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

PAIN ( 4017 FDA reports)
ANXIETY ( 3863 FDA reports)
NAUSEA ( 3561 FDA reports)
FATIGUE ( 3059 FDA reports)
DEPRESSION ( 3003 FDA reports)
DYSPNOEA ( 2968 FDA reports)
INSOMNIA ( 2896 FDA reports)
HEADACHE ( 2538 FDA reports)
FALL ( 2516 FDA reports)
DIZZINESS ( 2378 FDA reports)
ASTHENIA ( 2342 FDA reports)
DRUG INEFFECTIVE ( 2272 FDA reports)
BACK PAIN ( 2198 FDA reports)
DIARRHOEA ( 2189 FDA reports)
VOMITING ( 2128 FDA reports)
ARTHRALGIA ( 2068 FDA reports)
CHEST PAIN ( 2052 FDA reports)
AMNESIA ( 1990 FDA reports)
ANAEMIA ( 1888 FDA reports)
HYPERTENSION ( 1864 FDA reports)
OEDEMA PERIPHERAL ( 1802 FDA reports)
PAIN IN EXTREMITY ( 1792 FDA reports)
INJURY ( 1684 FDA reports)
ABDOMINAL PAIN ( 1642 FDA reports)
WEIGHT DECREASED ( 1590 FDA reports)
CONSTIPATION ( 1547 FDA reports)
PNEUMONIA ( 1542 FDA reports)
PYREXIA ( 1527 FDA reports)
CONFUSIONAL STATE ( 1495 FDA reports)
OSTEONECROSIS OF JAW ( 1393 FDA reports)
HYPOAESTHESIA ( 1387 FDA reports)
WEIGHT INCREASED ( 1327 FDA reports)
DEHYDRATION ( 1269 FDA reports)
DIABETES MELLITUS ( 1212 FDA reports)
URINARY TRACT INFECTION ( 1205 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1190 FDA reports)
HYPOTENSION ( 1174 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1171 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1161 FDA reports)
OSTEOARTHRITIS ( 1138 FDA reports)
BONE DISORDER ( 1111 FDA reports)
MALAISE ( 1088 FDA reports)
RASH ( 1065 FDA reports)
EMOTIONAL DISTRESS ( 1054 FDA reports)
MYOCARDIAL INFARCTION ( 1041 FDA reports)
SUICIDAL IDEATION ( 1031 FDA reports)
PARAESTHESIA ( 1028 FDA reports)
SOMNOLENCE ( 1020 FDA reports)
LOSS OF CONSCIOUSNESS ( 1012 FDA reports)
FEELING ABNORMAL ( 975 FDA reports)
TREMOR ( 974 FDA reports)
DYSPHAGIA ( 973 FDA reports)
PLEURAL EFFUSION ( 965 FDA reports)
OSTEOMYELITIS ( 964 FDA reports)
NEUROPATHY PERIPHERAL ( 959 FDA reports)
CEREBROVASCULAR ACCIDENT ( 954 FDA reports)
GAIT DISTURBANCE ( 949 FDA reports)
COUGH ( 943 FDA reports)
MUSCLE SPASMS ( 943 FDA reports)
DEEP VEIN THROMBOSIS ( 919 FDA reports)
DECREASED APPETITE ( 914 FDA reports)
ABDOMINAL PAIN UPPER ( 905 FDA reports)
SPINAL OSTEOARTHRITIS ( 874 FDA reports)
RENAL FAILURE ( 872 FDA reports)
CONTUSION ( 863 FDA reports)
CONVULSION ( 847 FDA reports)
SINUSITIS ( 836 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 832 FDA reports)
BRONCHITIS ( 830 FDA reports)
VISION BLURRED ( 826 FDA reports)
HYPERHIDROSIS ( 805 FDA reports)
PULMONARY EMBOLISM ( 792 FDA reports)
SYNCOPE ( 788 FDA reports)
ATRIAL FIBRILLATION ( 779 FDA reports)
MYALGIA ( 775 FDA reports)
TYPE 2 DIABETES MELLITUS ( 775 FDA reports)
CORONARY ARTERY DISEASE ( 772 FDA reports)
DEATH ( 769 FDA reports)
CONDITION AGGRAVATED ( 766 FDA reports)
NECK PAIN ( 759 FDA reports)
ANHEDONIA ( 755 FDA reports)
SOMNAMBULISM ( 753 FDA reports)
SWELLING ( 744 FDA reports)
PRURITUS ( 743 FDA reports)
ATELECTASIS ( 740 FDA reports)
CELLULITIS ( 737 FDA reports)
HALLUCINATION ( 735 FDA reports)
IMPAIRED HEALING ( 725 FDA reports)
RENAL FAILURE ACUTE ( 724 FDA reports)
PAIN IN JAW ( 714 FDA reports)
OSTEONECROSIS ( 713 FDA reports)
DYSPEPSIA ( 712 FDA reports)
MUSCULAR WEAKNESS ( 711 FDA reports)
DYSGEUSIA ( 706 FDA reports)
PALPITATIONS ( 706 FDA reports)
BLOOD GLUCOSE INCREASED ( 702 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 702 FDA reports)
TOOTH EXTRACTION ( 699 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 698 FDA reports)
HYPERLIPIDAEMIA ( 698 FDA reports)
ABNORMAL BEHAVIOUR ( 683 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 674 FDA reports)
THROMBOCYTOPENIA ( 673 FDA reports)
HYPOKALAEMIA ( 669 FDA reports)
ARTHRITIS ( 664 FDA reports)
MEMORY IMPAIRMENT ( 662 FDA reports)
METASTASES TO BONE ( 658 FDA reports)
SUICIDE ATTEMPT ( 645 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 644 FDA reports)
CHILLS ( 642 FDA reports)
RESPIRATORY FAILURE ( 632 FDA reports)
IMPAIRED DRIVING ABILITY ( 631 FDA reports)
BONE PAIN ( 621 FDA reports)
INFECTION ( 620 FDA reports)
OVERDOSE ( 620 FDA reports)
MUSCULOSKELETAL PAIN ( 615 FDA reports)
MITRAL VALVE INCOMPETENCE ( 606 FDA reports)
SEPSIS ( 604 FDA reports)
ERYTHEMA ( 603 FDA reports)
OSTEOPENIA ( 582 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 581 FDA reports)
CARDIOMEGALY ( 575 FDA reports)
DRY MOUTH ( 572 FDA reports)
BLOOD PRESSURE INCREASED ( 571 FDA reports)
AGITATION ( 554 FDA reports)
HAEMORRHOIDS ( 551 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 550 FDA reports)
DRUG DEPENDENCE ( 549 FDA reports)
HAEMOGLOBIN DECREASED ( 546 FDA reports)
HYPERGLYCAEMIA ( 543 FDA reports)
DENTAL CARIES ( 542 FDA reports)
ASTHMA ( 539 FDA reports)
CHOLELITHIASIS ( 534 FDA reports)
SLEEP WALKING ( 534 FDA reports)
GASTRITIS ( 531 FDA reports)
HIATUS HERNIA ( 531 FDA reports)
MENTAL STATUS CHANGES ( 530 FDA reports)
OSTEOPOROSIS ( 525 FDA reports)
TACHYCARDIA ( 514 FDA reports)
CHEST DISCOMFORT ( 508 FDA reports)
BALANCE DISORDER ( 506 FDA reports)
MIGRAINE ( 500 FDA reports)
CARDIAC DISORDER ( 497 FDA reports)
NERVOUSNESS ( 492 FDA reports)
PANCREATITIS ( 491 FDA reports)
LYMPHADENOPATHY ( 475 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 473 FDA reports)
STRESS ( 471 FDA reports)
DYSURIA ( 468 FDA reports)
SLEEP APNOEA SYNDROME ( 466 FDA reports)
DEFORMITY ( 459 FDA reports)
EATING DISORDER ( 459 FDA reports)
LETHARGY ( 458 FDA reports)
ABDOMINAL DISTENSION ( 456 FDA reports)
PANCYTOPENIA ( 455 FDA reports)
RECTAL HAEMORRHAGE ( 455 FDA reports)
RIB FRACTURE ( 455 FDA reports)
DECREASED INTEREST ( 442 FDA reports)
EXOSTOSIS ( 442 FDA reports)
NEUTROPENIA ( 440 FDA reports)
NEOPLASM MALIGNANT ( 438 FDA reports)
RENAL FAILURE CHRONIC ( 436 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 434 FDA reports)
HEART RATE INCREASED ( 431 FDA reports)
VERTIGO ( 426 FDA reports)
CATARACT ( 424 FDA reports)
ABDOMINAL DISCOMFORT ( 421 FDA reports)
DIVERTICULUM ( 420 FDA reports)
JOINT SWELLING ( 417 FDA reports)
DRUG INTERACTION ( 412 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 406 FDA reports)
HYPOXIA ( 403 FDA reports)
COMPLETED SUICIDE ( 400 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 400 FDA reports)
PANIC ATTACK ( 399 FDA reports)
AGGRESSION ( 394 FDA reports)
RENAL CYST ( 394 FDA reports)
TOOTHACHE ( 394 FDA reports)
SLEEP DISORDER ( 393 FDA reports)
TOOTH DISORDER ( 389 FDA reports)
HERPES ZOSTER ( 389 FDA reports)
DYSARTHRIA ( 386 FDA reports)
DISORIENTATION ( 384 FDA reports)
BURSITIS ( 380 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 380 FDA reports)
ARTHROPATHY ( 379 FDA reports)
OBESITY ( 377 FDA reports)
IRRITABILITY ( 376 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 375 FDA reports)
HYPONATRAEMIA ( 375 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 373 FDA reports)
DYSPNOEA EXERTIONAL ( 373 FDA reports)
LUNG NEOPLASM ( 372 FDA reports)
PULMONARY OEDEMA ( 369 FDA reports)
HOT FLUSH ( 368 FDA reports)
HYPOTHYROIDISM ( 368 FDA reports)
THROMBOSIS ( 364 FDA reports)
TOOTH LOSS ( 364 FDA reports)
BLOOD CREATININE INCREASED ( 360 FDA reports)
DISTURBANCE IN ATTENTION ( 359 FDA reports)
ALOPECIA ( 356 FDA reports)
STOMATITIS ( 356 FDA reports)
BONE LESION ( 355 FDA reports)
CARDIAC ARREST ( 350 FDA reports)
MULTIPLE MYELOMA ( 350 FDA reports)
OEDEMA ( 349 FDA reports)
OROPHARYNGEAL PAIN ( 348 FDA reports)
ORAL PAIN ( 347 FDA reports)
PLATELET COUNT DECREASED ( 347 FDA reports)
MENTAL DISORDER ( 343 FDA reports)
MOUTH ULCERATION ( 343 FDA reports)
PRIMARY SEQUESTRUM ( 337 FDA reports)
HAEMATOCHEZIA ( 336 FDA reports)
HAEMATOCRIT DECREASED ( 333 FDA reports)
HEPATIC STEATOSIS ( 332 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 331 FDA reports)
SCOLIOSIS ( 331 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 327 FDA reports)
INFLUENZA LIKE ILLNESS ( 325 FDA reports)
POLLAKIURIA ( 325 FDA reports)
HYPERSENSITIVITY ( 324 FDA reports)
NEPHROLITHIASIS ( 324 FDA reports)
LUNG INFILTRATION ( 323 FDA reports)
DISABILITY ( 322 FDA reports)
SWELLING FACE ( 322 FDA reports)
STAPHYLOCOCCAL INFECTION ( 318 FDA reports)
NIGHT SWEATS ( 318 FDA reports)
ROTATOR CUFF SYNDROME ( 315 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 312 FDA reports)
FEBRILE NEUTROPENIA ( 312 FDA reports)
ANOREXIA ( 311 FDA reports)
ARTERIOSCLEROSIS ( 311 FDA reports)
HYPOPHAGIA ( 311 FDA reports)
ANGER ( 309 FDA reports)
INTENTIONAL OVERDOSE ( 309 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 307 FDA reports)
HAEMORRHAGE ( 306 FDA reports)
VISUAL IMPAIRMENT ( 305 FDA reports)
TINNITUS ( 304 FDA reports)
URINARY INCONTINENCE ( 303 FDA reports)
EPISTAXIS ( 303 FDA reports)
ECONOMIC PROBLEM ( 297 FDA reports)
HAEMATURIA ( 297 FDA reports)
CARPAL TUNNEL SYNDROME ( 296 FDA reports)
ENDODONTIC PROCEDURE ( 296 FDA reports)
ANGINA PECTORIS ( 295 FDA reports)
TENDERNESS ( 295 FDA reports)
TOOTH ABSCESS ( 295 FDA reports)
URTICARIA ( 293 FDA reports)
BRADYCARDIA ( 293 FDA reports)
CARDIOMYOPATHY ( 293 FDA reports)
DIABETIC NEUROPATHY ( 293 FDA reports)
FOOT FRACTURE ( 292 FDA reports)
CRYING ( 290 FDA reports)
HEAD INJURY ( 290 FDA reports)
FLUSHING ( 287 FDA reports)
SPEECH DISORDER ( 287 FDA reports)
SCAR ( 285 FDA reports)
BURNING SENSATION ( 283 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 282 FDA reports)
NIGHTMARE ( 280 FDA reports)
DRUG DOSE OMISSION ( 279 FDA reports)
OFF LABEL USE ( 279 FDA reports)
SINUS TACHYCARDIA ( 278 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 277 FDA reports)
HYPERCHOLESTEROLAEMIA ( 277 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 276 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 276 FDA reports)
PSYCHOTIC DISORDER ( 275 FDA reports)
ABNORMAL DREAMS ( 275 FDA reports)
EAR PAIN ( 274 FDA reports)
NASAL CONGESTION ( 273 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 273 FDA reports)
SPINAL COLUMN STENOSIS ( 272 FDA reports)
PULMONARY HYPERTENSION ( 271 FDA reports)
ARRHYTHMIA ( 271 FDA reports)
CARDIAC MURMUR ( 270 FDA reports)
FEAR ( 268 FDA reports)
INJECTION SITE PAIN ( 268 FDA reports)
COMPRESSION FRACTURE ( 267 FDA reports)
BLOOD PRESSURE DECREASED ( 266 FDA reports)
METASTASES TO LIVER ( 266 FDA reports)
RESTLESS LEGS SYNDROME ( 266 FDA reports)
TENDONITIS ( 266 FDA reports)
TREATMENT NONCOMPLIANCE ( 266 FDA reports)
ERECTILE DYSFUNCTION ( 264 FDA reports)
ABASIA ( 263 FDA reports)
URINARY RETENTION ( 263 FDA reports)
FIBROMYALGIA ( 262 FDA reports)
INTENTIONAL DRUG MISUSE ( 261 FDA reports)
MIDDLE INSOMNIA ( 261 FDA reports)
DISEASE PROGRESSION ( 258 FDA reports)
PARANOIA ( 256 FDA reports)
INFLAMMATION ( 254 FDA reports)
NEURALGIA ( 254 FDA reports)
GINGIVAL PAIN ( 253 FDA reports)
HYPOGLYCAEMIA ( 253 FDA reports)
IRRITABLE BOWEL SYNDROME ( 253 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 253 FDA reports)
RESPIRATORY DISTRESS ( 253 FDA reports)
SURGERY ( 253 FDA reports)
TOOTH FRACTURE ( 250 FDA reports)
TOOTH INFECTION ( 250 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 250 FDA reports)
DRUG ABUSE ( 249 FDA reports)
LOOSE TOOTH ( 249 FDA reports)
DRUG HYPERSENSITIVITY ( 248 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 247 FDA reports)
LUNG DISORDER ( 247 FDA reports)
HIP FRACTURE ( 246 FDA reports)
UNEVALUABLE EVENT ( 246 FDA reports)
DISCOMFORT ( 245 FDA reports)
DYSPHONIA ( 243 FDA reports)
COMA ( 242 FDA reports)
INCORRECT DOSE ADMINISTERED ( 242 FDA reports)
BLOOD POTASSIUM DECREASED ( 240 FDA reports)
DIVERTICULITIS ( 239 FDA reports)
DYSKINESIA ( 239 FDA reports)
GALLBLADDER DISORDER ( 238 FDA reports)
HAEMATOMA ( 237 FDA reports)
BLOOD UREA INCREASED ( 236 FDA reports)
OESOPHAGITIS ( 236 FDA reports)
DRUG ABUSER ( 235 FDA reports)
HEPATIC ENZYME INCREASED ( 235 FDA reports)
MOBILITY DECREASED ( 234 FDA reports)
EYE PAIN ( 232 FDA reports)
GINGIVITIS ( 232 FDA reports)
LEUKOPENIA ( 232 FDA reports)
LEUKOCYTOSIS ( 231 FDA reports)
MAJOR DEPRESSION ( 231 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 230 FDA reports)
SPINAL COMPRESSION FRACTURE ( 230 FDA reports)
VIRAL INFECTION ( 230 FDA reports)
PRODUCT QUALITY ISSUE ( 229 FDA reports)
BONE DEBRIDEMENT ( 229 FDA reports)
OSTEITIS ( 229 FDA reports)
NASOPHARYNGITIS ( 228 FDA reports)
CYST ( 226 FDA reports)
DRUG EFFECT DECREASED ( 226 FDA reports)
DEBRIDEMENT ( 224 FDA reports)
LUMBAR SPINAL STENOSIS ( 224 FDA reports)
OSTEOSCLEROSIS ( 224 FDA reports)
DEPRESSED MOOD ( 221 FDA reports)
PERICARDIAL EFFUSION ( 221 FDA reports)
AORTIC VALVE INCOMPETENCE ( 220 FDA reports)
FLUID RETENTION ( 219 FDA reports)
RESTLESSNESS ( 219 FDA reports)
SYNOVIAL CYST ( 219 FDA reports)
WHEEZING ( 218 FDA reports)
DRUG TOXICITY ( 216 FDA reports)
GASTROENTERITIS ( 216 FDA reports)
MALNUTRITION ( 216 FDA reports)
JOINT INJURY ( 215 FDA reports)
FLATULENCE ( 214 FDA reports)
MOOD SWINGS ( 213 FDA reports)
HEPATIC CYST ( 212 FDA reports)
CHOLECYSTITIS CHRONIC ( 211 FDA reports)
HEART RATE IRREGULAR ( 211 FDA reports)
COGNITIVE DISORDER ( 210 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 208 FDA reports)
CANDIDIASIS ( 207 FDA reports)
DIPLOPIA ( 207 FDA reports)
GINGIVAL BLEEDING ( 207 FDA reports)
MULTIPLE INJURIES ( 207 FDA reports)
CHRONIC SINUSITIS ( 206 FDA reports)
SCIATICA ( 206 FDA reports)
RADICULOPATHY ( 205 FDA reports)
MUCOSAL INFLAMMATION ( 204 FDA reports)
BONE DENSITY DECREASED ( 203 FDA reports)
GINGIVAL SWELLING ( 202 FDA reports)
DELIRIUM ( 200 FDA reports)
FEMUR FRACTURE ( 200 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 200 FDA reports)
MEDICATION ERROR ( 199 FDA reports)
PRODUCTIVE COUGH ( 199 FDA reports)
NOCTURIA ( 198 FDA reports)
PULMONARY CONGESTION ( 197 FDA reports)
VENTRICULAR TACHYCARDIA ( 197 FDA reports)
RENAL IMPAIRMENT ( 196 FDA reports)
UNRESPONSIVE TO STIMULI ( 196 FDA reports)
JAW DISORDER ( 196 FDA reports)
OSTEOLYSIS ( 196 FDA reports)
EJECTION FRACTION DECREASED ( 195 FDA reports)
ORAL CANDIDIASIS ( 195 FDA reports)
INITIAL INSOMNIA ( 194 FDA reports)
JOINT EFFUSION ( 194 FDA reports)
SLEEP TALKING ( 194 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 192 FDA reports)
PERIODONTITIS ( 192 FDA reports)
DIVERTICULUM INTESTINAL ( 191 FDA reports)
GASTRIC ULCER ( 191 FDA reports)
PATHOLOGICAL FRACTURE ( 191 FDA reports)
ACTINOMYCOSIS ( 190 FDA reports)
HAEMOPTYSIS ( 190 FDA reports)
METASTASES TO SPINE ( 189 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 189 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 189 FDA reports)
TARDIVE DYSKINESIA ( 189 FDA reports)
PURULENT DISCHARGE ( 188 FDA reports)
SKIN ULCER ( 188 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 188 FDA reports)
SINUS DISORDER ( 187 FDA reports)
ADVERSE EVENT ( 187 FDA reports)
ENCEPHALOPATHY ( 185 FDA reports)
MULTIPLE SCLEROSIS ( 185 FDA reports)
DEAFNESS ( 184 FDA reports)
FUNGAL INFECTION ( 184 FDA reports)
BLOOD CALCIUM DECREASED ( 183 FDA reports)
HALLUCINATION, VISUAL ( 183 FDA reports)
VISUAL ACUITY REDUCED ( 183 FDA reports)
COLITIS ( 182 FDA reports)
EMOTIONAL DISORDER ( 181 FDA reports)
ILL-DEFINED DISORDER ( 181 FDA reports)
METASTASES TO LUNG ( 181 FDA reports)
PANCREATITIS ACUTE ( 181 FDA reports)
RHEUMATOID ARTHRITIS ( 181 FDA reports)
THINKING ABNORMAL ( 181 FDA reports)
GASTROINTESTINAL DISORDER ( 180 FDA reports)
JAW FRACTURE ( 180 FDA reports)
BIPOLAR DISORDER ( 179 FDA reports)
HEPATIC FAILURE ( 179 FDA reports)
MASTICATION DISORDER ( 179 FDA reports)
RASH PRURITIC ( 179 FDA reports)
PHYSICAL DISABILITY ( 178 FDA reports)
ABSCESS ( 177 FDA reports)
ACCIDENTAL OVERDOSE ( 177 FDA reports)
RENAL DISORDER ( 176 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 175 FDA reports)
LUMBAR RADICULOPATHY ( 175 FDA reports)
MENISCUS LESION ( 175 FDA reports)
FISTULA ( 174 FDA reports)
JOINT DISLOCATION ( 174 FDA reports)
PERIODONTAL DISEASE ( 174 FDA reports)
UTERINE LEIOMYOMA ( 174 FDA reports)
RHINORRHOEA ( 172 FDA reports)
TYPE 1 DIABETES MELLITUS ( 172 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 172 FDA reports)
ORAL INFECTION ( 172 FDA reports)
COLONIC POLYP ( 171 FDA reports)
GINGIVAL INFECTION ( 171 FDA reports)
MASS ( 171 FDA reports)
INFLUENZA ( 169 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 169 FDA reports)
PRESYNCOPE ( 168 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 168 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 168 FDA reports)
FLANK PAIN ( 168 FDA reports)
MUSCLE TWITCHING ( 168 FDA reports)
CARDIAC FAILURE ( 167 FDA reports)
DIABETIC KETOACIDOSIS ( 167 FDA reports)
EXCORIATION ( 167 FDA reports)
BLOOD SODIUM DECREASED ( 166 FDA reports)
FOOT DEFORMITY ( 166 FDA reports)
HAEMATEMESIS ( 166 FDA reports)
LACERATION ( 166 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 166 FDA reports)
SKIN LESION ( 165 FDA reports)
CHOLECYSTITIS ( 165 FDA reports)
DRY EYE ( 164 FDA reports)
HYPERCALCAEMIA ( 164 FDA reports)
PROTHROMBIN TIME PROLONGED ( 164 FDA reports)
RHABDOMYOLYSIS ( 164 FDA reports)
WOUND DEHISCENCE ( 162 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 162 FDA reports)
ORAL DISORDER ( 162 FDA reports)
CARDIO-RESPIRATORY ARREST ( 161 FDA reports)
SKIN LACERATION ( 161 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 161 FDA reports)
SEBORRHOEIC KERATOSIS ( 160 FDA reports)
JOINT SPRAIN ( 160 FDA reports)
MYOCARDIAL ISCHAEMIA ( 158 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 157 FDA reports)
COORDINATION ABNORMAL ( 157 FDA reports)
GROIN PAIN ( 157 FDA reports)
ORTHOSTATIC HYPOTENSION ( 157 FDA reports)
BREAST CANCER ( 156 FDA reports)
MICTURITION URGENCY ( 156 FDA reports)
RHINITIS ALLERGIC ( 156 FDA reports)
SEDATION ( 155 FDA reports)
BLOOD GLUCOSE DECREASED ( 155 FDA reports)
CAROTID ARTERY STENOSIS ( 155 FDA reports)
CYSTITIS ( 155 FDA reports)
JOINT STIFFNESS ( 155 FDA reports)
LYMPHOEDEMA ( 155 FDA reports)
PHARYNGITIS ( 155 FDA reports)
CEREBRAL ATROPHY ( 154 FDA reports)
HUMERUS FRACTURE ( 154 FDA reports)
HYPOCALCAEMIA ( 154 FDA reports)
METABOLIC ACIDOSIS ( 154 FDA reports)
MULTI-ORGAN FAILURE ( 154 FDA reports)
FIBROSIS ( 153 FDA reports)
SEPTIC SHOCK ( 153 FDA reports)
FEELING HOT ( 152 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 152 FDA reports)
DRY SKIN ( 151 FDA reports)
HYPERKALAEMIA ( 151 FDA reports)
INJECTION SITE ERYTHEMA ( 151 FDA reports)
SEQUESTRECTOMY ( 151 FDA reports)
SKIN DISORDER ( 150 FDA reports)
UPPER LIMB FRACTURE ( 150 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 150 FDA reports)
EXPOSED BONE IN JAW ( 149 FDA reports)
PNEUMOTHORAX ( 149 FDA reports)
MITRAL VALVE PROLAPSE ( 148 FDA reports)
RESPIRATORY ARREST ( 148 FDA reports)
WITHDRAWAL SYNDROME ( 148 FDA reports)
DENTAL FISTULA ( 147 FDA reports)
GASTRIC DISORDER ( 147 FDA reports)
JAW OPERATION ( 147 FDA reports)
EMPHYSEMA ( 146 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 146 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 146 FDA reports)
SKIN DISCOLOURATION ( 146 FDA reports)
SPINAL FRACTURE ( 146 FDA reports)
SPONDYLOLISTHESIS ( 146 FDA reports)
VISUAL DISTURBANCE ( 146 FDA reports)
RHINITIS ( 145 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 145 FDA reports)
HALLUCINATION, AUDITORY ( 145 FDA reports)
MANIA ( 145 FDA reports)
ANGINA UNSTABLE ( 144 FDA reports)
FACIAL PAIN ( 144 FDA reports)
FLUID OVERLOAD ( 144 FDA reports)
ACUTE RESPIRATORY FAILURE ( 143 FDA reports)
LIBIDO DECREASED ( 143 FDA reports)
BLOOD BILIRUBIN INCREASED ( 142 FDA reports)
LIMB INJURY ( 142 FDA reports)
SKIN EXFOLIATION ( 142 FDA reports)
FAILURE TO THRIVE ( 141 FDA reports)
ANKLE FRACTURE ( 140 FDA reports)
HYPERSOMNIA ( 140 FDA reports)
LOCALISED INFECTION ( 140 FDA reports)
DECUBITUS ULCER ( 139 FDA reports)
PERONEAL NERVE PALSY ( 139 FDA reports)
ABDOMINAL PAIN LOWER ( 138 FDA reports)
NEOPLASM PROGRESSION ( 138 FDA reports)
NERVOUS SYSTEM DISORDER ( 137 FDA reports)
OXYGEN SATURATION DECREASED ( 137 FDA reports)
SINUS BRADYCARDIA ( 137 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 136 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 136 FDA reports)
BLISTER ( 136 FDA reports)
DEPENDENCE ( 136 FDA reports)
BLINDNESS ( 135 FDA reports)
COAGULOPATHY ( 135 FDA reports)
DERMATITIS ( 135 FDA reports)
DEVICE RELATED INFECTION ( 135 FDA reports)
FACIAL BONES FRACTURE ( 135 FDA reports)
FAECAL INCONTINENCE ( 135 FDA reports)
ATRIAL SEPTAL DEFECT ( 134 FDA reports)
GENERALISED OEDEMA ( 134 FDA reports)
PLATELET COUNT INCREASED ( 134 FDA reports)
PNEUMONIA ASPIRATION ( 134 FDA reports)
ASCITES ( 133 FDA reports)
DYSSTASIA ( 133 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 133 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 133 FDA reports)
ULCER ( 133 FDA reports)
VENTRICULAR HYPERTROPHY ( 132 FDA reports)
CEREBRAL INFARCTION ( 132 FDA reports)
IMPAIRED WORK ABILITY ( 132 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 132 FDA reports)
CERVICAL SPINAL STENOSIS ( 131 FDA reports)
MENTAL IMPAIRMENT ( 131 FDA reports)
MOOD ALTERED ( 131 FDA reports)
EAR INFECTION ( 130 FDA reports)
PSORIASIS ( 130 FDA reports)
PULMONARY FIBROSIS ( 129 FDA reports)
APHASIA ( 129 FDA reports)
ECZEMA ( 129 FDA reports)
KYPHOSIS ( 129 FDA reports)
SPLENOMEGALY ( 128 FDA reports)
HYPOVOLAEMIA ( 127 FDA reports)
DEMENTIA ( 126 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 125 FDA reports)
BASAL CELL CARCINOMA ( 124 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 124 FDA reports)
ORAL CAVITY FISTULA ( 124 FDA reports)
POST PROCEDURAL COMPLICATION ( 124 FDA reports)
SINUS HEADACHE ( 124 FDA reports)
STRESS FRACTURE ( 124 FDA reports)
CEREBRAL ISCHAEMIA ( 123 FDA reports)
MOVEMENT DISORDER ( 123 FDA reports)
BACK DISORDER ( 122 FDA reports)
GLAUCOMA ( 122 FDA reports)
RASH GENERALISED ( 122 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 121 FDA reports)
DELUSION ( 121 FDA reports)
GOITRE ( 121 FDA reports)
GRAND MAL CONVULSION ( 121 FDA reports)
INTESTINAL OBSTRUCTION ( 121 FDA reports)
ABSCESS ORAL ( 120 FDA reports)
HAND FRACTURE ( 120 FDA reports)
INCONTINENCE ( 120 FDA reports)
VAGINAL HAEMORRHAGE ( 120 FDA reports)
SWOLLEN TONGUE ( 119 FDA reports)
CORONARY ARTERY OCCLUSION ( 119 FDA reports)
PLEURAL FIBROSIS ( 119 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 118 FDA reports)
SPINAL DISORDER ( 118 FDA reports)
DENTAL OPERATION ( 117 FDA reports)
IRON DEFICIENCY ANAEMIA ( 117 FDA reports)
LIVER DISORDER ( 116 FDA reports)
ODYNOPHAGIA ( 116 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 116 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 115 FDA reports)
HEPATIC LESION ( 115 FDA reports)
HYPOMAGNESAEMIA ( 115 FDA reports)
INADEQUATE ANALGESIA ( 115 FDA reports)
NODULE ( 115 FDA reports)
PATHOLOGICAL GAMBLING ( 115 FDA reports)
PELVIC FRACTURE ( 115 FDA reports)
AORTIC ANEURYSM ( 114 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 114 FDA reports)
HEPATITIS ( 114 FDA reports)
INTERSTITIAL LUNG DISEASE ( 114 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 114 FDA reports)
BRUXISM ( 113 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 113 FDA reports)
ONYCHOMYCOSIS ( 113 FDA reports)
OVARIAN CYST ( 113 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 112 FDA reports)
HOMICIDAL IDEATION ( 112 FDA reports)
HEMIPARESIS ( 111 FDA reports)
HEPATIC CIRRHOSIS ( 111 FDA reports)
PLEURITIC PAIN ( 111 FDA reports)
BONE FRAGMENTATION ( 110 FDA reports)
ECCHYMOSIS ( 110 FDA reports)
GUN SHOT WOUND ( 110 FDA reports)
ORAL SURGERY ( 110 FDA reports)
CROHN'S DISEASE ( 109 FDA reports)
DERMAL CYST ( 109 FDA reports)
GINGIVAL ULCERATION ( 109 FDA reports)
HEPATOMEGALY ( 109 FDA reports)
PALLOR ( 109 FDA reports)
THYROID DISORDER ( 109 FDA reports)
RASH MACULAR ( 108 FDA reports)
HAEMANGIOMA ( 108 FDA reports)
HYDRONEPHROSIS ( 108 FDA reports)
LEFT ATRIAL DILATATION ( 108 FDA reports)
ACUTE SINUSITIS ( 107 FDA reports)
BACTERIAL INFECTION ( 107 FDA reports)
BLOOD ALBUMIN DECREASED ( 107 FDA reports)
BREAST MASS ( 107 FDA reports)
COLD SWEAT ( 107 FDA reports)
INJECTION SITE HAEMATOMA ( 107 FDA reports)
INJECTION SITE HAEMORRHAGE ( 107 FDA reports)
OCULAR HYPERAEMIA ( 107 FDA reports)
PELVIC PAIN ( 107 FDA reports)
POOR QUALITY SLEEP ( 107 FDA reports)
RETCHING ( 107 FDA reports)
WRIST FRACTURE ( 107 FDA reports)
BREAST CANCER METASTATIC ( 106 FDA reports)
COLON CANCER ( 106 FDA reports)
EYE IRRITATION ( 106 FDA reports)
PARAESTHESIA ORAL ( 106 FDA reports)
DRUG SCREEN POSITIVE ( 105 FDA reports)
INCOHERENT ( 105 FDA reports)
ORAL DISCOMFORT ( 105 FDA reports)
PEPTIC ULCER ( 105 FDA reports)
BODY TEMPERATURE INCREASED ( 104 FDA reports)
CARDIOVASCULAR DISORDER ( 104 FDA reports)
CHOLECYSTECTOMY ( 104 FDA reports)
GOUT ( 104 FDA reports)
HERPES SIMPLEX ( 104 FDA reports)
JAUNDICE ( 104 FDA reports)
LOBAR PNEUMONIA ( 104 FDA reports)
MELAENA ( 104 FDA reports)
MUSCLE STRAIN ( 104 FDA reports)
MYOPATHY ( 104 FDA reports)
POLYURIA ( 104 FDA reports)
SENSITIVITY OF TEETH ( 104 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 103 FDA reports)
BLOOD CALCIUM INCREASED ( 103 FDA reports)
BLOOD URINE PRESENT ( 103 FDA reports)
CONCUSSION ( 103 FDA reports)
FACE OEDEMA ( 103 FDA reports)
LACRIMATION INCREASED ( 103 FDA reports)
ACTINIC KERATOSIS ( 102 FDA reports)
APPENDICITIS ( 102 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 102 FDA reports)
METASTATIC NEOPLASM ( 102 FDA reports)
AZOTAEMIA ( 101 FDA reports)
DEVICE FAILURE ( 101 FDA reports)
LUNG NEOPLASM MALIGNANT ( 101 FDA reports)
MULTIPLE DRUG OVERDOSE ( 101 FDA reports)
SLEEP-RELATED EATING DISORDER ( 101 FDA reports)
DENTURE WEARER ( 100 FDA reports)
EYE SWELLING ( 100 FDA reports)
POLYP ( 100 FDA reports)
BONE LOSS ( 99 FDA reports)
RESPIRATORY DISORDER ( 99 FDA reports)
TENDON DISORDER ( 99 FDA reports)
VENOUS INSUFFICIENCY ( 99 FDA reports)
RASH ERYTHEMATOUS ( 98 FDA reports)
ABSCESS JAW ( 98 FDA reports)
ESCHERICHIA INFECTION ( 98 FDA reports)
HYPERKERATOSIS ( 98 FDA reports)
LOCAL SWELLING ( 98 FDA reports)
ATAXIA ( 97 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 97 FDA reports)
DRUG ADMINISTRATION ERROR ( 97 FDA reports)
FEELING JITTERY ( 97 FDA reports)
HEART RATE DECREASED ( 97 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 97 FDA reports)
LIMB DISCOMFORT ( 97 FDA reports)
SEXUAL DYSFUNCTION ( 97 FDA reports)
STOMACH DISCOMFORT ( 97 FDA reports)
VARICOSE VEIN ( 97 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 97 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 96 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 96 FDA reports)
ANAPHYLACTIC REACTION ( 96 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 95 FDA reports)
CORONARY ARTERY STENOSIS ( 95 FDA reports)
HYPOAESTHESIA ORAL ( 95 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 95 FDA reports)
METASTASES TO LYMPH NODES ( 95 FDA reports)
PARALYSIS ( 95 FDA reports)
BREAST PAIN ( 94 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 94 FDA reports)
PANCREATITIS CHRONIC ( 94 FDA reports)
PHARYNGEAL OEDEMA ( 94 FDA reports)
PROCEDURAL PAIN ( 94 FDA reports)
PROSTATE CANCER ( 94 FDA reports)
SINUS CONGESTION ( 94 FDA reports)
SOFT TISSUE DISORDER ( 94 FDA reports)
STEM CELL TRANSPLANT ( 94 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 94 FDA reports)
PROTEINURIA ( 93 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 93 FDA reports)
ADRENAL INSUFFICIENCY ( 93 FDA reports)
FACET JOINT SYNDROME ( 93 FDA reports)
NEURITIS ( 93 FDA reports)
PLANTAR FASCIITIS ( 93 FDA reports)
ANXIETY DISORDER ( 92 FDA reports)
BACTERAEMIA ( 92 FDA reports)
DILATATION VENTRICULAR ( 92 FDA reports)
ELECTROLYTE IMBALANCE ( 92 FDA reports)
EPICONDYLITIS ( 92 FDA reports)
LIFE EXPECTANCY SHORTENED ( 92 FDA reports)
NECK INJURY ( 92 FDA reports)
RENAL INJURY ( 92 FDA reports)
ADVERSE DRUG REACTION ( 91 FDA reports)
CIRCULATORY COLLAPSE ( 91 FDA reports)
FEELING COLD ( 91 FDA reports)
GINGIVAL DISORDER ( 91 FDA reports)
INCREASED APPETITE ( 91 FDA reports)
PERSONALITY CHANGE ( 91 FDA reports)
AFFECTIVE DISORDER ( 90 FDA reports)
ASPIRATION ( 90 FDA reports)
ATRIAL FLUTTER ( 90 FDA reports)
HYPOKINESIA ( 90 FDA reports)
THROAT TIGHTNESS ( 90 FDA reports)
PSEUDOMONAS INFECTION ( 89 FDA reports)
SENSORY LOSS ( 89 FDA reports)
AFFECT LABILITY ( 89 FDA reports)
ALCOHOL USE ( 89 FDA reports)
BONE NEOPLASM MALIGNANT ( 89 FDA reports)
COLITIS ULCERATIVE ( 89 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 89 FDA reports)
LARYNGITIS ( 89 FDA reports)
OPEN WOUND ( 89 FDA reports)
ABSCESS DRAINAGE ( 88 FDA reports)
BACK INJURY ( 88 FDA reports)
BREATH ODOUR ( 88 FDA reports)
ILEUS ( 88 FDA reports)
NON-CARDIAC CHEST PAIN ( 88 FDA reports)
PNEUMONITIS ( 88 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 88 FDA reports)
VENTRICULAR FIBRILLATION ( 88 FDA reports)
SUBCUTANEOUS ABSCESS ( 87 FDA reports)
SUBDURAL HAEMATOMA ( 87 FDA reports)
TACHYPNOEA ( 87 FDA reports)
AORTIC VALVE SCLEROSIS ( 87 FDA reports)
BEDRIDDEN ( 87 FDA reports)
INGROWING NAIL ( 87 FDA reports)
FEELING DRUNK ( 86 FDA reports)
HYPOACUSIS ( 86 FDA reports)
LOWER LIMB FRACTURE ( 86 FDA reports)
MALIGNANT MELANOMA ( 86 FDA reports)
NEUTROPHIL COUNT DECREASED ( 86 FDA reports)
SPINAL CORD COMPRESSION ( 86 FDA reports)
THIRST ( 85 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 85 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 85 FDA reports)
BIPOLAR I DISORDER ( 85 FDA reports)
DRUG INTOLERANCE ( 85 FDA reports)
ENTEROCOCCAL INFECTION ( 85 FDA reports)
HEPATITIS C ( 85 FDA reports)
CATARACT OPERATION ( 84 FDA reports)
CERUMEN IMPACTION ( 84 FDA reports)
COSTOCHONDRITIS ( 84 FDA reports)
DEAFNESS NEUROSENSORY ( 84 FDA reports)
FAECES DISCOLOURED ( 84 FDA reports)
HYPERTONIC BLADDER ( 84 FDA reports)
PERIPHERAL COLDNESS ( 84 FDA reports)
PULMONARY MASS ( 84 FDA reports)
PULPITIS DENTAL ( 84 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 84 FDA reports)
GLOSSODYNIA ( 83 FDA reports)
INJECTION SITE REACTION ( 83 FDA reports)
ISCHAEMIA ( 83 FDA reports)
PHOTOPHOBIA ( 83 FDA reports)
BLOOD POTASSIUM INCREASED ( 82 FDA reports)
DIABETIC COMA ( 82 FDA reports)
DIALYSIS ( 82 FDA reports)
DIFFICULTY IN WALKING ( 82 FDA reports)
DUODENITIS ( 82 FDA reports)
HERNIA ( 82 FDA reports)
OTITIS MEDIA ( 82 FDA reports)
BONE EROSION ( 81 FDA reports)
CHOLECYSTITIS ACUTE ( 81 FDA reports)
CHROMATURIA ( 81 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 81 FDA reports)
GASTRITIS EROSIVE ( 81 FDA reports)
HYPOALBUMINAEMIA ( 81 FDA reports)
NERVE INJURY ( 81 FDA reports)
VAGINAL INFECTION ( 81 FDA reports)
VASCULITIS ( 81 FDA reports)
RADIUS FRACTURE ( 80 FDA reports)
SENSORY DISTURBANCE ( 80 FDA reports)
BONE MARROW FAILURE ( 80 FDA reports)
DERMATITIS CONTACT ( 80 FDA reports)
DYSLIPIDAEMIA ( 80 FDA reports)
INGUINAL HERNIA ( 80 FDA reports)
OEDEMA MOUTH ( 80 FDA reports)
OTITIS EXTERNA ( 80 FDA reports)
CYANOSIS ( 79 FDA reports)
DIASTOLIC DYSFUNCTION ( 79 FDA reports)
DISEASE RECURRENCE ( 79 FDA reports)
ESSENTIAL HYPERTENSION ( 79 FDA reports)
INFUSION RELATED REACTION ( 79 FDA reports)
MYOCLONUS ( 79 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 79 FDA reports)
PROCTALGIA ( 79 FDA reports)
TENDON INJURY ( 79 FDA reports)
RADIOTHERAPY ( 78 FDA reports)
SICK SINUS SYNDROME ( 78 FDA reports)
BLOOD MAGNESIUM DECREASED ( 78 FDA reports)
INTERMITTENT CLAUDICATION ( 78 FDA reports)
LIGAMENT SPRAIN ( 78 FDA reports)
ORAL HERPES ( 78 FDA reports)
PARKINSON'S DISEASE ( 78 FDA reports)
EUPHORIC MOOD ( 77 FDA reports)
SKELETAL INJURY ( 77 FDA reports)
PURULENCE ( 76 FDA reports)
STEVENS-JOHNSON SYNDROME ( 76 FDA reports)
AKATHISIA ( 76 FDA reports)
ANGIOEDEMA ( 76 FDA reports)
BARRETT'S OESOPHAGUS ( 76 FDA reports)
BRONCHOPNEUMONIA ( 76 FDA reports)
KNEE ARTHROPLASTY ( 76 FDA reports)
NEOPLASM ( 76 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 76 FDA reports)
BLADDER DISORDER ( 75 FDA reports)
MUSCLE INJURY ( 75 FDA reports)
ACUTE CORONARY SYNDROME ( 74 FDA reports)
BONE OPERATION ( 74 FDA reports)
KIDNEY INFECTION ( 74 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 74 FDA reports)
PHLEBITIS ( 74 FDA reports)
SPINAL LAMINECTOMY ( 74 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 74 FDA reports)
WALKING AID USER ( 74 FDA reports)
SKIN HYPERTROPHY ( 73 FDA reports)
SPINAL FUSION SURGERY ( 73 FDA reports)
WOUND INFECTION ( 73 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 73 FDA reports)
CYSTOCELE ( 73 FDA reports)
DRUG TOLERANCE ( 73 FDA reports)
EYE DISORDER ( 73 FDA reports)
FACIAL PALSY ( 73 FDA reports)
GASTROINTESTINAL PAIN ( 73 FDA reports)
INTENTIONAL SELF-INJURY ( 73 FDA reports)
MENORRHAGIA ( 73 FDA reports)
ABDOMINAL HERNIA ( 72 FDA reports)
ORTHOPNOEA ( 72 FDA reports)
ALVEOLOPLASTY ( 71 FDA reports)
DEVICE MALFUNCTION ( 71 FDA reports)
HEARING IMPAIRED ( 71 FDA reports)
MUSCLE TIGHTNESS ( 71 FDA reports)
PETECHIAE ( 71 FDA reports)
VAGINAL DISCHARGE ( 71 FDA reports)
PRURITUS GENERALISED ( 70 FDA reports)
ACNE ( 70 FDA reports)
AORTIC STENOSIS ( 70 FDA reports)
BLEPHARITIS ( 70 FDA reports)
NERVE COMPRESSION ( 70 FDA reports)
APATHY ( 69 FDA reports)
FACE INJURY ( 69 FDA reports)
HOSPITALISATION ( 69 FDA reports)
NASAL SEPTUM DEVIATION ( 69 FDA reports)
RECTOCELE ( 69 FDA reports)
SKIN TIGHTNESS ( 69 FDA reports)
THYROID NEOPLASM ( 69 FDA reports)
WOUND ( 69 FDA reports)
PYELONEPHRITIS ( 68 FDA reports)
SKIN BURNING SENSATION ( 68 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 68 FDA reports)
TRISMUS ( 68 FDA reports)
CHOKING ( 68 FDA reports)
METABOLIC ENCEPHALOPATHY ( 68 FDA reports)
MYELODYSPLASTIC SYNDROME ( 68 FDA reports)
PANIC DISORDER ( 68 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 67 FDA reports)
BREAST TENDERNESS ( 67 FDA reports)
CARDIAC VALVE DISEASE ( 67 FDA reports)
CLAVICLE FRACTURE ( 67 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 67 FDA reports)
MITRAL VALVE CALCIFICATION ( 67 FDA reports)
MYOSITIS ( 67 FDA reports)
OESOPHAGEAL STENOSIS ( 67 FDA reports)
PSYCHIATRIC SYMPTOM ( 67 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 67 FDA reports)
TONGUE ULCERATION ( 67 FDA reports)
UROSEPSIS ( 67 FDA reports)
VASCULAR CALCIFICATION ( 67 FDA reports)
POST HERPETIC NEURALGIA ( 66 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 66 FDA reports)
TOOTH REPAIR ( 66 FDA reports)
BRONCHOSPASM ( 66 FDA reports)
DECREASED ACTIVITY ( 66 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 66 FDA reports)
FRACTURE ( 66 FDA reports)
ORAL INTAKE REDUCED ( 66 FDA reports)
BLINDNESS UNILATERAL ( 65 FDA reports)
BONE SCAN ABNORMAL ( 65 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 65 FDA reports)
ENTERITIS ( 65 FDA reports)
ERUCTATION ( 65 FDA reports)
HYPOAESTHESIA FACIAL ( 65 FDA reports)
INCREASED TENDENCY TO BRUISE ( 65 FDA reports)
MALOCCLUSION ( 65 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 65 FDA reports)
PLASMACYTOSIS ( 65 FDA reports)
PLEURISY ( 65 FDA reports)
PREGNANCY ( 65 FDA reports)
SKIN INDURATION ( 65 FDA reports)
TENOSYNOVITIS ( 65 FDA reports)
VITAMIN D DECREASED ( 65 FDA reports)
WOUND DRAINAGE ( 65 FDA reports)
PREMATURE BABY ( 64 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 64 FDA reports)
ABDOMINAL TENDERNESS ( 64 FDA reports)
AORTIC CALCIFICATION ( 64 FDA reports)
GINGIVAL ERYTHEMA ( 64 FDA reports)
GRANULOMA ( 64 FDA reports)
HIP ARTHROPLASTY ( 64 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 64 FDA reports)
NEUROGENIC BLADDER ( 64 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 64 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 63 FDA reports)
HOMICIDE ( 63 FDA reports)
PARAPLEGIA ( 63 FDA reports)
PLASMACYTOMA ( 63 FDA reports)
STRESS URINARY INCONTINENCE ( 63 FDA reports)
TRIGGER FINGER ( 63 FDA reports)
RENAL PAIN ( 62 FDA reports)
TEMPERATURE INTOLERANCE ( 62 FDA reports)
URINARY HESITATION ( 62 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 62 FDA reports)
CEREBRAL HAEMORRHAGE ( 62 FDA reports)
GINGIVAL RECESSION ( 62 FDA reports)
MACULAR DEGENERATION ( 62 FDA reports)
MUSCLE CRAMP ( 62 FDA reports)
COLON ADENOMA ( 61 FDA reports)
CULTURE URINE POSITIVE ( 61 FDA reports)
DENTAL CARE ( 61 FDA reports)
DILATATION ATRIAL ( 61 FDA reports)
GLOSSITIS ( 61 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 61 FDA reports)
INTENTIONAL MISUSE ( 61 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 61 FDA reports)
PHYSICAL ASSAULT ( 61 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 61 FDA reports)
SKIN HYPERPIGMENTATION ( 61 FDA reports)
RASH PAPULAR ( 60 FDA reports)
SCAB ( 60 FDA reports)
THROAT IRRITATION ( 60 FDA reports)
BLOOD CHLORIDE DECREASED ( 60 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 60 FDA reports)
CAESAREAN SECTION ( 60 FDA reports)
CARDIOGENIC SHOCK ( 60 FDA reports)
HYSTERECTOMY ( 60 FDA reports)
LABORATORY TEST ABNORMAL ( 60 FDA reports)
MOUTH HAEMORRHAGE ( 60 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 60 FDA reports)
APHAGIA ( 59 FDA reports)
BREAST CANCER RECURRENT ( 59 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 59 FDA reports)
LACUNAR INFARCTION ( 59 FDA reports)
LIPOMA ( 59 FDA reports)
PRESCRIBED OVERDOSE ( 59 FDA reports)
PULMONARY GRANULOMA ( 59 FDA reports)
REFLUX OESOPHAGITIS ( 59 FDA reports)
SEASONAL ALLERGY ( 59 FDA reports)
SKIN FIBROSIS ( 59 FDA reports)
VITREOUS FLOATERS ( 59 FDA reports)
PRESBYOPIA ( 58 FDA reports)
PROTEIN URINE PRESENT ( 58 FDA reports)
RENAL TUBULAR NECROSIS ( 58 FDA reports)
RHONCHI ( 58 FDA reports)
VITAMIN B12 DEFICIENCY ( 58 FDA reports)
AGRANULOCYTOSIS ( 58 FDA reports)
CARDIAC PACEMAKER INSERTION ( 58 FDA reports)
CONJUNCTIVITIS ( 58 FDA reports)
DYSTONIA ( 58 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 58 FDA reports)
OSTEORADIONECROSIS ( 58 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 57 FDA reports)
BRONCHITIS ACUTE ( 57 FDA reports)
GENITAL HERPES ( 57 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 57 FDA reports)
NEURODERMATITIS ( 57 FDA reports)
OLIGURIA ( 57 FDA reports)
OVARIAN CANCER ( 57 FDA reports)
PAIN OF SKIN ( 57 FDA reports)
RASH MACULO-PAPULAR ( 57 FDA reports)
RECTAL POLYP ( 57 FDA reports)
THYROID CANCER ( 57 FDA reports)
VENTRICULAR HYPOKINESIA ( 57 FDA reports)
SNORING ( 56 FDA reports)
TRANSAMINASES INCREASED ( 56 FDA reports)
VERTEBROPLASTY ( 56 FDA reports)
ABDOMINAL ADHESIONS ( 56 FDA reports)
ANGIOPATHY ( 56 FDA reports)
CATHETER RELATED INFECTION ( 56 FDA reports)
HYPOPHOSPHATAEMIA ( 56 FDA reports)
INJECTION SITE PRURITUS ( 56 FDA reports)
LIGAMENT INJURY ( 56 FDA reports)
PERIORBITAL HAEMATOMA ( 56 FDA reports)
ASTIGMATISM ( 55 FDA reports)
CACHEXIA ( 55 FDA reports)
CLOSTRIDIAL INFECTION ( 55 FDA reports)
DIABETIC COMPLICATION ( 55 FDA reports)
GASTROENTERITIS VIRAL ( 55 FDA reports)
INTRAOCULAR LENS IMPLANT ( 55 FDA reports)
RESPIRATORY TRACT CONGESTION ( 55 FDA reports)
TOOTH INJURY ( 55 FDA reports)
RESPIRATORY RATE INCREASED ( 54 FDA reports)
TENSION ( 54 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 54 FDA reports)
CERVICOBRACHIAL SYNDROME ( 54 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 54 FDA reports)
DYSPHORIA ( 54 FDA reports)
HEPATIC MASS ( 54 FDA reports)
HERPES VIRUS INFECTION ( 54 FDA reports)
IMPRISONMENT ( 54 FDA reports)
PHOTOSENSITIVITY REACTION ( 54 FDA reports)
ABORTION SPONTANEOUS ( 53 FDA reports)
COLLAPSE OF LUNG ( 53 FDA reports)
EAR DISORDER ( 53 FDA reports)
HYPERTENSIVE HEART DISEASE ( 53 FDA reports)
LABYRINTHITIS ( 53 FDA reports)
NO THERAPEUTIC RESPONSE ( 53 FDA reports)
AGEUSIA ( 52 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 52 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 52 FDA reports)
BONE GRAFT ( 52 FDA reports)
EYE INFECTION ( 52 FDA reports)
FISTULA DISCHARGE ( 52 FDA reports)
GINGIVAL OEDEMA ( 52 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 52 FDA reports)
LUNG CONSOLIDATION ( 52 FDA reports)
MUSCLE ATROPHY ( 52 FDA reports)
OESOPHAGEAL DISORDER ( 52 FDA reports)
RADICULAR PAIN ( 52 FDA reports)
RALES ( 52 FDA reports)
SEXUAL ABUSE ( 52 FDA reports)
TONGUE DISORDER ( 52 FDA reports)
WOUND SECRETION ( 52 FDA reports)
RESPIRATORY TRACT INFECTION ( 51 FDA reports)
VENTRICULAR DYSFUNCTION ( 51 FDA reports)
BODY TEMPERATURE DECREASED ( 51 FDA reports)
CATHETERISATION CARDIAC ( 51 FDA reports)
EYELID PTOSIS ( 51 FDA reports)
FORMICATION ( 51 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 51 FDA reports)
LIP SWELLING ( 51 FDA reports)
MELANOCYTIC NAEVUS ( 51 FDA reports)
PERIARTHRITIS ( 51 FDA reports)
PERICARDITIS ( 51 FDA reports)
ALCOHOL POISONING ( 50 FDA reports)
APNOEA ( 50 FDA reports)
BODY HEIGHT DECREASED ( 50 FDA reports)
CARDIAC FLUTTER ( 50 FDA reports)
CONGENITAL ANOMALY ( 50 FDA reports)
DIABETIC NEPHROPATHY ( 50 FDA reports)
FIBULA FRACTURE ( 50 FDA reports)
GASTRIC POLYPS ( 50 FDA reports)
INJECTION SITE SWELLING ( 50 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 50 FDA reports)
MITRAL VALVE DISEASE ( 50 FDA reports)
MUSCULOSKELETAL DISORDER ( 50 FDA reports)
POST CONCUSSION SYNDROME ( 50 FDA reports)
TENDON RUPTURE ( 50 FDA reports)
STREPTOCOCCAL INFECTION ( 49 FDA reports)
TIBIA FRACTURE ( 49 FDA reports)
VIITH NERVE PARALYSIS ( 49 FDA reports)
ANEURYSM ( 49 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 49 FDA reports)
BREATH SOUNDS ABNORMAL ( 49 FDA reports)
DRUG LEVEL INCREASED ( 49 FDA reports)
GANGRENE ( 49 FDA reports)
HANGOVER ( 49 FDA reports)
HYPOTONIA ( 49 FDA reports)
INJECTION SITE IRRITATION ( 49 FDA reports)
LOGORRHOEA ( 49 FDA reports)
MYDRIASIS ( 49 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 49 FDA reports)
ADNEXA UTERI MASS ( 48 FDA reports)
BLOOD IRON DECREASED ( 48 FDA reports)
BREAST RECONSTRUCTION ( 48 FDA reports)
CATHETER PLACEMENT ( 48 FDA reports)
COMMUNICATION DISORDER ( 48 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 48 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 48 FDA reports)
INCISIONAL DRAINAGE ( 48 FDA reports)
LUNG INFECTION ( 48 FDA reports)
METASTASIS ( 48 FDA reports)
PANCREATIC DISORDER ( 48 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 48 FDA reports)
PULSE ABSENT ( 48 FDA reports)
SEROMA ( 48 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 48 FDA reports)
PROSTATITIS ( 47 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 47 FDA reports)
RETINAL HAEMORRHAGE ( 47 FDA reports)
SHOULDER PAIN ( 47 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 47 FDA reports)
TENSION HEADACHE ( 47 FDA reports)
TOBACCO ABUSE ( 47 FDA reports)
TRAUMATIC BRAIN INJURY ( 47 FDA reports)
URINE OUTPUT DECREASED ( 47 FDA reports)
VITAMIN D DEFICIENCY ( 47 FDA reports)
ATROPHIC VULVOVAGINITIS ( 47 FDA reports)
BILIARY DILATATION ( 47 FDA reports)
ENDOTRACHEAL INTUBATION ( 47 FDA reports)
HYPERCOAGULATION ( 47 FDA reports)
HYPERPHAGIA ( 47 FDA reports)
LARYNGOSPASM ( 47 FDA reports)
LIGAMENT RUPTURE ( 47 FDA reports)
LUNG HYPERINFLATION ( 47 FDA reports)
MYELOMA RECURRENCE ( 47 FDA reports)
NASAL DISORDER ( 47 FDA reports)
NEUROPATHY ( 47 FDA reports)
PANIC REACTION ( 47 FDA reports)
PERITONITIS ( 47 FDA reports)
POLYSUBSTANCE ABUSE ( 47 FDA reports)
APPENDICECTOMY ( 46 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 46 FDA reports)
BRONCHIECTASIS ( 46 FDA reports)
DRUG PRESCRIBING ERROR ( 46 FDA reports)
HAEMOLYTIC ANAEMIA ( 46 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 46 FDA reports)
MYELOPATHY ( 46 FDA reports)
OSTEITIS DEFORMANS ( 46 FDA reports)
OTORRHOEA ( 46 FDA reports)
OVERWEIGHT ( 46 FDA reports)
QUALITY OF LIFE DECREASED ( 46 FDA reports)
THROMBOCYTOSIS ( 46 FDA reports)
PUPIL FIXED ( 45 FDA reports)
SPONDYLITIS ( 45 FDA reports)
VULVOVAGINAL DRYNESS ( 45 FDA reports)
ACIDOSIS ( 45 FDA reports)
ADENOMA BENIGN ( 45 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 45 FDA reports)
BREAST CANCER FEMALE ( 45 FDA reports)
CHONDROMALACIA ( 45 FDA reports)
DIABETIC RETINOPATHY ( 45 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 45 FDA reports)
FRACTURE NONUNION ( 45 FDA reports)
HEPATITIS ACUTE ( 45 FDA reports)
LYMPHOMA ( 45 FDA reports)
ORGAN FAILURE ( 45 FDA reports)
ACCIDENT ( 44 FDA reports)
APHTHOUS STOMATITIS ( 44 FDA reports)
COLITIS ISCHAEMIC ( 44 FDA reports)
FLAT AFFECT ( 44 FDA reports)
GYNAECOMASTIA ( 44 FDA reports)
HAEMANGIOMA OF LIVER ( 44 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 44 FDA reports)
IMMUNOSUPPRESSION ( 44 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 44 FDA reports)
KLEBSIELLA INFECTION ( 44 FDA reports)
LOW TURNOVER OSTEOPATHY ( 44 FDA reports)
MUSCLE DISORDER ( 44 FDA reports)
SCLERODERMA ( 44 FDA reports)
SHOCK ( 44 FDA reports)
SKIN REACTION ( 44 FDA reports)
UMBILICAL HERNIA ( 44 FDA reports)
VERTIGO POSITIONAL ( 44 FDA reports)
PROTEIN TOTAL INCREASED ( 43 FDA reports)
UTERINE HAEMORRHAGE ( 43 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 43 FDA reports)
BLOOD CULTURE POSITIVE ( 43 FDA reports)
BRAIN DEATH ( 43 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 43 FDA reports)
CERVICAL DYSPLASIA ( 43 FDA reports)
DYSPHEMIA ( 43 FDA reports)
ENDOCARDITIS ( 43 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 43 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 43 FDA reports)
HAEMODIALYSIS ( 43 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 43 FDA reports)
INTRACRANIAL ANEURYSM ( 43 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 43 FDA reports)
POOR DENTAL CONDITION ( 43 FDA reports)
BACTERIAL TEST POSITIVE ( 42 FDA reports)
BIOPSY ( 42 FDA reports)
DEVELOPMENTAL DELAY ( 42 FDA reports)
DYSAESTHESIA ( 42 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 42 FDA reports)
EDENTULOUS ( 42 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 42 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 42 FDA reports)
HEPATOSPLENOMEGALY ( 42 FDA reports)
HYPERTHYROIDISM ( 42 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 42 FDA reports)
MEDICAL DEVICE COMPLICATION ( 42 FDA reports)
MEDICATION RESIDUE ( 42 FDA reports)
POLYNEUROPATHY ( 42 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 42 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 42 FDA reports)
SELF-INJURIOUS IDEATION ( 41 FDA reports)
THERAPY NON-RESPONDER ( 41 FDA reports)
ACETABULUM FRACTURE ( 41 FDA reports)
EYE PRURITUS ( 41 FDA reports)
LARYNGEAL OEDEMA ( 41 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 41 FDA reports)
MECHANICAL VENTILATION ( 41 FDA reports)
MENINGIOMA ( 41 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 41 FDA reports)
POOR PERIPHERAL CIRCULATION ( 41 FDA reports)
ABNORMAL SENSATION IN EYE ( 40 FDA reports)
ACUTE PRERENAL FAILURE ( 40 FDA reports)
ADJUSTMENT DISORDER ( 40 FDA reports)
APHONIA ( 40 FDA reports)
APTYALISM ( 40 FDA reports)
BRAIN OEDEMA ( 40 FDA reports)
CALCULUS URETERIC ( 40 FDA reports)
CHRONIC FATIGUE SYNDROME ( 40 FDA reports)
FOREIGN BODY ( 40 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 40 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 40 FDA reports)
HOSTILITY ( 40 FDA reports)
HYPERBILIRUBINAEMIA ( 40 FDA reports)
ILEUS PARALYTIC ( 40 FDA reports)
KNEE OPERATION ( 40 FDA reports)
LYMPHADENITIS ( 40 FDA reports)
MENIERE'S DISEASE ( 40 FDA reports)
NYSTAGMUS ( 40 FDA reports)
OCCULT BLOOD POSITIVE ( 40 FDA reports)
OESOPHAGITIS ULCERATIVE ( 40 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 40 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 40 FDA reports)
SLEEP TERROR ( 40 FDA reports)
SLUGGISHNESS ( 40 FDA reports)
SPLENIC LESION ( 40 FDA reports)
SPONDYLOLYSIS ( 40 FDA reports)
SQUAMOUS CELL CARCINOMA ( 40 FDA reports)
TOOTH IMPACTED ( 40 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 39 FDA reports)
PROSTATOMEGALY ( 39 FDA reports)
RADIATION INJURY ( 39 FDA reports)
SINUS OPERATION ( 39 FDA reports)
BILE DUCT STENOSIS ( 39 FDA reports)
BINGE EATING ( 39 FDA reports)
BONE SWELLING ( 39 FDA reports)
BREAST CALCIFICATIONS ( 39 FDA reports)
CAROTID BRUIT ( 39 FDA reports)
DRUG DISPENSING ERROR ( 39 FDA reports)
FAMILY STRESS ( 39 FDA reports)
FURUNCLE ( 39 FDA reports)
HEART DISEASE CONGENITAL ( 39 FDA reports)
HYPERVENTILATION ( 39 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 39 FDA reports)
MENSTRUATION IRREGULAR ( 39 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 39 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 39 FDA reports)
NON-SMALL CELL LUNG CANCER ( 39 FDA reports)
OPTIC NEURITIS ( 39 FDA reports)
ORTHOSIS USER ( 39 FDA reports)
OSTEOMYELITIS CHRONIC ( 39 FDA reports)
ARTHROPOD BITE ( 38 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 38 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 38 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 38 FDA reports)
CRANIOTOMY ( 38 FDA reports)
FOLLICULITIS ( 38 FDA reports)
HODGKIN'S DISEASE ( 38 FDA reports)
JUGULAR VEIN THROMBOSIS ( 38 FDA reports)
KETOACIDOSIS ( 38 FDA reports)
LIPASE INCREASED ( 38 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 38 FDA reports)
MASTECTOMY ( 38 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 38 FDA reports)
METAPLASIA ( 38 FDA reports)
OESOPHAGEAL ULCER ( 38 FDA reports)
OPEN REDUCTION OF FRACTURE ( 38 FDA reports)
OTITIS MEDIA ACUTE ( 38 FDA reports)
RENAL ATROPHY ( 38 FDA reports)
RETINAL TEAR ( 38 FDA reports)
SCREAMING ( 38 FDA reports)
SEROTONIN SYNDROME ( 38 FDA reports)
SKIN CANCER ( 38 FDA reports)
SKIN PAPILLOMA ( 38 FDA reports)
TESTICULAR PAIN ( 38 FDA reports)
THROMBOPHLEBITIS ( 38 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 38 FDA reports)
TONGUE INJURY ( 38 FDA reports)
TRIGEMINAL NEURALGIA ( 38 FDA reports)
TROPONIN INCREASED ( 38 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 38 FDA reports)
PROSTATE CANCER METASTATIC ( 37 FDA reports)
RENAL CANCER ( 37 FDA reports)
SACROILIITIS ( 37 FDA reports)
TEARFULNESS ( 37 FDA reports)
TEMPORAL ARTERITIS ( 37 FDA reports)
TONGUE DISCOLOURATION ( 37 FDA reports)
WALKING DISABILITY ( 37 FDA reports)
WHEELCHAIR USER ( 37 FDA reports)
ABNORMAL FAECES ( 37 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 37 FDA reports)
ATRIOVENTRICULAR BLOCK ( 37 FDA reports)
BLINDNESS TRANSIENT ( 37 FDA reports)
CHEST X-RAY ABNORMAL ( 37 FDA reports)
CLAUSTROPHOBIA ( 37 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 37 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 37 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 37 FDA reports)
EOSINOPHILIA ( 37 FDA reports)
FEELING OF DESPAIR ( 37 FDA reports)
FEMORAL NECK FRACTURE ( 37 FDA reports)
INTESTINAL ULCER ( 37 FDA reports)
MITRAL VALVE SCLEROSIS ( 37 FDA reports)
NAIL DISORDER ( 37 FDA reports)
NASAL MUCOSAL DISORDER ( 37 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 37 FDA reports)
ADENOCARCINOMA ( 36 FDA reports)
ANAPHYLACTIC SHOCK ( 36 FDA reports)
BRAIN INJURY ( 36 FDA reports)
DEPRESSION SUICIDAL ( 36 FDA reports)
DIABETIC FOOT ( 36 FDA reports)
FACIAL NEURALGIA ( 36 FDA reports)
FRACTURED SACRUM ( 36 FDA reports)
GENERALISED ANXIETY DISORDER ( 36 FDA reports)
HEPATIC ENCEPHALOPATHY ( 36 FDA reports)
HYPERAESTHESIA ( 36 FDA reports)
HYPERMETROPIA ( 36 FDA reports)
HYPOMANIA ( 36 FDA reports)
IMMUNODEFICIENCY ( 36 FDA reports)
LEGAL PROBLEM ( 36 FDA reports)
METASTASES TO THORAX ( 36 FDA reports)
PARADOXICAL DRUG REACTION ( 36 FDA reports)
PARAPROTEINAEMIA ( 36 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 36 FDA reports)
PULMONARY THROMBOSIS ( 36 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 36 FDA reports)
SCHIZOPHRENIA ( 36 FDA reports)
SENSATION OF HEAVINESS ( 36 FDA reports)
SKIN IRRITATION ( 36 FDA reports)
STENT PLACEMENT ( 36 FDA reports)
SUICIDAL BEHAVIOUR ( 36 FDA reports)
SYNOVITIS ( 36 FDA reports)
TONGUE BITING ( 36 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 36 FDA reports)
URINARY TRACT OBSTRUCTION ( 36 FDA reports)
VASCULAR PSEUDOANEURYSM ( 36 FDA reports)
VENOUS THROMBOSIS ( 36 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 36 FDA reports)
POSTURE ABNORMAL ( 35 FDA reports)
PREMATURE LABOUR ( 35 FDA reports)
PROTEIN TOTAL DECREASED ( 35 FDA reports)
RENAL MASS ( 35 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 35 FDA reports)
VICTIM OF SEXUAL ABUSE ( 35 FDA reports)
WEGENER'S GRANULOMATOSIS ( 35 FDA reports)
ADRENAL MASS ( 35 FDA reports)
ANAEMIA POSTOPERATIVE ( 35 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 35 FDA reports)
BILIARY DYSKINESIA ( 35 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 35 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 35 FDA reports)
BUNDLE BRANCH BLOCK ( 35 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 35 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 35 FDA reports)
COLONOSCOPY ABNORMAL ( 35 FDA reports)
DRUG TOLERANCE INCREASED ( 35 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 35 FDA reports)
HUNGER ( 35 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 35 FDA reports)
LYMPHOPENIA ( 35 FDA reports)
MOTOR DYSFUNCTION ( 35 FDA reports)
NEPHROPATHY ( 35 FDA reports)
PERIPHERAL ISCHAEMIA ( 35 FDA reports)
POLYDIPSIA ( 35 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 34 FDA reports)
ACUTE PULMONARY OEDEMA ( 34 FDA reports)
ASPIRATION PLEURAL CAVITY ( 34 FDA reports)
ASTHENOPIA ( 34 FDA reports)
BLADDER CANCER ( 34 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 34 FDA reports)
BRAIN NEOPLASM ( 34 FDA reports)
CATHETER REMOVAL ( 34 FDA reports)
CORONARY ARTERY BYPASS ( 34 FDA reports)
DEPRESSIVE SYMPTOM ( 34 FDA reports)
DRY THROAT ( 34 FDA reports)
ENCEPHALOMALACIA ( 34 FDA reports)
EROSIVE OESOPHAGITIS ( 34 FDA reports)
EYE HAEMORRHAGE ( 34 FDA reports)
GRAFT VERSUS HOST DISEASE ( 34 FDA reports)
HAEMOLYSIS ( 34 FDA reports)
ISCHAEMIC STROKE ( 34 FDA reports)
MULTIPLE FRACTURES ( 34 FDA reports)
NEUTROPHIL COUNT INCREASED ( 34 FDA reports)
ONYCHALGIA ( 34 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 34 FDA reports)
PYURIA ( 34 FDA reports)
RADICULITIS LUMBOSACRAL ( 34 FDA reports)
REFLUX GASTRITIS ( 34 FDA reports)
RIGHT VENTRICULAR FAILURE ( 34 FDA reports)
SENSATION OF FOREIGN BODY ( 34 FDA reports)
TIC ( 34 FDA reports)
VITREOUS DETACHMENT ( 34 FDA reports)
PROSTATE CANCER RECURRENT ( 33 FDA reports)
RESORPTION BONE INCREASED ( 33 FDA reports)
SUBSTANCE ABUSE ( 33 FDA reports)
ULNA FRACTURE ( 33 FDA reports)
VULVOVAGINAL PRURITUS ( 33 FDA reports)
BURNS SECOND DEGREE ( 33 FDA reports)
CHEST WALL MASS ( 33 FDA reports)
EARLY SATIETY ( 33 FDA reports)
EYE MOVEMENT DISORDER ( 33 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 33 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 33 FDA reports)
HALLUCINATIONS, MIXED ( 33 FDA reports)
HELICOBACTER INFECTION ( 33 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 33 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 33 FDA reports)
IMPETIGO ( 33 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 33 FDA reports)
LACTOSE INTOLERANCE ( 33 FDA reports)
MYOPIA ( 33 FDA reports)
NECK MASS ( 33 FDA reports)
OESOPHAGEAL SPASM ( 33 FDA reports)
BONE CYST ( 32 FDA reports)
BRONCHIOLITIS ( 32 FDA reports)
CEREBELLAR INFARCTION ( 32 FDA reports)
CHEILITIS ( 32 FDA reports)
DISSOCIATION ( 32 FDA reports)
EAR CONGESTION ( 32 FDA reports)
GINGIVAL EROSION ( 32 FDA reports)
HAEMORRHAGIC STROKE ( 32 FDA reports)
HEAD DISCOMFORT ( 32 FDA reports)
HYPERTENSIVE CRISIS ( 32 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 32 FDA reports)
JOINT CREPITATION ( 32 FDA reports)
LOSS OF EMPLOYMENT ( 32 FDA reports)
METABOLIC DISORDER ( 32 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 32 FDA reports)
PAPILLOMA ( 32 FDA reports)
PERIODONTAL OPERATION ( 32 FDA reports)
POLYTRAUMATISM ( 32 FDA reports)
RADICULITIS ( 32 FDA reports)
RECTAL FISSURE ( 32 FDA reports)
RIGHT ATRIAL DILATATION ( 32 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 32 FDA reports)
SINUS ARRHYTHMIA ( 32 FDA reports)
SKIN HAEMORRHAGE ( 32 FDA reports)
SNEEZING ( 32 FDA reports)
STREPTOCOCCAL SEPSIS ( 32 FDA reports)
THERMAL BURN ( 32 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 32 FDA reports)
X-RAY ABNORMAL ( 32 FDA reports)
PUBIS FRACTURE ( 31 FDA reports)
ROSACEA ( 31 FDA reports)
SKIN INFECTION ( 31 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 31 FDA reports)
STRESS INCONTINENCE ( 31 FDA reports)
URINARY TRACT DISORDER ( 31 FDA reports)
UTERINE PROLAPSE ( 31 FDA reports)
ACCIDENT AT WORK ( 31 FDA reports)
ACUTE PSYCHOSIS ( 31 FDA reports)
ANOXIC ENCEPHALOPATHY ( 31 FDA reports)
AREFLEXIA ( 31 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 31 FDA reports)
ARTERIOSPASM CORONARY ( 31 FDA reports)
ASPHYXIA ( 31 FDA reports)
BRAIN CONTUSION ( 31 FDA reports)
CHEST WALL PAIN ( 31 FDA reports)
CLOSTRIDIUM COLITIS ( 31 FDA reports)
DIZZINESS POSTURAL ( 31 FDA reports)
EAR DISCOMFORT ( 31 FDA reports)
EMBOLIC STROKE ( 31 FDA reports)
EXTRASYSTOLES ( 31 FDA reports)
FLUID INTAKE REDUCED ( 31 FDA reports)
HERNIA REPAIR ( 31 FDA reports)
HIGH FREQUENCY ABLATION ( 31 FDA reports)
HYPERPLASIA ( 31 FDA reports)
HYPOTHERMIA ( 31 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 31 FDA reports)
JUDGEMENT IMPAIRED ( 31 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 31 FDA reports)
MENOPAUSAL SYMPTOMS ( 31 FDA reports)
MUSCLE RIGIDITY ( 31 FDA reports)
PANCREATIC CARCINOMA ( 31 FDA reports)
PNEUMONIA BACTERIAL ( 31 FDA reports)
POISONING ( 31 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 30 FDA reports)
ANOSMIA ( 30 FDA reports)
BLADDER SPASM ( 30 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 30 FDA reports)
BLOOD TEST ABNORMAL ( 30 FDA reports)
BONE MARROW OEDEMA ( 30 FDA reports)
BOWEN'S DISEASE ( 30 FDA reports)
CATARACT NUCLEAR ( 30 FDA reports)
DEVICE BREAKAGE ( 30 FDA reports)
DYSTHYMIC DISORDER ( 30 FDA reports)
FOOT OPERATION ( 30 FDA reports)
HEART VALVE INCOMPETENCE ( 30 FDA reports)
HEPATIC CONGESTION ( 30 FDA reports)
HEPATOTOXICITY ( 30 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 30 FDA reports)
INTESTINAL RESECTION ( 30 FDA reports)
MALABSORPTION ( 30 FDA reports)
MONOCYTE COUNT INCREASED ( 30 FDA reports)
OEDEMA MUCOSAL ( 30 FDA reports)
OESOPHAGEAL PAIN ( 30 FDA reports)
PATELLA FRACTURE ( 30 FDA reports)
PROCEDURAL COMPLICATION ( 30 FDA reports)
RENAL CELL CARCINOMA ( 30 FDA reports)
RESPIRATORY DEPRESSION ( 30 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 30 FDA reports)
SALIVARY HYPERSECRETION ( 30 FDA reports)
SHOULDER ARTHROPLASTY ( 30 FDA reports)
SHOULDER OPERATION ( 30 FDA reports)
SPUTUM DISCOLOURED ( 30 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 30 FDA reports)
URINE FLOW DECREASED ( 30 FDA reports)
UTERINE ENLARGEMENT ( 30 FDA reports)
VENA CAVA FILTER INSERTION ( 30 FDA reports)
POSTNASAL DRIP ( 29 FDA reports)
PROSTATIC OBSTRUCTION ( 29 FDA reports)
PURPURA ( 29 FDA reports)
SERUM FERRITIN INCREASED ( 29 FDA reports)
SUDDEN DEATH ( 29 FDA reports)
TRANSFUSION ( 29 FDA reports)
VENA CAVA THROMBOSIS ( 29 FDA reports)
VENOUS OCCLUSION ( 29 FDA reports)
AMENORRHOEA ( 29 FDA reports)
ATRIAL TACHYCARDIA ( 29 FDA reports)
AUTOIMMUNE HEPATITIS ( 29 FDA reports)
AXILLARY MASS ( 29 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 29 FDA reports)
BLOOD COUNT ABNORMAL ( 29 FDA reports)
BONE NEOPLASM ( 29 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 29 FDA reports)
DEVICE OCCLUSION ( 29 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 29 FDA reports)
DRUG ERUPTION ( 29 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 29 FDA reports)
EPIGASTRIC DISCOMFORT ( 29 FDA reports)
FAT TISSUE INCREASED ( 29 FDA reports)
HEPATIC NECROSIS ( 29 FDA reports)
HIP SURGERY ( 29 FDA reports)
HYPOVENTILATION ( 29 FDA reports)
JOINT ARTHROPLASTY ( 29 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 29 FDA reports)
MUSCLE SPASTICITY ( 29 FDA reports)
NARCOLEPSY ( 29 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 29 FDA reports)
OROANTRAL FISTULA ( 29 FDA reports)
PERSONALITY DISORDER ( 29 FDA reports)
ABSCESS LIMB ( 28 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 28 FDA reports)
AMBLYOPIA ( 28 FDA reports)
ANAL FISSURE ( 28 FDA reports)
ATROPHY ( 28 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 28 FDA reports)
BIOPSY BONE ( 28 FDA reports)
BLOOD CHLORIDE INCREASED ( 28 FDA reports)
BRONCHITIS CHRONIC ( 28 FDA reports)
CAROTID ARTERY DISEASE ( 28 FDA reports)
CHANGE OF BOWEL HABIT ( 28 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 28 FDA reports)
EMBOLISM ( 28 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 28 FDA reports)
GASTRODUODENITIS ( 28 FDA reports)
GASTROENTERITIS RADIATION ( 28 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 28 FDA reports)
HEPATOCELLULAR DAMAGE ( 28 FDA reports)
HYPERMETABOLISM ( 28 FDA reports)
INTESTINAL POLYP ( 28 FDA reports)
INTRACARDIAC THROMBUS ( 28 FDA reports)
IRITIS ( 28 FDA reports)
IRON DEFICIENCY ( 28 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 28 FDA reports)
LIVEDO RETICULARIS ( 28 FDA reports)
LIVER INJURY ( 28 FDA reports)
MASTOIDITIS ( 28 FDA reports)
MAXILLOFACIAL OPERATION ( 28 FDA reports)
MENINGITIS VIRAL ( 28 FDA reports)
MENISCUS REMOVAL ( 28 FDA reports)
MONOCLONAL GAMMOPATHY ( 28 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 28 FDA reports)
NEGATIVE THOUGHTS ( 28 FDA reports)
POOR VENOUS ACCESS ( 28 FDA reports)
POST PROCEDURAL HAEMATOMA ( 28 FDA reports)
PRODUCT ADHESION ISSUE ( 28 FDA reports)
RAYNAUD'S PHENOMENON ( 28 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 28 FDA reports)
SKIN PLAQUE ( 28 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 28 FDA reports)
STENT OCCLUSION ( 28 FDA reports)
TACHYPHRENIA ( 28 FDA reports)
TOOTH DEPOSIT ( 28 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 28 FDA reports)
VISUAL FIELD DEFECT ( 28 FDA reports)
POST LAMINECTOMY SYNDROME ( 27 FDA reports)
PSORIATIC ARTHROPATHY ( 27 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 27 FDA reports)
TELANGIECTASIA ( 27 FDA reports)
THYROIDECTOMY ( 27 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 27 FDA reports)
TUMOUR LYSIS SYNDROME ( 27 FDA reports)
WEIGHT BEARING DIFFICULTY ( 27 FDA reports)
WOUND COMPLICATION ( 27 FDA reports)
WRONG DRUG ADMINISTERED ( 27 FDA reports)
ALCOHOLISM ( 27 FDA reports)
ALVEOLAR OSTEITIS ( 27 FDA reports)
BLADDER DIVERTICULUM ( 27 FDA reports)
BRADYPHRENIA ( 27 FDA reports)
BUNION ( 27 FDA reports)
CAROTID ARTERY OCCLUSION ( 27 FDA reports)
COR PULMONALE CHRONIC ( 27 FDA reports)
CYSTITIS HAEMORRHAGIC ( 27 FDA reports)
CYSTITIS INTERSTITIAL ( 27 FDA reports)
DYSGRAPHIA ( 27 FDA reports)
EFFUSION ( 27 FDA reports)
EOSINOPHIL COUNT INCREASED ( 27 FDA reports)
FAECALOMA ( 27 FDA reports)
GASTRIC HAEMORRHAGE ( 27 FDA reports)
GLARE ( 27 FDA reports)
HAEMORRHAGIC ANAEMIA ( 27 FDA reports)
HAEMORRHAGIC DIATHESIS ( 27 FDA reports)
HILAR LYMPHADENOPATHY ( 27 FDA reports)
HYPERPARATHYROIDISM ( 27 FDA reports)
IMPULSIVE BEHAVIOUR ( 27 FDA reports)
MACROCYTOSIS ( 27 FDA reports)
MICROCYTIC ANAEMIA ( 27 FDA reports)
MYASTHENIA GRAVIS ( 27 FDA reports)
NARCOTIC INTOXICATION ( 27 FDA reports)
NASAL ULCER ( 27 FDA reports)
NO ADVERSE EVENT ( 27 FDA reports)
ORAL FUNGAL INFECTION ( 27 FDA reports)
PAROSMIA ( 27 FDA reports)
PELVIC HAEMATOMA ( 27 FDA reports)
AORTIC VALVE STENOSIS ( 26 FDA reports)
BASEDOW'S DISEASE ( 26 FDA reports)
BILE DUCT STONE ( 26 FDA reports)
BILIARY COLIC ( 26 FDA reports)
BIOPSY BONE ABNORMAL ( 26 FDA reports)
CARTILAGE INJURY ( 26 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 26 FDA reports)
CONDUCTION DISORDER ( 26 FDA reports)
CONVERSION DISORDER ( 26 FDA reports)
CORNEAL DYSTROPHY ( 26 FDA reports)
DEAFNESS UNILATERAL ( 26 FDA reports)
EXOPHTHALMOS ( 26 FDA reports)
FAT NECROSIS ( 26 FDA reports)
FIBRIN D DIMER INCREASED ( 26 FDA reports)
FISTULA REPAIR ( 26 FDA reports)
GALLBLADDER POLYP ( 26 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 26 FDA reports)
JOINT CONTRACTURE ( 26 FDA reports)
KERATITIS ( 26 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 26 FDA reports)
METABOLIC SYNDROME ( 26 FDA reports)
NEPHROSCLEROSIS ( 26 FDA reports)
OROPHARYNGEAL BLISTERING ( 26 FDA reports)
OSTEOCHONDROSIS ( 26 FDA reports)
OSTEOMA ( 26 FDA reports)
OVARIAN MASS ( 26 FDA reports)
PNEUMONIA VIRAL ( 26 FDA reports)
POOR PERSONAL HYGIENE ( 26 FDA reports)
PORTAL HYPERTENSION ( 26 FDA reports)
RECTAL ABSCESS ( 26 FDA reports)
REFLUX LARYNGITIS ( 26 FDA reports)
SKIN WARM ( 26 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 26 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 26 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 25 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 25 FDA reports)
QRS AXIS ABNORMAL ( 25 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 25 FDA reports)
ROTATOR CUFF REPAIR ( 25 FDA reports)
SELF-MEDICATION ( 25 FDA reports)
SJOGREN'S SYNDROME ( 25 FDA reports)
SOFT TISSUE INFECTION ( 25 FDA reports)
SPINAL CORPECTOMY ( 25 FDA reports)
STUPOR ( 25 FDA reports)
UMBILICAL CORD ABNORMALITY ( 25 FDA reports)
UNDERDOSE ( 25 FDA reports)
VESICAL FISTULA ( 25 FDA reports)
WEIGHT FLUCTUATION ( 25 FDA reports)
ADHESION ( 25 FDA reports)
ANIMAL BITE ( 25 FDA reports)
BALANITIS ( 25 FDA reports)
BLADDER MASS ( 25 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 25 FDA reports)
BLOOD PRESSURE ABNORMAL ( 25 FDA reports)
CUBITAL TUNNEL SYNDROME ( 25 FDA reports)
DEMYELINATION ( 25 FDA reports)
DROWNING ( 25 FDA reports)
DUODENAL ULCER ( 25 FDA reports)
DYSMENORRHOEA ( 25 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 25 FDA reports)
ENTHESOPATHY ( 25 FDA reports)
EXERCISE TOLERANCE DECREASED ( 25 FDA reports)
EYE NAEVUS ( 25 FDA reports)
FORAMEN MAGNUM STENOSIS ( 25 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 25 FDA reports)
HAEMATOCRIT INCREASED ( 25 FDA reports)
HEART INJURY ( 25 FDA reports)
HEPATIC FIBROSIS ( 25 FDA reports)
HICCUPS ( 25 FDA reports)
IMMOBILE ( 25 FDA reports)
INJECTION SITE RASH ( 25 FDA reports)
LENTIGO ( 25 FDA reports)
MACROGLOSSIA ( 25 FDA reports)
MENOPAUSE ( 25 FDA reports)
METRORRHAGIA ( 25 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 25 FDA reports)
OPTIC NERVE CUPPING ( 25 FDA reports)
PERIORBITAL OEDEMA ( 25 FDA reports)
AMMONIA INCREASED ( 24 FDA reports)
ANAEMIA MACROCYTIC ( 24 FDA reports)
APPLICATION SITE ERYTHEMA ( 24 FDA reports)
ARTHROSCOPY ( 24 FDA reports)
BLOOD DISORDER ( 24 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 24 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 24 FDA reports)
BRAIN HERNIATION ( 24 FDA reports)
BREAKTHROUGH PAIN ( 24 FDA reports)
CARDIAC ANEURYSM ( 24 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 24 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 24 FDA reports)
CLEFT PALATE ( 24 FDA reports)
COARCTATION OF THE AORTA ( 24 FDA reports)
COELIAC DISEASE ( 24 FDA reports)
COLON POLYPECTOMY ( 24 FDA reports)
DENTAL DISCOMFORT ( 24 FDA reports)
DERMATITIS ATOPIC ( 24 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 24 FDA reports)
EYE LASER SURGERY ( 24 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 24 FDA reports)
INJECTION SITE WARMTH ( 24 FDA reports)
INTESTINAL PERFORATION ( 24 FDA reports)
LEG AMPUTATION ( 24 FDA reports)
LYMPHADENECTOMY ( 24 FDA reports)
MICROANGIOPATHY ( 24 FDA reports)
MYELITIS TRANSVERSE ( 24 FDA reports)
PAIN EXACERBATED ( 24 FDA reports)
PAPILLOEDEMA ( 24 FDA reports)
POLYP COLORECTAL ( 24 FDA reports)
SCAN BONE MARROW ABNORMAL ( 24 FDA reports)
STOMATITIS NECROTISING ( 24 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 24 FDA reports)
TOXIC ENCEPHALOPATHY ( 24 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 24 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 24 FDA reports)
VOCAL CORD PARALYSIS ( 24 FDA reports)
VOCAL CORD POLYP ( 24 FDA reports)
PROCTITIS ( 23 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 23 FDA reports)
SEBORRHOEIC DERMATITIS ( 23 FDA reports)
SELF MUTILATION ( 23 FDA reports)
SEPSIS SYNDROME ( 23 FDA reports)
SIGMOIDITIS ( 23 FDA reports)
SPINAL CORD DISORDER ( 23 FDA reports)
SPINAL OPERATION ( 23 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 23 FDA reports)
VASCULAR ANOMALY ( 23 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 23 FDA reports)
ANISOCYTOSIS ( 23 FDA reports)
AORTIC DISORDER ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 23 FDA reports)
BLADDER OPERATION ( 23 FDA reports)
BLADDER PROLAPSE ( 23 FDA reports)
BONE MARROW TRANSPLANT ( 23 FDA reports)
BRAIN SCAN ABNORMAL ( 23 FDA reports)
BREAST CYST ( 23 FDA reports)
CARDIAC TAMPONADE ( 23 FDA reports)
CLUMSINESS ( 23 FDA reports)
COMMINUTED FRACTURE ( 23 FDA reports)
DIAPHRAGMATIC HERNIA ( 23 FDA reports)
DROOLING ( 23 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 23 FDA reports)
FACIAL PARESIS ( 23 FDA reports)
FOREIGN BODY TRAUMA ( 23 FDA reports)
FRUSTRATION ( 23 FDA reports)
HAEMOPHILUS INFECTION ( 23 FDA reports)
HEPATITIS B ( 23 FDA reports)
HIP DYSPLASIA ( 23 FDA reports)
HORNER'S SYNDROME ( 23 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 23 FDA reports)
INJECTION SITE DISCOLOURATION ( 23 FDA reports)
INTESTINAL MASS ( 23 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 23 FDA reports)
LACTIC ACIDOSIS ( 23 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 23 FDA reports)
OCULAR HYPERTENSION ( 23 FDA reports)
ORAL FIBROMA ( 23 FDA reports)
PAINFUL RESPIRATION ( 23 FDA reports)
PERITONITIS BACTERIAL ( 23 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 23 FDA reports)
PHONOPHOBIA ( 23 FDA reports)
AORTIC DILATATION ( 22 FDA reports)
AORTIC VALVE CALCIFICATION ( 22 FDA reports)
APPLICATION SITE PRURITUS ( 22 FDA reports)
BACTERIAL SEPSIS ( 22 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 22 FDA reports)
BONE TRIMMING ( 22 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 22 FDA reports)
BULLOUS LUNG DISEASE ( 22 FDA reports)
CARDIOPULMONARY FAILURE ( 22 FDA reports)
CAUDA EQUINA SYNDROME ( 22 FDA reports)
CHAPPED LIPS ( 22 FDA reports)
CORNEAL ABRASION ( 22 FDA reports)
DIABETES INSIPIDUS ( 22 FDA reports)
ENCEPHALITIS ( 22 FDA reports)
FEAR OF DEATH ( 22 FDA reports)
FIBROMA ( 22 FDA reports)
GALLBLADDER ENLARGEMENT ( 22 FDA reports)
GASTROINTESTINAL INFECTION ( 22 FDA reports)
GESTATIONAL DIABETES ( 22 FDA reports)
HAEMODYNAMIC INSTABILITY ( 22 FDA reports)
INJECTION SITE NODULE ( 22 FDA reports)
INJURY ASPHYXIATION ( 22 FDA reports)
LUNG INJURY ( 22 FDA reports)
MASS EXCISION ( 22 FDA reports)
METASTASES TO SKIN ( 22 FDA reports)
NECROSIS ( 22 FDA reports)
OTITIS MEDIA CHRONIC ( 22 FDA reports)
PCO2 DECREASED ( 22 FDA reports)
PERFORMANCE STATUS DECREASED ( 22 FDA reports)
POST THROMBOTIC SYNDROME ( 22 FDA reports)
RADIAL NERVE PALSY ( 22 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 22 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 22 FDA reports)
SKIN NECROSIS ( 22 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 22 FDA reports)
TONGUE COATED ( 22 FDA reports)
TUBERCULOSIS ( 22 FDA reports)
TUMOUR MARKER INCREASED ( 22 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 22 FDA reports)
POST PROCEDURAL INFECTION ( 21 FDA reports)
POSTOPERATIVE ILEUS ( 21 FDA reports)
SKULL FRACTURE ( 21 FDA reports)
SPINAL DEFORMITY ( 21 FDA reports)
STARING ( 21 FDA reports)
SUBDURAL HAEMORRHAGE ( 21 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 21 FDA reports)
URETHRAL STENOSIS ( 21 FDA reports)
ANTISOCIAL BEHAVIOUR ( 21 FDA reports)
APPLICATION SITE RASH ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 21 FDA reports)
B-CELL LYMPHOMA ( 21 FDA reports)
BLOOD CREATININE DECREASED ( 21 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 21 FDA reports)
BLOOD URIC ACID INCREASED ( 21 FDA reports)
BREAST ENLARGEMENT ( 21 FDA reports)
CARDIAC ENZYMES INCREASED ( 21 FDA reports)
CHEST WALL OPERATION ( 21 FDA reports)
CHOLECYSTITIS INFECTIVE ( 21 FDA reports)
CORONARY ARTERY THROMBOSIS ( 21 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 21 FDA reports)
DISSOCIATIVE FUGUE ( 21 FDA reports)
EPILEPSY ( 21 FDA reports)
FIBROUS HISTIOCYTOMA ( 21 FDA reports)
FOOD POISONING ( 21 FDA reports)
HAIR GROWTH ABNORMAL ( 21 FDA reports)
HEMIPLEGIA ( 21 FDA reports)
ILIAC ARTERY STENOSIS ( 21 FDA reports)
INCISION SITE COMPLICATION ( 21 FDA reports)
INJECTION SITE BRUISING ( 21 FDA reports)
INJECTION SITE URTICARIA ( 21 FDA reports)
INNER EAR DISORDER ( 21 FDA reports)
INTESTINAL ISCHAEMIA ( 21 FDA reports)
ISCHAEMIC HEPATITIS ( 21 FDA reports)
JOINT LOCK ( 21 FDA reports)
LEUKOENCEPHALOPATHY ( 21 FDA reports)
MUSCLE CONTRACTURE ( 21 FDA reports)
OBSESSIVE THOUGHTS ( 21 FDA reports)
ORAL DISCHARGE ( 21 FDA reports)
PERIODONTAL INFECTION ( 21 FDA reports)
PLASTIC SURGERY ( 21 FDA reports)
POLYMYALGIA RHEUMATICA ( 21 FDA reports)
ADRENAL NEOPLASM ( 20 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 20 FDA reports)
AORTIC VALVE DISEASE ( 20 FDA reports)
APLASIA PURE RED CELL ( 20 FDA reports)
APPETITE DISORDER ( 20 FDA reports)
BLOOD CREATINE INCREASED ( 20 FDA reports)
BREAST SWELLING ( 20 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 20 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 20 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 20 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 20 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 20 FDA reports)
EYELID OEDEMA ( 20 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 20 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 20 FDA reports)
LICHENOID KERATOSIS ( 20 FDA reports)
LOWER EXTREMITY MASS ( 20 FDA reports)
MENINGITIS ( 20 FDA reports)
MUCOSAL ULCERATION ( 20 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 20 FDA reports)
ORAL NEOPLASM BENIGN ( 20 FDA reports)
PARONYCHIA ( 20 FDA reports)
PHOTOPSIA ( 20 FDA reports)
PULMONARY HAEMORRHAGE ( 20 FDA reports)
PYODERMA GANGRENOSUM ( 20 FDA reports)
SARCOIDOSIS ( 20 FDA reports)
SCAN ABNORMAL ( 20 FDA reports)
SKIN ATROPHY ( 20 FDA reports)
SKIN FISSURES ( 20 FDA reports)
SKIN GRAFT ( 20 FDA reports)
SOCIAL PROBLEM ( 20 FDA reports)
SPINAL DECOMPRESSION ( 20 FDA reports)
STILLBIRTH ( 20 FDA reports)
SUDDEN CARDIAC DEATH ( 20 FDA reports)
TALIPES ( 20 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 20 FDA reports)
TINEA PEDIS ( 20 FDA reports)
TOE AMPUTATION ( 20 FDA reports)
TORSADE DE POINTES ( 20 FDA reports)
TRACHEOBRONCHITIS ( 20 FDA reports)
UTERINE POLYP ( 20 FDA reports)
VERBAL ABUSE ( 20 FDA reports)
VOCAL CORD DISORDER ( 20 FDA reports)
WOUND DEBRIDEMENT ( 20 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 19 FDA reports)
RECTAL CANCER ( 19 FDA reports)
RETINOPATHY ( 19 FDA reports)
SINUS POLYP ( 19 FDA reports)
SOFT TISSUE INJURY ( 19 FDA reports)
SPLENIC CALCIFICATION ( 19 FDA reports)
TENOSYNOVITIS STENOSANS ( 19 FDA reports)
THYROID CYST ( 19 FDA reports)
TOOTH EROSION ( 19 FDA reports)
TRACHEITIS ( 19 FDA reports)
URGE INCONTINENCE ( 19 FDA reports)
VEIN DISORDER ( 19 FDA reports)
VULVOVAGINITIS ( 19 FDA reports)
WOUND HAEMORRHAGE ( 19 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 19 FDA reports)
ABDOMINAL ABSCESS ( 19 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 19 FDA reports)
AGORAPHOBIA ( 19 FDA reports)
ANAL CANDIDIASIS ( 19 FDA reports)
BENIGN OVARIAN TUMOUR ( 19 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 19 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 19 FDA reports)
BREAST LUMP REMOVAL ( 19 FDA reports)
CARDIAC OPERATION ( 19 FDA reports)
CATATONIA ( 19 FDA reports)
CATHETER RELATED COMPLICATION ( 19 FDA reports)
CATHETER SITE HAEMORRHAGE ( 19 FDA reports)
DERMATOMYOSITIS ( 19 FDA reports)
DEVICE RELATED SEPSIS ( 19 FDA reports)
DIVERTICULAR PERFORATION ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
FOAMING AT MOUTH ( 19 FDA reports)
FRACTURE DELAYED UNION ( 19 FDA reports)
FRACTURE DISPLACEMENT ( 19 FDA reports)
GALACTORRHOEA ( 19 FDA reports)
GINGIVAL ABSCESS ( 19 FDA reports)
HYPERTHERMIA ( 19 FDA reports)
INAPPROPRIATE AFFECT ( 19 FDA reports)
INGUINAL HERNIA REPAIR ( 19 FDA reports)
KYPHOSCOLIOSIS ( 19 FDA reports)
METASTASES TO PLEURA ( 19 FDA reports)
MONOCYTOSIS ( 19 FDA reports)
MOUTH INJURY ( 19 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 19 FDA reports)
MUMPS ( 19 FDA reports)
NEPHROTIC SYNDROME ( 19 FDA reports)
OBSTRUCTION ( 19 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 19 FDA reports)
PARAPARESIS ( 19 FDA reports)
PARKINSONISM ( 19 FDA reports)
PHYSIOTHERAPY ( 19 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 19 FDA reports)
ABDOMINAL MASS ( 18 FDA reports)
ALCOHOL ABUSE ( 18 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 18 FDA reports)
ARTHRITIS INFECTIVE ( 18 FDA reports)
BEREAVEMENT REACTION ( 18 FDA reports)
BLADDER NECK OPERATION ( 18 FDA reports)
BLOOD BLISTER ( 18 FDA reports)
BREAST CANCER IN SITU ( 18 FDA reports)
CARCINOID SYNDROME ( 18 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 18 FDA reports)
CENTRAL LINE INFECTION ( 18 FDA reports)
CHEST INJURY ( 18 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 18 FDA reports)
COLECTOMY ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 18 FDA reports)
EPIDIDYMITIS ( 18 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 18 FDA reports)
FALLOT'S TETRALOGY ( 18 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 18 FDA reports)
FOOD CRAVING ( 18 FDA reports)
GASTRIC BYPASS ( 18 FDA reports)
GASTRIC DILATATION ( 18 FDA reports)
GLOMERULONEPHRITIS ( 18 FDA reports)
HEARING AID USER ( 18 FDA reports)
IMPULSE-CONTROL DISORDER ( 18 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 18 FDA reports)
INFECTED SEBACEOUS CYST ( 18 FDA reports)
INJECTION SITE MASS ( 18 FDA reports)
KIDNEY SMALL ( 18 FDA reports)
LEUKAEMIA ( 18 FDA reports)
LIBIDO INCREASED ( 18 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 18 FDA reports)
MAMMOPLASTY ( 18 FDA reports)
MIOSIS ( 18 FDA reports)
MORTON'S NEUROMA ( 18 FDA reports)
MULTIPLE ALLERGIES ( 18 FDA reports)
NEUROLOGICAL SYMPTOM ( 18 FDA reports)
OBSTRUCTION GASTRIC ( 18 FDA reports)
OSTEOTOMY ( 18 FDA reports)
PANCREATIC CYST ( 18 FDA reports)
PANCREATIC INSUFFICIENCY ( 18 FDA reports)
PERINEAL PAIN ( 18 FDA reports)
PHARYNGEAL ERYTHEMA ( 18 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 18 FDA reports)
PROTEIN URINE ( 18 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RESPIRATORY RATE DECREASED ( 18 FDA reports)
SCRATCH ( 18 FDA reports)
SKIN EROSION ( 18 FDA reports)
SKIN ODOUR ABNORMAL ( 18 FDA reports)
SKULL FRACTURED BASE ( 18 FDA reports)
SKULL MALFORMATION ( 18 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 18 FDA reports)
STASIS DERMATITIS ( 18 FDA reports)
STOMATOCYTES PRESENT ( 18 FDA reports)
TEETH BRITTLE ( 18 FDA reports)
THYROID MASS ( 18 FDA reports)
VASCULAR OCCLUSION ( 18 FDA reports)
VENOUS THROMBOSIS LIMB ( 18 FDA reports)
VESTIBULAR DISORDER ( 18 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
PORTAL VEIN THROMBOSIS ( 17 FDA reports)
PROSTATIC DISORDER ( 17 FDA reports)
PROSTHESIS USER ( 17 FDA reports)
PULMONARY HILUM MASS ( 17 FDA reports)
PULMONARY INFARCTION ( 17 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 17 FDA reports)
RECTAL ULCER ( 17 FDA reports)
RED BLOOD CELL ABNORMALITY ( 17 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 17 FDA reports)
REGURGITATION ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 17 FDA reports)
SPINAL CORD OEDEMA ( 17 FDA reports)
SPLENIC INFARCTION ( 17 FDA reports)
SPUTUM PURULENT ( 17 FDA reports)
SUBCUTANEOUS NODULE ( 17 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 17 FDA reports)
TOE DEFORMITY ( 17 FDA reports)
TREATMENT FAILURE ( 17 FDA reports)
ULNAR NEURITIS ( 17 FDA reports)
VARICELLA ( 17 FDA reports)
VENTRICULAR DYSKINESIA ( 17 FDA reports)
WOUND TREATMENT ( 17 FDA reports)
YELLOW SKIN ( 17 FDA reports)
ABSCESS INTESTINAL ( 17 FDA reports)
ADENOMYOSIS ( 17 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 17 FDA reports)
ANDROGENS ABNORMAL ( 17 FDA reports)
ANORECTAL DISCOMFORT ( 17 FDA reports)
APLASTIC ANAEMIA ( 17 FDA reports)
ATHEROSCLEROSIS ( 17 FDA reports)
BELLIGERENCE ( 17 FDA reports)
BLADDER PAIN ( 17 FDA reports)
BLEPHAROSPASM ( 17 FDA reports)
BLOOD PH DECREASED ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 17 FDA reports)
BLOOD UREA DECREASED ( 17 FDA reports)
CAECITIS ( 17 FDA reports)
CARDIAC OUTPUT DECREASED ( 17 FDA reports)
CEREBRAL CYST ( 17 FDA reports)
CHORIOAMNIONITIS ( 17 FDA reports)
COLOSTOMY ( 17 FDA reports)
CUTIS LAXA ( 17 FDA reports)
DIABETIC GASTROPARESIS ( 17 FDA reports)
DROP ATTACKS ( 17 FDA reports)
EAR NEOPLASM ( 17 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 17 FDA reports)
EMBOLISM VENOUS ( 17 FDA reports)
EMPYEMA ( 17 FDA reports)
ENDOMETRIOSIS ( 17 FDA reports)
ENTEROCELE ( 17 FDA reports)
ERYTHEMA MULTIFORME ( 17 FDA reports)
EXPIRED DRUG ADMINISTERED ( 17 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 17 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 17 FDA reports)
GALLBLADDER INJURY ( 17 FDA reports)
GAMMOPATHY ( 17 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 17 FDA reports)
GLYCOSURIA ( 17 FDA reports)
HYPERREFLEXIA ( 17 FDA reports)
HYPERTROPHY ( 17 FDA reports)
HYPOPARATHYROIDISM ( 17 FDA reports)
IMPAIRED SELF-CARE ( 17 FDA reports)
INTESTINAL HAEMORRHAGE ( 17 FDA reports)
LARGE INTESTINE PERFORATION ( 17 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 17 FDA reports)
MORBID THOUGHTS ( 17 FDA reports)
MOUTH CYST ( 17 FDA reports)
MYOFASCITIS ( 17 FDA reports)
NEUTROPENIC SEPSIS ( 17 FDA reports)
OESOPHAGEAL CARCINOMA ( 17 FDA reports)
ORAL PUSTULE ( 17 FDA reports)
PANCREATIC PSEUDOCYST ( 17 FDA reports)
PARTIAL SEIZURES ( 17 FDA reports)
PARTNER STRESS ( 17 FDA reports)
PEYRONIE'S DISEASE ( 17 FDA reports)
PHLEBITIS SUPERFICIAL ( 17 FDA reports)
PLACENTAL INFARCTION ( 17 FDA reports)
PLACENTAL INSUFFICIENCY ( 17 FDA reports)
ACCIDENTAL EXPOSURE ( 16 FDA reports)
ADRENAL DISORDER ( 16 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 16 FDA reports)
ANURIA ( 16 FDA reports)
AUTOIMMUNE DISORDER ( 16 FDA reports)
BARTHOLIN'S ABSCESS ( 16 FDA reports)
BARTHOLIN'S CYST ( 16 FDA reports)
BLADDER OBSTRUCTION ( 16 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 16 FDA reports)
BLOOD SODIUM INCREASED ( 16 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 16 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
CHONDROPATHY ( 16 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 16 FDA reports)
COMPLEX PARTIAL SEIZURES ( 16 FDA reports)
CONGENITAL AORTIC ATRESIA ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
CORONARY ARTERY RESTENOSIS ( 16 FDA reports)
DENTAL TREATMENT ( 16 FDA reports)
ENTEROCUTANEOUS FISTULA ( 16 FDA reports)
EYE INJURY ( 16 FDA reports)
FACIAL OPERATION ( 16 FDA reports)
FASCIITIS ( 16 FDA reports)
FEELING GUILTY ( 16 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 16 FDA reports)
GALLOP RHYTHM PRESENT ( 16 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 16 FDA reports)
GENITAL RASH ( 16 FDA reports)
HAEMOCHROMATOSIS ( 16 FDA reports)
HAEMORRHOID OPERATION ( 16 FDA reports)
HAIR TEXTURE ABNORMAL ( 16 FDA reports)
HISTOPLASMOSIS ( 16 FDA reports)
HYPERCHLORHYDRIA ( 16 FDA reports)
HYPERNATRAEMIA ( 16 FDA reports)
HYPERPHOSPHATAEMIA ( 16 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 16 FDA reports)
INFECTED SKIN ULCER ( 16 FDA reports)
INTERTRIGO ( 16 FDA reports)
LYME DISEASE ( 16 FDA reports)
LYMPH NODE PAIN ( 16 FDA reports)
MALIGNANT HYPERTENSION ( 16 FDA reports)
MONOPLEGIA ( 16 FDA reports)
MULTI-ORGAN DISORDER ( 16 FDA reports)
OCULAR ICTERUS ( 16 FDA reports)
ORAL SOFT TISSUE DISORDER ( 16 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 16 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 16 FDA reports)
PRESSURE OF SPEECH ( 16 FDA reports)
PROCEDURAL HYPERTENSION ( 16 FDA reports)
PROLAPSE REPAIR ( 16 FDA reports)
RASH VESICULAR ( 16 FDA reports)
RUBELLA ( 16 FDA reports)
SCARLET FEVER ( 16 FDA reports)
SEXUAL ASSAULT VICTIM ( 16 FDA reports)
SPINAL COLUMN INJURY ( 16 FDA reports)
TOBACCO USER ( 16 FDA reports)
TONGUE PARALYSIS ( 16 FDA reports)
TONSILLITIS ( 16 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 16 FDA reports)
TRAUMATIC ARTHRITIS ( 16 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 16 FDA reports)
URINE ODOUR ABNORMAL ( 16 FDA reports)
VARICES OESOPHAGEAL ( 16 FDA reports)
VERTEBRAL WEDGING ( 16 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 15 FDA reports)
PROSTATE TENDERNESS ( 15 FDA reports)
RADICAL MASTECTOMY ( 15 FDA reports)
RASH PUSTULAR ( 15 FDA reports)
RENAL ANEURYSM ( 15 FDA reports)
RENAL CANCER METASTATIC ( 15 FDA reports)
RENAL TUBULAR ACIDOSIS ( 15 FDA reports)
RESUSCITATION ( 15 FDA reports)
RETICULOCYTE COUNT INCREASED ( 15 FDA reports)
RHINALGIA ( 15 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 15 FDA reports)
SALPINGO-OOPHORECTOMY ( 15 FDA reports)
SECRETION DISCHARGE ( 15 FDA reports)
SENSATION OF PRESSURE ( 15 FDA reports)
SINUS TARSI SYNDROME ( 15 FDA reports)
SMALL INTESTINE OPERATION ( 15 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 15 FDA reports)
THERAPY REGIMEN CHANGED ( 15 FDA reports)
THORACOTOMY ( 15 FDA reports)
TOE OPERATION ( 15 FDA reports)
TRANCE ( 15 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 15 FDA reports)
UTERINE CANCER ( 15 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 15 FDA reports)
VENTRICULAR ARRHYTHMIA ( 15 FDA reports)
VERTEBRAL COLUMN MASS ( 15 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 15 FDA reports)
ACCIDENTAL DEATH ( 15 FDA reports)
ADRENAL ADENOMA ( 15 FDA reports)
AMAUROSIS FUGAX ( 15 FDA reports)
ANGIONEUROTIC OEDEMA ( 15 FDA reports)
APPENDIX DISORDER ( 15 FDA reports)
ASBESTOSIS ( 15 FDA reports)
AUTONOMIC NEUROPATHY ( 15 FDA reports)
BACTERIAL DISEASE CARRIER ( 15 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 15 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 15 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 15 FDA reports)
BRADYARRHYTHMIA ( 15 FDA reports)
CALCINOSIS ( 15 FDA reports)
CALCULUS BLADDER ( 15 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 15 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 15 FDA reports)
CEREBROVASCULAR DISORDER ( 15 FDA reports)
CHEST TUBE INSERTION ( 15 FDA reports)
CHOKING SENSATION ( 15 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 15 FDA reports)
COMPULSIVE SHOPPING ( 15 FDA reports)
CONNECTIVE TISSUE DISORDER ( 15 FDA reports)
DENTAL IMPLANTATION ( 15 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 15 FDA reports)
EAR HAEMORRHAGE ( 15 FDA reports)
EXTREMITY CONTRACTURE ( 15 FDA reports)
FOOD ALLERGY ( 15 FDA reports)
GALLBLADDER OPERATION ( 15 FDA reports)
GOUTY ARTHRITIS ( 15 FDA reports)
HAEMOTHORAX ( 15 FDA reports)
HEPATIC ENZYME ABNORMAL ( 15 FDA reports)
HYPERACUSIS ( 15 FDA reports)
HYPERAEMIA ( 15 FDA reports)
IMMUNE SYSTEM DISORDER ( 15 FDA reports)
INCISIONAL HERNIA ( 15 FDA reports)
INFARCTION ( 15 FDA reports)
INFUSION SITE SWELLING ( 15 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 15 FDA reports)
INTERNAL INJURY ( 15 FDA reports)
INTESTINAL DILATATION ( 15 FDA reports)
INTRACRANIAL HYPOTENSION ( 15 FDA reports)
JAUNDICE NEONATAL ( 15 FDA reports)
JUGULAR VEIN DISTENSION ( 15 FDA reports)
KNEE DEFORMITY ( 15 FDA reports)
LAZINESS ( 15 FDA reports)
LISTLESS ( 15 FDA reports)
LOCALISED OEDEMA ( 15 FDA reports)
MARITAL PROBLEM ( 15 FDA reports)
MELANOSIS COLI ( 15 FDA reports)
MENINGITIS ASEPTIC ( 15 FDA reports)
MONONUCLEOSIS SYNDROME ( 15 FDA reports)
NASAL DISCOMFORT ( 15 FDA reports)
NERVE ROOT COMPRESSION ( 15 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 15 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 15 FDA reports)
OPTIC NEUROPATHY ( 15 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 15 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 15 FDA reports)
ABSCESS NECK ( 14 FDA reports)
ANAL FISTULA ( 14 FDA reports)
ANGIOPLASTY ( 14 FDA reports)
ANOGENITAL WARTS ( 14 FDA reports)
ANORECTAL DISORDER ( 14 FDA reports)
APPLICATION SITE IRRITATION ( 14 FDA reports)
APPLICATION SITE REACTION ( 14 FDA reports)
ARTERIAL DISORDER ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
BIOPSY TONGUE ABNORMAL ( 14 FDA reports)
BK VIRUS INFECTION ( 14 FDA reports)
BLOOD ALCOHOL INCREASED ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 14 FDA reports)
BONE ATROPHY ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 14 FDA reports)
BRAIN COMPRESSION ( 14 FDA reports)
BREAST CELLULITIS ( 14 FDA reports)
BREAST OPERATION ( 14 FDA reports)
CARDIAC FAILURE CHRONIC ( 14 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 14 FDA reports)
CEREBRAL ARTERY STENOSIS ( 14 FDA reports)
CERVICAL CORD COMPRESSION ( 14 FDA reports)
CLOSED HEAD INJURY ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
CYSTOSCOPY ( 14 FDA reports)
DERMATITIS EXFOLIATIVE ( 14 FDA reports)
DRUG EFFECT INCREASED ( 14 FDA reports)
DYSPLASIA ( 14 FDA reports)
ECZEMA ASTEATOTIC ( 14 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 14 FDA reports)
ENDOSCOPY ( 14 FDA reports)
ENERGY INCREASED ( 14 FDA reports)
FAILURE OF IMPLANT ( 14 FDA reports)
FEELING HOT AND COLD ( 14 FDA reports)
FUNGAEMIA ( 14 FDA reports)
GASTRITIS HAEMORRHAGIC ( 14 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 14 FDA reports)
GLOMERULOSCLEROSIS ( 14 FDA reports)
HAEMOGLOBINURIA ( 14 FDA reports)
HYDROCEPHALUS ( 14 FDA reports)
HYPERPROTEINAEMIA ( 14 FDA reports)
ICHTHYOSIS ( 14 FDA reports)
INFUSION SITE PAIN ( 14 FDA reports)
INJECTION SITE DISCOMFORT ( 14 FDA reports)
INJECTION SITE INDURATION ( 14 FDA reports)
JAW CYST ( 14 FDA reports)
LARGE INTESTINAL ULCER ( 14 FDA reports)
LERICHE SYNDROME ( 14 FDA reports)
LIP ULCERATION ( 14 FDA reports)
LIVER TRANSPLANT REJECTION ( 14 FDA reports)
LOSS OF LIBIDO ( 14 FDA reports)
LUPUS-LIKE SYNDROME ( 14 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 14 FDA reports)
MEGACOLON ( 14 FDA reports)
METASTASES TO ABDOMINAL WALL ( 14 FDA reports)
MITRAL VALVE STENOSIS ( 14 FDA reports)
MIXED HYPERLIPIDAEMIA ( 14 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
NEOPLASM RECURRENCE ( 14 FDA reports)
NEPHRITIC SYNDROME ( 14 FDA reports)
NERVE ROOT LESION ( 14 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 14 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 14 FDA reports)
OOPHORECTOMY ( 14 FDA reports)
ORAL MUCOSA ATROPHY ( 14 FDA reports)
ORAL MUCOSAL BLISTERING ( 14 FDA reports)
ORAL NEOPLASM ( 14 FDA reports)
ORTHODONTIC APPLIANCE USER ( 14 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 14 FDA reports)
PELVIC ABSCESS ( 14 FDA reports)
PERICARDIAL DISEASE ( 14 FDA reports)
PERNICIOUS ANAEMIA ( 14 FDA reports)
PIRIFORMIS SYNDROME ( 14 FDA reports)
PITTING OEDEMA ( 14 FDA reports)
POLYARTHRITIS ( 14 FDA reports)
POLYCYSTIC OVARIES ( 14 FDA reports)
POLYPECTOMY ( 14 FDA reports)
PROSTHESIS IMPLANTATION ( 14 FDA reports)
PSEUDOMONAL SEPSIS ( 14 FDA reports)
PSYCHOTIC BEHAVIOUR ( 14 FDA reports)
RESPIRATION ABNORMAL ( 14 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 14 FDA reports)
SCAPULA FRACTURE ( 14 FDA reports)
SERUM SICKNESS ( 14 FDA reports)
SKIN HYPOPIGMENTATION ( 14 FDA reports)
SMALL FOR DATES BABY ( 14 FDA reports)
SPINAL X-RAY ABNORMAL ( 14 FDA reports)
STRESS SYMPTOMS ( 14 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 14 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 14 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 14 FDA reports)
TRICUSPID VALVE DISEASE ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VOCAL CORD THICKENING ( 14 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 13 FDA reports)
PROTEUS INFECTION ( 13 FDA reports)
PSEUDOMONAS BRONCHITIS ( 13 FDA reports)
PUBIC RAMI FRACTURE ( 13 FDA reports)
PULMONARY VASCULAR DISORDER ( 13 FDA reports)
RADICULITIS BRACHIAL ( 13 FDA reports)
RADIOTHERAPY TO BRAIN ( 13 FDA reports)
RENAL COLIC ( 13 FDA reports)
RENAL STONE REMOVAL ( 13 FDA reports)
RETINOPATHY HYPERTENSIVE ( 13 FDA reports)
RETROPERITONEAL HAEMATOMA ( 13 FDA reports)
RHINITIS SEASONAL ( 13 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 13 FDA reports)
SCOTOMA ( 13 FDA reports)
SKIN CANDIDA ( 13 FDA reports)
SKIN NEOPLASM EXCISION ( 13 FDA reports)
SPINAL HAEMANGIOMA ( 13 FDA reports)
SYNCOPE VASOVAGAL ( 13 FDA reports)
THERAPY CESSATION ( 13 FDA reports)
THROMBOSIS IN DEVICE ( 13 FDA reports)
THYROIDITIS ( 13 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 13 FDA reports)
TRANSFUSION REACTION ( 13 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 13 FDA reports)
URINE COLOUR ABNORMAL ( 13 FDA reports)
URINE KETONE BODY PRESENT ( 13 FDA reports)
VAGINITIS BACTERIAL ( 13 FDA reports)
VASCULAR OPERATION ( 13 FDA reports)
WEIGHT GAIN POOR ( 13 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 13 FDA reports)
ALVEOLITIS ALLERGIC ( 13 FDA reports)
ANAL PRURITUS ( 13 FDA reports)
ANORGASMIA ( 13 FDA reports)
ARTHROPOD STING ( 13 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 13 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
BILE DUCT OBSTRUCTION ( 13 FDA reports)
BLADDER CATHETERISATION ( 13 FDA reports)
BLOOD BICARBONATE DECREASED ( 13 FDA reports)
BRAIN OPERATION ( 13 FDA reports)
BRAIN STEM SYNDROME ( 13 FDA reports)
CARBON DIOXIDE INCREASED ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 13 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 13 FDA reports)
CHRONIC HEPATITIS ( 13 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 13 FDA reports)
COLONOSCOPY ( 13 FDA reports)
COMPARTMENT SYNDROME ( 13 FDA reports)
CONGENITAL AORTIC STENOSIS ( 13 FDA reports)
CRANIAL NERVE DISORDER ( 13 FDA reports)
DENTAL PROSTHESIS USER ( 13 FDA reports)
DIABETIC EYE DISEASE ( 13 FDA reports)
DIABETIC ULCER ( 13 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 13 FDA reports)
ENTEROBACTER INFECTION ( 13 FDA reports)
EXCESSIVE EYE BLINKING ( 13 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 13 FDA reports)
FOOD INTOLERANCE ( 13 FDA reports)
FULL BLOOD COUNT DECREASED ( 13 FDA reports)
GRAVITATIONAL OEDEMA ( 13 FDA reports)
GRIMACING ( 13 FDA reports)
HEART RATE ABNORMAL ( 13 FDA reports)
HELICOBACTER TEST POSITIVE ( 13 FDA reports)
HYPERSEXUALITY ( 13 FDA reports)
ILEITIS ( 13 FDA reports)
INDURATION ( 13 FDA reports)
INFUSION SITE IRRITATION ( 13 FDA reports)
KERATOMILEUSIS ( 13 FDA reports)
LIP DRY ( 13 FDA reports)
LIP PAIN ( 13 FDA reports)
LOCALISED OSTEOARTHRITIS ( 13 FDA reports)
MALE SEXUAL DYSFUNCTION ( 13 FDA reports)
METASTASES TO MENINGES ( 13 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 13 FDA reports)
MICTURITION FREQUENCY DECREASED ( 13 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 13 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 13 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 13 FDA reports)
NASAL DRYNESS ( 13 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 13 FDA reports)
NEPHRECTOMY ( 13 FDA reports)
ONYCHOCLASIS ( 13 FDA reports)
ONYCHOLYSIS ( 13 FDA reports)
OPEN ANGLE GLAUCOMA ( 13 FDA reports)
OVARIAN DISORDER ( 13 FDA reports)
PANCREATIC ATROPHY ( 13 FDA reports)
PAPILLARY THYROID CANCER ( 13 FDA reports)
PARACENTESIS ( 13 FDA reports)
PERIPHERAL NERVE INJURY ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 13 FDA reports)
ADVERSE REACTION ( 12 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 12 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 12 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 12 FDA reports)
ASPERGILLOSIS ( 12 FDA reports)
BENIGN COLONIC NEOPLASM ( 12 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 12 FDA reports)
BLADDER DISCOMFORT ( 12 FDA reports)
BLADDER DYSFUNCTION ( 12 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 12 FDA reports)
BLOOD PROLACTIN INCREASED ( 12 FDA reports)
BUNION OPERATION ( 12 FDA reports)
BURN INFECTION ( 12 FDA reports)
BUTTOCK PAIN ( 12 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 12 FDA reports)
CARBON DIOXIDE DECREASED ( 12 FDA reports)
CARDIOVERSION ( 12 FDA reports)
CATHETER SEPSIS ( 12 FDA reports)
CATHETER SITE INFECTION ( 12 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 12 FDA reports)
CEREBRAL DISORDER ( 12 FDA reports)
CERVICITIS ( 12 FDA reports)
CHOLANGITIS ( 12 FDA reports)
CHOLESTEATOMA ( 12 FDA reports)
CLEFT LIP ( 12 FDA reports)
CONJUNCTIVAL ABRASION ( 12 FDA reports)
CRYPTORCHISM ( 12 FDA reports)
CULTURE WOUND POSITIVE ( 12 FDA reports)
CUSHINGOID ( 12 FDA reports)
CYST RUPTURE ( 12 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
DYSPAREUNIA ( 12 FDA reports)
EJECTION FRACTION ABNORMAL ( 12 FDA reports)
ENDOMETRIAL CANCER ( 12 FDA reports)
EYE ROLLING ( 12 FDA reports)
FEAR OF DISEASE ( 12 FDA reports)
FUNGAL SKIN INFECTION ( 12 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 12 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 12 FDA reports)
GRIP STRENGTH DECREASED ( 12 FDA reports)
HAEMARTHROSIS ( 12 FDA reports)
HAND DEFORMITY ( 12 FDA reports)
HEAD DEFORMITY ( 12 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 12 FDA reports)
HEPATIC ISCHAEMIA ( 12 FDA reports)
HEPATOJUGULAR REFLUX ( 12 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 12 FDA reports)
HYPOREFLEXIA ( 12 FDA reports)
ILIAC ARTERY THROMBOSIS ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
INFUSION SITE EXTRAVASATION ( 12 FDA reports)
INJECTION SITE EXTRAVASATION ( 12 FDA reports)
INTRA-UTERINE DEATH ( 12 FDA reports)
KELOID SCAR ( 12 FDA reports)
LIVER ABSCESS ( 12 FDA reports)
LOSS OF PROPRIOCEPTION ( 12 FDA reports)
MACROPHAGES INCREASED ( 12 FDA reports)
MEDIASTINAL MASS ( 12 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 12 FDA reports)
METASTASES TO LARGE INTESTINE ( 12 FDA reports)
METASTASES TO PELVIS ( 12 FDA reports)
METASTATIC PAIN ( 12 FDA reports)
NASAL POLYPS ( 12 FDA reports)
NEUROENDOCRINE TUMOUR ( 12 FDA reports)
OBSTRUCTIVE UROPATHY ( 12 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 12 FDA reports)
PALATAL DISORDER ( 12 FDA reports)
PEAU D'ORANGE ( 12 FDA reports)
PERIODONTAL DESTRUCTION ( 12 FDA reports)
PERITONEAL ADHESIONS ( 12 FDA reports)
PNEUMOCEPHALUS ( 12 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 12 FDA reports)
PNEUMONIA FUNGAL ( 12 FDA reports)
PNEUMONIA LEGIONELLA ( 12 FDA reports)
POSTICTAL STATE ( 12 FDA reports)
POSTOPERATIVE INFECTION ( 12 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 12 FDA reports)
PSYCHOMOTOR RETARDATION ( 12 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 12 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 12 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 12 FDA reports)
RETINAL ARTERY OCCLUSION ( 12 FDA reports)
RHEUMATOID FACTOR INCREASED ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 12 FDA reports)
SKIN TURGOR DECREASED ( 12 FDA reports)
SKIN WRINKLING ( 12 FDA reports)
SOCIAL PHOBIA ( 12 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 12 FDA reports)
SPLENIC GRANULOMA ( 12 FDA reports)
SPLENIC VEIN THROMBOSIS ( 12 FDA reports)
SPONDYLOARTHROPATHY ( 12 FDA reports)
SPONDYLOSIS ( 12 FDA reports)
THERAPEUTIC PROCEDURE ( 12 FDA reports)
TINEA CRURIS ( 12 FDA reports)
TUMOUR INVASION ( 12 FDA reports)
URACHAL ABNORMALITY ( 12 FDA reports)
URETHRAL DISORDER ( 12 FDA reports)
UTERINE DISORDER ( 12 FDA reports)
VENOOCCLUSIVE DISEASE ( 12 FDA reports)
VICTIM OF CRIME ( 12 FDA reports)
WHIPLASH INJURY ( 12 FDA reports)
YAWNING ( 12 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 11 FDA reports)
PRECANCEROUS CELLS PRESENT ( 11 FDA reports)
PROTEIN URINE ABSENT ( 11 FDA reports)
PROTRUSION TONGUE ( 11 FDA reports)
PULMONARY MYCOSIS ( 11 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
RESIDUAL URINE ( 11 FDA reports)
RETINAL VEIN OCCLUSION ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SLEEP SEX ( 11 FDA reports)
STERNOTOMY ( 11 FDA reports)
TERMINAL INSOMNIA ( 11 FDA reports)
THROAT CANCER ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 11 FDA reports)
TRANSPLANT REJECTION ( 11 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 11 FDA reports)
TUMOUR FLARE ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 11 FDA reports)
UVEITIS ( 11 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 11 FDA reports)
ABDOMINAL SEPSIS ( 11 FDA reports)
ABORTION INDUCED ( 11 FDA reports)
ACUTE HEPATIC FAILURE ( 11 FDA reports)
ACUTE LEUKAEMIA ( 11 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 11 FDA reports)
ANAL SPHINCTER ATONY ( 11 FDA reports)
ANDROGEN DEFICIENCY ( 11 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 11 FDA reports)
BASOSQUAMOUS CARCINOMA ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BREAST DISCHARGE ( 11 FDA reports)
CANDIDURIA ( 11 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 11 FDA reports)
CEREBRAL THROMBOSIS ( 11 FDA reports)
CERVIX CARCINOMA ( 11 FDA reports)
CHOLESTEROSIS ( 11 FDA reports)
CLUSTER HEADACHE ( 11 FDA reports)
COCCYDYNIA ( 11 FDA reports)
COITAL BLEEDING ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
CONJUNCTIVITIS VIRAL ( 11 FDA reports)
CREPITATIONS ( 11 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 11 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 11 FDA reports)
DISINHIBITION ( 11 FDA reports)
DIURETIC THERAPY ( 11 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
DRUG SCREEN NEGATIVE ( 11 FDA reports)
DYSPNOEA EXACERBATED ( 11 FDA reports)
EJECTION FRACTION ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
ESCHERICHIA BACTERAEMIA ( 11 FDA reports)
EYE DISCHARGE ( 11 FDA reports)
FEMORAL ARTERY OCCLUSION ( 11 FDA reports)
FLIGHT OF IDEAS ( 11 FDA reports)
FOETAL CARDIAC DISORDER ( 11 FDA reports)
FOREIGN BODY REACTION ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
GASTRIC CANCER ( 11 FDA reports)
GASTRIC PERFORATION ( 11 FDA reports)
GASTRIC PH DECREASED ( 11 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 11 FDA reports)
GINGIVAL GRAFT ( 11 FDA reports)
GRANULOCYTOPENIA ( 11 FDA reports)
GRIEF REACTION ( 11 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 11 FDA reports)
HALLUCINATION, OLFACTORY ( 11 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 11 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 11 FDA reports)
HYPOGONADISM ( 11 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 11 FDA reports)
INFUSION SITE ERYTHEMA ( 11 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 11 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 11 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 11 FDA reports)
INTRAOCULAR MELANOMA ( 11 FDA reports)
JOINT WARMTH ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 11 FDA reports)
LIGHT CHAIN ANALYSIS ( 11 FDA reports)
LUNG CANCER METASTATIC ( 11 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 11 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 11 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 11 FDA reports)
MEDICAL DEVICE REMOVAL ( 11 FDA reports)
METASTASES TO ADRENALS ( 11 FDA reports)
METASTASES TO BONE MARROW ( 11 FDA reports)
METASTASES TO THE MEDIASTINUM ( 11 FDA reports)
MICTURITION DISORDER ( 11 FDA reports)
MUCOSAL DRYNESS ( 11 FDA reports)
MYELOFIBROSIS ( 11 FDA reports)
MYOCARDITIS ( 11 FDA reports)
NEPHROCALCINOSIS ( 11 FDA reports)
NEUROMA ( 11 FDA reports)
NEUROMYOPATHY ( 11 FDA reports)
NEUROPATHIC ARTHROPATHY ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
NICOTINE DEPENDENCE ( 11 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 11 FDA reports)
ORTHOPEDIC PROCEDURE ( 11 FDA reports)
OSTEOMYELITIS ACUTE ( 11 FDA reports)
PARATHYROID TUMOUR BENIGN ( 11 FDA reports)
PCO2 INCREASED ( 11 FDA reports)
PETIT MAL EPILEPSY ( 11 FDA reports)
PILONIDAL CYST ( 11 FDA reports)
PNEUMATOSIS INTESTINALIS ( 11 FDA reports)
POLYMEDICATION ( 11 FDA reports)
POLYMYOSITIS ( 11 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 11 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 10 FDA reports)
ACANTHOLYSIS ( 10 FDA reports)
ACCELERATED HYPERTENSION ( 10 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 10 FDA reports)
AXILLARY PAIN ( 10 FDA reports)
BIPOLAR II DISORDER ( 10 FDA reports)
BLEEDING TIME ABNORMAL ( 10 FDA reports)
BLOOD AMYLASE INCREASED ( 10 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 10 FDA reports)
BLOOD PH INCREASED ( 10 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 10 FDA reports)
BLOOD URINE ( 10 FDA reports)
BLOODY DISCHARGE ( 10 FDA reports)
BREAST HYPERPLASIA ( 10 FDA reports)
CARDIAC ABLATION ( 10 FDA reports)
CATARACT CONGENITAL ( 10 FDA reports)
CATHETER SITE PAIN ( 10 FDA reports)
CEREBELLAR ATROPHY ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 10 FDA reports)
CERVICAL CYST ( 10 FDA reports)
CHOREA ( 10 FDA reports)
CLUBBING ( 10 FDA reports)
COLLATERAL CIRCULATION ( 10 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 10 FDA reports)
CORONARY ARTERY REOCCLUSION ( 10 FDA reports)
CROUP INFECTIOUS ( 10 FDA reports)
CULTURE POSITIVE ( 10 FDA reports)
DEATH OF RELATIVE ( 10 FDA reports)
DEPERSONALISATION ( 10 FDA reports)
DERMATITIS ACNEIFORM ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DIAPHRAGMATIC DISORDER ( 10 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 10 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 10 FDA reports)
DRUG DIVERSION ( 10 FDA reports)
DUODENAL STENOSIS ( 10 FDA reports)
DYSPHASIA ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
EPIDURAL LIPOMATOSIS ( 10 FDA reports)
EROSIVE DUODENITIS ( 10 FDA reports)
FEMALE STERILISATION ( 10 FDA reports)
FOOD AVERSION ( 10 FDA reports)
FOREIGN BODY IN EYE ( 10 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 10 FDA reports)
FUNGAL SEPSIS ( 10 FDA reports)
GASTRECTOMY ( 10 FDA reports)
GASTROSTOMY TUBE INSERTION ( 10 FDA reports)
GLIOSIS ( 10 FDA reports)
GUILLAIN-BARRE SYNDROME ( 10 FDA reports)
HALLUCINATION, TACTILE ( 10 FDA reports)
HEART TRANSPLANT ( 10 FDA reports)
HEART VALVE STENOSIS ( 10 FDA reports)
HELICOBACTER GASTRITIS ( 10 FDA reports)
HORDEOLUM ( 10 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 10 FDA reports)
HYPERPROLACTINAEMIA ( 10 FDA reports)
HYPERTENSIVE EMERGENCY ( 10 FDA reports)
HYPOTRICHOSIS ( 10 FDA reports)
INCISION SITE HAEMORRHAGE ( 10 FDA reports)
INCISION SITE INFECTION ( 10 FDA reports)
INCORRECT STORAGE OF DRUG ( 10 FDA reports)
INTERNAL HERNIA ( 10 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 10 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 10 FDA reports)
KERATOACANTHOMA ( 10 FDA reports)
LICHEN PLANUS ( 10 FDA reports)
LIMB CRUSHING INJURY ( 10 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 10 FDA reports)
LUNG OPERATION ( 10 FDA reports)
MANDIBULECTOMY ( 10 FDA reports)
METATARSALGIA ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MITRAL VALVE REPAIR ( 10 FDA reports)
MUCOSAL ATROPHY ( 10 FDA reports)
MUCOSAL EROSION ( 10 FDA reports)
NEPHRITIS INTERSTITIAL ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEUROGENIC SHOCK ( 10 FDA reports)
NIPPLE PAIN ( 10 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 10 FDA reports)
OESOPHAGEAL INFECTION ( 10 FDA reports)
OVARIAN ADHESION ( 10 FDA reports)
PANCREATIC ENZYMES INCREASED ( 10 FDA reports)
PANCREATITIS RELAPSING ( 10 FDA reports)
PAPULE ( 10 FDA reports)
PARAPSORIASIS ( 10 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 10 FDA reports)
PELVIC ADHESIONS ( 10 FDA reports)
PENIS DISORDER ( 10 FDA reports)
PHARYNGEAL DISORDER ( 10 FDA reports)
PNEUMOPERITONEUM ( 10 FDA reports)
POST PROCEDURAL DIARRHOEA ( 10 FDA reports)
PREMENSTRUAL SYNDROME ( 10 FDA reports)
PREPUCE REDUNDANT ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PSYCHOLOGICAL TRAUMA ( 10 FDA reports)
PULMONARY ARTERY ATRESIA ( 10 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 10 FDA reports)
PULMONARY MALFORMATION ( 10 FDA reports)
RADICULAR CYST ( 10 FDA reports)
REHABILITATION THERAPY ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RESPIRATORY ACIDOSIS ( 10 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 10 FDA reports)
RETROGRADE EJACULATION ( 10 FDA reports)
SEBACEOUS GLAND DISORDER ( 10 FDA reports)
SEPTIC EMBOLUS ( 10 FDA reports)
SOFT TISSUE INFLAMMATION ( 10 FDA reports)
SPLEEN CONGESTION ( 10 FDA reports)
SPUTUM CULTURE POSITIVE ( 10 FDA reports)
SPUTUM INCREASED ( 10 FDA reports)
STATUS ASTHMATICUS ( 10 FDA reports)
STRABISMUS ( 10 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 10 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 10 FDA reports)
TOOTH RESORPTION ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VASCULAR GRAFT OCCLUSION ( 10 FDA reports)
VASCULAR INJURY ( 10 FDA reports)
VICTIM OF HOMICIDE ( 10 FDA reports)
WEIGHT ABNORMAL ( 10 FDA reports)
WOUND CLOSURE ( 10 FDA reports)
PRE-ECLAMPSIA ( 9 FDA reports)
PRINZMETAL ANGINA ( 9 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
QUADRIPARESIS ( 9 FDA reports)
REBOUND EFFECT ( 9 FDA reports)
REPETITIVE SPEECH ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SINUS ANTROSTOMY ( 9 FDA reports)
SKIN CHAPPED ( 9 FDA reports)
SMEAR CERVIX ABNORMAL ( 9 FDA reports)
SPHENOID SINUS OPERATION ( 9 FDA reports)
SPINAL CORD INJURY ( 9 FDA reports)
SPINAL CORD INJURY THORACIC ( 9 FDA reports)
SPLENECTOMY ( 9 FDA reports)
STAG HORN CALCULUS ( 9 FDA reports)
STERNAL FRACTURE ( 9 FDA reports)
STRESS ULCER ( 9 FDA reports)
STRIDOR ( 9 FDA reports)
SUFFOCATION FEELING ( 9 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 9 FDA reports)
TENDON SHEATH INCISION ( 9 FDA reports)
TONSILLAR DISORDER ( 9 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 9 FDA reports)
TUBERCULIN TEST POSITIVE ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 9 FDA reports)
URETHRAL CARUNCLE ( 9 FDA reports)
URETHRAL OBSTRUCTION ( 9 FDA reports)
UTERINE FIBROSIS ( 9 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 9 FDA reports)
VITAMIN B12 DECREASED ( 9 FDA reports)
VOLVULUS ( 9 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 9 FDA reports)
VULVOVAGINAL DISCOMFORT ( 9 FDA reports)
ACANTHOSIS ( 9 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 9 FDA reports)
AKINESIA ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANKYLOSING SPONDYLITIS ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
APPLICATION SITE PAIN ( 9 FDA reports)
AURA ( 9 FDA reports)
AUTOIMMUNE THYROIDITIS ( 9 FDA reports)
BENIGN GASTRIC NEOPLASM ( 9 FDA reports)
BICUSPID AORTIC VALVE ( 9 FDA reports)
BILE DUCT CANCER ( 9 FDA reports)
BILIARY TRACT DISORDER ( 9 FDA reports)
BLADDER TRABECULATION ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 9 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 9 FDA reports)
BONE FISTULA ( 9 FDA reports)
BRAIN MASS ( 9 FDA reports)
BREAST ABSCESS ( 9 FDA reports)
BURNING MOUTH SYNDROME ( 9 FDA reports)
CARDIAC VALVE VEGETATION ( 9 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATHETER SITE ERYTHEMA ( 9 FDA reports)
CHONDROPLASTY ( 9 FDA reports)
COLON CANCER METASTATIC ( 9 FDA reports)
COMPULSIONS ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CRANIOCEREBRAL INJURY ( 9 FDA reports)
CYSTITIS KLEBSIELLA ( 9 FDA reports)
CYSTOPEXY ( 9 FDA reports)
DELUSION OF GRANDEUR ( 9 FDA reports)
DENTAL PLAQUE ( 9 FDA reports)
DIARRHOEA INFECTIOUS ( 9 FDA reports)
DIPLEGIA ( 9 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
EAR PRURITUS ( 9 FDA reports)
EAR TUBE INSERTION ( 9 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 9 FDA reports)
ENEMA ADMINISTRATION ( 9 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 9 FDA reports)
ESCHERICHIA SEPSIS ( 9 FDA reports)
ETHMOID SINUS SURGERY ( 9 FDA reports)
EYE BURNS ( 9 FDA reports)
EYEBALL RUPTURE ( 9 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 9 FDA reports)
FAECES HARD ( 9 FDA reports)
FEMALE ORGASMIC DISORDER ( 9 FDA reports)
FOETAL HEART RATE DECREASED ( 9 FDA reports)
FOETAL MACROSOMIA ( 9 FDA reports)
FRONTAL SINUS OPERATION ( 9 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 9 FDA reports)
GASTROINTESTINAL PERFORATION ( 9 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HEAD BANGING ( 9 FDA reports)
HEPATIC NEOPLASM ( 9 FDA reports)
HEPATIC VEIN THROMBOSIS ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HORMONE LEVEL ABNORMAL ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 9 FDA reports)
HYPERTONIA ( 9 FDA reports)
HYPERURICAEMIA ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
ILLUSION ( 9 FDA reports)
IMPLANT SITE SWELLING ( 9 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 9 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 9 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 9 FDA reports)
LASER THERAPY ( 9 FDA reports)
LATEX ALLERGY ( 9 FDA reports)
LEIOMYOMA ( 9 FDA reports)
LIPOMA EXCISION ( 9 FDA reports)
LYMPHATIC DISORDER ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MAMMOGRAM ABNORMAL ( 9 FDA reports)
METABOLIC ALKALOSIS ( 9 FDA reports)
MIDDLE EAR EFFUSION ( 9 FDA reports)
MIGRAINE WITH AURA ( 9 FDA reports)
MUCOUS STOOLS ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 9 FDA reports)
NEONATAL TACHYPNOEA ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NEPHROGENIC ANAEMIA ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 9 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 9 FDA reports)
OSTEOMALACIA ( 9 FDA reports)
PARASOMNIA ( 9 FDA reports)
PELVIC VENOUS THROMBOSIS ( 9 FDA reports)
PERIOSTITIS ( 9 FDA reports)
PERITONEAL DIALYSIS ( 9 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 9 FDA reports)
PNEUMONIA KLEBSIELLA ( 9 FDA reports)
POLYCYTHAEMIA ( 9 FDA reports)
ACARODERMATITIS ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ADRENAL HAEMORRHAGE ( 8 FDA reports)
AMNESTIC DISORDER ( 8 FDA reports)
AMYLOIDOSIS ( 8 FDA reports)
ANAL SKIN TAGS ( 8 FDA reports)
ANEURYSM RUPTURED ( 8 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 8 FDA reports)
AORTIC ATHEROSCLEROSIS ( 8 FDA reports)
AORTIC THROMBOSIS ( 8 FDA reports)
APPENDICITIS PERFORATED ( 8 FDA reports)
ARTERIOVENOUS MALFORMATION ( 8 FDA reports)
ARTHROSCOPIC SURGERY ( 8 FDA reports)
BIOPSY LIVER ABNORMAL ( 8 FDA reports)
BLOOD CHOLESTEROL ( 8 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 8 FDA reports)
BLOOD OESTROGEN DECREASED ( 8 FDA reports)
BRAIN ABSCESS ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 8 FDA reports)
CARBON MONOXIDE POISONING ( 8 FDA reports)
CARDIAC PSEUDOANEURYSM ( 8 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 8 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 8 FDA reports)
CERVICAL SPINE FLATTENING ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 8 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 8 FDA reports)
DEAFNESS BILATERAL ( 8 FDA reports)
DENTOFACIAL ANOMALY ( 8 FDA reports)
DEVICE LEAKAGE ( 8 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 8 FDA reports)
DISSOCIATIVE DISORDER ( 8 FDA reports)
DREAMY STATE ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ECTOPIC PREGNANCY ( 8 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 8 FDA reports)
ENCEPHALITIS HERPES ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENCEPHALITIS VIRAL ( 8 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 8 FDA reports)
EUTHYROID SICK SYNDROME ( 8 FDA reports)
EXTRADURAL ABSCESS ( 8 FDA reports)
EYE OEDEMA ( 8 FDA reports)
FLASHBACK ( 8 FDA reports)
GAMBLING ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTRIC HYPOMOTILITY ( 8 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GENERAL SYMPTOM ( 8 FDA reports)
GLOBULINS INCREASED ( 8 FDA reports)
GRANDIOSITY ( 8 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 8 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 8 FDA reports)
HEMICEPHALALGIA ( 8 FDA reports)
HEPATITIS FULMINANT ( 8 FDA reports)
HEPATORENAL SYNDROME ( 8 FDA reports)
HYDROCELE ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
HYPERCHLORAEMIA ( 8 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 8 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 8 FDA reports)
HYPOCHROMASIA ( 8 FDA reports)
INFERTILITY ( 8 FDA reports)
INJECTION SITE ABSCESS ( 8 FDA reports)
INJECTION SITE CELLULITIS ( 8 FDA reports)
INJECTION SITE PAPULE ( 8 FDA reports)
IRON METABOLISM DISORDER ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LABILE HYPERTENSION ( 8 FDA reports)
LABORATORY TEST INTERFERENCE ( 8 FDA reports)
LIP BLISTER ( 8 FDA reports)
LIPOGRANULOMA ( 8 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 8 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 8 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 8 FDA reports)
MARROW HYPERPLASIA ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
MEAN CELL VOLUME DECREASED ( 8 FDA reports)
MEAN CELL VOLUME INCREASED ( 8 FDA reports)
METASTASES TO HEART ( 8 FDA reports)
METASTATIC CARCINOID TUMOUR ( 8 FDA reports)
MICROCYTOSIS ( 8 FDA reports)
MORPHOEA ( 8 FDA reports)
MUCOUS MEMBRANE DISORDER ( 8 FDA reports)
MUSCLE FATIGUE ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NAIL OPERATION ( 8 FDA reports)
NASAL SEPTUM PERFORATION ( 8 FDA reports)
NEOPLASM PROSTATE ( 8 FDA reports)
NEUTROPENIC INFECTION ( 8 FDA reports)
NIGHT BLINDNESS ( 8 FDA reports)
NODULE ON EXTREMITY ( 8 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
OESOPHAGEAL DILATATION ( 8 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 8 FDA reports)
OPPORTUNISTIC INFECTION ( 8 FDA reports)
ORGASM ABNORMAL ( 8 FDA reports)
OSTEOMYELITIS FUNGAL ( 8 FDA reports)
PAINFUL DEFAECATION ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 8 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 8 FDA reports)
PHOBIA ( 8 FDA reports)
PIGMENTATION DISORDER ( 8 FDA reports)
PLASTIC SURGERY TO THE FACE ( 8 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 8 FDA reports)
POST-TRAUMATIC HEADACHE ( 8 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 8 FDA reports)
POSTERIOR CAPSULOTOMY ( 8 FDA reports)
POSTOPERATIVE FEVER ( 8 FDA reports)
POSTPARTUM HAEMORRHAGE ( 8 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 8 FDA reports)
PRODUCT TASTE ABNORMAL ( 8 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 8 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
PYELONEPHRITIS ACUTE ( 8 FDA reports)
RADIATION NEUROPATHY ( 8 FDA reports)
RENAL CYST HAEMORRHAGE ( 8 FDA reports)
RESIDUAL URINE VOLUME ( 8 FDA reports)
RETINAL DISORDER ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SHORT-BOWEL SYNDROME ( 8 FDA reports)
SKELETAL SURVEY ABNORMAL ( 8 FDA reports)
SKIN MASS ( 8 FDA reports)
SMOKER ( 8 FDA reports)
SPINAL MYELOGRAM ( 8 FDA reports)
SPLENIC CYST ( 8 FDA reports)
STEATORRHOEA ( 8 FDA reports)
STENOTROPHOMONAS INFECTION ( 8 FDA reports)
SUBMANDIBULAR MASS ( 8 FDA reports)
TESTICULAR ATROPHY ( 8 FDA reports)
THEFT ( 8 FDA reports)
TONGUE BLISTERING ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TORTICOLLIS ( 8 FDA reports)
TRANSPLANT ( 8 FDA reports)
ULNAR NERVE INJURY ( 8 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 8 FDA reports)
VAGINAL EROSION ( 8 FDA reports)
VASCULAR BYPASS GRAFT ( 8 FDA reports)
VASCULAR DEMENTIA ( 8 FDA reports)
VASOSPASM ( 8 FDA reports)
VOCAL CORD PARESIS ( 8 FDA reports)
WHITE BLOOD CELL DISORDER ( 8 FDA reports)
POST POLIO SYNDROME ( 7 FDA reports)
POST PROCEDURAL PNEUMONIA ( 7 FDA reports)
PRIAPISM ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PROSTATECTOMY ( 7 FDA reports)
PULMONARY CALCIFICATION ( 7 FDA reports)
PULSE ABNORMAL ( 7 FDA reports)
RADIATION NECROSIS ( 7 FDA reports)
READING DISORDER ( 7 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
RENAL TRANSPLANT ( 7 FDA reports)
RENAL TUBULAR DISORDER ( 7 FDA reports)
SALIVA ALTERED ( 7 FDA reports)
SELF ESTEEM DECREASED ( 7 FDA reports)
SHOPLIFTING ( 7 FDA reports)
SIGMOIDECTOMY ( 7 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 7 FDA reports)
SKIN FRAGILITY ( 7 FDA reports)
SKIN OPERATION ( 7 FDA reports)
SPINAL CLAUDICATION ( 7 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SPLENIC RUPTURE ( 7 FDA reports)
STARVATION ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
SWEAT GLAND TUMOUR ( 7 FDA reports)
SYMBOLIC DYSFUNCTION ( 7 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 7 FDA reports)
THORACIC OPERATION ( 7 FDA reports)
THROAT LESION ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
THYROIDITIS CHRONIC ( 7 FDA reports)
TOOTH DISCOLOURATION ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 7 FDA reports)
TUMOUR HAEMORRHAGE ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
URETERIC OBSTRUCTION ( 7 FDA reports)
URINE ABNORMALITY ( 7 FDA reports)
VAGINAL ULCERATION ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VASCULAR RUPTURE ( 7 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 7 FDA reports)
VITAMIN K DEFICIENCY ( 7 FDA reports)
WRIST SURGERY ( 7 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 7 FDA reports)
ACTINOMYCES TEST POSITIVE ( 7 FDA reports)
ADNEXA UTERI CYST ( 7 FDA reports)
ALCOHOL INTERACTION ( 7 FDA reports)
ALCOHOLIC PANCREATITIS ( 7 FDA reports)
ALLERGIC SINUSITIS ( 7 FDA reports)
ALLERGY TO CHEMICALS ( 7 FDA reports)
ALOPECIA AREATA ( 7 FDA reports)
ANION GAP INCREASED ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
AORTIC VALVE REPLACEMENT ( 7 FDA reports)
APGAR SCORE LOW ( 7 FDA reports)
APPLICATION SITE SWELLING ( 7 FDA reports)
ARTERIAL STENOSIS ( 7 FDA reports)
ARTHRITIS BACTERIAL ( 7 FDA reports)
ASEPTIC NECROSIS BONE ( 7 FDA reports)
ASTERIXIS ( 7 FDA reports)
BACTERIAL TEST ( 7 FDA reports)
BENIGN BREAST NEOPLASM ( 7 FDA reports)
BILIARY CIRRHOSIS ( 7 FDA reports)
BIOPSY BONE MARROW ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD CORTISOL DECREASED ( 7 FDA reports)
BLOOD CREATININE ABNORMAL ( 7 FDA reports)
BLOOD MAGNESIUM INCREASED ( 7 FDA reports)
BLOOD PRESSURE ( 7 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 7 FDA reports)
BODY TINEA ( 7 FDA reports)
BONE CANCER METASTATIC ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 7 FDA reports)
BRACHIAL PLEXOPATHY ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
CANDIDA SEPSIS ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIAC PERFORATION ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CEREBRAL CALCIFICATION ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
CHOLESTEROL GRANULOMA ( 7 FDA reports)
COLONIC OBSTRUCTION ( 7 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 7 FDA reports)
CONJUNCTIVAL OEDEMA ( 7 FDA reports)
CORNEAL DEPOSITS ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CULTURE STOOL POSITIVE ( 7 FDA reports)
DENTAL NECROSIS ( 7 FDA reports)
DEVICE DISLOCATION ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DRUG ADDICT ( 7 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 7 FDA reports)
ENDOMETRIAL ATROPHY ( 7 FDA reports)
ENURESIS ( 7 FDA reports)
ESSENTIAL TREMOR ( 7 FDA reports)
EYE INFECTION VIRAL ( 7 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 7 FDA reports)
FEELING OF RELAXATION ( 7 FDA reports)
FEELINGS OF WORTHLESSNESS ( 7 FDA reports)
FINGER DEFORMITY ( 7 FDA reports)
FOREARM FRACTURE ( 7 FDA reports)
GASTRIC INFECTION ( 7 FDA reports)
GASTROENTERITIS SALMONELLA ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
GAZE PALSY ( 7 FDA reports)
GENITAL PRURITUS FEMALE ( 7 FDA reports)
GINGIVAL ATROPHY ( 7 FDA reports)
GLIOMA ( 7 FDA reports)
GRAFT DYSFUNCTION ( 7 FDA reports)
GRANULOMA ANNULARE ( 7 FDA reports)
HAEMATOTOXICITY ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HEPATITIS ALCOHOLIC ( 7 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 7 FDA reports)
HOARSENESS ( 7 FDA reports)
HYPOPHOSPHATASIA ( 7 FDA reports)
HYPOPROTHROMBINAEMIA ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
IMPATIENCE ( 7 FDA reports)
INCISION SITE PAIN ( 7 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
INFUSION SITE REACTION ( 7 FDA reports)
INJECTION SITE INFECTION ( 7 FDA reports)
INJECTION SITE INFLAMMATION ( 7 FDA reports)
INJECTION SITE VESICLES ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 7 FDA reports)
KAWASAKI'S DISEASE ( 7 FDA reports)
LABIA ENLARGED ( 7 FDA reports)
LHERMITTE'S SIGN ( 7 FDA reports)
LIMB ASYMMETRY ( 7 FDA reports)
LIMB DEFORMITY ( 7 FDA reports)
LIPIDS INCREASED ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
LOSS OF CONTROL OF LEGS ( 7 FDA reports)
MACROCEPHALY ( 7 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
MENINGITIS BACTERIAL ( 7 FDA reports)
MENINGOMYELOCELE ( 7 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 7 FDA reports)
MITRAL VALVE ATRESIA ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
NIGHT CRAMPS ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
OCCIPITAL NEURALGIA ( 7 FDA reports)
OESOPHAGEAL ACHALASIA ( 7 FDA reports)
OPTIC ATROPHY ( 7 FDA reports)
ORCHITIS ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
PANCREATIC DUCT DILATATION ( 7 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 7 FDA reports)
PERIRECTAL ABSCESS ( 7 FDA reports)
PILOERECTION ( 7 FDA reports)
PO2 DECREASED ( 7 FDA reports)
POLYMENORRHOEA ( 7 FDA reports)
ABDOMINAL INJURY ( 6 FDA reports)
ABORTION THREATENED ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
AIR EMBOLISM ( 6 FDA reports)
ALOPECIA TOTALIS ( 6 FDA reports)
ALOPECIA UNIVERSALIS ( 6 FDA reports)
ANGIOMYOLIPOMA ( 6 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 6 FDA reports)
ANTIBODY TEST POSITIVE ( 6 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 6 FDA reports)
AORTIC BYPASS ( 6 FDA reports)
APHAKIA ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
APPLICATION SITE DERMATITIS ( 6 FDA reports)
ARTERIAL THROMBOSIS ( 6 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 6 FDA reports)
BLADDER CANCER RECURRENT ( 6 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 6 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 6 FDA reports)
BLOOD LACTIC ACID INCREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 6 FDA reports)
BLUNTED AFFECT ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BRAIN CANCER METASTATIC ( 6 FDA reports)
BREAST DISORDER ( 6 FDA reports)
BREAST FIBROSIS ( 6 FDA reports)
BREECH PRESENTATION ( 6 FDA reports)
BULIMIA NERVOSA ( 6 FDA reports)
BURNS THIRD DEGREE ( 6 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 6 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 6 FDA reports)
CARDIORENAL SYNDROME ( 6 FDA reports)
CATHETERISATION VENOUS ( 6 FDA reports)
CELLULITIS ORBITAL ( 6 FDA reports)
CENTRAL OBESITY ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CERVIX INFLAMMATION ( 6 FDA reports)
CHEMOTHERAPY ( 6 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
COLONIC STENOSIS ( 6 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 6 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 6 FDA reports)
CYTOGENETIC ABNORMALITY ( 6 FDA reports)
DERMATITIS ALLERGIC ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DEVICE INTERACTION ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DRUG TOLERANCE DECREASED ( 6 FDA reports)
DUPUYTREN'S CONTRACTURE ( 6 FDA reports)
DYSKINESIA OESOPHAGEAL ( 6 FDA reports)
DYSMORPHISM ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
EARLY MORNING AWAKENING ( 6 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 6 FDA reports)
ENDOCRINE DISORDER ( 6 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 6 FDA reports)
ESCHERICHIA TEST POSITIVE ( 6 FDA reports)
EUSTACHIAN TUBE DISORDER ( 6 FDA reports)
EXOMPHALOS ( 6 FDA reports)
EXTRADURAL HAEMATOMA ( 6 FDA reports)
EYE INFLAMMATION ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FALLOPIAN TUBE DISORDER ( 6 FDA reports)
FALLOPIAN TUBE OPERATION ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
GASTRIC VARICES ( 6 FDA reports)
GASTROINTESTINAL CARCINOMA ( 6 FDA reports)
GASTROINTESTINAL INJURY ( 6 FDA reports)
GASTROINTESTINAL OEDEMA ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GENITAL ULCERATION ( 6 FDA reports)
GLIOBLASTOMA MULTIFORME ( 6 FDA reports)
GRAFT INFECTION ( 6 FDA reports)
GRANULOCYTES MATURATION ARREST ( 6 FDA reports)
HAEMANGIOMA OF SKIN ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HEAT RASH ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATIC CANCER METASTATIC ( 6 FDA reports)
HIDRADENITIS ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
HOSPICE CARE ( 6 FDA reports)
HYPERCAPNIA ( 6 FDA reports)
HYPERKINETIC HEART SYNDROME ( 6 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 6 FDA reports)
HYPERTHERMIA MALIGNANT ( 6 FDA reports)
IMMUNOGLOBULINS INCREASED ( 6 FDA reports)
IMPAIRED FASTING GLUCOSE ( 6 FDA reports)
IMPLANT SITE INDURATION ( 6 FDA reports)
IMPLANT SITE REACTION ( 6 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 6 FDA reports)
INSULIN RESISTANCE ( 6 FDA reports)
IRON OVERLOAD ( 6 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
KLEBSIELLA BACTERAEMIA ( 6 FDA reports)
LEARNING DISORDER ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LEFT VENTRICULAR FAILURE ( 6 FDA reports)
LIGAMENT DISORDER ( 6 FDA reports)
LIMB MALFORMATION ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LIP DISORDER ( 6 FDA reports)
LIPOMATOSIS ( 6 FDA reports)
LOOSE STOOLS ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 6 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MACULOPATHY ( 6 FDA reports)
MASTITIS ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MEDICAL DIET ( 6 FDA reports)
METASTASES TO BLADDER ( 6 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 6 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MYRINGOTOMY ( 6 FDA reports)
NAIL RIDGING ( 6 FDA reports)
NASAL OBSTRUCTION ( 6 FDA reports)
NASAL OEDEMA ( 6 FDA reports)
NASAL SEPTAL OPERATION ( 6 FDA reports)
NEONATAL ASPIRATION ( 6 FDA reports)
NEONATAL DISORDER ( 6 FDA reports)
NEURAL TUBE DEFECT ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NEUROMYELITIS OPTICA ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
NIPPLE DISORDER ( 6 FDA reports)
NO ADVERSE DRUG EFFECT ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 6 FDA reports)
OEDEMA GENITAL ( 6 FDA reports)
OPERATIVE HAEMORRHAGE ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
OROPHARYNGEAL SPASM ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OVARIAN ABSCESS ( 6 FDA reports)
OVARIAN LOW MALIGNANT POTENTIAL TUMOUR ( 6 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 6 FDA reports)
PANCREATIC DUCT STENOSIS ( 6 FDA reports)
PANNICULITIS ( 6 FDA reports)
PENILE PAIN ( 6 FDA reports)
PERICARDIAL CYST ( 6 FDA reports)
PERIDIVERTICULAR ABSCESS ( 6 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
PLATELET AGGREGATION INCREASED ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
PLEURAL ADHESION ( 6 FDA reports)
PLEURAL DISORDER ( 6 FDA reports)
POST PROCEDURAL DRAINAGE ( 6 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
PROCEDURAL SITE REACTION ( 6 FDA reports)
PROTEIN C INCREASED ( 6 FDA reports)
PSEUDOCYST ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
PULMONARY VEIN STENOSIS ( 6 FDA reports)
PULSE PRESSURE DECREASED ( 6 FDA reports)
RADIATION OESOPHAGITIS ( 6 FDA reports)
RECURRENT CANCER ( 6 FDA reports)
RELAPSING FEVER ( 6 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 6 FDA reports)
RENAL OSTEODYSTROPHY ( 6 FDA reports)
RESPIRATORY TRACT OEDEMA ( 6 FDA reports)
RETINAL DEGENERATION ( 6 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 6 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 6 FDA reports)
SEPTOPLASTY ( 6 FDA reports)
SERRATIA INFECTION ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SMALL INTESTINAL RESECTION ( 6 FDA reports)
SPLEEN SCAN ABNORMAL ( 6 FDA reports)
STILL'S DISEASE ADULT ONSET ( 6 FDA reports)
SUBRETINAL FIBROSIS ( 6 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 6 FDA reports)
SUDDEN ONSET OF SLEEP ( 6 FDA reports)
SUPRAPUBIC PAIN ( 6 FDA reports)
SURGICAL FAILURE ( 6 FDA reports)
SURGICAL PROCEDURE REPEATED ( 6 FDA reports)
SYSTEMIC CANDIDA ( 6 FDA reports)
TACHYARRHYTHMIA ( 6 FDA reports)
TAENIASIS ( 6 FDA reports)
TANGENTIALITY ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
THYROGLOBULIN INCREASED ( 6 FDA reports)
TINEA VERSICOLOUR ( 6 FDA reports)
TONGUE HAEMORRHAGE ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TOXOPLASMOSIS ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TRAUMATIC LIVER INJURY ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRISOMY 21 ( 6 FDA reports)
TROPONIN I INCREASED ( 6 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 6 FDA reports)
URAEMIC ENCEPHALOPATHY ( 6 FDA reports)
URINE OUTPUT INCREASED ( 6 FDA reports)
URTICARIA PAPULAR ( 6 FDA reports)
UTERINE MALPOSITION ( 6 FDA reports)
VENOUS STENOSIS ( 6 FDA reports)
VITREOUS DEGENERATION ( 6 FDA reports)
VULVAL DISORDER ( 6 FDA reports)
WEIGHT LOSS POOR ( 6 FDA reports)
WOUND NECROSIS ( 6 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 5 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 5 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
PSEUDARTHROSIS ( 5 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 5 FDA reports)
PULMONARY CAVITATION ( 5 FDA reports)
PULMONARY VALVE STENOSIS ( 5 FDA reports)
PYOGENIC GRANULOMA ( 5 FDA reports)
RADIATION PNEUMONITIS ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
RED BLOOD CELL MICROCYTES PRESENT ( 5 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
REFLEXES ABNORMAL ( 5 FDA reports)
REPERFUSION ARRHYTHMIA ( 5 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 5 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 5 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 5 FDA reports)
RESPIRATORY TRACT IRRITATION ( 5 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 5 FDA reports)
SALIVARY GLAND PAIN ( 5 FDA reports)
SALPINGITIS ( 5 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 5 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SERUM SEROTONIN DECREASED ( 5 FDA reports)
SHUNT INFECTION ( 5 FDA reports)
SHUNT OCCLUSION ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
SOMATIC DELUSION ( 5 FDA reports)
SOMATISATION DISORDER ( 5 FDA reports)
SPINAL CORD OPERATION ( 5 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
THYROID CANCER METASTATIC ( 5 FDA reports)
TIBIAL TORSION ( 5 FDA reports)
TONIC CLONIC MOVEMENTS ( 5 FDA reports)
TONSILLAR HYPERTROPHY ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TRAUMATIC ULCER ( 5 FDA reports)
TRENDELENBURG'S SYMPTOM ( 5 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 5 FDA reports)
TUMOUR EXCISION ( 5 FDA reports)
UMBILICAL CORD AROUND NECK ( 5 FDA reports)
UMBILICAL HERNIA REPAIR ( 5 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 5 FDA reports)
URETERAL STENT INSERTION ( 5 FDA reports)
URETHRAL DILATATION ( 5 FDA reports)
URETHRAL FISTULA ( 5 FDA reports)
URETHRAL STRICTURE ( 5 FDA reports)
URINARY TRACT OPERATION ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VAGINAL SWELLING ( 5 FDA reports)
VARICOPHLEBITIS ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VENOUS BRUIT ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VERTEBRAL INJURY ( 5 FDA reports)
VIRAL LABYRINTHITIS ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 5 FDA reports)
VULVOVAGINAL PAIN ( 5 FDA reports)
WOUND INFECTION BACTERIAL ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
ABDOMINAL HAEMATOMA ( 5 FDA reports)
ABORTION ( 5 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 5 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 5 FDA reports)
AEROPHAGIA ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANDROGENS DECREASED ( 5 FDA reports)
ANION GAP DECREASED ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 5 FDA reports)
APPLICATION SITE VESICLES ( 5 FDA reports)
ARACHNOIDITIS ( 5 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ATRIAL THROMBOSIS ( 5 FDA reports)
BACTERIURIA ( 5 FDA reports)
BACTEROIDES TEST POSITIVE ( 5 FDA reports)
BEHCET'S SYNDROME ( 5 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 5 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 5 FDA reports)
BIOPSY BREAST ( 5 FDA reports)
BLADDER DILATATION ( 5 FDA reports)
BLAST CELL COUNT INCREASED ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BLOOD OESTROGEN INCREASED ( 5 FDA reports)
BONE DENSITOMETRY ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BOTULISM ( 5 FDA reports)
BRAIN MIDLINE SHIFT ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BREAST MICROCALCIFICATION ( 5 FDA reports)
BURN DRESSING ( 5 FDA reports)
CALCIUM DEFICIENCY ( 5 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 5 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 5 FDA reports)
CATHETER SITE CELLULITIS ( 5 FDA reports)
CHILD ABUSE ( 5 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 5 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 5 FDA reports)
CONGENITAL HIP DEFORMITY ( 5 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 5 FDA reports)
CRANIOSYNOSTOSIS ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 5 FDA reports)
DELIRIUM TREMENS ( 5 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELUSIONS ( 5 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 5 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 5 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DISEASE COMPLICATION ( 5 FDA reports)
DISLOCATION OF VERTEBRA ( 5 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSLEXIA ( 5 FDA reports)
DYSTROPHIC CALCIFICATION ( 5 FDA reports)
EJACULATION DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
ELECTROCONVULSIVE THERAPY ( 5 FDA reports)
ENTEROVESICAL FISTULA ( 5 FDA reports)
EPIDERMAL NECROSIS ( 5 FDA reports)
EPISCLERITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXPLORATORY OPERATION ( 5 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 5 FDA reports)
EXTRAVASATION ( 5 FDA reports)
EYE PENETRATION ( 5 FDA reports)
EYELID PTOSIS CONGENITAL ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FEMORAL ANTEVERSION ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FUNGAL RASH ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GENITAL PAIN ( 5 FDA reports)
GIARDIASIS ( 5 FDA reports)
GINGIVAL BLISTER ( 5 FDA reports)
GINGIVAL HYPERTROPHY ( 5 FDA reports)
GLIOBLASTOMA ( 5 FDA reports)
GRUNTING ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMATOSPERMIA ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMORRHAGE URINARY TRACT ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEPATECTOMY ( 5 FDA reports)
HEPATITIS A ( 5 FDA reports)
HEPATITIS VIRAL ( 5 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPEROSMOLAR STATE ( 5 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 5 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 5 FDA reports)
HYPOVITAMINOSIS ( 5 FDA reports)
IMPINGEMENT SYNDROME ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 5 FDA reports)
INDIFFERENCE ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE INFECTION ( 5 FDA reports)
INGROWN HAIR ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 5 FDA reports)
INTERVERTEBRAL DISCITIS ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 5 FDA reports)
IODINE ALLERGY ( 5 FDA reports)
JOINT INJECTION ( 5 FDA reports)
KERATITIS INTERSTITIAL ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
KLEBSIELLA SEPSIS ( 5 FDA reports)
LACTOBACILLUS INFECTION ( 5 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 5 FDA reports)
LARYNGEAL DISORDER ( 5 FDA reports)
LATENT TUBERCULOSIS ( 5 FDA reports)
LEARNING DISABILITY ( 5 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 5 FDA reports)
MACULAR HOLE ( 5 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 5 FDA reports)
MENSTRUAL DISORDER ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
METASTASES TO OVARY ( 5 FDA reports)
METASTASES TO RETROPERITONEUM ( 5 FDA reports)
MITRAL VALVE REPLACEMENT ( 5 FDA reports)
MIXED DEAFNESS ( 5 FDA reports)
MOANING ( 5 FDA reports)
MOEBIUS II SYNDROME ( 5 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
MUSCLE ABSCESS ( 5 FDA reports)
MUSCLE RUPTURE ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYELOMALACIA ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
NAIL DISCOLOURATION ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEUTROPENIC COLITIS ( 5 FDA reports)
NO ADVERSE EFFECT ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 5 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 5 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
ORCHIDECTOMY ( 5 FDA reports)
OSTEOGENESIS IMPERFECTA ( 5 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 5 FDA reports)
PANCREATITIS NECROTISING ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
PERITONEAL HAEMORRHAGE ( 5 FDA reports)
PERTUSSIS ( 5 FDA reports)
PHANTOM PAIN ( 5 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 5 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 5 FDA reports)
PHIMOSIS ( 5 FDA reports)
PLATELET TRANSFUSION ( 5 FDA reports)
PLEURODESIS ( 5 FDA reports)
PNEUMATOSIS ( 5 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 5 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABDOMINAL WALL CYST ( 4 FDA reports)
ABORTION MISSED ( 4 FDA reports)
ACID BASE BALANCE ABNORMAL ( 4 FDA reports)
ACNE CYSTIC ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ADACTYLY ( 4 FDA reports)
AGITATED DEPRESSION ( 4 FDA reports)
AKINAESTHESIA ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 4 FDA reports)
ALBUMIN URINE PRESENT ( 4 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 4 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 4 FDA reports)
ANAESTHETIC COMPLICATION ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APPLICATION SITE DRYNESS ( 4 FDA reports)
ARACHNOID CYST ( 4 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ATELECTASIS NEONATAL ( 4 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
AUTISM ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BASAL GANGLIA INFARCTION ( 4 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BIOPSY BREAST ABNORMAL ( 4 FDA reports)
BLADDER IRRITATION ( 4 FDA reports)
BLASTOCYSTIS INFECTION ( 4 FDA reports)
BLEEDING VARICOSE VEIN ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST CANCER STAGE II ( 4 FDA reports)
BREAST PROSTHESIS USER ( 4 FDA reports)
BRONCHIAL HYPERACTIVITY ( 4 FDA reports)
CALCULUS URETHRAL ( 4 FDA reports)
CARNITINE DECREASED ( 4 FDA reports)
CARNITINE DEFICIENCY ( 4 FDA reports)
CATHETER SITE DISCHARGE ( 4 FDA reports)
CAUSTIC INJURY ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CHRONIC HEPATIC FAILURE ( 4 FDA reports)
CLEFT LIP AND PALATE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
COAGULATION TEST ABNORMAL ( 4 FDA reports)
COLD AGGLUTININS ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
CONFABULATION ( 4 FDA reports)
CONGENITAL HAND MALFORMATION ( 4 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CORNEAL OEDEMA ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CORONARY BYPASS THROMBOSIS ( 4 FDA reports)
CORONARY OSTIAL STENOSIS ( 4 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CSF OLIGOCLONAL BAND PRESENT ( 4 FDA reports)
CSF PROTEIN INCREASED ( 4 FDA reports)
CYCLOTHYMIC DISORDER ( 4 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 4 FDA reports)
DACRYOCYSTORHINOSTOMY ( 4 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 4 FDA reports)
DEVICE COMPONENT ISSUE ( 4 FDA reports)
DEVICE MIGRATION ( 4 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 4 FDA reports)
DIABETIC VASCULAR DISORDER ( 4 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 4 FDA reports)
DISTRACTIBILITY ( 4 FDA reports)
DRUG EFFECT PROLONGED ( 4 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 4 FDA reports)
EATING DISORDER SYMPTOM ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 4 FDA reports)
EMPTY SELLA SYNDROME ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EXPLORATIVE LAPAROTOMY ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
FACIAL WASTING ( 4 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 4 FDA reports)
FEBRILE INFECTION ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FEMALE GENITAL OPERATION ( 4 FDA reports)
FOETAL HEART RATE ABNORMAL ( 4 FDA reports)
FOETAL HEART RATE DECELERATION ( 4 FDA reports)
FRACTURED COCCYX ( 4 FDA reports)
GANGLION ( 4 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROENTERITIS HELICOBACTER ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
HAEMOGLOBIN ABNORMAL ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEART VALVE REPLACEMENT ( 4 FDA reports)
HEPATIC INFARCTION ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
HYPERVIGILANCE ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
HYPOCOMPLEMENTAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
HYPOSPADIAS ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
ILEOSTOMY ( 4 FDA reports)
IMMUNOGLOBULINS DECREASED ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
IMPLANT SITE EFFUSION ( 4 FDA reports)
INCISION SITE HAEMATOMA ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCORRECT PRODUCT STORAGE ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INFUSION SITE RASH ( 4 FDA reports)
INJECTION SITE OEDEMA ( 4 FDA reports)
INTESTINAL FISTULA ( 4 FDA reports)
INTESTINAL OPERATION ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 4 FDA reports)
IRIS ADHESIONS ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 4 FDA reports)
IUCD COMPLICATION ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
KUSSMAUL RESPIRATION ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LACRIMAL DUCT PROCEDURE ( 4 FDA reports)
LACRIMATION DECREASED ( 4 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LIBIDO DISORDER ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 4 FDA reports)
LYMPH NODE TUBERCULOSIS ( 4 FDA reports)
MACROSOMIA ( 4 FDA reports)
MALIGNANT TUMOUR EXCISION ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MEDICAL DEVICE PAIN ( 4 FDA reports)
MENOMETRORRHAGIA ( 4 FDA reports)
METAMORPHOPSIA ( 4 FDA reports)
MONARTHRITIS ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONONEURITIS ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 4 FDA reports)
MURDER ( 4 FDA reports)
MUSCLE ENZYME INCREASED ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
MYOPATHY STEROID ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NEONATAL TACHYCARDIA ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OCULAR VASCULAR DISORDER ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 4 FDA reports)
OESOPHAGEAL DISCOMFORT ( 4 FDA reports)
OESOPHAGEAL OPERATION ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
ONYCHOPHAGIA ( 4 FDA reports)
ORAL PRURITUS ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
ORTHOSTATIC HYPERTENSION ( 4 FDA reports)
OSTEOARTHROPATHY ( 4 FDA reports)
OVARIAN NEOPLASM ( 4 FDA reports)
OVULATION PAIN ( 4 FDA reports)
PARACENTESIS ABDOMEN ( 4 FDA reports)
PARAKERATOSIS ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PERFORATED ULCER ( 4 FDA reports)
PERICARDIAL FIBROSIS ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PHAGOPHOBIA ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 4 FDA reports)
PHARYNGEAL MASS ( 4 FDA reports)
PHLEBOLITH ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PLACENTA PRAEVIA ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
PNEUMONIA HAEMOPHILUS ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
POIKILOCYTOSIS ( 4 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
POST PROCEDURAL CONSTIPATION ( 4 FDA reports)
POSTPARTUM DISORDER ( 4 FDA reports)
POTENTIATING DRUG INTERACTION ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PULMONARY ARTERY STENOSIS ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PYROMANIA ( 4 FDA reports)
RADIATION FIBROSIS ( 4 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 4 FDA reports)
REACTION TO PRESERVATIVES ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RENAL TUMOUR EXCISION ( 4 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 4 FDA reports)
RETROGRADE AMNESIA ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
RHYTHM IDIOVENTRICULAR ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SEPSIS NEONATAL ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SINUS PAIN ( 4 FDA reports)
SINUSITIS FUNGAL ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SKIN GRAFT FAILURE ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SLOW SPEECH ( 4 FDA reports)
SOMATOFORM DISORDER ( 4 FDA reports)
SPLENIC HAEMORRHAGE ( 4 FDA reports)
SPLINTER HAEMORRHAGES ( 4 FDA reports)
SPONTANEOUS PENILE ERECTION ( 4 FDA reports)
STOOL ANALYSIS ABNORMAL ( 4 FDA reports)
STRESS AT WORK ( 4 FDA reports)
SUPERFICIAL INJURY OF EYE ( 4 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 4 FDA reports)
SUTURE INSERTION ( 4 FDA reports)
SWEAT GLAND INFECTION ( 4 FDA reports)
SYSTOLIC HYPERTENSION ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
TEMPORAL LOBE EPILEPSY ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
THYROTOXIC CRISIS ( 4 FDA reports)
TINEA CAPITIS ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TRAUMATIC ARTHROPATHY ( 4 FDA reports)
TRAUMATIC FRACTURE ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URETHRAL STENT INSERTION ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT PAIN ( 4 FDA reports)
UTERINE ATONY ( 4 FDA reports)
UTERINE ATROPHY ( 4 FDA reports)
UTERINE CYST ( 4 FDA reports)
UTERINE DILATION AND CURETTAGE ( 4 FDA reports)
UTERINE NEOPLASM ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VASCULAR INSUFFICIENCY ( 4 FDA reports)
VASCULITIS CEREBRAL ( 4 FDA reports)
VASODILATATION ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 4 FDA reports)
VICTIM OF ABUSE ( 4 FDA reports)
VIRAL LOAD INCREASED ( 4 FDA reports)
VISCERAL CONGESTION ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
VITAMIN D ABNORMAL ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WEIGHT ( 4 FDA reports)
WHITE BLOOD CELL COUNT ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POST PROCEDURAL OEDEMA ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POSTOPERATIVE HERNIA ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 3 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 3 FDA reports)
PRODUCT PACKAGING ISSUE ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATE INFECTION ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 3 FDA reports)
PSEUDOPHAKIA ( 3 FDA reports)
PTERYGIUM ( 3 FDA reports)
PUBIC PAIN ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY BULLA ( 3 FDA reports)
PUNCTATE KERATITIS ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RADICULITIS CERVICAL ( 3 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETICULOCYTOSIS ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCAN LYMPH NODES ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SICKLE CELL TRAIT ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOCIAL FEAR ( 3 FDA reports)
SPHEROCYTIC ANAEMIA ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPINAL CORD NEOPLASM ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUDDEN VISUAL LOSS ( 3 FDA reports)
SUTURE RELATED COMPLICATION ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
TACHYCARDIA FOETAL ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 3 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYMOMA ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TONGUE ERUPTION ( 3 FDA reports)
TOXIC OPTIC NEUROPATHY ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 3 FDA reports)
TRICHOTILLOMANIA ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
ULNAR NERVE PALSY ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER EXTREMITY MASS ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINE KETONE BODY ( 3 FDA reports)
UROBILINOGEN URINE INCREASED ( 3 FDA reports)
VAGINAL LESION ( 3 FDA reports)
VAGINAL ODOUR ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 3 FDA reports)
VITAL CAPACITY DECREASED ( 3 FDA reports)
VITAMIN A DEFICIENCY ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
WEANING FAILURE ( 3 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 3 FDA reports)
WHOLE BLOOD TRANSFUSION ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 3 FDA reports)
ZINC DEFICIENCY ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ACETONAEMIA ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE CHEST SYNDROME ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
ALCOHOL INTOLERANCE ( 3 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANALGESIC EFFECT ( 3 FDA reports)
ANALGESIC INTERVENTION SUPPORTIVE THERAPY ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC VALVE DISEASE MIXED ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE EROSION ( 3 FDA reports)
APPLICATION SITE EXFOLIATION ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 3 FDA reports)
ASTHMA EXERCISE INDUCED ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
B-CELL LYMPHOMA STAGE III ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BENIGN BONE NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BILIARY FIBROSIS ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BIOPSY STOMACH ( 3 FDA reports)
BIRTH TRAUMA ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLINDNESS TRAUMATIC ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE DECREASED ( 3 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BONE FORMATION INCREASED ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BREAST COSMETIC SURGERY ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
BRONCHIAL NEOPLASM ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BURGLARY VICTIM ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 3 FDA reports)
CARDIAC DISCOMFORT ( 3 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CARDIAC SEPTAL DEFECT ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CARDIOLIPIN ANTIBODY ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID ARTERY DISSECTION ( 3 FDA reports)
CAROTID ENDARTERECTOMY ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 3 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 3 FDA reports)
CHEST WALL CYST ( 3 FDA reports)
CHEST WALL NECROSIS ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
CNS VENTRICULITIS ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CONDUCTIVE DEAFNESS ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
COR TRIATRIATUM ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CYST REMOVAL ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DIABETIC GASTROPATHY ( 3 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 3 FDA reports)
DIVORCED ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 3 FDA reports)
DRESSLER'S SYNDROME ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DRY GANGRENE ( 3 FDA reports)
DRY SOCKET ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DURAL TEAR ( 3 FDA reports)
EDUCATIONAL PROBLEM ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
ELEVATED MOOD ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
ENCHONDROMATOSIS ( 3 FDA reports)
ENDOMETRIAL DISORDER ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 3 FDA reports)
EXTRASKELETAL OSSIFICATION ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 3 FDA reports)
FIBROADENOMA OF BREAST ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
FUNGAL TEST POSITIVE ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GENITAL DISORDER MALE ( 3 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 3 FDA reports)
GERSTMANN'S SYNDROME ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GINGIVAL PRURITUS ( 3 FDA reports)
GLOBULIN ABNORMAL ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HAIRY CELL LEUKAEMIA ( 3 FDA reports)
HEART AND LUNG TRANSPLANT ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HELLP SYNDROME ( 3 FDA reports)
HEMIANOPIA HETERONYMOUS ( 3 FDA reports)
HEPATIC ARTERY OCCLUSION ( 3 FDA reports)
HEPATIC ATROPHY ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HYALOSIS ASTEROID ( 3 FDA reports)
HYPERADRENALISM ( 3 FDA reports)
HYPEREMESIS GRAVIDARUM ( 3 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 3 FDA reports)
HYPERTROPHY BREAST ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
IMPLANT SITE EROSION ( 3 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFUSION SITE EROSION ( 3 FDA reports)
INFUSION SITE INFLAMMATION ( 3 FDA reports)
INFUSION SITE MASS ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTESTINAL GANGRENE ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JOB DISSATISFACTION ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KNEE MENISCECTOMY ( 3 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 3 FDA reports)
LESION EXCISION ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LOOSE ASSOCIATIONS ( 3 FDA reports)
LOW BIRTH WEIGHT BABY ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LYMPH NODE CANCER METASTATIC ( 3 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MASTOID DISORDER ( 3 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 3 FDA reports)
MENINGOCELE ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
MESOTHELIOMA MALIGNANT ( 3 FDA reports)
METASTASES TO CHEST WALL ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MIGRAINE WITHOUT AURA ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 3 FDA reports)
MURPHY'S SIGN POSITIVE ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NEEDLE ISSUE ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NEUTRALISING ANTIBODIES ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIA ( 3 FDA reports)
NORMAL DELIVERY ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OBTURATOR HERNIA ( 3 FDA reports)
OPEN FRACTURE ( 3 FDA reports)
OPIATES POSITIVE ( 3 FDA reports)
OPTIC DISC HAEMORRHAGE ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OVARIAN GRANULOSA-THECA CELL TUMOUR ( 3 FDA reports)
PACEMAKER GENERATED RHYTHM ( 3 FDA reports)
PANCREAS DIVISUM ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 3 FDA reports)
PELVIC DISCOMFORT ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PERFORATION BILE DUCT ( 3 FDA reports)
PERINEPHRIC COLLECTION ( 3 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 3 FDA reports)
PHLEBOTHROMBOSIS ( 3 FDA reports)
PINEAL GLAND CYST ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
PNEUMOPERICARDIUM ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 2 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO ( 2 FDA reports)
ALCOHOL DETOXIFICATION ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANISOMETROPIA ( 2 FDA reports)
ANKLE RECONSTRUCTION ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTITHROMBIN III INCREASED ( 2 FDA reports)
AORTIC VALVE ATRESIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE PAPULES ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTICULAR DISC DISORDER ( 2 FDA reports)
ASPIRATION BIOPSY ( 2 FDA reports)
ASPIRATION JOINT ABNORMAL ( 2 FDA reports)
ASPIRATION TRACHEAL ( 2 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
AVERSION ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BASE EXCESS POSITIVE ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 2 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN VAGINAL NEOPLASM ( 2 FDA reports)
BEREAVEMENT ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BILIARY ADENOMA ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BIOPSY ENDOMETRIUM ( 2 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER DYSPLASIA ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLAST CELLS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD SODIUM ( 2 FDA reports)
BLOOD STEM CELL HARVEST ( 2 FDA reports)
BODY DYSMORPHIC DISORDER ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BOREDOM ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BREAST CANCER STAGE IV ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST INFLAMMATION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BRUCELLOSIS ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
BURNS FIRST DEGREE ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
CALCIUM METABOLISM DISORDER ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CAPSULE PHYSICAL ISSUE ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CENTRAL PAIN SYNDROME ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLESTASIS OF PREGNANCY ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHOROIDITIS ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CHRONIC TONSILLITIS ( 2 FDA reports)
CLOSED FRACTURE MANIPULATION ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONGENITAL BLADDER ANOMALY ( 2 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 2 FDA reports)
CONJUNCTIVAL NEOPLASM ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRUSH SYNDROME ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CSF CULTURE POSITIVE ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 2 FDA reports)
DACTYLITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DELAYED FONTANELLE CLOSURE ( 2 FDA reports)
DEPENDENT RUBOR ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DEVICE ADHESION ISSUE ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DEVICE PACING ISSUE ( 2 FDA reports)
DIABETIC BLINDNESS ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
DIGEORGE'S SYNDROME ( 2 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EAR MALFORMATION ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECTOPIC KIDNEY ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELDERLY ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENCOPRESIS ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOCARDITIS VIRAL ( 2 FDA reports)
ENDOVENOUS ABLATION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EX-SMOKER ( 2 FDA reports)
EXHIBITIONISM ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTERNAL EAR CELLULITIS ( 2 FDA reports)
EXTERNAL EAR INFLAMMATION ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FALLOPIAN TUBE CANCER ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FORAMINOTOMY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FRACTURE REDUCTION ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC VOLVULUS ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 2 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GINGIVAL INJURY ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
GROSS MOTOR DELAY ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEARING DISABILITY ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEAT EXHAUSTION ( 2 FDA reports)
HEAT OEDEMA ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 2 FDA reports)
HERMAPHRODITISM ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HIV TEST POSITIVE ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERCALCIURIA ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPOAESTHESIA TEETH ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOMETABOLISM ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILEOSTOMY CLOSURE ( 2 FDA reports)
IMPACTED FRACTURE ( 2 FDA reports)
IMPLANT SITE ERYTHEMA ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFERIOR VENA CAVA DILATATION ( 2 FDA reports)
INFERTILITY MALE ( 2 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTERMEDIATE DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE REMOVAL ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
INTUBATION COMPLICATION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
JEJUNAL ULCER PERFORATION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOINT ADHESION ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
KERATOSIS PILARIS ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
LABOUR INDUCTION ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LAXATIVE ABUSE ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LICE INFESTATION ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIPOSUCTION ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LUDWIG ANGINA ( 2 FDA reports)
LUMBAR HERNIA ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR ISCHAEMIA ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL DUCT ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MARFAN'S SYNDROME ( 2 FDA reports)
MASTOPTOSIS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
MENINGITIS HERPES ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
METASTASES TO BREAST ( 2 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROPENIS ( 2 FDA reports)
MILK ALLERGY ( 2 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYOFASCIAL SPASM ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
NAIL BED DISORDER ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NEURILEMMOMA BENIGN ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NUCLEATED RED CELLS ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR CANCER METASTATIC ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OLFACTORY NERVE DISORDER ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOCHONDRITIS ( 2 FDA reports)
OTITIS MEDIA VIRAL ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN CANCER STAGE I ( 2 FDA reports)
OVARIAN RUPTURE ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAEDOPHILIA ( 2 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PAROPHTHALMIA ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC PROLAPSE ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERINEAL LACERATION ( 2 FDA reports)
PERINEAL OPERATION ( 2 FDA reports)
PERINEURIAL CYST ( 2 FDA reports)
PERIORBITAL CELLULITIS ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PH BODY FLUID DECREASED ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL DYSKINESIA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHYSICAL ABUSE ( 2 FDA reports)
PILONIDAL CYST CONGENITAL ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
PORENCEPHALY ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PRESCRIPTION FORM TAMPERING ( 2 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROLACTINOMA ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
RADIAL TUNNEL SYNDROME ( 2 FDA reports)
RADIATION ASSOCIATED PAIN ( 2 FDA reports)
RAOULTELLA TEST POSITIVE ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL PROLAPSE REPAIR ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 2 FDA reports)
REGRESSIVE BEHAVIOUR ( 2 FDA reports)
REITER'S SYNDROME ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 2 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SALPINGOSTOMY ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SECONDARY HYPERTHYROIDISM ( 2 FDA reports)
SEIZURE LIKE PHENOMENA ( 2 FDA reports)
SENSORY GANGLIONITIS ( 2 FDA reports)
SEXUAL ACTIVITY INCREASED ( 2 FDA reports)
SHARED PSYCHOTIC DISORDER ( 2 FDA reports)
SIALOMETAPLASIA ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SKELETON DYSPLASIA ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SMALL CELL CARCINOMA ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE NEOPLASM ( 2 FDA reports)
SOLAR ELASTOSIS ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPINA BIFIDA OCCULTA ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STIFF-MAN SYNDROME ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBDURAL EFFUSION ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SYRINGE ISSUE ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TESTICULAR CYST ( 2 FDA reports)
TESTIS DISCOMFORT ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOEMBOLIC STROKE ( 2 FDA reports)
THYMUS DISORDER ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRANSVERSE PRESENTATION ( 2 FDA reports)
TRAUMATIC SHOCK ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TUBAL RUPTURE ( 2 FDA reports)
TUBEROUS SCLEROSIS ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 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 STENOSIS ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
UROGENITAL DISORDER ( 2 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL FISTULA ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINITIS ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASODILATION PROCEDURE ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VEIN WALL HYPERTROPHY ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VERBIGERATION ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VESTIBULOPLASTY ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN B1 DEFICIENCY ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
XANTHOCHROMIA ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
PORTAL TRIADITIS ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRIMARY HYPOGONADISM ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOLOGICAL ABUSE ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RABIES ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RADIOTHERAPY TO THROAT ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM GASTROINTESTINAL TRACT ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL VENOUS CONGESTION ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEBACEOUS ADENOMA ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBACEOUS HYPERPLASIA ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN LIQUEFACTION ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPIGELIAN HERNIA ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
ST. LOUIS ENCEPHALITIS ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT EMBOLISATION ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUBSTANCE ABUSER ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUICIDE OF RELATIVE ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SYMPATHECTOMY ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYNOVIAL SARCOMA METASTATIC ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST DECREASED ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TERTIARY SYPHILIS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TETANUS IMMUNISATION ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THORACOSTOMY ( 1 FDA reports)
THOUGHT BROADCASTING ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROIDITIS ACUTE ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
TYRAMINE REACTION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ABNORMAL ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNINTENTIONAL MEDICAL DEVICE REMOVAL BY PATIENT ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERAL SPASM ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URETHRITIS CHLAMYDIAL ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE BARBITURATES INCREASED ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE VISCOSITY INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VAGINOPLASTY ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VIRAL TONSILLITIS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOGRANULOMA ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ABSCESS STERILE ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACQUIRED TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
ACRAL LENTIGINOUS MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL CANCER STAGE 0 ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANAPHYLAXIS TREATMENT ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANENCEPHALY ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM RETINA ABNORMAL ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANORECTAL AGENESIS ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANOVULATORY CYCLE ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTI-HBS ANTIBODY ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE MASS ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARACHNOPHOBIA ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM CORONARY NORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS MOENCKEBERG-TYPE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS VIRAL ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BANKRUPTCY ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF EYELID ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT CANCER RECURRENT ( 1 FDA reports)
BILE DUCT PRESSURE ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BRAIN NORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEPHAROPACHYNSIS ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALCOHOL ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD COPPER DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES NORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BORDERLINE MENTAL IMPAIRMENT ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST HYPOPLASIA ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 1 FDA reports)
BRONCHIAL CYST ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC IMAGING PROCEDURE ABNORMAL ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBRAL OEDEMA MANAGEMENT ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL VERTEBRA INJURY ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLESTATIC PRURITUS ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON DYSPLASIA ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE WOUND ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF PET ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DERMOID CYST OF OVARY ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DIABETES COMPLICATING PREGNANCY ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFUSE AXONAL INJURY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DIPHTHERIA IMMUNISATION ( 1 FDA reports)
DISORDER OF GLOBE ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL THERAPEUTIC ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
EAR CANAL STENOSIS ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EBSTEIN'S ANOMALY ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 1 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROLYTE SUBSTITUTION THERAPY ( 1 FDA reports)
ELECTRON RADIATION THERAPY TO PROSTATE ( 1 FDA reports)
EMOTIONAL POVERTY ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS POST VARICELLA ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EPIDIDYMAL TENDERNESS ( 1 FDA reports)
EPIDIDYMECTOMY ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE LUXATION ( 1 FDA reports)
EYEGLASSES THERAPY ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR VII DEFICIENCY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL FAT INCREASED ( 1 FDA reports)
FAILED TRIAL OF LABOUR ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALLOPIAN TUBE ABSCESS ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING TUBE INSERTION ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRONECTIN INCREASED ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETAL MALPRESENTATION ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FRONTAL SINUS OPERATIONS ( 1 FDA reports)
FULL BLOOD COUNT ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRANULOCYTE COUNT ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN S INCREASED ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A IMMUNISATION ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS B ANTIBODY ABNORMAL ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS POST TRANSFUSION ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN ANTI-MOUSE ANTIBODY POSITIVE ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTHYROIDISM POSTOPERATIVE ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEAL GANGRENE ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTIOUS DISEASE CARRIER ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE CYST ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE SCAR ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSTILLATION SITE FOREIGN BODY SENSATION ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL FISTULA INFECTION ( 1 FDA reports)
INTESTINAL FISTULA REPAIR ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STOMA SITE BLEEDING ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KERATOSIS OBTURANS ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGITIS VIRAL ( 1 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
LEUKAEMIC LYMPHOMA ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPASE URINE INCREASED ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER FUNCTION TEST NORMAL ( 1 FDA reports)
LIVER GRAFT LOSS ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOSS OF DREAMING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUMBOSACRAL PLEXUS INJURY ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MAGICAL THINKING ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MARCUS GUNN SYNDROME ( 1 FDA reports)
MASTOIDECTOMY ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MECONIUM INCREASED ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICATION DILUTION ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSE DELAYED ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE POLYMORPHISM ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL GROWTH CESSATION ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECK SURGERY ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING SPINAL CORD ABNORMAL ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL STENT INSERTION ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO DECREASED ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHODONTIC PROCEDURE ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PARACENTESIS EYE ABNORMAL ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL CYST ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIORBITAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL MEMBRANE FAILURE ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERONEAL NERVE INJURY ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERTUSSIS IMMUNISATION ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PHARMACOPHOBIA ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET FACTOR 4 ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use