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

FALL ( 9614 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 9166 FDA reports)
INFLUENZA LIKE ILLNESS ( 8823 FDA reports)
MULTIPLE SCLEROSIS ( 7132 FDA reports)
FATIGUE ( 6418 FDA reports)
GAIT DISTURBANCE ( 4635 FDA reports)
ASTHENIA ( 4623 FDA reports)
HEADACHE ( 4430 FDA reports)
PAIN ( 4390 FDA reports)
PNEUMONIA ( 4193 FDA reports)
DEPRESSION ( 3912 FDA reports)
URINARY TRACT INFECTION ( 3813 FDA reports)
CONDITION AGGRAVATED ( 3416 FDA reports)
PYREXIA ( 3381 FDA reports)
PAIN IN EXTREMITY ( 3233 FDA reports)
HYPOAESTHESIA ( 3214 FDA reports)
MEMORY IMPAIRMENT ( 3137 FDA reports)
MYOCARDIAL INFARCTION ( 3096 FDA reports)
BALANCE DISORDER ( 3057 FDA reports)
CONVULSION ( 2696 FDA reports)
HYPERTENSION ( 2689 FDA reports)
DEATH ( 2603 FDA reports)
MUSCLE SPASMS ( 2583 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2478 FDA reports)
BACK PAIN ( 2420 FDA reports)
VOMITING ( 2383 FDA reports)
NAUSEA ( 2337 FDA reports)
MUSCULAR WEAKNESS ( 2306 FDA reports)
TREMOR ( 2239 FDA reports)
DIZZINESS ( 2214 FDA reports)
ABASIA ( 2153 FDA reports)
INJECTION SITE PAIN ( 2122 FDA reports)
MOBILITY DECREASED ( 2052 FDA reports)
WEIGHT DECREASED ( 2045 FDA reports)
DYSPNOEA ( 2025 FDA reports)
ANXIETY ( 1982 FDA reports)
DEHYDRATION ( 1976 FDA reports)
ARTHRALGIA ( 1975 FDA reports)
INSOMNIA ( 1807 FDA reports)
STRESS ( 1780 FDA reports)
BREAST CANCER ( 1757 FDA reports)
CHILLS ( 1709 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1655 FDA reports)
OEDEMA PERIPHERAL ( 1583 FDA reports)
MALAISE ( 1573 FDA reports)
NASOPHARYNGITIS ( 1557 FDA reports)
DIARRHOEA ( 1538 FDA reports)
LOSS OF CONSCIOUSNESS ( 1528 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1517 FDA reports)
PARAESTHESIA ( 1494 FDA reports)
DRUG INEFFECTIVE ( 1471 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1465 FDA reports)
CHEST PAIN ( 1423 FDA reports)
THROMBOSIS ( 1415 FDA reports)
CYSTITIS ( 1307 FDA reports)
CONTUSION ( 1288 FDA reports)
COGNITIVE DISORDER ( 1257 FDA reports)
AMNESIA ( 1250 FDA reports)
BREAST CANCER FEMALE ( 1172 FDA reports)
FEELING ABNORMAL ( 1169 FDA reports)
WEIGHT INCREASED ( 1137 FDA reports)
ARTHRITIS ( 1136 FDA reports)
HIP FRACTURE ( 1125 FDA reports)
MIGRAINE ( 1104 FDA reports)
VISUAL IMPAIRMENT ( 1055 FDA reports)
DIABETES MELLITUS ( 1044 FDA reports)
CELLULITIS ( 1039 FDA reports)
VISION BLURRED ( 1025 FDA reports)
URINARY INCONTINENCE ( 1018 FDA reports)
CONFUSIONAL STATE ( 1015 FDA reports)
INFECTION ( 1006 FDA reports)
DECUBITUS ULCER ( 992 FDA reports)
INFLUENZA ( 988 FDA reports)
POST PROCEDURAL COMPLICATION ( 984 FDA reports)
ANKLE FRACTURE ( 972 FDA reports)
HYPOTENSION ( 972 FDA reports)
CORONARY ARTERY OCCLUSION ( 957 FDA reports)
COORDINATION ABNORMAL ( 930 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 930 FDA reports)
MYALGIA ( 925 FDA reports)
ANAEMIA ( 920 FDA reports)
BLOOD PRESSURE INCREASED ( 911 FDA reports)
STAPHYLOCOCCAL INFECTION ( 904 FDA reports)
NEPHROLITHIASIS ( 903 FDA reports)
OPTIC NEURITIS ( 886 FDA reports)
LOWER LIMB FRACTURE ( 882 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 869 FDA reports)
INJECTION SITE HAEMATOMA ( 864 FDA reports)
CHOLELITHIASIS ( 861 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 856 FDA reports)
SEPSIS ( 853 FDA reports)
HYPERSENSITIVITY ( 851 FDA reports)
HYSTERECTOMY ( 837 FDA reports)
MUSCLE SPASTICITY ( 836 FDA reports)
KNEE ARTHROPLASTY ( 822 FDA reports)
SPEECH DISORDER ( 805 FDA reports)
LOSS OF CONTROL OF LEGS ( 794 FDA reports)
CONSTIPATION ( 726 FDA reports)
CARDIAC DISORDER ( 725 FDA reports)
OSTEOARTHRITIS ( 724 FDA reports)
ASTHMA ( 722 FDA reports)
BLOOD POTASSIUM DECREASED ( 715 FDA reports)
SINUSITIS ( 715 FDA reports)
COUGH ( 711 FDA reports)
PRURITUS ( 710 FDA reports)
DYSSTASIA ( 709 FDA reports)
DIFFICULTY IN WALKING ( 700 FDA reports)
BRONCHITIS ( 692 FDA reports)
HEAD INJURY ( 687 FDA reports)
RENAL FAILURE ( 687 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 680 FDA reports)
HEART RATE INCREASED ( 677 FDA reports)
UPPER LIMB FRACTURE ( 659 FDA reports)
SYNCOPE ( 652 FDA reports)
ABDOMINAL PAIN UPPER ( 650 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 649 FDA reports)
DYSPHAGIA ( 648 FDA reports)
HAEMORRHAGE ( 644 FDA reports)
BURNING SENSATION ( 643 FDA reports)
DRUG HYPERSENSITIVITY ( 642 FDA reports)
PULMONARY EMBOLISM ( 634 FDA reports)
HEMIPARESIS ( 632 FDA reports)
SURGERY ( 623 FDA reports)
MUSCULOSKELETAL DISORDER ( 622 FDA reports)
BLOOD GLUCOSE INCREASED ( 621 FDA reports)
RASH ( 621 FDA reports)
HYPERHIDROSIS ( 614 FDA reports)
VERTIGO ( 611 FDA reports)
UTERINE LEIOMYOMA ( 609 FDA reports)
HEPATIC ENZYME INCREASED ( 602 FDA reports)
LUNG NEOPLASM MALIGNANT ( 600 FDA reports)
BLADDER DISORDER ( 592 FDA reports)
ARTHROPATHY ( 591 FDA reports)
COMA ( 584 FDA reports)
GENERAL SYMPTOM ( 579 FDA reports)
OSTEOPOROSIS ( 577 FDA reports)
DYSARTHRIA ( 568 FDA reports)
APHASIA ( 567 FDA reports)
INJECTION SITE ERYTHEMA ( 567 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 565 FDA reports)
KIDNEY INFECTION ( 562 FDA reports)
URTICARIA ( 542 FDA reports)
CORONARY ARTERY DISEASE ( 541 FDA reports)
PANCREATITIS ( 537 FDA reports)
VISUAL ACUITY REDUCED ( 537 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 529 FDA reports)
NECK PAIN ( 527 FDA reports)
HIP ARTHROPLASTY ( 526 FDA reports)
ALOPECIA ( 522 FDA reports)
ADVERSE DRUG REACTION ( 521 FDA reports)
DEEP VEIN THROMBOSIS ( 518 FDA reports)
ABORTION SPONTANEOUS ( 505 FDA reports)
NEOPLASM MALIGNANT ( 502 FDA reports)
CHEST DISCOMFORT ( 501 FDA reports)
COLON CANCER ( 501 FDA reports)
HERPES ZOSTER ( 497 FDA reports)
JOINT INJURY ( 495 FDA reports)
RIB FRACTURE ( 494 FDA reports)
FEMUR FRACTURE ( 491 FDA reports)
JOINT SWELLING ( 491 FDA reports)
URINARY RETENTION ( 489 FDA reports)
BLINDNESS ( 488 FDA reports)
FEELING COLD ( 487 FDA reports)
SOMNOLENCE ( 485 FDA reports)
PARALYSIS ( 483 FDA reports)
GASTROINTESTINAL DISORDER ( 482 FDA reports)
PROCEDURAL PAIN ( 481 FDA reports)
FEELING HOT ( 476 FDA reports)
GRAND MAL CONVULSION ( 475 FDA reports)
CARDIAC ARREST ( 474 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 472 FDA reports)
DECREASED APPETITE ( 469 FDA reports)
FOOT FRACTURE ( 469 FDA reports)
ABDOMINAL PAIN ( 463 FDA reports)
ATRIAL FIBRILLATION ( 459 FDA reports)
PALPITATIONS ( 453 FDA reports)
INTESTINAL OBSTRUCTION ( 452 FDA reports)
SCAR ( 451 FDA reports)
PERONEAL NERVE PALSY ( 436 FDA reports)
OVARIAN CYST ( 434 FDA reports)
TRIGEMINAL NEURALGIA ( 425 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 420 FDA reports)
DEPRESSED MOOD ( 420 FDA reports)
DIPLOPIA ( 418 FDA reports)
DIVERTICULITIS ( 418 FDA reports)
SPINAL COLUMN STENOSIS ( 413 FDA reports)
INJECTION SITE MASS ( 411 FDA reports)
PULMONARY THROMBOSIS ( 398 FDA reports)
ERYTHEMA ( 397 FDA reports)
MUSCULOSKELETAL PAIN ( 396 FDA reports)
NERVOUSNESS ( 396 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 394 FDA reports)
DYSURIA ( 390 FDA reports)
ROTATOR CUFF SYNDROME ( 387 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 383 FDA reports)
IMPAIRED HEALING ( 381 FDA reports)
MENTAL IMPAIRMENT ( 376 FDA reports)
SUICIDAL IDEATION ( 376 FDA reports)
LIMB INJURY ( 374 FDA reports)
SPINAL FRACTURE ( 368 FDA reports)
GALLBLADDER DISORDER ( 363 FDA reports)
CONCUSSION ( 361 FDA reports)
NERVE COMPRESSION ( 360 FDA reports)
HALLUCINATION ( 358 FDA reports)
SENSORY DISTURBANCE ( 358 FDA reports)
INTRACRANIAL ANEURYSM ( 356 FDA reports)
HERNIA ( 354 FDA reports)
MALIGNANT MELANOMA ( 354 FDA reports)
VIRAL INFECTION ( 354 FDA reports)
BLINDNESS UNILATERAL ( 351 FDA reports)
BLOOD PRESSURE DECREASED ( 351 FDA reports)
POLLAKIURIA ( 350 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 348 FDA reports)
PREGNANCY ( 347 FDA reports)
NEURALGIA ( 346 FDA reports)
SENSATION OF HEAVINESS ( 344 FDA reports)
OROPHARYNGEAL PAIN ( 343 FDA reports)
CHOLECYSTECTOMY ( 342 FDA reports)
PNEUMONIA ASPIRATION ( 341 FDA reports)
PROSTATE CANCER ( 341 FDA reports)
FLUID RETENTION ( 340 FDA reports)
PROCEDURAL COMPLICATION ( 339 FDA reports)
NERVOUS SYSTEM DISORDER ( 337 FDA reports)
OVARIAN CANCER ( 336 FDA reports)
DISORIENTATION ( 335 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 335 FDA reports)
OSTEONECROSIS ( 334 FDA reports)
TEMPERATURE INTOLERANCE ( 334 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 333 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 332 FDA reports)
MOVEMENT DISORDER ( 332 FDA reports)
CATARACT ( 327 FDA reports)
CRYING ( 325 FDA reports)
BODY TEMPERATURE INCREASED ( 324 FDA reports)
HAEMOGLOBIN DECREASED ( 322 FDA reports)
OVERDOSE ( 321 FDA reports)
THYROID DISORDER ( 320 FDA reports)
SPINAL DISORDER ( 318 FDA reports)
CAESAREAN SECTION ( 317 FDA reports)
HYPOTHYROIDISM ( 317 FDA reports)
FIBROMYALGIA ( 315 FDA reports)
JOINT DISLOCATION ( 314 FDA reports)
SWELLING ( 312 FDA reports)
WRIST FRACTURE ( 311 FDA reports)
INJECTION SITE REACTION ( 311 FDA reports)
FEAR ( 307 FDA reports)
RENAL DISORDER ( 306 FDA reports)
THYROID CANCER ( 299 FDA reports)
LIVER DISORDER ( 299 FDA reports)
MUSCLE TIGHTNESS ( 298 FDA reports)
ABDOMINAL DISCOMFORT ( 295 FDA reports)
FAECAL INCONTINENCE ( 294 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 293 FDA reports)
RESPIRATORY FAILURE ( 292 FDA reports)
POOR VENOUS ACCESS ( 292 FDA reports)
VISUAL DISTURBANCE ( 291 FDA reports)
DYSPEPSIA ( 288 FDA reports)
GASTRIC DISORDER ( 288 FDA reports)
NEUROPATHY PERIPHERAL ( 288 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 287 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 287 FDA reports)
EXOSTOSIS ( 286 FDA reports)
SKIN CANCER ( 286 FDA reports)
BACK DISORDER ( 284 FDA reports)
BASAL CELL CARCINOMA ( 284 FDA reports)
INCONTINENCE ( 284 FDA reports)
HEART RATE DECREASED ( 280 FDA reports)
UNDERDOSE ( 279 FDA reports)
EPILEPSY ( 278 FDA reports)
MENTAL DISORDER ( 278 FDA reports)
INJECTION SITE SWELLING ( 276 FDA reports)
CLOSTRIDIAL INFECTION ( 275 FDA reports)
SUICIDE ATTEMPT ( 274 FDA reports)
RESPIRATORY ARREST ( 273 FDA reports)
SLEEP DISORDER ( 267 FDA reports)
PULMONARY OEDEMA ( 266 FDA reports)
LETHARGY ( 265 FDA reports)
BONE PAIN ( 262 FDA reports)
LYMPHOMA ( 260 FDA reports)
SKIN LACERATION ( 259 FDA reports)
DISEASE PROGRESSION ( 256 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 254 FDA reports)
DYSGRAPHIA ( 252 FDA reports)
COLITIS ( 251 FDA reports)
CYST ( 251 FDA reports)
LUNG DISORDER ( 249 FDA reports)
EYE PAIN ( 248 FDA reports)
ARRHYTHMIA ( 246 FDA reports)
BREAST CANCER IN SITU ( 244 FDA reports)
SKIN ULCER ( 244 FDA reports)
OSTEOMYELITIS ( 242 FDA reports)
INJURY ( 241 FDA reports)
UROSEPSIS ( 240 FDA reports)
PELVIC FRACTURE ( 239 FDA reports)
EYE DISORDER ( 238 FDA reports)
OBESITY ( 238 FDA reports)
CEREBRAL HAEMORRHAGE ( 237 FDA reports)
MUSCLE ATROPHY ( 236 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 236 FDA reports)
SPINAL FUSION SURGERY ( 236 FDA reports)
RENAL FAILURE ACUTE ( 234 FDA reports)
SPINAL OSTEOARTHRITIS ( 234 FDA reports)
BLOOD SODIUM DECREASED ( 234 FDA reports)
HOT FLUSH ( 233 FDA reports)
SLEEP APNOEA SYNDROME ( 233 FDA reports)
PANIC ATTACK ( 232 FDA reports)
CROHN'S DISEASE ( 231 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 231 FDA reports)
PLATELET COUNT DECREASED ( 231 FDA reports)
APPENDICITIS ( 229 FDA reports)
DISEASE RECURRENCE ( 227 FDA reports)
BACTERIAL INFECTION ( 226 FDA reports)
TACHYCARDIA ( 226 FDA reports)
FLUSHING ( 225 FDA reports)
BIPOLAR DISORDER ( 223 FDA reports)
HEPATIC STEATOSIS ( 223 FDA reports)
NEUROGENIC BLADDER ( 220 FDA reports)
ADVERSE EVENT ( 219 FDA reports)
LACERATION ( 219 FDA reports)
MOTOR DYSFUNCTION ( 218 FDA reports)
NO ADVERSE EVENT ( 217 FDA reports)
SKIN DISCOLOURATION ( 217 FDA reports)
SWELLING FACE ( 217 FDA reports)
DISTURBANCE IN ATTENTION ( 215 FDA reports)
INJECTION SITE RASH ( 215 FDA reports)
GASTRITIS ( 214 FDA reports)
GASTRIC BYPASS ( 211 FDA reports)
CARDIAC FAILURE ( 210 FDA reports)
DYSKINESIA ( 210 FDA reports)
DYSPHONIA ( 210 FDA reports)
FUNGAL INFECTION ( 208 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 207 FDA reports)
MENORRHAGIA ( 206 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 205 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 205 FDA reports)
ENDOMETRIOSIS ( 203 FDA reports)
RENAL IMPAIRMENT ( 202 FDA reports)
BACK INJURY ( 201 FDA reports)
ABDOMINAL DISTENSION ( 199 FDA reports)
BLOOD GLUCOSE DECREASED ( 199 FDA reports)
CHOLECYSTITIS ( 199 FDA reports)
SCOLIOSIS ( 199 FDA reports)
APHAGIA ( 198 FDA reports)
GASTRIC ULCER ( 198 FDA reports)
IRRITABILITY ( 198 FDA reports)
MENISCUS LESION ( 197 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 196 FDA reports)
COLLAPSE OF LUNG ( 196 FDA reports)
RESTLESS LEGS SYNDROME ( 196 FDA reports)
BONE DISORDER ( 195 FDA reports)
DRUG EFFECT DECREASED ( 195 FDA reports)
SCIATICA ( 194 FDA reports)
HIATUS HERNIA ( 193 FDA reports)
HEPATIC FAILURE ( 192 FDA reports)
JOINT SPRAIN ( 192 FDA reports)
MEDICAL DEVICE COMPLICATION ( 192 FDA reports)
TIBIA FRACTURE ( 192 FDA reports)
ANGINA PECTORIS ( 191 FDA reports)
COLONIC POLYP ( 190 FDA reports)
DRUG DOSE OMISSION ( 190 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 190 FDA reports)
LOCALISED INFECTION ( 190 FDA reports)
LYMPHADENOPATHY ( 189 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 188 FDA reports)
BLOOD COUNT ABNORMAL ( 187 FDA reports)
WOUND ( 186 FDA reports)
CARPAL TUNNEL SYNDROME ( 185 FDA reports)
BLOOD DISORDER ( 183 FDA reports)
LUNG INFECTION ( 182 FDA reports)
EMOTIONAL DISORDER ( 180 FDA reports)
GASTROENTERITIS VIRAL ( 180 FDA reports)
OXYGEN SATURATION DECREASED ( 180 FDA reports)
BLISTER ( 179 FDA reports)
HYPERSOMNIA ( 179 FDA reports)
DRUG INTOLERANCE ( 178 FDA reports)
HEPATITIS ( 178 FDA reports)
STRESS SYMPTOMS ( 178 FDA reports)
DEVICE RELATED INFECTION ( 177 FDA reports)
COLITIS ULCERATIVE ( 176 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 175 FDA reports)
TREATMENT NONCOMPLIANCE ( 175 FDA reports)
VEIN DISORDER ( 175 FDA reports)
RECTAL HAEMORRHAGE ( 174 FDA reports)
INFLAMMATION ( 174 FDA reports)
ANOREXIA ( 173 FDA reports)
BREAST CANCER STAGE I ( 173 FDA reports)
IMMUNE SYSTEM DISORDER ( 173 FDA reports)
NERVE INJURY ( 173 FDA reports)
BRAIN NEOPLASM ( 172 FDA reports)
FIBULA FRACTURE ( 172 FDA reports)
HYPOTONIA ( 172 FDA reports)
MUSCLE TWITCHING ( 171 FDA reports)
THERMAL BURN ( 171 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 170 FDA reports)
VAGINAL HAEMORRHAGE ( 169 FDA reports)
HEARING IMPAIRED ( 168 FDA reports)
HYPERAESTHESIA ( 168 FDA reports)
PLEURAL EFFUSION ( 168 FDA reports)
ILL-DEFINED DISORDER ( 167 FDA reports)
MENTAL STATUS CHANGES ( 167 FDA reports)
NASAL CONGESTION ( 167 FDA reports)
UNEVALUABLE EVENT ( 167 FDA reports)
KNEE OPERATION ( 166 FDA reports)
MICTURITION URGENCY ( 165 FDA reports)
NIGHT SWEATS ( 165 FDA reports)
RHEUMATOID ARTHRITIS ( 165 FDA reports)
UTERINE CANCER ( 165 FDA reports)
MOOD SWINGS ( 164 FDA reports)
CARDIOMYOPATHY ( 163 FDA reports)
DIALYSIS ( 163 FDA reports)
PERIPHERAL COLDNESS ( 163 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 163 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 161 FDA reports)
ARTHRITIS INFECTIVE ( 161 FDA reports)
EXCORIATION ( 161 FDA reports)
MITRAL VALVE INCOMPETENCE ( 161 FDA reports)
CARDIOMEGALY ( 159 FDA reports)
WOUND INFECTION ( 159 FDA reports)
GALLBLADDER OPERATION ( 158 FDA reports)
INJECTION SITE PRURITUS ( 158 FDA reports)
PANCREATIC CARCINOMA ( 158 FDA reports)
HAEMORRHOIDS ( 157 FDA reports)
INFUSION RELATED REACTION ( 157 FDA reports)
INJECTION SITE INDURATION ( 157 FDA reports)
JOINT STIFFNESS ( 157 FDA reports)
BLADDER CANCER ( 156 FDA reports)
MULTIPLE ALLERGIES ( 156 FDA reports)
ANAPHYLACTIC SHOCK ( 154 FDA reports)
HAEMATOMA ( 154 FDA reports)
INJECTION SITE INFECTION ( 154 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 154 FDA reports)
ARTHROPOD BITE ( 153 FDA reports)
PERICARDIAL EFFUSION ( 153 FDA reports)
HAEMATOCRIT DECREASED ( 152 FDA reports)
DRY MOUTH ( 151 FDA reports)
COLITIS ISCHAEMIC ( 150 FDA reports)
EAR INFECTION ( 150 FDA reports)
RHINORRHOEA ( 150 FDA reports)
SARCOIDOSIS ( 150 FDA reports)
THYROID NEOPLASM ( 150 FDA reports)
HEART RATE IRREGULAR ( 149 FDA reports)
HEPATITIS C ( 148 FDA reports)
ABSCESS ( 147 FDA reports)
HEMIPLEGIA ( 147 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 146 FDA reports)
PREMATURE LABOUR ( 146 FDA reports)
ANGER ( 145 FDA reports)
BREAST CANCER METASTATIC ( 145 FDA reports)
BREAST CANCER STAGE II ( 145 FDA reports)
APPENDICITIS PERFORATED ( 144 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 144 FDA reports)
GASTROINTESTINAL INFECTION ( 144 FDA reports)
OSTEOPENIA ( 144 FDA reports)
EPISTAXIS ( 143 FDA reports)
METASTASES TO LYMPH NODES ( 143 FDA reports)
DEMENTIA ( 142 FDA reports)
PULMONARY HYPERTENSION ( 142 FDA reports)
SKIN LESION ( 142 FDA reports)
FRUSTRATION ( 141 FDA reports)
EMOTIONAL DISTRESS ( 140 FDA reports)
HUMERUS FRACTURE ( 140 FDA reports)
TINNITUS ( 140 FDA reports)
RESPIRATORY DISORDER ( 139 FDA reports)
INCOHERENT ( 139 FDA reports)
ACCIDENT ( 138 FDA reports)
CHONDROPATHY ( 138 FDA reports)
LIGAMENT RUPTURE ( 138 FDA reports)
MUSCLE DISORDER ( 138 FDA reports)
BLOOD URINE PRESENT ( 137 FDA reports)
FACIAL BONES FRACTURE ( 137 FDA reports)
LUNG NEOPLASM ( 137 FDA reports)
HAEMATOCHEZIA ( 136 FDA reports)
HYPOPHAGIA ( 136 FDA reports)
RETINAL DETACHMENT ( 136 FDA reports)
CLAVICLE FRACTURE ( 135 FDA reports)
FACIAL PAIN ( 135 FDA reports)
DENTAL CARIES ( 134 FDA reports)
EMPHYSEMA ( 134 FDA reports)
PETIT MAL EPILEPSY ( 134 FDA reports)
RASH PRURITIC ( 134 FDA reports)
LEUKAEMIA ( 133 FDA reports)
POOR PERIPHERAL CIRCULATION ( 133 FDA reports)
CARDIAC VALVE DISEASE ( 132 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 132 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 130 FDA reports)
CERVIX CARCINOMA ( 130 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 130 FDA reports)
INTESTINAL PERFORATION ( 130 FDA reports)
MASS ( 130 FDA reports)
MENOPAUSE ( 130 FDA reports)
THROAT TIGHTNESS ( 130 FDA reports)
WHEEZING ( 129 FDA reports)
ANAPHYLACTIC REACTION ( 129 FDA reports)
APPENDICECTOMY ( 129 FDA reports)
AORTIC ANEURYSM ( 128 FDA reports)
ABDOMINAL HERNIA ( 127 FDA reports)
LUMBAR SPINAL STENOSIS ( 127 FDA reports)
CHOKING ( 126 FDA reports)
DRUG INTERACTION ( 126 FDA reports)
IATROGENIC INJURY ( 126 FDA reports)
HYPONATRAEMIA ( 125 FDA reports)
INFECTED SKIN ULCER ( 124 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 124 FDA reports)
PSYCHOTIC DISORDER ( 124 FDA reports)
TOOTH FRACTURE ( 124 FDA reports)
ULCER HAEMORRHAGE ( 124 FDA reports)
DELIRIUM ( 123 FDA reports)
BRAIN OEDEMA ( 122 FDA reports)
GOITRE ( 122 FDA reports)
HAND FRACTURE ( 122 FDA reports)
AGITATION ( 121 FDA reports)
DEAFNESS ( 121 FDA reports)
HYPOAESTHESIA FACIAL ( 121 FDA reports)
DIPLEGIA ( 120 FDA reports)
RESPIRATORY DISTRESS ( 120 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 119 FDA reports)
BLOOD IRON DECREASED ( 119 FDA reports)
BLOOD TEST ABNORMAL ( 119 FDA reports)
DYSGEUSIA ( 119 FDA reports)
FEAR OF NEEDLES ( 119 FDA reports)
HYPERLIPIDAEMIA ( 118 FDA reports)
HYPERTHYROIDISM ( 118 FDA reports)
PREMATURE BABY ( 118 FDA reports)
TOOTH ABSCESS ( 117 FDA reports)
UTERINE HAEMORRHAGE ( 117 FDA reports)
PYELONEPHRITIS ( 116 FDA reports)
RASH PAPULAR ( 116 FDA reports)
ULCER ( 116 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 116 FDA reports)
HEPATIC CIRRHOSIS ( 116 FDA reports)
POST PROCEDURAL INFECTION ( 116 FDA reports)
PRURITUS GENERALISED ( 116 FDA reports)
PNEUMOTHORAX ( 115 FDA reports)
RETCHING ( 114 FDA reports)
HEPATOMEGALY ( 113 FDA reports)
HYPOACUSIS ( 113 FDA reports)
INCREASED TENDENCY TO BRUISE ( 113 FDA reports)
CEREBRAL ATROPHY ( 112 FDA reports)
TYPE 2 DIABETES MELLITUS ( 112 FDA reports)
SEPTIC SHOCK ( 111 FDA reports)
INJECTION SITE SCAR ( 111 FDA reports)
JAUNDICE ( 111 FDA reports)
BEDRIDDEN ( 110 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 110 FDA reports)
EJECTION FRACTION DECREASED ( 110 FDA reports)
SWOLLEN TONGUE ( 110 FDA reports)
TOOTH DISORDER ( 110 FDA reports)
BREAST CANCER RECURRENT ( 109 FDA reports)
CARDIAC OPERATION ( 109 FDA reports)
DEVICE FAILURE ( 109 FDA reports)
FOOD POISONING ( 109 FDA reports)
INJECTION SITE CELLULITIS ( 109 FDA reports)
MULTIPLE MYELOMA ( 109 FDA reports)
MUSCLE STRAIN ( 109 FDA reports)
PRE-ECLAMPSIA ( 109 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 108 FDA reports)
EATING DISORDER ( 108 FDA reports)
TENDONITIS ( 108 FDA reports)
PALLOR ( 107 FDA reports)
BURSITIS ( 106 FDA reports)
METASTASES TO LIVER ( 106 FDA reports)
SEASONAL ALLERGY ( 106 FDA reports)
ANEURYSM ( 105 FDA reports)
CERVICAL SPINAL STENOSIS ( 105 FDA reports)
HOSPITALISATION ( 105 FDA reports)
PRECANCEROUS CELLS PRESENT ( 105 FDA reports)
ENDOMETRIAL CANCER ( 104 FDA reports)
ATAXIA ( 103 FDA reports)
BODY HEIGHT DECREASED ( 103 FDA reports)
MONOPLEGIA ( 103 FDA reports)
SPINAL CORD DISORDER ( 103 FDA reports)
ASPIRATION ( 102 FDA reports)
BLOOD PRESSURE ABNORMAL ( 102 FDA reports)
CALCULUS BLADDER ( 102 FDA reports)
COLON CANCER METASTATIC ( 102 FDA reports)
ECTOPIC PREGNANCY ( 102 FDA reports)
LARGE INTESTINE PERFORATION ( 102 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 102 FDA reports)
MEDICATION ERROR ( 102 FDA reports)
ATROPHY ( 101 FDA reports)
HYPERGLYCAEMIA ( 101 FDA reports)
MENINGIOMA ( 101 FDA reports)
OESOPHAGEAL CARCINOMA ( 101 FDA reports)
OVERWEIGHT ( 101 FDA reports)
FACIAL PALSY ( 100 FDA reports)
GLAUCOMA ( 100 FDA reports)
INCISION SITE COMPLICATION ( 100 FDA reports)
ABDOMINAL ADHESIONS ( 99 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 99 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 99 FDA reports)
CORONARY ARTERY STENOSIS ( 99 FDA reports)
EAR PAIN ( 99 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 99 FDA reports)
BLADDER SPASM ( 98 FDA reports)
EYE SWELLING ( 98 FDA reports)
HYPOKALAEMIA ( 98 FDA reports)
PARAPLEGIA ( 98 FDA reports)
RASH ERYTHEMATOUS ( 98 FDA reports)
SPINAL COMPRESSION FRACTURE ( 98 FDA reports)
RASH GENERALISED ( 97 FDA reports)
ABSCESS LIMB ( 97 FDA reports)
APHONIA ( 97 FDA reports)
AUTOIMMUNE HEPATITIS ( 97 FDA reports)
BRADYCARDIA ( 97 FDA reports)
HYPOAESTHESIA ORAL ( 97 FDA reports)
IRRITABLE BOWEL SYNDROME ( 97 FDA reports)
LOWER EXTREMITY MASS ( 97 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 97 FDA reports)
CAROTID ARTERY OCCLUSION ( 96 FDA reports)
CATHETER RELATED COMPLICATION ( 96 FDA reports)
DYSPHEMIA ( 96 FDA reports)
MENSTRUATION IRREGULAR ( 96 FDA reports)
SLUGGISHNESS ( 96 FDA reports)
THROMBOCYTOPENIA ( 95 FDA reports)
ABNORMAL BEHAVIOUR ( 95 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 95 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 95 FDA reports)
BLINDNESS TRANSIENT ( 94 FDA reports)
BLOOD POTASSIUM INCREASED ( 94 FDA reports)
CARDIO-RESPIRATORY ARREST ( 94 FDA reports)
ESCHERICHIA INFECTION ( 94 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 93 FDA reports)
IMMOBILE ( 93 FDA reports)
VITAMIN D DECREASED ( 93 FDA reports)
RESPIRATORY TRACT INFECTION ( 92 FDA reports)
SINUS DISORDER ( 92 FDA reports)
DRY SKIN ( 92 FDA reports)
FACE INJURY ( 92 FDA reports)
IMPAIRED DRIVING ABILITY ( 92 FDA reports)
INJECTION SITE WARMTH ( 92 FDA reports)
LEUKOPENIA ( 92 FDA reports)
ARTERIOSCLEROSIS ( 91 FDA reports)
CEREBRAL INFARCTION ( 91 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 91 FDA reports)
INJECTION SITE ABSCESS ( 91 FDA reports)
LIVER INJURY ( 91 FDA reports)
ADVERSE REACTION ( 90 FDA reports)
BLOOD BILIRUBIN INCREASED ( 90 FDA reports)
DERMATITIS CONTACT ( 90 FDA reports)
HERNIA REPAIR ( 90 FDA reports)
MALNUTRITION ( 90 FDA reports)
WHEELCHAIR USER ( 90 FDA reports)
TOOTHACHE ( 89 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 89 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 89 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 89 FDA reports)
LABORATORY TEST ABNORMAL ( 89 FDA reports)
METASTASES TO BONE ( 89 FDA reports)
MUSCLE RIGIDITY ( 88 FDA reports)
PAIN OF SKIN ( 88 FDA reports)
RENAL CANCER ( 88 FDA reports)
SPINAL OPERATION ( 88 FDA reports)
TENDON RUPTURE ( 87 FDA reports)
AGGRESSION ( 87 FDA reports)
BREAST MASS ( 87 FDA reports)
CARTILAGE INJURY ( 87 FDA reports)
GASTRIC CANCER ( 87 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 87 FDA reports)
PATELLA FRACTURE ( 87 FDA reports)
SENSORY LOSS ( 86 FDA reports)
THERAPY NON-RESPONDER ( 86 FDA reports)
URINARY TRACT DISORDER ( 86 FDA reports)
VISUAL FIELD DEFECT ( 86 FDA reports)
SUBDURAL HAEMATOMA ( 85 FDA reports)
SYNOVIAL CYST ( 85 FDA reports)
TOOTH LOSS ( 85 FDA reports)
MENINGITIS ( 85 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 85 FDA reports)
AGRAPHIA ( 84 FDA reports)
ANAESTHETIC COMPLICATION ( 84 FDA reports)
INTRACARDIAC THROMBUS ( 84 FDA reports)
MOOD ALTERED ( 84 FDA reports)
DELUSION ( 83 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 83 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 83 FDA reports)
ORAL INTAKE REDUCED ( 83 FDA reports)
ORTHOSTATIC HYPOTENSION ( 83 FDA reports)
SPINAL CORD COMPRESSION ( 83 FDA reports)
SKIN DISORDER ( 82 FDA reports)
ABDOMINAL ABSCESS ( 82 FDA reports)
OEDEMA ( 82 FDA reports)
PHOBIA ( 82 FDA reports)
COLD SWEAT ( 81 FDA reports)
INCISION SITE INFECTION ( 81 FDA reports)
NEOPLASM ( 81 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 81 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 81 FDA reports)
POSTOPERATIVE INFECTION ( 81 FDA reports)
THROAT IRRITATION ( 81 FDA reports)
RECTAL CANCER ( 80 FDA reports)
RESPIRATORY TRACT CONGESTION ( 80 FDA reports)
TOOTH INFECTION ( 80 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 80 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 80 FDA reports)
CATHETER RELATED INFECTION ( 80 FDA reports)
DEVICE DISLOCATION ( 80 FDA reports)
HYPOXIA ( 80 FDA reports)
ORAL HERPES ( 80 FDA reports)
POOR QUALITY SLEEP ( 79 FDA reports)
SKELETAL INJURY ( 79 FDA reports)
SKIN GRAFT ( 79 FDA reports)
SPONDYLITIS ( 78 FDA reports)
THINKING ABNORMAL ( 78 FDA reports)
VAGINAL INFECTION ( 78 FDA reports)
BACTERAEMIA ( 78 FDA reports)
CHOLECYSTITIS INFECTIVE ( 78 FDA reports)
H1N1 INFLUENZA ( 78 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 78 FDA reports)
INJECTION SITE DISCOLOURATION ( 78 FDA reports)
PULMONARY FIBROSIS ( 78 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 77 FDA reports)
FURUNCLE ( 77 FDA reports)
OPEN WOUND ( 77 FDA reports)
BASEDOW'S DISEASE ( 76 FDA reports)
GASTROENTERITIS ( 76 FDA reports)
HYPERCHOLESTEROLAEMIA ( 76 FDA reports)
INJECTION SITE IRRITATION ( 76 FDA reports)
POLYP ( 76 FDA reports)
SURGICAL PROCEDURE REPEATED ( 76 FDA reports)
WALKING AID USER ( 76 FDA reports)
ATELECTASIS ( 75 FDA reports)
BLADDER PROLAPSE ( 75 FDA reports)
CARDIOVASCULAR DISORDER ( 75 FDA reports)
LARYNGITIS ( 75 FDA reports)
METASTATIC NEOPLASM ( 75 FDA reports)
MULTI-ORGAN FAILURE ( 75 FDA reports)
PARANOIA ( 75 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 74 FDA reports)
BLADDER OPERATION ( 74 FDA reports)
HAEMATEMESIS ( 74 FDA reports)
METASTASES TO LUNG ( 74 FDA reports)
PERITONITIS ( 74 FDA reports)
VITAMIN D DEFICIENCY ( 74 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 73 FDA reports)
ECONOMIC PROBLEM ( 73 FDA reports)
PLATELET COUNT INCREASED ( 73 FDA reports)
ACCIDENTAL OVERDOSE ( 72 FDA reports)
EYE MOVEMENT DISORDER ( 72 FDA reports)
INJECTION SITE EXTRAVASATION ( 72 FDA reports)
PAIN IN JAW ( 72 FDA reports)
SCRATCH ( 72 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 71 FDA reports)
STOMACH DISCOMFORT ( 71 FDA reports)
BONE DENSITY DECREASED ( 71 FDA reports)
COMPLETED SUICIDE ( 71 FDA reports)
DEMYELINATION ( 71 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 71 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 71 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 70 FDA reports)
ENCEPHALOPATHY ( 70 FDA reports)
FULL BLOOD COUNT DECREASED ( 70 FDA reports)
NEUROMYELITIS OPTICA ( 70 FDA reports)
PERIORBITAL HAEMATOMA ( 70 FDA reports)
REACTION TO PRESERVATIVES ( 70 FDA reports)
SPONDYLOLISTHESIS ( 70 FDA reports)
TENDON DISORDER ( 69 FDA reports)
BIPOLAR I DISORDER ( 69 FDA reports)
BLOOD MAGNESIUM DECREASED ( 69 FDA reports)
BRAIN NEOPLASM BENIGN ( 69 FDA reports)
CONVERSION DISORDER ( 69 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 69 FDA reports)
PLEURISY ( 69 FDA reports)
BREAST CANCER STAGE III ( 68 FDA reports)
CARDIAC MURMUR ( 68 FDA reports)
DRUG DEPENDENCE ( 68 FDA reports)
GOUT ( 68 FDA reports)
SHOCK ( 68 FDA reports)
SPLENECTOMY ( 68 FDA reports)
VIITH NERVE PARALYSIS ( 68 FDA reports)
RHABDOMYOLYSIS ( 67 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 67 FDA reports)
UTERINE PROLAPSE ( 67 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 67 FDA reports)
LIGAMENT SPRAIN ( 67 FDA reports)
MANIA ( 67 FDA reports)
PHOTOSENSITIVITY REACTION ( 67 FDA reports)
BONE NEOPLASM MALIGNANT ( 66 FDA reports)
HAEMOPTYSIS ( 66 FDA reports)
LIP SWELLING ( 66 FDA reports)
MENINGITIS VIRAL ( 66 FDA reports)
MYOCARDIAL ISCHAEMIA ( 66 FDA reports)
PARTIAL SEIZURES ( 66 FDA reports)
RESTLESSNESS ( 66 FDA reports)
RENAL CELL CARCINOMA ( 65 FDA reports)
RENAL FAILURE CHRONIC ( 65 FDA reports)
SINUS CONGESTION ( 65 FDA reports)
SNEEZING ( 65 FDA reports)
SPLENOMEGALY ( 65 FDA reports)
CANDIDIASIS ( 65 FDA reports)
CARDIAC PACEMAKER INSERTION ( 65 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 65 FDA reports)
HALLUCINATION, VISUAL ( 65 FDA reports)
HANGOVER ( 65 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 65 FDA reports)
PHARYNGEAL OEDEMA ( 65 FDA reports)
PHOTOPHOBIA ( 65 FDA reports)
ANIMAL BITE ( 64 FDA reports)
CEREBRAL THROMBOSIS ( 64 FDA reports)
CHROMATURIA ( 64 FDA reports)
DRUG ABUSE ( 64 FDA reports)
HEPATIC CYST ( 64 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 64 FDA reports)
OPERATIVE HAEMORRHAGE ( 64 FDA reports)
PERICARDITIS ( 64 FDA reports)
SQUAMOUS CELL CARCINOMA ( 64 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 64 FDA reports)
SPLENIC RUPTURE ( 63 FDA reports)
STENT PLACEMENT ( 63 FDA reports)
VARICOSE VEIN ( 63 FDA reports)
COLOSTOMY ( 63 FDA reports)
CORONARY ARTERY BYPASS ( 63 FDA reports)
HAEMATURIA ( 63 FDA reports)
HYPOGLYCAEMIA ( 63 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 63 FDA reports)
NARCOLEPSY ( 63 FDA reports)
LIGAMENT INJURY ( 62 FDA reports)
PRODUCTIVE COUGH ( 62 FDA reports)
RASH MACULAR ( 62 FDA reports)
STATUS EPILEPTICUS ( 62 FDA reports)
THIRST ( 62 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 61 FDA reports)
ROTATOR CUFF REPAIR ( 61 FDA reports)
VITAMIN B12 DECREASED ( 61 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 61 FDA reports)
IRON DEFICIENCY ANAEMIA ( 61 FDA reports)
LUMBAR RADICULOPATHY ( 61 FDA reports)
LUNG CANCER METASTATIC ( 61 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 61 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 61 FDA reports)
BODY TEMPERATURE DECREASED ( 60 FDA reports)
DRUG TOXICITY ( 60 FDA reports)
HYPERTONIC BLADDER ( 60 FDA reports)
IMMUNOSUPPRESSION ( 60 FDA reports)
INJECTION SITE URTICARIA ( 60 FDA reports)
JC VIRUS TEST POSITIVE ( 60 FDA reports)
NON-SMALL CELL LUNG CANCER ( 60 FDA reports)
NYSTAGMUS ( 60 FDA reports)
PANCREATITIS ACUTE ( 60 FDA reports)
PNEUMONIA BACTERIAL ( 60 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 60 FDA reports)
SKIN INFECTION ( 60 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 60 FDA reports)
STREPTOCOCCAL INFECTION ( 59 FDA reports)
THYROIDECTOMY ( 59 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 59 FDA reports)
UTERINE ENLARGEMENT ( 59 FDA reports)
AUTOIMMUNE THYROIDITIS ( 59 FDA reports)
COLON CANCER STAGE III ( 59 FDA reports)
GROIN PAIN ( 59 FDA reports)
ASCITES ( 58 FDA reports)
ASEPTIC NECROSIS BONE ( 58 FDA reports)
BRONCHOPNEUMONIA ( 58 FDA reports)
CIRCULATORY COLLAPSE ( 58 FDA reports)
ECZEMA ( 58 FDA reports)
HAEMORRHAGIC STROKE ( 58 FDA reports)
INFUSION SITE PAIN ( 58 FDA reports)
OOPHORECTOMY ( 58 FDA reports)
ATRIAL FLUTTER ( 57 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 57 FDA reports)
DRY EYE ( 57 FDA reports)
DYSMENORRHOEA ( 57 FDA reports)
ENTERITIS INFECTIOUS ( 57 FDA reports)
FOOD ALLERGY ( 57 FDA reports)
LEG AMPUTATION ( 57 FDA reports)
LYMPHOEDEMA ( 57 FDA reports)
MENSTRUAL DISORDER ( 57 FDA reports)
OPEN FRACTURE ( 57 FDA reports)
SKIN BURNING SENSATION ( 57 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 56 FDA reports)
AGEUSIA ( 56 FDA reports)
ANTIBODY TEST POSITIVE ( 56 FDA reports)
BRONCHOSPASM ( 56 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 56 FDA reports)
ELECTROLYTE IMBALANCE ( 56 FDA reports)
LOBAR PNEUMONIA ( 56 FDA reports)
LYME DISEASE ( 56 FDA reports)
PARAPARESIS ( 56 FDA reports)
PITUITARY TUMOUR ( 56 FDA reports)
AMENORRHOEA ( 55 FDA reports)
AORTIC VALVE DISEASE ( 55 FDA reports)
APATHY ( 55 FDA reports)
BENIGN BREAST NEOPLASM ( 55 FDA reports)
CARDIAC ENZYMES INCREASED ( 55 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 55 FDA reports)
EMBOLISM ( 55 FDA reports)
FRACTURED COCCYX ( 55 FDA reports)
INJECTION SITE BRUISING ( 55 FDA reports)
NECROTISING FASCIITIS ( 55 FDA reports)
OPTIC NERVE DISORDER ( 55 FDA reports)
PSORIASIS ( 55 FDA reports)
TOOTH EXTRACTION ( 55 FDA reports)
SJOGREN'S SYNDROME ( 54 FDA reports)
STILLBIRTH ( 54 FDA reports)
SUBCUTANEOUS ABSCESS ( 54 FDA reports)
WOUND DEHISCENCE ( 54 FDA reports)
ABDOMINAL PAIN LOWER ( 54 FDA reports)
COAGULOPATHY ( 54 FDA reports)
DIVERTICULUM ( 54 FDA reports)
HEPATIC NECROSIS ( 54 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 54 FDA reports)
LEUKOCYTOSIS ( 54 FDA reports)
LIMB CRUSHING INJURY ( 54 FDA reports)
LUNG ADENOCARCINOMA ( 54 FDA reports)
MYASTHENIA GRAVIS ( 54 FDA reports)
NO THERAPEUTIC RESPONSE ( 54 FDA reports)
OESOPHAGITIS ( 54 FDA reports)
ANGINA UNSTABLE ( 53 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 53 FDA reports)
BREAST CYST ( 53 FDA reports)
CLUMSINESS ( 53 FDA reports)
EYE IRRITATION ( 53 FDA reports)
FEMORAL NECK FRACTURE ( 53 FDA reports)
FLATULENCE ( 53 FDA reports)
LOCAL SWELLING ( 53 FDA reports)
MITRAL VALVE PROLAPSE ( 53 FDA reports)
MUSCLE CRAMP ( 53 FDA reports)
PHARYNGITIS ( 53 FDA reports)
PHLEBITIS ( 53 FDA reports)
PITUITARY TUMOUR BENIGN ( 53 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 52 FDA reports)
COMPLEX PARTIAL SEIZURES ( 52 FDA reports)
DEAFNESS UNILATERAL ( 52 FDA reports)
DISCOMFORT ( 52 FDA reports)
GESTATIONAL DIABETES ( 52 FDA reports)
HALLUCINATION, AUDITORY ( 52 FDA reports)
HEART VALVE INCOMPETENCE ( 52 FDA reports)
INJECTION SITE ATROPHY ( 52 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 52 FDA reports)
NECK INJURY ( 52 FDA reports)
RENAL CYST ( 52 FDA reports)
RECTOCELE ( 51 FDA reports)
SCIATIC NERVE INJURY ( 51 FDA reports)
ALCOHOLISM ( 51 FDA reports)
ENCEPHALITIS ( 51 FDA reports)
FAECALOMA ( 51 FDA reports)
HEPATOCELLULAR DAMAGE ( 51 FDA reports)
HIP SURGERY ( 51 FDA reports)
MAJOR DEPRESSION ( 51 FDA reports)
OPHTHALMOPLEGIA ( 51 FDA reports)
PANCYTOPENIA ( 51 FDA reports)
PSEUDOMONAS INFECTION ( 51 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 50 FDA reports)
BLOOD ALBUMIN DECREASED ( 50 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 50 FDA reports)
EYE HAEMORRHAGE ( 50 FDA reports)
FAECES DISCOLOURED ( 50 FDA reports)
FEELING JITTERY ( 50 FDA reports)
GANGRENE ( 50 FDA reports)
HEAT EXHAUSTION ( 50 FDA reports)
LATEX ALLERGY ( 50 FDA reports)
MYELODYSPLASTIC SYNDROME ( 50 FDA reports)
OESOPHAGEAL DISORDER ( 50 FDA reports)
POST PROCEDURAL HAEMATOMA ( 50 FDA reports)
RAYNAUD'S PHENOMENON ( 50 FDA reports)
RENAL PAIN ( 50 FDA reports)
SINUS TACHYCARDIA ( 50 FDA reports)
TENSION ( 50 FDA reports)
UTERINE DISORDER ( 50 FDA reports)
SKULL FRACTURE ( 49 FDA reports)
STOMATITIS ( 49 FDA reports)
VITREOUS FLOATERS ( 49 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 49 FDA reports)
AUTOIMMUNE DISORDER ( 49 FDA reports)
DERMATITIS ALLERGIC ( 49 FDA reports)
DIZZINESS POSTURAL ( 49 FDA reports)
FEELING DRUNK ( 49 FDA reports)
FRACTURE ( 49 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 49 FDA reports)
INTERVERTEBRAL DISC INJURY ( 49 FDA reports)
METRORRHAGIA ( 49 FDA reports)
MIDDLE INSOMNIA ( 49 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 49 FDA reports)
OVARIAN NEOPLASM ( 49 FDA reports)
ABNORMAL DREAMS ( 48 FDA reports)
BUNION ( 48 FDA reports)
CATHETERISATION CARDIAC ( 48 FDA reports)
GASTRIC HAEMORRHAGE ( 48 FDA reports)
PLEURITIC PAIN ( 48 FDA reports)
SHOULDER PAIN ( 48 FDA reports)
VENOUS INJURY ( 48 FDA reports)
SCOTOMA ( 47 FDA reports)
SHOULDER OPERATION ( 47 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 47 FDA reports)
ANGIONEUROTIC OEDEMA ( 47 FDA reports)
ATRIAL SEPTAL DEFECT ( 47 FDA reports)
CEREBRAL DISORDER ( 47 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 47 FDA reports)
HYDROCEPHALUS ( 47 FDA reports)
ILEUS ( 47 FDA reports)
MYELITIS TRANSVERSE ( 47 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 46 FDA reports)
ANKLE OPERATION ( 46 FDA reports)
B-CELL LYMPHOMA ( 46 FDA reports)
BONE MARROW FAILURE ( 46 FDA reports)
EYELID PTOSIS ( 46 FDA reports)
GASTRIC INFECTION ( 46 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 46 FDA reports)
OCULAR HYPERAEMIA ( 46 FDA reports)
SINUS HEADACHE ( 46 FDA reports)
SMEAR CERVIX ABNORMAL ( 46 FDA reports)
THYROID GLAND CANCER ( 46 FDA reports)
VASCULITIS ( 46 FDA reports)
VITAMIN B12 DEFICIENCY ( 46 FDA reports)
UMBILICAL CORD AROUND NECK ( 45 FDA reports)
ABNORMAL LABOUR ( 45 FDA reports)
ADHESION ( 45 FDA reports)
AFFECT LABILITY ( 45 FDA reports)
AORTIC VALVE INCOMPETENCE ( 45 FDA reports)
APNOEA ( 45 FDA reports)
BRAIN OPERATION ( 45 FDA reports)
BREAST PAIN ( 45 FDA reports)
CATHETER PLACEMENT ( 45 FDA reports)
INCISION SITE HAEMORRHAGE ( 45 FDA reports)
MUSCLE INJURY ( 45 FDA reports)
MUSCLE RUPTURE ( 45 FDA reports)
NIGHTMARE ( 45 FDA reports)
PANCREATIC DISORDER ( 45 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 45 FDA reports)
PULMONARY MASS ( 45 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 44 FDA reports)
BREECH PRESENTATION ( 44 FDA reports)
CORONARY ARTERY THROMBOSIS ( 44 FDA reports)
DROOLING ( 44 FDA reports)
GRIP STRENGTH DECREASED ( 44 FDA reports)
INJECTION SITE VESICLES ( 44 FDA reports)
INTRACRANIAL HYPOTENSION ( 44 FDA reports)
LIPOMA ( 44 FDA reports)
NECROSIS ( 44 FDA reports)
NEUTROPENIA ( 44 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 44 FDA reports)
PRESYNCOPE ( 44 FDA reports)
QUADRIPLEGIA ( 44 FDA reports)
SKIN EXFOLIATION ( 44 FDA reports)
SKIN MASS ( 44 FDA reports)
SPINAL LAMINECTOMY ( 44 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 44 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 44 FDA reports)
SCHIZOPHRENIA ( 43 FDA reports)
SHOULDER ARTHROPLASTY ( 43 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 43 FDA reports)
TOE AMPUTATION ( 43 FDA reports)
TUBERCULOSIS ( 43 FDA reports)
VASCULAR RUPTURE ( 43 FDA reports)
WEIGHT BEARING DIFFICULTY ( 43 FDA reports)
ABORTION INDUCED ( 43 FDA reports)
BRADYPHRENIA ( 43 FDA reports)
FRACTURE NONUNION ( 43 FDA reports)
HERPES SIMPLEX ( 43 FDA reports)
INITIAL INSOMNIA ( 43 FDA reports)
MENINGIOMA BENIGN ( 43 FDA reports)
MITRAL VALVE DISEASE ( 43 FDA reports)
MULTIPLE FRACTURES ( 43 FDA reports)
NEUROPATHY ( 43 FDA reports)
ORAL CANDIDIASIS ( 43 FDA reports)
POSTOPERATIVE FEVER ( 43 FDA reports)
ACNE ( 42 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 42 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 42 FDA reports)
CERVICOBRACHIAL SYNDROME ( 42 FDA reports)
INJECTION SITE INFLAMMATION ( 42 FDA reports)
INJECTION SITE NECROSIS ( 42 FDA reports)
ISCHAEMIC STROKE ( 42 FDA reports)
LYMPHADENECTOMY ( 42 FDA reports)
MASTECTOMY ( 42 FDA reports)
MYOSITIS ( 42 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 42 FDA reports)
RECTAL PROLAPSE ( 42 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 42 FDA reports)
RETINAL TEAR ( 42 FDA reports)
THROAT CANCER ( 42 FDA reports)
TRAUMATIC BRAIN INJURY ( 42 FDA reports)
VENTRICULAR HYPERTROPHY ( 42 FDA reports)
WEIGHT FLUCTUATION ( 42 FDA reports)
RESPIRATORY RATE INCREASED ( 41 FDA reports)
SKIN WARM ( 41 FDA reports)
STRABISMUS ( 41 FDA reports)
THYROID CYST ( 41 FDA reports)
BILE DUCT OBSTRUCTION ( 41 FDA reports)
CARCINOMA ( 41 FDA reports)
DILATATION VENTRICULAR ( 41 FDA reports)
ERYTHEMA NODOSUM ( 41 FDA reports)
EXTRASYSTOLES ( 41 FDA reports)
FOOT OPERATION ( 41 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 41 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 41 FDA reports)
MENOPAUSAL SYMPTOMS ( 41 FDA reports)
NEPHRECTOMY ( 41 FDA reports)
NOCTURIA ( 41 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 40 FDA reports)
ANGIOPATHY ( 40 FDA reports)
CHOLECYSTITIS CHRONIC ( 40 FDA reports)
CYSTOPEXY ( 40 FDA reports)
DYSPNOEA EXERTIONAL ( 40 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 40 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 40 FDA reports)
HEPATIC ENZYME ABNORMAL ( 40 FDA reports)
HYPOVENTILATION ( 40 FDA reports)
PLACENTA PRAEVIA ( 40 FDA reports)
PNEUMONITIS ( 40 FDA reports)
POST PROCEDURAL PAIN ( 40 FDA reports)
SPINAL DEFORMITY ( 40 FDA reports)
UTERINE POLYP ( 40 FDA reports)
SARCOMA ( 39 FDA reports)
UNRESPONSIVE TO STIMULI ( 39 FDA reports)
UVEITIS ( 39 FDA reports)
VOLVULUS ( 39 FDA reports)
BLOOD CALCIUM INCREASED ( 39 FDA reports)
CYANOSIS ( 39 FDA reports)
FISTULA ( 39 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 39 FDA reports)
GINGIVAL BLEEDING ( 39 FDA reports)
HEART RATE ABNORMAL ( 39 FDA reports)
HEPATIC LESION ( 39 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 39 FDA reports)
INFECTED CYST ( 39 FDA reports)
JAW FRACTURE ( 39 FDA reports)
PAPILLARY THYROID CANCER ( 39 FDA reports)
PARAESTHESIA ORAL ( 39 FDA reports)
PHOTOPSIA ( 39 FDA reports)
POLYMENORRHOEA ( 39 FDA reports)
ABORTION MISSED ( 38 FDA reports)
ADENOMYOSIS ( 38 FDA reports)
BLOOD CALCIUM DECREASED ( 38 FDA reports)
CALCINOSIS ( 38 FDA reports)
CEREBRAL CYST ( 38 FDA reports)
DEVICE BREAKAGE ( 38 FDA reports)
GASTRIC PERFORATION ( 38 FDA reports)
GENERALISED OEDEMA ( 38 FDA reports)
HEAT STROKE ( 38 FDA reports)
INCORRECT DOSE ADMINISTERED ( 38 FDA reports)
INCREASED APPETITE ( 38 FDA reports)
JOINT HYPEREXTENSION ( 38 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 38 FDA reports)
PARKINSON'S DISEASE ( 38 FDA reports)
PEMPHIGOID ( 38 FDA reports)
UTERINE CYST ( 38 FDA reports)
SALIVARY GLAND CANCER ( 37 FDA reports)
SMALL FOR DATES BABY ( 37 FDA reports)
URINE ODOUR ABNORMAL ( 37 FDA reports)
ABNORMAL SENSATION IN EYE ( 37 FDA reports)
BAND SENSATION ( 37 FDA reports)
BARRETT'S OESOPHAGUS ( 37 FDA reports)
BILE DUCT STONE ( 37 FDA reports)
BONE GRAFT ( 37 FDA reports)
BONE NEOPLASM ( 37 FDA reports)
BURNS SECOND DEGREE ( 37 FDA reports)
CARDIAC FLUTTER ( 37 FDA reports)
COLECTOMY ( 37 FDA reports)
DRUG ERUPTION ( 37 FDA reports)
ERECTILE DYSFUNCTION ( 37 FDA reports)
FOOT DEFORMITY ( 37 FDA reports)
HUNGER ( 37 FDA reports)
INTERSTITIAL LUNG DISEASE ( 37 FDA reports)
NERVE ROOT COMPRESSION ( 37 FDA reports)
BENIGN OVARIAN TUMOUR ( 36 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 36 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 36 FDA reports)
COMMUNICATION DISORDER ( 36 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 36 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 36 FDA reports)
DIABETIC COMA ( 36 FDA reports)
DYSTONIA ( 36 FDA reports)
EYE OPERATION ( 36 FDA reports)
FORMICATION ( 36 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 36 FDA reports)
INTRA-UTERINE DEATH ( 36 FDA reports)
LIMB OPERATION ( 36 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 36 FDA reports)
OVARIAN MASS ( 36 FDA reports)
SUTURE RELATED COMPLICATION ( 36 FDA reports)
THYROID MASS ( 36 FDA reports)
TONGUE INJURY ( 36 FDA reports)
UMBILICAL HERNIA ( 36 FDA reports)
UPPER EXTREMITY MASS ( 36 FDA reports)
URTICARIA GENERALISED ( 36 FDA reports)
WRONG DRUG ADMINISTERED ( 36 FDA reports)
TENDON INJURY ( 35 FDA reports)
URINARY HESITATION ( 35 FDA reports)
VIITH NERVE INJURY ( 35 FDA reports)
VOCAL CORD DISORDER ( 35 FDA reports)
VOCAL CORD PARALYSIS ( 35 FDA reports)
ARTERIOSPASM CORONARY ( 35 FDA reports)
BLADDER CATHETERISATION ( 35 FDA reports)
BLEPHAROSPASM ( 35 FDA reports)
BRAIN INJURY ( 35 FDA reports)
BURNS THIRD DEGREE ( 35 FDA reports)
CLOSTRIDIUM COLITIS ( 35 FDA reports)
DYSLIPIDAEMIA ( 35 FDA reports)
INGROWING NAIL ( 35 FDA reports)
LUNG INFILTRATION ( 35 FDA reports)
LUNG INJURY ( 35 FDA reports)
MULTIPLE DRUG OVERDOSE ( 35 FDA reports)
NOSOCOMIAL INFECTION ( 35 FDA reports)
OESOPHAGEAL SPASM ( 35 FDA reports)
OPTIC NERVE INJURY ( 35 FDA reports)
ORAL PAIN ( 35 FDA reports)
POSTURE ABNORMAL ( 35 FDA reports)
PULSE ABSENT ( 35 FDA reports)
ABDOMINAL INFECTION ( 34 FDA reports)
ABSCESS INTESTINAL ( 34 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 34 FDA reports)
CARDIOGENIC SHOCK ( 34 FDA reports)
CYSTITIS INTERSTITIAL ( 34 FDA reports)
EYELID OEDEMA ( 34 FDA reports)
FUNGAL SKIN INFECTION ( 34 FDA reports)
GASTROINTESTINAL CARCINOMA ( 34 FDA reports)
GASTROINTESTINAL INJURY ( 34 FDA reports)
HAEMANGIOMA ( 34 FDA reports)
HYDRONEPHROSIS ( 34 FDA reports)
IMPLANT SITE INFECTION ( 34 FDA reports)
JOINT EFFUSION ( 34 FDA reports)
NODULE ( 34 FDA reports)
PELVIC PAIN ( 34 FDA reports)
PERSONALITY DISORDER ( 34 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 34 FDA reports)
RADICULOPATHY ( 34 FDA reports)
SCAB ( 34 FDA reports)
RETINAL HAEMORRHAGE ( 33 FDA reports)
SEXUAL DYSFUNCTION ( 33 FDA reports)
STEROID THERAPY ( 33 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 33 FDA reports)
VENTRICULAR TACHYCARDIA ( 33 FDA reports)
BENIGN NEOPLASM ( 33 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 33 FDA reports)
BREAST INFECTION ( 33 FDA reports)
CAROTID ARTERY STENOSIS ( 33 FDA reports)
CHOLECYSTITIS ACUTE ( 33 FDA reports)
COELIAC DISEASE ( 33 FDA reports)
DECREASED ACTIVITY ( 33 FDA reports)
GUN SHOT WOUND ( 33 FDA reports)
HELICOBACTER INFECTION ( 33 FDA reports)
INCISION SITE PAIN ( 33 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 33 FDA reports)
MYOCARDITIS ( 33 FDA reports)
NASAL SEPTUM DEVIATION ( 33 FDA reports)
NEUROPATHIC PAIN ( 33 FDA reports)
OBESITY SURGERY ( 33 FDA reports)
OESOPHAGEAL STENOSIS ( 33 FDA reports)
PANIC REACTION ( 33 FDA reports)
BLADDER PAIN ( 32 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 32 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 32 FDA reports)
BONE FRAGMENTATION ( 32 FDA reports)
BRAIN STEM SYNDROME ( 32 FDA reports)
DEVICE MALFUNCTION ( 32 FDA reports)
DUODENAL ULCER ( 32 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 32 FDA reports)
HYPERVENTILATION ( 32 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 32 FDA reports)
INFUSION SITE REACTION ( 32 FDA reports)
LIMB DEFORMITY ( 32 FDA reports)
NONSPECIFIC REACTION ( 32 FDA reports)
PULMONARY SARCOIDOSIS ( 32 FDA reports)
SUDDEN DEATH ( 32 FDA reports)
TRANSFUSION ( 32 FDA reports)
VACCINATION COMPLICATION ( 32 FDA reports)
VAGINAL DISCHARGE ( 32 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 32 FDA reports)
RHINITIS ( 31 FDA reports)
SPINAL CORD INJURY ( 31 FDA reports)
SUTURE RUPTURE ( 31 FDA reports)
THROMBOSIS IN DEVICE ( 31 FDA reports)
TRISOMY 21 ( 31 FDA reports)
UNDERWEIGHT ( 31 FDA reports)
ACCIDENTAL NEEDLE STICK ( 31 FDA reports)
ARTHROPOD STING ( 31 FDA reports)
CEREBROVASCULAR DISORDER ( 31 FDA reports)
DRY THROAT ( 31 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 31 FDA reports)
HEART VALVE REPLACEMENT ( 31 FDA reports)
HODGKIN'S DISEASE ( 31 FDA reports)
INFUSION SITE HAEMATOMA ( 31 FDA reports)
METASTASES TO SPINE ( 31 FDA reports)
PERSONALITY CHANGE ( 31 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 31 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 31 FDA reports)
POSTOPERATIVE ILEUS ( 31 FDA reports)
PROSTATE CANCER METASTATIC ( 31 FDA reports)
PULMONARY HAEMORRHAGE ( 31 FDA reports)
BLOOD CREATININE INCREASED ( 30 FDA reports)
COLONOSCOPY ( 30 FDA reports)
COLORECTAL CANCER ( 30 FDA reports)
COMPARTMENT SYNDROME ( 30 FDA reports)
COMPLICATION OF DELIVERY ( 30 FDA reports)
CYTOLYTIC HEPATITIS ( 30 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 30 FDA reports)
ENTEROCOCCAL INFECTION ( 30 FDA reports)
EYE PRURITUS ( 30 FDA reports)
FLUID INTAKE REDUCED ( 30 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 30 FDA reports)
HEPATOTOXICITY ( 30 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 30 FDA reports)
INTENTIONAL OVERDOSE ( 30 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 30 FDA reports)
PEPTIC ULCER ( 30 FDA reports)
PERFORATED ULCER ( 30 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 30 FDA reports)
POSTOPERATIVE THROMBOSIS ( 30 FDA reports)
RECURRENT CANCER ( 30 FDA reports)
RENAL NEOPLASM ( 30 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
RADIUS FRACTURE ( 29 FDA reports)
SALMONELLOSIS ( 29 FDA reports)
STREPTOCOCCAL SEPSIS ( 29 FDA reports)
SYNCOPE VASOVAGAL ( 29 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 29 FDA reports)
VENOUS INSUFFICIENCY ( 29 FDA reports)
VERTIGO POSITIONAL ( 29 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 29 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 29 FDA reports)
CATARACT OPERATION ( 29 FDA reports)
DROWNING ( 29 FDA reports)
DRUG ABUSER ( 29 FDA reports)
EXERCISE TOLERANCE DECREASED ( 29 FDA reports)
EYE INFECTION ( 29 FDA reports)
FACE OEDEMA ( 29 FDA reports)
FAILURE TO THRIVE ( 29 FDA reports)
GINGIVAL PAIN ( 29 FDA reports)
LACUNAR INFARCTION ( 29 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 29 FDA reports)
NEUROLOGICAL SYMPTOM ( 29 FDA reports)
PAIN EXACERBATED ( 29 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 29 FDA reports)
PELVIC SEPSIS ( 29 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 29 FDA reports)
ABDOMINAL RIGIDITY ( 28 FDA reports)
BLOOD UREA INCREASED ( 28 FDA reports)
BONE CYST ( 28 FDA reports)
BRONCHIECTASIS ( 28 FDA reports)
COLON CANCER STAGE II ( 28 FDA reports)
FEMALE STERILISATION ( 28 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 28 FDA reports)
GALLBLADDER PAIN ( 28 FDA reports)
GLOSSODYNIA ( 28 FDA reports)
HEPATIC FIBROSIS ( 28 FDA reports)
HEPATIC PAIN ( 28 FDA reports)
IMPAIRED WORK ABILITY ( 28 FDA reports)
JOINT LOCK ( 28 FDA reports)
LIMB DISCOMFORT ( 28 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 28 FDA reports)
NEURITIS ( 28 FDA reports)
NO ADVERSE EFFECT ( 28 FDA reports)
OESOPHAGEAL ULCER ( 28 FDA reports)
ORGAN FAILURE ( 28 FDA reports)
OVARIAN DISORDER ( 28 FDA reports)
POST PROCEDURAL SWELLING ( 28 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 28 FDA reports)
PROSTATIC DISORDER ( 28 FDA reports)
VENTRICULAR DYSFUNCTION ( 28 FDA reports)
WHIPLASH INJURY ( 28 FDA reports)
SKIN REACTION ( 27 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 27 FDA reports)
UTERINE NEOPLASM ( 27 FDA reports)
VASCULAR INJURY ( 27 FDA reports)
VENTRICULAR FIBRILLATION ( 27 FDA reports)
ANOXIC ENCEPHALOPATHY ( 27 FDA reports)
AUTOMATIC BLADDER ( 27 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 27 FDA reports)
CENTRAL LINE INFECTION ( 27 FDA reports)
CEREBRAL ISCHAEMIA ( 27 FDA reports)
CERVIX DISORDER ( 27 FDA reports)
CHOLESTASIS ( 27 FDA reports)
CYSTOCELE ( 27 FDA reports)
DISLOCATION OF VERTEBRA ( 27 FDA reports)
DISSOCIATION ( 27 FDA reports)
GASTRIC OPERATION ( 27 FDA reports)
GENITAL HERPES ( 27 FDA reports)
HEAD AND NECK CANCER ( 27 FDA reports)
HEPATIC INFECTION ( 27 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 27 FDA reports)
INTESTINAL GANGRENE ( 27 FDA reports)
ISCHAEMIA ( 27 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 27 FDA reports)
MACULAR DEGENERATION ( 27 FDA reports)
MYELOPATHY ( 27 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 27 FDA reports)
PANCREATIC CYST ( 27 FDA reports)
POSTOPERATIVE ADHESION ( 27 FDA reports)
PSYCHIATRIC SYMPTOM ( 27 FDA reports)
ABDOMINAL MASS ( 26 FDA reports)
ACCIDENT AT WORK ( 26 FDA reports)
ADENOCARCINOMA ( 26 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 26 FDA reports)
AORTIC THROMBOSIS ( 26 FDA reports)
BACTERIAL SEPSIS ( 26 FDA reports)
BENIGN LUNG NEOPLASM ( 26 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 26 FDA reports)
BLOOD CULTURE POSITIVE ( 26 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 26 FDA reports)
BONE DEFORMITY ( 26 FDA reports)
BREAST MICROCALCIFICATION ( 26 FDA reports)
BREAST RECONSTRUCTION ( 26 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 26 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 26 FDA reports)
ECCHYMOSIS ( 26 FDA reports)
FOETAL GROWTH RETARDATION ( 26 FDA reports)
HEART DISEASE CONGENITAL ( 26 FDA reports)
HEPATITIS B ( 26 FDA reports)
HYPERKERATOSIS ( 26 FDA reports)
HYPOKINESIA ( 26 FDA reports)
HYPOTHERMIA ( 26 FDA reports)
INJECTION SITE LACERATION ( 26 FDA reports)
INTESTINAL PROLAPSE ( 26 FDA reports)
LACRIMATION INCREASED ( 26 FDA reports)
MENINGITIS ASEPTIC ( 26 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 26 FDA reports)
MITRAL VALVE STENOSIS ( 26 FDA reports)
NEUTROPHIL COUNT DECREASED ( 26 FDA reports)
PELVIC FLUID COLLECTION ( 26 FDA reports)
PLANTAR FASCIITIS ( 26 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 26 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 26 FDA reports)
SEDATION ( 26 FDA reports)
SKIN TIGHTNESS ( 26 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 26 FDA reports)
TENDERNESS ( 26 FDA reports)
TENSION HEADACHE ( 26 FDA reports)
TRISMUS ( 26 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 26 FDA reports)
WOUND SECRETION ( 26 FDA reports)
SKIN INDURATION ( 25 FDA reports)
ALCOHOL ABUSE ( 25 FDA reports)
ALLERGY TO METALS ( 25 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 25 FDA reports)
ANEURYSM RUPTURED ( 25 FDA reports)
ANGIOEDEMA ( 25 FDA reports)
ARTHRITIS BACTERIAL ( 25 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 25 FDA reports)
BREAST COSMETIC SURGERY ( 25 FDA reports)
BRUXISM ( 25 FDA reports)
CARDIAC INFECTION ( 25 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 25 FDA reports)
CHEST INJURY ( 25 FDA reports)
COLON NEOPLASM ( 25 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 25 FDA reports)
DIASTOLIC DYSFUNCTION ( 25 FDA reports)
EAR DISCOMFORT ( 25 FDA reports)
EAR DISORDER ( 25 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 25 FDA reports)
EYE INJURY ( 25 FDA reports)
FACIAL NEURALGIA ( 25 FDA reports)
GASTRIC ULCER PERFORATION ( 25 FDA reports)
GENITAL DISORDER FEMALE ( 25 FDA reports)
HAEMORRHAGIC DISORDER ( 25 FDA reports)
HEART VALVE INSUFFICIENCY ( 25 FDA reports)
HOMICIDAL IDEATION ( 25 FDA reports)
HYPERREFLEXIA ( 25 FDA reports)
INJECTION SITE ANAESTHESIA ( 25 FDA reports)
INTESTINAL HAEMORRHAGE ( 25 FDA reports)
JAW DISORDER ( 25 FDA reports)
MEDICAL DEVICE REMOVAL ( 25 FDA reports)
MELANOCYTIC NAEVUS ( 25 FDA reports)
MENINGITIS BACTERIAL ( 25 FDA reports)
NO ADVERSE DRUG EFFECT ( 25 FDA reports)
PAINFUL RESPIRATION ( 25 FDA reports)
ADJUSTMENT DISORDER ( 24 FDA reports)
ARTERIAL DISORDER ( 24 FDA reports)
ASTHENOPIA ( 24 FDA reports)
BLADDER CANCER STAGE II ( 24 FDA reports)
BONE MARROW DISORDER ( 24 FDA reports)
CATHETER SITE PAIN ( 24 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 24 FDA reports)
DERMATITIS ( 24 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 24 FDA reports)
DISEASE COMPLICATION ( 24 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 24 FDA reports)
ILEUS PARALYTIC ( 24 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 24 FDA reports)
OOPHORECTOMY BILATERAL ( 24 FDA reports)
OPPORTUNISTIC INFECTION ( 24 FDA reports)
OPTIC NEUROPATHY ( 24 FDA reports)
OROPHARYNGEAL BLISTERING ( 24 FDA reports)
PROSTATOMEGALY ( 24 FDA reports)
PROTHROMBIN TIME PROLONGED ( 24 FDA reports)
PULMONARY GRANULOMA ( 24 FDA reports)
STARING ( 24 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 24 FDA reports)
URETHRAL DISORDER ( 24 FDA reports)
VENTRICULAR HYPOKINESIA ( 24 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 23 FDA reports)
SENSATION OF PRESSURE ( 23 FDA reports)
SMALL CELL CARCINOMA ( 23 FDA reports)
STEVENS-JOHNSON SYNDROME ( 23 FDA reports)
VERTEBRAL INJURY ( 23 FDA reports)
AORTIC STENOSIS ( 23 FDA reports)
ARTERIAL INJURY ( 23 FDA reports)
ARTHROSCOPY ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 23 FDA reports)
BLADDER DYSFUNCTION ( 23 FDA reports)
BLADDER NEOPLASM ( 23 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 23 FDA reports)
CATHETER SEPSIS ( 23 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 23 FDA reports)
CERVICAL DYSPLASIA ( 23 FDA reports)
DEVICE ISSUE ( 23 FDA reports)
DILATATION ATRIAL ( 23 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 23 FDA reports)
EMBOLIC STROKE ( 23 FDA reports)
ESCHERICHIA SEPSIS ( 23 FDA reports)
GALLBLADDER ENLARGEMENT ( 23 FDA reports)
GRANULOMA ( 23 FDA reports)
HERPES VIRUS INFECTION ( 23 FDA reports)
HYPOVOLAEMIA ( 23 FDA reports)
INCISIONAL HERNIA ( 23 FDA reports)
INJECTION SITE BURNING ( 23 FDA reports)
LOCALISED OEDEMA ( 23 FDA reports)
LOCALISED OSTEOARTHRITIS ( 23 FDA reports)
MALIGNANT MELANOMA IN SITU ( 23 FDA reports)
MOUTH HAEMORRHAGE ( 23 FDA reports)
MYOPIA ( 23 FDA reports)
NEOPLASM PROGRESSION ( 23 FDA reports)
NEPHROTIC SYNDROME ( 23 FDA reports)
NEUTROPHIL COUNT INCREASED ( 23 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 23 FDA reports)
PANCREAS INFECTION ( 23 FDA reports)
PERICARDIAL HAEMORRHAGE ( 23 FDA reports)
PETECHIAE ( 23 FDA reports)
POISONING ( 23 FDA reports)
ABDOMINOPLASTY ( 22 FDA reports)
AFFECTIVE DISORDER ( 22 FDA reports)
ANURIA ( 22 FDA reports)
BENIGN COLONIC NEOPLASM ( 22 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 22 FDA reports)
BLADDER REPAIR ( 22 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 22 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 22 FDA reports)
CEREBELLAR SYNDROME ( 22 FDA reports)
COCCYDYNIA ( 22 FDA reports)
CONGENITAL ANOMALY ( 22 FDA reports)
DIABETES INSIPIDUS ( 22 FDA reports)
DIABETIC COMPLICATION ( 22 FDA reports)
ENDOCARDITIS ( 22 FDA reports)
FLANK PAIN ( 22 FDA reports)
FLUID OVERLOAD ( 22 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 22 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 22 FDA reports)
HAEMOCHROMATOSIS ( 22 FDA reports)
HYPERCOAGULATION ( 22 FDA reports)
INCISION SITE ABSCESS ( 22 FDA reports)
INGUINAL HERNIA ( 22 FDA reports)
IRON DEFICIENCY ( 22 FDA reports)
LABYRINTHITIS ( 22 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 22 FDA reports)
MAMMOPLASTY ( 22 FDA reports)
METASTASIS ( 22 FDA reports)
NON-CARDIAC CHEST PAIN ( 22 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 22 FDA reports)
OEDEMA MOUTH ( 22 FDA reports)
OVARIAN CANCER RECURRENT ( 22 FDA reports)
PAPILLOMA VIRAL INFECTION ( 22 FDA reports)
PELVIC MASS ( 22 FDA reports)
PLASMAPHERESIS ( 22 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 22 FDA reports)
PROTEIN TOTAL INCREASED ( 22 FDA reports)
PUPILLARY DISORDER ( 22 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 22 FDA reports)
RENAL TRANSPLANT ( 22 FDA reports)
SCAPULA FRACTURE ( 22 FDA reports)
STRESS FRACTURE ( 22 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 22 FDA reports)
TWIN PREGNANCY ( 22 FDA reports)
UTERINE DILATION AND CURETTAGE ( 22 FDA reports)
QUALITY OF LIFE DECREASED ( 21 FDA reports)
READING DISORDER ( 21 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 21 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 21 FDA reports)
STENT OCCLUSION ( 21 FDA reports)
TEMPERATURE REGULATION DISORDER ( 21 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 21 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 21 FDA reports)
URINE OUTPUT DECREASED ( 21 FDA reports)
VARICELLA ( 21 FDA reports)
VICTIM OF CRIME ( 21 FDA reports)
VULVOVAGINAL PRURITUS ( 21 FDA reports)
WOUND HAEMORRHAGE ( 21 FDA reports)
ACUTE CORONARY SYNDROME ( 21 FDA reports)
ACUTE PULMONARY OEDEMA ( 21 FDA reports)
ALCOHOLIC LIVER DISEASE ( 21 FDA reports)
BRONCHITIS CHRONIC ( 21 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 21 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 21 FDA reports)
CARDIOVASCULAR EVALUATION ( 21 FDA reports)
CERVICAL MYELOPATHY ( 21 FDA reports)
COLOSTOMY CLOSURE ( 21 FDA reports)
DARK CIRCLES UNDER EYES ( 21 FDA reports)
DEPRESSION SUICIDAL ( 21 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 21 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 21 FDA reports)
GASTROINTESTINAL NECROSIS ( 21 FDA reports)
GLIOBLASTOMA ( 21 FDA reports)
GLIOBLASTOMA MULTIFORME ( 21 FDA reports)
HAIR TEXTURE ABNORMAL ( 21 FDA reports)
HERPES OPHTHALMIC ( 21 FDA reports)
LEIOMYOMA ( 21 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
LYMPHOPENIA ( 21 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 21 FDA reports)
MUSCLE CONTRACTURE ( 21 FDA reports)
NECK MASS ( 21 FDA reports)
NEOPLASM SKIN ( 21 FDA reports)
OESOPHAGEAL FISTULA ( 21 FDA reports)
PLATELET DISORDER ( 21 FDA reports)
PNEUMONIA VIRAL ( 21 FDA reports)
PROTEIN TOTAL DECREASED ( 21 FDA reports)
ABDOMINAL OPERATION ( 20 FDA reports)
ADRENAL INSUFFICIENCY ( 20 FDA reports)
ANORECTAL DISORDER ( 20 FDA reports)
APHTHOUS STOMATITIS ( 20 FDA reports)
ARTERIAL STENOSIS ( 20 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 20 FDA reports)
BLOOD SODIUM ABNORMAL ( 20 FDA reports)
BLOOD URINE ( 20 FDA reports)
BREAST CANCER STAGE IV ( 20 FDA reports)
BREAST CELLULITIS ( 20 FDA reports)
CAROTID ARTERY DISEASE ( 20 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 20 FDA reports)
COLONIC STENOSIS ( 20 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 20 FDA reports)
CORONARY ARTERY SURGERY ( 20 FDA reports)
DIVERTICULUM INTESTINAL ( 20 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 20 FDA reports)
DYSPLASIA ( 20 FDA reports)
EXTREMITY CONTRACTURE ( 20 FDA reports)
FEELING HOT AND COLD ( 20 FDA reports)
FIBRIN D DIMER INCREASED ( 20 FDA reports)
FOETAL HEART RATE DECREASED ( 20 FDA reports)
FRACTURE DELAYED UNION ( 20 FDA reports)
FRACTURED SACRUM ( 20 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 20 FDA reports)
HEAD TITUBATION ( 20 FDA reports)
HEMICEPHALALGIA ( 20 FDA reports)
HICCUPS ( 20 FDA reports)
HYPERTROPHIC SCAR ( 20 FDA reports)
IMPLANT SITE REACTION ( 20 FDA reports)
JOINT ARTHROPLASTY ( 20 FDA reports)
JOINT CREPITATION ( 20 FDA reports)
KLEBSIELLA INFECTION ( 20 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 20 FDA reports)
MYCOSIS FUNGOIDES ( 20 FDA reports)
NIGHT BLINDNESS ( 20 FDA reports)
OBSTRUCTIVE UROPATHY ( 20 FDA reports)
OESOPHAGEAL RUPTURE ( 20 FDA reports)
OVARIAN CYST RUPTURED ( 20 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 20 FDA reports)
POST PROCEDURAL VOMITING ( 20 FDA reports)
SCREAMING ( 20 FDA reports)
SECRETION DISCHARGE ( 20 FDA reports)
SINUS OPERATION ( 20 FDA reports)
SKIN HAEMORRHAGE ( 20 FDA reports)
SMALL INTESTINAL PERFORATION ( 20 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 20 FDA reports)
STRESS URINARY INCONTINENCE ( 20 FDA reports)
SUNBURN ( 20 FDA reports)
TRACHEOSTOMY ( 20 FDA reports)
TRANSAMINASES INCREASED ( 20 FDA reports)
VAGINAL MYCOSIS ( 20 FDA reports)
VASCULAR PSEUDOANEURYSM ( 20 FDA reports)
VENOUS THROMBOSIS ( 20 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 19 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 19 FDA reports)
TERMINAL STATE ( 19 FDA reports)
TRIGEMINAL NERVE DISORDER ( 19 FDA reports)
ULNA FRACTURE ( 19 FDA reports)
ULNAR NERVE INJURY ( 19 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 19 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 19 FDA reports)
AORTIC DISSECTION ( 19 FDA reports)
APLASTIC ANAEMIA ( 19 FDA reports)
BENIGN RENAL NEOPLASM ( 19 FDA reports)
BLOOD SODIUM INCREASED ( 19 FDA reports)
BREAST NEOPLASM ( 19 FDA reports)
CHEST X-RAY ABNORMAL ( 19 FDA reports)
COCCIDIOIDOMYCOSIS ( 19 FDA reports)
COLONIC OBSTRUCTION ( 19 FDA reports)
CYSTITIS PSEUDOMONAL ( 19 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 19 FDA reports)
FACIAL SPASM ( 19 FDA reports)
FAT NECROSIS ( 19 FDA reports)
FEMORAL ARTERY OCCLUSION ( 19 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 19 FDA reports)
GLOSSITIS ( 19 FDA reports)
HEPATIC ENCEPHALOPATHY ( 19 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 19 FDA reports)
ILEOSTOMY ( 19 FDA reports)
IMMUNODEFICIENCY ( 19 FDA reports)
IMMUNOGLOBULINS DECREASED ( 19 FDA reports)
INFECTIVE THROMBOSIS ( 19 FDA reports)
LIVEDO RETICULARIS ( 19 FDA reports)
MUSCLE FATIGUE ( 19 FDA reports)
MYOCARDIAL CALCIFICATION ( 19 FDA reports)
OCULAR ICTERUS ( 19 FDA reports)
OPTIC ATROPHY ( 19 FDA reports)
ORAL FUNGAL INFECTION ( 19 FDA reports)
ORAL INFECTION ( 19 FDA reports)
ORGANISING PNEUMONIA ( 19 FDA reports)
POLYARTHRITIS ( 19 FDA reports)
PRECANCEROUS SKIN LESION ( 19 FDA reports)
ABDOMINAL TENDERNESS ( 18 FDA reports)
ACOUSTIC NEUROMA ( 18 FDA reports)
ACUTE HEPATIC FAILURE ( 18 FDA reports)
ACUTE RESPIRATORY FAILURE ( 18 FDA reports)
ACUTE SINUSITIS ( 18 FDA reports)
ANAEMIA POSTOPERATIVE ( 18 FDA reports)
AORTIC ANEURYSM RUPTURE ( 18 FDA reports)
AORTIC VALVE REPLACEMENT ( 18 FDA reports)
AORTIC VALVE STENOSIS ( 18 FDA reports)
AREFLEXIA ( 18 FDA reports)
ARTERIAL RUPTURE ( 18 FDA reports)
BENIGN UTERINE NEOPLASM ( 18 FDA reports)
BREAST CALCIFICATIONS ( 18 FDA reports)
CARDIAC ANEURYSM ( 18 FDA reports)
CATHETER SITE INFECTION ( 18 FDA reports)
COLORECTAL CANCER METASTATIC ( 18 FDA reports)
COW'S MILK INTOLERANCE ( 18 FDA reports)
DEVICE OCCLUSION ( 18 FDA reports)
DRUG TOLERANCE ( 18 FDA reports)
DRUG TOLERANCE DECREASED ( 18 FDA reports)
DYSAESTHESIA ( 18 FDA reports)
ERYSIPELAS ( 18 FDA reports)
ESSENTIAL HYPERTENSION ( 18 FDA reports)
EXCESSIVE SKIN ( 18 FDA reports)
FAMILY STRESS ( 18 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 18 FDA reports)
GASTROINTESTINAL ULCER ( 18 FDA reports)
HAEMOLYTIC ANAEMIA ( 18 FDA reports)
HEPATITIS ACUTE ( 18 FDA reports)
HYPERCHLORHYDRIA ( 18 FDA reports)
HYPERPARATHYROIDISM ( 18 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 18 FDA reports)
LIBIDO DECREASED ( 18 FDA reports)
MAMMOGRAM ABNORMAL ( 18 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
METABOLIC ACIDOSIS ( 18 FDA reports)
MIDDLE EAR EFFUSION ( 18 FDA reports)
MUSCLE ABSCESS ( 18 FDA reports)
OBSTRUCTION ( 18 FDA reports)
OVARIAN FIBROMA ( 18 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 18 FDA reports)
PEPTIC ULCER PERFORATION ( 18 FDA reports)
POLYURIA ( 18 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 18 FDA reports)
RADIATION INJURY ( 18 FDA reports)
RECTAL POLYP ( 18 FDA reports)
SERUM FERRITIN INCREASED ( 18 FDA reports)
SKIN IRRITATION ( 18 FDA reports)
SKIN NECROSIS ( 18 FDA reports)
SPINAL COLUMN INJURY ( 18 FDA reports)
SPINAL DECOMPRESSION ( 18 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 18 FDA reports)
TRAUMATIC LUNG INJURY ( 18 FDA reports)
TYPE 1 DIABETES MELLITUS ( 18 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 18 FDA reports)
VASCULAR OCCLUSION ( 18 FDA reports)
VENOUS OCCLUSION ( 18 FDA reports)
PURULENCE ( 17 FDA reports)
QUADRIPARESIS ( 17 FDA reports)
RESPIRATORY RATE DECREASED ( 17 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 17 FDA reports)
SENSATION OF FOREIGN BODY ( 17 FDA reports)
SINUS BRADYCARDIA ( 17 FDA reports)
SKIN BACTERIAL INFECTION ( 17 FDA reports)
STRESS CARDIOMYOPATHY ( 17 FDA reports)
THROMBOTIC STROKE ( 17 FDA reports)
UTERINE RUPTURE ( 17 FDA reports)
VAGINAL PROLAPSE ( 17 FDA reports)
WEGENER'S GRANULOMATOSIS ( 17 FDA reports)
ALCOHOL POISONING ( 17 FDA reports)
ANGIOPLASTY ( 17 FDA reports)
APPENDIX DISORDER ( 17 FDA reports)
ARTERIAL THROMBOSIS ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK ( 17 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 17 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 17 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 17 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 17 FDA reports)
CARDIOTOXICITY ( 17 FDA reports)
CHRONIC HEPATITIS ( 17 FDA reports)
COLON OPERATION ( 17 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 17 FDA reports)
CONFUSION POSTOPERATIVE ( 17 FDA reports)
CORONARY ARTERY DISSECTION ( 17 FDA reports)
DERMAL CYST ( 17 FDA reports)
DIABETIC FOOT ( 17 FDA reports)
DIABETIC VASCULAR DISORDER ( 17 FDA reports)
DIAPHRAGMATIC DISORDER ( 17 FDA reports)
DRUG ADMINISTRATION ERROR ( 17 FDA reports)
EAR CONGESTION ( 17 FDA reports)
FACET JOINT SYNDROME ( 17 FDA reports)
FALLOPIAN TUBE CYST ( 17 FDA reports)
FEELING OF DESPAIR ( 17 FDA reports)
GASTROENTERITIS SALMONELLA ( 17 FDA reports)
GASTROINTESTINAL NEOPLASM ( 17 FDA reports)
HALLUCINATIONS, MIXED ( 17 FDA reports)
HEAD DISCOMFORT ( 17 FDA reports)
HORMONE LEVEL ABNORMAL ( 17 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 17 FDA reports)
INFUSION SITE EXTRAVASATION ( 17 FDA reports)
INNER EAR DISORDER ( 17 FDA reports)
INTERVERTEBRAL DISCITIS ( 17 FDA reports)
LYMPHADENITIS ( 17 FDA reports)
MENSTRUATION DELAYED ( 17 FDA reports)
MONARTHRITIS ( 17 FDA reports)
MYELITIS ( 17 FDA reports)
OSTEOCHONDROSIS ( 17 FDA reports)
PATHOGEN RESISTANCE ( 17 FDA reports)
PHARYNGEAL ULCERATION ( 17 FDA reports)
POLYNEUROPATHY ( 17 FDA reports)
POSTICTAL STATE ( 17 FDA reports)
PROCTALGIA ( 17 FDA reports)
PROTEIN S DEFICIENCY ( 17 FDA reports)
PROTEUS INFECTION ( 17 FDA reports)
PRURITUS ALLERGIC ( 17 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 16 FDA reports)
ALCOHOL PROBLEM ( 16 FDA reports)
ANAL CANCER ( 16 FDA reports)
ANAL FISTULA ( 16 FDA reports)
ANXIETY DISORDER ( 16 FDA reports)
ARTERIAL REPAIR ( 16 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 16 FDA reports)
BILIARY DYSKINESIA ( 16 FDA reports)
BLEEDING TIME PROLONGED ( 16 FDA reports)
BLISTER INFECTED ( 16 FDA reports)
BLOOD ALBUMIN INCREASED ( 16 FDA reports)
BLOOD CHLORIDE DECREASED ( 16 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 16 FDA reports)
BRAIN DAMAGE ( 16 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 16 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 16 FDA reports)
CHRONIC SINUSITIS ( 16 FDA reports)
COLON CANCER RECURRENT ( 16 FDA reports)
CONDUCTION DISORDER ( 16 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 16 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 16 FDA reports)
DEVICE INEFFECTIVE ( 16 FDA reports)
DIABETIC KETOACIDOSIS ( 16 FDA reports)
DISTRACTIBILITY ( 16 FDA reports)
DIVERTICULAR PERFORATION ( 16 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 16 FDA reports)
ENZYME ABNORMALITY ( 16 FDA reports)
EROSIVE OESOPHAGITIS ( 16 FDA reports)
EUPHORIC MOOD ( 16 FDA reports)
FALLOPIAN TUBE DISORDER ( 16 FDA reports)
FOETAL HEART RATE ABNORMAL ( 16 FDA reports)
FOLLICULITIS ( 16 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 16 FDA reports)
GESTATIONAL HYPERTENSION ( 16 FDA reports)
HEART INJURY ( 16 FDA reports)
HEPATIC NEOPLASM ( 16 FDA reports)
HEPATITIS TOXIC ( 16 FDA reports)
INJECTION SITE DISCOMFORT ( 16 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 16 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 16 FDA reports)
LIVER TRANSPLANT ( 16 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 16 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 16 FDA reports)
MUSCLE NECROSIS ( 16 FDA reports)
NEOPLASM RECURRENCE ( 16 FDA reports)
NEUROFIBROMA ( 16 FDA reports)
OCULAR VASCULAR DISORDER ( 16 FDA reports)
OSTEOSCLEROSIS ( 16 FDA reports)
OVARIAN EPITHELIAL CANCER ( 16 FDA reports)
PERIARTHRITIS ( 16 FDA reports)
PERIPHERAL ISCHAEMIA ( 16 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 16 FDA reports)
PLACENTAL DISORDER ( 16 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 16 FDA reports)
PORTAL HYPERTENSION ( 16 FDA reports)
POST PROCEDURAL NAUSEA ( 16 FDA reports)
PROLONGED LABOUR ( 16 FDA reports)
PROSTATE CANCER STAGE II ( 16 FDA reports)
PULMONARY CONGESTION ( 16 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 16 FDA reports)
REFLEXES ABNORMAL ( 16 FDA reports)
RENAL MASS ( 16 FDA reports)
SHUNT INFECTION ( 16 FDA reports)
SIALOADENITIS ( 16 FDA reports)
SKIN ATROPHY ( 16 FDA reports)
SPLEEN DISORDER ( 16 FDA reports)
STERNAL FRACTURE ( 16 FDA reports)
TEARFULNESS ( 16 FDA reports)
THROMBOCYTHAEMIA ( 16 FDA reports)
TONGUE DISORDER ( 16 FDA reports)
TONSILLECTOMY ( 16 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 16 FDA reports)
URINARY BLADDER POLYP ( 16 FDA reports)
VOLVULUS OF BOWEL ( 16 FDA reports)
RADICULITIS LUMBOSACRAL ( 15 FDA reports)
REFLUX OESOPHAGITIS ( 15 FDA reports)
RHINITIS ALLERGIC ( 15 FDA reports)
SICK SINUS SYNDROME ( 15 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 15 FDA reports)
SOFT TISSUE INJURY ( 15 FDA reports)
SPLENIC CYST ( 15 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 15 FDA reports)
SUPERFICIAL INJURY OF EYE ( 15 FDA reports)
TRAUMATIC HAEMATOMA ( 15 FDA reports)
TUBAL LIGATION ( 15 FDA reports)
VAGINAL NEOPLASM ( 15 FDA reports)
VIBRATORY SENSE INCREASED ( 15 FDA reports)
YELLOW SKIN ( 15 FDA reports)
ABDOMINAL PANNICULECTOMY ( 15 FDA reports)
ADRENAL NEOPLASM ( 15 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 15 FDA reports)
ANOSMIA ( 15 FDA reports)
AORTIC DISORDER ( 15 FDA reports)
ARTHRITIS FUNGAL ( 15 FDA reports)
ATHEROSCLEROSIS ( 15 FDA reports)
BACTERIAL DISEASE CARRIER ( 15 FDA reports)
BASAL GANGLIA INFARCTION ( 15 FDA reports)
BILIARY TRACT DISORDER ( 15 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 15 FDA reports)
BONE EROSION ( 15 FDA reports)
BRAIN DEATH ( 15 FDA reports)
BRAIN HYPOXIA ( 15 FDA reports)
BURNOUT SYNDROME ( 15 FDA reports)
CALCULUS URETERIC ( 15 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 15 FDA reports)
CEREBRAL SARCOIDOSIS ( 15 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 15 FDA reports)
COLON CANCER STAGE IV ( 15 FDA reports)
COSTOCHONDRITIS ( 15 FDA reports)
DEPRESSIVE SYMPTOM ( 15 FDA reports)
DEVICE LEAKAGE ( 15 FDA reports)
DRUG RESISTANCE ( 15 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 15 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 15 FDA reports)
FASCIITIS ( 15 FDA reports)
FOETAL DISTRESS SYNDROME ( 15 FDA reports)
GASTRIC POLYPS ( 15 FDA reports)
HAEMODIALYSIS ( 15 FDA reports)
HEPATITIS A ( 15 FDA reports)
HYPERPHAGIA ( 15 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 15 FDA reports)
INTERMITTENT CLAUDICATION ( 15 FDA reports)
INVESTIGATION ABNORMAL ( 15 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 15 FDA reports)
LARYNGEAL CANCER ( 15 FDA reports)
LARYNGEAL DISORDER ( 15 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 15 FDA reports)
LIPOSUCTION ( 15 FDA reports)
LISTLESS ( 15 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 15 FDA reports)
LUNG ABSCESS ( 15 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 15 FDA reports)
MEAN CELL VOLUME INCREASED ( 15 FDA reports)
MICTURITION DISORDER ( 15 FDA reports)
NEEDLE ISSUE ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 15 FDA reports)
PAROSMIA ( 15 FDA reports)
PNEUMONIA LEGIONELLA ( 15 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 15 FDA reports)
ABDOMINAL HERNIA REPAIR ( 14 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 14 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 14 FDA reports)
BILIARY CIRRHOSIS ( 14 FDA reports)
BLOOD BLISTER ( 14 FDA reports)
BREAST DISORDER ( 14 FDA reports)
BREAST LUMP REMOVAL ( 14 FDA reports)
BREATH ODOUR ( 14 FDA reports)
CATATONIA ( 14 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 14 FDA reports)
CERVICAL POLYP ( 14 FDA reports)
CHEST WALL MASS ( 14 FDA reports)
COMPLICATION OF PREGNANCY ( 14 FDA reports)
DYSPHASIA ( 14 FDA reports)
FAILURE OF IMPLANT ( 14 FDA reports)
FOETAL MALPOSITION ( 14 FDA reports)
GINGIVAL INFECTION ( 14 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 14 FDA reports)
HAEMORRHAGIC ANAEMIA ( 14 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
HYPERKALAEMIA ( 14 FDA reports)
INDIFFERENCE ( 14 FDA reports)
INFUSION SITE INFECTION ( 14 FDA reports)
INJECTION SITE NODULE ( 14 FDA reports)
INTENTIONAL SELF-INJURY ( 14 FDA reports)
JAUNDICE CHOLESTATIC ( 14 FDA reports)
JAW OPERATION ( 14 FDA reports)
LACTOSE INTOLERANCE ( 14 FDA reports)
LEFT VENTRICULAR FAILURE ( 14 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 14 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 14 FDA reports)
MEDICAL DEVICE PAIN ( 14 FDA reports)
MENINGITIS HERPES ( 14 FDA reports)
METABOLIC ENCEPHALOPATHY ( 14 FDA reports)
METAMORPHOPSIA ( 14 FDA reports)
MICROCYTIC ANAEMIA ( 14 FDA reports)
MITRAL VALVE REPAIR ( 14 FDA reports)
MOUTH INJURY ( 14 FDA reports)
MYDRIASIS ( 14 FDA reports)
NAIL DISORDER ( 14 FDA reports)
NASOPHARYNGEAL DISORDER ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BREAST ABNORMAL ( 14 FDA reports)
OESOPHAGEAL PERFORATION ( 14 FDA reports)
OESOPHAGITIS ULCERATIVE ( 14 FDA reports)
ONYCHOCLASIS ( 14 FDA reports)
PERIPHERAL EMBOLISM ( 14 FDA reports)
PHARYNGEAL DISORDER ( 14 FDA reports)
PNEUMONIA MYCOPLASMAL ( 14 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 14 FDA reports)
PSYCHOSOMATIC DISEASE ( 14 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 14 FDA reports)
RETINITIS ( 14 FDA reports)
SCLERODERMA ( 14 FDA reports)
THYROID ADENOMA ( 14 FDA reports)
TONIC CONVULSION ( 14 FDA reports)
TONSILLITIS ( 14 FDA reports)
TRAUMATIC HAEMORRHAGE ( 14 FDA reports)
TREATMENT FAILURE ( 14 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
WEIGHT GAIN POOR ( 14 FDA reports)
WHITE BLOOD CELL DISORDER ( 14 FDA reports)
RASH PUSTULAR ( 13 FDA reports)
RECTAL CANCER STAGE I ( 13 FDA reports)
RENAL ARTERY OCCLUSION ( 13 FDA reports)
RENAL SURGERY ( 13 FDA reports)
ROSACEA ( 13 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 13 FDA reports)
SELF-INJURIOUS IDEATION ( 13 FDA reports)
SKIN ODOUR ABNORMAL ( 13 FDA reports)
SLEEP TALKING ( 13 FDA reports)
SOMNAMBULISM ( 13 FDA reports)
SUDDEN CARDIAC DEATH ( 13 FDA reports)
TENDON OPERATION ( 13 FDA reports)
THROMBOPHLEBITIS ( 13 FDA reports)
THYROIDITIS ( 13 FDA reports)
TONGUE CARCINOMA STAGE III ( 13 FDA reports)
TONGUE CARCINOMA STAGE IV ( 13 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 13 FDA reports)
UTERINE MASS ( 13 FDA reports)
VAGINAL CANCER ( 13 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 13 FDA reports)
VOCAL CORD POLYP ( 13 FDA reports)
WOUND SEPSIS ( 13 FDA reports)
ABDOMINAL NEOPLASM ( 13 FDA reports)
ALCOHOL USE ( 13 FDA reports)
AMMONIA INCREASED ( 13 FDA reports)
AORTIC OCCLUSION ( 13 FDA reports)
APNOEIC ATTACK ( 13 FDA reports)
ARRESTED LABOUR ( 13 FDA reports)
ARTERITIS ( 13 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 13 FDA reports)
BENIGN GASTRIC NEOPLASM ( 13 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 13 FDA reports)
BILE DUCT CANCER ( 13 FDA reports)
BILIARY COLIC ( 13 FDA reports)
BLIGHTED OVUM ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
BODY TEMPERATURE ( 13 FDA reports)
BONE INFECTION ( 13 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 13 FDA reports)
BRAIN MASS ( 13 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 13 FDA reports)
BUTTOCK PAIN ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 13 FDA reports)
CEREBRAL HAEMATOMA ( 13 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 13 FDA reports)
CERVICAL CORD COMPRESSION ( 13 FDA reports)
CERVIX CARCINOMA STAGE II ( 13 FDA reports)
CERVIX CARCINOMA STAGE III ( 13 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 13 FDA reports)
COAGULATION TIME PROLONGED ( 13 FDA reports)
COMPRESSION FRACTURE ( 13 FDA reports)
CSF PROTEIN INCREASED ( 13 FDA reports)
CSF TEST ABNORMAL ( 13 FDA reports)
DECREASED INTEREST ( 13 FDA reports)
DERMATOMYOSITIS ( 13 FDA reports)
DIABETIC NEUROPATHY ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 13 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 13 FDA reports)
EPICONDYLITIS ( 13 FDA reports)
EPIDIDYMITIS ( 13 FDA reports)
FACIAL PARESIS ( 13 FDA reports)
FIBROSIS ( 13 FDA reports)
GAIT SPASTIC ( 13 FDA reports)
GASTRIC BANDING ( 13 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 13 FDA reports)
GINGIVAL SWELLING ( 13 FDA reports)
GLARE ( 13 FDA reports)
HEPATIC HAEMORRHAGE ( 13 FDA reports)
INCISION SITE CELLULITIS ( 13 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 13 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 13 FDA reports)
INFUSION SITE SWELLING ( 13 FDA reports)
INJECTION SITE HYPERTROPHY ( 13 FDA reports)
INJECTION SITE THROMBOSIS ( 13 FDA reports)
INTRAOCULAR MELANOMA ( 13 FDA reports)
IRITIS ( 13 FDA reports)
JC VIRUS INFECTION ( 13 FDA reports)
JOINT WARMTH ( 13 FDA reports)
LARYNGOSPASM ( 13 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 13 FDA reports)
LIGAMENT DISORDER ( 13 FDA reports)
LIPOATROPHY ( 13 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 13 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 13 FDA reports)
LUMBAR PUNCTURE ( 13 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 13 FDA reports)
MARROW HYPERPLASIA ( 13 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 13 FDA reports)
MOUTH ULCERATION ( 13 FDA reports)
NEONATAL DISORDER ( 13 FDA reports)
NEPHROPATHY ( 13 FDA reports)
NERVE BLOCK ( 13 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 13 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 13 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 13 FDA reports)
OVARIAN CANCER METASTATIC ( 13 FDA reports)
PANCREATITIS RELAPSING ( 13 FDA reports)
PARVOVIRUS INFECTION ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PCO2 DECREASED ( 13 FDA reports)
PELVIC PROLAPSE ( 13 FDA reports)
PERIODONTAL DISEASE ( 13 FDA reports)
PHARYNGEAL MASS ( 13 FDA reports)
PHYSICAL ASSAULT ( 13 FDA reports)
PITTING OEDEMA ( 13 FDA reports)
PLEURAL FIBROSIS ( 13 FDA reports)
PORPHYRIA NON-ACUTE ( 13 FDA reports)
PROCEDURAL SITE REACTION ( 13 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 13 FDA reports)
ACCIDENTAL EXPOSURE ( 12 FDA reports)
ADRENAL CARCINOMA ( 12 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 12 FDA reports)
ALVEOLITIS ALLERGIC ( 12 FDA reports)
ANAL CANCER METASTATIC ( 12 FDA reports)
ANORECTAL OPERATION ( 12 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 12 FDA reports)
BIOPSY LIVER ( 12 FDA reports)
BLOOD CREATININE DECREASED ( 12 FDA reports)
BRACHIAL PLEXUS INJURY ( 12 FDA reports)
BREAST HYPERPLASIA ( 12 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 12 FDA reports)
CAROTID ARTERY DISSECTION ( 12 FDA reports)
CERVICAL CYST ( 12 FDA reports)
CHOROIDITIS ( 12 FDA reports)
COLON ADENOMA ( 12 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 12 FDA reports)
CONTRAST MEDIA ALLERGY ( 12 FDA reports)
CRUSH INJURY ( 12 FDA reports)
DRUG LEVEL INCREASED ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 12 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 12 FDA reports)
EOSINOPHILIA ( 12 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 12 FDA reports)
EXTREMITY NECROSIS ( 12 FDA reports)
EYE OEDEMA ( 12 FDA reports)
EYELID FUNCTION DISORDER ( 12 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 12 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 12 FDA reports)
GALLBLADDER CANCER ( 12 FDA reports)
GASTRIC NEOPLASM ( 12 FDA reports)
GASTROENTERITIS BACTERIAL ( 12 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 12 FDA reports)
GASTROINTESTINAL PAIN ( 12 FDA reports)
GENERALISED ERYTHEMA ( 12 FDA reports)
HAEMANGIOMA OF LIVER ( 12 FDA reports)
HEAD DEFORMITY ( 12 FDA reports)
HEPATITIS C POSITIVE ( 12 FDA reports)
HEPATITIS FULMINANT ( 12 FDA reports)
HILAR LYMPHADENOPATHY ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
HYPOREFLEXIA ( 12 FDA reports)
INAPPROPRIATE AFFECT ( 12 FDA reports)
INFERTILITY FEMALE ( 12 FDA reports)
INTENTION TREMOR ( 12 FDA reports)
INTESTINAL OPERATION ( 12 FDA reports)
JOINT CONTRACTURE ( 12 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 12 FDA reports)
LIVER INDURATION ( 12 FDA reports)
MACULOPATHY ( 12 FDA reports)
MEDICAL DEVICE CHANGE ( 12 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 12 FDA reports)
METASTASES TO NECK ( 12 FDA reports)
MIGRAINE WITH AURA ( 12 FDA reports)
MITRAL VALVE CALCIFICATION ( 12 FDA reports)
MONOPARESIS ( 12 FDA reports)
MYOCLONUS ( 12 FDA reports)
NASAL CAVITY CANCER ( 12 FDA reports)
NEUROFIBROMATOSIS ( 12 FDA reports)
ONYCHALGIA ( 12 FDA reports)
OTITIS MEDIA ( 12 FDA reports)
OVARIAN OPERATION ( 12 FDA reports)
PAPILLOEDEMA ( 12 FDA reports)
PERNICIOUS ANAEMIA ( 12 FDA reports)
POST PROCEDURAL DISCHARGE ( 12 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 12 FDA reports)
PROCEDURAL NAUSEA ( 12 FDA reports)
REFLUX GASTRITIS ( 12 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 12 FDA reports)
RETINAL SCAR ( 12 FDA reports)
RETROPERITONEAL HAEMATOMA ( 12 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 12 FDA reports)
SERUM FERRITIN DECREASED ( 12 FDA reports)
SEXUAL ASSAULT VICTIM ( 12 FDA reports)
SKIN FISSURES ( 12 FDA reports)
SKIN PAPILLOMA ( 12 FDA reports)
SPINAL PAIN ( 12 FDA reports)
SPONDYLITIC MYELOPATHY ( 12 FDA reports)
SPONDYLOARTHROPATHY ( 12 FDA reports)
SPONDYLOSIS ( 12 FDA reports)
STEM CELL TRANSPLANT ( 12 FDA reports)
T-CELL LYMPHOMA ( 12 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 12 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 12 FDA reports)
THYROID CANCER METASTATIC ( 12 FDA reports)
TINEA INFECTION ( 12 FDA reports)
TOE OPERATION ( 12 FDA reports)
TONGUE BITING ( 12 FDA reports)
TRAUMATIC LIVER INJURY ( 12 FDA reports)
TROPONIN INCREASED ( 12 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 12 FDA reports)
VAGINITIS BACTERIAL ( 12 FDA reports)
VASCULAR BYPASS GRAFT ( 12 FDA reports)
VASODILATATION ( 12 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
RADIATION SKIN INJURY ( 11 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 11 FDA reports)
RESPIRATORY ALKALOSIS ( 11 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 11 FDA reports)
RHEUMATOID FACTOR INCREASED ( 11 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SPIDER VEIN ( 11 FDA reports)
SURGICAL FAILURE ( 11 FDA reports)
THERMOANAESTHESIA ( 11 FDA reports)
THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
THYROID OPERATION ( 11 FDA reports)
TONGUE CANCER METASTATIC ( 11 FDA reports)
TOOTH INJURY ( 11 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 11 FDA reports)
TUMOUR EXCISION ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
URINARY TRACT OBSTRUCTION ( 11 FDA reports)
URINE ABNORMALITY ( 11 FDA reports)
UTERINE INFECTION ( 11 FDA reports)
VASCULAR GRAFT ( 11 FDA reports)
WOUND INFECTION BACTERIAL ( 11 FDA reports)
X-RAY ABNORMAL ( 11 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ADRENAL DISORDER ( 11 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 11 FDA reports)
ANTIBODY TEST ABNORMAL ( 11 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
ARTIFICIAL MENOPAUSE ( 11 FDA reports)
ATRIAL TACHYCARDIA ( 11 FDA reports)
AXILLARY PAIN ( 11 FDA reports)
BACTERIAL TOXAEMIA ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 11 FDA reports)
BLOOD IRON INCREASED ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 11 FDA reports)
BLOOD VISCOSITY INCREASED ( 11 FDA reports)
BODY TINEA ( 11 FDA reports)
BONE LESION ( 11 FDA reports)
BRAIN CONTUSION ( 11 FDA reports)
BRAIN SCAN ABNORMAL ( 11 FDA reports)
BREAST HAEMORRHAGE ( 11 FDA reports)
BREAST TENDERNESS ( 11 FDA reports)
CARDIAC OUTPUT DECREASED ( 11 FDA reports)
CATHETER SITE HAEMORRHAGE ( 11 FDA reports)
CELLULITIS STREPTOCOCCAL ( 11 FDA reports)
CONTRAST MEDIA REACTION ( 11 FDA reports)
CORNEAL DEGENERATION ( 11 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 11 FDA reports)
CUTANEOUS SARCOIDOSIS ( 11 FDA reports)
CYSTITIS ESCHERICHIA ( 11 FDA reports)
DEATH NEONATAL ( 11 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 11 FDA reports)
EAR HAEMORRHAGE ( 11 FDA reports)
ENERGY INCREASED ( 11 FDA reports)
ENTEROCELE ( 11 FDA reports)
ENURESIS ( 11 FDA reports)
ERUCTATION ( 11 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 11 FDA reports)
EYE INFLAMMATION ( 11 FDA reports)
FAT TISSUE INCREASED ( 11 FDA reports)
FEEDING DISORDER ( 11 FDA reports)
FEEDING TUBE COMPLICATION ( 11 FDA reports)
FOAMING AT MOUTH ( 11 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 11 FDA reports)
GASTRIC PH DECREASED ( 11 FDA reports)
GASTRITIS EROSIVE ( 11 FDA reports)
GASTROINTESTINAL STENOSIS ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
GRIEF REACTION ( 11 FDA reports)
HAEMORRHOID OPERATION ( 11 FDA reports)
HAIR DISORDER ( 11 FDA reports)
HEART VALVE STENOSIS ( 11 FDA reports)
HYPERMETROPIA ( 11 FDA reports)
HYPERTENSIVE HEART DISEASE ( 11 FDA reports)
HYPOPROTEINAEMIA ( 11 FDA reports)
IMPATIENCE ( 11 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 11 FDA reports)
INDUCED LABOUR ( 11 FDA reports)
INFECTIVE MYOSITIS ( 11 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 11 FDA reports)
INJECTION SITE PARAESTHESIA ( 11 FDA reports)
INTESTINAL ISCHAEMIA ( 11 FDA reports)
JUGULAR VEIN THROMBOSIS ( 11 FDA reports)
KYPHOSIS ( 11 FDA reports)
LENTIGO ( 11 FDA reports)
LICHEN PLANUS ( 11 FDA reports)
LIP INJURY ( 11 FDA reports)
LOGORRHOEA ( 11 FDA reports)
MESOTHELIOMA ( 11 FDA reports)
METASTASES TO PLEURA ( 11 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 11 FDA reports)
MUSCLE ENZYME INCREASED ( 11 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 11 FDA reports)
NAIL DISCOLOURATION ( 11 FDA reports)
NEUROGENIC BOWEL ( 11 FDA reports)
OBSTRUCTION GASTRIC ( 11 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 11 FDA reports)
OVARIAN ADENOMA ( 11 FDA reports)
OVARIAN ENLARGEMENT ( 11 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 11 FDA reports)
PANCREATIC PSEUDOCYST ( 11 FDA reports)
PARESIS ( 11 FDA reports)
PELVIC HAEMORRHAGE ( 11 FDA reports)
PERIRECTAL ABSCESS ( 11 FDA reports)
PERTUSSIS ( 11 FDA reports)
PLASMACYTOMA ( 11 FDA reports)
PLASTIC SURGERY ( 11 FDA reports)
POLYDIPSIA ( 11 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 11 FDA reports)
POSTOPERATIVE HERNIA ( 11 FDA reports)
PROCEDURAL VOMITING ( 11 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 10 FDA reports)
ABSCESS RUPTURE ( 10 FDA reports)
ACUTE PRERENAL FAILURE ( 10 FDA reports)
ADENOVIRUS INFECTION ( 10 FDA reports)
AKINESIA ( 10 FDA reports)
ANAL FISSURE ( 10 FDA reports)
ANKYLOSING SPONDYLITIS ( 10 FDA reports)
AORTIC VALVE SCLEROSIS ( 10 FDA reports)
ARTHROSCOPIC SURGERY ( 10 FDA reports)
ASPHYXIA ( 10 FDA reports)
BENIGN BONE NEOPLASM ( 10 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 10 FDA reports)
BLADDER PERFORATION ( 10 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 10 FDA reports)
BLOOD PH INCREASED ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 10 FDA reports)
BONE OPERATION ( 10 FDA reports)
BRAIN CANCER METASTATIC ( 10 FDA reports)
BRAIN TUMOUR OPERATION ( 10 FDA reports)
BREAST ENLARGEMENT ( 10 FDA reports)
BREAST FIBROMA ( 10 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 10 FDA reports)
CARDIAC ABLATION ( 10 FDA reports)
CARDIAC FIBRILLATION ( 10 FDA reports)
CARDIAC HYPERTROPHY ( 10 FDA reports)
CAROTID ARTERY ANEURYSM ( 10 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 10 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
CHOKING SENSATION ( 10 FDA reports)
CHOLANGITIS ( 10 FDA reports)
CHRONIC LEUKAEMIA ( 10 FDA reports)
CLAUSTROPHOBIA ( 10 FDA reports)
CULTURE URINE POSITIVE ( 10 FDA reports)
CULTURE WOUND POSITIVE ( 10 FDA reports)
CYTOGENETIC ABNORMALITY ( 10 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DEVELOPMENTAL DELAY ( 10 FDA reports)
DIABETIC NEPHROPATHY ( 10 FDA reports)
DRUG LEVEL DECREASED ( 10 FDA reports)
DYSPAREUNIA ( 10 FDA reports)
DYSTHYMIC DISORDER ( 10 FDA reports)
EAR PRURITUS ( 10 FDA reports)
ENDODONTIC PROCEDURE ( 10 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 10 FDA reports)
EXPOSURE TO TOXIC AGENT ( 10 FDA reports)
FEBRILE NEUTROPENIA ( 10 FDA reports)
FINGER AMPUTATION ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
GASTROENTERITIS NOROVIRUS ( 10 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 10 FDA reports)
GASTROSTOMY TUBE INSERTION ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GENITAL BURNING SENSATION ( 10 FDA reports)
HAEMARTHROSIS ( 10 FDA reports)
HAEMOGLOBIN INCREASED ( 10 FDA reports)
HEAT RASH ( 10 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 10 FDA reports)
HIV TEST POSITIVE ( 10 FDA reports)
HYPERTENSIVE CRISIS ( 10 FDA reports)
HYPOMANIA ( 10 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 10 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 10 FDA reports)
INJECTION SITE ULCER ( 10 FDA reports)
JAUNDICE NEONATAL ( 10 FDA reports)
JUDGEMENT IMPAIRED ( 10 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 10 FDA reports)
LIPASE INCREASED ( 10 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 10 FDA reports)
MACULAR HOLE ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
MEAN CELL VOLUME DECREASED ( 10 FDA reports)
MERALGIA PARAESTHETICA ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MUCOSAL INFLAMMATION ( 10 FDA reports)
MULTIPLE INJURIES ( 10 FDA reports)
NEURILEMMOMA ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 10 FDA reports)
NIPPLE PAIN ( 10 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 10 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 10 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 10 FDA reports)
OLIGODENDROGLIOMA ( 10 FDA reports)
ONYCHOMADESIS ( 10 FDA reports)
OROPHARYNGEAL SWELLING ( 10 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 10 FDA reports)
PANCREATIC NEOPLASM ( 10 FDA reports)
PARATHYROID TUMOUR BENIGN ( 10 FDA reports)
PARATHYROID TUMOUR MALIGNANT ( 10 FDA reports)
PO2 DECREASED ( 10 FDA reports)
POLYCYSTIC OVARIES ( 10 FDA reports)
POSITRON EMISSION TOMOGRAM ( 10 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 10 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 10 FDA reports)
PROLACTINOMA ( 10 FDA reports)
PROSTATITIS ( 10 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 10 FDA reports)
RADICULOTOMY ( 10 FDA reports)
RENAL ABSCESS ( 10 FDA reports)
RENAL CANCER METASTATIC ( 10 FDA reports)
RETINAL VEIN OCCLUSION ( 10 FDA reports)
SCIATIC NERVE NEUROPATHY ( 10 FDA reports)
SERUM SEROTONIN DECREASED ( 10 FDA reports)
SHORTENED CERVIX ( 10 FDA reports)
SKIN GRAFT INFECTION ( 10 FDA reports)
SPLENIC HAEMORRHAGE ( 10 FDA reports)
SPUTUM CULTURE POSITIVE ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
SUBSTANCE ABUSE ( 10 FDA reports)
SYNOVIAL DISORDER ( 10 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 10 FDA reports)
TACITURNITY ( 10 FDA reports)
TEMPORAL ARTERITIS ( 10 FDA reports)
TENDON CALCIFICATION ( 10 FDA reports)
TOOTH IMPACTED ( 10 FDA reports)
TORTICOLLIS ( 10 FDA reports)
TRIGGER FINGER ( 10 FDA reports)
UHTHOFF'S PHENOMENON ( 10 FDA reports)
ULTRASOUND SCAN ( 10 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 10 FDA reports)
VAGINAL DISORDER ( 10 FDA reports)
VASCULITIS CEREBRAL ( 10 FDA reports)
VASOCONSTRICTION ( 10 FDA reports)
VENTRICLE RUPTURE ( 10 FDA reports)
VULVITIS ( 10 FDA reports)
WEIGHT LOSS POOR ( 10 FDA reports)
WEST NILE VIRAL INFECTION ( 10 FDA reports)
WOUND EVISCERATION ( 10 FDA reports)
RADICULITIS ( 9 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 9 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 9 FDA reports)
RED BLOOD CELL ABNORMALITY ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 9 FDA reports)
RENAL ONCOCYTOMA ( 9 FDA reports)
SMALL INTESTINAL RESECTION ( 9 FDA reports)
SOMATOFORM DISORDER ( 9 FDA reports)
SPINA BIFIDA ( 9 FDA reports)
SPINAL FUSION ACQUIRED ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 9 FDA reports)
STRESS AT WORK ( 9 FDA reports)
THORACIC OUTLET SYNDROME ( 9 FDA reports)
TOBACCO USER ( 9 FDA reports)
TONSIL CANCER ( 9 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 9 FDA reports)
UMBILICAL CORD ABNORMALITY ( 9 FDA reports)
UROSTOMY COMPLICATION ( 9 FDA reports)
VESTIBULAR DISORDER ( 9 FDA reports)
WOUND COMPLICATION ( 9 FDA reports)
ABNORMAL FAECES ( 9 FDA reports)
ABORTION ( 9 FDA reports)
ADENOID CYSTIC CARCINOMA ( 9 FDA reports)
AMPUTATION ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 9 FDA reports)
APRAXIA ( 9 FDA reports)
ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
ARTHRITIS REACTIVE ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
AUTISM ( 9 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 9 FDA reports)
BIOPSY LUNG ( 9 FDA reports)
BLOOD FOLATE DECREASED ( 9 FDA reports)
BRAIN ABSCESS ( 9 FDA reports)
BRAIN STEM HAEMORRHAGE ( 9 FDA reports)
BREAST DISCHARGE ( 9 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 9 FDA reports)
CARCINOID TUMOUR ( 9 FDA reports)
CARDIAC FAILURE CHRONIC ( 9 FDA reports)
CARDIAC PERFORATION ( 9 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 9 FDA reports)
CEREBRAL PALSY ( 9 FDA reports)
CERVICAL INCOMPETENCE ( 9 FDA reports)
CERVIX NEOPLASM ( 9 FDA reports)
COLOUR BLINDNESS ( 9 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 9 FDA reports)
CRANIOTOMY ( 9 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 9 FDA reports)
CYST REMOVAL ( 9 FDA reports)
DIABETIC ULCER ( 9 FDA reports)
DRUG DETOXIFICATION ( 9 FDA reports)
ECG P WAVE INVERTED ( 9 FDA reports)
ECZEMA NUMMULAR ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 9 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 9 FDA reports)
EPIGASTRIC DISCOMFORT ( 9 FDA reports)
EPIGLOTTITIS ( 9 FDA reports)
FACTOR V DEFICIENCY ( 9 FDA reports)
FACTOR V LEIDEN MUTATION ( 9 FDA reports)
FAILED INDUCTION OF LABOUR ( 9 FDA reports)
FAT EMBOLISM ( 9 FDA reports)
FIBROMA ( 9 FDA reports)
FOOT AMPUTATION ( 9 FDA reports)
FOREIGN BODY TRAUMA ( 9 FDA reports)
FRONTAL LOBE EPILEPSY ( 9 FDA reports)
GASTRIC CYST ( 9 FDA reports)
GASTRIC STAPLING ( 9 FDA reports)
GASTRIC ULCER HELICOBACTER ( 9 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 9 FDA reports)
GINGIVAL ABSCESS ( 9 FDA reports)
HAEMORRHAGE URINARY TRACT ( 9 FDA reports)
HAEMOTHORAX ( 9 FDA reports)
HEART VALVE OPERATION ( 9 FDA reports)
HEPATIC ADENOMA ( 9 FDA reports)
HEPATOSPLENOMEGALY ( 9 FDA reports)
HIDRADENITIS ( 9 FDA reports)
HIGH RISK PREGNANCY ( 9 FDA reports)
HIP DYSPLASIA ( 9 FDA reports)
HOARSENESS ( 9 FDA reports)
HOMICIDE ( 9 FDA reports)
HYPEREMESIS GRAVIDARUM ( 9 FDA reports)
HYPERTONIA ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 9 FDA reports)
INCISION SITE OEDEMA ( 9 FDA reports)
INDURATION ( 9 FDA reports)
INFECTED BITES ( 9 FDA reports)
INSULIN RESISTANCE ( 9 FDA reports)
INTERNAL HERNIA ( 9 FDA reports)
INTESTINAL RESECTION ( 9 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 9 FDA reports)
INVESTIGATION ( 9 FDA reports)
IODINE ALLERGY ( 9 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 9 FDA reports)
JOINT IRRIGATION ( 9 FDA reports)
LARGE FOR DATES BABY ( 9 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 9 FDA reports)
LIMB ASYMMETRY ( 9 FDA reports)
LIP DRY ( 9 FDA reports)
LIVER ABSCESS ( 9 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 9 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MALIGNANT PALATE NEOPLASM ( 9 FDA reports)
MASS EXCISION ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 9 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 9 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 9 FDA reports)
MELAENA ( 9 FDA reports)
METABOLIC DISORDER ( 9 FDA reports)
METASTASES TO ADRENALS ( 9 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
MORTON'S NEUROMA ( 9 FDA reports)
MYELOFIBROSIS ( 9 FDA reports)
NAIL INJURY ( 9 FDA reports)
NASAL OPERATION ( 9 FDA reports)
NEUROPATHIC ARTHROPATHY ( 9 FDA reports)
ODYNOPHAGIA ( 9 FDA reports)
OLIGOHYDRAMNIOS ( 9 FDA reports)
ORAL MUCOSAL BLISTERING ( 9 FDA reports)
ORAL NEOPLASM ( 9 FDA reports)
PANNICULITIS ( 9 FDA reports)
PELVIC ADHESIONS ( 9 FDA reports)
PELVIC HAEMATOMA ( 9 FDA reports)
PHANTOM PAIN ( 9 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 9 FDA reports)
PHYSIOTHERAPY ( 9 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 9 FDA reports)
PO2 INCREASED ( 9 FDA reports)
POST-TRAUMATIC HEADACHE ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
PROCEDURAL HEADACHE ( 9 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 9 FDA reports)
ABSCESS BACTERIAL ( 8 FDA reports)
ABSCESS SWEAT GLAND ( 8 FDA reports)
ACCIDENTAL DEATH ( 8 FDA reports)
ALCOHOL INTOLERANCE ( 8 FDA reports)
ALLERGY TO ANIMAL ( 8 FDA reports)
ALOPECIA AREATA ( 8 FDA reports)
AMNIORRHOEA ( 8 FDA reports)
ANAL ABSCESS ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
ANTIBODY TEST ( 8 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 8 FDA reports)
ARTHROFIBROSIS ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
ATRIAL THROMBOSIS ( 8 FDA reports)
BENIGN HEPATIC NEOPLASM ( 8 FDA reports)
BENIGN SPLEEN TUMOUR ( 8 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 8 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
BLOOD OESTROGEN INCREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
BONE MARROW DEPRESSION ( 8 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 8 FDA reports)
BREAST ABSCESS ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BRONCHIAL INFECTION ( 8 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 8 FDA reports)
BUNION OPERATION ( 8 FDA reports)
CALCULUS URINARY ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 8 FDA reports)
CAROTID ARTERY ATHEROMA ( 8 FDA reports)
CEREBELLAR ATAXIA ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY ( 8 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 8 FDA reports)
CERVICITIS ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
CHOLANGITIS SCLEROSING ( 8 FDA reports)
CHORIOCARCINOMA ( 8 FDA reports)
CHRONIC FATIGUE SYNDROME ( 8 FDA reports)
CIRRHOSIS ALCOHOLIC ( 8 FDA reports)
CLEAR CELL ENDOMETRIAL CARCINOMA ( 8 FDA reports)
COLON CANCER STAGE I ( 8 FDA reports)
COMMINUTED FRACTURE ( 8 FDA reports)
CONGENITAL HIP DEFORMITY ( 8 FDA reports)
CYSTITIS EROSIVE ( 8 FDA reports)
CYSTITIS RADIATION ( 8 FDA reports)
DENTAL IMPLANTATION ( 8 FDA reports)
DERMATITIS INFECTED ( 8 FDA reports)
DERMOID CYST ( 8 FDA reports)
DEVICE EXTRUSION ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 8 FDA reports)
DIZZINESS EXERTIONAL ( 8 FDA reports)
DUODENAL PERFORATION ( 8 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 8 FDA reports)
ENCEPHALITIS HERPES ( 8 FDA reports)
ENCEPHALITIS VIRAL ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
EYE ROLLING ( 8 FDA reports)
FEBRILE CONVULSION ( 8 FDA reports)
FORCEPS DELIVERY ( 8 FDA reports)
FOREARM FRACTURE ( 8 FDA reports)
FOREIGN BODY ASPIRATION ( 8 FDA reports)
GALLBLADDER PERFORATION ( 8 FDA reports)
GARDNERELLA INFECTION ( 8 FDA reports)
GASTRITIS BACTERIAL ( 8 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 8 FDA reports)
GASTROINTESTINAL MALFORMATION ( 8 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
GLUCOSE URINE PRESENT ( 8 FDA reports)
GROIN INFECTION ( 8 FDA reports)
HAEMANGIOBLASTOMA ( 8 FDA reports)
HAEMODYNAMIC INSTABILITY ( 8 FDA reports)
HEMIANOPIA ( 8 FDA reports)
HEPATIC CANCER METASTATIC ( 8 FDA reports)
HEPATITIS VIRAL ( 8 FDA reports)
HERPES ZOSTER DISSEMINATED ( 8 FDA reports)
HOUSE DUST ALLERGY ( 8 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 8 FDA reports)
HYPERTROPHY ( 8 FDA reports)
HYPOPITUITARISM ( 8 FDA reports)
ILIAC ARTERY THROMBOSIS ( 8 FDA reports)
ILIUM FRACTURE ( 8 FDA reports)
IMPETIGO ( 8 FDA reports)
INCISION SITE HAEMATOMA ( 8 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 8 FDA reports)
INFERTILITY ( 8 FDA reports)
INFUSION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE SCAB ( 8 FDA reports)
INJECTION SITE STINGING ( 8 FDA reports)
INSULINOMA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 8 FDA reports)
INTESTINAL MASS ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
LABILE BLOOD PRESSURE ( 8 FDA reports)
LABOUR COMPLICATION ( 8 FDA reports)
LARGE INTESTINAL ULCER ( 8 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
LEUKOENCEPHALOMYELITIS ( 8 FDA reports)
LOWER LIMB DEFORMITY ( 8 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 8 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
MACROSOMIA ( 8 FDA reports)
MADAROSIS ( 8 FDA reports)
MALIGNANT ANORECTAL NEOPLASM ( 8 FDA reports)
MALIGNANT MELANOMA STAGE I ( 8 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 8 FDA reports)
MANTLE CELL LYMPHOMA ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
MEDICAL DEVICE SITE REACTION ( 8 FDA reports)
MENOMETRORRHAGIA ( 8 FDA reports)
METASTASES TO PERITONEUM ( 8 FDA reports)
MONOCLONAL GAMMOPATHY ( 8 FDA reports)
MOTION SICKNESS ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
MYOSCLEROSIS ( 8 FDA reports)
N-TELOPEPTIDE URINE INCREASED ( 8 FDA reports)
NAIL INFECTION ( 8 FDA reports)
NASAL DISCOMFORT ( 8 FDA reports)
NEEDLE TRACK MARKS ( 8 FDA reports)
NEOPLASM PROSTATE ( 8 FDA reports)
NEPHROSCLEROSIS ( 8 FDA reports)
NO ADVERSE REACTION ( 8 FDA reports)
OEDEMATOUS PANCREATITIS ( 8 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
OSCILLOPSIA ( 8 FDA reports)
OVARIAN CANCER STAGE I ( 8 FDA reports)
PANCREATIC INSUFFICIENCY ( 8 FDA reports)
PANCREATIC LEAK ( 8 FDA reports)
PANCREATITIS NECROTISING ( 8 FDA reports)
PANIC DISORDER ( 8 FDA reports)
PARATHYROID DISORDER ( 8 FDA reports)
PELVIC INFECTION ( 8 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 8 FDA reports)
PHARYNGEAL INJURY ( 8 FDA reports)
PHLEBOTHROMBOSIS ( 8 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 8 FDA reports)
POST CONCUSSION SYNDROME ( 8 FDA reports)
POST PROCEDURAL STROKE ( 8 FDA reports)
POSTICTAL HEADACHE ( 8 FDA reports)
POSTMENOPAUSE ( 8 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 8 FDA reports)
PROTEIN URINE PRESENT ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
PSYCHIATRIC EVALUATION ( 8 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 8 FDA reports)
REFRACTORY CANCER ( 8 FDA reports)
RENAL STONE REMOVAL ( 8 FDA reports)
RESORPTION BONE INCREASED ( 8 FDA reports)
RESPIRATORY COMPLICATION ASSOCIATED WITH DEVICE ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
RETINAL TELANGIECTASIA ( 8 FDA reports)
RHINALGIA ( 8 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 8 FDA reports)
SALPINGITIS ( 8 FDA reports)
SCAR EXCISION ( 8 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 8 FDA reports)
SKIN WRINKLING ( 8 FDA reports)
SNORING ( 8 FDA reports)
SPINAL ARTERY EMBOLISM ( 8 FDA reports)
SPINAL HAEMATOMA ( 8 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 8 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 8 FDA reports)
TALIPES ( 8 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 8 FDA reports)
TOOTH EROSION ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
TRANSFUSION REACTION ( 8 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 8 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 8 FDA reports)
TUMOUR HAEMORRHAGE ( 8 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 8 FDA reports)
UNINTENDED PREGNANCY ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
URETERIC RUPTURE ( 8 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 8 FDA reports)
URINE KETONE BODY PRESENT ( 8 FDA reports)
UTERINE PAIN ( 8 FDA reports)
VAGINAL CYST ( 8 FDA reports)
VAGINAL POLYP ( 8 FDA reports)
VARICOSE VEIN OPERATION ( 8 FDA reports)
VASOSPASM ( 8 FDA reports)
VEIN PAIN ( 8 FDA reports)
VICTIM OF HOMICIDE ( 8 FDA reports)
VULVAL CANCER STAGE I ( 8 FDA reports)
WISDOM TEETH REMOVAL ( 8 FDA reports)
WOUND TREATMENT ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 7 FDA reports)
RECTAL ULCER ( 7 FDA reports)
RED MAN SYNDROME ( 7 FDA reports)
REHABILITATION THERAPY ( 7 FDA reports)
RENAL INJURY ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 7 FDA reports)
RETINAL EXUDATES ( 7 FDA reports)
RETINAL ISCHAEMIA ( 7 FDA reports)
RETINOPATHY PROLIFERATIVE ( 7 FDA reports)
RETROGRADE AMNESIA ( 7 FDA reports)
SCARLET FEVER ( 7 FDA reports)
SELF-MEDICATION ( 7 FDA reports)
SENSITIVITY OF TEETH ( 7 FDA reports)
SICKLE CELL ANAEMIA ( 7 FDA reports)
SIMPLE PARTIAL SEIZURES ( 7 FDA reports)
SKIN CANCER METASTATIC ( 7 FDA reports)
SKIN INJURY ( 7 FDA reports)
SOPOR ( 7 FDA reports)
SPINAL HAEMANGIOMA ( 7 FDA reports)
SPORTS INJURY ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
SYRINGE ISSUE ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
TEMPORAL LOBE EPILEPSY ( 7 FDA reports)
THERAPEUTIC PROCEDURE ( 7 FDA reports)
THERAPY CESSATION ( 7 FDA reports)
THYMOMA ( 7 FDA reports)
TIC ( 7 FDA reports)
TOE DEFORMITY ( 7 FDA reports)
TONGUE ULCERATION ( 7 FDA reports)
TOOTH AVULSION ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TRACHEAL OPERATION ( 7 FDA reports)
UMBILICAL HERNIA REPAIR ( 7 FDA reports)
URINE FLOW DECREASED ( 7 FDA reports)
UTEROVAGINAL PROLAPSE ( 7 FDA reports)
VAGINAL HYSTERECTOMY ( 7 FDA reports)
VAGINAL LESION ( 7 FDA reports)
VENOUS STASIS ( 7 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 7 FDA reports)
VIRAL PERICARDITIS ( 7 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 7 FDA reports)
VITAMIN K DEFICIENCY ( 7 FDA reports)
VON WILLEBRAND'S DISEASE ( 7 FDA reports)
VTH NERVE INJURY ( 7 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 7 FDA reports)
WATER INTOXICATION ( 7 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 7 FDA reports)
ABDOMINAL HYSTERECTOMY ( 7 FDA reports)
ABDOMINAL WALL DISORDER ( 7 FDA reports)
ABDOMINAL WALL NEOPLASM ( 7 FDA reports)
ACCIDENT AT HOME ( 7 FDA reports)
ACIDOSIS ( 7 FDA reports)
ADENOMA BENIGN ( 7 FDA reports)
ADNEXA UTERI PAIN ( 7 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
AGORAPHOBIA ( 7 FDA reports)
ALLERGY TO CHEMICALS ( 7 FDA reports)
ANGIOGRAM ( 7 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 7 FDA reports)
AORTIC CALCIFICATION ( 7 FDA reports)
AORTIC VALVE REPAIR ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
APPARENT DEATH ( 7 FDA reports)
APPENDICEAL ABSCESS ( 7 FDA reports)
ARACHNOID CYST ( 7 FDA reports)
ARTERIAL SPASM ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
ATROPHIC VULVOVAGINITIS ( 7 FDA reports)
AXILLARY MASS ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BARIUM SWALLOW ABNORMAL ( 7 FDA reports)
BENIGN COLONIC POLYP ( 7 FDA reports)
BENIGN NEOPLASM OF SKIN ( 7 FDA reports)
BILIARY CYST ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BILIARY TRACT OPERATION ( 7 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
BLOOD AMYLASE INCREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 7 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 7 FDA reports)
BODY MASS INDEX DECREASED ( 7 FDA reports)
BONE MARROW TRANSPLANT ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BRAIN STEM INFARCTION ( 7 FDA reports)
BREECH DELIVERY ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRONCHITIS ACUTE ( 7 FDA reports)
CARCINOID TUMOUR PULMONARY ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 7 FDA reports)
CEREBRAL ARTERITIS ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 7 FDA reports)
CHOLELITHOTOMY ( 7 FDA reports)
CHROMATOPSIA ( 7 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 7 FDA reports)
COLITIS COLLAGENOUS ( 7 FDA reports)
COLON CANCER STAGE 0 ( 7 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
CONNECTIVE TISSUE DISORDER ( 7 FDA reports)
CONTRACTED BLADDER ( 7 FDA reports)
CRANIAL NERVE DISORDER ( 7 FDA reports)
CRANIOCEREBRAL INJURY ( 7 FDA reports)
CREST SYNDROME ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DEPENDENCE ON RESPIRATOR ( 7 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 7 FDA reports)
DIAPHRAGMATIC HERNIA ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
ELECTROCARDIOGRAM ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
EMBOLISM ARTERIAL ( 7 FDA reports)
ENDOCRINE DISORDER ( 7 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 7 FDA reports)
ERYTHEMA INFECTIOSUM ( 7 FDA reports)
EXTRADURAL ABSCESS ( 7 FDA reports)
EXTRUSION OF DEVICE ( 7 FDA reports)
EYE DISCHARGE ( 7 FDA reports)
EYE INFECTION BACTERIAL ( 7 FDA reports)
FEMORAL ARTERY ANEURYSM ( 7 FDA reports)
FOETAL GROWTH RESTRICTION ( 7 FDA reports)
FOETAL MALPRESENTATION ( 7 FDA reports)
FOLLICULAR THYROID CANCER ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
GASTROENTERITIS RADIATION ( 7 FDA reports)
GASTROINTESTINAL GANGRENE ( 7 FDA reports)
GENITAL HYPOAESTHESIA ( 7 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 7 FDA reports)
HAEMORRHAGIC DIATHESIS ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
HIV INFECTION ( 7 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE TYPE STAGE III ( 7 FDA reports)
HUMAN EHRLICHIOSIS ( 7 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYPOSPADIAS ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
INCORRECT STORAGE OF DRUG ( 7 FDA reports)
INFUSION SITE BRUISING ( 7 FDA reports)
INTESTINAL POLYP ( 7 FDA reports)
INTUSSUSCEPTION ( 7 FDA reports)
KELOID SCAR ( 7 FDA reports)
KYPHOSCOLIOSIS ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LIVER OPERATION ( 7 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 7 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 7 FDA reports)
LYMPH GLAND INFECTION ( 7 FDA reports)
LYMPH NODE PAIN ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 7 FDA reports)
MASTITIS ( 7 FDA reports)
METASTASES TO CHEST WALL ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 7 FDA reports)
MYCOTIC ALLERGY ( 7 FDA reports)
MYOFASCITIS ( 7 FDA reports)
NASAL DISORDER ( 7 FDA reports)
NEGATIVE THOUGHTS ( 7 FDA reports)
NEPHRITIS ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
OESOPHAGEAL ACHALASIA ( 7 FDA reports)
OPTIC NERVE NEOPLASM ( 7 FDA reports)
OPTICOKINETIC NYSTAGMUS TESTS ABNORMAL ( 7 FDA reports)
OTORRHOEA ( 7 FDA reports)
PANCREATIC DUCT STENOSIS ( 7 FDA reports)
PANCREATOLITHIASIS ( 7 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 7 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 7 FDA reports)
PELVIC FLOOR REPAIR ( 7 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 7 FDA reports)
PERIPHLEBITIS ( 7 FDA reports)
PITUITARY CYST ( 7 FDA reports)
POST PROCEDURAL PNEUMONIA ( 7 FDA reports)
POSTICTAL PARALYSIS ( 7 FDA reports)
POSTOPERATIVE ABSCESS ( 7 FDA reports)
POSTPARTUM DISORDER ( 7 FDA reports)
PREMATURE MENOPAUSE ( 7 FDA reports)
PROSTATE CANCER STAGE IV ( 7 FDA reports)
PROSTATIC OPERATION ( 7 FDA reports)
ABDOMINAL INJURY ( 6 FDA reports)
ABSCESS ORAL ( 6 FDA reports)
ACARODERMATITIS ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
AMNIOTIC BAND SYNDROME ( 6 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 6 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 6 FDA reports)
ANAL SPHINCTER ATONY ( 6 FDA reports)
ANGIOSARCOMA ( 6 FDA reports)
ANIMAL SCRATCH ( 6 FDA reports)
ANISOCYTOSIS ( 6 FDA reports)
ANOGENITAL WARTS ( 6 FDA reports)
ANOXIA ( 6 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
APALLIC SYNDROME ( 6 FDA reports)
APPLICATION SITE PAIN ( 6 FDA reports)
ARTERIOVENOUS FISTULA ( 6 FDA reports)
ASTROCYTOMA ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 6 FDA reports)
BIOPSY BREAST ( 6 FDA reports)
BIOPSY BREAST ABNORMAL ( 6 FDA reports)
BIOPSY THYROID GLAND ABNORMAL ( 6 FDA reports)
BLADDER DILATATION ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
BONE INFARCTION ( 6 FDA reports)
BREAST DISCOLOURATION ( 6 FDA reports)
BREAST NECROSIS ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CANCER GENE CARRIER ( 6 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 6 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CATHETER SITE ERYTHEMA ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM DERMOID TUMOUR ( 6 FDA reports)
CHEMICAL POISONING ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 6 FDA reports)
CIRCULATING ANTICOAGULANT ( 6 FDA reports)
CLOSED HEAD INJURY ( 6 FDA reports)
CLUSTER HEADACHE ( 6 FDA reports)
COAGULATION TEST ABNORMAL ( 6 FDA reports)
COGNITIVE DETERIORATION ( 6 FDA reports)
COLITIS MICROSCOPIC ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 6 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 6 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 6 FDA reports)
DEAFNESS BILATERAL ( 6 FDA reports)
DEATH OF RELATIVE ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DEVICE MIGRATION ( 6 FDA reports)
DIABETIC RETINOPATHY ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ELECTROLYTE DEPLETION ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 6 FDA reports)
ENDOMETRIAL ABLATION ( 6 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
ENTERITIS ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
ESCHERICHIA TEST POSITIVE ( 6 FDA reports)
EWING'S SARCOMA ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
EYE LASER SURGERY ( 6 FDA reports)
EYEBALL RUPTURE ( 6 FDA reports)
FIBROADENOMA ( 6 FDA reports)
FLUID IMBALANCE ( 6 FDA reports)
GALLBLADDER OBSTRUCTION ( 6 FDA reports)
GASTRECTOMY ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GINGIVAL INJURY ( 6 FDA reports)
GLIOMA ( 6 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 6 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 6 FDA reports)
GLOSSOPTOSIS ( 6 FDA reports)
GROIN ABSCESS ( 6 FDA reports)
HAEMATOCRIT INCREASED ( 6 FDA reports)
HAIR COLOUR CHANGES ( 6 FDA reports)
HELICOBACTER GASTRITIS ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATIC MASS ( 6 FDA reports)
HERNIA HIATUS REPAIR ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
HYPERTROPHY BREAST ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 6 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 6 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 6 FDA reports)
INFUSION SITE DISCOMFORT ( 6 FDA reports)
INFUSION SITE HAEMORRHAGE ( 6 FDA reports)
INFUSION SITE PRURITUS ( 6 FDA reports)
INJECTION SITE FIBROSIS ( 6 FDA reports)
INJECTION SITE INJURY ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
INTESTINAL ADHESION LYSIS ( 6 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
LACRIMATION DECREASED ( 6 FDA reports)
LARYNGEAL INJURY ( 6 FDA reports)
LARYNGEAL OEDEMA ( 6 FDA reports)
LAZINESS ( 6 FDA reports)
LESION OF SCIATIC NERVE ( 6 FDA reports)
LIGAMENT LAXITY ( 6 FDA reports)
LIGAMENT OPERATION ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
LOSS OF EMPLOYMENT ( 6 FDA reports)
LOW BIRTH WEIGHT BABY ( 6 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 6 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 6 FDA reports)
MACROCYTOSIS ( 6 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA METASTATIC ( 6 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 6 FDA reports)
MARCUS GUNN SYNDROME ( 6 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 6 FDA reports)
METASTATIC GASTRIC CANCER ( 6 FDA reports)
METASTATIC SALIVARY GLAND CANCER ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MITRAL VALVE REPLACEMENT ( 6 FDA reports)
MOLE EXCISION ( 6 FDA reports)
MOYAMOYA DISEASE ( 6 FDA reports)
MYOCARDIAL OEDEMA ( 6 FDA reports)
NASAL MUCOSAL DISORDER ( 6 FDA reports)
NEPHROPATHY TOXIC ( 6 FDA reports)
NERVE DEGENERATION ( 6 FDA reports)
NEUROLOGICAL COMPLICATION ASSOCIATED WITH DEVICE ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NEUTRALISING ANTIBODIES ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 6 FDA reports)
OESOPHAGECTOMY ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
ORAL DISORDER ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OSTEITIS DEFORMANS ( 6 FDA reports)
OVARIAN GRANULOSA-THECA CELL TUMOUR ( 6 FDA reports)
OVARIAN HYPERFUNCTION ( 6 FDA reports)
PANCREATIC ENZYMES DECREASED ( 6 FDA reports)
PATHOLOGICAL GAMBLING ( 6 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 6 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 6 FDA reports)
PERIPHERAL NERVE LESION ( 6 FDA reports)
PERITONITIS BACTERIAL ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PIGMENTED NAEVUS ( 6 FDA reports)
PITUITARY ENLARGEMENT ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
PNEUMOPERITONEUM ( 6 FDA reports)
POST PROCEDURAL CELLULITIS ( 6 FDA reports)
POST PROCEDURAL DIARRHOEA ( 6 FDA reports)
POST PROCEDURAL DISCOMFORT ( 6 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 6 FDA reports)
PTERYGIUM ( 6 FDA reports)
PULMONARY BULLA ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PUPILS UNEQUAL ( 6 FDA reports)
PURPURA ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RADIAL NERVE PALSY ( 6 FDA reports)
RADICAL HYSTERECTOMY ( 6 FDA reports)
RADICULAR PAIN ( 6 FDA reports)
RALES ( 6 FDA reports)
RECTAL ADENOMA ( 6 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
RENAL HAEMATOMA ( 6 FDA reports)
RENAL HYPERTENSION ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 6 FDA reports)
REVISION OF INTERNAL FIXATION ( 6 FDA reports)
RIB EXCISION ( 6 FDA reports)
RIGHT VENTRICULAR FAILURE ( 6 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 6 FDA reports)
SALIVARY GLAND MASS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SALPINGO-OOPHORECTOMY ( 6 FDA reports)
SEBORRHOEIC KERATOSIS ( 6 FDA reports)
SHIFT TO THE LEFT ( 6 FDA reports)
SHOCK HYPOGLYCAEMIC ( 6 FDA reports)
SINUS PERFORATION ( 6 FDA reports)
SKIN DESQUAMATION ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SMALL INTESTINE OPERATION ( 6 FDA reports)
SMOKER ( 6 FDA reports)
SPINAL CORD INFECTION ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 6 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
STATUS ASTHMATICUS ( 6 FDA reports)
STATUS MIGRAINOSUS ( 6 FDA reports)
SUDDEN ONSET OF SLEEP ( 6 FDA reports)
SUPPORTIVE CARE ( 6 FDA reports)
SUTURE INSERTION ( 6 FDA reports)
TACHYARRHYTHMIA ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
TINEA PEDIS ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOXIC ENCEPHALOPATHY ( 6 FDA reports)
TRAUMATIC ARTHRITIS ( 6 FDA reports)
TRAUMATIC FRACTURE ( 6 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 6 FDA reports)
TUMOUR MARKER INCREASED ( 6 FDA reports)
TUNNEL VISION ( 6 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 6 FDA reports)
UNINTENTIONAL MEDICAL DEVICE REMOVAL BY PATIENT ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
URETERIC CANCER ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
URINARY SEDIMENT PRESENT ( 6 FDA reports)
URINARY TRACT OPERATION ( 6 FDA reports)
UTERINE PERFORATION ( 6 FDA reports)
UTERINE SPASM ( 6 FDA reports)
VAGINITIS ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VENOUS OPERATION ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VIBRATION TEST ABNORMAL ( 6 FDA reports)
VICTIM OF SEXUAL ABUSE ( 6 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 6 FDA reports)
VIRAEMIA ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 6 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 6 FDA reports)
WRIST SURGERY ( 6 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RECTAL TENESMUS ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RETROPERITONEAL FIBROSIS ( 5 FDA reports)
RIB HYPOPLASIA ( 5 FDA reports)
SALPINGECTOMY ( 5 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 5 FDA reports)
SALPINGO-OOPHORITIS ( 5 FDA reports)
SCAN ABDOMEN ABNORMAL ( 5 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 5 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 5 FDA reports)
SEMINOMA ( 5 FDA reports)
SICKLE CELL TRAIT ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SPASTIC PARALYSIS ( 5 FDA reports)
SPLEEN CONGESTION ( 5 FDA reports)
SPUTUM ABNORMAL ( 5 FDA reports)
STENT REMOVAL ( 5 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 5 FDA reports)
SUBDURAL EMPYEMA ( 5 FDA reports)
SUBSTANCE USE ( 5 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE I ( 5 FDA reports)
TESTIS CANCER ( 5 FDA reports)
THYROIDITIS CHRONIC ( 5 FDA reports)
TINEA CRURIS ( 5 FDA reports)
TONSILLAR HYPERTROPHY ( 5 FDA reports)
TOXIC NODULAR GOITRE ( 5 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 5 FDA reports)
TRICHORRHEXIS ( 5 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 5 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 5 FDA reports)
URETERAL STENT INSERTION ( 5 FDA reports)
URETERIC DIVERSION OPERATION ( 5 FDA reports)
URINE BILIRUBIN INCREASED ( 5 FDA reports)
UTERINE MALPOSITION ( 5 FDA reports)
VACCINATION SITE PAIN ( 5 FDA reports)
VAGINAL DYSPLASIA ( 5 FDA reports)
VASCULAR ACCESS COMPLICATION ( 5 FDA reports)
VASCULAR DEMENTIA ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
VIRAL LABYRINTHITIS ( 5 FDA reports)
VIRAL MYOCARDITIS ( 5 FDA reports)
VIRAL TEST POSITIVE ( 5 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 5 FDA reports)
VISUAL PATHWAY DISORDER ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
WEIGHT DECREASE NEONATAL ( 5 FDA reports)
WOUND ABSCESS ( 5 FDA reports)
ABNORMAL PRODUCT OF CONCEPTION ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ADNEXA UTERI MASS ( 5 FDA reports)
ADRENALECTOMY ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALCOHOL DETOXIFICATION ( 5 FDA reports)
ALLERGIC COUGH ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
ARTERIAL BYPASS OPERATION ( 5 FDA reports)
AURA ( 5 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 5 FDA reports)
BELLIGERENCE ( 5 FDA reports)
BEREAVEMENT REACTION ( 5 FDA reports)
BILIARY NEOPLASM ( 5 FDA reports)
BITE ( 5 FDA reports)
BLADDER CANCER RECURRENT ( 5 FDA reports)
BLADDER DISCOMFORT ( 5 FDA reports)
BLADDER NECK SUSPENSION ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 5 FDA reports)
BLOOD AMYLASE DECREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 5 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BONE LESION EXCISION ( 5 FDA reports)
BREAST OEDEMA ( 5 FDA reports)
BREAST OPERATION ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHITIS VIRAL ( 5 FDA reports)
BURSITIS INFECTIVE ( 5 FDA reports)
CAPILLARY DISORDER ( 5 FDA reports)
CARBON MONOXIDE POISONING ( 5 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 5 FDA reports)
CARDIAC MYXOMA ( 5 FDA reports)
CARDIAC SEPTAL DEFECT ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CAUSTIC INJURY ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 5 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 5 FDA reports)
CHAPPED LIPS ( 5 FDA reports)
CHROMOSOME ABNORMALITY ( 5 FDA reports)
CHRONIC HEPATIC FAILURE ( 5 FDA reports)
COLONIC FISTULA ( 5 FDA reports)
COLONOSCOPY ABNORMAL ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 5 FDA reports)
CSF OLIGOCLONAL BAND PRESENT ( 5 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 5 FDA reports)
CYSTITIS BACTERIAL ( 5 FDA reports)
DEATH OF PARENT ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DEVICE COMPONENT ISSUE ( 5 FDA reports)
DEVICE CONNECTION ISSUE ( 5 FDA reports)
DIET REFUSAL ( 5 FDA reports)
DRUG EFFECT INCREASED ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DRUG THERAPY CHANGED ( 5 FDA reports)
DUPUYTREN'S CONTRACTURE ( 5 FDA reports)
DURAL TEAR ( 5 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
ENDOMETRIOMA ( 5 FDA reports)
ENTEROCOLITIS BACTERIAL ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
EYE DEGENERATIVE DISORDER ( 5 FDA reports)
FALLOPIAN TUBE NEOPLASM ( 5 FDA reports)
FEAR OF FALLING ( 5 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 5 FDA reports)
FOETAL DISORDER ( 5 FDA reports)
GALLBLADDER OEDEMA ( 5 FDA reports)
GALLBLADDER POLYP ( 5 FDA reports)
GAMMOPATHY ( 5 FDA reports)
GAS POISONING ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC VOLVULUS ( 5 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GLIOSIS ( 5 FDA reports)
GLOBULINS INCREASED ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GONORRHOEA ( 5 FDA reports)
GRAFT COMPLICATION ( 5 FDA reports)
GRANULOCYTE COUNT DECREASED ( 5 FDA reports)
GUILLAIN-BARRE SYNDROME ( 5 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HELLP SYNDROME ( 5 FDA reports)
HEPATIC TRAUMA ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERPLASIA ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCISIONAL DRAINAGE ( 5 FDA reports)
INFECTIOUS PERITONITIS ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE RASH ( 5 FDA reports)
INGUINAL MASS ( 5 FDA reports)
INJECTION SITE CALCIFICATION ( 5 FDA reports)
INJECTION SITE DYSAESTHESIA ( 5 FDA reports)
INJECTION SITE EROSION ( 5 FDA reports)
INJECTION SITE OEDEMA ( 5 FDA reports)
INJURY ASPHYXIATION ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
INTESTINAL CYST ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 5 FDA reports)
INTRASPINAL ABSCESS ( 5 FDA reports)
JOINT ADHESION ( 5 FDA reports)
JUVENILE ARTHRITIS ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
LABORATORY TEST INTERFERENCE ( 5 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 5 FDA reports)
LEIOMYOSARCOMA ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LIFE SUPPORT ( 5 FDA reports)
LIGHT CHAIN DISEASE ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LOSS OF LIBIDO ( 5 FDA reports)
MACULAR FIBROSIS ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 5 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
MENINGITIS LISTERIA ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 5 FDA reports)
MITRAL VALVE SCLEROSIS ( 5 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
MONOCYTE COUNT DECREASED ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
NAIL AVULSION ( 5 FDA reports)
NASAL NEOPLASM ( 5 FDA reports)
NECK CRUSHING ( 5 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 5 FDA reports)
NERVE ROOT LESION ( 5 FDA reports)
NEURILEMMOMA BENIGN ( 5 FDA reports)
NEUROBLASTOMA ( 5 FDA reports)
NEUROMA ( 5 FDA reports)
OBSTRUCTED LABOUR ( 5 FDA reports)
OCCIPITAL NEURALGIA ( 5 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PANCREATECTOMY ( 5 FDA reports)
PANCREATIC NECROSIS ( 5 FDA reports)
PARATHYROIDECTOMY ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 5 FDA reports)
PEAU D'ORANGE ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERIPHERAL NERVE INJURY ( 5 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 5 FDA reports)
PHYSICAL DISABILITY ( 5 FDA reports)
PILONIDAL CYST ( 5 FDA reports)
PLASMA VISCOSITY DECREASED ( 5 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 5 FDA reports)
POLYTRAUMATISM ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POSTPARTUM DEPRESSION ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 5 FDA reports)
PREMENSTRUAL SYNDROME ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROCTITIS ( 5 FDA reports)
PROCTITIS ULCERATIVE ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PROSTATECTOMY ( 5 FDA reports)
PSYCHOTIC BEHAVIOUR ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
ACNE CYSTIC ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ADENOIDECTOMY ( 4 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 4 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
AMBLYOPIA ( 4 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAL CANCER STAGE II ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
ANORECTAL INFECTION ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
APTYALISM ( 4 FDA reports)
ARM AMPUTATION ( 4 FDA reports)
ARTERIAL HAEMORRHAGE ( 4 FDA reports)
ARTERY DISSECTION ( 4 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 4 FDA reports)
ASBESTOSIS ( 4 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
AUTONOMIC NERVE OPERATION ( 4 FDA reports)
AVIAN INFLUENZA ( 4 FDA reports)
AXILLARY VEIN THROMBOSIS ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
B-CELL LYMPHOMA STAGE I ( 4 FDA reports)
BACTERIAL FOOD POISONING ( 4 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 4 FDA reports)
BASAL GANGLIA STROKE ( 4 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BENIGN NEOPLASM OF EYE ( 4 FDA reports)
BICUSPID AORTIC VALVE ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BIOPSY BLADDER ( 4 FDA reports)
BIOPSY KIDNEY ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER DISTENSION ( 4 FDA reports)
BLADDER DIVERTICULUM ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
BORDERLINE OVARIAN TUMOUR ( 4 FDA reports)
BRAIN MIDLINE SHIFT ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
BURN INFECTION ( 4 FDA reports)
BURSA DISORDER ( 4 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CALCULUS PROSTATIC ( 4 FDA reports)
CAPNOCYTOPHAGIA INFECTION ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 4 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 4 FDA reports)
CARDIAC PACEMAKER REMOVAL ( 4 FDA reports)
CARDIOLIPIN ANTIBODY ( 4 FDA reports)
CARDITIS ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CATHETER SITE OEDEMA ( 4 FDA reports)
CATHETER SITE RELATED REACTION ( 4 FDA reports)
CATHETER THROMBOSIS ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 4 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 4 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 4 FDA reports)
CERVIX CARCINOMA STAGE I ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHEMICAL INJURY ( 4 FDA reports)
CHEST WALL CYST ( 4 FDA reports)
CHOLANGITIS CHRONIC ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CHONDRITIS ( 4 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 4 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COAGULATION FACTOR VIII LEVEL ABNORMAL ( 4 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 4 FDA reports)
COLON GANGRENE ( 4 FDA reports)
COLON INJURY ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 4 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 4 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 4 FDA reports)
CONGENITAL EYE NAEVUS ( 4 FDA reports)
CONGENITAL FOOT MALFORMATION ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CORNEAL DYSTROPHY ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
COUGH DECREASED ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CRYPTORCHISM ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DERMAL SINUS ( 4 FDA reports)
DERMATILLOMANIA ( 4 FDA reports)
DIABETES MELLITUS MANAGEMENT ( 4 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
EAR OPERATION ( 4 FDA reports)
ELECTRIC SHOCK ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
ENTEROSTOMY ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EXTRASKELETAL OSSIFICATION ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
EYE INFECTION INTRAOCULAR ( 4 FDA reports)
EYE OPERATION COMPLICATION ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FACTOR X DEFICIENCY ( 4 FDA reports)
FACTOR XIII DEFICIENCY ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FALLOPIAN TUBE CANCER ( 4 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
FILARIASIS ( 4 FDA reports)
FOETAL DEATH ( 4 FDA reports)
FRACTURED ISCHIUM ( 4 FDA reports)
FROSTBITE ( 4 FDA reports)
FUNGAL CYSTITIS ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GALLBLADDER CANCER METASTATIC ( 4 FDA reports)
GALLBLADDER NECROSIS ( 4 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 4 FDA reports)
GASTRIC SARCOMA ( 4 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 4 FDA reports)
GENITAL INFECTION FEMALE ( 4 FDA reports)
GENITAL PROLAPSE ( 4 FDA reports)
GINGIVAL BLISTER ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEAD BANGING ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEART VALVE CALCIFICATION ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HIP DEFORMITY ( 4 FDA reports)
HUNTINGTON'S CHOREA ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
HYPOHIDROSIS ( 4 FDA reports)
HYPOPLASTIC ANAEMIA ( 4 FDA reports)
HYSTEROPEXY ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 4 FDA reports)
IMMUNOGLOBULINS INCREASED ( 4 FDA reports)
IMPLANT SITE ABSCESS ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INJECTION SITE DISCHARGE ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERNAL INJURY ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTESTINAL ULCER PERFORATION ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
IRIS ATROPHY ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
KIDNEY RUPTURE ( 4 FDA reports)
KLEBSIELLA BACTERAEMIA ( 4 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 4 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
LEFT ATRIAL DILATATION ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LHERMITTE'S SIGN ( 4 FDA reports)
LIBIDO INCREASED ( 4 FDA reports)
LIP DISCOLOURATION ( 4 FDA reports)
LIPID METABOLISM DISORDER ( 4 FDA reports)
LIPOPROTEIN (A) INCREASED ( 4 FDA reports)
LUNG CYST BENIGN ( 4 FDA reports)
LYMPH NODE CANCER METASTATIC ( 4 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 4 FDA reports)
MALIGNANT GLIOMA ( 4 FDA reports)
MALIGNANT MELANOMA STAGE III ( 4 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 4 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 4 FDA reports)
MENINGITIS CHEMICAL ( 4 FDA reports)
MENOPAUSAL DISORDER ( 4 FDA reports)
METASTASES TO BREAST ( 4 FDA reports)
METASTASES TO KIDNEY ( 4 FDA reports)
METASTASES TO STOMACH ( 4 FDA reports)
METASTASES TO THE MEDIASTINUM ( 4 FDA reports)
MILK-ALKALI SYNDROME ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 4 FDA reports)
MUSCLE FIBROSIS ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYELOID LEUKAEMIA ( 4 FDA reports)
MYELOID METAPLASIA ( 4 FDA reports)
NASAL CYST ( 4 FDA reports)
NASAL SEPTUM DISORDER ( 4 FDA reports)
NASAL SINUS DRAINAGE ( 4 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 4 FDA reports)
NEONATAL INFECTION ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEPHROANGIOSCLEROSIS ( 4 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 4 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 4 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSTETRIC PROCEDURE COMPLICATION ( 4 FDA reports)
OCULAR MYASTHENIA ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OESOPHAGEAL CARCINOMA RECURRENT ( 4 FDA reports)
OESOPHAGEAL INFECTION ( 4 FDA reports)
OESOPHAGEAL IRRITATION ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
OSTEOGENESIS IMPERFECTA ( 4 FDA reports)
OTITIS MEDIA CHRONIC ( 4 FDA reports)
OVARIAN CANCER STAGE III ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 4 FDA reports)
PAGET'S DISEASE OF THE VULVA ( 4 FDA reports)
PANCREATICOSPLENECTOMY ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PAPILLOMA ( 4 FDA reports)
PARADOXICAL EMBOLISM ( 4 FDA reports)
PARAGANGLION NEOPLASM MALIGNANT ( 4 FDA reports)
PECTUS EXCAVATUM ( 4 FDA reports)
PELVIC DISCOMFORT ( 4 FDA reports)
PERICARDITIS INFECTIVE ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PHAEOCHROMOCYTOMA ( 4 FDA reports)
PHYSICAL ABUSE ( 4 FDA reports)
PITUITARY HAEMORRHAGE ( 4 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PREDISPOSITION TO DISEASE ( 4 FDA reports)
PREGNANCY OF PARTNER ( 4 FDA reports)
PROCEDURAL HYPERTENSION ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PSEUDARTHROSIS ( 4 FDA reports)
PSEUDOCYST ( 4 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 4 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
PYOMYOSITIS ( 4 FDA reports)
RABIES IMMUNISATION ( 4 FDA reports)
RECALL PHENOMENON ( 4 FDA reports)
RECTAL ABSCESS ( 4 FDA reports)
RECTAL CANCER STAGE III ( 4 FDA reports)
RECTOCELE REPAIR ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
REPETITIVE STRAIN INJURY ( 4 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RETINAL DYSTROPHY ( 4 FDA reports)
RHEUMATIC HEART DISEASE ( 4 FDA reports)
SARCOMA METASTATIC ( 4 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 4 FDA reports)
SCINTILLATING SCOTOMA ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SEPTIC NECROSIS ( 4 FDA reports)
SEXUAL ABUSE ( 4 FDA reports)
SHUNT OCCLUSION ( 4 FDA reports)
SINUSITIS FUNGAL ( 4 FDA reports)
SKIN INFLAMMATION ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKIN SWELLING ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 4 FDA reports)
SOCIAL PHOBIA ( 4 FDA reports)
SODIUM RETENTION ( 4 FDA reports)
SOLILOQUY ( 4 FDA reports)
SPINAL CORD NEOPLASM ( 4 FDA reports)
SPINAL MENINGIOMA BENIGN ( 4 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 4 FDA reports)
STITCH ABSCESS ( 4 FDA reports)
STREPTOCOCCAL ABSCESS ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SWEAT GLAND DISORDER ( 4 FDA reports)
TANNING ( 4 FDA reports)
TARDIVE DYSKINESIA ( 4 FDA reports)
TETHERED CORD SYNDROME ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THIRST DECREASED ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
THYMUS HYPERTROPHY ( 4 FDA reports)
THYROXINE FREE ABNORMAL ( 4 FDA reports)
TOBACCO ABUSE ( 4 FDA reports)
TONGUE ABSCESS ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TOXOPLASMOSIS ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 4 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER REGIONAL ( 4 FDA reports)
TRAUMATIC AMPUTATION ( 4 FDA reports)
TRI-IODOTHYRONINE ABNORMAL ( 4 FDA reports)
TROUSSEAU'S SYNDROME ( 4 FDA reports)
TUMOUR NECROSIS ( 4 FDA reports)
TUMOUR RUPTURE ( 4 FDA reports)
TURNER'S SYNDROME ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 4 FDA reports)
URETERIC OBSTRUCTION ( 4 FDA reports)
URETERIC REPAIR ( 4 FDA reports)
URETHRAL DISCHARGE ( 4 FDA reports)
URINARY BLADDER EXCISION ( 4 FDA reports)
URINARY BLADDER RUPTURE ( 4 FDA reports)
URINARY CONTROL NEUROSTIMULATOR IMPLANTATION ( 4 FDA reports)
URINARY TRACT INFLAMMATION ( 4 FDA reports)
URINARY TRACT PAIN ( 4 FDA reports)
UROSTOMY ( 4 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 4 FDA reports)
VACCINATION SITE CELLULITIS ( 4 FDA reports)
VAGINAL CANCER RECURRENT ( 4 FDA reports)
VAGINAL OPERATION ( 4 FDA reports)
VAGINAL PAIN ( 4 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 4 FDA reports)
VENOUS STENT INSERTION ( 4 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 4 FDA reports)
VIRAL PHARYNGITIS ( 4 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 4 FDA reports)
VITAMIN B12 ABNORMAL ( 4 FDA reports)
VITREOUS DEGENERATION ( 4 FDA reports)
VOLUME BLOOD INCREASED ( 4 FDA reports)
VOLVULUS OF SMALL BOWEL ( 4 FDA reports)
VOMITING IN PREGNANCY ( 4 FDA reports)
VULVAL ABSCESS ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
YAWNING ( 4 FDA reports)
PYURIA ( 3 FDA reports)
RADIOTHERAPY TO BRAIN ( 3 FDA reports)
RECTAL CANCER STAGE IV ( 3 FDA reports)
RECTAL PERFORATION ( 3 FDA reports)
RECTAL PROLAPSE REPAIR ( 3 FDA reports)
RECTOSIGMOID CANCER ( 3 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 3 FDA reports)
RED BLOOD CELL MORPHOLOGY NORMAL ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL ADENOMA ( 3 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
RETINAL ANEURYSM ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RETINAL NEOPLASM ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RETINITIS PIGMENTOSA ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 3 FDA reports)
SALIVARY GLAND CALCULUS ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SELECTIVE IGG SUBCLASS DEFICIENCY ( 3 FDA reports)
SENSATION OF PRESSURE IN EAR ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SINGLE UMBILICAL ARTERY ( 3 FDA reports)
SKIN GRAFT FAILURE ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SLOW SPEECH ( 3 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 3 FDA reports)
SMALL INTESTINE GANGRENE ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPASTIC PARAPLEGIA ( 3 FDA reports)
SPINAL CORD DRAINAGE ( 3 FDA reports)
SPINAL CORD OPERATION ( 3 FDA reports)
SPINAL CORPECTOMY ( 3 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THERMOHYPOAESTHESIA ( 3 FDA reports)
THORACOTOMY ( 3 FDA reports)
THROMBOANGIITIS OBLITERANS ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
THYROTOXIC CRISIS ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TONSILLAR NEOPLASM ( 3 FDA reports)
TOXIC SHOCK SYNDROME ( 3 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TRISOMY 8 ( 3 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 3 FDA reports)
UMBILICAL ERYTHEMA ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY BLADDER ABSCESS ( 3 FDA reports)
URINARY BLADDER ATROPHY ( 3 FDA reports)
UTERINE ATONY ( 3 FDA reports)
UTERINE LEIOMYOSARCOMA ( 3 FDA reports)
UTERINE OPERATION ( 3 FDA reports)
VACCINATION SITE ERYTHEMA ( 3 FDA reports)
VAGINAL LACERATION ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
VESICOURETERIC REFLUX ( 3 FDA reports)
VICTIM OF ABUSE ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VIRAL SINUSITIS ( 3 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VITREOUS DETACHMENT ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVAL CANCER STAGE 0 ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
VULVOVAGINITIS ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WOUND INFECTION FUNGAL ( 3 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 3 FDA reports)
XANTHOPSIA ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 3 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 3 FDA reports)
ABORTION THREATENED ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 3 FDA reports)
ALLERGIC SINUSITIS ( 3 FDA reports)
ALLERGY TO ARTHROPOD STING ( 3 FDA reports)
ALLERGY TO PLANTS ( 3 FDA reports)
ALLODYNIA ( 3 FDA reports)
ALVEOLAR OSTEITIS ( 3 FDA reports)
AMNIOCENTESIS ABNORMAL ( 3 FDA reports)
AMNIOTIC CAVITY DISORDER ( 3 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 3 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANORECTAL ULCER ( 3 FDA reports)
ANORGASMIA ( 3 FDA reports)
ANOVULATORY CYCLE ( 3 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 3 FDA reports)
ANTIDEPRESSANT THERAPY ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
AORTIC SURGERY ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTIFICIAL BLADDER IMPLANTATION ( 3 FDA reports)
ASPIRATION BONE MARROW ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AUTOANTIBODY POSITIVE ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
BABESIOSIS ( 3 FDA reports)
BACTERIAL PYELONEPHRITIS ( 3 FDA reports)
BACTEROIDES INFECTION ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BASOPHIL COUNT DECREASED ( 3 FDA reports)
BED BUG INFESTATION ( 3 FDA reports)
BENIGN BILIARY NEOPLASM ( 3 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 3 FDA reports)
BEREAVEMENT ( 3 FDA reports)
BILIARY TRACT INFECTION ( 3 FDA reports)
BIOPSY BREAST NORMAL ( 3 FDA reports)
BIOPSY LYMPH GLAND ( 3 FDA reports)
BIRTH MARK ( 3 FDA reports)
BLADDER CANCER STAGE III ( 3 FDA reports)
BLADDER CYST ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD ETHANOL INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
BONE CANCER METASTATIC ( 3 FDA reports)
BONE SWELLING ( 3 FDA reports)
BORRELIA INFECTION ( 3 FDA reports)
BRACHYTHERAPY ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BREAST DISORDER FEMALE ( 3 FDA reports)
BREAST PROSTHESIS REMOVAL ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 3 FDA reports)
CALCIFICATION OF MUSCLE ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 3 FDA reports)
CAROTID ARTERY STENT INSERTION ( 3 FDA reports)
CAROTID ARTERY THROMBOSIS ( 3 FDA reports)
CARTILAGE ATROPHY ( 3 FDA reports)
CATHETER REMOVAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL DECOMPRESSION ( 3 FDA reports)
CEREBROSPINAL FLUID RHINORRHOEA ( 3 FDA reports)
CHEST WALL ABSCESS ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLELITHIASIS MIGRATION ( 3 FDA reports)
CHOLESTEROL GRANULOMA ( 3 FDA reports)
CHORIOAMNIONITIS ( 3 FDA reports)
CHOROIDAL NAEVUS ( 3 FDA reports)
CHROMOSOMAL MUTATION ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CLEFT PALATE ( 3 FDA reports)
COAGULATION FACTOR DECREASED ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COLORECTAL CANCER STAGE IV ( 3 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 3 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 3 FDA reports)
COMPLICATED MIGRAINE ( 3 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 3 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 3 FDA reports)
CONGENITAL AORTIC ANOMALY ( 3 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 3 FDA reports)
CONGENITAL INTESTINAL MALFORMATION ( 3 FDA reports)
CONGENITAL OESOPHAGEAL ANOMALY ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CRYOGLOBULINAEMIA ( 3 FDA reports)
CSF CELL COUNT ABNORMAL ( 3 FDA reports)
CSF CELL COUNT INCREASED ( 3 FDA reports)
CSF GLUCOSE INCREASED ( 3 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 3 FDA reports)
CSF VIRUS IDENTIFIED ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CYSTOCELE REPAIR ( 3 FDA reports)
CYSTOSTOMY ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DENTAL CARE ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DERMOID CYST OF OVARY ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DEVICE DIFFICULT TO USE ( 3 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 3 FDA reports)
DISBACTERIOSIS ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
DYSPLASTIC NAEVUS ( 3 FDA reports)
EAR NEOPLASM ( 3 FDA reports)
EAR NEOPLASM MALIGNANT ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
EMOTIONAL POVERTY ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
ENDOMETRIAL DISORDER ( 3 FDA reports)
ENDOSALPINGIOSIS ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
EPIDURAL ANAESTHESIA ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 3 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 3 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 3 FDA reports)
EYE INFECTION TOXOPLASMAL ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
FACTOR XI DEFICIENCY ( 3 FDA reports)
FAECAL VOMITING ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FALSE LABOUR ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FIBROADENOMA OF BREAST ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FITZ-HUGH-CURTIS SYNDROME ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
FRACTURE MALUNION ( 3 FDA reports)
FRACTURE TREATMENT ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GASTRIC HYPOMOTILITY ( 3 FDA reports)
GASTRITIS FUNGAL ( 3 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GASTROOESOPHAGEAL CANCER ( 3 FDA reports)
GENE MUTATION ( 3 FDA reports)
GENITAL ABSCESS ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GILBERT'S SYNDROME ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GINGIVAL RECESSION ( 3 FDA reports)
GINGIVAL ULCERATION ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMANGIOPERICYTOMA ( 3 FDA reports)
HAEMATOMA INFECTION ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMOPHILIA ( 3 FDA reports)
HEAD LAG ( 3 FDA reports)
HEADACHE POSTOPERATIVE ( 3 FDA reports)
HEAT ILLNESS ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATECTOMY ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HERPES DERMATITIS ( 3 FDA reports)
HIATUS HERNIA, OBSTRUCTIVE ( 3 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE I INFECTION ( 3 FDA reports)
HYDROCHOLECYSTIS ( 3 FDA reports)
HYPER IGE SYNDROME ( 3 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 3 FDA reports)
HYPERMETABOLISM ( 3 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERPATHIA ( 3 FDA reports)
HYPERSPLENISM ( 3 FDA reports)
HYPOAESTHESIA EYE ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
IMMINENT ABORTION ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCISION SITE ERYTHEMA ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFECTED NEOPLASM ( 3 FDA reports)
INFLAMMATION LOCALISED ( 3 FDA reports)
INFUSION SITE DISCOLOURATION ( 3 FDA reports)
INFUSION SITE MASS ( 3 FDA reports)
INFUSION SITE PHLEBITIS ( 3 FDA reports)
INJECTION ( 3 FDA reports)
INJECTION SITE COLDNESS ( 3 FDA reports)
INJECTION SITE DRYNESS ( 3 FDA reports)
INJECTION SITE STREAKING ( 3 FDA reports)
INTERTRIGO ( 3 FDA reports)
INTESTINAL STOMA ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTRACRANIAL HAEMANGIOMA ( 3 FDA reports)
INTRAOCULAR LENS IMPLANT ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
IRON METABOLISM DISORDER ( 3 FDA reports)
JOINT LIGAMENT RUPTURE ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LABORATORY TEST ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LARYNGITIS ALLERGIC ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LIBIDO DISORDER ( 3 FDA reports)
LIMB MALFORMATION ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER RECURRENT ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
LIPOMA EXCISION ( 3 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUDWIG ANGINA ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 3 FDA reports)
LUNG LOBECTOMY ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MALIGNANT MELANOMA OF EYELID ( 3 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 3 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEGACOLON ACQUIRED ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
MENINGOCOCCAL BACTERAEMIA ( 3 FDA reports)
MENISCUS OPERATION ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
METAPLASIA ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MUSCLE GRAFT ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MYOCARDITIS INFECTIOUS ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
MYOKYMIA ( 3 FDA reports)
MYOMECTOMY ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
MYOTONIC DYSTROPHY ( 3 FDA reports)
NAEVUS FLAMMEUS ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEONATAL ASPIRATION ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NERVE ROOT INJURY ( 3 FDA reports)
NERVE ROOT INJURY LUMBAR ( 3 FDA reports)
NEUROSURGERY ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NOREPINEPHRINE INCREASED ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 3 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 3 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 3 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL POLYP ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPIATES POSITIVE ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
ORBIT PLASTIC REPAIR ( 3 FDA reports)
ORGASM ABNORMAL ( 3 FDA reports)
OROPHARYNGEAL CANCER STAGE I ( 3 FDA reports)
ORTHOSIS USER ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PAIN MANAGEMENT ( 3 FDA reports)
PALLANAESTHESIA ( 3 FDA reports)
PANCREATIC ENLARGEMENT ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PARANASAL SINUS NEOPLASM ( 3 FDA reports)
PARASITIC INFECTION INTESTINAL ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PENILE PAIN ( 3 FDA reports)
PERIOSTITIS ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PHARYNGEAL NEOPLASM ( 3 FDA reports)
PHARYNGEAL OPERATION ( 3 FDA reports)
PHLEBOPLASTY ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYCYTHAEMIA VERA ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
POOR PERSONAL HYGIENE ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
POSTOPERATIVE CONSTIPATION ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PROSTATE CANCER STAGE I ( 3 FDA reports)
PROSTATIC MASS ( 3 FDA reports)
PROSTATIC OBSTRUCTION ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
5-ALPHA-REDUCTASE DEFICIENCY ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACANTHAMOEBA INFECTION ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADACTYLY ( 2 FDA reports)
ADENOIDAL DISORDER ( 2 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
ADRENOLEUKODYSTROPHY ( 2 FDA reports)
AFFERENT LOOP SYNDROME ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOL REHABILITATION ( 2 FDA reports)
ALCOHOLIC SEIZURE ( 2 FDA reports)
ALEXIA ( 2 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 2 FDA reports)
ALLERGY TO VACCINE ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
AMPULLA OF VATER STENOSIS ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAEMIC HYPOXIA ( 2 FDA reports)
ANAL FISTULA EXCISION ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANEURYSMAL BONE CYST ( 2 FDA reports)
ANGIOFIBROMA ( 2 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 2 FDA reports)
ANKLE DEFORMITY ( 2 FDA reports)
ANTICIPATORY ANXIETY ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTICULAR DISC DISORDER ( 2 FDA reports)
ASPERGER'S DISORDER ( 2 FDA reports)
ASPIRATION JOINT ABNORMAL ( 2 FDA reports)
ASTROCYTOMA MALIGNANT ( 2 FDA reports)
ATONIC URINARY BLADDER ( 2 FDA reports)
ATRIAL BIGEMINY ( 2 FDA reports)
ATRIAL PRESSURE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AUTOIMMUNE MYOCARDITIS ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
BED REST ( 2 FDA reports)
BENIGN MESOTHELIOMA ( 2 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 2 FDA reports)
BENIGN PERITONEAL NEOPLASM ( 2 FDA reports)
BENIGN VAGINAL NEOPLASM ( 2 FDA reports)
BILE DUCT CANCER STAGE IV ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BIOPSY CERVIX ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BIOPSY THYROID GLAND ( 2 FDA reports)
BIPOLAR II DISORDER ( 2 FDA reports)
BLADDER CALCULUS REMOVAL ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER PAPILLOMA ( 2 FDA reports)
BLADDER STENOSIS ( 2 FDA reports)
BLAST CELL CRISIS ( 2 FDA reports)
BLEEDING ANOVULATORY ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CORTICOSTERONE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 2 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BREAST CANCER MALE ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST INJURY ( 2 FDA reports)
BREAST PROSTHESIS USER ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHITIS ACUTE VIRAL ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURSA INJURY ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CAPILLARY FRAGILITY ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOMA EXCISION ( 2 FDA reports)
CARDIAC ARREST NEONATAL ( 2 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 2 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 2 FDA reports)
CARDIAC SARCOIDOSIS ( 2 FDA reports)
CARDIAC SEPTAL DEFECT REPAIR ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIAC VALVE RUPTURE ( 2 FDA reports)
CARDIOSPASM ( 2 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
CEPHALHAEMATOMA ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CEREBROVASCULAR OPERATION ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CERVIX CARCINOMA RECURRENT ( 2 FDA reports)
CERVIX ENLARGEMENT ( 2 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 2 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHONDRECTOMY ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CIRCUMCISED ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
COLPOCELE ( 2 FDA reports)
COLPOSCOPY ABNORMAL ( 2 FDA reports)
COLPOSUSPENSION ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CONDYLOMA ACUMINATUM ( 2 FDA reports)
CONGENITAL ABSENCE OF BILE DUCTS ( 2 FDA reports)
CONGENITAL ACROCHORDON ( 2 FDA reports)
CONGENITAL BOWING OF LONG BONES ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL CYSTIC LUNG ( 2 FDA reports)
CONGENITAL EYE DISORDER ( 2 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 2 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 2 FDA reports)
CONGENITAL TORTICOLLIS ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
CREATINE URINE DECREASED ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CRYSTAL URINE ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CSF BACTERIA IDENTIFIED ( 2 FDA reports)
CSF GLUCOSE DECREASED ( 2 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYSTOURETHROCELE ( 2 FDA reports)
CYTOLOGY ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DACRYOLITH ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEAFNESS CONGENITAL ( 2 FDA reports)
DEATH OF FRIEND ( 2 FDA reports)
DELAYED DELIVERY ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DEPRESSION POSTOPERATIVE ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMABRASION ( 2 FDA reports)
DERMATITIS DIAPER ( 2 FDA reports)
DETACHMENT OF MACULAR RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIAPHRAGMALGIA ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA REFRACTORY ( 2 FDA reports)
DIPHTHERIA ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 2 FDA reports)
DOUBLE URETER ( 2 FDA reports)
DOUBLE VESSEL BYPASS GRAFT ( 2 FDA reports)
DRUG ADDICT ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG THERAPY ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
DYSTROPHIC CALCIFICATION ( 2 FDA reports)
EAR INFECTION FUNGAL ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EAR TUBE INSERTION ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECTOPIC PARATHORMONE PRODUCTION ( 2 FDA reports)
ECZEMA INFECTED ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELECTROCUTION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENCEPHALITIS TOXIC ( 2 FDA reports)
ENCEPHALOMYELITIS ( 2 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE 0 ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENEMA ADMINISTRATION ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
ENZYME INHIBITION ( 2 FDA reports)
EPENDYMOMA MALIGNANT ( 2 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURAL TEST DOSE ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
ERB'S PALSY ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXPOSURE TO ALLERGEN ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTENSIVE SWELLING OF VACCINATED LIMB ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) STAGE I ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYE PROSTHESIS INSERTION ( 2 FDA reports)
EYEBALL AVULSION ( 2 FDA reports)
EYELID BLEEDING ( 2 FDA reports)
EYELID OPERATION ( 2 FDA reports)
EYELID PTOSIS CONGENITAL ( 2 FDA reports)
FACE LIFT ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FACIAL OPERATION ( 2 FDA reports)
FACTOR II DEFICIENCY ( 2 FDA reports)
FALLOPIAN TUBE ABSCESS ( 2 FDA reports)
FALLOPIAN TUBE CANCER STAGE IV ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMALE GENITAL OPERATION ( 2 FDA reports)
FEVER NEONATAL ( 2 FDA reports)
FIBROSARCOMA ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FOETAL CYSTIC HYGROMA ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC ILEUS ( 2 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC STENOSIS ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRINOMA ( 2 FDA reports)
GASTRO-INTESTINAL FISTULA ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROPARESIS POSTOPERATIVE ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL DISCOMFORT ( 2 FDA reports)
GENITAL INFECTION BACTERIAL ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITAL SWELLING ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRAFT ISCHAEMIA ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAMARTOMA ( 2 FDA reports)
HEAT EXPOSURE INJURY ( 2 FDA reports)
HEMIANOPIA HETERONYMOUS ( 2 FDA reports)
HEPATIC CANCER STAGE II ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HEREDITARY DISORDER ( 2 FDA reports)
HERNIA OBSTRUCTIVE ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HISTONE ANTIBODY POSITIVE ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE STAGE II SITE UNSPEC ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE II SUPRADIAPHRAGMATIC ( 2 FDA reports)
HOMOCYSTINAEMIA ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HORMONE REPLACEMENT THERAPY ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERMOBILITY SYNDROME ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTONIC URINARY BLADDER ( 2 FDA reports)
HYPOTONY OF EYE ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
IDEAS OF REFERENCE ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANT SITE IRRITATION ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INCISION SITE PRURITUS ( 2 FDA reports)
INFANTILE ASTHMA ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFECTIVE EXACERBATION OF BRONCHIECTASIS ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFUSION SITE CELLULITIS ( 2 FDA reports)
INFUSION SITE SCAR ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INJECTION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ABSCESS STERILE ( 2 FDA reports)
INJECTION SITE CYST ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INJECTION SITE PHOTOSENSITIVITY REACTION ( 2 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTESTINAL ADENOCARCINOMA ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTESTINAL STRANGULATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 2 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ( 2 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ISCHIORECTAL HERNIA ( 2 FDA reports)
IVTH NERVE INJURY ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT DISLOCATION PATHOLOGICAL ( 2 FDA reports)
JOINT RECONSTRUCTION ( 2 FDA reports)
JOINT RESURFACING SURGERY ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KERATOMILEUSIS ( 2 FDA reports)
KIDNEY DUPLEX ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LAPAROSCOPY ( 2 FDA reports)
LARYNGEAL CANCER STAGE IV ( 2 FDA reports)
LARYNGEAL INFILTRATION ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIP INFECTION ( 2 FDA reports)
LIP PRURITUS ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LISSENCEPHALY ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LIVER FUNCTION TEST ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 2 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 2 FDA reports)
MALIGNANT MELANOMA STAGE II ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 2 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MARBURG'S VARIANT MULTIPLE SCLEROSIS ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTOCYTOSIS ( 2 FDA reports)
MAXILLOFACIAL OPERATION ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MEASLES ANTIBODY POSITIVE ( 2 FDA reports)
MEDIASTINAL FIBROSIS ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MEGAKARYOCYTES ( 2 FDA reports)
MEIGS' SYNDROME ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
MENINGORADICULITIS ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO MUSCLE ( 2 FDA reports)
METASTASES TO RECTUM ( 2 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
METASTATIC LYMPHOMA ( 2 FDA reports)
METASTATIC OCULAR MELANOMA ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MIGRATION OF IMPLANT ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MORTON'S NEURALGIA ( 2 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE PREGNANCY ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MUSCLE OPERATION ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL GROWTH CESSATION ( 2 FDA reports)
NASAL SINUS CANCER ( 2 FDA reports)
NEONATAL APNOEIC ATTACK ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM OF APPENDIX ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE ROOT INJURY CERVICAL ( 2 FDA reports)
NEUROGENIC SHOCK ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTRALISING ANTIBODIES NEGATIVE ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NIPPLE EXUDATE BLOODY ( 2 FDA reports)
NITRITE URINE ( 2 FDA reports)
NO ADVERSE DRUG REACTION ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NORMAL DELIVERY ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OBSTETRICAL PULMONARY EMBOLISM ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OESOPHAGEAL STENT REMOVAL ( 2 FDA reports)
OESTROGENIC EFFECT ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPTIC DISCS BLURRED ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
ORO-PHARYNGEAL ASPERGILLOSIS ( 2 FDA reports)
OROPHARYNGITIS FUNGAL ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE IV ( 2 FDA reports)
OVARIAN FIBROSIS ( 2 FDA reports)
OVARIAN INFECTION ( 2 FDA reports)
OVARIAN PROLAPSE ( 2 FDA reports)
OVARIAN TORSION ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OXYGEN SATURATION INCREASED ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALATAL DYSPLASIA ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC CARCINOMA NON-RESECTABLE ( 2 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC FISTULA ( 2 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 2 FDA reports)
PANCREATICODUODENECTOMY ( 2 FDA reports)
PARAESTHESIA MUCOSAL ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARAPSORIASIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PAROPHTHALMIA ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL NERVE INFECTION ( 2 FDA reports)
PERIPHERAL NERVE PALSY ( 2 FDA reports)
PERIPROSTHETIC FRACTURE ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL MESOTHELIOMA ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST PROCEDURAL HEADACHE ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 2 FDA reports)
POST-TRAUMATIC PAIN ( 2 FDA reports)
POSTMATURE BABY ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
POVERTY OF THOUGHT CONTENT ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PREMATURE AGEING ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRIMITIVE NEUROECTODERMAL TUMOUR ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC HAEMORRHAGE ( 2 FDA reports)
PROTEIN C DEFICIENCY ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSEUDODEMENTIA ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PSEUDOMONAS BRONCHITIS ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PSYCHOTHERAPY ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY CALCIFICATION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY HAEMATOMA ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RATHKE'S CLEFT CYST ( 2 FDA reports)
REACTION TO COLOURING ( 2 FDA reports)
REACTION TO FOOD ADDITIVE ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REDUCED BLADDER CAPACITY ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RENAL CANCER STAGE III ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RENAL VEIN OCCLUSION ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL MELANOMA ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALIVARY GLAND ADENOMA ( 2 FDA reports)
SALIVARY GLAND CANCER RECURRENT ( 2 FDA reports)
SALIVARY GLAND CYST ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SCAR PAIN ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCOLIOSIS SURGERY ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SECONDARY HYPOTHYROIDISM ( 2 FDA reports)
SELECTIVE ABORTION ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SENSATION OF BLOCK IN EAR ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SEPTIC PHLEBITIS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SKIN GRAFT REJECTION ( 2 FDA reports)
SKIN OPERATION ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SLEEP STUDY ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SOMATIC DELUSION ( 2 FDA reports)
SPINAL CORD HERNIATION ( 2 FDA reports)
SPINAL CORD INJURY CAUDA EQUINA ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPINAL X-RAY ABNORMAL ( 2 FDA reports)
SPINDLE CELL SARCOMA ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 2 FDA reports)
STASIS SYNDROME ( 2 FDA reports)
STOMA SITE REACTION ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STRUCK BY LIGHTNING ( 2 FDA reports)
SUBACUTE SCLEROSING PANENCEPHALITIS ( 2 FDA reports)
SUBCHORIONIC HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPRAPUBIC CATHETER INSERTION ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TESTICULAR CANCER METASTATIC ( 2 FDA reports)
TESTICULAR GERM CELL CANCER ( 2 FDA reports)
TESTICULAR HYPERTROPHY ( 2 FDA reports)
TESTICULAR OEDEMA ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THALASSAEMIA ( 2 FDA reports)
THYMUS ENLARGEMENT ( 2 FDA reports)
THYROGLOSSAL CYST ( 2 FDA reports)
THYROID CANCER STAGE IV ( 2 FDA reports)
THYROIDECTOMY PARTIAL ( 2 FDA reports)
THYROXINE ABNORMAL ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 2 FDA reports)
TOTAL HYSTERECTOMY ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRAUMATIC COMA ( 2 FDA reports)
TRISOMY 22 ( 2 FDA reports)
ULTRASOUND BLADDER ABNORMAL ( 2 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 2 FDA reports)
UNEQUAL LIMB LENGTH ( 2 FDA reports)
URETERAL CYST ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL PERFORATION ( 2 FDA reports)
URETHRAL STENT INSERTION ( 2 FDA reports)
URINARY TRACT INFECTION VIRAL ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URINE POTASSIUM ABNORMAL ( 2 FDA reports)
URINE POTASSIUM INCREASED ( 2 FDA reports)
UTERINE ABSCESS ( 2 FDA reports)
UTERINE CERVIX HYPERTROPHY ( 2 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 2 FDA reports)
UTERINE FIBROID EMBOLISATION ( 2 FDA reports)
UTERINE INJURY ( 2 FDA reports)
UTERINE INVERSION ( 2 FDA reports)
VACCINATION SITE INDURATION ( 2 FDA reports)
VACCINATION SITE INFLAMMATION ( 2 FDA reports)
VAGINAL ABSCESS ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINITIS GARDNERELLA ( 2 FDA reports)
VAGUS NERVE DISORDER ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VARICOPHLEBITIS ( 2 FDA reports)
VARICOSE VEIN RUPTURED ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULAR TEST ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 2 FDA reports)
VENOUS REPAIR ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VERTIGO CNS ORIGIN ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
VESSEL PUNCTURE SITE DISCHARGE ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL SKIN INFECTION ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN B1 DEFICIENCY ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VITREOUS LOSS ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VOCAL CORD POLYPECTOMY ( 2 FDA reports)
VULVAL CANCER STAGE III ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WATER POLLUTION ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
PYELOCYSTITIS ( 1 FDA reports)
PYLORIC ABSCESS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIATION SICKNESS SYNDROME ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RED BLOOD CELL ACANTHOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 1 FDA reports)
REFLEX TEST ABNORMAL ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REMOVAL OF FOREIGN BODY ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL GRANULAR CELL CARCINOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUMOUR EXCISION ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOSCHISIS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
RHABDOID TUMOUR OF THE KIDNEY ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLEREMA ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SENILE PSYCHOSIS ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SEVERED DIGIT REIMPLANTATION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL CELL LUNG CANCER LIMITED STAGE ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE ATROPHY ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPINAL CORD INJURY LUMBAR ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL INFECTION VIRAL ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STRANGULATED HERNIA REPAIR ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUBTOTAL HYSTERECTOMY ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYMPATHECTOMY ( 1 FDA reports)
SYMPHYSIOLYSIS ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TATTOO ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TENOTOMY ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROID CANCER STAGE I ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TICK-BORNE FEVER ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRANSVERSE PRESENTATION ( 1 FDA reports)
TRAUMATIC ARTHROPATHY ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TYMPANIC MEMBRANE SCARRING ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND BLADDER ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
URETHRAL CARUNCLE ( 1 FDA reports)
URETHRAL DILATATION ( 1 FDA reports)
URETHRAL INTRINSIC SPHINCTER DEFICIENCY ( 1 FDA reports)
URETHRAL PROLAPSE ( 1 FDA reports)
URETHRAL ULCER ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE KETONE BODY ABSENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
UTERINE CERVICAL LACERATION ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE TENDERNESS ( 1 FDA reports)
UTERINE TUMOUR EXCISION ( 1 FDA reports)
VACCINATION SITE REACTION ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL LEUKOPLAKIA ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASECTOMY ( 1 FDA reports)
VENOM POISONING ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBRAL ABSCESS ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VIIITH NERVE LESION ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VISION ABNORMAL NEONATAL ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITAMIN SUPPLEMENTATION ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
VULVAL LACERATION ( 1 FDA reports)
VULVAL NEOPLASM ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHITE BLOOD CELL SCAN ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABSCESS STERILE ( 1 FDA reports)
ACCESSORY LIVER LOBE ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUPUNCTURE ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE II ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMBLYOPIA CONGENITAL ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPUTATION REVISION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SPHINCTER REPAIR ( 1 FDA reports)
ANAL TINEA ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTHROPOD INFESTATION ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASTROCYTOMA, LOW GRADE ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BASOSQUAMOUS CARCINOMA ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 1 FDA reports)
BENIGN EAR NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF TESTIS ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY CERVIX ABNORMAL ( 1 FDA reports)
BIOPSY FALLOPIAN TUBE ABNORMAL ( 1 FDA reports)
BIOPSY PARATHYROID GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY VOCAL CORD ABNORMAL ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER MALPOSITION ACQUIRED ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER SUSPENSION ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD LEAD INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TEST NORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST ADENOMA ( 1 FDA reports)
BREAST FIBROSIS ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST MALFORMATION ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BROWN-SEQUARD SYNDROME ( 1 FDA reports)
BURN OPERATION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELL MARKER ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR HYPOPLASIA ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMOSIDERIN DEPOSITION ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CERVICAL RIB ( 1 FDA reports)
CERVICAL SPASM ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHOLESTEATOMA REMOVAL ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 1 ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COLORECTAL CANCER STAGE III ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONFUSIONAL AROUSAL ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONVULSION PROPHYLAXIS ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL OPERATION ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIOPLASTY ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CRYPTOCOCCUS ANTIGEN POSITIVE ( 1 FDA reports)
CSF CULTURE NEGATIVE ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN ABNORMAL ( 1 FDA reports)
CSF SHUNT REMOVAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUPULOLITHIASIS ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEEP BRAIN STIMULATION ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSIONAL DISORDER, SOMATIC TYPE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DESMOID TUMOUR ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE INFUSION ISSUE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE INVERSION ( 1 FDA reports)
DEVICE POWER SOURCE ISSUE ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC MACROANGIOPATHY ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DRUG DELIVERY DEVICE REMOVAL ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DURAL FISTULA ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 1 FDA reports)
EHLERS-DANLOS SYNDROME ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTIVE PROCEDURE ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL METAPLASIA ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDIDYMAL NEOPLASM ( 1 FDA reports)
EPIGLOTTIC CARCINOMA ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EPSTEIN-BARR VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA VAGINITIS ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE COLOUR CHANGE ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID INJURY ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID SENSORY DISORDER ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACTOR II MUTATION ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAILED TRIAL OF LABOUR ( 1 FDA reports)
FALLOPIAN TUBE OPERATION ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL ARTERY DISSECTION ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FINGER HYPOPLASIA ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALLBLADDER CANCER STAGE I ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC CANCER STAGE II ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL INFECTION ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL PAIN MALE ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GLIOMATOSIS CEREBRI ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE LEVEL ABNORMAL ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMANGIOMA CONGENITAL ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE NEONATAL ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B ANTIBODY ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEREDITARY ATAXIA ( 1 FDA reports)
HEREDITARY OPTIC ATROPHY ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HODGKIN'S DISEASE STAGE II ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPODONTIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNISATION REACTION ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
IMPLANT EXPULSION ( 1 FDA reports)
IMPLANT SITE BRUISING ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE LUBRICATION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INFECTED INSECT BITE ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTED VARICOSE VEIN ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF BREAST STAGE III ( 1 FDA reports)
INFUSION SITE COLDNESS ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INNER EAR OPERATION ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL VARICES ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IODINE DEFICIENCY ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT LAXITY ( 1 FDA reports)
JOINT MANIPULATION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY PERFORATION ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL CANCER STAGE II ( 1 FDA reports)
LARYNGEAL CANCER STAGE III ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LEAD URINE INCREASED ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKAEMIC LYMPHOMA ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE III ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIPECTOMY ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LORDOSIS POST SURGICAL ( 1 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 1 FDA reports)
LOW SET EARS ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOMA OPERATION ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
MAGICAL THINKING ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT HAEMANGIOPERICYTOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MALIGNANT PITUITARY TUMOUR ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEGALOBLASTS INCREASED ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MENINGITIS NEONATAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PHARYNX ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE POLYMORPHISM ( 1 FDA reports)
MICROSURGERY TO HAND ( 1 FDA reports)
MIXED HEPATOCELLULAR CHOLANGIOCARCINOMA ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDIAL STRAIN ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
NAEVUS CELL NAEVUS ( 1 FDA reports)
NAIL BED INJURY ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NAIL RIDGING ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEOPLASM SWELLING ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
NERVOUS SYSTEM SURGERY ( 1 FDA reports)
NEUROBORRELIOSIS ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROSTIMULATOR IMPLANTATION ( 1 FDA reports)
NEUROSTIMULATOR REMOVAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY AGGRESSIVE STAGE I ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING THORACIC ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTETRIC INFECTION ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OCULAR VASCULITIS ( 1 FDA reports)
OEDEMA NEONATAL ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA STAGE I ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODENDROGLIOMA BENIGN ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIVOPONTOCEREBELLAR ATROPHY ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OOPHORITIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL POLYPECTOMY ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOPEDIC EXAMINATION ABNORMAL ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OVARIAN CYST TORSION ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANENCEPHALITIS ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROVARIAN CYST ( 1 FDA reports)
PAROXYSMAL PERCEPTUAL ALTERATION ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATELLECTOMY ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICHONDRITIS ( 1 FDA reports)
PERINEAL OPERATION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHYSICAL EXAMINATION ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PRIMARY AMYLOIDOSIS ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY NEGATIVE ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROSTATIC ATROPHY ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY OEDEMA NEONATAL ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)

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