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

DYSPNOEA ( 4321 FDA reports)
NAUSEA ( 4309 FDA reports)
DIARRHOEA ( 3884 FDA reports)
VOMITING ( 3832 FDA reports)
PAIN ( 3409 FDA reports)
PYREXIA ( 3235 FDA reports)
FATIGUE ( 3032 FDA reports)
ANAEMIA ( 2915 FDA reports)
DIZZINESS ( 2836 FDA reports)
ASTHENIA ( 2796 FDA reports)
DRUG INEFFECTIVE ( 2771 FDA reports)
PNEUMONIA ( 2722 FDA reports)
FALL ( 2689 FDA reports)
HEADACHE ( 2564 FDA reports)
DRUG INTERACTION ( 2503 FDA reports)
RENAL FAILURE ACUTE ( 2423 FDA reports)
MALAISE ( 2308 FDA reports)
ARTHRALGIA ( 2273 FDA reports)
ABDOMINAL PAIN ( 2269 FDA reports)
OEDEMA PERIPHERAL ( 2129 FDA reports)
HYPOTENSION ( 2049 FDA reports)
PAIN IN EXTREMITY ( 2028 FDA reports)
ANXIETY ( 2027 FDA reports)
CHEST PAIN ( 1967 FDA reports)
DEHYDRATION ( 1955 FDA reports)
WEIGHT DECREASED ( 1932 FDA reports)
HYPERTENSION ( 1891 FDA reports)
CONFUSIONAL STATE ( 1853 FDA reports)
BACK PAIN ( 1823 FDA reports)
RENAL FAILURE ( 1753 FDA reports)
THROMBOCYTOPENIA ( 1689 FDA reports)
URINARY TRACT INFECTION ( 1666 FDA reports)
COUGH ( 1599 FDA reports)
DEPRESSION ( 1571 FDA reports)
CONSTIPATION ( 1567 FDA reports)
PRURITUS ( 1556 FDA reports)
HAEMOGLOBIN DECREASED ( 1480 FDA reports)
DECREASED APPETITE ( 1478 FDA reports)
ABDOMINAL PAIN UPPER ( 1476 FDA reports)
RASH ( 1467 FDA reports)
DEATH ( 1429 FDA reports)
INSOMNIA ( 1424 FDA reports)
SEPSIS ( 1421 FDA reports)
CONDITION AGGRAVATED ( 1411 FDA reports)
MYOCARDIAL INFARCTION ( 1312 FDA reports)
ATRIAL FIBRILLATION ( 1300 FDA reports)
SOMNOLENCE ( 1281 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1274 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1260 FDA reports)
TREMOR ( 1248 FDA reports)
CONVULSION ( 1219 FDA reports)
MYALGIA ( 1204 FDA reports)
NEUTROPENIA ( 1199 FDA reports)
PARAESTHESIA ( 1173 FDA reports)
GAIT DISTURBANCE ( 1151 FDA reports)
PULMONARY EMBOLISM ( 1125 FDA reports)
WEIGHT INCREASED ( 1102 FDA reports)
RESPIRATORY FAILURE ( 1094 FDA reports)
HYPONATRAEMIA ( 1088 FDA reports)
BLOOD CREATININE INCREASED ( 1086 FDA reports)
ERYTHEMA ( 1068 FDA reports)
SYNCOPE ( 1065 FDA reports)
MUSCLE SPASMS ( 1063 FDA reports)
LOSS OF CONSCIOUSNESS ( 1046 FDA reports)
DYSPEPSIA ( 1041 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1037 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1016 FDA reports)
MUSCULAR WEAKNESS ( 1007 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1004 FDA reports)
HYPOAESTHESIA ( 1003 FDA reports)
HYPERHIDROSIS ( 977 FDA reports)
PLATELET COUNT DECREASED ( 975 FDA reports)
PLEURAL EFFUSION ( 973 FDA reports)
DYSPHAGIA ( 964 FDA reports)
HYPOMAGNESAEMIA ( 925 FDA reports)
BLOOD GLUCOSE INCREASED ( 923 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 910 FDA reports)
BLOOD PRESSURE INCREASED ( 904 FDA reports)
FEELING ABNORMAL ( 902 FDA reports)
INFECTION ( 895 FDA reports)
TACHYCARDIA ( 841 FDA reports)
HYPOKALAEMIA ( 840 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 830 FDA reports)
INJURY ( 827 FDA reports)
DEEP VEIN THROMBOSIS ( 820 FDA reports)
VISION BLURRED ( 812 FDA reports)
PANCYTOPENIA ( 808 FDA reports)
HYPOCALCAEMIA ( 798 FDA reports)
CHILLS ( 796 FDA reports)
FLUSHING ( 783 FDA reports)
FEBRILE NEUTROPENIA ( 778 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 771 FDA reports)
PALPITATIONS ( 769 FDA reports)
CARDIAC ARREST ( 766 FDA reports)
GASTRITIS ( 762 FDA reports)
AGITATION ( 759 FDA reports)
CARDIAC FAILURE ( 758 FDA reports)
RENAL IMPAIRMENT ( 756 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 741 FDA reports)
CELLULITIS ( 740 FDA reports)
HYPERSENSITIVITY ( 732 FDA reports)
HYPERKALAEMIA ( 697 FDA reports)
CHOLELITHIASIS ( 696 FDA reports)
DIABETES MELLITUS ( 692 FDA reports)
CONTUSION ( 689 FDA reports)
ABDOMINAL DISTENSION ( 677 FDA reports)
SEPTIC SHOCK ( 666 FDA reports)
RHABDOMYOLYSIS ( 662 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 662 FDA reports)
OSTEOARTHRITIS ( 654 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 653 FDA reports)
MULTI-ORGAN FAILURE ( 649 FDA reports)
BRADYCARDIA ( 644 FDA reports)
CHEST DISCOMFORT ( 635 FDA reports)
BALANCE DISORDER ( 629 FDA reports)
HYPOGLYCAEMIA ( 625 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 620 FDA reports)
OSTEONECROSIS OF JAW ( 617 FDA reports)
LEUKOPENIA ( 616 FDA reports)
OVERDOSE ( 614 FDA reports)
NEUROPATHY PERIPHERAL ( 611 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 603 FDA reports)
BRONCHITIS ( 603 FDA reports)
DRUG DOSE OMISSION ( 600 FDA reports)
ARTHRITIS ( 598 FDA reports)
ABDOMINAL DISCOMFORT ( 597 FDA reports)
OEDEMA ( 595 FDA reports)
MEMORY IMPAIRMENT ( 591 FDA reports)
RECTAL HAEMORRHAGE ( 585 FDA reports)
BONE PAIN ( 584 FDA reports)
DISEASE PROGRESSION ( 583 FDA reports)
HAEMORRHAGE ( 581 FDA reports)
EPISTAXIS ( 575 FDA reports)
INTERSTITIAL LUNG DISEASE ( 575 FDA reports)
JOINT SWELLING ( 568 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 561 FDA reports)
URTICARIA ( 559 FDA reports)
HEART RATE INCREASED ( 555 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 547 FDA reports)
SWELLING ( 547 FDA reports)
PULMONARY OEDEMA ( 543 FDA reports)
MUSCULOSKELETAL PAIN ( 541 FDA reports)
HALLUCINATION ( 538 FDA reports)
DISORIENTATION ( 534 FDA reports)
BLOOD PRESSURE DECREASED ( 533 FDA reports)
BLOOD BILIRUBIN INCREASED ( 530 FDA reports)
DRY MOUTH ( 528 FDA reports)
INJECTION SITE PAIN ( 527 FDA reports)
ARRHYTHMIA ( 520 FDA reports)
SINUSITIS ( 519 FDA reports)
BONE DISORDER ( 515 FDA reports)
LETHARGY ( 515 FDA reports)
NECK PAIN ( 514 FDA reports)
SWELLING FACE ( 510 FDA reports)
HAEMATEMESIS ( 507 FDA reports)
PANCREATITIS ( 505 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 500 FDA reports)
RHEUMATOID ARTHRITIS ( 495 FDA reports)
CATARACT ( 492 FDA reports)
CORONARY ARTERY DISEASE ( 492 FDA reports)
ASTHMA ( 488 FDA reports)
LIVER DISORDER ( 482 FDA reports)
EMOTIONAL DISTRESS ( 481 FDA reports)
HAEMATURIA ( 473 FDA reports)
RENAL FAILURE CHRONIC ( 467 FDA reports)
BLOOD UREA INCREASED ( 464 FDA reports)
JAUNDICE ( 463 FDA reports)
HAEMATOCRIT DECREASED ( 462 FDA reports)
INFLAMMATION ( 461 FDA reports)
OROPHARYNGEAL PAIN ( 458 FDA reports)
ALOPECIA ( 457 FDA reports)
HEPATIC FAILURE ( 457 FDA reports)
ANOREXIA ( 451 FDA reports)
STAPHYLOCOCCAL INFECTION ( 444 FDA reports)
VISUAL IMPAIRMENT ( 442 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 442 FDA reports)
ASCITES ( 440 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 437 FDA reports)
SUICIDAL IDEATION ( 434 FDA reports)
MELAENA ( 431 FDA reports)
CARDIAC DISORDER ( 431 FDA reports)
HAEMORRHOIDS ( 428 FDA reports)
HIATUS HERNIA ( 428 FDA reports)
THROMBOSIS ( 423 FDA reports)
SPEECH DISORDER ( 422 FDA reports)
HYPOXIA ( 420 FDA reports)
HEPATITIS ( 416 FDA reports)
MENTAL STATUS CHANGES ( 416 FDA reports)
MULTIPLE MYELOMA ( 415 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 415 FDA reports)
PAIN IN JAW ( 414 FDA reports)
ATELECTASIS ( 412 FDA reports)
OFF LABEL USE ( 410 FDA reports)
COMA ( 407 FDA reports)
FLATULENCE ( 404 FDA reports)
AMNESIA ( 401 FDA reports)
BLOOD SODIUM DECREASED ( 401 FDA reports)
IMPAIRED HEALING ( 401 FDA reports)
NEOPLASM MALIGNANT ( 399 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 399 FDA reports)
ANGINA PECTORIS ( 397 FDA reports)
LUNG DISORDER ( 397 FDA reports)
NASOPHARYNGITIS ( 396 FDA reports)
CARDIO-RESPIRATORY ARREST ( 395 FDA reports)
STOMATITIS ( 393 FDA reports)
FEELING HOT ( 391 FDA reports)
URINARY RETENTION ( 390 FDA reports)
DYSARTHRIA ( 389 FDA reports)
BURNING SENSATION ( 387 FDA reports)
HYPERGLYCAEMIA ( 386 FDA reports)
MUCOSAL INFLAMMATION ( 385 FDA reports)
LYMPHADENOPATHY ( 376 FDA reports)
SPINAL OSTEOARTHRITIS ( 375 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 374 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 368 FDA reports)
OSTEONECROSIS ( 367 FDA reports)
NERVOUSNESS ( 365 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 364 FDA reports)
FEMUR FRACTURE ( 362 FDA reports)
BLOOD POTASSIUM DECREASED ( 361 FDA reports)
OSTEOPOROSIS ( 361 FDA reports)
DELIRIUM ( 360 FDA reports)
DYSGEUSIA ( 360 FDA reports)
DRUG HYPERSENSITIVITY ( 359 FDA reports)
HERPES ZOSTER ( 359 FDA reports)
INCORRECT DOSE ADMINISTERED ( 357 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 357 FDA reports)
DYSPNOEA EXERTIONAL ( 353 FDA reports)
HAEMOPTYSIS ( 352 FDA reports)
HEPATIC ENZYME INCREASED ( 352 FDA reports)
MITRAL VALVE INCOMPETENCE ( 351 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 345 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 344 FDA reports)
NEUTROPHIL COUNT DECREASED ( 344 FDA reports)
OSTEOMYELITIS ( 342 FDA reports)
CARDIOMEGALY ( 342 FDA reports)
HAEMATOCHEZIA ( 338 FDA reports)
BLISTER ( 337 FDA reports)
VERTIGO ( 334 FDA reports)
NEPHROLITHIASIS ( 333 FDA reports)
CHOLESTASIS ( 332 FDA reports)
GASTRIC ULCER ( 332 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 331 FDA reports)
LUNG INFILTRATION ( 331 FDA reports)
HYPERLIPIDAEMIA ( 330 FDA reports)
STEVENS-JOHNSON SYNDROME ( 330 FDA reports)
ARTHROPATHY ( 329 FDA reports)
OXYGEN SATURATION DECREASED ( 327 FDA reports)
RESPIRATORY DISTRESS ( 327 FDA reports)
METABOLIC ACIDOSIS ( 326 FDA reports)
INFLUENZA LIKE ILLNESS ( 326 FDA reports)
DYSKINESIA ( 325 FDA reports)
DRUG TOXICITY ( 324 FDA reports)
DYSURIA ( 323 FDA reports)
AGGRESSION ( 322 FDA reports)
DYSPHONIA ( 322 FDA reports)
HYPOPHAGIA ( 322 FDA reports)
ANHEDONIA ( 318 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 317 FDA reports)
PALLOR ( 317 FDA reports)
RASH PRURITIC ( 317 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 316 FDA reports)
GASTROINTESTINAL DISORDER ( 316 FDA reports)
COLITIS ( 312 FDA reports)
TETANY ( 311 FDA reports)
ABASIA ( 309 FDA reports)
LEUKOCYTOSIS ( 309 FDA reports)
HAEMODIALYSIS ( 307 FDA reports)
PRODUCT QUALITY ISSUE ( 307 FDA reports)
DRUG EFFECT DECREASED ( 306 FDA reports)
HYPOTHYROIDISM ( 306 FDA reports)
PRODUCTIVE COUGH ( 305 FDA reports)
SKIN EXFOLIATION ( 302 FDA reports)
CROHN'S DISEASE ( 302 FDA reports)
MOBILITY DECREASED ( 301 FDA reports)
VISUAL ACUITY REDUCED ( 301 FDA reports)
SLEEP DISORDER ( 300 FDA reports)
SWOLLEN TONGUE ( 300 FDA reports)
RENAL DISORDER ( 299 FDA reports)
HEPATIC STEATOSIS ( 299 FDA reports)
INFLUENZA ( 298 FDA reports)
CHOLECYSTITIS CHRONIC ( 296 FDA reports)
PULMONARY HYPERTENSION ( 296 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 295 FDA reports)
URINARY INCONTINENCE ( 295 FDA reports)
ANGIOEDEMA ( 295 FDA reports)
INTESTINAL OBSTRUCTION ( 295 FDA reports)
OSTEOPENIA ( 294 FDA reports)
ABNORMAL BEHAVIOUR ( 292 FDA reports)
CHOLECYSTITIS ( 290 FDA reports)
GALLBLADDER DISORDER ( 290 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 290 FDA reports)
OESOPHAGITIS ( 289 FDA reports)
PULMONARY FIBROSIS ( 289 FDA reports)
RESTLESSNESS ( 289 FDA reports)
TINNITUS ( 287 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 287 FDA reports)
MOUTH ULCERATION ( 285 FDA reports)
RIB FRACTURE ( 285 FDA reports)
STRESS ( 284 FDA reports)
RASH ERYTHEMATOUS ( 283 FDA reports)
NEUTROPHIL COUNT INCREASED ( 282 FDA reports)
WHEEZING ( 282 FDA reports)
ENCEPHALOPATHY ( 280 FDA reports)
HAEMATOMA ( 280 FDA reports)
CIRCULATORY COLLAPSE ( 278 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 277 FDA reports)
CYTOLYTIC HEPATITIS ( 273 FDA reports)
EYE PAIN ( 273 FDA reports)
DIVERTICULUM ( 271 FDA reports)
CEREBRAL HAEMORRHAGE ( 269 FDA reports)
BRONCHOPNEUMONIA ( 268 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 268 FDA reports)
MIGRAINE ( 268 FDA reports)
INJECTION SITE ERYTHEMA ( 266 FDA reports)
METASTASES TO BONE ( 264 FDA reports)
SKIN DISCOLOURATION ( 263 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 263 FDA reports)
GASTROENTERITIS ( 263 FDA reports)
BLOOD POTASSIUM INCREASED ( 260 FDA reports)
TOOTH EXTRACTION ( 259 FDA reports)
PNEUMONITIS ( 256 FDA reports)
HIP FRACTURE ( 256 FDA reports)
TOOTH LOSS ( 253 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 252 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 252 FDA reports)
PANCREATITIS ACUTE ( 251 FDA reports)
RASH MACULO-PAPULAR ( 251 FDA reports)
SKIN ULCER ( 251 FDA reports)
SUICIDE ATTEMPT ( 251 FDA reports)
BLOOD CALCIUM DECREASED ( 249 FDA reports)
DENTAL CARIES ( 248 FDA reports)
ECZEMA ( 248 FDA reports)
MYOCARDIAL ISCHAEMIA ( 248 FDA reports)
UNRESPONSIVE TO STIMULI ( 247 FDA reports)
SHOCK ( 246 FDA reports)
DISTURBANCE IN ATTENTION ( 246 FDA reports)
ANAPHYLACTIC REACTION ( 245 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 245 FDA reports)
PSORIASIS ( 243 FDA reports)
TREATMENT NONCOMPLIANCE ( 243 FDA reports)
RENAL CYST ( 242 FDA reports)
CEREBRAL INFARCTION ( 242 FDA reports)
DIVERTICULITIS ( 241 FDA reports)
ECONOMIC PROBLEM ( 241 FDA reports)
POLLAKIURIA ( 240 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 240 FDA reports)
MEDICATION ERROR ( 239 FDA reports)
SINUS TACHYCARDIA ( 239 FDA reports)
PSYCHOTIC DISORDER ( 238 FDA reports)
ORAL PAIN ( 236 FDA reports)
ROAD TRAFFIC ACCIDENT ( 236 FDA reports)
TRANSAMINASES INCREASED ( 235 FDA reports)
BLOOD ALBUMIN DECREASED ( 235 FDA reports)
EPILEPSY ( 235 FDA reports)
FACE OEDEMA ( 235 FDA reports)
IRRITABILITY ( 235 FDA reports)
PERICARDIAL EFFUSION ( 233 FDA reports)
ROTATOR CUFF SYNDROME ( 232 FDA reports)
COAGULOPATHY ( 231 FDA reports)
BLOOD GLUCOSE DECREASED ( 230 FDA reports)
HYPERCHOLESTEROLAEMIA ( 230 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 228 FDA reports)
LACTIC ACIDOSIS ( 228 FDA reports)
MENTAL DISORDER ( 228 FDA reports)
EOSINOPHILIA ( 227 FDA reports)
CYSTITIS ( 226 FDA reports)
SKIN LESION ( 226 FDA reports)
NIGHTMARE ( 224 FDA reports)
UNEVALUABLE EVENT ( 224 FDA reports)
HEPATOMEGALY ( 224 FDA reports)
BONE MARROW FAILURE ( 223 FDA reports)
INFUSION RELATED REACTION ( 223 FDA reports)
NEURALGIA ( 223 FDA reports)
SURGERY ( 223 FDA reports)
SLEEP APNOEA SYNDROME ( 222 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 222 FDA reports)
ORTHOSTATIC HYPOTENSION ( 221 FDA reports)
GRAND MAL CONVULSION ( 221 FDA reports)
ILL-DEFINED DISORDER ( 221 FDA reports)
PULMONARY CONGESTION ( 220 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 220 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 219 FDA reports)
APHASIA ( 219 FDA reports)
HALLUCINATION, VISUAL ( 218 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 217 FDA reports)
AGRANULOCYTOSIS ( 217 FDA reports)
HOT FLUSH ( 217 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 217 FDA reports)
TYPE 2 DIABETES MELLITUS ( 216 FDA reports)
DRY SKIN ( 216 FDA reports)
HEAD INJURY ( 216 FDA reports)
DIPLOPIA ( 215 FDA reports)
RESPIRATORY TRACT INFECTION ( 215 FDA reports)
DRUG LEVEL INCREASED ( 214 FDA reports)
FUNGAL INFECTION ( 214 FDA reports)
GASTRIC DISORDER ( 214 FDA reports)
HEART RATE IRREGULAR ( 214 FDA reports)
RASH GENERALISED ( 213 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 212 FDA reports)
LIP SWELLING ( 212 FDA reports)
BURSITIS ( 211 FDA reports)
MOVEMENT DISORDER ( 211 FDA reports)
POST PROCEDURAL COMPLICATION ( 211 FDA reports)
VENTRICULAR TACHYCARDIA ( 210 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 210 FDA reports)
RASH MACULAR ( 209 FDA reports)
EMOTIONAL DISORDER ( 208 FDA reports)
PERITONITIS ( 207 FDA reports)
MALNUTRITION ( 206 FDA reports)
EAR PAIN ( 206 FDA reports)
ABNORMAL DREAMS ( 205 FDA reports)
DEPRESSED MOOD ( 205 FDA reports)
INTENTIONAL DRUG MISUSE ( 205 FDA reports)
NASAL CONGESTION ( 205 FDA reports)
VASCULITIS ( 205 FDA reports)
PROTHROMBIN TIME PROLONGED ( 202 FDA reports)
VIRAL INFECTION ( 202 FDA reports)
CYANOSIS ( 202 FDA reports)
HEPATOTOXICITY ( 202 FDA reports)
CHROMATURIA ( 201 FDA reports)
HEPATIC ENCEPHALOPATHY ( 201 FDA reports)
FLUID RETENTION ( 200 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 200 FDA reports)
TOOTHACHE ( 200 FDA reports)
NEUTROPENIC SEPSIS ( 199 FDA reports)
PNEUMONIA ASPIRATION ( 199 FDA reports)
TOOTH DISORDER ( 199 FDA reports)
INJECTION SITE HAEMATOMA ( 199 FDA reports)
INJECTION SITE HAEMORRHAGE ( 199 FDA reports)
EATING DISORDER ( 198 FDA reports)
LUNG INFECTION ( 198 FDA reports)
ARTERIOSCLEROSIS ( 197 FDA reports)
CANDIDIASIS ( 197 FDA reports)
CARDIOMYOPATHY ( 197 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 197 FDA reports)
RHINORRHOEA ( 197 FDA reports)
ORAL CANDIDIASIS ( 195 FDA reports)
BACTERIAL INFECTION ( 195 FDA reports)
DIALYSIS ( 195 FDA reports)
DRUG ERUPTION ( 195 FDA reports)
SUDDEN DEATH ( 194 FDA reports)
RESPIRATORY DISORDER ( 193 FDA reports)
BONE LESION ( 193 FDA reports)
CORONARY ARTERY OCCLUSION ( 193 FDA reports)
COMPLETED SUICIDE ( 192 FDA reports)
FEAR ( 192 FDA reports)
GINGIVAL BLEEDING ( 192 FDA reports)
SCAR ( 192 FDA reports)
OBESITY ( 191 FDA reports)
LUNG NEOPLASM ( 191 FDA reports)
DYSSTASIA ( 190 FDA reports)
NIGHT SWEATS ( 190 FDA reports)
NO THERAPEUTIC RESPONSE ( 189 FDA reports)
SEDATION ( 189 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 188 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 188 FDA reports)
DRY EYE ( 188 FDA reports)
FLUID OVERLOAD ( 188 FDA reports)
METASTASES TO LIVER ( 187 FDA reports)
PANIC ATTACK ( 187 FDA reports)
PLATELET COUNT INCREASED ( 187 FDA reports)
PRESYNCOPE ( 187 FDA reports)
DEFORMITY ( 186 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 185 FDA reports)
COGNITIVE DISORDER ( 185 FDA reports)
HEART RATE DECREASED ( 185 FDA reports)
FEELING COLD ( 184 FDA reports)
NERVOUS SYSTEM DISORDER ( 184 FDA reports)
PETECHIAE ( 184 FDA reports)
BODY TEMPERATURE INCREASED ( 183 FDA reports)
BREAST CANCER ( 181 FDA reports)
PNEUMOTHORAX ( 181 FDA reports)
RESPIRATORY ARREST ( 181 FDA reports)
COORDINATION ABNORMAL ( 179 FDA reports)
FIBROMYALGIA ( 179 FDA reports)
SEROTONIN SYNDROME ( 178 FDA reports)
PROTEINURIA ( 177 FDA reports)
ABSCESS ( 177 FDA reports)
PRURITUS GENERALISED ( 176 FDA reports)
ULCER ( 176 FDA reports)
MYOCLONUS ( 175 FDA reports)
ATAXIA ( 175 FDA reports)
BASAL CELL CARCINOMA ( 174 FDA reports)
BLINDNESS ( 174 FDA reports)
DUODENAL ULCER ( 174 FDA reports)
EJECTION FRACTION DECREASED ( 174 FDA reports)
GOUT ( 174 FDA reports)
RENAL TUBULAR NECROSIS ( 174 FDA reports)
DECREASED INTEREST ( 172 FDA reports)
HYDRONEPHROSIS ( 171 FDA reports)
GENERALISED OEDEMA ( 170 FDA reports)
ILEUS ( 170 FDA reports)
ORAL DISORDER ( 170 FDA reports)
NEOPLASM PROGRESSION ( 169 FDA reports)
BRONCHOSPASM ( 169 FDA reports)
DRUG INTOLERANCE ( 169 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 168 FDA reports)
CEREBRAL ISCHAEMIA ( 168 FDA reports)
EMPHYSEMA ( 168 FDA reports)
FAECES DISCOLOURED ( 168 FDA reports)
HYPOPHOSPHATAEMIA ( 168 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 168 FDA reports)
HEMIPARESIS ( 167 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 167 FDA reports)
LYMPHOPENIA ( 166 FDA reports)
MYELODYSPLASTIC SYNDROME ( 166 FDA reports)
VENTRICULAR FIBRILLATION ( 166 FDA reports)
TOOTH ABSCESS ( 165 FDA reports)
DISEASE RECURRENCE ( 165 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 165 FDA reports)
SPINAL COLUMN STENOSIS ( 164 FDA reports)
URINE OUTPUT DECREASED ( 164 FDA reports)
THROAT IRRITATION ( 163 FDA reports)
EXOSTOSIS ( 163 FDA reports)
HEPATIC CIRRHOSIS ( 163 FDA reports)
COLONIC POLYP ( 162 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 162 FDA reports)
HYPOVOLAEMIA ( 162 FDA reports)
SKIN DISORDER ( 162 FDA reports)
OSTEITIS ( 161 FDA reports)
ANURIA ( 160 FDA reports)
ASPIRATION ( 160 FDA reports)
IRON DEFICIENCY ANAEMIA ( 160 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 160 FDA reports)
JOINT INJURY ( 158 FDA reports)
DISCOMFORT ( 157 FDA reports)
LUNG NEOPLASM MALIGNANT ( 157 FDA reports)
DEVICE RELATED INFECTION ( 156 FDA reports)
HYPERCALCAEMIA ( 156 FDA reports)
OLIGURIA ( 156 FDA reports)
SPINAL FRACTURE ( 156 FDA reports)
ATRIAL FLUTTER ( 155 FDA reports)
BRAIN OEDEMA ( 155 FDA reports)
JOINT EFFUSION ( 155 FDA reports)
DEMENTIA ( 154 FDA reports)
FAECAL INCONTINENCE ( 154 FDA reports)
PURPURA ( 154 FDA reports)
SPLENOMEGALY ( 154 FDA reports)
ACUTE RESPIRATORY FAILURE ( 153 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 153 FDA reports)
ANGINA UNSTABLE ( 152 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 152 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 152 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 151 FDA reports)
DEAFNESS ( 150 FDA reports)
PSEUDOMONAS INFECTION ( 150 FDA reports)
SPINAL COMPRESSION FRACTURE ( 150 FDA reports)
ANGER ( 149 FDA reports)
HYPERSOMNIA ( 149 FDA reports)
CARDIOGENIC SHOCK ( 148 FDA reports)
HEPATITIS CHOLESTATIC ( 148 FDA reports)
HYPOAESTHESIA ORAL ( 147 FDA reports)
PATHOLOGICAL FRACTURE ( 147 FDA reports)
PHARYNGITIS ( 147 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 147 FDA reports)
RETCHING ( 147 FDA reports)
SINUS BRADYCARDIA ( 147 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 147 FDA reports)
MYOSITIS ( 146 FDA reports)
ACCIDENTAL OVERDOSE ( 146 FDA reports)
DRUG ADMINISTRATION ERROR ( 146 FDA reports)
ESCHERICHIA INFECTION ( 146 FDA reports)
ERECTILE DYSFUNCTION ( 145 FDA reports)
INJECTION SITE REACTION ( 145 FDA reports)
KNEE ARTHROPLASTY ( 145 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 145 FDA reports)
TOXIC SKIN ERUPTION ( 145 FDA reports)
CRYING ( 144 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 143 FDA reports)
HYPOALBUMINAEMIA ( 143 FDA reports)
TACHYPNOEA ( 143 FDA reports)
MICTURITION URGENCY ( 142 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 142 FDA reports)
TENDONITIS ( 142 FDA reports)
TOOTH FRACTURE ( 142 FDA reports)
EYE SWELLING ( 142 FDA reports)
INCONTINENCE ( 142 FDA reports)
AZOTAEMIA ( 141 FDA reports)
FOOT DEFORMITY ( 141 FDA reports)
SCIATICA ( 141 FDA reports)
MULTIPLE INJURIES ( 140 FDA reports)
TUBERCULOSIS ( 140 FDA reports)
EYE DISORDER ( 140 FDA reports)
HAEMOLYTIC ANAEMIA ( 140 FDA reports)
LYMPHOMA ( 140 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 139 FDA reports)
SPINAL DISORDER ( 139 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 138 FDA reports)
SKIN BURNING SENSATION ( 138 FDA reports)
TOOTH INFECTION ( 138 FDA reports)
LACERATION ( 138 FDA reports)
PHARYNGEAL OEDEMA ( 137 FDA reports)
SUBDURAL HAEMATOMA ( 137 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 136 FDA reports)
COMPRESSION FRACTURE ( 136 FDA reports)
ISCHAEMIC STROKE ( 136 FDA reports)
ADVERSE EVENT ( 135 FDA reports)
GASTRITIS EROSIVE ( 135 FDA reports)
HEPATITIS C ( 135 FDA reports)
HYPERTHYROIDISM ( 135 FDA reports)
CARDIOVASCULAR DISORDER ( 134 FDA reports)
CARPAL TUNNEL SYNDROME ( 134 FDA reports)
CONJUNCTIVITIS ( 134 FDA reports)
CHOLECYSTECTOMY ( 133 FDA reports)
HOSPITALISATION ( 133 FDA reports)
LIMB INJURY ( 133 FDA reports)
NEPHRITIS INTERSTITIAL ( 133 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 133 FDA reports)
SCOLIOSIS ( 133 FDA reports)
SENSORY LOSS ( 133 FDA reports)
CARDIAC MURMUR ( 132 FDA reports)
GLAUCOMA ( 132 FDA reports)
ERUCTATION ( 131 FDA reports)
CLOSTRIDIAL INFECTION ( 130 FDA reports)
ELECTROLYTE IMBALANCE ( 130 FDA reports)
INTESTINAL PERFORATION ( 130 FDA reports)
UPPER LIMB FRACTURE ( 130 FDA reports)
MENTAL IMPAIRMENT ( 129 FDA reports)
PROSTATE CANCER ( 129 FDA reports)
TARDIVE DYSKINESIA ( 129 FDA reports)
FISTULA ( 129 FDA reports)
ABDOMINAL PAIN LOWER ( 128 FDA reports)
LOCALISED INFECTION ( 128 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 128 FDA reports)
RASH PAPULAR ( 128 FDA reports)
MOOD SWINGS ( 127 FDA reports)
PEPTIC ULCER ( 127 FDA reports)
ACUTE CORONARY SYNDROME ( 127 FDA reports)
BARRETT'S OESOPHAGUS ( 127 FDA reports)
COLON CANCER ( 127 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 126 FDA reports)
ALVEOLITIS ( 126 FDA reports)
CORONARY ARTERY STENOSIS ( 126 FDA reports)
DISABILITY ( 126 FDA reports)
FACIAL PAIN ( 126 FDA reports)
THYROID DISORDER ( 126 FDA reports)
PARAESTHESIA ORAL ( 125 FDA reports)
TENDON RUPTURE ( 125 FDA reports)
AGEUSIA ( 125 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 125 FDA reports)
CHOLECYSTITIS ACUTE ( 125 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 125 FDA reports)
METASTASES TO LUNG ( 124 FDA reports)
NECROSIS ( 123 FDA reports)
RALES ( 123 FDA reports)
WOUND INFECTION ( 123 FDA reports)
APLASIA PURE RED CELL ( 123 FDA reports)
BACTERAEMIA ( 123 FDA reports)
INTENTIONAL OVERDOSE ( 123 FDA reports)
DIVERTICULUM INTESTINAL ( 122 FDA reports)
HEPATITIS ACUTE ( 122 FDA reports)
PARANOIA ( 122 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 122 FDA reports)
WITHDRAWAL SYNDROME ( 122 FDA reports)
MUSCLE TWITCHING ( 121 FDA reports)
RESTLESS LEGS SYNDROME ( 121 FDA reports)
INJECTION SITE PRURITUS ( 121 FDA reports)
ERYTHEMA MULTIFORME ( 120 FDA reports)
PURULENT DISCHARGE ( 120 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 119 FDA reports)
GLOSSODYNIA ( 119 FDA reports)
HYPERBILIRUBINAEMIA ( 119 FDA reports)
ACIDOSIS ( 118 FDA reports)
ACUTE PULMONARY OEDEMA ( 118 FDA reports)
ATRIOVENTRICULAR BLOCK ( 118 FDA reports)
ECCHYMOSIS ( 118 FDA reports)
LABORATORY TEST ABNORMAL ( 118 FDA reports)
THROAT TIGHTNESS ( 118 FDA reports)
MECHANICAL VENTILATION ( 117 FDA reports)
ANAPHYLACTIC SHOCK ( 117 FDA reports)
COLITIS ULCERATIVE ( 117 FDA reports)
DERMATITIS ( 116 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 116 FDA reports)
MUSCLE RIGIDITY ( 116 FDA reports)
OCULAR HYPERAEMIA ( 116 FDA reports)
RHINITIS ALLERGIC ( 116 FDA reports)
SINUS DISORDER ( 115 FDA reports)
ADVERSE DRUG REACTION ( 115 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 114 FDA reports)
ADRENAL INSUFFICIENCY ( 114 FDA reports)
CEREBRAL ATROPHY ( 114 FDA reports)
FOOT FRACTURE ( 114 FDA reports)
GYNAECOMASTIA ( 114 FDA reports)
HYPOKINESIA ( 114 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 114 FDA reports)
ODYNOPHAGIA ( 114 FDA reports)
TUMOUR LYSIS SYNDROME ( 114 FDA reports)
SENSORY DISTURBANCE ( 113 FDA reports)
VISUAL DISTURBANCE ( 113 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 113 FDA reports)
COLD SWEAT ( 113 FDA reports)
DERMATITIS EXFOLIATIVE ( 113 FDA reports)
EYE IRRITATION ( 113 FDA reports)
ACUTE HEPATIC FAILURE ( 112 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 112 FDA reports)
GROIN PAIN ( 112 FDA reports)
GASTRIC HAEMORRHAGE ( 111 FDA reports)
JOINT STIFFNESS ( 111 FDA reports)
NODULE ( 111 FDA reports)
PROTEIN TOTAL DECREASED ( 111 FDA reports)
TONGUE DISORDER ( 110 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 110 FDA reports)
APHAGIA ( 109 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 109 FDA reports)
DERMATITIS BULLOUS ( 109 FDA reports)
EROSIVE OESOPHAGITIS ( 108 FDA reports)
JOINT DISLOCATION ( 108 FDA reports)
MASTICATION DISORDER ( 108 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 108 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 107 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 107 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 107 FDA reports)
JAUNDICE CHOLESTATIC ( 107 FDA reports)
CHOLANGITIS ( 106 FDA reports)
RASH PUSTULAR ( 106 FDA reports)
THIRST ( 105 FDA reports)
WOUND ( 105 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 105 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 105 FDA reports)
EXCORIATION ( 105 FDA reports)
FAILURE TO THRIVE ( 105 FDA reports)
HAEMODYNAMIC INSTABILITY ( 105 FDA reports)
BLOOD PRESSURE ABNORMAL ( 104 FDA reports)
BONE DENSITY DECREASED ( 104 FDA reports)
RIGHT VENTRICULAR FAILURE ( 104 FDA reports)
PARALYSIS ( 103 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 103 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 103 FDA reports)
VITAMIN D DEFICIENCY ( 103 FDA reports)
BLOOD URINE PRESENT ( 103 FDA reports)
DELUSION ( 103 FDA reports)
LOCAL SWELLING ( 103 FDA reports)
ANKLE FRACTURE ( 102 FDA reports)
ENTEROCOCCAL INFECTION ( 102 FDA reports)
RESPIRATORY DEPRESSION ( 102 FDA reports)
MULTIPLE SCLEROSIS ( 101 FDA reports)
MUSCLE DISORDER ( 101 FDA reports)
OSTEOLYSIS ( 101 FDA reports)
PHOTOPHOBIA ( 101 FDA reports)
SQUAMOUS CELL CARCINOMA ( 101 FDA reports)
TENDERNESS ( 101 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 101 FDA reports)
HICCUPS ( 101 FDA reports)
KIDNEY INFECTION ( 101 FDA reports)
DYSTONIA ( 100 FDA reports)
IRRITABLE BOWEL SYNDROME ( 100 FDA reports)
MASS ( 100 FDA reports)
PHOTOSENSITIVITY REACTION ( 100 FDA reports)
TROPONIN INCREASED ( 100 FDA reports)
PRIMARY SEQUESTRUM ( 99 FDA reports)
FEELING JITTERY ( 99 FDA reports)
LARYNGEAL OEDEMA ( 99 FDA reports)
LIPASE INCREASED ( 99 FDA reports)
AORTIC VALVE INCOMPETENCE ( 98 FDA reports)
BLOOD AMYLASE INCREASED ( 98 FDA reports)
LOOSE TOOTH ( 98 FDA reports)
NYSTAGMUS ( 98 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 98 FDA reports)
SENSATION OF HEAVINESS ( 98 FDA reports)
VIITH NERVE PARALYSIS ( 98 FDA reports)
MYOPATHY ( 97 FDA reports)
OESOPHAGEAL ULCER ( 97 FDA reports)
ORAL DISCOMFORT ( 97 FDA reports)
TORSADE DE POINTES ( 97 FDA reports)
ABDOMINAL TENDERNESS ( 97 FDA reports)
BLADDER CANCER ( 97 FDA reports)
HEPATITIS TOXIC ( 97 FDA reports)
ACTINOMYCOSIS ( 96 FDA reports)
COMA SCALE ABNORMAL ( 96 FDA reports)
PERIPHERAL COLDNESS ( 96 FDA reports)
PHYSICAL DISABILITY ( 95 FDA reports)
CHOKING ( 95 FDA reports)
CYST ( 95 FDA reports)
DECUBITUS ULCER ( 95 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 95 FDA reports)
EXPOSED BONE IN JAW ( 95 FDA reports)
HALLUCINATION, AUDITORY ( 95 FDA reports)
INTESTINAL ISCHAEMIA ( 95 FDA reports)
BEDRIDDEN ( 94 FDA reports)
GINGIVITIS ( 94 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 94 FDA reports)
MOOD ALTERED ( 94 FDA reports)
OEDEMA MOUTH ( 94 FDA reports)
POOR QUALITY SLEEP ( 94 FDA reports)
WOUND DEHISCENCE ( 93 FDA reports)
ARTHRITIS BACTERIAL ( 93 FDA reports)
DIABETIC KETOACIDOSIS ( 93 FDA reports)
ENDOCARDITIS ( 93 FDA reports)
FLANK PAIN ( 93 FDA reports)
ENDODONTIC PROCEDURE ( 92 FDA reports)
GENERALISED ERYTHEMA ( 92 FDA reports)
LARGE INTESTINE PERFORATION ( 92 FDA reports)
MUSCULOSKELETAL DISORDER ( 92 FDA reports)
NOCTURIA ( 92 FDA reports)
SCHIZOPHRENIA ( 92 FDA reports)
ORAL INTAKE REDUCED ( 91 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 91 FDA reports)
REFLUX OESOPHAGITIS ( 91 FDA reports)
UROSEPSIS ( 91 FDA reports)
VAGINAL HAEMORRHAGE ( 91 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 91 FDA reports)
HYPERKERATOSIS ( 91 FDA reports)
FAECALOMA ( 90 FDA reports)
FIBROSIS ( 90 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 90 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 90 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 90 FDA reports)
VITREOUS FLOATERS ( 90 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 89 FDA reports)
POLYURIA ( 89 FDA reports)
PYELONEPHRITIS ( 89 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 89 FDA reports)
BILIARY DYSKINESIA ( 89 FDA reports)
CARDIOPULMONARY FAILURE ( 89 FDA reports)
COLITIS ISCHAEMIC ( 89 FDA reports)
DILATATION VENTRICULAR ( 89 FDA reports)
LIVER INJURY ( 89 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 88 FDA reports)
EOSINOPHIL COUNT INCREASED ( 88 FDA reports)
GLOSSITIS ( 88 FDA reports)
GRANULOCYTOPENIA ( 88 FDA reports)
HYPERTENSIVE CRISIS ( 88 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 88 FDA reports)
WRIST FRACTURE ( 88 FDA reports)
NEPHROTIC SYNDROME ( 87 FDA reports)
PERICARDITIS ( 87 FDA reports)
POLYNEUROPATHY ( 87 FDA reports)
RENAL PAIN ( 87 FDA reports)
ANGIOPATHY ( 87 FDA reports)
DEVICE FAILURE ( 87 FDA reports)
GINGIVAL PAIN ( 87 FDA reports)
HYPOTHERMIA ( 87 FDA reports)
IMMUNOSUPPRESSION ( 87 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 87 FDA reports)
ACNE ( 86 FDA reports)
DROOLING ( 86 FDA reports)
DYSLIPIDAEMIA ( 86 FDA reports)
HAND FRACTURE ( 86 FDA reports)
HEARING IMPAIRED ( 86 FDA reports)
HYPERTHERMIA ( 86 FDA reports)
HYPOACUSIS ( 86 FDA reports)
THERAPY NON-RESPONDER ( 86 FDA reports)
MALIGNANT MELANOMA ( 85 FDA reports)
MANIA ( 85 FDA reports)
PERIPHERAL ISCHAEMIA ( 85 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 85 FDA reports)
RHINITIS ( 85 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 85 FDA reports)
BLOOD MAGNESIUM DECREASED ( 85 FDA reports)
DRUG DEPENDENCE ( 85 FDA reports)
BLOOD CULTURE POSITIVE ( 84 FDA reports)
GASTROINTESTINAL PAIN ( 84 FDA reports)
GOITRE ( 84 FDA reports)
INJECTION SITE SWELLING ( 84 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 84 FDA reports)
ORAL HERPES ( 84 FDA reports)
OVARIAN CYST ( 84 FDA reports)
SKIN NECROSIS ( 84 FDA reports)
THYROID NEOPLASM ( 84 FDA reports)
PULMONARY MASS ( 83 FDA reports)
AORTIC ANEURYSM ( 83 FDA reports)
HERNIA ( 83 FDA reports)
HUMERUS FRACTURE ( 83 FDA reports)
LEFT VENTRICULAR FAILURE ( 83 FDA reports)
LOWER LIMB FRACTURE ( 83 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 83 FDA reports)
APHTHOUS STOMATITIS ( 82 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 82 FDA reports)
LOBAR PNEUMONIA ( 82 FDA reports)
SALIVARY HYPERSECRETION ( 82 FDA reports)
SYNOVIAL CYST ( 82 FDA reports)
THINKING ABNORMAL ( 82 FDA reports)
METASTASES TO LYMPH NODES ( 81 FDA reports)
MUSCLE ATROPHY ( 81 FDA reports)
SINUS HEADACHE ( 81 FDA reports)
ACCIDENTAL EXPOSURE ( 81 FDA reports)
BLINDNESS UNILATERAL ( 81 FDA reports)
EXTRASYSTOLES ( 81 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 81 FDA reports)
HAEMOLYSIS ( 81 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 81 FDA reports)
JAW DISORDER ( 80 FDA reports)
PREGNANCY ( 80 FDA reports)
PULMONARY HAEMORRHAGE ( 80 FDA reports)
SPONDYLOLISTHESIS ( 80 FDA reports)
OCCULT BLOOD POSITIVE ( 79 FDA reports)
STATUS EPILEPTICUS ( 79 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 79 FDA reports)
CERVICAL SPINAL STENOSIS ( 79 FDA reports)
CHEST X-RAY ABNORMAL ( 79 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 79 FDA reports)
DRY THROAT ( 79 FDA reports)
ERYSIPELAS ( 79 FDA reports)
HAEMANGIOMA ( 79 FDA reports)
HEPATIC NECROSIS ( 79 FDA reports)
BONE DEBRIDEMENT ( 78 FDA reports)
DEMYELINATION ( 78 FDA reports)
DIFFICULTY IN WALKING ( 78 FDA reports)
IMMUNODEFICIENCY ( 78 FDA reports)
INCOHERENT ( 78 FDA reports)
MYDRIASIS ( 78 FDA reports)
MUSCLE TIGHTNESS ( 77 FDA reports)
BREATH SOUNDS ABNORMAL ( 77 FDA reports)
DIABETIC NEUROPATHY ( 77 FDA reports)
HEMIPLEGIA ( 77 FDA reports)
LUMBAR SPINAL STENOSIS ( 77 FDA reports)
BLOOD CREATINE INCREASED ( 76 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 76 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 76 FDA reports)
GINGIVAL DISORDER ( 76 FDA reports)
HIP ARTHROPLASTY ( 76 FDA reports)
PERIODONTAL DISEASE ( 76 FDA reports)
PERITONITIS BACTERIAL ( 76 FDA reports)
SPINAL CORD COMPRESSION ( 76 FDA reports)
ORTHOPNOEA ( 75 FDA reports)
RESPIRATORY RATE INCREASED ( 75 FDA reports)
VISUAL FIELD DEFECT ( 75 FDA reports)
ABDOMINAL HERNIA ( 75 FDA reports)
BLOOD CALCIUM INCREASED ( 75 FDA reports)
CATARACT OPERATION ( 75 FDA reports)
HELICOBACTER INFECTION ( 75 FDA reports)
INGUINAL HERNIA ( 75 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 75 FDA reports)
MACULAR DEGENERATION ( 75 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 74 FDA reports)
ESCHERICHIA SEPSIS ( 74 FDA reports)
GINGIVAL RECESSION ( 74 FDA reports)
HYPOTONIA ( 74 FDA reports)
IMPAIRED WORK ABILITY ( 74 FDA reports)
ISCHAEMIA ( 74 FDA reports)
LACRIMATION INCREASED ( 74 FDA reports)
NO ADVERSE EVENT ( 74 FDA reports)
UTERINE LEIOMYOMA ( 74 FDA reports)
METASTASES TO SPINE ( 73 FDA reports)
MIDDLE INSOMNIA ( 73 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 73 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 73 FDA reports)
BIPOLAR DISORDER ( 73 FDA reports)
BLOOD URIC ACID INCREASED ( 73 FDA reports)
CHRONIC SINUSITIS ( 73 FDA reports)
DEVICE MALFUNCTION ( 73 FDA reports)
HEPATIC CYST ( 73 FDA reports)
ILEUS PARALYTIC ( 73 FDA reports)
MAJOR DEPRESSION ( 73 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 72 FDA reports)
EAR INFECTION ( 72 FDA reports)
FORMICATION ( 72 FDA reports)
GASTRIC POLYPS ( 72 FDA reports)
INFARCTION ( 72 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 72 FDA reports)
SHOCK HAEMORRHAGIC ( 72 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 72 FDA reports)
WALKING AID USER ( 72 FDA reports)
BREAST PAIN ( 71 FDA reports)
CACHEXIA ( 71 FDA reports)
CEREBELLAR SYNDROME ( 71 FDA reports)
GASTROENTERITIS VIRAL ( 71 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 71 FDA reports)
LYMPHOEDEMA ( 71 FDA reports)
AREFLEXIA ( 70 FDA reports)
BILE DUCT STONE ( 70 FDA reports)
DERMATOMYOSITIS ( 70 FDA reports)
GRAFT VERSUS HOST DISEASE ( 70 FDA reports)
POLYP ( 70 FDA reports)
SERUM FERRITIN INCREASED ( 70 FDA reports)
SPUTUM DISCOLOURED ( 70 FDA reports)
VENTRICULAR HYPERTROPHY ( 70 FDA reports)
OTITIS MEDIA ( 69 FDA reports)
PLEURISY ( 69 FDA reports)
PREMATURE LABOUR ( 69 FDA reports)
STREPTOCOCCAL INFECTION ( 69 FDA reports)
ABNORMAL FAECES ( 69 FDA reports)
BILIARY COLIC ( 69 FDA reports)
BLOOD CHLORIDE DECREASED ( 69 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 69 FDA reports)
INJECTION SITE IRRITATION ( 69 FDA reports)
ANGIONEUROTIC OEDEMA ( 68 FDA reports)
BLOOD COUNT ABNORMAL ( 68 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 68 FDA reports)
FACIAL BONES FRACTURE ( 68 FDA reports)
FRACTURE ( 68 FDA reports)
HYPOVOLAEMIC SHOCK ( 68 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 68 FDA reports)
NEOPLASM ( 68 FDA reports)
OESOPHAGEAL DISORDER ( 68 FDA reports)
PARKINSONISM ( 68 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 68 FDA reports)
RADICULOPATHY ( 68 FDA reports)
TRANSPLANT REJECTION ( 68 FDA reports)
PANCREATIC CARCINOMA ( 67 FDA reports)
PELVIC FRACTURE ( 67 FDA reports)
RENAL INJURY ( 67 FDA reports)
SKIN REACTION ( 67 FDA reports)
VENOUS INSUFFICIENCY ( 67 FDA reports)
ACUTE PRERENAL FAILURE ( 67 FDA reports)
LUMBAR RADICULOPATHY ( 67 FDA reports)
ABORTION SPONTANEOUS ( 66 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 66 FDA reports)
ENTEROCOLITIS ( 66 FDA reports)
EYELID OEDEMA ( 66 FDA reports)
MOUTH HAEMORRHAGE ( 66 FDA reports)
MULTIPLE DRUG OVERDOSE ( 66 FDA reports)
PREMATURE BABY ( 66 FDA reports)
PROCEDURAL COMPLICATION ( 66 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 66 FDA reports)
TIBIA FRACTURE ( 66 FDA reports)
PARKINSON'S DISEASE ( 65 FDA reports)
STOMACH DISCOMFORT ( 65 FDA reports)
VARICOSE VEIN ( 65 FDA reports)
VENTRICULAR HYPOKINESIA ( 65 FDA reports)
GENITAL HERPES ( 65 FDA reports)
GRANULOMA ( 65 FDA reports)
HYPERAESTHESIA ( 65 FDA reports)
IMMUNE SYSTEM DISORDER ( 65 FDA reports)
INTERMITTENT CLAUDICATION ( 65 FDA reports)
LEFT ATRIAL DILATATION ( 65 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 65 FDA reports)
ANAEMIA MACROCYTIC ( 64 FDA reports)
BONE EROSION ( 64 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 64 FDA reports)
CAROTID ARTERY STENOSIS ( 64 FDA reports)
DERMATITIS ALLERGIC ( 64 FDA reports)
DRUG PRESCRIBING ERROR ( 64 FDA reports)
EYE INFECTION ( 64 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 64 FDA reports)
HYPERNATRAEMIA ( 64 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 64 FDA reports)
MENISCUS LESION ( 64 FDA reports)
METASTATIC NEOPLASM ( 64 FDA reports)
ORAL CAVITY FISTULA ( 64 FDA reports)
PERIODONTITIS ( 64 FDA reports)
SINUS CONGESTION ( 64 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 64 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 64 FDA reports)
NEPHROPATHY ( 63 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 63 FDA reports)
PROCTALGIA ( 63 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 63 FDA reports)
ENCEPHALITIS ( 63 FDA reports)
HYPERVENTILATION ( 63 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 63 FDA reports)
JAW FRACTURE ( 63 FDA reports)
LIMB DISCOMFORT ( 63 FDA reports)
APHONIA ( 62 FDA reports)
APPENDICITIS ( 62 FDA reports)
BONE NEOPLASM MALIGNANT ( 62 FDA reports)
BREAST MASS ( 62 FDA reports)
CARDIAC FAILURE ACUTE ( 62 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 62 FDA reports)
DISSOCIATION ( 62 FDA reports)
EMBOLISM ( 62 FDA reports)
HYPERTONIC BLADDER ( 62 FDA reports)
JAW OPERATION ( 62 FDA reports)
KYPHOSIS ( 62 FDA reports)
LEUKOENCEPHALOPATHY ( 62 FDA reports)
ORAL INFECTION ( 62 FDA reports)
OESOPHAGEAL STENOSIS ( 61 FDA reports)
OPEN WOUND ( 61 FDA reports)
OPTIC NEURITIS ( 61 FDA reports)
OSTEOSCLEROSIS ( 61 FDA reports)
PELVIC PAIN ( 61 FDA reports)
PHLEBITIS ( 61 FDA reports)
PLASMACYTOMA ( 61 FDA reports)
PROCEDURAL PAIN ( 61 FDA reports)
SKIN LACERATION ( 61 FDA reports)
VITAMIN D DECREASED ( 61 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 61 FDA reports)
BLOOD BICARBONATE DECREASED ( 61 FDA reports)
HYPERURICAEMIA ( 61 FDA reports)
INJECTION SITE RASH ( 61 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 60 FDA reports)
BRONCHIECTASIS ( 60 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 60 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 60 FDA reports)
FEELING OF DESPAIR ( 60 FDA reports)
GASTROINTESTINAL INFECTION ( 60 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 60 FDA reports)
MENORRHAGIA ( 60 FDA reports)
NEUROTOXICITY ( 60 FDA reports)
PAROSMIA ( 60 FDA reports)
PULMONARY THROMBOSIS ( 60 FDA reports)
STEM CELL TRANSPLANT ( 60 FDA reports)
MEDICAL DEVICE COMPLICATION ( 59 FDA reports)
MOTOR DYSFUNCTION ( 59 FDA reports)
PERFORMANCE STATUS DECREASED ( 59 FDA reports)
SYNOVITIS ( 59 FDA reports)
BLOOD DISORDER ( 59 FDA reports)
CARDIAC VALVE DISEASE ( 59 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 59 FDA reports)
DRUG DISPENSING ERROR ( 59 FDA reports)
EYE PRURITUS ( 59 FDA reports)
IMPAIRED DRIVING ABILITY ( 59 FDA reports)
JUGULAR VEIN THROMBOSIS ( 59 FDA reports)
KLEBSIELLA INFECTION ( 59 FDA reports)
BRADYPHRENIA ( 58 FDA reports)
DERMATITIS CONTACT ( 58 FDA reports)
DUODENITIS ( 58 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 58 FDA reports)
HEART VALVE INCOMPETENCE ( 58 FDA reports)
HYPOAESTHESIA FACIAL ( 58 FDA reports)
LEG AMPUTATION ( 58 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 58 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 58 FDA reports)
POISONING ( 58 FDA reports)
SKIN INDURATION ( 58 FDA reports)
SOFT TISSUE DISORDER ( 58 FDA reports)
STENT OCCLUSION ( 58 FDA reports)
NOSOCOMIAL INFECTION ( 57 FDA reports)
PERONEAL NERVE PALSY ( 57 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 57 FDA reports)
SKIN INFECTION ( 57 FDA reports)
SUBILEUS ( 57 FDA reports)
SUDDEN CARDIAC DEATH ( 57 FDA reports)
TRISMUS ( 57 FDA reports)
APATHY ( 57 FDA reports)
BONE LOSS ( 57 FDA reports)
CARDIAC PACEMAKER INSERTION ( 57 FDA reports)
DRUG ABUSE ( 57 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 57 FDA reports)
AORTIC STENOSIS ( 56 FDA reports)
ASPERGILLOSIS ( 56 FDA reports)
DEBRIDEMENT ( 56 FDA reports)
DRUG RESISTANCE ( 56 FDA reports)
ENTERITIS ( 56 FDA reports)
HALLUCINATIONS, MIXED ( 56 FDA reports)
HEPATITIS FULMINANT ( 56 FDA reports)
HERPES SIMPLEX ( 56 FDA reports)
MEDICATION RESIDUE ( 56 FDA reports)
NON-CARDIAC CHEST PAIN ( 56 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 55 FDA reports)
STRESS FRACTURE ( 55 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 55 FDA reports)
ABSCESS JAW ( 55 FDA reports)
ALCOHOL USE ( 55 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 55 FDA reports)
DIASTOLIC DYSFUNCTION ( 55 FDA reports)
FIBRIN D DIMER INCREASED ( 55 FDA reports)
GALLBLADDER INJURY ( 55 FDA reports)
GASTRIC CANCER ( 55 FDA reports)
HEPATOCELLULAR DAMAGE ( 55 FDA reports)
INCREASED TENDENCY TO BRUISE ( 55 FDA reports)
INGROWING NAIL ( 55 FDA reports)
APNOEA ( 54 FDA reports)
BLOOD PH DECREASED ( 54 FDA reports)
BREATH ODOUR ( 54 FDA reports)
DRUG LEVEL DECREASED ( 54 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 54 FDA reports)
LARYNGITIS ( 54 FDA reports)
LOCALISED OEDEMA ( 54 FDA reports)
MITRAL VALVE PROLAPSE ( 54 FDA reports)
NERVE INJURY ( 54 FDA reports)
PROTEIN URINE PRESENT ( 54 FDA reports)
METASTASIS ( 53 FDA reports)
NERVE COMPRESSION ( 53 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 53 FDA reports)
SEBORRHOEIC KERATOSIS ( 53 FDA reports)
SINUS ARRHYTHMIA ( 53 FDA reports)
TONGUE ULCERATION ( 53 FDA reports)
BACK DISORDER ( 53 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 53 FDA reports)
CARDIAC TAMPONADE ( 53 FDA reports)
COGWHEEL RIGIDITY ( 53 FDA reports)
DILATATION ATRIAL ( 53 FDA reports)
EAR DISCOMFORT ( 53 FDA reports)
FLUID INTAKE REDUCED ( 53 FDA reports)
FOREIGN BODY ( 53 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 53 FDA reports)
GASTROINTESTINAL NECROSIS ( 53 FDA reports)
HYPERAMMONAEMIA ( 53 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 53 FDA reports)
ACCIDENT ( 52 FDA reports)
AMMONIA INCREASED ( 52 FDA reports)
BRONCHITIS CHRONIC ( 52 FDA reports)
CREPITATIONS ( 52 FDA reports)
DENTURE WEARER ( 52 FDA reports)
FEAR OF EATING ( 52 FDA reports)
GINGIVAL SWELLING ( 52 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 52 FDA reports)
ONYCHOMYCOSIS ( 52 FDA reports)
OROPHARYNGEAL BLISTERING ( 52 FDA reports)
PAIN OF SKIN ( 52 FDA reports)
SENSATION OF FOREIGN BODY ( 52 FDA reports)
SNEEZING ( 52 FDA reports)
STENT PLACEMENT ( 52 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 52 FDA reports)
WRONG DRUG ADMINISTERED ( 52 FDA reports)
MICROCYTIC ANAEMIA ( 51 FDA reports)
MYELOPATHY ( 51 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 51 FDA reports)
PROSTATITIS ( 51 FDA reports)
PROSTATOMEGALY ( 51 FDA reports)
SUBCUTANEOUS ABSCESS ( 51 FDA reports)
TROPONIN I INCREASED ( 51 FDA reports)
VITREOUS DETACHMENT ( 51 FDA reports)
AKATHISIA ( 51 FDA reports)
APPLICATION SITE ERYTHEMA ( 51 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 51 FDA reports)
AUTOIMMUNE HEPATITIS ( 51 FDA reports)
BODY TEMPERATURE DECREASED ( 51 FDA reports)
COLLAPSE OF LUNG ( 51 FDA reports)
DISSEMINATED TUBERCULOSIS ( 51 FDA reports)
H1N1 INFLUENZA ( 51 FDA reports)
INCREASED APPETITE ( 51 FDA reports)
LACUNAR INFARCTION ( 51 FDA reports)
CAESAREAN SECTION ( 50 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 50 FDA reports)
CORONARY ARTERY BYPASS ( 50 FDA reports)
CYSTOCELE ( 50 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 50 FDA reports)
HAEMORRHAGIC ANAEMIA ( 50 FDA reports)
MALABSORPTION ( 50 FDA reports)
METABOLIC DISORDER ( 50 FDA reports)
MONOCYTE COUNT INCREASED ( 50 FDA reports)
MUSCLE STRAIN ( 50 FDA reports)
NAIL DISORDER ( 50 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 50 FDA reports)
TONGUE OEDEMA ( 50 FDA reports)
MUSCLE HAEMORRHAGE ( 49 FDA reports)
PLEURITIC PAIN ( 49 FDA reports)
PULMONARY GRANULOMA ( 49 FDA reports)
PULMONARY INFARCTION ( 49 FDA reports)
PULSE ABSENT ( 49 FDA reports)
PURULENCE ( 49 FDA reports)
QUALITY OF LIFE DECREASED ( 49 FDA reports)
SEQUESTRECTOMY ( 49 FDA reports)
TENDON DISORDER ( 49 FDA reports)
ANAL HAEMORRHAGE ( 49 FDA reports)
BODY HEIGHT DECREASED ( 49 FDA reports)
COELIAC DISEASE ( 49 FDA reports)
DIZZINESS POSTURAL ( 49 FDA reports)
EXPIRED DRUG ADMINISTERED ( 49 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 49 FDA reports)
HEPATOCELLULAR INJURY ( 49 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 48 FDA reports)
BUNION ( 48 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 48 FDA reports)
EYE HAEMORRHAGE ( 48 FDA reports)
HEPATIC PAIN ( 48 FDA reports)
HYPERTONIA ( 48 FDA reports)
INJECTION SITE NODULE ( 48 FDA reports)
LICHENOID KERATOSIS ( 48 FDA reports)
LISTLESS ( 48 FDA reports)
PANIC REACTION ( 48 FDA reports)
RETINAL HAEMORRHAGE ( 48 FDA reports)
SICK SINUS SYNDROME ( 48 FDA reports)
THROMBOPHLEBITIS ( 48 FDA reports)
MEAN CELL VOLUME INCREASED ( 47 FDA reports)
PAROTITIS ( 47 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 47 FDA reports)
POLYDIPSIA ( 47 FDA reports)
PYURIA ( 47 FDA reports)
RENAL CELL CARCINOMA ( 47 FDA reports)
THROMBOCYTHAEMIA ( 47 FDA reports)
THYROID CANCER ( 47 FDA reports)
VAGINAL INFECTION ( 47 FDA reports)
BLOOD IRON DECREASED ( 47 FDA reports)
BLOOD LACTIC ACID INCREASED ( 47 FDA reports)
BLOOD TEST ABNORMAL ( 47 FDA reports)
EYE MOVEMENT DISORDER ( 47 FDA reports)
FACIAL PALSY ( 47 FDA reports)
GASTROINTESTINAL ULCER ( 47 FDA reports)
HEPATIC ENZYME ABNORMAL ( 47 FDA reports)
HYPOPARATHYROIDISM ( 47 FDA reports)
APLASTIC ANAEMIA ( 46 FDA reports)
BILE DUCT OBSTRUCTION ( 46 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 46 FDA reports)
BONE FRAGMENTATION ( 46 FDA reports)
BRAIN NEOPLASM ( 46 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 46 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 46 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 46 FDA reports)
GASTROINTESTINAL PERFORATION ( 46 FDA reports)
GINGIVAL INFECTION ( 46 FDA reports)
HAEMORRHAGIC STROKE ( 46 FDA reports)
HYDROCEPHALUS ( 46 FDA reports)
INTENTIONAL SELF-INJURY ( 46 FDA reports)
LABYRINTHITIS ( 46 FDA reports)
LIVEDO RETICULARIS ( 46 FDA reports)
METABOLIC ENCEPHALOPATHY ( 46 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 46 FDA reports)
NON-SMALL CELL LUNG CANCER ( 46 FDA reports)
OESOPHAGEAL PAIN ( 46 FDA reports)
PERIORBITAL OEDEMA ( 46 FDA reports)
PNEUMONIA BACTERIAL ( 46 FDA reports)
PO2 DECREASED ( 46 FDA reports)
POLYARTHRITIS ( 46 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 46 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 46 FDA reports)
STRIDOR ( 46 FDA reports)
VARICES OESOPHAGEAL ( 46 FDA reports)
WOUND DRAINAGE ( 46 FDA reports)
WOUND SECRETION ( 46 FDA reports)
MONOPLEGIA ( 45 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 45 FDA reports)
SKIN CANCER ( 45 FDA reports)
SKIN HAEMORRHAGE ( 45 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 45 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 45 FDA reports)
ANOSMIA ( 45 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 45 FDA reports)
BRAIN INJURY ( 45 FDA reports)
CHEILITIS ( 45 FDA reports)
ESSENTIAL HYPERTENSION ( 45 FDA reports)
FEELING DRUNK ( 45 FDA reports)
GASTRIC PH DECREASED ( 45 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 45 FDA reports)
HAEMORRHAGIC DIATHESIS ( 45 FDA reports)
INTESTINAL ULCER ( 45 FDA reports)
LUNG ADENOCARCINOMA ( 45 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 44 FDA reports)
ACTINIC KERATOSIS ( 44 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 44 FDA reports)
ATRIAL SEPTAL DEFECT ( 44 FDA reports)
BREAST CANCER METASTATIC ( 44 FDA reports)
DIABETIC NEPHROPATHY ( 44 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 44 FDA reports)
FACET JOINT SYNDROME ( 44 FDA reports)
HERPES VIRUS INFECTION ( 44 FDA reports)
IRON DEFICIENCY ( 44 FDA reports)
LUNG CONSOLIDATION ( 44 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 44 FDA reports)
NECROTISING FASCIITIS ( 44 FDA reports)
PROSTATE CANCER METASTATIC ( 44 FDA reports)
RECTAL ABSCESS ( 44 FDA reports)
STRESS URINARY INCONTINENCE ( 44 FDA reports)
TONGUE INJURY ( 44 FDA reports)
VENTRICULAR DYSFUNCTION ( 44 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 43 FDA reports)
PANCREATIC DISORDER ( 43 FDA reports)
PERSONALITY CHANGE ( 43 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 43 FDA reports)
PULMONARY TUBERCULOSIS ( 43 FDA reports)
PUSTULAR PSORIASIS ( 43 FDA reports)
RADIOTHERAPY ( 43 FDA reports)
RECTOCELE ( 43 FDA reports)
SCLERODERMA ( 43 FDA reports)
SUPERINFECTION ( 43 FDA reports)
TACHYARRHYTHMIA ( 43 FDA reports)
TRANSFUSION ( 43 FDA reports)
TUMOUR HAEMORRHAGE ( 43 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 43 FDA reports)
AFFECT LABILITY ( 43 FDA reports)
ANAL ABSCESS ( 43 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 43 FDA reports)
BLOOD SODIUM INCREASED ( 43 FDA reports)
BREAST CANCER RECURRENT ( 43 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 43 FDA reports)
CEREBROVASCULAR DISORDER ( 43 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 43 FDA reports)
FACE INJURY ( 43 FDA reports)
HEPATIC CONGESTION ( 43 FDA reports)
HYPOVENTILATION ( 43 FDA reports)
INHIBITORY DRUG INTERACTION ( 43 FDA reports)
INJECTION SITE DISCOLOURATION ( 43 FDA reports)
LEUKAEMIA ( 43 FDA reports)
LIPOMA ( 43 FDA reports)
LUNG CANCER METASTATIC ( 43 FDA reports)
ABSCESS ORAL ( 42 FDA reports)
ACUTE ABDOMEN ( 42 FDA reports)
AORTIC CALCIFICATION ( 42 FDA reports)
BONE SCAN ABNORMAL ( 42 FDA reports)
HUNGER ( 42 FDA reports)
NEUROGENIC BLADDER ( 42 FDA reports)
NEUROLOGICAL SYMPTOM ( 42 FDA reports)
RENAL MASS ( 42 FDA reports)
RESORPTION BONE INCREASED ( 42 FDA reports)
SCAB ( 42 FDA reports)
SPUTUM CULTURE POSITIVE ( 42 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 42 FDA reports)
URINE OUTPUT INCREASED ( 42 FDA reports)
NEPHROPATHY TOXIC ( 41 FDA reports)
NEUROPATHY ( 41 FDA reports)
OCULAR ICTERUS ( 41 FDA reports)
PARAPLEGIA ( 41 FDA reports)
PLASMACYTOSIS ( 41 FDA reports)
PORTAL VEIN THROMBOSIS ( 41 FDA reports)
RAYNAUD'S PHENOMENON ( 41 FDA reports)
RENAL TUBULAR ACIDOSIS ( 41 FDA reports)
SELF-MEDICATION ( 41 FDA reports)
SKIN TIGHTNESS ( 41 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 41 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 41 FDA reports)
TOOTH DISCOLOURATION ( 41 FDA reports)
YELLOW SKIN ( 41 FDA reports)
B-CELL LYMPHOMA ( 41 FDA reports)
BILIARY DILATATION ( 41 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 41 FDA reports)
BLADDER DISORDER ( 41 FDA reports)
BLOOD CREATININE DECREASED ( 41 FDA reports)
CATHETER RELATED INFECTION ( 41 FDA reports)
CLAVICLE FRACTURE ( 41 FDA reports)
DRUG SCREEN POSITIVE ( 41 FDA reports)
EAR DISORDER ( 41 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 41 FDA reports)
HAEMOGLOBIN ABNORMAL ( 41 FDA reports)
HEPATITIS B ( 41 FDA reports)
INTESTINAL HAEMORRHAGE ( 41 FDA reports)
BACK INJURY ( 40 FDA reports)
CARDIAC FAILURE CHRONIC ( 40 FDA reports)
DYSPHEMIA ( 40 FDA reports)
HYPERCAPNIA ( 40 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 40 FDA reports)
INJECTION SITE URTICARIA ( 40 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 40 FDA reports)
MITRAL VALVE DISEASE ( 40 FDA reports)
OESOPHAGEAL CARCINOMA ( 40 FDA reports)
PNEUMONIA KLEBSIELLA ( 40 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 40 FDA reports)
POSTURE ABNORMAL ( 40 FDA reports)
PROTEIN TOTAL INCREASED ( 40 FDA reports)
UNDERDOSE ( 40 FDA reports)
URINE ANALYSIS ABNORMAL ( 40 FDA reports)
MELANOCYTIC NAEVUS ( 39 FDA reports)
OESOPHAGITIS ULCERATIVE ( 39 FDA reports)
REGURGITATION ( 39 FDA reports)
RETINAL DETACHMENT ( 39 FDA reports)
RETINOPATHY ( 39 FDA reports)
SKIN PAPILLOMA ( 39 FDA reports)
URINARY TRACT OBSTRUCTION ( 39 FDA reports)
APLASIA ( 39 FDA reports)
ATRIAL TACHYCARDIA ( 39 FDA reports)
ATROPHY ( 39 FDA reports)
BACTERIAL SEPSIS ( 39 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 39 FDA reports)
CLOSTRIDIUM COLITIS ( 39 FDA reports)
DENTAL FISTULA ( 39 FDA reports)
EPIGASTRIC DISCOMFORT ( 39 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 39 FDA reports)
HYPERCHLORHYDRIA ( 39 FDA reports)
INTRACARDIAC THROMBUS ( 39 FDA reports)
LIVER TRANSPLANT REJECTION ( 39 FDA reports)
LOW TURNOVER OSTEOPATHY ( 39 FDA reports)
LUPUS-LIKE SYNDROME ( 39 FDA reports)
ABORTION INDUCED ( 38 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 38 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 38 FDA reports)
BONE MARROW DEPRESSION ( 38 FDA reports)
CHONDROMALACIA ( 38 FDA reports)
COMMUNICATION DISORDER ( 38 FDA reports)
CULTURE URINE POSITIVE ( 38 FDA reports)
DEVICE DISLOCATION ( 38 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 38 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 38 FDA reports)
HYPERCOAGULATION ( 38 FDA reports)
LUPUS NEPHRITIS ( 38 FDA reports)
OVERWEIGHT ( 38 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 38 FDA reports)
RENAL ATROPHY ( 38 FDA reports)
SEROMA ( 38 FDA reports)
SKIN MASS ( 38 FDA reports)
SPINAL LAMINECTOMY ( 38 FDA reports)
VASCULAR CALCIFICATION ( 38 FDA reports)
VITAMIN B12 DEFICIENCY ( 38 FDA reports)
PANCREATITIS CHRONIC ( 37 FDA reports)
PEMPHIGOID ( 37 FDA reports)
RASH VESICULAR ( 37 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 37 FDA reports)
SENSATION OF PRESSURE ( 37 FDA reports)
SEXUAL DYSFUNCTION ( 37 FDA reports)
TEARFULNESS ( 37 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 37 FDA reports)
VENOUS THROMBOSIS ( 37 FDA reports)
VENTRICULAR ARRHYTHMIA ( 37 FDA reports)
WHEELCHAIR USER ( 37 FDA reports)
WOUND COMPLICATION ( 37 FDA reports)
APPLICATION SITE PRURITUS ( 37 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 37 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 37 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 37 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 37 FDA reports)
FACIAL PARESIS ( 37 FDA reports)
FEBRILE BONE MARROW APLASIA ( 37 FDA reports)
FOLLICULITIS ( 37 FDA reports)
FURUNCLE ( 37 FDA reports)
HEAD DISCOMFORT ( 37 FDA reports)
INJECTION SITE WARMTH ( 37 FDA reports)
ABDOMINAL ABSCESS ( 36 FDA reports)
ALCOHOL POISONING ( 36 FDA reports)
ANKYLOSING SPONDYLITIS ( 36 FDA reports)
AUTOIMMUNE DISORDER ( 36 FDA reports)
CAROTID ARTERY OCCLUSION ( 36 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 36 FDA reports)
DEAFNESS UNILATERAL ( 36 FDA reports)
EDENTULOUS ( 36 FDA reports)
ENTEROBACTER INFECTION ( 36 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 36 FDA reports)
GUILLAIN-BARRE SYNDROME ( 36 FDA reports)
INADEQUATE ANALGESIA ( 36 FDA reports)
INJECTION SITE INDURATION ( 36 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 36 FDA reports)
LIBIDO DECREASED ( 36 FDA reports)
MENINGIOMA ( 36 FDA reports)
MENINGITIS ( 36 FDA reports)
NECK INJURY ( 36 FDA reports)
PANIC DISORDER ( 36 FDA reports)
PLEURAL FIBROSIS ( 36 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 36 FDA reports)
ULCER HAEMORRHAGE ( 36 FDA reports)
MARROW HYPERPLASIA ( 35 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 35 FDA reports)
PERICARDIAL HAEMORRHAGE ( 35 FDA reports)
PNEUMONIA FUNGAL ( 35 FDA reports)
RADIUS FRACTURE ( 35 FDA reports)
RESPIRATORY TRACT CONGESTION ( 35 FDA reports)
SKIN HYPERTROPHY ( 35 FDA reports)
ATROPHIC VULVOVAGINITIS ( 35 FDA reports)
CHANGE OF BOWEL HABIT ( 35 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 35 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 35 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 35 FDA reports)
HEPATIC FIBROSIS ( 35 FDA reports)
HEPATOSPLENOMEGALY ( 35 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 35 FDA reports)
INFECTIOUS PERITONITIS ( 35 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 35 FDA reports)
INTERVERTEBRAL DISCITIS ( 35 FDA reports)
ACUTE SINUSITIS ( 34 FDA reports)
AFFECTIVE DISORDER ( 34 FDA reports)
AORTIC VALVE SCLEROSIS ( 34 FDA reports)
BACTERIAL DISEASE CARRIER ( 34 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 34 FDA reports)
CEREBRAL HAEMATOMA ( 34 FDA reports)
CORONARY ARTERY THROMBOSIS ( 34 FDA reports)
COSTOCHONDRITIS ( 34 FDA reports)
EARLY SATIETY ( 34 FDA reports)
HAEMANGIOMA OF LIVER ( 34 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 34 FDA reports)
HEPATIC NEOPLASM ( 34 FDA reports)
HYPERPARATHYROIDISM ( 34 FDA reports)
ILEAL STENOSIS ( 34 FDA reports)
INTESTINAL DILATATION ( 34 FDA reports)
INTESTINAL STENOSIS ( 34 FDA reports)
JOINT SPRAIN ( 34 FDA reports)
LARGE INTESTINAL ULCER ( 34 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 34 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 34 FDA reports)
MENSTRUAL DISORDER ( 34 FDA reports)
MENSTRUATION IRREGULAR ( 34 FDA reports)
METRORRHAGIA ( 34 FDA reports)
NEPHROGENIC ANAEMIA ( 34 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 34 FDA reports)
PCO2 DECREASED ( 34 FDA reports)
PITTING OEDEMA ( 34 FDA reports)
PLANTAR FASCIITIS ( 34 FDA reports)
POLYMYALGIA RHEUMATICA ( 34 FDA reports)
PSORIATIC ARTHROPATHY ( 34 FDA reports)
RESPIRATORY ACIDOSIS ( 34 FDA reports)
SELF-INJURIOUS IDEATION ( 34 FDA reports)
METAPLASIA ( 33 FDA reports)
MICROANGIOPATHY ( 33 FDA reports)
MONOCLONAL GAMMOPATHY ( 33 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 33 FDA reports)
NEUTROPHILIA ( 33 FDA reports)
PAPILLOEDEMA ( 33 FDA reports)
PARTIAL SEIZURES ( 33 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 33 FDA reports)
RASH MORBILLIFORM ( 33 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 33 FDA reports)
SECRETION DISCHARGE ( 33 FDA reports)
SKIN TEST POSITIVE ( 33 FDA reports)
TENOSYNOVITIS ( 33 FDA reports)
VASCULAR PURPURA ( 33 FDA reports)
VENOOCCLUSIVE DISEASE ( 33 FDA reports)
WALKING DISABILITY ( 33 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 33 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 33 FDA reports)
CARDIAC FLUTTER ( 33 FDA reports)
DECREASED ACTIVITY ( 33 FDA reports)
EXFOLIATIVE RASH ( 33 FDA reports)
FEMORAL NECK FRACTURE ( 33 FDA reports)
GASTROINTESTINAL EROSION ( 33 FDA reports)
GINGIVAL ULCERATION ( 33 FDA reports)
HEART RATE ABNORMAL ( 33 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 33 FDA reports)
HYPERPYREXIA ( 33 FDA reports)
HYPERREFLEXIA ( 33 FDA reports)
HYPOGLYCAEMIC COMA ( 33 FDA reports)
INCISIONAL HERNIA ( 33 FDA reports)
LYMPHOCYTOSIS ( 33 FDA reports)
ABSCESS DRAINAGE ( 32 FDA reports)
ANAEMIA POSTOPERATIVE ( 32 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 32 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 32 FDA reports)
BLOOD UREA DECREASED ( 32 FDA reports)
BONE MARROW TOXICITY ( 32 FDA reports)
CAROTID BRUIT ( 32 FDA reports)
CEREBRAL DISORDER ( 32 FDA reports)
ENTEROCUTANEOUS FISTULA ( 32 FDA reports)
FISTULA DISCHARGE ( 32 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 32 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 32 FDA reports)
LIGAMENT SPRAIN ( 32 FDA reports)
MYOGLOBINURIA ( 32 FDA reports)
OPTIC ATROPHY ( 32 FDA reports)
PETIT MAL EPILEPSY ( 32 FDA reports)
PHOTOPSIA ( 32 FDA reports)
PRESBYOPIA ( 32 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 32 FDA reports)
PROTHROMBIN TIME SHORTENED ( 32 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 32 FDA reports)
RENAL TUBULAR DISORDER ( 32 FDA reports)
RETINAL VEIN OCCLUSION ( 32 FDA reports)
STUPOR ( 32 FDA reports)
VASCULAR PSEUDOANEURYSM ( 32 FDA reports)
MYOPIA ( 31 FDA reports)
NEURITIS ( 31 FDA reports)
NEURODERMATITIS ( 31 FDA reports)
ORGAN FAILURE ( 31 FDA reports)
PARESIS ( 31 FDA reports)
POST PROCEDURAL INFECTION ( 31 FDA reports)
PSYCHOMOTOR RETARDATION ( 31 FDA reports)
SCOTOMA ( 31 FDA reports)
SKIN HYPERPIGMENTATION ( 31 FDA reports)
SKIN IRRITATION ( 31 FDA reports)
THERMAL BURN ( 31 FDA reports)
THROMBOCYTOPENIC PURPURA ( 31 FDA reports)
TREATMENT FAILURE ( 31 FDA reports)
URINARY HESITATION ( 31 FDA reports)
VITAMIN B12 DECREASED ( 31 FDA reports)
ABDOMINAL MASS ( 31 FDA reports)
ABSCESS LIMB ( 31 FDA reports)
ADENOCARCINOMA ( 31 FDA reports)
APPLICATION SITE PAIN ( 31 FDA reports)
ARTERIAL DISORDER ( 31 FDA reports)
BACTERIAL TEST POSITIVE ( 31 FDA reports)
BRUXISM ( 31 FDA reports)
CATHETERISATION CARDIAC ( 31 FDA reports)
CHOKING SENSATION ( 31 FDA reports)
CONVERSION DISORDER ( 31 FDA reports)
DERMAL CYST ( 31 FDA reports)
DIABETIC RETINOPATHY ( 31 FDA reports)
EYELID PTOSIS ( 31 FDA reports)
FOOD INTOLERANCE ( 31 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 31 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 31 FDA reports)
GASTROINTESTINAL TOXICITY ( 31 FDA reports)
IMMOBILE ( 31 FDA reports)
INFECTED SKIN ULCER ( 31 FDA reports)
INITIAL INSOMNIA ( 31 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 31 FDA reports)
LACTOSE INTOLERANCE ( 31 FDA reports)
LIVE BIRTH ( 31 FDA reports)
ACUTE PSYCHOSIS ( 30 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 30 FDA reports)
BLOOD CHLORIDE INCREASED ( 30 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 30 FDA reports)
CERVICAL MYELOPATHY ( 30 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 30 FDA reports)
DERMATITIS ACNEIFORM ( 30 FDA reports)
DYSGRAPHIA ( 30 FDA reports)
GASTRITIS ATROPHIC ( 30 FDA reports)
HAEMOGLOBIN INCREASED ( 30 FDA reports)
HAIR TEXTURE ABNORMAL ( 30 FDA reports)
ILEITIS ( 30 FDA reports)
INCORRECT STORAGE OF DRUG ( 30 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 30 FDA reports)
LIGAMENT RUPTURE ( 30 FDA reports)
LIP DRY ( 30 FDA reports)
MYOCARDITIS ( 30 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 30 FDA reports)
NODAL ARRHYTHMIA ( 30 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 30 FDA reports)
PLATELET COUNT ABNORMAL ( 30 FDA reports)
PORTAL HYPERTENSION ( 30 FDA reports)
POSTNASAL DRIP ( 30 FDA reports)
TENSION ( 30 FDA reports)
TYPE 1 DIABETES MELLITUS ( 30 FDA reports)
URGE INCONTINENCE ( 30 FDA reports)
VIRAL LOAD INCREASED ( 30 FDA reports)
MUCOUS MEMBRANE DISORDER ( 29 FDA reports)
MUSCLE SPASTICITY ( 29 FDA reports)
POOR PERIPHERAL CIRCULATION ( 29 FDA reports)
PSYCHIATRIC SYMPTOM ( 29 FDA reports)
RECTAL CANCER ( 29 FDA reports)
RECTAL FISSURE ( 29 FDA reports)
RHINALGIA ( 29 FDA reports)
RHONCHI ( 29 FDA reports)
SENSITIVITY OF TEETH ( 29 FDA reports)
SKIN FISSURES ( 29 FDA reports)
SOMNAMBULISM ( 29 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 29 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 29 FDA reports)
TONSILLITIS ( 29 FDA reports)
TOOTH EROSION ( 29 FDA reports)
URETHRAL STENOSIS ( 29 FDA reports)
UTERINE POLYP ( 29 FDA reports)
WHITE BLOOD CELL DISORDER ( 29 FDA reports)
ABDOMINAL RIGIDITY ( 29 FDA reports)
ADJUSTMENT DISORDER ( 29 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 29 FDA reports)
BLINDNESS TRANSIENT ( 29 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 29 FDA reports)
CERUMEN IMPACTION ( 29 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 29 FDA reports)
DYSAESTHESIA ( 29 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 29 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 29 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 29 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 29 FDA reports)
ENURESIS ( 29 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 29 FDA reports)
FIBULA FRACTURE ( 29 FDA reports)
FRACTURE NONUNION ( 29 FDA reports)
GANGRENE ( 29 FDA reports)
HAEMATOTOXICITY ( 29 FDA reports)
INTESTINAL RESECTION ( 29 FDA reports)
INTRACRANIAL ANEURYSM ( 29 FDA reports)
KERATITIS ( 29 FDA reports)
KNEE OPERATION ( 29 FDA reports)
ANAL FISTULA ( 28 FDA reports)
ANGIOPLASTY ( 28 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 28 FDA reports)
BEHCET'S SYNDROME ( 28 FDA reports)
BONE OPERATION ( 28 FDA reports)
BRAIN HERNIATION ( 28 FDA reports)
BREAST CANCER FEMALE ( 28 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 28 FDA reports)
COLONIC STENOSIS ( 28 FDA reports)
CORNEAL DYSTROPHY ( 28 FDA reports)
DEAFNESS NEUROSENSORY ( 28 FDA reports)
DEREALISATION ( 28 FDA reports)
DIABETIC COMPLICATION ( 28 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 28 FDA reports)
EUPHORIC MOOD ( 28 FDA reports)
EYE DISCHARGE ( 28 FDA reports)
FULL BLOOD COUNT DECREASED ( 28 FDA reports)
GALLBLADDER ENLARGEMENT ( 28 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 28 FDA reports)
HEPATORENAL SYNDROME ( 28 FDA reports)
HOMICIDAL IDEATION ( 28 FDA reports)
HORDEOLUM ( 28 FDA reports)
HYPOPROTEINAEMIA ( 28 FDA reports)
INDURATION ( 28 FDA reports)
INJECTION SITE EXTRAVASATION ( 28 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 28 FDA reports)
LYMPHADENITIS ( 28 FDA reports)
METABOLIC ALKALOSIS ( 28 FDA reports)
NASAL SEPTUM DEVIATION ( 28 FDA reports)
PANCREATIC ATROPHY ( 28 FDA reports)
PERIARTHRITIS ( 28 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 28 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 28 FDA reports)
REFLUX GASTRITIS ( 28 FDA reports)
RENAL CANCER ( 28 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 28 FDA reports)
RETINAL TEAR ( 28 FDA reports)
SARCOIDOSIS ( 28 FDA reports)
SKIN WARM ( 28 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 28 FDA reports)
THROMBOSIS IN DEVICE ( 28 FDA reports)
TOE AMPUTATION ( 28 FDA reports)
TONGUE BLISTERING ( 28 FDA reports)
URINE COLOUR ABNORMAL ( 28 FDA reports)
VENA CAVA THROMBOSIS ( 28 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 28 FDA reports)
MENIERE'S DISEASE ( 27 FDA reports)
MONOCYTOSIS ( 27 FDA reports)
MUCOSAL DRYNESS ( 27 FDA reports)
NASAL DISCOMFORT ( 27 FDA reports)
ONYCHOCLASIS ( 27 FDA reports)
PARAPROTEINAEMIA ( 27 FDA reports)
PATHOGEN RESISTANCE ( 27 FDA reports)
PROSTATIC DISORDER ( 27 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 27 FDA reports)
RENAL COLIC ( 27 FDA reports)
SOPOR ( 27 FDA reports)
SPINAL FUSION SURGERY ( 27 FDA reports)
SYNCOPE VASOVAGAL ( 27 FDA reports)
TENDON INJURY ( 27 FDA reports)
TONGUE DISCOLOURATION ( 27 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 27 FDA reports)
TRIGGER FINGER ( 27 FDA reports)
URINE ABNORMALITY ( 27 FDA reports)
AMYLOIDOSIS ( 27 FDA reports)
APPENDICECTOMY ( 27 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 27 FDA reports)
ARTHRITIS INFECTIVE ( 27 FDA reports)
ASTHMATIC CRISIS ( 27 FDA reports)
BILIARY TRACT DISORDER ( 27 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 27 FDA reports)
BONE SWELLING ( 27 FDA reports)
BREAST ENLARGEMENT ( 27 FDA reports)
CAPILLARY LEAK SYNDROME ( 27 FDA reports)
COLOSTOMY ( 27 FDA reports)
DEPERSONALISATION ( 27 FDA reports)
DEVICE OCCLUSION ( 27 FDA reports)
EXERCISE TOLERANCE DECREASED ( 27 FDA reports)
FOOT OPERATION ( 27 FDA reports)
HAEMOTHORAX ( 27 FDA reports)
HYPOMANIA ( 27 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 27 FDA reports)
LIFE EXPECTANCY SHORTENED ( 27 FDA reports)
ABNORMAL SENSATION IN EYE ( 26 FDA reports)
ALVEOLITIS ALLERGIC ( 26 FDA reports)
ANAL PRURITUS ( 26 FDA reports)
AORTIC VALVE STENOSIS ( 26 FDA reports)
ARTERIOSPASM CORONARY ( 26 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 26 FDA reports)
BRAIN ABSCESS ( 26 FDA reports)
BREAST DISORDER ( 26 FDA reports)
CANCER PAIN ( 26 FDA reports)
CATARACT NUCLEAR ( 26 FDA reports)
CERVICAL DYSPLASIA ( 26 FDA reports)
CLEFT PALATE ( 26 FDA reports)
COLON ADENOMA ( 26 FDA reports)
CYSTITIS INTERSTITIAL ( 26 FDA reports)
DUODENAL ULCER PERFORATION ( 26 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 26 FDA reports)
FRUSTRATION ( 26 FDA reports)
GASTRITIS HAEMORRHAGIC ( 26 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 26 FDA reports)
HAIR COLOUR CHANGES ( 26 FDA reports)
HYPERLACTACIDAEMIA ( 26 FDA reports)
HYPOPERFUSION ( 26 FDA reports)
INTESTINAL POLYP ( 26 FDA reports)
LABILE BLOOD PRESSURE ( 26 FDA reports)
MALLORY-WEISS SYNDROME ( 26 FDA reports)
NEPHROSCLEROSIS ( 26 FDA reports)
NIKOLSKY'S SIGN ( 26 FDA reports)
NODAL RHYTHM ( 26 FDA reports)
OBSTRUCTION GASTRIC ( 26 FDA reports)
OPTIC NERVE CUPPING ( 26 FDA reports)
ORGANISING PNEUMONIA ( 26 FDA reports)
RESUSCITATION ( 26 FDA reports)
SALMONELLOSIS ( 26 FDA reports)
SERUM SICKNESS ( 26 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 26 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 26 FDA reports)
SOFT TISSUE INFECTION ( 26 FDA reports)
SPUTUM INCREASED ( 26 FDA reports)
SPUTUM PURULENT ( 26 FDA reports)
SUFFOCATION FEELING ( 26 FDA reports)
TERMINAL STATE ( 26 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 26 FDA reports)
TOBACCO USER ( 26 FDA reports)
TRANSPLANT FAILURE ( 26 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 26 FDA reports)
VASCULITIC RASH ( 26 FDA reports)
VEIN DISORDER ( 26 FDA reports)
VERTEBROPLASTY ( 26 FDA reports)
VESTIBULAR DISORDER ( 26 FDA reports)
MAXILLOFACIAL OPERATION ( 25 FDA reports)
MENOPAUSE ( 25 FDA reports)
NASAL MUCOSAL DISORDER ( 25 FDA reports)
NEUTROPENIC COLITIS ( 25 FDA reports)
OCULAR HYPERTENSION ( 25 FDA reports)
OESOPHAGEAL SPASM ( 25 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 25 FDA reports)
OPERATIVE HAEMORRHAGE ( 25 FDA reports)
OSTEORADIONECROSIS ( 25 FDA reports)
PAINFUL RESPIRATION ( 25 FDA reports)
PCO2 INCREASED ( 25 FDA reports)
POLYPECTOMY ( 25 FDA reports)
POST HERPETIC NEURALGIA ( 25 FDA reports)
PROTEUS INFECTION ( 25 FDA reports)
PRURIGO ( 25 FDA reports)
PSEUDOMONAL SEPSIS ( 25 FDA reports)
QUADRIPARESIS ( 25 FDA reports)
RETROPERITONEAL FIBROSIS ( 25 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 25 FDA reports)
SEBORRHOEIC DERMATITIS ( 25 FDA reports)
SJOGREN'S SYNDROME ( 25 FDA reports)
STRESS CARDIOMYOPATHY ( 25 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 25 FDA reports)
URINE ODOUR ABNORMAL ( 25 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 25 FDA reports)
ABSCESS NECK ( 25 FDA reports)
ACINETOBACTER TEST POSITIVE ( 25 FDA reports)
ACUTE LEUKAEMIA ( 25 FDA reports)
AMENORRHOEA ( 25 FDA reports)
ANAL FISSURE ( 25 FDA reports)
ANORECTAL DISORDER ( 25 FDA reports)
AORTIC VALVE DISEASE ( 25 FDA reports)
APPENDIX DISORDER ( 25 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 25 FDA reports)
BLEPHAROSPASM ( 25 FDA reports)
BUNDLE BRANCH BLOCK ( 25 FDA reports)
CALCULUS URETERIC ( 25 FDA reports)
CARDIAC ENZYMES INCREASED ( 25 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 25 FDA reports)
DERMATITIS ATOPIC ( 25 FDA reports)
DEVICE BREAKAGE ( 25 FDA reports)
DRUG EFFECT INCREASED ( 25 FDA reports)
DYSPHASIA ( 25 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 25 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 25 FDA reports)
FAMILY STRESS ( 25 FDA reports)
FUNGAL SKIN INFECTION ( 25 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 25 FDA reports)
GALLBLADDER OPERATION ( 25 FDA reports)
HAND DEFORMITY ( 25 FDA reports)
HEPATIC MASS ( 25 FDA reports)
HIP SURGERY ( 25 FDA reports)
IATROGENIC INJURY ( 25 FDA reports)
ANAPHYLACTOID REACTION ( 24 FDA reports)
ANORECTAL DISCOMFORT ( 24 FDA reports)
APPENDICITIS PERFORATED ( 24 FDA reports)
ASTHENOPIA ( 24 FDA reports)
CALCULUS URINARY ( 24 FDA reports)
CARDIAC OPERATION ( 24 FDA reports)
CAROTID ARTERY DISEASE ( 24 FDA reports)
CHOLESTASIS OF PREGNANCY ( 24 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 24 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 24 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 24 FDA reports)
GASTRIC PERFORATION ( 24 FDA reports)
HAEMOPHILUS INFECTION ( 24 FDA reports)
HYPOREFLEXIA ( 24 FDA reports)
ICHTHYOSIS ( 24 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 24 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 24 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 24 FDA reports)
JOINT ARTHROPLASTY ( 24 FDA reports)
MACULAR OEDEMA ( 24 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 24 FDA reports)
MEGACOLON ( 24 FDA reports)
MICTURITION DISORDER ( 24 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 24 FDA reports)
OSTEOMYELITIS CHRONIC ( 24 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 24 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 24 FDA reports)
PERITONEAL TUBERCULOSIS ( 24 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 24 FDA reports)
PYELONEPHRITIS ACUTE ( 24 FDA reports)
PYODERMA GANGRENOSUM ( 24 FDA reports)
SCREAMING ( 24 FDA reports)
SKELETAL INJURY ( 24 FDA reports)
SPINAL DEFORMITY ( 24 FDA reports)
TOXIC ENCEPHALOPATHY ( 24 FDA reports)
TRACHEOBRONCHITIS ( 24 FDA reports)
TUMOUR NECROSIS ( 24 FDA reports)
UVEITIS ( 24 FDA reports)
VAGINAL DISCHARGE ( 24 FDA reports)
VENOUS THROMBOSIS LIMB ( 24 FDA reports)
MIOSIS ( 23 FDA reports)
ORAL FUNGAL INFECTION ( 23 FDA reports)
OVARIAN CANCER ( 23 FDA reports)
PNEUMOMEDIASTINUM ( 23 FDA reports)
POSTOPERATIVE ILEUS ( 23 FDA reports)
POTENTIATING DRUG INTERACTION ( 23 FDA reports)
PRIAPISM ( 23 FDA reports)
QUADRIPLEGIA ( 23 FDA reports)
SCRATCH ( 23 FDA reports)
SKIN SWELLING ( 23 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 23 FDA reports)
SMALL FOR DATES BABY ( 23 FDA reports)
TONGUE BITING ( 23 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 23 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 23 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 23 FDA reports)
X-RAY ABNORMAL ( 23 FDA reports)
ABSCESS INTESTINAL ( 23 FDA reports)
ADRENAL MASS ( 23 FDA reports)
APPARENT DEATH ( 23 FDA reports)
APPETITE DISORDER ( 23 FDA reports)
BK VIRUS INFECTION ( 23 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 23 FDA reports)
BRADYARRHYTHMIA ( 23 FDA reports)
BRADYKINESIA ( 23 FDA reports)
BRAIN SCAN ABNORMAL ( 23 FDA reports)
CHONDROPATHY ( 23 FDA reports)
COLITIS COLLAGENOUS ( 23 FDA reports)
CONCUSSION ( 23 FDA reports)
CUBITAL TUNNEL SYNDROME ( 23 FDA reports)
DIPLEGIA ( 23 FDA reports)
DRUG ABUSER ( 23 FDA reports)
EMPYEMA ( 23 FDA reports)
EPIGLOTTIC OEDEMA ( 23 FDA reports)
FLAT AFFECT ( 23 FDA reports)
FOOD POISONING ( 23 FDA reports)
GLOMERULONEPHRITIS ( 23 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 23 FDA reports)
INJECTION SITE MASS ( 23 FDA reports)
INTRAOCULAR LENS IMPLANT ( 23 FDA reports)
LIMB OPERATION ( 23 FDA reports)
LIP OEDEMA ( 23 FDA reports)
LIP PAIN ( 23 FDA reports)
ABDOMINAL ADHESIONS ( 22 FDA reports)
ABDOMINAL SEPSIS ( 22 FDA reports)
ANEURYSM ( 22 FDA reports)
AORTIC DISORDER ( 22 FDA reports)
ASPHYXIA ( 22 FDA reports)
BLOOD CREATININE ABNORMAL ( 22 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 22 FDA reports)
BRONCHIOLITIS ( 22 FDA reports)
CALCINOSIS ( 22 FDA reports)
CEREBRAL THROMBOSIS ( 22 FDA reports)
DEPENDENCE ( 22 FDA reports)
DEPRESSIVE SYMPTOM ( 22 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 22 FDA reports)
EAR HAEMORRHAGE ( 22 FDA reports)
GLARE ( 22 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 22 FDA reports)
HELICOBACTER GASTRITIS ( 22 FDA reports)
HEPATIC HAEMATOMA ( 22 FDA reports)
HYPERPHOSPHATAEMIA ( 22 FDA reports)
HYPERTENSIVE HEART DISEASE ( 22 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 22 FDA reports)
IMPULSIVE BEHAVIOUR ( 22 FDA reports)
INJECTION SITE DISCOMFORT ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 22 FDA reports)
INTESTINAL FISTULA ( 22 FDA reports)
KIDNEY FIBROSIS ( 22 FDA reports)
LIMB DEFORMITY ( 22 FDA reports)
LOGORRHOEA ( 22 FDA reports)
METABOLIC SYNDROME ( 22 FDA reports)
MUSCLE CRAMP ( 22 FDA reports)
OBSTRUCTION ( 22 FDA reports)
OESOPHAGEAL INJURY ( 22 FDA reports)
PNEUMONIA LEGIONELLA ( 22 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 22 FDA reports)
PROSTHESIS USER ( 22 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 22 FDA reports)
PUPILS UNEQUAL ( 22 FDA reports)
RETINAL DISORDER ( 22 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 22 FDA reports)
SKIN ATROPHY ( 22 FDA reports)
SKIN GRAFT ( 22 FDA reports)
SLUGGISHNESS ( 22 FDA reports)
SNORING ( 22 FDA reports)
SPINAL OPERATION ( 22 FDA reports)
SPONDYLITIS ( 22 FDA reports)
STASIS DERMATITIS ( 22 FDA reports)
STRONGYLOIDIASIS ( 22 FDA reports)
TINEA PEDIS ( 22 FDA reports)
TONSIL CANCER ( 22 FDA reports)
UTERINE DISORDER ( 22 FDA reports)
VASCULAR OCCLUSION ( 22 FDA reports)
VENOUS OCCLUSION ( 22 FDA reports)
VITREOUS HAEMORRHAGE ( 22 FDA reports)
WEIGHT FLUCTUATION ( 22 FDA reports)
MALIGNANT MELANOMA IN SITU ( 21 FDA reports)
MASTITIS ( 21 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 21 FDA reports)
MONOPARESIS ( 21 FDA reports)
MOUTH INJURY ( 21 FDA reports)
MUSCLE INJURY ( 21 FDA reports)
MUSCLE RUPTURE ( 21 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 21 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 21 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 21 FDA reports)
ORTHOSIS USER ( 21 FDA reports)
OSTEOMALACIA ( 21 FDA reports)
PARONYCHIA ( 21 FDA reports)
PERNICIOUS ANAEMIA ( 21 FDA reports)
POLYP COLORECTAL ( 21 FDA reports)
POST PROCEDURAL HAEMATOMA ( 21 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 21 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 21 FDA reports)
PUBIS FRACTURE ( 21 FDA reports)
RENAL HAEMORRHAGE ( 21 FDA reports)
RHEUMATOID NODULE ( 21 FDA reports)
SHOULDER PAIN ( 21 FDA reports)
SKIN NEOPLASM EXCISION ( 21 FDA reports)
TONGUE COATED ( 21 FDA reports)
TRAUMATIC BRAIN INJURY ( 21 FDA reports)
TRIGEMINAL NEURALGIA ( 21 FDA reports)
URINE FLOW DECREASED ( 21 FDA reports)
WOUND HAEMORRHAGE ( 21 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 21 FDA reports)
ABDOMINAL INFECTION ( 21 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 21 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 21 FDA reports)
ARTERIAL THROMBOSIS ( 21 FDA reports)
ASTIGMATISM ( 21 FDA reports)
BILE DUCT CANCER ( 21 FDA reports)
BLEPHARITIS ( 21 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 21 FDA reports)
BONE MARROW TRANSPLANT ( 21 FDA reports)
CHOLECYSTITIS INFECTIVE ( 21 FDA reports)
COMPARTMENT SYNDROME ( 21 FDA reports)
CONDUCTION DISORDER ( 21 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 21 FDA reports)
DENTAL CARE ( 21 FDA reports)
DEVELOPMENTAL DELAY ( 21 FDA reports)
DIVERTICULAR PERFORATION ( 21 FDA reports)
DUODENAL PERFORATION ( 21 FDA reports)
ENDOTRACHEAL INTUBATION ( 21 FDA reports)
ESCHERICHIA BACTERAEMIA ( 21 FDA reports)
FAT NECROSIS ( 21 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 21 FDA reports)
HOMICIDE ( 21 FDA reports)
HYPERTRANSAMINASAEMIA ( 21 FDA reports)
ILLUSION ( 21 FDA reports)
INJECTION SITE BRUISING ( 21 FDA reports)
LARYNGOSPASM ( 21 FDA reports)
LIVER ABSCESS ( 21 FDA reports)
LUNG ABSCESS ( 21 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 21 FDA reports)
MACULOPATHY ( 21 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 20 FDA reports)
ANAESTHETIC COMPLICATION ( 20 FDA reports)
ANXIETY DISORDER ( 20 FDA reports)
BLADDER OPERATION ( 20 FDA reports)
BRONCHIAL CARCINOMA ( 20 FDA reports)
CATHETER RELATED COMPLICATION ( 20 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 20 FDA reports)
CERVICOBRACHIAL SYNDROME ( 20 FDA reports)
COLECTOMY ( 20 FDA reports)
DIABETIC COMA ( 20 FDA reports)
EMBOLIC STROKE ( 20 FDA reports)
FEEDING DISORDER ( 20 FDA reports)
FINGER DEFORMITY ( 20 FDA reports)
GALLBLADDER POLYP ( 20 FDA reports)
GASTRIC INFECTION ( 20 FDA reports)
GASTROINTESTINAL CARCINOMA ( 20 FDA reports)
HAEMARTHROSIS ( 20 FDA reports)
HAEMATOCRIT INCREASED ( 20 FDA reports)
HILAR LYMPHADENOPATHY ( 20 FDA reports)
HIP DYSPLASIA ( 20 FDA reports)
HYPERPROLACTINAEMIA ( 20 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 20 FDA reports)
INJECTION SITE BURNING ( 20 FDA reports)
JOINT CONTRACTURE ( 20 FDA reports)
LEUKOCYTURIA ( 20 FDA reports)
LIP ULCERATION ( 20 FDA reports)
METASTASES TO PERITONEUM ( 20 FDA reports)
MITRAL VALVE CALCIFICATION ( 20 FDA reports)
MONOCYTE COUNT DECREASED ( 20 FDA reports)
MUCOSAL ULCERATION ( 20 FDA reports)
MULTIPLE FRACTURES ( 20 FDA reports)
MUSCLE FATIGUE ( 20 FDA reports)
NEGATIVE THOUGHTS ( 20 FDA reports)
OEDEMA GENITAL ( 20 FDA reports)
ORAL SURGERY ( 20 FDA reports)
PANCREATIC NEOPLASM ( 20 FDA reports)
PHARYNGEAL ERYTHEMA ( 20 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 20 FDA reports)
PNEUMONIA VIRAL ( 20 FDA reports)
POSTOPERATIVE INFECTION ( 20 FDA reports)
RETICULOCYTE COUNT INCREASED ( 20 FDA reports)
RETROPERITONEAL HAEMATOMA ( 20 FDA reports)
UMBILICAL HERNIA ( 20 FDA reports)
URINARY TRACT DISORDER ( 20 FDA reports)
VERTIGO POSITIONAL ( 20 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
MELANOSIS COLI ( 19 FDA reports)
MICTURITION FREQUENCY DECREASED ( 19 FDA reports)
MYCOSIS FUNGOIDES ( 19 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 19 FDA reports)
NASAL DRYNESS ( 19 FDA reports)
NEPHRITIS ( 19 FDA reports)
OBSTRUCTIVE UROPATHY ( 19 FDA reports)
OPPORTUNISTIC INFECTION ( 19 FDA reports)
PANCREATIC CYST ( 19 FDA reports)
PANCREATIC PSEUDOCYST ( 19 FDA reports)
PATELLA FRACTURE ( 19 FDA reports)
PHARYNGEAL INFLAMMATION ( 19 FDA reports)
PO2 INCREASED ( 19 FDA reports)
POSTICTAL STATE ( 19 FDA reports)
PULMONARY MYCOSIS ( 19 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 19 FDA reports)
SEPTIC EMBOLUS ( 19 FDA reports)
SPLENIC INFARCTION ( 19 FDA reports)
STENOTROPHOMONAS INFECTION ( 19 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 19 FDA reports)
SUBDURAL HAEMORRHAGE ( 19 FDA reports)
TRANSFUSION REACTION ( 19 FDA reports)
URETHRITIS ( 19 FDA reports)
VARICELLA ( 19 FDA reports)
WEGENER'S GRANULOMATOSIS ( 19 FDA reports)
ACINETOBACTER INFECTION ( 19 FDA reports)
ADVERSE REACTION ( 19 FDA reports)
AKINESIA ( 19 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 19 FDA reports)
ANGIOFIBROMA ( 19 FDA reports)
ANOXIC ENCEPHALOPATHY ( 19 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 19 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 19 FDA reports)
APPLICATION SITE RASH ( 19 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 19 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 19 FDA reports)
BLOOD BICARBONATE INCREASED ( 19 FDA reports)
BLOOD OSMOLARITY DECREASED ( 19 FDA reports)
BLOOD PH INCREASED ( 19 FDA reports)
BLOODY DISCHARGE ( 19 FDA reports)
BONE INFARCTION ( 19 FDA reports)
BRONCHIAL OBSTRUCTION ( 19 FDA reports)
CARDIAC DEATH ( 19 FDA reports)
CHEST WALL MASS ( 19 FDA reports)
CHONDROCALCINOSIS ( 19 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 19 FDA reports)
COR PULMONALE ( 19 FDA reports)
CUSHINGOID ( 19 FDA reports)
DENTAL PLAQUE ( 19 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 19 FDA reports)
DROP ATTACKS ( 19 FDA reports)
EFFUSION ( 19 FDA reports)
ENTEROBACTER TEST POSITIVE ( 19 FDA reports)
EYE OEDEMA ( 19 FDA reports)
FANCONI SYNDROME ( 19 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 19 FDA reports)
GESTATIONAL DIABETES ( 19 FDA reports)
HODGKIN'S DISEASE ( 19 FDA reports)
HYPERPHAGIA ( 19 FDA reports)
ILEAL ULCER ( 19 FDA reports)
ILIUM FRACTURE ( 19 FDA reports)
IMPAIRED SELF-CARE ( 19 FDA reports)
INDIFFERENCE ( 19 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 19 FDA reports)
INTERTRIGO ( 19 FDA reports)
IRITIS ( 19 FDA reports)
JOINT CREPITATION ( 19 FDA reports)
LYMPH NODE TUBERCULOSIS ( 19 FDA reports)
LYMPHOCELE ( 19 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 19 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 18 FDA reports)
ADHESION ( 18 FDA reports)
ALVEOLITIS FIBROSING ( 18 FDA reports)
ARTHROPOD BITE ( 18 FDA reports)
ASTERIXIS ( 18 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 18 FDA reports)
BLOOD ALBUMIN INCREASED ( 18 FDA reports)
BLOOD MAGNESIUM INCREASED ( 18 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 18 FDA reports)
BONE CYST ( 18 FDA reports)
BRONCHIAL INFECTION ( 18 FDA reports)
CALCIPHYLAXIS ( 18 FDA reports)
CARDIOTOXICITY ( 18 FDA reports)
CHOLESTEROSIS ( 18 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 18 FDA reports)
COAGULATION TIME PROLONGED ( 18 FDA reports)
COLONIC FISTULA ( 18 FDA reports)
COLORECTAL CANCER ( 18 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 18 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 18 FDA reports)
DEVICE RELATED SEPSIS ( 18 FDA reports)
DIABETES INSIPIDUS ( 18 FDA reports)
DISEASE COMPLICATION ( 18 FDA reports)
EOSINOPHILIC PNEUMONIA ( 18 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 18 FDA reports)
EXOPHTHALMOS ( 18 FDA reports)
EYE INFLAMMATION ( 18 FDA reports)
FAECES HARD ( 18 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 18 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
FOETAL GROWTH RESTRICTION ( 18 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 18 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 18 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 18 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 18 FDA reports)
GOUTY ARTHRITIS ( 18 FDA reports)
HEART INJURY ( 18 FDA reports)
HEPATITIS E ( 18 FDA reports)
HERNIA REPAIR ( 18 FDA reports)
HOSTILITY ( 18 FDA reports)
IRON OVERLOAD ( 18 FDA reports)
JUVENILE ARTHRITIS ( 18 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 18 FDA reports)
MOUTH CYST ( 18 FDA reports)
MUSCLE CONTRACTURE ( 18 FDA reports)
NAIL DISCOLOURATION ( 18 FDA reports)
NODULE ON EXTREMITY ( 18 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 18 FDA reports)
PATHOLOGICAL GAMBLING ( 18 FDA reports)
PERIRECTAL ABSCESS ( 18 FDA reports)
PLASTIC SURGERY ( 18 FDA reports)
PROCEDURAL HYPERTENSION ( 18 FDA reports)
PULMONARY SEPSIS ( 18 FDA reports)
RECTAL POLYP ( 18 FDA reports)
RECTAL ULCER ( 18 FDA reports)
RENAL ARTERY STENOSIS ( 18 FDA reports)
RENAL OSTEODYSTROPHY ( 18 FDA reports)
RENAL TRANSPLANT ( 18 FDA reports)
ROTATOR CUFF REPAIR ( 18 FDA reports)
SIGMOIDITIS ( 18 FDA reports)
SPINAL COLUMN INJURY ( 18 FDA reports)
SPINAL DECOMPRESSION ( 18 FDA reports)
SPINAL PAIN ( 18 FDA reports)
STRABISMUS ( 18 FDA reports)
STREPTOCOCCAL SEPSIS ( 18 FDA reports)
ULCERATIVE KERATITIS ( 18 FDA reports)
UTERINE CANCER ( 18 FDA reports)
VASCULAR GRAFT ( 18 FDA reports)
VASCULITIS NECROTISING ( 18 FDA reports)
WEIGHT BEARING DIFFICULTY ( 18 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 17 FDA reports)
MYELITIS ( 17 FDA reports)
NARCOTIC INTOXICATION ( 17 FDA reports)
NASAL DISORDER ( 17 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 17 FDA reports)
NERVE ROOT LESION ( 17 FDA reports)
ONYCHOMADESIS ( 17 FDA reports)
PANCREATITIS NECROTISING ( 17 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 17 FDA reports)
PNEUMOPERITONEUM ( 17 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 17 FDA reports)
PROCTITIS ( 17 FDA reports)
PRODUCT ADHESION ISSUE ( 17 FDA reports)
PULMONARY TOXICITY ( 17 FDA reports)
RENAL ANEURYSM ( 17 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 17 FDA reports)
RESPIRATORY ALKALOSIS ( 17 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 17 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 17 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 17 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 17 FDA reports)
SINUS POLYP DEGENERATION ( 17 FDA reports)
SKIN PLAQUE ( 17 FDA reports)
SMALL INTESTINE CARCINOMA ( 17 FDA reports)
STRESS SYMPTOMS ( 17 FDA reports)
SURGICAL PROCEDURE REPEATED ( 17 FDA reports)
THERAPY CESSATION ( 17 FDA reports)
TUBERCULIN TEST POSITIVE ( 17 FDA reports)
TUMOUR EMBOLISM ( 17 FDA reports)
TYPE I HYPERSENSITIVITY ( 17 FDA reports)
ULNAR NEURITIS ( 17 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 17 FDA reports)
URTICARIA GENERALISED ( 17 FDA reports)
VASODILATATION ( 17 FDA reports)
ABDOMINAL HAEMATOMA ( 17 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 17 FDA reports)
ALCOHOLISM ( 17 FDA reports)
APRAXIA ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 17 FDA reports)
ASPIRATION BRONCHIAL ( 17 FDA reports)
ATRIAL THROMBOSIS ( 17 FDA reports)
BASEDOW'S DISEASE ( 17 FDA reports)
BILE DUCT STENOSIS ( 17 FDA reports)
BRAIN CONTUSION ( 17 FDA reports)
BRAIN DEATH ( 17 FDA reports)
BREAST SWELLING ( 17 FDA reports)
CAUDA EQUINA SYNDROME ( 17 FDA reports)
CLONUS ( 17 FDA reports)
COLITIS MICROSCOPIC ( 17 FDA reports)
COLON POLYPECTOMY ( 17 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 17 FDA reports)
CULTURE POSITIVE ( 17 FDA reports)
DUODENAL STENOSIS ( 17 FDA reports)
DYSENTERY ( 17 FDA reports)
DYSPNOEA AT REST ( 17 FDA reports)
ECZEMA ASTEATOTIC ( 17 FDA reports)
EMBOLISM VENOUS ( 17 FDA reports)
ENCEPHALITIS VIRAL ( 17 FDA reports)
ENDOMETRIOSIS ( 17 FDA reports)
ENTERITIS INFECTIOUS ( 17 FDA reports)
ERYTHEMA NODOSUM ( 17 FDA reports)
ESCHERICHIA TEST POSITIVE ( 17 FDA reports)
EXANTHEM ( 17 FDA reports)
FIBROUS HISTIOCYTOMA ( 17 FDA reports)
GASTRODUODENITIS ( 17 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 17 FDA reports)
GRIMACING ( 17 FDA reports)
HEMIANOPIA ( 17 FDA reports)
HEPATITIS VIRAL ( 17 FDA reports)
HYSTERECTOMY ( 17 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 17 FDA reports)
KETOACIDOSIS ( 17 FDA reports)
KLEBSIELLA SEPSIS ( 17 FDA reports)
LIP BLISTER ( 17 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 17 FDA reports)
LYMPHANGITIS ( 17 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 16 FDA reports)
AMYLASE INCREASED ( 16 FDA reports)
ANION GAP INCREASED ( 16 FDA reports)
BRAIN STEM INFARCTION ( 16 FDA reports)
BRONCHIAL SECRETION RETENTION ( 16 FDA reports)
CARDIAC OUTPUT DECREASED ( 16 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 16 FDA reports)
CATHETER PLACEMENT ( 16 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 16 FDA reports)
CHEST INJURY ( 16 FDA reports)
CHEST WALL OPERATION ( 16 FDA reports)
CHRONIC HEPATITIS ( 16 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 16 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
CSF PROTEIN INCREASED ( 16 FDA reports)
DIABETIC FOOT ( 16 FDA reports)
DIARRHOEA INFECTIOUS ( 16 FDA reports)
DYSPHORIA ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 16 FDA reports)
ENCEPHALITIS HERPES ( 16 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 16 FDA reports)
FOETAL GROWTH RETARDATION ( 16 FDA reports)
GAMMOPATHY ( 16 FDA reports)
GASTRIC MUCOSAL LESION ( 16 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 16 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 16 FDA reports)
GENITAL RASH ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HEPATITIS A ( 16 FDA reports)
HYPOCHLORAEMIA ( 16 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 16 FDA reports)
INCREASED BRONCHIAL SECRETION ( 16 FDA reports)
INTESTINAL INFARCTION ( 16 FDA reports)
ISCHAEMIC HEPATITIS ( 16 FDA reports)
LARYNGEAL CANCER ( 16 FDA reports)
LEGIONELLA INFECTION ( 16 FDA reports)
LOSS OF LIBIDO ( 16 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 16 FDA reports)
MEAN CELL VOLUME DECREASED ( 16 FDA reports)
METASTATIC PAIN ( 16 FDA reports)
NARCOLEPSY ( 16 FDA reports)
NEOPLASM SKIN ( 16 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 16 FDA reports)
NONSPECIFIC REACTION ( 16 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 16 FDA reports)
OESOPHAGEAL DISCOMFORT ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
ORAL MUCOSA ATROPHY ( 16 FDA reports)
ORTHODONTIC APPLIANCE USER ( 16 FDA reports)
PAPULE ( 16 FDA reports)
PELVIC ABSCESS ( 16 FDA reports)
PERIPHERAL EMBOLISM ( 16 FDA reports)
PERITONEAL HAEMORRHAGE ( 16 FDA reports)
PERSECUTORY DELUSION ( 16 FDA reports)
PHARYNGEAL DISORDER ( 16 FDA reports)
PIGMENTATION DISORDER ( 16 FDA reports)
PRESCRIBED OVERDOSE ( 16 FDA reports)
PROCEDURAL HYPOTENSION ( 16 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 16 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 16 FDA reports)
RADICULAR PAIN ( 16 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 16 FDA reports)
REFRACTORY ANAEMIA ( 16 FDA reports)
SCLERITIS ( 16 FDA reports)
SERUM FERRITIN DECREASED ( 16 FDA reports)
SIALOADENITIS ( 16 FDA reports)
SKIN FIBROSIS ( 16 FDA reports)
SPLEEN DISORDER ( 16 FDA reports)
URETERIC OBSTRUCTION ( 16 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 16 FDA reports)
UTERINE ENLARGEMENT ( 16 FDA reports)
VERBAL ABUSE ( 16 FDA reports)
WEIGHT LOSS POOR ( 16 FDA reports)
MANDIBULAR PROSTHESIS USER ( 15 FDA reports)
METASTASES TO MENINGES ( 15 FDA reports)
NEUTROPENIC INFECTION ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 15 FDA reports)
OCCULT BLOOD ( 15 FDA reports)
PARATHYROID TUMOUR BENIGN ( 15 FDA reports)
PELVIC DEFORMITY ( 15 FDA reports)
PERITONEAL DISORDER ( 15 FDA reports)
POLYCYTHAEMIA ( 15 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 15 FDA reports)
PUPIL FIXED ( 15 FDA reports)
PYLORIC STENOSIS ( 15 FDA reports)
QRS AXIS ABNORMAL ( 15 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 15 FDA reports)
RED BLOOD CELL ABNORMALITY ( 15 FDA reports)
RESPIRATION ABNORMAL ( 15 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 15 FDA reports)
RHEUMATOID FACTOR INCREASED ( 15 FDA reports)
SKULL FRACTURE ( 15 FDA reports)
SPUTUM RETENTION ( 15 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 15 FDA reports)
SUBMANDIBULAR MASS ( 15 FDA reports)
SUDDEN HEARING LOSS ( 15 FDA reports)
SYNOVIAL RUPTURE ( 15 FDA reports)
TEMPERATURE REGULATION DISORDER ( 15 FDA reports)
TONGUE DRY ( 15 FDA reports)
TONSILLAR HYPERTROPHY ( 15 FDA reports)
TRACHEAL OBSTRUCTION ( 15 FDA reports)
UNINTENDED PREGNANCY ( 15 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 15 FDA reports)
VULVITIS ( 15 FDA reports)
VULVOVAGINAL DRYNESS ( 15 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 15 FDA reports)
ADRENAL DISORDER ( 15 FDA reports)
AMAUROSIS ( 15 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 15 FDA reports)
BACTERIA STOOL IDENTIFIED ( 15 FDA reports)
BENIGN TUMOUR EXCISION ( 15 FDA reports)
BLADDER PAIN ( 15 FDA reports)
BLADDER PROLAPSE ( 15 FDA reports)
BLOOD BLISTER ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 15 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 15 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 15 FDA reports)
BONE TRIMMING ( 15 FDA reports)
BRAIN MIDLINE SHIFT ( 15 FDA reports)
CALCULUS BLADDER ( 15 FDA reports)
CARDIAC AMYLOIDOSIS ( 15 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 15 FDA reports)
CENTRAL LINE INFECTION ( 15 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 15 FDA reports)
CHAPPED LIPS ( 15 FDA reports)
CHOLANGITIS ACUTE ( 15 FDA reports)
CITROBACTER INFECTION ( 15 FDA reports)
COAGULATION TEST ABNORMAL ( 15 FDA reports)
COMPLEX PARTIAL SEIZURES ( 15 FDA reports)
CORONARY ANGIOPLASTY ( 15 FDA reports)
DENTAL OPERATION ( 15 FDA reports)
DRUG CLEARANCE DECREASED ( 15 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 15 FDA reports)
DYSHIDROSIS ( 15 FDA reports)
EAR CONGESTION ( 15 FDA reports)
ELECTROLYTE DEPLETION ( 15 FDA reports)
ENDOCARDITIS BACTERIAL ( 15 FDA reports)
ENGRAFT FAILURE ( 15 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 15 FDA reports)
EPICONDYLITIS ( 15 FDA reports)
ESSENTIAL TREMOR ( 15 FDA reports)
GINGIVAL ERYTHEMA ( 15 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 15 FDA reports)
HEART SOUNDS ABNORMAL ( 15 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 15 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 15 FDA reports)
HYPERTHERMIA MALIGNANT ( 15 FDA reports)
HYPOCOAGULABLE STATE ( 15 FDA reports)
INFLAMMATION OF WOUND ( 15 FDA reports)
INFLAMMATORY MARKER INCREASED ( 15 FDA reports)
INFUSION SITE PAIN ( 15 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 15 FDA reports)
KIDNEY ENLARGEMENT ( 15 FDA reports)
KIDNEY MALFORMATION ( 15 FDA reports)
LICHEN PLANUS ( 15 FDA reports)
LIPIDS INCREASED ( 15 FDA reports)
LIVER TRANSPLANT ( 15 FDA reports)
MACULE ( 15 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 14 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 14 FDA reports)
AEROMONA INFECTION ( 14 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 14 FDA reports)
ANKLE OPERATION ( 14 FDA reports)
APPLICATION SITE REACTION ( 14 FDA reports)
APTYALISM ( 14 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 14 FDA reports)
AXILLARY MASS ( 14 FDA reports)
BICYTOPENIA ( 14 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 14 FDA reports)
BLOOD CORTISOL DECREASED ( 14 FDA reports)
BONE FORMATION INCREASED ( 14 FDA reports)
BONE GRAFT ( 14 FDA reports)
CALCIUM DEFICIENCY ( 14 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 14 FDA reports)
CEREBELLAR INFARCTION ( 14 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 14 FDA reports)
CHOLESTATIC LIVER INJURY ( 14 FDA reports)
CONGENITAL ANOMALY ( 14 FDA reports)
CONTRAST MEDIA REACTION ( 14 FDA reports)
CRANIOCEREBRAL INJURY ( 14 FDA reports)
DEAFNESS BILATERAL ( 14 FDA reports)
DENTAL DISCOMFORT ( 14 FDA reports)
DEPRESSION SUICIDAL ( 14 FDA reports)
DIAPHRAGMATIC HERNIA ( 14 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 14 FDA reports)
DISSOCIATIVE DISORDER ( 14 FDA reports)
ENTEROCELE ( 14 FDA reports)
ENTEROCOCCAL SEPSIS ( 14 FDA reports)
EXCESSIVE EYE BLINKING ( 14 FDA reports)
FASCIITIS ( 14 FDA reports)
FRACTURE DELAYED UNION ( 14 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 14 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 14 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 14 FDA reports)
GLIOBLASTOMA ( 14 FDA reports)
GRAFT DYSFUNCTION ( 14 FDA reports)
HAEMORRHAGE URINARY TRACT ( 14 FDA reports)
HEPATIC HAEMORRHAGE ( 14 FDA reports)
HYDROCELE ( 14 FDA reports)
HYDROPNEUMOTHORAX ( 14 FDA reports)
HYPERMETABOLISM ( 14 FDA reports)
HYPERPLASIA ( 14 FDA reports)
INCISION SITE COMPLICATION ( 14 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 14 FDA reports)
INJECTION SITE INFLAMMATION ( 14 FDA reports)
INTENTIONAL MISUSE ( 14 FDA reports)
KERATOACANTHOMA ( 14 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 14 FDA reports)
MENINGITIS ASEPTIC ( 14 FDA reports)
MITRAL VALVE STENOSIS ( 14 FDA reports)
MUCORMYCOSIS ( 14 FDA reports)
MUCOSAL EROSION ( 14 FDA reports)
NASAL ULCER ( 14 FDA reports)
NECK MASS ( 14 FDA reports)
NEOPLASM PROSTATE ( 14 FDA reports)
NEUROFIBROMA ( 14 FDA reports)
OPHTHALMOPLEGIA ( 14 FDA reports)
OVARIAN NEOPLASM ( 14 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 14 FDA reports)
PERITONEAL EFFUSION ( 14 FDA reports)
PLASMAPHERESIS ( 14 FDA reports)
PLEURAL DISORDER ( 14 FDA reports)
PNEUMATOSIS INTESTINALIS ( 14 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 14 FDA reports)
PREMATURE DELIVERY ( 14 FDA reports)
PRODUCT ODOUR ABNORMAL ( 14 FDA reports)
PULMONARY VASCULITIS ( 14 FDA reports)
PULSE ABNORMAL ( 14 FDA reports)
SELF ESTEEM DECREASED ( 14 FDA reports)
SINUS POLYP ( 14 FDA reports)
SKULL FRACTURED BASE ( 14 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 14 FDA reports)
SOCIAL PROBLEM ( 14 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 14 FDA reports)
SYSTEMIC MYCOSIS ( 14 FDA reports)
TACHYPHRENIA ( 14 FDA reports)
TEETH BRITTLE ( 14 FDA reports)
THERAPY REGIMEN CHANGED ( 14 FDA reports)
THROMBOCYTOSIS ( 14 FDA reports)
TOBACCO ABUSE ( 14 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 14 FDA reports)
TOXOPLASMOSIS ( 14 FDA reports)
TRAUMATIC HAEMATOMA ( 14 FDA reports)
TUMOUR FLARE ( 14 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 14 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 14 FDA reports)
UTERINE HAEMORRHAGE ( 14 FDA reports)
VASCULAR DEMENTIA ( 14 FDA reports)
VOCAL CORD DISORDER ( 14 FDA reports)
VULVOVAGINAL PAIN ( 14 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 13 FDA reports)
METAMORPHOPSIA ( 13 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 13 FDA reports)
MULTIPLE ALLERGIES ( 13 FDA reports)
MYELOFIBROSIS ( 13 FDA reports)
NEUROENDOCRINE CARCINOMA ( 13 FDA reports)
NOCTURNAL DYSPNOEA ( 13 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 13 FDA reports)
OESOPHAGEAL DILATATION ( 13 FDA reports)
ORAL MUCOSAL BLISTERING ( 13 FDA reports)
PANCREATIC HAEMORRHAGE ( 13 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 13 FDA reports)
PELVIC MASS ( 13 FDA reports)
PHYSICAL ASSAULT ( 13 FDA reports)
POLYHYDRAMNIOS ( 13 FDA reports)
PROCEDURAL VOMITING ( 13 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 13 FDA reports)
RENAL NEOPLASM ( 13 FDA reports)
RETROPERITONEAL ABSCESS ( 13 FDA reports)
RHEUMATOID LUNG ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 13 FDA reports)
SARCOMA ( 13 FDA reports)
SCROTAL SWELLING ( 13 FDA reports)
SEASONAL ALLERGY ( 13 FDA reports)
SHUNT OCCLUSION ( 13 FDA reports)
SINOATRIAL BLOCK ( 13 FDA reports)
SKIN DESQUAMATION ( 13 FDA reports)
SKIN NODULE ( 13 FDA reports)
SKIN TOXICITY ( 13 FDA reports)
STARING ( 13 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 13 FDA reports)
TEMPERATURE INTOLERANCE ( 13 FDA reports)
TENDON PAIN ( 13 FDA reports)
TENOSYNOVITIS STENOSANS ( 13 FDA reports)
TOOTH REPAIR ( 13 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 13 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 13 FDA reports)
URETERIC STENOSIS ( 13 FDA reports)
VASCULAR GRAFT OCCLUSION ( 13 FDA reports)
VESTIBULAR NEURONITIS ( 13 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 13 FDA reports)
ABDOMINAL NEOPLASM ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 13 FDA reports)
ADENOMYOSIS ( 13 FDA reports)
ADNEXA UTERI MASS ( 13 FDA reports)
ADRENAL ADENOMA ( 13 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 13 FDA reports)
ALCOHOL ABUSE ( 13 FDA reports)
AORTIC DISSECTION ( 13 FDA reports)
APALLIC SYNDROME ( 13 FDA reports)
APPARENT LIFE THREATENING EVENT ( 13 FDA reports)
APPLICATION SITE IRRITATION ( 13 FDA reports)
ARTERIAL STENOSIS ( 13 FDA reports)
ARTERIOVENOUS MALFORMATION ( 13 FDA reports)
AUTOIMMUNE THYROIDITIS ( 13 FDA reports)
BIOPSY TONGUE ABNORMAL ( 13 FDA reports)
BLADDER CATHETERISATION ( 13 FDA reports)
BLEEDING TIME PROLONGED ( 13 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 13 FDA reports)
BONE MARROW DISORDER ( 13 FDA reports)
BREAST TENDERNESS ( 13 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 13 FDA reports)
BURNS SECOND DEGREE ( 13 FDA reports)
CARBON DIOXIDE DECREASED ( 13 FDA reports)
CARDIOVERSION ( 13 FDA reports)
CELL DEATH ( 13 FDA reports)
CHOLURIA ( 13 FDA reports)
CHOREA ( 13 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 13 FDA reports)
CORNEAL DISORDER ( 13 FDA reports)
CUSHING'S SYNDROME ( 13 FDA reports)
CYSTITIS NONINFECTIVE ( 13 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 13 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 13 FDA reports)
DIET REFUSAL ( 13 FDA reports)
DIURETIC THERAPY ( 13 FDA reports)
DYSPNOEA EXACERBATED ( 13 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 13 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 13 FDA reports)
ENERGY INCREASED ( 13 FDA reports)
ENTEROBACTER BACTERAEMIA ( 13 FDA reports)
EPIDERMOLYSIS ( 13 FDA reports)
EXSANGUINATION ( 13 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 13 FDA reports)
FEELING GUILTY ( 13 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 13 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 13 FDA reports)
GIARDIASIS ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
GLYCOSURIA ( 13 FDA reports)
HAEMATOMA INFECTION ( 13 FDA reports)
HAEMOCHROMATOSIS ( 13 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 13 FDA reports)
HAPTOGLOBIN DECREASED ( 13 FDA reports)
HEPATIC ATROPHY ( 13 FDA reports)
HERNIA PAIN ( 13 FDA reports)
HIRSUTISM ( 13 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 13 FDA reports)
HYPERCREATININAEMIA ( 13 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 13 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 13 FDA reports)
LABORATORY TEST INTERFERENCE ( 13 FDA reports)
LEUKAEMIA PLASMACYTIC ( 13 FDA reports)
MACROGLOSSIA ( 13 FDA reports)
ACROCHORDON ( 12 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 12 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 12 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
AORTIC DILATATION ( 12 FDA reports)
APGAR SCORE LOW ( 12 FDA reports)
APPLICATION SITE BURN ( 12 FDA reports)
ARTERITIS ( 12 FDA reports)
BIPOLAR I DISORDER ( 12 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 12 FDA reports)
BONE MARROW OEDEMA ( 12 FDA reports)
BRAIN DAMAGE ( 12 FDA reports)
BREAST RECONSTRUCTION ( 12 FDA reports)
CARDIAC HYPERTROPHY ( 12 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 12 FDA reports)
CEREBRAL MICROANGIOPATHY ( 12 FDA reports)
CLUSTER HEADACHE ( 12 FDA reports)
COITAL BLEEDING ( 12 FDA reports)
COMA HEPATIC ( 12 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 12 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 12 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 12 FDA reports)
CRYOGLOBULINAEMIA ( 12 FDA reports)
CYSTITIS HAEMORRHAGIC ( 12 FDA reports)
DENTAL PROSTHESIS USER ( 12 FDA reports)
DRUG INTERACTION POTENTIATION ( 12 FDA reports)
DYSLALIA ( 12 FDA reports)
DYSPAREUNIA ( 12 FDA reports)
EJECTION FRACTION ABNORMAL ( 12 FDA reports)
EROSIVE DUODENITIS ( 12 FDA reports)
ERYTHEMA OF EYELID ( 12 FDA reports)
EXTREMITY NECROSIS ( 12 FDA reports)
FACTOR VIII INHIBITION ( 12 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 12 FDA reports)
FRACTURE DISPLACEMENT ( 12 FDA reports)
GALLBLADDER PAIN ( 12 FDA reports)
GASTRIC BYPASS ( 12 FDA reports)
GASTRIC ULCER PERFORATION ( 12 FDA reports)
GAZE PALSY ( 12 FDA reports)
GENITAL HAEMORRHAGE ( 12 FDA reports)
GLIOBLASTOMA MULTIFORME ( 12 FDA reports)
GRAFT COMPLICATION ( 12 FDA reports)
GRANULOCYTE COUNT DECREASED ( 12 FDA reports)
GRAVITATIONAL OEDEMA ( 12 FDA reports)
HELICOBACTER TEST POSITIVE ( 12 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 12 FDA reports)
HYPERKINESIA ( 12 FDA reports)
HYPERTENSIVE EMERGENCY ( 12 FDA reports)
HYPERVOLAEMIA ( 12 FDA reports)
HYPOTONIA NEONATAL ( 12 FDA reports)
ILEOSTOMY ( 12 FDA reports)
INCISION SITE INFECTION ( 12 FDA reports)
INCISION SITE PAIN ( 12 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 12 FDA reports)
INFUSION SITE SWELLING ( 12 FDA reports)
IRIDOCYCLITIS ( 12 FDA reports)
JUGULAR VEIN DISTENSION ( 12 FDA reports)
KAPOSI'S SARCOMA ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
KNEE DEFORMITY ( 12 FDA reports)
LIP EROSION ( 12 FDA reports)
LOSS OF EMPLOYMENT ( 12 FDA reports)
LOWER EXTREMITY MASS ( 12 FDA reports)
MACROCYTOSIS ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
MIGRAINE WITH AURA ( 12 FDA reports)
MULTI-ORGAN DISORDER ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
NERVE ROOT COMPRESSION ( 12 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 12 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 12 FDA reports)
OEDEMA MUCOSAL ( 12 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 12 FDA reports)
OOPHORECTOMY ( 12 FDA reports)
OTITIS EXTERNA ( 12 FDA reports)
PAIN EXACERBATED ( 12 FDA reports)
PANCREATIC MASS ( 12 FDA reports)
PARTNER STRESS ( 12 FDA reports)
PERICARDIAL DISEASE ( 12 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 12 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 12 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 12 FDA reports)
PO2 ABNORMAL ( 12 FDA reports)
POLYSEROSITIS ( 12 FDA reports)
POOR PERSONAL HYGIENE ( 12 FDA reports)
PROCEDURAL NAUSEA ( 12 FDA reports)
PROCEDURAL SITE REACTION ( 12 FDA reports)
PROSTATISM ( 12 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 12 FDA reports)
READING DISORDER ( 12 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 12 FDA reports)
RESIDUAL URINE ( 12 FDA reports)
RETINAL ARTERY OCCLUSION ( 12 FDA reports)
RETINAL DEGENERATION ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SINUSITIS FUNGAL ( 12 FDA reports)
SKIN EROSION ( 12 FDA reports)
SKIN INJURY ( 12 FDA reports)
SKIN ODOUR ABNORMAL ( 12 FDA reports)
SLOW SPEECH ( 12 FDA reports)
SPLENECTOMY ( 12 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 12 FDA reports)
SYSTEMIC CANDIDA ( 12 FDA reports)
THYROIDITIS ( 12 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 12 FDA reports)
TRACHEITIS ( 12 FDA reports)
TUBERCULOUS PLEURISY ( 12 FDA reports)
TUMOUR PAIN ( 12 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 12 FDA reports)
URINE KETONE BODY PRESENT ( 12 FDA reports)
URINE OSMOLARITY INCREASED ( 12 FDA reports)
VAGINAL CANDIDIASIS ( 12 FDA reports)
VASCULAR INSUFFICIENCY ( 12 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 12 FDA reports)
MARITAL PROBLEM ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MENINGITIS BACTERIAL ( 11 FDA reports)
METASTASES TO ADRENALS ( 11 FDA reports)
METASTASES TO EYE ( 11 FDA reports)
MUCOSAL HAEMORRHAGE ( 11 FDA reports)
MYASTHENIA GRAVIS ( 11 FDA reports)
NASAL INFLAMMATION ( 11 FDA reports)
NASAL POLYPS ( 11 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 11 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 11 FDA reports)
OPTIC NEUROPATHY ( 11 FDA reports)
ORAL MUCOSA EROSION ( 11 FDA reports)
OSTEOCHONDROSIS ( 11 FDA reports)
PALATAL DISORDER ( 11 FDA reports)
PANCREATITIS RELAPSING ( 11 FDA reports)
PARAPARESIS ( 11 FDA reports)
PAROTIDECTOMY ( 11 FDA reports)
PELVIC DISCOMFORT ( 11 FDA reports)
PERIORBITAL HAEMATOMA ( 11 FDA reports)
PERIPHERAL NERVE LESION ( 11 FDA reports)
PNEUMOCOCCAL SEPSIS ( 11 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 11 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 11 FDA reports)
PULSE PRESSURE DECREASED ( 11 FDA reports)
PYELOCALIECTASIS ( 11 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 11 FDA reports)
RETINAL VEIN THROMBOSIS ( 11 FDA reports)
RETINOPATHY HYPERTENSIVE ( 11 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 11 FDA reports)
ROSACEA ( 11 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 11 FDA reports)
SECONDARY HYPOGONADISM ( 11 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 11 FDA reports)
SINUS OPERATION ( 11 FDA reports)
SKIN OEDEMA ( 11 FDA reports)
SMALL INTESTINAL PERFORATION ( 11 FDA reports)
SUICIDAL BEHAVIOUR ( 11 FDA reports)
TEMPORAL ARTERITIS ( 11 FDA reports)
THROAT CANCER ( 11 FDA reports)
TRACHEOSTOMY ( 11 FDA reports)
TRANSAMINASES ABNORMAL ( 11 FDA reports)
URETHRAL PAIN ( 11 FDA reports)
URINE SODIUM DECREASED ( 11 FDA reports)
UTERINE PROLAPSE ( 11 FDA reports)
VASCULAR CAUTERISATION ( 11 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 11 FDA reports)
VENOUS STENOSIS ( 11 FDA reports)
VOCAL CORD PARALYSIS ( 11 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 11 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 11 FDA reports)
AGITATED DEPRESSION ( 11 FDA reports)
ALCOHOLIC LIVER DISEASE ( 11 FDA reports)
AMAUROSIS FUGAX ( 11 FDA reports)
ANEURYSM RUPTURED ( 11 FDA reports)
AORTIC VALVE REPLACEMENT ( 11 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 11 FDA reports)
BACILLUS INFECTION ( 11 FDA reports)
BACTERIA URINE IDENTIFIED ( 11 FDA reports)
BILIARY SEPSIS ( 11 FDA reports)
BLADDER SPASM ( 11 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 11 FDA reports)
BONE METABOLISM DISORDER ( 11 FDA reports)
BRAIN COMPRESSION ( 11 FDA reports)
BREAKTHROUGH PAIN ( 11 FDA reports)
BREAST CALCIFICATIONS ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BRONCHITIS ACUTE ( 11 FDA reports)
CALCULUS URETHRAL ( 11 FDA reports)
CARDIAC ANEURYSM ( 11 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 11 FDA reports)
CATHETER SITE ERYTHEMA ( 11 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 11 FDA reports)
CHLAMYDIAL INFECTION ( 11 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 11 FDA reports)
CLAUSTROPHOBIA ( 11 FDA reports)
COLLAGEN DISORDER ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 11 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 11 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 11 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 11 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 11 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 11 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 11 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 11 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 11 FDA reports)
ENDOMETRIAL CANCER ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
ENZYME ABNORMALITY ( 11 FDA reports)
EXTREMITY CONTRACTURE ( 11 FDA reports)
EYE ALLERGY ( 11 FDA reports)
EYE ROLLING ( 11 FDA reports)
FACIAL ASYMMETRY ( 11 FDA reports)
FIBRINOLYSIS ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
FOOD ALLERGY ( 11 FDA reports)
FOREIGN BODY IN EYE ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 11 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 11 FDA reports)
GASTROINTESTINAL OEDEMA ( 11 FDA reports)
GENERAL SYMPTOM ( 11 FDA reports)
GENITAL EROSION ( 11 FDA reports)
HAEMORRHOID OPERATION ( 11 FDA reports)
HAIR DISORDER ( 11 FDA reports)
HAIR GROWTH ABNORMAL ( 11 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 11 FDA reports)
HOARSENESS ( 11 FDA reports)
HYPERAEMIA ( 11 FDA reports)
HYPERCHLORAEMIA ( 11 FDA reports)
HYPEROSMOLAR STATE ( 11 FDA reports)
HYPOGONADISM ( 11 FDA reports)
HYPOSPADIAS ( 11 FDA reports)
HYPOVITAMINOSIS ( 11 FDA reports)
IMPRISONMENT ( 11 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 11 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 11 FDA reports)
INJECTION SITE ULCER ( 11 FDA reports)
INNER EAR DISORDER ( 11 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 11 FDA reports)
JOINT ANKYLOSIS ( 11 FDA reports)
JOINT PROSTHESIS USER ( 11 FDA reports)
LEARNING DISORDER ( 11 FDA reports)
LEUKAEMIA RECURRENT ( 11 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 11 FDA reports)
LISTERIA SEPSIS ( 11 FDA reports)
LOOSE BODY IN JOINT ( 11 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 10 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
AGORAPHOBIA ( 10 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 10 FDA reports)
AMPUTATION ( 10 FDA reports)
ANAL SKIN TAGS ( 10 FDA reports)
ANTIBODY TEST POSITIVE ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
ANTITHROMBIN III DECREASED ( 10 FDA reports)
AORTIC ANEURYSM RUPTURE ( 10 FDA reports)
AORTIC ATHEROSCLEROSIS ( 10 FDA reports)
APPLICATION SITE INFLAMMATION ( 10 FDA reports)
APPLICATION SITE VESICLES ( 10 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 10 FDA reports)
ARTERIOVENOUS FISTULA ( 10 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 10 FDA reports)
ASBESTOSIS ( 10 FDA reports)
ASPIRATION PLEURAL CAVITY ( 10 FDA reports)
BASE EXCESS DECREASED ( 10 FDA reports)
BEZOAR ( 10 FDA reports)
BIOPSY LIP ( 10 FDA reports)
BLOOD OESTROGEN INCREASED ( 10 FDA reports)
BURNING MOUTH SYNDROME ( 10 FDA reports)
CATHETER SITE HAEMORRHAGE ( 10 FDA reports)
CATHETER SITE INFECTION ( 10 FDA reports)
CEREBELLAR HAEMORRHAGE ( 10 FDA reports)
COLON CANCER METASTATIC ( 10 FDA reports)
COLON NEOPLASM ( 10 FDA reports)
CULTURE STOOL POSITIVE ( 10 FDA reports)
CUTANEOUS VASCULITIS ( 10 FDA reports)
CYANOSIS NEONATAL ( 10 FDA reports)
CYTOKINE RELEASE SYNDROME ( 10 FDA reports)
DEATH OF RELATIVE ( 10 FDA reports)
DEFAECATION URGENCY ( 10 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 10 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 10 FDA reports)
DERMATITIS PSORIASIFORM ( 10 FDA reports)
DIAPHRAGMATIC DISORDER ( 10 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 10 FDA reports)
EPIDERMAL NECROSIS ( 10 FDA reports)
EPIDIDYMITIS ( 10 FDA reports)
EVAN'S SYNDROME ( 10 FDA reports)
EXTRADURAL HAEMATOMA ( 10 FDA reports)
EYELID FUNCTION DISORDER ( 10 FDA reports)
FAECES PALE ( 10 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 10 FDA reports)
FORCEPS DELIVERY ( 10 FDA reports)
FOREIGN BODY ASPIRATION ( 10 FDA reports)
GASTROENTERITIS RADIATION ( 10 FDA reports)
GASTROINTESTINAL NEOPLASM ( 10 FDA reports)
GLOMERULOSCLEROSIS ( 10 FDA reports)
GLUCOSE URINE PRESENT ( 10 FDA reports)
GRIEF REACTION ( 10 FDA reports)
HAEMANGIOMA CONGENITAL ( 10 FDA reports)
HEART TRANSPLANT REJECTION ( 10 FDA reports)
HEPATIC VEIN THROMBOSIS ( 10 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 10 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 10 FDA reports)
HIDRADENITIS ( 10 FDA reports)
HORMONE LEVEL ABNORMAL ( 10 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 10 FDA reports)
HYPERMETROPIA ( 10 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 10 FDA reports)
HYPOCHROMIC ANAEMIA ( 10 FDA reports)
HYPOGEUSIA ( 10 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 10 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 10 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 10 FDA reports)
HYPOPITUITARISM ( 10 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 10 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 10 FDA reports)
INAPPROPRIATE AFFECT ( 10 FDA reports)
INJECTION SITE CELLULITIS ( 10 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
INTUBATION ( 10 FDA reports)
INVESTIGATION ( 10 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 10 FDA reports)
LESION EXCISION ( 10 FDA reports)
LIPODYSTROPHY ACQUIRED ( 10 FDA reports)
LONG QT SYNDROME ( 10 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 10 FDA reports)
LYME DISEASE ( 10 FDA reports)
MAMMOGRAM ABNORMAL ( 10 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 10 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 10 FDA reports)
MICROALBUMINURIA ( 10 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 10 FDA reports)
MONONUCLEOSIS SYNDROME ( 10 FDA reports)
MYCOBACTERIAL INFECTION ( 10 FDA reports)
MYELITIS TRANSVERSE ( 10 FDA reports)
MYELOID LEUKAEMIA ( 10 FDA reports)
NAIL DYSTROPHY ( 10 FDA reports)
NAIL INFECTION ( 10 FDA reports)
NAIL OPERATION ( 10 FDA reports)
NEOPLASM RECURRENCE ( 10 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 10 FDA reports)
NICOTINE DEPENDENCE ( 10 FDA reports)
NIPPLE PAIN ( 10 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 10 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
OSTEOPOROTIC FRACTURE ( 10 FDA reports)
OXYGEN SUPPLEMENTATION ( 10 FDA reports)
PANCREATIC ENZYMES INCREASED ( 10 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 10 FDA reports)
PANNICULITIS ( 10 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 10 FDA reports)
PARANEOPLASTIC SYNDROME ( 10 FDA reports)
PAROTID GLAND INFLAMMATION ( 10 FDA reports)
PAST-POINTING ( 10 FDA reports)
PEMPHIGUS ( 10 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 10 FDA reports)
POLYMYOSITIS ( 10 FDA reports)
PRINZMETAL ANGINA ( 10 FDA reports)
PRODUCT COUNTERFEIT ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PROSTATE INFECTION ( 10 FDA reports)
PSEUDARTHROSIS ( 10 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 10 FDA reports)
REACTIVE PSYCHOSIS ( 10 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 10 FDA reports)
RESPIRATORY RATE DECREASED ( 10 FDA reports)
SALPINGO-OOPHORECTOMY ( 10 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 10 FDA reports)
SCLERAL DISCOLOURATION ( 10 FDA reports)
SCLERODACTYLIA ( 10 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 10 FDA reports)
SINUS ARREST ( 10 FDA reports)
SKIN INFLAMMATION ( 10 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 10 FDA reports)
SOFT TISSUE INJURY ( 10 FDA reports)
SOFT TISSUE NECROSIS ( 10 FDA reports)
SUPERINFECTION LUNG ( 10 FDA reports)
T-CELL LYMPHOMA ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TONIC CLONIC MOVEMENTS ( 10 FDA reports)
TONIC CONVULSION ( 10 FDA reports)
TOXIC SHOCK SYNDROME ( 10 FDA reports)
TROPONIN T INCREASED ( 10 FDA reports)
URINARY TRACT PAIN ( 10 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
VASCULITIS CEREBRAL ( 10 FDA reports)
VENTRICULAR FAILURE ( 10 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 10 FDA reports)
WOUND DECOMPOSITION ( 10 FDA reports)
XEROSIS ( 10 FDA reports)
MASTECTOMY ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 9 FDA reports)
MEDIASTINAL DISORDER ( 9 FDA reports)
MEDIASTINAL SHIFT ( 9 FDA reports)
MENINGITIS TOXOPLASMAL ( 9 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 9 FDA reports)
MIXED LIVER INJURY ( 9 FDA reports)
MONONEUROPATHY MULTIPLEX ( 9 FDA reports)
MOTION SICKNESS ( 9 FDA reports)
MUSCLE ENZYME INCREASED ( 9 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 9 FDA reports)
NEUROMYOPATHY ( 9 FDA reports)
NEUROPATHIC ARTHROPATHY ( 9 FDA reports)
NEUROSENSORY HYPOACUSIS ( 9 FDA reports)
NOCARDIOSIS ( 9 FDA reports)
OCULAR DISCOMFORT ( 9 FDA reports)
OESOPHAGEAL OEDEMA ( 9 FDA reports)
ONYCHALGIA ( 9 FDA reports)
ORAL MUCOSAL ERUPTION ( 9 FDA reports)
OTORRHOEA ( 9 FDA reports)
PERIODONTAL OPERATION ( 9 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 9 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 9 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 9 FDA reports)
PRODUCT TASTE ABNORMAL ( 9 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
PROTRUSION TONGUE ( 9 FDA reports)
PSEUDODEMENTIA ( 9 FDA reports)
PSYCHOLOGICAL TRAUMA ( 9 FDA reports)
PULMONARY CAVITATION ( 9 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 9 FDA reports)
RADICULITIS ( 9 FDA reports)
RENAL TUBULAR ATROPHY ( 9 FDA reports)
RESPIRATORY TRACT IRRITATION ( 9 FDA reports)
SENSORIMOTOR DISORDER ( 9 FDA reports)
SERRATIA INFECTION ( 9 FDA reports)
SICCA SYNDROME ( 9 FDA reports)
SPLENIC RUPTURE ( 9 FDA reports)
STEATORRHOEA ( 9 FDA reports)
SUDDEN ONSET OF SLEEP ( 9 FDA reports)
SUNBURN ( 9 FDA reports)
SUPERINFECTION BACTERIAL ( 9 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 9 FDA reports)
SUTURE RELATED COMPLICATION ( 9 FDA reports)
TACHYCARDIA PAROXYSMAL ( 9 FDA reports)
TESTICULAR ATROPHY ( 9 FDA reports)
TESTICULAR PAIN ( 9 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 9 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 9 FDA reports)
TOOTH DEPOSIT ( 9 FDA reports)
TOOTH IMPACTED ( 9 FDA reports)
TORTICOLLIS ( 9 FDA reports)
UPPER EXTREMITY MASS ( 9 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 9 FDA reports)
VAGINITIS BACTERIAL ( 9 FDA reports)
VIRAL TEST POSITIVE ( 9 FDA reports)
VITREOUS OPACITIES ( 9 FDA reports)
VULVOVAGINAL SWELLING ( 9 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 9 FDA reports)
WHITE BLOOD CELL COUNT ( 9 FDA reports)
XANTHOPSIA ( 9 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 9 FDA reports)
ABDOMINAL OPERATION ( 9 FDA reports)
ABDOMINAL WALL ABSCESS ( 9 FDA reports)
ABDOMINAL WALL MASS ( 9 FDA reports)
ACCIDENTAL NEEDLE STICK ( 9 FDA reports)
ADDISON'S DISEASE ( 9 FDA reports)
ADENOMA BENIGN ( 9 FDA reports)
ADRENAL NEOPLASM ( 9 FDA reports)
ADRENAL SUPPRESSION ( 9 FDA reports)
ALLERGIC BRONCHITIS ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANAL SPHINCTER ATONY ( 9 FDA reports)
ANAL ULCER ( 9 FDA reports)
ANIMAL BITE ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANOXIA ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 9 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 9 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
AORTIC THROMBOSIS ( 9 FDA reports)
APPLICATION SITE HAEMATOMA ( 9 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 9 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 9 FDA reports)
AXONAL NEUROPATHY ( 9 FDA reports)
BASAL GANGLIA INFARCTION ( 9 FDA reports)
BASOPHIL COUNT INCREASED ( 9 FDA reports)
BENCE JONES PROTEINURIA ( 9 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 9 FDA reports)
BLOOD AMYLASE DECREASED ( 9 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 9 FDA reports)
BLOOD CALCIUM ABNORMAL ( 9 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 9 FDA reports)
BLOOD GASTRIN INCREASED ( 9 FDA reports)
BLOOD SODIUM ABNORMAL ( 9 FDA reports)
BONE FORMATION DECREASED ( 9 FDA reports)
BRAIN MASS ( 9 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 9 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 9 FDA reports)
CAMPYLOBACTER INFECTION ( 9 FDA reports)
CARBON DIOXIDE INCREASED ( 9 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 9 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 9 FDA reports)
CAROTID ARTERY THROMBOSIS ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 9 FDA reports)
CHEYNE-STOKES RESPIRATION ( 9 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 9 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 9 FDA reports)
COLORECTAL CANCER METASTATIC ( 9 FDA reports)
CONNECTIVE TISSUE DISORDER ( 9 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 9 FDA reports)
CORRECTIVE LENS USER ( 9 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 9 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 9 FDA reports)
DISLOCATION OF VERTEBRA ( 9 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 9 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 9 FDA reports)
DRY GANGRENE ( 9 FDA reports)
DUPUYTREN'S CONTRACTURE ( 9 FDA reports)
EMBOLISM ARTERIAL ( 9 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 9 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 9 FDA reports)
ERYTHRODERMIC PSORIASIS ( 9 FDA reports)
EXTRAVASATION ( 9 FDA reports)
FACIAL OPERATION ( 9 FDA reports)
FANCONI SYNDROME ACQUIRED ( 9 FDA reports)
FAT TISSUE INCREASED ( 9 FDA reports)
FOOD INTERACTION ( 9 FDA reports)
FOREIGN BODY TRAUMA ( 9 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 9 FDA reports)
FUNGAEMIA ( 9 FDA reports)
GASTRIC FISTULA ( 9 FDA reports)
GASTRIC VARICES ( 9 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 9 FDA reports)
GRIP STRENGTH DECREASED ( 9 FDA reports)
HANGOVER ( 9 FDA reports)
HEART VALVE CALCIFICATION ( 9 FDA reports)
HEPATOJUGULAR REFLUX ( 9 FDA reports)
HEPATORENAL FAILURE ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HOSPICE CARE ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 9 FDA reports)
HYPERSPLENISM ( 9 FDA reports)
HYPOPNOEA ( 9 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 9 FDA reports)
INCISION SITE HAEMORRHAGE ( 9 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 9 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 9 FDA reports)
INJECTION SITE VESICLES ( 9 FDA reports)
INTESTINAL CYST ( 9 FDA reports)
JOINT FLUID DRAINAGE ( 9 FDA reports)
JOINT INSTABILITY ( 9 FDA reports)
LENTICULAR OPACITIES ( 9 FDA reports)
LIGAMENT INJURY ( 9 FDA reports)
LIP EXFOLIATION ( 9 FDA reports)
LIPOATROPHY ( 9 FDA reports)
LOSS OF CONTROL OF LEGS ( 9 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 9 FDA reports)
ABNORMAL CLOTTING FACTOR ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 8 FDA reports)
AGNOSIA ( 8 FDA reports)
ALANINE AMINOTRANSFERASE ( 8 FDA reports)
ALBUMINURIA ( 8 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 8 FDA reports)
ANOGENITAL WARTS ( 8 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 8 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 8 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 8 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 8 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 8 FDA reports)
AORTIC VALVE CALCIFICATION ( 8 FDA reports)
APPLICATION SITE SCAR ( 8 FDA reports)
ARACHNOID CYST ( 8 FDA reports)
ARTERIAL RUPTURE ( 8 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 8 FDA reports)
ASPERGILLUS TEST POSITIVE ( 8 FDA reports)
ATHEROSCLEROSIS ( 8 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
BENIGN BONE NEOPLASM ( 8 FDA reports)
BLADDER DYSFUNCTION ( 8 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 8 FDA reports)
BLOOD IRON INCREASED ( 8 FDA reports)
BLOOD URIC ACID DECREASED ( 8 FDA reports)
BLOOD URINE ( 8 FDA reports)
BODY MASS INDEX INCREASED ( 8 FDA reports)
BODY TEMPERATURE ( 8 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 8 FDA reports)
BONE FISTULA ( 8 FDA reports)
BRAIN STEM HAEMORRHAGE ( 8 FDA reports)
BRONCHIAL HAEMORRHAGE ( 8 FDA reports)
BRUGADA SYNDROME ( 8 FDA reports)
CAECITIS ( 8 FDA reports)
CANDIDA SEPSIS ( 8 FDA reports)
CARBON DIOXIDE ABNORMAL ( 8 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 8 FDA reports)
CAROTID ARTERY DISSECTION ( 8 FDA reports)
CATHETER REMOVAL ( 8 FDA reports)
CATHETER SEPSIS ( 8 FDA reports)
CELL MARKER INCREASED ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 8 FDA reports)
CERVIX CARCINOMA ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
CHOLINERGIC SYNDROME ( 8 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 8 FDA reports)
CLUMSINESS ( 8 FDA reports)
COGNITIVE DETERIORATION ( 8 FDA reports)
COLOUR BLINDNESS ( 8 FDA reports)
CORNEAL OPACITY ( 8 FDA reports)
DENGUE FEVER ( 8 FDA reports)
DISBACTERIOSIS ( 8 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 8 FDA reports)
DRUG-INDUCED LIVER INJURY ( 8 FDA reports)
DUODENAL POLYP ( 8 FDA reports)
EJACULATION FAILURE ( 8 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 8 FDA reports)
ENCEPHALOMALACIA ( 8 FDA reports)
ENDOPHTHALMITIS ( 8 FDA reports)
EOSINOPHIL COUNT DECREASED ( 8 FDA reports)
ESCHAR ( 8 FDA reports)
EYELID OPERATION ( 8 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 8 FDA reports)
FOOD CRAVING ( 8 FDA reports)
FRACTURED SACRUM ( 8 FDA reports)
GALACTORRHOEA ( 8 FDA reports)
GAMBLING ( 8 FDA reports)
GASTROENTERITIS BACTERIAL ( 8 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 8 FDA reports)
GINGIVECTOMY ( 8 FDA reports)
GLOBULINS INCREASED ( 8 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 8 FDA reports)
GUN SHOT WOUND ( 8 FDA reports)
HEPATIC CANCER METASTATIC ( 8 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 8 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 8 FDA reports)
HYPERAMYLASAEMIA ( 8 FDA reports)
HYPERVIGILANCE ( 8 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 8 FDA reports)
IGA NEPHROPATHY ( 8 FDA reports)
IMMUNOGLOBULINS INCREASED ( 8 FDA reports)
INDUCED LABOUR ( 8 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 8 FDA reports)
INJECTION SITE INFECTION ( 8 FDA reports)
INJECTION SITE PAPULE ( 8 FDA reports)
INTESTINAL MASS ( 8 FDA reports)
INTRA-UTERINE DEATH ( 8 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 8 FDA reports)
JOINT LOCK ( 8 FDA reports)
KOUNIS SYNDROME ( 8 FDA reports)
LACTOBACILLUS INFECTION ( 8 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 8 FDA reports)
LATENT TUBERCULOSIS ( 8 FDA reports)
LEUKOARAIOSIS ( 8 FDA reports)
LEUKOPLAKIA ( 8 FDA reports)
LIBIDO INCREASED ( 8 FDA reports)
LIGAMENT DISORDER ( 8 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 8 FDA reports)
LORDOSIS ( 8 FDA reports)
LOW BIRTH WEIGHT BABY ( 8 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 8 FDA reports)
LUNG CREPITATION ( 8 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 8 FDA reports)
MAGNESIUM DEFICIENCY ( 8 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 8 FDA reports)
MALIGNANT HYPERTENSION ( 8 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 8 FDA reports)
MASKED FACIES ( 8 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 8 FDA reports)
MICROTIA ( 8 FDA reports)
MOANING ( 8 FDA reports)
MUCOUS STOOLS ( 8 FDA reports)
MUSCLE NECROSIS ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
MYELOMA RECURRENCE ( 8 FDA reports)
MYOCARDIAL RUPTURE ( 8 FDA reports)
NECROTISING COLITIS ( 8 FDA reports)
NEPHROCALCINOSIS ( 8 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 8 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 8 FDA reports)
NIGHT BLINDNESS ( 8 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 8 FDA reports)
OBSESSIVE THOUGHTS ( 8 FDA reports)
OEDEMATOUS PANCREATITIS ( 8 FDA reports)
OPEN ANGLE GLAUCOMA ( 8 FDA reports)
ORAL SOFT TISSUE DISORDER ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PANCREATOLITHIASIS ( 8 FDA reports)
PAPILLOMA ( 8 FDA reports)
PARANASAL SINUS NEOPLASM ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 8 FDA reports)
PERIANAL ABSCESS ( 8 FDA reports)
PERITONITIS SCLEROSING ( 8 FDA reports)
PERSONALITY DISORDER ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
PLATELET DISORDER ( 8 FDA reports)
PNEUMOCOCCAL INFECTION ( 8 FDA reports)
PNEUMONIA HERPES VIRAL ( 8 FDA reports)
PNEUMONIA NECROTISING ( 8 FDA reports)
POOR VENOUS ACCESS ( 8 FDA reports)
PROTEIN URINE ( 8 FDA reports)
PSYCHOTIC BEHAVIOUR ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
PUPILLARY DISORDER ( 8 FDA reports)
RADIAL NERVE PALSY ( 8 FDA reports)
RADIATION OESOPHAGITIS ( 8 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 8 FDA reports)
REBOUND EFFECT ( 8 FDA reports)
RECTAL DISCHARGE ( 8 FDA reports)
RECTAL NEOPLASM ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 8 FDA reports)
REFLEXES ABNORMAL ( 8 FDA reports)
RENAL CANCER METASTATIC ( 8 FDA reports)
RENAL INFARCT ( 8 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 8 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 8 FDA reports)
RETINAL ARTERY EMBOLISM ( 8 FDA reports)
RHEUMATOID VASCULITIS ( 8 FDA reports)
SALPINGITIS ( 8 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 8 FDA reports)
SHUNT THROMBOSIS ( 8 FDA reports)
SINUS ANTROSTOMY ( 8 FDA reports)
SLEEP INERTIA ( 8 FDA reports)
SOMATISATION DISORDER ( 8 FDA reports)
SPINAL CORD INJURY ( 8 FDA reports)
SPUTUM ABNORMAL ( 8 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 8 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUTURE INSERTION ( 8 FDA reports)
TESTICULAR SWELLING ( 8 FDA reports)
THROMBECTOMY ( 8 FDA reports)
THYROID CYST ( 8 FDA reports)
TONGUE PARALYSIS ( 8 FDA reports)
URINARY FISTULA ( 8 FDA reports)
URTICARIA VESICULOSA ( 8 FDA reports)
VASOCONSTRICTION ( 8 FDA reports)
VOMITING PROJECTILE ( 8 FDA reports)
VULVOVAGINAL DISCOMFORT ( 8 FDA reports)
WOUND TREATMENT ( 8 FDA reports)
YAWNING ( 8 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MANTLE CELL LYMPHOMA ( 7 FDA reports)
MASS EXCISION ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 7 FDA reports)
MEDICAL DEVICE REMOVAL ( 7 FDA reports)
MEGAKARYOCYTES INCREASED ( 7 FDA reports)
MENINGEAL DISORDER ( 7 FDA reports)
MENINGITIS VIRAL ( 7 FDA reports)
MENINGORRHAGIA ( 7 FDA reports)
MENSTRUATION DELAYED ( 7 FDA reports)
METASTASES TO KIDNEY ( 7 FDA reports)
METASTASES TO PANCREAS ( 7 FDA reports)
METASTASES TO SKIN ( 7 FDA reports)
MORBID THOUGHTS ( 7 FDA reports)
MOUTH BREATHING ( 7 FDA reports)
MUCOSAL DISCOLOURATION ( 7 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 7 FDA reports)
NAIL HYPERTROPHY ( 7 FDA reports)
NASAL OEDEMA ( 7 FDA reports)
NASAL SEPTUM DISORDER ( 7 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 7 FDA reports)
NO ADVERSE EFFECT ( 7 FDA reports)
NUCHAL RIGIDITY ( 7 FDA reports)
OESOPHAGEAL ATRESIA ( 7 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
OPTIC NERVE DISORDER ( 7 FDA reports)
OPTIC NERVE INJURY ( 7 FDA reports)
ORAL PRURITUS ( 7 FDA reports)
ORCHITIS ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
OTITIS MEDIA CHRONIC ( 7 FDA reports)
OTOTOXICITY ( 7 FDA reports)
OVARIAN DISORDER ( 7 FDA reports)
OVERGROWTH BACTERIAL ( 7 FDA reports)
PANOPHTHALMITIS ( 7 FDA reports)
PEAU D'ORANGE ( 7 FDA reports)
PELVIC VENOUS THROMBOSIS ( 7 FDA reports)
PERFORATED ULCER ( 7 FDA reports)
PERIHEPATIC ABSCESS ( 7 FDA reports)
PERINEPHRIC COLLECTION ( 7 FDA reports)
PERITONEAL ADHESIONS ( 7 FDA reports)
PHARYNGEAL LESION ( 7 FDA reports)
PHARYNGEAL ULCERATION ( 7 FDA reports)
PHIMOSIS ( 7 FDA reports)
PHOTODERMATOSIS ( 7 FDA reports)
PNEUMONIA ESCHERICHIA ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
POOR DENTAL CONDITION ( 7 FDA reports)
POST PROCEDURAL FISTULA ( 7 FDA reports)
PROCTOCOLITIS ( 7 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 7 FDA reports)
PSEUDOPORPHYRIA ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 7 FDA reports)
PULMONARY VALVE STENOSIS ( 7 FDA reports)
PULPITIS DENTAL ( 7 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 7 FDA reports)
PYOTHORAX ( 7 FDA reports)
RASH SCARLATINIFORM ( 7 FDA reports)
RECTAL PERFORATION ( 7 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
RECURRENT CANCER ( 7 FDA reports)
RHEUMATIC FEVER ( 7 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
ROTAVIRUS INFECTION ( 7 FDA reports)
SCROTAL ULCER ( 7 FDA reports)
SENILE DEMENTIA ( 7 FDA reports)
SHIFT TO THE LEFT ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 7 FDA reports)
SKIN STRIAE ( 7 FDA reports)
SLOW RESPONSE TO STIMULI ( 7 FDA reports)
SMALL INTESTINAL RESECTION ( 7 FDA reports)
STITCH ABSCESS ( 7 FDA reports)
STOMATITIS HAEMORRHAGIC ( 7 FDA reports)
SUTURE RUPTURE ( 7 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 7 FDA reports)
SYSTEMIC SCLEROSIS ( 7 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
TERMINAL INSOMNIA ( 7 FDA reports)
TESTICULAR MASS ( 7 FDA reports)
THORACIC OUTLET SYNDROME ( 7 FDA reports)
THROMBOLYSIS ( 7 FDA reports)
TIC ( 7 FDA reports)
TOOTH INJURY ( 7 FDA reports)
TRANSPLANT ( 7 FDA reports)
TROUSSEAU'S SYNDROME ( 7 FDA reports)
TUMOUR COMPRESSION ( 7 FDA reports)
ULNA FRACTURE ( 7 FDA reports)
UMBILICAL HERNIA REPAIR ( 7 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 7 FDA reports)
VARICOSE VEIN OPERATION ( 7 FDA reports)
VENTRICULAR ASYSTOLE ( 7 FDA reports)
VENTRICULAR FLUTTER ( 7 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 7 FDA reports)
VIRAEMIA ( 7 FDA reports)
VOLVULUS ( 7 FDA reports)
VULVAL CANCER ( 7 FDA reports)
VULVOVAGINAL PRURITUS ( 7 FDA reports)
VULVOVAGINITIS ( 7 FDA reports)
WHIPPLE'S DISEASE ( 7 FDA reports)
WISDOM TEETH REMOVAL ( 7 FDA reports)
WOUND NECROSIS ( 7 FDA reports)
XERODERMA ( 7 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 7 FDA reports)
ACARODERMATITIS ( 7 FDA reports)
ACCIDENT AT WORK ( 7 FDA reports)
ACCOMMODATION DISORDER ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 7 FDA reports)
ADRENOMEGALY ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
AMINOACIDURIA ( 7 FDA reports)
AMYOTROPHY ( 7 FDA reports)
ANASTOMOTIC COMPLICATION ( 7 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
APNOEIC ATTACK ( 7 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 7 FDA reports)
ARTHRITIS SALMONELLA ( 7 FDA reports)
ARTHROPOD STING ( 7 FDA reports)
ASPIRATION JOINT ( 7 FDA reports)
ASTHMA LATE ONSET ( 7 FDA reports)
AURICULAR SWELLING ( 7 FDA reports)
BACTERIURIA ( 7 FDA reports)
BARTHOLIN'S CYST ( 7 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 7 FDA reports)
BIOPSY LIVER ( 7 FDA reports)
BLADDER NEOPLASM ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 7 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 7 FDA reports)
BLOOD GASES ABNORMAL ( 7 FDA reports)
BLOOD OSMOLARITY INCREASED ( 7 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 7 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 7 FDA reports)
BLOOD VISCOSITY INCREASED ( 7 FDA reports)
BONE NEOPLASM ( 7 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 7 FDA reports)
BREAST ABSCESS ( 7 FDA reports)
BREAST NEOPLASM ( 7 FDA reports)
BRONCHIAL FISTULA ( 7 FDA reports)
BULLOUS LUNG DISEASE ( 7 FDA reports)
CANDIDA TEST POSITIVE ( 7 FDA reports)
CANDIDURIA ( 7 FDA reports)
CARDIAC ASTHMA ( 7 FDA reports)
CARDIAC FIBRILLATION ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
CARDIORENAL SYNDROME ( 7 FDA reports)
CATAPLEXY ( 7 FDA reports)
CATHETER SITE RELATED REACTION ( 7 FDA reports)
CERVICAL NEURITIS ( 7 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 7 FDA reports)
CHEST WALL ABSCESS ( 7 FDA reports)
CHROMATOPSIA ( 7 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 7 FDA reports)
CIRRHOSIS ALCOHOLIC ( 7 FDA reports)
CLONIC CONVULSION ( 7 FDA reports)
COCCIDIOIDOMYCOSIS ( 7 FDA reports)
COLON CANCER STAGE III ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
COLONIC OBSTRUCTION ( 7 FDA reports)
COLONOSCOPY ( 7 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 7 FDA reports)
COOMBS TEST POSITIVE ( 7 FDA reports)
CORNEAL ABRASION ( 7 FDA reports)
CORNEAL EROSION ( 7 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 7 FDA reports)
CSF TEST ABNORMAL ( 7 FDA reports)
CULTURE WOUND POSITIVE ( 7 FDA reports)
CYST RUPTURE ( 7 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 7 FDA reports)
DAYDREAMING ( 7 FDA reports)
DEVICE LEAKAGE ( 7 FDA reports)
DIABETIC GASTROPARESIS ( 7 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 7 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 7 FDA reports)
DRUG INTERACTION INHIBITION ( 7 FDA reports)
DRUG NAME CONFUSION ( 7 FDA reports)
DUODENAL OBSTRUCTION ( 7 FDA reports)
DYSMENORRHOEA ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 7 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 7 FDA reports)
EPENDYMOMA ( 7 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 7 FDA reports)
EXTRADURAL ABSCESS ( 7 FDA reports)
EYELID DISORDER ( 7 FDA reports)
FACIAL NERVE DISORDER ( 7 FDA reports)
FIBROMA ( 7 FDA reports)
FLUID INTAKE RESTRICTION ( 7 FDA reports)
FOAMING AT MOUTH ( 7 FDA reports)
FOETAL DISTRESS SYNDROME ( 7 FDA reports)
FOLATE DEFICIENCY ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
FUNGAL OESOPHAGITIS ( 7 FDA reports)
FUNGAL PERITONITIS ( 7 FDA reports)
FUNGAL TEST POSITIVE ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 7 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 7 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 7 FDA reports)
GINGIVAL HYPERPLASIA ( 7 FDA reports)
GRAFT INFECTION ( 7 FDA reports)
GRANULOCYTES ABNORMAL ( 7 FDA reports)
GROIN ABSCESS ( 7 FDA reports)
GRUNTING ( 7 FDA reports)
HAEMOBILIA ( 7 FDA reports)
HAEMOGLOBIN ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HEPATIC SIDEROSIS ( 7 FDA reports)
HISTOPLASMOSIS ( 7 FDA reports)
HYPERACUSIS ( 7 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 7 FDA reports)
IIIRD NERVE PARESIS ( 7 FDA reports)
IMMUNOGLOBULINS DECREASED ( 7 FDA reports)
IMPAIRED FASTING GLUCOSE ( 7 FDA reports)
INFUSION SITE ERYTHEMA ( 7 FDA reports)
INFUSION SITE EXTRAVASATION ( 7 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 7 FDA reports)
INTESTINAL FISTULA INFECTION ( 7 FDA reports)
INTESTINAL OPERATION ( 7 FDA reports)
INTUSSUSCEPTION ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
KIDNEY RUPTURE ( 7 FDA reports)
KIDNEY SMALL ( 7 FDA reports)
KLEBSIELLA BACTERAEMIA ( 7 FDA reports)
LAPAROTOMY ( 7 FDA reports)
LARGE INTESTINE CARCINOMA ( 7 FDA reports)
LARYNGEAL STENOSIS ( 7 FDA reports)
LEUKAEMOID REACTION ( 7 FDA reports)
LEUKOPLAKIA ORAL ( 7 FDA reports)
LIP DISORDER ( 7 FDA reports)
LIP HAEMORRHAGE ( 7 FDA reports)
LIVER TENDERNESS ( 7 FDA reports)
LUNG INJURY ( 7 FDA reports)
MADAROSIS ( 7 FDA reports)
MALIGNANT ASCITES ( 7 FDA reports)
ABDOMINAL WALL DISORDER ( 6 FDA reports)
ABULIA ( 6 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 6 FDA reports)
ACUTE LUNG INJURY ( 6 FDA reports)
ADENOIDAL HYPERTROPHY ( 6 FDA reports)
ADENOVIRUS INFECTION ( 6 FDA reports)
ADRENAL CARCINOMA ( 6 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ALOPECIA EFFLUVIUM ( 6 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 6 FDA reports)
ANAL CANCER ( 6 FDA reports)
ANGIODYSPLASIA ( 6 FDA reports)
ANIMAL SCRATCH ( 6 FDA reports)
ANORECTAL OPERATION ( 6 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 6 FDA reports)
ANTINUCLEAR ANTIBODY ( 6 FDA reports)
ANTISOCIAL BEHAVIOUR ( 6 FDA reports)
AORTIC ANEURYSM REPAIR ( 6 FDA reports)
APPLICATION SITE EXFOLIATION ( 6 FDA reports)
APPLICATION SITE WARMTH ( 6 FDA reports)
ARTERIAL STENOSIS LIMB ( 6 FDA reports)
ASPIRATION BONE MARROW ( 6 FDA reports)
ATRIAL HYPERTROPHY ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BENIGN BREAST NEOPLASM ( 6 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 6 FDA reports)
BIFASCICULAR BLOCK ( 6 FDA reports)
BILIARY CYST ( 6 FDA reports)
BILIARY TRACT OPERATION ( 6 FDA reports)
BLADDER CANCER RECURRENT ( 6 FDA reports)
BLADDER DISTENSION ( 6 FDA reports)
BLOOD CORTISOL INCREASED ( 6 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 6 FDA reports)
BLOOD ETHANOL INCREASED ( 6 FDA reports)
BLOOD HIV RNA INCREASED ( 6 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 6 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 6 FDA reports)
BLOOD UREA ABNORMAL ( 6 FDA reports)
BODY FAT DISORDER ( 6 FDA reports)
BONE DEFORMITY ( 6 FDA reports)
BONE DENSITY ABNORMAL ( 6 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 6 FDA reports)
BORRELIA INFECTION ( 6 FDA reports)
BOWEN'S DISEASE ( 6 FDA reports)
BRADYPNOEA ( 6 FDA reports)
BRAIN HYPOXIA ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 6 FDA reports)
BRAIN STEM ISCHAEMIA ( 6 FDA reports)
BRAIN STEM SYNDROME ( 6 FDA reports)
BREAST INFLAMMATION ( 6 FDA reports)
BREAST LUMP REMOVAL ( 6 FDA reports)
BREAST OPERATION ( 6 FDA reports)
BRONCHIAL DISORDER ( 6 FDA reports)
BRONCHOPNEUMOPATHY ( 6 FDA reports)
BUNION OPERATION ( 6 FDA reports)
CALCIUM IONISED DECREASED ( 6 FDA reports)
CAPSULE ISSUE ( 6 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 6 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CATARACT SUBCAPSULAR ( 6 FDA reports)
CATATONIA ( 6 FDA reports)
CATHETER SITE DISCHARGE ( 6 FDA reports)
CELLULITIS ORBITAL ( 6 FDA reports)
CEREBELLAR ATROPHY ( 6 FDA reports)
CEREBELLAR ISCHAEMIA ( 6 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 6 FDA reports)
CEREBRAL CYST ( 6 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 6 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 6 FDA reports)
COLONOSCOPY ABNORMAL ( 6 FDA reports)
COMMINUTED FRACTURE ( 6 FDA reports)
CONGENITAL AORTIC ATRESIA ( 6 FDA reports)
CORNEAL ABSCESS ( 6 FDA reports)
CRANIAL NERVE INFECTION ( 6 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 6 FDA reports)
CRYPTORCHISM ( 6 FDA reports)
CUTANEOUS SARCOIDOSIS ( 6 FDA reports)
CYSTIC FIBROSIS ( 6 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 6 FDA reports)
DEHYDROEPIANDROSTERONE DECREASED ( 6 FDA reports)
DELIRIUM TREMENS ( 6 FDA reports)
DENERVATION ATROPHY ( 6 FDA reports)
DENTAL TREATMENT ( 6 FDA reports)
DERMATITIS INFECTED ( 6 FDA reports)
DEVICE COMPONENT ISSUE ( 6 FDA reports)
DEVICE MISUSE ( 6 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 6 FDA reports)
DIABETIC EYE DISEASE ( 6 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 6 FDA reports)
DRUG EFFECT DELAYED ( 6 FDA reports)
DRUG TOLERANCE ( 6 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSMORPHISM ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 6 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 6 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 6 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 6 FDA reports)
ENTEROBACTER SEPSIS ( 6 FDA reports)
ENTHESOPATHY ( 6 FDA reports)
EPIGLOTTITIS ( 6 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 6 FDA reports)
EXOMPHALOS ( 6 FDA reports)
EYELID CYST ( 6 FDA reports)
EYELIDS PRURITUS ( 6 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 6 FDA reports)
FEBRILE INFECTION ( 6 FDA reports)
FEEDING DISORDER NEONATAL ( 6 FDA reports)
FEELINGS OF WORTHLESSNESS ( 6 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 6 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 6 FDA reports)
FLUID REPLACEMENT ( 6 FDA reports)
FOETAL DISORDER ( 6 FDA reports)
FOETAL MOVEMENTS DECREASED ( 6 FDA reports)
FOOD AVERSION ( 6 FDA reports)
FUNGAL RHINITIS ( 6 FDA reports)
FUNGAL SEPSIS ( 6 FDA reports)
GALLBLADDER CANCER ( 6 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 6 FDA reports)
GASTROENTERITIS NOROVIRUS ( 6 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 6 FDA reports)
GASTROINTESTINAL FISTULA ( 6 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 6 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 6 FDA reports)
GINGIVAL OEDEMA ( 6 FDA reports)
GLAUCOMA SURGERY ( 6 FDA reports)
GLOBAL AMNESIA ( 6 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 6 FDA reports)
GRAFT LOSS ( 6 FDA reports)
GRAFT THROMBOSIS ( 6 FDA reports)
GRANULOCYTOSIS ( 6 FDA reports)
HAEMATOCRIT ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEART VALVE REPLACEMENT ( 6 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 6 FDA reports)
HEPATITIS ALCOHOLIC ( 6 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 6 FDA reports)
HIGH GRADE B-CELL LYMPHOMA BURKITT-LIKE LYMPHOMA ( 6 FDA reports)
HYPERTRICHOSIS ( 6 FDA reports)
HYPERTROPHY ( 6 FDA reports)
HYPOCHOLESTEROLAEMIA ( 6 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 6 FDA reports)
HYPOGONADISM MALE ( 6 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 6 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 6 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 6 FDA reports)
INCISION SITE CELLULITIS ( 6 FDA reports)
INCISION SITE HAEMATOMA ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 6 FDA reports)
INFECTED CYST ( 6 FDA reports)
INFUSION SITE HAEMORRHAGE ( 6 FDA reports)
INFUSION SITE REACTION ( 6 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 6 FDA reports)
IVTH NERVE PARALYSIS ( 6 FDA reports)
JC VIRUS INFECTION ( 6 FDA reports)
JOINT DESTRUCTION ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
JOINT TUBERCULOSIS ( 6 FDA reports)
JUDGEMENT IMPAIRED ( 6 FDA reports)
KLEBSIELLA TEST POSITIVE ( 6 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 6 FDA reports)
LASER THERAPY ( 6 FDA reports)
LENS DISORDER ( 6 FDA reports)
LEPROSY ( 6 FDA reports)
LICHEN SCLEROSUS ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LIMB ASYMMETRY ( 6 FDA reports)
LINEAR IGA DISEASE ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
LYMPH NODE PAIN ( 6 FDA reports)
LYMPHOCYTIC INFILTRATION ( 6 FDA reports)
LYMPHORRHOEA ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MASTOIDITIS ( 6 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 6 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 6 FDA reports)
METASTASES TO LARGE INTESTINE ( 6 FDA reports)
METASTASES TO PLEURA ( 6 FDA reports)
MICROGNATHIA ( 6 FDA reports)
MIDDLE EAR INFLAMMATION ( 6 FDA reports)
MITRAL VALVE REPLACEMENT ( 6 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 6 FDA reports)
MUSCLE GRAFT ( 6 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 6 FDA reports)
MYOCLONIC EPILEPSY ( 6 FDA reports)
NEONATAL DISORDER ( 6 FDA reports)
NEPHRECTOMY ( 6 FDA reports)
NEPHROANGIOSCLEROSIS ( 6 FDA reports)
NEUROMYELITIS OPTICA ( 6 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 6 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 6 FDA reports)
OESOPHAGEAL ACHALASIA ( 6 FDA reports)
OLIGODIPSIA ( 6 FDA reports)
ORAL TORUS ( 6 FDA reports)
ORBITAL OEDEMA ( 6 FDA reports)
OROPHARYNGEAL SWELLING ( 6 FDA reports)
ORTHOSTATIC INTOLERANCE ( 6 FDA reports)
OVARIAN CYST RUPTURED ( 6 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 6 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 6 FDA reports)
PANCREATIC ABSCESS ( 6 FDA reports)
PAPILLARY THYROID CANCER ( 6 FDA reports)
PARASOMNIA ( 6 FDA reports)
PARATHYROIDECTOMY ( 6 FDA reports)
PENILE OEDEMA ( 6 FDA reports)
PENIS CARCINOMA ( 6 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PERITONEAL ABSCESS ( 6 FDA reports)
PHLEBITIS SUPERFICIAL ( 6 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
PLACENTAL INFARCTION ( 6 FDA reports)
POLYMENORRHOEA ( 6 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 6 FDA reports)
POSTOPERATIVE ABSCESS ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 6 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 6 FDA reports)
PRODUCT FORMULATION ISSUE ( 6 FDA reports)
PTERYGIUM COLLI ( 6 FDA reports)
PULMONARY ARTERY DILATATION ( 6 FDA reports)
PULMONARY CALCIFICATION ( 6 FDA reports)
PULMONARY EOSINOPHILIA ( 6 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 6 FDA reports)
RADIATION PNEUMONITIS ( 6 FDA reports)
RECTAL CANCER METASTATIC ( 6 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 6 FDA reports)
REHABILITATION THERAPY ( 6 FDA reports)
RENAL ARTERY OCCLUSION ( 6 FDA reports)
RENAL STONE REMOVAL ( 6 FDA reports)
REPETITIVE SPEECH ( 6 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 6 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 6 FDA reports)
RETICULOCYTE COUNT DECREASED ( 6 FDA reports)
RETINAL OEDEMA ( 6 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 6 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SALMONELLA SEPSIS ( 6 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 6 FDA reports)
SCROTAL DISORDER ( 6 FDA reports)
SIDEROBLASTIC ANAEMIA ( 6 FDA reports)
SIMPLE PARTIAL SEIZURES ( 6 FDA reports)
SINGLE UMBILICAL ARTERY ( 6 FDA reports)
SKIN CANDIDA ( 6 FDA reports)
SKIN FRAGILITY ( 6 FDA reports)
SKIN TURGOR DECREASED ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
SLEEP-RELATED EATING DISORDER ( 6 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 6 FDA reports)
SMALL INTESTINAL STENOSIS ( 6 FDA reports)
SMALL INTESTINE ULCER ( 6 FDA reports)
SODIUM RETENTION ( 6 FDA reports)
SPLEEN CONGESTION ( 6 FDA reports)
SPLENIC ABSCESS ( 6 FDA reports)
SPLENIC GRANULOMA ( 6 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 6 FDA reports)
STATUS ASTHMATICUS ( 6 FDA reports)
SWEAT GLAND DISORDER ( 6 FDA reports)
SYNOVIAL DISORDER ( 6 FDA reports)
THERMOHYPERAESTHESIA ( 6 FDA reports)
THYROID MASS ( 6 FDA reports)
THYROID OPERATION ( 6 FDA reports)
THYROXINE INCREASED ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TOE OPERATION ( 6 FDA reports)
TONGUE BLACK HAIRY ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOOTH DECALCIFICATION ( 6 FDA reports)
TOXIC OPTIC NEUROPATHY ( 6 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 6 FDA reports)
TUMOUR MARKER INCREASED ( 6 FDA reports)
TUNNEL VISION ( 6 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
URAEMIC GASTROPATHY ( 6 FDA reports)
URETHRAL DISORDER ( 6 FDA reports)
URETHRAL HAEMORRHAGE ( 6 FDA reports)
URETHRITIS NONINFECTIVE ( 6 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 6 FDA reports)
VAGINAL ULCERATION ( 6 FDA reports)
VASCULAR ENCEPHALOPATHY ( 6 FDA reports)
VASCULAR RUPTURE ( 6 FDA reports)
VENA CAVA FILTER INSERTION ( 6 FDA reports)
VIRAL LABYRINTHITIS ( 6 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 5 FDA reports)
MECONIUM ABNORMAL ( 5 FDA reports)
MENINGISM ( 5 FDA reports)
MENISCUS REMOVAL ( 5 FDA reports)
MESENTERIC ARTERY STENOSIS ( 5 FDA reports)
MESENTERIC OCCLUSION ( 5 FDA reports)
METASTASES TO BONE MARROW ( 5 FDA reports)
METASTASES TO SPLEEN ( 5 FDA reports)
METATARSUS PRIMUS VARUS ( 5 FDA reports)
MICROCOCCUS INFECTION ( 5 FDA reports)
MITOCHONDRIAL MYOPATHY ( 5 FDA reports)
MITRAL VALVE SCLEROSIS ( 5 FDA reports)
MOTOR NEURONE DISEASE ( 5 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 5 FDA reports)
MUSCLE ABSCESS ( 5 FDA reports)
MUSCULAR DYSTROPHY ( 5 FDA reports)
MYASTHENIC SYNDROME ( 5 FDA reports)
MYCOPLASMA INFECTION ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 5 FDA reports)
MYOCARDIAC ABSCESS ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
MYOGLOBIN URINE PRESENT ( 5 FDA reports)
MYOPATHY STEROID ( 5 FDA reports)
NAIL BED BLEEDING ( 5 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 5 FDA reports)
NEUROENDOCRINE TUMOUR ( 5 FDA reports)
NEUROFIBROMATOSIS ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NEUTROPHIL COUNT ( 5 FDA reports)
NO ADVERSE DRUG EFFECT ( 5 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 5 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 5 FDA reports)
OSTEITIS DEFORMANS ( 5 FDA reports)
OSTEOARTHROPATHY ( 5 FDA reports)
OSTEOMYELITIS ACUTE ( 5 FDA reports)
OSTEOSYNTHESIS ( 5 FDA reports)
OVARIAN CANCER METASTATIC ( 5 FDA reports)
OVARIAN CANCER RECURRENT ( 5 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 5 FDA reports)
PALATAL OEDEMA ( 5 FDA reports)
PANCREATIC NECROSIS ( 5 FDA reports)
PARACENTESIS ( 5 FDA reports)
PARATHYROID DISORDER ( 5 FDA reports)
PARIETAL CELL ANTIBODY POSITIVE ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
PELVIC FLUID COLLECTION ( 5 FDA reports)
PERICARDITIS CONSTRICTIVE ( 5 FDA reports)
PERIPHERAL PARALYSIS ( 5 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 5 FDA reports)
PHANTOM PAIN ( 5 FDA reports)
PHARYNGEAL ABSCESS ( 5 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 5 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 5 FDA reports)
PILOERECTION ( 5 FDA reports)
PITUITARY TUMOUR RECURRENT ( 5 FDA reports)
PLASMA CELL DISORDER ( 5 FDA reports)
POISONING DELIBERATE ( 5 FDA reports)
POLYCYTHAEMIA VERA ( 5 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 5 FDA reports)
POST PROCEDURAL DRAINAGE ( 5 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 5 FDA reports)
POTTER'S SYNDROME ( 5 FDA reports)
PRECANCEROUS CELLS PRESENT ( 5 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 5 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
PROPIONIBACTERIUM INFECTION ( 5 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 5 FDA reports)
PRURITUS ALLERGIC ( 5 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 5 FDA reports)
PUS IN STOOL ( 5 FDA reports)
PYELONEPHRITIS CHRONIC ( 5 FDA reports)
PYOGENIC GRANULOMA ( 5 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 5 FDA reports)
RADIATION INJURY ( 5 FDA reports)
RADIATION MUCOSITIS ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
RECTAL ADENOMA ( 5 FDA reports)
RECTAL OBSTRUCTION ( 5 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
RENAL AMYLOIDOSIS ( 5 FDA reports)
RENAL CANCER STAGE III ( 5 FDA reports)
RENAL CYST INFECTION ( 5 FDA reports)
RENAL CYST RUPTURED ( 5 FDA reports)
RENAL HAEMATOMA ( 5 FDA reports)
RENAL VEIN THROMBOSIS ( 5 FDA reports)
RENAL VESSEL DISORDER ( 5 FDA reports)
RETINAL PIGMENTATION ( 5 FDA reports)
RETINOIC ACID SYNDROME ( 5 FDA reports)
SACROILIITIS ( 5 FDA reports)
SCEDOSPORIUM INFECTION ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SEBORRHOEA ( 5 FDA reports)
SEMEN VOLUME DECREASED ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SINUS RHYTHM ( 5 FDA reports)
SKIN CANCER METASTATIC ( 5 FDA reports)
SKIN DEPIGMENTATION ( 5 FDA reports)
SKIN GRAFT FAILURE ( 5 FDA reports)
SKIN SENSITISATION ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SLEEP TERROR ( 5 FDA reports)
SMOKER ( 5 FDA reports)
SPINAL CORD HAEMORRHAGE ( 5 FDA reports)
SPINAL CORD INFARCTION ( 5 FDA reports)
SPINAL HAEMATOMA ( 5 FDA reports)
SPINDLE CELL SARCOMA ( 5 FDA reports)
SPLENIC ARTERY ANEURYSM ( 5 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 5 FDA reports)
STERNAL FRACTURE ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STRESS ULCER ( 5 FDA reports)
SUPRAPUBIC PAIN ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
SYNDACTYLY ( 5 FDA reports)
SYNOVIAL SARCOMA ( 5 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
TELANGIECTASIA ( 5 FDA reports)
TESTICULAR NEOPLASM ( 5 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 5 FDA reports)
THYROXINE FREE INCREASED ( 5 FDA reports)
TINEA INFECTION ( 5 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 5 FDA reports)
TRAUMATIC FRACTURE ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 5 FDA reports)
TUMOUR INVASION ( 5 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
URETERIC CANCER ( 5 FDA reports)
URINARY BLADDER POLYP ( 5 FDA reports)
URINOMA ( 5 FDA reports)
VASCULAR STENOSIS ( 5 FDA reports)
VASOSPASM ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VESTIBULITIS ( 5 FDA reports)
VIRAL SINUSITIS ( 5 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 5 FDA reports)
VITAL CAPACITY DECREASED ( 5 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
VOCAL CORD POLYP ( 5 FDA reports)
WEANING FAILURE ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ABORTION THREATENED ( 5 FDA reports)
ACHLORHYDRIA ( 5 FDA reports)
ACQUIRED PIGMENTED RETINOPATHY ( 5 FDA reports)
ADRENAL HAEMORRHAGE ( 5 FDA reports)
ADRENAL INSUFFICIENCY NEONATAL ( 5 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ANGIOGRAM ( 5 FDA reports)
ANISOMETROPIA ( 5 FDA reports)
ANORECTAL INFECTION ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ( 5 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 5 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 5 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 5 FDA reports)
ASCITES INFECTION ( 5 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 5 FDA reports)
ASTEATOSIS ( 5 FDA reports)
ASTROCYTOMA ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
AXILLARY PAIN ( 5 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 5 FDA reports)
BALANITIS ( 5 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BIOPSY BREAST ( 5 FDA reports)
BLADDER DILATATION ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 5 FDA reports)
BLINDNESS DAY ( 5 FDA reports)
BLOOD BILIRUBIN DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 5 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 5 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 5 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 5 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 5 FDA reports)
BONE ATROPHY ( 5 FDA reports)
BOWEL SOUNDS ABNORMAL ( 5 FDA reports)
BREAST CANCER STAGE I ( 5 FDA reports)
BREAST CYST ( 5 FDA reports)
BREAST HAEMORRHAGE ( 5 FDA reports)
BRONCHIAL HYPERACTIVITY ( 5 FDA reports)
BRONCHOPLEURAL FISTULA ( 5 FDA reports)
BRONCHOSCOPY ( 5 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 5 FDA reports)
BURN OESOPHAGEAL ( 5 FDA reports)
BURNOUT SYNDROME ( 5 FDA reports)
BUTTERFLY RASH ( 5 FDA reports)
BUTTOCK PAIN ( 5 FDA reports)
CALCIUM IONISED INCREASED ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 5 FDA reports)
CARCINOID TUMOUR PULMONARY ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIAC ABLATION ( 5 FDA reports)
CARDIAC DISCOMFORT ( 5 FDA reports)
CARDIAC INFECTION ( 5 FDA reports)
CARDIAC OUTPUT INCREASED ( 5 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDITIS ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CEREBRAL HYGROMA ( 5 FDA reports)
CEREBRAL HYPOPERFUSION ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHEMICAL INJURY ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
CHONDROLYSIS ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CHRONIC FATIGUE SYNDROME ( 5 FDA reports)
CHRONIC HEPATIC FAILURE ( 5 FDA reports)
CLEFT LIP AND PALATE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 5 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 5 FDA reports)
COLONIC HAEMATOMA ( 5 FDA reports)
COMPULSIVE SHOPPING ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CONJUNCTIVAL PALLOR ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CORONA VIRUS INFECTION ( 5 FDA reports)
CORONARY ARTERY DISSECTION ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 5 FDA reports)
CROSS SENSITIVITY REACTION ( 5 FDA reports)
DEAFNESS TRANSITORY ( 5 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 5 FDA reports)
DENTAL CLEANING ( 5 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 5 FDA reports)
DEVICE INEFFECTIVE ( 5 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 5 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 5 FDA reports)
DISINHIBITION ( 5 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 5 FDA reports)
DNA ANTIBODY POSITIVE ( 5 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 5 FDA reports)
DRUG LEVEL FLUCTUATING ( 5 FDA reports)
DRUG TOLERANCE DECREASED ( 5 FDA reports)
EAR NEOPLASM ( 5 FDA reports)
EAR PRURITUS ( 5 FDA reports)
ECHOLALIA ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 5 FDA reports)
ENDOSCOPY ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 5 FDA reports)
EPIDURITIS ( 5 FDA reports)
ERYTHEMA ANNULARE ( 5 FDA reports)
EXPOSURE TO TOXIC AGENT ( 5 FDA reports)
EXTRASKELETAL OSSIFICATION ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
EYE LASER SURGERY ( 5 FDA reports)
EYES SUNKEN ( 5 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 5 FDA reports)
FAILURE OF IMPLANT ( 5 FDA reports)
FLASHBACK ( 5 FDA reports)
FOETAL ARRHYTHMIA ( 5 FDA reports)
FREEZING PHENOMENON ( 5 FDA reports)
GASTRIC NEOPLASM ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 5 FDA reports)
GASTROINTESTINAL INJURY ( 5 FDA reports)
GASTROOESOPHAGITIS ( 5 FDA reports)
GASTROSTOMY TUBE INSERTION ( 5 FDA reports)
GENITAL INFECTION FEMALE ( 5 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 5 FDA reports)
HAEMOCONCENTRATION ( 5 FDA reports)
HAEMOGLOBINURIA ( 5 FDA reports)
HAEMOSIDEROSIS ( 5 FDA reports)
HEAD AND NECK CANCER ( 5 FDA reports)
HEAD BANGING ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEAT ILLNESS ( 5 FDA reports)
HEPATIC CALCIFICATION ( 5 FDA reports)
HEPATIC INFARCTION ( 5 FDA reports)
HEPATIC INFECTION ( 5 FDA reports)
HEPATIC ISCHAEMIA ( 5 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 5 FDA reports)
HEPATITIS GRANULOMATOUS ( 5 FDA reports)
HERNIA OBSTRUCTIVE ( 5 FDA reports)
HISTOLOGY ABNORMAL ( 5 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HIV TEST POSITIVE ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERGLOBULINAEMIA ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 5 FDA reports)
HYPOAESTHESIA EYE ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
HYPOSPERMIA ( 5 FDA reports)
ILEAL PERFORATION ( 5 FDA reports)
IMPLANT SITE INFECTION ( 5 FDA reports)
INCLUSION BODY MYOSITIS ( 5 FDA reports)
INFANTILE APNOEIC ATTACK ( 5 FDA reports)
INFECTION PARASITIC ( 5 FDA reports)
INFERIOR VENA CAVA DILATATION ( 5 FDA reports)
INJECTION SITE ABSCESS ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INJURY ASPHYXIATION ( 5 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 5 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 5 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 5 FDA reports)
IUCD COMPLICATION ( 5 FDA reports)
JOINT WARMTH ( 5 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 5 FDA reports)
LARYNGEAL DISORDER ( 5 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 5 FDA reports)
LIMB IMMOBILISATION ( 5 FDA reports)
LIMB MALFORMATION ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 5 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 5 FDA reports)
LIVIDITY ( 5 FDA reports)
LOOSE STOOLS ( 5 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
LUNG LOBECTOMY ( 5 FDA reports)
LYMPHATIC OBSTRUCTION ( 5 FDA reports)
LYMPHOMATOID PAPULOSIS ( 5 FDA reports)
MACROSOMIA ( 5 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 4 FDA reports)
ABORTION ( 4 FDA reports)
ACETABULUM FRACTURE ( 4 FDA reports)
ACHOLIA ( 4 FDA reports)
ACNE PUSTULAR ( 4 FDA reports)
ACTINIC ELASTOSIS ( 4 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 4 FDA reports)
ADENOIDECTOMY ( 4 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 4 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 4 FDA reports)
AEROPHAGIA ( 4 FDA reports)
AIR EMBOLISM ( 4 FDA reports)
ALCOHOLIC ( 4 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 4 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 4 FDA reports)
ALLERGIC COUGH ( 4 FDA reports)
AMNIOCENTESIS ABNORMAL ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANASTOMOTIC LEAK ( 4 FDA reports)
ANDROGEN DEFICIENCY ( 4 FDA reports)
ANGIOLIPOMA ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 4 FDA reports)
ANORECTAL CELLULITIS ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 4 FDA reports)
AORTITIS ( 4 FDA reports)
APICAL GRANULOMA ( 4 FDA reports)
APPLICATION SITE PARAESTHESIA ( 4 FDA reports)
APPLICATION SITE PUSTULES ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIAL HAEMORRHAGE ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ARTERIAL REPAIR ( 4 FDA reports)
ARTERIAL STENT INSERTION ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASPERGER'S DISORDER ( 4 FDA reports)
AUTOIMMUNE PANCREATITIS ( 4 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 4 FDA reports)
AVERSION ( 4 FDA reports)
BACTERIAL PYELONEPHRITIS ( 4 FDA reports)
BASE EXCESS ABNORMAL ( 4 FDA reports)
BASOPHIL COUNT DECREASED ( 4 FDA reports)
BENIGN NEOPLASM ( 4 FDA reports)
BILE DUCT STENT INSERTION ( 4 FDA reports)
BILIARY CIRRHOSIS ( 4 FDA reports)
BILIARY DRAINAGE ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BIOPSY LUNG ABNORMAL ( 4 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 4 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 4 FDA reports)
BITE ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLAST CELLS PRESENT ( 4 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 4 FDA reports)
BLOOD CREATINE DECREASED ( 4 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 4 FDA reports)
BLOOD INSULIN INCREASED ( 4 FDA reports)
BLOOD IRON ABNORMAL ( 4 FDA reports)
BLOOD LACTIC ACID ( 4 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 4 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 4 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 4 FDA reports)
BONE FISSURE ( 4 FDA reports)
BONE TUBERCULOSIS ( 4 FDA reports)
BREAST CANCER STAGE II ( 4 FDA reports)
BREAST DISCOMFORT ( 4 FDA reports)
BREECH PRESENTATION ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
CAMPTODACTYLY CONGENITAL ( 4 FDA reports)
CANDIDA PNEUMONIA ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARCINOID TUMOUR ( 4 FDA reports)
CARDIAC PERFORATION ( 4 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 4 FDA reports)
CAROTID ARTERY ATHEROMA ( 4 FDA reports)
CATHETER SITE HAEMATOMA ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM FUNCTION TEST ABNORMAL ( 4 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CERVIX CARCINOMA STAGE III ( 4 FDA reports)
CERVIX NEOPLASM ( 4 FDA reports)
CHEMICAL PERITONITIS ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 4 FDA reports)
CLEFT LIP ( 4 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 4 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 4 FDA reports)
COLON CANCER STAGE II ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 4 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONDYLOMA ACUMINATUM ( 4 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 4 FDA reports)
CONJUNCTIVAL OEDEMA ( 4 FDA reports)
CONJUNCTIVITIS VIRAL ( 4 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
COR PULMONALE CHRONIC ( 4 FDA reports)
CORNEAL OEDEMA ( 4 FDA reports)
CORNEAL PIGMENTATION ( 4 FDA reports)
CORNEAL TRANSPLANT ( 4 FDA reports)
CRANIAL NERVE DISORDER ( 4 FDA reports)
CRANIAL NERVE PARALYSIS ( 4 FDA reports)
CRANIAL NEUROPATHY ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CSF CELL COUNT INCREASED ( 4 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
CYSTITIS ESCHERICHIA ( 4 FDA reports)
CYSTOID MACULAR OEDEMA ( 4 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 4 FDA reports)
DECEREBRATION ( 4 FDA reports)
DELAYED FONTANELLE CLOSURE ( 4 FDA reports)
DERMATITIS HERPETIFORMIS ( 4 FDA reports)
DIAPHRAGMATIC RUPTURE ( 4 FDA reports)
DISUSE SYNDROME ( 4 FDA reports)
DOUBLE HETEROZYGOUS SICKLING DISORDERS ( 4 FDA reports)
DRUG ADDICT ( 4 FDA reports)
DRUG THERAPY CHANGED ( 4 FDA reports)
DYSLEXIA ( 4 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 4 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 4 FDA reports)
ECZEMA NUMMULAR ( 4 FDA reports)
ELECTRIC SHOCK ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 4 FDA reports)
ENCHONDROMATOSIS ( 4 FDA reports)
ENDOSCOPY ABNORMAL ( 4 FDA reports)
ENTERAL NUTRITION ( 4 FDA reports)
ENTEROSTOMY ( 4 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 4 FDA reports)
EPIPHYSIOLYSIS ( 4 FDA reports)
ERECTION INCREASED ( 4 FDA reports)
ERYTHROPENIA ( 4 FDA reports)
EXCITABILITY ( 4 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EXTERNAL EAR PAIN ( 4 FDA reports)
EYE INFECTION FUNGAL ( 4 FDA reports)
EYELID INFECTION ( 4 FDA reports)
FACTOR VIII DEFICIENCY ( 4 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 4 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FEMORAL NERVE INJURY ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOETAL CARDIAC DISORDER ( 4 FDA reports)
FOETAL HAEMOGLOBIN INCREASED ( 4 FDA reports)
FOREARM FRACTURE ( 4 FDA reports)
FRACTURED COCCYX ( 4 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 4 FDA reports)
FROSTBITE ( 4 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 4 FDA reports)
GALLBLADDER EMPYEMA ( 4 FDA reports)
GALLBLADDER NECROSIS ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 4 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 4 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 4 FDA reports)
GASTROPLEURAL FISTULA ( 4 FDA reports)
GASTROSTOMY ( 4 FDA reports)
GENITAL CANDIDIASIS ( 4 FDA reports)
GILBERT'S SYNDROME ( 4 FDA reports)
GINGIVITIS ULCERATIVE ( 4 FDA reports)
GLOSSOPTOSIS ( 4 FDA reports)
GUTTATE PSORIASIS ( 4 FDA reports)
HAEMATOCRIT ABNORMAL ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HEAT THERAPY ( 4 FDA reports)
HEMISENSORY NEGLECT ( 4 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 4 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 4 FDA reports)
HEPATITIS INFECTIOUS ( 4 FDA reports)
HERPES OPHTHALMIC ( 4 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 4 FDA reports)
HYPERALDOSTERONISM ( 4 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPERLIPASAEMIA ( 4 FDA reports)
HYPERMAGNESAEMIA ( 4 FDA reports)
HYPOPHYSITIS ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 4 FDA reports)
INCORRECT PRODUCT STORAGE ( 4 FDA reports)
INFECTED BITES ( 4 FDA reports)
INFECTED NEOPLASM ( 4 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INFUSION SITE PRURITUS ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INJECTION SITE ANAESTHESIA ( 4 FDA reports)
INJECTION SITE INJURY ( 4 FDA reports)
INJECTION SITE OEDEMA ( 4 FDA reports)
INTENTION TREMOR ( 4 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
INTRASPINAL ABSCESS ( 4 FDA reports)
IRIS COLOBOMA ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 4 FDA reports)
JEJUNAL PERFORATION ( 4 FDA reports)
JEJUNAL STENOSIS ( 4 FDA reports)
JOINT HYPEREXTENSION ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
KUSSMAUL RESPIRATION ( 4 FDA reports)
KYPHOSCOLIOSIS ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LATENT TETANY ( 4 FDA reports)
LEARNING DISABILITY ( 4 FDA reports)
LERICHE SYNDROME ( 4 FDA reports)
LESION OF ULNAR NERVE ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LYMPH GLAND INFECTION ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MECHANICAL ILEUS ( 4 FDA reports)
MEDICATION TAMPERING ( 4 FDA reports)
MENINGITIS ENTEROCOCCAL ( 4 FDA reports)
MENINGITIS HERPES ( 4 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 4 FDA reports)
METASTASES TO ABDOMINAL WALL ( 4 FDA reports)
METASTASES TO CHEST WALL ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTASES TO SMALL INTESTINE ( 4 FDA reports)
METASTASES TO THORAX ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MICROPHTHALMOS ( 4 FDA reports)
MICROSOMIA ( 4 FDA reports)
MORAXELLA INFECTION ( 4 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 4 FDA reports)
MYOCARDIAL CALCIFICATION ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 4 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 4 FDA reports)
NEEDLE ISSUE ( 4 FDA reports)
NEONATAL CHOLESTASIS ( 4 FDA reports)
NEPHRITIC SYNDROME ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
NEURILEMMOMA ( 4 FDA reports)
NEURODEGENERATIVE DISORDER ( 4 FDA reports)
NEUROGENIC SHOCK ( 4 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 4 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OCULAR VASCULAR DISORDER ( 4 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 4 FDA reports)
OESOPHAGEAL INFECTION ( 4 FDA reports)
OESOPHAGEAL NEOPLASM ( 4 FDA reports)
OESOPHAGEAL PERFORATION ( 4 FDA reports)
OESTRADIOL DECREASED ( 4 FDA reports)
OLIGODENDROGLIOMA ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
ONCOCYTOMA ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
OROMANDIBULAR DYSTONIA ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 4 FDA reports)
OVARIAN ENLARGEMENT ( 4 FDA reports)
OVARIAN INFECTION ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PALMAR ERYTHEMA ( 4 FDA reports)
PALPABLE PURPURA ( 4 FDA reports)
PANCREATIC CALCIFICATION ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PENILE HAEMORRHAGE ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PEPTIC ULCER PERFORATION ( 4 FDA reports)
PERIANAL ERYTHEMA ( 4 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 4 FDA reports)
PERIORBITAL CELLULITIS ( 4 FDA reports)
PERIPHERAL PULSE DECREASED ( 4 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
PEYRONIE'S DISEASE ( 4 FDA reports)
PHAEHYPHOMYCOSIS ( 4 FDA reports)
PHARYNGEAL MASS ( 4 FDA reports)
PHLEBOTHROMBOSIS ( 4 FDA reports)
PIGMENTED NAEVUS ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PLATELET DESTRUCTION INCREASED ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
PNEUMONIA CHLAMYDIAL ( 4 FDA reports)
POIKILOCYTOSIS ( 4 FDA reports)
POLYARTERITIS NODOSA ( 4 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POST PROCEDURAL BILE LEAK ( 4 FDA reports)
POST PROCEDURAL CONSTIPATION ( 4 FDA reports)
POST PROCEDURAL DISCHARGE ( 4 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 4 FDA reports)
PRODUCT CONTAMINATION ( 4 FDA reports)
PRODUCT PACKAGING ISSUE ( 4 FDA reports)
PROLONGED EXPIRATION ( 4 FDA reports)
PROSTATIC ADENOMA ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PROTEUS TEST POSITIVE ( 4 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 4 FDA reports)
PULMONARY NECROSIS ( 4 FDA reports)
PULMONARY SARCOIDOSIS ( 4 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 4 FDA reports)
RADICULAR SYNDROME ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 4 FDA reports)
REFRACTION DISORDER ( 4 FDA reports)
RENAL NECROSIS ( 4 FDA reports)
RENAL SALT-WASTING SYNDROME ( 4 FDA reports)
RESPIRATORY PARALYSIS ( 4 FDA reports)
RETINAL ANEURYSM ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RETINAL ISCHAEMIA ( 4 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 4 FDA reports)
RETINITIS PIGMENTOSA ( 4 FDA reports)
RETINOGRAM ABNORMAL ( 4 FDA reports)
SALIVA DISCOLOURATION ( 4 FDA reports)
SCLERODERMA RENAL CRISIS ( 4 FDA reports)
SEBACEOUS CARCINOMA ( 4 FDA reports)
SENSE OF OPPRESSION ( 4 FDA reports)
SERONEGATIVE ARTHRITIS ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SERUM SEROTONIN DECREASED ( 4 FDA reports)
SHOULDER DEFORMITY ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN ULCER HAEMORRHAGE ( 4 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
SOFT TISSUE INFLAMMATION ( 4 FDA reports)
SOLILOQUY ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL CLAUDICATION ( 4 FDA reports)
SPINAL MUSCULAR ATROPHY ( 4 FDA reports)
SPINAL SHOCK ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
SPONDYLOLYSIS ( 4 FDA reports)
SPONDYLOSIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 4 FDA reports)
STENT REMOVAL ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
STRESS AT WORK ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SUPERFICIAL INJURY OF EYE ( 4 FDA reports)
SURFACTANT PROTEIN INCREASED ( 4 FDA reports)
SUSPICIOUSNESS ( 4 FDA reports)
SYDENHAM'S CHOREA ( 4 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 4 FDA reports)
SYMPTOM MASKED ( 4 FDA reports)
SYNOVECTOMY ( 4 FDA reports)
TARSAL TUNNEL SYNDROME ( 4 FDA reports)
TENDON CALCIFICATION ( 4 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYROIDECTOMY ( 4 FDA reports)
THYROXINE FREE DECREASED ( 4 FDA reports)
TOE DEFORMITY ( 4 FDA reports)
TONGUE HAEMATOMA ( 4 FDA reports)
TONGUE NEOPLASM ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TRANCE ( 4 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 4 FDA reports)
TUBERCULOSIS LIVER ( 4 FDA reports)
TUBO-OVARIAN ABSCESS ( 4 FDA reports)
URATE NEPHROPATHY ( 4 FDA reports)
URINARY CASTS ( 4 FDA reports)
URINARY CASTS PRESENT ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
URINARY TRACT INFLAMMATION ( 4 FDA reports)
URINARY TRACT OPERATION ( 4 FDA reports)
VANISHING BILE DUCT SYNDROME ( 4 FDA reports)
VASCULAR ACCESS COMPLICATION ( 4 FDA reports)
VASCULAR INJURY ( 4 FDA reports)
VASOMOTOR RHINITIS ( 4 FDA reports)
VENOUS INJURY ( 4 FDA reports)
VENTRICULAR HYPOPLASIA ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VISCERAL CONGESTION ( 4 FDA reports)
VITAMIN B1 DEFICIENCY ( 4 FDA reports)
VITAMIN B6 DEFICIENCY ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VULVOVAGINAL ERYTHEMA ( 4 FDA reports)
WEIGHT GAIN POOR ( 4 FDA reports)
WOUND EVISCERATION ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 3 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 3 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 3 FDA reports)
MEDIASTINUM NEOPLASM ( 3 FDA reports)
MENINGITIS LEPTOSPIRAL ( 3 FDA reports)
MENINGORADICULITIS ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
METANEPHRINE URINE INCREASED ( 3 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 3 FDA reports)
METASTASES TO BREAST ( 3 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MICROCEPHALY ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MICROVASCULAR ANGINA ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 3 FDA reports)
MITOCHONDRIAL TOXICITY ( 3 FDA reports)
MITRAL VALVE ATRESIA ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MULTIPLE EPIPHYSEAL DYSPLASIA ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MURPHY'S SIGN POSITIVE ( 3 FDA reports)
MUSCLE HYPERTROPHY ( 3 FDA reports)
MYELOCYTE PRESENT ( 3 FDA reports)
MYELOID MATURATION ARREST ( 3 FDA reports)
MYOCARDIAL STRAIN ( 3 FDA reports)
MYOSITIS OSSIFICANS ( 3 FDA reports)
NAIL BED INFECTION ( 3 FDA reports)
NASAL OBSTRUCTION ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NECROSIS ISCHAEMIC ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 3 FDA reports)
NEUROBLASTOMA ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 3 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 3 FDA reports)
NIGHT CRAMPS ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 3 FDA reports)
NUCLEATED RED CELLS ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
OESOPHAGEAL FISTULA ( 3 FDA reports)
OESOPHAGEAL OPERATION ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 3 FDA reports)
OMENTUM NEOPLASM ( 3 FDA reports)
ONYCHOPHAGIA ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
ORAL MUCOSAL DISORDER ( 3 FDA reports)
ORCHITIS NONINFECTIVE ( 3 FDA reports)
OROPHARYNGITIS FUNGAL ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
OVARIAN ATROPHY ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PACEMAKER COMPLICATION ( 3 FDA reports)
PAIN MANAGEMENT ( 3 FDA reports)
PANCOAST'S TUMOUR ( 3 FDA reports)
PANCREAS DIVISUM ( 3 FDA reports)
PANCREAS LIPOMATOSIS ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PANCREATIC FISTULA ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PARAKERATOSIS ( 3 FDA reports)
PARAPHARYNGEAL ABSCESS ( 3 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 3 FDA reports)
PARESIS ANAL SPHINCTER ( 3 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 3 FDA reports)
PENILE INFECTION ( 3 FDA reports)
PERICARDIAL RUB ( 3 FDA reports)
PERINEAL ABSCESS ( 3 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 3 FDA reports)
PERIPHLEBITIS ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERITONEAL INFECTION ( 3 FDA reports)
PERITONEAL LESION ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PERTUSSIS ( 3 FDA reports)
PH BODY FLUID DECREASED ( 3 FDA reports)
PHAEOCHROMOCYTOMA ( 3 FDA reports)
PHLEBITIS INFECTIVE ( 3 FDA reports)
PHOBIA OF DRIVING ( 3 FDA reports)
PHOBIC AVOIDANCE ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PHOSPHENES ( 3 FDA reports)
PHRENIC NERVE PARALYSIS ( 3 FDA reports)
PHYSIOTHERAPY ( 3 FDA reports)
PICKWICKIAN SYNDROME ( 3 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 3 FDA reports)
PLATELET AGGREGATION ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PLATELET PRODUCTION DECREASED ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PNEUMATOSIS ( 3 FDA reports)
PNEUMATURIA ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POROCARCINOMA ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 3 FDA reports)
POST POLIO SYNDROME ( 3 FDA reports)
POSTRENAL FAILURE ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PRECANCEROUS SKIN LESION ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PROCALCITONIN INCREASED ( 3 FDA reports)
PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PRODUCT DROPPER ISSUE ( 3 FDA reports)
PROSTATECTOMY ( 3 FDA reports)
PROSTATIC CALCIFICATION ( 3 FDA reports)
PROSTATIC HAEMORRHAGE ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 3 FDA reports)
PROSTRATION ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PSEUDOMONAS BRONCHITIS ( 3 FDA reports)
PSYCHOMOTOR AGITATION ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PUTAMEN HAEMORRHAGE ( 3 FDA reports)
PYLORUS DILATATION ( 3 FDA reports)
Q FEVER ( 3 FDA reports)
RASH FOLLICULAR ( 3 FDA reports)
RECALL PHENOMENON ( 3 FDA reports)
RED BLOOD CELLS URINE ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
REGRESSIVE BEHAVIOUR ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 3 FDA reports)
RENAL ARTERY THROMBOSIS ( 3 FDA reports)
RENAL CYST HAEMORRHAGE ( 3 FDA reports)
RENAL TUBERCULOSIS ( 3 FDA reports)
RESECTION OF RECTUM ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETINAL DYSTROPHY ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETROGRADE EJACULATION ( 3 FDA reports)
RETROPERITONEAL NEOPLASM ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RHINOVIRUS INFECTION ( 3 FDA reports)
SALIVARY GLAND CALCULUS ( 3 FDA reports)
SALIVARY GLAND DISORDER ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCINTILLATING SCOTOMA ( 3 FDA reports)
SCROTAL ABSCESS ( 3 FDA reports)
SCROTAL ERYTHEMA ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SECONDARY HYPOTHYROIDISM ( 3 FDA reports)
SELF-INDUCED VOMITING ( 3 FDA reports)
SEMINAL VESICULAR CALCULUS ( 3 FDA reports)
SENSATION OF BLOOD FLOW ( 3 FDA reports)
SEPTIC ENCEPHALOPATHY ( 3 FDA reports)
SEPTOPLASTY ( 3 FDA reports)
SERRATIA TEST POSITIVE ( 3 FDA reports)
SERUM FERRITIN ABNORMAL ( 3 FDA reports)
SERUM SEROTONIN INCREASED ( 3 FDA reports)
SHORT-BOWEL SYNDROME ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SKIN DEGENERATIVE DISORDER ( 3 FDA reports)
SOLITARY KIDNEY ( 3 FDA reports)
SOMATIC DELUSION ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPERMATOGENESIS ABNORMAL ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL CORD OEDEMA ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPLENIC INFECTION ( 3 FDA reports)
SPLENIC LESION ( 3 FDA reports)
STAB WOUND ( 3 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 3 FDA reports)
STICKY SKIN ( 3 FDA reports)
SUBDURAL EMPYEMA ( 3 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 3 FDA reports)
SUCROSE INTOLERANCE ( 3 FDA reports)
SURGICAL STAPLING ( 3 FDA reports)
SYRINGE ISSUE ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
TABLET ISSUE ( 3 FDA reports)
TACITURNITY ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TENDON OPERATION ( 3 FDA reports)
TERATOMA ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
TETANUS ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBIN TIME SHORTENED ( 3 FDA reports)
THROMBOANGIITIS OBLITERANS ( 3 FDA reports)
THYMOMA ( 3 FDA reports)
THYROID ADENOMA ( 3 FDA reports)
THYROID ATROPHY ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 3 FDA reports)
TONGUE ERUPTION ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOOTH HYPOPLASIA ( 3 FDA reports)
TOOTH MALFORMATION ( 3 FDA reports)
TOXIC NODULAR GOITRE ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRACHEAL FISTULA ( 3 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER REGIONAL ( 3 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TROPONIN I ( 3 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 3 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 3 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
URAEMIC ENCEPHALOPATHY ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETERAL NECROSIS ( 3 FDA reports)
URETERIC DILATATION ( 3 FDA reports)
URETERITIS ( 3 FDA reports)
URETHRAL DILATATION ( 3 FDA reports)
URETHRAL INJURY ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINE ANALYSIS ( 3 FDA reports)
URINE BILIRUBIN INCREASED ( 3 FDA reports)
URINE CALCIUM INCREASED ( 3 FDA reports)
URINE POTASSIUM INCREASED ( 3 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
UTERINE CYST ( 3 FDA reports)
VACCINATION FAILURE ( 3 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VAGINITIS ATROPHIC ( 3 FDA reports)
VARICOSE ULCERATION ( 3 FDA reports)
VARICOSE VEIN RUPTURED ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASCULAR TEST ABNORMAL ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VITAMIN D ABNORMAL ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
VULVAL ABSCESS ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 3 FDA reports)
WEIGHT ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
WRIST DEFORMITY ( 3 FDA reports)
WRIST SURGERY ( 3 FDA reports)
XANTHOGRANULOMA ( 3 FDA reports)
ZINC DEFICIENCY ( 3 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 3 FDA reports)
ACANTHOMA ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACID BASE BALANCE ABNORMAL ( 3 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACUTE STRESS DISORDER ( 3 FDA reports)
ADENOCARCINOMA PANCREAS ( 3 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 3 FDA reports)
ADRENOCORTICAL CARCINOMA ( 3 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALCOHOL INTOLERANCE ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
ALLERGY TO CHEMICALS ( 3 FDA reports)
ALLODYNIA ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
AMBLYOPIA ( 3 FDA reports)
AMPHETAMINES POSITIVE ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANAL EROSION ( 3 FDA reports)
ANAL NEOPLASM ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 3 FDA reports)
ANGIOSARCOMA ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
ANOREXIA NERVOSA ( 3 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC DISSECTION RUPTURE ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE DISCOMFORT ( 3 FDA reports)
APPLICATION SITE ULCER ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
ARTERIOPATHIC DISEASE ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ASOCIAL BEHAVIOUR ( 3 FDA reports)
ATONIC SEIZURES ( 3 FDA reports)
ATOPY ( 3 FDA reports)
ATRIAL PRESSURE INCREASED ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 3 FDA reports)
AUTOPHONY ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
AXILLARY VEIN THROMBOSIS ( 3 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 3 FDA reports)
BACTERIAL TEST NEGATIVE ( 3 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BARTTER'S SYNDROME ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BASE EXCESS ( 3 FDA reports)
BENIGN NEOPLASM OF SKIN ( 3 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 3 FDA reports)
BENIGN OVARIAN TUMOUR ( 3 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 3 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 3 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 3 FDA reports)
BILIARY SPHINCTEROTOMY ( 3 FDA reports)
BIOPSY BONE MARROW ( 3 FDA reports)
BIOPSY LYMPH GLAND ( 3 FDA reports)
BIOPSY STOMACH ABNORMAL ( 3 FDA reports)
BLADDER MASS ( 3 FDA reports)
BLADDER NECK OBSTRUCTION ( 3 FDA reports)
BLISTER INFECTED ( 3 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 3 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 3 FDA reports)
BLOOD FOLATE ABNORMAL ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BLOOD ZINC ABNORMAL ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE DENSITOMETRY ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BONE MARROW NECROSIS ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRACHIAL PLEXOPATHY ( 3 FDA reports)
BREAST DISCHARGE ( 3 FDA reports)
BREAST ENGORGEMENT ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 3 FDA reports)
BRONCHOPULMONARY DISEASE ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BURN INFECTION ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 3 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 3 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARDIAC MYXOMA ( 3 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CATECHOLAMINES URINE INCREASED ( 3 FDA reports)
CATHETER SITE PHLEBITIS ( 3 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 3 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL FUNGAL INFECTION ( 3 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
CERVICAL CORD COMPRESSION ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEST EXPANSION DECREASED ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLEDOCHAL CYST ( 3 FDA reports)
CHORIORETINAL ATROPHY ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 3 FDA reports)
CONDUCTIVE DEAFNESS ( 3 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 3 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 3 FDA reports)
CONGENITAL DEFORMITY OF CLAVICLE ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONGENITAL HAND MALFORMATION ( 3 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 3 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CONTRALATERAL BREAST CANCER ( 3 FDA reports)
CONTRAST MEDIA ALLERGY ( 3 FDA reports)
COR PULMONALE ACUTE ( 3 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 3 FDA reports)
CORNEAL STRIAE ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CORONARY REVASCULARISATION ( 3 FDA reports)
CRANIOPHARYNGIOMA ( 3 FDA reports)
CRANIOSYNOSTOSIS ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CSF GLUCOSE DECREASED ( 3 FDA reports)
CSF PROTEIN DECREASED ( 3 FDA reports)
CYSTIC LYMPHANGIOMA ( 3 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DERMATITIS DIAPER ( 3 FDA reports)
DEVICE ADHESION ISSUE ( 3 FDA reports)
DEVICE CONNECTION ISSUE ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC GANGRENE ( 3 FDA reports)
DIAPEDESIS ( 3 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 3 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 3 FDA reports)
DOLICHOCOLON ( 3 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 3 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 3 FDA reports)
DRUG EFFECT PROLONGED ( 3 FDA reports)
DRUG THERAPY ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
DUODENAL ULCER, OBSTRUCTIVE ( 3 FDA reports)
DURAL TEAR ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ECZEMA WEEPING ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
ENDOMETRIAL DISORDER ( 3 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXERCISE TEST ABNORMAL ( 3 FDA reports)
EXTERNAL EAR CELLULITIS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EYE INFECTION INTRAOCULAR ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE PENETRATION ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
EYELID EXFOLIATION ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FACTOR V LEIDEN MUTATION ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEAR OF FALLING ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEELING HOT AND COLD ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FINE MOTOR DELAY ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FIXED ERUPTION ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
GANGLION ( 3 FDA reports)
GASTRIC CANCER STAGE IV ( 3 FDA reports)
GASTRIC CYST ( 3 FDA reports)
GASTRIC XANTHOMA ( 3 FDA reports)
GASTRITIS BACTERIAL ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROENTERITIS SALMONELLA ( 3 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GENITAL INFECTION ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GENITAL ULCERATION ( 3 FDA reports)
GESTATIONAL HYPERTENSION ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GINGIVAL DISCOLOURATION ( 3 FDA reports)
GINGIVAL OPERATION ( 3 FDA reports)
GLIOMA ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GRAFT HAEMORRHAGE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GROWTH HORMONE DEFICIENCY ( 3 FDA reports)
GROWTH RETARDATION ( 3 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 3 FDA reports)
HAEMOPHILIA ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAIRY CELL LEUKAEMIA ( 3 FDA reports)
HAPTOGLOBIN INCREASED ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HEPATIC ARTERY ANEURYSM ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HERNIA HIATUS REPAIR ( 3 FDA reports)
HERNIAL EVENTRATION ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 3 FDA reports)
HOLMES-ADIE PUPIL ( 3 FDA reports)
HYDROMETRA ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 3 FDA reports)
HYPOKINESIA NEONATAL ( 3 FDA reports)
HYPOPYON ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 3 FDA reports)
HYPOURICAEMIA ( 3 FDA reports)
ILEOSTOMY CLOSURE ( 3 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INABILITY TO CRAWL ( 3 FDA reports)
INCISION SITE ERYTHEMA ( 3 FDA reports)
INFECTED LYMPHOCELE ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
INFUSION SITE IRRITATION ( 3 FDA reports)
INFUSION SITE WARMTH ( 3 FDA reports)
INHALATION THERAPY ( 3 FDA reports)
INJECTION SITE COLDNESS ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE MACULE ( 3 FDA reports)
INJECTION SITE THROMBOSIS ( 3 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 3 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 3 FDA reports)
INTERNAL INJURY ( 3 FDA reports)
INTERTRIGO CANDIDA ( 3 FDA reports)
INTESTINAL ANASTOMOSIS ( 3 FDA reports)
INTESTINAL HAEMATOMA ( 3 FDA reports)
INTESTINAL MALROTATION ( 3 FDA reports)
INTESTINAL STRANGULATION ( 3 FDA reports)
INTESTINAL VILLI ATROPHY ( 3 FDA reports)
INTOXICATION BY BREAST FEEDING ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTUBATION COMPLICATION ( 3 FDA reports)
IODINE UPTAKE INCREASED ( 3 FDA reports)
JAUNDICE HEPATOCELLULAR ( 3 FDA reports)
JOINT STABILISATION ( 3 FDA reports)
KERATOCONUS ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LDL/HDL RATIO DECREASED ( 3 FDA reports)
LEISHMANIASIS ( 3 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 3 FDA reports)
LEUKAEMIC INFILTRATION RENAL ( 3 FDA reports)
LICE INFESTATION ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LIGAMENT PAIN ( 3 FDA reports)
LIPASE ABNORMAL ( 3 FDA reports)
LIPOEDEMA ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LIVER CARCINOMA RUPTURED ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LOCAL REACTION ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LYMPHANGIECTASIA INTESTINAL ( 3 FDA reports)
LYMPHANGIOMA ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MACROCEPHALY ( 3 FDA reports)
MACULAR FIBROSIS ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID DECREASED ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE DECREASED ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABDOMINAL WALL OPERATION ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
ACQUIRED PORPHYRIA ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 2 FDA reports)
ADENOIDAL DISORDER ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADRENALECTOMY ( 2 FDA reports)
AGONAL DEATH STRUGGLE ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALDOSTERONE URINE DECREASED ( 2 FDA reports)
ALEXIA ( 2 FDA reports)
ALLERGIC PHARYNGITIS ( 2 FDA reports)
ALPHA 1 GLOBULIN ABNORMAL ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALVEOLAR SOFT PART SARCOMA METASTATIC ( 2 FDA reports)
AMBLYOPIA STRABISMIC ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANAL FUNGAL INFECTION ( 2 FDA reports)
ANAL INFECTION ( 2 FDA reports)
ANDROGENETIC ALOPECIA ( 2 FDA reports)
ANDROGENS DECREASED ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 2 FDA reports)
ANGIOSCLEROSIS ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANKLE DEFORMITY ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC BRUIT ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC VALVE PROLAPSE ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 2 FDA reports)
ASPERGILLOMA ( 2 FDA reports)
ASPIRATION JOINT ABNORMAL ( 2 FDA reports)
ASPIRATION TRACHEAL ( 2 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BALANOPOSTHITIS ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASE EXCESS NEGATIVE ( 2 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BENIGN EAR NEOPLASM ( 2 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BENIGN MUSCLE NEOPLASM ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BILIARY ANASTOMOSIS ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 2 FDA reports)
BLADDER CATHETER REPLACEMENT ( 2 FDA reports)
BLADDER CONSTRICTION ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER DYSPLASIA ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLADDER PAPILLOMA ( 2 FDA reports)
BLADDER TRABECULATION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLEEDING PERIPARTUM ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATINE ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD PROLACTIN DECREASED ( 2 FDA reports)
BLOOD STEM CELL HARVEST ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE NORMAL ( 2 FDA reports)
BLOODY AIRWAY DISCHARGE ( 2 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY MASS INDEX DECREASED ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHOMALACIA ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BURNS FIRST DEGREE ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALLUS FORMATION DELAYED ( 2 FDA reports)
CAMPYLOBACTER SEPSIS ( 2 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 2 FDA reports)
CARCINOMA IN SITU ( 2 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC MASSAGE ( 2 FDA reports)
CARDIAC PACEMAKER REVISION ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CATHETER CULTURE POSITIVE ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CATHETERISATION VENOUS ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CAUTERY TO NOSE ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CD4/CD8 RATIO DECREASED ( 2 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL VASOCONSTRICTION ( 2 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CEREBROVASCULAR OPERATION ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CERVICAL ROOT PAIN ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHOLANGITIS CHRONIC ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHOROIDAL EFFUSION ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CHVOSTEK'S SIGN ( 2 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 2 FDA reports)
CLUTTERING ( 2 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 2 FDA reports)
COELIAC ARTERY STENOSIS ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLON DYSPLASIA ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLORECTAL CANCER RECURRENT ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
COMPLICATION OF PREGNANCY ( 2 FDA reports)
COMPULSIVE HOARDING ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 2 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 2 FDA reports)
CONGENITAL VISUAL ACUITY REDUCED ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COOMBS TEST NEGATIVE ( 2 FDA reports)
CORNEAL INFILTRATES ( 2 FDA reports)
CORNEAL LEUKOMA ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORONARY BYPASS THROMBOSIS ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CREATINE URINE ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE ( 2 FDA reports)
CREATININE URINE DECREASED ( 2 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRYOGLOBULINS PRESENT ( 2 FDA reports)
CULTURE URINE ( 2 FDA reports)
CYSTIC FIBROSIS LUNG ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEFICIENCY OF BILE SECRETION ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DERMATOSIS ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 2 FDA reports)
DRUG HALF-LIFE INCREASED ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DUODENAL FISTULA ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DYSACUSIS ( 2 FDA reports)
DYSLOGIA ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
ECZEMA IMPETIGINOUS ( 2 FDA reports)
ECZEMA INFECTED ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ELLIPTOCYTOSIS ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 2 FDA reports)
ENLARGED UVULA ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
ENZYME INDUCTION ( 2 FDA reports)
EOSINOPHILIC PUSTULOSIS ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
EPIDURAL LIPOMATOSIS ( 2 FDA reports)
EPINEPHRINE INCREASED ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
ERGOT POISONING ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXTERNAL EAR DISORDER ( 2 FDA reports)
EXTERNAL EAR INFLAMMATION ( 2 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 2 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EYE INFECTION TOXOPLASMAL ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYE NAEVUS ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELID EROSION ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 2 FDA reports)
FEAR OF WEIGHT GAIN ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
FEMALE STERILISATION ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOLLICULAR THYROID CANCER ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL ENDOCARDITIS ( 2 FDA reports)
FUNGUS CULTURE POSITIVE ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 2 FDA reports)
GASTRIC ATONY ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC CANCER STAGE III ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTRINOMA MALIGNANT ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GASTROPARESIS POSTOPERATIVE ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GENITAL TRACT INFLAMMATION ( 2 FDA reports)
GERSTMANN'S SYNDROME ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 2 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE IV ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATIDROSIS ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMODILUTION ( 2 FDA reports)
HAEMORRHAGIC ASCITES ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HAPTOGLOBIN ABNORMAL ( 2 FDA reports)
HEARING DISABILITY ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 2 FDA reports)
HEPATITIS B DNA INCREASED ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HEPATOCELLULAR FOAMY CELL SYNDROME ( 2 FDA reports)
HEPATOPULMONARY SYNDROME ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HERPETIC GINGIVOSTOMATITIS ( 2 FDA reports)
HOFFMANN'S SIGN ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HUMORAL IMMUNE DEFECT ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYALOSIS ASTEROID ( 2 FDA reports)
HYDROCHOLECYSTIS ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOCALCIURIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
IDIOPATHIC URTICARIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
INBORN ERROR OF METABOLISM ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCISION SITE BLISTER ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTIOUS DISEASE CARRIER ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFECTIVE GLOSSITIS ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 2 FDA reports)
INJECTION SITE PALLOR ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INJECTION SITE SCAB ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INJURY CORNEAL ( 2 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 2 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INTERCEPTED MEDICATION ERROR ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL ABNORMAL ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
JAUNDICE ACHOLURIC ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
JOINT DISLOCATION PATHOLOGICAL ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 2 FDA reports)
KARNOFSKY SCALE WORSENED ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABORATORY TEST ( 2 FDA reports)
LABOUR COMPLICATION ( 2 FDA reports)
LACTATION DISORDER ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LARYNGEAL INFLAMMATION ( 2 FDA reports)
LARYNGOMALACIA ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIGHT CHAIN DISEASE ( 2 FDA reports)
LIMB PROSTHESIS USER ( 2 FDA reports)
LIPOGRANULOMA ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LIVER INDURATION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LUMBAR HERNIA ( 2 FDA reports)
LUMBAR SPINE FLATTENING ( 2 FDA reports)
LUNG WEDGE RESECTION ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCYTOTOXIC ANTIBODY POSITIVE ( 2 FDA reports)
MACROPHAGES INCREASED ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA NON-METASTATIC ( 2 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 2 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 2 FDA reports)
MALIGNANT MELANOMA STAGE II ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 2 FDA reports)
MASTOCYTIC LEUKAEMIA ( 2 FDA reports)
MASTOID EFFUSION ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEDICAL DEVICE SITE REACTION ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 2 FDA reports)
MESENTERITIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO GALLBLADDER ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
MILD MENTAL RETARDATION ( 2 FDA reports)
MILK ALLERGY ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MINERAL DEFICIENCY ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MUCOSA VESICLE ( 2 FDA reports)
MUCOSAL EXFOLIATION ( 2 FDA reports)
MUCOSAL PIGMENTATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 2 FDA reports)
MURDER ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYELOCYTE COUNT INCREASED ( 2 FDA reports)
MYELOCYTOSIS ( 2 FDA reports)
MYOGLOBINAEMIA ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NAIL AVULSION ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NAIL PSORIASIS ( 2 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 2 FDA reports)
NASAL NEOPLASM BENIGN ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL SEPTUM ULCERATION ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECROSIS OF BRONCHIOLI ( 2 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 2 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL HYPOXIA ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NEURAL TUBE DEFECT ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NIPPLE SWELLING ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
NODULAR VASCULITIS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 2 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL IRRITATION ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 2 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
OPTIC DISC HAEMORRHAGE ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
ORAL VIRAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
ORTHOPOX VIRUS INFECTION ( 2 FDA reports)
OSTEOMA ( 2 FDA reports)
OVARIAN ADENOMA ( 2 FDA reports)
OVARIAN EPITHELIAL CANCER ( 2 FDA reports)
OVULATION DISORDER ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PALLANAESTHESIA ( 2 FDA reports)
PANCREATIC ENZYMES DECREASED ( 2 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARAESTHESIA CIRCUMORAL ( 2 FDA reports)
PARAMETRITIS ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PASSIVE SMOKING ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PENILE ABSCESS ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PENILE ULCERATION ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERICARDIAL FIBROSIS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL NERVE INJURY ( 2 FDA reports)
PERIPROCTITIS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL NECROSIS ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PH BODY FLUID INCREASED ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL EROSION ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHLEBECTOMY ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PITYRIASIS ROSEA ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET AGGREGATION INCREASED ( 2 FDA reports)
PLEURA CARCINOMA ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL DECORTICATION ( 2 FDA reports)
PLEURAL FISTULA ( 2 FDA reports)
PLEURAL INFECTION ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA ADENOVIRAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYMERASE CHAIN REACTION ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
PORTAL HYPERTENSIVE ENTEROPATHY ( 2 FDA reports)
PORTAL VEIN FLOW DECREASED ( 2 FDA reports)
PORTOPULMONARY HYPERTENSION ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POST-TRAUMATIC PAIN ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POSTMENOPAUSE ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRERENAL FAILURE ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PRIMARY IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROTEIN C DECREASED ( 2 FDA reports)
PROTEIN C DEFICIENCY ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDO LYMPHOMA ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOENDOPHTHALMITIS ( 2 FDA reports)
PSEUDOHYPERKALAEMIA ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOPOLYPOSIS ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PUBIC PAIN ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 2 FDA reports)
PULMONARY BULLA ( 2 FDA reports)
PULMONARY COCCIDIOIDES ( 2 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 2 FDA reports)
PULSE PRESSURE ABNORMAL ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYONEPHROSIS ( 2 FDA reports)
PYOPNEUMOTHORAX ( 2 FDA reports)
PYROGLUTAMATE INCREASED ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION MYELOPATHY ( 2 FDA reports)
RADIATION PROSTATITIS ( 2 FDA reports)
RADICULITIS BRACHIAL ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RELAPSING POLYCHONDRITIS ( 2 FDA reports)
RENAL ADENOMA ( 2 FDA reports)
RENAL CANCER RECURRENT ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RENAL LYMPHOCELE ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY THERAPY ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RESPIRATORY TRACT OEDEMA ( 2 FDA reports)
RETICULIN INCREASED ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINAL ARTERY STENOSIS ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RETINAL OPERATION ( 2 FDA reports)
RETINAL SCAR ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RETROGRADE P-WAVES ( 2 FDA reports)
RETROPERITONEAL EFFUSION ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
ROSEOLA ( 2 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SALMONELLA TEST POSITIVE ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHISTOSOMIASIS ( 2 FDA reports)
SCHIZOPHRENIA SIMPLE ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCLEROEDEMA ( 2 FDA reports)
SCROTAL HAEMATOCOELE ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SECONDARY AMYLOIDOSIS ( 2 FDA reports)
SEDATIVE THERAPY ( 2 FDA reports)
SENSATION OF PRESSURE IN EAR ( 2 FDA reports)
SEPTIC ARTHRITIS STREPTOCOCCAL ( 2 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SINOBRONCHITIS ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 2 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SOMATOFORM DISORDER CARDIOVASCULAR ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC INFECTION BACTERIAL ( 2 FDA reports)
SPLINTER HAEMORRHAGES ( 2 FDA reports)
SPONDYLITIC MYELOPATHY ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
SPORTS INJURY ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STEROID THERAPY ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STREPTOCOCCAL ABSCESS ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
SUBSTANCE USE ( 2 FDA reports)
SUDDEN VISUAL LOSS ( 2 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 2 FDA reports)
SURGICAL VASCULAR SHUNT ( 2 FDA reports)
SWEAT DISCOLOURATION ( 2 FDA reports)
SYMBLEPHARON ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 2 FDA reports)
TACHYPHYLAXIS ( 2 FDA reports)
TENDON SHEATH INCISION ( 2 FDA reports)
TESTICULAR CANCER METASTATIC ( 2 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THERAPY NAIVE ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THYMECTOMY ( 2 FDA reports)
THYROID CANCER RECURRENT ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TILT TABLE TEST ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONGUE PRURITUS ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRANSFERRIN DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TROUSSEAU'S SIGN ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TUMOUR RUPTURE ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETHRAL DISCHARGE ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URINARY ANASTOMOTIC LEAK ( 2 FDA reports)
URINARY SEDIMENT ABNORMAL ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 2 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 2 FDA reports)
URINE MAGNESIUM DECREASED ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE HAEMATOMA ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UTERINE NEOPLASM ( 2 FDA reports)
UTERINE OPERATION ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL LACERATION ( 2 FDA reports)
VASCULAR ANOMALY ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 2 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 2 FDA reports)
VASCULITIS GASTROINTESTINAL ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VESSEL PERFORATION ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VIIITH NERVE LESION ( 2 FDA reports)
VIRAL DIARRHOEA ( 2 FDA reports)
VIRAL DNA TEST POSITIVE ( 2 FDA reports)
VIRAL MUTATION IDENTIFIED ( 2 FDA reports)
VIRAL MYOSITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
VIRUS URINE TEST POSITIVE ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN C DEFICIENCY ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VOCAL CORD PARESIS ( 2 FDA reports)
VULVAR EROSION ( 2 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 2 FDA reports)
WANDERING PACEMAKER ( 2 FDA reports)
WART EXCISION ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 2 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WITHDRAWAL HYPERTENSION ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
YERSINIA INFECTION ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MALIGNANT MUSCLE NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 1 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MALNUTRITION-INFLAMMATION-ATHEROSCLEROSIS SYNDROME ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MATERNAL ALCOHOL USE ( 1 FDA reports)
MATERNAL DISTRESS DURING LABOUR ( 1 FDA reports)
MATERNAL EXPOSURE DURING DELIVERY ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 1 FDA reports)
MEDICATION DILUTION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MEGALOBLASTS INCREASED ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS NEONATAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC FIBROSIS ( 1 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO DIAPHRAGM ( 1 FDA reports)
METASTASES TO MUSCLE ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTASES TO THE RESPIRATORY SYSTEM ( 1 FDA reports)
METASTASES TO THYROID ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC PULMONARY EMBOLISM ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MIKULICZ'S DISEASE ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED HEPATOCELLULAR CHOLANGIOCARCINOMA ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCOSAL HYPERAEMIA ( 1 FDA reports)
MULTI-VITAMIN DEFICIENCY ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MYALGIA INTERCOSTAL ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYCOTIC ALLERGY ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN URINE ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
MYRINGITIS ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL GROWTH CESSATION ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY ARREST ( 1 FDA reports)
NEOPLASM OF ORBIT ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEUROBORRELIOSIS ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUTRALISING ANTIBODIES ( 1 FDA reports)
NEUTRALISING ANTIBODIES NEGATIVE ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NITRITOID CRISIS ( 1 FDA reports)
NOCTIPHOBIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO DRUG ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULOAURICULOVERTEBRAL DYSPLASIA ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE III ( 1 FDA reports)
OESOPHAGEAL CARCINOMA RECURRENT ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 1 FDA reports)
OESOPHAGOSCOPY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOGRYPHOSIS ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPHTHALMIC FLUID DRAINAGE ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOCALCIN INCREASED ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OTITIS EXTERNA BACTERIAL ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PALINDROMIC RHEUMATISM ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA NON-RESECTABLE ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PARASITIC GASTROENTERITIS ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARATYPHOID FEVER ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PELVIC FIBROSIS ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE VEIN THROMBOSIS ( 1 FDA reports)
PERFORMANCE FEAR ( 1 FDA reports)
PERICARDIAL DRAINAGE TEST ABNORMAL ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERICARDITIS LUPUS ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONEAL CYST ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERTUSSIS IMMUNISATION ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHAGOCYTOSIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANCER METASTATIC ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL NEOPLASM BENIGN ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLAGUE ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA EXPANDER TRANSFUSION ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA SALMONELLA ( 1 FDA reports)
PNEUMONIA TOXOPLASMAL ( 1 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
PO2 ( 1 FDA reports)
POIKILODERMA ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POLYNEUROPATHY CHRONIC ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL DIZZINESS ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PRECURSOR B-LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROGESTERONE ABNORMAL ( 1 FDA reports)
PROGRESSIVE BULBAR PALSY ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEIN S ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN URINE ABSENT ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOANGINA ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FISTULA ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
PUVA ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION EXPOSURE ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RATHKE'S CLEFT CYST ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
REBOUND TACHYCARDIA ( 1 FDA reports)
RECTAL ATRESIA ( 1 FDA reports)
RECTAL CANCER RECURRENT ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL MICROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY HYPERPLASIA ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL FUNCTION TEST ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL PALLOR ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL TOXICITY ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RETROPERITONEAL MASS ( 1 FDA reports)
RETROVIRAL INFECTION ( 1 FDA reports)
REYE'S SYNDROME ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIB DEFORMITY ( 1 FDA reports)
RIB HYPOPLASIA ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALIVARY GLAND ADENOMA ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALIVARY GLAND RESECTION ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SALPINGO-OOPHORITIS ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SEPSIS PASTEURELLA ( 1 FDA reports)
SEPTIC RASH ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHRINKING LUNG SYNDROME ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SINUSITIS NONINFECTIVE ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN DYSTROPHY ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN MALFORMATION ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOLAR DERMATITIS ( 1 FDA reports)
SOMATOFORM DISORDER NEUROLOGIC ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPHEROCYTIC ANAEMIA ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL MENINGEAL CYST ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRANGURY ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOBACILLUS INFECTION ( 1 FDA reports)
STROKE IN EVOLUTION ( 1 FDA reports)
STROKE VOLUME DECREASED ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYMPATHETIC NERVE INJURY ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON NEOPLASM ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TESTICULAR OPERATION ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
TETANUS IMMUNISATION ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBIN TIME ABNORMAL ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOENDARTERECTOMY ( 1 FDA reports)
THROMBOPHLEBITIS PELVIC VEIN ( 1 FDA reports)
THYMUS HYPOPLASIA ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROID HAEMORRHAGE ( 1 FDA reports)
THYROID THERAPY ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE ABNORMAL ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TISSUE ANOXIA ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONSILLAR ATROPHY ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH AVULSION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANSAMINASES ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 1 FDA reports)
TRANSMYOCARDIAL REVASCULARISATION ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TRISOMY 8 ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR LOCAL INVASION ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
UMBILICAL ARTERY HYPOPLASIA ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
URAEMIC PRURITUS ( 1 FDA reports)
UREA RENAL CLEARANCE DECREASED ( 1 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 1 FDA reports)
URETERIC FISTULA ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URINARY BLADDER ABSCESS ( 1 FDA reports)
URINARY CYSTECTOMY ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 1 FDA reports)
URINARY TRACT INFECTION VIRAL ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINE AMINO ACID LEVEL INCREASED ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE CALCIUM DECREASED ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINE SODIUM ABNORMAL ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA CHOLINERGIC ( 1 FDA reports)
URTICARIA PIGMENTOSA ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VACTERL SYNDROME ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL HAEMATOMA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR WALL THICKENING ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTIGO CNS ORIGIN ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIBRIO TEST POSITIVE ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISCERAL OEDEMA ( 1 FDA reports)
VISION CORRECTION OPERATION ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 1 FDA reports)
VITAMIN SUPPLEMENTATION ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 1 FDA reports)
VON WILLEBRAND'S FACTOR ANTIGEN INCREASED ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL ULCERATION ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT NORMAL ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL SINUS REPAIR ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABORTION OF ECTOPIC PREGNANCY ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCESSORY LIVER LOBE ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED GENE MUTATION ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED PROTEIN S DEFICIENCY ( 1 FDA reports)
ACRODERMATITIS ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHASE REACTION ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AIDS RELATED COMPLEX ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALKAPTONURIA ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALLOIMMUNISATION ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 1 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMINO ACID LEVEL ABNORMAL ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMOEBIC DYSENTERY ( 1 FDA reports)
AMYLASE DECREASED ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANAPHYLAXIS TREATMENT ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGENS ABNORMAL ( 1 FDA reports)
ANEURYSM ARTERIOVENOUS ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANKLE ARTHROPLASTY ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOMALY OF MIDDLE EAR CONGENITAL ( 1 FDA reports)
ANORECTAL AGENESIS ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANOTIA ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTIPYRESIS ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASSISTED DELIVERY ( 1 FDA reports)
ASTROCYTOMA MALIGNANT ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATLANTOAXIAL INSTABILITY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE NEUROPATHY ( 1 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 1 FDA reports)
AUTOPHOBIA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BARTHOLINITIS ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASOPHIL COUNT ABNORMAL ( 1 FDA reports)
BED REST ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC POLYP ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BILE DUCT CANCER STAGE III ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE OUTPUT ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIARY ISCHAEMIA ( 1 FDA reports)
BIOPSY BLADDER ( 1 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY PHARYNX ( 1 FDA reports)
BIOPSY PROSTATE ( 1 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ( 1 FDA reports)
BLADDER CANCER STAGE II ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER NECK OPERATION ( 1 FDA reports)
BLADDER NECK SCLEROSIS ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHARAL PAPILLOMA ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BROMIDE DECREASED ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELASTASE INCREASED ( 1 FDA reports)
BLOOD ETHANOL DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD TEST NORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRYPSIN INCREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URINE ABSENT ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE GIANT CELL TUMOUR ( 1 FDA reports)
BONE MARROW EOSINOPHILIC LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE OEDEMA ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BRANCHIAL CYST ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH ALCOHOL TEST NEGATIVE ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHOLITHIASIS ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURN DRESSING ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CAPNOCYTOPHAGA INFECTION ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC TELEMETRY ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CEMENTOPLASTY ( 1 FDA reports)
CENTRAL AUDITORY PROCESSING DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERITIS ( 1 FDA reports)
CEREBRAL DYSGENESIS ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHEMOTHERAPY EXTRAVASATION MANAGEMENT ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHLOASMA ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLAMPING OF BLOOD VESSEL ( 1 FDA reports)
CLINICALLY ISOLATED SYNDROME ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COCCYGECTOMY ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLITIS HERPES ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLORECTAL CANCER STAGE III ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMBINED IMMUNODEFICIENCY ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 INCREASED ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL ACROCHORDON ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 1 FDA reports)
CONGENITAL HEPATOMEGALY ( 1 FDA reports)
CONGENITAL INGUINAL HERNIA ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL POIKILODERMA ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 1 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONTRAINDICATION TO VACCINATION ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL CYST ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
COXIELLA INFECTION ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CROSSMATCH INCOMPATIBLE ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CSF PRESSURE DECREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CULTURE STOOL NEGATIVE ( 1 FDA reports)
CUTANEOUS TUBERCULOSIS ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
CYTOMEGALOVIRUS DUODENITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DACRYOADENITIS ACQUIRED ( 1 FDA reports)
DEAFNESS PERMANENT ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DELAYED DELIVERY ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 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)
DEPRESSIVE DELUSION ( 1 FDA reports)
DERAILMENT ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
DERMATITIS PAPILLARIS CAPILLITII ( 1 FDA reports)
DERMATOLOGIC EXAMINATION ABNORMAL ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE PHYSICAL PROPERTY ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC MACROANGIOPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DIHYDROTESTOSTERONE LEVEL ( 1 FDA reports)
DIPHTHERIA IMMUNISATION ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE VESSEL BYPASS GRAFT ( 1 FDA reports)
DOUGLAS' ABSCESS ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENAL ATRESIA ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR IRRIGATION ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROPHORESIS ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
EMPHYSEMATOUS PYELONEPHRITIS ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENTEROBIASIS ( 1 FDA reports)
ENTEROCHROMAFFIN CELL HYPERPLASIA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIDIDYMAL INFECTION ( 1 FDA reports)
EPIDURAL INJECTION ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
ESCHAROTOMY ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPANDED DISABILITY STATUS SCALE SCORE INCREASED ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASATION OF URINE ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID SCALES ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FACTOR II DEFICIENCY ( 1 FDA reports)
FACTOR IX INHIBITION ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FALSE POSITIVE TUBERCULOSIS TEST ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FLAVOBACTERIUM INFECTION ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOETAL CYSTIC HYGROMA ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETAL MACROSOMIA ( 1 FDA reports)
FOETAL MALNUTRITION ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FRACTURED ZYGOMATIC ARCH ELEVATION ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTRINOMA ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 1 FDA reports)
GIANT CELL EPULIS ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLASGOW COMA SCALE ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAM STAIN NEGATIVE ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIP STRENGTH ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMOPHILIA A WITH ANTI FACTOR VIII ( 1 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HAIR DYE USER ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HARTNUP DISEASE ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC ARTERY EMBOLISM ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS A IMMUNISATION ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS NON-A NON-B ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HLA MARKER STUDY POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE STAGE II ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HY'S LAW CASE ( 1 FDA reports)
HYDROCELE FEMALE ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERFIBRINOGENAEMIA ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPEROXIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOCHONDROPLASIA ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 1 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNISATION ( 1 FDA reports)
IMMUNOBLASTIC LYMPHOMA ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
IMPLANT TISSUE NECROSIS ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INDIRECT INFECTION TRANSMISSION ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERNAL CAROTID ARTERY KINKING ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS ATROPHY ( 1 FDA reports)
IRIS BOMBE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT IRRIGATION ( 1 FDA reports)
JOINT RESURFACING SURGERY ( 1 FDA reports)
KIDNEY MALROTATION ( 1 FDA reports)
KIDNEY PERFORATION ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTOBACILLUS TEST POSITIVE ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGEAL DISCOMFORT ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGITIS ALLERGIC ( 1 FDA reports)
LARYNGITIS BACTERIAL ( 1 FDA reports)
LARYNGOTRACHEITIS ( 1 FDA reports)
LASEGUE'S TEST POSITIVE ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEIOMYOSARCOMA RECURRENT ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIGAMENTITIS ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIPECTOMY ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIPOSARCOMA METASTATIC ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT ANORECTAL NEOPLASM ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)