELL TUMOUR ( 3 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 3 FDA reports)
BRACHYCEPHALY ( 3 FDA reports)
BRAIN MIDLINE SHIFT ( 3 FDA reports)
BREAST ADENOMA ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CAMPTODACTYLY CONGENITAL ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 3 FDA reports)
CAST APPLICATION ( 3 FDA reports)
CATECHOLAMINES URINE INCREASED ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 3 FDA reports)
CERVIX INFLAMMATION ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHLAMYDIA TEST POSITIVE ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHOLANGIOLITIS ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLONAL EVOLUTION ( 3 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLOBOMA ( 3 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 3 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORNEAL LESION ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CSF MONONUCLEAR CELL COUNT INCREASED ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DEPERSONALISATION ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMAL SINUS ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DNA ANTIBODY POSITIVE ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DUODENAL ULCER REPAIR ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
EARLY SATIETY ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EXCESSIVE SKIN ( 3 FDA reports)
EXPLORATIVE LAPAROTOMY ( 3 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYELID INFECTION ( 3 FDA reports)
FACIAL NERVE DISORDER ( 3 FDA reports)
FEAR OF FALLING ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FEMORAL BRUIT ( 3 FDA reports)
FEMOROACETABULAR IMPINGEMENT ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FROSTBITE ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GANGLIONEUROMA ( 3 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 3 FDA reports)
GASTRIC PH DECREASED ( 3 FDA reports)
GASTRIC VARICES ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 3 FDA reports)
GASTROENTERITIS RADIATION ( 3 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GINGIVAL BLISTER ( 3 FDA reports)
GINGIVAL ERYTHEMA ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GINGIVAL OEDEMA ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 3 FDA reports)
GRIP STRENGTH ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 3 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERTELORISM OF ORBIT ( 3 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 3 FDA reports)
HYPOGONADISM MALE ( 3 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
ILIUM FRACTURE ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFECTED DERMAL CYST ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INJECTION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTESTINAL MALROTATION ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
JEJUNAL ULCER ( 3 FDA reports)
JOINT ABSCESS ( 3 FDA reports)
JOINT ADHESION ( 3 FDA reports)
JOINT ANKYLOSIS ( 3 FDA reports)
JOINT INJECTION ( 3 FDA reports)
KELOID SCAR ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LIMB IMMOBILISATION ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MEASLES ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MEIBOMIAN GLAND DYSFUNCTION ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS TUBERCULOUS ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METANEPHRINE URINE INCREASED ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
METATARSUS PRIMUS VARUS ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MICROGNATHIA ( 3 FDA reports)
MICROTIA ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYCOPLASMA TEST POSITIVE ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NECROTISING OESOPHAGITIS ( 3 FDA reports)
NEOPLASM OF ORBIT ( 3 FDA reports)
NERVE ROOT INJURY LUMBAR ( 3 FDA reports)
NEURILEMMOMA ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 3 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL ATRESIA ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
OLFACTORY NERVE DISORDER ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
OSTEOMA CUTIS ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PELVIC DEFORMITY ( 3 FDA reports)
PERICARDITIS RHEUMATIC ( 3 FDA reports)
PERONEAL NERVE INJURY ( 3 FDA reports)
PHANTOM PAIN ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PICKWICKIAN SYNDROME ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMONIA ESCHERICHIA ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA INFLUENZAL ( 3 FDA reports)
PNEUMONIA NECROTISING ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POOR DENTAL CONDITION ( 3 FDA reports)
POST POLIO SYNDROME ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PROGRESSIVE MUSCULAR ATROPHY ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PUS IN STOOL ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
REFRACTION DISORDER ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL NEOPLASM ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
SALIVARY GLAND CALCULUS ( 3 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SCLEROTHERAPY ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SLOW SPEECH ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPLINTER ( 3 FDA reports)
SPONDYLOLYSIS ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SURFACTANT PROTEIN INCREASED ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
SYRINGE ISSUE ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TEETHING ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THALAMIC INFARCTION ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THYMOMA ( 3 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TOOTH INJURY ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TRENDELENBURG'S SYMPTOM ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
URETHRAL CYST ( 3 FDA reports)
URINARY CASTS PRESENT ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
UTERINE ENLARGEMENT ( 3 FDA reports)
VAGINAL STRICTURE ( 3 FDA reports)
VAGINISMUS ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR HEADACHE ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASCULAR STENT INSERTION ( 3 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VIRAL SINUSITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
YAWNING ( 3 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 2 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYMUS DISORDER ( 2 FDA reports)
THYMUS ENLARGEMENT ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE NEOPLASM BENIGN ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRACHEAL DEVIATION ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRAUMATIC ULCER ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URACHAL ABSCESS ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT OPERATION ( 2 FDA reports)
URINE POTASSIUM INCREASED ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
UTERINE CARCINOMA IN SITU ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VACCINATION FAILURE ( 2 FDA reports)
VAGINAL DYSPLASIA ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL PROLAPSE REPAIR ( 2 FDA reports)
VAGINITIS ( 2 FDA reports)
VAGINOPLASTY ( 2 FDA reports)
VARICOPHLEBITIS ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VITAMIN A INCREASED ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WRIST SURGERY ( 2 FDA reports)
WRONG DEVICE DISPENSED ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
YELLOW NAIL SYNDROME ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID DECREASED ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE DECREASED ( 2 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACTINIC ELASTOSIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AIDS DEMENTIA COMPLEX ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL NEOPLASM ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANEURYSMECTOMY ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIAL SPASM ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
AUTOINFLAMMATORY DISEASE ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF CONJUNCTIVA ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BIOPSY BONE ( 2 FDA reports)
BIOPSY BREAST NORMAL ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BLADDER FIBROSIS ( 2 FDA reports)
BLINDNESS CONGENITAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BREAST CANCER MALE ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
CALLUS FORMATION DELAYED ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID PULSE ABNORMAL ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEST WALL ABSCESS ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CLINODACTYLY ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL OPERATION ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS ARTEFACTA ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE INTOLERANCE ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DIVERTICULITIS OESOPHAGEAL ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FASCIAL HERNIA ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FATTY LIVER ALCOHOLIC ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEMORAL ARTERY EMBOLISM ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE TREATMENT ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GAIT DEVIATION ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC LAVAGE ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE III ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
INCISIONAL HERNIA REPAIR ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LAPAROSCOPY ( 2 FDA reports)
LARYNGEAL INJURY ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIGAMENT OPERATION ( 2 FDA reports)
LIMB RECONSTRUCTIVE SURGERY ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOPERICARDITIS ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NEISSERIA INFECTION ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NEUROSTIMULATOR IMPLANTATION ( 2 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 2 FDA reports)
NEUTROPHILIC PANNICULITIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY AGGRESSIVE ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 2 FDA reports)
OESTROGEN REPLACEMENT THERAPY ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOCALCIN DECREASED ( 2 FDA reports)
OTITIS EXTERNA FUNGAL ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN FAILURE ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 2 FDA reports)
PARTIAL LIPODYSTROPHY ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATIENT ISOLATION ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIORBITAL HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHARYNGEAL FISTULA ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLICA SYNDROME ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 2 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PRESBYACUSIS ( 2 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADICULAR CYST ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESTING TREMOR ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
ROSAI-DORFMAN SYNDROME ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
RUBELLA ( 2 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 2 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSITISATION ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 2 FDA reports)
SHIGELLA TEST POSITIVE ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP DISORDER THERAPY ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL HAEMANGIOMA ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS OF EYELID ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACROCHORDON EXCISION ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANENCEPHALY ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANKLE ARTHROPLASTY ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST SENSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
APPLICATION SITE ATROPHY ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTICULAR DISC DISORDER ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATLANTOAXIAL INSTABILITY ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL ALLERGY ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ACID PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN D DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C-TELOPEPTIDE INCREASED ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTIDYNIA ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMANGIOMA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVIX ERYTHEMA ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEMICAL BURN OF RESPIRATORY TRACT ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DOLICHOCOLON ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECTOPIC KIDNEY ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOMETRIOMA ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
EOSINOPHILS URINE ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTIS ULCER ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EX-DRUG ABUSER ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING PROBLEM IN CHILD ( 1 FDA reports)
FEMALE GENITAL TRACT TUBERCULOSIS ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC CANCER STAGE II ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATINURIA ( 1 FDA reports)
HAEMOPHILIA ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYGROMA COLLI ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOAESTHESIA TEETH ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPLANT SITE SCAR ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INHIBITING ANTIBODIES ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL T-CELL LYMPHOMA ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR LENS EXTRACTION ( 1 FDA reports)
INTRATHECAL PUMP INSERTION ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
JUVENILE MELANOMA BENIGN ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACULAR PIGMENTATION ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL GLAND ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MELAS SYNDROME ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGIOMA MALIGNANT ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENISCUS REMOVAL ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO URINARY TRACT ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METASTATIC UTERINE CANCER ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE LENTIGINES SYNDROME ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEOLOGISM ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODULAR VASCULITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE II ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC PSEUDOCYST DRAINAGE ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE HAEMATOMA ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERINEAL INFECTION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTPARTUM VENOUS THROMBOSIS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY CILIARY DYSKINESIA ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PSEUDOCHOLINESTERASE DEFICIENCY ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBACEOUS HYPERPLASIA ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEROCONVERSION TEST POSITIVE ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINGLE VESSEL BYPASS GRAFT ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL MENINGEAL CYST ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENSION ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRI-IODOTHYRONINE FREE ABNORMAL ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 1 FDA reports)
TUBERCULOSIS OF PERIPHERAL LYMPH NODES ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TYPHUS ( 1 FDA reports)
ULTRASOUND BLADDER ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 1 FDA reports)
URETHRAL CARBUNCLE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WEIL'S DISEASE ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)

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