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

NAUSEA ( 3657 FDA reports)
PYREXIA ( 3597 FDA reports)
VOMITING ( 3495 FDA reports)
COMPLETED SUICIDE ( 3301 FDA reports)
PAIN ( 3172 FDA reports)
DYSPNOEA ( 3076 FDA reports)
DIARRHOEA ( 2691 FDA reports)
HEADACHE ( 2562 FDA reports)
OVERDOSE ( 2520 FDA reports)
FATIGUE ( 2394 FDA reports)
ANAEMIA ( 2296 FDA reports)
ASTHENIA ( 2251 FDA reports)
HYPOTENSION ( 2228 FDA reports)
DRUG TOXICITY ( 2215 FDA reports)
PNEUMONIA ( 2204 FDA reports)
RENAL FAILURE ACUTE ( 1965 FDA reports)
FALL ( 1950 FDA reports)
ANXIETY ( 1915 FDA reports)
ABDOMINAL PAIN ( 1872 FDA reports)
DIZZINESS ( 1845 FDA reports)
RENAL FAILURE ( 1769 FDA reports)
OEDEMA PERIPHERAL ( 1620 FDA reports)
DEATH ( 1609 FDA reports)
CHEST PAIN ( 1604 FDA reports)
CONFUSIONAL STATE ( 1601 FDA reports)
ARTHRALGIA ( 1588 FDA reports)
DEHYDRATION ( 1576 FDA reports)
MALAISE ( 1576 FDA reports)
HYPERTENSION ( 1566 FDA reports)
DRUG INTERACTION ( 1551 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1532 FDA reports)
BACK PAIN ( 1493 FDA reports)
THROMBOCYTOPENIA ( 1483 FDA reports)
DEPRESSION ( 1445 FDA reports)
INTENTIONAL OVERDOSE ( 1439 FDA reports)
RASH ( 1438 FDA reports)
PAIN IN EXTREMITY ( 1397 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1376 FDA reports)
SEPSIS ( 1354 FDA reports)
WEIGHT DECREASED ( 1292 FDA reports)
HEPATIC FAILURE ( 1285 FDA reports)
DRUG INEFFECTIVE ( 1279 FDA reports)
HAEMOGLOBIN DECREASED ( 1279 FDA reports)
URINARY TRACT INFECTION ( 1268 FDA reports)
CONSTIPATION ( 1232 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1214 FDA reports)
SOMNOLENCE ( 1211 FDA reports)
PULMONARY EMBOLISM ( 1183 FDA reports)
PLEURAL EFFUSION ( 1179 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1161 FDA reports)
INJURY ( 1152 FDA reports)
CARDIAC ARREST ( 1142 FDA reports)
PRURITUS ( 1125 FDA reports)
ATRIAL FIBRILLATION ( 1120 FDA reports)
CONVULSION ( 1114 FDA reports)
COUGH ( 1095 FDA reports)
TACHYCARDIA ( 1069 FDA reports)
RESPIRATORY FAILURE ( 1068 FDA reports)
DECREASED APPETITE ( 1055 FDA reports)
DEEP VEIN THROMBOSIS ( 1047 FDA reports)
NEUTROPENIA ( 1015 FDA reports)
CONDITION AGGRAVATED ( 1008 FDA reports)
LOSS OF CONSCIOUSNESS ( 978 FDA reports)
MYOCARDIAL INFARCTION ( 977 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 966 FDA reports)
CHILLS ( 964 FDA reports)
ACUTE HEPATIC FAILURE ( 944 FDA reports)
BLOOD CREATININE INCREASED ( 935 FDA reports)
INSOMNIA ( 925 FDA reports)
CEREBROVASCULAR ACCIDENT ( 911 FDA reports)
ABDOMINAL PAIN UPPER ( 909 FDA reports)
FEBRILE NEUTROPENIA ( 888 FDA reports)
GAIT DISTURBANCE ( 876 FDA reports)
ERYTHEMA ( 851 FDA reports)
HYPOAESTHESIA ( 848 FDA reports)
MYALGIA ( 848 FDA reports)
MULTI-ORGAN FAILURE ( 842 FDA reports)
MULTIPLE DRUG OVERDOSE ( 839 FDA reports)
PLATELET COUNT DECREASED ( 833 FDA reports)
DYSPHAGIA ( 828 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 811 FDA reports)
CARDIO-RESPIRATORY ARREST ( 785 FDA reports)
SUICIDE ATTEMPT ( 783 FDA reports)
TREMOR ( 774 FDA reports)
HYPOKALAEMIA ( 767 FDA reports)
METABOLIC ACIDOSIS ( 760 FDA reports)
MUSCULAR WEAKNESS ( 753 FDA reports)
INFECTION ( 752 FDA reports)
HYPERHIDROSIS ( 748 FDA reports)
SYNCOPE ( 741 FDA reports)
PANCYTOPENIA ( 738 FDA reports)
OSTEONECROSIS OF JAW ( 737 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 736 FDA reports)
RENAL IMPAIRMENT ( 728 FDA reports)
COMA ( 726 FDA reports)
PARAESTHESIA ( 714 FDA reports)
HYPONATRAEMIA ( 688 FDA reports)
INTENTIONAL DRUG MISUSE ( 687 FDA reports)
PULMONARY OEDEMA ( 676 FDA reports)
VISION BLURRED ( 662 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 659 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 653 FDA reports)
INFUSION RELATED REACTION ( 651 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 648 FDA reports)
EMOTIONAL DISTRESS ( 646 FDA reports)
MUSCLE SPASMS ( 643 FDA reports)
AGITATION ( 637 FDA reports)
BRADYCARDIA ( 634 FDA reports)
OSTEOARTHRITIS ( 609 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 601 FDA reports)
HYPERSENSITIVITY ( 592 FDA reports)
HYPOXIA ( 592 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 588 FDA reports)
WEIGHT INCREASED ( 582 FDA reports)
BLOOD GLUCOSE INCREASED ( 579 FDA reports)
BLOOD PRESSURE INCREASED ( 577 FDA reports)
URTICARIA ( 570 FDA reports)
RHABDOMYOLYSIS ( 567 FDA reports)
CELLULITIS ( 564 FDA reports)
CHOLELITHIASIS ( 564 FDA reports)
RESPIRATORY ARREST ( 563 FDA reports)
MENTAL STATUS CHANGES ( 552 FDA reports)
OEDEMA ( 550 FDA reports)
ACCIDENTAL OVERDOSE ( 546 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 536 FDA reports)
ATELECTASIS ( 534 FDA reports)
BRONCHITIS ( 534 FDA reports)
HEART RATE INCREASED ( 534 FDA reports)
JAUNDICE ( 531 FDA reports)
LIVER INJURY ( 530 FDA reports)
FEELING ABNORMAL ( 528 FDA reports)
RECTAL HAEMORRHAGE ( 520 FDA reports)
HYPERKALAEMIA ( 518 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 516 FDA reports)
DYSPEPSIA ( 511 FDA reports)
BLOOD BILIRUBIN INCREASED ( 510 FDA reports)
SEPTIC SHOCK ( 510 FDA reports)
SINUSITIS ( 509 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 503 FDA reports)
LETHARGY ( 502 FDA reports)
HEPATIC NECROSIS ( 500 FDA reports)
BONE DISORDER ( 496 FDA reports)
HALLUCINATION ( 496 FDA reports)
BLOOD PRESSURE DECREASED ( 490 FDA reports)
CARDIAC FAILURE ( 489 FDA reports)
CHEST DISCOMFORT ( 488 FDA reports)
ABDOMINAL DISTENSION ( 487 FDA reports)
ENCEPHALOPATHY ( 481 FDA reports)
NEUROPATHY PERIPHERAL ( 478 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 476 FDA reports)
ASTHMA ( 474 FDA reports)
DISEASE PROGRESSION ( 473 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 471 FDA reports)
HEPATIC ENZYME INCREASED ( 469 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 468 FDA reports)
STEVENS-JOHNSON SYNDROME ( 467 FDA reports)
CARDIOMEGALY ( 467 FDA reports)
UNRESPONSIVE TO STIMULI ( 461 FDA reports)
BONE PAIN ( 458 FDA reports)
COAGULOPATHY ( 457 FDA reports)
MUSCULOSKELETAL PAIN ( 456 FDA reports)
LEUKOPENIA ( 455 FDA reports)
OSTEOMYELITIS ( 453 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 449 FDA reports)
HEPATOTOXICITY ( 448 FDA reports)
PALPITATIONS ( 447 FDA reports)
HYPOGLYCAEMIA ( 446 FDA reports)
EPISTAXIS ( 441 FDA reports)
HAEMORRHAGE ( 440 FDA reports)
CYTOLYTIC HEPATITIS ( 436 FDA reports)
MEDICATION ERROR ( 433 FDA reports)
MEMORY IMPAIRMENT ( 433 FDA reports)
ARTHRITIS ( 429 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 427 FDA reports)
NECK PAIN ( 427 FDA reports)
RESPIRATORY DISTRESS ( 423 FDA reports)
CHOLESTASIS ( 422 FDA reports)
CONTUSION ( 422 FDA reports)
HEPATITIS ( 421 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 420 FDA reports)
CORONARY ARTERY DISEASE ( 420 FDA reports)
INFLUENZA LIKE ILLNESS ( 420 FDA reports)
ANHEDONIA ( 417 FDA reports)
ABDOMINAL DISCOMFORT ( 415 FDA reports)
BALANCE DISORDER ( 415 FDA reports)
HAEMATOCRIT DECREASED ( 415 FDA reports)
DELIRIUM ( 414 FDA reports)
ARRHYTHMIA ( 413 FDA reports)
LIVER DISORDER ( 404 FDA reports)
LYMPHADENOPATHY ( 404 FDA reports)
SPINAL OSTEOARTHRITIS ( 403 FDA reports)
SUICIDAL IDEATION ( 397 FDA reports)
NEOPLASM MALIGNANT ( 396 FDA reports)
ABNORMAL BEHAVIOUR ( 396 FDA reports)
SWELLING FACE ( 393 FDA reports)
SWELLING ( 390 FDA reports)
ASCITES ( 390 FDA reports)
BLOOD UREA INCREASED ( 387 FDA reports)
AMNESIA ( 385 FDA reports)
OXYGEN SATURATION DECREASED ( 385 FDA reports)
STAPHYLOCOCCAL INFECTION ( 382 FDA reports)
CARDIAC DISORDER ( 382 FDA reports)
TRANSAMINASES INCREASED ( 381 FDA reports)
INFLAMMATION ( 380 FDA reports)
DIABETES MELLITUS ( 377 FDA reports)
THROMBOSIS ( 374 FDA reports)
LUNG DISORDER ( 373 FDA reports)
OSTEOPOROSIS ( 371 FDA reports)
DISORIENTATION ( 371 FDA reports)
HYPERGLYCAEMIA ( 371 FDA reports)
HAEMATEMESIS ( 369 FDA reports)
LEUKOCYTOSIS ( 366 FDA reports)
RENAL FAILURE CHRONIC ( 362 FDA reports)
PROTHROMBIN TIME PROLONGED ( 358 FDA reports)
OSTEOPENIA ( 354 FDA reports)
PAIN IN JAW ( 354 FDA reports)
HEPATIC STEATOSIS ( 354 FDA reports)
PANCREATITIS ( 353 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 353 FDA reports)
VERTIGO ( 350 FDA reports)
ALOPECIA ( 350 FDA reports)
MITRAL VALVE INCOMPETENCE ( 349 FDA reports)
SINUS TACHYCARDIA ( 348 FDA reports)
DRUG HYPERSENSITIVITY ( 348 FDA reports)
HAEMATURIA ( 346 FDA reports)
DYSARTHRIA ( 344 FDA reports)
MIGRAINE ( 344 FDA reports)
MOBILITY DECREASED ( 341 FDA reports)
MELAENA ( 338 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 338 FDA reports)
JOINT SWELLING ( 336 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 336 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 335 FDA reports)
HYPERLIPIDAEMIA ( 332 FDA reports)
OROPHARYNGEAL PAIN ( 332 FDA reports)
FLUSHING ( 329 FDA reports)
BLOOD SODIUM DECREASED ( 327 FDA reports)
VISUAL IMPAIRMENT ( 325 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 324 FDA reports)
AGGRESSION ( 323 FDA reports)
GASTRITIS ( 323 FDA reports)
CATARACT ( 322 FDA reports)
METASTASES TO BONE ( 321 FDA reports)
SHOCK ( 320 FDA reports)
NEUTROPHIL COUNT DECREASED ( 314 FDA reports)
PERICARDIAL EFFUSION ( 313 FDA reports)
PULMONARY HYPERTENSION ( 313 FDA reports)
MUCOSAL INFLAMMATION ( 312 FDA reports)
NEPHROLITHIASIS ( 312 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 311 FDA reports)
HAEMORRHOIDS ( 308 FDA reports)
BLOOD POTASSIUM DECREASED ( 307 FDA reports)
HAEMATOMA ( 307 FDA reports)
INTENTIONAL MISUSE ( 307 FDA reports)
SPEECH DISORDER ( 306 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 305 FDA reports)
HIATUS HERNIA ( 305 FDA reports)
NASOPHARYNGITIS ( 303 FDA reports)
WHEEZING ( 303 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 302 FDA reports)
URINARY RETENTION ( 300 FDA reports)
DRUG ABUSE ( 300 FDA reports)
INTERSTITIAL LUNG DISEASE ( 300 FDA reports)
INJECTION SITE ERYTHEMA ( 298 FDA reports)
UNEVALUABLE EVENT ( 298 FDA reports)
ANAPHYLACTIC REACTION ( 296 FDA reports)
RASH MACULO-PAPULAR ( 293 FDA reports)
INCORRECT DOSE ADMINISTERED ( 290 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 288 FDA reports)
DRY MOUTH ( 287 FDA reports)
INJECTION SITE PAIN ( 287 FDA reports)
RHEUMATOID ARTHRITIS ( 286 FDA reports)
HERPES ZOSTER ( 284 FDA reports)
HYPOPHAGIA ( 284 FDA reports)
CROHN'S DISEASE ( 281 FDA reports)
GASTRIC ULCER ( 281 FDA reports)
STOMATITIS ( 279 FDA reports)
PALLOR ( 278 FDA reports)
MULTIPLE MYELOMA ( 276 FDA reports)
ANGIOEDEMA ( 276 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 275 FDA reports)
HAEMOPTYSIS ( 272 FDA reports)
BODY TEMPERATURE INCREASED ( 270 FDA reports)
BRAIN OEDEMA ( 270 FDA reports)
CHOLECYSTITIS CHRONIC ( 270 FDA reports)
GALLBLADDER DISORDER ( 270 FDA reports)
RASH ERYTHEMATOUS ( 270 FDA reports)
COLITIS ( 269 FDA reports)
LUNG INFILTRATION ( 267 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 267 FDA reports)
ANOREXIA ( 266 FDA reports)
FEAR ( 266 FDA reports)
HYPOTHYROIDISM ( 266 FDA reports)
ACIDOSIS ( 264 FDA reports)
AGRANULOCYTOSIS ( 264 FDA reports)
HYPOTHERMIA ( 263 FDA reports)
RENAL DISORDER ( 263 FDA reports)
RESTLESSNESS ( 263 FDA reports)
URINARY INCONTINENCE ( 263 FDA reports)
OFF LABEL USE ( 262 FDA reports)
HAEMATOCHEZIA ( 262 FDA reports)
GASTROENTERITIS ( 261 FDA reports)
VENTRICULAR TACHYCARDIA ( 259 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 258 FDA reports)
SKIN EXFOLIATION ( 257 FDA reports)
OSTEONECROSIS ( 254 FDA reports)
IMPAIRED HEALING ( 254 FDA reports)
ANGINA PECTORIS ( 252 FDA reports)
CEREBRAL HAEMORRHAGE ( 252 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 249 FDA reports)
INFLUENZA ( 249 FDA reports)
CYANOSIS ( 247 FDA reports)
STRESS ( 247 FDA reports)
POLLAKIURIA ( 244 FDA reports)
LUNG NEOPLASM ( 242 FDA reports)
PRODUCT QUALITY ISSUE ( 242 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 242 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 241 FDA reports)
PNEUMONIA ASPIRATION ( 240 FDA reports)
FEELING HOT ( 239 FDA reports)
HAEMODIALYSIS ( 239 FDA reports)
SLEEP APNOEA SYNDROME ( 238 FDA reports)
DEFORMITY ( 237 FDA reports)
BRONCHOPNEUMONIA ( 236 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 236 FDA reports)
DECREASED INTEREST ( 235 FDA reports)
HEPATIC ENCEPHALOPATHY ( 235 FDA reports)
MENTAL DISORDER ( 234 FDA reports)
RENAL TUBULAR NECROSIS ( 233 FDA reports)
ORTHOSTATIC HYPOTENSION ( 230 FDA reports)
PULMONARY CONGESTION ( 230 FDA reports)
DRUG ADMINISTRATION ERROR ( 229 FDA reports)
DYSURIA ( 229 FDA reports)
GRAND MAL CONVULSION ( 228 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 228 FDA reports)
CHOLECYSTITIS ( 227 FDA reports)
DRUG LEVEL INCREASED ( 226 FDA reports)
TOXIC SKIN ERUPTION ( 226 FDA reports)
MALNUTRITION ( 225 FDA reports)
POISONING ( 225 FDA reports)
CEREBRAL INFARCTION ( 224 FDA reports)
DYSPHONIA ( 224 FDA reports)
PANCREATITIS ACUTE ( 223 FDA reports)
RESPIRATORY DEPRESSION ( 223 FDA reports)
ABASIA ( 222 FDA reports)
BURNING SENSATION ( 222 FDA reports)
HEAD INJURY ( 222 FDA reports)
DYSGEUSIA ( 221 FDA reports)
COGNITIVE DISORDER ( 220 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 218 FDA reports)
SKIN DISCOLOURATION ( 216 FDA reports)
OESOPHAGITIS ( 215 FDA reports)
DYSKINESIA ( 215 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 214 FDA reports)
SPINAL COMPRESSION FRACTURE ( 214 FDA reports)
TOOTH EXTRACTION ( 214 FDA reports)
PNEUMOTHORAX ( 213 FDA reports)
RIB FRACTURE ( 213 FDA reports)
SLEEP DISORDER ( 213 FDA reports)
TACHYPNOEA ( 213 FDA reports)
DIVERTICULUM ( 213 FDA reports)
GASTROINTESTINAL DISORDER ( 213 FDA reports)
RENAL CYST ( 212 FDA reports)
FLUID OVERLOAD ( 211 FDA reports)
BLOOD ALBUMIN DECREASED ( 210 FDA reports)
PHARYNGITIS ( 209 FDA reports)
DISTURBANCE IN ATTENTION ( 208 FDA reports)
ABORTION SPONTANEOUS ( 207 FDA reports)
HYPERCHOLESTEROLAEMIA ( 207 FDA reports)
MOUTH ULCERATION ( 205 FDA reports)
RHINORRHOEA ( 204 FDA reports)
METASTASES TO LIVER ( 203 FDA reports)
NEOPLASM PROGRESSION ( 203 FDA reports)
ARTERIOSCLEROSIS ( 203 FDA reports)
ARTHROPATHY ( 202 FDA reports)
CARDIAC MURMUR ( 202 FDA reports)
CIRCULATORY COLLAPSE ( 202 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 202 FDA reports)
HALLUCINATION, VISUAL ( 202 FDA reports)
SKIN LESION ( 202 FDA reports)
DYSPNOEA EXERTIONAL ( 201 FDA reports)
HEPATOMEGALY ( 200 FDA reports)
VIRAL INFECTION ( 200 FDA reports)
DENTAL CARIES ( 199 FDA reports)
BLISTER ( 197 FDA reports)
BLOOD POTASSIUM INCREASED ( 197 FDA reports)
SCAR ( 197 FDA reports)
MYOCARDIAL ISCHAEMIA ( 196 FDA reports)
RESPIRATORY DISORDER ( 195 FDA reports)
TREATMENT NONCOMPLIANCE ( 195 FDA reports)
ORAL PAIN ( 194 FDA reports)
EXOSTOSIS ( 194 FDA reports)
EOSINOPHILIA ( 192 FDA reports)
DIPLOPIA ( 191 FDA reports)
SWOLLEN TONGUE ( 191 FDA reports)
RASH PRURITIC ( 190 FDA reports)
SINUS BRADYCARDIA ( 190 FDA reports)
BONE LESION ( 190 FDA reports)
CANDIDIASIS ( 189 FDA reports)
DRY SKIN ( 189 FDA reports)
INTESTINAL OBSTRUCTION ( 189 FDA reports)
CHROMATURIA ( 188 FDA reports)
DRUG ERUPTION ( 188 FDA reports)
TOOTHACHE ( 188 FDA reports)
NASAL CONGESTION ( 186 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 186 FDA reports)
ECONOMIC PROBLEM ( 185 FDA reports)
FACE OEDEMA ( 185 FDA reports)
NERVOUSNESS ( 185 FDA reports)
POST PROCEDURAL COMPLICATION ( 185 FDA reports)
PRODUCTIVE COUGH ( 184 FDA reports)
PROTEINURIA ( 184 FDA reports)
VISUAL ACUITY REDUCED ( 184 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 184 FDA reports)
OBESITY ( 182 FDA reports)
RASH GENERALISED ( 182 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 182 FDA reports)
HYPOCALCAEMIA ( 182 FDA reports)
DIALYSIS ( 180 FDA reports)
BONE MARROW FAILURE ( 179 FDA reports)
HYPERCALCAEMIA ( 179 FDA reports)
SKIN ULCER ( 179 FDA reports)
BLOOD CALCIUM DECREASED ( 178 FDA reports)
BACTERIAL INFECTION ( 177 FDA reports)
HYPERBILIRUBINAEMIA ( 177 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 176 FDA reports)
ANURIA ( 176 FDA reports)
PETECHIAE ( 176 FDA reports)
TOOTH ABSCESS ( 174 FDA reports)
TYPE 2 DIABETES MELLITUS ( 174 FDA reports)
ROAD TRAFFIC ACCIDENT ( 172 FDA reports)
NEURALGIA ( 171 FDA reports)
PNEUMONITIS ( 171 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 171 FDA reports)
ECZEMA ( 171 FDA reports)
HEPATITIS ACUTE ( 171 FDA reports)
CARDIOMYOPATHY ( 170 FDA reports)
EYE PAIN ( 170 FDA reports)
HEPATITIS CHOLESTATIC ( 170 FDA reports)
IRRITABILITY ( 170 FDA reports)
LACTIC ACIDOSIS ( 170 FDA reports)
APHASIA ( 169 FDA reports)
EMPHYSEMA ( 169 FDA reports)
TINNITUS ( 169 FDA reports)
PULMONARY FIBROSIS ( 168 FDA reports)
BURSITIS ( 168 FDA reports)
EJECTION FRACTION DECREASED ( 168 FDA reports)
ERYTHEMA MULTIFORME ( 167 FDA reports)
FUNGAL INFECTION ( 167 FDA reports)
BLOOD GLUCOSE DECREASED ( 166 FDA reports)
ABSCESS ( 165 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 165 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 165 FDA reports)
PREMATURE BABY ( 165 FDA reports)
CYSTITIS ( 164 FDA reports)
DECUBITUS ULCER ( 162 FDA reports)
EPILEPSY ( 162 FDA reports)
FEMUR FRACTURE ( 162 FDA reports)
FLATULENCE ( 162 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 162 FDA reports)
DIVERTICULITIS ( 161 FDA reports)
TOOTH LOSS ( 161 FDA reports)
HOT FLUSH ( 160 FDA reports)
CEREBRAL ISCHAEMIA ( 159 FDA reports)
ILEUS ( 159 FDA reports)
PURPURA ( 159 FDA reports)
RASH MACULAR ( 159 FDA reports)
SCOLIOSIS ( 159 FDA reports)
RESPIRATORY RATE INCREASED ( 158 FDA reports)
LUNG INFECTION ( 157 FDA reports)
SEROTONIN SYNDROME ( 156 FDA reports)
DEVICE RELATED INFECTION ( 156 FDA reports)
EAR PAIN ( 156 FDA reports)
SUDDEN DEATH ( 155 FDA reports)
URINE OUTPUT DECREASED ( 155 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 154 FDA reports)
ASPIRATION ( 154 FDA reports)
CONJUNCTIVITIS ( 154 FDA reports)
DRUG EFFECT DECREASED ( 154 FDA reports)
COMPRESSION FRACTURE ( 153 FDA reports)
HYPERTHERMIA ( 153 FDA reports)
RESPIRATORY TRACT INFECTION ( 153 FDA reports)
JOINT STIFFNESS ( 152 FDA reports)
CEREBRAL ATROPHY ( 151 FDA reports)
LYMPHOPENIA ( 151 FDA reports)
NERVOUS SYSTEM DISORDER ( 151 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 151 FDA reports)
DEAFNESS ( 150 FDA reports)
HEMIPARESIS ( 150 FDA reports)
NIGHT SWEATS ( 149 FDA reports)
DRUG DOSE OMISSION ( 148 FDA reports)
HEART RATE IRREGULAR ( 148 FDA reports)
AZOTAEMIA ( 147 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 147 FDA reports)
BRONCHOSPASM ( 147 FDA reports)
CARDIOGENIC SHOCK ( 147 FDA reports)
HYDRONEPHROSIS ( 147 FDA reports)
ACUTE RESPIRATORY FAILURE ( 146 FDA reports)
COLITIS ULCERATIVE ( 146 FDA reports)
EXPOSED BONE IN JAW ( 146 FDA reports)
INTENTIONAL SELF-INJURY ( 146 FDA reports)
BLINDNESS ( 145 FDA reports)
CLOSTRIDIAL INFECTION ( 144 FDA reports)
PANIC ATTACK ( 144 FDA reports)
PLATELET COUNT INCREASED ( 144 FDA reports)
METASTASES TO LUNG ( 143 FDA reports)
ORAL CANDIDIASIS ( 143 FDA reports)
RESTLESS LEGS SYNDROME ( 143 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 143 FDA reports)
DRUG INTOLERANCE ( 143 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 142 FDA reports)
DISCOMFORT ( 142 FDA reports)
HYPOALBUMINAEMIA ( 142 FDA reports)
IRRITABLE BOWEL SYNDROME ( 142 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 142 FDA reports)
PRURITUS GENERALISED ( 142 FDA reports)
PYELONEPHRITIS ( 142 FDA reports)
RENAL INJURY ( 142 FDA reports)
ODYNOPHAGIA ( 140 FDA reports)
PHARYNGEAL OEDEMA ( 140 FDA reports)
GENERALISED OEDEMA ( 140 FDA reports)
CYST ( 139 FDA reports)
FISTULA ( 139 FDA reports)
ATRIAL FLUTTER ( 138 FDA reports)
DERMATITIS EXFOLIATIVE ( 138 FDA reports)
OSTEOLYSIS ( 138 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 138 FDA reports)
FEELING COLD ( 137 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 136 FDA reports)
PATHOLOGICAL FRACTURE ( 135 FDA reports)
HEART RATE DECREASED ( 135 FDA reports)
DEPRESSED MOOD ( 134 FDA reports)
INJECTION SITE HAEMATOMA ( 134 FDA reports)
OLIGURIA ( 134 FDA reports)
SPINAL COLUMN STENOSIS ( 134 FDA reports)
TOOTH DISORDER ( 134 FDA reports)
SCIATICA ( 133 FDA reports)
BLOOD PH DECREASED ( 133 FDA reports)
DISABILITY ( 133 FDA reports)
HAEMODYNAMIC INSTABILITY ( 133 FDA reports)
ANAPHYLACTIC SHOCK ( 132 FDA reports)
DYSTONIA ( 132 FDA reports)
ELECTROLYTE IMBALANCE ( 132 FDA reports)
MOVEMENT DISORDER ( 132 FDA reports)
SPLENOMEGALY ( 132 FDA reports)
TUMOUR LYSIS SYNDROME ( 132 FDA reports)
PERITONITIS ( 131 FDA reports)
PSORIASIS ( 131 FDA reports)
FAILURE TO THRIVE ( 131 FDA reports)
LARGE INTESTINE PERFORATION ( 131 FDA reports)
BLOOD CULTURE POSITIVE ( 130 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 130 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 130 FDA reports)
DEMENTIA ( 130 FDA reports)
GOUT ( 130 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 130 FDA reports)
SUBDURAL HAEMATOMA ( 130 FDA reports)
VENTRICULAR FIBRILLATION ( 130 FDA reports)
PSYCHOTIC DISORDER ( 129 FDA reports)
EMOTIONAL DISORDER ( 129 FDA reports)
ILL-DEFINED DISORDER ( 129 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 128 FDA reports)
DISEASE RECURRENCE ( 128 FDA reports)
HIP FRACTURE ( 128 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 128 FDA reports)
NIGHTMARE ( 128 FDA reports)
SEDATION ( 128 FDA reports)
PRESYNCOPE ( 127 FDA reports)
CARDIOVASCULAR DISORDER ( 127 FDA reports)
HYPOMAGNESAEMIA ( 127 FDA reports)
DRUG DEPENDENCE ( 126 FDA reports)
ROTATOR CUFF SYNDROME ( 126 FDA reports)
SKIN DISORDER ( 125 FDA reports)
TOOTH FRACTURE ( 125 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 125 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 125 FDA reports)
DYSSTASIA ( 124 FDA reports)
FLUID RETENTION ( 124 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 124 FDA reports)
MYOCLONUS ( 123 FDA reports)
PHYSICAL DISABILITY ( 122 FDA reports)
ULCER ( 122 FDA reports)
LYMPHOMA ( 121 FDA reports)
VASCULITIS ( 121 FDA reports)
EATING DISORDER ( 121 FDA reports)
HAEMOLYTIC ANAEMIA ( 121 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 121 FDA reports)
CHOLECYSTITIS ACUTE ( 120 FDA reports)
ERECTILE DYSFUNCTION ( 120 FDA reports)
APNOEA ( 119 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 119 FDA reports)
BACTERAEMIA ( 119 FDA reports)
BASAL CELL CARCINOMA ( 119 FDA reports)
HEPATOCELLULAR INJURY ( 119 FDA reports)
DRUG ABUSER ( 118 FDA reports)
NEUTROPENIC SEPSIS ( 118 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 118 FDA reports)
TENDONITIS ( 117 FDA reports)
THROAT TIGHTNESS ( 117 FDA reports)
ECCHYMOSIS ( 117 FDA reports)
ESCHERICHIA INFECTION ( 117 FDA reports)
HEPATOCELLULAR DAMAGE ( 117 FDA reports)
DRUG SCREEN POSITIVE ( 116 FDA reports)
PURULENT DISCHARGE ( 116 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 116 FDA reports)
VAGINAL HAEMORRHAGE ( 116 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 115 FDA reports)
PSEUDOMONAS INFECTION ( 115 FDA reports)
SURGERY ( 115 FDA reports)
HYPOPHOSPHATAEMIA ( 115 FDA reports)
ALCOHOL USE ( 114 FDA reports)
COORDINATION ABNORMAL ( 114 FDA reports)
CRYING ( 114 FDA reports)
DERMATITIS ( 114 FDA reports)
HYPOVOLAEMIA ( 114 FDA reports)
ANGINA UNSTABLE ( 113 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 113 FDA reports)
MYELODYSPLASTIC SYNDROME ( 113 FDA reports)
NEUTROPHIL COUNT INCREASED ( 113 FDA reports)
ORAL HERPES ( 112 FDA reports)
ATRIAL SEPTAL DEFECT ( 112 FDA reports)
HEPATIC CIRRHOSIS ( 112 FDA reports)
HEPATITIS FULMINANT ( 112 FDA reports)
ATAXIA ( 111 FDA reports)
LIP SWELLING ( 111 FDA reports)
PELVIC PAIN ( 111 FDA reports)
PRIMARY SEQUESTRUM ( 111 FDA reports)
LUNG NEOPLASM MALIGNANT ( 110 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 110 FDA reports)
PHOTOPHOBIA ( 110 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 110 FDA reports)
DRY EYE ( 109 FDA reports)
GLAUCOMA ( 109 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 109 FDA reports)
LIPASE INCREASED ( 109 FDA reports)
LIVER TRANSPLANT ( 109 FDA reports)
PREGNANCY ( 109 FDA reports)
MULTIPLE INJURIES ( 108 FDA reports)
MUSCLE RIGIDITY ( 108 FDA reports)
MYOSITIS ( 108 FDA reports)
EAR INFECTION ( 108 FDA reports)
EYELID OEDEMA ( 108 FDA reports)
ENTEROCOCCAL INFECTION ( 107 FDA reports)
AMMONIA INCREASED ( 106 FDA reports)
AORTIC VALVE INCOMPETENCE ( 106 FDA reports)
BODY TEMPERATURE DECREASED ( 106 FDA reports)
PEPTIC ULCER ( 106 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 106 FDA reports)
SINUS DISORDER ( 106 FDA reports)
PERIPHERAL COLDNESS ( 105 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 105 FDA reports)
THIRST ( 105 FDA reports)
BREAST CANCER ( 105 FDA reports)
DIVERTICULUM INTESTINAL ( 105 FDA reports)
EXCORIATION ( 105 FDA reports)
FOOT FRACTURE ( 105 FDA reports)
GASTRIC DISORDER ( 105 FDA reports)
GINGIVITIS ( 105 FDA reports)
HAEMOLYSIS ( 105 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 104 FDA reports)
COLONIC POLYP ( 104 FDA reports)
FAECES DISCOLOURED ( 104 FDA reports)
MULTIPLE SCLEROSIS ( 104 FDA reports)
PERICARDITIS ( 104 FDA reports)
UTERINE LEIOMYOMA ( 104 FDA reports)
OSTEOSCLEROSIS ( 103 FDA reports)
PLEURAL FIBROSIS ( 103 FDA reports)
RALES ( 102 FDA reports)
CORONARY ARTERY OCCLUSION ( 102 FDA reports)
EYE DISORDER ( 102 FDA reports)
ACUTE CORONARY SYNDROME ( 101 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 101 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 101 FDA reports)
HEPATIC CYST ( 100 FDA reports)
INCONTINENCE ( 100 FDA reports)
MASS ( 100 FDA reports)
NEPHROPATHY TOXIC ( 100 FDA reports)
LOOSE TOOTH ( 99 FDA reports)
OCULAR HYPERAEMIA ( 99 FDA reports)
SKIN TIGHTNESS ( 99 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 99 FDA reports)
ADVERSE DRUG REACTION ( 99 FDA reports)
BLOOD URINE PRESENT ( 99 FDA reports)
COLD SWEAT ( 99 FDA reports)
HEPATITIS C ( 99 FDA reports)
ABDOMINAL PAIN LOWER ( 98 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 98 FDA reports)
NO THERAPEUTIC RESPONSE ( 98 FDA reports)
PARANOIA ( 98 FDA reports)
LUMBAR SPINAL STENOSIS ( 97 FDA reports)
NOCTURIA ( 97 FDA reports)
OVARIAN CYST ( 97 FDA reports)
PROTEIN TOTAL DECREASED ( 97 FDA reports)
TENDERNESS ( 97 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 97 FDA reports)
CHOLECYSTECTOMY ( 97 FDA reports)
EYE SWELLING ( 97 FDA reports)
HYDROCEPHALUS ( 97 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 97 FDA reports)
INTESTINAL ISCHAEMIA ( 97 FDA reports)
COLITIS ISCHAEMIC ( 96 FDA reports)
COLON CANCER ( 96 FDA reports)
DUODENAL ULCER ( 96 FDA reports)
FIBROMYALGIA ( 96 FDA reports)
ISCHAEMIA ( 96 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 96 FDA reports)
PLEURITIC PAIN ( 96 FDA reports)
THERAPY NON-RESPONDER ( 96 FDA reports)
WRONG DRUG ADMINISTERED ( 96 FDA reports)
ACCIDENTAL EXPOSURE ( 95 FDA reports)
DILATATION VENTRICULAR ( 95 FDA reports)
ISCHAEMIC STROKE ( 95 FDA reports)
JOINT INJURY ( 95 FDA reports)
ABDOMINAL TENDERNESS ( 94 FDA reports)
INJECTION SITE REACTION ( 94 FDA reports)
LABORATORY TEST ABNORMAL ( 94 FDA reports)
LOBAR PNEUMONIA ( 94 FDA reports)
MASTICATION DISORDER ( 94 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 94 FDA reports)
WITHDRAWAL SYNDROME ( 94 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 93 FDA reports)
FAECAL INCONTINENCE ( 93 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 93 FDA reports)
LACERATION ( 93 FDA reports)
APPENDICITIS ( 92 FDA reports)
BLOOD BICARBONATE DECREASED ( 92 FDA reports)
INJECTION SITE HAEMORRHAGE ( 92 FDA reports)
RETCHING ( 92 FDA reports)
SKIN INDURATION ( 92 FDA reports)
SPONDYLOLISTHESIS ( 92 FDA reports)
MYDRIASIS ( 91 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 91 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 91 FDA reports)
PROSTATE CANCER ( 91 FDA reports)
BRAIN HERNIATION ( 91 FDA reports)
BEDRIDDEN ( 90 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 90 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 90 FDA reports)
ILEUS PARALYTIC ( 90 FDA reports)
UROSEPSIS ( 90 FDA reports)
VISUAL DISTURBANCE ( 90 FDA reports)
MIOSIS ( 89 FDA reports)
OTITIS MEDIA ( 89 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 89 FDA reports)
BIPOLAR DISORDER ( 89 FDA reports)
CAESAREAN SECTION ( 89 FDA reports)
ANGER ( 88 FDA reports)
FACIAL PAIN ( 88 FDA reports)
GINGIVAL BLEEDING ( 88 FDA reports)
LACRIMATION INCREASED ( 88 FDA reports)
METASTASES TO SPINE ( 88 FDA reports)
PREMATURE LABOUR ( 88 FDA reports)
SERUM FERRITIN INCREASED ( 87 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 87 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 87 FDA reports)
HYPERAESTHESIA ( 87 FDA reports)
BLOOD AMYLASE INCREASED ( 86 FDA reports)
BLOOD CHLORIDE DECREASED ( 86 FDA reports)
INTESTINAL PERFORATION ( 86 FDA reports)
IRON DEFICIENCY ANAEMIA ( 86 FDA reports)
NO ADVERSE EVENT ( 86 FDA reports)
SKIN HYPERPIGMENTATION ( 86 FDA reports)
TROPONIN INCREASED ( 86 FDA reports)
LUNG CONSOLIDATION ( 85 FDA reports)
MUSCLE TWITCHING ( 85 FDA reports)
ORAL INTAKE REDUCED ( 85 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 85 FDA reports)
PULSE ABSENT ( 85 FDA reports)
RASH PAPULAR ( 85 FDA reports)
RHINITIS ALLERGIC ( 85 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 85 FDA reports)
APHTHOUS STOMATITIS ( 85 FDA reports)
BLINDNESS TRANSIENT ( 85 FDA reports)
CHRONIC SINUSITIS ( 85 FDA reports)
HOSPITALISATION ( 85 FDA reports)
CAROTID ARTERY STENOSIS ( 84 FDA reports)
KYPHOSIS ( 84 FDA reports)
MENTAL IMPAIRMENT ( 84 FDA reports)
RASH PUSTULAR ( 84 FDA reports)
SENSORY DISTURBANCE ( 84 FDA reports)
VENTRICULAR HYPERTROPHY ( 84 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 83 FDA reports)
CACHEXIA ( 83 FDA reports)
FIBROSIS ( 83 FDA reports)
HYPOKINESIA ( 83 FDA reports)
JAUNDICE CHOLESTATIC ( 83 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 82 FDA reports)
DELUSION ( 82 FDA reports)
GASTRIC HAEMORRHAGE ( 82 FDA reports)
LOCAL SWELLING ( 82 FDA reports)
MICTURITION URGENCY ( 82 FDA reports)
OEDEMA MOUTH ( 82 FDA reports)
THROAT IRRITATION ( 81 FDA reports)
ANAPHYLACTOID REACTION ( 81 FDA reports)
HEPATIC LESION ( 81 FDA reports)
HYPOTONIA ( 81 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 81 FDA reports)
ADVERSE EVENT ( 80 FDA reports)
MOTOR DYSFUNCTION ( 80 FDA reports)
SUBSTANCE ABUSE ( 80 FDA reports)
THYROID CANCER ( 80 FDA reports)
RESPIRATORY ACIDOSIS ( 79 FDA reports)
SKIN HYPERTROPHY ( 79 FDA reports)
ACUTE PULMONARY OEDEMA ( 79 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 79 FDA reports)
GINGIVAL DISORDER ( 79 FDA reports)
HYPERSOMNIA ( 79 FDA reports)
HYPERURICAEMIA ( 79 FDA reports)
FLANK PAIN ( 78 FDA reports)
GENERALISED ERYTHEMA ( 78 FDA reports)
IMPAIRED WORK ABILITY ( 78 FDA reports)
TORSADE DE POINTES ( 78 FDA reports)
WOUND INFECTION ( 78 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 77 FDA reports)
MYOPATHY ( 77 FDA reports)
PERIODONTITIS ( 77 FDA reports)
PLEURISY ( 77 FDA reports)
WOUND ( 77 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 77 FDA reports)
BACTERIAL SEPSIS ( 76 FDA reports)
CARPAL TUNNEL SYNDROME ( 76 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 76 FDA reports)
GINGIVAL PAIN ( 76 FDA reports)
IMMUNOSUPPRESSION ( 76 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 76 FDA reports)
JAW FRACTURE ( 76 FDA reports)
MUSCLE ATROPHY ( 76 FDA reports)
TOOTH INFECTION ( 76 FDA reports)
NEPHROTIC SYNDROME ( 75 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 75 FDA reports)
BLOOD LACTIC ACID INCREASED ( 75 FDA reports)
DUODENITIS ( 75 FDA reports)
GASTROENTERITIS VIRAL ( 75 FDA reports)
JOINT EFFUSION ( 75 FDA reports)
LEFT ATRIAL DILATATION ( 75 FDA reports)
NECROSIS ( 74 FDA reports)
UPPER LIMB FRACTURE ( 74 FDA reports)
PHLEBITIS ( 73 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 73 FDA reports)
CHEST X-RAY ABNORMAL ( 72 FDA reports)
DIASTOLIC DYSFUNCTION ( 72 FDA reports)
DIFFICULTY IN WALKING ( 72 FDA reports)
EMBOLISM ( 72 FDA reports)
GROIN PAIN ( 72 FDA reports)
INJECTION SITE SWELLING ( 72 FDA reports)
LOCALISED INFECTION ( 72 FDA reports)
STREPTOCOCCAL INFECTION ( 72 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 72 FDA reports)
MOOD ALTERED ( 71 FDA reports)
MOUTH HAEMORRHAGE ( 71 FDA reports)
PERIPHERAL ISCHAEMIA ( 71 FDA reports)
SPINAL FRACTURE ( 71 FDA reports)
STATUS EPILEPTICUS ( 71 FDA reports)
SYNOVIAL CYST ( 71 FDA reports)
ADRENAL INSUFFICIENCY ( 71 FDA reports)
ANKLE FRACTURE ( 71 FDA reports)
AREFLEXIA ( 71 FDA reports)
GINGIVAL INFECTION ( 71 FDA reports)
HYPERNATRAEMIA ( 71 FDA reports)
BREAST MASS ( 70 FDA reports)
DEBRIDEMENT ( 70 FDA reports)
ENDODONTIC PROCEDURE ( 70 FDA reports)
FAECALOMA ( 70 FDA reports)
INGUINAL HERNIA ( 70 FDA reports)
LOWER LIMB FRACTURE ( 70 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 70 FDA reports)
PULMONARY HAEMORRHAGE ( 70 FDA reports)
SENSATION OF HEAVINESS ( 70 FDA reports)
SKIN NECROSIS ( 70 FDA reports)
VENOUS THROMBOSIS ( 70 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 70 FDA reports)
OPEN WOUND ( 69 FDA reports)
OSTEITIS ( 69 FDA reports)
WALKING AID USER ( 69 FDA reports)
ACTINOMYCOSIS ( 69 FDA reports)
ANGIONEUROTIC OEDEMA ( 69 FDA reports)
ASPERGILLOSIS ( 69 FDA reports)
BILIARY DYSKINESIA ( 69 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 69 FDA reports)
JOINT DISLOCATION ( 69 FDA reports)
ANGIOPATHY ( 68 FDA reports)
GANGRENE ( 68 FDA reports)
HEPATOSPLENOMEGALY ( 68 FDA reports)
INJECTION SITE PRURITUS ( 68 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 68 FDA reports)
PCO2 DECREASED ( 68 FDA reports)
RADICULOPATHY ( 68 FDA reports)
SPINAL DISORDER ( 68 FDA reports)
ORGAN FAILURE ( 67 FDA reports)
PROCEDURAL COMPLICATION ( 67 FDA reports)
SKIN REACTION ( 67 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 67 FDA reports)
DERMATITIS BULLOUS ( 67 FDA reports)
ENDOCARDITIS ( 67 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 67 FDA reports)
HYPOACUSIS ( 67 FDA reports)
KLEBSIELLA INFECTION ( 67 FDA reports)
AORTIC ANEURYSM ( 66 FDA reports)
BLOOD CREATINE INCREASED ( 66 FDA reports)
CORONARY ARTERY STENOSIS ( 66 FDA reports)
CULTURE URINE POSITIVE ( 66 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 66 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 66 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 66 FDA reports)
TUBERCULOSIS ( 66 FDA reports)
MAJOR DEPRESSION ( 65 FDA reports)
METABOLIC ENCEPHALOPATHY ( 65 FDA reports)
OCULAR ICTERUS ( 65 FDA reports)
ORTHOPNOEA ( 65 FDA reports)
SHOCK HAEMORRHAGIC ( 65 FDA reports)
THROMBOCYTOSIS ( 65 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 65 FDA reports)
CHEILITIS ( 65 FDA reports)
ENTEROCOLITIS ( 65 FDA reports)
FOOT DEFORMITY ( 65 FDA reports)
LIFE EXPECTANCY SHORTENED ( 65 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 64 FDA reports)
CHOKING ( 64 FDA reports)
GINGIVAL SWELLING ( 64 FDA reports)
HALLUCINATION, AUDITORY ( 64 FDA reports)
HEPATITIS TOXIC ( 64 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 64 FDA reports)
INCOHERENT ( 64 FDA reports)
LIMB INJURY ( 64 FDA reports)
MACULAR DEGENERATION ( 64 FDA reports)
PYROGLUTAMATE INCREASED ( 64 FDA reports)
TARDIVE DYSKINESIA ( 64 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 64 FDA reports)
POLYURIA ( 63 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 63 FDA reports)
SENSATION OF FOREIGN BODY ( 63 FDA reports)
VENTRICULAR DYSFUNCTION ( 63 FDA reports)
YELLOW SKIN ( 63 FDA reports)
ABNORMAL DREAMS ( 63 FDA reports)
HAEMORRHAGIC ANAEMIA ( 63 FDA reports)
CEREBROVASCULAR DISORDER ( 62 FDA reports)
DIABETIC KETOACIDOSIS ( 62 FDA reports)
DIABETIC NEUROPATHY ( 62 FDA reports)
FRACTURE ( 62 FDA reports)
HEMIPLEGIA ( 62 FDA reports)
HERPES VIRUS INFECTION ( 62 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 62 FDA reports)
HYPERVENTILATION ( 62 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 62 FDA reports)
MOOD SWINGS ( 62 FDA reports)
PARALYSIS ( 62 FDA reports)
POLYNEUROPATHY ( 62 FDA reports)
RHINITIS ( 62 FDA reports)
SINUS CONGESTION ( 62 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 61 FDA reports)
ORAL DISORDER ( 61 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 61 FDA reports)
ULCER HAEMORRHAGE ( 61 FDA reports)
ABSCESS DRAINAGE ( 61 FDA reports)
ALCOHOL POISONING ( 61 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 61 FDA reports)
DILATATION ATRIAL ( 61 FDA reports)
ENCEPHALITIS ( 61 FDA reports)
HEARING IMPAIRED ( 61 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 61 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 61 FDA reports)
JAW DISORDER ( 61 FDA reports)
BRAIN DEATH ( 60 FDA reports)
BREAST PAIN ( 60 FDA reports)
DYSLIPIDAEMIA ( 60 FDA reports)
GASTRITIS EROSIVE ( 60 FDA reports)
HERPES SIMPLEX ( 60 FDA reports)
IMMUNODEFICIENCY ( 60 FDA reports)
LACUNAR INFARCTION ( 60 FDA reports)
MUSCLE TIGHTNESS ( 60 FDA reports)
ONYCHOMYCOSIS ( 60 FDA reports)
PYELONEPHRITIS ACUTE ( 60 FDA reports)
SNORING ( 60 FDA reports)
STEM CELL TRANSPLANT ( 60 FDA reports)
TRANSPLANT REJECTION ( 60 FDA reports)
LUMBAR RADICULOPATHY ( 59 FDA reports)
MUSCLE STRAIN ( 59 FDA reports)
OESOPHAGEAL ULCER ( 59 FDA reports)
SENSORY LOSS ( 59 FDA reports)
SEXUAL DYSFUNCTION ( 59 FDA reports)
VENTRICULAR HYPOKINESIA ( 59 FDA reports)
AORTIC STENOSIS ( 59 FDA reports)
CEREBRAL HAEMATOMA ( 59 FDA reports)
CERVICAL SPINAL STENOSIS ( 59 FDA reports)
HYPERTENSIVE HEART DISEASE ( 59 FDA reports)
HYPERTHYROIDISM ( 59 FDA reports)
ABDOMINAL ABSCESS ( 58 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 58 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 58 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 58 FDA reports)
HIP ARTHROPLASTY ( 58 FDA reports)
POLYP ( 58 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 58 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 58 FDA reports)
PHOTOSENSITIVITY REACTION ( 57 FDA reports)
PULMONARY MASS ( 57 FDA reports)
PUPIL FIXED ( 57 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 57 FDA reports)
VENOUS THROMBOSIS LIMB ( 57 FDA reports)
ABORTION INDUCED ( 57 FDA reports)
BREATH SOUNDS ABNORMAL ( 57 FDA reports)
CREPITATIONS ( 57 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 57 FDA reports)
HYPOVENTILATION ( 57 FDA reports)
INGROWING NAIL ( 57 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 56 FDA reports)
APATHY ( 56 FDA reports)
APLASTIC ANAEMIA ( 56 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 56 FDA reports)
BLINDNESS UNILATERAL ( 56 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 56 FDA reports)
ESSENTIAL HYPERTENSION ( 56 FDA reports)
GOITRE ( 56 FDA reports)
INADEQUATE ANALGESIA ( 56 FDA reports)
JUGULAR VEIN THROMBOSIS ( 56 FDA reports)
PO2 DECREASED ( 56 FDA reports)
SQUAMOUS CELL CARCINOMA ( 56 FDA reports)
SUBCUTANEOUS ABSCESS ( 56 FDA reports)
LUNG CANCER METASTATIC ( 55 FDA reports)
NODULE ( 55 FDA reports)
OESOPHAGEAL STENOSIS ( 55 FDA reports)
PARAESTHESIA ORAL ( 55 FDA reports)
POOR QUALITY SLEEP ( 55 FDA reports)
RESPIRATORY ALKALOSIS ( 55 FDA reports)
SEBORRHOEIC DERMATITIS ( 55 FDA reports)
WRIST FRACTURE ( 55 FDA reports)
ARTHRITIS BACTERIAL ( 55 FDA reports)
FACIAL BONES FRACTURE ( 55 FDA reports)
HEPATIC CONGESTION ( 55 FDA reports)
INTRA-UTERINE DEATH ( 55 FDA reports)
ANAL ABSCESS ( 54 FDA reports)
APHAGIA ( 54 FDA reports)
BREAST CANCER METASTATIC ( 54 FDA reports)
CHOLANGITIS ( 54 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 54 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 54 FDA reports)
DENTURE WEARER ( 54 FDA reports)
EXTRASYSTOLES ( 54 FDA reports)
EYE IRRITATION ( 54 FDA reports)
GALLBLADDER INJURY ( 54 FDA reports)
OPTIC NEURITIS ( 54 FDA reports)
ORAL INFECTION ( 54 FDA reports)
PNEUMONIA BACTERIAL ( 54 FDA reports)
RENAL PAIN ( 54 FDA reports)
SERUM SICKNESS ( 54 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 53 FDA reports)
METABOLIC DISORDER ( 53 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 53 FDA reports)
POISONING DELIBERATE ( 53 FDA reports)
SELF-MEDICATION ( 53 FDA reports)
TENDON RUPTURE ( 53 FDA reports)
ABDOMINAL HERNIA ( 53 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 53 FDA reports)
ANAL FISTULA ( 53 FDA reports)
AUTOIMMUNE HEPATITIS ( 53 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 53 FDA reports)
GRANULOCYTOPENIA ( 53 FDA reports)
GYNAECOMASTIA ( 53 FDA reports)
HYPOAESTHESIA ORAL ( 53 FDA reports)
ABSCESS JAW ( 52 FDA reports)
BILIARY COLIC ( 52 FDA reports)
BLOOD MAGNESIUM DECREASED ( 52 FDA reports)
BRONCHIECTASIS ( 52 FDA reports)
COMA HEPATIC ( 52 FDA reports)
DRUG PRESCRIBING ERROR ( 52 FDA reports)
DUODENAL ULCER PERFORATION ( 52 FDA reports)
FACET JOINT SYNDROME ( 52 FDA reports)
KERATITIS ( 52 FDA reports)
OESOPHAGEAL PAIN ( 52 FDA reports)
THROMBOPHLEBITIS ( 52 FDA reports)
VENOUS INSUFFICIENCY ( 52 FDA reports)
VIITH NERVE PARALYSIS ( 52 FDA reports)
MENORRHAGIA ( 51 FDA reports)
MUSCLE HAEMORRHAGE ( 51 FDA reports)
NERVE COMPRESSION ( 51 FDA reports)
PAIN OF SKIN ( 51 FDA reports)
PERIODONTAL DISEASE ( 51 FDA reports)
SCAB ( 51 FDA reports)
TRISMUS ( 51 FDA reports)
BONE DENSITY DECREASED ( 51 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 51 FDA reports)
ERUCTATION ( 51 FDA reports)
FIBRIN D DIMER INCREASED ( 51 FDA reports)
HUMERUS FRACTURE ( 51 FDA reports)
KNEE ARTHROPLASTY ( 51 FDA reports)
ACNE ( 50 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 50 FDA reports)
BLOOD CHLORIDE INCREASED ( 50 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 50 FDA reports)
CARDIAC VALVE DISEASE ( 50 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 50 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 50 FDA reports)
HYPOPROTEINAEMIA ( 50 FDA reports)
LIGAMENT SPRAIN ( 50 FDA reports)
METASTATIC NEOPLASM ( 50 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 50 FDA reports)
PERONEAL NERVE PALSY ( 50 FDA reports)
POLYARTHRITIS ( 50 FDA reports)
PULMONARY INFARCTION ( 50 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 50 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 49 FDA reports)
QUALITY OF LIFE DECREASED ( 49 FDA reports)
RETROPERITONEAL HAEMATOMA ( 49 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 49 FDA reports)
SUBDURAL HAEMORRHAGE ( 49 FDA reports)
TONGUE OEDEMA ( 49 FDA reports)
VENOOCCLUSIVE DISEASE ( 49 FDA reports)
VITAMIN D DEFICIENCY ( 49 FDA reports)
ACCIDENTAL DEATH ( 49 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 49 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 49 FDA reports)
FEMORAL NECK FRACTURE ( 49 FDA reports)
GLOSSODYNIA ( 49 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 49 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 49 FDA reports)
JOINT SPRAIN ( 49 FDA reports)
KIDNEY INFECTION ( 49 FDA reports)
LIMB DISCOMFORT ( 49 FDA reports)
ABSCESS ORAL ( 48 FDA reports)
CARDIAC FAILURE ACUTE ( 48 FDA reports)
CATHETER RELATED INFECTION ( 48 FDA reports)
DERMATITIS CONTACT ( 48 FDA reports)
DEVELOPMENTAL DELAY ( 48 FDA reports)
MENINGITIS ( 48 FDA reports)
METASTASIS ( 48 FDA reports)
MYOPIA ( 48 FDA reports)
PERSONALITY CHANGE ( 48 FDA reports)
PULMONARY TUBERCULOSIS ( 48 FDA reports)
PURULENCE ( 48 FDA reports)
RENAL TUBULAR DISORDER ( 48 FDA reports)
RESPIRATORY TRACT CONGESTION ( 48 FDA reports)
SKIN INFECTION ( 48 FDA reports)
SPINAL CORD COMPRESSION ( 48 FDA reports)
STOMACH DISCOMFORT ( 48 FDA reports)
LOCALISED OEDEMA ( 47 FDA reports)
NEUROPATHY ( 47 FDA reports)
PARKINSON'S DISEASE ( 47 FDA reports)
PSYCHIATRIC SYMPTOM ( 47 FDA reports)
ATRIOVENTRICULAR BLOCK ( 47 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 47 FDA reports)
CARDIAC TAMPONADE ( 47 FDA reports)
DRUG DISPENSING ERROR ( 47 FDA reports)
DYSAESTHESIA ( 47 FDA reports)
FACIAL PALSY ( 47 FDA reports)
FEBRILE BONE MARROW APLASIA ( 47 FDA reports)
FUNGAEMIA ( 47 FDA reports)
LARYNGEAL OEDEMA ( 47 FDA reports)
ADRENAL NEOPLASM ( 46 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 46 FDA reports)
BREAST TENDERNESS ( 46 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 46 FDA reports)
CALCULUS URETERIC ( 46 FDA reports)
COLON ADENOMA ( 46 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 46 FDA reports)
GRAFT VERSUS HOST DISEASE ( 46 FDA reports)
HODGKIN'S DISEASE ( 46 FDA reports)
MEDICAL DEVICE COMPLICATION ( 46 FDA reports)
MENISCUS LESION ( 46 FDA reports)
NEPHROPATHY ( 46 FDA reports)
PAPILLOEDEMA ( 46 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 46 FDA reports)
SCHIZOPHRENIA ( 46 FDA reports)
URETERIC OBSTRUCTION ( 46 FDA reports)
VASCULAR PSEUDOANEURYSM ( 46 FDA reports)
NEUROLOGICAL SYMPTOM ( 45 FDA reports)
PROTEIN URINE PRESENT ( 45 FDA reports)
THYROID NEOPLASM ( 45 FDA reports)
VISUAL FIELD DEFECT ( 45 FDA reports)
AORTIC CALCIFICATION ( 45 FDA reports)
CARDIOPULMONARY FAILURE ( 45 FDA reports)
CYSTITIS HAEMORRHAGIC ( 45 FDA reports)
DERMAL CYST ( 45 FDA reports)
DYSGRAPHIA ( 45 FDA reports)
EPIGASTRIC DISCOMFORT ( 45 FDA reports)
GASTROINTESTINAL NECROSIS ( 45 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 45 FDA reports)
HERNIA ( 45 FDA reports)
HYPERAMYLASAEMIA ( 45 FDA reports)
HYPERKERATOSIS ( 45 FDA reports)
BODY HEIGHT DECREASED ( 44 FDA reports)
BONE NEOPLASM MALIGNANT ( 44 FDA reports)
BREATH ODOUR ( 44 FDA reports)
CLEFT PALATE ( 44 FDA reports)
EYE MOVEMENT DISORDER ( 44 FDA reports)
LEG AMPUTATION ( 44 FDA reports)
METASTASES TO LYMPH NODES ( 44 FDA reports)
PERIORBITAL OEDEMA ( 44 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 44 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 44 FDA reports)
WOUND SECRETION ( 44 FDA reports)
PLASMACYTOSIS ( 43 FDA reports)
PROTHROMBIN TIME SHORTENED ( 43 FDA reports)
RENAL CELL CARCINOMA ( 43 FDA reports)
RIGHT VENTRICULAR FAILURE ( 43 FDA reports)
SKIN CANCER ( 43 FDA reports)
SKIN LACERATION ( 43 FDA reports)
STRABISMUS ( 43 FDA reports)
VARICOSE VEIN ( 43 FDA reports)
APPETITE DISORDER ( 43 FDA reports)
BACK INJURY ( 43 FDA reports)
CATHETER RELATED COMPLICATION ( 43 FDA reports)
EOSINOPHIL COUNT INCREASED ( 43 FDA reports)
ESCHERICHIA SEPSIS ( 43 FDA reports)
HAEMOTHORAX ( 43 FDA reports)
INTESTINAL HAEMORRHAGE ( 43 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 42 FDA reports)
ACTINIC KERATOSIS ( 42 FDA reports)
AFFECTIVE DISORDER ( 42 FDA reports)
BLOOD CALCIUM INCREASED ( 42 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 42 FDA reports)
BLOOD TEST ABNORMAL ( 42 FDA reports)
COLLAPSE OF LUNG ( 42 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 42 FDA reports)
GASTROINTESTINAL PAIN ( 42 FDA reports)
GRANULOMA ( 42 FDA reports)
INJECTION SITE IRRITATION ( 42 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 42 FDA reports)
KLEBSIELLA SEPSIS ( 42 FDA reports)
MANIA ( 42 FDA reports)
MUCOUS MEMBRANE DISORDER ( 42 FDA reports)
MULTI-ORGAN DISORDER ( 42 FDA reports)
OLIGOHYDRAMNIOS ( 42 FDA reports)
PANIC REACTION ( 42 FDA reports)
PNEUMONIA FUNGAL ( 42 FDA reports)
PROCTALGIA ( 42 FDA reports)
SKIN FISSURES ( 42 FDA reports)
SYNCOPE VASOVAGAL ( 42 FDA reports)
VENA CAVA THROMBOSIS ( 42 FDA reports)
LYMPHOEDEMA ( 41 FDA reports)
MALIGNANT MELANOMA ( 41 FDA reports)
MELANOCYTIC NAEVUS ( 41 FDA reports)
MITRAL VALVE DISEASE ( 41 FDA reports)
NEPHRITIS INTERSTITIAL ( 41 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 41 FDA reports)
PRURIGO ( 41 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 41 FDA reports)
SINUS ARRHYTHMIA ( 41 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 41 FDA reports)
VAGINAL DISCHARGE ( 41 FDA reports)
AGEUSIA ( 41 FDA reports)
BACK DISORDER ( 41 FDA reports)
BLOOD SODIUM INCREASED ( 41 FDA reports)
CAECITIS ( 41 FDA reports)
CANDIDA TEST POSITIVE ( 41 FDA reports)
COMMUNICATION DISORDER ( 41 FDA reports)
CONCUSSION ( 41 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 41 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 41 FDA reports)
ERYSIPELAS ( 41 FDA reports)
FOLLICULITIS ( 41 FDA reports)
HYPOVOLAEMIC SHOCK ( 41 FDA reports)
LARYNGITIS ( 41 FDA reports)
AORTIC VALVE SCLEROSIS ( 40 FDA reports)
BLEPHARITIS ( 40 FDA reports)
BLOOD COUNT ABNORMAL ( 40 FDA reports)
BLOOD DISORDER ( 40 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 40 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 40 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 40 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 40 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 40 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 40 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 40 FDA reports)
HAEMORRHAGIC STROKE ( 40 FDA reports)
IMMOBILE ( 40 FDA reports)
INJECTION SITE RASH ( 40 FDA reports)
MITRAL VALVE PROLAPSE ( 40 FDA reports)
NAIL DISORDER ( 40 FDA reports)
NYSTAGMUS ( 40 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 40 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 40 FDA reports)
RENAL ATROPHY ( 40 FDA reports)
RENAL PAPILLARY NECROSIS ( 40 FDA reports)
SYNOVITIS ( 40 FDA reports)
NASAL SEPTUM DEVIATION ( 39 FDA reports)
NEOPLASM ( 39 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 39 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 39 FDA reports)
SICK SINUS SYNDROME ( 39 FDA reports)
SKIN FIBROSIS ( 39 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 39 FDA reports)
SUBILEUS ( 39 FDA reports)
THYROID DISORDER ( 39 FDA reports)
VITREOUS FLOATERS ( 39 FDA reports)
ALVEOLITIS ( 39 FDA reports)
ANION GAP INCREASED ( 39 FDA reports)
AORTIC DISSECTION ( 39 FDA reports)
BILE DUCT STONE ( 39 FDA reports)
BLADDER DISORDER ( 39 FDA reports)
BRONCHITIS CHRONIC ( 39 FDA reports)
BUNDLE BRANCH BLOCK ( 39 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 39 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 39 FDA reports)
FLUID INTAKE REDUCED ( 39 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 39 FDA reports)
HELICOBACTER INFECTION ( 39 FDA reports)
HEPATIC FIBROSIS ( 39 FDA reports)
HILAR LYMPHADENOPATHY ( 39 FDA reports)
HYPERCAPNIA ( 39 FDA reports)
ISCHAEMIC HEPATITIS ( 39 FDA reports)
LIVEDO RETICULARIS ( 39 FDA reports)
ACCIDENT ( 38 FDA reports)
ADNEXA UTERI MASS ( 38 FDA reports)
BLOOD CREATININE DECREASED ( 38 FDA reports)
BONE LOSS ( 38 FDA reports)
DIZZINESS POSTURAL ( 38 FDA reports)
EYE HAEMORRHAGE ( 38 FDA reports)
HAEMANGIOMA OF LIVER ( 38 FDA reports)
HYPERCOAGULATION ( 38 FDA reports)
HYPERTENSIVE CRISIS ( 38 FDA reports)
HYPERTONIA ( 38 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 38 FDA reports)
JOINT CONTRACTURE ( 38 FDA reports)
NEUROTOXICITY ( 38 FDA reports)
PARKINSONISM ( 38 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 38 FDA reports)
PRE-ECLAMPSIA ( 38 FDA reports)
RASH MORBILLIFORM ( 38 FDA reports)
SARCOIDOSIS ( 38 FDA reports)
SPUTUM DISCOLOURED ( 38 FDA reports)
TENDON DISORDER ( 38 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 38 FDA reports)
MIDDLE INSOMNIA ( 37 FDA reports)
MUSCULOSKELETAL DISORDER ( 37 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 37 FDA reports)
NON-CARDIAC CHEST PAIN ( 37 FDA reports)
PERIARTHRITIS ( 37 FDA reports)
PIGMENTATION DISORDER ( 37 FDA reports)
PRESBYOPIA ( 37 FDA reports)
RETINAL HAEMORRHAGE ( 37 FDA reports)
TREATMENT FAILURE ( 37 FDA reports)
UMBILICAL HERNIA ( 37 FDA reports)
ANEURYSM ( 37 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 37 FDA reports)
BONE OPERATION ( 37 FDA reports)
BRAIN INJURY ( 37 FDA reports)
CAPILLARY LEAK SYNDROME ( 37 FDA reports)
CATARACT OPERATION ( 37 FDA reports)
DRUG LEVEL DECREASED ( 37 FDA reports)
GINGIVAL ULCERATION ( 37 FDA reports)
HEPATORENAL SYNDROME ( 37 FDA reports)
INCREASED TENDENCY TO BRUISE ( 37 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 37 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 36 FDA reports)
ACUTE SINUSITIS ( 36 FDA reports)
BLOOD UREA DECREASED ( 36 FDA reports)
BRUXISM ( 36 FDA reports)
CERUMEN IMPACTION ( 36 FDA reports)
CHANGE OF BOWEL HABIT ( 36 FDA reports)
COMA SCALE ABNORMAL ( 36 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 36 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 36 FDA reports)
DERMATITIS ALLERGIC ( 36 FDA reports)
FACE INJURY ( 36 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 36 FDA reports)
HAEMORRHAGIC DIATHESIS ( 36 FDA reports)
HYPERAMMONAEMIA ( 36 FDA reports)
INFECTIOUS PERITONITIS ( 36 FDA reports)
LIP HAEMORRHAGE ( 36 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 36 FDA reports)
MYOTONIA ( 36 FDA reports)
POSTOPERATIVE INFECTION ( 36 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 36 FDA reports)
PULMONARY THROMBOSIS ( 36 FDA reports)
RADIUS FRACTURE ( 36 FDA reports)
SKIN WARM ( 36 FDA reports)
SPUTUM CULTURE POSITIVE ( 36 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 36 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 35 FDA reports)
MASTOIDITIS ( 35 FDA reports)
PELVIC ABSCESS ( 35 FDA reports)
PO2 INCREASED ( 35 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 35 FDA reports)
PULMONARY TOXICITY ( 35 FDA reports)
RASH VESICULAR ( 35 FDA reports)
RHONCHI ( 35 FDA reports)
SCREAMING ( 35 FDA reports)
SKIN BURNING SENSATION ( 35 FDA reports)
SKIN HAEMORRHAGE ( 35 FDA reports)
SKIN PAPILLOMA ( 35 FDA reports)
TONGUE DISORDER ( 35 FDA reports)
UVEITIS ( 35 FDA reports)
APLASIA PURE RED CELL ( 35 FDA reports)
CONGENITAL ANOMALY ( 35 FDA reports)
DECREASED ACTIVITY ( 35 FDA reports)
DISSEMINATED TUBERCULOSIS ( 35 FDA reports)
DYSMENORRHOEA ( 35 FDA reports)
EROSIVE OESOPHAGITIS ( 35 FDA reports)
EYE INFECTION ( 35 FDA reports)
HAEMANGIOMA ( 35 FDA reports)
IMMUNE SYSTEM DISORDER ( 35 FDA reports)
ABSCESS LIMB ( 34 FDA reports)
ACUTE PRERENAL FAILURE ( 34 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 34 FDA reports)
BLOOD PH INCREASED ( 34 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 34 FDA reports)
BONE NEOPLASM ( 34 FDA reports)
CLEFT LIP AND PALATE ( 34 FDA reports)
DEVICE MALFUNCTION ( 34 FDA reports)
EYELID PTOSIS ( 34 FDA reports)
FEELING JITTERY ( 34 FDA reports)
HICCUPS ( 34 FDA reports)
HYPERREFLEXIA ( 34 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 34 FDA reports)
INJECTION SITE NODULE ( 34 FDA reports)
INTRACARDIAC THROMBUS ( 34 FDA reports)
LIPOMA ( 34 FDA reports)
MENINGIOMA ( 34 FDA reports)
MUSCLE SPASTICITY ( 34 FDA reports)
OVARIAN CANCER ( 34 FDA reports)
PLASMACYTOMA ( 34 FDA reports)
PROTEIN TOTAL INCREASED ( 34 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 34 FDA reports)
STREPTOCOCCAL SEPSIS ( 34 FDA reports)
TACHYARRHYTHMIA ( 34 FDA reports)
TENSION ( 34 FDA reports)
THINKING ABNORMAL ( 34 FDA reports)
MITRAL VALVE CALCIFICATION ( 33 FDA reports)
MONOPLEGIA ( 33 FDA reports)
ORAL DISCOMFORT ( 33 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 33 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 33 FDA reports)
TONGUE ULCERATION ( 33 FDA reports)
TONSILLITIS ( 33 FDA reports)
TYPE 1 DIABETES MELLITUS ( 33 FDA reports)
URINARY HESITATION ( 33 FDA reports)
WOUND COMPLICATION ( 33 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 33 FDA reports)
BACTERIAL TEST POSITIVE ( 33 FDA reports)
BEHCET'S SYNDROME ( 33 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 33 FDA reports)
BRADYPHRENIA ( 33 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 33 FDA reports)
DEAFNESS NEUROSENSORY ( 33 FDA reports)
DEMYELINATION ( 33 FDA reports)
DIABETIC RETINOPATHY ( 33 FDA reports)
DROOLING ( 33 FDA reports)
ENDOTRACHEAL INTUBATION ( 33 FDA reports)
ERYTHEMA NODOSUM ( 33 FDA reports)
EXFOLIATIVE RASH ( 33 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 33 FDA reports)
FEEDING DISORDER ( 33 FDA reports)
GLOMERULONEPHRITIS ( 33 FDA reports)
HOSTILITY ( 33 FDA reports)
IMPAIRED DRIVING ABILITY ( 33 FDA reports)
INJECTION SITE MASS ( 33 FDA reports)
ADENOMA BENIGN ( 32 FDA reports)
DIVERTICULAR PERFORATION ( 32 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 32 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 32 FDA reports)
EYE PRURITUS ( 32 FDA reports)
GASTROINTESTINAL INFECTION ( 32 FDA reports)
INJECTION SITE DISCOLOURATION ( 32 FDA reports)
LISTLESS ( 32 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 32 FDA reports)
PETIT MAL EPILEPSY ( 32 FDA reports)
PROCEDURAL PAIN ( 32 FDA reports)
PROSTATITIS ( 32 FDA reports)
REFLUX OESOPHAGITIS ( 32 FDA reports)
SKIN PLAQUE ( 32 FDA reports)
STRIDOR ( 32 FDA reports)
WOUND DEHISCENCE ( 32 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 31 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 31 FDA reports)
NEURODERMATITIS ( 31 FDA reports)
PARAPLEGIA ( 31 FDA reports)
PERFORMANCE STATUS DECREASED ( 31 FDA reports)
PNEUMOPERITONEUM ( 31 FDA reports)
PREMATURE DELIVERY ( 31 FDA reports)
PSEUDOMONAL SEPSIS ( 31 FDA reports)
SALIVARY HYPERSECRETION ( 31 FDA reports)
SKIN TEST POSITIVE ( 31 FDA reports)
SOCIAL PROBLEM ( 31 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 31 FDA reports)
VASCULAR CALCIFICATION ( 31 FDA reports)
ANAEMIA MACROCYTIC ( 31 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 31 FDA reports)
BILIARY DILATATION ( 31 FDA reports)
BLOOD IRON DECREASED ( 31 FDA reports)
CATHETER SITE HAEMORRHAGE ( 31 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 31 FDA reports)
DEVICE RELATED SEPSIS ( 31 FDA reports)
FAECES HARD ( 31 FDA reports)
GASTRIC CANCER ( 31 FDA reports)
HALLUCINATIONS, MIXED ( 31 FDA reports)
ILEAL STENOSIS ( 31 FDA reports)
INTERMITTENT CLAUDICATION ( 31 FDA reports)
IRON DEFICIENCY ( 31 FDA reports)
KIDNEY ENLARGEMENT ( 31 FDA reports)
LEUKOENCEPHALOPATHY ( 31 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 30 FDA reports)
BLOOD PRESSURE ABNORMAL ( 30 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 30 FDA reports)
BRAIN ABSCESS ( 30 FDA reports)
CAROTID ARTERY OCCLUSION ( 30 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 30 FDA reports)
COAGULATION TIME PROLONGED ( 30 FDA reports)
EMPYEMA ( 30 FDA reports)
FIBULA FRACTURE ( 30 FDA reports)
FRACTURED SACRUM ( 30 FDA reports)
GASTRIC POLYPS ( 30 FDA reports)
HEPATIC MASS ( 30 FDA reports)
IATROGENIC INJURY ( 30 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 30 FDA reports)
LEFT VENTRICULAR FAILURE ( 30 FDA reports)
LUNG HYPERINFLATION ( 30 FDA reports)
METASTASES TO MENINGES ( 30 FDA reports)
MICROCYTIC ANAEMIA ( 30 FDA reports)
MUSCLE DISORDER ( 30 FDA reports)
PHARYNGEAL ERYTHEMA ( 30 FDA reports)
PHOTOPSIA ( 30 FDA reports)
POST HERPETIC NEURALGIA ( 30 FDA reports)
RENAL ARTERY STENOSIS ( 30 FDA reports)
SCLERODACTYLIA ( 30 FDA reports)
SCLERODERMA ( 30 FDA reports)
SEBORRHOEIC KERATOSIS ( 30 FDA reports)
SKIN IRRITATION ( 30 FDA reports)
SOFT TISSUE DISORDER ( 30 FDA reports)
SPINAL LAMINECTOMY ( 30 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 30 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 30 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 30 FDA reports)
TRANSFUSION REACTION ( 30 FDA reports)
VULVOVAGINAL DRYNESS ( 30 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 29 FDA reports)
MACULOPATHY ( 29 FDA reports)
NERVE INJURY ( 29 FDA reports)
OPPORTUNISTIC INFECTION ( 29 FDA reports)
PEMPHIGOID ( 29 FDA reports)
PERSONALITY DISORDER ( 29 FDA reports)
PITTING OEDEMA ( 29 FDA reports)
REFLUX GASTRITIS ( 29 FDA reports)
RESPIRATORY RATE DECREASED ( 29 FDA reports)
SHOULDER PAIN ( 29 FDA reports)
SOFT TISSUE INFECTION ( 29 FDA reports)
TEARFULNESS ( 29 FDA reports)
TENSION HEADACHE ( 29 FDA reports)
THROMBOCYTOPENIC PURPURA ( 29 FDA reports)
TONGUE DISCOLOURATION ( 29 FDA reports)
TOXIC ENCEPHALOPATHY ( 29 FDA reports)
WEIGHT BEARING DIFFICULTY ( 29 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 29 FDA reports)
APHONIA ( 29 FDA reports)
ASPHYXIA ( 29 FDA reports)
ATROPHIC VULVOVAGINITIS ( 29 FDA reports)
BONE DEBRIDEMENT ( 29 FDA reports)
BONE MARROW DEPRESSION ( 29 FDA reports)
CONVERSION DISORDER ( 29 FDA reports)
CYTOKINE RELEASE SYNDROME ( 29 FDA reports)
DENTAL OPERATION ( 29 FDA reports)
DEPENDENCE ( 29 FDA reports)
DERMATITIS ATOPIC ( 29 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 29 FDA reports)
ENTEROCOCCAL SEPSIS ( 29 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 29 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 29 FDA reports)
INTESTINAL FISTULA ( 29 FDA reports)
JAUNDICE NEONATAL ( 29 FDA reports)
JAW OPERATION ( 29 FDA reports)
LABYRINTHITIS ( 29 FDA reports)
AMENORRHOEA ( 28 FDA reports)
ANORECTAL DISORDER ( 28 FDA reports)
ARTHROPOD BITE ( 28 FDA reports)
ATROPHY ( 28 FDA reports)
BLADDER CANCER ( 28 FDA reports)
BLOOD ALCOHOL INCREASED ( 28 FDA reports)
BLOOD URIC ACID INCREASED ( 28 FDA reports)
CENTRAL LINE INFECTION ( 28 FDA reports)
CEREBRAL THROMBOSIS ( 28 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 28 FDA reports)
DRY THROAT ( 28 FDA reports)
GINGIVAL ERYTHEMA ( 28 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 28 FDA reports)
GUILLAIN-BARRE SYNDROME ( 28 FDA reports)
HYPEROSMOLAR STATE ( 28 FDA reports)
HYPOAESTHESIA FACIAL ( 28 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 28 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 28 FDA reports)
KLEBSIELLA BACTERAEMIA ( 28 FDA reports)
LIVER ABSCESS ( 28 FDA reports)
OESOPHAGEAL DISORDER ( 28 FDA reports)
OROANTRAL FISTULA ( 28 FDA reports)
PARESIS ( 28 FDA reports)
PARVOVIRUS INFECTION ( 28 FDA reports)
PELVIC FRACTURE ( 28 FDA reports)
PORTAL VEIN THROMBOSIS ( 28 FDA reports)
POST PROCEDURAL HAEMATOMA ( 28 FDA reports)
PROCTITIS ( 28 FDA reports)
PROSTATOMEGALY ( 28 FDA reports)
SINUS HEADACHE ( 28 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 28 FDA reports)
SNEEZING ( 28 FDA reports)
TIBIA FRACTURE ( 28 FDA reports)
TRAUMATIC HAEMATOMA ( 28 FDA reports)
TROPONIN I INCREASED ( 28 FDA reports)
MONOCYTE COUNT INCREASED ( 27 FDA reports)
MYOCARDITIS ( 27 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 27 FDA reports)
OESOPHAGEAL SPASM ( 27 FDA reports)
PAINFUL RESPIRATION ( 27 FDA reports)
PANIC DISORDER ( 27 FDA reports)
PARAPARESIS ( 27 FDA reports)
POST PROCEDURAL INFECTION ( 27 FDA reports)
RECTAL PROLAPSE ( 27 FDA reports)
RECTAL ULCER ( 27 FDA reports)
RETINAL DETACHMENT ( 27 FDA reports)
SCOTOMA ( 27 FDA reports)
SEQUESTRECTOMY ( 27 FDA reports)
SKIN EROSION ( 27 FDA reports)
SPINAL OPERATION ( 27 FDA reports)
SPLENIC INFARCTION ( 27 FDA reports)
TENDON INJURY ( 27 FDA reports)
TRACHEOBRONCHITIS ( 27 FDA reports)
VASCULAR PURPURA ( 27 FDA reports)
ABNORMAL FAECES ( 27 FDA reports)
ABNORMAL SENSATION IN EYE ( 27 FDA reports)
ALCOHOLISM ( 27 FDA reports)
ANOSMIA ( 27 FDA reports)
APLASIA ( 27 FDA reports)
ATRIAL TACHYCARDIA ( 27 FDA reports)
AUTOIMMUNE DISORDER ( 27 FDA reports)
BIPOLAR I DISORDER ( 27 FDA reports)
BRAIN STEM SYNDROME ( 27 FDA reports)
COARCTATION OF THE AORTA ( 27 FDA reports)
CULTURE POSITIVE ( 27 FDA reports)
ESCHERICHIA BACTERAEMIA ( 27 FDA reports)
FEELING DRUNK ( 27 FDA reports)
GLOSSITIS ( 27 FDA reports)
HEPATORENAL FAILURE ( 27 FDA reports)
HYPOMANIA ( 27 FDA reports)
INTESTINAL STENOSIS ( 27 FDA reports)
INTRACRANIAL ANEURYSM ( 27 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 27 FDA reports)
LARGE INTESTINAL ULCER ( 27 FDA reports)
LIP OEDEMA ( 27 FDA reports)
ACUTE ABDOMEN ( 26 FDA reports)
AFFECT LABILITY ( 26 FDA reports)
AKATHISIA ( 26 FDA reports)
ARTHRITIS INFECTIVE ( 26 FDA reports)
BARRETT'S OESOPHAGUS ( 26 FDA reports)
BILIARY TRACT DISORDER ( 26 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 26 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 26 FDA reports)
BREAST CANCER RECURRENT ( 26 FDA reports)
CAROTID BRUIT ( 26 FDA reports)
CELL DEATH ( 26 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 26 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 26 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 26 FDA reports)
ESCHERICHIA TEST POSITIVE ( 26 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 26 FDA reports)
FORMICATION ( 26 FDA reports)
GASTROINTESTINAL ULCER ( 26 FDA reports)
HAEMARTHROSIS ( 26 FDA reports)
HEART INJURY ( 26 FDA reports)
HEPATITIS B ( 26 FDA reports)
HYPERPYREXIA ( 26 FDA reports)
HYSTERECTOMY ( 26 FDA reports)
INFARCTION ( 26 FDA reports)
IRITIS ( 26 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 26 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 26 FDA reports)
LUNG ADENOCARCINOMA ( 26 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 26 FDA reports)
MUCOSAL ULCERATION ( 26 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 26 FDA reports)
OCCULT BLOOD POSITIVE ( 26 FDA reports)
ONYCHOCLASIS ( 26 FDA reports)
PATHOGEN RESISTANCE ( 26 FDA reports)
PLANTAR FASCIITIS ( 26 FDA reports)
PNEUMONIA KLEBSIELLA ( 26 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 26 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 26 FDA reports)
PUSTULAR PSORIASIS ( 26 FDA reports)
QUADRIPLEGIA ( 26 FDA reports)
RAYNAUD'S PHENOMENON ( 26 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 26 FDA reports)
RENAL TRANSPLANT ( 26 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 26 FDA reports)
SENSITIVITY OF TEETH ( 26 FDA reports)
SEPSIS SYNDROME ( 26 FDA reports)
SEPTIC EMBOLUS ( 26 FDA reports)
SMALL FOR DATES BABY ( 26 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 26 FDA reports)
STUPOR ( 26 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 26 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 26 FDA reports)
VENTRICULAR ARRHYTHMIA ( 26 FDA reports)
VOCAL CORD PARALYSIS ( 26 FDA reports)
MECHANICAL VENTILATION ( 25 FDA reports)
MENSTRUATION IRREGULAR ( 25 FDA reports)
METAPLASIA ( 25 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 25 FDA reports)
NASAL DRYNESS ( 25 FDA reports)
NEUROGENIC BLADDER ( 25 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 25 FDA reports)
OPEN REDUCTION OF FRACTURE ( 25 FDA reports)
OTITIS EXTERNA ( 25 FDA reports)
OVERWEIGHT ( 25 FDA reports)
PERITONEAL DIALYSIS ( 25 FDA reports)
POLYSUBSTANCE ABUSE ( 25 FDA reports)
RENAL TUBULAR ACIDOSIS ( 25 FDA reports)
SEASONAL ALLERGY ( 25 FDA reports)
SPONDYLOLYSIS ( 25 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 25 FDA reports)
TEMPORAL ARTERITIS ( 25 FDA reports)
TUMOUR HAEMORRHAGE ( 25 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 25 FDA reports)
VAGINAL INFECTION ( 25 FDA reports)
AORTIC DILATATION ( 25 FDA reports)
BLOOD BICARBONATE INCREASED ( 25 FDA reports)
CEREBELLAR INFARCTION ( 25 FDA reports)
CEREBRAL DISORDER ( 25 FDA reports)
CERVICAL DYSPLASIA ( 25 FDA reports)
CORONARY ARTERY BYPASS ( 25 FDA reports)
DERMATITIS ACNEIFORM ( 25 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 25 FDA reports)
DIPLEGIA ( 25 FDA reports)
DRUG-INDUCED LIVER INJURY ( 25 FDA reports)
ENTERITIS ( 25 FDA reports)
FACIAL PARESIS ( 25 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 25 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 25 FDA reports)
GLIOSIS ( 25 FDA reports)
HYDROCELE ( 25 FDA reports)
INJECTION SITE INDURATION ( 25 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 25 FDA reports)
INTRAOCULAR LENS IMPLANT ( 25 FDA reports)
ABDOMINAL RIGIDITY ( 24 FDA reports)
ACCIDENTAL POISONING ( 24 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 24 FDA reports)
AORTIC ANEURYSM RUPTURE ( 24 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 24 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 24 FDA reports)
BREAST ENLARGEMENT ( 24 FDA reports)
CEREBELLAR HAEMORRHAGE ( 24 FDA reports)
CHONDROCALCINOSIS ( 24 FDA reports)
COLON CANCER METASTATIC ( 24 FDA reports)
CYSTOCELE ( 24 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 24 FDA reports)
DEAFNESS UNILATERAL ( 24 FDA reports)
DEVICE FAILURE ( 24 FDA reports)
DIABETES INSIPIDUS ( 24 FDA reports)
DIABETIC NEPHROPATHY ( 24 FDA reports)
EOSINOPHILIC PNEUMONIA ( 24 FDA reports)
EUPHORIC MOOD ( 24 FDA reports)
FOOD INTOLERANCE ( 24 FDA reports)
FURUNCLE ( 24 FDA reports)
HAEMOPHILUS INFECTION ( 24 FDA reports)
HEPATIC NEOPLASM ( 24 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 24 FDA reports)
HOMICIDE ( 24 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 24 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 24 FDA reports)
LICHENOID KERATOSIS ( 24 FDA reports)
LIVER TRANSPLANT REJECTION ( 24 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 24 FDA reports)
LYMPHOCYTOSIS ( 24 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 24 FDA reports)
MIXED LIVER INJURY ( 24 FDA reports)
MULTIPLE ALLERGIES ( 24 FDA reports)
MYELOPATHY ( 24 FDA reports)
NARCOTIC INTOXICATION ( 24 FDA reports)
NEURITIS ( 24 FDA reports)
PARTIAL SEIZURES ( 24 FDA reports)
PERITONEAL HAEMORRHAGE ( 24 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 24 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 24 FDA reports)
POLYDIPSIA ( 24 FDA reports)
POOR PERIPHERAL CIRCULATION ( 24 FDA reports)
POSTPARTUM HAEMORRHAGE ( 24 FDA reports)
RENAL INFARCT ( 24 FDA reports)
RESUSCITATION ( 24 FDA reports)
SELF-INJURIOUS IDEATION ( 24 FDA reports)
SERRATIA INFECTION ( 24 FDA reports)
STARING ( 24 FDA reports)
STRESS FRACTURE ( 24 FDA reports)
SUPRAPUBIC PAIN ( 24 FDA reports)
THERMAL BURN ( 24 FDA reports)
VITAMIN B12 DEFICIENCY ( 24 FDA reports)
LUPUS-LIKE SYNDROME ( 23 FDA reports)
MUSCLE INJURY ( 23 FDA reports)
NECK MASS ( 23 FDA reports)
NEUTROPHILIA ( 23 FDA reports)
NON-SMALL CELL LUNG CANCER ( 23 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 23 FDA reports)
OSTEORADIONECROSIS ( 23 FDA reports)
OTITIS MEDIA CHRONIC ( 23 FDA reports)
PRODUCT PACKAGING ISSUE ( 23 FDA reports)
PSYCHOMOTOR RETARDATION ( 23 FDA reports)
PYURIA ( 23 FDA reports)
QRS AXIS ABNORMAL ( 23 FDA reports)
RADICULITIS ( 23 FDA reports)
RELAPSING FEVER ( 23 FDA reports)
SMALL INTESTINE OPERATION ( 23 FDA reports)
SOMNAMBULISM ( 23 FDA reports)
TENOSYNOVITIS ( 23 FDA reports)
THROMBOSIS IN DEVICE ( 23 FDA reports)
TRANSFUSION ( 23 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 23 FDA reports)
UTERINE POLYP ( 23 FDA reports)
VASODILATATION ( 23 FDA reports)
VENOUS OCCLUSION ( 23 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 23 FDA reports)
ABSCESS INTESTINAL ( 23 FDA reports)
ASPERGILLOMA ( 23 FDA reports)
BLOOD MAGNESIUM INCREASED ( 23 FDA reports)
CARDIAC FLUTTER ( 23 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 23 FDA reports)
CLAVICLE FRACTURE ( 23 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 23 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 23 FDA reports)
EFFUSION ( 23 FDA reports)
ENTEROBACTER INFECTION ( 23 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 23 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 23 FDA reports)
FOETAL GROWTH RESTRICTION ( 23 FDA reports)
GLOMERULOSCLEROSIS ( 23 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 23 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 23 FDA reports)
HYPERPHOSPHATAEMIA ( 23 FDA reports)
IMPETIGO ( 23 FDA reports)
INCREASED APPETITE ( 23 FDA reports)
INJECTION SITE URTICARIA ( 23 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 23 FDA reports)
LACTOSE INTOLERANCE ( 23 FDA reports)
LEUKAEMIA ( 23 FDA reports)
LIP DRY ( 23 FDA reports)
ABDOMINAL SEPSIS ( 22 FDA reports)
ABDOMINAL WALL ABSCESS ( 22 FDA reports)
ADENOCARCINOMA ( 22 FDA reports)
ADJUSTMENT DISORDER ( 22 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 22 FDA reports)
ASTERIXIS ( 22 FDA reports)
ASTHENOPIA ( 22 FDA reports)
B-CELL LYMPHOMA ( 22 FDA reports)
CARBON DIOXIDE DECREASED ( 22 FDA reports)
CARDIOTOXICITY ( 22 FDA reports)
CATHETER SITE INFECTION ( 22 FDA reports)
CLOSTRIDIUM COLITIS ( 22 FDA reports)
DIABETIC COMA ( 22 FDA reports)
EXANTHEM ( 22 FDA reports)
FAMILY STRESS ( 22 FDA reports)
FEEDING DISORDER NEONATAL ( 22 FDA reports)
FOETAL GROWTH RETARDATION ( 22 FDA reports)
FRACTURE NONUNION ( 22 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 22 FDA reports)
GASTRIC MUCOSAL LESION ( 22 FDA reports)
GASTRIC ULCER PERFORATION ( 22 FDA reports)
HAEMOGLOBIN INCREASED ( 22 FDA reports)
HEART RATE ABNORMAL ( 22 FDA reports)
HEPATIC TRAUMA ( 22 FDA reports)
HYPERPHAGIA ( 22 FDA reports)
HYPERPLASIA ( 22 FDA reports)
INCREASED BRONCHIAL SECRETION ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 22 FDA reports)
LOGORRHOEA ( 22 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 22 FDA reports)
MENINGITIS ASEPTIC ( 22 FDA reports)
METASTASES TO PLEURA ( 22 FDA reports)
MOUTH CYST ( 22 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 22 FDA reports)
PANCREATIC DISORDER ( 22 FDA reports)
PARONYCHIA ( 22 FDA reports)
PSEUDOLYMPHOMA ( 22 FDA reports)
PSORIATIC ARTHROPATHY ( 22 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 22 FDA reports)
SJOGREN'S SYNDROME ( 22 FDA reports)
SOPOR ( 22 FDA reports)
STENOTROPHOMONAS INFECTION ( 22 FDA reports)
STENT PLACEMENT ( 22 FDA reports)
SUPERINFECTION ( 22 FDA reports)
TEMPERATURE INTOLERANCE ( 22 FDA reports)
URINE ANALYSIS ABNORMAL ( 22 FDA reports)
LYMPHADENITIS ( 21 FDA reports)
LYMPHOCYTIC INFILTRATION ( 21 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 21 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 21 FDA reports)
MUSCLE CRAMP ( 21 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 21 FDA reports)
NEPHROGENIC ANAEMIA ( 21 FDA reports)
NEURODEGENERATIVE DISORDER ( 21 FDA reports)
NEUTROPENIC INFECTION ( 21 FDA reports)
NIGHT BLINDNESS ( 21 FDA reports)
OPTIC ATROPHY ( 21 FDA reports)
ORAL MUCOSA EROSION ( 21 FDA reports)
OTITIS MEDIA ACUTE ( 21 FDA reports)
PANCREATIC CARCINOMA ( 21 FDA reports)
PANCREATITIS NECROTISING ( 21 FDA reports)
PAPULE ( 21 FDA reports)
PCO2 INCREASED ( 21 FDA reports)
POLYMYALGIA RHEUMATICA ( 21 FDA reports)
PROSTATE CANCER METASTATIC ( 21 FDA reports)
PULPITIS DENTAL ( 21 FDA reports)
PUPILS UNEQUAL ( 21 FDA reports)
RENAL MASS ( 21 FDA reports)
RESORPTION BONE INCREASED ( 21 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 21 FDA reports)
SKIN OEDEMA ( 21 FDA reports)
SPLENIC LESION ( 21 FDA reports)
THROMBOCYTHAEMIA ( 21 FDA reports)
TRAUMATIC BRAIN INJURY ( 21 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 21 FDA reports)
URGE INCONTINENCE ( 21 FDA reports)
VEIN DISORDER ( 21 FDA reports)
VITREOUS DETACHMENT ( 21 FDA reports)
VITREOUS HAEMORRHAGE ( 21 FDA reports)
ABDOMINAL ADHESIONS ( 21 FDA reports)
ADHESION ( 21 FDA reports)
AKINESIA ( 21 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 21 FDA reports)
ANXIETY DISORDER ( 21 FDA reports)
AORTIC VALVE STENOSIS ( 21 FDA reports)
BLEEDING TIME PROLONGED ( 21 FDA reports)
BLOOD ALBUMIN INCREASED ( 21 FDA reports)
BONE EROSION ( 21 FDA reports)
BONE MARROW OEDEMA ( 21 FDA reports)
BONE SCAN ABNORMAL ( 21 FDA reports)
BRONCHIAL OBSTRUCTION ( 21 FDA reports)
CALCULUS URINARY ( 21 FDA reports)
CARDIAC FIBRILLATION ( 21 FDA reports)
CERVICOBRACHIAL SYNDROME ( 21 FDA reports)
COLECTOMY ( 21 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 21 FDA reports)
CONDUCTION DISORDER ( 21 FDA reports)
CORONARY ARTERY THROMBOSIS ( 21 FDA reports)
CRANIOSYNOSTOSIS ( 21 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 21 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 21 FDA reports)
EROSIVE DUODENITIS ( 21 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 21 FDA reports)
EXPIRED DRUG ADMINISTERED ( 21 FDA reports)
EXTREMITY NECROSIS ( 21 FDA reports)
FEAR OF DEATH ( 21 FDA reports)
FEBRILE CONVULSION ( 21 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 21 FDA reports)
GASTRITIS HAEMORRHAGIC ( 21 FDA reports)
GASTROINTESTINAL PERFORATION ( 21 FDA reports)
GOUTY ARTHRITIS ( 21 FDA reports)
HAEMATOMA INFECTION ( 21 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 21 FDA reports)
HEART DISEASE CONGENITAL ( 21 FDA reports)
ILEITIS ( 21 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 21 FDA reports)
ADRENAL MASS ( 20 FDA reports)
ALCOHOL ABUSE ( 20 FDA reports)
ALCOHOL INTERACTION ( 20 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 20 FDA reports)
ANAL FISSURE ( 20 FDA reports)
ANOXIC ENCEPHALOPATHY ( 20 FDA reports)
ASPIRATION PLEURAL CAVITY ( 20 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 20 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 20 FDA reports)
BRADYARRHYTHMIA ( 20 FDA reports)
BRAIN STEM INFARCTION ( 20 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 20 FDA reports)
CANCER PAIN ( 20 FDA reports)
CANDIDURIA ( 20 FDA reports)
CARDIAC OUTPUT DECREASED ( 20 FDA reports)
CERVICAL CORD COMPRESSION ( 20 FDA reports)
CORNEAL REFLEX DECREASED ( 20 FDA reports)
CULTURE WOUND POSITIVE ( 20 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 20 FDA reports)
EAR DISCOMFORT ( 20 FDA reports)
ENCEPHALOMALACIA ( 20 FDA reports)
ENDOMETRIOSIS ( 20 FDA reports)
GASTROINTESTINAL INJURY ( 20 FDA reports)
GINGIVITIS ULCERATIVE ( 20 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 20 FDA reports)
HEAD DISCOMFORT ( 20 FDA reports)
HEPATIC CALCIFICATION ( 20 FDA reports)
HOMICIDAL IDEATION ( 20 FDA reports)
HYPERTONIC BLADDER ( 20 FDA reports)
INFUSION SITE ERYTHEMA ( 20 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 20 FDA reports)
MEAN CELL VOLUME INCREASED ( 20 FDA reports)
METASTASES TO ADRENALS ( 20 FDA reports)
METRORRHAGIA ( 20 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 20 FDA reports)
NEPHROSCLEROSIS ( 20 FDA reports)
OEDEMA MUCOSAL ( 20 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 20 FDA reports)
ORAL FUNGAL INFECTION ( 20 FDA reports)
OROPHARYNGEAL BLISTERING ( 20 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 20 FDA reports)
OTORRHOEA ( 20 FDA reports)
PANCREATIC CYST ( 20 FDA reports)
PERIRECTAL ABSCESS ( 20 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 20 FDA reports)
RECTOCELE ( 20 FDA reports)
RESPIRATION ABNORMAL ( 20 FDA reports)
RIGHT ATRIAL DILATATION ( 20 FDA reports)
SKULL FRACTURE ( 20 FDA reports)
SUFFOCATION FEELING ( 20 FDA reports)
THYROID CYST ( 20 FDA reports)
TUMOUR PAIN ( 20 FDA reports)
URINARY TRACT OBSTRUCTION ( 20 FDA reports)
VARICELLA ( 20 FDA reports)
MACROCYTOSIS ( 19 FDA reports)
MALABSORPTION ( 19 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 19 FDA reports)
MONONUCLEOSIS SYNDROME ( 19 FDA reports)
MUCOSAL EROSION ( 19 FDA reports)
MUSCLE CONTRACTURE ( 19 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 19 FDA reports)
NERVE ROOT COMPRESSION ( 19 FDA reports)
NIKOLSKY'S SIGN ( 19 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 19 FDA reports)
PARAPROTEINAEMIA ( 19 FDA reports)
PERIPHERAL EMBOLISM ( 19 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 19 FDA reports)
PERITONITIS BACTERIAL ( 19 FDA reports)
PHAEOCHROMOCYTOMA ( 19 FDA reports)
PLEURAL DISORDER ( 19 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 19 FDA reports)
PULMONARY GRANULOMA ( 19 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 19 FDA reports)
RENAL CANCER ( 19 FDA reports)
RENAL COLIC ( 19 FDA reports)
SCRATCH ( 19 FDA reports)
SECRETION DISCHARGE ( 19 FDA reports)
SKIN NEOPLASM EXCISION ( 19 FDA reports)
SKIN TOXICITY ( 19 FDA reports)
SUICIDAL BEHAVIOUR ( 19 FDA reports)
TERMINAL STATE ( 19 FDA reports)
TOXIC SHOCK SYNDROME ( 19 FDA reports)
UTERINE HAEMORRHAGE ( 19 FDA reports)
VANISHING BILE DUCT SYNDROME ( 19 FDA reports)
VASOCONSTRICTION ( 19 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 19 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 19 FDA reports)
ADENOVIRUS INFECTION ( 19 FDA reports)
ADVERSE REACTION ( 19 FDA reports)
ANKYLOSING SPONDYLITIS ( 19 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 19 FDA reports)
ARTERIAL DISORDER ( 19 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 19 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 19 FDA reports)
BK VIRUS INFECTION ( 19 FDA reports)
BLEPHAROSPASM ( 19 FDA reports)
BLOOD BLISTER ( 19 FDA reports)
BONE MARROW TRANSPLANT ( 19 FDA reports)
BONE SWELLING ( 19 FDA reports)
BREAST CANCER FEMALE ( 19 FDA reports)
BREAST INFECTION ( 19 FDA reports)
BURNS THIRD DEGREE ( 19 FDA reports)
CARDIAC ENZYMES INCREASED ( 19 FDA reports)
CATATONIA ( 19 FDA reports)
COELIAC DISEASE ( 19 FDA reports)
COLOSTOMY ( 19 FDA reports)
COMPARTMENT SYNDROME ( 19 FDA reports)
COSTOCHONDRITIS ( 19 FDA reports)
CULTURE STOOL POSITIVE ( 19 FDA reports)
DENTAL FISTULA ( 19 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 19 FDA reports)
DIAPHRAGMATIC HERNIA ( 19 FDA reports)
DYSTHYMIC DISORDER ( 19 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 19 FDA reports)
EXOMPHALOS ( 19 FDA reports)
FRUSTRATION ( 19 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 19 FDA reports)
IMPAIRED SELF-CARE ( 19 FDA reports)
INJECTION SITE INFLAMMATION ( 19 FDA reports)
KNEE OPERATION ( 19 FDA reports)
ABDOMINAL MASS ( 18 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 18 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 18 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 18 FDA reports)
BILIARY CYST ( 18 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 18 FDA reports)
BRAIN SCAN ABNORMAL ( 18 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 18 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 18 FDA reports)
CHOKING SENSATION ( 18 FDA reports)
CHOREA ( 18 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 18 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 18 FDA reports)
DISEASE COMPLICATION ( 18 FDA reports)
EPIDERMAL NECROSIS ( 18 FDA reports)
ERB'S PALSY ( 18 FDA reports)
EXTRADURAL ABSCESS ( 18 FDA reports)
FUNGAL SKIN INFECTION ( 18 FDA reports)
GASTRODUODENITIS ( 18 FDA reports)
GENERAL SYMPTOM ( 18 FDA reports)
GENERALISED ANXIETY DISORDER ( 18 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 18 FDA reports)
GRIP STRENGTH DECREASED ( 18 FDA reports)
HEPATIC ENZYME ABNORMAL ( 18 FDA reports)
HEPATIC PAIN ( 18 FDA reports)
HYPERAEMIA ( 18 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 18 FDA reports)
INCISIONAL HERNIA ( 18 FDA reports)
INFECTED SKIN ULCER ( 18 FDA reports)
LIP BLISTER ( 18 FDA reports)
MYELITIS TRANSVERSE ( 18 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 18 FDA reports)
NEUTROPENIC COLITIS ( 18 FDA reports)
NODAL RHYTHM ( 18 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 18 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 18 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 18 FDA reports)
OVARIAN MASS ( 18 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 18 FDA reports)
PANCREATIC MASS ( 18 FDA reports)
PNEUMONIA VIRAL ( 18 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 18 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 18 FDA reports)
PSYCHOTIC BEHAVIOUR ( 18 FDA reports)
PYELOCALIECTASIS ( 18 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 18 FDA reports)
ROSACEA ( 18 FDA reports)
SUBCUTANEOUS NODULE ( 18 FDA reports)
SUDDEN CARDIAC DEATH ( 18 FDA reports)
SYSTEMIC CANDIDA ( 18 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 18 FDA reports)
THALAMIC INFARCTION ( 18 FDA reports)
TROPONIN T INCREASED ( 18 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 18 FDA reports)
VERTEBROPLASTY ( 18 FDA reports)
VIRAEMIA ( 18 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
MACULAR OEDEMA ( 17 FDA reports)
MALLORY-WEISS SYNDROME ( 17 FDA reports)
MEAN CELL VOLUME DECREASED ( 17 FDA reports)
MENINGITIS VIRAL ( 17 FDA reports)
MITRAL VALVE STENOSIS ( 17 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 17 FDA reports)
NECROTISING FASCIITIS ( 17 FDA reports)
NEUROMYOPATHY ( 17 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 17 FDA reports)
OPERATIVE HAEMORRHAGE ( 17 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 17 FDA reports)
PAROTID GLAND ENLARGEMENT ( 17 FDA reports)
PAROTITIS ( 17 FDA reports)
PATELLA FRACTURE ( 17 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 17 FDA reports)
PLAGIOCEPHALY ( 17 FDA reports)
POSTOPERATIVE ILEUS ( 17 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 17 FDA reports)
PROCEDURAL HYPOTENSION ( 17 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 17 FDA reports)
PSEUDODEMENTIA ( 17 FDA reports)
PULMONARY CAVITATION ( 17 FDA reports)
RADICULAR PAIN ( 17 FDA reports)
RADIOTHERAPY ( 17 FDA reports)
RENAL FAILURE NEONATAL ( 17 FDA reports)
SPLEEN DISORDER ( 17 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 17 FDA reports)
TINEA INFECTION ( 17 FDA reports)
TORTICOLLIS ( 17 FDA reports)
UNDERDOSE ( 17 FDA reports)
URINE COLOUR ABNORMAL ( 17 FDA reports)
URINE SODIUM DECREASED ( 17 FDA reports)
VULVOVAGINAL PAIN ( 17 FDA reports)
XEROSIS ( 17 FDA reports)
AMYLOIDOSIS ( 17 FDA reports)
ANAL ULCER ( 17 FDA reports)
ANASTOMOTIC LEAK ( 17 FDA reports)
ARTERIAL THROMBOSIS ( 17 FDA reports)
ARTERIOSPASM CORONARY ( 17 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 17 FDA reports)
BILE DUCT OBSTRUCTION ( 17 FDA reports)
BONE MARROW DISORDER ( 17 FDA reports)
BRAIN COMPRESSION ( 17 FDA reports)
CARDIAC PACEMAKER INSERTION ( 17 FDA reports)
CAROTID ARTERY DISEASE ( 17 FDA reports)
CERVIX CARCINOMA ( 17 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 17 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 17 FDA reports)
CYSTITIS NONINFECTIVE ( 17 FDA reports)
DENTAL PLAQUE ( 17 FDA reports)
DISSOCIATION ( 17 FDA reports)
DYSPHASIA ( 17 FDA reports)
EAR DISORDER ( 17 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 17 FDA reports)
FALLOT'S TETRALOGY ( 17 FDA reports)
FEAR OF EATING ( 17 FDA reports)
FOAMING AT MOUTH ( 17 FDA reports)
FOETAL DEATH ( 17 FDA reports)
GASTROINTESTINAL CARCINOMA ( 17 FDA reports)
GENITAL HERPES ( 17 FDA reports)
GINGIVAL RECESSION ( 17 FDA reports)
HAEMOGLOBIN ABNORMAL ( 17 FDA reports)
HYPERKINESIA ( 17 FDA reports)
HYPOREFLEXIA ( 17 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 17 FDA reports)
INFUSION SITE PAIN ( 17 FDA reports)
INJECTION SITE WARMTH ( 17 FDA reports)
INTESTINAL DILATATION ( 17 FDA reports)
INTESTINAL INFARCTION ( 17 FDA reports)
KIDNEY MALFORMATION ( 17 FDA reports)
LICHEN PLANUS ( 17 FDA reports)
ACUTE PSYCHOSIS ( 16 FDA reports)
ALVEOLOPLASTY ( 16 FDA reports)
ANAL CANCER ( 16 FDA reports)
ANTIBODY TEST POSITIVE ( 16 FDA reports)
AORTIC THROMBOSIS ( 16 FDA reports)
APPLICATION SITE RASH ( 16 FDA reports)
ATONIC SEIZURES ( 16 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 16 FDA reports)
BREAST DISCHARGE ( 16 FDA reports)
BRONCHIOLITIS ( 16 FDA reports)
CALCINOSIS ( 16 FDA reports)
CEREBELLAR SYNDROME ( 16 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 16 FDA reports)
CONJUNCTIVAL OEDEMA ( 16 FDA reports)
CONNECTIVE TISSUE DISORDER ( 16 FDA reports)
EMBOLISM ARTERIAL ( 16 FDA reports)
ENANTHEMA ( 16 FDA reports)
EXOPHTHALMOS ( 16 FDA reports)
EXTRASKELETAL OSSIFICATION ( 16 FDA reports)
EXTRAVASATION ( 16 FDA reports)
EYE INJURY ( 16 FDA reports)
GASTRINOMA ( 16 FDA reports)
HIP DYSPLASIA ( 16 FDA reports)
HORDEOLUM ( 16 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 16 FDA reports)
HUNGER ( 16 FDA reports)
HYDROURETER ( 16 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 16 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 16 FDA reports)
INJECTION SITE BURNING ( 16 FDA reports)
JUVENILE ARTHRITIS ( 16 FDA reports)
KNEE DEFORMITY ( 16 FDA reports)
LOSS OF EMPLOYMENT ( 16 FDA reports)
MACROGLOSSIA ( 16 FDA reports)
MEGACOLON ( 16 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 16 FDA reports)
MONOCYTE COUNT DECREASED ( 16 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 16 FDA reports)
NASAL DISCOMFORT ( 16 FDA reports)
NONSPECIFIC REACTION ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 16 FDA reports)
OPTIC NERVE DISORDER ( 16 FDA reports)
ORGANISING PNEUMONIA ( 16 FDA reports)
OXYGEN SATURATION ABNORMAL ( 16 FDA reports)
PANCREATITIS CHRONIC ( 16 FDA reports)
PAROSMIA ( 16 FDA reports)
PLATELET COUNT ABNORMAL ( 16 FDA reports)
POLYHYDRAMNIOS ( 16 FDA reports)
PROSTATISM ( 16 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 16 FDA reports)
RETINAL EXUDATES ( 16 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 16 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 16 FDA reports)
SUNBURN ( 16 FDA reports)
T-CELL LYMPHOMA ( 16 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 16 FDA reports)
ULCERATIVE KERATITIS ( 16 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 16 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 16 FDA reports)
UTERINE ENLARGEMENT ( 16 FDA reports)
LUNG INJURY ( 15 FDA reports)
MALIGNANT HYPERTENSION ( 15 FDA reports)
MEDICATION RESIDUE ( 15 FDA reports)
MENSTRUAL DISORDER ( 15 FDA reports)
METABOLIC SYNDROME ( 15 FDA reports)
MIGRAINE WITH AURA ( 15 FDA reports)
MYELOMA RECURRENCE ( 15 FDA reports)
MYOCARDIAL FIBROSIS ( 15 FDA reports)
NEONATAL DISORDER ( 15 FDA reports)
ONYCHOLYSIS ( 15 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 15 FDA reports)
PAPILLOMA VIRAL INFECTION ( 15 FDA reports)
PATHOLOGICAL GAMBLING ( 15 FDA reports)
PORPHYRIA ( 15 FDA reports)
PORTAL HYPERTENSION ( 15 FDA reports)
POST PROCEDURAL BILE LEAK ( 15 FDA reports)
PROCTOCOLECTOMY ( 15 FDA reports)
PULSE PRESSURE DECREASED ( 15 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 15 FDA reports)
SKIN ATROPHY ( 15 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 15 FDA reports)
SYNOVIAL RUPTURE ( 15 FDA reports)
TETANY ( 15 FDA reports)
THROAT CANCER ( 15 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 15 FDA reports)
TINEA PEDIS ( 15 FDA reports)
TOE AMPUTATION ( 15 FDA reports)
TRIGEMINAL NEURALGIA ( 15 FDA reports)
TUMOUR NECROSIS ( 15 FDA reports)
ULNA FRACTURE ( 15 FDA reports)
URETERIC STENOSIS ( 15 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 15 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 15 FDA reports)
WHEELCHAIR USER ( 15 FDA reports)
ABDOMINAL INFECTION ( 15 FDA reports)
ACROCHORDON ( 15 FDA reports)
ANAL HAEMORRHAGE ( 15 FDA reports)
ANORECTAL DISCOMFORT ( 15 FDA reports)
ANTICHOLINERGIC SYNDROME ( 15 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 15 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 15 FDA reports)
AORTIC DISORDER ( 15 FDA reports)
AORTIC VALVE DISEASE ( 15 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 15 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 15 FDA reports)
ARTERIAL INSUFFICIENCY ( 15 FDA reports)
AUTOIMMUNE THYROIDITIS ( 15 FDA reports)
BLADDER PROLAPSE ( 15 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 15 FDA reports)
BLOOD GASES ABNORMAL ( 15 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 15 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 15 FDA reports)
BONE FRAGMENTATION ( 15 FDA reports)
BOWEL SOUNDS ABNORMAL ( 15 FDA reports)
BRADYPNOEA ( 15 FDA reports)
BRAIN MIDLINE SHIFT ( 15 FDA reports)
BRAIN NEOPLASM ( 15 FDA reports)
BREAKTHROUGH PAIN ( 15 FDA reports)
BRONCHIAL CARCINOMA ( 15 FDA reports)
CERVICAL MYELOPATHY ( 15 FDA reports)
CHAPPED LIPS ( 15 FDA reports)
CHOLECYSTITIS INFECTIVE ( 15 FDA reports)
CLONUS ( 15 FDA reports)
COLITIS MICROSCOPIC ( 15 FDA reports)
COLONIC STENOSIS ( 15 FDA reports)
CONDUCTIVE DEAFNESS ( 15 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 15 FDA reports)
CUTANEOUS VASCULITIS ( 15 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 15 FDA reports)
DUODENAL PERFORATION ( 15 FDA reports)
DYSPLASIA ( 15 FDA reports)
ECTROPION ( 15 FDA reports)
EDENTULOUS ( 15 FDA reports)
EJACULATION DISORDER ( 15 FDA reports)
EMBOLIC STROKE ( 15 FDA reports)
ENTEROCUTANEOUS FISTULA ( 15 FDA reports)
EPIDERMOLYSIS ( 15 FDA reports)
EYE ROLLING ( 15 FDA reports)
FAECES PALE ( 15 FDA reports)
FOREIGN BODY ( 15 FDA reports)
FUNGAL SEPSIS ( 15 FDA reports)
GASTROINTESTINAL OEDEMA ( 15 FDA reports)
GLIOBLASTOMA ( 15 FDA reports)
GRANULOCYTE COUNT DECREASED ( 15 FDA reports)
HAEMATOTOXICITY ( 15 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 15 FDA reports)
HYPERMETROPIA ( 15 FDA reports)
HYPOCOAGULABLE STATE ( 15 FDA reports)
INJECTION SITE CELLULITIS ( 15 FDA reports)
INJECTION SITE DISCOMFORT ( 15 FDA reports)
INTERVERTEBRAL DISCITIS ( 15 FDA reports)
IRIDOCYCLITIS ( 15 FDA reports)
IRON OVERLOAD ( 15 FDA reports)
JUGULAR VEIN DISTENSION ( 15 FDA reports)
LARYNGOSPASM ( 15 FDA reports)
LIP PAIN ( 15 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 14 FDA reports)
ADRENAL DISORDER ( 14 FDA reports)
AEROMONA INFECTION ( 14 FDA reports)
ALLODYNIA ( 14 FDA reports)
ANAEMIA POSTOPERATIVE ( 14 FDA reports)
AORTIC VALVE CALCIFICATION ( 14 FDA reports)
APRAXIA ( 14 FDA reports)
ASPERGILLUS TEST POSITIVE ( 14 FDA reports)
ATHEROSCLEROSIS ( 14 FDA reports)
BIOPSY TONGUE ABNORMAL ( 14 FDA reports)
BRADYCARDIA NEONATAL ( 14 FDA reports)
BREAST DISORDER ( 14 FDA reports)
BURNS SECOND DEGREE ( 14 FDA reports)
CANDIDA SEPSIS ( 14 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 14 FDA reports)
CATARACT NUCLEAR ( 14 FDA reports)
CATHETERISATION CARDIAC ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 14 FDA reports)
CERVICITIS ( 14 FDA reports)
CHRONIC HEPATITIS ( 14 FDA reports)
CLAUSTROPHOBIA ( 14 FDA reports)
CRYPTORCHISM ( 14 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 14 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 14 FDA reports)
DEFAECATION URGENCY ( 14 FDA reports)
DEVICE DISLOCATION ( 14 FDA reports)
DIET REFUSAL ( 14 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 14 FDA reports)
EAR PRURITUS ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 14 FDA reports)
ENDOCARDITIS BACTERIAL ( 14 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 14 FDA reports)
ENTEROVESICAL FISTULA ( 14 FDA reports)
EYE DISCHARGE ( 14 FDA reports)
FAT NECROSIS ( 14 FDA reports)
FLAT AFFECT ( 14 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 14 FDA reports)
GASTRIC PERFORATION ( 14 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 14 FDA reports)
GRAFT DYSFUNCTION ( 14 FDA reports)
HAEMORRHAGIC DISORDER ( 14 FDA reports)
HAIR GROWTH ABNORMAL ( 14 FDA reports)
HEART SOUNDS ABNORMAL ( 14 FDA reports)
HISTOPLASMOSIS ( 14 FDA reports)
HYPERALBUMINAEMIA ( 14 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 14 FDA reports)
HYPOSPADIAS ( 14 FDA reports)
ILIAC ARTERY OCCLUSION ( 14 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 14 FDA reports)
INCISION SITE ERYTHEMA ( 14 FDA reports)
INCISION SITE INFECTION ( 14 FDA reports)
INFANTILE APNOEIC ATTACK ( 14 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 14 FDA reports)
INFUSION SITE EXTRAVASATION ( 14 FDA reports)
INJECTION SITE EXTRAVASATION ( 14 FDA reports)
LIMB DEFORMITY ( 14 FDA reports)
LIP DISORDER ( 14 FDA reports)
LUMBAR SPINE FLATTENING ( 14 FDA reports)
LYMPHADENECTOMY ( 14 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 14 FDA reports)
MENOPAUSAL SYMPTOMS ( 14 FDA reports)
METASTASES TO SKIN ( 14 FDA reports)
MITOCHONDRIAL TOXICITY ( 14 FDA reports)
MUCOSAL DRYNESS ( 14 FDA reports)
MULTIPLE FRACTURES ( 14 FDA reports)
MYCOBACTERIAL INFECTION ( 14 FDA reports)
MYCOPLASMA INFECTION ( 14 FDA reports)
NASAL SEPTUM PERFORATION ( 14 FDA reports)
NEPHRITIS ( 14 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 14 FDA reports)
NOSOCOMIAL INFECTION ( 14 FDA reports)
OEDEMA GENITAL ( 14 FDA reports)
OESOPHAGEAL CARCINOMA ( 14 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 14 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 14 FDA reports)
PERITONEAL EFFUSION ( 14 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 14 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 14 FDA reports)
PLACENTAL DISORDER ( 14 FDA reports)
PNEUMOMEDIASTINUM ( 14 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 14 FDA reports)
POLYTRAUMATISM ( 14 FDA reports)
POOR DENTAL CONDITION ( 14 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 14 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 14 FDA reports)
PSOAS ABSCESS ( 14 FDA reports)
RECTAL ABSCESS ( 14 FDA reports)
RECTAL CANCER ( 14 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 14 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 14 FDA reports)
RENAL HAEMORRHAGE ( 14 FDA reports)
RETINAL DEPOSITS ( 14 FDA reports)
RETINOPATHY ( 14 FDA reports)
RHEUMATOID NODULE ( 14 FDA reports)
SENSATION OF PRESSURE ( 14 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 14 FDA reports)
SKIN GRAFT ( 14 FDA reports)
SPINA BIFIDA ( 14 FDA reports)
SPINAL CORD DISORDER ( 14 FDA reports)
SPLENIC GRANULOMA ( 14 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 14 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 14 FDA reports)
TOOTH DISCOLOURATION ( 14 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 14 FDA reports)
URINE ABNORMALITY ( 14 FDA reports)
VARICES OESOPHAGEAL ( 14 FDA reports)
MARROW HYPERPLASIA ( 13 FDA reports)
MENINGISM ( 13 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 13 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 13 FDA reports)
METASTASES TO LARGE INTESTINE ( 13 FDA reports)
MICROCYTOSIS ( 13 FDA reports)
MUCOSAL HAEMORRHAGE ( 13 FDA reports)
NERVE ROOT LESION ( 13 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 13 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 13 FDA reports)
OCCULT BLOOD ( 13 FDA reports)
OSTEOMYELITIS CHRONIC ( 13 FDA reports)
OVERGROWTH BACTERIAL ( 13 FDA reports)
PENIS DISORDER ( 13 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 13 FDA reports)
PHLEBITIS SUPERFICIAL ( 13 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 13 FDA reports)
POLYMYOSITIS ( 13 FDA reports)
PRESCRIBED OVERDOSE ( 13 FDA reports)
PRODUCT ADHESION ISSUE ( 13 FDA reports)
PRODUCT ODOUR ABNORMAL ( 13 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 13 FDA reports)
PROTEIN URINE ( 13 FDA reports)
PUPILLARY DISORDER ( 13 FDA reports)
QUADRIPARESIS ( 13 FDA reports)
RECTAL POLYP ( 13 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 13 FDA reports)
SIALOADENITIS ( 13 FDA reports)
SKELETAL INJURY ( 13 FDA reports)
SKIN SWELLING ( 13 FDA reports)
SKIN TURGOR DECREASED ( 13 FDA reports)
SMEAR CERVIX ABNORMAL ( 13 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 13 FDA reports)
STERNAL FRACTURE ( 13 FDA reports)
STILLBIRTH ( 13 FDA reports)
STRESS CARDIOMYOPATHY ( 13 FDA reports)
TESTICULAR SWELLING ( 13 FDA reports)
TIC ( 13 FDA reports)
TONGUE BITING ( 13 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 13 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 13 FDA reports)
TUBERCULIN TEST POSITIVE ( 13 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 13 FDA reports)
URETHRAL OBSTRUCTION ( 13 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 13 FDA reports)
UTERINE PROLAPSE ( 13 FDA reports)
VASCULITIS NECROTISING ( 13 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
VITAMIN B12 DECREASED ( 13 FDA reports)
VITAMIN D DECREASED ( 13 FDA reports)
WEIGHT FLUCTUATION ( 13 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 13 FDA reports)
WOUND DECOMPOSITION ( 13 FDA reports)
X-RAY ABNORMAL ( 13 FDA reports)
ABDOMINAL NEOPLASM ( 13 FDA reports)
ABORTION ( 13 FDA reports)
ACCIDENT AT HOME ( 13 FDA reports)
ACINETOBACTER INFECTION ( 13 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 13 FDA reports)
ALVEOLAR OSTEITIS ( 13 FDA reports)
ANOGENITAL WARTS ( 13 FDA reports)
APALLIC SYNDROME ( 13 FDA reports)
APPARENT DEATH ( 13 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 13 FDA reports)
BLAST CELL CRISIS ( 13 FDA reports)
BLOOD OESTROGEN INCREASED ( 13 FDA reports)
BRADYKINESIA ( 13 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 13 FDA reports)
CARDIAC FAILURE CHRONIC ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 13 FDA reports)
CEREBELLAR ISCHAEMIA ( 13 FDA reports)
CEREBRAL VASOCONSTRICTION ( 13 FDA reports)
CHOROIDAL DETACHMENT ( 13 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 13 FDA reports)
COMPULSIVE SHOPPING ( 13 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 13 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 13 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 13 FDA reports)
CORYNEBACTERIUM INFECTION ( 13 FDA reports)
CUSHINGOID ( 13 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 13 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 13 FDA reports)
DUCTUS ARTERIOSUS STENOSIS FOETAL ( 13 FDA reports)
EAR HAEMORRHAGE ( 13 FDA reports)
ENTERITIS INFECTIOUS ( 13 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 13 FDA reports)
EXERCISE TOLERANCE DECREASED ( 13 FDA reports)
EXTREMITY CONTRACTURE ( 13 FDA reports)
FASCIITIS ( 13 FDA reports)
FEELING OF DESPAIR ( 13 FDA reports)
FIBRINOLYSIS ( 13 FDA reports)
FIBROUS HISTIOCYTOMA ( 13 FDA reports)
FOETAL HEART RATE ABNORMAL ( 13 FDA reports)
FOOT OPERATION ( 13 FDA reports)
FOREIGN BODY IN EYE ( 13 FDA reports)
FULL BLOOD COUNT DECREASED ( 13 FDA reports)
GINGIVAL EROSION ( 13 FDA reports)
GLUCOSE URINE PRESENT ( 13 FDA reports)
HAEMORRHAGE URINARY TRACT ( 13 FDA reports)
HAND FRACTURE ( 13 FDA reports)
HERNIA REPAIR ( 13 FDA reports)
HERPES ZOSTER DISSEMINATED ( 13 FDA reports)
HIP SURGERY ( 13 FDA reports)
HYDROPNEUMOTHORAX ( 13 FDA reports)
HYPERPARATHYROIDISM ( 13 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 13 FDA reports)
IMMUNOGLOBULINS INCREASED ( 13 FDA reports)
IMPLANT SITE INFECTION ( 13 FDA reports)
INITIAL INSOMNIA ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 13 FDA reports)
INTESTINAL RESECTION ( 13 FDA reports)
KETOACIDOSIS ( 13 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 12 FDA reports)
ALVEOLITIS ALLERGIC ( 12 FDA reports)
AMIMIA ( 12 FDA reports)
AMYLASE INCREASED ( 12 FDA reports)
ANAESTHETIC COMPLICATION ( 12 FDA reports)
ANASTOMOTIC FISTULA ( 12 FDA reports)
ANORECTAL OPERATION ( 12 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 12 FDA reports)
APGAR SCORE LOW ( 12 FDA reports)
APPENDICITIS PERFORATED ( 12 FDA reports)
ATRIAL THROMBOSIS ( 12 FDA reports)
AURICULAR SWELLING ( 12 FDA reports)
AUTISM ( 12 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 12 FDA reports)
BILE DUCT STENOSIS ( 12 FDA reports)
BLOOD CREATININE ABNORMAL ( 12 FDA reports)
BLOOD ETHANOL INCREASED ( 12 FDA reports)
BLOOD IRON INCREASED ( 12 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 12 FDA reports)
BRONCHOSTENOSIS ( 12 FDA reports)
CAECUM OPERATION ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
CHOLESTATIC LIVER INJURY ( 12 FDA reports)
CIRRHOSIS ALCOHOLIC ( 12 FDA reports)
CLEFT LIP ( 12 FDA reports)
COITAL BLEEDING ( 12 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 12 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 12 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 12 FDA reports)
CRANIOCEREBRAL INJURY ( 12 FDA reports)
CSF GLUCOSE DECREASED ( 12 FDA reports)
CSF PROTEIN INCREASED ( 12 FDA reports)
CSF TEST ABNORMAL ( 12 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 12 FDA reports)
DEATH OF RELATIVE ( 12 FDA reports)
DERMOID CYST ( 12 FDA reports)
DUODENAL STENOSIS ( 12 FDA reports)
DYSPHEMIA ( 12 FDA reports)
DYSPNOEA EXACERBATED ( 12 FDA reports)
EARLY SATIETY ( 12 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 12 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 12 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 12 FDA reports)
ENDOMETRIAL CANCER ( 12 FDA reports)
ENGRAFT FAILURE ( 12 FDA reports)
EXTRADURAL HAEMATOMA ( 12 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 12 FDA reports)
EYE OEDEMA ( 12 FDA reports)
EYELID DISORDER ( 12 FDA reports)
FINGER DEFORMITY ( 12 FDA reports)
FOETAL DISTRESS SYNDROME ( 12 FDA reports)
GASTROENTERITIS RADIATION ( 12 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 12 FDA reports)
GINGIVAL OEDEMA ( 12 FDA reports)
HAEMATOCRIT INCREASED ( 12 FDA reports)
HAIR COLOUR CHANGES ( 12 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 12 FDA reports)
HAPTOGLOBIN DECREASED ( 12 FDA reports)
HEPATIC HAEMATOMA ( 12 FDA reports)
HEPATIC HAEMORRHAGE ( 12 FDA reports)
HEPATITIS VIRAL ( 12 FDA reports)
HIV PERIPHERAL NEUROPATHY ( 12 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 12 FDA reports)
INFUSION SITE SWELLING ( 12 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 12 FDA reports)
INTESTINAL MASS ( 12 FDA reports)
INTESTINAL OPERATION ( 12 FDA reports)
LABORATORY TEST INTERFERENCE ( 12 FDA reports)
LEARNING DISORDER ( 12 FDA reports)
LIGAMENT RUPTURE ( 12 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 12 FDA reports)
LYMPHANGITIS ( 12 FDA reports)
METASTASES TO PERITONEUM ( 12 FDA reports)
MOUTH INJURY ( 12 FDA reports)
MYELOFIBROSIS ( 12 FDA reports)
NAIL DISCOLOURATION ( 12 FDA reports)
NEUTROPHIL COUNT ( 12 FDA reports)
OESOPHAGITIS ULCERATIVE ( 12 FDA reports)
ORAL SURGERY ( 12 FDA reports)
PERICARDIAL HAEMORRHAGE ( 12 FDA reports)
PERITONEAL ADHESIONS ( 12 FDA reports)
PERITONEAL TUBERCULOSIS ( 12 FDA reports)
PHLEBOLITH ( 12 FDA reports)
PLATELET DISORDER ( 12 FDA reports)
PNEUMOCOCCAL INFECTION ( 12 FDA reports)
PNEUMONIA MYCOPLASMAL ( 12 FDA reports)
PORPHYRIA ACUTE ( 12 FDA reports)
PRODUCT TASTE ABNORMAL ( 12 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 12 FDA reports)
PULMONARY VALVE STENOSIS ( 12 FDA reports)
RADIATION INJURY ( 12 FDA reports)
RECTAL PROLAPSE REPAIR ( 12 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 12 FDA reports)
SCAPULA FRACTURE ( 12 FDA reports)
SERRATIA BACTERAEMIA ( 12 FDA reports)
SKIN MASS ( 12 FDA reports)
SKULL FRACTURED BASE ( 12 FDA reports)
SLUGGISHNESS ( 12 FDA reports)
SMALL INTESTINAL STENOSIS ( 12 FDA reports)
SPONDYLITIS ( 12 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 12 FDA reports)
STRESS SYMPTOMS ( 12 FDA reports)
THYMUS DISORDER ( 12 FDA reports)
TRACHEITIS ( 12 FDA reports)
TUMOUR FLARE ( 12 FDA reports)
TYPE I HYPERSENSITIVITY ( 12 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 12 FDA reports)
URETHRAL STENOSIS ( 12 FDA reports)
URINARY TRACT DISORDER ( 12 FDA reports)
URTICARIA GENERALISED ( 12 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 12 FDA reports)
VERTIGO POSITIONAL ( 12 FDA reports)
VIROLOGIC FAILURE ( 12 FDA reports)
WEANING FAILURE ( 12 FDA reports)
LOSS OF LIBIDO ( 11 FDA reports)
LUDWIG ANGINA ( 11 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 11 FDA reports)
METABOLIC ALKALOSIS ( 11 FDA reports)
METASTASES TO ABDOMINAL WALL ( 11 FDA reports)
METASTATIC PAIN ( 11 FDA reports)
MICTURITION DISORDER ( 11 FDA reports)
MIDDLE EAR EFFUSION ( 11 FDA reports)
MONOCLONAL GAMMOPATHY ( 11 FDA reports)
MUSCLE ABSCESS ( 11 FDA reports)
MYASTHENIA GRAVIS ( 11 FDA reports)
MYELITIS ( 11 FDA reports)
NARCOLEPSY ( 11 FDA reports)
OCULAR DISCOMFORT ( 11 FDA reports)
ORAL PRURITUS ( 11 FDA reports)
OSTEOPOROTIC FRACTURE ( 11 FDA reports)
PANCREATIC NECROSIS ( 11 FDA reports)
PANCREATIC PSEUDOCYST ( 11 FDA reports)
PELVIC HAEMATOMA ( 11 FDA reports)
PELVIC VENOUS THROMBOSIS ( 11 FDA reports)
PERICARDIAL DISEASE ( 11 FDA reports)
PILOERECTION ( 11 FDA reports)
POLYCYTHAEMIA ( 11 FDA reports)
POTENTIATING DRUG INTERACTION ( 11 FDA reports)
PROCTOCOLITIS ( 11 FDA reports)
PROSTATE INFECTION ( 11 FDA reports)
PSYCHOLOGICAL TRAUMA ( 11 FDA reports)
PUBIS FRACTURE ( 11 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 11 FDA reports)
PULMONARY VASCULAR DISORDER ( 11 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 11 FDA reports)
RETINITIS ( 11 FDA reports)
SALPINGO-OOPHORECTOMY ( 11 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 11 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 11 FDA reports)
SEROMA ( 11 FDA reports)
SERUM FERRITIN DECREASED ( 11 FDA reports)
SIGMOIDITIS ( 11 FDA reports)
SINUS POLYP ( 11 FDA reports)
SKIN DESQUAMATION ( 11 FDA reports)
SOFT TISSUE INFLAMMATION ( 11 FDA reports)
SPINAL FUSION SURGERY ( 11 FDA reports)
SPINAL PAIN ( 11 FDA reports)
SPUTUM INCREASED ( 11 FDA reports)
STASIS DERMATITIS ( 11 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 11 FDA reports)
TELANGIECTASIA ( 11 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 11 FDA reports)
TONIC CONVULSION ( 11 FDA reports)
TOOTH EROSION ( 11 FDA reports)
TRANSPLANT FAILURE ( 11 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 11 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 11 FDA reports)
UNINTENDED PREGNANCY ( 11 FDA reports)
URETHRAL DISORDER ( 11 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 11 FDA reports)
URINE KETONE BODY PRESENT ( 11 FDA reports)
VAGINITIS BACTERIAL ( 11 FDA reports)
VASOSPASM ( 11 FDA reports)
VITH NERVE PARALYSIS ( 11 FDA reports)
VOMITING PROJECTILE ( 11 FDA reports)
VULVAL DISORDER ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WOUND HAEMORRHAGE ( 11 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 11 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 11 FDA reports)
ACUTE LEUKAEMIA ( 11 FDA reports)
ANEURYSM REPAIR ( 11 FDA reports)
ANIMAL BITE ( 11 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 11 FDA reports)
APPLICATION SITE ERYTHEMA ( 11 FDA reports)
ARTERITIS ( 11 FDA reports)
AXILLARY PAIN ( 11 FDA reports)
AXILLARY VEIN THROMBOSIS ( 11 FDA reports)
BACILLUS INFECTION ( 11 FDA reports)
BACTERIA URINE IDENTIFIED ( 11 FDA reports)
BILE DUCT CANCER ( 11 FDA reports)
BLAST CELL COUNT INCREASED ( 11 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 11 FDA reports)
BRAIN CONTUSION ( 11 FDA reports)
BREAST CYST ( 11 FDA reports)
BRONCHIAL SECRETION RETENTION ( 11 FDA reports)
BUNION ( 11 FDA reports)
BUTTERFLY RASH ( 11 FDA reports)
CALCULUS BLADDER ( 11 FDA reports)
CALCULUS URETHRAL ( 11 FDA reports)
CARBON MONOXIDE POISONING ( 11 FDA reports)
CARDIAC SEPTAL DEFECT ( 11 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 11 FDA reports)
CATARACT CORTICAL ( 11 FDA reports)
CATHETER PLACEMENT ( 11 FDA reports)
CATHETER SITE PAIN ( 11 FDA reports)
CEREBELLAR ATAXIA ( 11 FDA reports)
CEREBELLAR ATROPHY ( 11 FDA reports)
CEREBRAL CALCIFICATION ( 11 FDA reports)
CERVICAL CYST ( 11 FDA reports)
CHOLANGITIS SCLEROSING ( 11 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 11 FDA reports)
CORNEAL DISORDER ( 11 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 11 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 11 FDA reports)
DAYDREAMING ( 11 FDA reports)
DECEREBRATION ( 11 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 11 FDA reports)
DERMATITIS PSORIASIFORM ( 11 FDA reports)
DEVICE BREAKAGE ( 11 FDA reports)
DIABETIC FOOT INFECTION ( 11 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 11 FDA reports)
DROWNING ( 11 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 11 FDA reports)
DYSPHORIA ( 11 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 11 FDA reports)
ENURESIS ( 11 FDA reports)
ERECTION INCREASED ( 11 FDA reports)
EXCITABILITY ( 11 FDA reports)
GALLBLADDER ENLARGEMENT ( 11 FDA reports)
GLOBULINS INCREASED ( 11 FDA reports)
GLYCOSURIA ( 11 FDA reports)
HAEMOCHROMATOSIS ( 11 FDA reports)
HEAT RASH ( 11 FDA reports)
HEMIANOPIA HOMONYMOUS ( 11 FDA reports)
HIDRADENITIS ( 11 FDA reports)
HYPERLACTACIDAEMIA ( 11 FDA reports)
HYPERTRANSAMINASAEMIA ( 11 FDA reports)
HYPOPERFUSION ( 11 FDA reports)
IIIRD NERVE PARALYSIS ( 11 FDA reports)
ILEOSTOMY ( 11 FDA reports)
IMMUNOGLOBULINS DECREASED ( 11 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 11 FDA reports)
INJECTION SITE ABSCESS ( 11 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 11 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 11 FDA reports)
JOINT ARTHROPLASTY ( 11 FDA reports)
JOINT CREPITATION ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
KLEBSIELLA TEST POSITIVE ( 11 FDA reports)
LARYNGEAL HAEMORRHAGE ( 11 FDA reports)
LIBIDO DECREASED ( 11 FDA reports)
LIGAMENT DISORDER ( 11 FDA reports)
LIMB OPERATION ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 10 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 10 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 10 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 10 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 10 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 10 FDA reports)
ANTITHROMBIN III DECREASED ( 10 FDA reports)
APPARENT LIFE THREATENING EVENT ( 10 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 10 FDA reports)
BLOOD OSMOLARITY DECREASED ( 10 FDA reports)
BLOOD OSMOLARITY INCREASED ( 10 FDA reports)
BLOOD PROLACTIN INCREASED ( 10 FDA reports)
BLOODY DISCHARGE ( 10 FDA reports)
BONE GRAFT ( 10 FDA reports)
BRAIN DAMAGE ( 10 FDA reports)
BRAIN OPERATION ( 10 FDA reports)
BREECH PRESENTATION ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
CARDIAC ASTHMA ( 10 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 10 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 10 FDA reports)
CEPHALHAEMATOMA ( 10 FDA reports)
CEREBRAL MICROANGIOPATHY ( 10 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
CHYLOTHORAX ( 10 FDA reports)
COAGULATION TEST ABNORMAL ( 10 FDA reports)
COGWHEEL RIGIDITY ( 10 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 10 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 10 FDA reports)
COR PULMONALE ( 10 FDA reports)
CRYOGLOBULINAEMIA ( 10 FDA reports)
CYST ASPIRATION ( 10 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 10 FDA reports)
DEAFNESS BILATERAL ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DEPRESSION SUICIDAL ( 10 FDA reports)
DIABETIC COMPLICATION ( 10 FDA reports)
DIAPHRAGMATIC DISORDER ( 10 FDA reports)
DISINHIBITION ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 10 FDA reports)
DRUG TOLERANCE ( 10 FDA reports)
DYSPRAXIA ( 10 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 10 FDA reports)
ENCEPHALITIS VIRAL ( 10 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 10 FDA reports)
EPIDIDYMITIS ( 10 FDA reports)
FEAR OF DISEASE ( 10 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 10 FDA reports)
FOOD POISONING ( 10 FDA reports)
FRACTURE DISPLACEMENT ( 10 FDA reports)
GALACTORRHOEA ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 10 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 10 FDA reports)
GLIOBLASTOMA MULTIFORME ( 10 FDA reports)
GROIN ABSCESS ( 10 FDA reports)
HAND DEFORMITY ( 10 FDA reports)
HEMIANOPIA ( 10 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 10 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 10 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 10 FDA reports)
HYPOCHROMASIA ( 10 FDA reports)
HYPOTONIA NEONATAL ( 10 FDA reports)
INCISION SITE HAEMORRHAGE ( 10 FDA reports)
INFLAMMATION OF WOUND ( 10 FDA reports)
INJECTION SITE VESICLES ( 10 FDA reports)
KETOSIS ( 10 FDA reports)
LABILE BLOOD PRESSURE ( 10 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 10 FDA reports)
LENTIGO ( 10 FDA reports)
LIBIDO DISORDER ( 10 FDA reports)
LIP EROSION ( 10 FDA reports)
LIVE BIRTH ( 10 FDA reports)
LOWER EXTREMITY MASS ( 10 FDA reports)
LUNG ABSCESS ( 10 FDA reports)
LUPUS NEPHRITIS ( 10 FDA reports)
LYMPHOCELE ( 10 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 10 FDA reports)
MEDIASTINAL MASS ( 10 FDA reports)
MENIERE'S DISEASE ( 10 FDA reports)
MERALGIA PARAESTHETICA ( 10 FDA reports)
MICROANGIOPATHY ( 10 FDA reports)
MICROCEPHALY ( 10 FDA reports)
MOANING ( 10 FDA reports)
MUSCLE RUPTURE ( 10 FDA reports)
NAIL INFECTION ( 10 FDA reports)
NAIL RIDGING ( 10 FDA reports)
NEUROSIS ( 10 FDA reports)
NICOTINE DEPENDENCE ( 10 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 10 FDA reports)
OBSTRUCTIVE UROPATHY ( 10 FDA reports)
PALATAL DISORDER ( 10 FDA reports)
PANCREATIC ENLARGEMENT ( 10 FDA reports)
PARAKERATOSIS ( 10 FDA reports)
PARATHYROIDECTOMY ( 10 FDA reports)
PEAU D'ORANGE ( 10 FDA reports)
PERIODONTAL INFECTION ( 10 FDA reports)
PERITONEAL DISORDER ( 10 FDA reports)
PERNICIOUS ANAEMIA ( 10 FDA reports)
PILONIDAL CYST ( 10 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 10 FDA reports)
POOR VENOUS ACCESS ( 10 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 10 FDA reports)
POST THROMBOTIC SYNDROME ( 10 FDA reports)
POST-TRAUMATIC PAIN ( 10 FDA reports)
POSTURING ( 10 FDA reports)
PROCEDURAL VOMITING ( 10 FDA reports)
PROSTATIC OBSTRUCTION ( 10 FDA reports)
PULSE ABNORMAL ( 10 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 10 FDA reports)
RADIATION ASSOCIATED PAIN ( 10 FDA reports)
RED BLOOD CELL ABNORMALITY ( 10 FDA reports)
RED MAN SYNDROME ( 10 FDA reports)
RENAL ISCHAEMIA ( 10 FDA reports)
RESPIRATORY TRACT OEDEMA ( 10 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 10 FDA reports)
SCHAMBERG'S DISEASE ( 10 FDA reports)
SERRATIA SEPSIS ( 10 FDA reports)
SINOATRIAL BLOCK ( 10 FDA reports)
SINUSITIS FUNGAL ( 10 FDA reports)
SPINAL DEFORMITY ( 10 FDA reports)
SPLEEN CONGESTION ( 10 FDA reports)
SPLENIC CALCIFICATION ( 10 FDA reports)
SPONTANEOUS HAEMATOMA ( 10 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 10 FDA reports)
SUBGALEAL HAEMATOMA ( 10 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
SYSTEMIC MYCOSIS ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TENDON PAIN ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
THYROXINE FREE DECREASED ( 10 FDA reports)
TOBACCO ABUSE ( 10 FDA reports)
TONGUE DRY ( 10 FDA reports)
TONGUE HAEMORRHAGE ( 10 FDA reports)
TUMOUR INVASION ( 10 FDA reports)
TURNER'S SYNDROME ( 10 FDA reports)
URINE OUTPUT INCREASED ( 10 FDA reports)
UTERINE DISORDER ( 10 FDA reports)
VOCAL CORD PARESIS ( 10 FDA reports)
VULVOVAGINITIS ( 10 FDA reports)
WALKING DISABILITY ( 10 FDA reports)
WATER INTOXICATION ( 10 FDA reports)
YAWNING ( 10 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 9 FDA reports)
LYME DISEASE ( 9 FDA reports)
LYMPH NODE CALCIFICATION ( 9 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 9 FDA reports)
MEDICAL DEVICE REMOVAL ( 9 FDA reports)
MENINGORRHAGIA ( 9 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 9 FDA reports)
METASTASES TO PANCREAS ( 9 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 9 FDA reports)
MONOPARESIS ( 9 FDA reports)
MORAXELLA INFECTION ( 9 FDA reports)
MUCORMYCOSIS ( 9 FDA reports)
MYCOSIS FUNGOIDES ( 9 FDA reports)
MYOGLOBINURIA ( 9 FDA reports)
MYOPERICARDITIS ( 9 FDA reports)
NASAL DISORDER ( 9 FDA reports)
NASAL MUCOSAL DISORDER ( 9 FDA reports)
NECK INJURY ( 9 FDA reports)
NEGATIVE THOUGHTS ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NODAL ARRHYTHMIA ( 9 FDA reports)
NUCHAL RIGIDITY ( 9 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 9 FDA reports)
OPTIC DISC DISORDER ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
ORAL CAVITY FISTULA ( 9 FDA reports)
ORAL DISCHARGE ( 9 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 9 FDA reports)
OROPHARYNGEAL SPASM ( 9 FDA reports)
OVARIAN CANCER METASTATIC ( 9 FDA reports)
OVARIAN DISORDER ( 9 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 9 FDA reports)
PANCREATIC ENZYMES INCREASED ( 9 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 9 FDA reports)
PELVIC MASS ( 9 FDA reports)
PERIANAL ABSCESS ( 9 FDA reports)
PERINEAL LACERATION ( 9 FDA reports)
PERIORBITAL HAEMATOMA ( 9 FDA reports)
PHYSICAL ASSAULT ( 9 FDA reports)
PITUITARY TUMOUR ( 9 FDA reports)
PITUITARY TUMOUR BENIGN ( 9 FDA reports)
PLEURAL ADHESION ( 9 FDA reports)
PNEUMATOSIS INTESTINALIS ( 9 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 9 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 9 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 9 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 9 FDA reports)
POSTURE ABNORMAL ( 9 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 9 FDA reports)
PROCEDURAL NAUSEA ( 9 FDA reports)
PROTRUSION TONGUE ( 9 FDA reports)
PTERYGIUM COLLI ( 9 FDA reports)
RECTAL LESION ( 9 FDA reports)
RECURRENT CANCER ( 9 FDA reports)
REFRACTORY ANAEMIA ( 9 FDA reports)
RETICULOCYTE COUNT INCREASED ( 9 FDA reports)
RETINAL ARTERY OCCLUSION ( 9 FDA reports)
RHINITIS SEASONAL ( 9 FDA reports)
SALIVARY GLAND DISORDER ( 9 FDA reports)
SALIVARY GLAND MASS ( 9 FDA reports)
SCROTAL SWELLING ( 9 FDA reports)
SKIN INJURY ( 9 FDA reports)
SKIN ODOUR ABNORMAL ( 9 FDA reports)
SOFT TISSUE INJURY ( 9 FDA reports)
SOFT TISSUE MASS ( 9 FDA reports)
SPINAL COLUMN INJURY ( 9 FDA reports)
SYMBLEPHARON ( 9 FDA reports)
TONGUE INJURY ( 9 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 9 FDA reports)
TRACHEAL INJURY ( 9 FDA reports)
TRACHEOSTOMY ( 9 FDA reports)
TRANSAMINASES ABNORMAL ( 9 FDA reports)
UHTHOFF'S PHENOMENON ( 9 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 9 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
UTERINE CANCER ( 9 FDA reports)
VAGINAL CANDIDIASIS ( 9 FDA reports)
VAGINAL MYCOSIS ( 9 FDA reports)
VENA CAVA FILTER INSERTION ( 9 FDA reports)
VENOUS STENOSIS ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 9 FDA reports)
ADRENAL ADENOMA ( 9 FDA reports)
ADRENOGENITAL SYNDROME ( 9 FDA reports)
ANAL SPHINCTER ATONY ( 9 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
ANKLE OPERATION ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
APPLICATION SITE BURN ( 9 FDA reports)
ARTERIOVENOUS FISTULA ( 9 FDA reports)
ASBESTOSIS ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
AURA ( 9 FDA reports)
BACTERIA STOOL IDENTIFIED ( 9 FDA reports)
BIOPSY LIVER ABNORMAL ( 9 FDA reports)
BIOPSY SKIN ABNORMAL ( 9 FDA reports)
BLADDER DILATATION ( 9 FDA reports)
BLADDER DISTENSION ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 9 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 9 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 9 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 9 FDA reports)
BLOOD URINE ( 9 FDA reports)
BONE ABSCESS ( 9 FDA reports)
BONE FORMATION INCREASED ( 9 FDA reports)
BRAIN STEM HAEMORRHAGE ( 9 FDA reports)
BREAST CANCER IN SITU ( 9 FDA reports)
BREAST NECROSIS ( 9 FDA reports)
BRONCHOPNEUMOPATHY ( 9 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 9 FDA reports)
CARDIAC ANEURYSM ( 9 FDA reports)
CARDIAC HYPERTROPHY ( 9 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 9 FDA reports)
CAUDA EQUINA SYNDROME ( 9 FDA reports)
CHEYNE-STOKES RESPIRATION ( 9 FDA reports)
CHLAMYDIAL INFECTION ( 9 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 9 FDA reports)
CHROMATOPSIA ( 9 FDA reports)
COMMINUTED FRACTURE ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 9 FDA reports)
CONGENITAL HAIR DISORDER ( 9 FDA reports)
CONGENITAL JAW MALFORMATION ( 9 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 9 FDA reports)
CONJUNCTIVAL DISORDER ( 9 FDA reports)
CORNEAL ABRASION ( 9 FDA reports)
DEATH NEONATAL ( 9 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 9 FDA reports)
DEFORMITY THORAX ( 9 FDA reports)
DEREALISATION ( 9 FDA reports)
DERMATOMYOSITIS ( 9 FDA reports)
DIARRHOEA INFECTIOUS ( 9 FDA reports)
DRUG RESISTANCE ( 9 FDA reports)
DYSENTERY ( 9 FDA reports)
ENCEPHALITIS HERPES ( 9 FDA reports)
ENGRAFTMENT SYNDROME ( 9 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 9 FDA reports)
EOSINOPHIL COUNT DECREASED ( 9 FDA reports)
ESCHAR ( 9 FDA reports)
EYE LASER SURGERY ( 9 FDA reports)
FOREARM FRACTURE ( 9 FDA reports)
GALLBLADDER OPERATION ( 9 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 9 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 9 FDA reports)
GESTATIONAL HYPERTENSION ( 9 FDA reports)
GRAFT LOSS ( 9 FDA reports)
GRIMACING ( 9 FDA reports)
GUN SHOT WOUND ( 9 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 9 FDA reports)
HAEMOSIDEROSIS ( 9 FDA reports)
HAIR TEXTURE ABNORMAL ( 9 FDA reports)
HALO VISION ( 9 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 9 FDA reports)
HELICOBACTER TEST POSITIVE ( 9 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 9 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 9 FDA reports)
HEPATIC CANCER METASTATIC ( 9 FDA reports)
HYDROTHORAX ( 9 FDA reports)
HYPERACUSIS ( 9 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 9 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 9 FDA reports)
HYPOGONADISM ( 9 FDA reports)
ILIAC ARTERY STENOSIS ( 9 FDA reports)
ILLUSION ( 9 FDA reports)
INCISION SITE PAIN ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INFUSION SITE REACTION ( 9 FDA reports)
INJECTION SITE INFECTION ( 9 FDA reports)
INJECTION SITE ULCER ( 9 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 9 FDA reports)
KIDNEY FIBROSIS ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LEUKOCYTURIA ( 9 FDA reports)
LIGAMENT INJURY ( 9 FDA reports)
ABDOMINAL BRUIT ( 8 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 8 FDA reports)
ACNE PUSTULAR ( 8 FDA reports)
ADRENAL SUPPRESSION ( 8 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 8 FDA reports)
ALKALOSIS ( 8 FDA reports)
AMPUTATION ( 8 FDA reports)
ANASTOMOTIC STENOSIS ( 8 FDA reports)
ANISOCYTOSIS ( 8 FDA reports)
APPENDICECTOMY ( 8 FDA reports)
APPLICATION SITE PAIN ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
APPLICATION SITE REACTION ( 8 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 8 FDA reports)
ASPIRATION JOINT ( 8 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BACTEROIDES TEST POSITIVE ( 8 FDA reports)
BILIRUBINURIA ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 8 FDA reports)
BLADDER DYSFUNCTION ( 8 FDA reports)
BLADDER NEOPLASM ( 8 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 8 FDA reports)
BLOOD UREA ABNORMAL ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BONE MARROW TOXICITY ( 8 FDA reports)
BREAST ABSCESS ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
BREAST RECONSTRUCTION ( 8 FDA reports)
CALCIUM DEFICIENCY ( 8 FDA reports)
CARDIAC OPERATION ( 8 FDA reports)
CATHETER SITE RELATED REACTION ( 8 FDA reports)
CELLULITIS ORBITAL ( 8 FDA reports)
CEREBRAL PALSY ( 8 FDA reports)
CERVIX INFLAMMATION ( 8 FDA reports)
CHONDROMALACIA ( 8 FDA reports)
CLONIC CONVULSION ( 8 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 8 FDA reports)
CONGENITAL ECTODERMAL DYSPLASIA ( 8 FDA reports)
CONJUNCTIVAL IRRITATION ( 8 FDA reports)
CORONARY ANGIOPLASTY ( 8 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 8 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 8 FDA reports)
CUSHING'S SYNDROME ( 8 FDA reports)
CUTANEOUS SARCOIDOSIS ( 8 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 8 FDA reports)
DELIRIUM TREMENS ( 8 FDA reports)
DEVICE OCCLUSION ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DRUG TOLERANCE DECREASED ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 8 FDA reports)
DUANE'S SYNDROME ( 8 FDA reports)
DYSHIDROSIS ( 8 FDA reports)
DYSTROPHIC CALCIFICATION ( 8 FDA reports)
ECTOPIC PREGNANCY ( 8 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 8 FDA reports)
ENDOMETRIAL ATROPHY ( 8 FDA reports)
ENDOTHELIN INCREASED ( 8 FDA reports)
EYE REDNESS ( 8 FDA reports)
EYELIDS PRURITUS ( 8 FDA reports)
FISTULA DISCHARGE ( 8 FDA reports)
FLASHBACK ( 8 FDA reports)
FOLATE DEFICIENCY ( 8 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 8 FDA reports)
GAZE PALSY ( 8 FDA reports)
GENITAL RASH ( 8 FDA reports)
GENITAL ULCERATION ( 8 FDA reports)
HELICOBACTER GASTRITIS ( 8 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 8 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 8 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 8 FDA reports)
HOARSENESS ( 8 FDA reports)
HORMONE LEVEL ABNORMAL ( 8 FDA reports)
HYPERCREATININAEMIA ( 8 FDA reports)
HYPERMAGNESAEMIA ( 8 FDA reports)
HYPERVISCOSITY SYNDROME ( 8 FDA reports)
HYPOCHROMIC ANAEMIA ( 8 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 8 FDA reports)
IMPULSIVE BEHAVIOUR ( 8 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 8 FDA reports)
INFLAMMATORY MARKER INCREASED ( 8 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 8 FDA reports)
INTRACRANIAL HYPOTENSION ( 8 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 8 FDA reports)
LACRIMAL DISORDER ( 8 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 8 FDA reports)
LATEX ALLERGY ( 8 FDA reports)
LONG QT SYNDROME ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 8 FDA reports)
LYMPH NODE PAIN ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
MELANOMATOUS MENINGITIS ( 8 FDA reports)
MENINGEAL DISORDER ( 8 FDA reports)
METAL POISONING ( 8 FDA reports)
METASTASES TO SPLEEN ( 8 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 8 FDA reports)
METHAEMOGLOBINAEMIA ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MUSCLE FATIGUE ( 8 FDA reports)
MYCOTIC ALLERGY ( 8 FDA reports)
MYOPATHY TOXIC ( 8 FDA reports)
NASAL POLYPS ( 8 FDA reports)
NOSE DEFORMITY ( 8 FDA reports)
OBSESSIVE THOUGHTS ( 8 FDA reports)
OCULAR VASCULAR DISORDER ( 8 FDA reports)
ONYCHALGIA ( 8 FDA reports)
ORAL MUCOSAL BLISTERING ( 8 FDA reports)
ORAL MUCOSAL ERUPTION ( 8 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 8 FDA reports)
OSTEOCHONDROSIS ( 8 FDA reports)
PACHYMENINGITIS ( 8 FDA reports)
PANCREATIC ATROPHY ( 8 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 8 FDA reports)
PARTNER STRESS ( 8 FDA reports)
PENILE PAIN ( 8 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 8 FDA reports)
PERFORATED ULCER ( 8 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 8 FDA reports)
PERSECUTORY DELUSION ( 8 FDA reports)
PHONOPHOBIA ( 8 FDA reports)
PLACENTAL INSUFFICIENCY ( 8 FDA reports)
PNEUMONIA NECROTISING ( 8 FDA reports)
POST PROCEDURAL PAIN ( 8 FDA reports)
POSTMENOPAUSE ( 8 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 8 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 8 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 8 FDA reports)
PRIAPISM ( 8 FDA reports)
PRODUCT TAMPERING ( 8 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 8 FDA reports)
PULMONARY NECROSIS ( 8 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 8 FDA reports)
REGURGITATION ( 8 FDA reports)
RENAL CORTICAL NECROSIS ( 8 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 8 FDA reports)
RETINAL DISORDER ( 8 FDA reports)
SACROILIITIS ( 8 FDA reports)
SEPSIS NEONATAL ( 8 FDA reports)
SHONE COMPLEX ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SKIN DEGENERATIVE DISORDER ( 8 FDA reports)
SMALL INTESTINE CARCINOMA ( 8 FDA reports)
SPINAL CORD INJURY CERVICAL ( 8 FDA reports)
SPLENIC HAEMORRHAGE ( 8 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 8 FDA reports)
STENT OCCLUSION ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SURGICAL FAILURE ( 8 FDA reports)
SYSTOLIC DYSFUNCTION ( 8 FDA reports)
TENOSYNOVITIS STENOSANS ( 8 FDA reports)
TERATOGENICITY ( 8 FDA reports)
TINEA CRURIS ( 8 FDA reports)
TONSILLAR HYPERTROPHY ( 8 FDA reports)
TOOTH DEPOSIT ( 8 FDA reports)
TOOTH IMPACTED ( 8 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 8 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 8 FDA reports)
TRICUSPID VALVE DISEASE ( 8 FDA reports)
TWIN PREGNANCY ( 8 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 8 FDA reports)
URETERIC DILATATION ( 8 FDA reports)
URINE ODOUR ABNORMAL ( 8 FDA reports)
VASCULITIC RASH ( 8 FDA reports)
VICTIM OF SEXUAL ABUSE ( 8 FDA reports)
VITAMIN K DEFICIENCY ( 8 FDA reports)
VOCAL CORD DISORDER ( 8 FDA reports)
LOCKED-IN SYNDROME ( 7 FDA reports)
LOSS OF CONTROL OF LEGS ( 7 FDA reports)
LOSS OF PROPRIOCEPTION ( 7 FDA reports)
LYMPHATIC DISORDER ( 7 FDA reports)
MACROSOMIA ( 7 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 7 FDA reports)
MENOMETRORRHAGIA ( 7 FDA reports)
METASTASES TO BONE MARROW ( 7 FDA reports)
METASTASES TO KIDNEY ( 7 FDA reports)
METASTASES TO OVARY ( 7 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 7 FDA reports)
MITRAL VALVE SCLEROSIS ( 7 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 7 FDA reports)
MIXED DEAFNESS ( 7 FDA reports)
MORTON'S NEUROMA ( 7 FDA reports)
MUTISM ( 7 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 7 FDA reports)
NAIL GROWTH ABNORMAL ( 7 FDA reports)
NEPHRITIC SYNDROME ( 7 FDA reports)
NORMAL NEWBORN ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
OESOPHAGEAL DILATATION ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
OPISTHOTONUS ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
OROPHARYNGITIS FUNGAL ( 7 FDA reports)
OXYGEN SUPPLEMENTATION ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PANNICULITIS ( 7 FDA reports)
PAPILLOMA ( 7 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 7 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 7 FDA reports)
PENILE DISCHARGE ( 7 FDA reports)
PENILE SWELLING ( 7 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 7 FDA reports)
PERIPHERAL NERVE LESION ( 7 FDA reports)
PERITONEAL ABSCESS ( 7 FDA reports)
PHIMOSIS ( 7 FDA reports)
PLEURAL CALCIFICATION ( 7 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 7 FDA reports)
PNEUMONIA LEGIONELLA ( 7 FDA reports)
POIKILOCYTOSIS ( 7 FDA reports)
PORPHYRIA NON-ACUTE ( 7 FDA reports)
POST LAMINECTOMY SYNDROME ( 7 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 7 FDA reports)
POSTPARTUM DEPRESSION ( 7 FDA reports)
PRIMARY HYPOGONADISM ( 7 FDA reports)
PROCEDURAL HYPERTENSION ( 7 FDA reports)
PROSTATIC DISORDER ( 7 FDA reports)
PROTEUS INFECTION ( 7 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 7 FDA reports)
PULMONARY VASCULITIS ( 7 FDA reports)
RADIATION SKIN INJURY ( 7 FDA reports)
RADICULAR CYST ( 7 FDA reports)
REHABILITATION THERAPY ( 7 FDA reports)
RENAL TUBULAR ATROPHY ( 7 FDA reports)
RESPIRATORY MONILIASIS ( 7 FDA reports)
RETROGNATHIA ( 7 FDA reports)
SCAN ABDOMEN ABNORMAL ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
SKIN HYPOPIGMENTATION ( 7 FDA reports)
SLEEP ATTACKS ( 7 FDA reports)
SMALL INTESTINAL PERFORATION ( 7 FDA reports)
SOMATISATION DISORDER ( 7 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 7 FDA reports)
SPLENIC ABSCESS ( 7 FDA reports)
SPLENIC VEIN THROMBOSIS ( 7 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 7 FDA reports)
SUBRETINAL FIBROSIS ( 7 FDA reports)
SUDDEN ONSET OF SLEEP ( 7 FDA reports)
SYNOVIAL DISORDER ( 7 FDA reports)
SYSTEMIC SCLEROSIS ( 7 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 7 FDA reports)
TAKAYASU'S ARTERITIS ( 7 FDA reports)
THYROXINE INCREASED ( 7 FDA reports)
TONIC CLONIC MOVEMENTS ( 7 FDA reports)
TRACHEAL HAEMORRHAGE ( 7 FDA reports)
TRACHEAL OEDEMA ( 7 FDA reports)
UMBILICAL CORD ABNORMALITY ( 7 FDA reports)
URETHRAL HAEMORRHAGE ( 7 FDA reports)
VASCULAR GRAFT OCCLUSION ( 7 FDA reports)
VASCULAR INJURY ( 7 FDA reports)
VASCULAR OCCLUSION ( 7 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 7 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 7 FDA reports)
VISCERAL CONGESTION ( 7 FDA reports)
VULVAR EROSION ( 7 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 7 FDA reports)
WEIGHT ABNORMAL ( 7 FDA reports)
WHITE BLOOD CELL DISORDER ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
XANTHOPSIA ( 7 FDA reports)
ABDOMINAL HAEMATOMA ( 7 FDA reports)
ABORTION MISSED ( 7 FDA reports)
ABSCESS BACTERIAL ( 7 FDA reports)
ADRENAL HAEMORRHAGE ( 7 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 7 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 7 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 7 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
AORTA HYPOPLASIA ( 7 FDA reports)
APPENDIX DISORDER ( 7 FDA reports)
APPLICATION SITE IRRITATION ( 7 FDA reports)
APPLICATION SITE VESICLES ( 7 FDA reports)
ARTERIAL HAEMORRHAGE ( 7 FDA reports)
ARTERIAL INJURY ( 7 FDA reports)
ASTHMATIC CRISIS ( 7 FDA reports)
ATELECTASIS NEONATAL ( 7 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 7 FDA reports)
BACTERIAL DISEASE CARRIER ( 7 FDA reports)
BACTERIAL TEST ( 7 FDA reports)
BACTERIURIA ( 7 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 7 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 7 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 7 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 7 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 7 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 7 FDA reports)
BREAST DISCOMFORT ( 7 FDA reports)
BREAST FEEDING ( 7 FDA reports)
BREAST NEOPLASM ( 7 FDA reports)
BRONCHIAL DISORDER ( 7 FDA reports)
BRONCHOMALACIA ( 7 FDA reports)
CALCIPHYLAXIS ( 7 FDA reports)
CARDIAC DEATH ( 7 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 7 FDA reports)
CARDIAC PSEUDOANEURYSM ( 7 FDA reports)
CARDIORENAL SYNDROME ( 7 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 7 FDA reports)
CARDIOVERSION ( 7 FDA reports)
CATHETER SITE ERYTHEMA ( 7 FDA reports)
CATHETER SITE PHLEBITIS ( 7 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 7 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 7 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 7 FDA reports)
CHARLES BONNET SYNDROME ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
CHILD ABUSE ( 7 FDA reports)
CHLOROMA ( 7 FDA reports)
CHOLANGITIS ACUTE ( 7 FDA reports)
CHOLESTEROSIS ( 7 FDA reports)
CHRONIC FATIGUE SYNDROME ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 7 FDA reports)
COLD AGGLUTININS POSITIVE ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
COLONIC FISTULA ( 7 FDA reports)
COLORECTAL CANCER ( 7 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 7 FDA reports)
CONJUNCTIVITIS VIRAL ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 7 FDA reports)
CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
CRANIAL NERVE DISORDER ( 7 FDA reports)
CRANIAL NERVE PARALYSIS ( 7 FDA reports)
CYSTIC LYMPHANGIOMA ( 7 FDA reports)
CYTARABINE SYNDROME ( 7 FDA reports)
DENGUE FEVER ( 7 FDA reports)
DEPRESSIVE SYMPTOM ( 7 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 7 FDA reports)
DRUG INTERACTION POTENTIATION ( 7 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 7 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 7 FDA reports)
DYSPNOEA AT REST ( 7 FDA reports)
EARLY MORNING AWAKENING ( 7 FDA reports)
ENEMA ADMINISTRATION ( 7 FDA reports)
EPICONDYLITIS ( 7 FDA reports)
EPIDURAL LIPOMATOSIS ( 7 FDA reports)
ESSENTIAL TREMOR ( 7 FDA reports)
FACTITIOUS DISORDER ( 7 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 7 FDA reports)
FIBROMA ( 7 FDA reports)
FINE MOTOR DELAY ( 7 FDA reports)
FIXED ERUPTION ( 7 FDA reports)
FLIGHT OF IDEAS ( 7 FDA reports)
FOETAL MOVEMENTS DECREASED ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 7 FDA reports)
FUNGAL OESOPHAGITIS ( 7 FDA reports)
GALLBLADDER CANCER ( 7 FDA reports)
GALLBLADDER PAIN ( 7 FDA reports)
GAMMOPATHY ( 7 FDA reports)
GASTRIC BYPASS ( 7 FDA reports)
GASTRIC INFECTION ( 7 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 7 FDA reports)
GASTROENTERITIS BACTERIAL ( 7 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 7 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 7 FDA reports)
GASTROSCHISIS ( 7 FDA reports)
GENITAL EROSION ( 7 FDA reports)
GLOMERULONEPHROPATHY ( 7 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 7 FDA reports)
GRAFT INFECTION ( 7 FDA reports)
GROWTH RETARDATION ( 7 FDA reports)
HAEMOGLOBINURIA ( 7 FDA reports)
HEAD TITUBATION ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HEPATECTOMY ( 7 FDA reports)
HEPATIC INFARCTION ( 7 FDA reports)
HEPATIC INFECTION FUNGAL ( 7 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 7 FDA reports)
HEPATOBILIARY DISEASE ( 7 FDA reports)
HYPERTELORISM OF ORBIT ( 7 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 7 FDA reports)
INCISION SITE OEDEMA ( 7 FDA reports)
INDURATION ( 7 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
INGUINAL MASS ( 7 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 7 FDA reports)
IRIS ADHESIONS ( 7 FDA reports)
KIDNEY SMALL ( 7 FDA reports)
LEUKOPLAKIA ORAL ( 7 FDA reports)
LIMB CRUSHING INJURY ( 7 FDA reports)
LINEAR IGA DISEASE ( 7 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 6 FDA reports)
ABORTION THREATENED ( 6 FDA reports)
ACARODERMATITIS ( 6 FDA reports)
ACUTE LUNG INJURY ( 6 FDA reports)
ADENOCARCINOMA PANCREAS ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 6 FDA reports)
ALBUMIN URINE PRESENT ( 6 FDA reports)
AMBLYOPIA ( 6 FDA reports)
AMINOACIDURIA ( 6 FDA reports)
ANAEMIA MEGALOBLASTIC ( 6 FDA reports)
ANGIOMYOLIPOMA ( 6 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 6 FDA reports)
ANION GAP ABNORMAL ( 6 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 6 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 6 FDA reports)
ANTEROGRADE AMNESIA ( 6 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 6 FDA reports)
ANTISOCIAL BEHAVIOUR ( 6 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 6 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 6 FDA reports)
BACTERIAL TRACHEITIS ( 6 FDA reports)
BALANITIS ( 6 FDA reports)
BASE EXCESS DECREASED ( 6 FDA reports)
BELLIGERENCE ( 6 FDA reports)
BENIGN NEOPLASM ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BENIGN OVARIAN TUMOUR ( 6 FDA reports)
BITE ( 6 FDA reports)
BLOOD BILIRUBIN DECREASED ( 6 FDA reports)
BLOOD FOLATE DECREASED ( 6 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 6 FDA reports)
BODY DYSMORPHIC DISORDER ( 6 FDA reports)
BONE FISTULA ( 6 FDA reports)
BORRELIA INFECTION ( 6 FDA reports)
BRAIN HYPOXIA ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BREAST CALCIFICATIONS ( 6 FDA reports)
BURKITT'S LYMPHOMA ( 6 FDA reports)
BURSITIS INFECTIVE ( 6 FDA reports)
CAMPYLOBACTER INFECTION ( 6 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 6 FDA reports)
CARDIAC ABLATION ( 6 FDA reports)
CARDIAC DISCOMFORT ( 6 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 6 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 6 FDA reports)
CATHETER SITE DISCHARGE ( 6 FDA reports)
CATHETER SITE SWELLING ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 6 FDA reports)
CHEST WALL OPERATION ( 6 FDA reports)
CHONDROPATHY ( 6 FDA reports)
CHRONIC HEPATIC FAILURE ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COLOUR BLINDNESS ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 6 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 6 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 6 FDA reports)
COOMBS TEST POSITIVE ( 6 FDA reports)
COR PULMONALE CHRONIC ( 6 FDA reports)
CORNEAL PERFORATION ( 6 FDA reports)
CYANOSIS NEONATAL ( 6 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 6 FDA reports)
DANDRUFF ( 6 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 6 FDA reports)
DEMENTIA WITH LEWY BODIES ( 6 FDA reports)
DENTAL TREATMENT ( 6 FDA reports)
DEPERSONALISATION ( 6 FDA reports)
DEVICE LEAKAGE ( 6 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 6 FDA reports)
DIABETIC ULCER ( 6 FDA reports)
DNA ANTIBODY POSITIVE ( 6 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 6 FDA reports)
EAR CONGESTION ( 6 FDA reports)
EJECTION FRACTION ABNORMAL ( 6 FDA reports)
ENERGY INCREASED ( 6 FDA reports)
ERYTHEMA ANNULARE ( 6 FDA reports)
ERYTHEMA OF EYELID ( 6 FDA reports)
ERYTHRODERMIC PSORIASIS ( 6 FDA reports)
ERYTHROPENIA ( 6 FDA reports)
FACTOR VIII INHIBITION ( 6 FDA reports)
FALLOPIAN TUBE OPERATION ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
FEMORAL NERVE PALSY ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
FOOD ALLERGY ( 6 FDA reports)
FOOD CRAVING ( 6 FDA reports)
FUNGAL TEST POSITIVE ( 6 FDA reports)
GASTROENTERITIS NOROVIRUS ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GASTROINTESTINAL FISTULA ( 6 FDA reports)
GASTROINTESTINAL NEOPLASM ( 6 FDA reports)
GASTROINTESTINAL TOXICITY ( 6 FDA reports)
GENITAL DISCOMFORT ( 6 FDA reports)
GESTATIONAL DIABETES ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 6 FDA reports)
H1N1 INFLUENZA ( 6 FDA reports)
HAEMANGIOMA CONGENITAL ( 6 FDA reports)
HEART TRANSPLANT REJECTION ( 6 FDA reports)
HELMINTHIC INFECTION ( 6 FDA reports)
HEPATIC INFECTION ( 6 FDA reports)
HEPATITIS A ( 6 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 6 FDA reports)
HEPATITIS ALCOHOLIC ( 6 FDA reports)
HEPATITIS INFECTIOUS ( 6 FDA reports)
HETEROTAXIA ( 6 FDA reports)
HIV INFECTION ( 6 FDA reports)
HOSPICE CARE ( 6 FDA reports)
HYPERCHLORHYDRIA ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 6 FDA reports)
HYPERPROLACTINAEMIA ( 6 FDA reports)
HYPERPROTEINAEMIA ( 6 FDA reports)
HYPERSEXUALITY ( 6 FDA reports)
HYPERTENSIVE EMERGENCY ( 6 FDA reports)
HYPERTHERMIA MALIGNANT ( 6 FDA reports)
HYPERTROPHY ( 6 FDA reports)
HYPOPHYSITIS ( 6 FDA reports)
ILEAL ULCER ( 6 FDA reports)
ILIAC ARTERY THROMBOSIS ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INFUSION SITE HAEMATOMA ( 6 FDA reports)
INFUSION SITE HAEMORRHAGE ( 6 FDA reports)
INGUINAL HERNIA REPAIR ( 6 FDA reports)
INGUINAL HERNIA STRANGULATED ( 6 FDA reports)
INHIBITORY DRUG INTERACTION ( 6 FDA reports)
INJECTION SITE OEDEMA ( 6 FDA reports)
INJECTION SITE PAPULE ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
INTRACRANIAL HAEMATOMA ( 6 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 6 FDA reports)
JOINT DESTRUCTION ( 6 FDA reports)
KAWASAKI'S DISEASE ( 6 FDA reports)
KERATITIS INTERSTITIAL ( 6 FDA reports)
LARYNGEAL STENOSIS ( 6 FDA reports)
LEUKAEMIA RECURRENT ( 6 FDA reports)
LIPOMA EXCISION ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
LYMPH NODE PALPABLE ( 6 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 6 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 6 FDA reports)
LYMPHOHISTIOCYTOSIS ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MANTLE CELL LYMPHOMA ( 6 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 6 FDA reports)
MENINGEAL NEOPLASM ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
METAPNEUMOVIRUS INFECTION ( 6 FDA reports)
METASTASES TO HEART ( 6 FDA reports)
METASTASES TO THE MEDIASTINUM ( 6 FDA reports)
MICROGNATHIA ( 6 FDA reports)
MICROTIA ( 6 FDA reports)
MITOCHONDRIAL MYOPATHY ( 6 FDA reports)
MONONEUROPATHY ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MUNCHAUSEN'S SYNDROME ( 6 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
MYRINGOTOMY ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEONATAL EXCHANGE BLOOD TRANSFUSION ( 6 FDA reports)
NERVE ROOT INJURY LUMBAR ( 6 FDA reports)
NEUROENDOCRINE CARCINOMA ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NOCTURNAL DYSPNOEA ( 6 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 6 FDA reports)
OBSTRUCTION GASTRIC ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 6 FDA reports)
ONYCHOGRYPHOSIS ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
OPTIC NERVE CUPPING ( 6 FDA reports)
ORAL DYSAESTHESIA ( 6 FDA reports)
ORAL MUCOSAL DISORDER ( 6 FDA reports)
ORAL SOFT TISSUE DISORDER ( 6 FDA reports)
ORTHOSIS USER ( 6 FDA reports)
OSTEOCHONDRITIS ( 6 FDA reports)
PAIN EXACERBATED ( 6 FDA reports)
PALMAR ERYTHEMA ( 6 FDA reports)
PARALYSIS FLACCID ( 6 FDA reports)
PARANASAL CYST ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
PERICARDIAL CYST ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PERITONEAL CARCINOMA ( 6 FDA reports)
PHARYNGEAL ABSCESS ( 6 FDA reports)
PHARYNGITIS BACTERIAL ( 6 FDA reports)
PLEURAL INFECTION ( 6 FDA reports)
PNEUMATOSIS ( 6 FDA reports)
PNEUMOCOCCAL SEPSIS ( 6 FDA reports)
PNEUMONIA ESCHERICHIA ( 6 FDA reports)
POLYCYSTIC OVARIES ( 6 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 6 FDA reports)
POSTNASAL DRIP ( 6 FDA reports)
PRESSURE OF SPEECH ( 6 FDA reports)
PROCEDURAL SITE REACTION ( 6 FDA reports)
PROPOFOL INFUSION SYNDROME ( 6 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
PULMONARY ARTERY ATRESIA ( 6 FDA reports)
PULMONARY HILUM MASS ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
READING DISORDER ( 6 FDA reports)
RECTAL TENESMUS ( 6 FDA reports)
RECTOSIGMOID CANCER ( 6 FDA reports)
RENAL ANEURYSM ( 6 FDA reports)
RENAL CYST HAEMORRHAGE ( 6 FDA reports)
RENAL NEOPLASM ( 6 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 6 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 6 FDA reports)
RHEUMATOID LUNG ( 6 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SCROTAL PAIN ( 6 FDA reports)
SECONDARY SYPHILIS ( 6 FDA reports)
SENSORIMOTOR DISORDER ( 6 FDA reports)
SHIFT TO THE LEFT ( 6 FDA reports)
SINUS OPERATION ( 6 FDA reports)
SKIN ULCER HAEMORRHAGE ( 6 FDA reports)
SPINAL CLAUDICATION ( 6 FDA reports)
SPINAL CORD INJURY ( 6 FDA reports)
SPINAL FUSION ACQUIRED ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
SPLENIC INJURY ( 6 FDA reports)
SPUTUM ABNORMAL ( 6 FDA reports)
STATUS ASTHMATICUS ( 6 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 6 FDA reports)
TABLET PHYSICAL ISSUE ( 6 FDA reports)
TACHYCARDIA PAROXYSMAL ( 6 FDA reports)
THEFT ( 6 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 6 FDA reports)
THERMOHYPOAESTHESIA ( 6 FDA reports)
THREATENED LABOUR ( 6 FDA reports)
THYMOMA ( 6 FDA reports)
THYROID CANCER METASTATIC ( 6 FDA reports)
THYROID MASS ( 6 FDA reports)
TOE DEFORMITY ( 6 FDA reports)
TOE OPERATION ( 6 FDA reports)
TOOTH INJURY ( 6 FDA reports)
TRAUMATIC FRACTURE ( 6 FDA reports)
TRYPTASE INCREASED ( 6 FDA reports)
TUMOUR ASSOCIATED FEVER ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
URINARY BLADDER POLYP ( 6 FDA reports)
URINOMA ( 6 FDA reports)
UTERINE DILATION AND CURETTAGE ( 6 FDA reports)
VAGINAL DISORDER ( 6 FDA reports)
VAGINAL EROSION ( 6 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 6 FDA reports)
VASCULITIS CEREBRAL ( 6 FDA reports)
VENTRICULAR FAILURE ( 6 FDA reports)
VIBRATORY SENSE INCREASED ( 6 FDA reports)
VIRAL MYOCARDITIS ( 6 FDA reports)
VIRAL OESOPHAGITIS ( 6 FDA reports)
VITAL CAPACITY DECREASED ( 6 FDA reports)
VOCAL CORD POLYP ( 6 FDA reports)
VULVAL ABSCESS ( 6 FDA reports)
VULVOVAGINAL PRURITUS ( 6 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 6 FDA reports)
WOUND INFECTION BACTERIAL ( 6 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 6 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 5 FDA reports)
LYMPHATIC OBSTRUCTION ( 5 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 5 FDA reports)
MALARIA ( 5 FDA reports)
MALIGNANT MELANOMA IN SITU ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
MEDIASTINAL HAEMATOMA ( 5 FDA reports)
MESOTHELIOMA ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MONOCYTOSIS ( 5 FDA reports)
MOTION SICKNESS ( 5 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 5 FDA reports)
MUSCLE ENZYME INCREASED ( 5 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 5 FDA reports)
MYOCLONIC EPILEPSY ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
NECROSIS ISCHAEMIC ( 5 FDA reports)
NECROTISING RETINITIS ( 5 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 5 FDA reports)
NEONATAL TACHYCARDIA ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 5 FDA reports)
NO ADVERSE EFFECT ( 5 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 5 FDA reports)
OESOPHAGEAL ACHALASIA ( 5 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 5 FDA reports)
OPIATES POSITIVE ( 5 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 5 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
OSTEOTOMY ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PAINFUL ERECTION ( 5 FDA reports)
PANCREATIC HAEMORRHAGE ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARATHYROID DISORDER ( 5 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 5 FDA reports)
PELVIC FLUID COLLECTION ( 5 FDA reports)
PERIODONTAL OPERATION ( 5 FDA reports)
PERIVASCULAR DERMATITIS ( 5 FDA reports)
PHARYNGEAL EROSION ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PHLEBOTHROMBOSIS ( 5 FDA reports)
PHOSPHENES ( 5 FDA reports)
POOR PERSONAL HYGIENE ( 5 FDA reports)
POOR SUCKING REFLEX ( 5 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 5 FDA reports)
POST PROCEDURAL DISCOMFORT ( 5 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROCALCITONIN INCREASED ( 5 FDA reports)
PRODUCT CONTAMINATION ( 5 FDA reports)
PROSTATIC CALCIFICATION ( 5 FDA reports)
PROSTHESIS IMPLANTATION ( 5 FDA reports)
PROTEIN TOTAL ABNORMAL ( 5 FDA reports)
PSEUDOPARALYSIS ( 5 FDA reports)
PTERYGIUM ( 5 FDA reports)
PULMONARY ARTERY STENOSIS ( 5 FDA reports)
PULMONARY EOSINOPHILIA ( 5 FDA reports)
PULMONARY HYPOPLASIA ( 5 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 5 FDA reports)
PULMONARY VEIN STENOSIS ( 5 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
PYODERMA ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 5 FDA reports)
RADIATION NECROSIS ( 5 FDA reports)
REBOUND EFFECT ( 5 FDA reports)
RED BLOOD CELLS URINE ( 5 FDA reports)
RENAL APLASIA ( 5 FDA reports)
RENAL LIPOMATOSIS ( 5 FDA reports)
RENAL NECROSIS ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 5 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
RETINAL INFARCTION ( 5 FDA reports)
RETINAL OEDEMA ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RETINAL VEIN OCCLUSION ( 5 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 5 FDA reports)
REYE'S SYNDROME ( 5 FDA reports)
RHEUMATIC FEVER ( 5 FDA reports)
SALIVARY GLAND CALCULUS ( 5 FDA reports)
SCAN BONE MARROW ABNORMAL ( 5 FDA reports)
SCROTAL IRRITATION ( 5 FDA reports)
SEIZURE LIKE PHENOMENA ( 5 FDA reports)
SENSATION OF BLOCK IN EAR ( 5 FDA reports)
SENSE OF OPPRESSION ( 5 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 5 FDA reports)
SIMPLE PARTIAL SEIZURES ( 5 FDA reports)
SKIN BACTERIAL INFECTION ( 5 FDA reports)
SKIN FRAGILITY ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SPASTIC DIPLEGIA ( 5 FDA reports)
SPONDYLOARTHROPATHY ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
STEATORRHOEA ( 5 FDA reports)
SUBACUTE ENDOCARDITIS ( 5 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 5 FDA reports)
SYPHILIS ( 5 FDA reports)
TESTICULAR ATROPHY ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 5 FDA reports)
THERAPY CESSATION ( 5 FDA reports)
THERMOHYPERAESTHESIA ( 5 FDA reports)
THOUGHT BLOCKING ( 5 FDA reports)
THYROIDECTOMY ( 5 FDA reports)
TONGUE BLISTERING ( 5 FDA reports)
TOOTH REPAIR ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
TRANCE ( 5 FDA reports)
TRIGGER FINGER ( 5 FDA reports)
TRISOMY 21 ( 5 FDA reports)
TROUSSEAU'S SYNDROME ( 5 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 5 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
UMBILICAL HERNIA REPAIR ( 5 FDA reports)
UTERINE INFECTION ( 5 FDA reports)
VAGINAL CANCER ( 5 FDA reports)
VAGINAL FISTULA ( 5 FDA reports)
VAGINAL LESION ( 5 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 5 FDA reports)
VASCULAR INSUFFICIENCY ( 5 FDA reports)
VENOUS STASIS ( 5 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 5 FDA reports)
VIRAL LOAD INCREASED ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ABNORMAL CHEST SOUND ( 5 FDA reports)
ACTINIC ELASTOSIS ( 5 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 5 FDA reports)
ACUTE TONSILLITIS ( 5 FDA reports)
ADDISON'S DISEASE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
ALDOLASE INCREASED ( 5 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 5 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 5 FDA reports)
ALVEOLITIS FIBROSING ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
ANION GAP ( 5 FDA reports)
ANION GAP DECREASED ( 5 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 5 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 5 FDA reports)
APPLICATION SITE DISCOLOURATION ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ATOPY ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
AXILLARY MASS ( 5 FDA reports)
AXONAL NEUROPATHY ( 5 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 5 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 5 FDA reports)
BACTERIA URINE ( 5 FDA reports)
BALINT'S SYNDROME ( 5 FDA reports)
BASE EXCESS ( 5 FDA reports)
BASE EXCESS INCREASED ( 5 FDA reports)
BASEDOW'S DISEASE ( 5 FDA reports)
BEZOAR ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BIFASCICULAR BLOCK ( 5 FDA reports)
BIOPSY BREAST ABNORMAL ( 5 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 5 FDA reports)
BLADDER CANCER STAGE III ( 5 FDA reports)
BLADDER DISCOMFORT ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLADDER PERFORATION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 5 FDA reports)
BLOOD CREATINE DECREASED ( 5 FDA reports)
BLOOD CREATININE ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BLUNTED AFFECT ( 5 FDA reports)
BODY MASS INDEX DECREASED ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BONE DEFORMITY ( 5 FDA reports)
BONE DENSITY INCREASED ( 5 FDA reports)
BONE METABOLISM DISORDER ( 5 FDA reports)
BOWEN'S DISEASE ( 5 FDA reports)
BREAST INDURATION ( 5 FDA reports)
BREAST SWELLING ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
BUNION OPERATION ( 5 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 5 FDA reports)
CAROTID ARTERY ATHEROMA ( 5 FDA reports)
CAROTID ARTERY DISSECTION ( 5 FDA reports)
CARTILAGE INJURY ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CATHETER SITE HAEMATOMA ( 5 FDA reports)
CATHETER SITE INFLAMMATION ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 5 FDA reports)
CEREBRAL CYST ( 5 FDA reports)
CEREBROVASCULAR SPASM ( 5 FDA reports)
CHEMICAL POISONING ( 5 FDA reports)
CHOLESTEATOMA ( 5 FDA reports)
CHOLURIA ( 5 FDA reports)
CHOREOATHETOSIS ( 5 FDA reports)
CITROBACTER INFECTION ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
CNS VENTRICULITIS ( 5 FDA reports)
COLON CANCER RECURRENT ( 5 FDA reports)
CONGENITAL AORTIC STENOSIS ( 5 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 5 FDA reports)
CONGENITAL NAEVUS ( 5 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 5 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 5 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 5 FDA reports)
CONTRAST MEDIA REACTION ( 5 FDA reports)
CORNEAL NEOVASCULARISATION ( 5 FDA reports)
CORONARY ARTERY EMBOLISM ( 5 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 5 FDA reports)
CYANOPSIA ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DENTAL PULP DISORDER ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 5 FDA reports)
DROP ATTACKS ( 5 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 5 FDA reports)
DRUG DIVERSION ( 5 FDA reports)
DRUG HALF-LIFE INCREASED ( 5 FDA reports)
DRUG TOLERANCE INCREASED ( 5 FDA reports)
DRY GANGRENE ( 5 FDA reports)
DUODENAL OBSTRUCTION ( 5 FDA reports)
DYSCHEZIA ( 5 FDA reports)
DYSPLASTIC NAEVUS ( 5 FDA reports)
EAR NEOPLASM ( 5 FDA reports)
EATING DISORDER SYMPTOM ( 5 FDA reports)
ENCEPHALITIC INFECTION ( 5 FDA reports)
ENDOCARDIAL FIBROSIS ( 5 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 5 FDA reports)
ENTEROBACTER PNEUMONIA ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 5 FDA reports)
EPIDERMOLYSIS BULLOSA ( 5 FDA reports)
EPIDURITIS ( 5 FDA reports)
EPISCLERITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 5 FDA reports)
EXCESSIVE EYE BLINKING ( 5 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 5 FDA reports)
EXSANGUINATION ( 5 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 5 FDA reports)
EYE ABSCESS ( 5 FDA reports)
EYELID FUNCTION DISORDER ( 5 FDA reports)
FACIAL DYSMORPHISM ( 5 FDA reports)
FACIAL NERVE DISORDER ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FACTOR V DEFICIENCY ( 5 FDA reports)
FAT EMBOLISM ( 5 FDA reports)
FEELING GUILTY ( 5 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 5 FDA reports)
FIBROADENOMA OF BREAST ( 5 FDA reports)
FINGER AMPUTATION ( 5 FDA reports)
FOETAL DISORDER ( 5 FDA reports)
FOOD INTERACTION ( 5 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 5 FDA reports)
FOREIGN BODY ASPIRATION ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
FUNGAL RHINITIS ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL SURGERY ( 5 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 5 FDA reports)
GLARE ( 5 FDA reports)
GLOBAL AMNESIA ( 5 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 5 FDA reports)
GRANULOMA SKIN ( 5 FDA reports)
HAEMANGIOMA OF SKIN ( 5 FDA reports)
HAEMATOCRIT ABNORMAL ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMOCONCENTRATION ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEPATIC ISCHAEMIA ( 5 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 5 FDA reports)
HEREDITARY ANGIOEDEMA ( 5 FDA reports)
HIRSUTISM ( 5 FDA reports)
HY'S LAW CASE ( 5 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
HYPOCAPNIA ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INAPPROPRIATE AFFECT ( 5 FDA reports)
INDIFFERENCE ( 5 FDA reports)
INFECTED CYST ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE COLDNESS ( 5 FDA reports)
INJECTION SITE DISCHARGE ( 5 FDA reports)
INJECTION SITE DRYNESS ( 5 FDA reports)
INTERCEPTED MEDICATION ERROR ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
JOINT ANKYLOSIS ( 5 FDA reports)
JOINT WARMTH ( 5 FDA reports)
KETONURIA ( 5 FDA reports)
KYPHOSCOLIOSIS ( 5 FDA reports)
LABIA ENLARGED ( 5 FDA reports)
LARYNGOMALACIA ( 5 FDA reports)
LEUKAEMIA PLASMACYTIC ( 5 FDA reports)
LICHEN SCLEROSUS ( 5 FDA reports)
LIMB REDUCTION DEFECT ( 5 FDA reports)
LIP INJURY ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
LIPOATROPHY ( 5 FDA reports)
LIPODYSTROPHY ACQUIRED ( 5 FDA reports)
LIPOMATOSIS ( 5 FDA reports)
ABDOMINAL WALL INFECTION ( 4 FDA reports)
ACID FAST STAIN POSITIVE ( 4 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 4 FDA reports)
ACUTE CHEST SYNDROME ( 4 FDA reports)
ACUTE PHASE REACTION ( 4 FDA reports)
ACUTE STRESS DISORDER ( 4 FDA reports)
AGITATION NEONATAL ( 4 FDA reports)
AGITATION POSTOPERATIVE ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
ALCOHOLIC SEIZURE ( 4 FDA reports)
ALLERGIC BRONCHITIS ( 4 FDA reports)
AMAUROSIS ( 4 FDA reports)
AMINO ACID LEVEL INCREASED ( 4 FDA reports)
ANAEMIA NEONATAL ( 4 FDA reports)
ANAL CANDIDIASIS ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 4 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 4 FDA reports)
ANASTOMOTIC COMPLICATION ( 4 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 4 FDA reports)
ANEURYSM RUPTURED ( 4 FDA reports)
ANGIODERMATITIS ( 4 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 4 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 4 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AORTIC EMBOLUS ( 4 FDA reports)
APICAL GRANULOMA ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APOPTOSIS ( 4 FDA reports)
APPLICATION SITE SCAB ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARACHNOID CYST ( 4 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 4 FDA reports)
ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
ARTHROPOD STING ( 4 FDA reports)
ASCITES INFECTION ( 4 FDA reports)
ASPERGER'S DISORDER ( 4 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
ATRIAL PRESSURE INCREASED ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
AUTISM SPECTRUM DISORDER ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
BALANITIS CANDIDA ( 4 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 4 FDA reports)
BENIGN BREAST NEOPLASM ( 4 FDA reports)
BENIGN LUNG NEOPLASM ( 4 FDA reports)
BENIGN RESPIRATORY TRACT NEOPLASM ( 4 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 4 FDA reports)
BICUSPID AORTIC VALVE ( 4 FDA reports)
BILE DUCT NECROSIS ( 4 FDA reports)
BILIARY SEPSIS ( 4 FDA reports)
BLADDER CYST ( 4 FDA reports)
BLEEDING TIME ABNORMAL ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD AMYLASE DECREASED ( 4 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 4 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BOVINE TUBERCULOSIS ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST OEDEMA ( 4 FDA reports)
BRONCHIAL HAEMORRHAGE ( 4 FDA reports)
BRONCHIAL IRRITATION ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 4 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CALCIUM IONISED INCREASED ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 4 FDA reports)
CARDIOMYOPATHY ACUTE ( 4 FDA reports)
CATHETER SITE RASH ( 4 FDA reports)
CELL MARKER INCREASED ( 4 FDA reports)
CENTRAL OBESITY ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 4 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 4 FDA reports)
CHEMICAL INJURY ( 4 FDA reports)
CHEST INJURY ( 4 FDA reports)
CHROMOSOMAL DELETION ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
COAGULATION FACTOR INCREASED ( 4 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 4 FDA reports)
COLLAGEN DISORDER ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 4 FDA reports)
COLORECTAL CANCER METASTATIC ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CONFUSION POSTOPERATIVE ( 4 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 4 FDA reports)
CONGENITAL HYDROCEPHALUS ( 4 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
CONVULSION NEONATAL ( 4 FDA reports)
CORNEAL TRANSPLANT ( 4 FDA reports)
CRANIOPHARYNGIOMA ( 4 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
CROSS SENSITIVITY REACTION ( 4 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 4 FDA reports)
CULTURE THROAT POSITIVE ( 4 FDA reports)
CYST REMOVAL ( 4 FDA reports)
CYSTITIS ESCHERICHIA ( 4 FDA reports)
CYSTOPEXY ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DENTAL NECROSIS ( 4 FDA reports)
DENTOFACIAL ANOMALY ( 4 FDA reports)
DESQUAMATION MOUTH ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIASTOLIC HYPERTENSION ( 4 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 4 FDA reports)
DOUBLE HETEROZYGOUS SICKLING DISORDERS ( 4 FDA reports)
DRUG EFFECT PROLONGED ( 4 FDA reports)
DUODENAL POLYP ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
ECHOLALIA ( 4 FDA reports)
ECZEMA NUMMULAR ( 4 FDA reports)
EDUCATIONAL PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
ENCEPHALOMYELITIS ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
ENDOMETRIAL DISORDER ( 4 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 4 FDA reports)
ENZYME ABNORMALITY ( 4 FDA reports)
EPIGLOTTITIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 4 FDA reports)
ERYTHROSIS ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYELID MARGIN CRUSTING ( 4 FDA reports)
EYES SUNKEN ( 4 FDA reports)
FAECAL VOLUME DECREASED ( 4 FDA reports)
FAILURE TO ANASTOMOSE ( 4 FDA reports)
FALLOPIAN TUBE DISORDER ( 4 FDA reports)
FANCONI SYNDROME ACQUIRED ( 4 FDA reports)
FEBRILE INFECTION ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 4 FDA reports)
FEMORAL ARTERY ANEURYSM ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOETAL HAEMOGLOBIN INCREASED ( 4 FDA reports)
GALLBLADDER OBSTRUCTION ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GAMBLING ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTRIC LAVAGE ( 4 FDA reports)
GASTRIC VOLVULUS ( 4 FDA reports)
GASTRITIS HYPERTROPHIC ( 4 FDA reports)
GASTROINTESTINAL STENOSIS ( 4 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GENITAL INFECTION FEMALE ( 4 FDA reports)
GENITAL LABIAL ADHESIONS ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 4 FDA reports)
GLOSSOPTOSIS ( 4 FDA reports)
GOUTY TOPHUS ( 4 FDA reports)
GRANULOCYTES MATURATION ARREST ( 4 FDA reports)
GROWTH OF EYELASHES ( 4 FDA reports)
HAEMOPHILUS SEPSIS ( 4 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 4 FDA reports)
HEAT EXHAUSTION ( 4 FDA reports)
HEAT STROKE ( 4 FDA reports)
HEMICEPHALALGIA ( 4 FDA reports)
HEPATIC VEIN THROMBOSIS ( 4 FDA reports)
HEPATITIS C RNA INCREASED ( 4 FDA reports)
HEPATITIS C VIRUS ( 4 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOPITUITARISM ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 4 FDA reports)
IMPLANT SITE EROSION ( 4 FDA reports)
IMPRISONMENT ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INCISION SITE ABSCESS ( 4 FDA reports)
INCLUSION BODY MYOSITIS ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INDUCED LABOUR ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INFERTILITY FEMALE ( 4 FDA reports)
INFUSION SITE IRRITATION ( 4 FDA reports)
INFUSION SITE PRURITUS ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
INJECTION SITE PUSTULE ( 4 FDA reports)
INJECTION SITE SCAR ( 4 FDA reports)
INJECTION SITE THROMBOSIS ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTERTRIGO ( 4 FDA reports)
INTESTINAL ANASTOMOSIS ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LASER THERAPY ( 4 FDA reports)
LEGAL PROBLEM ( 4 FDA reports)
LEGIONELLA INFECTION ( 4 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 4 FDA reports)
LIMB ASYMMETRY ( 4 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 4 FDA reports)
LIVER TENDERNESS ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LOW TURNOVER OSTEOPATHY ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
LYMPHOCYTE COUNT ( 4 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MARITAL PROBLEM ( 4 FDA reports)
MASTITIS ( 4 FDA reports)
MAXILLOFACIAL OPERATION ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 4 FDA reports)
MEASLES ( 4 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 4 FDA reports)
MELAS SYNDROME ( 4 FDA reports)
MENINGITIS MENINGOCOCCAL ( 4 FDA reports)
MENSTRUATION DELAYED ( 4 FDA reports)
METASTASES TO BREAST ( 4 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 4 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 4 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 4 FDA reports)
MITRAL VALVE HYPOPLASIA ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MOTOR NEURONE DISEASE ( 4 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 4 FDA reports)
MUSCLE SWELLING ( 4 FDA reports)
MYELOID LEUKAEMIA ( 4 FDA reports)
MYOCARDIAL STRAIN ( 4 FDA reports)
NASAL OEDEMA ( 4 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NEONATAL HYPOTENSION ( 4 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 4 FDA reports)
NEONATAL TACHYPNOEA ( 4 FDA reports)
NEOPLASM PROSTATE ( 4 FDA reports)
NEPHRITIS ALLERGIC ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 4 FDA reports)
NEUROBLASTOMA ( 4 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NON-HIGH-DENSITY LIPOPROTEIN CHOLESTEROL INCREASED ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OEDEMATOUS PANCREATITIS ( 4 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 4 FDA reports)
OESOPHAGEAL INFECTION ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
OSTEITIS DEFORMANS ( 4 FDA reports)
OSTEOCHONDROMA ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
OVARIAN ENLARGEMENT ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PANCREATIC ABSCESS ( 4 FDA reports)
PANCREATIC NEOPLASM ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PARAPHARYNGEAL ABSCESS ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 4 FDA reports)
PELIOSIS HEPATIS ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PENILE OEDEMA ( 4 FDA reports)
PENILE ULCERATION ( 4 FDA reports)
PERINEPHRIC COLLECTION ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PERTUSSIS ( 4 FDA reports)
PEYRONIE'S DISEASE ( 4 FDA reports)
PHANTOM PAIN ( 4 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 4 FDA reports)
PHOTODERMATOSIS ( 4 FDA reports)
PHOTOSENSITIVE RASH ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 4 FDA reports)
PLATELET AGGREGATION ( 4 FDA reports)
PLATELET TRANSFUSION ( 4 FDA reports)
POLYARTERITIS NODOSA ( 4 FDA reports)
POLYCYTHAEMIA VERA ( 4 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 4 FDA reports)
PORTAL VEIN PHLEBITIS ( 4 FDA reports)
POSITIVE ROMBERGISM ( 4 FDA reports)
POST CONCUSSION SYNDROME ( 4 FDA reports)
POST PROCEDURAL DISCHARGE ( 4 FDA reports)
POSTERIOR CAPSULOTOMY ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PROCTITIS ULCERATIVE ( 4 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 4 FDA reports)
PROTEIN S DECREASED ( 4 FDA reports)
PROTHROMBIN TIME ( 4 FDA reports)
PSEUDOPOLYP ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
RADIATION MUCOSITIS ( 4 FDA reports)
RADIATION OESOPHAGITIS ( 4 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 4 FDA reports)
RASH SCARLATINIFORM ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RECTAL PERFORATION ( 4 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
REFRACTIVE AMBLYOPIA ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
RENAL ARTERY THROMBOSIS ( 4 FDA reports)
RENAL CANCER METASTATIC ( 4 FDA reports)
RENAL HAEMATOMA ( 4 FDA reports)
RENAL VESSEL DISORDER ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETICULOCYTOSIS ( 4 FDA reports)
RETINAL ARTERY EMBOLISM ( 4 FDA reports)
RETINAL SCAR ( 4 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 4 FDA reports)
RETINAL VASCULITIS ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
RIB DEFORMITY ( 4 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 4 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SKIN INFLAMMATION ( 4 FDA reports)
SKULL MALFORMATION ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SLEEP WALKING ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 4 FDA reports)
SPLENIC ARTERY ANEURYSM ( 4 FDA reports)
SPONDYLITIC MYELOPATHY ( 4 FDA reports)
SPUTUM RETENTION ( 4 FDA reports)
STATUS MIGRAINOSUS ( 4 FDA reports)
SUBDURAL HYGROMA ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SUPERINFECTION BACTERIAL ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TEMPORAL LOBE EPILEPSY ( 4 FDA reports)
THALAMUS HAEMORRHAGE ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THORACIC CAVITY DRAINAGE ( 4 FDA reports)
THROMBIN TIME PROLONGED ( 4 FDA reports)
THYROID ADENOMA ( 4 FDA reports)
THYROTOXIC CRISIS ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TONSILLECTOMY ( 4 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRACHEOMALACIA ( 4 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 4 FDA reports)
TRAUMATIC LIVER INJURY ( 4 FDA reports)
TRICHOMONIASIS ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 4 FDA reports)
UMBILICAL CORD AROUND NECK ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
URINARY TRACT INFECTION VIRAL ( 4 FDA reports)
URINE BILIRUBIN INCREASED ( 4 FDA reports)
URINE CYTOLOGY ABNORMAL ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
URINE SODIUM INCREASED ( 4 FDA reports)
UROBILIN URINE PRESENT ( 4 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 4 FDA reports)
UTERINE HYPERTONUS ( 4 FDA reports)
UTERINE NEOPLASM ( 4 FDA reports)
VAGINAL PROLAPSE ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VEILLONELLA INFECTION ( 4 FDA reports)
VENOUS INJURY ( 4 FDA reports)
VESICOURETERIC REFLUX ( 4 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 4 FDA reports)
VICTIM OF HOMICIDE ( 4 FDA reports)
VIRAL RASH ( 4 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 4 FDA reports)
VISCERAL OEDEMA ( 4 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 4 FDA reports)
VISUAL BRIGHTNESS ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
VOCAL CORD THICKENING ( 4 FDA reports)
VOLUME BLOOD DECREASED ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 4 FDA reports)
WHIPLASH INJURY ( 4 FDA reports)
WOUND ABSCESS ( 4 FDA reports)
XANTHOCHROMIA ( 4 FDA reports)
LONG THORACIC NERVE PALSY ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
MACULE ( 3 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 3 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 3 FDA reports)
MASTOCYTOSIS ( 3 FDA reports)
MEDIASTINAL BIOPSY ( 3 FDA reports)
MEDICAL DEVICE PAIN ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 3 FDA reports)
MEGAKARYOCYTES DECREASED ( 3 FDA reports)
MEIBOMIANITIS ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENINGIOMA BENIGN ( 3 FDA reports)
MENINGOCOCCAL SEPSIS ( 3 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 3 FDA reports)
MESENTERIC PANNICULITIS ( 3 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 3 FDA reports)
METASTASES TO DIAPHRAGM ( 3 FDA reports)
METASTASES TO PELVIS ( 3 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 3 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
MIGRAINE WITHOUT AURA ( 3 FDA reports)
MILIA ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
MYOGLOBINAEMIA ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NAIL HYPERTROPHY ( 3 FDA reports)
NASAL CYST ( 3 FDA reports)
NASAL OBSTRUCTION ( 3 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 3 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEONATAL APNOEIC ATTACK ( 3 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 3 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROANGIOSCLEROSIS ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NERVE BLOCK ( 3 FDA reports)
NERVE DEGENERATION ( 3 FDA reports)
NEUROENDOCRINE TUMOUR ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
NEUROMYELITIS OPTICA ( 3 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 3 FDA reports)
NITRITE URINE ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OCULAR MYASTHENIA ( 3 FDA reports)
OCULOGYRIC CRISIS ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL IRRITATION ( 3 FDA reports)
OESTROGEN DEFICIENCY ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
ORTHOSTATIC INTOLERANCE ( 3 FDA reports)
OSTEOARTHROPATHY ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
OVARIAN EPITHELIAL CANCER ( 3 FDA reports)
OVARIAN FAILURE ( 3 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PANCOAST'S SYNDROME ( 3 FDA reports)
PANCREAS LIPOMATOSIS ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PANOPHTHALMITIS ( 3 FDA reports)
PARASPINAL ABSCESS ( 3 FDA reports)
PARATHYROID TUMOUR ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PEPTIC ULCER PERFORATION ( 3 FDA reports)
PERIDIVERTICULAR ABSCESS ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 3 FDA reports)
PERITONEAL NEOPLASM ( 3 FDA reports)
PERSISTENT LEFT SUPERIOR VENA CAVA ( 3 FDA reports)
PH BODY FLUID DECREASED ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PLEURAL INFECTION BACTERIAL ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PNEUMONIA ASPERGILLUS ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMONIA HERPES VIRAL ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYMENORRHOEA ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
PORTAL TRIADITIS ( 3 FDA reports)
POSITIONAL PLAGIOCEPHALY ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 3 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POSTOPERATIVE ABSCESS ( 3 FDA reports)
POSTRENAL FAILURE ( 3 FDA reports)
POVERTY OF SPEECH ( 3 FDA reports)
PREGNANCY TEST POSITIVE ( 3 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 3 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 3 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROTEIN C INCREASED ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PSEUDOPORPHYRIA ( 3 FDA reports)
PUBIC PAIN ( 3 FDA reports)
PULMONARY MALFORMATION ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
RADIATION FIBROSIS ( 3 FDA reports)
RADIATION PNEUMONITIS ( 3 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 3 FDA reports)
REBOUND HYPERTENSION ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
REFLUX LARYNGITIS ( 3 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 3 FDA reports)
RENAL SURGERY ( 3 FDA reports)
RESIDUAL URINE VOLUME ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
ROTATOR CUFF REPAIR ( 3 FDA reports)
ROTAVIRUS INFECTION ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALIVA DISCOLOURATION ( 3 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 3 FDA reports)
SALMONELLA SEPSIS ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SCROTAL DISORDER ( 3 FDA reports)
SCROTAL ERYTHEMA ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
SEIZURE CLUSTER ( 3 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SERUM FERRITIN ABNORMAL ( 3 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SINGLE UMBILICAL ARTERY ( 3 FDA reports)
SKIN BLEEDING ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOCIAL PHOBIA ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 3 FDA reports)
SPINE MALFORMATION ( 3 FDA reports)
SPONTANEOUS PENILE ERECTION ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STRESS ULCER ( 3 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 3 FDA reports)
SUBDURAL EMPYEMA ( 3 FDA reports)
SUBMANDIBULAR MASS ( 3 FDA reports)
SUPERINFECTION LUNG ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
TEETH BRITTLE ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 3 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 3 FDA reports)
THYROIDITIS ACUTE ( 3 FDA reports)
THYROIDITIS CHRONIC ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONGUE NEOPLASM ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 3 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TRICUSPID VALVE STENOSIS ( 3 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 3 FDA reports)
TUMOUR COMPRESSION ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
URETERAL NECROSIS ( 3 FDA reports)
URETERIC CANCER ( 3 FDA reports)
URETHRAL INJURY ( 3 FDA reports)
URETHRAL STRICTURE ( 3 FDA reports)
URINARY SEDIMENT ABNORMAL ( 3 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 3 FDA reports)
UTERINE ATONY ( 3 FDA reports)
UTERINE SPASM ( 3 FDA reports)
VAGINAL ULCERATION ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VARICOSE VEIN OPERATION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR STENOSIS ( 3 FDA reports)
VASCULAR STENT INSERTION ( 3 FDA reports)
VASOPLEGIA SYNDROME ( 3 FDA reports)
VENTRICULAR HYPOPLASIA ( 3 FDA reports)
VERBAL ABUSE ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VIRUS URINE TEST POSITIVE ( 3 FDA reports)
VITREOUS DEGENERATION ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
WAXY FLEXIBILITY ( 3 FDA reports)
WEIGHT ( 3 FDA reports)
WHITE BLOOD CELL ANALYSIS ( 3 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 3 FDA reports)
WHITE CLOT SYNDROME ( 3 FDA reports)
WOUND EVISCERATION ( 3 FDA reports)
WOUND INFECTION FUNGAL ( 3 FDA reports)
XERODERMA ( 3 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ABNORMAL CLOTTING FACTOR ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ABSCESS RUPTURE ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACINETOBACTER TEST POSITIVE ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 3 FDA reports)
ACTINOMYCES TEST POSITIVE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ADNEXA UTERI CYST ( 3 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 3 FDA reports)
ALLERGIC COLITIS ( 3 FDA reports)
ALLERGIC SINUSITIS ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANAL ATRESIA ( 3 FDA reports)
ANAL INFECTION ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANASTOMOTIC ULCER ( 3 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC BYPASS ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ARRESTED LABOUR ( 3 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 3 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ASPIRATION BONE MARROW ( 3 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 3 FDA reports)
ASPIRATION BRONCHIAL ( 3 FDA reports)
ASTHMA EXERCISE INDUCED ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
ATROPHIC GLOSSITIS ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 3 FDA reports)
AVERSION ( 3 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL PERICARDITIS ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BASE EXCESS NEGATIVE ( 3 FDA reports)
BENIGN NEOPLASM OF SKIN ( 3 FDA reports)
BILIARY CIRRHOSIS ( 3 FDA reports)
BIOPSY GINGIVAL ( 3 FDA reports)
BIOPSY LUNG ABNORMAL ( 3 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 3 FDA reports)
BIOPSY SKIN ( 3 FDA reports)
BIRTH TRAUMA ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER PAPILLOMA ( 3 FDA reports)
BLADDER SPHINCTER ATONY ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD ALCOHOL ( 3 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 3 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD FOLATE INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 3 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BONE DENSITY ABNORMAL ( 3 FDA reports)
BONE MARROW NECROSIS ( 3 FDA reports)
BONE SARCOMA ( 3 FDA reports)
BOTULISM ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BREATH SOUNDS ABSENT ( 3 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHITIS CHEMICAL ( 3 FDA reports)
CALCIFICATION METASTATIC ( 3 FDA reports)
CALLUS FORMATION DELAYED ( 3 FDA reports)
CARBUNCLE ( 3 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIAC VALVE SCLEROSIS ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 3 FDA reports)
CARDIOLIPIN ANTIBODY ( 3 FDA reports)
CATABOLIC STATE ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 3 FDA reports)
CEREBELLAR HAEMATOMA ( 3 FDA reports)
CERVIX DYSTOCIA ( 3 FDA reports)
CERVIX NEOPLASM ( 3 FDA reports)
CHALAZION ( 3 FDA reports)
CHEMICAL BURN OF SKIN ( 3 FDA reports)
CHEMICAL CYSTITIS ( 3 FDA reports)
CHLAMYDIA TEST POSITIVE ( 3 FDA reports)
CHONDROSARCOMA ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 3 FDA reports)
CLONAL EVOLUTION ( 3 FDA reports)
CLOSED FRACTURE MANIPULATION ( 3 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
COAGULATION FACTOR DECREASED ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COCCYDYNIA ( 3 FDA reports)
COGNITIVE DETERIORATION ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON INJURY ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLONIC HAEMORRHAGE ( 3 FDA reports)
CONFABULATION ( 3 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONGENITAL HAND MALFORMATION ( 3 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 3 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 3 FDA reports)
CONJUNCTIVAL ABRASION ( 3 FDA reports)
CONJUNCTIVAL EROSION ( 3 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 3 FDA reports)
COPPER DEFICIENCY ( 3 FDA reports)
CORNEAL INFECTION ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 3 FDA reports)
CRYPTOCOCCOSIS ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
CUBITAL TUNNEL SYNDROME ( 3 FDA reports)
CYCLOPIA ( 3 FDA reports)
CYSTOCELE REPAIR ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
CYTOKINE STORM ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 3 FDA reports)
DARK CIRCLES UNDER EYES ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DEATH OF PARENT ( 3 FDA reports)
DENTAL CARE ( 3 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DEXTROCARDIA ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC MICROANGIOPATHY ( 3 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 3 FDA reports)
DIPHTHERIA ( 3 FDA reports)
DISSOCIATIVE DISORDER ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG LEVEL ( 3 FDA reports)
DRUG NAME CONFUSION ( 3 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DUODENAL SCARRING ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
EAR MALFORMATION ( 3 FDA reports)
EBSTEIN'S ANOMALY ( 3 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ECZEMA EYELIDS ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROPHORESIS ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOTOXAEMIA ( 3 FDA reports)
ENTEROBACTER BACTERAEMIA ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 3 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 3 FDA reports)
EPIGLOTTIC OEDEMA ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 3 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EYE ALLERGY ( 3 FDA reports)
EYE INFECTION FUNGAL ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYELID CYST ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FACTOR V LEIDEN MUTATION ( 3 FDA reports)
FACTOR VII DEFICIENCY ( 3 FDA reports)
FAILURE OF CHILD RESISTANT MECHANISM FOR PHARMACEUTICAL PRODUCT ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FLUID IMBALANCE ( 3 FDA reports)
FLUID REPLACEMENT ( 3 FDA reports)
FOETAL HEART RATE DECREASED ( 3 FDA reports)
FOETAL HEART RATE DISORDER ( 3 FDA reports)
FORAMEN MAGNUM STENOSIS ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
FRACTURE TREATMENT ( 3 FDA reports)
FUNGAL ENDOCARDITIS ( 3 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 3 FDA reports)
FUNGUS URINE TEST POSITIVE ( 3 FDA reports)
FUSOBACTERIUM INFECTION ( 3 FDA reports)
GALLBLADDER NECROSIS ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 3 FDA reports)
GENITAL ABSCESS ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
GRUNTING ( 3 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 3 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATIC SIDEROSIS ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HEPATITIS C POSITIVE ( 3 FDA reports)
HEPATITIS E ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
HERPETIC GINGIVOSTOMATITIS ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HODGKIN'S DISEASE STAGE III ( 3 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 3 FDA reports)
HUNTINGTON'S DISEASE ( 3 FDA reports)
HYDROPS FOETALIS ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERPATHIA ( 3 FDA reports)
HYPERTONIA NEONATAL ( 3 FDA reports)
HYPOCHONDRIASIS ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
HYPOTHERMIA NEONATAL ( 3 FDA reports)
ILIUM FRACTURE ( 3 FDA reports)
IMPLANT SITE EFFUSION ( 3 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 3 FDA reports)
IMPLANT SITE INDURATION ( 3 FDA reports)
IMPLANT SITE PAIN ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 3 FDA reports)
INCISION SITE CELLULITIS ( 3 FDA reports)
INCISION SITE HAEMATOMA ( 3 FDA reports)
INCORRECT PRODUCT STORAGE ( 3 FDA reports)
INFANTILE SPITTING UP ( 3 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 3 FDA reports)
INFUSION SITE RASH ( 3 FDA reports)
INFUSION SITE URTICARIA ( 3 FDA reports)
INJECTION SITE ATROPHY ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INTERCOSTAL RETRACTION ( 3 FDA reports)
INTESTINAL ADENOCARCINOMA ( 3 FDA reports)
INTESTINAL GANGRENE ( 3 FDA reports)
INTRACARDIAC MASS ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 3 FDA reports)
INVESTIGATION ( 3 FDA reports)
JOINT ABSCESS ( 3 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 3 FDA reports)
JOINT STABILISATION ( 3 FDA reports)
JOINT SURGERY ( 3 FDA reports)
KELOID SCAR ( 3 FDA reports)
KERATOACANTHOMA ( 3 FDA reports)
KERATOPATHY ( 3 FDA reports)
KLIPPEL-FEIL SYNDROME ( 3 FDA reports)
KUSSMAUL RESPIRATION ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LACRIMATION DECREASED ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LENTICULAR OPACITIES ( 3 FDA reports)
LEUKODYSTROPHY ( 3 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ABNORMAL LABOUR ( 2 FDA reports)
ABORTION INFECTED ( 2 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACUTE FATTY LIVER OF PREGNANCY ( 2 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 2 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALPHA 1 MICROGLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
AMAUROSIS FUGAX ( 2 FDA reports)
AMAUROTIC FAMILIAL IDIOCY ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
AMNIORRHOEA ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL CANCER STAGE III ( 2 FDA reports)
ANAL INJURY ( 2 FDA reports)
ANALGESIC DRUG LEVEL ( 2 FDA reports)
ANALGESIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANALGESIC THERAPY ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
ANGIOSCLEROSIS ( 2 FDA reports)
ANTERIOR DISPLACED ANUS ( 2 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE COLD FEELING ( 2 FDA reports)
APPLICATION SITE PAPULES ( 2 FDA reports)
APPLICATION SITE PARAESTHESIA ( 2 FDA reports)
APPLICATION SITE PUSTULES ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARGININOSUCCINATE SYNTHETASE DEFICIENCY ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 2 FDA reports)
ATHERECTOMY ( 2 FDA reports)
ATRIOVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
AUTOANTIBODY POSITIVE ( 2 FDA reports)
BACILLUS TEST POSITIVE ( 2 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BENIGN TUMOUR EXCISION ( 2 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
BETA GLOBULIN INCREASED ( 2 FDA reports)
BILE CULTURE POSITIVE ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY BONE ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BIPOLAR II DISORDER ( 2 FDA reports)
BLADDER CANCER STAGE I, WITHOUT CANCER IN SITU ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLEEDING TIME ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CALCITONIN INCREASED ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD KETONE BODY INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 2 FDA reports)
BONE FISSURE ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRANCHIAL CYST ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 2 FDA reports)
BREAST PROSTHESIS USER ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BULLOUS IMPETIGO ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CAECAL LESION EXCISION ( 2 FDA reports)
CAFE AU LAIT SPOTS ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CANDIDA OSTEOMYELITIS ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARCINOID HEART DISEASE ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 2 FDA reports)
CARDIAC INDEX DECREASED ( 2 FDA reports)
CARDIAC SEPTAL DEFECT REPAIR ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIOSPASM ( 2 FDA reports)
CARNITINE DECREASED ( 2 FDA reports)
CARNITINE DEFICIENCY ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CAROTID PULSE ABNORMAL ( 2 FDA reports)
CARTILAGE ATROPHY ( 2 FDA reports)
CATARACT CONGENITAL ( 2 FDA reports)
CATHETER CULTURE POSITIVE ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 2 FDA reports)
CEREBELLAR HYPOPLASIA ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CEREBRAL FUNGAL INFECTION ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
CERVICAL NEURITIS ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHEST WALL CYST ( 2 FDA reports)
CHLOROPSIA ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHORIORETINAL DISORDER ( 2 FDA reports)
CHOROIDITIS ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CHRONIC TONSILLITIS ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
CLEFT UVULA ( 2 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 2 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLON CANCER STAGE II ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONGENITAL ACROCHORDON ( 2 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 2 FDA reports)
CONGENITAL GENITAL MALFORMATION FEMALE ( 2 FDA reports)
CONGENITAL HEARING DISORDER ( 2 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 2 FDA reports)
CONGENITAL INTESTINAL MALFORMATION ( 2 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 2 FDA reports)
CONGENITAL URETERIC ANOMALY ( 2 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONJUNCTIVAL PALLOR ( 2 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL GRAFT REJECTION ( 2 FDA reports)
CORNEAL LESION ( 2 FDA reports)
CORNEAL STAINING ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
COXSACKIE VIRAL INFECTION ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 2 FDA reports)
CRYOFIBRINOGENAEMIA ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
CSF PRESSURE ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYSTOSCOPY ABNORMAL ( 2 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 2 FDA reports)
DANDY-WALKER SYNDROME ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DEPENDENT RUBOR ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DERMATOSIS ( 2 FDA reports)
DERMO-HYPODERMITIS ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIASTOLIC HYPOTENSION ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISORDER OF ORBIT ( 2 FDA reports)
DISTICHIASIS ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG CLEARANCE INCREASED ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
DRUG LABEL CONFUSION ( 2 FDA reports)
DUODENAL FISTULA ( 2 FDA reports)
DURAL FISTULA ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELECTROLYTE DEPLETION ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENDOCARDIAL DISEASE ( 2 FDA reports)
ENDOCARDITIS PSEUDOMONAL ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENTEROSTOMY ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EVERSION OF LACRIMAL PUNCTUM ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EYE NAEVUS ( 2 FDA reports)
EYELID EROSION ( 2 FDA reports)
FACIAL NEURALGIA ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FASCIOTOMY ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FATTY ACID DEFICIENCY ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
FEVER NEONATAL ( 2 FDA reports)
FISTULA REPAIR ( 2 FDA reports)
FLUID INTAKE RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FOETAL HEART RATE INCREASED ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FONTANELLE DEPRESSED ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRO-JEJUNOSTOMY ( 2 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 2 FDA reports)
GASTROOESOPHAGITIS ( 2 FDA reports)
GAUCHER'S DISEASE ( 2 FDA reports)
GENDER IDENTITY DISORDER ( 2 FDA reports)
GENITAL CYST ( 2 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 2 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 2 FDA reports)
GLUCOSE URINE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GROSS MOTOR DELAY ( 2 FDA reports)
HAEMATINURIA ( 2 FDA reports)
HAEMATOCRIT ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 2 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
HAEMORRHAGIC ASCITES ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEARING DISABILITY ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEAT OEDEMA ( 2 FDA reports)
HEMIPLEGIA TRANSIENT ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATITIS A POSITIVE ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HERPES SEPSIS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HISTIOCYTOSIS ( 2 FDA reports)
HIV ANTIBODY POSITIVE ( 2 FDA reports)
HLA MARKER STUDY POSITIVE ( 2 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE III ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 2 FDA reports)
HUNTINGTON'S CHOREA ( 2 FDA reports)
HYALURONIC ACID INCREASED ( 2 FDA reports)
HYDROMETRA ( 2 FDA reports)
HYDROXYPROLINURIA ( 2 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOTELORISM OF ORBIT ( 2 FDA reports)
HYPOTONIC URINARY BLADDER ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
IMMOBILISATION PROLONGED ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCISION SITE BLISTER ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFANTILE SPASMS ( 2 FDA reports)
INFECTION MASKED ( 2 FDA reports)
INFECTION PROPHYLAXIS ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFERTILITY MALE ( 2 FDA reports)
INFLAMMATION LOCALISED ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE DISCOMFORT ( 2 FDA reports)
INFUSION SITE INDURATION ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INFUSION SITE WARMTH ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE CALCIFICATION ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERMEDIATE UVEITIS ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTERNAL INJURY ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL CYST ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IODINE ALLERGY ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
ISCHAEMIC NEUROPATHY ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
JAUNDICE ACHOLURIC ( 2 FDA reports)
JAUNDICE HEPATOCELLULAR ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
JEJUNAL STENOSIS ( 2 FDA reports)
JEJUNAL ULCER PERFORATION ( 2 FDA reports)
JEJUNOSTOMY ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KARNOFSKY SCALE WORSENED ( 2 FDA reports)
KIDNEY MALROTATION ( 2 FDA reports)
KIDNEY RUPTURE ( 2 FDA reports)
KOUNIS SYNDROME ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACTATION DISORDER ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LAGOPHTHALMOS ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGEAL DYSPNOEA ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LARYNX IRRITATION ( 2 FDA reports)
LATENT SYPHILIS ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LENS DISORDER ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 2 FDA reports)
LEPROSY ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIPOGRANULOMA ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUMBAR HERNIA ( 2 FDA reports)
LUMBAR PUNCTURE ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG WEDGE RESECTION ( 2 FDA reports)
LYMPH NODE CANCER METASTATIC ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
LYMPHOMA TRANSFORMATION ( 2 FDA reports)
MACROCEPHALY ( 2 FDA reports)
MACROPHAGE ACTIVATION ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULAR PIGMENTATION ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MALIGNANT GLIOMA ( 2 FDA reports)
MALIGNANT MELANOMA STAGE I ( 2 FDA reports)
MALIGNANT MUSCLE NEOPLASM ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 2 FDA reports)
MAMMARY DUCT ECTASIA ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MANDIBULAR PROSTHESIS USER ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEDIAN NERVE INJURY ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDICAL OBSERVATION ( 2 FDA reports)
MEGACOLON ACQUIRED ( 2 FDA reports)
MENINGOCOCCAL INFECTION ( 2 FDA reports)
MENISCAL DEGENERATION ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 2 FDA reports)
METASTATIC CARCINOID TUMOUR ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MISCARRIAGE OF PARTNER ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MODERATE MENTAL RETARDATION ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 2 FDA reports)
MUCOPOLYSACCHARIDOSIS ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MUMPS ANTIBODY TEST POSITIVE ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYELOCYTOSIS ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
MYXOEDEMA COMA ( 2 FDA reports)
NAIL BED INFLAMMATION ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NASAL NECROSIS ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NECK DEFORMITY ( 2 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEONATAL INTESTINAL OBSTRUCTION ( 2 FDA reports)
NEUROBORRELIOSIS ( 2 FDA reports)
NEUROMUSCULAR BLOCKADE ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
NOROVIRUS TEST POSITIVE ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OEDEMA NEONATAL ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC DISCS BLURRED ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OSMOPHOBIA ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN FIBROMA ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
OVARIAN TORSION ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 2 FDA reports)
OXYGEN SATURATION INCREASED ( 2 FDA reports)
PANCREAS DIVISUM ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAPSORIASIS ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PAROTID DUCT OBSTRUCTION ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PEDAL PULSE ABSENT ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PELVIC PROLAPSE ( 2 FDA reports)
PENILE PROSTHESIS INSERTION ( 2 FDA reports)
PENILE VASCULAR DISORDER ( 2 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 2 FDA reports)
PERCUSSION TEST ABNORMAL ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERICARDIAL RUB ( 2 FDA reports)
PERIHEPATIC ABSCESS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERINEPHRIC ABSCESS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERIPORTAL OEDEMA ( 2 FDA reports)
PERITONEAL FIBROSIS ( 2 FDA reports)
PH BODY FLUID ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PHYSICAL ABUSE ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PLACENTAL INFARCTION ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL NEOPLASM ( 2 FDA reports)
PLEURAL RUB ( 2 FDA reports)
PLICATED TONGUE ( 2 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
PORTAL VEIN FLOW DECREASED ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
PORTAL VENOUS GAS ( 2 FDA reports)
POST PROCEDURAL CONSTIPATION ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 2 FDA reports)
POST STROKE DEPRESSION ( 2 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 2 FDA reports)
POSTMATURE BABY ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PROCTITIS HAEMORRHAGIC ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PRODUCT DOSAGE FORM CONFUSION ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROPIONIBACTERIUM INFECTION ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATE TENDERNESS ( 2 FDA reports)
PROSTATIC MASS ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTEIN C DECREASED ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY OEDEMA NEONATAL ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
PYELECTASIA ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
PYELONEPHRITIS FUNGAL ( 2 FDA reports)
PYONEPHROSIS ( 2 FDA reports)
RADIATION FIBROSIS - LUNG ( 2 FDA reports)
RADICAL HYSTERECTOMY ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
RECTAL CANCER STAGE IV ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CYST INFECTION ( 2 FDA reports)
RENAL IMPAIRMENT NEONATAL ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RENAL SCAN ABNORMAL ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
REOCCLUSION ( 2 FDA reports)
REPETITIVE STRAIN INJURY ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 2 FDA reports)
RETINOL BINDING PROTEIN INCREASED ( 2 FDA reports)
RETINOPATHY OF PREMATURITY ( 2 FDA reports)
RHABDOMYOMA ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RIB HYPOPLASIA ( 2 FDA reports)
SACCADIC EYE MOVEMENT ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 2 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SCROTAL HAEMATOCOELE ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SECONDARY SEQUESTRUM ( 2 FDA reports)
SEIZURE ANOXIC ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
SMALL INTESTINAL RESECTION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOMATIC DELUSION ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SOMNOLENCE NEONATAL ( 2 FDA reports)
SPHEROCYTIC ANAEMIA ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINA BIFIDA OCCULTA ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 2 FDA reports)
STAPHYLOMA ( 2 FDA reports)
STASIS SYNDROME ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STREPTOCOCCAL ABSCESS ( 2 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 2 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SULPHAEMOGLOBINAEMIA ( 2 FDA reports)
SUPRAPUBIC CATHETER INSERTION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SWOLLEN TEAR DUCT ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
TAENIASIS ( 2 FDA reports)
THALASSAEMIA ALPHA ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPY NAIVE ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 2 FDA reports)
THROMBOEMBOLIC STROKE ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYMECTOMY ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TONSILLITIS BACTERIAL ( 2 FDA reports)
TOTAL BILE ACIDS INCREASED ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 2 FDA reports)
TRACHEAL DEVIATION ( 2 FDA reports)
TRACHEAL INFLAMMATION ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEAL ULCER ( 2 FDA reports)
TRANSAMINASES DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRANSIENT PSYCHOSIS ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRANSVERSE PRESENTATION ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
TUBEROUS SCLEROSIS ( 2 FDA reports)
TUBO-OVARIAN ABSCESS ( 2 FDA reports)
TULARAEMIA ( 2 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URAEMIC ACIDOSIS ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETHRAL DILATATION ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
URINE ELECTROLYTES ABNORMAL ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
UROGENITAL HAEMORRHAGE ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL EXFOLIATION ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL OEDEMA ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR FRAGILITY ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 2 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 2 FDA reports)
VENTRICLE RUPTURE ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VICTIM OF CHILD ABUSE ( 2 FDA reports)
VIRAL MYOSITIS ( 2 FDA reports)
VITAMIN B1 DEFICIENCY ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITELLO-INTESTINAL DUCT REMNANT ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOLUME BLOOD INCREASED ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VOMITING NEONATAL ( 2 FDA reports)
VULVAL CELLULITIS ( 2 FDA reports)
VULVAL OEDEMA ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL INJURY ( 2 FDA reports)
WATERHOUSE-FRIDERICHSEN SYNDROME ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 2 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 2 FDA reports)
XEROPHTHALMIA ( 2 FDA reports)
YERSINIA INFECTION ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOW SET EARS ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS MYOCARDITIS ( 1 FDA reports)
LUPUS VULGARIS ( 1 FDA reports)
LYMPHANGIOMA ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
MALE REPRODUCTIVE TRACT NEOPLASM ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MARRIED ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MATERNAL EXPOSURE DURING DELIVERY ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENINGITIS HERPES ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS NONINFECTIVE ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ADVANCED ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHYLOBACTERIUM INFECTION ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROSURGERY TO HAND ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MINIMUM INHIBITORY CONCENTRATION ( 1 FDA reports)
MITOCHONDRIAL ENZYME DEFICIENCY ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS IH ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MYALGIA INTERCOSTAL ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIA BLOOD TEST POSITIVE ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES STAGE I ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCARDITIS POST INFECTION ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOGLOBIN URINE ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL NEOPLASM ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEEDLE BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL CANDIDA INFECTION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL LEUKAEMIA ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEPHRITIS RADIATION ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROCYSTICERCOSIS ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
NITRITOID CRISIS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCTIPHOBIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE II ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSTETRICAL PULMONARY EMBOLISM ( 1 FDA reports)
OBSTRUCTED LABOUR ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPHTHALMIA NODOSA ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORGAN DONOR ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
ORTHOSTATIC HEART RATE RESPONSE INCREASED ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN INFECTION ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARADOXICAL PAIN ( 1 FDA reports)
PARAESTHESIA MUCOSAL ( 1 FDA reports)
PARAGANGLION NEOPLASM ( 1 FDA reports)
PARANASAL SINUS NEOPLASM ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 1 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE ARTERY OCCLUSION ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIOTOMY ( 1 FDA reports)
PERICARDITIS LUPUS ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL CYST ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIODONTAL DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARMACOPHOBIA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHOTOONYCHOLYSIS ( 1 FDA reports)
PHOTOPHERESIS ( 1 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PIGMENTARY GLAUCOMA ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PINEAL GLAND CYST ( 1 FDA reports)
PITUITARY INFARCTION ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLACENTAL NEOPLASM ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLEURAL DECORTICATION ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ADVANCED ( 1 FDA reports)
PLEURECTOMY ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
PO2 ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMORPHIC ERUPTION OF PREGNANCY ( 1 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POPLITEAL PULSE ABNORMAL ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTPARTUM DISORDER ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREAURICULAR CYST ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PRECURSOR B-LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROLACTIN-PRODUCING PITUITARY TUMOUR ( 1 FDA reports)
PROLAPSE REPAIR ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELOCYSTITIS ( 1 FDA reports)
PYLOROSPASM ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADICULOTOMY ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ADENOMA ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL FUNCTION TEST ( 1 FDA reports)
RENAL GLYCOSURIA ( 1 FDA reports)
RENAL HAEMANGIOMA ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY RATE ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RESPITE CARE ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOENDOTHELIAL SYSTEM STIMULATED ( 1 FDA reports)
RETINAL ANOMALY CONGENITAL ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
RETROPERITONEAL OEDEMA ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
RHABDOMYOSARCOMA RECURRENT ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHINITIS PERENNIAL ( 1 FDA reports)
RHINOLARYNGITIS ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RICHTER'S SYNDROME ( 1 FDA reports)
RICKETS ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCHIZOPHRENIA, RESIDUAL TYPE ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORY LEVEL ABNORMAL ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SEVER'S DISEASE ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SINUS TARSI SYNDROME ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SLE ARTHRITIS ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL ARTERY THROMBOSIS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC INFECTION FUNGAL ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STAG HORN CALCULUS ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE I ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
SUPERINFECTION FUNGAL ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SYMPHYSIOLYSIS ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON GRAFT ( 1 FDA reports)
TENDON REPAIR ( 1 FDA reports)
TENONECTOMY ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR RETRACTION ( 1 FDA reports)
THERAPEUTIC ASPIRATION ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERMOMETRY ABNORMAL ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THYMUS HYPOPLASIA ( 1 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 1 FDA reports)
THYROXINE FREE ABNORMAL ( 1 FDA reports)
TISSUE ANOXIA ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL FISTULA REPAIR ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEAL OPERATION ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOSTOMY INFECTION ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TRIGEMINAL NERVE ABLATION ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TURBINECTOMY ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN VAGINA ABNORMAL ( 1 FDA reports)
UMBILICAL HAEMATOMA ( 1 FDA reports)
UNDERSENSING ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URAEMIC PRURITUS ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC OPERATION ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URETHRAL VALVES ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE AMINO ACID LEVEL INCREASED ( 1 FDA reports)
URINE ANALYSIS ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE CHLORIDE DECREASED ( 1 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE URIC ACID DECREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE FIBROSIS ( 1 FDA reports)
UTERINE HAEMATOMA ( 1 FDA reports)
UTERINE INJURY ( 1 FDA reports)
UTERINE ISCHAEMIA ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL HAEMATOMA ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL OPERATION ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR COMPRESSION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENIPUNCTURE SITE THROMBOSIS ( 1 FDA reports)
VENOM POISONING ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS OXYGEN SATURATION DECREASED ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIBRIO TEST POSITIVE ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVAL HAEMATOMA ( 1 FDA reports)
VULVAL LEUKOPLAKIA ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WEIGHT BELOW NORMAL ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABORTION COMPLETE ( 1 FDA reports)
ABSCESS MANAGEMENT ( 1 FDA reports)
ABSCESS OF EYELID ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACNE CONGLOBATA ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACQUIRED FORAMEN MAGNUM STENOSIS ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACQUIRED TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME NORMAL ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RADIATION SYNDROME ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADENOTONSILLECTOMY ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADMINISTRATION RELATED REACTION ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENALECTOMY ( 1 FDA reports)
ADRENALITIS ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALLERGENIC DESENSITISATION PROCEDURE ( 1 FDA reports)
ALLERGIC COUGH ( 1 FDA reports)
ALLERGIC PHARYNGITIS ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DECREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
AMINO ACID LEVEL DECREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYLASE ABNORMAL ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANENCEPHALY ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 1 FDA reports)
ANGIOKERATOMA ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANORECTAL AGENESIS ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTERIOR CHAMBER FLARE ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APLASIA CUTIS CONGENITA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRITIS SALMONELLA ( 1 FDA reports)
ARTHROPOD INFESTATION ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROTOXICITY ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPLENIA ( 1 FDA reports)
ASSISTED DELIVERY ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
ATYPICAL FIBROXANTHOMA ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL PNEUMONIA ( 1 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
AUTOIMMUNE MYOCARDITIS ( 1 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BAROTITIS MEDIA ( 1 FDA reports)
BARTHOLINITIS ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN MUSCLE NEOPLASM ( 1 FDA reports)
BENZODIAZEPINE DRUG LEVEL ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA 2 GLOBULIN ( 1 FDA reports)
BILE DUCT CANCER NON-RESECTABLE ( 1 FDA reports)
BILE DUCT EXPLORATION ( 1 FDA reports)
BILE DUCT PRESSURE ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY ANASTOMOSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY ABDOMINAL WALL ABNORMAL ( 1 FDA reports)
BIOPSY BRAIN NORMAL ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY MUSCLE ( 1 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ( 1 FDA reports)
BIOPSY THYROID GLAND ( 1 FDA reports)
BIOPSY VAGINA ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NECK OPERATION ( 1 FDA reports)
BLADDER NECROSIS ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLEPHARAL PAPILLOMA ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD BERYLLIUM DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CORTICOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CULTURE ( 1 FDA reports)
BLOOD ETHANOL ( 1 FDA reports)
BLOOD GALACTOSE ABNORMAL ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORDERLINE MENTAL IMPAIRMENT ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREATH SOUNDS ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL INJURY ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX SEPSIS ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSAL OPERATION ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CALCIUM IONISED ( 1 FDA reports)
CALCULUS PROSTATIC ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE EROSION ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CEMENTOPLASTY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERITIS ( 1 FDA reports)
CEREBRAL CYST EXCISION ( 1 FDA reports)
CEREBRAL DYSGENESIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE FOETAL ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBROVASCULAR OPERATION ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL ABUSER ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHLAMYDIA IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLELITHIASIS MIGRATION ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCUMSTANTIALITY ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL ABNORMAL ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COLPOSCOPY ( 1 FDA reports)
COLPOSCOPY ABNORMAL ( 1 FDA reports)
COMA SCALE ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL AORTIC ATRESIA ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL CEREBELLAR AGENESIS ( 1 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CONGENITAL ENDOCRINE ANOMALY ( 1 FDA reports)
CONGENITAL HIP DEFORMITY ( 1 FDA reports)
CONGENITAL KYPHOSCOLIOSIS ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONJUNCTIVAL VASCULAR DISORDER ( 1 FDA reports)
CONTRACEPTION ( 1 FDA reports)
CONTRAINDICATION TO SURGERY ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL DIAMETER INCREASED ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL INFILTRATES ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRANIAL NERVE OPERATION ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CROSSMATCH INCOMPATIBLE ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYOGLOBULINS ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUTANEOUS TUBERCULOSIS ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYP2D6 POLYMORPHISM ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED DELIVERY ( 1 FDA reports)
DELAYED FONTANELLE CLOSURE ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIAPHRAGM NEOPLASM ( 1 FDA reports)
DIARRHOEA NEONATAL ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DIFFUSE VASCULITIS ( 1 FDA reports)
DIGEORGE'S SYNDROME ( 1 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DISSOCIATIVE AMNESIA ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUGLAS' ABSCESS ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENAL OPERATION ( 1 FDA reports)
DUODENAL ULCER REPAIR ( 1 FDA reports)
DUODENECTOMY ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DUST INHALATION PNEUMOPATHY ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
DYSPONESIS ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 1 FDA reports)
ELECTROCUTION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMBOLECTOMY ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENCEPHALITIS POST VARICELLA ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENCHONDROMATOSIS ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
END-TIDAL CO2 DECREASED ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHILIA MYALGIA SYNDROME ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRACORPOREAL CIRCULATION ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYELID INJURY ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACE CRUSHING ( 1 FDA reports)
FACE PRESENTATION ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACTOR II DEFICIENCY ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FACTOR XI DEFICIENCY ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
FAMILIAL HEMIPLEGIC MIGRAINE ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FATTY LIVER ALCOHOLIC ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FIBRINOUS BRONCHITIS ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FLOPPY INFANT ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL ALCOHOL SYNDROME ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 1 FDA reports)
FOETAL CYSTIC HYGROMA ( 1 FDA reports)
FOETAL WARFARIN SYNDROME ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FRAGILE X SYNDROME ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CANCER STAGE IV ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC CANCER STAGE 0 ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROSTOMY CLOSURE ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLUTATHIONE DECREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRIP STRENGTH ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GUM NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMANGIOPERICYTOMA ( 1 FDA reports)
HAEMATOCOLPOS ( 1 FDA reports)
HAEMATOTYMPANUM ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMOPHILIA A WITH ANTI FACTOR VIII ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HALLUCINATION, SYNAESTHETIC ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HANTAVIRAL INFECTION ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CYST INFECTION ( 1 FDA reports)
HEPATIC CYST RUPTURED ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C RNA FLUCTUATION ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOBLASTOMA ( 1 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 1 FDA reports)
HERBAL INTERACTION ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIPPUS ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE DEPLETION TYPE STAGE III ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROXYPROLINE INCREASED ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPHOSPHATASIA ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
IIIRD NERVE INJURY ( 1 FDA reports)
ILEOCOLECTOMY ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNISATION ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE EXTRAVASATION ( 1 FDA reports)
IMPLANT SITE FIBROSIS ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INDIRECT INFECTION TRANSMISSION ( 1 FDA reports)
INDUCED ABORTION FAILED ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFECTIVE ANEURYSM ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFLAMMATION OF LACRIMAL PASSAGE ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE ANAESTHESIA ( 1 FDA reports)
INFUSION SITE CYST ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE JOINT WARMTH ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERCEPTED DRUG PRESCRIBING ERROR ( 1 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL ATRESIA ( 1 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTRAUTERINE INFECTION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED DECREASED ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT CAPSULE RUPTURE ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
KERNIG'S SIGN ( 1 FDA reports)
KOEBNER PHENOMENON ( 1 FDA reports)
KWASHIORKOR ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL PASSAGE GRANULOMA ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARYNGEAL CYST ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL REPAIR ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
LEUKAEMIC INFILTRATION ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LEUKOTRIENE INCREASED ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LIGAMENT OPERATION ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP REPAIR ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIPOSARCOMA METASTATIC ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER FUNCTION TEST NORMAL ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)

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