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

NAUSEA ( 4086 FDA reports)
DIZZINESS ( 3642 FDA reports)
PAIN ( 3587 FDA reports)
DYSPNOEA ( 3545 FDA reports)
FATIGUE ( 3076 FDA reports)
DIARRHOEA ( 3014 FDA reports)
ASTHENIA ( 2931 FDA reports)
DRUG INEFFECTIVE ( 2820 FDA reports)
ANXIETY ( 2728 FDA reports)
HEADACHE ( 2625 FDA reports)
FALL ( 2605 FDA reports)
VOMITING ( 2571 FDA reports)
HYPERTENSION ( 2550 FDA reports)
CHEST PAIN ( 2421 FDA reports)
OEDEMA PERIPHERAL ( 2305 FDA reports)
MYOCARDIAL INFARCTION ( 2220 FDA reports)
HYPOTENSION ( 2155 FDA reports)
ARTHRALGIA ( 2146 FDA reports)
PAIN IN EXTREMITY ( 2042 FDA reports)
DEPRESSION ( 1992 FDA reports)
WEIGHT DECREASED ( 1893 FDA reports)
BACK PAIN ( 1866 FDA reports)
ANAEMIA ( 1842 FDA reports)
RENAL FAILURE ACUTE ( 1800 FDA reports)
MALAISE ( 1772 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1703 FDA reports)
PYREXIA ( 1688 FDA reports)
INSOMNIA ( 1653 FDA reports)
ATRIAL FIBRILLATION ( 1643 FDA reports)
MYALGIA ( 1626 FDA reports)
RENAL FAILURE ( 1624 FDA reports)
BLOOD PRESSURE INCREASED ( 1579 FDA reports)
DEHYDRATION ( 1559 FDA reports)
ABDOMINAL PAIN ( 1536 FDA reports)
PNEUMONIA ( 1521 FDA reports)
DRUG INTERACTION ( 1495 FDA reports)
CONFUSIONAL STATE ( 1493 FDA reports)
BLOOD GLUCOSE INCREASED ( 1437 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1408 FDA reports)
INJURY ( 1408 FDA reports)
PRURITUS ( 1388 FDA reports)
RASH ( 1352 FDA reports)
SYNCOPE ( 1317 FDA reports)
COUGH ( 1276 FDA reports)
WEIGHT INCREASED ( 1274 FDA reports)
CONSTIPATION ( 1259 FDA reports)
URINARY TRACT INFECTION ( 1240 FDA reports)
FEELING ABNORMAL ( 1228 FDA reports)
PARAESTHESIA ( 1174 FDA reports)
MUSCLE SPASMS ( 1173 FDA reports)
BRADYCARDIA ( 1166 FDA reports)
PALPITATIONS ( 1153 FDA reports)
HYPOAESTHESIA ( 1137 FDA reports)
DIABETES MELLITUS ( 1124 FDA reports)
CORONARY ARTERY DISEASE ( 1118 FDA reports)
SOMNOLENCE ( 1106 FDA reports)
DEATH ( 1089 FDA reports)
HYPERHIDROSIS ( 1082 FDA reports)
ABDOMINAL PAIN UPPER ( 1076 FDA reports)
GAIT DISTURBANCE ( 1074 FDA reports)
DECREASED APPETITE ( 1042 FDA reports)
LOSS OF CONSCIOUSNESS ( 1038 FDA reports)
TREMOR ( 1026 FDA reports)
FLUSHING ( 1024 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 994 FDA reports)
MUSCULAR WEAKNESS ( 993 FDA reports)
CONDITION AGGRAVATED ( 981 FDA reports)
BLOOD CREATININE INCREASED ( 922 FDA reports)
EMOTIONAL DISTRESS ( 912 FDA reports)
HAEMOGLOBIN DECREASED ( 899 FDA reports)
VISION BLURRED ( 897 FDA reports)
CONVULSION ( 865 FDA reports)
OSTEOARTHRITIS ( 848 FDA reports)
PULMONARY EMBOLISM ( 846 FDA reports)
ERYTHEMA ( 810 FDA reports)
DYSPEPSIA ( 787 FDA reports)
CARDIAC DISORDER ( 778 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 777 FDA reports)
CHEST DISCOMFORT ( 768 FDA reports)
CARDIAC ARREST ( 764 FDA reports)
THROMBOCYTOPENIA ( 717 FDA reports)
RENAL IMPAIRMENT ( 709 FDA reports)
HEART RATE INCREASED ( 707 FDA reports)
DYSPHAGIA ( 705 FDA reports)
CHILLS ( 702 FDA reports)
PLEURAL EFFUSION ( 702 FDA reports)
DEEP VEIN THROMBOSIS ( 695 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 694 FDA reports)
ANGINA PECTORIS ( 682 FDA reports)
ANHEDONIA ( 676 FDA reports)
RHABDOMYOLYSIS ( 675 FDA reports)
INFECTION ( 669 FDA reports)
OSTEONECROSIS OF JAW ( 664 FDA reports)
SEPSIS ( 659 FDA reports)
NEUROPATHY PERIPHERAL ( 656 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 634 FDA reports)
TACHYCARDIA ( 633 FDA reports)
RESPIRATORY FAILURE ( 628 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 628 FDA reports)
BLOOD PRESSURE DECREASED ( 625 FDA reports)
HYPOKALAEMIA ( 623 FDA reports)
LETHARGY ( 613 FDA reports)
HYPERSENSITIVITY ( 611 FDA reports)
UNEVALUABLE EVENT ( 611 FDA reports)
AMNESIA ( 603 FDA reports)
OEDEMA ( 600 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 598 FDA reports)
OVERDOSE ( 595 FDA reports)
PLATELET COUNT DECREASED ( 594 FDA reports)
JOINT SWELLING ( 590 FDA reports)
ABDOMINAL DISTENSION ( 588 FDA reports)
DRY MOUTH ( 588 FDA reports)
COMPLETED SUICIDE ( 583 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 579 FDA reports)
CONTUSION ( 577 FDA reports)
HYPONATRAEMIA ( 576 FDA reports)
BRONCHITIS ( 572 FDA reports)
ARTHRITIS ( 571 FDA reports)
HYPERKALAEMIA ( 563 FDA reports)
BALANCE DISORDER ( 559 FDA reports)
CELLULITIS ( 556 FDA reports)
ARRHYTHMIA ( 555 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 547 FDA reports)
SINUSITIS ( 545 FDA reports)
URTICARIA ( 545 FDA reports)
MEMORY IMPAIRMENT ( 544 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 543 FDA reports)
SWELLING ( 542 FDA reports)
OSTEOMYELITIS ( 540 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 537 FDA reports)
MULTI-ORGAN FAILURE ( 537 FDA reports)
HAEMORRHAGE ( 536 FDA reports)
PANCREATITIS ( 534 FDA reports)
FEAR ( 530 FDA reports)
CARDIOMEGALY ( 523 FDA reports)
BONE DISORDER ( 522 FDA reports)
MUSCULOSKELETAL PAIN ( 522 FDA reports)
PULMONARY OEDEMA ( 517 FDA reports)
STRESS ( 514 FDA reports)
BLOOD UREA INCREASED ( 513 FDA reports)
ALOPECIA ( 508 FDA reports)
CATARACT ( 507 FDA reports)
NECK PAIN ( 507 FDA reports)
RECTAL HAEMORRHAGE ( 506 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 500 FDA reports)
HYPERLIPIDAEMIA ( 497 FDA reports)
ABDOMINAL DISCOMFORT ( 496 FDA reports)
HYPERGLYCAEMIA ( 484 FDA reports)
FEELING HOT ( 480 FDA reports)
HYPOGLYCAEMIA ( 480 FDA reports)
BONE PAIN ( 476 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 471 FDA reports)
BURNING SENSATION ( 468 FDA reports)
OSTEONECROSIS ( 468 FDA reports)
RENAL FAILURE CHRONIC ( 456 FDA reports)
IMPAIRED HEALING ( 455 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 451 FDA reports)
EPISTAXIS ( 450 FDA reports)
SWELLING FACE ( 447 FDA reports)
NERVOUSNESS ( 444 FDA reports)
PANCYTOPENIA ( 441 FDA reports)
DYSGEUSIA ( 440 FDA reports)
MYOCARDIAL ISCHAEMIA ( 440 FDA reports)
CHOLELITHIASIS ( 438 FDA reports)
HALLUCINATION ( 437 FDA reports)
NEUTROPENIA ( 436 FDA reports)
ANOREXIA ( 432 FDA reports)
OSTEOPOROSIS ( 430 FDA reports)
AGITATION ( 429 FDA reports)
INJECTION SITE PAIN ( 424 FDA reports)
PAIN IN JAW ( 424 FDA reports)
THROMBOSIS ( 422 FDA reports)
TYPE 2 DIABETES MELLITUS ( 418 FDA reports)
VERTIGO ( 418 FDA reports)
HAEMATOCRIT DECREASED ( 418 FDA reports)
GASTRITIS ( 411 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 407 FDA reports)
CARDIO-RESPIRATORY ARREST ( 406 FDA reports)
SPEECH DISORDER ( 404 FDA reports)
INFLUENZA LIKE ILLNESS ( 403 FDA reports)
INCORRECT DOSE ADMINISTERED ( 401 FDA reports)
DRUG HYPERSENSITIVITY ( 397 FDA reports)
HEART RATE DECREASED ( 395 FDA reports)
HAEMORRHOIDS ( 394 FDA reports)
CORONARY ARTERY OCCLUSION ( 393 FDA reports)
FLATULENCE ( 390 FDA reports)
MITRAL VALVE INCOMPETENCE ( 390 FDA reports)
DIVERTICULUM ( 389 FDA reports)
ATELECTASIS ( 388 FDA reports)
BLOOD GLUCOSE DECREASED ( 384 FDA reports)
SPINAL OSTEOARTHRITIS ( 384 FDA reports)
SUICIDAL IDEATION ( 382 FDA reports)
HAEMATURIA ( 382 FDA reports)
HOT FLUSH ( 379 FDA reports)
URINARY INCONTINENCE ( 379 FDA reports)
TOOTH EXTRACTION ( 378 FDA reports)
MENTAL STATUS CHANGES ( 378 FDA reports)
NASOPHARYNGITIS ( 378 FDA reports)
ABASIA ( 376 FDA reports)
NEPHROLITHIASIS ( 372 FDA reports)
DYSARTHRIA ( 370 FDA reports)
HEART RATE IRREGULAR ( 369 FDA reports)
CARDIAC FAILURE ( 368 FDA reports)
DRUG TOXICITY ( 368 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 368 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 367 FDA reports)
ARTHROPATHY ( 363 FDA reports)
SINUS BRADYCARDIA ( 363 FDA reports)
RENAL INJURY ( 360 FDA reports)
ASTHMA ( 358 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 358 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 355 FDA reports)
DYSURIA ( 354 FDA reports)
HYPOXIA ( 354 FDA reports)
MIGRAINE ( 353 FDA reports)
STAPHYLOCOCCAL INFECTION ( 353 FDA reports)
HAEMATOCHEZIA ( 351 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 347 FDA reports)
DISORIENTATION ( 347 FDA reports)
ROAD TRAFFIC ACCIDENT ( 347 FDA reports)
TINNITUS ( 346 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 345 FDA reports)
HERPES ZOSTER ( 342 FDA reports)
OROPHARYNGEAL PAIN ( 341 FDA reports)
OSTEOPENIA ( 341 FDA reports)
DYSPNOEA EXERTIONAL ( 339 FDA reports)
ANGINA UNSTABLE ( 338 FDA reports)
OFF LABEL USE ( 338 FDA reports)
TREATMENT NONCOMPLIANCE ( 337 FDA reports)
RHEUMATOID ARTHRITIS ( 335 FDA reports)
BLOOD POTASSIUM DECREASED ( 335 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 331 FDA reports)
DRUG DOSE OMISSION ( 328 FDA reports)
DYSPHONIA ( 327 FDA reports)
DISTURBANCE IN ATTENTION ( 325 FDA reports)
POLLAKIURIA ( 325 FDA reports)
SEPTIC SHOCK ( 325 FDA reports)
VISUAL ACUITY REDUCED ( 325 FDA reports)
METABOLIC ACIDOSIS ( 324 FDA reports)
MOBILITY DECREASED ( 320 FDA reports)
HIATUS HERNIA ( 318 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 310 FDA reports)
SKIN DISCOLOURATION ( 307 FDA reports)
SLEEP DISORDER ( 307 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 305 FDA reports)
DISEASE PROGRESSION ( 305 FDA reports)
VISUAL IMPAIRMENT ( 303 FDA reports)
BLOOD SODIUM DECREASED ( 301 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 300 FDA reports)
SCAR ( 299 FDA reports)
SLEEP APNOEA SYNDROME ( 298 FDA reports)
RASH PRURITIC ( 297 FDA reports)
WHEEZING ( 297 FDA reports)
HYPOTHYROIDISM ( 297 FDA reports)
ARTERIOSCLEROSIS ( 296 FDA reports)
DRUG EFFECT DECREASED ( 295 FDA reports)
BREAST CANCER ( 292 FDA reports)
COMA ( 289 FDA reports)
ECONOMIC PROBLEM ( 286 FDA reports)
DEFORMITY ( 284 FDA reports)
LACTIC ACIDOSIS ( 284 FDA reports)
NEOPLASM MALIGNANT ( 284 FDA reports)
BURSITIS ( 283 FDA reports)
DYSKINESIA ( 279 FDA reports)
INFLAMMATION ( 279 FDA reports)
INJECTION SITE ERYTHEMA ( 279 FDA reports)
DENTAL CARIES ( 275 FDA reports)
TOOTH DISORDER ( 275 FDA reports)
ERECTILE DYSFUNCTION ( 274 FDA reports)
FEBRILE NEUTROPENIA ( 273 FDA reports)
PULMONARY HYPERTENSION ( 273 FDA reports)
RHINORRHOEA ( 273 FDA reports)
RENAL CYST ( 272 FDA reports)
RENAL DISORDER ( 271 FDA reports)
AGGRESSION ( 268 FDA reports)
BLOOD POTASSIUM INCREASED ( 267 FDA reports)
PANIC ATTACK ( 266 FDA reports)
PRODUCT QUALITY ISSUE ( 266 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 266 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 266 FDA reports)
MEDICATION ERROR ( 265 FDA reports)
URINARY RETENTION ( 264 FDA reports)
ROTATOR CUFF SYNDROME ( 261 FDA reports)
GASTRIC ULCER ( 261 FDA reports)
DIPLOPIA ( 260 FDA reports)
EXOSTOSIS ( 260 FDA reports)
ABNORMAL DREAMS ( 259 FDA reports)
LEUKOPENIA ( 259 FDA reports)
SUICIDE ATTEMPT ( 259 FDA reports)
VENTRICULAR TACHYCARDIA ( 259 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 258 FDA reports)
ORTHOSTATIC HYPOTENSION ( 257 FDA reports)
BLOOD BILIRUBIN INCREASED ( 257 FDA reports)
CIRCULATORY COLLAPSE ( 257 FDA reports)
HEPATIC STEATOSIS ( 256 FDA reports)
IRRITABILITY ( 254 FDA reports)
HAEMATOMA ( 253 FDA reports)
NASAL CONGESTION ( 253 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 253 FDA reports)
BLISTER ( 252 FDA reports)
ADVERSE EVENT ( 251 FDA reports)
HEPATIC ENZYME INCREASED ( 251 FDA reports)
DIVERTICULITIS ( 249 FDA reports)
SWOLLEN TONGUE ( 246 FDA reports)
RESPIRATORY ARREST ( 245 FDA reports)
LUNG DISORDER ( 245 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 244 FDA reports)
FEMUR FRACTURE ( 244 FDA reports)
GOUT ( 244 FDA reports)
SKIN ULCER ( 243 FDA reports)
PANCREATITIS ACUTE ( 241 FDA reports)
STOMATITIS ( 241 FDA reports)
LYMPHADENOPATHY ( 241 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 238 FDA reports)
HAEMATEMESIS ( 238 FDA reports)
GASTROINTESTINAL DISORDER ( 237 FDA reports)
INFLUENZA ( 237 FDA reports)
COLITIS ( 236 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 236 FDA reports)
DRY SKIN ( 235 FDA reports)
OESOPHAGITIS ( 235 FDA reports)
SURGERY ( 235 FDA reports)
METASTASES TO BONE ( 233 FDA reports)
ABNORMAL BEHAVIOUR ( 231 FDA reports)
SPINAL COLUMN STENOSIS ( 231 FDA reports)
FLUID RETENTION ( 230 FDA reports)
HEAD INJURY ( 227 FDA reports)
PERICARDIAL EFFUSION ( 226 FDA reports)
SHOCK ( 226 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 225 FDA reports)
RESPIRATORY DISTRESS ( 225 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 225 FDA reports)
POST PROCEDURAL COMPLICATION ( 224 FDA reports)
SKIN EXFOLIATION ( 223 FDA reports)
LUNG INFILTRATION ( 223 FDA reports)
NOCTURIA ( 223 FDA reports)
CYSTITIS ( 222 FDA reports)
OXYGEN SATURATION DECREASED ( 220 FDA reports)
BLINDNESS ( 219 FDA reports)
OBESITY ( 218 FDA reports)
HAEMOPTYSIS ( 216 FDA reports)
JAUNDICE ( 216 FDA reports)
RIB FRACTURE ( 216 FDA reports)
UNRESPONSIVE TO STIMULI ( 216 FDA reports)
ASCITES ( 215 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 214 FDA reports)
HYPERCHOLESTEROLAEMIA ( 214 FDA reports)
HYPOMAGNESAEMIA ( 214 FDA reports)
ORAL PAIN ( 214 FDA reports)
SINUS TACHYCARDIA ( 214 FDA reports)
MENTAL DISORDER ( 213 FDA reports)
HEPATIC FAILURE ( 212 FDA reports)
NIGHT SWEATS ( 212 FDA reports)
EYE PAIN ( 211 FDA reports)
PALLOR ( 211 FDA reports)
TOOTHACHE ( 210 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 209 FDA reports)
HAEMODIALYSIS ( 209 FDA reports)
BLOOD CALCIUM DECREASED ( 208 FDA reports)
CORONARY ARTERY STENOSIS ( 207 FDA reports)
APHASIA ( 205 FDA reports)
RESTLESSNESS ( 205 FDA reports)
RASH GENERALISED ( 204 FDA reports)
CARDIOVASCULAR DISORDER ( 204 FDA reports)
MULTIPLE MYELOMA ( 204 FDA reports)
EATING DISORDER ( 203 FDA reports)
EMOTIONAL DISORDER ( 203 FDA reports)
PRESYNCOPE ( 202 FDA reports)
VENTRICULAR HYPERTROPHY ( 202 FDA reports)
VISUAL DISTURBANCE ( 202 FDA reports)
CARDIAC MURMUR ( 198 FDA reports)
ILL-DEFINED DISORDER ( 198 FDA reports)
DIFFICULTY IN WALKING ( 197 FDA reports)
PRODUCTIVE COUGH ( 197 FDA reports)
VIRAL INFECTION ( 197 FDA reports)
MUCOSAL INFLAMMATION ( 196 FDA reports)
CAROTID ARTERY STENOSIS ( 195 FDA reports)
CARPAL TUNNEL SYNDROME ( 195 FDA reports)
TENDONITIS ( 194 FDA reports)
FAECES DISCOLOURED ( 193 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 193 FDA reports)
PNEUMONIA ASPIRATION ( 192 FDA reports)
PROTHROMBIN TIME PROLONGED ( 191 FDA reports)
SKIN LESION ( 191 FDA reports)
STOMACH DISCOMFORT ( 191 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 191 FDA reports)
GRAND MAL CONVULSION ( 191 FDA reports)
INJECTION SITE HAEMORRHAGE ( 191 FDA reports)
INTENTIONAL DRUG MISUSE ( 191 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 190 FDA reports)
FIBROMYALGIA ( 190 FDA reports)
MUSCLE TWITCHING ( 190 FDA reports)
SCIATICA ( 189 FDA reports)
PRURITUS GENERALISED ( 188 FDA reports)
DELIRIUM ( 188 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 188 FDA reports)
DISABILITY ( 187 FDA reports)
LUNG NEOPLASM ( 186 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 186 FDA reports)
ABDOMINAL PAIN LOWER ( 185 FDA reports)
INTESTINAL OBSTRUCTION ( 185 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 185 FDA reports)
PSORIASIS ( 184 FDA reports)
BLOOD URINE PRESENT ( 184 FDA reports)
DIABETIC NEUROPATHY ( 184 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 184 FDA reports)
NEURALGIA ( 183 FDA reports)
BREAST CANCER FEMALE ( 181 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 180 FDA reports)
ANGER ( 179 FDA reports)
COLONIC POLYP ( 179 FDA reports)
EYE SWELLING ( 179 FDA reports)
TOOTH ABSCESS ( 179 FDA reports)
SKIN BURNING SENSATION ( 178 FDA reports)
BASAL CELL CARCINOMA ( 178 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 177 FDA reports)
HYPOPHAGIA ( 177 FDA reports)
INTERSTITIAL LUNG DISEASE ( 177 FDA reports)
MUSCLE ATROPHY ( 177 FDA reports)
DYSSTASIA ( 176 FDA reports)
HIP FRACTURE ( 175 FDA reports)
VENTRICULAR FIBRILLATION ( 175 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 174 FDA reports)
LIMB INJURY ( 174 FDA reports)
MELAENA ( 174 FDA reports)
DRY EYE ( 173 FDA reports)
LEUKOCYTOSIS ( 173 FDA reports)
BONE DENSITY DECREASED ( 172 FDA reports)
DEAFNESS ( 172 FDA reports)
HEMIPARESIS ( 172 FDA reports)
DIALYSIS ( 171 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 171 FDA reports)
CEREBRAL HAEMORRHAGE ( 170 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 170 FDA reports)
RASH ERYTHEMATOUS ( 170 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 169 FDA reports)
ANAPHYLACTIC REACTION ( 169 FDA reports)
BLOOD ALBUMIN DECREASED ( 169 FDA reports)
CHOLECYSTITIS ( 169 FDA reports)
CARDIOMYOPATHY ( 168 FDA reports)
ANGIOEDEMA ( 167 FDA reports)
CHROMATURIA ( 166 FDA reports)
PROTEINURIA ( 166 FDA reports)
SINUS DISORDER ( 165 FDA reports)
THROAT IRRITATION ( 165 FDA reports)
PERIPHERAL COLDNESS ( 163 FDA reports)
EYE DISORDER ( 163 FDA reports)
GLAUCOMA ( 163 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 163 FDA reports)
COGNITIVE DISORDER ( 161 FDA reports)
AORTIC ANEURYSM ( 160 FDA reports)
TOOTH INFECTION ( 160 FDA reports)
TOOTH LOSS ( 160 FDA reports)
ADVERSE DRUG REACTION ( 159 FDA reports)
ATRIAL FLUTTER ( 159 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 159 FDA reports)
DEPRESSED MOOD ( 159 FDA reports)
EAR PAIN ( 159 FDA reports)
FLUID OVERLOAD ( 159 FDA reports)
IRRITABLE BOWEL SYNDROME ( 159 FDA reports)
MIDDLE INSOMNIA ( 159 FDA reports)
NIGHTMARE ( 159 FDA reports)
COORDINATION ABNORMAL ( 158 FDA reports)
DISCOMFORT ( 158 FDA reports)
GALLBLADDER DISORDER ( 158 FDA reports)
JOINT STIFFNESS ( 158 FDA reports)
MENTAL IMPAIRMENT ( 158 FDA reports)
GASTROENTERITIS ( 157 FDA reports)
HEPATITIS ( 157 FDA reports)
PROSTATE CANCER ( 157 FDA reports)
THROAT TIGHTNESS ( 156 FDA reports)
DEMENTIA ( 156 FDA reports)
FEELING COLD ( 156 FDA reports)
HALLUCINATION, VISUAL ( 156 FDA reports)
HYPOCALCAEMIA ( 156 FDA reports)
HYPOVOLAEMIA ( 156 FDA reports)
ACUTE CORONARY SYNDROME ( 155 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 155 FDA reports)
MULTIPLE DRUG OVERDOSE ( 155 FDA reports)
CEREBRAL ATROPHY ( 154 FDA reports)
NERVOUS SYSTEM DISORDER ( 154 FDA reports)
SEDATION ( 154 FDA reports)
PURULENT DISCHARGE ( 153 FDA reports)
RESTLESS LEGS SYNDROME ( 153 FDA reports)
ABSCESS ( 153 FDA reports)
MULTIPLE INJURIES ( 153 FDA reports)
CYANOSIS ( 152 FDA reports)
DECREASED INTEREST ( 152 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 152 FDA reports)
PULMONARY FIBROSIS ( 152 FDA reports)
BACK INJURY ( 151 FDA reports)
COAGULOPATHY ( 151 FDA reports)
HYPOAESTHESIA ORAL ( 151 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 150 FDA reports)
GLOSSODYNIA ( 150 FDA reports)
DYSLIPIDAEMIA ( 149 FDA reports)
MOUTH ULCERATION ( 149 FDA reports)
CEREBRAL INFARCTION ( 148 FDA reports)
CRYING ( 148 FDA reports)
RASH MACULAR ( 148 FDA reports)
TENDERNESS ( 147 FDA reports)
AGEUSIA ( 147 FDA reports)
LIVER DISORDER ( 147 FDA reports)
ACCIDENTAL OVERDOSE ( 146 FDA reports)
EJECTION FRACTION DECREASED ( 146 FDA reports)
IRON DEFICIENCY ANAEMIA ( 146 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 145 FDA reports)
PULMONARY CONGESTION ( 145 FDA reports)
RESPIRATORY DISORDER ( 145 FDA reports)
SKIN DISORDER ( 145 FDA reports)
TOOTH FRACTURE ( 145 FDA reports)
SPINAL COMPRESSION FRACTURE ( 144 FDA reports)
CARDIOGENIC SHOCK ( 144 FDA reports)
FUNGAL INFECTION ( 144 FDA reports)
CANDIDIASIS ( 143 FDA reports)
EMPHYSEMA ( 143 FDA reports)
MOVEMENT DISORDER ( 143 FDA reports)
PNEUMONITIS ( 143 FDA reports)
RETCHING ( 142 FDA reports)
JOINT INJURY ( 142 FDA reports)
MYOCLONUS ( 142 FDA reports)
DRUG INTOLERANCE ( 141 FDA reports)
GASTRIC DISORDER ( 141 FDA reports)
ISCHAEMIC STROKE ( 141 FDA reports)
MYOSITIS ( 141 FDA reports)
PARAESTHESIA ORAL ( 141 FDA reports)
PSYCHOTIC DISORDER ( 141 FDA reports)
ULCER ( 139 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 139 FDA reports)
COLD SWEAT ( 139 FDA reports)
LOOSE TOOTH ( 139 FDA reports)
ATAXIA ( 138 FDA reports)
CYST ( 138 FDA reports)
INTENTIONAL OVERDOSE ( 138 FDA reports)
LIMB DISCOMFORT ( 138 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 137 FDA reports)
LIP SWELLING ( 137 FDA reports)
DIVERTICULUM INTESTINAL ( 135 FDA reports)
FEELING JITTERY ( 135 FDA reports)
JAW DISORDER ( 135 FDA reports)
MASS ( 135 FDA reports)
FAECAL INCONTINENCE ( 134 FDA reports)
VAGINAL HAEMORRHAGE ( 134 FDA reports)
SEROTONIN SYNDROME ( 133 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 133 FDA reports)
HYPERSOMNIA ( 133 FDA reports)
ANKLE FRACTURE ( 132 FDA reports)
COLON CANCER ( 132 FDA reports)
AORTIC VALVE INCOMPETENCE ( 130 FDA reports)
ATRIOVENTRICULAR BLOCK ( 130 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 130 FDA reports)
FOOT FRACTURE ( 129 FDA reports)
LACRIMATION INCREASED ( 128 FDA reports)
PHARYNGEAL OEDEMA ( 128 FDA reports)
PRIMARY SEQUESTRUM ( 128 FDA reports)
THINKING ABNORMAL ( 128 FDA reports)
LUMBAR SPINAL STENOSIS ( 127 FDA reports)
LUNG NEOPLASM MALIGNANT ( 127 FDA reports)
OCULAR HYPERAEMIA ( 127 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 126 FDA reports)
INJECTION SITE REACTION ( 126 FDA reports)
BODY TEMPERATURE INCREASED ( 125 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 125 FDA reports)
GINGIVAL BLEEDING ( 125 FDA reports)
ORAL DISORDER ( 125 FDA reports)
CEREBRAL ISCHAEMIA ( 124 FDA reports)
LACERATION ( 124 FDA reports)
SKIN LACERATION ( 124 FDA reports)
OSTEOLYSIS ( 123 FDA reports)
LOCALISED INFECTION ( 123 FDA reports)
DISEASE RECURRENCE ( 122 FDA reports)
INJECTION SITE PRURITUS ( 122 FDA reports)
MUSCLE TIGHTNESS ( 122 FDA reports)
BACTERIAL INFECTION ( 121 FDA reports)
BONE LESION ( 120 FDA reports)
DRUG DEPENDENCE ( 120 FDA reports)
GINGIVAL PAIN ( 120 FDA reports)
HEPATIC CYST ( 120 FDA reports)
HEPATOMEGALY ( 120 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 119 FDA reports)
ECCHYMOSIS ( 119 FDA reports)
OSTEITIS ( 119 FDA reports)
PHYSICAL DISABILITY ( 118 FDA reports)
SQUAMOUS CELL CARCINOMA ( 117 FDA reports)
STENT PLACEMENT ( 117 FDA reports)
STEVENS-JOHNSON SYNDROME ( 117 FDA reports)
VASCULITIS ( 117 FDA reports)
CHRONIC SINUSITIS ( 117 FDA reports)
DRUG ADMINISTRATION ERROR ( 117 FDA reports)
ORAL INTAKE REDUCED ( 117 FDA reports)
DRUG LEVEL INCREASED ( 116 FDA reports)
HEPATIC CIRRHOSIS ( 116 FDA reports)
MULTIPLE SCLEROSIS ( 116 FDA reports)
SKIN INDURATION ( 116 FDA reports)
SPINAL DISORDER ( 116 FDA reports)
PERITONITIS ( 115 FDA reports)
RASH PAPULAR ( 115 FDA reports)
ANGIONEUROTIC OEDEMA ( 115 FDA reports)
BLINDNESS UNILATERAL ( 114 FDA reports)
CHOLESTASIS ( 114 FDA reports)
ECZEMA ( 114 FDA reports)
HYPERCALCAEMIA ( 114 FDA reports)
NEUTROPHIL COUNT DECREASED ( 114 FDA reports)
SICK SINUS SYNDROME ( 114 FDA reports)
SUDDEN DEATH ( 114 FDA reports)
THYROID DISORDER ( 114 FDA reports)
UPPER LIMB FRACTURE ( 114 FDA reports)
SPINAL FRACTURE ( 113 FDA reports)
DUODENAL ULCER ( 113 FDA reports)
FIBROSIS ( 113 FDA reports)
JOINT DISLOCATION ( 113 FDA reports)
CHOLECYSTITIS CHRONIC ( 112 FDA reports)
ERUCTATION ( 112 FDA reports)
EXTRASYSTOLES ( 112 FDA reports)
INJECTION SITE HAEMATOMA ( 112 FDA reports)
MYOPATHY ( 112 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 112 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 112 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 112 FDA reports)
RHINITIS ALLERGIC ( 111 FDA reports)
BIPOLAR DISORDER ( 111 FDA reports)
IMPAIRED DRIVING ABILITY ( 111 FDA reports)
BACK DISORDER ( 110 FDA reports)
DRUG ABUSE ( 110 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 110 FDA reports)
INTESTINAL ISCHAEMIA ( 110 FDA reports)
RASH MACULO-PAPULAR ( 110 FDA reports)
PARALYSIS ( 109 FDA reports)
BODY HEIGHT DECREASED ( 109 FDA reports)
BRONCHOSPASM ( 109 FDA reports)
DIABETIC KETOACIDOSIS ( 109 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 109 FDA reports)
INCONTINENCE ( 109 FDA reports)
INFUSION RELATED REACTION ( 109 FDA reports)
MICTURITION URGENCY ( 108 FDA reports)
MUSCLE DISORDER ( 108 FDA reports)
SKIN TIGHTNESS ( 108 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 108 FDA reports)
CARDIAC VALVE DISEASE ( 107 FDA reports)
CATARACT OPERATION ( 107 FDA reports)
INITIAL INSOMNIA ( 107 FDA reports)
MUSCLE STRAIN ( 107 FDA reports)
COMPRESSION FRACTURE ( 106 FDA reports)
FISTULA ( 106 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 106 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 106 FDA reports)
PULSE ABSENT ( 106 FDA reports)
SENSORY DISTURBANCE ( 106 FDA reports)
SKIN HYPERTROPHY ( 106 FDA reports)
RESPIRATORY RATE INCREASED ( 105 FDA reports)
TARDIVE DYSKINESIA ( 105 FDA reports)
HYPERTENSIVE CRISIS ( 105 FDA reports)
LABORATORY TEST ABNORMAL ( 105 FDA reports)
MAJOR DEPRESSION ( 105 FDA reports)
ORAL CANDIDIASIS ( 105 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 104 FDA reports)
FLANK PAIN ( 104 FDA reports)
MUSCLE CRAMP ( 104 FDA reports)
RADICULOPATHY ( 104 FDA reports)
SKIN CANCER ( 104 FDA reports)
PATHOLOGICAL FRACTURE ( 103 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 102 FDA reports)
SPLENOMEGALY ( 102 FDA reports)
ACUTE RESPIRATORY FAILURE ( 102 FDA reports)
AZOTAEMIA ( 102 FDA reports)
BRONCHOPNEUMONIA ( 102 FDA reports)
CLOSTRIDIAL INFECTION ( 102 FDA reports)
DECUBITUS ULCER ( 102 FDA reports)
EXPOSED BONE IN JAW ( 102 FDA reports)
GINGIVITIS ( 102 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 102 FDA reports)
ONYCHOMYCOSIS ( 102 FDA reports)
GENERALISED OEDEMA ( 101 FDA reports)
MENISCUS LESION ( 101 FDA reports)
RENAL TUBULAR NECROSIS ( 101 FDA reports)
SUBDURAL HAEMATOMA ( 101 FDA reports)
THERAPY NON-RESPONDER ( 101 FDA reports)
SINUS CONGESTION ( 100 FDA reports)
APNOEA ( 100 FDA reports)
EYE HAEMORRHAGE ( 100 FDA reports)
GOITRE ( 100 FDA reports)
LACUNAR INFARCTION ( 100 FDA reports)
LOCAL SWELLING ( 100 FDA reports)
METASTASES TO LUNG ( 100 FDA reports)
CROHN'S DISEASE ( 99 FDA reports)
BONE MARROW FAILURE ( 98 FDA reports)
ENCEPHALOPATHY ( 98 FDA reports)
HYPOACUSIS ( 98 FDA reports)
MOOD ALTERED ( 98 FDA reports)
UROSEPSIS ( 98 FDA reports)
WRIST FRACTURE ( 98 FDA reports)
GINGIVAL DISORDER ( 97 FDA reports)
HYPOKINESIA ( 97 FDA reports)
LIPASE INCREASED ( 97 FDA reports)
OLIGURIA ( 97 FDA reports)
ORAL INFECTION ( 97 FDA reports)
HALLUCINATION, AUDITORY ( 96 FDA reports)
IMPAIRED WORK ABILITY ( 96 FDA reports)
METASTASES TO LIVER ( 96 FDA reports)
OPEN WOUND ( 96 FDA reports)
PARANOIA ( 96 FDA reports)
POISONING ( 96 FDA reports)
URINE OUTPUT DECREASED ( 95 FDA reports)
VENTRICULAR HYPOKINESIA ( 95 FDA reports)
BLOOD PRESSURE ABNORMAL ( 95 FDA reports)
CHOKING ( 95 FDA reports)
JOINT EFFUSION ( 95 FDA reports)
ORAL DISCOMFORT ( 95 FDA reports)
CORONARY ARTERY BYPASS ( 94 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 94 FDA reports)
MOOD SWINGS ( 94 FDA reports)
WITHDRAWAL SYNDROME ( 94 FDA reports)
SENSATION OF HEAVINESS ( 93 FDA reports)
DERMATITIS ( 93 FDA reports)
ANURIA ( 92 FDA reports)
DEBRIDEMENT ( 92 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 92 FDA reports)
KNEE ARTHROPLASTY ( 92 FDA reports)
MACULAR DEGENERATION ( 92 FDA reports)
NO THERAPEUTIC RESPONSE ( 92 FDA reports)
RESPIRATORY TRACT INFECTION ( 92 FDA reports)
PHARYNGITIS ( 91 FDA reports)
RADIOTHERAPY ( 91 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 91 FDA reports)
MALNUTRITION ( 91 FDA reports)
OEDEMA MOUTH ( 91 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 90 FDA reports)
DILATATION ATRIAL ( 90 FDA reports)
DUODENITIS ( 90 FDA reports)
GYNAECOMASTIA ( 90 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 90 FDA reports)
HIP ARTHROPLASTY ( 90 FDA reports)
PETECHIAE ( 90 FDA reports)
PHOTOPHOBIA ( 90 FDA reports)
SCOLIOSIS ( 90 FDA reports)
TRANSAMINASES INCREASED ( 90 FDA reports)
RHINITIS ( 89 FDA reports)
SENSORY LOSS ( 89 FDA reports)
DIASTOLIC DYSFUNCTION ( 89 FDA reports)
EXCORIATION ( 89 FDA reports)
ILEUS ( 89 FDA reports)
COLITIS ISCHAEMIC ( 88 FDA reports)
ISCHAEMIA ( 88 FDA reports)
POLYP ( 88 FDA reports)
RALES ( 88 FDA reports)
PLATELET COUNT INCREASED ( 87 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 87 FDA reports)
TUBERCULOSIS ( 87 FDA reports)
VENTRICULAR DYSFUNCTION ( 87 FDA reports)
CAROTID ARTERY OCCLUSION ( 87 FDA reports)
ELECTROLYTE IMBALANCE ( 87 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 87 FDA reports)
BEDRIDDEN ( 86 FDA reports)
EYE IRRITATION ( 86 FDA reports)
KIDNEY INFECTION ( 86 FDA reports)
KYPHOSIS ( 86 FDA reports)
SOMNAMBULISM ( 86 FDA reports)
THIRST ( 85 FDA reports)
BLADDER CANCER ( 85 FDA reports)
CHOLECYSTECTOMY ( 85 FDA reports)
INFARCTION ( 85 FDA reports)
AORTIC STENOSIS ( 84 FDA reports)
ASPIRATION ( 84 FDA reports)
BLOOD CHLORIDE DECREASED ( 84 FDA reports)
OTITIS MEDIA ( 84 FDA reports)
PERIODONTITIS ( 83 FDA reports)
POLYURIA ( 83 FDA reports)
THYROID NEOPLASM ( 83 FDA reports)
ANGIOPATHY ( 83 FDA reports)
HERNIA ( 83 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 83 FDA reports)
FACE OEDEMA ( 82 FDA reports)
CONJUNCTIVITIS ( 81 FDA reports)
DELUSION ( 81 FDA reports)
GROIN PAIN ( 81 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 81 FDA reports)
MASTICATION DISORDER ( 81 FDA reports)
FAILURE TO THRIVE ( 80 FDA reports)
HYPERTHYROIDISM ( 80 FDA reports)
MOTOR DYSFUNCTION ( 80 FDA reports)
NEUROPATHY ( 80 FDA reports)
PERFORMANCE STATUS DECREASED ( 80 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 79 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 79 FDA reports)
JAW FRACTURE ( 79 FDA reports)
LEFT VENTRICULAR FAILURE ( 79 FDA reports)
LUNG INFECTION ( 79 FDA reports)
ANOSMIA ( 78 FDA reports)
BLOOD MAGNESIUM DECREASED ( 78 FDA reports)
METASTASES TO SPINE ( 78 FDA reports)
METASTATIC NEOPLASM ( 78 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 78 FDA reports)
PERONEAL NERVE PALSY ( 78 FDA reports)
PROCEDURAL COMPLICATION ( 78 FDA reports)
RENAL ARTERY STENOSIS ( 78 FDA reports)
PERIODONTAL DISEASE ( 77 FDA reports)
UMBILICAL HERNIA ( 77 FDA reports)
COLITIS ULCERATIVE ( 77 FDA reports)
FACIAL PALSY ( 77 FDA reports)
HEPATOTOXICITY ( 77 FDA reports)
HOSPITALISATION ( 77 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 77 FDA reports)
NON-CARDIAC CHEST PAIN ( 77 FDA reports)
BLADDER DISORDER ( 76 FDA reports)
CARDIAC FLUTTER ( 76 FDA reports)
HAND FRACTURE ( 76 FDA reports)
HEART INJURY ( 76 FDA reports)
NEUTROPENIC SEPSIS ( 76 FDA reports)
PERSONALITY CHANGE ( 76 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 76 FDA reports)
ACIDOSIS ( 75 FDA reports)
APLASIA PURE RED CELL ( 75 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 75 FDA reports)
FACET JOINT SYNDROME ( 75 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 74 FDA reports)
BLOOD CALCIUM INCREASED ( 74 FDA reports)
EYE PRURITUS ( 74 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 74 FDA reports)
HYDRONEPHROSIS ( 74 FDA reports)
INJECTION SITE SWELLING ( 74 FDA reports)
PEPTIC ULCER ( 74 FDA reports)
VISUAL FIELD DEFECT ( 74 FDA reports)
POOR QUALITY SLEEP ( 73 FDA reports)
RESORPTION BONE INCREASED ( 73 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 73 FDA reports)
DIABETIC RETINOPATHY ( 73 FDA reports)
DILATATION VENTRICULAR ( 73 FDA reports)
GASTROENTERITIS VIRAL ( 73 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 73 FDA reports)
ACCIDENTAL EXPOSURE ( 72 FDA reports)
DRUG ERUPTION ( 72 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 72 FDA reports)
GASTRITIS EROSIVE ( 72 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 72 FDA reports)
NEOPLASM PROGRESSION ( 72 FDA reports)
RENAL PAIN ( 72 FDA reports)
SPINAL FUSION SURGERY ( 72 FDA reports)
WALKING AID USER ( 72 FDA reports)
BACTERAEMIA ( 71 FDA reports)
HYPERKERATOSIS ( 71 FDA reports)
HYPOALBUMINAEMIA ( 71 FDA reports)
JAW OPERATION ( 71 FDA reports)
LOBAR PNEUMONIA ( 71 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 70 FDA reports)
ANAPHYLACTIC SHOCK ( 70 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 70 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 70 FDA reports)
MYDRIASIS ( 70 FDA reports)
OSTEOSCLEROSIS ( 70 FDA reports)
PLASMACYTOMA ( 70 FDA reports)
SEBORRHOEIC KERATOSIS ( 70 FDA reports)
PROTEIN URINE PRESENT ( 69 FDA reports)
TENDON RUPTURE ( 69 FDA reports)
WOUND ( 69 FDA reports)
AREFLEXIA ( 69 FDA reports)
ENDODONTIC PROCEDURE ( 69 FDA reports)
INJECTION SITE NODULE ( 69 FDA reports)
INTESTINAL PERFORATION ( 69 FDA reports)
LYMPHOMA ( 69 FDA reports)
MALIGNANT MELANOMA ( 69 FDA reports)
ACUTE PULMONARY OEDEMA ( 68 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 68 FDA reports)
CATHETERISATION CARDIAC ( 68 FDA reports)
FOOT DEFORMITY ( 68 FDA reports)
NEOPLASM ( 68 FDA reports)
NO ADVERSE EVENT ( 68 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 68 FDA reports)
OESOPHAGEAL ULCER ( 68 FDA reports)
ORTHOPNOEA ( 68 FDA reports)
OVARIAN CANCER ( 68 FDA reports)
RESPIRATORY TRACT CONGESTION ( 68 FDA reports)
DERMATITIS CONTACT ( 67 FDA reports)
FACIAL PAIN ( 67 FDA reports)
FRACTURE ( 67 FDA reports)
LIFE EXPECTANCY SHORTENED ( 67 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 67 FDA reports)
MITRAL VALVE PROLAPSE ( 67 FDA reports)
AGRANULOCYTOSIS ( 66 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 66 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 66 FDA reports)
EPILEPSY ( 66 FDA reports)
INCREASED APPETITE ( 66 FDA reports)
INGUINAL HERNIA ( 66 FDA reports)
INJECTION SITE IRRITATION ( 66 FDA reports)
LOWER LIMB FRACTURE ( 66 FDA reports)
MEDICATION RESIDUE ( 66 FDA reports)
METABOLIC ENCEPHALOPATHY ( 66 FDA reports)
ORAL CAVITY FISTULA ( 66 FDA reports)
PURPURA ( 66 FDA reports)
TENDON DISORDER ( 66 FDA reports)
VITREOUS FLOATERS ( 66 FDA reports)
SKIN INFECTION ( 65 FDA reports)
TROPONIN INCREASED ( 65 FDA reports)
TYPE 1 DIABETES MELLITUS ( 65 FDA reports)
ACCIDENT ( 65 FDA reports)
APPLICATION SITE PRURITUS ( 65 FDA reports)
BONE DEBRIDEMENT ( 65 FDA reports)
DIZZINESS POSTURAL ( 65 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 65 FDA reports)
LEFT ATRIAL DILATATION ( 65 FDA reports)
LIVER INJURY ( 65 FDA reports)
ALCOHOL USE ( 64 FDA reports)
BREAST MASS ( 64 FDA reports)
CEREBROVASCULAR DISORDER ( 64 FDA reports)
DRUG DISPENSING ERROR ( 64 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 64 FDA reports)
INTERMITTENT CLAUDICATION ( 64 FDA reports)
MENINGIOMA ( 64 FDA reports)
WOUND INFECTION ( 64 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 64 FDA reports)
PROCTALGIA ( 63 FDA reports)
SEQUESTRECTOMY ( 63 FDA reports)
SYNOVITIS ( 63 FDA reports)
TENDON INJURY ( 63 FDA reports)
CHEST X-RAY ABNORMAL ( 63 FDA reports)
DEVICE FAILURE ( 63 FDA reports)
ESCHERICHIA INFECTION ( 63 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 63 FDA reports)
HEARING IMPAIRED ( 63 FDA reports)
HYPOAESTHESIA FACIAL ( 63 FDA reports)
INCREASED TENDENCY TO BRUISE ( 63 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 63 FDA reports)
BLOOD AMYLASE INCREASED ( 62 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 62 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 62 FDA reports)
CYTOLYTIC HEPATITIS ( 62 FDA reports)
DRY THROAT ( 62 FDA reports)
ERYTHEMA MULTIFORME ( 62 FDA reports)
INCOHERENT ( 62 FDA reports)
LIBIDO DECREASED ( 62 FDA reports)
NERVE COMPRESSION ( 62 FDA reports)
NERVE INJURY ( 62 FDA reports)
APHONIA ( 61 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 61 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 61 FDA reports)
GASTRIC HAEMORRHAGE ( 61 FDA reports)
HYPERTENSIVE HEART DISEASE ( 61 FDA reports)
LARYNGEAL OEDEMA ( 61 FDA reports)
MUSCLE INJURY ( 61 FDA reports)
MYELODYSPLASTIC SYNDROME ( 61 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 61 FDA reports)
SKIN FISSURES ( 61 FDA reports)
SKIN IRRITATION ( 61 FDA reports)
PROSTATOMEGALY ( 60 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 60 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 60 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 60 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 60 FDA reports)
BLOOD BICARBONATE DECREASED ( 59 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 59 FDA reports)
INGROWING NAIL ( 59 FDA reports)
MANIA ( 59 FDA reports)
VITAMIN D DEFICIENCY ( 59 FDA reports)
PARKINSON'S DISEASE ( 58 FDA reports)
PERIPHERAL ISCHAEMIA ( 58 FDA reports)
PLEURITIC PAIN ( 58 FDA reports)
SEXUAL DYSFUNCTION ( 58 FDA reports)
UTERINE LEIOMYOMA ( 58 FDA reports)
ABSCESS DRAINAGE ( 58 FDA reports)
BLOOD CREATINE INCREASED ( 58 FDA reports)
CARDIAC PACEMAKER INSERTION ( 58 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 58 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 58 FDA reports)
DEVICE RELATED INFECTION ( 58 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 58 FDA reports)
ESSENTIAL HYPERTENSION ( 58 FDA reports)
GRANULOMA ( 58 FDA reports)
ABNORMAL SENSATION IN EYE ( 57 FDA reports)
CHOLECYSTITIS ACUTE ( 57 FDA reports)
DIABETIC NEPHROPATHY ( 57 FDA reports)
GINGIVAL SWELLING ( 57 FDA reports)
HYPOTHERMIA ( 57 FDA reports)
JOINT SPRAIN ( 57 FDA reports)
LUMBAR RADICULOPATHY ( 57 FDA reports)
NEPHROPATHY TOXIC ( 57 FDA reports)
PELVIC PAIN ( 57 FDA reports)
POLYMYALGIA RHEUMATICA ( 57 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 57 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 56 FDA reports)
SENSATION OF FOREIGN BODY ( 56 FDA reports)
STRESS FRACTURE ( 56 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 56 FDA reports)
ACTINIC KERATOSIS ( 56 FDA reports)
APHAGIA ( 56 FDA reports)
APPLICATION SITE ERYTHEMA ( 56 FDA reports)
ARTERIAL DISORDER ( 56 FDA reports)
HAEMANGIOMA ( 56 FDA reports)
HAEMORRHAGIC STROKE ( 56 FDA reports)
HEPATITIS C ( 56 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 56 FDA reports)
LYMPHOEDEMA ( 56 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 56 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 56 FDA reports)
BREATH SOUNDS ABNORMAL ( 55 FDA reports)
EAR INFECTION ( 55 FDA reports)
FACIAL BONES FRACTURE ( 55 FDA reports)
HYPERAESTHESIA ( 55 FDA reports)
NEUTROPHIL COUNT INCREASED ( 55 FDA reports)
NODULE ( 55 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 55 FDA reports)
ORAL SURGERY ( 55 FDA reports)
PROTEIN TOTAL DECREASED ( 55 FDA reports)
SALIVARY HYPERSECRETION ( 55 FDA reports)
SHOULDER PAIN ( 55 FDA reports)
PELVIC FRACTURE ( 54 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 54 FDA reports)
SEASONAL ALLERGY ( 54 FDA reports)
TORSADE DE POINTES ( 54 FDA reports)
WHEELCHAIR USER ( 54 FDA reports)
BRAIN OEDEMA ( 54 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 54 FDA reports)
EOSINOPHILIA ( 54 FDA reports)
FISTULA DISCHARGE ( 54 FDA reports)
JAUNDICE CHOLESTATIC ( 54 FDA reports)
LIGAMENT SPRAIN ( 54 FDA reports)
ANGIOPLASTY ( 53 FDA reports)
ASTIGMATISM ( 53 FDA reports)
DECREASED ACTIVITY ( 53 FDA reports)
DRUG PRESCRIBING ERROR ( 53 FDA reports)
FAECALOMA ( 53 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 53 FDA reports)
HEART VALVE INCOMPETENCE ( 53 FDA reports)
HEPATOCELLULAR DAMAGE ( 53 FDA reports)
INADEQUATE ANALGESIA ( 53 FDA reports)
METABOLIC DISORDER ( 53 FDA reports)
MUSCLE RIGIDITY ( 53 FDA reports)
OESOPHAGEAL DISORDER ( 53 FDA reports)
ORGAN FAILURE ( 53 FDA reports)
PNEUMOTHORAX ( 53 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 53 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 53 FDA reports)
TONGUE DISCOLOURATION ( 53 FDA reports)
PHOTOSENSITIVITY REACTION ( 52 FDA reports)
PULMONARY MASS ( 52 FDA reports)
SINUS ARRHYTHMIA ( 52 FDA reports)
TONGUE DISORDER ( 52 FDA reports)
ABDOMINAL HERNIA ( 52 FDA reports)
AFFECTIVE DISORDER ( 52 FDA reports)
CACHEXIA ( 52 FDA reports)
CAROTID ARTERY DISEASE ( 52 FDA reports)
CERVICAL MYELOPATHY ( 52 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 52 FDA reports)
FEAR OF EATING ( 52 FDA reports)
INJECTION SITE BRUISING ( 52 FDA reports)
LARGE INTESTINAL ULCER ( 52 FDA reports)
LOW TURNOVER OSTEOPATHY ( 52 FDA reports)
APATHY ( 51 FDA reports)
BLOOD IRON DECREASED ( 51 FDA reports)
EROSIVE OESOPHAGITIS ( 51 FDA reports)
HEPATIC ENCEPHALOPATHY ( 51 FDA reports)
HICCUPS ( 51 FDA reports)
HUMERUS FRACTURE ( 51 FDA reports)
NAIL DISORDER ( 51 FDA reports)
NECROSIS ( 51 FDA reports)
NEUROGENIC BLADDER ( 51 FDA reports)
PAIN OF SKIN ( 51 FDA reports)
PSEUDOMONAS INFECTION ( 51 FDA reports)
RECTOCELE ( 51 FDA reports)
SNEEZING ( 51 FDA reports)
TACHYPNOEA ( 51 FDA reports)
THYROID CANCER ( 51 FDA reports)
TRANSFUSION ( 51 FDA reports)
VASCULAR CALCIFICATION ( 51 FDA reports)
SEROMA ( 50 FDA reports)
SYNCOPE VASOVAGAL ( 50 FDA reports)
SYNOVIAL CYST ( 50 FDA reports)
ABDOMINAL TENDERNESS ( 50 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 50 FDA reports)
EXERCISE TOLERANCE DECREASED ( 50 FDA reports)
FINGER DEFORMITY ( 50 FDA reports)
HEPATITIS ACUTE ( 50 FDA reports)
ANEURYSM ( 49 FDA reports)
AORTIC CALCIFICATION ( 49 FDA reports)
BLINDNESS TRANSIENT ( 49 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 49 FDA reports)
BODY TEMPERATURE DECREASED ( 49 FDA reports)
CERUMEN IMPACTION ( 49 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 49 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 49 FDA reports)
FIBULA FRACTURE ( 49 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 49 FDA reports)
HYPERVENTILATION ( 49 FDA reports)
INJECTION SITE RASH ( 49 FDA reports)
LARYNGOSPASM ( 49 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 49 FDA reports)
PLASMACYTOSIS ( 49 FDA reports)
PANIC REACTION ( 48 FDA reports)
POST HERPETIC NEURALGIA ( 48 FDA reports)
PREMATURE BABY ( 48 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 48 FDA reports)
PULMONARY HAEMORRHAGE ( 48 FDA reports)
SPINAL CORD COMPRESSION ( 48 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 48 FDA reports)
ACNE ( 48 FDA reports)
AFFECT LABILITY ( 48 FDA reports)
BRADYARRHYTHMIA ( 48 FDA reports)
DEPENDENCE ( 48 FDA reports)
DRUG SCREEN POSITIVE ( 48 FDA reports)
EYELID OEDEMA ( 48 FDA reports)
HYDROCEPHALUS ( 48 FDA reports)
HYPOPHOSPHATAEMIA ( 48 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 48 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 48 FDA reports)
METASTASES TO LYMPH NODES ( 48 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 48 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 48 FDA reports)
ABORTION SPONTANEOUS ( 47 FDA reports)
APHTHOUS STOMATITIS ( 47 FDA reports)
ATHEROSCLEROSIS ( 47 FDA reports)
BARRETT'S OESOPHAGUS ( 47 FDA reports)
EPICONDYLITIS ( 47 FDA reports)
GANGRENE ( 47 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 47 FDA reports)
LARYNGITIS ( 47 FDA reports)
NEPHROPATHY ( 47 FDA reports)
PYELONEPHRITIS ( 47 FDA reports)
SINUS HEADACHE ( 47 FDA reports)
VAGINAL INFECTION ( 47 FDA reports)
PANCREATITIS CHRONIC ( 46 FDA reports)
SCAB ( 46 FDA reports)
SKIN FIBROSIS ( 46 FDA reports)
VITAMIN D DECREASED ( 46 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 46 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 46 FDA reports)
ATRIAL SEPTAL DEFECT ( 46 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 46 FDA reports)
BREAST CANCER RECURRENT ( 46 FDA reports)
CYSTOCELE ( 46 FDA reports)
DRUG LEVEL DECREASED ( 46 FDA reports)
HEMIPLEGIA ( 46 FDA reports)
HUNGER ( 46 FDA reports)
HYPERPARATHYROIDISM ( 46 FDA reports)
HYPOVOLAEMIC SHOCK ( 46 FDA reports)
ARTHROPOD BITE ( 45 FDA reports)
BONE OPERATION ( 45 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 45 FDA reports)
EOSINOPHIL COUNT INCREASED ( 45 FDA reports)
EYELID PTOSIS ( 45 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 45 FDA reports)
MACROCYTOSIS ( 45 FDA reports)
MITRAL VALVE DISEASE ( 45 FDA reports)
NODAL RHYTHM ( 45 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 45 FDA reports)
PHOTOPSIA ( 45 FDA reports)
POLYNEUROPATHY ( 45 FDA reports)
RESPIRATORY DEPRESSION ( 45 FDA reports)
URINE ODOUR ABNORMAL ( 45 FDA reports)
PANCREATIC CARCINOMA ( 44 FDA reports)
PARKINSONISM ( 44 FDA reports)
PULMONARY THROMBOSIS ( 44 FDA reports)
PURULENCE ( 44 FDA reports)
RADIUS FRACTURE ( 44 FDA reports)
REFLUX OESOPHAGITIS ( 44 FDA reports)
SKELETAL INJURY ( 44 FDA reports)
VENOUS OCCLUSION ( 44 FDA reports)
WOUND DEHISCENCE ( 44 FDA reports)
WRONG DRUG ADMINISTERED ( 44 FDA reports)
ACUTE SINUSITIS ( 44 FDA reports)
CLOSTRIDIUM COLITIS ( 44 FDA reports)
CORONARY ARTERY THROMBOSIS ( 44 FDA reports)
DERMATITIS EXFOLIATIVE ( 44 FDA reports)
GINGIVAL RECESSION ( 44 FDA reports)
IMMUNODEFICIENCY ( 44 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 44 FDA reports)
METABOLIC SYNDROME ( 44 FDA reports)
NEPHRITIS INTERSTITIAL ( 44 FDA reports)
NEPHROTIC SYNDROME ( 44 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 43 FDA reports)
AKATHISIA ( 43 FDA reports)
ATROPHY ( 43 FDA reports)
BRADYPHRENIA ( 43 FDA reports)
BRONCHIECTASIS ( 43 FDA reports)
DYSGRAPHIA ( 43 FDA reports)
FORMICATION ( 43 FDA reports)
MENORRHAGIA ( 43 FDA reports)
PARAPLEGIA ( 43 FDA reports)
PAROSMIA ( 43 FDA reports)
PERSONALITY DISORDER ( 43 FDA reports)
PHLEBITIS ( 43 FDA reports)
POST PROCEDURAL HAEMATOMA ( 43 FDA reports)
PROCEDURAL PAIN ( 43 FDA reports)
RIGHT VENTRICULAR FAILURE ( 43 FDA reports)
SKIN HYPERPIGMENTATION ( 43 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 43 FDA reports)
TIBIA FRACTURE ( 43 FDA reports)
PANCREATIC DISORDER ( 42 FDA reports)
PLANTAR FASCIITIS ( 42 FDA reports)
POOR PERIPHERAL CIRCULATION ( 42 FDA reports)
RETINAL DETACHMENT ( 42 FDA reports)
SCHIZOPHRENIA ( 42 FDA reports)
STRIDOR ( 42 FDA reports)
TEARFULNESS ( 42 FDA reports)
TENOSYNOVITIS ( 42 FDA reports)
TOE AMPUTATION ( 42 FDA reports)
TOOTH INJURY ( 42 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 42 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 42 FDA reports)
ACUTE PRERENAL FAILURE ( 42 FDA reports)
ANXIETY DISORDER ( 42 FDA reports)
BLOOD DISORDER ( 42 FDA reports)
BLOOD TEST ABNORMAL ( 42 FDA reports)
CARDIAC FIBRILLATION ( 42 FDA reports)
CATHETER RELATED INFECTION ( 42 FDA reports)
DEMYELINATION ( 42 FDA reports)
DRUG ABUSER ( 42 FDA reports)
EYE INFECTION ( 42 FDA reports)
FEELING DRUNK ( 42 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 42 FDA reports)
HELICOBACTER INFECTION ( 42 FDA reports)
HYPERURICAEMIA ( 42 FDA reports)
LABYRINTHITIS ( 42 FDA reports)
MUSCULOSKELETAL DISORDER ( 42 FDA reports)
APPLICATION SITE IRRITATION ( 41 FDA reports)
CATHETER RELATED COMPLICATION ( 41 FDA reports)
DERMAL CYST ( 41 FDA reports)
ENTEROCOCCAL INFECTION ( 41 FDA reports)
EXPIRED DRUG ADMINISTERED ( 41 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 41 FDA reports)
HYPOMANIA ( 41 FDA reports)
LIVER TENDERNESS ( 41 FDA reports)
NODAL ARRHYTHMIA ( 41 FDA reports)
PANIC DISORDER ( 41 FDA reports)
PERICARDITIS ( 41 FDA reports)
TEMPERATURE INTOLERANCE ( 41 FDA reports)
TRISMUS ( 41 FDA reports)
VARICOSE VEIN ( 41 FDA reports)
PANCREATITIS RELAPSING ( 40 FDA reports)
POSTURE ABNORMAL ( 40 FDA reports)
PUPIL FIXED ( 40 FDA reports)
RENAL COLIC ( 40 FDA reports)
SELF-MEDICATION ( 40 FDA reports)
SKIN ATROPHY ( 40 FDA reports)
SLUGGISHNESS ( 40 FDA reports)
SPONDYLOLISTHESIS ( 40 FDA reports)
THROMBOSIS IN DEVICE ( 40 FDA reports)
WOUND COMPLICATION ( 40 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 40 FDA reports)
BONE EROSION ( 40 FDA reports)
BONE LOSS ( 40 FDA reports)
CARDIAC ENZYMES INCREASED ( 40 FDA reports)
DENTURE WEARER ( 40 FDA reports)
DYSTONIA ( 40 FDA reports)
EMBOLISM ( 40 FDA reports)
EUPHORIC MOOD ( 40 FDA reports)
FACE INJURY ( 40 FDA reports)
HEPATIC NECROSIS ( 40 FDA reports)
IMMUNOSUPPRESSION ( 40 FDA reports)
MEDICAL DEVICE COMPLICATION ( 40 FDA reports)
MITRAL VALVE CALCIFICATION ( 40 FDA reports)
ODYNOPHAGIA ( 40 FDA reports)
OESOPHAGEAL STENOSIS ( 40 FDA reports)
ATRIAL TACHYCARDIA ( 39 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 39 FDA reports)
BREAST PAIN ( 39 FDA reports)
CHEILITIS ( 39 FDA reports)
DEAFNESS NEUROSENSORY ( 39 FDA reports)
DIABETIC FOOT ( 39 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 39 FDA reports)
EMBOLIC STROKE ( 39 FDA reports)
FAMILY STRESS ( 39 FDA reports)
JOINT CONTRACTURE ( 39 FDA reports)
LEUKAEMIA ( 39 FDA reports)
ORAL HERPES ( 39 FDA reports)
PERIORBITAL OEDEMA ( 39 FDA reports)
PSORIATIC ARTHROPATHY ( 39 FDA reports)
TENSION ( 39 FDA reports)
TRANSPLANT REJECTION ( 39 FDA reports)
VEIN DISORDER ( 39 FDA reports)
VITAMIN B12 DEFICIENCY ( 39 FDA reports)
OROPHARYNGEAL BLISTERING ( 38 FDA reports)
OTITIS EXTERNA ( 38 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 38 FDA reports)
PREGNANCY ( 38 FDA reports)
RETINAL HAEMORRHAGE ( 38 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 38 FDA reports)
RHONCHI ( 38 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 38 FDA reports)
SNORING ( 38 FDA reports)
TRIGGER FINGER ( 38 FDA reports)
BILE DUCT OBSTRUCTION ( 38 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 38 FDA reports)
BLOOD URIC ACID INCREASED ( 38 FDA reports)
CAESAREAN SECTION ( 38 FDA reports)
CHOLANGITIS ( 38 FDA reports)
DEAFNESS UNILATERAL ( 38 FDA reports)
DEVICE MALFUNCTION ( 38 FDA reports)
DROOLING ( 38 FDA reports)
EAR DISCOMFORT ( 38 FDA reports)
HYPERBILIRUBINAEMIA ( 38 FDA reports)
HYPERNATRAEMIA ( 38 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 38 FDA reports)
INTRACARDIAC THROMBUS ( 38 FDA reports)
LICHEN PLANUS ( 38 FDA reports)
LIGAMENT RUPTURE ( 38 FDA reports)
METASTASIS ( 38 FDA reports)
OCCULT BLOOD POSITIVE ( 38 FDA reports)
ADRENAL MASS ( 37 FDA reports)
ANOXIC ENCEPHALOPATHY ( 37 FDA reports)
AORTIC DILATATION ( 37 FDA reports)
APPENDICITIS ( 37 FDA reports)
BACTERIAL SEPSIS ( 37 FDA reports)
BREAST CANCER METASTATIC ( 37 FDA reports)
BRONCHITIS ACUTE ( 37 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 37 FDA reports)
CONDUCTION DISORDER ( 37 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 37 FDA reports)
GUILLAIN-BARRE SYNDROME ( 37 FDA reports)
HAEMODYNAMIC INSTABILITY ( 37 FDA reports)
HYPOCHONDRIASIS ( 37 FDA reports)
INDURATION ( 37 FDA reports)
INTRAOCULAR LENS IMPLANT ( 37 FDA reports)
MARROW HYPERPLASIA ( 37 FDA reports)
MIGRAINE WITH AURA ( 37 FDA reports)
MONOPLEGIA ( 37 FDA reports)
NEPHROSCLEROSIS ( 37 FDA reports)
NYSTAGMUS ( 37 FDA reports)
OESOPHAGEAL PAIN ( 37 FDA reports)
RETINOPATHY ( 37 FDA reports)
SERUM FERRITIN INCREASED ( 37 FDA reports)
SINUS ARREST ( 37 FDA reports)
SKIN HAEMORRHAGE ( 37 FDA reports)
SLEEP TALKING ( 37 FDA reports)
TENDON PAIN ( 37 FDA reports)
ULCER HAEMORRHAGE ( 37 FDA reports)
URINE ANALYSIS ABNORMAL ( 37 FDA reports)
WOUND DRAINAGE ( 37 FDA reports)
PATHOLOGICAL GAMBLING ( 36 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 36 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 36 FDA reports)
PROSTATE CANCER METASTATIC ( 36 FDA reports)
RASH PUSTULAR ( 36 FDA reports)
SOFT TISSUE DISORDER ( 36 FDA reports)
THERMAL BURN ( 36 FDA reports)
WALKING DISABILITY ( 36 FDA reports)
AMMONIA INCREASED ( 36 FDA reports)
ANAL FISSURE ( 36 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 36 FDA reports)
BLOOD PROLACTIN INCREASED ( 36 FDA reports)
BONE FRAGMENTATION ( 36 FDA reports)
CATHETER PLACEMENT ( 36 FDA reports)
CONCUSSION ( 36 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 36 FDA reports)
EXTREMITY CONTRACTURE ( 36 FDA reports)
FEMORAL NECK FRACTURE ( 36 FDA reports)
FURUNCLE ( 36 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 36 FDA reports)
GENERALISED ANXIETY DISORDER ( 36 FDA reports)
HEAD DISCOMFORT ( 36 FDA reports)
HERNIA REPAIR ( 36 FDA reports)
ILEUS PARALYTIC ( 36 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 36 FDA reports)
LARGE INTESTINE PERFORATION ( 36 FDA reports)
LUNG CONSOLIDATION ( 36 FDA reports)
MACULAR OEDEMA ( 36 FDA reports)
MENINGITIS ( 36 FDA reports)
METRORRHAGIA ( 36 FDA reports)
MOUTH HAEMORRHAGE ( 36 FDA reports)
NEUROLOGICAL SYMPTOM ( 36 FDA reports)
ABSCESS JAW ( 35 FDA reports)
APPENDICITIS PERFORATED ( 35 FDA reports)
BLEPHARITIS ( 35 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 35 FDA reports)
CARDIAC OPERATION ( 35 FDA reports)
GASTROINTESTINAL PAIN ( 35 FDA reports)
GENERALISED ERYTHEMA ( 35 FDA reports)
HERPES SIMPLEX ( 35 FDA reports)
HYPERTONIC BLADDER ( 35 FDA reports)
INJECTION SITE WARMTH ( 35 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 35 FDA reports)
LYMPHOPENIA ( 35 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 35 FDA reports)
MYOPIA ( 35 FDA reports)
OBSTRUCTIVE UROPATHY ( 35 FDA reports)
POLYMYOSITIS ( 35 FDA reports)
RENAL CANCER ( 35 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 35 FDA reports)
SPINAL CORPECTOMY ( 35 FDA reports)
THROAT CANCER ( 35 FDA reports)
VERTIGO POSITIONAL ( 35 FDA reports)
VIITH NERVE PARALYSIS ( 35 FDA reports)
PEMPHIGOID ( 34 FDA reports)
PRESCRIBED OVERDOSE ( 34 FDA reports)
ROTATOR CUFF REPAIR ( 34 FDA reports)
SKIN PLAQUE ( 34 FDA reports)
VESICAL FISTULA ( 34 FDA reports)
AORTIC VALVE SCLEROSIS ( 34 FDA reports)
APLASTIC ANAEMIA ( 34 FDA reports)
CERVICAL CORD COMPRESSION ( 34 FDA reports)
CERVICAL SPINAL STENOSIS ( 34 FDA reports)
COLON ADENOMA ( 34 FDA reports)
CREPITATIONS ( 34 FDA reports)
DENTAL CARE ( 34 FDA reports)
DIABETIC COMPLICATION ( 34 FDA reports)
EYE NAEVUS ( 34 FDA reports)
HEPATIC LESION ( 34 FDA reports)
HOMICIDAL IDEATION ( 34 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 34 FDA reports)
HYPOTONIA ( 34 FDA reports)
IMMUNE SYSTEM DISORDER ( 34 FDA reports)
INJECTION SITE EXTRAVASATION ( 34 FDA reports)
MEGACOLON ( 34 FDA reports)
MELANOCYTIC NAEVUS ( 34 FDA reports)
MYELOPATHY ( 34 FDA reports)
APPETITE DISORDER ( 33 FDA reports)
BREAST TENDERNESS ( 33 FDA reports)
BRONCHITIS CHRONIC ( 33 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 33 FDA reports)
CEREBRAL HAEMATOMA ( 33 FDA reports)
COSTOCHONDRITIS ( 33 FDA reports)
CYSTITIS HAEMORRHAGIC ( 33 FDA reports)
DIABETIC COMA ( 33 FDA reports)
FACIAL PARESIS ( 33 FDA reports)
FIBRIN D DIMER INCREASED ( 33 FDA reports)
GRIP STRENGTH DECREASED ( 33 FDA reports)
HYSTERECTOMY ( 33 FDA reports)
MACULOPATHY ( 33 FDA reports)
MICTURITION DISORDER ( 33 FDA reports)
MYELOMA RECURRENCE ( 33 FDA reports)
NASAL DISCOMFORT ( 33 FDA reports)
POLYTRAUMATISM ( 33 FDA reports)
PROSTATITIS ( 33 FDA reports)
SENSITIVITY OF TEETH ( 33 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 33 FDA reports)
STEM CELL TRANSPLANT ( 33 FDA reports)
UNDERDOSE ( 33 FDA reports)
URINARY TRACT DISORDER ( 33 FDA reports)
VASCULITIC RASH ( 33 FDA reports)
OVARIAN CYST ( 32 FDA reports)
PAROTITIS ( 32 FDA reports)
PITTING OEDEMA ( 32 FDA reports)
PLEURAL FIBROSIS ( 32 FDA reports)
POLYDIPSIA ( 32 FDA reports)
RENAL ATROPHY ( 32 FDA reports)
RENAL CELL CARCINOMA ( 32 FDA reports)
SACROILIITIS ( 32 FDA reports)
STARING ( 32 FDA reports)
STREPTOCOCCAL INFECTION ( 32 FDA reports)
TACHYARRHYTHMIA ( 32 FDA reports)
TOBACCO ABUSE ( 32 FDA reports)
VITREOUS DETACHMENT ( 32 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 32 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 32 FDA reports)
BILIARY DILATATION ( 32 FDA reports)
BLOOD CHLORIDE INCREASED ( 32 FDA reports)
CHEST WALL PAIN ( 32 FDA reports)
DENTAL OPERATION ( 32 FDA reports)
EDENTULOUS ( 32 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 32 FDA reports)
FLUID INTAKE REDUCED ( 32 FDA reports)
GRANULOCYTOPENIA ( 32 FDA reports)
HAIR GROWTH ABNORMAL ( 32 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 32 FDA reports)
INJECTION SITE BURNING ( 32 FDA reports)
LICHENOID KERATOSIS ( 32 FDA reports)
MENSTRUATION IRREGULAR ( 32 FDA reports)
ONYCHALGIA ( 32 FDA reports)
ACUTE HEPATIC FAILURE ( 31 FDA reports)
ARTERIOSPASM CORONARY ( 31 FDA reports)
ARTHRITIS BACTERIAL ( 31 FDA reports)
BLOOD COUNT ABNORMAL ( 31 FDA reports)
BOWEN'S DISEASE ( 31 FDA reports)
BRAIN DEATH ( 31 FDA reports)
BRAIN NEOPLASM ( 31 FDA reports)
BRUXISM ( 31 FDA reports)
CARDIAC TAMPONADE ( 31 FDA reports)
CORONARY ARTERY RESTENOSIS ( 31 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 31 FDA reports)
EAR DISORDER ( 31 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 31 FDA reports)
FAECES PALE ( 31 FDA reports)
GINGIVAL INFECTION ( 31 FDA reports)
HAEMOLYTIC ANAEMIA ( 31 FDA reports)
HEPATITIS TOXIC ( 31 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 31 FDA reports)
INTENTIONAL MISUSE ( 31 FDA reports)
LACTOSE INTOLERANCE ( 31 FDA reports)
LOSS OF EMPLOYMENT ( 31 FDA reports)
LUNG HYPERINFLATION ( 31 FDA reports)
LUPUS-LIKE SYNDROME ( 31 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 31 FDA reports)
MYOCARDITIS ( 31 FDA reports)
NASAL DRYNESS ( 31 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 31 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 31 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 31 FDA reports)
RADICULAR PAIN ( 31 FDA reports)
RESPIRATORY RATE DECREASED ( 31 FDA reports)
SKIN ODOUR ABNORMAL ( 31 FDA reports)
SKIN PAPILLOMA ( 31 FDA reports)
SPUTUM DISCOLOURED ( 31 FDA reports)
STENT OCCLUSION ( 31 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 31 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 31 FDA reports)
URINARY HESITATION ( 31 FDA reports)
VENTRICULAR ARRHYTHMIA ( 31 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 31 FDA reports)
YELLOW SKIN ( 31 FDA reports)
ORTHOSIS USER ( 30 FDA reports)
PSYCHIATRIC SYMPTOM ( 30 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 30 FDA reports)
QUALITY OF LIFE DECREASED ( 30 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 30 FDA reports)
RENAL TRANSPLANT ( 30 FDA reports)
SKIN NECROSIS ( 30 FDA reports)
STRESS SYMPTOMS ( 30 FDA reports)
VASCULAR GRAFT ( 30 FDA reports)
VENOUS INSUFFICIENCY ( 30 FDA reports)
ABSCESS ORAL ( 30 FDA reports)
ANAL HAEMORRHAGE ( 30 FDA reports)
BLOOD CULTURE POSITIVE ( 30 FDA reports)
BLOOD PH DECREASED ( 30 FDA reports)
BRAIN INJURY ( 30 FDA reports)
BREATH ODOUR ( 30 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 30 FDA reports)
FRACTURE NONUNION ( 30 FDA reports)
GALLBLADDER POLYP ( 30 FDA reports)
HAEMORRHAGIC ANAEMIA ( 30 FDA reports)
HEART RATE ABNORMAL ( 30 FDA reports)
HEPATIC NEOPLASM ( 30 FDA reports)
IMMOBILE ( 30 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 30 FDA reports)
MALIGNANT HYPERTENSION ( 30 FDA reports)
MEAN CELL VOLUME INCREASED ( 30 FDA reports)
OESOPHAGEAL CARCINOMA ( 30 FDA reports)
ABDOMINAL ABSCESS ( 29 FDA reports)
BLOOD LACTIC ACID INCREASED ( 29 FDA reports)
BREAST CANCER IN SITU ( 29 FDA reports)
CULTURE URINE POSITIVE ( 29 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 29 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 29 FDA reports)
FULL BLOOD COUNT DECREASED ( 29 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 29 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 29 FDA reports)
MICROANGIOPATHY ( 29 FDA reports)
NEPHRITIS ( 29 FDA reports)
PCO2 DECREASED ( 29 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 29 FDA reports)
PERITONITIS BACTERIAL ( 29 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 29 FDA reports)
POST PROCEDURAL FISTULA ( 29 FDA reports)
RESPIRATORY ACIDOSIS ( 29 FDA reports)
URETERIC OBSTRUCTION ( 29 FDA reports)
URINE FLOW DECREASED ( 29 FDA reports)
PARAPROTEINAEMIA ( 28 FDA reports)
PITUITARY HAEMORRHAGE ( 28 FDA reports)
POSTNASAL DRIP ( 28 FDA reports)
PREMATURE LABOUR ( 28 FDA reports)
RECTAL POLYP ( 28 FDA reports)
RESUSCITATION ( 28 FDA reports)
TONGUE ULCERATION ( 28 FDA reports)
TROPONIN I INCREASED ( 28 FDA reports)
URINE ABNORMALITY ( 28 FDA reports)
VENOUS THROMBOSIS LIMB ( 28 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 28 FDA reports)
WOUND HAEMORRHAGE ( 28 FDA reports)
BILE DUCT STONE ( 28 FDA reports)
BIPOLAR I DISORDER ( 28 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 28 FDA reports)
BONE SWELLING ( 28 FDA reports)
CAROTID BRUIT ( 28 FDA reports)
CLAVICLE FRACTURE ( 28 FDA reports)
COELIAC DISEASE ( 28 FDA reports)
EARLY SATIETY ( 28 FDA reports)
FEAR OF DEATH ( 28 FDA reports)
FOREIGN BODY ( 28 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 28 FDA reports)
HANGOVER ( 28 FDA reports)
HYPERPHOSPHATAEMIA ( 28 FDA reports)
HYPOPITUITARISM ( 28 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 28 FDA reports)
INJECTION SITE INDURATION ( 28 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 28 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 28 FDA reports)
MONOCYTE COUNT INCREASED ( 28 FDA reports)
NECK INJURY ( 28 FDA reports)
NEURITIS ( 28 FDA reports)
ACROCHORDON ( 27 FDA reports)
ANAEMIA POSTOPERATIVE ( 27 FDA reports)
AORTIC VALVE DISEASE ( 27 FDA reports)
APPLICATION SITE REACTION ( 27 FDA reports)
AUTOIMMUNE HEPATITIS ( 27 FDA reports)
BONE NEOPLASM MALIGNANT ( 27 FDA reports)
BREAST CALCIFICATIONS ( 27 FDA reports)
BUNDLE BRANCH BLOCK ( 27 FDA reports)
CHOKING SENSATION ( 27 FDA reports)
CHOLECYSTITIS INFECTIVE ( 27 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 27 FDA reports)
DYSTHYMIC DISORDER ( 27 FDA reports)
FLAT AFFECT ( 27 FDA reports)
GLARE ( 27 FDA reports)
HAEMOLYSIS ( 27 FDA reports)
HAND DEFORMITY ( 27 FDA reports)
HYPERMETROPIA ( 27 FDA reports)
IRITIS ( 27 FDA reports)
LIP DISORDER ( 27 FDA reports)
LIPIDS INCREASED ( 27 FDA reports)
MYASTHENIA GRAVIS ( 27 FDA reports)
MYELITIS TRANSVERSE ( 27 FDA reports)
OCULAR ICTERUS ( 27 FDA reports)
OESOPHAGEAL SPASM ( 27 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 27 FDA reports)
PERIORBITAL HAEMATOMA ( 27 FDA reports)
POST PROCEDURAL INFECTION ( 27 FDA reports)
RAYNAUD'S PHENOMENON ( 27 FDA reports)
RETINAL VEIN OCCLUSION ( 27 FDA reports)
SPLENIC INFARCTION ( 27 FDA reports)
TUMOUR LYSIS SYNDROME ( 27 FDA reports)
UTERINE DISORDER ( 27 FDA reports)
VAGINAL DISCHARGE ( 27 FDA reports)
VASCULAR GRAFT OCCLUSION ( 27 FDA reports)
PERICARDIAL HAEMORRHAGE ( 26 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 26 FDA reports)
QRS AXIS ABNORMAL ( 26 FDA reports)
RECTAL ABSCESS ( 26 FDA reports)
SCRATCH ( 26 FDA reports)
SOPOR ( 26 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 26 FDA reports)
TOOTH EROSION ( 26 FDA reports)
VASCULAR OCCLUSION ( 26 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 26 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 26 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 26 FDA reports)
ALCOHOL POISONING ( 26 FDA reports)
ANORECTAL DISCOMFORT ( 26 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 26 FDA reports)
ATROPHIC VULVOVAGINITIS ( 26 FDA reports)
BILE DUCT CANCER ( 26 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 26 FDA reports)
BREAST FIBROSIS ( 26 FDA reports)
BREAST NECROSIS ( 26 FDA reports)
BREAST SWELLING ( 26 FDA reports)
CARDIAC FAILURE ACUTE ( 26 FDA reports)
COLLAPSE OF LUNG ( 26 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 26 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 26 FDA reports)
FOLLICULITIS ( 26 FDA reports)
FOOD CRAVING ( 26 FDA reports)
GASTROINTESTINAL INFECTION ( 26 FDA reports)
HEPATOCELLULAR INJURY ( 26 FDA reports)
HEPATOSPLENOMEGALY ( 26 FDA reports)
HILAR LYMPHADENOPATHY ( 26 FDA reports)
HIP SURGERY ( 26 FDA reports)
HYPERREFLEXIA ( 26 FDA reports)
HYPOVENTILATION ( 26 FDA reports)
INJECTION SITE URTICARIA ( 26 FDA reports)
JOINT CREPITATION ( 26 FDA reports)
KNEE OPERATION ( 26 FDA reports)
LOCALISED OEDEMA ( 26 FDA reports)
METASTASES TO MENINGES ( 26 FDA reports)
MONOCLONAL GAMMOPATHY ( 26 FDA reports)
MULTIPLE FRACTURES ( 26 FDA reports)
NON-SMALL CELL LUNG CANCER ( 26 FDA reports)
ARTERIAL STENOSIS ( 25 FDA reports)
ARTERIAL THROMBOSIS ( 25 FDA reports)
BLADDER SPASM ( 25 FDA reports)
BLOOD URINE ( 25 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 25 FDA reports)
CATARACT NUCLEAR ( 25 FDA reports)
CHRONIC FATIGUE SYNDROME ( 25 FDA reports)
CORONARY ARTERY SURGERY ( 25 FDA reports)
DRUG TOLERANCE ( 25 FDA reports)
ENCEPHALITIS ( 25 FDA reports)
ENCEPHALOMALACIA ( 25 FDA reports)
ENDOTRACHEAL INTUBATION ( 25 FDA reports)
ENTERITIS ( 25 FDA reports)
EYE DISCHARGE ( 25 FDA reports)
HAEMOTHORAX ( 25 FDA reports)
HEPATIC FIBROSIS ( 25 FDA reports)
HOARSENESS ( 25 FDA reports)
HYPOREFLEXIA ( 25 FDA reports)
INJECTION SITE INFECTION ( 25 FDA reports)
JAUNDICE NEONATAL ( 25 FDA reports)
JOINT ARTHROPLASTY ( 25 FDA reports)
KLEBSIELLA INFECTION ( 25 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 25 FDA reports)
MUSCLE FATIGUE ( 25 FDA reports)
NEURODERMATITIS ( 25 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 25 FDA reports)
OPTIC NERVE CUPPING ( 25 FDA reports)
OVERWEIGHT ( 25 FDA reports)
PHARYNGEAL ERYTHEMA ( 25 FDA reports)
PITUITARY TUMOUR BENIGN ( 25 FDA reports)
RADICULITIS LUMBOSACRAL ( 25 FDA reports)
RECTAL CANCER ( 25 FDA reports)
SEBORRHOEIC DERMATITIS ( 25 FDA reports)
SOCIAL PROBLEM ( 25 FDA reports)
SPONDYLITIS ( 25 FDA reports)
TIC ( 25 FDA reports)
TOBACCO USER ( 25 FDA reports)
TOXIC SKIN ERUPTION ( 25 FDA reports)
URINARY TRACT OBSTRUCTION ( 25 FDA reports)
WOUND SECRETION ( 25 FDA reports)
OSTEOMYELITIS ACUTE ( 24 FDA reports)
PAPILLOEDEMA ( 24 FDA reports)
PATELLA FRACTURE ( 24 FDA reports)
PHAEOCHROMOCYTOMA ( 24 FDA reports)
POSTOPERATIVE INFECTION ( 24 FDA reports)
PROSTATIC DISORDER ( 24 FDA reports)
RENAL TUBULAR DISORDER ( 24 FDA reports)
RETROPERITONEAL HAEMATOMA ( 24 FDA reports)
SHOCK HAEMORRHAGIC ( 24 FDA reports)
TINEA PEDIS ( 24 FDA reports)
TRAUMATIC BRAIN INJURY ( 24 FDA reports)
TREATMENT FAILURE ( 24 FDA reports)
URINE COLOUR ABNORMAL ( 24 FDA reports)
VERTEBROPLASTY ( 24 FDA reports)
VITAMIN B12 DECREASED ( 24 FDA reports)
ABNORMAL FAECES ( 24 FDA reports)
ADHESION ( 24 FDA reports)
ANAEMIA MACROCYTIC ( 24 FDA reports)
ANIMAL BITE ( 24 FDA reports)
APPENDICECTOMY ( 24 FDA reports)
BLOOD CORTISOL DECREASED ( 24 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 24 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 24 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 24 FDA reports)
BONE MARROW DEPRESSION ( 24 FDA reports)
BUNION ( 24 FDA reports)
CARDIAC OUTPUT DECREASED ( 24 FDA reports)
CARTILAGE INJURY ( 24 FDA reports)
CEREBELLAR ATROPHY ( 24 FDA reports)
CORONARY ARTERY REOCCLUSION ( 24 FDA reports)
DERMATITIS ALLERGIC ( 24 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 24 FDA reports)
ENURESIS ( 24 FDA reports)
EPIGASTRIC DISCOMFORT ( 24 FDA reports)
EYE OEDEMA ( 24 FDA reports)
FEELING OF DESPAIR ( 24 FDA reports)
HALLUCINATIONS, MIXED ( 24 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 24 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 24 FDA reports)
HYPOGONADISM ( 24 FDA reports)
INJECTION SITE DISCOLOURATION ( 24 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 24 FDA reports)
LYMPHOCELE ( 24 FDA reports)
MASTECTOMY ( 24 FDA reports)
MECHANICAL VENTILATION ( 24 FDA reports)
MUSCLE HAEMORRHAGE ( 24 FDA reports)
ACTINOMYCOSIS ( 23 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 23 FDA reports)
AMENORRHOEA ( 23 FDA reports)
ANAPHYLACTOID REACTION ( 23 FDA reports)
ARTHRITIS INFECTIVE ( 23 FDA reports)
BACTERIA STOOL IDENTIFIED ( 23 FDA reports)
BLEPHAROSPASM ( 23 FDA reports)
BLOODY DISCHARGE ( 23 FDA reports)
BONE CYST ( 23 FDA reports)
BREAKTHROUGH PAIN ( 23 FDA reports)
CEREBELLAR INFARCTION ( 23 FDA reports)
COMMUNICATION DISORDER ( 23 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 23 FDA reports)
DERMATITIS BULLOUS ( 23 FDA reports)
DIABETIC FOOT INFECTION ( 23 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 23 FDA reports)
DYSPNOEA EXACERBATED ( 23 FDA reports)
ENTEROVESICAL FISTULA ( 23 FDA reports)
EYE MOVEMENT DISORDER ( 23 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 23 FDA reports)
HERPES VIRUS INFECTION ( 23 FDA reports)
HYPERAMMONAEMIA ( 23 FDA reports)
INJECTION SITE MASS ( 23 FDA reports)
LEG AMPUTATION ( 23 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 23 FDA reports)
MICROALBUMINURIA ( 23 FDA reports)
MULTIPLE ALLERGIES ( 23 FDA reports)
OROPHARYNGEAL SWELLING ( 23 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 23 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 23 FDA reports)
POLYARTHRITIS ( 23 FDA reports)
POLYCYTHAEMIA ( 23 FDA reports)
PRODUCT ODOUR ABNORMAL ( 23 FDA reports)
RENAL HAEMORRHAGE ( 23 FDA reports)
RESPIRATORY ALKALOSIS ( 23 FDA reports)
RETINAL DISORDER ( 23 FDA reports)
SKIN WARM ( 23 FDA reports)
SOFT TISSUE INFLAMMATION ( 23 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 23 FDA reports)
SPINAL COLUMN INJURY ( 23 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 23 FDA reports)
TRIGEMINAL NEURALGIA ( 23 FDA reports)
VULVOVAGINAL DISCOMFORT ( 23 FDA reports)
OSTEORADIONECROSIS ( 22 FDA reports)
PIGMENTATION DISORDER ( 22 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 22 FDA reports)
POST LAMINECTOMY SYNDROME ( 22 FDA reports)
PULMONARY INFARCTION ( 22 FDA reports)
PYODERMA GANGRENOSUM ( 22 FDA reports)
RETINAL ARTERY OCCLUSION ( 22 FDA reports)
SARCOIDOSIS ( 22 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 22 FDA reports)
SKIN SWELLING ( 22 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 22 FDA reports)
VARICES OESOPHAGEAL ( 22 FDA reports)
WEIGHT FLUCTUATION ( 22 FDA reports)
ABDOMINAL ADHESIONS ( 22 FDA reports)
ASTHENOPIA ( 22 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 22 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 22 FDA reports)
BURNS SECOND DEGREE ( 22 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 22 FDA reports)
CERVICOBRACHIAL SYNDROME ( 22 FDA reports)
CHAPPED LIPS ( 22 FDA reports)
CLUMSINESS ( 22 FDA reports)
CORONARY ANGIOPLASTY ( 22 FDA reports)
DIVERTICULAR PERFORATION ( 22 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 22 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 22 FDA reports)
GALLBLADDER OPERATION ( 22 FDA reports)
HYPERCOAGULATION ( 22 FDA reports)
HYPOPERFUSION ( 22 FDA reports)
IIIRD NERVE PARALYSIS ( 22 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 22 FDA reports)
INTESTINAL POLYP ( 22 FDA reports)
KETOACIDOSIS ( 22 FDA reports)
LUNG CANCER METASTATIC ( 22 FDA reports)
MUCOUS MEMBRANE DISORDER ( 22 FDA reports)
NEPHROGENIC ANAEMIA ( 22 FDA reports)
ACCIDENT AT WORK ( 21 FDA reports)
ADRENAL INSUFFICIENCY ( 21 FDA reports)
ALCOHOLISM ( 21 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 21 FDA reports)
ANORGASMIA ( 21 FDA reports)
BASEDOW'S DISEASE ( 21 FDA reports)
BLOOD ALBUMIN INCREASED ( 21 FDA reports)
BLOOD BLISTER ( 21 FDA reports)
BONE GRAFT ( 21 FDA reports)
BONE SCAN ABNORMAL ( 21 FDA reports)
BREAST RECONSTRUCTION ( 21 FDA reports)
CALCINOSIS ( 21 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 21 FDA reports)
CHEST TUBE INSERTION ( 21 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 21 FDA reports)
DERMATITIS ACNEIFORM ( 21 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 21 FDA reports)
EAR CONGESTION ( 21 FDA reports)
EJACULATION FAILURE ( 21 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 21 FDA reports)
GASTROINTESTINAL PERFORATION ( 21 FDA reports)
GENITAL HERPES ( 21 FDA reports)
HEART SOUNDS ABNORMAL ( 21 FDA reports)
IATROGENIC INJURY ( 21 FDA reports)
IMPETIGO ( 21 FDA reports)
INTRACRANIAL ANEURYSM ( 21 FDA reports)
LIPOMA ( 21 FDA reports)
MENSTRUAL DISORDER ( 21 FDA reports)
MUCOSAL ULCERATION ( 21 FDA reports)
NECROTISING FASCIITIS ( 21 FDA reports)
OLIGOHYDRAMNIOS ( 21 FDA reports)
PAINFUL RESPIRATION ( 21 FDA reports)
PNEUMONIA VIRAL ( 21 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 21 FDA reports)
PRODUCT ADHESION ISSUE ( 21 FDA reports)
PROTEIN TOTAL INCREASED ( 21 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 21 FDA reports)
RECTAL FISSURE ( 21 FDA reports)
RENAL MASS ( 21 FDA reports)
SCLERODACTYLIA ( 21 FDA reports)
SENSATION OF PRESSURE ( 21 FDA reports)
SKIN NODULE ( 21 FDA reports)
STUPOR ( 21 FDA reports)
SUDDEN CARDIAC DEATH ( 21 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 21 FDA reports)
THYROID CYST ( 21 FDA reports)
TRICUSPID VALVE DISEASE ( 21 FDA reports)
VASODILATATION ( 21 FDA reports)
VITREOUS HAEMORRHAGE ( 21 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 20 FDA reports)
PLATELET COUNT ABNORMAL ( 20 FDA reports)
PO2 DECREASED ( 20 FDA reports)
QUADRIPLEGIA ( 20 FDA reports)
RENAL OSTEODYSTROPHY ( 20 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 20 FDA reports)
SCROTAL SWELLING ( 20 FDA reports)
SINUS OPERATION ( 20 FDA reports)
SKIN GRAFT ( 20 FDA reports)
SKIN REACTION ( 20 FDA reports)
SPINAL DECOMPRESSION ( 20 FDA reports)
SPLENIC GRANULOMA ( 20 FDA reports)
STATUS EPILEPTICUS ( 20 FDA reports)
TENSION HEADACHE ( 20 FDA reports)
TINEA CRURIS ( 20 FDA reports)
VASCULAR PSEUDOANEURYSM ( 20 FDA reports)
ALCOHOL ABUSE ( 20 FDA reports)
BICYTOPENIA ( 20 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 20 FDA reports)
BLADDER PROLAPSE ( 20 FDA reports)
BLEEDING TIME PROLONGED ( 20 FDA reports)
BLOOD CREATININE ABNORMAL ( 20 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 20 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 20 FDA reports)
BREAST CYST ( 20 FDA reports)
BREAST ENLARGEMENT ( 20 FDA reports)
BUTTOCK PAIN ( 20 FDA reports)
CALCULUS BLADDER ( 20 FDA reports)
CARDIOPULMONARY FAILURE ( 20 FDA reports)
CEREBRAL THROMBOSIS ( 20 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 20 FDA reports)
DUODENAL ULCER PERFORATION ( 20 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 20 FDA reports)
ESCHERICHIA SEPSIS ( 20 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 20 FDA reports)
FRUSTRATION ( 20 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 20 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 20 FDA reports)
HAEMORRHAGE URINARY TRACT ( 20 FDA reports)
HEPATORENAL SYNDROME ( 20 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 20 FDA reports)
INGUINAL HERNIA REPAIR ( 20 FDA reports)
INTESTINAL HAEMORRHAGE ( 20 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 20 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 20 FDA reports)
IRON OVERLOAD ( 20 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 20 FDA reports)
LIP DRY ( 20 FDA reports)
LIVEDO RETICULARIS ( 20 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 20 FDA reports)
MACULAR HOLE ( 20 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 20 FDA reports)
NAIL INFECTION ( 20 FDA reports)
NASAL DISORDER ( 20 FDA reports)
NICOTINE DEPENDENCE ( 20 FDA reports)
OEDEMA MUCOSAL ( 20 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 20 FDA reports)
ACUTE PSYCHOSIS ( 19 FDA reports)
ADJUSTMENT DISORDER ( 19 FDA reports)
AORTIC DISSECTION ( 19 FDA reports)
APPLICATION SITE RASH ( 19 FDA reports)
ARTHROSCOPY ( 19 FDA reports)
BILIARY DYSKINESIA ( 19 FDA reports)
BREAST DISCHARGE ( 19 FDA reports)
BREAST DISORDER ( 19 FDA reports)
CARDIAC FAILURE CHRONIC ( 19 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 19 FDA reports)
CEREBRAL CALCIFICATION ( 19 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 19 FDA reports)
DEFAECATION URGENCY ( 19 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 19 FDA reports)
EJECTION FRACTION ABNORMAL ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
GLOMERULONEPHRITIS ( 19 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 19 FDA reports)
GLYCOSURIA ( 19 FDA reports)
HAEMOGLOBIN ABNORMAL ( 19 FDA reports)
HEPATIC ENZYME ABNORMAL ( 19 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 19 FDA reports)
INTERTRIGO ( 19 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 19 FDA reports)
LIP OEDEMA ( 19 FDA reports)
LISTLESS ( 19 FDA reports)
MALABSORPTION ( 19 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 19 FDA reports)
MASTOIDITIS ( 19 FDA reports)
MELANOSIS COLI ( 19 FDA reports)
MONARTHRITIS ( 19 FDA reports)
OPTIC NEURITIS ( 19 FDA reports)
OVARIAN DISORDER ( 19 FDA reports)
PERIPHERAL EMBOLISM ( 19 FDA reports)
PLEURISY ( 19 FDA reports)
PORTAL VEIN THROMBOSIS ( 19 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 19 FDA reports)
SCLERODERMA ( 19 FDA reports)
SPUTUM CULTURE POSITIVE ( 19 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 19 FDA reports)
ULNAR NEURITIS ( 19 FDA reports)
VASCULAR BYPASS GRAFT ( 19 FDA reports)
VENA CAVA THROMBOSIS ( 19 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 19 FDA reports)
PANCREATIC CYST ( 18 FDA reports)
PEAU D'ORANGE ( 18 FDA reports)
PENILE PAIN ( 18 FDA reports)
PERIARTHRITIS ( 18 FDA reports)
PERITONEAL DIALYSIS ( 18 FDA reports)
PINGUECULA ( 18 FDA reports)
PLASTIC SURGERY ( 18 FDA reports)
PNEUMONIA BACTERIAL ( 18 FDA reports)
PORTAL HYPERTENSION ( 18 FDA reports)
PRODUCT TASTE ABNORMAL ( 18 FDA reports)
REFLUX GASTRITIS ( 18 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 18 FDA reports)
RENAL NEOPLASM ( 18 FDA reports)
SPINAL LAMINECTOMY ( 18 FDA reports)
SUICIDAL BEHAVIOUR ( 18 FDA reports)
THROMBOPHLEBITIS ( 18 FDA reports)
TONGUE BITING ( 18 FDA reports)
TONSILLAR DISORDER ( 18 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 18 FDA reports)
TUBERCULIN TEST POSITIVE ( 18 FDA reports)
UTERINE CANCER ( 18 FDA reports)
ABSCESS INTESTINAL ( 18 FDA reports)
ACCELERATED HYPERTENSION ( 18 FDA reports)
ADVERSE REACTION ( 18 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 18 FDA reports)
ANAESTHETIC COMPLICATION ( 18 FDA reports)
ANGIOFIBROMA ( 18 FDA reports)
AORTIC DISORDER ( 18 FDA reports)
AORTIC VALVE STENOSIS ( 18 FDA reports)
BIOPSY BONE MARROW ( 18 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 18 FDA reports)
BONE MARROW OEDEMA ( 18 FDA reports)
BRADYKINESIA ( 18 FDA reports)
CARDIAC HYPERTROPHY ( 18 FDA reports)
CHEST WALL OPERATION ( 18 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 18 FDA reports)
CORNEAL DYSTROPHY ( 18 FDA reports)
CUTIS LAXA ( 18 FDA reports)
DISSEMINATED TUBERCULOSIS ( 18 FDA reports)
EAR HAEMORRHAGE ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
GALACTORRHOEA ( 18 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 18 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 18 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 18 FDA reports)
HORMONE LEVEL ABNORMAL ( 18 FDA reports)
HOSTILITY ( 18 FDA reports)
HYPERPHAGIA ( 18 FDA reports)
HYPERTHERMIA ( 18 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 18 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 18 FDA reports)
INTESTINAL DILATATION ( 18 FDA reports)
LABILE HYPERTENSION ( 18 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 18 FDA reports)
METAPLASIA ( 18 FDA reports)
MUSCLE CONTRACTURE ( 18 FDA reports)
MUSCLE SPASTICITY ( 18 FDA reports)
MYELOFIBROSIS ( 18 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 18 FDA reports)
OBSTRUCTION ( 18 FDA reports)
ORAL TORUS ( 18 FDA reports)
ABDOMINAL RIGIDITY ( 17 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 17 FDA reports)
ADENOCARCINOMA ( 17 FDA reports)
ADRENAL ADENOMA ( 17 FDA reports)
ANOGENITAL WARTS ( 17 FDA reports)
APPENDIX DISORDER ( 17 FDA reports)
ASPERGILLOSIS ( 17 FDA reports)
AUTOIMMUNE DISORDER ( 17 FDA reports)
BACTERIAL TEST POSITIVE ( 17 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 17 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 17 FDA reports)
BREAST CANCER STAGE I ( 17 FDA reports)
CARDIAC DEATH ( 17 FDA reports)
CARDIOVERSION ( 17 FDA reports)
CATHETER SEPSIS ( 17 FDA reports)
CATHETER SITE HAEMATOMA ( 17 FDA reports)
CAUDA EQUINA SYNDROME ( 17 FDA reports)
COAGULATION TIME PROLONGED ( 17 FDA reports)
CRANIAL NERVE DISORDER ( 17 FDA reports)
CUSHINGOID ( 17 FDA reports)
DEPERSONALISATION ( 17 FDA reports)
ERECTION INCREASED ( 17 FDA reports)
EYE INFLAMMATION ( 17 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 17 FDA reports)
GINGIVAL EROSION ( 17 FDA reports)
HAEMATOCRIT ABNORMAL ( 17 FDA reports)
HAEMOGLOBIN INCREASED ( 17 FDA reports)
HEART VALVE REPLACEMENT ( 17 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 17 FDA reports)
HYPERTONIA ( 17 FDA reports)
HYPERTROPHY ( 17 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 17 FDA reports)
ILEITIS ( 17 FDA reports)
INCISIONAL HERNIA ( 17 FDA reports)
INCORRECT STORAGE OF DRUG ( 17 FDA reports)
KIDNEY FIBROSIS ( 17 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 17 FDA reports)
LIBIDO INCREASED ( 17 FDA reports)
LIP PAIN ( 17 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 17 FDA reports)
MOUTH INJURY ( 17 FDA reports)
NASAL SEPTUM DEVIATION ( 17 FDA reports)
NEUROMYOPATHY ( 17 FDA reports)
NIGHT BLINDNESS ( 17 FDA reports)
OSTEITIS DEFORMANS ( 17 FDA reports)
PANCREATITIS NECROTISING ( 17 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 17 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 17 FDA reports)
PYURIA ( 17 FDA reports)
RADIATION INJURY ( 17 FDA reports)
READING DISORDER ( 17 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 17 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 17 FDA reports)
SCOTOMA ( 17 FDA reports)
SERUM FERRITIN DECREASED ( 17 FDA reports)
SMALL FOR DATES BABY ( 17 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 17 FDA reports)
SPINAL OPERATION ( 17 FDA reports)
TONGUE INJURY ( 17 FDA reports)
TORTICOLLIS ( 17 FDA reports)
VENOUS THROMBOSIS ( 17 FDA reports)
POLYPECTOMY ( 16 FDA reports)
PRESBYOPIA ( 16 FDA reports)
PROCTITIS ( 16 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 16 FDA reports)
PSYCHOMOTOR RETARDATION ( 16 FDA reports)
PULSE PRESSURE DECREASED ( 16 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 16 FDA reports)
RIGHT ATRIAL DILATATION ( 16 FDA reports)
SECRETION DISCHARGE ( 16 FDA reports)
SKIN MASS ( 16 FDA reports)
SKIN NEOPLASM EXCISION ( 16 FDA reports)
SLEEP TERROR ( 16 FDA reports)
SPLEEN DISORDER ( 16 FDA reports)
STOMATOCYTES PRESENT ( 16 FDA reports)
SUBCUTANEOUS ABSCESS ( 16 FDA reports)
SUBDURAL HAEMORRHAGE ( 16 FDA reports)
TEMPORAL ARTERITIS ( 16 FDA reports)
VOCAL CORD DISORDER ( 16 FDA reports)
ABDOMINAL SEPSIS ( 16 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 16 FDA reports)
ABSCESS LIMB ( 16 FDA reports)
ACCIDENTAL NEEDLE STICK ( 16 FDA reports)
AMAUROSIS FUGAX ( 16 FDA reports)
ANION GAP INCREASED ( 16 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 16 FDA reports)
AUTOIMMUNE THYROIDITIS ( 16 FDA reports)
BILIARY COLIC ( 16 FDA reports)
BILIARY TRACT DISORDER ( 16 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 16 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 16 FDA reports)
BONE CALLUS EXCESSIVE ( 16 FDA reports)
BONE MARROW TOXICITY ( 16 FDA reports)
BONE MARROW TRANSPLANT ( 16 FDA reports)
BURSITIS INFECTIVE ( 16 FDA reports)
CATATONIA ( 16 FDA reports)
CATHETER SITE HAEMORRHAGE ( 16 FDA reports)
CHANGE OF BOWEL HABIT ( 16 FDA reports)
COLON POLYPECTOMY ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 16 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 16 FDA reports)
DIPLEGIA ( 16 FDA reports)
DYSAESTHESIA ( 16 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 16 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 16 FDA reports)
ENTEROCUTANEOUS FISTULA ( 16 FDA reports)
ENTHESOPATHY ( 16 FDA reports)
ERYTHEMA OF EYELID ( 16 FDA reports)
ESCHERICHIA BACTERAEMIA ( 16 FDA reports)
ESSENTIAL TREMOR ( 16 FDA reports)
FAECES HARD ( 16 FDA reports)
FEEDING DISORDER ( 16 FDA reports)
FEELING HOT AND COLD ( 16 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 16 FDA reports)
GALLBLADDER ENLARGEMENT ( 16 FDA reports)
GLIOSIS ( 16 FDA reports)
HAIR COLOUR CHANGES ( 16 FDA reports)
HELICOBACTER GASTRITIS ( 16 FDA reports)
HEREDITARY ANGIOEDEMA ( 16 FDA reports)
HYPOPARATHYROIDISM ( 16 FDA reports)
IRON DEFICIENCY ( 16 FDA reports)
KNEE DEFORMITY ( 16 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 16 FDA reports)
LUNG ABSCESS ( 16 FDA reports)
LUNG ADENOCARCINOMA ( 16 FDA reports)
MALLORY-WEISS SYNDROME ( 16 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 16 FDA reports)
MICROCYTIC ANAEMIA ( 16 FDA reports)
MIOSIS ( 16 FDA reports)
MITRAL VALVE STENOSIS ( 16 FDA reports)
NASAL POLYPS ( 16 FDA reports)
NASAL ULCER ( 16 FDA reports)
NECK MASS ( 16 FDA reports)
NERVE ROOT COMPRESSION ( 16 FDA reports)
OCULAR VASCULAR DISORDER ( 16 FDA reports)
ONYCHOCLASIS ( 16 FDA reports)
ALVEOLAR OSTEITIS ( 15 FDA reports)
ANAL FISTULA ( 15 FDA reports)
APPLICATION SITE VESICLES ( 15 FDA reports)
BLADDER OBSTRUCTION ( 15 FDA reports)
BLOOD SODIUM INCREASED ( 15 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 15 FDA reports)
BREAST MICROCALCIFICATION ( 15 FDA reports)
CHONDROPATHY ( 15 FDA reports)
COLON CANCER STAGE III ( 15 FDA reports)
COLOUR BLINDNESS ( 15 FDA reports)
COR PULMONALE ( 15 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 15 FDA reports)
DYSPNOEA AT REST ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 15 FDA reports)
ESCHAR ( 15 FDA reports)
EXOPHTHALMOS ( 15 FDA reports)
EYE OPERATION ( 15 FDA reports)
EYE ROLLING ( 15 FDA reports)
GINGIVAL ULCERATION ( 15 FDA reports)
GOUTY ARTHRITIS ( 15 FDA reports)
HEPATITIS CHOLESTATIC ( 15 FDA reports)
HYPERACUSIS ( 15 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 15 FDA reports)
HYPERVOLAEMIA ( 15 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 15 FDA reports)
INTENTIONAL SELF-INJURY ( 15 FDA reports)
INTRA-UTERINE DEATH ( 15 FDA reports)
LOOSE BODY IN JOINT ( 15 FDA reports)
LYME DISEASE ( 15 FDA reports)
MARFAN'S SYNDROME ( 15 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 15 FDA reports)
MYCOSIS FUNGOIDES ( 15 FDA reports)
NAIL DISCOLOURATION ( 15 FDA reports)
NEPHRECTOMY ( 15 FDA reports)
NEUROGENIC BOWEL ( 15 FDA reports)
NEUROMA ( 15 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 15 FDA reports)
OVERGROWTH BACTERIAL ( 15 FDA reports)
PANCREATIC MASS ( 15 FDA reports)
PAROTID GLAND ENLARGEMENT ( 15 FDA reports)
PENILE HAEMORRHAGE ( 15 FDA reports)
PERIRECTAL ABSCESS ( 15 FDA reports)
PHYSICAL ASSAULT ( 15 FDA reports)
POOR VENOUS ACCESS ( 15 FDA reports)
PROSTATIC OBSTRUCTION ( 15 FDA reports)
PROTEIN URINE ( 15 FDA reports)
PULSE ABNORMAL ( 15 FDA reports)
QUADRIPARESIS ( 15 FDA reports)
RECTAL ULCER ( 15 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 15 FDA reports)
SCREAMING ( 15 FDA reports)
SEPSIS SYNDROME ( 15 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 15 FDA reports)
TOE DEFORMITY ( 15 FDA reports)
TOXIC ENCEPHALOPATHY ( 15 FDA reports)
TROPONIN T INCREASED ( 15 FDA reports)
TUMOUR HAEMORRHAGE ( 15 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 15 FDA reports)
UTERINE HAEMORRHAGE ( 15 FDA reports)
UVEITIS ( 15 FDA reports)
VERTEBRAL WEDGING ( 15 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 15 FDA reports)
VULVOVAGINAL DRYNESS ( 15 FDA reports)
OVARIAN MASS ( 14 FDA reports)
PARATHYROID TUMOUR BENIGN ( 14 FDA reports)
PCO2 INCREASED ( 14 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 14 FDA reports)
PETIT MAL EPILEPSY ( 14 FDA reports)
PLACENTAL DISORDER ( 14 FDA reports)
PLEURAL DISORDER ( 14 FDA reports)
PROCEDURAL HYPOTENSION ( 14 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 14 FDA reports)
PUBIS FRACTURE ( 14 FDA reports)
PULMONARY GRANULOMA ( 14 FDA reports)
PUSTULAR PSORIASIS ( 14 FDA reports)
PYOGENIC GRANULOMA ( 14 FDA reports)
RADICULITIS ( 14 FDA reports)
REGURGITATION ( 14 FDA reports)
RHEUMATIC FEVER ( 14 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
SELF-INJURIOUS IDEATION ( 14 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 14 FDA reports)
SLEEP WALKING ( 14 FDA reports)
TESTICULAR PAIN ( 14 FDA reports)
TONSILLECTOMY ( 14 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 14 FDA reports)
TRACHEOBRONCHITIS ( 14 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 14 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 14 FDA reports)
VOCAL CORD PARALYSIS ( 14 FDA reports)
VULVAL DISORDER ( 14 FDA reports)
WOUND TREATMENT ( 14 FDA reports)
ALBUMIN URINE PRESENT ( 14 FDA reports)
ANAL ABSCESS ( 14 FDA reports)
ANORECTAL DISORDER ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 14 FDA reports)
AORTIC VALVE REPLACEMENT ( 14 FDA reports)
ARTERIAL STENT INSERTION ( 14 FDA reports)
ARTERIOVENOUS MALFORMATION ( 14 FDA reports)
ASPIRATION BONE MARROW ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
BACTERIURIA ( 14 FDA reports)
BLOOD CHOLESTEROL ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 14 FDA reports)
CALCULUS URETERIC ( 14 FDA reports)
CARBON DIOXIDE DECREASED ( 14 FDA reports)
CARDIAC ANEURYSM ( 14 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 14 FDA reports)
CERVIX CARCINOMA ( 14 FDA reports)
COLITIS COLLAGENOUS ( 14 FDA reports)
CORNEAL ABRASION ( 14 FDA reports)
CULTURE POSITIVE ( 14 FDA reports)
DENTAL PROSTHESIS USER ( 14 FDA reports)
DIABETIC GASTROPARESIS ( 14 FDA reports)
DRUG EFFECT INCREASED ( 14 FDA reports)
DYSPHASIA ( 14 FDA reports)
EFFUSION ( 14 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 14 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 14 FDA reports)
ENDOPHTHALMITIS ( 14 FDA reports)
ENTEROBACTER INFECTION ( 14 FDA reports)
ERYSIPELAS ( 14 FDA reports)
ESCHERICHIA TEST POSITIVE ( 14 FDA reports)
EYE INJURY ( 14 FDA reports)
FEMORAL ARTERY OCCLUSION ( 14 FDA reports)
FOOD POISONING ( 14 FDA reports)
GALLBLADDER INJURY ( 14 FDA reports)
GASTRIC CANCER ( 14 FDA reports)
GASTRIC PERFORATION ( 14 FDA reports)
GASTRIC POLYPS ( 14 FDA reports)
GASTRIC ULCER PERFORATION ( 14 FDA reports)
HAEMATOCRIT INCREASED ( 14 FDA reports)
HAEMOPHILUS INFECTION ( 14 FDA reports)
HEPATIC TRAUMA ( 14 FDA reports)
HYPERSEXUALITY ( 14 FDA reports)
IMPLANT SITE INFECTION ( 14 FDA reports)
INFECTED SKIN ULCER ( 14 FDA reports)
INTERVERTEBRAL DISCITIS ( 14 FDA reports)
JOINT LOCK ( 14 FDA reports)
KIDNEY ENLARGEMENT ( 14 FDA reports)
LEUKOPLAKIA ORAL ( 14 FDA reports)
LOGORRHOEA ( 14 FDA reports)
LOSS OF LIBIDO ( 14 FDA reports)
MACULE ( 14 FDA reports)
MENIERE'S DISEASE ( 14 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 14 FDA reports)
METABOLIC ALKALOSIS ( 14 FDA reports)
METASTASES TO ADRENALS ( 14 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 14 FDA reports)
NEUROMUSCULAR BLOCKADE ( 14 FDA reports)
NEUROTOXICITY ( 14 FDA reports)
OPERATIVE HAEMORRHAGE ( 14 FDA reports)
OPPORTUNISTIC INFECTION ( 14 FDA reports)
OPTIC NERVE DISORDER ( 14 FDA reports)
ORAL FUNGAL INFECTION ( 14 FDA reports)
ACANTHOMA ( 13 FDA reports)
AKINESIA ( 13 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ANTINUCLEAR ANTIBODY ( 13 FDA reports)
ASBESTOSIS ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 13 FDA reports)
B-CELL LYMPHOMA ( 13 FDA reports)
BENIGN NEOPLASM ( 13 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 13 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 13 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 13 FDA reports)
BOTULISM ( 13 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 13 FDA reports)
CARDIOTOXICITY ( 13 FDA reports)
CATARACT CORTICAL ( 13 FDA reports)
CELLULITIS ORBITAL ( 13 FDA reports)
CLONUS ( 13 FDA reports)
COLITIS MICROSCOPIC ( 13 FDA reports)
COLON NEOPLASM ( 13 FDA reports)
CSF PROTEIN INCREASED ( 13 FDA reports)
CUTANEOUS VASCULITIS ( 13 FDA reports)
CYANOPSIA ( 13 FDA reports)
DISSOCIATION ( 13 FDA reports)
DYSPHORIA ( 13 FDA reports)
EPIDIDYMITIS ( 13 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 13 FDA reports)
EYELID DISORDER ( 13 FDA reports)
FASCIITIS ( 13 FDA reports)
FOETAL GROWTH RESTRICTION ( 13 FDA reports)
FOREIGN BODY TRAUMA ( 13 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 13 FDA reports)
GASTROINTESTINAL ULCER ( 13 FDA reports)
GENERAL SYMPTOM ( 13 FDA reports)
GENITAL DISCOMFORT ( 13 FDA reports)
HAEMANGIOMA OF LIVER ( 13 FDA reports)
HAEMARTHROSIS ( 13 FDA reports)
HAEMORRHAGIC DIATHESIS ( 13 FDA reports)
HAIR TEXTURE ABNORMAL ( 13 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 13 FDA reports)
HISTOPLASMOSIS ( 13 FDA reports)
HYPERCHLORHYDRIA ( 13 FDA reports)
HYPOTRICHOSIS ( 13 FDA reports)
INCISION SITE HAEMORRHAGE ( 13 FDA reports)
INCREASED BRONCHIAL SECRETION ( 13 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 13 FDA reports)
JEALOUS DELUSION ( 13 FDA reports)
LABORATORY TEST INTERFERENCE ( 13 FDA reports)
LAGOPHTHALMOS ( 13 FDA reports)
LEUKOENCEPHALOPATHY ( 13 FDA reports)
LIGHT CHAIN DISEASE ( 13 FDA reports)
LIMB OPERATION ( 13 FDA reports)
LIP BLISTER ( 13 FDA reports)
LIPIDS ABNORMAL ( 13 FDA reports)
LIVER TRANSPLANT REJECTION ( 13 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 13 FDA reports)
LYMPH GLAND INFECTION ( 13 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 13 FDA reports)
MAMMOGRAM ABNORMAL ( 13 FDA reports)
MARITAL PROBLEM ( 13 FDA reports)
MENISCUS REMOVAL ( 13 FDA reports)
MITRAL VALVE SCLEROSIS ( 13 FDA reports)
MOANING ( 13 FDA reports)
NASAL OEDEMA ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NEUTROPENIC INFECTION ( 13 FDA reports)
NOCTURNAL DYSPNOEA ( 13 FDA reports)
ONYCHOLYSIS ( 13 FDA reports)
OPEN REDUCTION OF FRACTURE ( 13 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 13 FDA reports)
OSTEOMALACIA ( 13 FDA reports)
PALATAL DISORDER ( 13 FDA reports)
PAPILLOMA ( 13 FDA reports)
PARONYCHIA ( 13 FDA reports)
PARTIAL SEIZURES ( 13 FDA reports)
PERNICIOUS ANAEMIA ( 13 FDA reports)
PITUITARY TUMOUR ( 13 FDA reports)
PRECANCEROUS CELLS PRESENT ( 13 FDA reports)
PROCEDURAL HYPERTENSION ( 13 FDA reports)
PROTEUS INFECTION ( 13 FDA reports)
PRURITUS GENITAL ( 13 FDA reports)
PSEUDODEMENTIA ( 13 FDA reports)
PTERYGIUM ( 13 FDA reports)
RENAL ARTERY OCCLUSION ( 13 FDA reports)
RETINITIS ( 13 FDA reports)
RETINOGRAM ABNORMAL ( 13 FDA reports)
RETROGRADE EJACULATION ( 13 FDA reports)
RHYTHM IDIOVENTRICULAR ( 13 FDA reports)
SCAPULA FRACTURE ( 13 FDA reports)
SCHAMBERG'S DISEASE ( 13 FDA reports)
SERRATIA INFECTION ( 13 FDA reports)
SIGMOIDITIS ( 13 FDA reports)
SKULL FRACTURE ( 13 FDA reports)
SOFT TISSUE INJURY ( 13 FDA reports)
SPINAL CORD DISORDER ( 13 FDA reports)
STASIS DERMATITIS ( 13 FDA reports)
STEAL SYNDROME ( 13 FDA reports)
STRABISMUS ( 13 FDA reports)
STRESS URINARY INCONTINENCE ( 13 FDA reports)
SUDDEN ONSET OF SLEEP ( 13 FDA reports)
TEMPORAL LOBE EPILEPSY ( 13 FDA reports)
THROMBOCYTHAEMIA ( 13 FDA reports)
TONGUE BLISTERING ( 13 FDA reports)
URETHRAL DISORDER ( 13 FDA reports)
UTERINE PROLAPSE ( 13 FDA reports)
VASCULAR RUPTURE ( 13 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 13 FDA reports)
WHITE BLOOD CELL DISORDER ( 13 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 12 FDA reports)
PAPILLOMA VIRAL INFECTION ( 12 FDA reports)
PAROTIDECTOMY ( 12 FDA reports)
PENIS DISORDER ( 12 FDA reports)
PROTHROMBIN TIME SHORTENED ( 12 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
RASH VESICULAR ( 12 FDA reports)
RESPIRATION ABNORMAL ( 12 FDA reports)
RETINAL EXUDATES ( 12 FDA reports)
RETINAL TEAR ( 12 FDA reports)
RETINAL VEIN THROMBOSIS ( 12 FDA reports)
RETROGRADE AMNESIA ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SHOULDER ARTHROPLASTY ( 12 FDA reports)
SHOULDER OPERATION ( 12 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 12 FDA reports)
SOFT TISSUE INFECTION ( 12 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 12 FDA reports)
STEREOTYPY ( 12 FDA reports)
THROMBOCYTOSIS ( 12 FDA reports)
THROMBOTIC STROKE ( 12 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
TONGUE PARALYSIS ( 12 FDA reports)
TONSIL CANCER ( 12 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 12 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 12 FDA reports)
UTERINE POLYP ( 12 FDA reports)
VASCULAR DEMENTIA ( 12 FDA reports)
VASCULAR INJURY ( 12 FDA reports)
VENOUS INJURY ( 12 FDA reports)
YAWNING ( 12 FDA reports)
ABDOMINAL HAEMATOMA ( 12 FDA reports)
ADRENAL NEOPLASM ( 12 FDA reports)
AGORAPHOBIA ( 12 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 12 FDA reports)
ANOXIA ( 12 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 12 FDA reports)
APPARENT DEATH ( 12 FDA reports)
APPLICATION SITE DERMATITIS ( 12 FDA reports)
APRAXIA ( 12 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
BENIGN TUMOUR EXCISION ( 12 FDA reports)
BIOPSY LIVER ABNORMAL ( 12 FDA reports)
BK VIRUS INFECTION ( 12 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 12 FDA reports)
BONE FORMATION INCREASED ( 12 FDA reports)
BREAST LUMP REMOVAL ( 12 FDA reports)
BRONCHIOLITIS ( 12 FDA reports)
CALCIUM METABOLISM DISORDER ( 12 FDA reports)
CALCULUS URINARY ( 12 FDA reports)
CEREBRAL DISORDER ( 12 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 12 FDA reports)
CERVICAL DYSPLASIA ( 12 FDA reports)
CHROMATOPSIA ( 12 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 12 FDA reports)
COLECTOMY ( 12 FDA reports)
CONTRAST MEDIA REACTION ( 12 FDA reports)
CONVERSION DISORDER ( 12 FDA reports)
DEAFNESS TRANSITORY ( 12 FDA reports)
DENGUE FEVER ( 12 FDA reports)
DRUG RESISTANCE ( 12 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 12 FDA reports)
ENDOCARDITIS ( 12 FDA reports)
ENDOMETRIOSIS ( 12 FDA reports)
ENERGY INCREASED ( 12 FDA reports)
EOSINOPHILIC PNEUMONIA ( 12 FDA reports)
EXANTHEM ( 12 FDA reports)
EXTRAVASATION ( 12 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 12 FDA reports)
FAT TISSUE INCREASED ( 12 FDA reports)
FULGURATION ( 12 FDA reports)
GASTROINTESTINAL NECROSIS ( 12 FDA reports)
GLOSSITIS ( 12 FDA reports)
GRAFT COMPLICATION ( 12 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 12 FDA reports)
GRIEF REACTION ( 12 FDA reports)
HAIR DISORDER ( 12 FDA reports)
HEAD TITUBATION ( 12 FDA reports)
HEAT EXHAUSTION ( 12 FDA reports)
HEMIANOPIA ( 12 FDA reports)
HEPATIC CONGESTION ( 12 FDA reports)
HYPOPNOEA ( 12 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 12 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 12 FDA reports)
ILIAC ARTERY STENOSIS ( 12 FDA reports)
INCISION SITE INFECTION ( 12 FDA reports)
INJECTION SITE ABSCESS ( 12 FDA reports)
INJECTION SITE DISCOMFORT ( 12 FDA reports)
INTESTINAL MASS ( 12 FDA reports)
JAW LESION EXCISION ( 12 FDA reports)
JUGULAR VEIN DISTENSION ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
LIMB ASYMMETRY ( 12 FDA reports)
LIPODYSTROPHY ACQUIRED ( 12 FDA reports)
LUNG INJURY ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
MIDDLE EAR EFFUSION ( 12 FDA reports)
MIXED DEAFNESS ( 12 FDA reports)
MIXED HYPERLIPIDAEMIA ( 12 FDA reports)
MUCOSAL EROSION ( 12 FDA reports)
MYOPATHY TOXIC ( 12 FDA reports)
NEPHROCALCINOSIS ( 12 FDA reports)
NERVE ROOT LESION ( 12 FDA reports)
NOSOCOMIAL INFECTION ( 12 FDA reports)
OESOPHAGEAL RUPTURE ( 12 FDA reports)
OPEN ANGLE GLAUCOMA ( 12 FDA reports)
ADRENAL DISORDER ( 11 FDA reports)
ADRENAL HAEMORRHAGE ( 11 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 11 FDA reports)
ALVEOLOPLASTY ( 11 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 11 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 11 FDA reports)
AORTIC ANEURYSM RUPTURE ( 11 FDA reports)
APALLIC SYNDROME ( 11 FDA reports)
APPLICATION SITE PAIN ( 11 FDA reports)
APTYALISM ( 11 FDA reports)
ARTERIAL INJURY ( 11 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 11 FDA reports)
BIOPSY ( 11 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 11 FDA reports)
BLOOD UREA DECREASED ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
BULIMIA NERVOSA ( 11 FDA reports)
CAPILLARY LEAK SYNDROME ( 11 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 11 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 11 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 11 FDA reports)
CAUSTIC INJURY ( 11 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 11 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 11 FDA reports)
CHOLESTEROSIS ( 11 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 11 FDA reports)
CIRRHOSIS ALCOHOLIC ( 11 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 11 FDA reports)
CONNECTIVE TISSUE DISORDER ( 11 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 11 FDA reports)
DENTAL DISCOMFORT ( 11 FDA reports)
DEVICE BREAKAGE ( 11 FDA reports)
DEVICE DISLOCATION ( 11 FDA reports)
DIABETIC MICROANGIOPATHY ( 11 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 11 FDA reports)
DYSPHEMIA ( 11 FDA reports)
EPHELIDES ( 11 FDA reports)
EROSIVE DUODENITIS ( 11 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 11 FDA reports)
FOOD ALLERGY ( 11 FDA reports)
FUNGAL SKIN INFECTION ( 11 FDA reports)
GASTRITIS ATROPHIC ( 11 FDA reports)
GASTRITIS HAEMORRHAGIC ( 11 FDA reports)
GLOMERULOSCLEROSIS ( 11 FDA reports)
GRAFT THROMBOSIS ( 11 FDA reports)
GRAFT VERSUS HOST DISEASE ( 11 FDA reports)
GUN SHOT WOUND ( 11 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 11 FDA reports)
HEPATITIS A ( 11 FDA reports)
HEPATITIS B ( 11 FDA reports)
HYPEROSMOLAR STATE ( 11 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 11 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 11 FDA reports)
HYPERTRICHOSIS ( 11 FDA reports)
HYPOGLYCAEMIC COMA ( 11 FDA reports)
IMPRISONMENT ( 11 FDA reports)
INFUSION SITE IRRITATION ( 11 FDA reports)
INTENTION TREMOR ( 11 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 11 FDA reports)
INTESTINAL ULCER ( 11 FDA reports)
ISCHAEMIC HEPATITIS ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LENTIGO ( 11 FDA reports)
LIFE SUPPORT ( 11 FDA reports)
LIVER ABSCESS ( 11 FDA reports)
MASS EXCISION ( 11 FDA reports)
MEIBOMIANITIS ( 11 FDA reports)
MITRAL VALVE REPAIR ( 11 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 11 FDA reports)
MOTION SICKNESS ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 11 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 11 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 11 FDA reports)
NEUTROPHILIA ( 11 FDA reports)
NIPPLE PAIN ( 11 FDA reports)
ORTHOPEDIC PROCEDURE ( 11 FDA reports)
PAIN EXACERBATED ( 11 FDA reports)
PAINFUL DEFAECATION ( 11 FDA reports)
PALMAR ERYTHEMA ( 11 FDA reports)
PANCREATIC PSEUDOCYST ( 11 FDA reports)
PARAPARESIS ( 11 FDA reports)
PARATHYROID DISORDER ( 11 FDA reports)
PARTNER STRESS ( 11 FDA reports)
PELVIC ABSCESS ( 11 FDA reports)
PHYSIOTHERAPY ( 11 FDA reports)
PROSTATECTOMY ( 11 FDA reports)
PSEUDOMONAL SEPSIS ( 11 FDA reports)
PSYCHOTIC BEHAVIOUR ( 11 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 11 FDA reports)
PULMONARY HILUM MASS ( 11 FDA reports)
RADIATION SKIN INJURY ( 11 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 11 FDA reports)
RETINAL INJURY ( 11 FDA reports)
RETINAL OEDEMA ( 11 FDA reports)
RETINITIS PIGMENTOSA ( 11 FDA reports)
RHEUMATOID NODULE ( 11 FDA reports)
ROSACEA ( 11 FDA reports)
SARCOMA ( 11 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 11 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 11 FDA reports)
SKIN TOXICITY ( 11 FDA reports)
SOCIAL PHOBIA ( 11 FDA reports)
SOMATOFORM DISORDER ( 11 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 11 FDA reports)
SPUTUM PURULENT ( 11 FDA reports)
STREPTOCOCCAL SEPSIS ( 11 FDA reports)
SUPERFICIAL INJURY OF EYE ( 11 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 11 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 11 FDA reports)
TUMOUR NECROSIS ( 11 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 11 FDA reports)
URINE KETONE BODY PRESENT ( 11 FDA reports)
URINE OUTPUT INCREASED ( 11 FDA reports)
VENOOCCLUSIVE DISEASE ( 11 FDA reports)
VULVOVAGINAL PRURITUS ( 11 FDA reports)
XEROSIS ( 11 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 10 FDA reports)
OROPHARYNGEAL PLAQUE ( 10 FDA reports)
PARADOXICAL DRUG REACTION ( 10 FDA reports)
PATHOGEN RESISTANCE ( 10 FDA reports)
PENILE OEDEMA ( 10 FDA reports)
POLYSUBSTANCE ABUSE ( 10 FDA reports)
POST PROCEDURAL PAIN ( 10 FDA reports)
PRINZMETAL ANGINA ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PRURITUS ALLERGIC ( 10 FDA reports)
PULMONARY TOXICITY ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
RECURRENT CANCER ( 10 FDA reports)
RENAL TUBULAR ATROPHY ( 10 FDA reports)
RESPIRATORY TRACT OEDEMA ( 10 FDA reports)
RETINAL ANOMALY CONGENITAL ( 10 FDA reports)
RETINAL ISCHAEMIA ( 10 FDA reports)
RHEUMATOID FACTOR INCREASED ( 10 FDA reports)
ROTAVIRUS INFECTION ( 10 FDA reports)
SALPINGO-OOPHORECTOMY ( 10 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
SINOBRONCHITIS ( 10 FDA reports)
SKIN BLEEDING ( 10 FDA reports)
SMEAR CERVIX ABNORMAL ( 10 FDA reports)
SPONDYLOLYSIS ( 10 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 10 FDA reports)
STOOL ANALYSIS ABNORMAL ( 10 FDA reports)
SUFFOCATION FEELING ( 10 FDA reports)
SYRINGOMYELIA ( 10 FDA reports)
SYSTEMIC SCLEROSIS ( 10 FDA reports)
TESTICULAR SWELLING ( 10 FDA reports)
TETANY ( 10 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 10 FDA reports)
THORACOTOMY ( 10 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 10 FDA reports)
THYROXINE INCREASED ( 10 FDA reports)
TONGUE DRY ( 10 FDA reports)
TONGUE HAEMORRHAGE ( 10 FDA reports)
TONIC CLONIC MOVEMENTS ( 10 FDA reports)
TONSILLITIS ( 10 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 10 FDA reports)
TRACHEITIS ( 10 FDA reports)
TRANSFUSION REACTION ( 10 FDA reports)
TUMOUR MARKER INCREASED ( 10 FDA reports)
TUNNEL VISION ( 10 FDA reports)
ULCERATIVE KERATITIS ( 10 FDA reports)
URETERIC STENOSIS ( 10 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 10 FDA reports)
URTICARIA GENERALISED ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VAGINAL CANCER ( 10 FDA reports)
VOLUME BLOOD DECREASED ( 10 FDA reports)
WEIGHT BEARING DIFFICULTY ( 10 FDA reports)
ABDOMINAL INFECTION ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 10 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 10 FDA reports)
ADENOMA BENIGN ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
ANKYLOSING SPONDYLITIS ( 10 FDA reports)
APPLICATION SITE BURN ( 10 FDA reports)
ARTERIAL BYPASS OPERATION ( 10 FDA reports)
ARTHROPOD STING ( 10 FDA reports)
ASEPTIC NECROSIS BONE ( 10 FDA reports)
ATRIAL THROMBOSIS ( 10 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 10 FDA reports)
BACTEROIDES TEST POSITIVE ( 10 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 10 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 10 FDA reports)
BLOOD CREATININE DECREASED ( 10 FDA reports)
BLOOD UREA ABNORMAL ( 10 FDA reports)
BONE NEOPLASM ( 10 FDA reports)
BREAST DISCOMFORT ( 10 FDA reports)
BREAST HYPERPLASIA ( 10 FDA reports)
BRONCHIAL OBSTRUCTION ( 10 FDA reports)
BUNION OPERATION ( 10 FDA reports)
CAECITIS ( 10 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 10 FDA reports)
CALCIUM DEFICIENCY ( 10 FDA reports)
CARDIAC ABLATION ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
CEREBELLAR SYNDROME ( 10 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 10 FDA reports)
CERVICITIS ( 10 FDA reports)
CHEMOTHERAPY ( 10 FDA reports)
CHONDROCALCINOSIS ( 10 FDA reports)
CHORIORETINOPATHY ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
COAGULATION TEST ABNORMAL ( 10 FDA reports)
COLOSTOMY ( 10 FDA reports)
COMPARTMENT SYNDROME ( 10 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 10 FDA reports)
CRYSTAL URINE ( 10 FDA reports)
CUBITAL TUNNEL SYNDROME ( 10 FDA reports)
CYSTITIS NONINFECTIVE ( 10 FDA reports)
DEREALISATION ( 10 FDA reports)
DRUG LEVEL FLUCTUATING ( 10 FDA reports)
DRUG TOLERANCE DECREASED ( 10 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
EMBOLISM ARTERIAL ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 10 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 10 FDA reports)
FACIAL NERVE DISORDER ( 10 FDA reports)
FISTULA REPAIR ( 10 FDA reports)
FOAMING AT MOUTH ( 10 FDA reports)
FOETAL GROWTH RETARDATION ( 10 FDA reports)
FOOD INTOLERANCE ( 10 FDA reports)
FOOT AMPUTATION ( 10 FDA reports)
GAMMOPATHY ( 10 FDA reports)
GENITAL CANDIDIASIS ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 10 FDA reports)
GRANULOMA SKIN ( 10 FDA reports)
GROWTH RETARDATION ( 10 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 10 FDA reports)
HAEMORRHAGIC DISORDER ( 10 FDA reports)
HEAT RASH ( 10 FDA reports)
HEPATOBLASTOMA ( 10 FDA reports)
HORDEOLUM ( 10 FDA reports)
HYPERCAPNIA ( 10 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 10 FDA reports)
HYPERTROPHY BREAST ( 10 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 10 FDA reports)
HYPOVITAMINOSIS ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INJECTION SITE PAPULE ( 10 FDA reports)
INJECTION SITE STINGING ( 10 FDA reports)
INTUBATION ( 10 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 10 FDA reports)
LARYNGEAL CANCER ( 10 FDA reports)
LOCALISED OSTEOARTHRITIS ( 10 FDA reports)
LOSS OF CONTROL OF LEGS ( 10 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 10 FDA reports)
MEAN CELL VOLUME DECREASED ( 10 FDA reports)
METASTATIC PAIN ( 10 FDA reports)
MULTI-ORGAN DISORDER ( 10 FDA reports)
MUSCLE ENZYME INCREASED ( 10 FDA reports)
MYCOPLASMA INFECTION ( 10 FDA reports)
MYOGLOBINURIA ( 10 FDA reports)
NASAL MUCOSAL DISORDER ( 10 FDA reports)
NASOPHARYNGEAL DISORDER ( 10 FDA reports)
NEGATIVE THOUGHTS ( 10 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 10 FDA reports)
OESOPHAGEAL DILATATION ( 10 FDA reports)
OPTIC ATROPHY ( 10 FDA reports)
ABSCESS NECK ( 9 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 9 FDA reports)
ACCOMMODATION DISORDER ( 9 FDA reports)
ACETABULUM FRACTURE ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANAL SPHINCTER ATONY ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
AORTIC VALVE CALCIFICATION ( 9 FDA reports)
ARACHNOID CYST ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BASAL GANGLIA INFARCTION ( 9 FDA reports)
BEREAVEMENT ( 9 FDA reports)
BLADDER NEOPLASM ( 9 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 9 FDA reports)
BLADDER PAIN ( 9 FDA reports)
BLOOD ALCOHOL INCREASED ( 9 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 9 FDA reports)
BLOOD PH INCREASED ( 9 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 9 FDA reports)
BURNS THIRD DEGREE ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 9 FDA reports)
CATHETER SITE RELATED REACTION ( 9 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 9 FDA reports)
CEREBRAL CYST ( 9 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 9 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 9 FDA reports)
CLUSTER HEADACHE ( 9 FDA reports)
COGWHEEL RIGIDITY ( 9 FDA reports)
COLON CANCER RECURRENT ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONJUNCTIVAL OEDEMA ( 9 FDA reports)
CORNEAL OEDEMA ( 9 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 9 FDA reports)
CUSHING'S SYNDROME ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 9 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 9 FDA reports)
DENTAL TREATMENT ( 9 FDA reports)
DEVICE OCCLUSION ( 9 FDA reports)
DIAPHRAGMATIC DISORDER ( 9 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 9 FDA reports)
DYSENTERY ( 9 FDA reports)
EATING DISORDER SYMPTOM ( 9 FDA reports)
EMPYEMA ( 9 FDA reports)
ENDOMETRIAL CANCER ( 9 FDA reports)
ENTEROBACTER BACTERAEMIA ( 9 FDA reports)
ENTEROCOLITIS ( 9 FDA reports)
EXPOSURE TO TOXIC AGENT ( 9 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 9 FDA reports)
EXTRASKELETAL OSSIFICATION ( 9 FDA reports)
FAILURE OF IMPLANT ( 9 FDA reports)
FEELINGS OF WORTHLESSNESS ( 9 FDA reports)
FOETAL HEART RATE ABNORMAL ( 9 FDA reports)
FOOT OPERATION ( 9 FDA reports)
FOREARM FRACTURE ( 9 FDA reports)
FRACTURED COCCYX ( 9 FDA reports)
FUNGAL RASH ( 9 FDA reports)
GASTRIC BYPASS ( 9 FDA reports)
GASTRIC INFECTION ( 9 FDA reports)
GASTRIC OPERATION ( 9 FDA reports)
GASTROINTESTINAL CARCINOMA ( 9 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 9 FDA reports)
GRAVITATIONAL OEDEMA ( 9 FDA reports)
HEPATITIS FULMINANT ( 9 FDA reports)
HERPES OPHTHALMIC ( 9 FDA reports)
HIP DEFORMITY ( 9 FDA reports)
HODGKIN'S DISEASE ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
IMPAIRED FASTING GLUCOSE ( 9 FDA reports)
IMPAIRED SELF-CARE ( 9 FDA reports)
IMPATIENCE ( 9 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 9 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 9 FDA reports)
JUGULAR VEIN THROMBOSIS ( 9 FDA reports)
KELOID SCAR ( 9 FDA reports)
KERATITIS ( 9 FDA reports)
KERATOACANTHOMA ( 9 FDA reports)
LIP DISCOLOURATION ( 9 FDA reports)
LIP ULCERATION ( 9 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 9 FDA reports)
LYMPHADENECTOMY ( 9 FDA reports)
LYMPHANGIOMA ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 9 FDA reports)
MENINGITIS ASEPTIC ( 9 FDA reports)
MENOPAUSE ( 9 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 9 FDA reports)
METASTASES TO PERITONEUM ( 9 FDA reports)
METASTASES TO SKIN ( 9 FDA reports)
MUCOSAL DRYNESS ( 9 FDA reports)
MUSCLE RUPTURE ( 9 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 9 FDA reports)
MYELOMALACIA ( 9 FDA reports)
NAIL DYSTROPHY ( 9 FDA reports)
NAIL OPERATION ( 9 FDA reports)
NARCOLEPSY ( 9 FDA reports)
NARCOTIC INTOXICATION ( 9 FDA reports)
NEOPLASM RECURRENCE ( 9 FDA reports)
NEUTROPENIC COLITIS ( 9 FDA reports)
NODULE ON EXTREMITY ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
ORAL PRURITUS ( 9 FDA reports)
ORAL SOFT TISSUE DISORDER ( 9 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 9 FDA reports)
OSTEOPOROTIC FRACTURE ( 9 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 9 FDA reports)
PEMPHIGUS ( 9 FDA reports)
PERIANAL ABSCESS ( 9 FDA reports)
PERIODONTAL INFECTION ( 9 FDA reports)
PITUITARY TUMOUR RECURRENT ( 9 FDA reports)
PLACENTAL INSUFFICIENCY ( 9 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 9 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 9 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 9 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
PROSTATE CANCER RECURRENT ( 9 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 9 FDA reports)
PROTEIN TOTAL ABNORMAL ( 9 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 9 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 9 FDA reports)
PSEUDOPOLYPOSIS ( 9 FDA reports)
REBOUND EFFECT ( 9 FDA reports)
RESIDUAL URINE ( 9 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SELF ESTEEM DECREASED ( 9 FDA reports)
SJOGREN'S SYNDROME ( 9 FDA reports)
SKIN HYPOPIGMENTATION ( 9 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 9 FDA reports)
SURGICAL PROCEDURE REPEATED ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 9 FDA reports)
TARSAL TUNNEL SYNDROME ( 9 FDA reports)
TELANGIECTASIA ( 9 FDA reports)
THALAMIC INFARCTION ( 9 FDA reports)
THERAPEUTIC PROCEDURE ( 9 FDA reports)
THERAPY CESSATION ( 9 FDA reports)
THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
TOOTH DISCOLOURATION ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
URGE INCONTINENCE ( 9 FDA reports)
VAGINAL BURNING SENSATION ( 9 FDA reports)
VAGINAL MYCOSIS ( 9 FDA reports)
VASCULAR INSUFFICIENCY ( 9 FDA reports)
VASCULITIS CEREBRAL ( 9 FDA reports)
VENTRICULAR FAILURE ( 9 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 9 FDA reports)
VESTIBULAR NEURONITIS ( 9 FDA reports)
VOLVULUS ( 9 FDA reports)
VULVOVAGINAL PAIN ( 9 FDA reports)
WEIGHT LOSS POOR ( 9 FDA reports)
PACEMAKER COMPLICATION ( 8 FDA reports)
PANCREATIC ENZYMES INCREASED ( 8 FDA reports)
PANCREATOLITHIASIS ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PELVIC NEOPLASM ( 8 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 8 FDA reports)
PERITONEAL HAEMORRHAGE ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 8 FDA reports)
PHOBIA ( 8 FDA reports)
PLEURAL DECORTICATION ( 8 FDA reports)
PNEUMONIA FUNGAL ( 8 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 8 FDA reports)
POST POLIO SYNDROME ( 8 FDA reports)
POSTICTAL STATE ( 8 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 8 FDA reports)
POTENTIATING DRUG INTERACTION ( 8 FDA reports)
PRE-ECLAMPSIA ( 8 FDA reports)
PRIAPISM ( 8 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 8 FDA reports)
PROCEDURAL SITE REACTION ( 8 FDA reports)
PRODUCT COUNTERFEIT ( 8 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 8 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 8 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
RENAL TUBULAR ACIDOSIS ( 8 FDA reports)
RESPIRATORY TRACT IRRITATION ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 8 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 8 FDA reports)
SIALOADENITIS ( 8 FDA reports)
SKIN CHAPPED ( 8 FDA reports)
SOFT TISSUE NECROSIS ( 8 FDA reports)
SPLENIC RUPTURE ( 8 FDA reports)
SPONTANEOUS PENILE ERECTION ( 8 FDA reports)
STERNAL FRACTURE ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
SUPERINFECTION ( 8 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 8 FDA reports)
TERMINAL STATE ( 8 FDA reports)
THORACIC OPERATION ( 8 FDA reports)
TONGUE COATED ( 8 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
TRANSPLANT FAILURE ( 8 FDA reports)
TRAUMATIC HAEMATOMA ( 8 FDA reports)
TRIGONITIS ( 8 FDA reports)
ULNAR NERVE INJURY ( 8 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 8 FDA reports)
URETHRAL STRICTURE ( 8 FDA reports)
URINARY SEDIMENT PRESENT ( 8 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 8 FDA reports)
VARICOSE ULCERATION ( 8 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 8 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 8 FDA reports)
VITH NERVE PARALYSIS ( 8 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 8 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 8 FDA reports)
WANDERING PACEMAKER ( 8 FDA reports)
WEANING FAILURE ( 8 FDA reports)
WOUND ABSCESS ( 8 FDA reports)
ADENOTONSILLECTOMY ( 8 FDA reports)
ALDOLASE INCREASED ( 8 FDA reports)
ALVEOLITIS FIBROSING ( 8 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 8 FDA reports)
ANAL PRURITUS ( 8 FDA reports)
ANASTOMOTIC STENOSIS ( 8 FDA reports)
ANHIDROSIS ( 8 FDA reports)
ANIMAL SCRATCH ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ANTICONVULSANT TOXICITY ( 8 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
ANTISOCIAL BEHAVIOUR ( 8 FDA reports)
AORTIC OCCLUSION ( 8 FDA reports)
ARTERIAL SPASM ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 8 FDA reports)
AXONAL NEUROPATHY ( 8 FDA reports)
BACTERIAL DISEASE CARRIER ( 8 FDA reports)
BENIGN RENAL NEOPLASM ( 8 FDA reports)
BILIARY SEPSIS ( 8 FDA reports)
BIOPSY BONE ABNORMAL ( 8 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 8 FDA reports)
BITE ( 8 FDA reports)
BLADDER CYST ( 8 FDA reports)
BLADDER INJURY ( 8 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 8 FDA reports)
BLOOD GASES ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE ( 8 FDA reports)
BOWEL SOUNDS ABNORMAL ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
BRONCHITIS VIRAL ( 8 FDA reports)
BURN INFECTION ( 8 FDA reports)
CARCINOMA ( 8 FDA reports)
CELL DEATH ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 8 FDA reports)
CERVICAL CYST ( 8 FDA reports)
CHEYNE-STOKES RESPIRATION ( 8 FDA reports)
CHRONIC HEPATITIS ( 8 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 8 FDA reports)
COLON CANCER METASTATIC ( 8 FDA reports)
COMA HEPATIC ( 8 FDA reports)
CORNEAL OPACITY ( 8 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 8 FDA reports)
CORONARY OSTIAL STENOSIS ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 8 FDA reports)
CULTURE ( 8 FDA reports)
CYCLOTHYMIC DISORDER ( 8 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 8 FDA reports)
DENTAL CLEANING ( 8 FDA reports)
DENTAL FISTULA ( 8 FDA reports)
DENTAL IMPLANTATION ( 8 FDA reports)
DERMATITIS PSORIASIFORM ( 8 FDA reports)
DEVICE LEAKAGE ( 8 FDA reports)
DIABETES INSIPIDUS ( 8 FDA reports)
DIABETIC EYE DISEASE ( 8 FDA reports)
DIAPHRAGMATIC INJURY ( 8 FDA reports)
DIARRHOEA INFECTIOUS ( 8 FDA reports)
DISEASE COMPLICATION ( 8 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 8 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 8 FDA reports)
DYSMENORRHOEA ( 8 FDA reports)
DYSPAREUNIA ( 8 FDA reports)
EAR INFECTION VIRAL ( 8 FDA reports)
EJACULATION DISORDER ( 8 FDA reports)
ELECTRIC SHOCK ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 8 FDA reports)
ENDOCARDITIS BACTERIAL ( 8 FDA reports)
ENZYME ABNORMALITY ( 8 FDA reports)
EXCESSIVE EYE BLINKING ( 8 FDA reports)
EXCITABILITY ( 8 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 8 FDA reports)
FANCONI SYNDROME ( 8 FDA reports)
FEMALE ORGASMIC DISORDER ( 8 FDA reports)
FIBROADENOMA OF BREAST ( 8 FDA reports)
FOOD INTERACTION ( 8 FDA reports)
GALLBLADDER CANCER ( 8 FDA reports)
GASTROINTESTINAL NEOPLASM ( 8 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 8 FDA reports)
GASTROINTESTINAL OEDEMA ( 8 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 8 FDA reports)
GENITAL BURNING SENSATION ( 8 FDA reports)
GENITAL RASH ( 8 FDA reports)
GIANT CELL EPULIS ( 8 FDA reports)
GINGIVAL ERYTHEMA ( 8 FDA reports)
GINGIVAL OEDEMA ( 8 FDA reports)
GRAFT LOSS ( 8 FDA reports)
HAEMOCHROMATOSIS ( 8 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HEART VALVE STENOSIS ( 8 FDA reports)
HEMIANOPIA HOMONYMOUS ( 8 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 8 FDA reports)
HEPATIC CANCER METASTATIC ( 8 FDA reports)
HEPATITIS C POSITIVE ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 8 FDA reports)
HYPERMAGNESAEMIA ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
HYPERVIGILANCE ( 8 FDA reports)
IMMUNOGLOBULINS INCREASED ( 8 FDA reports)
INDIFFERENCE ( 8 FDA reports)
INFECTED CYST ( 8 FDA reports)
INFUSION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE INFLAMMATION ( 8 FDA reports)
INJECTION SITE OEDEMA ( 8 FDA reports)
INJECTION SITE SCAR ( 8 FDA reports)
INJECTION SITE ULCER ( 8 FDA reports)
INTESTINAL ADENOCARCINOMA ( 8 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 8 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 8 FDA reports)
JUDGEMENT IMPAIRED ( 8 FDA reports)
LIP INJURY ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 8 FDA reports)
MALIGNANT TUMOUR EXCISION ( 8 FDA reports)
MONOPARESIS ( 8 FDA reports)
MORBID THOUGHTS ( 8 FDA reports)
MUCOSAL HAEMORRHAGE ( 8 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 8 FDA reports)
NONSPECIFIC REACTION ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 8 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 8 FDA reports)
ORAL FIBROMA ( 8 FDA reports)
ORAL MUCOSAL BLISTERING ( 8 FDA reports)
ORCHITIS ( 8 FDA reports)
ABDOMINAL MASS ( 7 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 7 FDA reports)
AMYLOIDOSIS ( 7 FDA reports)
ANASTOMOTIC ULCER ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
AORTIC ATHEROSCLEROSIS ( 7 FDA reports)
APPLICATION SITE DISCOLOURATION ( 7 FDA reports)
APPLICATION SITE SWELLING ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
ASPIRATION PLEURAL CAVITY ( 7 FDA reports)
AURA ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BASOPHIL COUNT INCREASED ( 7 FDA reports)
BENIGN BREAST NEOPLASM ( 7 FDA reports)
BLADDER DISTENSION ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 7 FDA reports)
BLOOD IRON INCREASED ( 7 FDA reports)
BLOOD OSMOLARITY DECREASED ( 7 FDA reports)
BLUE TOE SYNDROME ( 7 FDA reports)
BONE DENSITOMETRY ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BRAIN CANCER METASTATIC ( 7 FDA reports)
BRAIN SCAN ABNORMAL ( 7 FDA reports)
BRAIN STEM INFARCTION ( 7 FDA reports)
BREAST NEOPLASM ( 7 FDA reports)
BRONCHIAL CARCINOMA ( 7 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 7 FDA reports)
CARTILAGE ATROPHY ( 7 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 7 FDA reports)
CHOREA ( 7 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
COMMINUTED FRACTURE ( 7 FDA reports)
COMPULSIVE SHOPPING ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 7 FDA reports)
CULTURE WOUND POSITIVE ( 7 FDA reports)
CYSTITIS INTERSTITIAL ( 7 FDA reports)
DEAFNESS BILATERAL ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
DEVELOPMENTAL DELAY ( 7 FDA reports)
DEVICE RELATED SEPSIS ( 7 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 7 FDA reports)
DIABETIC RETINAL OEDEMA ( 7 FDA reports)
DIABETIC VASCULAR DISORDER ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
ENAMEL ANOMALY ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
EYELID FUNCTION DISORDER ( 7 FDA reports)
FEEDING TUBE COMPLICATION ( 7 FDA reports)
FEMORAL ARTERY ANEURYSM ( 7 FDA reports)
FINGER AMPUTATION ( 7 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 7 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 7 FDA reports)
GALLBLADDER OEDEMA ( 7 FDA reports)
GALLBLADDER PAIN ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 7 FDA reports)
GENITAL LESION ( 7 FDA reports)
GILBERT'S SYNDROME ( 7 FDA reports)
GINGIVAL HYPERPLASIA ( 7 FDA reports)
GLUCOSE URINE ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
GROWTH OF EYELASHES ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HALO VISION ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HEPATIC INFECTION BACTERIAL ( 7 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 7 FDA reports)
HEPATITIS VIRAL ( 7 FDA reports)
HEPATORENAL FAILURE ( 7 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 7 FDA reports)
HIDRADENITIS ( 7 FDA reports)
HLA MARKER STUDY POSITIVE ( 7 FDA reports)
HYPERLACTACIDAEMIA ( 7 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 7 FDA reports)
HYPOCAPNIA ( 7 FDA reports)
INAPPROPRIATE AFFECT ( 7 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
INFUSION SITE EXTRAVASATION ( 7 FDA reports)
INFUSION SITE SWELLING ( 7 FDA reports)
INJECTION SITE CELLULITIS ( 7 FDA reports)
INJECTION SITE NECROSIS ( 7 FDA reports)
INNER EAR DISORDER ( 7 FDA reports)
INSULIN RESISTANCE ( 7 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
INTESTINAL INFARCTION ( 7 FDA reports)
INTESTINAL RESECTION ( 7 FDA reports)
JOINT STABILISATION ( 7 FDA reports)
JOINT WARMTH ( 7 FDA reports)
KAPOSI'S SARCOMA ( 7 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 7 FDA reports)
LATEX ALLERGY ( 7 FDA reports)
LENTICULAR OPACITIES ( 7 FDA reports)
LIGAMENT DISORDER ( 7 FDA reports)
LIGAMENT INJURY ( 7 FDA reports)
LINEAR IGA DISEASE ( 7 FDA reports)
LIP EXFOLIATION ( 7 FDA reports)
LIP HAEMORRHAGE ( 7 FDA reports)
LOOSE STOOLS ( 7 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 7 FDA reports)
MASTITIS ( 7 FDA reports)
MEGAKARYOCYTES INCREASED ( 7 FDA reports)
MERALGIA PARAESTHETICA ( 7 FDA reports)
METAMORPHOPSIA ( 7 FDA reports)
MICTURITION FREQUENCY DECREASED ( 7 FDA reports)
MITRAL VALVE REPLACEMENT ( 7 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 7 FDA reports)
MUSCLE SWELLING ( 7 FDA reports)
MYODESOPSIA ( 7 FDA reports)
NAIL BED TENDERNESS ( 7 FDA reports)
NASAL SINUS DRAINAGE ( 7 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 7 FDA reports)
NO ADVERSE EFFECT ( 7 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
OEDEMA GENITAL ( 7 FDA reports)
ORBITAL INFECTION ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
OXYGEN SATURATION ABNORMAL ( 7 FDA reports)
PANCREATIC NEOPLASM ( 7 FDA reports)
PARALYSIS FLACCID ( 7 FDA reports)
PELVIC VENOUS THROMBOSIS ( 7 FDA reports)
PERIDIVERTICULAR ABSCESS ( 7 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 7 FDA reports)
PHLEBITIS SUPERFICIAL ( 7 FDA reports)
PNEUMONIA KLEBSIELLA ( 7 FDA reports)
PO2 INCREASED ( 7 FDA reports)
POISONING DELIBERATE ( 7 FDA reports)
POLYP COLORECTAL ( 7 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 7 FDA reports)
POOR DENTAL CONDITION ( 7 FDA reports)
POST PROCEDURAL NAUSEA ( 7 FDA reports)
POST PROCEDURAL VOMITING ( 7 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 7 FDA reports)
POSTOPERATIVE ILEUS ( 7 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 7 FDA reports)
PRODUCT COLOUR ISSUE ( 7 FDA reports)
PROSTHESIS IMPLANTATION ( 7 FDA reports)
PRURIGO ( 7 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 7 FDA reports)
PURPURA SENILE ( 7 FDA reports)
RED BLOOD CELL ABNORMALITY ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 7 FDA reports)
RENAL ARTERY THROMBOSIS ( 7 FDA reports)
RENAL ISCHAEMIA ( 7 FDA reports)
RESIDUAL URINE VOLUME ( 7 FDA reports)
RETICULOCYTE COUNT DECREASED ( 7 FDA reports)
SALIVARY GLAND MASS ( 7 FDA reports)
SKIN OEDEMA ( 7 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
SPINAL DEFORMITY ( 7 FDA reports)
SPINAL SHOCK ( 7 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
SUBILEUS ( 7 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 7 FDA reports)
TALIPES ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 7 FDA reports)
THYROID MASS ( 7 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 7 FDA reports)
TRIGEMINAL NERVE PARESIS ( 7 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 7 FDA reports)
URETHRAL PROLAPSE ( 7 FDA reports)
URETHRAL STENOSIS ( 7 FDA reports)
URINARY FISTULA ( 7 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 7 FDA reports)
URINE OSMOLARITY DECREASED ( 7 FDA reports)
VAGINAL DISORDER ( 7 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 7 FDA reports)
VENA CAVA FILTER INSERTION ( 7 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 7 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 7 FDA reports)
WEIGHT ABNORMAL ( 7 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
PANNICULITIS ( 6 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 6 FDA reports)
PELVIC MASS ( 6 FDA reports)
PERFORATED ULCER ( 6 FDA reports)
PERINEPHRIC COLLECTION ( 6 FDA reports)
PERIRENAL HAEMATOMA ( 6 FDA reports)
PERITONEAL CARCINOMA ( 6 FDA reports)
PERITONEAL EFFUSION ( 6 FDA reports)
PERIVASCULAR DERMATITIS ( 6 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 6 FDA reports)
PHONOPHOBIA ( 6 FDA reports)
PHOTODERMATOSIS ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PLANTAR ERYTHEMA ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PNEUMATOSIS ( 6 FDA reports)
PNEUMOCOCCAL SEPSIS ( 6 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 6 FDA reports)
POLYMENORRHOEA ( 6 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 6 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 6 FDA reports)
PROTRUSION TONGUE ( 6 FDA reports)
PUBIC RAMI FRACTURE ( 6 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 6 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 6 FDA reports)
PULMONARY VASCULAR DISORDER ( 6 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 6 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 6 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 6 FDA reports)
RENAL STONE REMOVAL ( 6 FDA reports)
RETINOPATHY HYPERTENSIVE ( 6 FDA reports)
RETROPERITONEAL FIBROSIS ( 6 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 6 FDA reports)
RHEUMATIC HEART DISEASE ( 6 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 6 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 6 FDA reports)
SEMEN VOLUME DECREASED ( 6 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 6 FDA reports)
SIMPLE PARTIAL SEIZURES ( 6 FDA reports)
SINUS ANTROSTOMY ( 6 FDA reports)
SKIN DEPIGMENTATION ( 6 FDA reports)
SKIN INFLAMMATION ( 6 FDA reports)
SKIN INJURY ( 6 FDA reports)
SKIN STRIAE ( 6 FDA reports)
SKIN TEST POSITIVE ( 6 FDA reports)
SKIN TURGOR DECREASED ( 6 FDA reports)
SKULL MALFORMATION ( 6 FDA reports)
SLEEP-RELATED EATING DISORDER ( 6 FDA reports)
SLOW RESPONSE TO STIMULI ( 6 FDA reports)
SMOKER ( 6 FDA reports)
SPONDYLOSIS ( 6 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
THERAPEUTIC EMBOLISATION ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
THROAT LESION ( 6 FDA reports)
THYROID CANCER METASTATIC ( 6 FDA reports)
THYROIDECTOMY ( 6 FDA reports)
TONSILLAR HYPERTROPHY ( 6 FDA reports)
TOOTH REPAIR ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRACHEAL DISORDER ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRICHORRHEXIS ( 6 FDA reports)
TUBERCULOUS PLEURISY ( 6 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 6 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 6 FDA reports)
UMBILICAL ARTERY HYPOPLASIA ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
URETERAL NECROSIS ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
URINE URIC ACID DECREASED ( 6 FDA reports)
VARICELLA ( 6 FDA reports)
VASCULAR GRAFT COMPLICATION ( 6 FDA reports)
VASCULAR OPERATION ( 6 FDA reports)
VASCULAR PURPURA ( 6 FDA reports)
VASCULITIS NECROTISING ( 6 FDA reports)
VASOPLEGIA SYNDROME ( 6 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 6 FDA reports)
VENOUS STASIS ( 6 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
VIRAL RHINITIS ( 6 FDA reports)
VISUAL BRIGHTNESS ( 6 FDA reports)
VITILIGO ( 6 FDA reports)
WOUND DEBRIDEMENT ( 6 FDA reports)
ABDOMINAL SYMPTOM ( 6 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 6 FDA reports)
ABORTION INDUCED ( 6 FDA reports)
ACCIDENTAL DEATH ( 6 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 6 FDA reports)
ACUTE LEUKAEMIA ( 6 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 6 FDA reports)
ALCOHOL INTERACTION ( 6 FDA reports)
ALLERGIC SINUSITIS ( 6 FDA reports)
AMBLYOPIA ( 6 FDA reports)
AMNESTIC DISORDER ( 6 FDA reports)
AMYOTROPHY ( 6 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 6 FDA reports)
ANGIOGRAM ABNORMAL ( 6 FDA reports)
ANOSOGNOSIA ( 6 FDA reports)
APPLICATION SITE URTICARIA ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
ASTERIXIS ( 6 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 6 FDA reports)
AXILLARY MASS ( 6 FDA reports)
B-CELL LYMPHOMA STAGE I ( 6 FDA reports)
BELLIGERENCE ( 6 FDA reports)
BENIGN BONE NEOPLASM ( 6 FDA reports)
BENIGN COLONIC NEOPLASM ( 6 FDA reports)
BENIGN MESOTHELIOMA ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLADDER NECK OPERATION ( 6 FDA reports)
BLAST CELL COUNT INCREASED ( 6 FDA reports)
BLOOD CREATINE ABNORMAL ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 6 FDA reports)
BLOOD SODIUM ABNORMAL ( 6 FDA reports)
BODY MASS INDEX INCREASED ( 6 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 6 FDA reports)
BRAIN HERNIATION ( 6 FDA reports)
BRAIN STEM HAEMORRHAGE ( 6 FDA reports)
BREAST HAEMORRHAGE ( 6 FDA reports)
BRONCHIAL WALL THICKENING ( 6 FDA reports)
BURNING MOUTH SYNDROME ( 6 FDA reports)
BURSA DISORDER ( 6 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 6 FDA reports)
CALCULUS URETHRAL ( 6 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 6 FDA reports)
CAROTIDYNIA ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 6 FDA reports)
CEREBRAL HYPOPERFUSION ( 6 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 6 FDA reports)
CERVIX DISORDER ( 6 FDA reports)
CHOLESTATIC LIVER INJURY ( 6 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 6 FDA reports)
CLAUSTROPHOBIA ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COGNITIVE DETERIORATION ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
COMA SCALE ABNORMAL ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
CORONARY BYPASS THROMBOSIS ( 6 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 6 FDA reports)
CREATININE URINE DECREASED ( 6 FDA reports)
CREATININE URINE INCREASED ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 6 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 6 FDA reports)
DELIRIUM TREMENS ( 6 FDA reports)
DEVICE MISUSE ( 6 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 6 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
DISLOCATION OF VERTEBRA ( 6 FDA reports)
DIVERTICULAR FISTULA ( 6 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 6 FDA reports)
DYSMORPHISM ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
EAR TUBE INSERTION ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 6 FDA reports)
EMBOLISM VENOUS ( 6 FDA reports)
ENCEPHALITIS VIRAL ( 6 FDA reports)
ENDOCRINE DISORDER ( 6 FDA reports)
ENDOMETRIAL ABLATION ( 6 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 6 FDA reports)
ENEMA ADMINISTRATION ( 6 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
ERYTHEMA NODOSUM ( 6 FDA reports)
ETHMOID SINUS SURGERY ( 6 FDA reports)
FEAR OF DISEASE ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FOETAL DISORDER ( 6 FDA reports)
GALLBLADDER PERFORATION ( 6 FDA reports)
GASTRIC DILATATION ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GENITAL EROSION ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
HAEMATOMA EVACUATION ( 6 FDA reports)
HEART VALVE INSUFFICIENCY ( 6 FDA reports)
HEPATIC INFARCTION ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HERNIA HIATUS REPAIR ( 6 FDA reports)
HERPES ZOSTER DISSEMINATED ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERPLASIA ( 6 FDA reports)
HYPERSPLENISM ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
ILIAC ARTERY OCCLUSION ( 6 FDA reports)
INJECTION SITE VESICLES ( 6 FDA reports)
INJURY ASPHYXIATION ( 6 FDA reports)
INTESTINAL STENOSIS ( 6 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 6 FDA reports)
IRIS NEOPLASM ( 6 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 6 FDA reports)
JEJUNAL PERFORATION ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
JOINT SURGERY ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LAZINESS ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LEUKOARAIOSIS ( 6 FDA reports)
LEUKOCYTURIA ( 6 FDA reports)
LIMB DEFORMITY ( 6 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 6 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
LONG QT SYNDROME ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LYMPH NODE PAIN ( 6 FDA reports)
MEDIASTINAL DISORDER ( 6 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 6 FDA reports)
MENINGITIS VIRAL ( 6 FDA reports)
MENOMETRORRHAGIA ( 6 FDA reports)
METASTASES TO SPLEEN ( 6 FDA reports)
MONONEUROPATHY MULTIPLEX ( 6 FDA reports)
MUCORMYCOSIS ( 6 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 6 FDA reports)
MYELITIS ( 6 FDA reports)
NAIL GROWTH ABNORMAL ( 6 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 6 FDA reports)
NEONATAL HYPOTENSION ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NO ADVERSE DRUG EFFECT ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 6 FDA reports)
OCCIPITAL NEURALGIA ( 6 FDA reports)
OCULOGYRATION ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
OESOPHAGITIS ULCERATIVE ( 6 FDA reports)
OLIGODENDROGLIOMA ( 6 FDA reports)
ONYCHOMADESIS ( 6 FDA reports)
OPTIC NERVE INJURY ( 6 FDA reports)
ABDOMINAL INJURY ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 5 FDA reports)
ABDOMINOPLASTY ( 5 FDA reports)
ABSCESS SOFT TISSUE ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ACUTE ABDOMEN ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ADENOIDITIS ( 5 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 5 FDA reports)
ALCOHOL INTOLERANCE ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 5 FDA reports)
AMPUTATION ( 5 FDA reports)
AMYLASE INCREASED ( 5 FDA reports)
ANGIODYSPLASIA ( 5 FDA reports)
ANION GAP DECREASED ( 5 FDA reports)
ANKLE OPERATION ( 5 FDA reports)
ANTEROGRADE AMNESIA ( 5 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 5 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
APPLICATION SITE EXFOLIATION ( 5 FDA reports)
APPLICATION SITE HAEMATOMA ( 5 FDA reports)
ARTERIAL GRAFT ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
BACTERIAL DIARRHOEA ( 5 FDA reports)
BASE EXCESS NEGATIVE ( 5 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BIOPSY BREAST ABNORMAL ( 5 FDA reports)
BIOPSY LIVER ( 5 FDA reports)
BLADDER DILATATION ( 5 FDA reports)
BLADDER DISCOMFORT ( 5 FDA reports)
BLISTER INFECTED ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD COPPER DECREASED ( 5 FDA reports)
BLOOD CREATININE ( 5 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 5 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 5 FDA reports)
BRACHIAL PLEXOPATHY ( 5 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 5 FDA reports)
BREAST CANCER STAGE III ( 5 FDA reports)
BREAST CELLULITIS ( 5 FDA reports)
BREAST DISORDER FEMALE ( 5 FDA reports)
BREAST INDURATION ( 5 FDA reports)
BUTTERFLY RASH ( 5 FDA reports)
CALCIUM IONISED INCREASED ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 5 FDA reports)
CARDIAC STRESS TEST ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CENTRAL LINE INFECTION ( 5 FDA reports)
CEREBRAL PALSY ( 5 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 5 FDA reports)
CHALAZION ( 5 FDA reports)
CHOLANGITIS ACUTE ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHONDROMALACIA ( 5 FDA reports)
CHORDAE TENDINAE RUPTURE ( 5 FDA reports)
CLOSED HEAD INJURY ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
COLONIC HAEMORRHAGE ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
COLORECTAL CANCER ( 5 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CONJUNCTIVITIS VIRAL ( 5 FDA reports)
CORNEAL DEPOSITS ( 5 FDA reports)
CORNEAL TRANSPLANT ( 5 FDA reports)
CORONARY ARTERY EMBOLISM ( 5 FDA reports)
CULTURE URINE ( 5 FDA reports)
DENTOFACIAL ANOMALY ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DIABETIC BLINDNESS ( 5 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DIAPHRAGMATIC HERNIA ( 5 FDA reports)
DISSOCIATIVE DISORDER ( 5 FDA reports)
DIVORCED ( 5 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG SCREEN NEGATIVE ( 5 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 5 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 5 FDA reports)
EAR NEOPLASM ( 5 FDA reports)
EAR PRURITUS ( 5 FDA reports)
ECTROPION ( 5 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
ERYTHRODERMIC PSORIASIS ( 5 FDA reports)
EYE REDNESS ( 5 FDA reports)
FACIAL ASYMMETRY ( 5 FDA reports)
FAT NECROSIS ( 5 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FRACTURE DISPLACEMENT ( 5 FDA reports)
FUNGAEMIA ( 5 FDA reports)
FUNGAL PERITONITIS ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 5 FDA reports)
GASTRIC ATONY ( 5 FDA reports)
GASTRODUODENAL ULCER ( 5 FDA reports)
GASTROENTERITIS BACTERIAL ( 5 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GENE MUTATION ( 5 FDA reports)
GENITAL HAEMORRHAGE ( 5 FDA reports)
GENITAL INJURY ( 5 FDA reports)
GENITAL PRURITUS FEMALE ( 5 FDA reports)
GINGIVAL DISCOLOURATION ( 5 FDA reports)
GLOBAL AMNESIA ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
GROIN INFECTION ( 5 FDA reports)
HEART VALVE CALCIFICATION ( 5 FDA reports)
HEPATIC MASS ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 5 FDA reports)
HEPATITIS C RNA POSITIVE ( 5 FDA reports)
HEPATOBILIARY DISEASE ( 5 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 5 FDA reports)
HIRSUTISM ( 5 FDA reports)
HYPERALDOSTERONISM ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 5 FDA reports)
HYPERKINETIC HEART SYNDROME ( 5 FDA reports)
HYPERMETABOLISM ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
ILLUSION ( 5 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 5 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 5 FDA reports)
INFLAMMATORY PAIN ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INTERCOSTAL NEURALGIA ( 5 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 5 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 5 FDA reports)
INTUBATION COMPLICATION ( 5 FDA reports)
ITCHING SCAR ( 5 FDA reports)
JOINT DESTRUCTION ( 5 FDA reports)
JOINT FLUID DRAINAGE ( 5 FDA reports)
JOINT TUBERCULOSIS ( 5 FDA reports)
KERATITIS HERPETIC ( 5 FDA reports)
KIDNEY SMALL ( 5 FDA reports)
KLIPPEL-FEIL SYNDROME ( 5 FDA reports)
LAPAROTOMY ( 5 FDA reports)
LARYNGEAL HAEMORRHAGE ( 5 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 5 FDA reports)
LEUKOPLAKIA ( 5 FDA reports)
LIPID METABOLISM DISORDER ( 5 FDA reports)
LISTERIOSIS ( 5 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 5 FDA reports)
LUPUS NEPHRITIS ( 5 FDA reports)
LYMPH NODE CALCIFICATION ( 5 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 5 FDA reports)
MAMMOPLASTY ( 5 FDA reports)
MASKED FACIES ( 5 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 5 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 5 FDA reports)
MEDICAL DEVICE REMOVAL ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 5 FDA reports)
MESOTHELIOMA MALIGNANT ( 5 FDA reports)
MILK-ALKALI SYNDROME ( 5 FDA reports)
MORPHOEA ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 5 FDA reports)
NEUROPATHIC ARTHROPATHY ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OCULAR NEOPLASM ( 5 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 5 FDA reports)
OESOPHAGEAL OPERATION ( 5 FDA reports)
OPHTHALMOPLEGIA ( 5 FDA reports)
OPTIC DISC HAEMORRHAGE ( 5 FDA reports)
ORGASM ABNORMAL ( 5 FDA reports)
OVARIAN CANCER RECURRENT ( 5 FDA reports)
OVARIAN NEOPLASM ( 5 FDA reports)
PACEMAKER GENERATED RHYTHM ( 5 FDA reports)
PALATAL OEDEMA ( 5 FDA reports)
PANCREATIC NECROSIS ( 5 FDA reports)
PARACENTESIS ( 5 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 5 FDA reports)
PEPTIC ULCER PERFORATION ( 5 FDA reports)
PHAEOCHROMOCYTOMA CRISIS ( 5 FDA reports)
PHLEBOTHROMBOSIS ( 5 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 5 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMONIA HERPES VIRAL ( 5 FDA reports)
PNEUMONIA LEGIONELLA ( 5 FDA reports)
PNEUMONIA MYCOPLASMAL ( 5 FDA reports)
PNEUMOPERITONEUM ( 5 FDA reports)
PORPHYRIA NON-ACUTE ( 5 FDA reports)
PORTAL VEIN OCCLUSION ( 5 FDA reports)
POST PROCEDURAL PNEUMONIA ( 5 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 5 FDA reports)
POSTOPERATIVE ADHESION ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
PRECOCIOUS PUBERTY ( 5 FDA reports)
PREMENSTRUAL SYNDROME ( 5 FDA reports)
PROTEUS TEST POSITIVE ( 5 FDA reports)
PSYCHOLOGICAL TRAUMA ( 5 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 5 FDA reports)
PYLORIC STENOSIS ( 5 FDA reports)
PYOTHORAX ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RECTAL DISCHARGE ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RED BLOOD CELLS URINE ( 5 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RENAL SURGERY ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RETINAL INFARCTION ( 5 FDA reports)
SCIATIC NERVE INJURY ( 5 FDA reports)
SCROTAL ABSCESS ( 5 FDA reports)
SCROTAL HAEMATOMA ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SECONDARY HYPERTENSION ( 5 FDA reports)
SENILE OSTEOPOROSIS ( 5 FDA reports)
SEPTIC EMBOLUS ( 5 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 5 FDA reports)
SINGLE VESSEL BYPASS GRAFT ( 5 FDA reports)
SKIN DESQUAMATION ( 5 FDA reports)
SKIN LESION EXCISION ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SLEEP ATTACKS ( 5 FDA reports)
SMALL INTESTINAL STENOSIS ( 5 FDA reports)
SPEECH REHABILITATION ( 5 FDA reports)
SPINAL CORD INFARCTION ( 5 FDA reports)
SPLENIC HAEMORRHAGE ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STROKE IN EVOLUTION ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
T-CELL LYMPHOMA ( 5 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 5 FDA reports)
TACHYCARDIA PAROXYSMAL ( 5 FDA reports)
TERMINAL INSOMNIA ( 5 FDA reports)
THIRST DECREASED ( 5 FDA reports)
THORACOSTOMY ( 5 FDA reports)
THYMOMA ( 5 FDA reports)
THYROID OPERATION ( 5 FDA reports)
THYROTOXIC PERIODIC PARALYSIS ( 5 FDA reports)
TOE OPERATION ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 5 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 5 FDA reports)
TRAUMATIC SHOCK ( 5 FDA reports)
TRISOMY 21 ( 5 FDA reports)
TUMOUR EXCISION ( 5 FDA reports)
TUMOUR PAIN ( 5 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 5 FDA reports)
UPPER EXTREMITY MASS ( 5 FDA reports)
URETHRAL DILATATION ( 5 FDA reports)
URETHRAL FISTULA ( 5 FDA reports)
URINARY CASTS ( 5 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 5 FDA reports)
URINARY TRACT OPERATION ( 5 FDA reports)
UTERINE CERVIX STENOSIS ( 5 FDA reports)
VAGINITIS ( 5 FDA reports)
VAGINITIS BACTERIAL ( 5 FDA reports)
VASODILATION PROCEDURE ( 5 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 5 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 5 FDA reports)
VIRAL PERICARDITIS ( 5 FDA reports)
VIRAL PHARYNGITIS ( 5 FDA reports)
VITAL CAPACITY DECREASED ( 5 FDA reports)
VOCAL CORD POLYPECTOMY ( 5 FDA reports)
WOUND NECROSIS ( 5 FDA reports)
X-RAY ABNORMAL ( 5 FDA reports)
XANTHELASMA ( 5 FDA reports)
OROMANDIBULAR DYSTONIA ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
PANCREAS INFECTION ( 4 FDA reports)
PANCREAS LIPOMATOSIS ( 4 FDA reports)
PANCREATIC CALCIFICATION ( 4 FDA reports)
PANCREATIC INJURY ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PARASYSTOLE ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PATIENT RESTRAINT ( 4 FDA reports)
PERFORATED DUODENAL ULCER REPAIR ( 4 FDA reports)
PERICARDIAL DISEASE ( 4 FDA reports)
PERIORBITAL ABSCESS ( 4 FDA reports)
PERITONEAL INFECTION ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PHLEBOLITH ( 4 FDA reports)
PLATELET AGGREGATION INCREASED ( 4 FDA reports)
PLATELET DESTRUCTION INCREASED ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POLYCYTHAEMIA VERA ( 4 FDA reports)
POOR PERSONAL HYGIENE ( 4 FDA reports)
POST PROCEDURAL DIARRHOEA ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
PROCEDURAL DIZZINESS ( 4 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 4 FDA reports)
PRODUCT PACKAGING ISSUE ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROSTATIC CALCIFICATION ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 4 FDA reports)
PSEUDOCYST ( 4 FDA reports)
PSEUDOPORPHYRIA ( 4 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PULMONARY HYPOPLASIA ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 4 FDA reports)
RASH SCALY ( 4 FDA reports)
REBOUND HYPERTENSION ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
REITER'S SYNDROME ( 4 FDA reports)
RENAL CANCER METASTATIC ( 4 FDA reports)
RESPIRATORY DEPTH DECREASED ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RETINAL ANEURYSM ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINAL NEOVASCULARISATION ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
RHINITIS SEASONAL ( 4 FDA reports)
RHINOVIRUS INFECTION ( 4 FDA reports)
SALMONELLOSIS ( 4 FDA reports)
SCLERAL DISORDER ( 4 FDA reports)
SCLERAL HAEMORRHAGE ( 4 FDA reports)
SCROTAL ULCER ( 4 FDA reports)
SEIZURE ANOXIC ( 4 FDA reports)
SENSATION OF BLOOD FLOW ( 4 FDA reports)
SEPTIC ENCEPHALOPATHY ( 4 FDA reports)
SERONEGATIVE ARTHRITIS ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SOLAR ELASTOSIS ( 4 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 4 FDA reports)
SPINAL CORD NEOPLASM ( 4 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 4 FDA reports)
SPLENIC INJURY ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
SPUTUM RETENTION ( 4 FDA reports)
STICKY PLATELET SYNDROME ( 4 FDA reports)
STIFF-MAN SYNDROME ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
STRESS AT WORK ( 4 FDA reports)
SUPRAPUBIC PAIN ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
TETANUS ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THORACIC OUTLET SYNDROME ( 4 FDA reports)
THYROID GLAND CANCER ( 4 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 4 FDA reports)
THYROIDITIS ( 4 FDA reports)
THYROXINE DECREASED ( 4 FDA reports)
TINEA INFECTION ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TOOTH DEPOSIT ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 4 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 4 FDA reports)
ULNAR NERVE PALSY ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
UMBILICAL HERNIA REPAIR ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
URETHRAL CARUNCLE ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
URETHRITIS ( 4 FDA reports)
URINARY BLADDER POLYP ( 4 FDA reports)
URINARY TRACT PAIN ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
VAGINAL PROLAPSE ( 4 FDA reports)
VAGINAL SWELLING ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VENTRICULAR DYSKINESIA ( 4 FDA reports)
VERTEBRAL COLUMN MASS ( 4 FDA reports)
VERTEBRAL INJURY ( 4 FDA reports)
VITREOUS DISORDER ( 4 FDA reports)
VITRITIS ( 4 FDA reports)
WEIGHT GAIN POOR ( 4 FDA reports)
WEST NILE VIRAL INFECTION ( 4 FDA reports)
WHIPLASH INJURY ( 4 FDA reports)
WOUND DECOMPOSITION ( 4 FDA reports)
ABDOMINAL OPERATION ( 4 FDA reports)
ABDOMINAL WALL INFECTION ( 4 FDA reports)
ACID FAST BACILLI INFECTION ( 4 FDA reports)
ACID FAST STAIN POSITIVE ( 4 FDA reports)
ACUTE STRESS DISORDER ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ALLERGIC COUGH ( 4 FDA reports)
AMPHETAMINES POSITIVE ( 4 FDA reports)
ANTICHOLINERGIC SYNDROME ( 4 FDA reports)
ANTICOAGULANT THERAPY ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
AORTIC VALVE ATRESIA ( 4 FDA reports)
APLASIA ( 4 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ARTERY DISSECTION ( 4 FDA reports)
ARTHRITIS REACTIVE ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
AXILLARY VEIN THROMBOSIS ( 4 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 4 FDA reports)
BASE EXCESS ( 4 FDA reports)
BASOPHIL COUNT DECREASED ( 4 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BINGE EATING ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 4 FDA reports)
BLOOD ARSENIC INCREASED ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD FOLATE DECREASED ( 4 FDA reports)
BLOOD IRON ABNORMAL ( 4 FDA reports)
BLOOD KETONE BODY ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 4 FDA reports)
BODY DYSMORPHIC DISORDER ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE FORMATION DECREASED ( 4 FDA reports)
BOVINE TUBERCULOSIS ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BREAST INFLAMMATION ( 4 FDA reports)
BRONCHOPNEUMOPATHY ( 4 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 4 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 4 FDA reports)
CARDIOMYOPATHY ACUTE ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CATHETER SITE PHLEBITIS ( 4 FDA reports)
CEREBROSCLEROSIS ( 4 FDA reports)
CHEST INJURY ( 4 FDA reports)
CHEST WALL ABSCESS ( 4 FDA reports)
CHEST WALL MASS ( 4 FDA reports)
CHOLANGIOLITIS ( 4 FDA reports)
CHOROIDAL DETACHMENT ( 4 FDA reports)
CITROBACTER INFECTION ( 4 FDA reports)
CLINODACTYLY ( 4 FDA reports)
CLONIC CONVULSION ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CONJUNCTIVAL DISORDER ( 4 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
CORNEAL GRAFT REJECTION ( 4 FDA reports)
CORNEAL INFECTION ( 4 FDA reports)
CORNEAL STAINING ( 4 FDA reports)
CORRECTIVE LENS USER ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CYST RUPTURE ( 4 FDA reports)
CYSTIC LYMPHANGIOMA ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
CYSTOSCOPY ( 4 FDA reports)
CYTOKINE RELEASE SYNDROME ( 4 FDA reports)
DARK CIRCLES UNDER EYES ( 4 FDA reports)
DEATH OF RELATIVE ( 4 FDA reports)
DEATH OF SPOUSE ( 4 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 4 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 4 FDA reports)
DENTAL NECROSIS ( 4 FDA reports)
DETOXIFICATION ( 4 FDA reports)
DEVICE INTERACTION ( 4 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 4 FDA reports)
DIET REFUSAL ( 4 FDA reports)
DISBACTERIOSIS ( 4 FDA reports)
DRESSLER'S SYNDROME ( 4 FDA reports)
DROP ATTACKS ( 4 FDA reports)
DRUG NAME CONFUSION ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
DRUG TOLERANCE INCREASED ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 4 FDA reports)
ELECTROLYTE DEPLETION ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
EPINEPHRINE INCREASED ( 4 FDA reports)
EVERSION OF LACRIMAL PUNCTUM ( 4 FDA reports)
EXPOSURE TO CONTAMINATED AIR ( 4 FDA reports)
EXTERNAL EAR CELLULITIS ( 4 FDA reports)
EXTERNAL EAR INFLAMMATION ( 4 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 4 FDA reports)
EXTUBATION ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
EYE LASER SURGERY ( 4 FDA reports)
EYELASH THICKENING ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEELING GUILTY ( 4 FDA reports)
FEMALE GENITAL OPERATION ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FLUID REPLACEMENT ( 4 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GASTRIC HYPERTONIA ( 4 FDA reports)
GASTROENTERITIS RADIATION ( 4 FDA reports)
GASTROENTERITIS SALMONELLA ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENITAL DISORDER FEMALE ( 4 FDA reports)
GENITAL PAIN ( 4 FDA reports)
GLIOBLASTOMA MULTIFORME ( 4 FDA reports)
GLOBULINS DECREASED ( 4 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 4 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 4 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 4 FDA reports)
GRAFT INFECTION ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMOGLOBIN ( 4 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 4 FDA reports)
HALLUCINATION, OLFACTORY ( 4 FDA reports)
HAPTOGLOBIN DECREASED ( 4 FDA reports)
HEAT STROKE ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATITIS B POSITIVE ( 4 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 4 FDA reports)
HEPATOJUGULAR REFLUX ( 4 FDA reports)
HIP SWELLING ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
HYDROURETER ( 4 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 4 FDA reports)
HYPERCREATININAEMIA ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPOCHROMASIA ( 4 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 4 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 4 FDA reports)
HYPOTONIA NEONATAL ( 4 FDA reports)
ILIAC VEIN OCCLUSION ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INCISION SITE ERYTHEMA ( 4 FDA reports)
INCISION SITE HAEMATOMA ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFLAMMATION LOCALISED ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INJECTION SITE ATROPHY ( 4 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTERNAL INJURY ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
JC VIRUS TEST POSITIVE ( 4 FDA reports)
JOINT ABSCESS ( 4 FDA reports)
JOINT LIGAMENT RUPTURE ( 4 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIVER OPERATION ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
LUPUS PNEUMONITIS ( 4 FDA reports)
LYMPHANGITIS ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MACULAR PIGMENTATION ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 4 FDA reports)
MEDIASTINUM NEOPLASM ( 4 FDA reports)
MESENTERIC OCCLUSION ( 4 FDA reports)
METAL POISONING ( 4 FDA reports)
METASTASES TO CHEST WALL ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 4 FDA reports)
MIXED LIVER INJURY ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOSCLEROSIS ( 4 FDA reports)
NASAL NECROSIS ( 4 FDA reports)
NECROTISING RETINITIS ( 4 FDA reports)
NEONATAL ANURIA ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 4 FDA reports)
NIGHT CRAMPS ( 4 FDA reports)
NITRITOID REACTION ( 4 FDA reports)
NOREPINEPHRINE INCREASED ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 4 FDA reports)
ONCOLOGIC COMPLICATION ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
ORBITAL OEDEMA ( 4 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABSCESS OF SALIVARY GLAND ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACARODERMATITIS ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANASTOMOTIC LEAK ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
AORTIC DISSECTION RUPTURE ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE BURNING ( 3 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 3 FDA reports)
APPLICATION SITE SCAB ( 3 FDA reports)
APPLICATION SITE SCAR ( 3 FDA reports)
APPLICATION SITE ULCER ( 3 FDA reports)
ARCUS LIPOIDES ( 3 FDA reports)
ARTERIAL RESTENOSIS ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ARTERIAL STENOSIS LIMB ( 3 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
ATROPHODERMA OF PASINI AND PIERINI ( 3 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
AZOOSPERMIA ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACILLUS TEST POSITIVE ( 3 FDA reports)
BACTERIAL PERICARDITIS ( 3 FDA reports)
BACTEROIDES INFECTION ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BECKWITH-WIEDEMANN SYNDROME ( 3 FDA reports)
BENIGN NEOPLASM OF SKIN ( 3 FDA reports)
BILIRUBIN URINE ( 3 FDA reports)
BILIRUBINURIA ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER NECK OBSTRUCTION ( 3 FDA reports)
BLAST CELLS PRESENT ( 3 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 3 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 3 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE ( 3 FDA reports)
BLOOD CREATINE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD PROLACTIN DECREASED ( 3 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 3 FDA reports)
BLOOD VISCOSITY INCREASED ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BRADYCARDIA NEONATAL ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN MIDLINE SHIFT ( 3 FDA reports)
BRAIN NEOPLASM BENIGN ( 3 FDA reports)
BREAST CANCER MALE ( 3 FDA reports)
BRONCHIAL DISORDER ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
C-REACTIVE PROTEIN ( 3 FDA reports)
CARCINOID TUMOUR PULMONARY ( 3 FDA reports)
CARCINOMA IN SITU OF SKIN ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID ARTERY STENT INSERTION ( 3 FDA reports)
CAROTID PULSE DECREASED ( 3 FDA reports)
CAROTID SINUS SYNDROME ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CHOLURIA ( 3 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 3 FDA reports)
CITROBACTER TEST POSITIVE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COAGULATION TIME SHORTENED ( 3 FDA reports)
COLECTOMY PARTIAL ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPULSIVE LIP BITING ( 3 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 3 FDA reports)
CONGENITAL AORTIC STENOSIS ( 3 FDA reports)
CONGENITAL BLADDER ANOMALY ( 3 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
CRANIOCEREBRAL INJURY ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 3 FDA reports)
DANDY-WALKER SYNDROME ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DELUSION OF GRANDEUR ( 3 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 3 FDA reports)
DELUSIONAL DISORDER, JEALOUS TYPE ( 3 FDA reports)
DELUSIONAL PERCEPTION ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DERMATOPHYTOSIS ( 3 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DRUG EFFECT PROLONGED ( 3 FDA reports)
DRUG LEVEL CHANGED ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ECZEMA NUMMULAR ( 3 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE ALLERGY ( 3 FDA reports)
EYE INFECTION TOXOPLASMAL ( 3 FDA reports)
EYE OPERATION COMPLICATION ( 3 FDA reports)
EYELID INJURY ( 3 FDA reports)
EYELID IRRITATION ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FACTITIOUS DISORDER ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FALLOPIAN TUBE CANCER ( 3 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 3 FDA reports)
FELTY'S SYNDROME ( 3 FDA reports)
FEMORAL BRUIT ( 3 FDA reports)
FIBROMA ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTRIC PH DECREASED ( 3 FDA reports)
GASTRIC VARICES ( 3 FDA reports)
GASTROENTERITIS NOROVIRUS ( 3 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 3 FDA reports)
GRAFT HAEMORRHAGE ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOBILIA ( 3 FDA reports)
HAEMOCONCENTRATION ( 3 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 3 FDA reports)
HAEMOSIDEROSIS ( 3 FDA reports)
HEAD AND NECK CANCER ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
HISTAMINE LEVEL INCREASED ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HORNER'S SYNDROME ( 3 FDA reports)
HYDROCELE MALE INFECTED ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERINSULINISM ( 3 FDA reports)
HYPERKALIURIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERVITAMINOSIS ( 3 FDA reports)
HYPOCALCIURIA ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
HYPOPYON ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
IIIRD NERVE DISORDER ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
IMMUNISATION REACTION ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCISION SITE OEDEMA ( 3 FDA reports)
INCLUSION BODY MYOSITIS ( 3 FDA reports)
INCREASED ANTEROPOSTERIOR CHEST DIAMETER ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INFECTED INSECT BITE ( 3 FDA reports)
INFECTED LYMPHOCELE ( 3 FDA reports)
INFECTED NEOPLASM ( 3 FDA reports)
INFECTION PARASITIC ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INSTILLATION SITE PAIN ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 3 FDA reports)
INTERVERTEBRAL DISC INJURY ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
IODINE UPTAKE INCREASED ( 3 FDA reports)
JAW CYST ( 3 FDA reports)
JEJUNAL ULCER ( 3 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
KETOSIS ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LACRIMAL DISORDER ( 3 FDA reports)
LESION EXCISION ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
LIPOPROTEIN (A) INCREASED ( 3 FDA reports)
LITHOTRIPSY ( 3 FDA reports)
LIVER SCAN ABNORMAL ( 3 FDA reports)
LIVIDITY ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG CREPITATION ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MALIGNANT MELANOMA STAGE I ( 3 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
MENINGIOMA BENIGN ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENISCUS OPERATION ( 3 FDA reports)
METASTASES TO BONE MARROW ( 3 FDA reports)
METASTASES TO HEART ( 3 FDA reports)
METASTASES TO SOFT TISSUE ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MIGRAINE WITHOUT AURA ( 3 FDA reports)
MIXED INCONTINENCE ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MORTON'S NEUROMA ( 3 FDA reports)
MOUTH CYST ( 3 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE HYPERTROPHY ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 3 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
MYELOID LEUKAEMIA ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NEEDLE ISSUE ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEPHROSTOMY ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NITRITOID CRISIS ( 3 FDA reports)
NO ADVERSE REACTION ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
NUCLEATED RED CELLS ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
OPTIC DISCS BLURRED ( 3 FDA reports)
OPTIC NERVE INFARCTION ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
ORAL MUCOSAL DISORDER ( 3 FDA reports)
ORAL NEOPLASM ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
ORTHOSTATIC INTOLERANCE ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 3 FDA reports)
PALLIDOTOMY ( 3 FDA reports)
PANCREATIC ATROPHY ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 3 FDA reports)
PARAPSORIASIS ( 3 FDA reports)
PARASPINAL ABSCESS ( 3 FDA reports)
PAROPHTHALMIA ( 3 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 3 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 3 FDA reports)
PCO2 ABNORMAL ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PELVIC HAEMORRHAGE ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PERICARDITIS INFECTIVE ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PHARYNX DISCOMFORT ( 3 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 3 FDA reports)
PITUITARY CYST ( 3 FDA reports)
PITUITARY INFARCTION ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
POLYOMAVIRUS INTERSTITIAL NEPHRITIS ( 3 FDA reports)
POSTURING ( 3 FDA reports)
POVERTY OF SPEECH ( 3 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 3 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 3 FDA reports)
PRODUCT FORMULATION ISSUE ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PROGESTERONE DECREASED ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 3 FDA reports)
PSEUDOPOLYP ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
RADIATION PNEUMONITIS ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
RATHKE'S CLEFT CYST ( 3 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RECTOSIGMOID CANCER ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 3 FDA reports)
RENAL CYST HAEMORRHAGE ( 3 FDA reports)
RENAL HAEMATOMA ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RENAL HYPERTROPHY ( 3 FDA reports)
RENAL VEIN OCCLUSION ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETINOSCHISIS ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
SALIVARY GLAND CANCER ( 3 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 3 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCROTAL CYST ( 3 FDA reports)
SECONDARY SEQUESTRUM ( 3 FDA reports)
SENILE DEMENTIA ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SEPSIS NEONATAL ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SHIGELLA INFECTION ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SHUNT OCCLUSION ( 3 FDA reports)
SICKLE CELL ANAEMIA ( 3 FDA reports)
SINUS RHYTHM ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN GRAFT INFECTION ( 3 FDA reports)
SLEEP PARALYSIS ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOLILOQUY ( 3 FDA reports)
SOMATIC DELUSION ( 3 FDA reports)
SOMATISATION DISORDER ( 3 FDA reports)
SPINAL CORD INJURY CERVICAL ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPLEEN SCAN ABNORMAL ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLINTER ( 3 FDA reports)
SPLINTER HAEMORRHAGES ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
STICKY SKIN ( 3 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SURGICAL STAPLING ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THROMBOSED VARICOSE VEIN ( 3 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
ULTRASOUND LIVER ( 3 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 3 FDA reports)
UMBILICAL CORD ABNORMALITY ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URETHRAL PAIN ( 3 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 3 FDA reports)
URINE SODIUM ABNORMAL ( 3 FDA reports)
URTICARIA PAPULAR ( 3 FDA reports)
VAGINAL ABSCESS ( 3 FDA reports)
VAGINAL CYST ( 3 FDA reports)
VASCULAR NEOPLASM ( 3 FDA reports)
VASOCONSTRICTION ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENTRICULAR DRAINAGE ( 3 FDA reports)
VIRAEMIA ( 3 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 3 FDA reports)
VOCAL CORD THICKENING ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVOVAGINAL SWELLING ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
X-RAY LIMB ABNORMAL ( 3 FDA reports)
XANTHOPSIA ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
OSTECTOMY ( 2 FDA reports)
OSTEOGENESIS IMPERFECTA ( 2 FDA reports)
OSTEOMA ( 2 FDA reports)
OSTEOMYELITIS DRAINAGE ( 2 FDA reports)
OVARIAN EPITHELIAL CANCER ( 2 FDA reports)
PACHYMENINGITIS ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PANCOAST'S TUMOUR ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PARADOXICAL EMBOLISM ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARATHYROID TUMOUR ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PELVIC ORGAN INJURY ( 2 FDA reports)
PENILE ARTERY OCCLUSION ( 2 FDA reports)
PENILE SIZE REDUCED ( 2 FDA reports)
PERCUSSION TEST ABNORMAL ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PH BODY FLUID ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARMACOPHOBIA ( 2 FDA reports)
PHARYNGITIS BACTERIAL ( 2 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 2 FDA reports)
PHOSPHENES ( 2 FDA reports)
PHOTOSENSITIVE RASH ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PICA ( 2 FDA reports)
PIGMENTATION LIP ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POLYMERASE CHAIN REACTION ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
PORCELAIN GALLBLADDER ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTOPERATIVE HERNIA ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PRESBYACUSIS ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROMOTION OF WOUND HEALING ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTATIC HAEMORRHAGE ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROTEIN C DEFICIENCY ( 2 FDA reports)
PROTHROMBIN TIME ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PUBIC PAIN ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH FOLLICULAR ( 2 FDA reports)
RASH PSORIAFORM ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFLUX LARYNGITIS ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
RENIN DECREASED ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RHINITIS PERENNIAL ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
ROSEOLA ( 2 FDA reports)
SALIVA DISCOLOURATION ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SALIVARY GLAND RESECTION ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SENSORY LEVEL ABNORMAL ( 2 FDA reports)
SERUM FERRITIN ABNORMAL ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SKIN WOUND ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 2 FDA reports)
SPONDYLITIC MYELOPATHY ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 2 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENT-GRAFT MALFUNCTION ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL ABSCESS ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBDURAL EMPYEMA ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUBGALEAL HAEMATOMA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUNCT SYNDROME ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SWEATING FEVER ( 2 FDA reports)
SYMPTOM MASKED ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENOSYNOVITIS STENOSANS ( 2 FDA reports)
TENSILON TEST ABNORMAL ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOANGIITIS OBLITERANS ( 2 FDA reports)
THROMBOEMBOLIC STROKE ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TRANSMYOCARDIAL REVASCULARISATION ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC AMPUTATION ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 2 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TRIGEMINAL NERVE DISORDER ( 2 FDA reports)
TROPICAL SPRUE ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
TYPHOID FEVER ( 2 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UMBILICAL HAEMORRHAGE ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
URETHRAL CANCER ( 2 FDA reports)
URETHRAL DISCHARGE ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
UROGENITAL FISTULA ( 2 FDA reports)
URTICARIA LOCALISED ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UVULITIS ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARICOSE VEIN RUPTURED ( 2 FDA reports)
VASCULAR CAUTERISATION ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VERBAL ABUSE ( 2 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VITREOUS DEGENERATION ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VOMITING IN PREGNANCY ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVAL HAEMORRHAGE ( 2 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENALECTOMY ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 2 FDA reports)
ADRENOMEGALY ( 2 FDA reports)
AEROPHAGIA ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
ALOPECIA TOTALIS ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL FUNGAL INFECTION ( 2 FDA reports)
ANAL NEOPLASM ( 2 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 2 FDA reports)
ANDROGEN DEFICIENCY ( 2 FDA reports)
ANDROGENS DECREASED ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANISOMETROPIA ( 2 FDA reports)
ANTERIOR CHAMBER DISORDER ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC SURGERY ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE DESQUAMATION ( 2 FDA reports)
APPLICATION SITE EXCORIATION ( 2 FDA reports)
APPLICATION SITE INFECTION ( 2 FDA reports)
APPLICATION SITE PERSPIRATION ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 2 FDA reports)
ARTERIOGRAM ABNORMAL ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPERMIA ( 2 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 2 FDA reports)
ATONIC URINARY BLADDER ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASILAR ARTERY THROMBOSIS ( 2 FDA reports)
BASOPHILIA ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER PAPILLOMA ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD AMYLASE ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 2 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD HIV RNA INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BLOOD OESTROGEN INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD UREA ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY HEIGHT INCREASED ( 2 FDA reports)
BONE MARROW NECROSIS ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN STEM ISCHAEMIA ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST DISCOLOURATION ( 2 FDA reports)
BREAST FEEDING ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BREAST PROSTHESIS USER ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
BURSA CALCIFICATION ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC INDEX DECREASED ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC REHABILITATION THERAPY ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 2 FDA reports)
CARDIOPULMONARY BYPASS ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CAROTID SINUS MASSAGE ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
CAUTERY TO NOSE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL ARTERITIS ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CERVICOGENIC HEADACHE ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 2 FDA reports)
CHEMICAL BURN OF SKIN ( 2 FDA reports)
CHLOASMA ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLD AGGLUTININS POSITIVE ( 2 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLON CANCER STAGE II ( 2 FDA reports)
COLONIC ATONY ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONDYLOMA ACUMINATUM ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL CYST ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL DECOMPENSATION ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CREATINE URINE ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CSF CULTURE POSITIVE ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYST DRAINAGE ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTATIN C INCREASED ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEFICIENCY OF BILE SECRETION ( 2 FDA reports)
DELUSION OF REPLACEMENT ( 2 FDA reports)
DENTAL FLUORIDE THERAPY ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATOSIS ( 2 FDA reports)
DETACHED RETINA REPAIR ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DIFFUSE VASCULITIS ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSSOMNIA ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ELDERLY ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENDOCRINE PANCREATIC DISORDER ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 2 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT NORMAL ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EPIPLOIC APPENDAGITIS ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
ERYTHROPLASIA ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
EXERCISE CAPACITY DECREASED ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYELID BLEEDING ( 2 FDA reports)
EYELID EXFOLIATION ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 2 FDA reports)
FAMILIAL RISK FACTOR ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 2 FDA reports)
FLAIL CHEST ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FLUID INTAKE RESTRICTION ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
FOETOR HEPATICUS ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE III ( 2 FDA reports)
FOLLICULAR THYROID CANCER ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FUSOBACTERIUM INFECTION ( 2 FDA reports)
GALLBLADDER ABSCESS ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX PROPHYLAXIS ( 2 FDA reports)
GENITAL DISORDER MALE ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GENITAL TRACT INFLAMMATION ( 2 FDA reports)
GENITALIA EXTERNAL PAINFUL ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL INJURY ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLOMUS TYMPANICUM TUMOUR ( 2 FDA reports)
GRAFT DELAMINATION ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOTYMPANUM ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEART RATE ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC VEIN OCCLUSION ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS B ANTIBODY ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HEPATITIS INFECTIOUS ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HIV ANTIBODY POSITIVE ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 2 FDA reports)
HOMELESS ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERADRENALISM ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCHROMIC ANAEMIA ( 2 FDA reports)
HYPERGLOBULINAEMIA ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPOALDOSTERONISM ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOPHYSITIS ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFECTIVE GLOSSITIS ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INFECTIVE TENOSYNOVITIS ( 2 FDA reports)
INFUSION SITE DISCOLOURATION ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL HAEMATOMA ( 2 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRIDOCELE ( 2 FDA reports)
IVTH NERVE PARALYSIS ( 2 FDA reports)
JEJUNAL ULCER PERFORATION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT PROSTHESIS USER ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KLEPTOMANIA ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL PAPILLOMA ( 2 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 2 FDA reports)
LDL/HDL RATIO ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LIGAMENT LAXITY ( 2 FDA reports)
LIGAMENT PAIN ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUMBAR PUNCTURE ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUMBARISATION ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 2 FDA reports)
LYMPHADENITIS BACTERIAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MANDIBULAR PROSTHESIS USER ( 2 FDA reports)
MASTOID OPERATION ( 2 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 2 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDICAL INDUCTION OF COMA ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO FALLOPIAN TUBE ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
METASTASES TO UTERUS ( 2 FDA reports)
MILIA ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MUCOSAL ATROPHY ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTI-VITAMIN DEFICIENCY ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOCARDIAL BRIDGING ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYOCARDITIS RHEUMATIC ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
NAIL AVULSION ( 2 FDA reports)
NASAL ABSCESS ( 2 FDA reports)
NASAL CAVITY PACKING ( 2 FDA reports)
NASAL NEOPLASM BENIGN ( 2 FDA reports)
NASAL ODOUR ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NEEDLE TRACK MARKS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEISSERIA INFECTION ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 2 FDA reports)
NEUROGENIC SHOCK ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROLOGICAL INFECTION ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NOCTURNAL FEAR ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OMENTUM NEOPLASM ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACROKERATOSIS PARANEOPLASTICA ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA SCARRING ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL PAP SMEAR ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC FISTULA ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANEURYSM ARTERIOVENOUS ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
ARTERECTOMY ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY NORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATLANTOAXIAL INSTABILITY ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATYPICAL FIBROXANTHOMA ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 1 FDA reports)
AVERSION ( 1 FDA reports)
B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER CALCULUS REMOVAL ( 1 FDA reports)
BLADDER CANCER STAGE II ( 1 FDA reports)
BLADDER FIBROSIS ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
BLINDNESS HYSTERICAL ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BROMIDE DECREASED ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD INSULIN ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 1 FDA reports)
BLOOD METHANOL INCREASED ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BOWMAN'S MEMBRANE DISORDER ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST FIBROMA ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
BURSA INJURY ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIFICATION PANCREATIC DUCT ( 1 FDA reports)
CALCIUM IONISED ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANCER GENE CARRIER ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID TUMOUR OF THE CAECUM ( 1 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID PULSE INCREASED ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CAUDAL REGRESSION SYNDROME ( 1 FDA reports)
CD4 LYMPHOCYTES ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CENTRAL VENOUS PRESSURE ABNORMAL ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL CONISATION ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROIDAL EFFUSION ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LEUKAEMIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC PAROXYSMAL HEMICRANIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CILIARY MUSCLE SPASM ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLITORAL ENGORGEMENT ( 1 FDA reports)
CLOSED FRACTURE MANIPULATION ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL EYE NAEVUS ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 1 FDA reports)
CONGENITAL HYPERTHYROIDISM ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL BLEB ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVAL PIGMENTATION ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY NO-REFLOW PHENOMENON ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CULTURE STOOL NEGATIVE ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE PHYSICAL PROPERTY ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISORDER OF GLOBE ( 1 FDA reports)
DISTICHIASIS ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 1 FDA reports)
DOUBLE VESSEL BYPASS GRAFT ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUBIN-JOHNSON SYNDROME ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ( 1 FDA reports)
EATON-LAMBERT SYNDROME ( 1 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLECTOMY ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOMETRITIS DECIDUAL ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENZYME ACTIVITY DECREASED ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID PTOSIS CONGENITAL ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FATTY LIVER ALCOHOLIC ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEAR OF PREGNANCY ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROADENOMA ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE I ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC CANCER STAGE 0 ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL PROLAPSE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GLASGOW COMA SCALE ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLUCAGONOMA ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMOPHILUS SEPSIS ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAIR DYE USER ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART AND LUNG TRANSPLANT ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEMIPELVECTOMY ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC CYST RUPTURED ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTAMINE LEVEL DECREASED ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYDRAEMIA ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOAESTHESIA TEETH ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOSOMNIA ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEAL FISTULA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEUS SPASTIC ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMOBILIZATION PROLONGED ( 1 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE PRURITUS ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INSTILLATION SITE ERYTHEMA ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL FISTULA INFECTION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STOMA SITE BLEEDING ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAOCULAR LENS EXTRACTION ( 1 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNOSTOMY REFASHIONING ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JUVENILE MELANOMA BENIGN ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL GRANULOMA ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL OPERATION ( 1 FDA reports)
LARYNGITIS VIRAL ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOEDEMA ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOEFFLER'S SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT DYSPHAGIA ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MAXILLOFACIAL OPERATION ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECONIUM ILEUS ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDICAL DEVICE ENTRAPMENT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGITIS COCCIDIOIDES ( 1 FDA reports)
MENINGITIS NONINFECTIVE ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MENTALLY LATE DEVELOPER ( 1 FDA reports)
METABOLIC FUNCTION TEST ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METASTASES TO ABDOMINAL WALL ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASES TO THYROID ( 1 FDA reports)
METASTASES TO TRACHEA ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
METHYLMALONIC ACIDURIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICRODACTYLY ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MITOCHONDRIAL ENZYME DEFICIENCY ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOCUTANEOUS FLAP OPERATION ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIFOCAL MICRONODULAR PNEUMOCYTE HYPERPLASIA ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MYECTOMY ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAEVUS CELL NAEVUS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL-PATELLA SYNDROME ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROSTIMULATOR IMPLANTATION ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NOCTURNAL EMISSION ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING THORACIC ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO DUST ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTRADIOL DECREASED ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSSICLE DISORDER ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC CARCINOMA NON-RESECTABLE ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARADOXICAL PRESSOR RESPONSE ( 1 FDA reports)
PARAGANGLION NEOPLASM ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARATHYROID HAEMORRHAGE ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PARVOVIRUS B19 TEST ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FLOOR REPAIR ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC KIDNEY ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE NEOPLASM ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIODONTAL DESTRUCTION ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL ADHESIONS DIVISION ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERIUMBILICAL ABSCESS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHARYNGEAL RECONSTRUCTION ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHYSICAL EXAMINATION NORMAL ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASMINOGEN ACTIVATOR INHIBITOR INCREASED ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCYSTIC LIVER DISEASE ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORPHYROMONAS INFECTION ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DIZZINESS ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRIMARY CEREBELLAR DEGENERATION ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PROGESTERONE ABNORMAL ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROMISCUITY ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOCHOLINESTERASE DEFICIENCY ( 1 FDA reports)
PSEUDOENDOPHTHALMITIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY VEIN STENOSIS ( 1 FDA reports)
PULSE PRESSURE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
PYRUVATE KINASE INCREASED ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION THYROIDITIS ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
REBOUND TACHYCARDIA ( 1 FDA reports)
RED BLOOD CELL ACANTHOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY DISSECTION ( 1 FDA reports)
RENAL ARTERY HYPERPLASIA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL LIPOMATOSIS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPITE CARE ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL FIBROSIS ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL IMPLANT ( 1 FDA reports)
RETINAL MICROANEURYSMS ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL TOXICITY ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL PIGMENTATION ( 1 FDA reports)
SCLEROMALACIA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEBACEOUS GLAND DISORDER ( 1 FDA reports)
SEBACEOUS HYPERPLASIA ( 1 FDA reports)
SEBACEOUS NAEVUS ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SELECTIVE IGM IMMUNODEFICIENCY ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEMEN VOLUME ABNORMAL ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SEX HORMONE BINDING GLOBULIN DECREASED ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINUS PERFORATION ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN GRAFT REJECTION ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL CELL LUNG CANCER LIMITED STAGE ( 1 FDA reports)
SMALL INTESTINAL BACTERIAL OVERGROWTH ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SPERM COUNT ZERO ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL LIGAMENT OPERATION ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY CONGENITAL ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STENT-GRAFT ENDOLEAK ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCLAVIAN ARTERY EMBOLISM ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUBTOTAL HYSTERECTOMY ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERFICIAL SIDEROSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TENDON REPAIR ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THALASSAEMIA ALPHA ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOENDARTERECTOMY ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYMOMA MALIGNANT ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE FREE ABNORMAL ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH AVULSION ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
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TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRABECULOPLASTY ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
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TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFUSION WITH INCOMPATIBLE BLOOD ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE FREE ABNORMAL ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TRYPTASE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYMPANIC MEMBRANE SCARRING ( 1 FDA reports)
UBIQUINONE DECREASED ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND CHEST ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URETERIC CANCER RECURRENT ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC FISTULA ( 1 FDA reports)
URETERIC INJURY ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETHRAL PAPILLOMA ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URINARY BLADDER ATROPHY ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINE AMINO ACID LEVEL INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COPPER DECREASED ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE PHOSPHATE DECREASED ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO DECREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE MALPOSITION ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
UTEROVAGINAL PROLAPSE ( 1 FDA reports)
UVULAR SPASM ( 1 FDA reports)
UVULOPLASTY ( 1 FDA reports)
VAGINAL CANCER STAGE 0 ( 1 FDA reports)
VAGINAL CANCER STAGE III ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VENIPUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VENOUS OPERATION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR WALL THICKENING ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
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VIITH NERVE INJURY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
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VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISION CORRECTION OPERATION ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
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VITREOUS ADHESIONS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
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WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
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X-RAY ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
YELLOW NAIL SYNDROME ( 1 FDA reports)

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