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

PAIN ( 2334 FDA reports)
ANXIETY ( 1834 FDA reports)
NAUSEA ( 1786 FDA reports)
DYSPNOEA ( 1545 FDA reports)
BACK PAIN ( 1387 FDA reports)
FATIGUE ( 1305 FDA reports)
DEPRESSION ( 1304 FDA reports)
HEADACHE ( 1273 FDA reports)
VOMITING ( 1243 FDA reports)
ASTHENIA ( 1125 FDA reports)
CHEST PAIN ( 1074 FDA reports)
ARTHRALGIA ( 1050 FDA reports)
DIZZINESS ( 1026 FDA reports)
INJURY ( 1026 FDA reports)
PAIN IN EXTREMITY ( 992 FDA reports)
FALL ( 957 FDA reports)
ANAEMIA ( 952 FDA reports)
DIARRHOEA ( 950 FDA reports)
OEDEMA PERIPHERAL ( 915 FDA reports)
PNEUMONIA ( 900 FDA reports)
ABDOMINAL PAIN ( 894 FDA reports)
INSOMNIA ( 886 FDA reports)
HYPERTENSION ( 883 FDA reports)
WEIGHT DECREASED ( 796 FDA reports)
CONSTIPATION ( 787 FDA reports)
DRUG INEFFECTIVE ( 757 FDA reports)
PYREXIA ( 753 FDA reports)
OSTEONECROSIS OF JAW ( 699 FDA reports)
OSTEOARTHRITIS ( 655 FDA reports)
DEEP VEIN THROMBOSIS ( 651 FDA reports)
EMOTIONAL DISTRESS ( 628 FDA reports)
HYPOAESTHESIA ( 618 FDA reports)
MYOCARDIAL INFARCTION ( 615 FDA reports)
DEHYDRATION ( 598 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 563 FDA reports)
HYPOTENSION ( 561 FDA reports)
URINARY TRACT INFECTION ( 561 FDA reports)
MUSCLE SPASMS ( 559 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 551 FDA reports)
BONE DISORDER ( 538 FDA reports)
GAIT DISTURBANCE ( 531 FDA reports)
MALAISE ( 525 FDA reports)
ABDOMINAL PAIN UPPER ( 521 FDA reports)
PLEURAL EFFUSION ( 506 FDA reports)
COUGH ( 489 FDA reports)
CEREBROVASCULAR ACCIDENT ( 488 FDA reports)
CONFUSIONAL STATE ( 477 FDA reports)
PULMONARY EMBOLISM ( 472 FDA reports)
RENAL FAILURE ( 470 FDA reports)
INFECTION ( 464 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 463 FDA reports)
PARAESTHESIA ( 459 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 456 FDA reports)
BRONCHITIS ( 442 FDA reports)
CHOLELITHIASIS ( 442 FDA reports)
OSTEOMYELITIS ( 442 FDA reports)
CORONARY ARTERY DISEASE ( 441 FDA reports)
DECREASED APPETITE ( 439 FDA reports)
RASH ( 437 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 436 FDA reports)
NEUROPATHY PERIPHERAL ( 433 FDA reports)
WEIGHT INCREASED ( 432 FDA reports)
SOMNOLENCE ( 429 FDA reports)
ATELECTASIS ( 426 FDA reports)
LOSS OF CONSCIOUSNESS ( 423 FDA reports)
TREMOR ( 422 FDA reports)
FEELING ABNORMAL ( 421 FDA reports)
SWELLING ( 415 FDA reports)
ANHEDONIA ( 406 FDA reports)
SPINAL OSTEOARTHRITIS ( 406 FDA reports)
CONVULSION ( 403 FDA reports)
DEATH ( 401 FDA reports)
CELLULITIS ( 400 FDA reports)
SYNCOPE ( 399 FDA reports)
DYSPHAGIA ( 391 FDA reports)
VISION BLURRED ( 391 FDA reports)
SINUSITIS ( 390 FDA reports)
ATRIAL FIBRILLATION ( 389 FDA reports)
RENAL FAILURE ACUTE ( 385 FDA reports)
OSTEONECROSIS ( 378 FDA reports)
DYSPEPSIA ( 377 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 369 FDA reports)
MENTAL STATUS CHANGES ( 369 FDA reports)
DIABETES MELLITUS ( 366 FDA reports)
ERYTHEMA ( 363 FDA reports)
HYPERHIDROSIS ( 362 FDA reports)
ARTHRITIS ( 361 FDA reports)
PAIN IN JAW ( 355 FDA reports)
HYPERLIPIDAEMIA ( 351 FDA reports)
CONTUSION ( 343 FDA reports)
METASTASES TO BONE ( 343 FDA reports)
SUICIDAL IDEATION ( 342 FDA reports)
AMNESIA ( 341 FDA reports)
SEPSIS ( 336 FDA reports)
TOOTH EXTRACTION ( 328 FDA reports)
HYPOKALAEMIA ( 327 FDA reports)
OSTEOPOROSIS ( 327 FDA reports)
THROMBOCYTOPENIA ( 324 FDA reports)
MUSCULOSKELETAL PAIN ( 322 FDA reports)
BLOOD PRESSURE INCREASED ( 318 FDA reports)
RESPIRATORY FAILURE ( 317 FDA reports)
JOINT SWELLING ( 314 FDA reports)
IMPAIRED HEALING ( 312 FDA reports)
RIB FRACTURE ( 312 FDA reports)
MITRAL VALVE INCOMPETENCE ( 301 FDA reports)
DENTAL CARIES ( 297 FDA reports)
PRURITUS ( 297 FDA reports)
HAEMORRHOIDS ( 296 FDA reports)
NECK PAIN ( 290 FDA reports)
OSTEOPENIA ( 287 FDA reports)
MUSCULAR WEAKNESS ( 283 FDA reports)
MYALGIA ( 281 FDA reports)
CHILLS ( 278 FDA reports)
MEMORY IMPAIRMENT ( 277 FDA reports)
CARDIOMEGALY ( 273 FDA reports)
DRUG DEPENDENCE ( 273 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 271 FDA reports)
CHOLECYSTITIS CHRONIC ( 261 FDA reports)
CHEST DISCOMFORT ( 260 FDA reports)
PALPITATIONS ( 260 FDA reports)
GASTRITIS ( 259 FDA reports)
RECTAL HAEMORRHAGE ( 259 FDA reports)
BLOOD GLUCOSE INCREASED ( 257 FDA reports)
OEDEMA ( 257 FDA reports)
HALLUCINATION ( 254 FDA reports)
CONDITION AGGRAVATED ( 253 FDA reports)
ASTHMA ( 250 FDA reports)
MIGRAINE ( 248 FDA reports)
BONE PAIN ( 247 FDA reports)
IRRITABILITY ( 246 FDA reports)
HYPOXIA ( 242 FDA reports)
ECONOMIC PROBLEM ( 240 FDA reports)
DECREASED INTEREST ( 238 FDA reports)
NERVOUSNESS ( 234 FDA reports)
HIATUS HERNIA ( 233 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 231 FDA reports)
GALLBLADDER DISORDER ( 229 FDA reports)
CARDIAC DISORDER ( 228 FDA reports)
DEFORMITY ( 228 FDA reports)
NEPHROLITHIASIS ( 226 FDA reports)
HEART RATE INCREASED ( 225 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 224 FDA reports)
PANCYTOPENIA ( 224 FDA reports)
OVERDOSE ( 223 FDA reports)
ROAD TRAFFIC ACCIDENT ( 223 FDA reports)
CATARACT ( 222 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 220 FDA reports)
HAEMOGLOBIN DECREASED ( 219 FDA reports)
LYMPHADENOPATHY ( 216 FDA reports)
DIVERTICULUM ( 214 FDA reports)
ABDOMINAL DISTENSION ( 213 FDA reports)
EXOSTOSIS ( 209 FDA reports)
AGITATION ( 207 FDA reports)
ARTHROPATHY ( 207 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 207 FDA reports)
DYSURIA ( 206 FDA reports)
MOUTH ULCERATION ( 205 FDA reports)
COMPRESSION FRACTURE ( 204 FDA reports)
CARDIAC ARREST ( 201 FDA reports)
TYPE 2 DIABETES MELLITUS ( 201 FDA reports)
ARTERIOSCLEROSIS ( 200 FDA reports)
RENAL FAILURE CHRONIC ( 200 FDA reports)
NEOPLASM MALIGNANT ( 198 FDA reports)
NEUTROPENIA ( 198 FDA reports)
TACHYCARDIA ( 197 FDA reports)
TENDERNESS ( 196 FDA reports)
HERPES ZOSTER ( 195 FDA reports)
SINUS TACHYCARDIA ( 194 FDA reports)
SLEEP APNOEA SYNDROME ( 193 FDA reports)
SURGERY ( 193 FDA reports)
VERTIGO ( 193 FDA reports)
ABDOMINAL DISCOMFORT ( 192 FDA reports)
DYSPNOEA EXERTIONAL ( 190 FDA reports)
HYPERGLYCAEMIA ( 189 FDA reports)
EMPHYSEMA ( 188 FDA reports)
THROMBOSIS ( 188 FDA reports)
TOOTHACHE ( 187 FDA reports)
PULMONARY OEDEMA ( 186 FDA reports)
BALANCE DISORDER ( 185 FDA reports)
STAPHYLOCOCCAL INFECTION ( 185 FDA reports)
PANIC ATTACK ( 182 FDA reports)
URINARY RETENTION ( 181 FDA reports)
BONE LESION ( 180 FDA reports)
HOT FLUSH ( 179 FDA reports)
TOOTH ABSCESS ( 179 FDA reports)
TOOTH FRACTURE ( 179 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 177 FDA reports)
STRESS ( 176 FDA reports)
POLLAKIURIA ( 171 FDA reports)
PRIMARY SEQUESTRUM ( 171 FDA reports)
TOOTH LOSS ( 170 FDA reports)
HAEMOPTYSIS ( 169 FDA reports)
MULTIPLE MYELOMA ( 167 FDA reports)
BURSITIS ( 166 FDA reports)
ABASIA ( 165 FDA reports)
ANGINA PECTORIS ( 165 FDA reports)
HYPONATRAEMIA ( 165 FDA reports)
SCOLIOSIS ( 165 FDA reports)
HYPERSENSITIVITY ( 164 FDA reports)
LUNG NEOPLASM ( 164 FDA reports)
SWELLING FACE ( 164 FDA reports)
HYPOPHAGIA ( 163 FDA reports)
RENAL CYST ( 163 FDA reports)
CARDIAC MURMUR ( 161 FDA reports)
LOOSE TOOTH ( 161 FDA reports)
INFLUENZA LIKE ILLNESS ( 160 FDA reports)
PANCREATITIS ( 160 FDA reports)
MALNUTRITION ( 158 FDA reports)
HYPOTHYROIDISM ( 157 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 156 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 156 FDA reports)
TOOTH DISORDER ( 155 FDA reports)
ORAL PAIN ( 154 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 153 FDA reports)
DISABILITY ( 152 FDA reports)
HYPERCHOLESTEROLAEMIA ( 152 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 152 FDA reports)
OSTEOSCLEROSIS ( 152 FDA reports)
DISTURBANCE IN ATTENTION ( 151 FDA reports)
LUNG INFILTRATION ( 150 FDA reports)
MULTIPLE INJURIES ( 150 FDA reports)
SCAR ( 150 FDA reports)
FEAR ( 149 FDA reports)
PERICARDIAL EFFUSION ( 148 FDA reports)
RESTLESS LEGS SYNDROME ( 148 FDA reports)
UNEVALUABLE EVENT ( 148 FDA reports)
AGGRESSION ( 147 FDA reports)
CARPAL TUNNEL SYNDROME ( 147 FDA reports)
JOINT INJURY ( 147 FDA reports)
OROPHARYNGEAL PAIN ( 147 FDA reports)
ANOREXIA ( 146 FDA reports)
BLOOD CREATININE INCREASED ( 146 FDA reports)
OBESITY ( 146 FDA reports)
BRADYCARDIA ( 144 FDA reports)
EPISTAXIS ( 144 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 144 FDA reports)
DRUG HYPERSENSITIVITY ( 143 FDA reports)
LETHARGY ( 143 FDA reports)
LUNG DISORDER ( 143 FDA reports)
SLEEP DISORDER ( 143 FDA reports)
NEURALGIA ( 142 FDA reports)
VISUAL IMPAIRMENT ( 141 FDA reports)
TINNITUS ( 140 FDA reports)
LEUKOCYTOSIS ( 139 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 138 FDA reports)
MENTAL DISORDER ( 138 FDA reports)
URTICARIA ( 137 FDA reports)
DYSGEUSIA ( 136 FDA reports)
HAEMATOCHEZIA ( 135 FDA reports)
PULMONARY HYPERTENSION ( 134 FDA reports)
CHRONIC SINUSITIS ( 133 FDA reports)
HAEMATURIA ( 133 FDA reports)
INJECTION SITE PAIN ( 133 FDA reports)
COLONIC POLYP ( 132 FDA reports)
DRUG ABUSER ( 132 FDA reports)
DRUG DOSE OMISSION ( 132 FDA reports)
DRY MOUTH ( 132 FDA reports)
NIGHT SWEATS ( 132 FDA reports)
ALOPECIA ( 131 FDA reports)
SUICIDE ATTEMPT ( 131 FDA reports)
BLOOD CALCIUM DECREASED ( 130 FDA reports)
DYSARTHRIA ( 130 FDA reports)
HAEMATEMESIS ( 130 FDA reports)
HAEMATOCRIT DECREASED ( 130 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 130 FDA reports)
ROTATOR CUFF SYNDROME ( 130 FDA reports)
TREATMENT NONCOMPLIANCE ( 130 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 129 FDA reports)
BLOOD PRESSURE DECREASED ( 129 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 129 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 128 FDA reports)
HYPOGLYCAEMIA ( 128 FDA reports)
HEPATIC STEATOSIS ( 127 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 126 FDA reports)
SPONDYLOLISTHESIS ( 126 FDA reports)
CARDIOMYOPATHY ( 125 FDA reports)
FIBROMYALGIA ( 125 FDA reports)
GASTROINTESTINAL DISORDER ( 125 FDA reports)
HAEMORRHAGE ( 124 FDA reports)
BURNING SENSATION ( 123 FDA reports)
COGNITIVE DISORDER ( 123 FDA reports)
EAR PAIN ( 123 FDA reports)
HEAD INJURY ( 123 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 123 FDA reports)
RENAL DISORDER ( 123 FDA reports)
UNRESPONSIVE TO STIMULI ( 123 FDA reports)
DISCOMFORT ( 122 FDA reports)
CHOLECYSTITIS ( 121 FDA reports)
FLUSHING ( 121 FDA reports)
DRUG TOXICITY ( 120 FDA reports)
FEMUR FRACTURE ( 120 FDA reports)
OSTEITIS ( 120 FDA reports)
ARRHYTHMIA ( 119 FDA reports)
INFLAMMATION ( 119 FDA reports)
RESPIRATORY ARREST ( 119 FDA reports)
STOMATITIS ( 119 FDA reports)
WHEEZING ( 119 FDA reports)
FEBRILE NEUTROPENIA ( 118 FDA reports)
RHINORRHOEA ( 118 FDA reports)
SPEECH DISORDER ( 118 FDA reports)
PRODUCT QUALITY ISSUE ( 116 FDA reports)
VENTRICULAR TACHYCARDIA ( 116 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 115 FDA reports)
MEDICATION ERROR ( 115 FDA reports)
BLOOD POTASSIUM DECREASED ( 113 FDA reports)
METASTASES TO SPINE ( 113 FDA reports)
CARDIAC FAILURE ( 112 FDA reports)
DIVERTICULUM INTESTINAL ( 112 FDA reports)
EXPOSED BONE IN JAW ( 112 FDA reports)
LUMBAR SPINAL STENOSIS ( 112 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 112 FDA reports)
ANGER ( 111 FDA reports)
OSTEOLYSIS ( 111 FDA reports)
PLATELET COUNT DECREASED ( 111 FDA reports)
BONE DEBRIDEMENT ( 110 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 110 FDA reports)
RHEUMATOID ARTHRITIS ( 110 FDA reports)
URINARY INCONTINENCE ( 110 FDA reports)
COLITIS ( 109 FDA reports)
DRUG INTERACTION ( 109 FDA reports)
MASTICATION DISORDER ( 109 FDA reports)
RESPIRATORY DISTRESS ( 109 FDA reports)
CRYING ( 108 FDA reports)
NASAL CONGESTION ( 108 FDA reports)
AORTIC VALVE INCOMPETENCE ( 106 FDA reports)
BACK INJURY ( 106 FDA reports)
PNEUMOTHORAX ( 106 FDA reports)
PRESYNCOPE ( 106 FDA reports)
MUCOSAL INFLAMMATION ( 105 FDA reports)
PHYSICAL DISABILITY ( 105 FDA reports)
DYSKINESIA ( 104 FDA reports)
MASS ( 104 FDA reports)
PURULENT DISCHARGE ( 104 FDA reports)
ABNORMAL BEHAVIOUR ( 103 FDA reports)
CARDIO-RESPIRATORY ARREST ( 103 FDA reports)
DEPENDENCE ( 103 FDA reports)
DISORIENTATION ( 103 FDA reports)
FOOT FRACTURE ( 103 FDA reports)
INCORRECT DOSE ADMINISTERED ( 103 FDA reports)
JOINT EFFUSION ( 103 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 103 FDA reports)
IRRITABLE BOWEL SYNDROME ( 102 FDA reports)
LACERATION ( 102 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 102 FDA reports)
SKIN ULCER ( 102 FDA reports)
SPINAL COLUMN STENOSIS ( 102 FDA reports)
JAW OPERATION ( 101 FDA reports)
ORAL DISORDER ( 101 FDA reports)
VIRAL INFECTION ( 101 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 101 FDA reports)
ABNORMAL DREAMS ( 100 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 100 FDA reports)
DIABETIC NEUROPATHY ( 100 FDA reports)
DISEASE PROGRESSION ( 100 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 100 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 99 FDA reports)
DEBRIDEMENT ( 98 FDA reports)
JAW DISORDER ( 98 FDA reports)
LEUKOPENIA ( 98 FDA reports)
RHINITIS ALLERGIC ( 98 FDA reports)
GINGIVITIS ( 97 FDA reports)
CYST ( 96 FDA reports)
DRUG EFFECT DECREASED ( 96 FDA reports)
EMOTIONAL DISORDER ( 96 FDA reports)
ENDODONTIC PROCEDURE ( 96 FDA reports)
IMPAIRED DRIVING ABILITY ( 96 FDA reports)
NASOPHARYNGITIS ( 96 FDA reports)
SPINAL COMPRESSION FRACTURE ( 96 FDA reports)
LOBAR PNEUMONIA ( 95 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 95 FDA reports)
HIP FRACTURE ( 94 FDA reports)
INFLUENZA ( 94 FDA reports)
OXYGEN SATURATION DECREASED ( 94 FDA reports)
ABSCESS ( 93 FDA reports)
HYPERCALCAEMIA ( 93 FDA reports)
PANCREATITIS ACUTE ( 93 FDA reports)
THINKING ABNORMAL ( 93 FDA reports)
DELUSION ( 92 FDA reports)
DYSSTASIA ( 92 FDA reports)
HYPERKALAEMIA ( 92 FDA reports)
RASH PRURITIC ( 92 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 92 FDA reports)
BLOOD UREA INCREASED ( 91 FDA reports)
FACET JOINT SYNDROME ( 91 FDA reports)
GOUT ( 91 FDA reports)
HEPATIC ENZYME INCREASED ( 91 FDA reports)
RADICULOPATHY ( 91 FDA reports)
GASTROENTERITIS ( 90 FDA reports)
HAEMATOMA ( 90 FDA reports)
HYPOAESTHESIA ORAL ( 90 FDA reports)
INTENTIONAL DRUG MISUSE ( 90 FDA reports)
METASTASES TO LIVER ( 90 FDA reports)
TENDONITIS ( 90 FDA reports)
BLADDER DISORDER ( 89 FDA reports)
CYSTITIS ( 89 FDA reports)
DELIRIUM ( 89 FDA reports)
ILL-DEFINED DISORDER ( 89 FDA reports)
RENAL IMPAIRMENT ( 89 FDA reports)
TOOTH INFECTION ( 89 FDA reports)
ADVERSE EVENT ( 88 FDA reports)
GROIN PAIN ( 87 FDA reports)
HEART RATE IRREGULAR ( 87 FDA reports)
HYPOCALCAEMIA ( 87 FDA reports)
MOOD SWINGS ( 87 FDA reports)
OFF LABEL USE ( 87 FDA reports)
PNEUMONIA ASPIRATION ( 87 FDA reports)
PULMONARY FIBROSIS ( 87 FDA reports)
ASCITES ( 86 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 86 FDA reports)
GINGIVAL BLEEDING ( 86 FDA reports)
METABOLIC ACIDOSIS ( 86 FDA reports)
MYOCARDIAL ISCHAEMIA ( 86 FDA reports)
PATHOLOGICAL FRACTURE ( 86 FDA reports)
SINUS DISORDER ( 86 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 85 FDA reports)
AZOTAEMIA ( 85 FDA reports)
ERECTILE DYSFUNCTION ( 85 FDA reports)
HYDRONEPHROSIS ( 85 FDA reports)
PRODUCTIVE COUGH ( 85 FDA reports)
FLUID RETENTION ( 84 FDA reports)
FEELING HOT ( 83 FDA reports)
FISTULA ( 83 FDA reports)
MULTI-ORGAN FAILURE ( 83 FDA reports)
OESOPHAGITIS ( 83 FDA reports)
RHABDOMYOLYSIS ( 83 FDA reports)
UPPER LIMB FRACTURE ( 83 FDA reports)
ACCIDENTAL OVERDOSE ( 82 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 82 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 82 FDA reports)
KIDNEY INFECTION ( 82 FDA reports)
KYPHOSIS ( 82 FDA reports)
PERONEAL NERVE PALSY ( 82 FDA reports)
RESTLESSNESS ( 82 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 81 FDA reports)
ANGINA UNSTABLE ( 81 FDA reports)
CEREBRAL ATROPHY ( 81 FDA reports)
INADEQUATE ANALGESIA ( 81 FDA reports)
PERSONALITY CHANGE ( 81 FDA reports)
BREAST MASS ( 80 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 80 FDA reports)
DEPRESSED MOOD ( 80 FDA reports)
EXCORIATION ( 80 FDA reports)
GINGIVAL DISORDER ( 80 FDA reports)
MULTIPLE DRUG OVERDOSE ( 80 FDA reports)
NECROSIS ( 80 FDA reports)
SPINAL DISORDER ( 80 FDA reports)
FLANK PAIN ( 79 FDA reports)
FOOT DEFORMITY ( 79 FDA reports)
FUNGAL INFECTION ( 79 FDA reports)
LUNG NEOPLASM MALIGNANT ( 79 FDA reports)
MAJOR DEPRESSION ( 79 FDA reports)
SINUS BRADYCARDIA ( 79 FDA reports)
EJECTION FRACTION DECREASED ( 78 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 78 FDA reports)
HEPATIC CYST ( 78 FDA reports)
VISUAL ACUITY REDUCED ( 78 FDA reports)
DEAFNESS ( 77 FDA reports)
FLUID OVERLOAD ( 77 FDA reports)
GASTRIC ULCER ( 77 FDA reports)
MULTIPLE SCLEROSIS ( 77 FDA reports)
VENTRICULAR HYPERTROPHY ( 77 FDA reports)
DRUG ABUSE ( 76 FDA reports)
HEPATOMEGALY ( 76 FDA reports)
HYPOVOLAEMIA ( 76 FDA reports)
NOCTURIA ( 76 FDA reports)
PARANOIA ( 76 FDA reports)
PERIODONTITIS ( 76 FDA reports)
ACUTE RESPIRATORY FAILURE ( 75 FDA reports)
BLISTER ( 75 FDA reports)
BLOOD GLUCOSE DECREASED ( 75 FDA reports)
PEPTIC ULCER ( 75 FDA reports)
SCIATICA ( 75 FDA reports)
UTERINE LEIOMYOMA ( 75 FDA reports)
COMA ( 74 FDA reports)
CROHN'S DISEASE ( 74 FDA reports)
EATING DISORDER ( 74 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 74 FDA reports)
PHOTOPHOBIA ( 74 FDA reports)
CORONARY ARTERY OCCLUSION ( 73 FDA reports)
DRY SKIN ( 73 FDA reports)
MOBILITY DECREASED ( 73 FDA reports)
VENTRICULAR FIBRILLATION ( 73 FDA reports)
WITHDRAWAL SYNDROME ( 73 FDA reports)
CHOLECYSTECTOMY ( 72 FDA reports)
DIASTOLIC DYSFUNCTION ( 72 FDA reports)
DRUG TOLERANCE ( 72 FDA reports)
INTERSTITIAL LUNG DISEASE ( 72 FDA reports)
NIGHTMARE ( 72 FDA reports)
ORAL INFECTION ( 72 FDA reports)
BILIARY DYSKINESIA ( 71 FDA reports)
MENISCUS LESION ( 71 FDA reports)
OTITIS MEDIA ( 71 FDA reports)
PLASMACYTOMA ( 71 FDA reports)
ACUTE SINUSITIS ( 70 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 69 FDA reports)
BIPOLAR DISORDER ( 69 FDA reports)
BREAST CANCER METASTATIC ( 69 FDA reports)
CANDIDIASIS ( 69 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 69 FDA reports)
LYMPHOEDEMA ( 69 FDA reports)
PYELONEPHRITIS ( 69 FDA reports)
SPINAL CORD COMPRESSION ( 69 FDA reports)
SPINAL FRACTURE ( 69 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 69 FDA reports)
DEVICE FAILURE ( 68 FDA reports)
ENCEPHALOPATHY ( 68 FDA reports)
FAECAL INCONTINENCE ( 68 FDA reports)
GOITRE ( 68 FDA reports)
JOINT DISLOCATION ( 68 FDA reports)
LIBIDO DECREASED ( 68 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 68 FDA reports)
PSORIASIS ( 68 FDA reports)
SOMNAMBULISM ( 68 FDA reports)
SYNOVIAL CYST ( 68 FDA reports)
BLINDNESS ( 67 FDA reports)
BLOOD POTASSIUM INCREASED ( 67 FDA reports)
COORDINATION ABNORMAL ( 67 FDA reports)
SKIN DISCOLOURATION ( 67 FDA reports)
ATRIAL FLUTTER ( 66 FDA reports)
BLOOD SODIUM DECREASED ( 66 FDA reports)
FLATULENCE ( 66 FDA reports)
HYPERKERATOSIS ( 66 FDA reports)
LIMB DISCOMFORT ( 66 FDA reports)
ORTHOSTATIC HYPOTENSION ( 66 FDA reports)
OSTEORADIONECROSIS ( 66 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 66 FDA reports)
BONE DENSITY DECREASED ( 65 FDA reports)
DIVERTICULITIS ( 65 FDA reports)
DYSPHONIA ( 65 FDA reports)
MOOD ALTERED ( 65 FDA reports)
MUSCLE STRAIN ( 65 FDA reports)
PROTHROMBIN TIME PROLONGED ( 65 FDA reports)
STOMACH DISCOMFORT ( 65 FDA reports)
VISUAL DISTURBANCE ( 65 FDA reports)
GINGIVAL PAIN ( 64 FDA reports)
LOCALISED INFECTION ( 64 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 64 FDA reports)
PHARYNGITIS ( 64 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 64 FDA reports)
ULCER ( 64 FDA reports)
CEREBRAL ISCHAEMIA ( 63 FDA reports)
COMPLETED SUICIDE ( 63 FDA reports)
DEMENTIA ( 63 FDA reports)
DYSPHEMIA ( 63 FDA reports)
FAILURE TO THRIVE ( 63 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 63 FDA reports)
POST PROCEDURAL COMPLICATION ( 63 FDA reports)
SEQUESTRECTOMY ( 63 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 63 FDA reports)
VAGINAL INFECTION ( 63 FDA reports)
ABDOMINAL PAIN LOWER ( 62 FDA reports)
CYANOSIS ( 62 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 62 FDA reports)
LUMBAR RADICULOPATHY ( 62 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 62 FDA reports)
ORAL CANDIDIASIS ( 62 FDA reports)
ORAL SURGERY ( 62 FDA reports)
OVARIAN CYST ( 62 FDA reports)
PLEURITIC PAIN ( 62 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 62 FDA reports)
ANXIETY DISORDER ( 61 FDA reports)
CONJUNCTIVITIS ( 61 FDA reports)
HEMIPARESIS ( 61 FDA reports)
HYSTERECTOMY ( 61 FDA reports)
INJECTION SITE ERYTHEMA ( 61 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 61 FDA reports)
PULMONARY CONGESTION ( 61 FDA reports)
SEPTIC SHOCK ( 61 FDA reports)
BLOOD CALCIUM INCREASED ( 60 FDA reports)
INTESTINAL OBSTRUCTION ( 60 FDA reports)
MELAENA ( 60 FDA reports)
MUSCLE TWITCHING ( 60 FDA reports)
NEOPLASM PROGRESSION ( 60 FDA reports)
PELVIC PAIN ( 60 FDA reports)
CARDIOVASCULAR DISORDER ( 59 FDA reports)
COLD SWEAT ( 59 FDA reports)
CORONARY ARTERY STENOSIS ( 59 FDA reports)
FIBROSIS ( 59 FDA reports)
HYPOMAGNESAEMIA ( 59 FDA reports)
LIVER DISORDER ( 59 FDA reports)
PERIODONTAL DISEASE ( 59 FDA reports)
PSYCHOTIC DISORDER ( 59 FDA reports)
SENSITIVITY OF TEETH ( 59 FDA reports)
TENDON INJURY ( 59 FDA reports)
CAROTID ARTERY STENOSIS ( 58 FDA reports)
HEPATIC FAILURE ( 58 FDA reports)
HEPATIC LESION ( 58 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 58 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 58 FDA reports)
NECK INJURY ( 58 FDA reports)
NERVE INJURY ( 58 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 58 FDA reports)
BACTERIAL INFECTION ( 57 FDA reports)
BLOOD BILIRUBIN INCREASED ( 57 FDA reports)
BREAST CANCER ( 57 FDA reports)
DEVICE RELATED INFECTION ( 57 FDA reports)
METASTASES TO LUNG ( 57 FDA reports)
NERVOUS SYSTEM DISORDER ( 57 FDA reports)
POLYURIA ( 57 FDA reports)
RHINITIS ( 57 FDA reports)
BONE NEOPLASM MALIGNANT ( 56 FDA reports)
DYSLIPIDAEMIA ( 56 FDA reports)
ILEUS ( 56 FDA reports)
INTENTIONAL OVERDOSE ( 56 FDA reports)
SKIN LESION ( 56 FDA reports)
VASCULAR CALCIFICATION ( 56 FDA reports)
APHASIA ( 55 FDA reports)
ASPIRATION ( 55 FDA reports)
CHOLECYSTITIS ACUTE ( 55 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 55 FDA reports)
FAECES DISCOLOURED ( 55 FDA reports)
HALLUCINATION, VISUAL ( 55 FDA reports)
SKIN DISORDER ( 55 FDA reports)
EAR INFECTION ( 54 FDA reports)
FISTULA DISCHARGE ( 54 FDA reports)
JOINT SPRAIN ( 54 FDA reports)
PROTEINURIA ( 54 FDA reports)
THYROID DISORDER ( 54 FDA reports)
EYE PAIN ( 53 FDA reports)
GINGIVAL INFECTION ( 53 FDA reports)
GRAND MAL CONVULSION ( 53 FDA reports)
SINUS CONGESTION ( 53 FDA reports)
SKIN LACERATION ( 53 FDA reports)
TENDON RUPTURE ( 53 FDA reports)
WALKING AID USER ( 53 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 52 FDA reports)
ADRENAL MASS ( 52 FDA reports)
HYPERSOMNIA ( 52 FDA reports)
METASTASES TO LYMPH NODES ( 52 FDA reports)
MICTURITION URGENCY ( 52 FDA reports)
SEDATION ( 52 FDA reports)
TONGUE ULCERATION ( 52 FDA reports)
TOOTH EROSION ( 52 FDA reports)
ADRENAL INSUFFICIENCY ( 51 FDA reports)
ATRIAL SEPTAL DEFECT ( 51 FDA reports)
BEDRIDDEN ( 51 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 51 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 51 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 51 FDA reports)
FEELING COLD ( 51 FDA reports)
HAND FRACTURE ( 51 FDA reports)
PURULENCE ( 51 FDA reports)
RADIOTHERAPY ( 51 FDA reports)
BONE SCAN ABNORMAL ( 50 FDA reports)
COAGULOPATHY ( 50 FDA reports)
DECUBITUS ULCER ( 50 FDA reports)
GLAUCOMA ( 50 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 50 FDA reports)
LIMB INJURY ( 50 FDA reports)
PHARYNGEAL OEDEMA ( 50 FDA reports)
PNEUMONITIS ( 50 FDA reports)
PROSTATOMEGALY ( 50 FDA reports)
ABSCESS JAW ( 49 FDA reports)
BASAL CELL CARCINOMA ( 49 FDA reports)
BILE DUCT STONE ( 49 FDA reports)
EROSIVE OESOPHAGITIS ( 49 FDA reports)
GYNAECOMASTIA ( 49 FDA reports)
HYPOACUSIS ( 49 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 49 FDA reports)
INJECTION SITE HAEMATOMA ( 49 FDA reports)
MENORRHAGIA ( 49 FDA reports)
ORAL HERPES ( 49 FDA reports)
SKIN EXFOLIATION ( 49 FDA reports)
VAGINAL HAEMORRHAGE ( 49 FDA reports)
WOUND DRAINAGE ( 49 FDA reports)
ABSCESS LIMB ( 48 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 48 FDA reports)
GANGRENE ( 48 FDA reports)
INCREASED TENDENCY TO BRUISE ( 48 FDA reports)
MYOPATHY ( 48 FDA reports)
OEDEMA MOUTH ( 48 FDA reports)
ORTHOPNOEA ( 48 FDA reports)
RENAL ATROPHY ( 48 FDA reports)
RHONCHI ( 48 FDA reports)
SEBORRHOEIC KERATOSIS ( 48 FDA reports)
SPINAL FUSION SURGERY ( 48 FDA reports)
SPLENOMEGALY ( 48 FDA reports)
SWOLLEN TONGUE ( 48 FDA reports)
TOOTH REPAIR ( 48 FDA reports)
ANOXIC ENCEPHALOPATHY ( 47 FDA reports)
BACK DISORDER ( 47 FDA reports)
BLOOD ALBUMIN DECREASED ( 47 FDA reports)
CEREBRAL INFARCTION ( 47 FDA reports)
DENTAL FISTULA ( 47 FDA reports)
DIPLOPIA ( 47 FDA reports)
DRUG INTOLERANCE ( 47 FDA reports)
DRUG SCREEN POSITIVE ( 47 FDA reports)
IRON DEFICIENCY ANAEMIA ( 47 FDA reports)
JOINT STIFFNESS ( 47 FDA reports)
RETCHING ( 47 FDA reports)
WOUND ( 47 FDA reports)
DENTAL OPERATION ( 46 FDA reports)
DILATATION VENTRICULAR ( 46 FDA reports)
DRY EYE ( 46 FDA reports)
HAEMANGIOMA ( 46 FDA reports)
JAUNDICE ( 46 FDA reports)
JAW FRACTURE ( 46 FDA reports)
LIFE EXPECTANCY SHORTENED ( 46 FDA reports)
RASH GENERALISED ( 46 FDA reports)
SUBDURAL HAEMATOMA ( 46 FDA reports)
TENDON DISORDER ( 46 FDA reports)
TRAUMATIC BRAIN INJURY ( 46 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 45 FDA reports)
BONE SWELLING ( 45 FDA reports)
CERVICAL SPINAL STENOSIS ( 45 FDA reports)
EUPHORIC MOOD ( 45 FDA reports)
GALLBLADDER INJURY ( 45 FDA reports)
HYPOALBUMINAEMIA ( 45 FDA reports)
HYPOTHERMIA ( 45 FDA reports)
INCONTINENCE ( 45 FDA reports)
MITRAL VALVE PROLAPSE ( 45 FDA reports)
MOVEMENT DISORDER ( 45 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 45 FDA reports)
BONE GRAFT ( 44 FDA reports)
BONE LOSS ( 44 FDA reports)
DISEASE RECURRENCE ( 44 FDA reports)
HIP ARTHROPLASTY ( 44 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 44 FDA reports)
AORTIC ANEURYSM ( 43 FDA reports)
CEREBRAL HAEMORRHAGE ( 43 FDA reports)
COSTOCHONDRITIS ( 43 FDA reports)
HEPATITIS C ( 43 FDA reports)
MUSCLE TIGHTNESS ( 43 FDA reports)
PREGNANCY ( 43 FDA reports)
SOFT TISSUE DISORDER ( 43 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 43 FDA reports)
ABDOMINAL HERNIA ( 42 FDA reports)
ACCIDENT AT WORK ( 42 FDA reports)
CALCULUS URETERIC ( 42 FDA reports)
HYPERAESTHESIA ( 42 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 42 FDA reports)
LOCAL SWELLING ( 42 FDA reports)
POLYP ( 42 FDA reports)
RESPIRATORY DISORDER ( 42 FDA reports)
VENOUS INSUFFICIENCY ( 42 FDA reports)
BARRETT'S OESOPHAGUS ( 41 FDA reports)
BREAST PAIN ( 41 FDA reports)
DIALYSIS ( 41 FDA reports)
FEELING DRUNK ( 41 FDA reports)
GRANULOMA ( 41 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 41 FDA reports)
PUPIL FIXED ( 41 FDA reports)
VITAMIN B12 DEFICIENCY ( 41 FDA reports)
ANAPHYLACTIC REACTION ( 40 FDA reports)
ATROPHY ( 40 FDA reports)
BREATH ODOUR ( 40 FDA reports)
BRONCHOPNEUMONIA ( 40 FDA reports)
GASTRIC DISORDER ( 40 FDA reports)
HEPATITIS ( 40 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 40 FDA reports)
KNEE ARTHROPLASTY ( 40 FDA reports)
LACRIMATION INCREASED ( 40 FDA reports)
MENTAL IMPAIRMENT ( 40 FDA reports)
PROCEDURAL PAIN ( 40 FDA reports)
RASH ERYTHEMATOUS ( 40 FDA reports)
RASH MACULAR ( 40 FDA reports)
SENSORY LOSS ( 40 FDA reports)
SINUS POLYP ( 40 FDA reports)
TARDIVE DYSKINESIA ( 40 FDA reports)
TRISMUS ( 40 FDA reports)
APPLICATION SITE PRURITUS ( 39 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 39 FDA reports)
COLITIS ISCHAEMIC ( 39 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 39 FDA reports)
HOMICIDAL IDEATION ( 39 FDA reports)
IMPAIRED WORK ABILITY ( 39 FDA reports)
METASTATIC NEOPLASM ( 39 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 39 FDA reports)
TIBIA FRACTURE ( 39 FDA reports)
VERTEBROPLASTY ( 39 FDA reports)
ACTINIC KERATOSIS ( 38 FDA reports)
ACTINOMYCOSIS ( 38 FDA reports)
ARTHROPOD BITE ( 38 FDA reports)
BODY TEMPERATURE INCREASED ( 38 FDA reports)
DENTURE WEARER ( 38 FDA reports)
DERMATITIS ( 38 FDA reports)
ECCHYMOSIS ( 38 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 38 FDA reports)
GINGIVAL ULCERATION ( 38 FDA reports)
OESOPHAGEAL PAIN ( 38 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 38 FDA reports)
POOR QUALITY SLEEP ( 38 FDA reports)
RENAL TUBULAR NECROSIS ( 38 FDA reports)
THYROID CANCER ( 38 FDA reports)
ABDOMINAL TENDERNESS ( 37 FDA reports)
ANKLE FRACTURE ( 37 FDA reports)
ATAXIA ( 37 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 37 FDA reports)
BONE EROSION ( 37 FDA reports)
BRAIN NEOPLASM ( 37 FDA reports)
CHROMATURIA ( 37 FDA reports)
CLOSTRIDIAL INFECTION ( 37 FDA reports)
EDENTULOUS ( 37 FDA reports)
GINGIVAL OEDEMA ( 37 FDA reports)
LEFT ATRIAL DILATATION ( 37 FDA reports)
NODULE ( 37 FDA reports)
PANIC DISORDER ( 37 FDA reports)
PARAESTHESIA ORAL ( 37 FDA reports)
PERITONITIS ( 37 FDA reports)
PULMONARY MASS ( 37 FDA reports)
RENAL INJURY ( 37 FDA reports)
THYROIDECTOMY ( 37 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 37 FDA reports)
WOUND INFECTION ( 37 FDA reports)
ALVEOLOPLASTY ( 36 FDA reports)
BIOPSY ( 36 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 36 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 36 FDA reports)
BONE FRAGMENTATION ( 36 FDA reports)
CERVICAL DYSPLASIA ( 36 FDA reports)
COMMUNICATION DISORDER ( 36 FDA reports)
DIABETIC KETOACIDOSIS ( 36 FDA reports)
ELECTROLYTE IMBALANCE ( 36 FDA reports)
ESSENTIAL HYPERTENSION ( 36 FDA reports)
GINGIVAL RECESSION ( 36 FDA reports)
HEART RATE DECREASED ( 36 FDA reports)
HERNIA ( 36 FDA reports)
HYPERCOAGULATION ( 36 FDA reports)
LIPOMA ( 36 FDA reports)
METAPLASIA ( 36 FDA reports)
OTORRHOEA ( 36 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 36 FDA reports)
ACUTE CORONARY SYNDROME ( 35 FDA reports)
AFFECTIVE DISORDER ( 35 FDA reports)
APNOEA ( 35 FDA reports)
APPLICATION SITE ERYTHEMA ( 35 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 35 FDA reports)
CHOLESTEROSIS ( 35 FDA reports)
DERMAL CYST ( 35 FDA reports)
EYE DISORDER ( 35 FDA reports)
GUN SHOT WOUND ( 35 FDA reports)
MELANOCYTIC NAEVUS ( 35 FDA reports)
MUSCLE INJURY ( 35 FDA reports)
NEURODERMATITIS ( 35 FDA reports)
OCCULT BLOOD POSITIVE ( 35 FDA reports)
PARKINSON'S DISEASE ( 35 FDA reports)
PATHOLOGICAL GAMBLING ( 35 FDA reports)
PLANTAR FASCIITIS ( 35 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 35 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 35 FDA reports)
WOUND SECRETION ( 35 FDA reports)
WRIST FRACTURE ( 34 FDA reports)
ALCOHOLISM ( 34 FDA reports)
BACTERAEMIA ( 34 FDA reports)
BRAIN CONTUSION ( 34 FDA reports)
BREAST CALCIFICATIONS ( 34 FDA reports)
BRONCHOSPASM ( 34 FDA reports)
CARDIAC VALVE DISEASE ( 34 FDA reports)
DEVICE MALFUNCTION ( 34 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 34 FDA reports)
FACIAL PAIN ( 34 FDA reports)
INCOHERENT ( 34 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 34 FDA reports)
INJECTION SITE REACTION ( 34 FDA reports)
INJECTION SITE SWELLING ( 34 FDA reports)
LOWER LIMB FRACTURE ( 34 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 34 FDA reports)
POST CONCUSSION SYNDROME ( 34 FDA reports)
RALES ( 34 FDA reports)
RECTAL POLYP ( 34 FDA reports)
RENAL PAIN ( 34 FDA reports)
SEASONAL ALLERGY ( 34 FDA reports)
SENSORY DISTURBANCE ( 34 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 34 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 34 FDA reports)
UROSEPSIS ( 34 FDA reports)
VARICOSE VEIN ( 34 FDA reports)
BILIARY COLIC ( 33 FDA reports)
CATARACT OPERATION ( 33 FDA reports)
CIRCULATORY COLLAPSE ( 33 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 33 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 33 FDA reports)
DROWNING ( 33 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 33 FDA reports)
FEELING JITTERY ( 33 FDA reports)
GASTRITIS EROSIVE ( 33 FDA reports)
INFUSION RELATED REACTION ( 33 FDA reports)
INGUINAL HERNIA ( 33 FDA reports)
INJECTION SITE HAEMORRHAGE ( 33 FDA reports)
LIP SWELLING ( 33 FDA reports)
MACULAR DEGENERATION ( 33 FDA reports)
MITRAL VALVE CALCIFICATION ( 33 FDA reports)
MUSCLE CRAMP ( 33 FDA reports)
ORAL CAVITY FISTULA ( 33 FDA reports)
PROSTATE CANCER METASTATIC ( 33 FDA reports)
STEM CELL TRANSPLANT ( 33 FDA reports)
STEVENS-JOHNSON SYNDROME ( 33 FDA reports)
STRESS FRACTURE ( 33 FDA reports)
TENSION ( 33 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 33 FDA reports)
WOUND DEHISCENCE ( 33 FDA reports)
ABSCESS ORAL ( 32 FDA reports)
ACETABULUM FRACTURE ( 32 FDA reports)
ACNE ( 32 FDA reports)
ANGIOPATHY ( 32 FDA reports)
APHTHOUS STOMATITIS ( 32 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 32 FDA reports)
BLINDNESS UNILATERAL ( 32 FDA reports)
CARDIAC ENZYMES INCREASED ( 32 FDA reports)
COLON ADENOMA ( 32 FDA reports)
CRANIOTOMY ( 32 FDA reports)
FRACTURE ( 32 FDA reports)
FURUNCLE ( 32 FDA reports)
GENERALISED OEDEMA ( 32 FDA reports)
HAEMANGIOMA OF LIVER ( 32 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 32 FDA reports)
NON-CARDIAC CHEST PAIN ( 32 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 32 FDA reports)
ODYNOPHAGIA ( 32 FDA reports)
PLATELET COUNT INCREASED ( 32 FDA reports)
PLEURAL FIBROSIS ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
POLYSUBSTANCE ABUSE ( 32 FDA reports)
VITAMIN D DECREASED ( 32 FDA reports)
VITAMIN D DEFICIENCY ( 32 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 31 FDA reports)
AORTIC STENOSIS ( 31 FDA reports)
BUNION ( 31 FDA reports)
CEREBROVASCULAR DISORDER ( 31 FDA reports)
CHANGE OF BOWEL HABIT ( 31 FDA reports)
DILATATION ATRIAL ( 31 FDA reports)
EXERCISE TOLERANCE DECREASED ( 31 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 31 FDA reports)
FIBULA FRACTURE ( 31 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 31 FDA reports)
INCREASED APPETITE ( 31 FDA reports)
PALLOR ( 31 FDA reports)
PROSTATITIS ( 31 FDA reports)
SQUAMOUS CELL CARCINOMA ( 31 FDA reports)
ADENOCARCINOMA ( 30 FDA reports)
AMENORRHOEA ( 30 FDA reports)
DERMATITIS CONTACT ( 30 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 30 FDA reports)
EAR DISORDER ( 30 FDA reports)
FACIAL PALSY ( 30 FDA reports)
ISCHAEMIA ( 30 FDA reports)
LABORATORY TEST ABNORMAL ( 30 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
OESOPHAGEAL ULCER ( 30 FDA reports)
OPEN WOUND ( 30 FDA reports)
PERICARDITIS ( 30 FDA reports)
PETECHIAE ( 30 FDA reports)
POLYARTHRITIS ( 30 FDA reports)
PROCTALGIA ( 30 FDA reports)
PSEUDOMONAS INFECTION ( 30 FDA reports)
PULSE ABSENT ( 30 FDA reports)
RADIUS FRACTURE ( 30 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 30 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 30 FDA reports)
ACIDOSIS ( 29 FDA reports)
ADVERSE DRUG REACTION ( 29 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 29 FDA reports)
ATHEROSCLEROSIS ( 29 FDA reports)
BILE DUCT STENOSIS ( 29 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 29 FDA reports)
BLOOD PRESSURE ABNORMAL ( 29 FDA reports)
HYPERTONIC BLADDER ( 29 FDA reports)
HYPOKINESIA ( 29 FDA reports)
INGROWING NAIL ( 29 FDA reports)
LUNG CONSOLIDATION ( 29 FDA reports)
LUNG INFECTION ( 29 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 29 FDA reports)
MUSCLE ATROPHY ( 29 FDA reports)
MUSCULOSKELETAL DISORDER ( 29 FDA reports)
NECK MASS ( 29 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 29 FDA reports)
NEUROMA ( 29 FDA reports)
ONYCHOMYCOSIS ( 29 FDA reports)
RASH MACULO-PAPULAR ( 29 FDA reports)
SHOCK ( 29 FDA reports)
SHOULDER ARTHROPLASTY ( 29 FDA reports)
SKIN BURNING SENSATION ( 29 FDA reports)
TONGUE INJURY ( 29 FDA reports)
ACCIDENT ( 28 FDA reports)
ANEURYSM ( 28 FDA reports)
APPENDICECTOMY ( 28 FDA reports)
APPENDICITIS ( 28 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 28 FDA reports)
DEAFNESS NEUROSENSORY ( 28 FDA reports)
ESCHERICHIA INFECTION ( 28 FDA reports)
GINGIVAL ERYTHEMA ( 28 FDA reports)
HEPATIC CIRRHOSIS ( 28 FDA reports)
INTENTIONAL SELF-INJURY ( 28 FDA reports)
JOINT CREPITATION ( 28 FDA reports)
KLEBSIELLA INFECTION ( 28 FDA reports)
MENOPAUSE ( 28 FDA reports)
MYDRIASIS ( 28 FDA reports)
NEUTROPHIL COUNT INCREASED ( 28 FDA reports)
OESOPHAGEAL STENOSIS ( 28 FDA reports)
PAROTITIS ( 28 FDA reports)
PHLEBITIS ( 28 FDA reports)
POOR PERSONAL HYGIENE ( 28 FDA reports)
PULMONARY INFARCTION ( 28 FDA reports)
RASH PAPULAR ( 28 FDA reports)
RESPIRATORY TRACT INFECTION ( 28 FDA reports)
SARCOIDOSIS ( 28 FDA reports)
SICK SINUS SYNDROME ( 28 FDA reports)
SKELETAL INJURY ( 28 FDA reports)
SKIN PAPILLOMA ( 28 FDA reports)
STREPTOCOCCAL INFECTION ( 28 FDA reports)
STREPTOCOCCAL SEPSIS ( 28 FDA reports)
TELANGIECTASIA ( 28 FDA reports)
THIRST ( 28 FDA reports)
THYROID NEOPLASM ( 28 FDA reports)
VASCULITIS ( 28 FDA reports)
WHEELCHAIR USER ( 28 FDA reports)
WEIGHT FLUCTUATION ( 27 FDA reports)
AORTIC DISORDER ( 27 FDA reports)
BREATH SOUNDS ABNORMAL ( 27 FDA reports)
BRONCHITIS ACUTE ( 27 FDA reports)
CARDIAC FLUTTER ( 27 FDA reports)
DRUG ADMINISTRATION ERROR ( 27 FDA reports)
DYSMENORRHOEA ( 27 FDA reports)
EMBOLIC STROKE ( 27 FDA reports)
HEART VALVE INCOMPETENCE ( 27 FDA reports)
HYPOAESTHESIA FACIAL ( 27 FDA reports)
ILEUS PARALYTIC ( 27 FDA reports)
INDURATION ( 27 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 27 FDA reports)
MONOCYTE COUNT INCREASED ( 27 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 27 FDA reports)
PLEURISY ( 27 FDA reports)
SNORING ( 27 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 27 FDA reports)
VITREOUS FLOATERS ( 27 FDA reports)
ANAEMIA POSTOPERATIVE ( 26 FDA reports)
BRAIN OEDEMA ( 26 FDA reports)
COLITIS ULCERATIVE ( 26 FDA reports)
CONCUSSION ( 26 FDA reports)
DECREASED ACTIVITY ( 26 FDA reports)
DENTAL CARE ( 26 FDA reports)
DUODENAL ULCER ( 26 FDA reports)
EPICONDYLITIS ( 26 FDA reports)
EYE INJURY ( 26 FDA reports)
GASTROINTESTINAL PAIN ( 26 FDA reports)
HYPOVENTILATION ( 26 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 26 FDA reports)
PRODUCT ADHESION ISSUE ( 26 FDA reports)
SCHIZOPHRENIA ( 26 FDA reports)
SEXUAL DYSFUNCTION ( 26 FDA reports)
SPINAL DEFORMITY ( 26 FDA reports)
TEARFULNESS ( 26 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 26 FDA reports)
ALCOHOL USE ( 25 FDA reports)
ANGIOEDEMA ( 25 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 25 FDA reports)
BLADDER CANCER ( 25 FDA reports)
BONE MARROW FAILURE ( 25 FDA reports)
FAMILY STRESS ( 25 FDA reports)
GLOSSODYNIA ( 25 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 25 FDA reports)
HYPERTENSIVE HEART DISEASE ( 25 FDA reports)
INJECTION SITE PRURITUS ( 25 FDA reports)
LARYNGEAL OEDEMA ( 25 FDA reports)
MENINGITIS ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
PELVIC FRACTURE ( 25 FDA reports)
RESUSCITATION ( 25 FDA reports)
STENT PLACEMENT ( 25 FDA reports)
THROAT TIGHTNESS ( 25 FDA reports)
TYPE 1 DIABETES MELLITUS ( 25 FDA reports)
VENA CAVA THROMBOSIS ( 25 FDA reports)
VISUAL FIELD DEFECT ( 25 FDA reports)
BRUXISM ( 24 FDA reports)
CLAVICLE FRACTURE ( 24 FDA reports)
DRUG ERUPTION ( 24 FDA reports)
DYSTHYMIC DISORDER ( 24 FDA reports)
EMPYEMA ( 24 FDA reports)
EYE SWELLING ( 24 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 24 FDA reports)
GALLBLADDER OPERATION ( 24 FDA reports)
GASTROENTERITIS VIRAL ( 24 FDA reports)
HAEMODIALYSIS ( 24 FDA reports)
HICCUPS ( 24 FDA reports)
HYPERCAPNIA ( 24 FDA reports)
HYPERVENTILATION ( 24 FDA reports)
LABYRINTHITIS ( 24 FDA reports)
MALIGNANT MELANOMA ( 24 FDA reports)
METASTASES TO MENINGES ( 24 FDA reports)
NERVE COMPRESSION ( 24 FDA reports)
NEUTROPHIL COUNT DECREASED ( 24 FDA reports)
ORAL INTAKE REDUCED ( 24 FDA reports)
PULMONARY VALVE STENOSIS ( 24 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 24 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 24 FDA reports)
STOMATITIS NECROTISING ( 24 FDA reports)
SYNOVITIS ( 24 FDA reports)
TOBACCO USER ( 24 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 24 FDA reports)
ABSCESS DRAINAGE ( 23 FDA reports)
AGRANULOCYTOSIS ( 23 FDA reports)
ANOGENITAL WARTS ( 23 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 23 FDA reports)
BONE MARROW OEDEMA ( 23 FDA reports)
BONE OPERATION ( 23 FDA reports)
BRONCHIECTASIS ( 23 FDA reports)
BRONCHIOLITIS ( 23 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 23 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 23 FDA reports)
CHRONIC FATIGUE SYNDROME ( 23 FDA reports)
DEVELOPMENTAL DELAY ( 23 FDA reports)
DUODENITIS ( 23 FDA reports)
FAECALOMA ( 23 FDA reports)
HODGKIN'S DISEASE ( 23 FDA reports)
HOSPITALISATION ( 23 FDA reports)
INJECTION SITE RASH ( 23 FDA reports)
INTESTINAL PERFORATION ( 23 FDA reports)
INTRACARDIAC THROMBUS ( 23 FDA reports)
KYPHOSCOLIOSIS ( 23 FDA reports)
LACTOSE INTOLERANCE ( 23 FDA reports)
LIGAMENT INJURY ( 23 FDA reports)
LIGAMENT SPRAIN ( 23 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 23 FDA reports)
MANIA ( 23 FDA reports)
OSTEITIS DEFORMANS ( 23 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 23 FDA reports)
PNEUMONIA VIRAL ( 23 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 23 FDA reports)
PULMONARY GRANULOMA ( 23 FDA reports)
RESPIRATORY TRACT CONGESTION ( 23 FDA reports)
SERUM FERRITIN INCREASED ( 23 FDA reports)
TESTICULAR PAIN ( 23 FDA reports)
THERMAL BURN ( 23 FDA reports)
TONGUE DISORDER ( 23 FDA reports)
URINE OUTPUT DECREASED ( 23 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 23 FDA reports)
VULVOVAGINAL DRYNESS ( 22 FDA reports)
ADENOMA BENIGN ( 22 FDA reports)
AORTIC DILATATION ( 22 FDA reports)
APATHY ( 22 FDA reports)
APPETITE DISORDER ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK ( 22 FDA reports)
ATROPHIC VULVOVAGINITIS ( 22 FDA reports)
BLADDER CATHETERISATION ( 22 FDA reports)
BLOOD CHLORIDE DECREASED ( 22 FDA reports)
BLOOD MAGNESIUM DECREASED ( 22 FDA reports)
BREAST TENDERNESS ( 22 FDA reports)
CERVICAL MYELOPATHY ( 22 FDA reports)
CHEST TUBE INSERTION ( 22 FDA reports)
CHEST X-RAY ABNORMAL ( 22 FDA reports)
DRUG DISPENSING ERROR ( 22 FDA reports)
ENTEROCOCCAL INFECTION ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 22 FDA reports)
HELICOBACTER INFECTION ( 22 FDA reports)
HUMERUS FRACTURE ( 22 FDA reports)
HYPERMETABOLISM ( 22 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 22 FDA reports)
IMMUNODEFICIENCY ( 22 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 22 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 22 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 22 FDA reports)
MIDDLE INSOMNIA ( 22 FDA reports)
MITRAL VALVE DISEASE ( 22 FDA reports)
MOUTH HAEMORRHAGE ( 22 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 22 FDA reports)
MYELODYSPLASTIC SYNDROME ( 22 FDA reports)
NASAL MUCOSAL DISORDER ( 22 FDA reports)
OSTEOMYELITIS ACUTE ( 22 FDA reports)
OVERWEIGHT ( 22 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 22 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 22 FDA reports)
SELF-INJURIOUS IDEATION ( 22 FDA reports)
SNEEZING ( 22 FDA reports)
ADNEXA UTERI CYST ( 21 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 21 FDA reports)
APHAGIA ( 21 FDA reports)
ARTERIAL STENOSIS ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 21 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 21 FDA reports)
CAUDA EQUINA SYNDROME ( 21 FDA reports)
DENTAL PROSTHESIS USER ( 21 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 21 FDA reports)
DIABETIC COMA ( 21 FDA reports)
DIFFICULTY IN WALKING ( 21 FDA reports)
DYSPLASTIC NAEVUS ( 21 FDA reports)
GLOMERULONEPHRITIS ( 21 FDA reports)
GOUTY ARTHRITIS ( 21 FDA reports)
HEARING IMPAIRED ( 21 FDA reports)
HEPATIC MASS ( 21 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 21 FDA reports)
ISCHAEMIC STROKE ( 21 FDA reports)
LIGAMENT RUPTURE ( 21 FDA reports)
NEPHROSCLEROSIS ( 21 FDA reports)
OESOPHAGEAL SPASM ( 21 FDA reports)
ORTHOSIS USER ( 21 FDA reports)
PARONYCHIA ( 21 FDA reports)
PHOTOSENSITIVITY REACTION ( 21 FDA reports)
RENAL MASS ( 21 FDA reports)
SELF-MEDICATION ( 21 FDA reports)
SLEEP TALKING ( 21 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 21 FDA reports)
SUDDEN DEATH ( 21 FDA reports)
TENOSYNOVITIS ( 21 FDA reports)
THERAPY NON-RESPONDER ( 21 FDA reports)
THROMBOPHLEBITIS ( 21 FDA reports)
THYROIDITIS ( 21 FDA reports)
TRANSFUSION ( 21 FDA reports)
UMBILICAL HERNIA ( 21 FDA reports)
UTERINE CANCER ( 21 FDA reports)
VITREOUS DETACHMENT ( 21 FDA reports)
WOUND COMPLICATION ( 21 FDA reports)
ABDOMINAL MASS ( 20 FDA reports)
APLASTIC ANAEMIA ( 20 FDA reports)
BLOOD CULTURE POSITIVE ( 20 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 20 FDA reports)
CUSHINGOID ( 20 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 20 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 20 FDA reports)
GINGIVAL SWELLING ( 20 FDA reports)
HERNIA REPAIR ( 20 FDA reports)
HYPERTHYROIDISM ( 20 FDA reports)
INTERMITTENT CLAUDICATION ( 20 FDA reports)
INTESTINAL HAEMORRHAGE ( 20 FDA reports)
INTRACRANIAL ANEURYSM ( 20 FDA reports)
LIPASE INCREASED ( 20 FDA reports)
LUNG HYPERINFLATION ( 20 FDA reports)
MENINGIOMA ( 20 FDA reports)
METASTATIC PAIN ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MULTI-ORGAN DISORDER ( 20 FDA reports)
MUMPS ( 20 FDA reports)
NEUROPATHY ( 20 FDA reports)
NO ADVERSE EVENT ( 20 FDA reports)
NO THERAPEUTIC RESPONSE ( 20 FDA reports)
NODAL RHYTHM ( 20 FDA reports)
OVARIAN MASS ( 20 FDA reports)
PERIARTHRITIS ( 20 FDA reports)
POLYDIPSIA ( 20 FDA reports)
PRESBYOPIA ( 20 FDA reports)
SALIVARY HYPERSECRETION ( 20 FDA reports)
SINUS HEADACHE ( 20 FDA reports)
SOCIAL PROBLEM ( 20 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 20 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 20 FDA reports)
TRANSAMINASES INCREASED ( 20 FDA reports)
VENTRICULAR HYPOKINESIA ( 20 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 19 FDA reports)
ADNEXA UTERI MASS ( 19 FDA reports)
ADRENAL ADENOMA ( 19 FDA reports)
ALCOHOL POISONING ( 19 FDA reports)
APPLICATION SITE REACTION ( 19 FDA reports)
APPLICATION SITE VESICLES ( 19 FDA reports)
AUTOIMMUNE THYROIDITIS ( 19 FDA reports)
BURNS SECOND DEGREE ( 19 FDA reports)
CAROTID ARTERY DISEASE ( 19 FDA reports)
COLON POLYPECTOMY ( 19 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 19 FDA reports)
DEPRESSIVE SYMPTOM ( 19 FDA reports)
DIABETIC GASTROPARESIS ( 19 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 19 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 19 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 19 FDA reports)
EYE IRRITATION ( 19 FDA reports)
FLAT AFFECT ( 19 FDA reports)
HALLUCINATION, AUDITORY ( 19 FDA reports)
HYDROURETER ( 19 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 19 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 19 FDA reports)
MYELOPATHY ( 19 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 19 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 19 FDA reports)
PARALYSIS ( 19 FDA reports)
PERFORMANCE STATUS DECREASED ( 19 FDA reports)
POST HERPETIC NEURALGIA ( 19 FDA reports)
RESPIRATORY RATE INCREASED ( 19 FDA reports)
RIGHT ATRIAL DILATATION ( 19 FDA reports)
RUBELLA ( 19 FDA reports)
SCARLET FEVER ( 19 FDA reports)
SKIN CANDIDA ( 19 FDA reports)
SPUTUM DISCOLOURED ( 19 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 19 FDA reports)
STRESS URINARY INCONTINENCE ( 19 FDA reports)
SUBCUTANEOUS ABSCESS ( 19 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 19 FDA reports)
VENOUS THROMBOSIS ( 19 FDA reports)
ADHESION ( 18 FDA reports)
ANAL FISSURE ( 18 FDA reports)
ANGIOPLASTY ( 18 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 18 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 18 FDA reports)
BREAST CYST ( 18 FDA reports)
BRONCHITIS CHRONIC ( 18 FDA reports)
CARBUNCLE ( 18 FDA reports)
CATHETER PLACEMENT ( 18 FDA reports)
COLON CANCER ( 18 FDA reports)
COMMINUTED FRACTURE ( 18 FDA reports)
CORONARY ARTERY BYPASS ( 18 FDA reports)
DEVICE OCCLUSION ( 18 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 18 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 18 FDA reports)
ECZEMA ( 18 FDA reports)
ENDOTRACHEAL INTUBATION ( 18 FDA reports)
ESCHERICHIA BACTERAEMIA ( 18 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 18 FDA reports)
GAMMOPATHY ( 18 FDA reports)
HEPATIC CANCER METASTATIC ( 18 FDA reports)
HEPATOSPLENOMEGALY ( 18 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 18 FDA reports)
HYPERPARATHYROIDISM ( 18 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 18 FDA reports)
INCISIONAL DRAINAGE ( 18 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 18 FDA reports)
INTESTINAL POLYP ( 18 FDA reports)
JOINT LOCK ( 18 FDA reports)
JUGULAR VEIN THROMBOSIS ( 18 FDA reports)
LEUKAEMIA ( 18 FDA reports)
LYMPHOMA ( 18 FDA reports)
MACROCYTOSIS ( 18 FDA reports)
MARROW HYPERPLASIA ( 18 FDA reports)
MAXILLOFACIAL OPERATION ( 18 FDA reports)
MEDICAL DEVICE REMOVAL ( 18 FDA reports)
MENSTRUATION IRREGULAR ( 18 FDA reports)
MICTURITION DISORDER ( 18 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 18 FDA reports)
PROSTATE CANCER ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RADIAL NERVE PALSY ( 18 FDA reports)
RESPIRATORY DEPRESSION ( 18 FDA reports)
SCIATIC NERVE INJURY ( 18 FDA reports)
SEROMA ( 18 FDA reports)
SHOULDER PAIN ( 18 FDA reports)
SKIN HYPERTROPHY ( 18 FDA reports)
VENTRICULAR DYSFUNCTION ( 18 FDA reports)
ABORTION SPONTANEOUS ( 17 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 17 FDA reports)
AORTIC VALVE DISEASE ( 17 FDA reports)
APPLICATION SITE RASH ( 17 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 17 FDA reports)
ARTHRITIS BACTERIAL ( 17 FDA reports)
ASPIRATION PLEURAL CAVITY ( 17 FDA reports)
BLOOD IRON DECREASED ( 17 FDA reports)
BONE DEFORMITY ( 17 FDA reports)
BONE GIANT CELL TUMOUR ( 17 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 17 FDA reports)
BRAIN CANCER METASTATIC ( 17 FDA reports)
BULLOUS LUNG DISEASE ( 17 FDA reports)
CACHEXIA ( 17 FDA reports)
CAESAREAN SECTION ( 17 FDA reports)
CARDIAC PACEMAKER INSERTION ( 17 FDA reports)
CATHETERISATION CARDIAC ( 17 FDA reports)
CHONDROMALACIA ( 17 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 17 FDA reports)
DERMATITIS ATOPIC ( 17 FDA reports)
DYSPAREUNIA ( 17 FDA reports)
DYSTONIA ( 17 FDA reports)
EAR DISCOMFORT ( 17 FDA reports)
EPIGASTRIC DISCOMFORT ( 17 FDA reports)
EXTRASYSTOLES ( 17 FDA reports)
FAT NECROSIS ( 17 FDA reports)
FEELING GUILTY ( 17 FDA reports)
FIBRIN D DIMER INCREASED ( 17 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 17 FDA reports)
GASTROINTESTINAL PERFORATION ( 17 FDA reports)
HALLUCINATIONS, MIXED ( 17 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HERPES SIMPLEX ( 17 FDA reports)
HYDROCEPHALUS ( 17 FDA reports)
HYPERPHOSPHATAEMIA ( 17 FDA reports)
HYPERPLASIA ( 17 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 17 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 17 FDA reports)
LARYNGITIS ( 17 FDA reports)
LEG AMPUTATION ( 17 FDA reports)
MEDICAL DEVICE COMPLICATION ( 17 FDA reports)
METABOLIC ENCEPHALOPATHY ( 17 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 17 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 17 FDA reports)
NASAL DISORDER ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
ORGAN FAILURE ( 17 FDA reports)
OTITIS EXTERNA ( 17 FDA reports)
PCO2 DECREASED ( 17 FDA reports)
PERIRECTAL ABSCESS ( 17 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 17 FDA reports)
PRURITUS GENERALISED ( 17 FDA reports)
PUPILS UNEQUAL ( 17 FDA reports)
REFLUX OESOPHAGITIS ( 17 FDA reports)
SCRATCH ( 17 FDA reports)
SKIN INDURATION ( 17 FDA reports)
SKIN INFECTION ( 17 FDA reports)
THYROID CYST ( 17 FDA reports)
TONSILLAR HYPERTROPHY ( 17 FDA reports)
TROPONIN INCREASED ( 17 FDA reports)
UTERINE POLYP ( 17 FDA reports)
YAWNING ( 17 FDA reports)
WEIGHT BEARING DIFFICULTY ( 17 FDA reports)
ACUTE LEUKAEMIA ( 16 FDA reports)
BLOOD DISORDER ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 16 FDA reports)
BLOOD URINE PRESENT ( 16 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 16 FDA reports)
CRANIOSYNOSTOSIS ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 16 FDA reports)
ENDOMETRIOSIS ( 16 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 16 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 16 FDA reports)
EYE HAEMORRHAGE ( 16 FDA reports)
HAEMORRHAGIC ANAEMIA ( 16 FDA reports)
HEART INJURY ( 16 FDA reports)
HEPATIC ENZYME ABNORMAL ( 16 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 16 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 16 FDA reports)
LOSS OF EMPLOYMENT ( 16 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 16 FDA reports)
NASAL POLYPS ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 16 FDA reports)
OEDEMA MUCOSAL ( 16 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 16 FDA reports)
PANCREATIC CARCINOMA ( 16 FDA reports)
PANCREATITIS CHRONIC ( 16 FDA reports)
PREMATURE LABOUR ( 16 FDA reports)
PROCEDURAL HYPERTENSION ( 16 FDA reports)
PROTEIN TOTAL DECREASED ( 16 FDA reports)
PULMONARY HAEMORRHAGE ( 16 FDA reports)
PULMONARY HILUM MASS ( 16 FDA reports)
QUALITY OF LIFE DECREASED ( 16 FDA reports)
RENAL CANCER ( 16 FDA reports)
ROTATOR CUFF REPAIR ( 16 FDA reports)
SENSATION OF HEAVINESS ( 16 FDA reports)
SPONDYLOSIS ( 16 FDA reports)
STARING ( 16 FDA reports)
STASIS DERMATITIS ( 16 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 16 FDA reports)
SUBSTANCE ABUSE ( 16 FDA reports)
SUICIDAL BEHAVIOUR ( 16 FDA reports)
TACHYARRHYTHMIA ( 16 FDA reports)
TACHYPNOEA ( 16 FDA reports)
TENOSYNOVITIS STENOSANS ( 16 FDA reports)
TOE AMPUTATION ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 15 FDA reports)
APPLICATION SITE PAIN ( 15 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 15 FDA reports)
ATRIAL TACHYCARDIA ( 15 FDA reports)
BEREAVEMENT REACTION ( 15 FDA reports)
BLADDER PROLAPSE ( 15 FDA reports)
BLEPHARITIS ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 15 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 15 FDA reports)
BODY HEIGHT DECREASED ( 15 FDA reports)
CARBON DIOXIDE INCREASED ( 15 FDA reports)
CARDIOGENIC SHOCK ( 15 FDA reports)
CATHETER SITE INFECTION ( 15 FDA reports)
CAUSTIC INJURY ( 15 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 15 FDA reports)
CERUMEN IMPACTION ( 15 FDA reports)
DEVICE BREAKAGE ( 15 FDA reports)
DIABETIC RETINOPATHY ( 15 FDA reports)
DIZZINESS POSTURAL ( 15 FDA reports)
FACIAL BONES FRACTURE ( 15 FDA reports)
FORMICATION ( 15 FDA reports)
GASTRIC HAEMORRHAGE ( 15 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 15 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 15 FDA reports)
IMMUNE SYSTEM DISORDER ( 15 FDA reports)
INITIAL INSOMNIA ( 15 FDA reports)
INTERTRIGO ( 15 FDA reports)
INTRAOCULAR LENS IMPLANT ( 15 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 15 FDA reports)
LOCALISED OEDEMA ( 15 FDA reports)
MASTECTOMY ( 15 FDA reports)
MONOPLEGIA ( 15 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 15 FDA reports)
MYOCLONIC EPILEPSY ( 15 FDA reports)
NERVE ROOT COMPRESSION ( 15 FDA reports)
NICOTINE DEPENDENCE ( 15 FDA reports)
NYSTAGMUS ( 15 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
PHYSICAL ASSAULT ( 15 FDA reports)
PROCEDURAL COMPLICATION ( 15 FDA reports)
PROTEIN TOTAL INCREASED ( 15 FDA reports)
PULMONARY THROMBOSIS ( 15 FDA reports)
RENAL CELL CARCINOMA ( 15 FDA reports)
SCAB ( 15 FDA reports)
SINUS OPERATION ( 15 FDA reports)
THORACOTOMY ( 15 FDA reports)
TOOTH IMPACTED ( 15 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 15 FDA reports)
TUMOUR EXCISION ( 15 FDA reports)
URINARY TRACT DISORDER ( 15 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 15 FDA reports)
ACUTE PSYCHOSIS ( 14 FDA reports)
AKATHISIA ( 14 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 14 FDA reports)
BACTERIAL DISEASE CARRIER ( 14 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 14 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 14 FDA reports)
BODY TEMPERATURE DECREASED ( 14 FDA reports)
BONE ATROPHY ( 14 FDA reports)
BREAST CANCER RECURRENT ( 14 FDA reports)
BREAST INFECTION ( 14 FDA reports)
CERVICITIS ( 14 FDA reports)
CERVICOBRACHIAL SYNDROME ( 14 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 14 FDA reports)
CSF PROTEIN INCREASED ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
DYSAESTHESIA ( 14 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 14 FDA reports)
EYE DISCHARGE ( 14 FDA reports)
FLUID INTAKE REDUCED ( 14 FDA reports)
GINGIVAL EROSION ( 14 FDA reports)
GRANULOCYTOPENIA ( 14 FDA reports)
HAIR PLUCKING ( 14 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 14 FDA reports)
INNER EAR DISORDER ( 14 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 14 FDA reports)
LYMPHADENECTOMY ( 14 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 14 FDA reports)
MUSCLE SPASTICITY ( 14 FDA reports)
MYELOMA RECURRENCE ( 14 FDA reports)
MYOCLONUS ( 14 FDA reports)
NEURECTOMY ( 14 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 14 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 14 FDA reports)
OESOPHAGEAL DISORDER ( 14 FDA reports)
ORAL FUNGAL INFECTION ( 14 FDA reports)
PANCREATIC DISORDER ( 14 FDA reports)
PARKINSONISM ( 14 FDA reports)
PERIODONTAL OPERATION ( 14 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 14 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 14 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 14 FDA reports)
RADICULITIS ( 14 FDA reports)
RENAL TUBULAR ACIDOSIS ( 14 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 14 FDA reports)
RETINAL MELANOMA ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
SEPSIS SYNDROME ( 14 FDA reports)
SEROTONIN SYNDROME ( 14 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 14 FDA reports)
SKIN ODOUR ABNORMAL ( 14 FDA reports)
SKIN TIGHTNESS ( 14 FDA reports)
SOFT TISSUE MASS ( 14 FDA reports)
SPINAL CORPECTOMY ( 14 FDA reports)
STRESS SYMPTOMS ( 14 FDA reports)
TEETH BRITTLE ( 14 FDA reports)
TEMPERATURE INTOLERANCE ( 14 FDA reports)
TENSION HEADACHE ( 14 FDA reports)
THALASSAEMIA ( 14 FDA reports)
URINE ABNORMALITY ( 14 FDA reports)
VULVAL CANCER ( 14 FDA reports)
X-RAY ABNORMAL ( 14 FDA reports)
WOUND HAEMORRHAGE ( 14 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 14 FDA reports)
ACUTE PRERENAL FAILURE ( 13 FDA reports)
ADRENAL HAEMORRHAGE ( 13 FDA reports)
AGEUSIA ( 13 FDA reports)
APPLICATION SITE IRRITATION ( 13 FDA reports)
BENCE JONES PROTEINURIA ( 13 FDA reports)
BENIGN TUMOUR EXCISION ( 13 FDA reports)
BIPOLAR I DISORDER ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 13 FDA reports)
BONE NEOPLASM ( 13 FDA reports)
BRAIN INJURY ( 13 FDA reports)
BREAST INDURATION ( 13 FDA reports)
CARDIOPULMONARY FAILURE ( 13 FDA reports)
CATHETER REMOVAL ( 13 FDA reports)
CLOSED HEAD INJURY ( 13 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 13 FDA reports)
DEMYELINATION ( 13 FDA reports)
DIABETIC COMPLICATION ( 13 FDA reports)
DROOLING ( 13 FDA reports)
DRUG PRESCRIBING ERROR ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FEAR OF DEATH ( 13 FDA reports)
FIBROADENOMA OF BREAST ( 13 FDA reports)
FIBROUS HISTIOCYTOMA ( 13 FDA reports)
GASTROINTESTINAL INFECTION ( 13 FDA reports)
GLOMERULOSCLEROSIS ( 13 FDA reports)
HEPATIC CALCIFICATION ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
HYDROPNEUMOTHORAX ( 13 FDA reports)
HYPERBILIRUBINAEMIA ( 13 FDA reports)
HYPERPROTEINAEMIA ( 13 FDA reports)
HYPERURICAEMIA ( 13 FDA reports)
HYPOPHOSPHATAEMIA ( 13 FDA reports)
ILEITIS ( 13 FDA reports)
INTERCOSTAL NEURALGIA ( 13 FDA reports)
LACUNAR INFARCTION ( 13 FDA reports)
LUNG CANCER METASTATIC ( 13 FDA reports)
MYOPIA ( 13 FDA reports)
NASOPHARYNGEAL DISORDER ( 13 FDA reports)
NEURITIS ( 13 FDA reports)
OCULAR HYPERAEMIA ( 13 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 13 FDA reports)
OROPHARYNGEAL PLAQUE ( 13 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 13 FDA reports)
PLAGIOCEPHALY ( 13 FDA reports)
PNEUMONIA BACTERIAL ( 13 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 13 FDA reports)
POLYPECTOMY ( 13 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 13 FDA reports)
PURPURA ( 13 FDA reports)
RADIATION INJURY ( 13 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 13 FDA reports)
REGURGITATION ( 13 FDA reports)
RENAL CANCER METASTATIC ( 13 FDA reports)
RENAL COLIC ( 13 FDA reports)
RETINAL DISORDER ( 13 FDA reports)
STERNOTOMY ( 13 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 13 FDA reports)
THROAT IRRITATION ( 13 FDA reports)
TOBACCO ABUSE ( 13 FDA reports)
VAGINITIS BACTERIAL ( 13 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
ABORTION INDUCED ( 12 FDA reports)
AFFECT LABILITY ( 12 FDA reports)
ALKALOSIS ( 12 FDA reports)
ANAL HAEMORRHAGE ( 12 FDA reports)
ANOSMIA ( 12 FDA reports)
ANTISOCIAL BEHAVIOUR ( 12 FDA reports)
APLASIA PURE RED CELL ( 12 FDA reports)
ARTHRITIS INFECTIVE ( 12 FDA reports)
ASPHYXIA ( 12 FDA reports)
AXILLARY MASS ( 12 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 12 FDA reports)
BLOOD COUNT ABNORMAL ( 12 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 12 FDA reports)
BLOODY DISCHARGE ( 12 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 12 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 12 FDA reports)
CAROTID ARTERY OCCLUSION ( 12 FDA reports)
CHONDROPATHY ( 12 FDA reports)
COELIAC DISEASE ( 12 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 12 FDA reports)
CONGENITAL ANOMALY ( 12 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 12 FDA reports)
DUODENAL OBSTRUCTION ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 12 FDA reports)
EMBOLISM VENOUS ( 12 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 12 FDA reports)
EXFOLIATIVE RASH ( 12 FDA reports)
EYELID OEDEMA ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
FOOD INTOLERANCE ( 12 FDA reports)
GALLBLADDER POLYP ( 12 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 12 FDA reports)
GRIP STRENGTH DECREASED ( 12 FDA reports)
HAEMARTHROSIS ( 12 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 12 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 12 FDA reports)
HAIR GROWTH ABNORMAL ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HEPATOTOXICITY ( 12 FDA reports)
INTENTIONAL MISUSE ( 12 FDA reports)
JAW LESION EXCISION ( 12 FDA reports)
LACTIC ACIDOSIS ( 12 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 12 FDA reports)
MALIGNANT MELANOMA IN SITU ( 12 FDA reports)
MASS EXCISION ( 12 FDA reports)
MASTOIDITIS ( 12 FDA reports)
METASTASIS ( 12 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 12 FDA reports)
MYOSITIS ( 12 FDA reports)
OSTEOMYELITIS CHRONIC ( 12 FDA reports)
OSTEOMYELITIS FUNGAL ( 12 FDA reports)
OSTEOSYNTHESIS ( 12 FDA reports)
OTITIS MEDIA ACUTE ( 12 FDA reports)
PAIN EXACERBATED ( 12 FDA reports)
PAINFUL RESPIRATION ( 12 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 12 FDA reports)
PAROTIDECTOMY ( 12 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 12 FDA reports)
PHARYNGEAL ULCERATION ( 12 FDA reports)
PIRIFORMIS SYNDROME ( 12 FDA reports)
PO2 DECREASED ( 12 FDA reports)
POST PROCEDURAL HAEMATOMA ( 12 FDA reports)
POSTOPERATIVE ADHESION ( 12 FDA reports)
PROTEUS INFECTION ( 12 FDA reports)
PULMONARY ARTERY DILATATION ( 12 FDA reports)
RADIATION OESOPHAGITIS ( 12 FDA reports)
RASH MORBILLIFORM ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
RENAL STONE REMOVAL ( 12 FDA reports)
SKIN CANCER ( 12 FDA reports)
SKIN SWELLING ( 12 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 12 FDA reports)
STATUS EPILEPTICUS ( 12 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 12 FDA reports)
TINEL'S SIGN ( 12 FDA reports)
URINE ANALYSIS ABNORMAL ( 12 FDA reports)
VAGINAL DISCHARGE ( 12 FDA reports)
ABDOMINAL ADHESIONS ( 11 FDA reports)
ABDOMINAL WALL MASS ( 11 FDA reports)
ABNORMAL FAECES ( 11 FDA reports)
ACCIDENTAL DEATH ( 11 FDA reports)
ADMINISTRATION SITE INFECTION ( 11 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 11 FDA reports)
ANISOCYTOSIS ( 11 FDA reports)
AORTIC CALCIFICATION ( 11 FDA reports)
ASTIGMATISM ( 11 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 11 FDA reports)
BACTERIA URINE IDENTIFIED ( 11 FDA reports)
BACTERIAL TEST NEGATIVE ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD PH DECREASED ( 11 FDA reports)
BRAIN SCAN ABNORMAL ( 11 FDA reports)
BREAKTHROUGH PAIN ( 11 FDA reports)
BREAST LUMP REMOVAL ( 11 FDA reports)
BREAST NECROSIS ( 11 FDA reports)
BRONCHIAL SECRETION RETENTION ( 11 FDA reports)
BUNDLE BRANCH BLOCK ( 11 FDA reports)
CALCIFICATION METASTATIC ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
CATARACT NUCLEAR ( 11 FDA reports)
CLAUSTROPHOBIA ( 11 FDA reports)
COR PULMONALE ( 11 FDA reports)
DENTAL DISCOMFORT ( 11 FDA reports)
DERMATITIS ALLERGIC ( 11 FDA reports)
DEVICE RELATED SEPSIS ( 11 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 11 FDA reports)
DIABETIC ULCER ( 11 FDA reports)
DRUG EFFECT INCREASED ( 11 FDA reports)
ENDOMETRIAL CANCER ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
EYE PRURITUS ( 11 FDA reports)
EYELID PTOSIS ( 11 FDA reports)
FACE INJURY ( 11 FDA reports)
FEMALE STERILISATION ( 11 FDA reports)
FRACTURE NONUNION ( 11 FDA reports)
GASTROSTOMY TUBE INSERTION ( 11 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 11 FDA reports)
HOSTILITY ( 11 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
INAPPROPRIATE AFFECT ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
KNEE OPERATION ( 11 FDA reports)
LOGORRHOEA ( 11 FDA reports)
LOOSE BODY IN JOINT ( 11 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MASTITIS ( 11 FDA reports)
MEDICATION RESIDUE ( 11 FDA reports)
MENINGITIS VIRAL ( 11 FDA reports)
METASTASES TO BONE MARROW ( 11 FDA reports)
MICROCYTIC ANAEMIA ( 11 FDA reports)
MORTON'S NEUROMA ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER ( 11 FDA reports)
OROPHARYNGEAL BLISTERING ( 11 FDA reports)
OSTECTOMY ( 11 FDA reports)
OSTEOSARCOMA METASTATIC ( 11 FDA reports)
PANCOAST'S TUMOUR ( 11 FDA reports)
PHARYNGEAL ERYTHEMA ( 11 FDA reports)
PHLEBOSCLEROSIS ( 11 FDA reports)
POLYP COLORECTAL ( 11 FDA reports)
PSEUDOMONAL SEPSIS ( 11 FDA reports)
RAYNAUD'S PHENOMENON ( 11 FDA reports)
RED BLOOD CELL ABNORMALITY ( 11 FDA reports)
REHABILITATION THERAPY ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
SELF ESTEEM DECREASED ( 11 FDA reports)
SINUS POLYP DEGENERATION ( 11 FDA reports)
SKIN HYPERPIGMENTATION ( 11 FDA reports)
SPLENIC INFARCTION ( 11 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 11 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 11 FDA reports)
THROMBOCYTOSIS ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TINEA PEDIS ( 11 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 11 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 11 FDA reports)
TRIGEMINAL NEURALGIA ( 11 FDA reports)
URINE ANALYSIS ( 11 FDA reports)
WHITE BLOOD CELL COUNT ( 11 FDA reports)
YELLOW SKIN ( 11 FDA reports)
WISDOM TEETH REMOVAL ( 11 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
ALCOHOL ABUSE ( 10 FDA reports)
APPLICATION SITE DERMATITIS ( 10 FDA reports)
ASTERIXIS ( 10 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 10 FDA reports)
BILIARY NEOPLASM ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
BREAST DISCHARGE ( 10 FDA reports)
BREAST SWELLING ( 10 FDA reports)
BRONCHITIS VIRAL ( 10 FDA reports)
BRONCHOPLEURAL FISTULA ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
CANCER PAIN ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
CAROTID BRUIT ( 10 FDA reports)
CATHETER RELATED INFECTION ( 10 FDA reports)
CEPHALHAEMATOMA ( 10 FDA reports)
CHOLECYSTITIS INFECTIVE ( 10 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 10 FDA reports)
CLOSED FRACTURE MANIPULATION ( 10 FDA reports)
CLOSTRIDIUM COLITIS ( 10 FDA reports)
COLLAPSE OF LUNG ( 10 FDA reports)
CORNEAL DYSTROPHY ( 10 FDA reports)
CORONARY ARTERY RESTENOSIS ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DEVICE LEAKAGE ( 10 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 10 FDA reports)
EMBOLISM ARTERIAL ( 10 FDA reports)
ENCEPHALOMALACIA ( 10 FDA reports)
EOSINOPHIL COUNT INCREASED ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 10 FDA reports)
FRUSTRATION ( 10 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 10 FDA reports)
GASTRIC POLYPS ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GASTRODUODENITIS ( 10 FDA reports)
GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
GRAVITATIONAL OEDEMA ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HEMIPLEGIA ( 10 FDA reports)
HERPES VIRUS INFECTION ( 10 FDA reports)
HORMONE LEVEL ABNORMAL ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
HYPERTENSIVE CRISIS ( 10 FDA reports)
HYPOCHROMASIA ( 10 FDA reports)
HYPOREFLEXIA ( 10 FDA reports)
HYPOVOLAEMIC SHOCK ( 10 FDA reports)
IMPULSIVE BEHAVIOUR ( 10 FDA reports)
INJECTION SITE IRRITATION ( 10 FDA reports)
INJECTION SITE MASS ( 10 FDA reports)
INJECTION SITE WARMTH ( 10 FDA reports)
INTESTINAL ISCHAEMIA ( 10 FDA reports)
KETOACIDOSIS ( 10 FDA reports)
LIP DRY ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
LUMBAR SPINE FLATTENING ( 10 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 10 FDA reports)
MENSTRUAL DISORDER ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
NAIL DISORDER ( 10 FDA reports)
NIGHT BLINDNESS ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
ORAL DISCHARGE ( 10 FDA reports)
OSTEOCHONDROSIS ( 10 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 10 FDA reports)
PELVIC FLUID COLLECTION ( 10 FDA reports)
PERINEURIAL CYST ( 10 FDA reports)
PERIORBITAL OEDEMA ( 10 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 10 FDA reports)
PERIPHERAL ISCHAEMIA ( 10 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 10 FDA reports)
PILOERECTION ( 10 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 10 FDA reports)
POLYCYSTIC OVARIES ( 10 FDA reports)
POLYMYALGIA RHEUMATICA ( 10 FDA reports)
PORTAL HYPERTENSION ( 10 FDA reports)
POST THROMBOTIC SYNDROME ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
PRESCRIBED OVERDOSE ( 10 FDA reports)
PROTEIN URINE PRESENT ( 10 FDA reports)
PSYCHOLOGICAL TRAUMA ( 10 FDA reports)
PULSE PRESSURE DECREASED ( 10 FDA reports)
RADICULAR PAIN ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RESPIRATORY ACIDOSIS ( 10 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 10 FDA reports)
RETINAL TEAR ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 10 FDA reports)
SKIN FIBROSIS ( 10 FDA reports)
SPINAL HAEMANGIOMA ( 10 FDA reports)
SPONDYLOLYSIS ( 10 FDA reports)
SUBDURAL HAEMORRHAGE ( 10 FDA reports)
SUBGALEAL HAEMATOMA ( 10 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
ULNA FRACTURE ( 10 FDA reports)
VASOCONSTRICTION ( 10 FDA reports)
VIITH NERVE PARALYSIS ( 10 FDA reports)
VISCERAL CONGESTION ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 9 FDA reports)
AMMONIA INCREASED ( 9 FDA reports)
ANAL FISTULA ( 9 FDA reports)
ANURIA ( 9 FDA reports)
ARTERIAL DISORDER ( 9 FDA reports)
ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
AURAL POLYP ( 9 FDA reports)
BLADDER DILATATION ( 9 FDA reports)
BLOOD BICARBONATE DECREASED ( 9 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BLOOD TEST ABNORMAL ( 9 FDA reports)
BREAST CANCER FEMALE ( 9 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 9 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 9 FDA reports)
CALCULUS BLADDER ( 9 FDA reports)
CARDIAC ANEURYSM ( 9 FDA reports)
CARDIAC FAILURE CHRONIC ( 9 FDA reports)
CEREBRAL HAEMATOMA ( 9 FDA reports)
CERVICAL CYST ( 9 FDA reports)
CHOKING ( 9 FDA reports)
COLECTOMY ( 9 FDA reports)
COLON CANCER RECURRENT ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONDUCTION DISORDER ( 9 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 9 FDA reports)
CONNECTIVE TISSUE DISORDER ( 9 FDA reports)
CORONARY ANGIOPLASTY ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
CUSHING'S SYNDROME ( 9 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 9 FDA reports)
DENTAL IMPLANTATION ( 9 FDA reports)
DENTAL PLAQUE ( 9 FDA reports)
DISSOCIATION ( 9 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
DUODENAL STENOSIS ( 9 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 9 FDA reports)
EMBOLISM ( 9 FDA reports)
ENDOCARDITIS ( 9 FDA reports)
ENTEROVESICAL FISTULA ( 9 FDA reports)
FACIAL OPERATION ( 9 FDA reports)
FALLOT'S TETRALOGY ( 9 FDA reports)
FUNGAL SEPSIS ( 9 FDA reports)
GALLBLADDER PAIN ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
GINGIVAL HYPERPLASIA ( 9 FDA reports)
HAEMOPHILUS INFECTION ( 9 FDA reports)
HEART RATE ABNORMAL ( 9 FDA reports)
HEPATIC NEOPLASM ( 9 FDA reports)
HUNGER ( 9 FDA reports)
HYPERPHAGIA ( 9 FDA reports)
HYPOTONIA ( 9 FDA reports)
INFARCTION ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INTERVERTEBRAL DISCITIS ( 9 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 9 FDA reports)
IRON DEFICIENCY ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 9 FDA reports)
LIP DISCOLOURATION ( 9 FDA reports)
LOW TURNOVER OSTEOPATHY ( 9 FDA reports)
LUNG INJURY ( 9 FDA reports)
LYMPHOPENIA ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MAMMOGRAM ABNORMAL ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MELANOSIS COLI ( 9 FDA reports)
METABOLIC SYNDROME ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MICROCYTOSIS ( 9 FDA reports)
MIXED HYPERLIPIDAEMIA ( 9 FDA reports)
MONOCLONAL GAMMOPATHY ( 9 FDA reports)
MUSCLE DISORDER ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NEPHROPATHY TOXIC ( 9 FDA reports)
NERVE BLOCK ( 9 FDA reports)
NEUROGENIC BLADDER ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 9 FDA reports)
OCULAR ICTERUS ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
ORAL NEOPLASM ( 9 FDA reports)
OVARIAN CANCER ( 9 FDA reports)
OVARIAN CYST RUPTURED ( 9 FDA reports)
PANCREATIC CYST ( 9 FDA reports)
PCO2 INCREASED ( 9 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 9 FDA reports)
PERITONITIS BACTERIAL ( 9 FDA reports)
PERSONALITY DISORDER ( 9 FDA reports)
PHOTODERMATOSIS ( 9 FDA reports)
PITTING OEDEMA ( 9 FDA reports)
PITUITARY TUMOUR ( 9 FDA reports)
POLYCHROMASIA ( 9 FDA reports)
POOR VENOUS ACCESS ( 9 FDA reports)
POST PROCEDURAL INFECTION ( 9 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 9 FDA reports)
PRE-ECLAMPSIA ( 9 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 9 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 9 FDA reports)
PSYCHIATRIC SYMPTOM ( 9 FDA reports)
PUBIC RAMI FRACTURE ( 9 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 9 FDA reports)
RADIATION SKIN INJURY ( 9 FDA reports)
RENAL ABSCESS ( 9 FDA reports)
RESORPTION BONE INCREASED ( 9 FDA reports)
ROULEAUX FORMATION ( 9 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SKIN FISSURES ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SLEEP WALKING ( 9 FDA reports)
SLOW RESPONSE TO STIMULI ( 9 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 9 FDA reports)
SPINAL CORD NEOPLASM ( 9 FDA reports)
SPINAL LAMINECTOMY ( 9 FDA reports)
STARVATION ( 9 FDA reports)
SUDDEN CARDIAC DEATH ( 9 FDA reports)
TENDON PAIN ( 9 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 9 FDA reports)
TINEA INFECTION ( 9 FDA reports)
TONSILLITIS ( 9 FDA reports)
TUMOUR MARKER INCREASED ( 9 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 9 FDA reports)
ULCERATIVE KERATITIS ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
VAGINAL PAIN ( 9 FDA reports)
VEIN DISORDER ( 9 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 9 FDA reports)
VERTIGO POSITIONAL ( 9 FDA reports)
VOMITING PROJECTILE ( 9 FDA reports)
VULVOVAGINAL PRURITUS ( 9 FDA reports)
VULVAL DISORDER ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
ALLERGIC SINUSITIS ( 8 FDA reports)
ALLODYNIA ( 8 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
AORTIC VALVE STENOSIS ( 8 FDA reports)
ARACHNOID CYST ( 8 FDA reports)
ARACHNOIDITIS ( 8 FDA reports)
ASEPTIC NECROSIS BONE ( 8 FDA reports)
AXILLARY PAIN ( 8 FDA reports)
BIOPSY GINGIVAL ( 8 FDA reports)
BLADDER SPASM ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD CANNABINOIDS ( 8 FDA reports)
BLOOD PH INCREASED ( 8 FDA reports)
BLOOD PROLACTIN INCREASED ( 8 FDA reports)
BONE FORMATION INCREASED ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BREAST ENLARGEMENT ( 8 FDA reports)
BREAST HAEMATOMA ( 8 FDA reports)
BREAST RECONSTRUCTION ( 8 FDA reports)
CARBON DIOXIDE DECREASED ( 8 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 8 FDA reports)
CARDIOTOXICITY ( 8 FDA reports)
CATHETER SITE HAEMORRHAGE ( 8 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 8 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 8 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
COLONIC STENOSIS ( 8 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DIABETIC NEPHROPATHY ( 8 FDA reports)
DRUG ADDICT ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
DRY THROAT ( 8 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
ERYTHEMA OF EYELID ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
EYE REDNESS ( 8 FDA reports)
FACIAL PARESIS ( 8 FDA reports)
FAT INTOLERANCE ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 8 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 8 FDA reports)
FULL BLOOD COUNT DECREASED ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GASTROSTOMY ( 8 FDA reports)
GENERALISED ANXIETY DISORDER ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
HAEMOCHROMATOSIS ( 8 FDA reports)
HEPATIC PAIN ( 8 FDA reports)
HILAR LYMPHADENOPATHY ( 8 FDA reports)
HYPERMETROPIA ( 8 FDA reports)
HYPERREFLEXIA ( 8 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 8 FDA reports)
IMPETIGO ( 8 FDA reports)
INGUINAL HERNIA REPAIR ( 8 FDA reports)
INJECTION SITE DISCOLOURATION ( 8 FDA reports)
INJECTION SITE INFECTION ( 8 FDA reports)
INJURY CORNEAL ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
INTESTINAL RESECTION ( 8 FDA reports)
ISCHAEMIC HEPATITIS ( 8 FDA reports)
LARGE INTESTINAL ULCER ( 8 FDA reports)
LAZINESS ( 8 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 8 FDA reports)
LISTLESS ( 8 FDA reports)
LYMPHOCYTIC INFILTRATION ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
METASTASES TO OVARY ( 8 FDA reports)
MUSCLE FATIGUE ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
NAIL AVULSION ( 8 FDA reports)
NARCOLEPSY ( 8 FDA reports)
NASAL DISCOMFORT ( 8 FDA reports)
NASAL SEPTUM DEVIATION ( 8 FDA reports)
NASAL ULCER ( 8 FDA reports)
NEOPLASM SKIN ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
NIPPLE PAIN ( 8 FDA reports)
PEAU D'ORANGE ( 8 FDA reports)
PERIPHERAL EMBOLISM ( 8 FDA reports)
PHOTOPSIA ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
PNEUMOCONIOSIS ( 8 FDA reports)
POLYDACTYLY ( 8 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 8 FDA reports)
POSTINFARCTION ANGINA ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
PULMONARY AIR LEAKAGE ( 8 FDA reports)
PULMONARY MYCOSIS ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
PYURIA ( 8 FDA reports)
RADIATION EXPOSURE ( 8 FDA reports)
RECTAL ULCER ( 8 FDA reports)
RENAL ARTERY STENOSIS ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SEBORRHOEIC DERMATITIS ( 8 FDA reports)
SENSATION OF PRESSURE ( 8 FDA reports)
SEPTIC EMBOLUS ( 8 FDA reports)
SINUS ARRHYTHMIA ( 8 FDA reports)
SKIN OEDEMA ( 8 FDA reports)
SKIN PLAQUE ( 8 FDA reports)
SPINE MALFORMATION ( 8 FDA reports)
SUBACUTE ENDOCARDITIS ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUPERINFECTION ( 8 FDA reports)
TARSAL TUNNEL SYNDROME ( 8 FDA reports)
THALASSAEMIA BETA ( 8 FDA reports)
THROMBOSIS IN DEVICE ( 8 FDA reports)
THYROID MASS ( 8 FDA reports)
TIC ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
TONGUE HAEMORRHAGE ( 8 FDA reports)
TOURETTE'S DISORDER ( 8 FDA reports)
TREATMENT FAILURE ( 8 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 8 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 8 FDA reports)
VAGINAL ERYTHEMA ( 8 FDA reports)
VENOUS STENOSIS ( 8 FDA reports)
VENOUS THROMBOSIS LIMB ( 8 FDA reports)
VOCAL CORD POLYP ( 8 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 7 FDA reports)
ABDOMINAL PANNICULECTOMY ( 7 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 7 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 7 FDA reports)
ADDISON'S DISEASE ( 7 FDA reports)
ADJUSTMENT DISORDER ( 7 FDA reports)
ADRENAL SUPPRESSION ( 7 FDA reports)
AMYLOIDOSIS ( 7 FDA reports)
ANAL CANCER ( 7 FDA reports)
APHONIA ( 7 FDA reports)
AURICULAR PSEUDOCYST ( 7 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 7 FDA reports)
BACTERIAL DIARRHOEA ( 7 FDA reports)
BASEDOW'S DISEASE ( 7 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BLOOD ETHANOL INCREASED ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 7 FDA reports)
BONE MARROW TRANSPLANT ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
BREAST CELLULITIS ( 7 FDA reports)
BREAST OEDEMA ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CANDIDURIA ( 7 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 7 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 7 FDA reports)
CARTILAGE ATROPHY ( 7 FDA reports)
CERVIX DISORDER ( 7 FDA reports)
CHOREA ( 7 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 7 FDA reports)
CONTRAST MEDIA REACTION ( 7 FDA reports)
CORNEAL SCAR ( 7 FDA reports)
DEPRESSION SUICIDAL ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
DRUG TOLERANCE INCREASED ( 7 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENDOMETRIAL ATROPHY ( 7 FDA reports)
EXTRASKELETAL OSSIFICATION ( 7 FDA reports)
FASCIITIS ( 7 FDA reports)
FISTULA REPAIR ( 7 FDA reports)
FOREIGN BODY ( 7 FDA reports)
FRACTURED SACRUM ( 7 FDA reports)
GALLBLADDER ENLARGEMENT ( 7 FDA reports)
GENITAL HERPES ( 7 FDA reports)
GLOBULINS INCREASED ( 7 FDA reports)
GLOSSITIS ( 7 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HIP SURGERY ( 7 FDA reports)
HISTOPLASMOSIS ( 7 FDA reports)
HYDROCELE ( 7 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 7 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 7 FDA reports)
ILIAC ARTERY STENOSIS ( 7 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 7 FDA reports)
INFECTIVE TENOSYNOVITIS ( 7 FDA reports)
INJECTION SITE VESICLES ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTESTINAL ULCER ( 7 FDA reports)
JUGULAR VEIN DISTENSION ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 7 FDA reports)
LUNG ADENOCARCINOMA ( 7 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 7 FDA reports)
LYMPH NODE CALCIFICATION ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MALIGNANT HYPERTENSION ( 7 FDA reports)
MENINGITIS ASEPTIC ( 7 FDA reports)
MENOMETRORRHAGIA ( 7 FDA reports)
MENSTRUATION DELAYED ( 7 FDA reports)
MIGRAINE WITH AURA ( 7 FDA reports)
MOLE EXCISION ( 7 FDA reports)
MONARTHRITIS ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MUSCLE RIGIDITY ( 7 FDA reports)
OCCIPITAL NEURALGIA ( 7 FDA reports)
ONYCHALGIA ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PELVIC MASS ( 7 FDA reports)
PELVIC VENOUS THROMBOSIS ( 7 FDA reports)
PERFORATED ULCER ( 7 FDA reports)
PERICARDIAL DRAINAGE ( 7 FDA reports)
PHARYNGEAL DISORDER ( 7 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 7 FDA reports)
PO2 INCREASED ( 7 FDA reports)
POOR DENTAL CONDITION ( 7 FDA reports)
POOR PERIPHERAL CIRCULATION ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
POST LAMINECTOMY SYNDROME ( 7 FDA reports)
POSTMENOPAUSE ( 7 FDA reports)
POSTNASAL DRIP ( 7 FDA reports)
POSTOPERATIVE INFECTION ( 7 FDA reports)
POSTURING ( 7 FDA reports)
PROTEIN C DEFICIENCY ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
PULMONARY VASCULITIS ( 7 FDA reports)
PYOGENIC GRANULOMA ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RADIATION PNEUMONITIS ( 7 FDA reports)
RADICULITIS LUMBOSACRAL ( 7 FDA reports)
RASH PUSTULAR ( 7 FDA reports)
RENAL VEIN THROMBOSIS ( 7 FDA reports)
RETINOPATHY ( 7 FDA reports)
ROSACEA ( 7 FDA reports)
SALIVARY GLAND CANCER ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SELF MUTILATION ( 7 FDA reports)
SHOULDER DEFORMITY ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKIN LESION EXCISION ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SKIN WARM ( 7 FDA reports)
SOFT TISSUE INFLAMMATION ( 7 FDA reports)
SOLILOQUY ( 7 FDA reports)
SPINAL CORD OPERATION ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SPLENIC CYST ( 7 FDA reports)
SPUTUM ABNORMAL ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 7 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 7 FDA reports)
THEFT ( 7 FDA reports)
THROMBECTOMY ( 7 FDA reports)
THROMBOLYSIS ( 7 FDA reports)
TRACHEAL DEVIATION ( 7 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 7 FDA reports)
TUBERCULIN TEST POSITIVE ( 7 FDA reports)
TUMOUR INVASION ( 7 FDA reports)
UNINTENDED PREGNANCY ( 7 FDA reports)
URETERAL STENT INSERTION ( 7 FDA reports)
URINARY HESITATION ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 7 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 7 FDA reports)
UTERINE ENLARGEMENT ( 7 FDA reports)
UTERINE HAEMORRHAGE ( 7 FDA reports)
VASCULAR CAUTERISATION ( 7 FDA reports)
VASCULAR INJURY ( 7 FDA reports)
VICTIM OF CRIME ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
WEIGHT ABNORMAL ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABDOMINAL BRUIT ( 6 FDA reports)
ABDOMINAL OPERATION ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
ALVEOLAR OSTEITIS ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 6 FDA reports)
APPLICATION SITE BLEEDING ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 6 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 6 FDA reports)
B-CELL LYMPHOMA ( 6 FDA reports)
BACTERIAL SEPSIS ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BASOPHIL COUNT INCREASED ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BIOPSY LIP ( 6 FDA reports)
BIOPSY LIVER ABNORMAL ( 6 FDA reports)
BLADDER DISCOMFORT ( 6 FDA reports)
BLADDER OBSTRUCTION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 6 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD GASES ABNORMAL ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BONE TRIMMING ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRAIN HYPOXIA ( 6 FDA reports)
BRAIN OPERATION ( 6 FDA reports)
BURNOUT SYNDROME ( 6 FDA reports)
CALCINOSIS ( 6 FDA reports)
CEREBROSCLEROSIS ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CHOKING SENSATION ( 6 FDA reports)
CHONDROSARCOMA ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 6 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 6 FDA reports)
CLEFT PALATE ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 6 FDA reports)
CORNEAL ABRASION ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DEATH OF RELATIVE ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DIASTOLIC HYPERTENSION ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
DRUG DIVERSION ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
ECTOPIC PREGNANCY ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENDOMETRIAL DISORDER ( 6 FDA reports)
ENTHESOPATHY ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
ESCHAR ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
FACIAL SPASM ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FEELINGS OF WORTHLESSNESS ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FOREARM FRACTURE ( 6 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 6 FDA reports)
FUSOBACTERIUM INFECTION ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GRANULOCYTES MATURATION ARREST ( 6 FDA reports)
GRIEF REACTION ( 6 FDA reports)
HAEMOGLOBIN ABNORMAL ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 6 FDA reports)
HEPATITIS C POSITIVE ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HOSPICE CARE ( 6 FDA reports)
HYPEROSMOLAR STATE ( 6 FDA reports)
HYPERTENSIVE EMERGENCY ( 6 FDA reports)
HYPOPROTHROMBINAEMIA ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
INTERNAL INJURY ( 6 FDA reports)
JOINT CONTRACTURE ( 6 FDA reports)
LEGAL PROBLEM ( 6 FDA reports)
LIMB CRUSHING INJURY ( 6 FDA reports)
LIMB DEFORMITY ( 6 FDA reports)
LIP INJURY ( 6 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 6 FDA reports)
LITHOTRIPSY ( 6 FDA reports)
LOCALISED OSTEOARTHRITIS ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYMPHOCYTOSIS ( 6 FDA reports)
MAGNESIUM DEFICIENCY ( 6 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 6 FDA reports)
MEAN CELL VOLUME INCREASED ( 6 FDA reports)
MEDIASTINAL DISORDER ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
METASTASES TO CHEST WALL ( 6 FDA reports)
METASTASES TO KIDNEY ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MIDDLE EAR EFFUSION ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
MUSCLE HAEMORRHAGE ( 6 FDA reports)
NERVE ROOT INJURY LUMBAR ( 6 FDA reports)
NEURILEMMOMA ( 6 FDA reports)
NEUROFIBROMA ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OESOPHAGEAL CARCINOMA ( 6 FDA reports)
OESOPHAGEAL PERFORATION ( 6 FDA reports)
OOPHORECTOMY BILATERAL ( 6 FDA reports)
OPEN ANGLE GLAUCOMA ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 6 FDA reports)
OSTEOARTHROPATHY ( 6 FDA reports)
OSTEOMALACIA ( 6 FDA reports)
OVARIAN ADHESION ( 6 FDA reports)
PAIN OF SKIN ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
PERICARDIAL EXCISION ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PHLEBITIS SUPERFICIAL ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 6 FDA reports)
PROSTATIC CALCIFICATION ( 6 FDA reports)
PROTHROMBIN TIME SHORTENED ( 6 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 6 FDA reports)
PURPURA SENILE ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RADIAL TUNNEL SYNDROME ( 6 FDA reports)
RECTAL DISCHARGE ( 6 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 6 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 6 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 6 FDA reports)
SECONDARY SEQUESTRUM ( 6 FDA reports)
SECRETION DISCHARGE ( 6 FDA reports)
SPINAL COLUMN INJURY ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
SYRINGOMYELIA ( 6 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 6 FDA reports)
TERMINAL STATE ( 6 FDA reports)
TESTICULAR DISORDER ( 6 FDA reports)
TONGUE COATED ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 6 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 6 FDA reports)
TUMOUR EMBOLISM ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
URINARY SEDIMENT PRESENT ( 6 FDA reports)
VASCULAR GRAFT ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VASCULAR OCCLUSION ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VENA CAVA FILTER INSERTION ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ADENOMYOSIS ( 5 FDA reports)
ADRENAL CARCINOMA ( 5 FDA reports)
ADRENAL NEOPLASM ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
AMPHETAMINES POSITIVE ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 5 FDA reports)
ANORECTAL DISCOMFORT ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
APPLICATION SITE EROSION ( 5 FDA reports)
APPLICATION SITE SCAR ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
BIPOLAR II DISORDER ( 5 FDA reports)
BLADDER MASS ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BODY TINEA ( 5 FDA reports)
BONE INFARCTION ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 5 FDA reports)
BRONCHIAL HYPERACTIVITY ( 5 FDA reports)
BUNION OPERATION ( 5 FDA reports)
BURN INFECTION ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
CAROTID ENDARTERECTOMY ( 5 FDA reports)
CATATONIA ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CERVIX CARCINOMA ( 5 FDA reports)
CHEST WALL MASS ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
COLON OPERATION ( 5 FDA reports)
CORONARY ARTERY REOCCLUSION ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DELUSIONAL PERCEPTION ( 5 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELUSIONS ( 5 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 5 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DETOXIFICATION ( 5 FDA reports)
DEVICE DISLOCATION ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DIARRHOEA INFECTIOUS ( 5 FDA reports)
DRESSLER'S SYNDROME ( 5 FDA reports)
DRUG SCREEN NEGATIVE ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
DYSPHORIA ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
EJECTION FRACTION ( 5 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ELECTROCUTION ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ENURESIS ( 5 FDA reports)
EXOPHTHALMOS ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FAILURE OF IMPLANT ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FINGER AMPUTATION ( 5 FDA reports)
FOOD POISONING ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL FISTULA ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GINGIVAL OPERATION ( 5 FDA reports)
HAEMOSIDEROSIS ( 5 FDA reports)
HEART BLOCK CONGENITAL ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPERSPLENISM ACQUIRED ( 5 FDA reports)
HYPERTROPHY ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
IMPRISONMENT ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INCISION SITE PAIN ( 5 FDA reports)
INFECTED CYST ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
KETONURIA ( 5 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 5 FDA reports)
LESION EXCISION ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LIP ULCERATION ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LUNG LOBECTOMY ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 5 FDA reports)
MEDIAN NERVE INJURY ( 5 FDA reports)
METAMORPHOPSIA ( 5 FDA reports)
METASTASES TO PLEURA ( 5 FDA reports)
METASTASES TO SKIN ( 5 FDA reports)
MIDDLE EAR DISORDER ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MULTIPLE ALLERGIES ( 5 FDA reports)
MULTIPLE FRACTURES ( 5 FDA reports)
MYASTHENIA GRAVIS ( 5 FDA reports)
NASAL SEPTUM DISORDER ( 5 FDA reports)
NEUROGENIC BOWEL ( 5 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
OPTIC NERVE INJURY ( 5 FDA reports)
ORTHOSTATIC INTOLERANCE ( 5 FDA reports)
PANCREATIC ATROPHY ( 5 FDA reports)
PAPILLOMA ( 5 FDA reports)
PAROSMIA ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PATHOGEN RESISTANCE ( 5 FDA reports)
PERIHEPATIC ABSCESS ( 5 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 5 FDA reports)
PERITONEAL DIALYSIS ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PLATELET COUNT ABNORMAL ( 5 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 5 FDA reports)
PROCTITIS ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PSEUDARTHROSIS ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
PUPILLARY DISORDER ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
RECTAL PROLAPSE ( 5 FDA reports)
REFRACTORY ANAEMIA ( 5 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 5 FDA reports)
RENAL EMBOLISM ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SALIVARY GLAND PAIN ( 5 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SENSATION OF PRESSURE IN EAR ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SHOCK HAEMORRHAGIC ( 5 FDA reports)
SICCA SYNDROME ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SOMATOFORM DISORDER ( 5 FDA reports)
SPONDYLITIC MYELOPATHY ( 5 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 5 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
SYSTOLIC HYPERTENSION ( 5 FDA reports)
T-CELL LYMPHOMA ( 5 FDA reports)
TESTICULAR SWELLING ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TOE DEFORMITY ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TRAUMATIC ULCER ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
URINE OUTPUT INCREASED ( 5 FDA reports)
VAGINAL NEOPLASM ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VENOOCCLUSIVE DISEASE ( 5 FDA reports)
WHITE BLOOD CELL DISORDER ( 5 FDA reports)
XANTHELASMA ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ADENOTONSILLECTOMY ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANKLE OPERATION ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
APPLICATION SITE BURN ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 4 FDA reports)
BACTERIURIA ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BENIGN BONE NEOPLASM ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLOOD ALCOHOL INCREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST CANCER STAGE III ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CAECITIS ( 4 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CENTRAL LINE INFECTION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COGNITIVE DETERIORATION ( 4 FDA reports)
COLON CANCER METASTATIC ( 4 FDA reports)
CONDUCTIVE DEAFNESS ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
CORRECTIVE LENS USER ( 4 FDA reports)
CSF TEST ABNORMAL ( 4 FDA reports)
CYSTITIS BACTERIAL ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
EMPTY SELLA SYNDROME ( 4 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ESCHERICHIA TEST POSITIVE ( 4 FDA reports)
ETHMOID SINUS SURGERY ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FOETAL CARDIAC DISORDER ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL OEDEMA ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GESTATIONAL DIABETES ( 4 FDA reports)
GLIOSIS ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAIR COLOUR CHANGES ( 4 FDA reports)
HEAD BANGING ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INFECTED SEBACEOUS CYST ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTRACRANIAL HAEMATOMA ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 4 FDA reports)
JOINT HYPEREXTENSION ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LIPOHYPERTROPHY ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
MAY-THURNER SYNDROME ( 4 FDA reports)
METASTASES TO NECK ( 4 FDA reports)
MITRAL VALVE SCLEROSIS ( 4 FDA reports)
MONONEURITIS ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NASAL OEDEMA ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PELVIC DISCOMFORT ( 4 FDA reports)
PERICARDIAL DISEASE ( 4 FDA reports)
PERIPHERAL NERVE LESION ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PLATELET AGGREGATION INCREASED ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PNEUMOCEPHALUS ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PRECANCEROUS CELLS PRESENT ( 4 FDA reports)
PROCEDURAL SITE REACTION ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
REFLUX GASTRITIS ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RENAL TRANSPLANT ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RETINAL INJURY ( 4 FDA reports)
RHEUMATOID NODULE ( 4 FDA reports)
SARCOMA ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SINUS ANTROSTOMY ( 4 FDA reports)
SKIN GRAFT FAILURE ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN MASS ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SMOKER ( 4 FDA reports)
SOLITARY KIDNEY ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPINAL DECOMPRESSION ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TALIPES ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THROAT CANCER ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYMOMA ( 4 FDA reports)
THYROID ADENOMA ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
URETHRAL OPERATION ( 4 FDA reports)
URETHRAL STENT INSERTION ( 4 FDA reports)
URETHRAL STRICTURE ( 4 FDA reports)
UTERINE SPASM ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VARICOPHLEBITIS ( 4 FDA reports)
VASCULAR INSUFFICIENCY ( 4 FDA reports)
VENOGRAM ( 4 FDA reports)
VENTRICULAR DYSKINESIA ( 4 FDA reports)
VERTEBRAL COLUMN MASS ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL TRANSPOSITION ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMMONIA DECREASED ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAL INFLAMMATION ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
APPLICATION SITE BURNING ( 3 FDA reports)
APPLICATION SITE SCAB ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPLENIA ( 3 FDA reports)
AUTOMATIC BLADDER ( 3 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACTEROIDES INFECTION ( 3 FDA reports)
BARBITURATES POSITIVE ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BASILAR MIGRAINE ( 3 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 3 FDA reports)
BENIGN COLONIC NEOPLASM ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIARY CYST ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
BRONCHOMALACIA ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 3 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLONIC OBSTRUCTION ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
CREST SYNDROME ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRUG THERAPY ( 3 FDA reports)
DRY GANGRENE ( 3 FDA reports)
DUODENAL ATRESIA ( 3 FDA reports)
EAR OPERATION ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EPENDYMOMA ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EYELID CYST ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FACIAL NEURALGIA ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FRACTURE DISPLACEMENT ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
FUNGATING WOUND ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GAS POISONING ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC ULCER HELICOBACTER ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GENITAL CANDIDIASIS ( 3 FDA reports)
GENITAL ERYTHEMA ( 3 FDA reports)
GENITAL SWELLING ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GROIN ABSCESS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEAT ILLNESS ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOBILIARY DISEASE ( 3 FDA reports)
HEREDITARY ANGIOEDEMA ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HORNER'S SYNDROME ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 3 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE OEDEMA ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 3 FDA reports)
INTERCEPTED MEDICATION ERROR ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTESTINAL MALROTATION ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRASPINAL ABSCESS ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
ITCHING SCAR ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
JOINT DESTRUCTION ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LIMB OPERATION ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
LIPOSUCTION ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LUNG WEDGE RESECTION ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 3 FDA reports)
MACROCEPHALY ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MAMMOPLASTY ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO ADRENALS ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASES TO SPLEEN ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MICROVASCULAR ANGINA ( 3 FDA reports)
MILIA ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NARCOTIC INTOXICATION ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 3 FDA reports)
NOSE DEFORMITY ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESOPHAGEAL INFECTION ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OESTROGEN DEFICIENCY ( 3 FDA reports)
OOPHORECTOMY ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PANCREATIC DUCT STENOSIS ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PENILE SWELLING ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIANAL ERYTHEMA ( 3 FDA reports)
PERICARDIAL CYST ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERIDIVERTICULAR ABSCESS ( 3 FDA reports)
PERIORBITAL DISORDER ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPROSTHETIC FRACTURE ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PHOBIC AVOIDANCE ( 3 FDA reports)
PHYSIOTHERAPY ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PNEUMOBILIA ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONECTOMY ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLYCYTHAEMIA VERA ( 3 FDA reports)
POLYHYDRAMNIOS ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST POLIO SYNDROME ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POST PROCEDURAL SWELLING ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PRESBYOESOPHAGUS ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROSTATIC ABSCESS ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PULMONARY ARTERIOVENOUS FISTULA ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RADIATION FIBROSIS ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RECALL PHENOMENON ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RECTAL CANCER METASTATIC ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
REFLUX LARYNGITIS ( 3 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
RIGHT AORTIC ARCH ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALPINGECTOMY ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SERRATIA INFECTION ( 3 FDA reports)
SERRATIA TEST POSITIVE ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SOFT TISSUE NECROSIS ( 3 FDA reports)
SOMATISATION DISORDER ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL FUSION ACQUIRED ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
SYNOVIAL RUPTURE ( 3 FDA reports)
TEETHING ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TESTICULAR CYST ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THYMUS DISORDER ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URTICARIA PAPULAR ( 3 FDA reports)
UTERINE CYST ( 3 FDA reports)
UTERINE DISORDER ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VAGINITIS GARDNERELLA ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
VULVAL CANCER METASTATIC ( 2 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABORTION COMPLETE ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANGIOFIBROMA ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 2 FDA reports)
AORTIC BRUIT ( 2 FDA reports)
AORTIC EMBOLUS ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AURA ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA STAGE IV ( 2 FDA reports)
BACTEROIDES BACTERAEMIA ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BANDAEMIA ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BILE DUCT CANCER STAGE IV ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BODY DYSMORPHIC DISORDER ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST HYPERPLASIA ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREECH DELIVERY ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CATHETERISATION VENOUS ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELLS IN URINE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLELITHOTOMY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 2 FDA reports)
CONGENITAL VESICOURETERIC REFLUX ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CORTISOL FREE URINE INCREASED ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CRUSH SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DETACHMENT OF MACULAR RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE INTOLERANCE ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISBACTERIOSIS ( 2 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EAR NEOPLASM ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
EXERTIONAL HEADACHE ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID OPERATION ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEAR OF PREGNANCY ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
GALLSTONE ILEUS ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENERAL NUTRITION DISORDER ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL GRAFT ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS B ANTIBODY ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HORMONE REPLACEMENT THERAPY ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPLANT SITE ERYTHEMA ( 2 FDA reports)
IMPLANT SITE SWELLING ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL STRANGULATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
IRITIS ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LARYNGECTOMY ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LATERAL PATELLAR COMPRESSION SYNDROME ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIPASE DECREASED ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MEDIASTINOSCOPY ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL TOXICITY ( 2 FDA reports)
NASAL POLYPECTOMY ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL OPERATION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OPTIC NERVE NEOPLASM ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PASTEURELLA INFECTION ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PERIARTICULAR DISORDER ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERIUMBILICAL ABSCESS ( 2 FDA reports)
PH BODY FLUID ABNORMAL ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 2 FDA reports)
PLEURISY VIRAL ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
POSTPARTUM VAGINAL LACERATION ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREGNANCY TEST POSITIVE ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY ARTERY STENOSIS ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY PNEUMATOCELE ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
RASH FOLLICULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REGRESSIVE BEHAVIOUR ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINITIS SEASONAL ( 2 FDA reports)
RHYTHM IDIOVENTRICULAR ( 2 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 2 FDA reports)
SCEDOSPORIUM INFECTION ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SEBACEOUS HYPERPLASIA ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SEIZURE LIKE PHENOMENA ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN CANCER METASTATIC ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 2 FDA reports)
STASIS SYNDROME ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TONSILLITIS BACTERIAL ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL CANCER ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETERIC CANCER METASTATIC ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
UTERINE ATROPHY ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
UTERINE HYPERTONUS ( 2 FDA reports)
UTERINE MASS ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENOUS VALVE RUPTURED ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VIRAL LABYRINTHITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 2 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 2 FDA reports)
VITAMIN C DEFICIENCY ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACCESSORY SALIVARY GLAND ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC BIFURCATION GRAFT ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRITIS VIRAL ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
AURICULOTEMPORAL SYNDROME ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY STOMACH ( 1 FDA reports)
BIOTIN DEFICIENCY ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALCOHOL ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL OEDEMA MANAGEMENT ( 1 FDA reports)
CERVICAL NEURITIS ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVIX CARCINOMA STAGE IV ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTEROL GRANULOMA ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORDEE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL AORTIC ATRESIA ( 1 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONGENITAL INGUINAL HERNIA ( 1 FDA reports)
CONGENITAL OESOPHAGEAL ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROSTOMY CLOSURE ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIA MYALGIA SYNDROME ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHROPLASIA ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FACTOR X DEFICIENCY ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FIBRONECTIN INCREASED ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OCCULT BLOOD POSITIVE ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS AEROMONAS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE VIII ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JAUNDICE EXTRAHEPATIC OBSTRUCTIVE ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGOSCOPY ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVER FUNCTION TEST NORMAL ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHOBLAST COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACRODACTYLY ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENISCUS REMOVAL ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO MUSCLE ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FLAP OPERATION ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYRINGITIS ( 1 FDA reports)
MYXOEDEMA COMA ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODDING OF HEAD ( 1 FDA reports)
NON-CONSUMMATION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL MUCOSA ERYTHEMA ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
OPIATES NEGATIVE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
ORBITAL CYST ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE III ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN THRESHOLD DECREASED ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANCREATOGENOUS DIABETES ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL CHOREOATHETOSIS ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIODONTAL DESTRUCTION ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL CANDIDIASIS ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOLOGICAL ABUSE ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY OEDEMA NEONATAL ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SCAPHOCEPHALY ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SOCIAL ALCOHOL DRINKER ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINA BIFIDA OCCULTA ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOBACILLUS INFECTION ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWEAT GLAND EXCISION ( 1 FDA reports)
SYNOVIAL SARCOMA ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TAENIASIS ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST DECREASED ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON NECROSIS ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THALASSAEMIA TRAIT ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LACTIC ACID ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROSTOMY COMPLICATION ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VARICOSE VEINS PELVIC ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR HEADACHE ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN SUPPLEMENTATION ( 1 FDA reports)
VITELLO-INTESTINAL DUCT REMNANT ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL SCAN ( 1 FDA reports)