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

DYSPNOEA ( 6247 FDA reports)
DRUG INEFFECTIVE ( 3287 FDA reports)
NAUSEA ( 3237 FDA reports)
PAIN ( 3202 FDA reports)
ASTHMA ( 2778 FDA reports)
ANXIETY ( 2731 FDA reports)
PNEUMONIA ( 2605 FDA reports)
FATIGUE ( 2328 FDA reports)
DIZZINESS ( 2309 FDA reports)
CHEST PAIN ( 2290 FDA reports)
HEADACHE ( 2287 FDA reports)
VOMITING ( 2272 FDA reports)
DEPRESSION ( 2143 FDA reports)
COUGH ( 2112 FDA reports)
ASTHENIA ( 1924 FDA reports)
OEDEMA PERIPHERAL ( 1853 FDA reports)
DIARRHOEA ( 1828 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1712 FDA reports)
BACK PAIN ( 1600 FDA reports)
FALL ( 1580 FDA reports)
PYREXIA ( 1571 FDA reports)
ABDOMINAL PAIN ( 1516 FDA reports)
ARTHRALGIA ( 1514 FDA reports)
ANAEMIA ( 1460 FDA reports)
HYPERTENSION ( 1453 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1423 FDA reports)
INSOMNIA ( 1417 FDA reports)
PAIN IN EXTREMITY ( 1402 FDA reports)
INJURY ( 1400 FDA reports)
HYPOTENSION ( 1296 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1280 FDA reports)
WEIGHT DECREASED ( 1276 FDA reports)
CONSTIPATION ( 1260 FDA reports)
MYOCARDIAL INFARCTION ( 1255 FDA reports)
PULMONARY EMBOLISM ( 1222 FDA reports)
BRONCHITIS ( 1221 FDA reports)
CHEST DISCOMFORT ( 1165 FDA reports)
MALAISE ( 1158 FDA reports)
WHEEZING ( 1056 FDA reports)
ATRIAL FIBRILLATION ( 1054 FDA reports)
DEHYDRATION ( 1004 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1001 FDA reports)
CONDITION AGGRAVATED ( 990 FDA reports)
WEIGHT INCREASED ( 988 FDA reports)
DEEP VEIN THROMBOSIS ( 983 FDA reports)
DEATH ( 982 FDA reports)
URINARY TRACT INFECTION ( 978 FDA reports)
RASH ( 972 FDA reports)
TREMOR ( 959 FDA reports)
HYPOAESTHESIA ( 955 FDA reports)
RENAL FAILURE ( 936 FDA reports)
MUSCLE SPASMS ( 919 FDA reports)
CEREBROVASCULAR ACCIDENT ( 886 FDA reports)
PLEURAL EFFUSION ( 883 FDA reports)
RESPIRATORY FAILURE ( 883 FDA reports)
EMOTIONAL DISTRESS ( 878 FDA reports)
ABDOMINAL PAIN UPPER ( 875 FDA reports)
CONFUSIONAL STATE ( 863 FDA reports)
PRURITUS ( 828 FDA reports)
SINUSITIS ( 819 FDA reports)
RENAL FAILURE ACUTE ( 818 FDA reports)
VISION BLURRED ( 817 FDA reports)
OSTEOARTHRITIS ( 794 FDA reports)
PALPITATIONS ( 776 FDA reports)
FEELING ABNORMAL ( 775 FDA reports)
HYPERHIDROSIS ( 774 FDA reports)
PARAESTHESIA ( 763 FDA reports)
DYSPHAGIA ( 762 FDA reports)
DECREASED APPETITE ( 761 FDA reports)
GAIT DISTURBANCE ( 759 FDA reports)
SEPSIS ( 755 FDA reports)
CONVULSION ( 748 FDA reports)
DIABETES MELLITUS ( 746 FDA reports)
MYALGIA ( 741 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 733 FDA reports)
SOMNOLENCE ( 730 FDA reports)
BLOOD GLUCOSE INCREASED ( 704 FDA reports)
LOSS OF CONSCIOUSNESS ( 701 FDA reports)
CORONARY ARTERY DISEASE ( 700 FDA reports)
TACHYCARDIA ( 695 FDA reports)
HYPERSENSITIVITY ( 679 FDA reports)
HEART RATE INCREASED ( 658 FDA reports)
SUICIDAL IDEATION ( 655 FDA reports)
SYNCOPE ( 621 FDA reports)
CELLULITIS ( 614 FDA reports)
DYSPEPSIA ( 610 FDA reports)
DYSPHONIA ( 609 FDA reports)
MUSCULAR WEAKNESS ( 609 FDA reports)
PRODUCT QUALITY ISSUE ( 608 FDA reports)
ERYTHEMA ( 601 FDA reports)
CHOLELITHIASIS ( 600 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 596 FDA reports)
OSTEONECROSIS OF JAW ( 593 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 587 FDA reports)
DRY MOUTH ( 586 FDA reports)
HAEMOGLOBIN DECREASED ( 573 FDA reports)
THROMBOCYTOPENIA ( 573 FDA reports)
URTICARIA ( 556 FDA reports)
OSTEOMYELITIS ( 555 FDA reports)
CHILLS ( 553 FDA reports)
BLOOD PRESSURE INCREASED ( 552 FDA reports)
BONE DISORDER ( 552 FDA reports)
CARDIAC ARREST ( 548 FDA reports)
ABDOMINAL DISTENSION ( 541 FDA reports)
CARDIOMEGALY ( 535 FDA reports)
HYPOXIA ( 528 FDA reports)
ATELECTASIS ( 525 FDA reports)
ANHEDONIA ( 522 FDA reports)
OSTEONECROSIS ( 521 FDA reports)
CONTUSION ( 517 FDA reports)
INFECTION ( 516 FDA reports)
PAIN IN JAW ( 515 FDA reports)
CARDIAC DISORDER ( 513 FDA reports)
RESPIRATORY DISTRESS ( 508 FDA reports)
NEUROPATHY PERIPHERAL ( 504 FDA reports)
DYSGEUSIA ( 477 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 473 FDA reports)
DRUG INTERACTION ( 472 FDA reports)
ECONOMIC PROBLEM ( 472 FDA reports)
SWELLING ( 471 FDA reports)
OVERDOSE ( 468 FDA reports)
HALLUCINATION ( 466 FDA reports)
MITRAL VALVE INCOMPETENCE ( 458 FDA reports)
NECK PAIN ( 457 FDA reports)
HYPERLIPIDAEMIA ( 452 FDA reports)
CATARACT ( 448 FDA reports)
MUSCULOSKELETAL PAIN ( 435 FDA reports)
SPINAL OSTEOARTHRITIS ( 431 FDA reports)
MIGRAINE ( 428 FDA reports)
MENTAL STATUS CHANGES ( 427 FDA reports)
OEDEMA ( 427 FDA reports)
CHOLECYSTITIS CHRONIC ( 426 FDA reports)
JOINT SWELLING ( 426 FDA reports)
MEMORY IMPAIRMENT ( 426 FDA reports)
GASTRITIS ( 424 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 424 FDA reports)
SLEEP APNOEA SYNDROME ( 421 FDA reports)
PRODUCTIVE COUGH ( 412 FDA reports)
NASOPHARYNGITIS ( 410 FDA reports)
TYPE 2 DIABETES MELLITUS ( 405 FDA reports)
EPISTAXIS ( 404 FDA reports)
RECTAL HAEMORRHAGE ( 395 FDA reports)
SWELLING FACE ( 395 FDA reports)
PULMONARY OEDEMA ( 394 FDA reports)
EMPHYSEMA ( 393 FDA reports)
ARTHRITIS ( 391 FDA reports)
PULMONARY HYPERTENSION ( 391 FDA reports)
RENAL FAILURE CHRONIC ( 390 FDA reports)
LETHARGY ( 389 FDA reports)
OSTEOPOROSIS ( 389 FDA reports)
GALLBLADDER DISORDER ( 388 FDA reports)
HYPERGLYCAEMIA ( 385 FDA reports)
LUNG DISORDER ( 385 FDA reports)
HYPOKALAEMIA ( 380 FDA reports)
AGGRESSION ( 379 FDA reports)
HIATUS HERNIA ( 379 FDA reports)
BLOOD CREATININE INCREASED ( 376 FDA reports)
HYPONATRAEMIA ( 376 FDA reports)
THROMBOSIS ( 375 FDA reports)
BRADYCARDIA ( 369 FDA reports)
OROPHARYNGEAL PAIN ( 368 FDA reports)
STRESS ( 368 FDA reports)
DYSPNOEA EXERTIONAL ( 366 FDA reports)
NERVOUSNESS ( 366 FDA reports)
LYMPHADENOPATHY ( 365 FDA reports)
BALANCE DISORDER ( 362 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 360 FDA reports)
AGITATION ( 357 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 355 FDA reports)
TOOTH EXTRACTION ( 355 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 354 FDA reports)
ANAPHYLACTIC REACTION ( 353 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 352 FDA reports)
DRUG HYPERSENSITIVITY ( 350 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 347 FDA reports)
OXYGEN SATURATION DECREASED ( 346 FDA reports)
ANGINA PECTORIS ( 345 FDA reports)
ABDOMINAL DISCOMFORT ( 344 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 340 FDA reports)
AMNESIA ( 339 FDA reports)
PANCREATITIS ( 338 FDA reports)
DYSURIA ( 336 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 335 FDA reports)
IMPAIRED HEALING ( 334 FDA reports)
CARDIO-RESPIRATORY ARREST ( 332 FDA reports)
HAEMOPTYSIS ( 332 FDA reports)
HAEMORRHOIDS ( 332 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 330 FDA reports)
CANDIDIASIS ( 326 FDA reports)
MENTAL DISORDER ( 326 FDA reports)
ALOPECIA ( 325 FDA reports)
OSTEOPENIA ( 325 FDA reports)
THROAT IRRITATION ( 324 FDA reports)
TREATMENT NONCOMPLIANCE ( 322 FDA reports)
ARRHYTHMIA ( 320 FDA reports)
NEUTROPENIA ( 320 FDA reports)
HAEMORRHAGE ( 316 FDA reports)
DRUG DOSE OMISSION ( 314 FDA reports)
SUICIDE ATTEMPT ( 314 FDA reports)
SINUS TACHYCARDIA ( 311 FDA reports)
PLATELET COUNT DECREASED ( 307 FDA reports)
DENTAL CARIES ( 307 FDA reports)
CARDIAC FAILURE ( 298 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 295 FDA reports)
HYPERKALAEMIA ( 295 FDA reports)
FLUSHING ( 294 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 293 FDA reports)
CARDIAC MURMUR ( 292 FDA reports)
PANCYTOPENIA ( 290 FDA reports)
NASAL CONGESTION ( 287 FDA reports)
BLOOD PRESSURE DECREASED ( 285 FDA reports)
DIVERTICULUM ( 285 FDA reports)
IRRITABILITY ( 284 FDA reports)
UNEVALUABLE EVENT ( 283 FDA reports)
ARTHROPATHY ( 282 FDA reports)
SLEEP DISORDER ( 281 FDA reports)
HYPOTHYROIDISM ( 280 FDA reports)
OBESITY ( 280 FDA reports)
VERTIGO ( 279 FDA reports)
ILL-DEFINED DISORDER ( 278 FDA reports)
DRUG EFFECT DECREASED ( 277 FDA reports)
TOOTHACHE ( 277 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 276 FDA reports)
BONE PAIN ( 275 FDA reports)
MULTIPLE INJURIES ( 274 FDA reports)
BRONCHOSPASM ( 273 FDA reports)
ANOREXIA ( 271 FDA reports)
CARDIOMYOPATHY ( 270 FDA reports)
CYANOSIS ( 270 FDA reports)
MEDICATION ERROR ( 270 FDA reports)
ABNORMAL DREAMS ( 269 FDA reports)
BLOOD POTASSIUM DECREASED ( 269 FDA reports)
PULMONARY CONGESTION ( 267 FDA reports)
HEART RATE IRREGULAR ( 265 FDA reports)
INFLUENZA LIKE ILLNESS ( 262 FDA reports)
LUNG NEOPLASM ( 262 FDA reports)
BURNING SENSATION ( 261 FDA reports)
RHINORRHOEA ( 261 FDA reports)
POLLAKIURIA ( 260 FDA reports)
SPEECH DISORDER ( 260 FDA reports)
LEUKOCYTOSIS ( 259 FDA reports)
EXOSTOSIS ( 258 FDA reports)
HAEMATURIA ( 258 FDA reports)
INFLUENZA ( 257 FDA reports)
VISUAL IMPAIRMENT ( 257 FDA reports)
ROAD TRAFFIC ACCIDENT ( 256 FDA reports)
ABNORMAL BEHAVIOUR ( 256 FDA reports)
HEPATIC STEATOSIS ( 253 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 252 FDA reports)
RESPIRATORY ARREST ( 249 FDA reports)
TOOTH DISORDER ( 249 FDA reports)
PANIC ATTACK ( 248 FDA reports)
DYSARTHRIA ( 246 FDA reports)
GASTROINTESTINAL DISORDER ( 246 FDA reports)
ROTATOR CUFF SYNDROME ( 244 FDA reports)
STAPHYLOCOCCAL INFECTION ( 244 FDA reports)
URINARY INCONTINENCE ( 242 FDA reports)
VENTRICULAR TACHYCARDIA ( 242 FDA reports)
MULTI-ORGAN FAILURE ( 241 FDA reports)
DRUG DEPENDENCE ( 240 FDA reports)
HYPOGLYCAEMIA ( 240 FDA reports)
ORAL CANDIDIASIS ( 240 FDA reports)
ACUTE RESPIRATORY FAILURE ( 237 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 237 FDA reports)
DRY SKIN ( 237 FDA reports)
DEFORMITY ( 236 FDA reports)
EMOTIONAL DISORDER ( 236 FDA reports)
INCORRECT DOSE ADMINISTERED ( 236 FDA reports)
HAEMATOCRIT DECREASED ( 235 FDA reports)
HERPES ZOSTER ( 235 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 235 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 232 FDA reports)
HOT FLUSH ( 232 FDA reports)
METASTASES TO BONE ( 232 FDA reports)
MYOCARDIAL ISCHAEMIA ( 232 FDA reports)
RESPIRATORY DISORDER ( 231 FDA reports)
RIB FRACTURE ( 231 FDA reports)
SINUS DISORDER ( 229 FDA reports)
COMA ( 229 FDA reports)
DISTURBANCE IN ATTENTION ( 228 FDA reports)
OFF LABEL USE ( 228 FDA reports)
SCAR ( 228 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 226 FDA reports)
NEPHROLITHIASIS ( 225 FDA reports)
VISUAL ACUITY REDUCED ( 225 FDA reports)
DYSKINESIA ( 222 FDA reports)
ABASIA ( 220 FDA reports)
DISEASE PROGRESSION ( 220 FDA reports)
MOBILITY DECREASED ( 220 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 219 FDA reports)
PERICARDIAL EFFUSION ( 219 FDA reports)
SURGERY ( 219 FDA reports)
FEAR ( 218 FDA reports)
INJECTION SITE PAIN ( 218 FDA reports)
ANGER ( 217 FDA reports)
NEOPLASM MALIGNANT ( 217 FDA reports)
RASH PRURITIC ( 217 FDA reports)
UNRESPONSIVE TO STIMULI ( 216 FDA reports)
LUNG INFILTRATION ( 216 FDA reports)
URINARY RETENTION ( 214 FDA reports)
TOOTH ABSCESS ( 213 FDA reports)
DEPRESSED MOOD ( 213 FDA reports)
ORAL PAIN ( 213 FDA reports)
ARTERIOSCLEROSIS ( 211 FDA reports)
BLOOD UREA INCREASED ( 211 FDA reports)
HEPATIC ENZYME INCREASED ( 211 FDA reports)
DECREASED INTEREST ( 209 FDA reports)
IRRITABLE BOWEL SYNDROME ( 209 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 208 FDA reports)
CRYING ( 208 FDA reports)
FLATULENCE ( 208 FDA reports)
STOMATITIS ( 207 FDA reports)
ATRIAL SEPTAL DEFECT ( 206 FDA reports)
COLITIS ( 206 FDA reports)
FLUID RETENTION ( 206 FDA reports)
SWOLLEN TONGUE ( 205 FDA reports)
RENAL IMPAIRMENT ( 204 FDA reports)
FEBRILE NEUTROPENIA ( 204 FDA reports)
MOOD SWINGS ( 204 FDA reports)
HAEMATOCHEZIA ( 203 FDA reports)
BURSITIS ( 201 FDA reports)
HYPOPHAGIA ( 201 FDA reports)
TINNITUS ( 201 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 200 FDA reports)
ADVERSE EVENT ( 199 FDA reports)
HYPERCHOLESTEROLAEMIA ( 199 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 199 FDA reports)
BLISTER ( 198 FDA reports)
DIVERTICULITIS ( 197 FDA reports)
NIGHTMARE ( 197 FDA reports)
RESPIRATORY TRACT INFECTION ( 197 FDA reports)
RHINITIS ALLERGIC ( 197 FDA reports)
MULTIPLE MYELOMA ( 196 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 195 FDA reports)
BLOOD GLUCOSE DECREASED ( 193 FDA reports)
COAGULOPATHY ( 193 FDA reports)
PHARYNGEAL OEDEMA ( 193 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 192 FDA reports)
THROAT TIGHTNESS ( 192 FDA reports)
SKIN LESION ( 191 FDA reports)
EAR PAIN ( 191 FDA reports)
CHOLECYSTITIS ( 188 FDA reports)
EYE PAIN ( 188 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 188 FDA reports)
VIRAL INFECTION ( 188 FDA reports)
BONE LESION ( 187 FDA reports)
FUNGAL INFECTION ( 185 FDA reports)
DRUG ADMINISTRATION ERROR ( 184 FDA reports)
DISORIENTATION ( 183 FDA reports)
SEPTIC SHOCK ( 182 FDA reports)
SKIN DISCOLOURATION ( 181 FDA reports)
PARANOIA ( 180 FDA reports)
TOOTH LOSS ( 180 FDA reports)
SPINAL COLUMN STENOSIS ( 179 FDA reports)
DISCOMFORT ( 179 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 179 FDA reports)
LIVER DISORDER ( 179 FDA reports)
FEELING HOT ( 178 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 178 FDA reports)
RESTLESS LEGS SYNDROME ( 177 FDA reports)
PULMONARY FIBROSIS ( 176 FDA reports)
BLINDNESS ( 176 FDA reports)
METABOLIC ACIDOSIS ( 176 FDA reports)
HEPATIC FAILURE ( 175 FDA reports)
INTERSTITIAL LUNG DISEASE ( 175 FDA reports)
EYE SWELLING ( 174 FDA reports)
GINGIVAL PAIN ( 174 FDA reports)
HAEMATEMESIS ( 174 FDA reports)
BIPOLAR DISORDER ( 173 FDA reports)
COLONIC POLYP ( 173 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 173 FDA reports)
PALLOR ( 173 FDA reports)
RHABDOMYOLYSIS ( 172 FDA reports)
SKIN ULCER ( 171 FDA reports)
INFLAMMATION ( 171 FDA reports)
CHRONIC SINUSITIS ( 169 FDA reports)
GLAUCOMA ( 167 FDA reports)
RENAL CYST ( 166 FDA reports)
RHEUMATOID ARTHRITIS ( 164 FDA reports)
PRESYNCOPE ( 163 FDA reports)
RENAL DISORDER ( 163 FDA reports)
RASH ERYTHEMATOUS ( 162 FDA reports)
HAEMATOMA ( 161 FDA reports)
DEAFNESS ( 160 FDA reports)
NIGHT SWEATS ( 160 FDA reports)
PHARYNGITIS ( 160 FDA reports)
PRURITUS GENERALISED ( 160 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 159 FDA reports)
CROHN'S DISEASE ( 159 FDA reports)
DIABETIC NEUROPATHY ( 158 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 158 FDA reports)
GASTRIC DISORDER ( 157 FDA reports)
HEAD INJURY ( 157 FDA reports)
PNEUMONIA ASPIRATION ( 157 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 157 FDA reports)
ENCEPHALOPATHY ( 156 FDA reports)
LUNG NEOPLASM MALIGNANT ( 156 FDA reports)
RESTLESSNESS ( 155 FDA reports)
SPLENOMEGALY ( 155 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 155 FDA reports)
MALNUTRITION ( 154 FDA reports)
OESOPHAGITIS ( 154 FDA reports)
APHASIA ( 153 FDA reports)
BONE DEBRIDEMENT ( 153 FDA reports)
JAUNDICE ( 153 FDA reports)
LUNG INFECTION ( 153 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 152 FDA reports)
MOUTH ULCERATION ( 152 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 151 FDA reports)
FIBROMYALGIA ( 151 FDA reports)
LUMBAR SPINAL STENOSIS ( 151 FDA reports)
ASCITES ( 150 FDA reports)
CYST ( 150 FDA reports)
ADVERSE DRUG REACTION ( 149 FDA reports)
COMPRESSION FRACTURE ( 149 FDA reports)
EJECTION FRACTION DECREASED ( 149 FDA reports)
ORAL DISORDER ( 149 FDA reports)
CHOKING ( 148 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 148 FDA reports)
INJECTION SITE ERYTHEMA ( 148 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 148 FDA reports)
GOUT ( 147 FDA reports)
FLUID OVERLOAD ( 146 FDA reports)
INTENTIONAL OVERDOSE ( 146 FDA reports)
LEUKOPENIA ( 146 FDA reports)
SPUTUM DISCOLOURED ( 146 FDA reports)
VENTRICULAR FIBRILLATION ( 146 FDA reports)
RETCHING ( 145 FDA reports)
AORTIC VALVE INCOMPETENCE ( 145 FDA reports)
BACTERIAL INFECTION ( 145 FDA reports)
BREAST CANCER ( 144 FDA reports)
DRUG TOXICITY ( 144 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 144 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 144 FDA reports)
SCOLIOSIS ( 143 FDA reports)
TACHYPNOEA ( 143 FDA reports)
GASTRIC ULCER ( 143 FDA reports)
GASTROENTERITIS ( 142 FDA reports)
LARYNGITIS ( 142 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 142 FDA reports)
MASS ( 142 FDA reports)
PEPTIC ULCER ( 142 FDA reports)
PROTHROMBIN TIME PROLONGED ( 142 FDA reports)
PERIODONTITIS ( 141 FDA reports)
SKIN EXFOLIATION ( 141 FDA reports)
HEPATOMEGALY ( 141 FDA reports)
JOINT STIFFNESS ( 141 FDA reports)
FEMUR FRACTURE ( 140 FDA reports)
PANCREATITIS ACUTE ( 140 FDA reports)
PNEUMOTHORAX ( 140 FDA reports)
DIPLOPIA ( 139 FDA reports)
HEPATITIS ( 139 FDA reports)
GINGIVITIS ( 138 FDA reports)
NEURALGIA ( 138 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 138 FDA reports)
POST PROCEDURAL COMPLICATION ( 136 FDA reports)
TENDONITIS ( 136 FDA reports)
ABDOMINAL PAIN LOWER ( 136 FDA reports)
DISABILITY ( 136 FDA reports)
LOBAR PNEUMONIA ( 136 FDA reports)
FEELING JITTERY ( 135 FDA reports)
BLOOD SODIUM DECREASED ( 134 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 134 FDA reports)
COGNITIVE DISORDER ( 134 FDA reports)
CORONARY ARTERY OCCLUSION ( 134 FDA reports)
FLANK PAIN ( 134 FDA reports)
SKIN DISORDER ( 134 FDA reports)
SPINAL COMPRESSION FRACTURE ( 133 FDA reports)
ANGIOEDEMA ( 133 FDA reports)
DYSLIPIDAEMIA ( 133 FDA reports)
HEART RATE DECREASED ( 133 FDA reports)
HIP FRACTURE ( 133 FDA reports)
HYPERCALCAEMIA ( 133 FDA reports)
INTENTIONAL DRUG MISUSE ( 132 FDA reports)
PSYCHOTIC DISORDER ( 132 FDA reports)
PRIMARY SEQUESTRUM ( 131 FDA reports)
VISUAL DISTURBANCE ( 131 FDA reports)
BONE DENSITY DECREASED ( 131 FDA reports)
MENISCUS LESION ( 131 FDA reports)
ANGINA UNSTABLE ( 130 FDA reports)
CIRCULATORY COLLAPSE ( 130 FDA reports)
DRY EYE ( 130 FDA reports)
MOOD ALTERED ( 130 FDA reports)
LIMB INJURY ( 129 FDA reports)
APNOEA ( 128 FDA reports)
ABSCESS ( 127 FDA reports)
APHONIA ( 127 FDA reports)
EYE DISORDER ( 127 FDA reports)
GENERALISED OEDEMA ( 127 FDA reports)
IRON DEFICIENCY ANAEMIA ( 127 FDA reports)
BLOOD BILIRUBIN INCREASED ( 126 FDA reports)
NERVOUS SYSTEM DISORDER ( 126 FDA reports)
NOCTURIA ( 126 FDA reports)
ERECTILE DYSFUNCTION ( 125 FDA reports)
HEMIPARESIS ( 125 FDA reports)
SEDATION ( 125 FDA reports)
SINUS CONGESTION ( 125 FDA reports)
BLOOD CALCIUM DECREASED ( 124 FDA reports)
JOINT INJURY ( 124 FDA reports)
LACERATION ( 124 FDA reports)
ASPIRATION ( 123 FDA reports)
TENDERNESS ( 123 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 122 FDA reports)
ENDODONTIC PROCEDURE ( 122 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 122 FDA reports)
ORTHOPNOEA ( 122 FDA reports)
LIP SWELLING ( 121 FDA reports)
AGEUSIA ( 120 FDA reports)
MASTICATION DISORDER ( 120 FDA reports)
PELVIC PAIN ( 120 FDA reports)
PNEUMONITIS ( 120 FDA reports)
CARPAL TUNNEL SYNDROME ( 119 FDA reports)
FAILURE TO THRIVE ( 119 FDA reports)
INTESTINAL OBSTRUCTION ( 119 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 118 FDA reports)
PERIODONTAL DISEASE ( 118 FDA reports)
COLITIS ULCERATIVE ( 117 FDA reports)
FISTULA ( 117 FDA reports)
ATRIAL FLUTTER ( 116 FDA reports)
CARDIOVASCULAR DISORDER ( 116 FDA reports)
CHOLECYSTECTOMY ( 116 FDA reports)
EAR INFECTION ( 116 FDA reports)
FEELING COLD ( 116 FDA reports)
INFUSION RELATED REACTION ( 116 FDA reports)
ORTHOSTATIC HYPOTENSION ( 116 FDA reports)
ECCHYMOSIS ( 115 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 115 FDA reports)
OVARIAN CYST ( 115 FDA reports)
ECZEMA ( 114 FDA reports)
JAW FRACTURE ( 114 FDA reports)
RADICULOPATHY ( 114 FDA reports)
VENTRICULAR HYPERTROPHY ( 114 FDA reports)
PURULENT DISCHARGE ( 113 FDA reports)
ULCER ( 113 FDA reports)
CAROTID ARTERY STENOSIS ( 113 FDA reports)
DILATATION VENTRICULAR ( 113 FDA reports)
HEPATIC CYST ( 113 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 113 FDA reports)
JOINT SPRAIN ( 113 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 113 FDA reports)
CEREBRAL ISCHAEMIA ( 112 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 112 FDA reports)
GLOSSODYNIA ( 112 FDA reports)
LOOSE TOOTH ( 112 FDA reports)
PHYSICAL DISABILITY ( 112 FDA reports)
STATUS ASTHMATICUS ( 112 FDA reports)
EATING DISORDER ( 111 FDA reports)
GINGIVAL BLEEDING ( 111 FDA reports)
HYPOVOLAEMIA ( 111 FDA reports)
MELAENA ( 111 FDA reports)
METASTASES TO LUNG ( 111 FDA reports)
BILIARY DYSKINESIA ( 110 FDA reports)
BODY TEMPERATURE INCREASED ( 110 FDA reports)
CHOLECYSTITIS ACUTE ( 110 FDA reports)
CHROMATURIA ( 110 FDA reports)
BREATH SOUNDS ABNORMAL ( 109 FDA reports)
AORTIC ANEURYSM ( 108 FDA reports)
DELIRIUM ( 108 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 108 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 107 FDA reports)
TENDON RUPTURE ( 107 FDA reports)
BLOOD ALBUMIN DECREASED ( 107 FDA reports)
GINGIVAL SWELLING ( 107 FDA reports)
MUCOSAL INFLAMMATION ( 107 FDA reports)
BRONCHOPNEUMONIA ( 106 FDA reports)
RESPIRATORY RATE INCREASED ( 106 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 105 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 104 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 104 FDA reports)
TARDIVE DYSKINESIA ( 104 FDA reports)
ILEUS ( 104 FDA reports)
JAW DISORDER ( 104 FDA reports)
ACCIDENTAL OVERDOSE ( 103 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 103 FDA reports)
FAECES DISCOLOURED ( 103 FDA reports)
GINGIVAL INFECTION ( 103 FDA reports)
MUSCLE TWITCHING ( 103 FDA reports)
OCULAR HYPERAEMIA ( 103 FDA reports)
COMPLETED SUICIDE ( 102 FDA reports)
GRAND MAL CONVULSION ( 102 FDA reports)
INJECTION SITE HAEMATOMA ( 102 FDA reports)
MUSCLE STRAIN ( 102 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 102 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 101 FDA reports)
DIASTOLIC DYSFUNCTION ( 101 FDA reports)
MAJOR DEPRESSION ( 101 FDA reports)
MUSCLE TIGHTNESS ( 101 FDA reports)
PLATELET COUNT INCREASED ( 101 FDA reports)
SHOCK ( 101 FDA reports)
RASH GENERALISED ( 100 FDA reports)
STOMACH DISCOMFORT ( 100 FDA reports)
CEREBRAL ATROPHY ( 100 FDA reports)
FOOT FRACTURE ( 100 FDA reports)
LACTIC ACIDOSIS ( 100 FDA reports)
LEFT ATRIAL DILATATION ( 100 FDA reports)
MENTAL IMPAIRMENT ( 100 FDA reports)
OSTEITIS ( 100 FDA reports)
ABDOMINAL HERNIA ( 99 FDA reports)
CARDIOGENIC SHOCK ( 99 FDA reports)
EXCORIATION ( 99 FDA reports)
HALLUCINATION, AUDITORY ( 99 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 99 FDA reports)
SINUS BRADYCARDIA ( 99 FDA reports)
STRESS FRACTURE ( 99 FDA reports)
THINKING ABNORMAL ( 99 FDA reports)
TOOTH INFECTION ( 99 FDA reports)
DEMENTIA ( 98 FDA reports)
DYSSTASIA ( 98 FDA reports)
GASTROENTERITIS VIRAL ( 98 FDA reports)
HYPERKERATOSIS ( 97 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 97 FDA reports)
WALKING AID USER ( 97 FDA reports)
SKIN TIGHTNESS ( 96 FDA reports)
HALLUCINATION, VISUAL ( 96 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 96 FDA reports)
METASTASES TO LIVER ( 96 FDA reports)
HYPOCALCAEMIA ( 95 FDA reports)
MOVEMENT DISORDER ( 95 FDA reports)
RALES ( 95 FDA reports)
SKIN HYPERTROPHY ( 95 FDA reports)
STEVENS-JOHNSON SYNDROME ( 95 FDA reports)
SCIATICA ( 94 FDA reports)
ABDOMINAL TENDERNESS ( 94 FDA reports)
DIABETIC KETOACIDOSIS ( 94 FDA reports)
ELECTROLYTE IMBALANCE ( 94 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 94 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 93 FDA reports)
IMPAIRED WORK ABILITY ( 93 FDA reports)
TOOTH FRACTURE ( 93 FDA reports)
RHINITIS ( 92 FDA reports)
SPINAL FRACTURE ( 92 FDA reports)
BLADDER DISORDER ( 92 FDA reports)
BLOOD POTASSIUM INCREASED ( 92 FDA reports)
DRUG ABUSER ( 92 FDA reports)
DYSPNOEA EXACERBATED ( 92 FDA reports)
HYPERSOMNIA ( 92 FDA reports)
OEDEMA MOUTH ( 92 FDA reports)
ABORTION SPONTANEOUS ( 91 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 91 FDA reports)
DECUBITUS ULCER ( 91 FDA reports)
DELUSION ( 91 FDA reports)
DERMATITIS ( 91 FDA reports)
LACRIMATION INCREASED ( 91 FDA reports)
PLEURITIC PAIN ( 91 FDA reports)
RESPIRATORY TRACT CONGESTION ( 91 FDA reports)
CEREBRAL INFARCTION ( 90 FDA reports)
COLD SWEAT ( 90 FDA reports)
CYSTITIS ( 90 FDA reports)
HEARING IMPAIRED ( 90 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 90 FDA reports)
LOCAL SWELLING ( 89 FDA reports)
MIDDLE INSOMNIA ( 89 FDA reports)
SKIN INDURATION ( 89 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 89 FDA reports)
ADRENAL INSUFFICIENCY ( 88 FDA reports)
DEVICE FAILURE ( 88 FDA reports)
DIVERTICULUM INTESTINAL ( 88 FDA reports)
CONJUNCTIVITIS ( 87 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 87 FDA reports)
DRUG ABUSE ( 87 FDA reports)
EXPOSED BONE IN JAW ( 87 FDA reports)
EYE IRRITATION ( 87 FDA reports)
LOCALISED INFECTION ( 87 FDA reports)
MYOCLONUS ( 87 FDA reports)
PERIPHERAL COLDNESS ( 87 FDA reports)
PYELONEPHRITIS ( 87 FDA reports)
REFLUX OESOPHAGITIS ( 86 FDA reports)
SYNOVIAL CYST ( 86 FDA reports)
VAGINAL HAEMORRHAGE ( 86 FDA reports)
ACUTE CORONARY SYNDROME ( 86 FDA reports)
BREAST PAIN ( 86 FDA reports)
CAESAREAN SECTION ( 86 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 86 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 85 FDA reports)
CARDIAC VALVE DISEASE ( 85 FDA reports)
DRUG INTOLERANCE ( 85 FDA reports)
DUODENITIS ( 85 FDA reports)
HOMICIDAL IDEATION ( 85 FDA reports)
AZOTAEMIA ( 84 FDA reports)
BODY HEIGHT DECREASED ( 84 FDA reports)
CORONARY ARTERY STENOSIS ( 84 FDA reports)
DRUG TOLERANCE ( 84 FDA reports)
HYDRONEPHROSIS ( 84 FDA reports)
LIMB DISCOMFORT ( 84 FDA reports)
MULTIPLE SCLEROSIS ( 84 FDA reports)
RHONCHI ( 84 FDA reports)
SPONDYLOLISTHESIS ( 84 FDA reports)
POOR QUALITY SLEEP ( 83 FDA reports)
PULSE ABSENT ( 83 FDA reports)
THIRST ( 83 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 83 FDA reports)
HAEMODIALYSIS ( 83 FDA reports)
HYPOACUSIS ( 83 FDA reports)
JAW OPERATION ( 83 FDA reports)
MACULAR DEGENERATION ( 83 FDA reports)
ACUTE SINUSITIS ( 82 FDA reports)
DRUG SCREEN POSITIVE ( 82 FDA reports)
GINGIVAL ULCERATION ( 82 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 82 FDA reports)
HERPES SIMPLEX ( 82 FDA reports)
MYOPATHY ( 82 FDA reports)
OSTEOLYSIS ( 82 FDA reports)
PSORIASIS ( 82 FDA reports)
RASH MACULAR ( 82 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 82 FDA reports)
SPINAL DISORDER ( 82 FDA reports)
VASCULITIS ( 82 FDA reports)
RENAL TUBULAR NECROSIS ( 81 FDA reports)
SKIN LACERATION ( 81 FDA reports)
TONGUE DISORDER ( 81 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 81 FDA reports)
GOITRE ( 81 FDA reports)
INADEQUATE ANALGESIA ( 81 FDA reports)
AORTIC STENOSIS ( 80 FDA reports)
MENORRHAGIA ( 80 FDA reports)
NON-CARDIAC CHEST PAIN ( 80 FDA reports)
PARALYSIS ( 80 FDA reports)
POLYURIA ( 79 FDA reports)
RASH MACULO-PAPULAR ( 79 FDA reports)
RENAL INJURY ( 79 FDA reports)
UTERINE LEIOMYOMA ( 79 FDA reports)
ANKLE FRACTURE ( 79 FDA reports)
APPENDICITIS ( 79 FDA reports)
ATAXIA ( 79 FDA reports)
COORDINATION ABNORMAL ( 79 FDA reports)
DYSTONIA ( 79 FDA reports)
HOSPITALISATION ( 79 FDA reports)
ANEURYSM ( 78 FDA reports)
FOOT DEFORMITY ( 78 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 78 FDA reports)
HEPATIC CIRRHOSIS ( 78 FDA reports)
WOUND DEHISCENCE ( 78 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 77 FDA reports)
PREGNANCY ( 77 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 77 FDA reports)
DIFFICULTY IN WALKING ( 77 FDA reports)
BASAL CELL CARCINOMA ( 76 FDA reports)
BLEPHARITIS ( 76 FDA reports)
BRONCHITIS CHRONIC ( 76 FDA reports)
GANGRENE ( 76 FDA reports)
INJECTION SITE HAEMORRHAGE ( 76 FDA reports)
MYELODYSPLASTIC SYNDROME ( 76 FDA reports)
ORAL DISCOMFORT ( 76 FDA reports)
ORAL INFECTION ( 76 FDA reports)
OSTEOSCLEROSIS ( 76 FDA reports)
SICK SINUS SYNDROME ( 76 FDA reports)
URINE OUTPUT DECREASED ( 76 FDA reports)
POLYP ( 75 FDA reports)
PROTEINURIA ( 75 FDA reports)
PSEUDOMONAS INFECTION ( 75 FDA reports)
RASH PAPULAR ( 75 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 75 FDA reports)
SNEEZING ( 75 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 75 FDA reports)
THYROID DISORDER ( 75 FDA reports)
TYPE 1 DIABETES MELLITUS ( 75 FDA reports)
BRONCHIECTASIS ( 75 FDA reports)
DIALYSIS ( 75 FDA reports)
DRY THROAT ( 75 FDA reports)
FAECAL INCONTINENCE ( 75 FDA reports)
INHALATION THERAPY ( 75 FDA reports)
MUSCLE ATROPHY ( 75 FDA reports)
ACTINOMYCOSIS ( 74 FDA reports)
ANAPHYLACTIC SHOCK ( 74 FDA reports)
FAMILY STRESS ( 74 FDA reports)
FIBROSIS ( 74 FDA reports)
METASTATIC NEOPLASM ( 74 FDA reports)
PREMATURE BABY ( 74 FDA reports)
ANOXIC ENCEPHALOPATHY ( 73 FDA reports)
BACK DISORDER ( 73 FDA reports)
CATARACT OPERATION ( 73 FDA reports)
HAND FRACTURE ( 73 FDA reports)
MANIA ( 73 FDA reports)
DEBRIDEMENT ( 72 FDA reports)
DEVICE RELATED INFECTION ( 72 FDA reports)
HYPOKINESIA ( 72 FDA reports)
INGUINAL HERNIA ( 72 FDA reports)
LOW TURNOVER OSTEOPATHY ( 72 FDA reports)
PLEURISY ( 72 FDA reports)
PROTEIN URINE PRESENT ( 72 FDA reports)
WOUND INFECTION ( 72 FDA reports)
SENSORY LOSS ( 71 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 71 FDA reports)
THERAPY NON-RESPONDER ( 71 FDA reports)
VITAMIN D DEFICIENCY ( 71 FDA reports)
BACTERAEMIA ( 71 FDA reports)
EXPIRED DRUG ADMINISTERED ( 71 FDA reports)
HYPOMAGNESAEMIA ( 71 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 71 FDA reports)
INCREASED APPETITE ( 71 FDA reports)
INJECTION SITE REACTION ( 71 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 71 FDA reports)
BACK INJURY ( 70 FDA reports)
BONE FRAGMENTATION ( 70 FDA reports)
FACE OEDEMA ( 70 FDA reports)
GALLBLADDER INJURY ( 70 FDA reports)
HYPERTENSIVE HEART DISEASE ( 70 FDA reports)
JOINT EFFUSION ( 70 FDA reports)
LYMPHOEDEMA ( 70 FDA reports)
MITRAL VALVE PROLAPSE ( 70 FDA reports)
PARAESTHESIA ORAL ( 70 FDA reports)
PELVIC FRACTURE ( 69 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 69 FDA reports)
TOOTH INJURY ( 69 FDA reports)
BLOOD CALCIUM INCREASED ( 69 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 69 FDA reports)
COR PULMONALE ( 69 FDA reports)
EYE PRURITUS ( 69 FDA reports)
HYPERTHYROIDISM ( 69 FDA reports)
METASTASES TO SPINE ( 69 FDA reports)
MICTURITION URGENCY ( 69 FDA reports)
NO THERAPEUTIC RESPONSE ( 69 FDA reports)
DISEASE RECURRENCE ( 68 FDA reports)
JOINT DISLOCATION ( 68 FDA reports)
LUNG HYPERINFLATION ( 68 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 68 FDA reports)
PULMONARY INFARCTION ( 68 FDA reports)
SENSORY DISTURBANCE ( 67 FDA reports)
BRUXISM ( 67 FDA reports)
GINGIVAL DISORDER ( 67 FDA reports)
ACNE ( 66 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 66 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 66 FDA reports)
CLOSTRIDIAL INFECTION ( 66 FDA reports)
DERMAL CYST ( 66 FDA reports)
DEVELOPMENTAL DELAY ( 66 FDA reports)
DILATATION ATRIAL ( 66 FDA reports)
FRACTURE ( 66 FDA reports)
GROIN PAIN ( 66 FDA reports)
HEPATITIS C ( 66 FDA reports)
HYPERVENTILATION ( 66 FDA reports)
KIDNEY INFECTION ( 66 FDA reports)
NEUTROPHIL COUNT DECREASED ( 66 FDA reports)
PULMONARY HAEMORRHAGE ( 66 FDA reports)
TROPONIN INCREASED ( 66 FDA reports)
VENTRICULAR HYPOKINESIA ( 66 FDA reports)
PATHOLOGICAL FRACTURE ( 65 FDA reports)
PROSTATE CANCER ( 65 FDA reports)
QUALITY OF LIFE DECREASED ( 65 FDA reports)
SNORING ( 65 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 65 FDA reports)
TRISMUS ( 65 FDA reports)
WITHDRAWAL SYNDROME ( 65 FDA reports)
SQUAMOUS CELL CARCINOMA ( 64 FDA reports)
BILIARY COLIC ( 64 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 64 FDA reports)
CHEST X-RAY ABNORMAL ( 64 FDA reports)
DERMATITIS CONTACT ( 64 FDA reports)
DEVICE MALFUNCTION ( 64 FDA reports)
INTERMITTENT CLAUDICATION ( 64 FDA reports)
LIGAMENT SPRAIN ( 64 FDA reports)
BLOOD CHLORIDE DECREASED ( 63 FDA reports)
BLOOD URINE PRESENT ( 63 FDA reports)
BRONCHITIS ACUTE ( 63 FDA reports)
CATHETERISATION CARDIAC ( 63 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 63 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 63 FDA reports)
HYPERMETROPIA ( 63 FDA reports)
LACUNAR INFARCTION ( 63 FDA reports)
MYOSITIS ( 63 FDA reports)
TONGUE DISCOLOURATION ( 63 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 63 FDA reports)
RESPIRATORY ACIDOSIS ( 62 FDA reports)
VIITH NERVE PARALYSIS ( 62 FDA reports)
VITAMIN B12 DEFICIENCY ( 62 FDA reports)
ACUTE PULMONARY OEDEMA ( 62 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 62 FDA reports)
BONE EROSION ( 62 FDA reports)
COLLAPSE OF LUNG ( 62 FDA reports)
HOARSENESS ( 62 FDA reports)
INCONTINENCE ( 62 FDA reports)
LABORATORY TEST ABNORMAL ( 62 FDA reports)
LYMPHOMA ( 62 FDA reports)
NASAL SEPTUM DEVIATION ( 62 FDA reports)
NECK INJURY ( 62 FDA reports)
HEART DISEASE CONGENITAL ( 61 FDA reports)
INTESTINAL HAEMORRHAGE ( 61 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 61 FDA reports)
METASTASES TO LYMPH NODES ( 61 FDA reports)
SUBCUTANEOUS ABSCESS ( 61 FDA reports)
VENTRICULAR DYSFUNCTION ( 61 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 60 FDA reports)
STREPTOCOCCAL INFECTION ( 60 FDA reports)
WRIST FRACTURE ( 60 FDA reports)
ACIDOSIS ( 60 FDA reports)
ANXIETY DISORDER ( 60 FDA reports)
AORTIC DISORDER ( 60 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 60 FDA reports)
CONGENITAL ANOMALY ( 60 FDA reports)
ESSENTIAL HYPERTENSION ( 60 FDA reports)
JOINT CONTRACTURE ( 60 FDA reports)
LIP DRY ( 60 FDA reports)
ORGAN FAILURE ( 60 FDA reports)
OTITIS MEDIA ( 60 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 59 FDA reports)
CHOKING SENSATION ( 59 FDA reports)
ESCHERICHIA INFECTION ( 59 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 59 FDA reports)
MUSCULOSKELETAL DISORDER ( 59 FDA reports)
NEUTROPHIL COUNT INCREASED ( 59 FDA reports)
PERONEAL NERVE PALSY ( 59 FDA reports)
PERSONALITY CHANGE ( 59 FDA reports)
PHOTOPHOBIA ( 59 FDA reports)
RENAL PAIN ( 59 FDA reports)
UROSEPSIS ( 59 FDA reports)
SINUS HEADACHE ( 58 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 58 FDA reports)
BLOOD MAGNESIUM DECREASED ( 58 FDA reports)
BREAST CANCER FEMALE ( 58 FDA reports)
CARDIAC PACEMAKER INSERTION ( 58 FDA reports)
COLITIS ISCHAEMIC ( 58 FDA reports)
EXERCISE TOLERANCE DECREASED ( 58 FDA reports)
ILEUS PARALYTIC ( 58 FDA reports)
NO ADVERSE EVENT ( 58 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 57 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 57 FDA reports)
CEREBRAL HAEMORRHAGE ( 57 FDA reports)
DENTAL FISTULA ( 57 FDA reports)
MUSCLE CRAMP ( 57 FDA reports)
NODULE ( 57 FDA reports)
ORAL SURGERY ( 57 FDA reports)
PNEUMONIA BACTERIAL ( 57 FDA reports)
POLYDIPSIA ( 57 FDA reports)
SKELETAL INJURY ( 57 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 57 FDA reports)
THROMBOCYTOSIS ( 57 FDA reports)
TONGUE ULCERATION ( 57 FDA reports)
VASCULAR CALCIFICATION ( 57 FDA reports)
PROCEDURAL PAIN ( 56 FDA reports)
SHOULDER PAIN ( 56 FDA reports)
THROMBOPHLEBITIS ( 56 FDA reports)
ABNORMAL SENSATION IN EYE ( 56 FDA reports)
CERVICAL DYSPLASIA ( 56 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 56 FDA reports)
HYPOAESTHESIA ORAL ( 56 FDA reports)
IMPAIRED DRIVING ABILITY ( 56 FDA reports)
KNEE ARTHROPLASTY ( 56 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 56 FDA reports)
ATRIAL TACHYCARDIA ( 55 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 55 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 55 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 55 FDA reports)
COLON CANCER ( 55 FDA reports)
FACIAL PALSY ( 55 FDA reports)
KYPHOSIS ( 55 FDA reports)
LUNG CONSOLIDATION ( 55 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 55 FDA reports)
ONYCHOMYCOSIS ( 55 FDA reports)
OTITIS EXTERNA ( 55 FDA reports)
RETINAL DETACHMENT ( 55 FDA reports)
SKIN HYPERPIGMENTATION ( 55 FDA reports)
SOCIAL PROBLEM ( 55 FDA reports)
SUDDEN DEATH ( 55 FDA reports)
PRESCRIBED OVERDOSE ( 54 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 54 FDA reports)
SKIN NECROSIS ( 54 FDA reports)
UMBILICAL HERNIA ( 54 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 54 FDA reports)
CERVICAL SPINAL STENOSIS ( 54 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 54 FDA reports)
GINGIVAL RECESSION ( 54 FDA reports)
HEART INJURY ( 54 FDA reports)
HEMIPLEGIA ( 54 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 54 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 54 FDA reports)
MULTIPLE DRUG OVERDOSE ( 54 FDA reports)
ODYNOPHAGIA ( 54 FDA reports)
ORAL INTAKE REDUCED ( 54 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 53 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 53 FDA reports)
COSTOCHONDRITIS ( 53 FDA reports)
ERUCTATION ( 53 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 53 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 53 FDA reports)
METRORRHAGIA ( 53 FDA reports)
MYDRIASIS ( 53 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 53 FDA reports)
PULMONARY MASS ( 53 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 53 FDA reports)
TEARFULNESS ( 53 FDA reports)
TOBACCO USER ( 53 FDA reports)
WEIGHT FLUCTUATION ( 53 FDA reports)
PERITONITIS ( 52 FDA reports)
PLANTAR FASCIITIS ( 52 FDA reports)
FACIAL PAIN ( 52 FDA reports)
HYPOVENTILATION ( 52 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 52 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 52 FDA reports)
ANGIOPATHY ( 51 FDA reports)
ASTIGMATISM ( 51 FDA reports)
ATRIOVENTRICULAR BLOCK ( 51 FDA reports)
GASTRITIS EROSIVE ( 51 FDA reports)
GRANULOMA ( 51 FDA reports)
HEPATIC LESION ( 51 FDA reports)
INCREASED TENDENCY TO BRUISE ( 51 FDA reports)
LIPASE INCREASED ( 51 FDA reports)
NEOPLASM PROGRESSION ( 51 FDA reports)
PROCEDURAL COMPLICATION ( 51 FDA reports)
RESPIRATORY DEPRESSION ( 51 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 51 FDA reports)
PAPILLOEDEMA ( 50 FDA reports)
PERIPHERAL ISCHAEMIA ( 50 FDA reports)
PLEURAL FIBROSIS ( 50 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 50 FDA reports)
SCREAMING ( 50 FDA reports)
SELF-INJURIOUS IDEATION ( 50 FDA reports)
ANOSMIA ( 50 FDA reports)
BARRETT'S OESOPHAGUS ( 50 FDA reports)
BONE LOSS ( 50 FDA reports)
DENTAL OPERATION ( 50 FDA reports)
DIABETIC RETINOPATHY ( 50 FDA reports)
DUODENAL ULCER ( 50 FDA reports)
EAR DISORDER ( 50 FDA reports)
EUPHORIC MOOD ( 50 FDA reports)
FORMICATION ( 50 FDA reports)
METASTASIS ( 50 FDA reports)
NERVE INJURY ( 50 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 49 FDA reports)
BILE DUCT STONE ( 49 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 49 FDA reports)
DEAFNESS NEUROSENSORY ( 49 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 49 FDA reports)
HERNIA ( 49 FDA reports)
HYSTERECTOMY ( 49 FDA reports)
INTENTIONAL SELF-INJURY ( 49 FDA reports)
LIPOMA ( 49 FDA reports)
ORAL HERPES ( 49 FDA reports)
PANIC DISORDER ( 49 FDA reports)
POLYNEUROPATHY ( 49 FDA reports)
RIGHT VENTRICULAR FAILURE ( 49 FDA reports)
SARCOIDOSIS ( 49 FDA reports)
SKIN CANCER ( 49 FDA reports)
VARICOSE VEIN ( 49 FDA reports)
PETECHIAE ( 48 FDA reports)
SKIN BURNING SENSATION ( 48 FDA reports)
UPPER LIMB FRACTURE ( 48 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 48 FDA reports)
ANGIONEUROTIC OEDEMA ( 48 FDA reports)
BRAIN OEDEMA ( 48 FDA reports)
BREAST MASS ( 48 FDA reports)
DECREASED ACTIVITY ( 48 FDA reports)
EROSIVE OESOPHAGITIS ( 48 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 48 FDA reports)
MEDICAL DEVICE COMPLICATION ( 48 FDA reports)
MITRAL VALVE CALCIFICATION ( 48 FDA reports)
OCULAR ICTERUS ( 48 FDA reports)
BREATH ODOUR ( 47 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 47 FDA reports)
ENTEROCOCCAL INFECTION ( 47 FDA reports)
HUMERUS FRACTURE ( 47 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 47 FDA reports)
HYPOAESTHESIA FACIAL ( 47 FDA reports)
INTRACRANIAL ANEURYSM ( 47 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 47 FDA reports)
OSTEITIS DEFORMANS ( 47 FDA reports)
PANIC REACTION ( 47 FDA reports)
PULMONARY VALVE STENOSIS ( 47 FDA reports)
SKIN INFECTION ( 47 FDA reports)
TRANSAMINASES INCREASED ( 47 FDA reports)
VERTEBROPLASTY ( 47 FDA reports)
PHOTOSENSITIVITY REACTION ( 46 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 46 FDA reports)
TORSADE DE POINTES ( 46 FDA reports)
BIPOLAR I DISORDER ( 46 FDA reports)
BONE SCAN ABNORMAL ( 46 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 46 FDA reports)
EMPYEMA ( 46 FDA reports)
HYPERCAPNIA ( 46 FDA reports)
HYPOPHOSPHATAEMIA ( 46 FDA reports)
LOWER LIMB FRACTURE ( 46 FDA reports)
MITRAL VALVE DISEASE ( 46 FDA reports)
CALCULUS URETERIC ( 45 FDA reports)
HILAR LYMPHADENOPATHY ( 45 FDA reports)
HYPERBILIRUBINAEMIA ( 45 FDA reports)
INITIAL INSOMNIA ( 45 FDA reports)
INTRAOCULAR LENS IMPLANT ( 45 FDA reports)
PROTEIN TOTAL DECREASED ( 45 FDA reports)
RESUSCITATION ( 45 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 45 FDA reports)
TALIPES ( 45 FDA reports)
URINARY HESITATION ( 45 FDA reports)
VENOUS INSUFFICIENCY ( 45 FDA reports)
VISUAL FIELD DEFECT ( 45 FDA reports)
WOUND DRAINAGE ( 45 FDA reports)
PERICARDITIS ( 44 FDA reports)
PLASMACYTOMA ( 44 FDA reports)
SINUS OPERATION ( 44 FDA reports)
STENT PLACEMENT ( 44 FDA reports)
TENDON DISORDER ( 44 FDA reports)
X-RAY ABNORMAL ( 44 FDA reports)
ABSCESS JAW ( 44 FDA reports)
BLADDER CANCER ( 44 FDA reports)
BLOOD DISORDER ( 44 FDA reports)
BONE OPERATION ( 44 FDA reports)
CERVICOBRACHIAL SYNDROME ( 44 FDA reports)
CHANGE OF BOWEL HABIT ( 44 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 44 FDA reports)
DERMATITIS ALLERGIC ( 44 FDA reports)
EYE DISCHARGE ( 44 FDA reports)
GLOSSITIS ( 44 FDA reports)
ISCHAEMIA ( 44 FDA reports)
LIFE EXPECTANCY SHORTENED ( 44 FDA reports)
LUMBAR RADICULOPATHY ( 44 FDA reports)
ABSCESS ORAL ( 43 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 43 FDA reports)
DRUG LEVEL INCREASED ( 43 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 43 FDA reports)
FRACTURE NONUNION ( 43 FDA reports)
HYPOALBUMINAEMIA ( 43 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 43 FDA reports)
INTESTINAL PERFORATION ( 43 FDA reports)
LARYNGEAL OEDEMA ( 43 FDA reports)
MOTOR DYSFUNCTION ( 43 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 43 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 43 FDA reports)
SCHIZOPHRENIA ( 43 FDA reports)
SPINAL FUSION SURGERY ( 43 FDA reports)
STEM CELL TRANSPLANT ( 43 FDA reports)
SUBCUTANEOUS NODULE ( 43 FDA reports)
TENSION ( 43 FDA reports)
PRESBYOPIA ( 42 FDA reports)
PROCTALGIA ( 42 FDA reports)
PULPITIS DENTAL ( 42 FDA reports)
SCAB ( 42 FDA reports)
SENSATION OF HEAVINESS ( 42 FDA reports)
WOUND ( 42 FDA reports)
AFFECTIVE DISORDER ( 42 FDA reports)
ASPIRATION PLEURAL CAVITY ( 42 FDA reports)
BLINDNESS UNILATERAL ( 42 FDA reports)
CREPITATIONS ( 42 FDA reports)
ENDOTRACHEAL INTUBATION ( 42 FDA reports)
EOSINOPHILIA ( 42 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 42 FDA reports)
HAEMANGIOMA ( 42 FDA reports)
INJECTION SITE SWELLING ( 42 FDA reports)
LIBIDO DECREASED ( 42 FDA reports)
MOUTH HAEMORRHAGE ( 42 FDA reports)
AMENORRHOEA ( 41 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 41 FDA reports)
BODY TEMPERATURE DECREASED ( 41 FDA reports)
CARDIAC FLUTTER ( 41 FDA reports)
CONCUSSION ( 41 FDA reports)
EXTRASYSTOLES ( 41 FDA reports)
FOLLICULITIS ( 41 FDA reports)
FURUNCLE ( 41 FDA reports)
ISCHAEMIC STROKE ( 41 FDA reports)
MENSTRUATION IRREGULAR ( 41 FDA reports)
NEUROGENIC BLADDER ( 41 FDA reports)
PARKINSON'S DISEASE ( 41 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 41 FDA reports)
POSTNASAL DRIP ( 41 FDA reports)
PRE-ECLAMPSIA ( 41 FDA reports)
PANCREATITIS CHRONIC ( 40 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 40 FDA reports)
PHLEBITIS ( 40 FDA reports)
PHYSICAL ASSAULT ( 40 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 40 FDA reports)
ROSACEA ( 40 FDA reports)
SEBORRHOEIC DERMATITIS ( 40 FDA reports)
SEQUESTRECTOMY ( 40 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 40 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 40 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 40 FDA reports)
VENOUS THROMBOSIS ( 40 FDA reports)
ACCIDENTAL EXPOSURE ( 40 FDA reports)
AFFECT LABILITY ( 40 FDA reports)
APPENDICECTOMY ( 40 FDA reports)
CACHEXIA ( 40 FDA reports)
ENDOCARDITIS ( 40 FDA reports)
FEELING OF DESPAIR ( 40 FDA reports)
FIBRIN D DIMER INCREASED ( 40 FDA reports)
GASTRIC HAEMORRHAGE ( 40 FDA reports)
INCOHERENT ( 40 FDA reports)
LARGE INTESTINE PERFORATION ( 40 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 40 FDA reports)
MULTI-ORGAN DISORDER ( 40 FDA reports)
OLIGURIA ( 40 FDA reports)
AORTIC CALCIFICATION ( 39 FDA reports)
AORTIC VALVE STENOSIS ( 39 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 39 FDA reports)
BONE NEOPLASM MALIGNANT ( 39 FDA reports)
BRAIN INJURY ( 39 FDA reports)
BRONCHIOLITIS ( 39 FDA reports)
EYE INFECTION ( 39 FDA reports)
EYE LASER SURGERY ( 39 FDA reports)
GYNAECOMASTIA ( 39 FDA reports)
HORDEOLUM ( 39 FDA reports)
HUNGER ( 39 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 39 FDA reports)
NASAL DISCOMFORT ( 39 FDA reports)
NASAL DISORDER ( 39 FDA reports)
NASAL DRYNESS ( 39 FDA reports)
OESOPHAGEAL STENOSIS ( 39 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 39 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 39 FDA reports)
PROSTATOMEGALY ( 39 FDA reports)
RECTAL POLYP ( 39 FDA reports)
WOUND SECRETION ( 39 FDA reports)
PAROSMIA ( 38 FDA reports)
PREMATURE LABOUR ( 38 FDA reports)
RESORPTION BONE INCREASED ( 38 FDA reports)
RETINOPATHY ( 38 FDA reports)
SALIVARY HYPERSECRETION ( 38 FDA reports)
SKIN FIBROSIS ( 38 FDA reports)
THORACIC OUTLET SYNDROME ( 38 FDA reports)
UTERINE POLYP ( 38 FDA reports)
VAGINAL DISCHARGE ( 38 FDA reports)
ALVEOLAR OSTEITIS ( 38 FDA reports)
APATHY ( 38 FDA reports)
CERVIX CARCINOMA ( 38 FDA reports)
EYELID PTOSIS ( 38 FDA reports)
HAEMORRHAGIC ANAEMIA ( 38 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 38 FDA reports)
HEPATIC ENCEPHALOPATHY ( 38 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 38 FDA reports)
METABOLIC SYNDROME ( 38 FDA reports)
NEPHROPATHY ( 38 FDA reports)
NEPHROSCLEROSIS ( 38 FDA reports)
NERVE COMPRESSION ( 38 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 38 FDA reports)
ABSCESS LIMB ( 37 FDA reports)
ACUTE PRERENAL FAILURE ( 37 FDA reports)
AMMONIA INCREASED ( 37 FDA reports)
ANAEMIA POSTOPERATIVE ( 37 FDA reports)
AORTIC VALVE SCLEROSIS ( 37 FDA reports)
BREAST CANCER METASTATIC ( 37 FDA reports)
CARDIAC ENZYMES INCREASED ( 37 FDA reports)
DYSPHEMIA ( 37 FDA reports)
ENTERITIS ( 37 FDA reports)
FALLOT'S TETRALOGY ( 37 FDA reports)
GROWTH RETARDATION ( 37 FDA reports)
GUILLAIN-BARRE SYNDROME ( 37 FDA reports)
HEPATOTOXICITY ( 37 FDA reports)
HYPERAESTHESIA ( 37 FDA reports)
IMMUNE SYSTEM DISORDER ( 37 FDA reports)
MALOCCLUSION ( 37 FDA reports)
NEOPLASM ( 37 FDA reports)
NON-SMALL CELL LUNG CANCER ( 37 FDA reports)
OESOPHAGEAL DISORDER ( 37 FDA reports)
OPEN WOUND ( 37 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 37 FDA reports)
PO2 DECREASED ( 37 FDA reports)
SENSITIVITY OF TEETH ( 37 FDA reports)
SLEEP TERROR ( 37 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 37 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 36 FDA reports)
PITTING OEDEMA ( 36 FDA reports)
PULMONARY GRANULOMA ( 36 FDA reports)
SOMNAMBULISM ( 36 FDA reports)
SUFFOCATION FEELING ( 36 FDA reports)
THYROID CANCER ( 36 FDA reports)
TIC ( 36 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 36 FDA reports)
ALVEOLOPLASTY ( 36 FDA reports)
BLOOD CULTURE POSITIVE ( 36 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 36 FDA reports)
CULTURE URINE POSITIVE ( 36 FDA reports)
DIABETIC COMA ( 36 FDA reports)
DIZZINESS POSTURAL ( 36 FDA reports)
DRUG ERUPTION ( 36 FDA reports)
EOSINOPHIL COUNT INCREASED ( 36 FDA reports)
FEMORAL NECK FRACTURE ( 36 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 36 FDA reports)
INJECTION SITE PRURITUS ( 36 FDA reports)
INTESTINAL ISCHAEMIA ( 36 FDA reports)
INTRACARDIAC THROMBUS ( 36 FDA reports)
LEG AMPUTATION ( 36 FDA reports)
MEDICATION RESIDUE ( 36 FDA reports)
OCCULT BLOOD POSITIVE ( 36 FDA reports)
PAIN OF SKIN ( 36 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 35 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 35 FDA reports)
ARTHROPOD BITE ( 35 FDA reports)
ATROPHY ( 35 FDA reports)
BLOOD IRON DECREASED ( 35 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 35 FDA reports)
CLOSTRIDIUM COLITIS ( 35 FDA reports)
CONDUCTION DISORDER ( 35 FDA reports)
DRUG DISPENSING ERROR ( 35 FDA reports)
DYSTHYMIC DISORDER ( 35 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 35 FDA reports)
EPILEPSY ( 35 FDA reports)
EYE HAEMORRHAGE ( 35 FDA reports)
FACE INJURY ( 35 FDA reports)
HEPATIC NECROSIS ( 35 FDA reports)
LOCALISED OEDEMA ( 35 FDA reports)
NEUROPATHY ( 35 FDA reports)
PUPIL FIXED ( 35 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 35 FDA reports)
SKIN PAPILLOMA ( 35 FDA reports)
VOCAL CORD PARALYSIS ( 35 FDA reports)
PERITONITIS BACTERIAL ( 34 FDA reports)
PLASMACYTOSIS ( 34 FDA reports)
PULMONARY THROMBOSIS ( 34 FDA reports)
RESPIRATION ABNORMAL ( 34 FDA reports)
SENSATION OF FOREIGN BODY ( 34 FDA reports)
STATUS EPILEPTICUS ( 34 FDA reports)
THYROID NEOPLASM ( 34 FDA reports)
UNDERDOSE ( 34 FDA reports)
UTERINE DISORDER ( 34 FDA reports)
VITAMIN D DECREASED ( 34 FDA reports)
ABDOMINAL MASS ( 34 FDA reports)
ACTINIC KERATOSIS ( 34 FDA reports)
APPLICATION SITE ERYTHEMA ( 34 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 34 FDA reports)
BLOOD PH DECREASED ( 34 FDA reports)
BRAIN NEOPLASM ( 34 FDA reports)
CAROTID BRUIT ( 34 FDA reports)
CERUMEN IMPACTION ( 34 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 34 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 34 FDA reports)
FIBULA FRACTURE ( 34 FDA reports)
FLAT AFFECT ( 34 FDA reports)
HEART RATE ABNORMAL ( 34 FDA reports)
HYPERTENSIVE CRISIS ( 34 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 34 FDA reports)
HYPOTHERMIA ( 34 FDA reports)
MULTIPLE ALLERGIES ( 34 FDA reports)
AUTISM ( 33 FDA reports)
BEDRIDDEN ( 33 FDA reports)
BREAST TENDERNESS ( 33 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 33 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 33 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 33 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 33 FDA reports)
FEELING DRUNK ( 33 FDA reports)
HEART VALVE INCOMPETENCE ( 33 FDA reports)
HYPERCOAGULATION ( 33 FDA reports)
HYPERPHAGIA ( 33 FDA reports)
HYPOSPADIAS ( 33 FDA reports)
INJECTION SITE IRRITATION ( 33 FDA reports)
LIGAMENT RUPTURE ( 33 FDA reports)
LOSS OF EMPLOYMENT ( 33 FDA reports)
MONOPLEGIA ( 33 FDA reports)
POOR DENTAL CONDITION ( 33 FDA reports)
REGURGITATION ( 33 FDA reports)
SINUS ARRHYTHMIA ( 33 FDA reports)
SPINAL CORD COMPRESSION ( 33 FDA reports)
VERTIGO POSITIONAL ( 33 FDA reports)
PANCREATIC DISORDER ( 32 FDA reports)
PHARYNGEAL ERYTHEMA ( 32 FDA reports)
RADIOTHERAPY ( 32 FDA reports)
RESPIRATORY TRACT IRRITATION ( 32 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 32 FDA reports)
THERMAL BURN ( 32 FDA reports)
TINEA PEDIS ( 32 FDA reports)
TOOTH IMPACTED ( 32 FDA reports)
TRIGEMINAL NEURALGIA ( 32 FDA reports)
VITREOUS FLOATERS ( 32 FDA reports)
ALCOHOL USE ( 32 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 32 FDA reports)
BONE MARROW FAILURE ( 32 FDA reports)
BREAST CYST ( 32 FDA reports)
CHOLESTASIS ( 32 FDA reports)
GASTRIC POLYPS ( 32 FDA reports)
HAEMOLYTIC ANAEMIA ( 32 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 32 FDA reports)
HYPERNATRAEMIA ( 32 FDA reports)
HYPOTONIA ( 32 FDA reports)
INFERTILITY ( 32 FDA reports)
INJECTION SITE RASH ( 32 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 32 FDA reports)
ANURIA ( 31 FDA reports)
APHAGIA ( 31 FDA reports)
BLOOD PRESSURE ABNORMAL ( 31 FDA reports)
BONE MARROW TRANSPLANT ( 31 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 31 FDA reports)
CHEILITIS ( 31 FDA reports)
CORONARY ARTERY BYPASS ( 31 FDA reports)
CYSTOCELE ( 31 FDA reports)
DENTURE WEARER ( 31 FDA reports)
DIABETIC NEPHROPATHY ( 31 FDA reports)
ENCEPHALOMALACIA ( 31 FDA reports)
FOETAL DISTRESS SYNDROME ( 31 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 31 FDA reports)
GASTROINTESTINAL PAIN ( 31 FDA reports)
HOSTILITY ( 31 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 31 FDA reports)
INCISIONAL DRAINAGE ( 31 FDA reports)
METABOLIC ENCEPHALOPATHY ( 31 FDA reports)
MUSCLE RIGIDITY ( 31 FDA reports)
PARKINSONISM ( 31 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 31 FDA reports)
SEASONAL ALLERGY ( 31 FDA reports)
SEROMA ( 31 FDA reports)
SMOKER ( 31 FDA reports)
WEGENER'S GRANULOMATOSIS ( 31 FDA reports)
PHOTOPSIA ( 30 FDA reports)
POSTURE ABNORMAL ( 30 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 30 FDA reports)
SERUM FERRITIN INCREASED ( 30 FDA reports)
STRESS URINARY INCONTINENCE ( 30 FDA reports)
TENSION HEADACHE ( 30 FDA reports)
TOBACCO ABUSE ( 30 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 30 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 30 FDA reports)
BLINDNESS TRANSIENT ( 30 FDA reports)
BLOOD URIC ACID INCREASED ( 30 FDA reports)
BRAIN DEATH ( 30 FDA reports)
COMMUNICATION DISORDER ( 30 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 30 FDA reports)
EYELID OEDEMA ( 30 FDA reports)
HAEMOTHORAX ( 30 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 30 FDA reports)
INCREASED BRONCHIAL SECRETION ( 30 FDA reports)
LIVEDO RETICULARIS ( 30 FDA reports)
LIVER INJURY ( 30 FDA reports)
MACROCYTOSIS ( 30 FDA reports)
MELANOCYTIC NAEVUS ( 30 FDA reports)
MENINGITIS ( 30 FDA reports)
MITRAL VALVE STENOSIS ( 30 FDA reports)
MUSCLE DISORDER ( 30 FDA reports)
MYELOMA RECURRENCE ( 30 FDA reports)
NEURITIS ( 30 FDA reports)
OTORRHOEA ( 30 FDA reports)
ABSCESS DRAINAGE ( 29 FDA reports)
ADENOCARCINOMA ( 29 FDA reports)
ADJUSTMENT DISORDER ( 29 FDA reports)
AKATHISIA ( 29 FDA reports)
BILIARY DILATATION ( 29 FDA reports)
BLOOD AMYLASE INCREASED ( 29 FDA reports)
DROOLING ( 29 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 29 FDA reports)
ENDOMETRIOSIS ( 29 FDA reports)
ENURESIS ( 29 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 29 FDA reports)
HEPATOSPLENOMEGALY ( 29 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 29 FDA reports)
IMPULSIVE BEHAVIOUR ( 29 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 29 FDA reports)
IRON DEFICIENCY ( 29 FDA reports)
JAUNDICE CHOLESTATIC ( 29 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 29 FDA reports)
MECHANICAL VENTILATION ( 29 FDA reports)
OROPHARYNGEAL BLISTERING ( 29 FDA reports)
OSTEOMYELITIS CHRONIC ( 29 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 29 FDA reports)
PANCREATIC CARCINOMA ( 29 FDA reports)
PATHOGEN RESISTANCE ( 29 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 29 FDA reports)
PSYCHOLOGICAL TRAUMA ( 29 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 29 FDA reports)
PURULENCE ( 29 FDA reports)
RAYNAUD'S PHENOMENON ( 29 FDA reports)
SKIN PLAQUE ( 29 FDA reports)
PERSONALITY DISORDER ( 28 FDA reports)
PILONIDAL CYST ( 28 FDA reports)
POISONING ( 28 FDA reports)
POLYPECTOMY ( 28 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 28 FDA reports)
SCLERODERMA ( 28 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 28 FDA reports)
STRIDOR ( 28 FDA reports)
TENOSYNOVITIS ( 28 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 28 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 28 FDA reports)
TUMOUR LYSIS SYNDROME ( 28 FDA reports)
URINE ANALYSIS ABNORMAL ( 28 FDA reports)
URINE FLOW DECREASED ( 28 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 28 FDA reports)
ANAL FISSURE ( 28 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 28 FDA reports)
COARCTATION OF THE AORTA ( 28 FDA reports)
COLON ADENOMA ( 28 FDA reports)
CONVERSION DISORDER ( 28 FDA reports)
DEAFNESS BILATERAL ( 28 FDA reports)
DRUG PRESCRIBING ERROR ( 28 FDA reports)
DYSAESTHESIA ( 28 FDA reports)
DYSMENORRHOEA ( 28 FDA reports)
EDENTULOUS ( 28 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 28 FDA reports)
FEEDING DISORDER NEONATAL ( 28 FDA reports)
GASTROINTESTINAL NECROSIS ( 28 FDA reports)
GENERALISED ANXIETY DISORDER ( 28 FDA reports)
GINGIVAL ERYTHEMA ( 28 FDA reports)
HAEMOLYSIS ( 28 FDA reports)
INJECTION SITE URTICARIA ( 28 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 28 FDA reports)
KLEBSIELLA INFECTION ( 28 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 28 FDA reports)
NICOTINE DEPENDENCE ( 28 FDA reports)
ORAL CAVITY FISTULA ( 28 FDA reports)
PAINFUL RESPIRATION ( 28 FDA reports)
ALCOHOL POISONING ( 27 FDA reports)
ANIMAL BITE ( 27 FDA reports)
AREFLEXIA ( 27 FDA reports)
AUTOIMMUNE HEPATITIS ( 27 FDA reports)
BLEPHAROSPASM ( 27 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 27 FDA reports)
BRONCHIAL SECRETION RETENTION ( 27 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 27 FDA reports)
CHRONIC FATIGUE SYNDROME ( 27 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 27 FDA reports)
DENTAL PROSTHESIS USER ( 27 FDA reports)
DIABETIC GASTROPARESIS ( 27 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 27 FDA reports)
DYSPLASTIC NAEVUS ( 27 FDA reports)
EPIGASTRIC DISCOMFORT ( 27 FDA reports)
EXOPHTHALMOS ( 27 FDA reports)
FOREIGN BODY ( 27 FDA reports)
HEAD DISCOMFORT ( 27 FDA reports)
HEPATIC FIBROSIS ( 27 FDA reports)
INDURATION ( 27 FDA reports)
IRITIS ( 27 FDA reports)
LEFT VENTRICULAR FAILURE ( 27 FDA reports)
METABOLIC DISORDER ( 27 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 27 FDA reports)
ORAL FUNGAL INFECTION ( 27 FDA reports)
PARAPLEGIA ( 27 FDA reports)
PATHOLOGICAL GAMBLING ( 27 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 27 FDA reports)
PROSTATITIS ( 27 FDA reports)
RETINAL HAEMORRHAGE ( 27 FDA reports)
SECRETION DISCHARGE ( 27 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 27 FDA reports)
SLUGGISHNESS ( 27 FDA reports)
SPUTUM CULTURE POSITIVE ( 27 FDA reports)
TRAUMATIC BRAIN INJURY ( 27 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
WHEELCHAIR USER ( 27 FDA reports)
PELVIC VENOUS THROMBOSIS ( 26 FDA reports)
POLYSUBSTANCE ABUSE ( 26 FDA reports)
PORTAL HYPERTENSION ( 26 FDA reports)
SKIN NODULE ( 26 FDA reports)
SMALL FOR DATES BABY ( 26 FDA reports)
SUDDEN CARDIAC DEATH ( 26 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 26 FDA reports)
VOCAL CORD DISORDER ( 26 FDA reports)
ADHESION ( 26 FDA reports)
ASTHMATIC CRISIS ( 26 FDA reports)
BLOOD BICARBONATE DECREASED ( 26 FDA reports)
BONE SWELLING ( 26 FDA reports)
CARDIAC TAMPONADE ( 26 FDA reports)
CLEFT PALATE ( 26 FDA reports)
DENTAL NECROSIS ( 26 FDA reports)
DEVICE OCCLUSION ( 26 FDA reports)
EAR DISCOMFORT ( 26 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 26 FDA reports)
EMBOLISM ( 26 FDA reports)
EXTREMITY CONTRACTURE ( 26 FDA reports)
FISTULA REPAIR ( 26 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 26 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 26 FDA reports)
HYDROCEPHALUS ( 26 FDA reports)
HYPERPARATHYROIDISM ( 26 FDA reports)
INTENTIONAL MISUSE ( 26 FDA reports)
MYOPIA ( 26 FDA reports)
NEUTROPENIC SEPSIS ( 26 FDA reports)
OPTIC NEURITIS ( 26 FDA reports)
ABNORMAL FAECES ( 25 FDA reports)
ADRENAL NEOPLASM ( 25 FDA reports)
ALCOHOL ABUSE ( 25 FDA reports)
APTYALISM ( 25 FDA reports)
AXILLARY PAIN ( 25 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 25 FDA reports)
CARDIOPULMONARY FAILURE ( 25 FDA reports)
CATHETER RELATED INFECTION ( 25 FDA reports)
CHOLECYSTITIS INFECTIVE ( 25 FDA reports)
CLAUSTROPHOBIA ( 25 FDA reports)
DIABETIC COMPLICATION ( 25 FDA reports)
FACET JOINT SYNDROME ( 25 FDA reports)
GINGIVAL ABSCESS ( 25 FDA reports)
IMPLANT SITE INFECTION ( 25 FDA reports)
INFARCTION ( 25 FDA reports)
JAUNDICE NEONATAL ( 25 FDA reports)
JOINT INSTABILITY ( 25 FDA reports)
LYMPHADENITIS ( 25 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 25 FDA reports)
OVERWEIGHT ( 25 FDA reports)
SEROTONIN SYNDROME ( 25 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 25 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 25 FDA reports)
TRAUMATIC LUNG INJURY ( 25 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 25 FDA reports)
VENTRICULAR ARRHYTHMIA ( 25 FDA reports)
VITREOUS DETACHMENT ( 25 FDA reports)
RENAL ARTERY STENOSIS ( 24 FDA reports)
RIGHT ATRIAL DILATATION ( 24 FDA reports)
SELF ESTEEM DECREASED ( 24 FDA reports)
SEXUAL DYSFUNCTION ( 24 FDA reports)
SKIN IRRITATION ( 24 FDA reports)
TIBIA FRACTURE ( 24 FDA reports)
UTERINE HAEMORRHAGE ( 24 FDA reports)
VAGINAL INFECTION ( 24 FDA reports)
ABDOMINAL ADHESIONS ( 24 FDA reports)
ADRENAL DISORDER ( 24 FDA reports)
AGRANULOCYTOSIS ( 24 FDA reports)
AORTIC DILATATION ( 24 FDA reports)
AORTIC VALVE CALCIFICATION ( 24 FDA reports)
APNOEIC ATTACK ( 24 FDA reports)
ARTERIOSPASM CORONARY ( 24 FDA reports)
AUTISM SPECTRUM DISORDER ( 24 FDA reports)
BLADDER OBSTRUCTION ( 24 FDA reports)
BOWEN'S DISEASE ( 24 FDA reports)
CEREBELLAR INFARCTION ( 24 FDA reports)
CUSHING'S SYNDROME ( 24 FDA reports)
FACIAL BONES FRACTURE ( 24 FDA reports)
FOETAL HEART RATE ABNORMAL ( 24 FDA reports)
GALLBLADDER POLYP ( 24 FDA reports)
HAEMODYNAMIC INSTABILITY ( 24 FDA reports)
HERPES VIRUS INFECTION ( 24 FDA reports)
HORMONE LEVEL ABNORMAL ( 24 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 24 FDA reports)
MACROGLOSSIA ( 24 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 24 FDA reports)
MUSCLE SPASTICITY ( 24 FDA reports)
MYELOPATHY ( 24 FDA reports)
NECROSIS ( 24 FDA reports)
ORAL MUCOSAL BLISTERING ( 24 FDA reports)
PALATAL DISORDER ( 24 FDA reports)
ACUTE HEPATIC FAILURE ( 23 FDA reports)
AMYLOIDOSIS ( 23 FDA reports)
ANAEMIA MACROCYTIC ( 23 FDA reports)
APPLICATION SITE PRURITUS ( 23 FDA reports)
BILE DUCT STENOSIS ( 23 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 23 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 23 FDA reports)
BLOOD TEST ABNORMAL ( 23 FDA reports)
CAROTID ARTERY DISEASE ( 23 FDA reports)
CAROTID ARTERY OCCLUSION ( 23 FDA reports)
CEREBROVASCULAR DISORDER ( 23 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 23 FDA reports)
DEPENDENCE ( 23 FDA reports)
DYSPHORIA ( 23 FDA reports)
ENCEPHALITIS ( 23 FDA reports)
ENTEROCUTANEOUS FISTULA ( 23 FDA reports)
FAECALOMA ( 23 FDA reports)
FEAR OF DEATH ( 23 FDA reports)
FRACTURED SACRUM ( 23 FDA reports)
GRIP STRENGTH DECREASED ( 23 FDA reports)
HAEMATOCRIT ABNORMAL ( 23 FDA reports)
HEPATOCELLULAR DAMAGE ( 23 FDA reports)
HICCUPS ( 23 FDA reports)
HIP ARTHROPLASTY ( 23 FDA reports)
IMPAIRED SELF-CARE ( 23 FDA reports)
ISCHAEMIC HEPATITIS ( 23 FDA reports)
LIGAMENT INJURY ( 23 FDA reports)
MICTURITION DISORDER ( 23 FDA reports)
NODAL ARRHYTHMIA ( 23 FDA reports)
OOPHORECTOMY ( 23 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 23 FDA reports)
POSTOPERATIVE INFECTION ( 23 FDA reports)
PSORIATIC ARTHROPATHY ( 23 FDA reports)
PURPURA ( 23 FDA reports)
RADIATION ASSOCIATED PAIN ( 23 FDA reports)
RECTOCELE ( 23 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 23 FDA reports)
SEBORRHOEIC KERATOSIS ( 23 FDA reports)
SHOULDER ARTHROPLASTY ( 23 FDA reports)
SPONDYLOARTHROPATHY ( 23 FDA reports)
STREPTOCOCCAL SEPSIS ( 23 FDA reports)
TELANGIECTASIA ( 23 FDA reports)
THYROIDECTOMY ( 23 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 23 FDA reports)
PAPILLOMA VIRAL INFECTION ( 22 FDA reports)
PIGMENTATION DISORDER ( 22 FDA reports)
POLYARTHRITIS ( 22 FDA reports)
POST THROMBOTIC SYNDROME ( 22 FDA reports)
PULMONARY HILUM MASS ( 22 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 22 FDA reports)
RENAL ATROPHY ( 22 FDA reports)
RENAL MASS ( 22 FDA reports)
SKIN WARM ( 22 FDA reports)
SPUTUM INCREASED ( 22 FDA reports)
STRESS SYMPTOMS ( 22 FDA reports)
SUBMANDIBULAR MASS ( 22 FDA reports)
SUNBURN ( 22 FDA reports)
TENDON INJURY ( 22 FDA reports)
THORACOTOMY ( 22 FDA reports)
TONGUE BLISTERING ( 22 FDA reports)
TOOTH DISCOLOURATION ( 22 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 22 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 22 FDA reports)
UNINTENDED PREGNANCY ( 22 FDA reports)
VENA CAVA FILTER INSERTION ( 22 FDA reports)
ACROCHORDON ( 22 FDA reports)
AGORAPHOBIA ( 22 FDA reports)
ANAL ABSCESS ( 22 FDA reports)
APPETITE DISORDER ( 22 FDA reports)
APPLICATION SITE RASH ( 22 FDA reports)
BASEDOW'S DISEASE ( 22 FDA reports)
BILIARY TRACT DISORDER ( 22 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 22 FDA reports)
BRAIN HERNIATION ( 22 FDA reports)
CHAPPED LIPS ( 22 FDA reports)
COLON POLYPECTOMY ( 22 FDA reports)
CYSTITIS INTERSTITIAL ( 22 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 22 FDA reports)
DEMYELINATION ( 22 FDA reports)
DEVICE BREAKAGE ( 22 FDA reports)
ESCHERICHIA SEPSIS ( 22 FDA reports)
GALLBLADDER PAIN ( 22 FDA reports)
GLYCOSURIA ( 22 FDA reports)
HEPATITIS ACUTE ( 22 FDA reports)
HEPATITIS B ( 22 FDA reports)
HISTOPLASMOSIS ( 22 FDA reports)
HYPERPLASIA ( 22 FDA reports)
INCISION SITE COMPLICATION ( 22 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 22 FDA reports)
INJECTION SITE DISCOLOURATION ( 22 FDA reports)
JOINT LOCK ( 22 FDA reports)
JUGULAR VEIN DISTENSION ( 22 FDA reports)
LIGAMENT DISORDER ( 22 FDA reports)
LUNG CANCER METASTATIC ( 22 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 22 FDA reports)
MULTIPLE FRACTURES ( 22 FDA reports)
MUSCLE INJURY ( 22 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 22 FDA reports)
MYCOSIS FUNGOIDES ( 22 FDA reports)
AORTIC VALVE DISEASE ( 21 FDA reports)
ATROPHIC VULVOVAGINITIS ( 21 FDA reports)
BLOOD UREA DECREASED ( 21 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 21 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 21 FDA reports)
BUNDLE BRANCH BLOCK ( 21 FDA reports)
CARBON DIOXIDE INCREASED ( 21 FDA reports)
COMPLEX PARTIAL SEIZURES ( 21 FDA reports)
CUSHINGOID ( 21 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 21 FDA reports)
DRUG LEVEL DECREASED ( 21 FDA reports)
DYSPAREUNIA ( 21 FDA reports)
DYSPLASIA ( 21 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 21 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 21 FDA reports)
EYE NAEVUS ( 21 FDA reports)
FACIAL NEURALGIA ( 21 FDA reports)
FOETAL GROWTH RETARDATION ( 21 FDA reports)
FOOD INTOLERANCE ( 21 FDA reports)
FOOD POISONING ( 21 FDA reports)
GESTATIONAL DIABETES ( 21 FDA reports)
HEPATIC CONGESTION ( 21 FDA reports)
HEPATIC NEOPLASM ( 21 FDA reports)
HYPERURICAEMIA ( 21 FDA reports)
INJECTION SITE WARMTH ( 21 FDA reports)
LARGE INTESTINAL ULCER ( 21 FDA reports)
LARYNGOSPASM ( 21 FDA reports)
LYMPHOPENIA ( 21 FDA reports)
MALIGNANT MELANOMA ( 21 FDA reports)
MAMMOGRAM ABNORMAL ( 21 FDA reports)
MYASTHENIA GRAVIS ( 21 FDA reports)
NASAL POLYPS ( 21 FDA reports)
OPTIC NERVE CUPPING ( 21 FDA reports)
ORAL PRURITUS ( 21 FDA reports)
PAROTITIS ( 21 FDA reports)
PERNICIOUS ANAEMIA ( 21 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 21 FDA reports)
POLYCYTHAEMIA ( 21 FDA reports)
POOR PERSONAL HYGIENE ( 21 FDA reports)
PORTAL VEIN THROMBOSIS ( 21 FDA reports)
PRODUCT TASTE ABNORMAL ( 21 FDA reports)
PSYCHIATRIC SYMPTOM ( 21 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 21 FDA reports)
RADIAL NERVE PALSY ( 21 FDA reports)
RADICULITIS LUMBOSACRAL ( 21 FDA reports)
RADIUS FRACTURE ( 21 FDA reports)
RESPIRATORY ALKALOSIS ( 21 FDA reports)
SEPSIS SYNDROME ( 21 FDA reports)
SIALOADENITIS ( 21 FDA reports)
SKIN FISSURES ( 21 FDA reports)
SKIN REACTION ( 21 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 21 FDA reports)
STOMATITIS NECROTISING ( 21 FDA reports)
SUBSTANCE ABUSE ( 21 FDA reports)
THYROIDITIS ( 21 FDA reports)
TONGUE BITING ( 21 FDA reports)
TONGUE COATED ( 21 FDA reports)
VESICAL FISTULA ( 21 FDA reports)
VULVOVAGINAL PRURITUS ( 21 FDA reports)
PERIORBITAL HAEMATOMA ( 20 FDA reports)
PERIORBITAL OEDEMA ( 20 FDA reports)
PNEUMONIA VIRAL ( 20 FDA reports)
PROTEUS INFECTION ( 20 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 20 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 20 FDA reports)
SELF-MEDICATION ( 20 FDA reports)
TEMPERATURE INTOLERANCE ( 20 FDA reports)
TONGUE INJURY ( 20 FDA reports)
TRACHEOBRONCHITIS ( 20 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 20 FDA reports)
TRIGGER FINGER ( 20 FDA reports)
UMBILICAL HERNIA REPAIR ( 20 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 20 FDA reports)
UTERINE CANCER ( 20 FDA reports)
VAGINITIS BACTERIAL ( 20 FDA reports)
VARICES OESOPHAGEAL ( 20 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 20 FDA reports)
ATRIAL THROMBOSIS ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 20 FDA reports)
CATHETER PLACEMENT ( 20 FDA reports)
CHEST WALL PAIN ( 20 FDA reports)
CHOLESTEROSIS ( 20 FDA reports)
CORNEAL DYSTROPHY ( 20 FDA reports)
DISSOCIATION ( 20 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 20 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 20 FDA reports)
EXTREMITY NECROSIS ( 20 FDA reports)
EYE MOVEMENT DISORDER ( 20 FDA reports)
FAECES PALE ( 20 FDA reports)
FOREIGN BODY TRAUMA ( 20 FDA reports)
FRUSTRATION ( 20 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 20 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 20 FDA reports)
GENERALISED ERYTHEMA ( 20 FDA reports)
GINGIVAL EROSION ( 20 FDA reports)
H1N1 INFLUENZA ( 20 FDA reports)
HELICOBACTER INFECTION ( 20 FDA reports)
HODGKIN'S DISEASE ( 20 FDA reports)
IMPETIGO ( 20 FDA reports)
INFUSION SITE ERYTHEMA ( 20 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 20 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 20 FDA reports)
LABYRINTHITIS ( 20 FDA reports)
LEUKAEMIA ( 20 FDA reports)
LEUKOPLAKIA ORAL ( 20 FDA reports)
MEAN CELL VOLUME INCREASED ( 20 FDA reports)
MENOPAUSE ( 20 FDA reports)
MORTON'S NEUROMA ( 20 FDA reports)
MUSCLE FATIGUE ( 20 FDA reports)
MUSCLE HAEMORRHAGE ( 20 FDA reports)
NEUROLOGICAL SYMPTOM ( 20 FDA reports)
ORAL DISCHARGE ( 20 FDA reports)
ORAL TORUS ( 20 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 20 FDA reports)
ADNEXA UTERI CYST ( 19 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
APLASIA PURE RED CELL ( 19 FDA reports)
BLOOD CREATINE INCREASED ( 19 FDA reports)
BRADYARRHYTHMIA ( 19 FDA reports)
CARDIAC FAILURE ACUTE ( 19 FDA reports)
CARDIAC OPERATION ( 19 FDA reports)
CHEST TUBE INSERTION ( 19 FDA reports)
CLEFT LIP ( 19 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 19 FDA reports)
FISTULA DISCHARGE ( 19 FDA reports)
GENITAL HERPES ( 19 FDA reports)
HAEMANGIOMA OF LIVER ( 19 FDA reports)
HAEMORRHAGIC STROKE ( 19 FDA reports)
HERNIA REPAIR ( 19 FDA reports)
HYPERTONIC BLADDER ( 19 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 19 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 19 FDA reports)
IMMUNOSUPPRESSION ( 19 FDA reports)
INCISIONAL HERNIA ( 19 FDA reports)
INGROWING NAIL ( 19 FDA reports)
INGUINAL HERNIA REPAIR ( 19 FDA reports)
INJECTION SITE BRUISING ( 19 FDA reports)
LYMPHOCYTIC INFILTRATION ( 19 FDA reports)
MACULAR HOLE ( 19 FDA reports)
MASTECTOMY ( 19 FDA reports)
MENSTRUAL DISORDER ( 19 FDA reports)
METABOLIC ALKALOSIS ( 19 FDA reports)
NECK MASS ( 19 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 19 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 19 FDA reports)
OESOPHAGEAL SPASM ( 19 FDA reports)
PNEUMONIA KLEBSIELLA ( 19 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 19 FDA reports)
PROTEIN TOTAL INCREASED ( 19 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 19 FDA reports)
SPLENIC LESION ( 19 FDA reports)
STARING ( 19 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 19 FDA reports)
STRESS INCONTINENCE ( 19 FDA reports)
SUICIDAL BEHAVIOUR ( 19 FDA reports)
TOE AMPUTATION ( 19 FDA reports)
TONGUE OEDEMA ( 19 FDA reports)
TOOTH REPAIR ( 19 FDA reports)
WRONG DRUG ADMINISTERED ( 19 FDA reports)
PEAU D'ORANGE ( 18 FDA reports)
PERIARTHRITIS ( 18 FDA reports)
PERICARDIAL HAEMORRHAGE ( 18 FDA reports)
POLYP COLORECTAL ( 18 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 18 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 18 FDA reports)
RECTAL PROLAPSE ( 18 FDA reports)
SACROILIITIS ( 18 FDA reports)
SPLENIC INFARCTION ( 18 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 18 FDA reports)
SYSTEMIC CANDIDA ( 18 FDA reports)
TOE DEFORMITY ( 18 FDA reports)
TOOTH DEPOSIT ( 18 FDA reports)
TORTICOLLIS ( 18 FDA reports)
UTERINE ENLARGEMENT ( 18 FDA reports)
ALCOHOLISM ( 18 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 18 FDA reports)
APHTHOUS STOMATITIS ( 18 FDA reports)
APPLICATION SITE PAIN ( 18 FDA reports)
ASPHYXIA ( 18 FDA reports)
AUTOIMMUNE DISORDER ( 18 FDA reports)
BACTERIAL DISEASE CARRIER ( 18 FDA reports)
BILE DUCT OBSTRUCTION ( 18 FDA reports)
BLOOD GASES ABNORMAL ( 18 FDA reports)
BONE ABSCESS ( 18 FDA reports)
BREAST CANCER RECURRENT ( 18 FDA reports)
BREAST LUMP REMOVAL ( 18 FDA reports)
CARBUNCLE ( 18 FDA reports)
CEREBRAL PALSY ( 18 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 18 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 18 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 18 FDA reports)
DENTAL CARE ( 18 FDA reports)
DIAPHRAGMATIC HERNIA ( 18 FDA reports)
DUPUYTREN'S CONTRACTURE ( 18 FDA reports)
ECHOCARDIOGRAM ( 18 FDA reports)
EJECTION FRACTION ABNORMAL ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 18 FDA reports)
FIBROMA ( 18 FDA reports)
FOOD ALLERGY ( 18 FDA reports)
GALACTORRHOEA ( 18 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 18 FDA reports)
HAIR GROWTH ABNORMAL ( 18 FDA reports)
HEREDITARY ANGIOEDEMA ( 18 FDA reports)
LOGORRHOEA ( 18 FDA reports)
LUNG ABSCESS ( 18 FDA reports)
MENOMETRORRHAGIA ( 18 FDA reports)
MILIA ( 18 FDA reports)
NASAL OEDEMA ( 18 FDA reports)
NOCTURNAL DYSPNOEA ( 18 FDA reports)
OBSTRUCTION ( 18 FDA reports)
OESOPHAGEAL ULCER ( 18 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 17 FDA reports)
ANAPHYLACTOID REACTION ( 17 FDA reports)
ANORECTAL DISCOMFORT ( 17 FDA reports)
APPARENT DEATH ( 17 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 17 FDA reports)
BACTERIAL SEPSIS ( 17 FDA reports)
BACTERIAL TEST POSITIVE ( 17 FDA reports)
BIOPSY SKIN ABNORMAL ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 17 FDA reports)
BLOOD PH INCREASED ( 17 FDA reports)
BLOOD SODIUM INCREASED ( 17 FDA reports)
BRAIN STEM INFARCTION ( 17 FDA reports)
BREAST DISORDER ( 17 FDA reports)
BRONCHIAL OBSTRUCTION ( 17 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 17 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 17 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 17 FDA reports)
CEREBRAL DISORDER ( 17 FDA reports)
CHOREA ( 17 FDA reports)
CLUMSINESS ( 17 FDA reports)
COMPARTMENT SYNDROME ( 17 FDA reports)
DERMATITIS EXFOLIATIVE ( 17 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 17 FDA reports)
GASTROINTESTINAL INFECTION ( 17 FDA reports)
GENITAL RASH ( 17 FDA reports)
HALO VISION ( 17 FDA reports)
HYPERKINESIA ( 17 FDA reports)
HYPERTROPHY ( 17 FDA reports)
IMPULSE-CONTROL DISORDER ( 17 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 17 FDA reports)
INFLAMMATION OF WOUND ( 17 FDA reports)
INFUSION SITE PAIN ( 17 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 17 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 17 FDA reports)
KNEE OPERATION ( 17 FDA reports)
LICHEN PLANUS ( 17 FDA reports)
LOSS OF LIBIDO ( 17 FDA reports)
MASTOIDITIS ( 17 FDA reports)
MEDICAL DEVICE REMOVAL ( 17 FDA reports)
MENINGITIS ASEPTIC ( 17 FDA reports)
MUCOUS MEMBRANE DISORDER ( 17 FDA reports)
OCCULT BLOOD ( 17 FDA reports)
OESOPHAGEAL CARCINOMA ( 17 FDA reports)
OPTIC ATROPHY ( 17 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 17 FDA reports)
OTITIS MEDIA CHRONIC ( 17 FDA reports)
PCO2 INCREASED ( 17 FDA reports)
POLYCYSTIC OVARIES ( 17 FDA reports)
POST HERPETIC NEURALGIA ( 17 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 17 FDA reports)
RASH PUSTULAR ( 17 FDA reports)
RENAL CANCER ( 17 FDA reports)
RETINAL DISORDER ( 17 FDA reports)
SINUS POLYP ( 17 FDA reports)
SOFT TISSUE INFLAMMATION ( 17 FDA reports)
SPINAL DECOMPRESSION ( 17 FDA reports)
SUBDURAL HAEMORRHAGE ( 17 FDA reports)
TRANSFUSION ( 17 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 17 FDA reports)
VASCULAR DEMENTIA ( 17 FDA reports)
VEIN DISORDER ( 17 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 17 FDA reports)
PCO2 DECREASED ( 16 FDA reports)
PERIPHERAL EMBOLISM ( 16 FDA reports)
PNEUMONIA FUNGAL ( 16 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 16 FDA reports)
POLYTRAUMATISM ( 16 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 16 FDA reports)
RADICULAR PAIN ( 16 FDA reports)
RASH VESICULAR ( 16 FDA reports)
RENAL CELL CARCINOMA ( 16 FDA reports)
RESPIRATORY RATE DECREASED ( 16 FDA reports)
SCRATCH ( 16 FDA reports)
SPINAL CORD DISORDER ( 16 FDA reports)
TESTICULAR PAIN ( 16 FDA reports)
TROPONIN I INCREASED ( 16 FDA reports)
VASCULAR INSUFFICIENCY ( 16 FDA reports)
ABDOMINAL SEPSIS ( 16 FDA reports)
ABORTION INDUCED ( 16 FDA reports)
ACUTE STRESS DISORDER ( 16 FDA reports)
ADRENAL MASS ( 16 FDA reports)
ADRENAL SUPPRESSION ( 16 FDA reports)
ALLERGIC COLITIS ( 16 FDA reports)
ANION GAP INCREASED ( 16 FDA reports)
ANOGENITAL WARTS ( 16 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 16 FDA reports)
ARTERIAL THROMBOSIS ( 16 FDA reports)
BIOPSY ( 16 FDA reports)
BLOOD BLISTER ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 16 FDA reports)
BONE GRAFT ( 16 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 16 FDA reports)
BREAKTHROUGH PAIN ( 16 FDA reports)
CAPILLARY LEAK SYNDROME ( 16 FDA reports)
CARDIAC STRESS TEST ( 16 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
CATHETER RELATED COMPLICATION ( 16 FDA reports)
CATHETER SITE HAEMORRHAGE ( 16 FDA reports)
CAUSTIC INJURY ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 16 FDA reports)
COLECTOMY ( 16 FDA reports)
COW'S MILK INTOLERANCE ( 16 FDA reports)
EAR NEOPLASM ( 16 FDA reports)
EDUCATIONAL PROBLEM ( 16 FDA reports)
EMBOLIC STROKE ( 16 FDA reports)
FACIAL PARESIS ( 16 FDA reports)
FEBRILE CONVULSION ( 16 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 16 FDA reports)
GALLBLADDER OPERATION ( 16 FDA reports)
GINGIVAL OEDEMA ( 16 FDA reports)
HAEMORRHOID OPERATION ( 16 FDA reports)
HYDROPNEUMOTHORAX ( 16 FDA reports)
HYPERPHOSPHATAEMIA ( 16 FDA reports)
HYPERREFLEXIA ( 16 FDA reports)
INFUSION SITE REACTION ( 16 FDA reports)
INJECTION SITE CELLULITIS ( 16 FDA reports)
LIMB OPERATION ( 16 FDA reports)
MASS EXCISION ( 16 FDA reports)
MENSTRUATION DELAYED ( 16 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 16 FDA reports)
MUSCLE RUPTURE ( 16 FDA reports)
MYOCARDITIS ( 16 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 16 FDA reports)
OLIGOHYDRAMNIOS ( 16 FDA reports)
ONYCHOMADESIS ( 16 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 16 FDA reports)
OROPHARYNGEAL SWELLING ( 16 FDA reports)
OXYGEN SUPPLEMENTATION ( 16 FDA reports)
PALATAL OEDEMA ( 16 FDA reports)
ABDOMINAL ABSCESS ( 15 FDA reports)
ANAL FISTULA ( 15 FDA reports)
APPLICATION SITE IRRITATION ( 15 FDA reports)
APPLICATION SITE REACTION ( 15 FDA reports)
ASTHENOPIA ( 15 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 15 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 15 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 15 FDA reports)
BIOPSY BLADDER ABNORMAL ( 15 FDA reports)
BIRTH TRAUMA ( 15 FDA reports)
BLADDER DISCOMFORT ( 15 FDA reports)
BLADDER PROLAPSE ( 15 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 15 FDA reports)
BLOOD CREATININE DECREASED ( 15 FDA reports)
BREAST CANCER IN SITU ( 15 FDA reports)
BREAST ENLARGEMENT ( 15 FDA reports)
BREAST SWELLING ( 15 FDA reports)
BULLOUS LUNG DISEASE ( 15 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 15 FDA reports)
CARDIOVERSION ( 15 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 15 FDA reports)
CATHETER REMOVAL ( 15 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 15 FDA reports)
CLAVICLE FRACTURE ( 15 FDA reports)
COCCYDYNIA ( 15 FDA reports)
COELIAC DISEASE ( 15 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 15 FDA reports)
CORONARY ARTERY THROMBOSIS ( 15 FDA reports)
DERMATITIS BULLOUS ( 15 FDA reports)
DEVICE DISLOCATION ( 15 FDA reports)
DYSGRAPHIA ( 15 FDA reports)
FLASHBACK ( 15 FDA reports)
FLUID INTAKE REDUCED ( 15 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 15 FDA reports)
GOUTY ARTHRITIS ( 15 FDA reports)
GRANULOCYTOPENIA ( 15 FDA reports)
HALLUCINATION, TACTILE ( 15 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 15 FDA reports)
HYPERPROLACTINAEMIA ( 15 FDA reports)
HYPOTHERMIA NEONATAL ( 15 FDA reports)
ILEITIS ( 15 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 15 FDA reports)
MACULAR OEDEMA ( 15 FDA reports)
MENOPAUSAL SYMPTOMS ( 15 FDA reports)
METASTASES TO BONE MARROW ( 15 FDA reports)
METASTATIC PAIN ( 15 FDA reports)
MICROCYTIC ANAEMIA ( 15 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 15 FDA reports)
MONOCYTE COUNT INCREASED ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 15 FDA reports)
OEDEMA MUCOSAL ( 15 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 15 FDA reports)
OESOPHAGEAL PAIN ( 15 FDA reports)
OLIGOMENORRHOEA ( 15 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 15 FDA reports)
OTITIS MEDIA ACUTE ( 15 FDA reports)
PAIN EXACERBATED ( 15 FDA reports)
PHARYNGEAL DISORDER ( 15 FDA reports)
PROCTITIS ( 15 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 15 FDA reports)
PULSE ABNORMAL ( 15 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 15 FDA reports)
QRS AXIS ABNORMAL ( 15 FDA reports)
RECTAL ABSCESS ( 15 FDA reports)
RECTAL FISSURE ( 15 FDA reports)
RENAL COLIC ( 15 FDA reports)
RETROPERITONEAL HAEMATOMA ( 15 FDA reports)
ROTATOR CUFF REPAIR ( 15 FDA reports)
SCAN BONE MARROW ABNORMAL ( 15 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 15 FDA reports)
SCOTOMA ( 15 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 15 FDA reports)
SKIN NEOPLASM EXCISION ( 15 FDA reports)
SPINAL CORPECTOMY ( 15 FDA reports)
SUDDEN ONSET OF SLEEP ( 15 FDA reports)
SYNOVITIS ( 15 FDA reports)
TACHYPHRENIA ( 15 FDA reports)
TRANSFUSION REACTION ( 15 FDA reports)
TUBERCULOSIS ( 15 FDA reports)
TURNER'S SYNDROME ( 15 FDA reports)
UMBILICAL CORD AROUND NECK ( 15 FDA reports)
URINE ODOUR ABNORMAL ( 15 FDA reports)
WEIGHT GAIN POOR ( 15 FDA reports)
PARTNER STRESS ( 14 FDA reports)
PERFORMANCE STATUS DECREASED ( 14 FDA reports)
PETIT MAL EPILEPSY ( 14 FDA reports)
PHYSIOTHERAPY ( 14 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 14 FDA reports)
POST CONCUSSION SYNDROME ( 14 FDA reports)
POST PROCEDURAL INFECTION ( 14 FDA reports)
POUCHITIS ( 14 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 14 FDA reports)
PRODUCT ADHESION ISSUE ( 14 FDA reports)
PYURIA ( 14 FDA reports)
RADICULITIS ( 14 FDA reports)
RENAL INFARCT ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SHOCK HAEMORRHAGIC ( 14 FDA reports)
SINUS ANTROSTOMY ( 14 FDA reports)
SKIN OEDEMA ( 14 FDA reports)
SKIN TURGOR DECREASED ( 14 FDA reports)
SPUTUM PURULENT ( 14 FDA reports)
SUBDURAL HAEMATOMA ( 14 FDA reports)
SYNCOPE VASOVAGAL ( 14 FDA reports)
TEMPORAL ARTERITIS ( 14 FDA reports)
TOXIC ENCEPHALOPATHY ( 14 FDA reports)
TRANSPLANT REJECTION ( 14 FDA reports)
TREATMENT FAILURE ( 14 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 14 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 14 FDA reports)
VENOUS STASIS ( 14 FDA reports)
VENOUS THROMBOSIS LIMB ( 14 FDA reports)
VOMITING PROJECTILE ( 14 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 14 FDA reports)
VULVOVAGINAL DRYNESS ( 14 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 14 FDA reports)
ADNEXA UTERI PAIN ( 14 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 14 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 14 FDA reports)
ANDROGEN DEFICIENCY ( 14 FDA reports)
ANGIOPLASTY ( 14 FDA reports)
ANKLE OPERATION ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 14 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 14 FDA reports)
APPENDIX DISORDER ( 14 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 14 FDA reports)
ASEPTIC NECROSIS BONE ( 14 FDA reports)
B-CELL LYMPHOMA ( 14 FDA reports)
BLOOD LACTIC ACID INCREASED ( 14 FDA reports)
BLOOD OSMOLARITY DECREASED ( 14 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 14 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 14 FDA reports)
BRONCHOSPASM PARADOXICAL ( 14 FDA reports)
BUTTOCK PAIN ( 14 FDA reports)
CARDIAC ANEURYSM ( 14 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 14 FDA reports)
CENTRAL LINE INFECTION ( 14 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 14 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 14 FDA reports)
CHEMOTHERAPY ( 14 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 14 FDA reports)
COR PULMONALE CHRONIC ( 14 FDA reports)
CORNEAL ABRASION ( 14 FDA reports)
CORONARY ARTERY EMBOLISM ( 14 FDA reports)
CRANIOTOMY ( 14 FDA reports)
DROP ATTACKS ( 14 FDA reports)
DUODENAL ULCER PERFORATION ( 14 FDA reports)
EARLY SATIETY ( 14 FDA reports)
ENZYME ABNORMALITY ( 14 FDA reports)
EXCESSIVE EYE BLINKING ( 14 FDA reports)
EXPOSURE TO TOXIC AGENT ( 14 FDA reports)
EYELID DISORDER ( 14 FDA reports)
FAECES HARD ( 14 FDA reports)
FLUID REPLACEMENT ( 14 FDA reports)
GRAVITATIONAL OEDEMA ( 14 FDA reports)
GUN SHOT WOUND ( 14 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 14 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 14 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
INFECTED SKIN ULCER ( 14 FDA reports)
INJECTION SITE NODULE ( 14 FDA reports)
INJECTION SITE OEDEMA ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 14 FDA reports)
INTESTINAL RESECTION ( 14 FDA reports)
JOINT CREPITATION ( 14 FDA reports)
LIP BLISTER ( 14 FDA reports)
LIVER ABSCESS ( 14 FDA reports)
MALLORY-WEISS SYNDROME ( 14 FDA reports)
MAMMOGRAM ( 14 FDA reports)
MAMMOPLASTY ( 14 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 14 FDA reports)
MONOCLONAL GAMMOPATHY ( 14 FDA reports)
MONOPARESIS ( 14 FDA reports)
MUSCLE CONTRACTURE ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
NEURAL TUBE DEFECT ( 14 FDA reports)
ADNEXA UTERI MASS ( 13 FDA reports)
ANGIOMYOLIPOMA ( 13 FDA reports)
ARTERIOVENOUS MALFORMATION ( 13 FDA reports)
ARTHRITIS BACTERIAL ( 13 FDA reports)
AXILLARY MASS ( 13 FDA reports)
BLOOD CHLORIDE INCREASED ( 13 FDA reports)
BONE CYST ( 13 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 13 FDA reports)
BRONCHOMALACIA ( 13 FDA reports)
CHEST INJURY ( 13 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 13 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 13 FDA reports)
CONVULSION NEONATAL ( 13 FDA reports)
CULTURE POSITIVE ( 13 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 13 FDA reports)
DERMATITIS ACNEIFORM ( 13 FDA reports)
DERMATITIS ATOPIC ( 13 FDA reports)
DEXTROCARDIA ( 13 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
EYE ROLLING ( 13 FDA reports)
EYELID MARGIN CRUSTING ( 13 FDA reports)
FOETAL GROWTH RESTRICTION ( 13 FDA reports)
GALLBLADDER ENLARGEMENT ( 13 FDA reports)
GASTRIC CANCER ( 13 FDA reports)
GASTRIC INFECTION ( 13 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 13 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 13 FDA reports)
HAEMATOCRIT INCREASED ( 13 FDA reports)
HAEMOCHROMATOSIS ( 13 FDA reports)
HAEMOGLOBIN INCREASED ( 13 FDA reports)
HAEMORRHAGE URINARY TRACT ( 13 FDA reports)
HEARING AID USER ( 13 FDA reports)
HEPATIC PAIN ( 13 FDA reports)
HYPEROSMOLAR STATE ( 13 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 13 FDA reports)
INFUSION SITE SWELLING ( 13 FDA reports)
INJECTION SITE BURNING ( 13 FDA reports)
INJECTION SITE EXTRAVASATION ( 13 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 13 FDA reports)
KETOACIDOSIS ( 13 FDA reports)
LIVE BIRTH ( 13 FDA reports)
LYMPHADENECTOMY ( 13 FDA reports)
MENINGITIS VIRAL ( 13 FDA reports)
METASTASES TO SPLEEN ( 13 FDA reports)
MIOSIS ( 13 FDA reports)
MONONEUROPATHY ( 13 FDA reports)
MOUTH INJURY ( 13 FDA reports)
MUCOUS STOOLS ( 13 FDA reports)
MYOMECTOMY ( 13 FDA reports)
NODAL RHYTHM ( 13 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 13 FDA reports)
OPEN REDUCTION OF FRACTURE ( 13 FDA reports)
OPTIC NERVE DISORDER ( 13 FDA reports)
OROANTRAL FISTULA ( 13 FDA reports)
OSTEORADIONECROSIS ( 13 FDA reports)
PATELLA FRACTURE ( 13 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 13 FDA reports)
PELVIC DEFORMITY ( 13 FDA reports)
PHOTOPHERESIS ( 13 FDA reports)
PLATELET COUNT ABNORMAL ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 13 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 13 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 13 FDA reports)
PROSTATE CANCER METASTATIC ( 13 FDA reports)
PUPILS UNEQUAL ( 13 FDA reports)
RESPIRATORY DEPTH INCREASED ( 13 FDA reports)
RETINAL TEAR ( 13 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 13 FDA reports)
SKIN MASS ( 13 FDA reports)
SPINAL DEFORMITY ( 13 FDA reports)
SPLEEN DISORDER ( 13 FDA reports)
SPUTUM ABNORMAL ( 13 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 13 FDA reports)
THROMBOSIS IN DEVICE ( 13 FDA reports)
TONSILLITIS ( 13 FDA reports)
TOOTH EROSION ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 13 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 13 FDA reports)
YELLOW SKIN ( 13 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PLEURAL CALCIFICATION ( 12 FDA reports)
POLYARTERITIS NODOSA ( 12 FDA reports)
PROCEDURAL SITE REACTION ( 12 FDA reports)
PULMONARY RADIATION INJURY ( 12 FDA reports)
PULMONARY TOXICITY ( 12 FDA reports)
PULMONARY VASCULAR DISORDER ( 12 FDA reports)
RADICAL HYSTERECTOMY ( 12 FDA reports)
RECTAL CANCER ( 12 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 12 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 12 FDA reports)
SOFT TISSUE DISORDER ( 12 FDA reports)
SOFT TISSUE INJURY ( 12 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 12 FDA reports)
SPONDYLOLYSIS ( 12 FDA reports)
STASIS DERMATITIS ( 12 FDA reports)
STILLBIRTH ( 12 FDA reports)
SUPERINFECTION ( 12 FDA reports)
TONGUE DRY ( 12 FDA reports)
TRACHEOMALACIA ( 12 FDA reports)
URINARY TRACT DISORDER ( 12 FDA reports)
UVEITIS ( 12 FDA reports)
VASCULAR OCCLUSION ( 12 FDA reports)
VITH NERVE PARALYSIS ( 12 FDA reports)
WALKING DISABILITY ( 12 FDA reports)
WEIGHT BEARING DIFFICULTY ( 12 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 12 FDA reports)
ABORTION ( 12 FDA reports)
ACCIDENT ( 12 FDA reports)
ACTINIC ELASTOSIS ( 12 FDA reports)
AKINESIA ( 12 FDA reports)
ANTISOCIAL BEHAVIOUR ( 12 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
ARTHRITIS INFECTIVE ( 12 FDA reports)
ASTERIXIS ( 12 FDA reports)
ASTROCYTOMA ( 12 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 12 FDA reports)
BLADDER DYSFUNCTION ( 12 FDA reports)
BLOOD BICARBONATE INCREASED ( 12 FDA reports)
BLOOD COUNT ABNORMAL ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 12 FDA reports)
BLOOD URINE ( 12 FDA reports)
BONE NEOPLASM ( 12 FDA reports)
BRADYPHRENIA ( 12 FDA reports)
BREAST DISCHARGE ( 12 FDA reports)
BRONCHIAL HYPERACTIVITY ( 12 FDA reports)
BURNS SECOND DEGREE ( 12 FDA reports)
CARDIAC SEPTAL DEFECT ( 12 FDA reports)
CATARACT NUCLEAR ( 12 FDA reports)
CATHETER SITE INFECTION ( 12 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 12 FDA reports)
CHOLANGITIS ( 12 FDA reports)
COLOSTOMY ( 12 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 12 FDA reports)
DENTAL DISCOMFORT ( 12 FDA reports)
DENTAL PLAQUE ( 12 FDA reports)
DEVICE LEAKAGE ( 12 FDA reports)
DIVERTICULAR PERFORATION ( 12 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 12 FDA reports)
EFFUSION ( 12 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 12 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 12 FDA reports)
EOSINOPHIL COUNT DECREASED ( 12 FDA reports)
FOAMING AT MOUTH ( 12 FDA reports)
FOETAL MOVEMENTS DECREASED ( 12 FDA reports)
FRACTURE DELAYED UNION ( 12 FDA reports)
GASTRODUODENITIS ( 12 FDA reports)
GASTROENTERITIS RADIATION ( 12 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 12 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 12 FDA reports)
HAEMOPHILUS INFECTION ( 12 FDA reports)
HANGOVER ( 12 FDA reports)
HEPATIC MASS ( 12 FDA reports)
ILIAC ARTERY STENOSIS ( 12 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 12 FDA reports)
IMMUNODEFICIENCY ( 12 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 12 FDA reports)
INJECTION SITE MASS ( 12 FDA reports)
INTESTINAL STENOSIS ( 12 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 12 FDA reports)
INTRAOSSEOUS ANGIOMA ( 12 FDA reports)
LABILE BLOOD PRESSURE ( 12 FDA reports)
LIP DISCOLOURATION ( 12 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 12 FDA reports)
MECHANICAL URTICARIA ( 12 FDA reports)
MENIERE'S DISEASE ( 12 FDA reports)
MUCOSAL ULCERATION ( 12 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 12 FDA reports)
NAIL DISORDER ( 12 FDA reports)
NEPHRITIS ( 12 FDA reports)
NEPHROPATHY TOXIC ( 12 FDA reports)
NEPHROTIC SYNDROME ( 12 FDA reports)
NEUROMA ( 12 FDA reports)
OROPHARYNGEAL PLAQUE ( 12 FDA reports)
ORTHOPEDIC PROCEDURE ( 12 FDA reports)
OSTEOCHONDROSIS ( 12 FDA reports)
OVARIAN CYST RUPTURED ( 12 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 11 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 11 FDA reports)
ANTIBODY TEST POSITIVE ( 11 FDA reports)
ARRESTED LABOUR ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 11 FDA reports)
BLADDER MASS ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 11 FDA reports)
BLOOD MAGNESIUM INCREASED ( 11 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 11 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 11 FDA reports)
BONE LESION EXCISION ( 11 FDA reports)
CALCINOSIS ( 11 FDA reports)
CANDIDURIA ( 11 FDA reports)
CARBON DIOXIDE DECREASED ( 11 FDA reports)
CEREBELLAR ATROPHY ( 11 FDA reports)
CHONDROMALACIA ( 11 FDA reports)
CHONDROPATHY ( 11 FDA reports)
CHOROIDAL DETACHMENT ( 11 FDA reports)
CRYPTORCHISM ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
DEFORMITY THORAX ( 11 FDA reports)
DERMOID CYST ( 11 FDA reports)
DIABETES INSIPIDUS ( 11 FDA reports)
DISEASE COMPLICATION ( 11 FDA reports)
DRUG EFFECT INCREASED ( 11 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
DRUG RESISTANCE ( 11 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 11 FDA reports)
EAR HAEMORRHAGE ( 11 FDA reports)
ECZEMA INFECTED ( 11 FDA reports)
ENTEROBACTER INFECTION ( 11 FDA reports)
EPICONDYLITIS ( 11 FDA reports)
ESCHERICHIA BACTERAEMIA ( 11 FDA reports)
FIBROADENOMA OF BREAST ( 11 FDA reports)
FIBROUS HISTIOCYTOMA ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 11 FDA reports)
GRAFT VERSUS HOST DISEASE ( 11 FDA reports)
HAEMORRHAGIC DIATHESIS ( 11 FDA reports)
HEPATITIS CHOLESTATIC ( 11 FDA reports)
HIP DYSPLASIA ( 11 FDA reports)
HIP SURGERY ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
HYPERLACTACIDAEMIA ( 11 FDA reports)
HYPOPERFUSION ( 11 FDA reports)
HYPOREFLEXIA ( 11 FDA reports)
INJECTION SITE INDURATION ( 11 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 11 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 11 FDA reports)
KLEBSIELLA TEST POSITIVE ( 11 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 11 FDA reports)
LARYNGOMALACIA ( 11 FDA reports)
LIPID METABOLISM DISORDER ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 11 FDA reports)
LYMPH NODE PAIN ( 11 FDA reports)
MALABSORPTION ( 11 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 11 FDA reports)
MAXILLOFACIAL OPERATION ( 11 FDA reports)
METAPLASIA ( 11 FDA reports)
METASTASES TO ADRENALS ( 11 FDA reports)
METASTASES TO PANCREAS ( 11 FDA reports)
MOTION SICKNESS ( 11 FDA reports)
MUCOSAL DISCOLOURATION ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 11 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 11 FDA reports)
NAIL DISCOLOURATION ( 11 FDA reports)
NEUROTOXICITY ( 11 FDA reports)
NIGHT BLINDNESS ( 11 FDA reports)
NYSTAGMUS ( 11 FDA reports)
ORTHOSIS USER ( 11 FDA reports)
OXYGEN SATURATION ABNORMAL ( 11 FDA reports)
PARONYCHIA ( 11 FDA reports)
PARTIAL SEIZURES ( 11 FDA reports)
PENILE TORSION ( 11 FDA reports)
PHONOPHOBIA ( 11 FDA reports)
PITUITARY TUMOUR ( 11 FDA reports)
PLATELET DISORDER ( 11 FDA reports)
PNEUMOPERITONEUM ( 11 FDA reports)
POSTMENOPAUSE ( 11 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 11 FDA reports)
PYLORIC STENOSIS ( 11 FDA reports)
RASH MORBILLIFORM ( 11 FDA reports)
REFLUX LARYNGITIS ( 11 FDA reports)
REFRACTION DISORDER ( 11 FDA reports)
RETICULOCYTE COUNT DECREASED ( 11 FDA reports)
RHYTHM IDIOVENTRICULAR ( 11 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 11 FDA reports)
SCLERAL OPERATION ( 11 FDA reports)
SELF MUTILATION ( 11 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 11 FDA reports)
SJOGREN'S SYNDROME ( 11 FDA reports)
SKIN HYPOPIGMENTATION ( 11 FDA reports)
SKIN WRINKLING ( 11 FDA reports)
SLEEP TALKING ( 11 FDA reports)
SPINA BIFIDA ( 11 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
TENDON PAIN ( 11 FDA reports)
TESTICULAR ATROPHY ( 11 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 11 FDA reports)
TINEA CRURIS ( 11 FDA reports)
TUBERCULIN TEST POSITIVE ( 11 FDA reports)
URETHRAL CARUNCLE ( 11 FDA reports)
URINE ABNORMALITY ( 11 FDA reports)
VARICELLA ( 11 FDA reports)
VENA CAVA THROMBOSIS ( 11 FDA reports)
VIRAL LOAD INCREASED ( 11 FDA reports)
VITAL CAPACITY DECREASED ( 11 FDA reports)
VITAMIN B12 DECREASED ( 11 FDA reports)
WEANING FAILURE ( 11 FDA reports)
PANCREATIC MASS ( 10 FDA reports)
PANCREATIC NEOPLASM ( 10 FDA reports)
PLAGIOCEPHALY ( 10 FDA reports)
PLEURECTOMY ( 10 FDA reports)
PNEUMOMEDIASTINUM ( 10 FDA reports)
PROCEDURAL HYPOTENSION ( 10 FDA reports)
PROSTATIC OBSTRUCTION ( 10 FDA reports)
PULMONARY ARTERY STENOSIS ( 10 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 10 FDA reports)
RECTAL PERFORATION ( 10 FDA reports)
REFLUX GASTRITIS ( 10 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 10 FDA reports)
SEBACEOUS GLAND DISORDER ( 10 FDA reports)
SERRATIA BACTERAEMIA ( 10 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 10 FDA reports)
SMEAR CERVIX ABNORMAL ( 10 FDA reports)
STENOTROPHOMONAS INFECTION ( 10 FDA reports)
STERNAL FRACTURE ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
STUPOR ( 10 FDA reports)
TESTICULAR SWELLING ( 10 FDA reports)
THROAT LESION ( 10 FDA reports)
THROMBOCYTHAEMIA ( 10 FDA reports)
TONSILLAR DISORDER ( 10 FDA reports)
TOXIC NEUROPATHY ( 10 FDA reports)
TRACHEOSTOMY ( 10 FDA reports)
URETERIC CANCER ( 10 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 10 FDA reports)
URINE COLOUR ABNORMAL ( 10 FDA reports)
VIRAL PHARYNGITIS ( 10 FDA reports)
VOLVULUS ( 10 FDA reports)
VULVOVAGINAL PAIN ( 10 FDA reports)
ADHESIOLYSIS ( 10 FDA reports)
ADVERSE REACTION ( 10 FDA reports)
ALBUMIN URINE PRESENT ( 10 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 10 FDA reports)
ANAESTHETIC COMPLICATION ( 10 FDA reports)
ANAL STENOSIS ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
AORTIC BYPASS ( 10 FDA reports)
ARTHROSCOPY ( 10 FDA reports)
ASPERGILLOSIS ( 10 FDA reports)
ASTEATOSIS ( 10 FDA reports)
ASTHMA EXERCISE INDUCED ( 10 FDA reports)
ATHEROSCLEROSIS ( 10 FDA reports)
AUTOIMMUNE THYROIDITIS ( 10 FDA reports)
BLOOD ALBUMIN INCREASED ( 10 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 10 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 10 FDA reports)
BODY TINEA ( 10 FDA reports)
CALCULUS URINARY ( 10 FDA reports)
CARDIAC ABLATION ( 10 FDA reports)
CEREBRAL CYST ( 10 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 10 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 10 FDA reports)
CONGENITAL FOOT MALFORMATION ( 10 FDA reports)
CONGENITAL TRACHEOMALACIA ( 10 FDA reports)
CROUP INFECTIOUS ( 10 FDA reports)
CYSTIC FIBROSIS ( 10 FDA reports)
DEAFNESS UNILATERAL ( 10 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 10 FDA reports)
DIABETIC FOOT ( 10 FDA reports)
DIAPHRAGMATIC DISORDER ( 10 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 10 FDA reports)
DIGEORGE'S SYNDROME ( 10 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 10 FDA reports)
DYSPNOEA AT REST ( 10 FDA reports)
ENDOCARDIAL FIBROSIS ( 10 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 10 FDA reports)
EPIDURAL LIPOMATOSIS ( 10 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
GANGLION ( 10 FDA reports)
GINGIVAL ATROPHY ( 10 FDA reports)
GLOBULINS INCREASED ( 10 FDA reports)
GRIMACING ( 10 FDA reports)
HAEMATOMA INFECTION ( 10 FDA reports)
HEPATIC ENZYME ABNORMAL ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 10 FDA reports)
HYPOVOLAEMIC SHOCK ( 10 FDA reports)
IMMOBILE ( 10 FDA reports)
INCORRECT STORAGE OF DRUG ( 10 FDA reports)
INTERTRIGO ( 10 FDA reports)
INTRA-UTERINE DEATH ( 10 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 10 FDA reports)
KERATITIS ( 10 FDA reports)
LABILE HYPERTENSION ( 10 FDA reports)
LEARNING DISABILITY ( 10 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LIP PAIN ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
LUNG OPERATION ( 10 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
MALIGNANT HYPERTENSION ( 10 FDA reports)
MANDIBULAR PROSTHESIS USER ( 10 FDA reports)
MARROW HYPERPLASIA ( 10 FDA reports)
MASTITIS ( 10 FDA reports)
MEDIASTINAL MASS ( 10 FDA reports)
MENINGOMYELOCELE ( 10 FDA reports)
METASTASES TO SKIN ( 10 FDA reports)
MIDDLE EAR EFFUSION ( 10 FDA reports)
MITRAL VALVE SCLEROSIS ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 10 FDA reports)
NEURODERMATITIS ( 10 FDA reports)
OEDEMA GENITAL ( 10 FDA reports)
OESOPHAGITIS ULCERATIVE ( 10 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 9 FDA reports)
ABDOMINAL OPERATION ( 9 FDA reports)
ABDOMINAL RIGIDITY ( 9 FDA reports)
ABSCESS INTESTINAL ( 9 FDA reports)
ADDISON'S DISEASE ( 9 FDA reports)
ALOPECIA EFFLUVIUM ( 9 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 9 FDA reports)
AORTIC VALVE REPLACEMENT ( 9 FDA reports)
APPLICATION SITE DERMATITIS ( 9 FDA reports)
APPLICATION SITE VESICLES ( 9 FDA reports)
AURA ( 9 FDA reports)
AURICULAR SWELLING ( 9 FDA reports)
BEREAVEMENT REACTION ( 9 FDA reports)
BIFASCICULAR BLOCK ( 9 FDA reports)
BLADDER DILATATION ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BLOOD PROLACTIN INCREASED ( 9 FDA reports)
BREAST CALCIFICATIONS ( 9 FDA reports)
BREAST FIBROSIS ( 9 FDA reports)
BREECH PRESENTATION ( 9 FDA reports)
BRONCHIAL DISORDER ( 9 FDA reports)
BRONCHITIS VIRAL ( 9 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 9 FDA reports)
BRONCHOSCOPY ( 9 FDA reports)
BURNING MOUTH SYNDROME ( 9 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 9 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 9 FDA reports)
CEREBRAL CALCIFICATION ( 9 FDA reports)
CHOLANGITIS ACUTE ( 9 FDA reports)
CLUBBING ( 9 FDA reports)
CNS VENTRICULITIS ( 9 FDA reports)
COGWHEEL RIGIDITY ( 9 FDA reports)
COMPULSIVE SHOPPING ( 9 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CONGENITAL HAIR DISORDER ( 9 FDA reports)
CORONARY ARTERY RESTENOSIS ( 9 FDA reports)
CORYNEBACTERIUM INFECTION ( 9 FDA reports)
CRANIOCEREBRAL INJURY ( 9 FDA reports)
CUTIS LAXA ( 9 FDA reports)
DENTAL PULP DISORDER ( 9 FDA reports)
DEPRESSION SUICIDAL ( 9 FDA reports)
DEVICE INEFFECTIVE ( 9 FDA reports)
DIARRHOEA INFECTIOUS ( 9 FDA reports)
DISORDER OF ORBIT ( 9 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 9 FDA reports)
DRUG TOLERANCE INCREASED ( 9 FDA reports)
EMBOLISM VENOUS ( 9 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 9 FDA reports)
EROSIVE DUODENITIS ( 9 FDA reports)
ERYTHEMA NODOSUM ( 9 FDA reports)
FACIAL SPASM ( 9 FDA reports)
FAT NECROSIS ( 9 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 9 FDA reports)
FEELINGS OF WORTHLESSNESS ( 9 FDA reports)
FEMORAL ARTERY OCCLUSION ( 9 FDA reports)
FOOD CRAVING ( 9 FDA reports)
FOREIGN BODY ASPIRATION ( 9 FDA reports)
FUNGAL SKIN INFECTION ( 9 FDA reports)
GASTROSTOMY TUBE INSERTION ( 9 FDA reports)
GLUCOSE URINE PRESENT ( 9 FDA reports)
HALLUCINATIONS, MIXED ( 9 FDA reports)
HELICOBACTER GASTRITIS ( 9 FDA reports)
HEPATIC TRAUMA ( 9 FDA reports)
HERNIA PAIN ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
HYPERACUSIS ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
HYPERTHERMIA MALIGNANT ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
HYPOGONADISM ( 9 FDA reports)
HYPOMANIA ( 9 FDA reports)
IMPLANT SITE THROMBOSIS ( 9 FDA reports)
INAPPROPRIATE AFFECT ( 9 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 9 FDA reports)
INJECTION SITE VESICLES ( 9 FDA reports)
INTESTINAL DILATATION ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
JUGULAR VEIN THROMBOSIS ( 9 FDA reports)
KIDNEY ENLARGEMENT ( 9 FDA reports)
KIDNEY FIBROSIS ( 9 FDA reports)
LASER THERAPY ( 9 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 9 FDA reports)
LIP ULCERATION ( 9 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 9 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 9 FDA reports)
LYME DISEASE ( 9 FDA reports)
LYMPHANGITIS ( 9 FDA reports)
MALIGNANT TUMOUR EXCISION ( 9 FDA reports)
MASTOCYTOSIS ( 9 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 9 FDA reports)
MELANOSIS COLI ( 9 FDA reports)
MERALGIA PARAESTHETICA ( 9 FDA reports)
METASTASES TO OVARY ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 9 FDA reports)
NERVE BLOCK ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
NEUTROPHILIA ( 9 FDA reports)
NIPPLE PAIN ( 9 FDA reports)
NONSPECIFIC REACTION ( 9 FDA reports)
OBSESSIVE THOUGHTS ( 9 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
ORBITAL OEDEMA ( 9 FDA reports)
ORGANISING PNEUMONIA ( 9 FDA reports)
OVARIAN CANCER ( 9 FDA reports)
PERIODONTAL OPERATION ( 9 FDA reports)
PHYSICAL TESTICLE EXAMINATION ABNORMAL ( 9 FDA reports)
PNEUMOCOCCAL SEPSIS ( 9 FDA reports)
PNEUMONECTOMY ( 9 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 9 FDA reports)
PROLONGED EXPIRATION ( 9 FDA reports)
PSOAS ABSCESS ( 9 FDA reports)
PTERYGIUM COLLI ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 9 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 9 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 9 FDA reports)
RHEUMATOID LUNG ( 9 FDA reports)
SENSATION OF PRESSURE ( 9 FDA reports)
SEPSIS NEONATAL ( 9 FDA reports)
SERRATIA INFECTION ( 9 FDA reports)
SITUS INVERSUS ( 9 FDA reports)
SKIN ATROPHY ( 9 FDA reports)
SKIN DEPIGMENTATION ( 9 FDA reports)
SKIN ODOUR ABNORMAL ( 9 FDA reports)
SOFT TISSUE MASS ( 9 FDA reports)
SPINAL CORD INJURY ( 9 FDA reports)
SPINAL X-RAY ABNORMAL ( 9 FDA reports)
STARVATION ( 9 FDA reports)
STRABISMUS ( 9 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 9 FDA reports)
TARSAL TUNNEL SYNDROME ( 9 FDA reports)
TENDON CALCIFICATION ( 9 FDA reports)
THROAT CANCER ( 9 FDA reports)
TONGUE HAEMORRHAGE ( 9 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 9 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 9 FDA reports)
TRACHEAL STENOSIS ( 9 FDA reports)
TRACHEITIS ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
VASCULAR CAUTERISATION ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
VASCULAR OPERATION ( 9 FDA reports)
VENTRICULAR HYPOPLASIA ( 9 FDA reports)
VITREOUS HAEMORRHAGE ( 9 FDA reports)
PELVIC ABSCESS ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 8 FDA reports)
PERITONEAL HAEMORRHAGE ( 8 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 8 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 8 FDA reports)
PICKWICKIAN SYNDROME ( 8 FDA reports)
POLYMYALGIA RHEUMATICA ( 8 FDA reports)
POST PROCEDURAL OEDEMA ( 8 FDA reports)
POSTERIOR CAPSULOTOMY ( 8 FDA reports)
POSTOPERATIVE ILEUS ( 8 FDA reports)
PREMATURE EJACULATION ( 8 FDA reports)
PROCTITIS ULCERATIVE ( 8 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
PROTEIN C DEFICIENCY ( 8 FDA reports)
PROTRUSION TONGUE ( 8 FDA reports)
RADIATION OESOPHAGITIS ( 8 FDA reports)
RENAL TUBULAR ACIDOSIS ( 8 FDA reports)
RESIDUAL URINE ( 8 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 8 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 8 FDA reports)
RETINITIS ( 8 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 8 FDA reports)
RHEUMATIC HEART DISEASE ( 8 FDA reports)
RIGHT AORTIC ARCH ( 8 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 8 FDA reports)
SALIVARY GLAND DISORDER ( 8 FDA reports)
SERUM SICKNESS ( 8 FDA reports)
SHIFT TO THE LEFT ( 8 FDA reports)
SINOBRONCHITIS ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SKIN SWELLING ( 8 FDA reports)
SKULL MALFORMATION ( 8 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 8 FDA reports)
SURGICAL PROCEDURE REPEATED ( 8 FDA reports)
SUTURE INSERTION ( 8 FDA reports)
SUTURE RELATED COMPLICATION ( 8 FDA reports)
TEMPERATURE REGULATION DISORDER ( 8 FDA reports)
TENOSYNOVITIS STENOSANS ( 8 FDA reports)
TESTICULAR MASS ( 8 FDA reports)
THERAPY REGIMEN CHANGED ( 8 FDA reports)
TONGUE PARALYSIS ( 8 FDA reports)
TUMOUR EMBOLISM ( 8 FDA reports)
TUNNEL VISION ( 8 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 8 FDA reports)
UPPER EXTREMITY MASS ( 8 FDA reports)
URGE INCONTINENCE ( 8 FDA reports)
URINARY TRACT OBSTRUCTION ( 8 FDA reports)
URINE KETONE BODY PRESENT ( 8 FDA reports)
URINE OUTPUT INCREASED ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 8 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 8 FDA reports)
ABDOMINAL PANNICULECTOMY ( 8 FDA reports)
ACARODERMATITIS ( 8 FDA reports)
ACCIDENTAL DEATH ( 8 FDA reports)
ACRODERMATITIS ( 8 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 8 FDA reports)
ALLERGY TO CHEMICALS ( 8 FDA reports)
AMAUROSIS FUGAX ( 8 FDA reports)
ANORECTAL DISORDER ( 8 FDA reports)
APALLIC SYNDROME ( 8 FDA reports)
APPLICATION SITE DISCOLOURATION ( 8 FDA reports)
ARTERIAL DISORDER ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 8 FDA reports)
BACTERIA URINE ( 8 FDA reports)
BACTERIAL DIARRHOEA ( 8 FDA reports)
BIOPSY BREAST ( 8 FDA reports)
BIOPSY LIVER ABNORMAL ( 8 FDA reports)
BLOODY DISCHARGE ( 8 FDA reports)
BONE DENSITY ABNORMAL ( 8 FDA reports)
BOWEL SOUNDS ABNORMAL ( 8 FDA reports)
BRAIN CONTUSION ( 8 FDA reports)
BRAIN SCAN ABNORMAL ( 8 FDA reports)
CARDIORENAL SYNDROME ( 8 FDA reports)
CARTILAGE INJURY ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 8 FDA reports)
CEREBELLAR HAEMORRHAGE ( 8 FDA reports)
CHOLANGITIS SCLEROSING ( 8 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 8 FDA reports)
CLONUS ( 8 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 8 FDA reports)
COMPLICATION OF DELIVERY ( 8 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 8 FDA reports)
CONGENITAL HAND MALFORMATION ( 8 FDA reports)
CONJUNCTIVAL ABRASION ( 8 FDA reports)
CONTRAST MEDIA REACTION ( 8 FDA reports)
CORONARY ANGIOPLASTY ( 8 FDA reports)
CYST REMOVAL ( 8 FDA reports)
CYSTIC FIBROSIS LUNG ( 8 FDA reports)
DAYDREAMING ( 8 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 8 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 8 FDA reports)
DEPRESSIVE SYMPTOM ( 8 FDA reports)
DEVICE INTERACTION ( 8 FDA reports)
DIPLEGIA ( 8 FDA reports)
DYSMORPHISM ( 8 FDA reports)
ECTOPIC PREGNANCY ( 8 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 8 FDA reports)
ENERGY INCREASED ( 8 FDA reports)
ENTEROCOCCAL SEPSIS ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
ETHMOID SINUS SURGERY ( 8 FDA reports)
EXOMPHALOS ( 8 FDA reports)
EYE INJURY ( 8 FDA reports)
EYELID FUNCTION DISORDER ( 8 FDA reports)
FEAR OF DISEASE ( 8 FDA reports)
FEELING GUILTY ( 8 FDA reports)
FEMALE STERILISATION ( 8 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 8 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 8 FDA reports)
GENERAL SYMPTOM ( 8 FDA reports)
GINGIVECTOMY ( 8 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 8 FDA reports)
HAEMOGLOBIN ABNORMAL ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HAIR COLOUR CHANGES ( 8 FDA reports)
HEAD TITUBATION ( 8 FDA reports)
HEPATITIS FULMINANT ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HOSPICE CARE ( 8 FDA reports)
HYPERVOLAEMIA ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
IMMUNOGLOBULINS INCREASED ( 8 FDA reports)
INFECTIVE TENOSYNOVITIS ( 8 FDA reports)
INFUSION SITE RASH ( 8 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
JUVENILE ARTHRITIS ( 8 FDA reports)
KUSSMAUL RESPIRATION ( 8 FDA reports)
LABORATORY TEST INTERFERENCE ( 8 FDA reports)
LATEX ALLERGY ( 8 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 8 FDA reports)
LHERMITTE'S SIGN ( 8 FDA reports)
LIP DISORDER ( 8 FDA reports)
LIPOMA EXCISION ( 8 FDA reports)
LIVER TRANSPLANT ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LORDOSIS ( 8 FDA reports)
LUNG INJURY ( 8 FDA reports)
LUPUS NEPHRITIS ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
MACROPHAGES INCREASED ( 8 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
MESOTHELIOMA ( 8 FDA reports)
MIGRAINE WITH AURA ( 8 FDA reports)
MOANING ( 8 FDA reports)
NASAL SINUS DRAINAGE ( 8 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 8 FDA reports)
NASAL ULCER ( 8 FDA reports)
NEONATAL DISORDER ( 8 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 8 FDA reports)
NEUROMYOPATHY ( 8 FDA reports)
NEUROPATHIC PAIN ( 8 FDA reports)
NODULE ON EXTREMITY ( 8 FDA reports)
NORMAL NEWBORN ( 8 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 8 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 8 FDA reports)
OPEN FRACTURE ( 8 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 8 FDA reports)
OSTEOMYELITIS DRAINAGE ( 8 FDA reports)
OSTEOSARCOMA LOCALISED ( 8 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 8 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 7 FDA reports)
ADENOIDAL HYPERTROPHY ( 7 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 7 FDA reports)
AGONAL DEATH STRUGGLE ( 7 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 7 FDA reports)
ALCOHOL DETOXIFICATION ( 7 FDA reports)
ANAL SPHINCTER ATONY ( 7 FDA reports)
ANKYLOSING SPONDYLITIS ( 7 FDA reports)
AORTIC ATHEROSCLEROSIS ( 7 FDA reports)
ARTIFICIAL MENOPAUSE ( 7 FDA reports)
AURICULAR PERICHONDRITIS ( 7 FDA reports)
BACTERIA STOOL IDENTIFIED ( 7 FDA reports)
BENIGN NEOPLASM ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BIOPSY BONE ( 7 FDA reports)
BLEEDING VARICOSE VEIN ( 7 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 7 FDA reports)
BLOOD OESTROGEN DECREASED ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BRAIN STEM SYNDROME ( 7 FDA reports)
BREAST MICROCALCIFICATION ( 7 FDA reports)
BRONCHIAL IRRITATION ( 7 FDA reports)
BURNING SENSATION MUCOSAL ( 7 FDA reports)
BURNS THIRD DEGREE ( 7 FDA reports)
CARDIAC DISCOMFORT ( 7 FDA reports)
CATHETER SEPSIS ( 7 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 7 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 7 FDA reports)
CHRONIC HEPATIC FAILURE ( 7 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
COLONOSCOPY ( 7 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 7 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 7 FDA reports)
CONNECTIVE TISSUE DISORDER ( 7 FDA reports)
CORNEAL DISORDER ( 7 FDA reports)
CORRECTIVE LENS USER ( 7 FDA reports)
CYSTITIS HAEMORRHAGIC ( 7 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 7 FDA reports)
DEATH OF RELATIVE ( 7 FDA reports)
DELAYED SLEEP PHASE ( 7 FDA reports)
DIABETIC ULCER ( 7 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DRUG TOLERANCE DECREASED ( 7 FDA reports)
DYSKINESIA OESOPHAGEAL ( 7 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 7 FDA reports)
EMPTY SELLA SYNDROME ( 7 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 7 FDA reports)
ENDOMETRIAL CANCER ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
ESCHAR ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
EYE INFLAMMATION ( 7 FDA reports)
EYE OPERATION ( 7 FDA reports)
EYE REDNESS ( 7 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 7 FDA reports)
FEMORAL ANTEVERSION ( 7 FDA reports)
FINGER AMPUTATION ( 7 FDA reports)
FLOPPY IRIS SYNDROME ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 7 FDA reports)
FUNGAL OESOPHAGITIS ( 7 FDA reports)
GAMMOPATHY ( 7 FDA reports)
GASTRIC BYPASS ( 7 FDA reports)
GASTRIC PERFORATION ( 7 FDA reports)
GASTROINTESTINAL ULCER ( 7 FDA reports)
GLIOSIS ( 7 FDA reports)
HAIR TEXTURE ABNORMAL ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HEART VALVE REPLACEMENT ( 7 FDA reports)
HEMICEPHALALGIA ( 7 FDA reports)
HLA MARKER STUDY POSITIVE ( 7 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 7 FDA reports)
HYPERINSULINAEMIA ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
HYPOVITAMINOSIS ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
IMPAIRED REASONING ( 7 FDA reports)
IMPATIENCE ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 7 FDA reports)
INJECTION SITE DISCOMFORT ( 7 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 7 FDA reports)
INNER EAR DISORDER ( 7 FDA reports)
INTENTION TREMOR ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
INTESTINAL ULCER ( 7 FDA reports)
INTRACRANIAL HYPOTENSION ( 7 FDA reports)
IUCD COMPLICATION ( 7 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 7 FDA reports)
LARYNGEAL STENOSIS ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LIBIDO INCREASED ( 7 FDA reports)
LICHENIFICATION ( 7 FDA reports)
LINEAR IGA DISEASE ( 7 FDA reports)
LIP OEDEMA ( 7 FDA reports)
LISTLESS ( 7 FDA reports)
LUNG ADENOCARCINOMA ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 7 FDA reports)
METAMORPHOPSIA ( 7 FDA reports)
METASTASES TO PLEURA ( 7 FDA reports)
METASTATIC LYMPHOMA ( 7 FDA reports)
MICROVASCULAR ANGINA ( 7 FDA reports)
MITRAL VALVE REPLACEMENT ( 7 FDA reports)
MOUTH PLAQUE ( 7 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 7 FDA reports)
NAIL BED TENDERNESS ( 7 FDA reports)
NASAL SEPTUM PERFORATION ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
NEOPLASM SKIN ( 7 FDA reports)
NEPHROCALCINOSIS ( 7 FDA reports)
NEPHROGENIC ANAEMIA ( 7 FDA reports)
NEURALGIC AMYOTROPHY ( 7 FDA reports)
NEUROFIBROMA ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 7 FDA reports)
OESOPHAGEAL RUPTURE ( 7 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 7 FDA reports)
ONYCHALGIA ( 7 FDA reports)
ORAL SOFT TISSUE DISORDER ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OSTEOSARCOMA METASTATIC ( 7 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 7 FDA reports)
PARANOID PERSONALITY DISORDER ( 7 FDA reports)
PAROTID GLAND ENLARGEMENT ( 7 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 7 FDA reports)
PERIORBITAL HAEMORRHAGE ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PERSECUTORY DELUSION ( 7 FDA reports)
PHARYNX DISCOMFORT ( 7 FDA reports)
PO2 INCREASED ( 7 FDA reports)
POLYDACTYLY ( 7 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 7 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 7 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 7 FDA reports)
POSTOPERATIVE FEVER ( 7 FDA reports)
PRESSURE OF SPEECH ( 7 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 7 FDA reports)
PROLONGED LABOUR ( 7 FDA reports)
PROSTATIC DISORDER ( 7 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PSEUDOMONAL SEPSIS ( 7 FDA reports)
PULMONARY EOSINOPHILIA ( 7 FDA reports)
RADIATION PNEUMONITIS ( 7 FDA reports)
RECTAL TENESMUS ( 7 FDA reports)
REGRESSIVE BEHAVIOUR ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RHEUMATIC FEVER ( 7 FDA reports)
RHINALGIA ( 7 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
SALPINGITIS ( 7 FDA reports)
SARCOMA ( 7 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SPLENIC RUPTURE ( 7 FDA reports)
SPONDYLOSIS ( 7 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 7 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 7 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 7 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 7 FDA reports)
TENDINOUS CONTRACTURE ( 7 FDA reports)
TERMINAL STATE ( 7 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 7 FDA reports)
TINEA VERSICOLOUR ( 7 FDA reports)
TONIC CLONIC MOVEMENTS ( 7 FDA reports)
TONSILLAR HYPERTROPHY ( 7 FDA reports)
TRACHEAL DISORDER ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
TUMOUR EXCISION ( 7 FDA reports)
TUMOUR NECROSIS ( 7 FDA reports)
URETHRAL STENOSIS ( 7 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 7 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 7 FDA reports)
VERTEBRAL COLUMN MASS ( 7 FDA reports)
VIRAL MYOCARDITIS ( 7 FDA reports)
VITRITIS ( 7 FDA reports)
WOUND DEBRIDEMENT ( 7 FDA reports)
PALMAR FASCIITIS ( 6 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PANCREATIC ENZYMES INCREASED ( 6 FDA reports)
PANCREATIC INSUFFICIENCY ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 6 FDA reports)
PARANASAL SINUS DISCOMFORT ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PHLEBOLITH ( 6 FDA reports)
PHOBIA ( 6 FDA reports)
PILOERECTION ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
POIKILOCYTOSIS ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
POST-TRAUMATIC PAIN ( 6 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 6 FDA reports)
POSTOPERATIVE CONSTIPATION ( 6 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 6 FDA reports)
PSYCHOTIC BEHAVIOUR ( 6 FDA reports)
PULMONARY HYPOPLASIA ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RATHKE'S CLEFT CYST ( 6 FDA reports)
READING DISORDER ( 6 FDA reports)
RECURRENT CANCER ( 6 FDA reports)
RED BLOOD CELLS URINE ( 6 FDA reports)
RENAL VEIN THROMBOSIS ( 6 FDA reports)
RETINAL ARTERY OCCLUSION ( 6 FDA reports)
RETINAL SCAR ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
RHEUMATOID FACTOR INCREASED ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SALIVARY GLAND PAIN ( 6 FDA reports)
SCLERAL HAEMORRHAGE ( 6 FDA reports)
SENSORY LEVEL ABNORMAL ( 6 FDA reports)
SHWACHMAN-DIAMOND SYNDROME ( 6 FDA reports)
SICCA SYNDROME ( 6 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SINUSITIS FUNGAL ( 6 FDA reports)
SKIN TOXICITY ( 6 FDA reports)
SOCIAL PHOBIA ( 6 FDA reports)
SOFT TISSUE INFECTION ( 6 FDA reports)
SPLEEN CONGESTION ( 6 FDA reports)
SPLINTER HAEMORRHAGES ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
STILL'S DISEASE ADULT ONSET ( 6 FDA reports)
STOMACH MASS ( 6 FDA reports)
TETANY ( 6 FDA reports)
THEFT ( 6 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 6 FDA reports)
THYROIDITIS CHRONIC ( 6 FDA reports)
TINEA INFECTION ( 6 FDA reports)
TONSILLECTOMY ( 6 FDA reports)
TRAUMATIC SHOCK ( 6 FDA reports)
TUMOUR FLARE ( 6 FDA reports)
ULNA FRACTURE ( 6 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 6 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 6 FDA reports)
UNDERWEIGHT ( 6 FDA reports)
URINE CALCIUM INCREASED ( 6 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 6 FDA reports)
VAGINAL MYCOSIS ( 6 FDA reports)
VAGINAL PAIN ( 6 FDA reports)
VAGINAL SWELLING ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VASCULAR HEADACHE ( 6 FDA reports)
VASCULAR INJURY ( 6 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 6 FDA reports)
VASCULAR RUPTURE ( 6 FDA reports)
VERBAL ABUSE ( 6 FDA reports)
WOUND COMPLICATION ( 6 FDA reports)
YAWNING ( 6 FDA reports)
ABDOMINAL SYMPTOM ( 6 FDA reports)
ACINETOBACTER INFECTION ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
ALCOHOL PROBLEM ( 6 FDA reports)
ALLERGY TO ARTHROPOD STING ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
ANAL INFLAMMATION ( 6 FDA reports)
ANGIOGRAM ( 6 FDA reports)
ANORCHISM ( 6 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
APGAR SCORE LOW ( 6 FDA reports)
APRAXIA ( 6 FDA reports)
ARTERIAL INSUFFICIENCY ( 6 FDA reports)
ARTERIAL RUPTURE ( 6 FDA reports)
ASBESTOSIS ( 6 FDA reports)
ASPLENIA ( 6 FDA reports)
AVULSION FRACTURE ( 6 FDA reports)
BACTERIA URINE IDENTIFIED ( 6 FDA reports)
BLADDER NEOPLASM ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BLEEDING TIME PROLONGED ( 6 FDA reports)
BLIGHTED OVUM ( 6 FDA reports)
BLOOD ALCOHOL INCREASED ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 6 FDA reports)
BODY MASS INDEX INCREASED ( 6 FDA reports)
BONE INFARCTION ( 6 FDA reports)
BRADYCARDIA FOETAL ( 6 FDA reports)
BRAIN HYPOXIA ( 6 FDA reports)
BREAST ABSCESS ( 6 FDA reports)
BREAST CELLULITIS ( 6 FDA reports)
BREAST OPERATION ( 6 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 6 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 6 FDA reports)
BRONCHITIS BACTERIAL ( 6 FDA reports)
BUNION ( 6 FDA reports)
BUTTERFLY RASH ( 6 FDA reports)
CALCIPHYLAXIS ( 6 FDA reports)
CARBON DIOXIDE ABNORMAL ( 6 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 6 FDA reports)
CARDIAC FAILURE CHRONIC ( 6 FDA reports)
CARDIAC INFECTION ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CARDIOTOXICITY ( 6 FDA reports)
CATHETER SITE PAIN ( 6 FDA reports)
CAUDA EQUINA SYNDROME ( 6 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 6 FDA reports)
CEREBELLAR SYNDROME ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CHEMICAL INJURY ( 6 FDA reports)
CHONDROSARCOMA ( 6 FDA reports)
CHRONIC HEPATITIS ( 6 FDA reports)
COAGULATION TEST ABNORMAL ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COITAL BLEEDING ( 6 FDA reports)
COMMINUTED FRACTURE ( 6 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 6 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 6 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 6 FDA reports)
CONGENITAL TERATOMA ( 6 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 6 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 6 FDA reports)
CRACKLES LUNG ( 6 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 6 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 6 FDA reports)
CUBITAL TUNNEL SYNDROME ( 6 FDA reports)
CUTANEOUS CONTOUR DEFORMITY ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DELUSIONAL PERCEPTION ( 6 FDA reports)
DEREALISATION ( 6 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 6 FDA reports)
DROWNING ( 6 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 6 FDA reports)
EAR CONGESTION ( 6 FDA reports)
EAR PRURITUS ( 6 FDA reports)
ECZEMA ASTEATOTIC ( 6 FDA reports)
ECZEMA NUMMULAR ( 6 FDA reports)
ELECTRIC SHOCK ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 6 FDA reports)
ENCEPHALITIS HERPES ( 6 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 6 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
FACTOR VIII DEFICIENCY ( 6 FDA reports)
FAILURE OF IMPLANT ( 6 FDA reports)
FEEDING TUBE COMPLICATION ( 6 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 6 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 6 FDA reports)
FUNGAEMIA ( 6 FDA reports)
GASTRIC OPERATION ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 6 FDA reports)
GASTROINTESTINAL TOXICITY ( 6 FDA reports)
GASTROSCHISIS ( 6 FDA reports)
GAZE PALSY ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
GLARE ( 6 FDA reports)
HAEMARTHROSIS ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HAND DEFORMITY ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEART VALVE STENOSIS ( 6 FDA reports)
HEPATIC ADENOMA ( 6 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HYPOGLYCAEMIC COMA ( 6 FDA reports)
IMPLANT SITE REACTION ( 6 FDA reports)
INFUSION SITE INFECTION ( 6 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 6 FDA reports)
INTERCOSTAL RETRACTION ( 6 FDA reports)
INTESTINAL GANGRENE ( 6 FDA reports)
INTESTINAL POLYP ( 6 FDA reports)
IODINE ALLERGY ( 6 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 6 FDA reports)
KERATOSIS PILARIS ( 6 FDA reports)
LEARNING DISORDER ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 6 FDA reports)
LUNG NEOPLASM SURGERY ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
MALIGNANT MELANOMA STAGE I ( 6 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 6 FDA reports)
MECONIUM STAIN ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 6 FDA reports)
METASTASES TO MOUTH ( 6 FDA reports)
METASTASES TO PERITONEUM ( 6 FDA reports)
METASTASES TO THE MEDIASTINUM ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 6 FDA reports)
MONOCYTE COUNT DECREASED ( 6 FDA reports)
MONOCYTOSIS ( 6 FDA reports)
MUCOSAL DRYNESS ( 6 FDA reports)
MYELITIS TRANSVERSE ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
NAIL TINEA ( 6 FDA reports)
NEGATIVISM ( 6 FDA reports)
NEONATAL HYPOTENSION ( 6 FDA reports)
NEURILEMMOMA ( 6 FDA reports)
NEUROGENIC BOWEL ( 6 FDA reports)
NEUTROPHIL COUNT ( 6 FDA reports)
NOCARDIOSIS ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
OBSTRUCTIVE UROPATHY ( 6 FDA reports)
OESOPHAGEAL OEDEMA ( 6 FDA reports)
OESOPHAGEAL POLYP ( 6 FDA reports)
OPPORTUNISTIC INFECTION ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OVARIAN LOW MALIGNANT POTENTIAL TUMOUR ( 6 FDA reports)
PACHYGYRIA ( 6 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 5 FDA reports)
ABORTION MISSED ( 5 FDA reports)
ACUTE PSYCHOSIS ( 5 FDA reports)
ADENOIDAL DISORDER ( 5 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 5 FDA reports)
ADENOMYOSIS ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ADRENAL CARCINOMA ( 5 FDA reports)
ANAL ULCER ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 5 FDA reports)
APPLICATION SITE BURN ( 5 FDA reports)
APPLICATION SITE EXFOLIATION ( 5 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 5 FDA reports)
AV DISSOCIATION ( 5 FDA reports)
AXILLARY VEIN THROMBOSIS ( 5 FDA reports)
BASOPHIL COUNT INCREASED ( 5 FDA reports)
BENIGN LUNG NEOPLASM ( 5 FDA reports)
BETA GLOBULIN INCREASED ( 5 FDA reports)
BIOPSY BONE ABNORMAL ( 5 FDA reports)
BLADDER CATHETERISATION ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD COPPER DECREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD INSULIN INCREASED ( 5 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 5 FDA reports)
BREAST CANCER STAGE II ( 5 FDA reports)
BREAST ENGORGEMENT ( 5 FDA reports)
BREAST NEOPLASM ( 5 FDA reports)
BREAST RECONSTRUCTION ( 5 FDA reports)
BRONCHIAL OEDEMA ( 5 FDA reports)
BURNOUT SYNDROME ( 5 FDA reports)
CANCER PAIN ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 5 FDA reports)
CATAPLEXY ( 5 FDA reports)
CATHETER SITE ERYTHEMA ( 5 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 5 FDA reports)
CERVICAL NEURITIS ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHLAMYDIAL INFECTION ( 5 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 5 FDA reports)
CLOSED HEAD INJURY ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
COLON GANGRENE ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CONJUNCTIVITIS VIRAL ( 5 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 5 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 5 FDA reports)
CYTOKINE RELEASE SYNDROME ( 5 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 5 FDA reports)
DEJA VU ( 5 FDA reports)
DELIRIUM TREMENS ( 5 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 5 FDA reports)
DEPERSONALISATION ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG SCREEN NEGATIVE ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 5 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 5 FDA reports)
ENDOMETRIAL ATROPHY ( 5 FDA reports)
ENTEROBACTER PNEUMONIA ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
ENTEROVESICAL FISTULA ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 5 FDA reports)
EYES SUNKEN ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FINGER DEFORMITY ( 5 FDA reports)
FLAIL CHEST ( 5 FDA reports)
FOETAL HYPOKINESIA ( 5 FDA reports)
FORCEPS DELIVERY ( 5 FDA reports)
FRACTURE DISPLACEMENT ( 5 FDA reports)
FUNGAL TEST POSITIVE ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC VARICES ( 5 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 5 FDA reports)
GASTROINTESTINAL OEDEMA ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GENITAL HAEMORRHAGE ( 5 FDA reports)
GROIN ABSCESS ( 5 FDA reports)
HAEMOGLOBINURIA ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HEPATIC ISCHAEMIA ( 5 FDA reports)
HEPATITIS VIRAL ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HIP DEFORMITY ( 5 FDA reports)
HOLOPROSENCEPHALY ( 5 FDA reports)
HYDROMETRA ( 5 FDA reports)
HYPERADRENALISM ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 5 FDA reports)
HYPERTRICHOSIS ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
ILIAC VEIN OCCLUSION ( 5 FDA reports)
ILLUSION ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INFECTED CYST ( 5 FDA reports)
INFUSION SITE EXTRAVASATION ( 5 FDA reports)
INFUSION SITE PRURITUS ( 5 FDA reports)
INFUSION SITE URTICARIA ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INTERNAL INJURY ( 5 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 5 FDA reports)
INTESTINAL MALROTATION ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
IRIS ADHESIONS ( 5 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
KETONURIA ( 5 FDA reports)
KLEBSIELLA SEPSIS ( 5 FDA reports)
LAZINESS ( 5 FDA reports)
LEUKOPLAKIA ( 5 FDA reports)
LIMB REDUCTION DEFECT ( 5 FDA reports)
LIVER TRANSPLANT REJECTION ( 5 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 5 FDA reports)
LUNG HERNIA ( 5 FDA reports)
LUNG WEDGE RESECTION ( 5 FDA reports)
LYMPHANGIECTASIA ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MARITAL PROBLEM ( 5 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 5 FDA reports)
METASTASES TO MUSCLE ( 5 FDA reports)
METASTATIC GASTRIC CANCER ( 5 FDA reports)
MILK ALLERGY ( 5 FDA reports)
MILK-ALKALI SYNDROME ( 5 FDA reports)
MITRAL VALVE REPAIR ( 5 FDA reports)
MIXED HYPERLIPIDAEMIA ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MUMPS ( 5 FDA reports)
MUSCLE FIBROSIS ( 5 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 5 FDA reports)
MYOCLONIC EPILEPSY ( 5 FDA reports)
MYOGLOBIN URINE PRESENT ( 5 FDA reports)
NECROSIS ISCHAEMIC ( 5 FDA reports)
NEOPLASM PROSTATE ( 5 FDA reports)
NEURODEGENERATIVE DISORDER ( 5 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 5 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 5 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 5 FDA reports)
OCCIPITAL NEURALGIA ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 5 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 5 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
OSTEOMALACIA ( 5 FDA reports)
OVARIAN MASS ( 5 FDA reports)
PAINFUL DEFAECATION ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 5 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 5 FDA reports)
PERIPHERAL NERVE INJURY ( 5 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 5 FDA reports)
PERITONEAL INFECTION ( 5 FDA reports)
PHARYNGEAL MASS ( 5 FDA reports)
PHLEBITIS SUPERFICIAL ( 5 FDA reports)
PHOTODERMATOSIS ( 5 FDA reports)
PICA ( 5 FDA reports)
PLACENTA PRAEVIA ( 5 FDA reports)
PLEURODESIS ( 5 FDA reports)
PNEUMOCOCCAL INFECTION ( 5 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 5 FDA reports)
POSTPARTUM DEPRESSION ( 5 FDA reports)
POSTURING ( 5 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 5 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PROCEDURAL NAUSEA ( 5 FDA reports)
PRODUCT TAMPERING ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
PULMONARY AIR LEAKAGE ( 5 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 5 FDA reports)
PULMONARY ARTERY ATRESIA ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
PYODERMA ( 5 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 5 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL EMBOLISM ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 5 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 5 FDA reports)
RETINOPATHY HYPERTENSIVE ( 5 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 5 FDA reports)
SHOULDER OPERATION ( 5 FDA reports)
SINGLE UMBILICAL ARTERY ( 5 FDA reports)
SKIN CANDIDA ( 5 FDA reports)
SKIN DEGENERATIVE DISORDER ( 5 FDA reports)
SKIN DISCOMFORT ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 5 FDA reports)
SOMATISATION DISORDER ( 5 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
SYRINGE ISSUE ( 5 FDA reports)
SYRINGOMYELIA ( 5 FDA reports)
TACHYCARDIA PAROXYSMAL ( 5 FDA reports)
TERATOMA ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
THYROXINE FREE DECREASED ( 5 FDA reports)
TIBIAL TORSION ( 5 FDA reports)
TRAUMATIC FRACTURE ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
UPPER LIMB DEFORMITY ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
URETHRAL STRICTURE ( 5 FDA reports)
UTERINE CYST ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
VASCULITIC RASH ( 5 FDA reports)
VASOCONSTRICTION ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENTILATION PERFUSION MISMATCH ( 5 FDA reports)
VERTEBRAL INJURY ( 5 FDA reports)
VESSEL PERFORATION ( 5 FDA reports)
VICTIM OF SEXUAL ABUSE ( 5 FDA reports)
VOCAL CORD THICKENING ( 5 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 4 FDA reports)
PARAKERATOSIS ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PARKINSONIAN GAIT ( 4 FDA reports)
PARVOVIRUS INFECTION ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PENILE SWELLING ( 4 FDA reports)
PENILE ULCERATION ( 4 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 4 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 4 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 4 FDA reports)
PERTUSSIS ( 4 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PHARYNGEAL ULCERATION ( 4 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 4 FDA reports)
PITUITARY TUMOUR BENIGN ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
POLYMENORRHOEA ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 4 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 4 FDA reports)
POST PROCEDURAL NAUSEA ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTICTAL STATE ( 4 FDA reports)
PREALBUMIN DECREASED ( 4 FDA reports)
PREGNANCY TEST POSITIVE ( 4 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 4 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 4 FDA reports)
PRODUCT FORMULATION ISSUE ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PROSTATIC PAIN ( 4 FDA reports)
PROSTATISM ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 4 FDA reports)
PUBIC RAMI FRACTURE ( 4 FDA reports)
PULMONARY SEQUESTRATION ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
RADIATION INJURY ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RECALL PHENOMENON ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RELAPSING FEVER ( 4 FDA reports)
RENAL ARTERY OCCLUSION ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RETICULOCYTE COUNT INCREASED ( 4 FDA reports)
RETINAL DEGENERATION ( 4 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 4 FDA reports)
SCAPULA FRACTURE ( 4 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 4 FDA reports)
SCLERITIS ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SEBACEOUS HYPERPLASIA ( 4 FDA reports)
SENSATION OF BLOOD FLOW ( 4 FDA reports)
SERONEGATIVE ARTHRITIS ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
SHONE COMPLEX ( 4 FDA reports)
SINUS RHYTHM ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN CYST EXCISION ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 4 FDA reports)
SOMATOFORM DISORDER ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPIDER VEIN ( 4 FDA reports)
SPINAL CORD INFARCTION ( 4 FDA reports)
SPINAL LAMINECTOMY ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SPLENIC CYST ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STOOL ANALYSIS ABNORMAL ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
TACHYCARDIA FOETAL ( 4 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 4 FDA reports)
THYROID CYST ( 4 FDA reports)
THYROID OPERATION ( 4 FDA reports)
THYROXINE FREE INCREASED ( 4 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TONSIL CANCER ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 4 FDA reports)
URINE CYTOLOGY ABNORMAL ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
UTERINE RUPTURE ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VAGINAL LESION ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VITREOUS DEGENERATION ( 4 FDA reports)
VULVAL CANCER ( 4 FDA reports)
VULVAL OEDEMA ( 4 FDA reports)
VULVAR EROSION ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
WAGNER'S DISEASE ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 4 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 4 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 4 FDA reports)
ABNORMAL WEIGHT GAIN ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 4 FDA reports)
AIR EMBOLISM ( 4 FDA reports)
ALCOHOLIC ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
AMPHETAMINES ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANGIOGRAM ABNORMAL ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTICHOLINERGIC SYNDROME ( 4 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
APPLICATION SITE HAEMATOMA ( 4 FDA reports)
ARACHNODACTYLY ( 4 FDA reports)
ARTERIAL CATHETERISATION ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 4 FDA reports)
ARTHROSCOPIC SURGERY ( 4 FDA reports)
ATONIC SEIZURES ( 4 FDA reports)
BACTERIAL CULTURE POSITIVE ( 4 FDA reports)
BACTERIAL TOXAEMIA ( 4 FDA reports)
BARBITURATES ( 4 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 4 FDA reports)
BENCE JONES PROTEINURIA ( 4 FDA reports)
BENIGN COLONIC NEOPLASM ( 4 FDA reports)
BICUSPID AORTIC VALVE ( 4 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BLADDER AGENESIS ( 4 FDA reports)
BLADDER DISTENSION ( 4 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 4 FDA reports)
BLOOD BILIRUBIN DECREASED ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD CREATINE DECREASED ( 4 FDA reports)
BLOOD PRESSURE ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BLUE TOE SYNDROME ( 4 FDA reports)
BODY HEIGHT ( 4 FDA reports)
BODY HEIGHT BELOW NORMAL ( 4 FDA reports)
BONE DEFORMITY ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 4 FDA reports)
BONE SARCOMA ( 4 FDA reports)
BONE TRIMMING ( 4 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN STEM THROMBOSIS ( 4 FDA reports)
BREAST CANCER STAGE III ( 4 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CAECITIS ( 4 FDA reports)
CALCIFICATION METASTATIC ( 4 FDA reports)
CALCULUS BLADDER ( 4 FDA reports)
CARBON MONOXIDE POISONING ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 4 FDA reports)
CARDIAC VALVE VEGETATION ( 4 FDA reports)
CAROTID ARTERY STENT INSERTION ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CENTRAL OBESITY ( 4 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERVICAL INCOMPETENCE ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
CHRONIC TONSILLITIS ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COLLATERAL CIRCULATION ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COMA SCALE ABNORMAL ( 4 FDA reports)
COMPLICATION OF PREGNANCY ( 4 FDA reports)
COMPULSIONS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONDUCT DISORDER ( 4 FDA reports)
CONGENITAL BLADDER ANOMALY ( 4 FDA reports)
CONGENITAL CEREBELLAR AGENESIS ( 4 FDA reports)
CONGENITAL NOSE MALFORMATION ( 4 FDA reports)
CONGENITAL TONGUE ANOMALY ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 4 FDA reports)
CORNEAL EROSION ( 4 FDA reports)
COUGH DECREASED ( 4 FDA reports)
CRANIOSYNOSTOSIS ( 4 FDA reports)
CREST SYNDROME ( 4 FDA reports)
CYST DRAINAGE ( 4 FDA reports)
CYSTITIS BACTERIAL ( 4 FDA reports)
CYSTITIS NONINFECTIVE ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DEVICE MISUSE ( 4 FDA reports)
DEVICE RELATED SEPSIS ( 4 FDA reports)
DISSEMINATED TUBERCULOSIS ( 4 FDA reports)
DISTRACTIBILITY ( 4 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 4 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 4 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 4 FDA reports)
DRUG DIVERSION ( 4 FDA reports)
DRUG INTERACTION INHIBITION ( 4 FDA reports)
DUODENAL POLYP ( 4 FDA reports)
DYSTROPHIC CALCIFICATION ( 4 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
EJACULATION FAILURE ( 4 FDA reports)
ELDERLY ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 4 FDA reports)
EMBOLISM ARTERIAL ( 4 FDA reports)
ENAMEL ANOMALY ( 4 FDA reports)
ENCEPHALITIS VIRAL ( 4 FDA reports)
ENCEPHALOCELE ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 4 FDA reports)
EOSINOPHILIA MYALGIA SYNDROME ( 4 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 4 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 4 FDA reports)
EPIDERMAL NAEVUS ( 4 FDA reports)
EPIDERMOID CYST EXCISION ( 4 FDA reports)
EPIGLOTTIC OEDEMA ( 4 FDA reports)
EPIGLOTTITIS ( 4 FDA reports)
ERYTHEMA INFECTIOSUM ( 4 FDA reports)
EXCITABILITY ( 4 FDA reports)
EXTRADURAL ABSCESS ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EXTRASKELETAL OSSIFICATION ( 4 FDA reports)
FABRY'S DISEASE ( 4 FDA reports)
FACE PRESENTATION ( 4 FDA reports)
FACTOR XI DEFICIENCY ( 4 FDA reports)
FAILED INDUCTION OF LABOUR ( 4 FDA reports)
FAT EMBOLISM ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FOETAL ALCOHOL SYNDROME ( 4 FDA reports)
FOETAL HEART RATE DECREASED ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
GASTRIC PH DECREASED ( 4 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
GENE MUTATION ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GINGIVAL HYPERPLASIA ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
GROIN INFECTION ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 4 FDA reports)
HAEMATOMETRA ( 4 FDA reports)
HEAD BANGING ( 4 FDA reports)
HEAD LAG ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATORENAL FAILURE ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
HYPOSMIA ( 4 FDA reports)
HYPOTONIC URINARY BLADDER ( 4 FDA reports)
ICHTHYOSIS ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
ILIAC ARTERY OCCLUSION ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCORRECT PRODUCT STORAGE ( 4 FDA reports)
INFLUENZA IMMUNISATION ( 4 FDA reports)
INFUSION SITE CELLULITIS ( 4 FDA reports)
INFUSION SITE WARMTH ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
INJECTION SITE PAPULE ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 4 FDA reports)
IRON OVERLOAD ( 4 FDA reports)
ISCHAEMIC NEPHROPATHY ( 4 FDA reports)
JAW CYST ( 4 FDA reports)
JAW LESION EXCISION ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
JOINT WARMTH ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
KERATECTOMY ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
KYPHOSCOLIOSIS ( 4 FDA reports)
LACTOBACILLUS INFECTION ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LATENT TUBERCULOSIS ( 4 FDA reports)
LEUKODYSTROPHY ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
LYMPH NODE PALPABLE ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
LYMPHOHISTIOCYTOSIS ( 4 FDA reports)
MALIGNANT MELANOMA IN SITU ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MAY-THURNER SYNDROME ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 4 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 4 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METAL POISONING ( 4 FDA reports)
METAPNEUMOVIRUS INFECTION ( 4 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 4 FDA reports)
METASTASES TO BLADDER ( 4 FDA reports)
METASTASES TO MENINGES ( 4 FDA reports)
METASTASES TO NECK ( 4 FDA reports)
METATARSALGIA ( 4 FDA reports)
MICROANGIOPATHY ( 4 FDA reports)
MICROCEPHALY ( 4 FDA reports)
MICROCOCCUS INFECTION ( 4 FDA reports)
MICROGNATHIA ( 4 FDA reports)
MICTURITION FREQUENCY DECREASED ( 4 FDA reports)
MOLE EXCISION ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 4 FDA reports)
MYOGLOBIN URINE ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NECK DEFORMITY ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NEGATIVE THOUGHTS ( 4 FDA reports)
NERVE DEGENERATION ( 4 FDA reports)
NEUROPATHIC ARTHROPATHY ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
NOREPINEPHRINE INCREASED ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORAL FIBROMA ( 4 FDA reports)
ORAL LICHEN PLANUS ( 4 FDA reports)
ORAL MUCOSA ATROPHY ( 4 FDA reports)
ORAL PAPILLOMA ( 4 FDA reports)
ORTHODONTIC APPLIANCE USER ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
OSTEOMYELITIS FUNGAL ( 4 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 4 FDA reports)
OVARIAN ENLARGEMENT ( 4 FDA reports)
ABDOMINAL AORTIC BRUIT ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 3 FDA reports)
ACUTE CHEST SYNDROME ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
ALLERGY TEST ( 3 FDA reports)
AMNIOTIC CAVITY DISORDER ( 3 FDA reports)
AMPHETAMINES POSITIVE ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANAEMIA NEONATAL ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 3 FDA reports)
ANDROGENS DECREASED ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPLICATION SITE PARAESTHESIA ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ARTHROPOD STING ( 3 FDA reports)
ATELECTASIS NEONATAL ( 3 FDA reports)
ATHETOSIS ( 3 FDA reports)
ATRIAL PRESSURE INCREASED ( 3 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 3 FDA reports)
AUTOMATIC BLADDER ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BALANITIS CANDIDA ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BITE ( 3 FDA reports)
BLADDER ABLATION ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 3 FDA reports)
BLOOD VISCOSITY INCREASED ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BODY TEMPERATURE ( 3 FDA reports)
BONE CANCER METASTATIC ( 3 FDA reports)
BONE METABOLISM DISORDER ( 3 FDA reports)
BORRELIA TEST POSITIVE ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 3 FDA reports)
BREAST HAEMATOMA ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
BURKHOLDERIA TEST POSITIVE ( 3 FDA reports)
BURNS FIRST DEGREE ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 3 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CARDIAC PSEUDOANEURYSM ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 3 FDA reports)
CAROTID SINUS SYNDROME ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHORDEE ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 3 FDA reports)
CIRCUMORAL OEDEMA ( 3 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 3 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 3 FDA reports)
COLON CANCER STAGE I ( 3 FDA reports)
COLON CANCER STAGE IV ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CRANIAL NERVE DISORDER ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
CREATININE URINE INCREASED ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
CYST RUPTURE ( 3 FDA reports)
CYSTIC FIBROSIS RELATED DIABETES ( 3 FDA reports)
CYSTITIS GLANDULARIS ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DERMATITIS DIAPER ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEVICE EXPULSION ( 3 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC FOOT INFECTION ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DNA ANTIBODY POSITIVE ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DUBIN-JOHNSON SYNDROME ( 3 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
EAGLES SYNDROME ( 3 FDA reports)
ECLAMPSIA ( 3 FDA reports)
ECZEMA HERPETICUM ( 3 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 3 FDA reports)
ENCHONDROMATOSIS ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTHESOPATHY ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXECUTIVE DYSFUNCTION ( 3 FDA reports)
EXPOSURE TO ALLERGEN ( 3 FDA reports)
EYELID CYST ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FACTITIOUS DISORDER ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FRACTURE TREATMENT ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROENTERITIS BACTERIAL ( 3 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 3 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 3 FDA reports)
GASTROINTESTINAL INJURY ( 3 FDA reports)
GASTROOESOPHAGITIS ( 3 FDA reports)
GENITAL CANDIDIASIS ( 3 FDA reports)
GENITAL PAIN ( 3 FDA reports)
GESTATIONAL HYPERTENSION ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HEART BLOCK CONGENITAL ( 3 FDA reports)
HEART VALVE INSUFFICIENCY ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATIC VEIN THROMBOSIS ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HIV TEST POSITIVE ( 3 FDA reports)
HOUSE DUST ALLERGY ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HYDROTHORAX ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOCOAGULABLE STATE ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
IMPLANT SITE EFFUSION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
IMPRISONMENT ( 3 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INFUSION SITE HAEMATOMA ( 3 FDA reports)
INFUSION SITE HAEMORRHAGE ( 3 FDA reports)
INGUINAL HERNIA STRANGULATED ( 3 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJURY CORNEAL ( 3 FDA reports)
INTERCEPTED MEDICATION ERROR ( 3 FDA reports)
INTERNAL HERNIA ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 3 FDA reports)
JOB DISSATISFACTION ( 3 FDA reports)
JOINT ABSCESS ( 3 FDA reports)
JOINT ANKYLOSIS ( 3 FDA reports)
JUVENILE MYOCLONIC EPILEPSY ( 3 FDA reports)
LABOUR COMPLICATION ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LAGOPHTHALMOS ( 3 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 3 FDA reports)
LDL/HDL RATIO INCREASED ( 3 FDA reports)
LEIOMYOSARCOMA ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOW BIRTH WEIGHT BABY ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MACULAR SCAR ( 3 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 3 FDA reports)
MANDIBULECTOMY ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MEDIASTINAL FIBROSIS ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
MEDICATION TAMPERING ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
METASTASES TO CHEST WALL ( 3 FDA reports)
METASTASES TO HEART ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MIXED OLIGO-ASTROCYTOMA ( 3 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
NAIL BED BLEEDING ( 3 FDA reports)
NAIL GROWTH ABNORMAL ( 3 FDA reports)
NARCOTIC INTOXICATION ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
OCULOGYRATION ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL MASS ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OILY SKIN ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
OPIATES POSITIVE ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL DYSAESTHESIA ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
OROPHARYNGEAL SPASM ( 3 FDA reports)
OROPHARYNGITIS FUNGAL ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
ORTHOSTATIC INTOLERANCE ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
OXYGEN SATURATION INCREASED ( 3 FDA reports)
PANCREATIC ATROPHY ( 3 FDA reports)
PANCREATICODUODENECTOMY ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARASOMNIA ( 3 FDA reports)
PCO2 ABNORMAL ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 3 FDA reports)
PECTUS EXCAVATUM ( 3 FDA reports)
PEDAL PULSE ABNORMAL ( 3 FDA reports)
PELVIC DISCOMFORT ( 3 FDA reports)
PELVIC FLUID COLLECTION ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PHAEOCHROMOCYTOMA ( 3 FDA reports)
PHARYNGEAL STENOSIS ( 3 FDA reports)
PITYRIASIS ( 3 FDA reports)
PLATELET AGGREGATION INCREASED ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PNEUMONIA ASPERGILLUS ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
PORENCEPHALY ( 3 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POST PROCEDURAL HAEMATURIA ( 3 FDA reports)
POST PROCEDURAL VOMITING ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PREMATURE MENOPAUSE ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROPOFOL INFUSION SYNDROME ( 3 FDA reports)
PROTEIN C DECREASED ( 3 FDA reports)
PROTEIN S DECREASED ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PSEUDOCYST ( 3 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PYELONEPHRITIS CHRONIC ( 3 FDA reports)
RADIATION SKIN INJURY ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
RASH SCALY ( 3 FDA reports)
REACTION TO COLOURING ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 3 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL OSTEODYSTROPHY ( 3 FDA reports)
RENAL PAPILLARY NECROSIS ( 3 FDA reports)
RENAL SURGERY ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL DYSTROPHY ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 3 FDA reports)
SALIVARY GLAND MASS ( 3 FDA reports)
SCAN ABDOMEN ABNORMAL ( 3 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 3 FDA reports)
SCROTAL GANGRENE ( 3 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 3 FDA reports)
SEBORRHOEA ( 3 FDA reports)
SEIZURE ANOXIC ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SHUNT STENOSIS ( 3 FDA reports)
SICKLE CELL ANAEMIA ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP PARALYSIS ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOCIAL FEAR ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
SPINAL CORD NEOPLASM ( 3 FDA reports)
SPINAL HAEMANGIOMA ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPIROMETRY ABNORMAL ( 3 FDA reports)
SPLENIC VARICES ( 3 FDA reports)
SPONDYLITIC MYELOPATHY ( 3 FDA reports)
SPONTANEOUS PENILE ERECTION ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
STRONGYLOIDIASIS ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SUBSTANCE ABUSER ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SYDENHAM'S CHOREA ( 3 FDA reports)
SYMBLEPHARON ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TEETH BRITTLE ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
THIRST DECREASED ( 3 FDA reports)
THORACIC HAEMORRHAGE ( 3 FDA reports)
THOUGHT INSERTION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID ADENOMA ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
THYROID PAIN ( 3 FDA reports)
TONSILLITIS BACTERIAL ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRAUMATIC RENAL INJURY ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
TRICHIASIS ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TRICHOTILLOMANIA ( 3 FDA reports)
TROPONIN I ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETERIC DILATATION ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
URINE BILIRUBIN INCREASED ( 3 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 3 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 3 FDA reports)
UTERINE MALPOSITION ( 3 FDA reports)
UVULECTOMY ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VIRAL RASH ( 3 FDA reports)
VISCERAL CONGESTION ( 3 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT ( 3 FDA reports)
WHITE CLOT SYNDROME ( 3 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
XANTHOGRANULOMA ( 3 FDA reports)
PANCOAST'S TUMOUR ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARASITE URINE TEST POSITIVE ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARENTERAL NUTRITION ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PENILE DISCHARGE ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PERINEAL FISTULA ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARMACOPHOBIA ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PILONIDAL CYST CONGENITAL ( 2 FDA reports)
PINEAL NEOPLASM ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLEURA CARCINOMA ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYCYSTIC LIVER DISEASE ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORTOPULMONARY HYPERTENSION ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POST-TUSSIVE VOMITING ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRODUCT SIZE ISSUE ( 2 FDA reports)
PROLONGED PREGNANCY ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSYCHIATRIC INVESTIGATION ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY OEDEMA NEONATAL ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
PUS IN STOOL ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION FIBROSIS ( 2 FDA reports)
REACTION TO DRUG EXCIPIENT ( 2 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
REACTIVE ATTACHMENT DISORDER OF INFANCY OR EARLY CHILDHOOD ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELLS SEMEN ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL AGENESIS ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL VEIN OCCLUSION ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPERFUSION ARRHYTHMIA ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY DEPTH DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIB HYPOPLASIA ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SALIVARY GLAND OPERATION ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEIZURE LIKE PHENOMENA ( 2 FDA reports)
SEMEN ABNORMAL ( 2 FDA reports)
SEMEN DISCOLOURATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SICKLE CELL TRAIT ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP STUDY ABNORMAL ( 2 FDA reports)
SMALL INTESTINAL RESECTION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMOKE SENSITIVITY ( 2 FDA reports)
SPERMATOZOA ABNORMAL ( 2 FDA reports)
SPINAL CLAUDICATION ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPOROTRICHOSIS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STUBBORNNESS ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TABLET ISSUE ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
THYMIC CANCER METASTATIC ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONGUE PRURITUS ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL CANCER ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRISOMY 21 ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
UNWANTED PREGNANCY ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINARY TRACT MALFORMATION ( 2 FDA reports)
URINE ANALYSIS ( 2 FDA reports)
URINE BARBITURATES ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UROGRAM ABNORMAL ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
UTERINE HYPERTONUS ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL DYSPLASIA ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINITIS ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR DISSECTION ( 2 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VEIN WALL HYPERTROPHY ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS RECANALISATION ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VIITH NERVE INJURY ( 2 FDA reports)
VIRAL CARDIOMYOPATHY ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN B6 DECREASED ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WITHDRAWAL BLEED ( 2 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
X-RAY DENTAL ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUPUNCTURE ( 2 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
AMMONIA DECREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANOREXIA NERVOSA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTOGRAM ABNORMAL ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPERMIA ( 2 FDA reports)
ASPIRATION BREAST ( 2 FDA reports)
ASTHMA PROPHYLAXIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL TEST NEGATIVE ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BENIGN UTERINE NEOPLASM ( 2 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY DRAINAGE ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIARY FISTULA ( 2 FDA reports)
BIOPSY ENDOMETRIUM ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLADDER CANDIDIASIS ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLEEDING PERIPARTUM ( 2 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CALCIUM ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 2 FDA reports)
BLOOD IRON ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN STEM GLIOMA ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST INDURATION ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHITIS ACUTE VIRAL ( 2 FDA reports)
BRONCHOGENIC CYST ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CAPSULE PHYSICAL ISSUE ( 2 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 2 FDA reports)
CARCINOMA IN SITU OF TRACHEA ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CAT SCRATCH DISEASE ( 2 FDA reports)
CATABOLIC STATE ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL SARCOIDOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHEMICAL PERITONITIS ( 2 FDA reports)
CHLORACNE ( 2 FDA reports)
CHOLEDOCHAL CYST ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLESTASIS OF PREGNANCY ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 2 FDA reports)
COLON CANCER STAGE III ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CONGENITAL CEREBRAL CYST ( 2 FDA reports)
CONGENITAL FLAT FEET ( 2 FDA reports)
CONGENITAL HEPATOBILIARY ANOMALY ( 2 FDA reports)
CONGENITAL PNEUMONIA ( 2 FDA reports)
CONJUNCTIVAL PALLOR ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORNEAL OPERATION ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CSF OLIGOCLONAL BAND PRESENT ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CSF VOLUME INCREASED ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTOPEXY ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DELIVERY ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEMENTIA WITH LEWY BODIES ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEPOSIT EYE ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DERMOID CYST OF OVARY ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE CONNECTION ISSUE ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DEVICE TOXICITY ( 2 FDA reports)
DIABETIC MACROANGIOPATHY ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIAPHRAGMALGIA ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DIVERTICULITIS MECKEL'S ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG ADDICT ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSACUSIS ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSSOMNIA ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECTOPIC KIDNEY ( 2 FDA reports)
ECTROPION OF CERVIX ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOCARDIAL DISEASE ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENDOVENOUS ABLATION ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCELE ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EXPOSURE TO CONTAMINATED DEVICE ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
FACIAL LESION EXCISION ( 2 FDA reports)
FALLOPIAN TUBE CYST ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FASCIOTOMY ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FIBRINOLYSIS ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FOREIGN BODY REACTION ( 2 FDA reports)
FREE FATTY ACIDS INCREASED ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGUS CULTURE POSITIVE ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALLBLADDER ABSCESS ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GAMMA RADIATION THERAPY TO PROSTATE ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 2 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
GENITAL INFECTION FEMALE ( 2 FDA reports)
GESTATIONAL TROPHOBLASTIC TUMOUR ( 2 FDA reports)
GINGIVAL HYPOPLASIA ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GRANULOCYTES ABNORMAL ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMOPHILUS SEPSIS ( 2 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HANGNAIL ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEART VALVE OPERATION ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 2 FDA reports)
HEPATIC EMBOLISATION ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC VEIN DILATATION ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
IDIOPATHIC URTICARIA ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPLANT SITE EXTRAVASATION ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE DERMATITIS ( 2 FDA reports)
INJECTION SITE MACULE ( 2 FDA reports)
INJECTION SITE SCAB ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE REMOVAL ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRIS HYPERPIGMENTATION ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JOINT ADHESION ( 2 FDA reports)
JOINT FLUID DRAINAGE ( 2 FDA reports)
JOINT STABILISATION ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
KELOID SCAR ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KNEE DEFORMITY ( 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)
LAPAROSCOPY ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARYNGEAL ERYTHEMA ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 2 FDA reports)
LIVER OPERATION ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LUDWIG ANGINA ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG CYST ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 2 FDA reports)
LYMPHATIC DUCT INJURY ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
MENTALLY LATE DEVELOPER ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MINERAL SUPPLEMENTATION ( 2 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYRINGITIS ( 2 FDA reports)
MYRINGOPLASTY ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASOPHARYNGEAL SURGERY ( 2 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEONATAL TACHYCARDIA ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NERVOUS SYSTEM SURGERY ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUTROPENIA NEONATAL ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NITRITE URINE ABSENT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OMENTUM NEOPLASM ( 2 FDA reports)
ONYCHOGRYPHOSIS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL ALLERGY SYNDROME ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
OSTEOARTHRITIS GENERALISED ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE DECREASED ( 1 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 1 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABORTION SPONTANEOUS INCOMPLETE ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABSCESS STERILE ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCESSORY SALIVARY GLAND ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADENOLIPOMA ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADENOTONSILLECTOMY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADMINISTRATION SITE INFECTION ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALKAPTONURIA ( 1 FDA reports)
ALLERGENIC DESENSITISATION PROCEDURE ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
AMINO ACID LEVEL ABNORMAL ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOCENTESIS ABNORMAL ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAL PAP SMEAR ( 1 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 1 FDA reports)
ANALGESIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTASTHMATIC DRUG LEVEL ( 1 FDA reports)
ANTASTHMATIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC BIFURCATION GRAFT ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERASCITES ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL RHINITIS ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASAL GANGLION DEGENERATION ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BED BUG INFESTATION ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY CARTILAGE ABNORMAL ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY HEART ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER IRRIGATION ( 1 FDA reports)
BLADDER SUSPENSION ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD PYRUVIC ACID ABNORMAL ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DENSITOMETRY ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE GIANT CELL TUMOUR ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST PROSTHESIS REMOVAL ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS CHEMICAL ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANDIDA NAPPY RASH ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARPUS CURVUS ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL DYSGENESIS ( 1 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL RIB ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CERVIX OPERATION ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST CRUSHING ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHOROID PLEXUS PAPILLOMA ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLITORAL ENGORGEMENT ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
CLOT RETRACTION TIME SHORTENED ( 1 FDA reports)
COLD-STIMULUS HEADACHE ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLORECTAL CANCER STAGE III ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLPOCELE ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL ABSENCE OF CRANIAL VAULT ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGENITAL EMPHYSEMA ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HEARING DISORDER ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL INGUINAL HERNIA ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL NAEVUS ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORONA VIRUS INFECTION ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORYNEBACTERIUM SEPSIS ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRANIAL SUTURES WIDENING ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF MONOCYTE COUNT DECREASED ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DECREASED BRONCHIAL SECRETION ( 1 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC BULLOSIS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DIURETIC THERAPY ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSPONESIS ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
EBSTEIN'S ANOMALY ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ECZEMA IMPETIGINOUS ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDITIS PSEUDOMONAL ( 1 FDA reports)
ENDOCARDITIS VIRAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHILIC BRONCHITIS ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTIC CARCINOMA ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTERNAL EAR PAIN ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION SYPHILITIC ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYEGLASSES THERAPY ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACTOR II DEFICIENCY ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALURIA ( 1 FDA reports)
FAILURE TO CAPTURE ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FALLOPIAN TUBE PERFORATION ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEAR OF PREGNANCY ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL HERNIA REPAIR ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBRINOUS BRONCHITIS ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FITZ-HUGH-CURTIS SYNDROME ( 1 FDA reports)
FLAT CHEST ( 1 FDA reports)
FLAVOBACTERIUM INFECTION ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOETAL MONITORING ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FRACTURED SKULL DEPRESSED ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC HYPERPLASIA ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMUS TUMOUR ( 1 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GROWTH ACCELERATED ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR PLUCKING ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEMIPLEGIC MIGRAINE ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HEREDITARY DISORDER ( 1 FDA reports)
HERNIA CONGENITAL ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUMAN HERPESVIRUS 7 INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST NEGATIVE ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL GANGRENE ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOLOGY TEST ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPLANT SITE INDURATION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE PARAESTHESIA ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERLEUKIN LEVEL DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRANASAL NUMBNESS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JUVENILE CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KOEBNER PHENOMENON ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGOCELE ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEMIERRE SYNDROME ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOID TISSUE OPERATION ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACULAR RUPTURE ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASSAGE ( 1 FDA reports)
MASTOID ABSCESS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MISCARRIAGE OF PARTNER ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE OEDEMA ( 1 FDA reports)
MYCOBACTERIA SPUTUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOMALACIA ( 1 FDA reports)
MYIASIS ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL BRIDGING ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOPLASTY ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL PICKING ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NATURAL KILLER CELL COUNT DECREASED ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NEISSERIA TEST POSITIVE ( 1 FDA reports)
NEONATAL ANOXIA ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OCULOFACIAL PARALYSIS ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL MUCOSA ERYTHEMA ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OFFICE VISIT ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO DECREASED ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN FIBROSIS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PANCREATIC PSEUDOCYST DRAINAGE ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERENNIAL ALLERGY ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL CYST ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDIOTOMY ( 1 FDA reports)
PERICARDITIS LUPUS ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERINEAL CYST ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL CANCER METASTATIC ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMA VISCOSITY ABNORMAL ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA MORAXELLA ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
PO2 ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
PODAGRA ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCOLLAGEN TYPE I C-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROMISCUITY ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE EXAMINATION ( 1 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULMONARY VEIN STENOSIS ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLOROSPASM ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADIOALLERGOSORBENT TEST POSITIVE ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLEX TEST ABNORMAL ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM GASTROINTESTINAL TRACT ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY SIGHS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESPITE CARE ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SALVAGE THERAPY ( 1 FDA reports)
SARCOMA OF SKIN ( 1 FDA reports)
SCAN GALLIUM ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL CYST ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SEBACEOUS ADENOMA ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBACEOUS NAEVUS ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SEPTUM PELLUCIDUM AGENESIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM PROCOLLAGEN TYPE I N-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
SEVER'S DISEASE ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SEXUAL INHIBITION ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER DYSTOCIA ( 1 FDA reports)
SIALOMETAPLASIA ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS PERFORATION ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPASTIC DIPLEGIA ( 1 FDA reports)
SPHEROCYTIC ANAEMIA ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPUTUM DECREASED ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STICKLER'S SYNDROME ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STREPTOCOCCAL IMPETIGO ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCHORIONIC HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBSTANCE USE ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERINFECTION ORAL ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYMPHYSIOLYSIS ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYPHILIS TEST POSITIVE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TATTOO ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON NEOPLASM ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR CANCER METASTATIC ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR GERM CELL CANCER ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THORACIC DUCT LIGATION ( 1 FDA reports)
THORACOSTOMY ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TOCOLYSIS ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC DELIVERY ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
TYPHUS RICKETTSIA TEST POSITIVE ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND FOETAL ( 1 FDA reports)
UMBILICAL HAEMORRHAGE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
UREAPLASMA INFECTION ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETHRITIS CHLAMYDIAL ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE COPPER DECREASED ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINE VISCOSITY INCREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
URTICARIA THERMAL ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE DILATION AND EVACUATION ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UVEITIS-GLAUCOMA-HYPHAEMA SYNDROME ( 1 FDA reports)
VACCINE EXPOSURE DURING PREGNANCY ( 1 FDA reports)
VAGINAL ABSCESS ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL CANCER RECURRENT ( 1 FDA reports)
VAGINAL CANCER STAGE III ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VAGINAL PH INCREASED ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINITIS CHLAMYDIAL ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF CHILD ABUSE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD POLYPECTOMY ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL ULCERATION ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHELASMA ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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