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

PAIN ( 2670 FDA reports)
NAUSEA ( 2242 FDA reports)
VOMITING ( 1758 FDA reports)
ANXIETY ( 1739 FDA reports)
DYSPNOEA ( 1635 FDA reports)
FATIGUE ( 1557 FDA reports)
DIARRHOEA ( 1458 FDA reports)
CONSTIPATION ( 1289 FDA reports)
BACK PAIN ( 1265 FDA reports)
PNEUMONIA ( 1233 FDA reports)
PYREXIA ( 1232 FDA reports)
ASTHENIA ( 1224 FDA reports)
ANAEMIA ( 1157 FDA reports)
HEADACHE ( 1127 FDA reports)
DEPRESSION ( 1118 FDA reports)
ARTHRALGIA ( 1085 FDA reports)
FALL ( 1085 FDA reports)
DIZZINESS ( 1028 FDA reports)
OEDEMA PERIPHERAL ( 997 FDA reports)
CONFUSIONAL STATE ( 989 FDA reports)
ABDOMINAL PAIN ( 987 FDA reports)
PAIN IN EXTREMITY ( 979 FDA reports)
DEATH ( 976 FDA reports)
DRUG INEFFECTIVE ( 976 FDA reports)
INSOMNIA ( 960 FDA reports)
WEIGHT DECREASED ( 954 FDA reports)
OSTEONECROSIS OF JAW ( 945 FDA reports)
INJURY ( 910 FDA reports)
DEHYDRATION ( 889 FDA reports)
SOMNOLENCE ( 878 FDA reports)
CHEST PAIN ( 834 FDA reports)
CARDIAC ARREST ( 788 FDA reports)
HYPOAESTHESIA ( 762 FDA reports)
HYPOTENSION ( 755 FDA reports)
RESPIRATORY ARREST ( 740 FDA reports)
DECREASED APPETITE ( 713 FDA reports)
MALAISE ( 708 FDA reports)
COMPLETED SUICIDE ( 686 FDA reports)
PLEURAL EFFUSION ( 654 FDA reports)
HYPERTENSION ( 641 FDA reports)
INFECTION ( 629 FDA reports)
URINARY TRACT INFECTION ( 625 FDA reports)
RENAL FAILURE ACUTE ( 615 FDA reports)
BONE DISORDER ( 615 FDA reports)
DEEP VEIN THROMBOSIS ( 615 FDA reports)
PAIN IN JAW ( 604 FDA reports)
NEUROPATHY PERIPHERAL ( 598 FDA reports)
RASH ( 595 FDA reports)
PARAESTHESIA ( 588 FDA reports)
OSTEOMYELITIS ( 584 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 583 FDA reports)
DRUG DEPENDENCE ( 574 FDA reports)
OSTEOARTHRITIS ( 572 FDA reports)
GAIT DISTURBANCE ( 559 FDA reports)
MUSCLE SPASMS ( 559 FDA reports)
OVERDOSE ( 557 FDA reports)
MULTIPLE DRUG OVERDOSE ( 542 FDA reports)
EMOTIONAL DISTRESS ( 539 FDA reports)
THROMBOCYTOPENIA ( 532 FDA reports)
PULMONARY EMBOLISM ( 531 FDA reports)
HYPERHIDROSIS ( 519 FDA reports)
ATELECTASIS ( 515 FDA reports)
CARDIO-RESPIRATORY ARREST ( 510 FDA reports)
RENAL FAILURE ( 503 FDA reports)
DYSPHAGIA ( 502 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 500 FDA reports)
COUGH ( 487 FDA reports)
DRUG INTERACTION ( 485 FDA reports)
BONE PAIN ( 484 FDA reports)
LOSS OF CONSCIOUSNESS ( 475 FDA reports)
SEPSIS ( 461 FDA reports)
TREMOR ( 459 FDA reports)
ANHEDONIA ( 458 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 453 FDA reports)
ACCIDENTAL OVERDOSE ( 448 FDA reports)
SPINAL OSTEOARTHRITIS ( 447 FDA reports)
CELLULITIS ( 442 FDA reports)
DENTAL CARIES ( 437 FDA reports)
DRUG TOXICITY ( 434 FDA reports)
METASTASES TO BONE ( 434 FDA reports)
MENTAL STATUS CHANGES ( 424 FDA reports)
ERYTHEMA ( 422 FDA reports)
SINUSITIS ( 414 FDA reports)
FEELING ABNORMAL ( 413 FDA reports)
DRUG ABUSE ( 412 FDA reports)
WEIGHT INCREASED ( 407 FDA reports)
ABDOMINAL PAIN UPPER ( 405 FDA reports)
DRUG ABUSER ( 404 FDA reports)
HAEMOGLOBIN DECREASED ( 403 FDA reports)
SUICIDAL IDEATION ( 402 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 401 FDA reports)
CHILLS ( 399 FDA reports)
CONDITION AGGRAVATED ( 396 FDA reports)
MUSCULAR WEAKNESS ( 396 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 393 FDA reports)
RESPIRATORY FAILURE ( 393 FDA reports)
PANCYTOPENIA ( 391 FDA reports)
NEOPLASM MALIGNANT ( 389 FDA reports)
MYALGIA ( 388 FDA reports)
DELIRIUM ( 387 FDA reports)
OSTEONECROSIS ( 386 FDA reports)
ATRIAL FIBRILLATION ( 384 FDA reports)
VISION BLURRED ( 380 FDA reports)
BRONCHITIS ( 375 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 374 FDA reports)
IMPAIRED HEALING ( 369 FDA reports)
NECK PAIN ( 369 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 369 FDA reports)
SWELLING ( 368 FDA reports)
ARTHRITIS ( 368 FDA reports)
CARDIOMEGALY ( 368 FDA reports)
TOOTH EXTRACTION ( 365 FDA reports)
OSTEOPENIA ( 361 FDA reports)
CONVULSION ( 360 FDA reports)
DISEASE PROGRESSION ( 358 FDA reports)
HYPOKALAEMIA ( 357 FDA reports)
NEUTROPENIA ( 355 FDA reports)
MUSCULOSKELETAL PAIN ( 350 FDA reports)
PRURITUS ( 343 FDA reports)
MYOCARDIAL INFARCTION ( 342 FDA reports)
BLOOD GLUCOSE INCREASED ( 337 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 337 FDA reports)
TACHYCARDIA ( 335 FDA reports)
AGITATION ( 333 FDA reports)
DEFORMITY ( 331 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 330 FDA reports)
SYNCOPE ( 330 FDA reports)
BLOOD PRESSURE INCREASED ( 319 FDA reports)
HYPOXIA ( 318 FDA reports)
CONTUSION ( 309 FDA reports)
CATARACT ( 308 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 307 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 302 FDA reports)
OEDEMA ( 302 FDA reports)
OSTEOPOROSIS ( 297 FDA reports)
ROAD TRAFFIC ACCIDENT ( 297 FDA reports)
AMNESIA ( 295 FDA reports)
DYSPEPSIA ( 295 FDA reports)
CEREBROVASCULAR ACCIDENT ( 294 FDA reports)
MULTIPLE MYELOMA ( 294 FDA reports)
BLOOD CREATININE INCREASED ( 289 FDA reports)
BONE LESION ( 289 FDA reports)
DECREASED INTEREST ( 289 FDA reports)
LETHARGY ( 288 FDA reports)
HYPOPHAGIA ( 287 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 286 FDA reports)
CHOLELITHIASIS ( 286 FDA reports)
PULMONARY OEDEMA ( 283 FDA reports)
MEMORY IMPAIRMENT ( 282 FDA reports)
HEART RATE INCREASED ( 277 FDA reports)
HYPONATRAEMIA ( 277 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 275 FDA reports)
INTENTIONAL DRUG MISUSE ( 274 FDA reports)
HERPES ZOSTER ( 268 FDA reports)
FEBRILE NEUTROPENIA ( 265 FDA reports)
HAEMORRHOIDS ( 264 FDA reports)
TOOTH LOSS ( 264 FDA reports)
CHEST DISCOMFORT ( 263 FDA reports)
DIABETES MELLITUS ( 261 FDA reports)
PLATELET COUNT DECREASED ( 261 FDA reports)
STAPHYLOCOCCAL INFECTION ( 261 FDA reports)
HALLUCINATION ( 258 FDA reports)
HYPERKALAEMIA ( 257 FDA reports)
RIB FRACTURE ( 257 FDA reports)
ABDOMINAL DISCOMFORT ( 255 FDA reports)
POISONING ( 250 FDA reports)
ORAL PAIN ( 247 FDA reports)
HIATUS HERNIA ( 244 FDA reports)
DYSURIA ( 242 FDA reports)
BALANCE DISORDER ( 240 FDA reports)
JOINT SWELLING ( 237 FDA reports)
CORONARY ARTERY DISEASE ( 235 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 233 FDA reports)
COMA ( 231 FDA reports)
HEPATIC STEATOSIS ( 231 FDA reports)
RECTAL HAEMORRHAGE ( 231 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 230 FDA reports)
VERTIGO ( 228 FDA reports)
HOT FLUSH ( 227 FDA reports)
NEPHROLITHIASIS ( 227 FDA reports)
UNRESPONSIVE TO STIMULI ( 226 FDA reports)
NERVOUSNESS ( 225 FDA reports)
SWELLING FACE ( 224 FDA reports)
TOOTHACHE ( 223 FDA reports)
LUNG NEOPLASM ( 223 FDA reports)
ABDOMINAL DISTENSION ( 222 FDA reports)
LYMPHADENOPATHY ( 222 FDA reports)
NEOPLASM PROGRESSION ( 222 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 220 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 220 FDA reports)
MIGRAINE ( 220 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 217 FDA reports)
MITRAL VALVE INCOMPETENCE ( 216 FDA reports)
DYSPNOEA EXERTIONAL ( 215 FDA reports)
HAEMATURIA ( 214 FDA reports)
STOMATITIS ( 214 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 214 FDA reports)
INADEQUATE ANALGESIA ( 213 FDA reports)
DYSARTHRIA ( 212 FDA reports)
ANOREXIA ( 211 FDA reports)
HAEMATOCRIT DECREASED ( 211 FDA reports)
PATHOLOGICAL FRACTURE ( 208 FDA reports)
COMPRESSION FRACTURE ( 203 FDA reports)
HEAD INJURY ( 203 FDA reports)
HYPERGLYCAEMIA ( 202 FDA reports)
METASTASES TO SPINE ( 202 FDA reports)
DRUG EFFECT DECREASED ( 201 FDA reports)
INTESTINAL OBSTRUCTION ( 199 FDA reports)
WITHDRAWAL SYNDROME ( 198 FDA reports)
MEDICATION ERROR ( 197 FDA reports)
LEUKOPENIA ( 196 FDA reports)
PALPITATIONS ( 195 FDA reports)
ARTHROPATHY ( 192 FDA reports)
SEDATION ( 191 FDA reports)
HAEMORRHAGE ( 190 FDA reports)
LUNG INFILTRATION ( 189 FDA reports)
METASTASES TO LIVER ( 189 FDA reports)
TOOTH DISORDER ( 189 FDA reports)
ASTHMA ( 188 FDA reports)
DYSGEUSIA ( 188 FDA reports)
HYPERLIPIDAEMIA ( 188 FDA reports)
INFLUENZA LIKE ILLNESS ( 188 FDA reports)
PRODUCT QUALITY ISSUE ( 188 FDA reports)
URINARY RETENTION ( 187 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 187 FDA reports)
EMPHYSEMA ( 184 FDA reports)
IRRITABILITY ( 184 FDA reports)
EXPOSED BONE IN JAW ( 183 FDA reports)
RESPIRATORY DISTRESS ( 182 FDA reports)
SINUS TACHYCARDIA ( 181 FDA reports)
DIVERTICULUM ( 180 FDA reports)
DRY MOUTH ( 180 FDA reports)
MUCOSAL INFLAMMATION ( 180 FDA reports)
HYPERSENSITIVITY ( 179 FDA reports)
OESOPHAGITIS ( 178 FDA reports)
RENAL FAILURE CHRONIC ( 178 FDA reports)
GASTRITIS ( 177 FDA reports)
MOUTH ULCERATION ( 177 FDA reports)
RENAL CYST ( 175 FDA reports)
DIPLOPIA ( 174 FDA reports)
DRUG DOSE OMISSION ( 174 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 174 FDA reports)
DISCOMFORT ( 173 FDA reports)
PRIMARY SEQUESTRUM ( 172 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 171 FDA reports)
DISORIENTATION ( 170 FDA reports)
OSTEOLYSIS ( 170 FDA reports)
COLITIS ( 169 FDA reports)
VISUAL IMPAIRMENT ( 169 FDA reports)
SEPTIC SHOCK ( 168 FDA reports)
URTICARIA ( 168 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 168 FDA reports)
ASCITES ( 167 FDA reports)
FIBROMYALGIA ( 167 FDA reports)
SPINAL COMPRESSION FRACTURE ( 167 FDA reports)
ROTATOR CUFF SYNDROME ( 166 FDA reports)
SLEEP APNOEA SYNDROME ( 166 FDA reports)
BURSITIS ( 166 FDA reports)
DISABILITY ( 163 FDA reports)
HIP FRACTURE ( 163 FDA reports)
PNEUMONIA ASPIRATION ( 163 FDA reports)
TYPE 2 DIABETES MELLITUS ( 163 FDA reports)
TOOTH ABSCESS ( 162 FDA reports)
ILEUS ( 162 FDA reports)
PULMONARY HYPERTENSION ( 162 FDA reports)
BLOOD CALCIUM DECREASED ( 160 FDA reports)
HYPERCHOLESTEROLAEMIA ( 160 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 160 FDA reports)
NIGHT SWEATS ( 160 FDA reports)
ACTINOMYCOSIS ( 159 FDA reports)
PANCREATITIS ( 158 FDA reports)
CARDIAC DISORDER ( 157 FDA reports)
INFLAMMATION ( 157 FDA reports)
SCOLIOSIS ( 157 FDA reports)
STRESS ( 155 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 155 FDA reports)
ARTERIOSCLEROSIS ( 155 FDA reports)
MULTI-ORGAN FAILURE ( 155 FDA reports)
ALOPECIA ( 153 FDA reports)
POLLAKIURIA ( 153 FDA reports)
HAEMOPTYSIS ( 152 FDA reports)
MOBILITY DECREASED ( 152 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 152 FDA reports)
OSTEITIS ( 152 FDA reports)
WHEEZING ( 152 FDA reports)
BLOOD POTASSIUM DECREASED ( 151 FDA reports)
DISTURBANCE IN ATTENTION ( 150 FDA reports)
EXOSTOSIS ( 150 FDA reports)
HAEMATOCHEZIA ( 150 FDA reports)
NEURALGIA ( 150 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 149 FDA reports)
INCORRECT DOSE ADMINISTERED ( 149 FDA reports)
BURNING SENSATION ( 148 FDA reports)
GINGIVAL PAIN ( 148 FDA reports)
SKIN ULCER ( 148 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 148 FDA reports)
SPEECH DISORDER ( 148 FDA reports)
OXYGEN SATURATION DECREASED ( 147 FDA reports)
SKIN LESION ( 146 FDA reports)
TREATMENT NONCOMPLIANCE ( 146 FDA reports)
URINARY INCONTINENCE ( 146 FDA reports)
THROMBOSIS ( 145 FDA reports)
EXCORIATION ( 144 FDA reports)
NEUTROPHIL COUNT DECREASED ( 144 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 142 FDA reports)
OSTEOSCLEROSIS ( 142 FDA reports)
JAW DISORDER ( 141 FDA reports)
OROPHARYNGEAL PAIN ( 141 FDA reports)
CANDIDIASIS ( 140 FDA reports)
CARDIOMYOPATHY ( 140 FDA reports)
MENTAL DISORDER ( 140 FDA reports)
RESTLESSNESS ( 140 FDA reports)
TOOTH FRACTURE ( 139 FDA reports)
LEUKOCYTOSIS ( 139 FDA reports)
MASS ( 139 FDA reports)
LOOSE TOOTH ( 138 FDA reports)
SURGERY ( 138 FDA reports)
HAEMATEMESIS ( 137 FDA reports)
INJECTION SITE PAIN ( 137 FDA reports)
EPISTAXIS ( 136 FDA reports)
FACIAL PAIN ( 136 FDA reports)
PULMONARY CONGESTION ( 136 FDA reports)
SUBSTANCE ABUSE ( 136 FDA reports)
SLEEP DISORDER ( 135 FDA reports)
ABASIA ( 135 FDA reports)
DYSPHONIA ( 134 FDA reports)
HEPATIC FAILURE ( 134 FDA reports)
FAILURE TO THRIVE ( 133 FDA reports)
FEELING HOT ( 133 FDA reports)
FLANK PAIN ( 133 FDA reports)
KYPHOSIS ( 133 FDA reports)
MASTICATION DISORDER ( 133 FDA reports)
ABNORMAL BEHAVIOUR ( 132 FDA reports)
HYDRONEPHROSIS ( 132 FDA reports)
ENCEPHALOPATHY ( 131 FDA reports)
LUMBAR SPINAL STENOSIS ( 131 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 130 FDA reports)
SCAR ( 130 FDA reports)
SEROTONIN SYNDROME ( 130 FDA reports)
BLOOD UREA INCREASED ( 129 FDA reports)
LUNG DISORDER ( 129 FDA reports)
INTENTIONAL OVERDOSE ( 128 FDA reports)
INTERSTITIAL LUNG DISEASE ( 128 FDA reports)
PRODUCTIVE COUGH ( 128 FDA reports)
RADICULOPATHY ( 128 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 127 FDA reports)
RENAL IMPAIRMENT ( 127 FDA reports)
CARDIAC MURMUR ( 127 FDA reports)
CARPAL TUNNEL SYNDROME ( 127 FDA reports)
DRUG HYPERSENSITIVITY ( 127 FDA reports)
ARRHYTHMIA ( 126 FDA reports)
METASTASES TO LUNG ( 126 FDA reports)
PARANOIA ( 126 FDA reports)
DYSKINESIA ( 125 FDA reports)
ERECTILE DYSFUNCTION ( 125 FDA reports)
HYPERCALCAEMIA ( 125 FDA reports)
HYPOGLYCAEMIA ( 125 FDA reports)
MALNUTRITION ( 124 FDA reports)
DRUG SCREEN POSITIVE ( 123 FDA reports)
EAR PAIN ( 123 FDA reports)
JAW FRACTURE ( 123 FDA reports)
ORTHOSTATIC HYPOTENSION ( 123 FDA reports)
PERICARDIAL EFFUSION ( 123 FDA reports)
UNEVALUABLE EVENT ( 123 FDA reports)
AGGRESSION ( 122 FDA reports)
ANGINA PECTORIS ( 122 FDA reports)
BLOOD PRESSURE DECREASED ( 122 FDA reports)
GINGIVITIS ( 121 FDA reports)
LACERATION ( 121 FDA reports)
LUNG NEOPLASM MALIGNANT ( 121 FDA reports)
RESPIRATORY DEPRESSION ( 121 FDA reports)
SPINAL COLUMN STENOSIS ( 120 FDA reports)
DEBRIDEMENT ( 120 FDA reports)
METABOLIC ACIDOSIS ( 120 FDA reports)
OFF LABEL USE ( 120 FDA reports)
CHOLECYSTITIS CHRONIC ( 119 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 119 FDA reports)
MIOSIS ( 119 FDA reports)
NASAL CONGESTION ( 119 FDA reports)
EJECTION FRACTION DECREASED ( 118 FDA reports)
GROIN PAIN ( 118 FDA reports)
ASPIRATION ( 117 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 117 FDA reports)
SUICIDE ATTEMPT ( 117 FDA reports)
VISUAL ACUITY REDUCED ( 116 FDA reports)
BLOOD BILIRUBIN INCREASED ( 116 FDA reports)
BACTERIAL INFECTION ( 115 FDA reports)
SPINAL FRACTURE ( 115 FDA reports)
TOOTH INFECTION ( 115 FDA reports)
PURULENT DISCHARGE ( 114 FDA reports)
BRADYCARDIA ( 114 FDA reports)
CROHN'S DISEASE ( 114 FDA reports)
CYSTITIS ( 113 FDA reports)
GASTROINTESTINAL DISORDER ( 113 FDA reports)
RHEUMATOID ARTHRITIS ( 113 FDA reports)
ANGER ( 112 FDA reports)
APHASIA ( 112 FDA reports)
COLONIC POLYP ( 112 FDA reports)
EYE PAIN ( 111 FDA reports)
FLUSHING ( 111 FDA reports)
GALLBLADDER DISORDER ( 111 FDA reports)
INFLUENZA ( 111 FDA reports)
PERIODONTITIS ( 111 FDA reports)
PROTHROMBIN TIME PROLONGED ( 110 FDA reports)
SINUS DISORDER ( 110 FDA reports)
SKIN EXFOLIATION ( 110 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 109 FDA reports)
CHRONIC SINUSITIS ( 109 FDA reports)
FLUID OVERLOAD ( 109 FDA reports)
HYPOTHYROIDISM ( 109 FDA reports)
CRYING ( 108 FDA reports)
FEMUR FRACTURE ( 108 FDA reports)
PANIC ATTACK ( 108 FDA reports)
BLOOD SODIUM DECREASED ( 107 FDA reports)
NASOPHARYNGITIS ( 107 FDA reports)
TENDONITIS ( 107 FDA reports)
TINNITUS ( 106 FDA reports)
CYST ( 106 FDA reports)
GASTRIC ULCER ( 106 FDA reports)
ORAL CANDIDIASIS ( 106 FDA reports)
DEAFNESS ( 105 FDA reports)
FUNGAL INFECTION ( 105 FDA reports)
RHINORRHOEA ( 105 FDA reports)
SCIATICA ( 105 FDA reports)
TENDERNESS ( 104 FDA reports)
ATAXIA ( 104 FDA reports)
DECUBITUS ULCER ( 104 FDA reports)
COGNITIVE DISORDER ( 103 FDA reports)
RENAL DISORDER ( 103 FDA reports)
ABSCESS ( 102 FDA reports)
HYPERSOMNIA ( 102 FDA reports)
BODY TEMPERATURE INCREASED ( 101 FDA reports)
FLATULENCE ( 100 FDA reports)
POLYSUBSTANCE ABUSE ( 100 FDA reports)
FISTULA ( 99 FDA reports)
RESPIRATORY DISORDER ( 99 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 98 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 98 FDA reports)
LYMPHOEDEMA ( 98 FDA reports)
CEREBRAL ATROPHY ( 97 FDA reports)
HEPATIC ENZYME INCREASED ( 97 FDA reports)
VIRAL INFECTION ( 97 FDA reports)
SKIN DISORDER ( 96 FDA reports)
ULCER ( 96 FDA reports)
FOOT FRACTURE ( 96 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 96 FDA reports)
MUSCLE TWITCHING ( 96 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 96 FDA reports)
NOCTURIA ( 96 FDA reports)
PERIODONTAL DISEASE ( 95 FDA reports)
IRON DEFICIENCY ANAEMIA ( 94 FDA reports)
MYOCARDIAL ISCHAEMIA ( 94 FDA reports)
ORAL DISORDER ( 94 FDA reports)
VAGINAL HAEMORRHAGE ( 94 FDA reports)
MYOCLONUS ( 93 FDA reports)
PHYSICAL DISABILITY ( 93 FDA reports)
PSYCHOTIC DISORDER ( 93 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 92 FDA reports)
METASTASES TO LYMPH NODES ( 92 FDA reports)
PNEUMONITIS ( 92 FDA reports)
UPPER LIMB FRACTURE ( 92 FDA reports)
JOINT EFFUSION ( 91 FDA reports)
LIVER DISORDER ( 91 FDA reports)
MELAENA ( 91 FDA reports)
PSORIASIS ( 91 FDA reports)
BLISTER ( 90 FDA reports)
GINGIVAL BLEEDING ( 90 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 90 FDA reports)
METASTATIC NEOPLASM ( 90 FDA reports)
OBESITY ( 90 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 89 FDA reports)
BONE DEBRIDEMENT ( 89 FDA reports)
CARDIAC FAILURE ( 89 FDA reports)
HAEMATOMA ( 89 FDA reports)
SPINAL DISORDER ( 89 FDA reports)
DEPRESSED MOOD ( 88 FDA reports)
ILL-DEFINED DISORDER ( 88 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 88 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 88 FDA reports)
CEREBRAL INFARCTION ( 87 FDA reports)
DRUG TOLERANCE ( 87 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 87 FDA reports)
ORAL DISCOMFORT ( 87 FDA reports)
SKIN DISCOLOURATION ( 87 FDA reports)
ABSCESS JAW ( 86 FDA reports)
BLOOD GLUCOSE DECREASED ( 86 FDA reports)
EATING DISORDER ( 86 FDA reports)
FEELING COLD ( 86 FDA reports)
JAW OPERATION ( 86 FDA reports)
LEFT ATRIAL DILATATION ( 86 FDA reports)
DIVERTICULUM INTESTINAL ( 85 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 85 FDA reports)
DRUG PRESCRIBING ERROR ( 84 FDA reports)
EMOTIONAL DISORDER ( 84 FDA reports)
NERVOUS SYSTEM DISORDER ( 84 FDA reports)
SPLENOMEGALY ( 84 FDA reports)
SQUAMOUS CELL CARCINOMA ( 84 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 84 FDA reports)
RESTLESS LEGS SYNDROME ( 83 FDA reports)
ABDOMINAL PAIN LOWER ( 83 FDA reports)
EAR INFECTION ( 83 FDA reports)
PELVIC PAIN ( 83 FDA reports)
JOINT STIFFNESS ( 82 FDA reports)
WOUND DEHISCENCE ( 82 FDA reports)
WALKING AID USER ( 81 FDA reports)
BLOOD ALBUMIN DECREASED ( 81 FDA reports)
MENISCUS LESION ( 81 FDA reports)
MOOD SWINGS ( 81 FDA reports)
BACTERAEMIA ( 80 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 80 FDA reports)
SINUS BRADYCARDIA ( 79 FDA reports)
SPONDYLOLISTHESIS ( 79 FDA reports)
ABNORMAL DREAMS ( 79 FDA reports)
APNOEA ( 79 FDA reports)
BLOOD POTASSIUM INCREASED ( 79 FDA reports)
BONE LOSS ( 79 FDA reports)
BRONCHOPNEUMONIA ( 79 FDA reports)
LIFE EXPECTANCY SHORTENED ( 79 FDA reports)
ORAL INFECTION ( 79 FDA reports)
PRESYNCOPE ( 79 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 78 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 78 FDA reports)
ENDODONTIC PROCEDURE ( 78 FDA reports)
HEPATOMEGALY ( 78 FDA reports)
RHABDOMYOLYSIS ( 78 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 77 FDA reports)
FLUID RETENTION ( 77 FDA reports)
HYPERBILIRUBINAEMIA ( 77 FDA reports)
ACCIDENTAL DEATH ( 76 FDA reports)
CERVICAL SPINAL STENOSIS ( 76 FDA reports)
HEPATIC CYST ( 76 FDA reports)
PALLOR ( 76 FDA reports)
SYNOVIAL CYST ( 76 FDA reports)
ACUTE RESPIRATORY FAILURE ( 75 FDA reports)
BREATH ODOUR ( 75 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 75 FDA reports)
GINGIVAL DISORDER ( 74 FDA reports)
GUN SHOT WOUND ( 74 FDA reports)
PLASMACYTOMA ( 74 FDA reports)
PROCTALGIA ( 74 FDA reports)
ECONOMIC PROBLEM ( 73 FDA reports)
FEAR ( 73 FDA reports)
GLAUCOMA ( 73 FDA reports)
HEPATIC LESION ( 73 FDA reports)
HEPATITIS ( 73 FDA reports)
RASH PRURITIC ( 73 FDA reports)
VENTRICULAR TACHYCARDIA ( 73 FDA reports)
COLD SWEAT ( 72 FDA reports)
LACRIMATION INCREASED ( 72 FDA reports)
NIGHTMARE ( 72 FDA reports)
COAGULOPATHY ( 71 FDA reports)
DELUSION ( 71 FDA reports)
DRY SKIN ( 71 FDA reports)
HYPOCALCAEMIA ( 71 FDA reports)
HYPOMAGNESAEMIA ( 71 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 71 FDA reports)
MUSCLE STRAIN ( 71 FDA reports)
SENSITIVITY OF TEETH ( 71 FDA reports)
SPINAL CORD COMPRESSION ( 71 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 71 FDA reports)
INGUINAL HERNIA ( 70 FDA reports)
MENTAL IMPAIRMENT ( 70 FDA reports)
BACK DISORDER ( 69 FDA reports)
DEMENTIA ( 69 FDA reports)
DENTAL FISTULA ( 69 FDA reports)
DENTURE WEARER ( 69 FDA reports)
FACET JOINT SYNDROME ( 69 FDA reports)
HUMERUS FRACTURE ( 69 FDA reports)
HYPOALBUMINAEMIA ( 69 FDA reports)
LUMBAR RADICULOPATHY ( 69 FDA reports)
RASH ERYTHEMATOUS ( 69 FDA reports)
RASH GENERALISED ( 68 FDA reports)
STEM CELL TRANSPLANT ( 68 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 68 FDA reports)
CHOLECYSTITIS ( 68 FDA reports)
DERMATITIS ( 68 FDA reports)
FIBROSIS ( 68 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 67 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 67 FDA reports)
ELECTROLYTE IMBALANCE ( 67 FDA reports)
INTENTIONAL MISUSE ( 67 FDA reports)
MYELODYSPLASTIC SYNDROME ( 67 FDA reports)
PNEUMOTHORAX ( 67 FDA reports)
POST HERPETIC NEURALGIA ( 67 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 67 FDA reports)
WOUND ( 67 FDA reports)
PYELONEPHRITIS ( 66 FDA reports)
SENSORY LOSS ( 66 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 66 FDA reports)
MUSCLE TIGHTNESS ( 66 FDA reports)
ORAL INTAKE REDUCED ( 66 FDA reports)
AORTIC ANEURYSM ( 65 FDA reports)
AORTIC VALVE SCLEROSIS ( 65 FDA reports)
DRY EYE ( 65 FDA reports)
GRAND MAL CONVULSION ( 65 FDA reports)
LIMB INJURY ( 65 FDA reports)
MULTIPLE SCLEROSIS ( 65 FDA reports)
POST PROCEDURAL COMPLICATION ( 65 FDA reports)
PULMONARY FIBROSIS ( 65 FDA reports)
ACCIDENT ( 64 FDA reports)
ADRENAL INSUFFICIENCY ( 64 FDA reports)
BONE MARROW FAILURE ( 64 FDA reports)
GASTROENTERITIS ( 64 FDA reports)
GINGIVAL INFECTION ( 64 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 64 FDA reports)
STOMACH DISCOMFORT ( 64 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 63 FDA reports)
BLINDNESS ( 63 FDA reports)
BONE DENSITY DECREASED ( 63 FDA reports)
DEVICE RELATED INFECTION ( 63 FDA reports)
EMBOLISM ( 63 FDA reports)
GINGIVAL SWELLING ( 63 FDA reports)
HYPERAESTHESIA ( 63 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 63 FDA reports)
DIVERTICULITIS ( 62 FDA reports)
DRUG ADMINISTRATION ERROR ( 62 FDA reports)
INTESTINAL PERFORATION ( 62 FDA reports)
MICTURITION URGENCY ( 62 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 62 FDA reports)
THINKING ABNORMAL ( 62 FDA reports)
VITREOUS FLOATERS ( 62 FDA reports)
RASH MACULAR ( 61 FDA reports)
ATRIAL FLUTTER ( 61 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 61 FDA reports)
GINGIVAL RECESSION ( 61 FDA reports)
HYPOAESTHESIA ORAL ( 61 FDA reports)
HYPOVOLAEMIA ( 61 FDA reports)
INJECTION SITE ERYTHEMA ( 61 FDA reports)
MOOD ALTERED ( 61 FDA reports)
NARCOTIC INTOXICATION ( 61 FDA reports)
NODULE ( 61 FDA reports)
ORAL CAVITY FISTULA ( 61 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 60 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 60 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 60 FDA reports)
GENERALISED OEDEMA ( 60 FDA reports)
HOSPITALISATION ( 60 FDA reports)
IRRITABLE BOWEL SYNDROME ( 60 FDA reports)
WOUND INFECTION ( 60 FDA reports)
ACTINIC KERATOSIS ( 59 FDA reports)
BONE OPERATION ( 59 FDA reports)
HALLUCINATION, VISUAL ( 59 FDA reports)
HEPATITIS C ( 59 FDA reports)
INFUSION RELATED REACTION ( 59 FDA reports)
LABYRINTHITIS ( 59 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 59 FDA reports)
OEDEMA MOUTH ( 59 FDA reports)
OPEN WOUND ( 59 FDA reports)
PERONEAL NERVE PALSY ( 59 FDA reports)
AORTIC VALVE INCOMPETENCE ( 58 FDA reports)
CYANOSIS ( 58 FDA reports)
HEART RATE IRREGULAR ( 58 FDA reports)
JOINT INJURY ( 58 FDA reports)
LUNG INFECTION ( 58 FDA reports)
PANCREATITIS ACUTE ( 58 FDA reports)
PARAESTHESIA ORAL ( 58 FDA reports)
PLATELET COUNT INCREASED ( 58 FDA reports)
VISUAL DISTURBANCE ( 58 FDA reports)
BASAL CELL CARCINOMA ( 57 FDA reports)
CACHEXIA ( 57 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 57 FDA reports)
FAECALOMA ( 57 FDA reports)
FRACTURE ( 57 FDA reports)
HALLUCINATION, AUDITORY ( 57 FDA reports)
HEMIPARESIS ( 57 FDA reports)
HEPATIC CIRRHOSIS ( 57 FDA reports)
INCOHERENT ( 57 FDA reports)
NERVE INJURY ( 57 FDA reports)
PARALYSIS ( 57 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 57 FDA reports)
POLYNEUROPATHY ( 57 FDA reports)
PRURITUS GENERALISED ( 57 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 56 FDA reports)
BRAIN OEDEMA ( 56 FDA reports)
CEREBRAL ISCHAEMIA ( 56 FDA reports)
ECZEMA ( 56 FDA reports)
EUPHORIC MOOD ( 56 FDA reports)
GOITRE ( 56 FDA reports)
MAJOR DEPRESSION ( 56 FDA reports)
PHARYNGITIS ( 56 FDA reports)
RESPIRATORY RATE INCREASED ( 56 FDA reports)
BEDRIDDEN ( 55 FDA reports)
BRUXISM ( 55 FDA reports)
HYPOACUSIS ( 55 FDA reports)
LYMPHOMA ( 55 FDA reports)
NON-CARDIAC CHEST PAIN ( 55 FDA reports)
ABDOMINAL HERNIA ( 54 FDA reports)
BLOOD URINE PRESENT ( 54 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 54 FDA reports)
GYNAECOMASTIA ( 54 FDA reports)
JAUNDICE ( 54 FDA reports)
LIBIDO DECREASED ( 54 FDA reports)
NEUTROPENIC SEPSIS ( 54 FDA reports)
NO THERAPEUTIC RESPONSE ( 54 FDA reports)
PROSTATOMEGALY ( 54 FDA reports)
SINUS CONGESTION ( 54 FDA reports)
TONGUE INJURY ( 54 FDA reports)
SEXUAL DYSFUNCTION ( 53 FDA reports)
AZOTAEMIA ( 53 FDA reports)
CERVICAL DYSPLASIA ( 53 FDA reports)
ENTEROCOCCAL INFECTION ( 53 FDA reports)
FEELING JITTERY ( 53 FDA reports)
ACCIDENTAL EXPOSURE ( 52 FDA reports)
BLOOD CULTURE POSITIVE ( 52 FDA reports)
GOUT ( 52 FDA reports)
IMPAIRED DRIVING ABILITY ( 52 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 52 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 52 FDA reports)
LUNG CONSOLIDATION ( 52 FDA reports)
METABOLIC ENCEPHALOPATHY ( 52 FDA reports)
METASTASIS ( 52 FDA reports)
OTITIS EXTERNA ( 52 FDA reports)
PULSE ABSENT ( 52 FDA reports)
SKIN LACERATION ( 52 FDA reports)
RADIUS FRACTURE ( 51 FDA reports)
SWOLLEN TONGUE ( 51 FDA reports)
THIRST ( 51 FDA reports)
VENOUS INSUFFICIENCY ( 51 FDA reports)
BARRETT'S OESOPHAGUS ( 51 FDA reports)
COSTOCHONDRITIS ( 51 FDA reports)
DYSSTASIA ( 51 FDA reports)
ESCHERICHIA INFECTION ( 51 FDA reports)
NEUROGENIC BLADDER ( 51 FDA reports)
OVARIAN CYST ( 51 FDA reports)
ANGIOEDEMA ( 50 FDA reports)
EDENTULOUS ( 50 FDA reports)
HAEMODIALYSIS ( 50 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 50 FDA reports)
ONYCHOMYCOSIS ( 50 FDA reports)
PROSTATE CANCER ( 50 FDA reports)
PROSTATE CANCER METASTATIC ( 50 FDA reports)
UROSEPSIS ( 50 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 50 FDA reports)
SEBORRHOEIC KERATOSIS ( 49 FDA reports)
URINARY HESITATION ( 49 FDA reports)
ACIDOSIS ( 49 FDA reports)
ADVERSE EVENT ( 49 FDA reports)
BLOOD CHLORIDE DECREASED ( 49 FDA reports)
COLON CANCER ( 49 FDA reports)
GASTROENTERITIS RADIATION ( 49 FDA reports)
HEARING IMPAIRED ( 49 FDA reports)
HEART RATE DECREASED ( 49 FDA reports)
HYPOPHOSPHATAEMIA ( 49 FDA reports)
INJECTION SITE HAEMATOMA ( 49 FDA reports)
NEURITIS ( 49 FDA reports)
NON-SMALL CELL LUNG CANCER ( 49 FDA reports)
AKATHISIA ( 48 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 48 FDA reports)
CEREBRAL HAEMORRHAGE ( 48 FDA reports)
CONJUNCTIVITIS ( 48 FDA reports)
DECREASED ACTIVITY ( 48 FDA reports)
DIABETIC NEUROPATHY ( 48 FDA reports)
GLOSSODYNIA ( 48 FDA reports)
HYPOKINESIA ( 48 FDA reports)
JOINT DISLOCATION ( 48 FDA reports)
PEPTIC ULCER ( 48 FDA reports)
PLASMACYTOSIS ( 48 FDA reports)
PRESBYOPIA ( 48 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 48 FDA reports)
SENSORY DISTURBANCE ( 48 FDA reports)
SPONDYLOLYSIS ( 48 FDA reports)
RADICULAR PAIN ( 47 FDA reports)
VARICOSE VEIN ( 47 FDA reports)
VENTRICULAR HYPERTROPHY ( 47 FDA reports)
ALCOHOL USE ( 47 FDA reports)
CHROMATURIA ( 47 FDA reports)
FRACTURED SACRUM ( 47 FDA reports)
IMPAIRED WORK ABILITY ( 47 FDA reports)
LARGE INTESTINE PERFORATION ( 47 FDA reports)
MULTIPLE INJURIES ( 47 FDA reports)
MYOPIA ( 47 FDA reports)
NEURODERMATITIS ( 47 FDA reports)
ODYNOPHAGIA ( 47 FDA reports)
PLEURAL FIBROSIS ( 47 FDA reports)
PRODUCT ADHESION ISSUE ( 47 FDA reports)
BLOOD MAGNESIUM DECREASED ( 46 FDA reports)
DENTAL OPERATION ( 46 FDA reports)
DERMATITIS CONTACT ( 46 FDA reports)
EYE SWELLING ( 46 FDA reports)
KIDNEY INFECTION ( 46 FDA reports)
MOVEMENT DISORDER ( 46 FDA reports)
OESOPHAGEAL ULCER ( 46 FDA reports)
PULMONARY MASS ( 46 FDA reports)
SKIN CANCER ( 46 FDA reports)
SKIN INDURATION ( 46 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 46 FDA reports)
TENDON DISORDER ( 46 FDA reports)
RESPIRATORY RATE DECREASED ( 45 FDA reports)
THROAT TIGHTNESS ( 45 FDA reports)
TRANSAMINASES INCREASED ( 45 FDA reports)
AFFECT LABILITY ( 45 FDA reports)
COORDINATION ABNORMAL ( 45 FDA reports)
DRUG INTOLERANCE ( 45 FDA reports)
DUODENAL ULCER ( 45 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 45 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 45 FDA reports)
MUSCLE ATROPHY ( 45 FDA reports)
MUSCLE INJURY ( 45 FDA reports)
AFFECTIVE DISORDER ( 44 FDA reports)
BREATH SOUNDS ABNORMAL ( 44 FDA reports)
ENTEROCOLITIS ( 44 FDA reports)
GASTRIC DISORDER ( 44 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 44 FDA reports)
LIGAMENT SPRAIN ( 44 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 44 FDA reports)
PLEURITIC PAIN ( 44 FDA reports)
SNORING ( 44 FDA reports)
TENSION ( 44 FDA reports)
WHEELCHAIR USER ( 44 FDA reports)
RALES ( 43 FDA reports)
RASH MACULO-PAPULAR ( 43 FDA reports)
SUBDURAL HAEMATOMA ( 43 FDA reports)
TACHYPNOEA ( 43 FDA reports)
TENDON INJURY ( 43 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 43 FDA reports)
DIALYSIS ( 43 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 43 FDA reports)
GINGIVAL EROSION ( 43 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 43 FDA reports)
INCONTINENCE ( 43 FDA reports)
LOBAR PNEUMONIA ( 43 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 43 FDA reports)
PURULENCE ( 43 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 42 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 42 FDA reports)
BREAST CANCER ( 42 FDA reports)
BREAST CANCER METASTATIC ( 42 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 42 FDA reports)
CHOLECYSTECTOMY ( 42 FDA reports)
HIP ARTHROPLASTY ( 42 FDA reports)
HYDROCEPHALUS ( 42 FDA reports)
HYPERKERATOSIS ( 42 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 42 FDA reports)
INCREASED APPETITE ( 42 FDA reports)
KNEE ARTHROPLASTY ( 42 FDA reports)
NEUTROPHIL COUNT INCREASED ( 42 FDA reports)
PETECHIAE ( 42 FDA reports)
PROCEDURAL PAIN ( 42 FDA reports)
VENTRICULAR HYPOKINESIA ( 42 FDA reports)
SKIN HYPERTROPHY ( 41 FDA reports)
SKIN TIGHTNESS ( 41 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 41 FDA reports)
URINE OUTPUT DECREASED ( 41 FDA reports)
BONE NEOPLASM MALIGNANT ( 41 FDA reports)
DRUG DISPENSING ERROR ( 41 FDA reports)
FAECAL INCONTINENCE ( 41 FDA reports)
MYOPATHY ( 41 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 41 FDA reports)
BLOOD CALCIUM INCREASED ( 40 FDA reports)
BONE EROSION ( 40 FDA reports)
CERVICOBRACHIAL SYNDROME ( 40 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 40 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 40 FDA reports)
MICROCYTIC ANAEMIA ( 40 FDA reports)
MOUTH HAEMORRHAGE ( 40 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 40 FDA reports)
OCULAR HYPERAEMIA ( 40 FDA reports)
PELVIC FRACTURE ( 40 FDA reports)
PROTEINURIA ( 40 FDA reports)
RHINITIS ALLERGIC ( 40 FDA reports)
SEQUESTRECTOMY ( 40 FDA reports)
STRESS FRACTURE ( 40 FDA reports)
VENTRICULAR FIBRILLATION ( 40 FDA reports)
SKIN HYPERPIGMENTATION ( 39 FDA reports)
STEVENS-JOHNSON SYNDROME ( 39 FDA reports)
TROPONIN INCREASED ( 39 FDA reports)
ANKLE FRACTURE ( 39 FDA reports)
BIPOLAR DISORDER ( 39 FDA reports)
DEVICE FAILURE ( 39 FDA reports)
ILEUS PARALYTIC ( 39 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 38 FDA reports)
BLOOD CHLORIDE INCREASED ( 38 FDA reports)
BUTTOCK PAIN ( 38 FDA reports)
CLOSTRIDIAL INFECTION ( 38 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 38 FDA reports)
INJECTION SITE HAEMORRHAGE ( 38 FDA reports)
MONOCLONAL GAMMOPATHY ( 38 FDA reports)
POLYDIPSIA ( 38 FDA reports)
PSEUDOMONAS INFECTION ( 38 FDA reports)
PUPIL FIXED ( 38 FDA reports)
RENAL TUBULAR NECROSIS ( 38 FDA reports)
SHOCK ( 38 FDA reports)
SOFT TISSUE DISORDER ( 38 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 38 FDA reports)
TOBACCO USER ( 37 FDA reports)
TOOTH DEPOSIT ( 37 FDA reports)
ANAPHYLACTIC REACTION ( 37 FDA reports)
APATHY ( 37 FDA reports)
BONE SWELLING ( 37 FDA reports)
DEVICE MALFUNCTION ( 37 FDA reports)
DILATATION ATRIAL ( 37 FDA reports)
DISEASE RECURRENCE ( 37 FDA reports)
ECCHYMOSIS ( 37 FDA reports)
FACIAL PALSY ( 37 FDA reports)
HERPES SIMPLEX ( 37 FDA reports)
LIMB DISCOMFORT ( 37 FDA reports)
LYMPHOPENIA ( 37 FDA reports)
PAIN OF SKIN ( 37 FDA reports)
PERITONITIS ( 37 FDA reports)
PERSONALITY CHANGE ( 37 FDA reports)
ABSCESS NECK ( 36 FDA reports)
ACUTE ABDOMEN ( 36 FDA reports)
ADVERSE DRUG REACTION ( 36 FDA reports)
AORTIC CALCIFICATION ( 36 FDA reports)
BIOPSY ( 36 FDA reports)
BODY TEMPERATURE DECREASED ( 36 FDA reports)
BRAIN INJURY ( 36 FDA reports)
CAROTID ARTERY STENOSIS ( 36 FDA reports)
CATARACT OPERATION ( 36 FDA reports)
CHOLANGITIS ( 36 FDA reports)
DIASTOLIC DYSFUNCTION ( 36 FDA reports)
FACE OEDEMA ( 36 FDA reports)
HEPATOTOXICITY ( 36 FDA reports)
LOCAL SWELLING ( 36 FDA reports)
METAPLASIA ( 36 FDA reports)
NASAL SEPTUM DEVIATION ( 36 FDA reports)
ORAL FUNGAL INFECTION ( 36 FDA reports)
OTITIS MEDIA ( 36 FDA reports)
RETCHING ( 36 FDA reports)
SELF-MEDICATION ( 36 FDA reports)
SUDDEN DEATH ( 36 FDA reports)
THERAPY NON-RESPONDER ( 36 FDA reports)
THORACOTOMY ( 36 FDA reports)
THROAT IRRITATION ( 36 FDA reports)
THROMBOPHLEBITIS ( 36 FDA reports)
UTERINE LEIOMYOMA ( 36 FDA reports)
REFLUX GASTRITIS ( 35 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 35 FDA reports)
UTERINE HAEMORRHAGE ( 35 FDA reports)
ANGINA UNSTABLE ( 35 FDA reports)
BACK INJURY ( 35 FDA reports)
COLITIS ULCERATIVE ( 35 FDA reports)
DIFFICULTY IN WALKING ( 35 FDA reports)
DYSLIPIDAEMIA ( 35 FDA reports)
EYE DISORDER ( 35 FDA reports)
GRANULOMA ( 35 FDA reports)
HAND FRACTURE ( 35 FDA reports)
LARYNGOSPASM ( 35 FDA reports)
MALIGNANT MELANOMA ( 35 FDA reports)
MITRAL VALVE SCLEROSIS ( 35 FDA reports)
MYDRIASIS ( 35 FDA reports)
PLEURISY ( 35 FDA reports)
PULMONARY GRANULOMA ( 35 FDA reports)
ADENOMA BENIGN ( 34 FDA reports)
APPLICATION SITE ERYTHEMA ( 34 FDA reports)
ARTERIAL DISORDER ( 34 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 34 FDA reports)
DRUG DIVERSION ( 34 FDA reports)
DRUG LEVEL INCREASED ( 34 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 34 FDA reports)
DYSTONIA ( 34 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 34 FDA reports)
GINGIVAL ERYTHEMA ( 34 FDA reports)
HAEMANGIOMA ( 34 FDA reports)
HEPATIC MASS ( 34 FDA reports)
HYPERNATRAEMIA ( 34 FDA reports)
PANCREATIC CARCINOMA ( 34 FDA reports)
PREMATURE BABY ( 34 FDA reports)
TENOSYNOVITIS STENOSANS ( 34 FDA reports)
TRISMUS ( 34 FDA reports)
VENOUS THROMBOSIS ( 34 FDA reports)
WOUND SECRETION ( 34 FDA reports)
RETINOPATHY ( 33 FDA reports)
SOMNAMBULISM ( 33 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 33 FDA reports)
TENOSYNOVITIS ( 33 FDA reports)
THYROID NEOPLASM ( 33 FDA reports)
WRIST FRACTURE ( 33 FDA reports)
BREAKTHROUGH PAIN ( 33 FDA reports)
CERUMEN IMPACTION ( 33 FDA reports)
DUODENITIS ( 33 FDA reports)
GASTROINTESTINAL PAIN ( 33 FDA reports)
HYPERPLASIA ( 33 FDA reports)
IMMUNOSUPPRESSION ( 33 FDA reports)
INGROWING NAIL ( 33 FDA reports)
LIPOMA ( 33 FDA reports)
LUNG CANCER METASTATIC ( 33 FDA reports)
LUNG HYPERINFLATION ( 33 FDA reports)
MENORRHAGIA ( 33 FDA reports)
METASTATIC PAIN ( 33 FDA reports)
NECK MASS ( 33 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 33 FDA reports)
PANCREATIC CYST ( 33 FDA reports)
PATELLA FRACTURE ( 33 FDA reports)
PHOTOPHOBIA ( 33 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 33 FDA reports)
ABSCESS DRAINAGE ( 32 FDA reports)
ABSCESS ORAL ( 32 FDA reports)
BLOOD BICARBONATE DECREASED ( 32 FDA reports)
BONE NEOPLASM ( 32 FDA reports)
CATHETER RELATED INFECTION ( 32 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 32 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 32 FDA reports)
ENTERITIS ( 32 FDA reports)
FORAMEN MAGNUM STENOSIS ( 32 FDA reports)
GRAFT VERSUS HOST DISEASE ( 32 FDA reports)
GRIP STRENGTH DECREASED ( 32 FDA reports)
HORDEOLUM ( 32 FDA reports)
PYELOCALIECTASIS ( 32 FDA reports)
RADIOTHERAPY ( 32 FDA reports)
SUBCUTANEOUS ABSCESS ( 32 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 32 FDA reports)
SEASONAL ALLERGY ( 31 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 31 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 31 FDA reports)
VIITH NERVE PARALYSIS ( 31 FDA reports)
WOUND DRAINAGE ( 31 FDA reports)
ABDOMINAL TENDERNESS ( 31 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 31 FDA reports)
ADENOMYOSIS ( 31 FDA reports)
BONE MARROW OEDEMA ( 31 FDA reports)
CARDIOVASCULAR DISORDER ( 31 FDA reports)
CHOLESTASIS ( 31 FDA reports)
CLAVICLE FRACTURE ( 31 FDA reports)
DILATATION VENTRICULAR ( 31 FDA reports)
ENDOCARDITIS ( 31 FDA reports)
GINGIVAL OEDEMA ( 31 FDA reports)
HEPATIC ENCEPHALOPATHY ( 31 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 31 FDA reports)
MUSCLE CRAMP ( 31 FDA reports)
MYELOPATHY ( 31 FDA reports)
ORAL HERPES ( 31 FDA reports)
ORTHOPNOEA ( 31 FDA reports)
PERIPHERAL COLDNESS ( 31 FDA reports)
POOR DENTAL CONDITION ( 31 FDA reports)
ABORTION SPONTANEOUS ( 30 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 30 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 30 FDA reports)
COCCYDYNIA ( 30 FDA reports)
DEPENDENCE ( 30 FDA reports)
ESSENTIAL HYPERTENSION ( 30 FDA reports)
HYPOVOLAEMIC SHOCK ( 30 FDA reports)
JOINT CONTRACTURE ( 30 FDA reports)
LACTIC ACIDOSIS ( 30 FDA reports)
MEDICAL DEVICE COMPLICATION ( 30 FDA reports)
METASTASES TO PELVIS ( 30 FDA reports)
MULTIPLE FRACTURES ( 30 FDA reports)
MUSCULOSKELETAL DISORDER ( 30 FDA reports)
ORAL SURGERY ( 30 FDA reports)
PHARYNGEAL OEDEMA ( 30 FDA reports)
PHLEBITIS ( 30 FDA reports)
POOR QUALITY SLEEP ( 30 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 30 FDA reports)
RASH PAPULAR ( 30 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 30 FDA reports)
RESPIRATORY TRACT INFECTION ( 30 FDA reports)
SPINAL FUSION SURGERY ( 30 FDA reports)
TOOTH INJURY ( 30 FDA reports)
VASCULAR CALCIFICATION ( 30 FDA reports)
RENAL PAIN ( 29 FDA reports)
SPUTUM DISCOLOURED ( 29 FDA reports)
VITAMIN D DECREASED ( 29 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 29 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 29 FDA reports)
AMMONIA INCREASED ( 29 FDA reports)
ASPIRATION PLEURAL CAVITY ( 29 FDA reports)
BACTERIAL SEPSIS ( 29 FDA reports)
BONE FRAGMENTATION ( 29 FDA reports)
BREAST MASS ( 29 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 29 FDA reports)
FAECES DISCOLOURED ( 29 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 29 FDA reports)
LABORATORY TEST ABNORMAL ( 29 FDA reports)
PAIN EXACERBATED ( 29 FDA reports)
PERIARTHRITIS ( 29 FDA reports)
ADRENAL DISORDER ( 28 FDA reports)
BLOODY DISCHARGE ( 28 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 28 FDA reports)
EMPYEMA ( 28 FDA reports)
EYE IRRITATION ( 28 FDA reports)
FACIAL BONES FRACTURE ( 28 FDA reports)
HYPERTENSIVE HEART DISEASE ( 28 FDA reports)
HYPOGONADISM ( 28 FDA reports)
LACUNAR INFARCTION ( 28 FDA reports)
MESOTHELIOMA ( 28 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 28 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 28 FDA reports)
REFLUX LARYNGITIS ( 28 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 28 FDA reports)
SINUS HEADACHE ( 28 FDA reports)
SKIN BURNING SENSATION ( 28 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 28 FDA reports)
URETERAL DISORDER ( 28 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 28 FDA reports)
SPLEEN DISORDER ( 27 FDA reports)
THROMBOCYTOSIS ( 27 FDA reports)
THYROID CYST ( 27 FDA reports)
TOOTH REPAIR ( 27 FDA reports)
ACCOMMODATION DISORDER ( 27 FDA reports)
AGRANULOCYTOSIS ( 27 FDA reports)
APHAGIA ( 27 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 27 FDA reports)
BLOOD CREATININE DECREASED ( 27 FDA reports)
CULTURE URINE POSITIVE ( 27 FDA reports)
FLUID INTAKE REDUCED ( 27 FDA reports)
FRUSTRATION ( 27 FDA reports)
GANGRENE ( 27 FDA reports)
HEMIPLEGIA ( 27 FDA reports)
HYPERTENSIVE CRISIS ( 27 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 27 FDA reports)
HYPOTHERMIA ( 27 FDA reports)
HYSTERECTOMY ( 27 FDA reports)
INTENTIONAL SELF-INJURY ( 27 FDA reports)
JOINT SPRAIN ( 27 FDA reports)
MEDICATION RESIDUE ( 27 FDA reports)
MENSTRUAL DISORDER ( 27 FDA reports)
NEUROTOXICITY ( 27 FDA reports)
OSTEORADIONECROSIS ( 27 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 27 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 27 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 27 FDA reports)
PROCEDURAL COMPLICATION ( 27 FDA reports)
PULMONARY INFARCTION ( 27 FDA reports)
APPLICATION SITE RASH ( 26 FDA reports)
BONE SCAN ABNORMAL ( 26 FDA reports)
CHOKING ( 26 FDA reports)
CIRCULATORY COLLAPSE ( 26 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 26 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 26 FDA reports)
DRUG SCREEN NEGATIVE ( 26 FDA reports)
ENURESIS ( 26 FDA reports)
FLAT AFFECT ( 26 FDA reports)
GASTROENTERITIS VIRAL ( 26 FDA reports)
GASTROINTESTINAL NECROSIS ( 26 FDA reports)
HIP SURGERY ( 26 FDA reports)
HYDROCELE ( 26 FDA reports)
INTESTINAL ISCHAEMIA ( 26 FDA reports)
LEUKOENCEPHALOPATHY ( 26 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 26 FDA reports)
MOTOR DYSFUNCTION ( 26 FDA reports)
NECK INJURY ( 26 FDA reports)
NEOPLASM SKIN ( 26 FDA reports)
NO ADVERSE EVENT ( 26 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 26 FDA reports)
OVARIAN CANCER ( 26 FDA reports)
PERFORMANCE STATUS DECREASED ( 26 FDA reports)
PERITONSILLITIS ( 26 FDA reports)
PROSTATITIS ( 26 FDA reports)
QUALITY OF LIFE DECREASED ( 26 FDA reports)
SCAB ( 26 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 26 FDA reports)
SPINAL CORD DISORDER ( 26 FDA reports)
TENDON RUPTURE ( 26 FDA reports)
RENAL INJURY ( 25 FDA reports)
TARDIVE DYSKINESIA ( 25 FDA reports)
UMBILICAL HERNIA ( 25 FDA reports)
WOUND HAEMORRHAGE ( 25 FDA reports)
WRONG DRUG ADMINISTERED ( 25 FDA reports)
ABDOMINAL ABSCESS ( 25 FDA reports)
ANAL FISTULA ( 25 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 25 FDA reports)
BLEPHARITIS ( 25 FDA reports)
BLINDNESS UNILATERAL ( 25 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 25 FDA reports)
BRAIN SCAN ABNORMAL ( 25 FDA reports)
CATHETERISATION CARDIAC ( 25 FDA reports)
CERVICAL CORD COMPRESSION ( 25 FDA reports)
GLARE ( 25 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 25 FDA reports)
HERNIA ( 25 FDA reports)
HERNIA REPAIR ( 25 FDA reports)
HYPERMETABOLISM ( 25 FDA reports)
HYPERTHYROIDISM ( 25 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 25 FDA reports)
LOCALISED INFECTION ( 25 FDA reports)
METASTASES TO SKIN ( 25 FDA reports)
MUSCLE DISORDER ( 25 FDA reports)
PANIC DISORDER ( 25 FDA reports)
PARONYCHIA ( 25 FDA reports)
PAROSMIA ( 25 FDA reports)
POISONING DELIBERATE ( 25 FDA reports)
POLYP ( 25 FDA reports)
POLYURIA ( 25 FDA reports)
ABDOMINAL MASS ( 24 FDA reports)
ACETABULUM FRACTURE ( 24 FDA reports)
AMBLYOPIA ( 24 FDA reports)
ANAL ABSCESS ( 24 FDA reports)
BLADDER PROLAPSE ( 24 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 24 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 24 FDA reports)
BLOOD UREA DECREASED ( 24 FDA reports)
BRAIN MASS ( 24 FDA reports)
BUNION ( 24 FDA reports)
CALCULUS URETERIC ( 24 FDA reports)
CHEMICAL POISONING ( 24 FDA reports)
CYTOLYTIC HEPATITIS ( 24 FDA reports)
DEAFNESS NEUROSENSORY ( 24 FDA reports)
DIABETIC KETOACIDOSIS ( 24 FDA reports)
DRUG TOLERANCE INCREASED ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 24 FDA reports)
FRACTURE NONUNION ( 24 FDA reports)
HAEMANGIOMA OF LIVER ( 24 FDA reports)
HIGH FREQUENCY ABLATION ( 24 FDA reports)
HYPOVENTILATION ( 24 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 24 FDA reports)
JUGULAR VEIN THROMBOSIS ( 24 FDA reports)
LIVER INJURY ( 24 FDA reports)
MIDDLE INSOMNIA ( 24 FDA reports)
NAIL DISORDER ( 24 FDA reports)
NEOPLASM ( 24 FDA reports)
PULPITIS DENTAL ( 24 FDA reports)
RENAL CELL CARCINOMA ( 24 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 24 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 24 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 24 FDA reports)
TEARFULNESS ( 24 FDA reports)
THYROID DISORDER ( 24 FDA reports)
VERTEBROPLASTY ( 24 FDA reports)
RADIATION SKIN INJURY ( 23 FDA reports)
RHINITIS ( 23 FDA reports)
STENT PLACEMENT ( 23 FDA reports)
URETHRAL CARUNCLE ( 23 FDA reports)
VAGINAL INFECTION ( 23 FDA reports)
ANAL CANDIDIASIS ( 23 FDA reports)
ANAL FISSURE ( 23 FDA reports)
ANURIA ( 23 FDA reports)
ASTIGMATISM ( 23 FDA reports)
BILE DUCT STENOSIS ( 23 FDA reports)
CERVIX CARCINOMA ( 23 FDA reports)
CHONDROMALACIA ( 23 FDA reports)
CYSTITIS HAEMORRHAGIC ( 23 FDA reports)
DERMAL CYST ( 23 FDA reports)
DYSTHYMIC DISORDER ( 23 FDA reports)
FORMICATION ( 23 FDA reports)
GASTRITIS EROSIVE ( 23 FDA reports)
ISCHAEMIA ( 23 FDA reports)
MALLORY-WEISS SYNDROME ( 23 FDA reports)
MITRAL VALVE PROLAPSE ( 23 FDA reports)
OBSTRUCTION ( 23 FDA reports)
PANCREATITIS CHRONIC ( 23 FDA reports)
PARESIS ( 23 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 23 FDA reports)
PROTEIN TOTAL INCREASED ( 23 FDA reports)
ADENOCARCINOMA ( 22 FDA reports)
ANOXIC ENCEPHALOPATHY ( 22 FDA reports)
APPENDICECTOMY ( 22 FDA reports)
BACTERIAL TEST POSITIVE ( 22 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 22 FDA reports)
BLOOD PH DECREASED ( 22 FDA reports)
BODY HEIGHT DECREASED ( 22 FDA reports)
BRAIN HERNIATION ( 22 FDA reports)
BRONCHIECTASIS ( 22 FDA reports)
BRONCHOSPASM ( 22 FDA reports)
CARDIAC VALVE DISEASE ( 22 FDA reports)
CARDIOGENIC SHOCK ( 22 FDA reports)
CHEST X-RAY ABNORMAL ( 22 FDA reports)
DERMATITIS EXFOLIATIVE ( 22 FDA reports)
DYSPHEMIA ( 22 FDA reports)
EAR DISCOMFORT ( 22 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 22 FDA reports)
EXTREMITY CONTRACTURE ( 22 FDA reports)
EYELID OEDEMA ( 22 FDA reports)
FISTULA DISCHARGE ( 22 FDA reports)
FOOT DEFORMITY ( 22 FDA reports)
FOREIGN BODY IN EYE ( 22 FDA reports)
GASTRIC CANCER ( 22 FDA reports)
HICCUPS ( 22 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 22 FDA reports)
INJECTION SITE IRRITATION ( 22 FDA reports)
ISCHAEMIC STROKE ( 22 FDA reports)
LOWER LIMB FRACTURE ( 22 FDA reports)
MANIA ( 22 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 22 FDA reports)
OESOPHAGEAL DISORDER ( 22 FDA reports)
PANCREATIC ATROPHY ( 22 FDA reports)
PERICARDITIS ( 22 FDA reports)
PERITONEAL DISORDER ( 22 FDA reports)
PUBIS FRACTURE ( 22 FDA reports)
RENAL ATROPHY ( 22 FDA reports)
SCLEROMALACIA ( 22 FDA reports)
SEBORRHOEIC DERMATITIS ( 22 FDA reports)
SKIN IRRITATION ( 22 FDA reports)
STUPOR ( 22 FDA reports)
TUMOUR LYSIS SYNDROME ( 22 FDA reports)
URINE FLOW DECREASED ( 22 FDA reports)
WOUND COMPLICATION ( 22 FDA reports)
REFLUX OESOPHAGITIS ( 21 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 21 FDA reports)
SLEEP TALKING ( 21 FDA reports)
VENOOCCLUSIVE DISEASE ( 21 FDA reports)
ACUTE SINUSITIS ( 21 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 21 FDA reports)
AORTIC STENOSIS ( 21 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 21 FDA reports)
BLOOD IRON DECREASED ( 21 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 21 FDA reports)
BRONCHITIS ACUTE ( 21 FDA reports)
CANCER PAIN ( 21 FDA reports)
CORONARY ARTERY OCCLUSION ( 21 FDA reports)
DRY THROAT ( 21 FDA reports)
DYSPHORIA ( 21 FDA reports)
EAR HAEMORRHAGE ( 21 FDA reports)
HEPATIC NECROSIS ( 21 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 21 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 21 FDA reports)
IRITIS ( 21 FDA reports)
JAUNDICE CHOLESTATIC ( 21 FDA reports)
MACULAR DEGENERATION ( 21 FDA reports)
MELANOCYTIC NAEVUS ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MYOSITIS ( 21 FDA reports)
NEUROPATHY ( 21 FDA reports)
OESOPHAGEAL PAIN ( 21 FDA reports)
OLIGURIA ( 21 FDA reports)
PARKINSON'S DISEASE ( 21 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 21 FDA reports)
POOR PERSONAL HYGIENE ( 21 FDA reports)
ADRENAL NEOPLASM ( 20 FDA reports)
ALVEOLAR OSTEITIS ( 20 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 20 FDA reports)
AORTIC VALVE STENOSIS ( 20 FDA reports)
BILE DUCT STONE ( 20 FDA reports)
BLOOD SODIUM INCREASED ( 20 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 20 FDA reports)
BONE GRAFT ( 20 FDA reports)
BRAIN DEATH ( 20 FDA reports)
BREAST CANCER RECURRENT ( 20 FDA reports)
CARDIAC PACEMAKER INSERTION ( 20 FDA reports)
DENTAL PLAQUE ( 20 FDA reports)
DEVICE BREAKAGE ( 20 FDA reports)
DYSTROPHIC CALCIFICATION ( 20 FDA reports)
ENDOTRACHEAL INTUBATION ( 20 FDA reports)
ENTEROCUTANEOUS FISTULA ( 20 FDA reports)
EXTRADURAL ABSCESS ( 20 FDA reports)
GASTRIC BYPASS ( 20 FDA reports)
GASTRIC POLYPS ( 20 FDA reports)
HODGKIN'S DISEASE ( 20 FDA reports)
HOMICIDAL IDEATION ( 20 FDA reports)
HYDROURETER ( 20 FDA reports)
HYPERPHAGIA ( 20 FDA reports)
INJECTION SITE PRURITUS ( 20 FDA reports)
INTRAOCULAR LENS IMPLANT ( 20 FDA reports)
KNEE OPERATION ( 20 FDA reports)
LIP SWELLING ( 20 FDA reports)
MASTOIDITIS ( 20 FDA reports)
MUCOSAL ULCERATION ( 20 FDA reports)
OCULAR ICTERUS ( 20 FDA reports)
OROANTRAL FISTULA ( 20 FDA reports)
OSTEOSARCOMA METASTATIC ( 20 FDA reports)
PROTEIN URINE PRESENT ( 20 FDA reports)
PURPURA ( 20 FDA reports)
RECTAL POLYP ( 20 FDA reports)
RESPIRATORY TRACT CONGESTION ( 20 FDA reports)
RETINAL HAEMORRHAGE ( 20 FDA reports)
SELF-INJURIOUS IDEATION ( 20 FDA reports)
TERMINAL STATE ( 20 FDA reports)
TONGUE DISORDER ( 20 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 20 FDA reports)
TYPE 1 DIABETES MELLITUS ( 20 FDA reports)
URINARY TRACT DISORDER ( 20 FDA reports)
VASCULITIS ( 20 FDA reports)
RASH PUSTULAR ( 19 FDA reports)
RECTOCELE ( 19 FDA reports)
RENAL ARTERY STENOSIS ( 19 FDA reports)
SARCOIDOSIS ( 19 FDA reports)
SENSATION OF FOREIGN BODY ( 19 FDA reports)
SENSATION OF HEAVINESS ( 19 FDA reports)
SHOULDER PAIN ( 19 FDA reports)
SPINAL LAMINECTOMY ( 19 FDA reports)
TEMPORAL ARTERITIS ( 19 FDA reports)
TOOTH IMPACTED ( 19 FDA reports)
TUBERCULOSIS ( 19 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 19 FDA reports)
ABSCESS INTESTINAL ( 19 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 19 FDA reports)
ADVERSE REACTION ( 19 FDA reports)
APHTHOUS STOMATITIS ( 19 FDA reports)
APPENDICITIS ( 19 FDA reports)
ARTHRITIS BACTERIAL ( 19 FDA reports)
B-CELL LYMPHOMA ( 19 FDA reports)
BLADDER DISORDER ( 19 FDA reports)
BLADDER SPASM ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 19 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 19 FDA reports)
BRONCHITIS CHRONIC ( 19 FDA reports)
COLLAPSE OF LUNG ( 19 FDA reports)
CORONARY ARTERY STENOSIS ( 19 FDA reports)
DIPLEGIA ( 19 FDA reports)
DRUG ERUPTION ( 19 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 19 FDA reports)
FOLLICULITIS ( 19 FDA reports)
FUNGAEMIA ( 19 FDA reports)
FURUNCLE ( 19 FDA reports)
GINGIVAL ABSCESS ( 19 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 19 FDA reports)
HEPATIC NEOPLASM ( 19 FDA reports)
INJECTION SITE REACTION ( 19 FDA reports)
LOCALISED OEDEMA ( 19 FDA reports)
NECROTISING FASCIITIS ( 19 FDA reports)
NEPHROSCLEROSIS ( 19 FDA reports)
PARAPLEGIA ( 19 FDA reports)
PELVIC HAEMATOMA ( 19 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 19 FDA reports)
PSORIATIC ARTHROPATHY ( 19 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 18 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 18 FDA reports)
ANEURYSM ( 18 FDA reports)
ANGIOPATHY ( 18 FDA reports)
APLASTIC ANAEMIA ( 18 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 18 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 18 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 18 FDA reports)
CARBON DIOXIDE DECREASED ( 18 FDA reports)
CARDIAC TAMPONADE ( 18 FDA reports)
COMMINUTED FRACTURE ( 18 FDA reports)
CONCUSSION ( 18 FDA reports)
DRUG EFFECT INCREASED ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 18 FDA reports)
FEELING OF DESPAIR ( 18 FDA reports)
FIBRIN D DIMER INCREASED ( 18 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 18 FDA reports)
FOREIGN BODY ( 18 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 18 FDA reports)
HEPATIC CONGESTION ( 18 FDA reports)
HYPERTONIC BLADDER ( 18 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 18 FDA reports)
MARROW HYPERPLASIA ( 18 FDA reports)
NERVE COMPRESSION ( 18 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 18 FDA reports)
OESOPHAGITIS ULCERATIVE ( 18 FDA reports)
OSTEOMYELITIS CHRONIC ( 18 FDA reports)
PCO2 DECREASED ( 18 FDA reports)
PERIORBITAL OEDEMA ( 18 FDA reports)
PERIOSTITIS ( 18 FDA reports)
PORTAL HYPERTENSION ( 18 FDA reports)
PSYCHIATRIC SYMPTOM ( 18 FDA reports)
RECTAL ULCER ( 18 FDA reports)
RENAL MASS ( 18 FDA reports)
RESORPTION BONE INCREASED ( 18 FDA reports)
RHONCHI ( 18 FDA reports)
SEROMA ( 18 FDA reports)
SKIN NECROSIS ( 18 FDA reports)
SKIN PLAQUE ( 18 FDA reports)
SNEEZING ( 18 FDA reports)
SOFT TISSUE INFECTION ( 18 FDA reports)
STASIS DERMATITIS ( 18 FDA reports)
SUBDURAL HAEMORRHAGE ( 18 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 18 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 18 FDA reports)
TRANSFUSION ( 18 FDA reports)
URETERIC OBSTRUCTION ( 18 FDA reports)
VENA CAVA THROMBOSIS ( 18 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
VITAMIN D DEFICIENCY ( 18 FDA reports)
VOCAL CORD PARALYSIS ( 18 FDA reports)
SICK SINUS SYNDROME ( 17 FDA reports)
STATUS MIGRAINOSUS ( 17 FDA reports)
SYNCOPE VASOVAGAL ( 17 FDA reports)
TESTICULAR PAIN ( 17 FDA reports)
THERMAL BURN ( 17 FDA reports)
TORSADE DE POINTES ( 17 FDA reports)
TOXIC ENCEPHALOPATHY ( 17 FDA reports)
TUMOUR ASSOCIATED FEVER ( 17 FDA reports)
VICTIM OF HOMICIDE ( 17 FDA reports)
VISUAL FIELD DEFECT ( 17 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 17 FDA reports)
ACUTE HEPATIC FAILURE ( 17 FDA reports)
ACUTE PRERENAL FAILURE ( 17 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 17 FDA reports)
ALCOHOL POISONING ( 17 FDA reports)
APPLICATION SITE PAIN ( 17 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 17 FDA reports)
BED REST ( 17 FDA reports)
BREAST HYPERPLASIA ( 17 FDA reports)
BRONCHIAL SECRETION RETENTION ( 17 FDA reports)
CEREBELLAR INFARCTION ( 17 FDA reports)
CORONARY ARTERY BYPASS ( 17 FDA reports)
CREPITATIONS ( 17 FDA reports)
CYSTITIS KLEBSIELLA ( 17 FDA reports)
DELIRIUM TREMENS ( 17 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 17 FDA reports)
EAR DISORDER ( 17 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 17 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 17 FDA reports)
ERYTHEMA OF EYELID ( 17 FDA reports)
EXERCISE TOLERANCE DECREASED ( 17 FDA reports)
FASCIITIS ( 17 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 17 FDA reports)
FIBULA FRACTURE ( 17 FDA reports)
GASTRIC HAEMORRHAGE ( 17 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 17 FDA reports)
HAEMORRHAGIC ANAEMIA ( 17 FDA reports)
HORMONE LEVEL ABNORMAL ( 17 FDA reports)
HYPERVENTILATION ( 17 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 17 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 17 FDA reports)
JOINT LOCK ( 17 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 17 FDA reports)
KLEBSIELLA INFECTION ( 17 FDA reports)
LICE INFESTATION ( 17 FDA reports)
MANTLE CELL LYMPHOMA ( 17 FDA reports)
MENINGITIS ( 17 FDA reports)
MUSCLE CONTRACTURE ( 17 FDA reports)
MYASTHENIA GRAVIS ( 17 FDA reports)
NECROSIS ( 17 FDA reports)
NEPHROTIC SYNDROME ( 17 FDA reports)
PERIPHERAL ISCHAEMIA ( 17 FDA reports)
PLANTAR FASCIITIS ( 17 FDA reports)
PROTEIN TOTAL DECREASED ( 17 FDA reports)
ACUTE CORONARY SYNDROME ( 16 FDA reports)
ALCOHOLISM ( 16 FDA reports)
ANIMAL BITE ( 16 FDA reports)
ASBESTOSIS ( 16 FDA reports)
BIOPSY BONE MARROW ( 16 FDA reports)
BLADDER OBSTRUCTION ( 16 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 16 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 16 FDA reports)
BONE CYST ( 16 FDA reports)
CEREBROVASCULAR DISORDER ( 16 FDA reports)
CHEILITIS ( 16 FDA reports)
CHOLECYSTITIS ACUTE ( 16 FDA reports)
CLONUS ( 16 FDA reports)
CLOSTRIDIUM COLITIS ( 16 FDA reports)
COLITIS ISCHAEMIC ( 16 FDA reports)
CONNECTIVE TISSUE DISORDER ( 16 FDA reports)
DERMATITIS ACNEIFORM ( 16 FDA reports)
DERMATITIS ATOPIC ( 16 FDA reports)
DIZZINESS POSTURAL ( 16 FDA reports)
DYSHIDROSIS ( 16 FDA reports)
EPICONDYLITIS ( 16 FDA reports)
ERUCTATION ( 16 FDA reports)
EXOPHTHALMOS ( 16 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 16 FDA reports)
HAEMOLYTIC ANAEMIA ( 16 FDA reports)
HERPES VIRUS INFECTION ( 16 FDA reports)
HOSTILITY ( 16 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 16 FDA reports)
INCISIONAL DRAINAGE ( 16 FDA reports)
INFECTED SKIN ULCER ( 16 FDA reports)
INTRACRANIAL ANEURYSM ( 16 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 16 FDA reports)
ISCHAEMIC HEPATITIS ( 16 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 16 FDA reports)
LARYNGITIS ( 16 FDA reports)
MASTECTOMY ( 16 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
METASTASES TO MENINGES ( 16 FDA reports)
MONOCYTE COUNT DECREASED ( 16 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 16 FDA reports)
NASAL MUCOSAL DISORDER ( 16 FDA reports)
NEPHROPATHY ( 16 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 16 FDA reports)
OCULAR HYPERTENSION ( 16 FDA reports)
ONYCHALGIA ( 16 FDA reports)
ORGAN FAILURE ( 16 FDA reports)
PATHOLOGICAL GAMBLING ( 16 FDA reports)
PERIRECTAL ABSCESS ( 16 FDA reports)
PERSONALITY DISORDER ( 16 FDA reports)
PHOTOPSIA ( 16 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 16 FDA reports)
RIGHT VENTRICULAR FAILURE ( 16 FDA reports)
SCRATCH ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SKIN FISSURES ( 16 FDA reports)
SUDDEN CARDIAC DEATH ( 16 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
TEMPERATURE INTOLERANCE ( 16 FDA reports)
TINEA PEDIS ( 16 FDA reports)
TRANSFUSION REACTION ( 16 FDA reports)
VENOUS THROMBOSIS LIMB ( 16 FDA reports)
QUADRIPLEGIA ( 15 FDA reports)
RADIATION ASSOCIATED PAIN ( 15 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 15 FDA reports)
SCLERODERMA ( 15 FDA reports)
SELF ESTEEM DECREASED ( 15 FDA reports)
SERUM FERRITIN INCREASED ( 15 FDA reports)
SKIN FIBROSIS ( 15 FDA reports)
SKIN PAPILLOMA ( 15 FDA reports)
SKIN REACTION ( 15 FDA reports)
SLUGGISHNESS ( 15 FDA reports)
SPINAL DEFORMITY ( 15 FDA reports)
SPINAL OPERATION ( 15 FDA reports)
SPONDYLITIS ( 15 FDA reports)
SPUTUM CULTURE POSITIVE ( 15 FDA reports)
TOOTH EROSION ( 15 FDA reports)
VITAMIN B12 DEFICIENCY ( 15 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 15 FDA reports)
WEIGHT FLUCTUATION ( 15 FDA reports)
ANAPHYLACTIC SHOCK ( 15 FDA reports)
ANOGENITAL WARTS ( 15 FDA reports)
AREFLEXIA ( 15 FDA reports)
ATHEROSCLEROSIS ( 15 FDA reports)
BILIARY DYSKINESIA ( 15 FDA reports)
BLADDER CANCER ( 15 FDA reports)
BLOOD BICARBONATE INCREASED ( 15 FDA reports)
BREAST SWELLING ( 15 FDA reports)
BURNS SECOND DEGREE ( 15 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 15 FDA reports)
DRUG LEVEL DECREASED ( 15 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 15 FDA reports)
EXTRASYSTOLES ( 15 FDA reports)
FACE INJURY ( 15 FDA reports)
FEMORAL NECK FRACTURE ( 15 FDA reports)
GALLBLADDER INJURY ( 15 FDA reports)
GENITAL HERPES ( 15 FDA reports)
HUNGER ( 15 FDA reports)
HYPERURICAEMIA ( 15 FDA reports)
INITIAL INSOMNIA ( 15 FDA reports)
LARGE INTESTINAL ULCER ( 15 FDA reports)
LIGAMENT INJURY ( 15 FDA reports)
LOWER EXTREMITY MASS ( 15 FDA reports)
LUDWIG ANGINA ( 15 FDA reports)
MENIERE'S DISEASE ( 15 FDA reports)
METABOLIC SYNDROME ( 15 FDA reports)
METASTASES TO ADRENALS ( 15 FDA reports)
MONOCYTE COUNT INCREASED ( 15 FDA reports)
MONOPLEGIA ( 15 FDA reports)
NYSTAGMUS ( 15 FDA reports)
OCCULT BLOOD POSITIVE ( 15 FDA reports)
OESOPHAGEAL CARCINOMA ( 15 FDA reports)
OPEN REDUCTION OF FRACTURE ( 15 FDA reports)
OROPHARYNGEAL PLAQUE ( 15 FDA reports)
PAPILLOEDEMA ( 15 FDA reports)
PARAPARESIS ( 15 FDA reports)
PARAPROTEINAEMIA ( 15 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 15 FDA reports)
PNEUMATOSIS INTESTINALIS ( 15 FDA reports)
PNEUMONIA FUNGAL ( 15 FDA reports)
PORTAL VEIN THROMBOSIS ( 15 FDA reports)
PREGNANCY ( 15 FDA reports)
PRODUCT FORMULATION ISSUE ( 15 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
PUPILS UNEQUAL ( 15 FDA reports)
ACNE ( 14 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 14 FDA reports)
ADRENAL MASS ( 14 FDA reports)
AMYLOIDOSIS ( 14 FDA reports)
AORTIC DILATATION ( 14 FDA reports)
APPENDICITIS PERFORATED ( 14 FDA reports)
APPLICATION SITE PRURITUS ( 14 FDA reports)
APPLICATION SITE REACTION ( 14 FDA reports)
ARTHROPOD BITE ( 14 FDA reports)
ASPERGILLOSIS ( 14 FDA reports)
AUTONOMIC NEUROPATHY ( 14 FDA reports)
BILE DUCT OBSTRUCTION ( 14 FDA reports)
BLINDNESS TRANSIENT ( 14 FDA reports)
BLOOD ALCOHOL INCREASED ( 14 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 14 FDA reports)
BONE MARROW TRANSPLANT ( 14 FDA reports)
BREAST CALCIFICATIONS ( 14 FDA reports)
BREAST PAIN ( 14 FDA reports)
BULLOUS LUNG DISEASE ( 14 FDA reports)
CALCULUS BLADDER ( 14 FDA reports)
CARBON MONOXIDE POISONING ( 14 FDA reports)
CARDIAC ENZYMES INCREASED ( 14 FDA reports)
CATARACT NUCLEAR ( 14 FDA reports)
CONJUNCTIVITIS VIRAL ( 14 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 14 FDA reports)
CYSTOCELE ( 14 FDA reports)
DEAFNESS BILATERAL ( 14 FDA reports)
DEVICE OCCLUSION ( 14 FDA reports)
ENDOMETRIOSIS ( 14 FDA reports)
ESSENTIAL TREMOR ( 14 FDA reports)
FACIAL PARESIS ( 14 FDA reports)
GENERALISED ANXIETY DISORDER ( 14 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 14 FDA reports)
GLOSSITIS ( 14 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 14 FDA reports)
HAIR GROWTH ABNORMAL ( 14 FDA reports)
HELICOBACTER INFECTION ( 14 FDA reports)
HEPATOSPLENOMEGALY ( 14 FDA reports)
HYPERCAPNIA ( 14 FDA reports)
HYPERREFLEXIA ( 14 FDA reports)
IMPLANT SITE INFECTION ( 14 FDA reports)
INJECTION SITE SWELLING ( 14 FDA reports)
LIPASE INCREASED ( 14 FDA reports)
LIVER TRANSPLANT REJECTION ( 14 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
MACROCYTOSIS ( 14 FDA reports)
MALOCCLUSION ( 14 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 14 FDA reports)
METASTASES TO EYE ( 14 FDA reports)
METASTASES TO PLEURA ( 14 FDA reports)
MUSCLE RIGIDITY ( 14 FDA reports)
MYELOMA RECURRENCE ( 14 FDA reports)
NASAL DISCOMFORT ( 14 FDA reports)
NEUROFIBROMA ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 14 FDA reports)
OESOPHAGEAL STENOSIS ( 14 FDA reports)
OSTEOMA ( 14 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 14 FDA reports)
PERINEAL PAIN ( 14 FDA reports)
PERIODONTAL OPERATION ( 14 FDA reports)
POLYTRAUMATISM ( 14 FDA reports)
POST PROCEDURAL INFECTION ( 14 FDA reports)
PROSTATE CANCER RECURRENT ( 14 FDA reports)
RECTAL CANCER ( 14 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 14 FDA reports)
RETINAL INFARCTION ( 14 FDA reports)
SALIVARY HYPERSECRETION ( 14 FDA reports)
SCHAMBERG'S DISEASE ( 14 FDA reports)
SKIN ATROPHY ( 14 FDA reports)
SKIN FRAGILITY ( 14 FDA reports)
STERNAL FRACTURE ( 14 FDA reports)
STRIDOR ( 14 FDA reports)
SUBCUTANEOUS NODULE ( 14 FDA reports)
TOBACCO ABUSE ( 14 FDA reports)
TUMOUR MARKER INCREASED ( 14 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 14 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 14 FDA reports)
RADIATION INJURY ( 13 FDA reports)
RECTAL PERFORATION ( 13 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 13 FDA reports)
REGURGITATION ( 13 FDA reports)
SCARLET FEVER ( 13 FDA reports)
SPINAL FUSION ACQUIRED ( 13 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 13 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 13 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 13 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 13 FDA reports)
URETHRAL STENOSIS ( 13 FDA reports)
VAGINAL PROLAPSE ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
VENTRICULAR DYSFUNCTION ( 13 FDA reports)
WEIGHT BEARING DIFFICULTY ( 13 FDA reports)
ACUTE PSYCHOSIS ( 13 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 13 FDA reports)
ANISOCYTOSIS ( 13 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 13 FDA reports)
ASPHYXIA ( 13 FDA reports)
BACTERIAL DISEASE CARRIER ( 13 FDA reports)
BLOOD COUNT ABNORMAL ( 13 FDA reports)
BLOOD DISORDER ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 13 FDA reports)
BLOOD TEST ABNORMAL ( 13 FDA reports)
BONE CALLUS EXCESSIVE ( 13 FDA reports)
BONE MARROW DISORDER ( 13 FDA reports)
CALCULUS URINARY ( 13 FDA reports)
CARDIAC ANEURYSM ( 13 FDA reports)
CHEST INJURY ( 13 FDA reports)
CHOLECYSTITIS INFECTIVE ( 13 FDA reports)
COLON ADENOMA ( 13 FDA reports)
COMMUNICATION DISORDER ( 13 FDA reports)
DENTAL PULP DISORDER ( 13 FDA reports)
DEVICE LEAKAGE ( 13 FDA reports)
DROOLING ( 13 FDA reports)
DYSGRAPHIA ( 13 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 13 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 13 FDA reports)
EMBOLIC STROKE ( 13 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 13 FDA reports)
EXTRASKELETAL OSSIFICATION ( 13 FDA reports)
EYE ROLLING ( 13 FDA reports)
EYELID PTOSIS ( 13 FDA reports)
HAEMOLYSIS ( 13 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 13 FDA reports)
HILAR LYMPHADENOPATHY ( 13 FDA reports)
HYPOPROTEINAEMIA ( 13 FDA reports)
HYPOTONIA ( 13 FDA reports)
HYPOTRICHOSIS ( 13 FDA reports)
IMMUNODEFICIENCY ( 13 FDA reports)
IMPAIRED SELF-CARE ( 13 FDA reports)
INHIBITORY DRUG INTERACTION ( 13 FDA reports)
LYMPH NODE PAIN ( 13 FDA reports)
MANDIBULAR PROSTHESIS USER ( 13 FDA reports)
MECHANICAL VENTILATION ( 13 FDA reports)
MEDIASTINAL DISORDER ( 13 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 13 FDA reports)
NASAL ULCER ( 13 FDA reports)
NEUROLOGICAL SYMPTOM ( 13 FDA reports)
NICOTINE DEPENDENCE ( 13 FDA reports)
NODAL RHYTHM ( 13 FDA reports)
OBSTRUCTION GASTRIC ( 13 FDA reports)
PANIC REACTION ( 13 FDA reports)
PNEUMONIA BACTERIAL ( 13 FDA reports)
PO2 DECREASED ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
PROTEIN URINE ( 13 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 13 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 13 FDA reports)
ACCIDENT AT WORK ( 12 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
ADNEXA UTERI MASS ( 12 FDA reports)
AGEUSIA ( 12 FDA reports)
ALLODYNIA ( 12 FDA reports)
ALVEOLOPLASTY ( 12 FDA reports)
ASTHENOPIA ( 12 FDA reports)
AUTOIMMUNE DISORDER ( 12 FDA reports)
BILIARY COLIC ( 12 FDA reports)
BLADDER NEOPLASM ( 12 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 12 FDA reports)
BLOOD PH INCREASED ( 12 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 12 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 12 FDA reports)
BODY TINEA ( 12 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 12 FDA reports)
CATHETER RELATED COMPLICATION ( 12 FDA reports)
CLUSTER HEADACHE ( 12 FDA reports)
COLONIC STENOSIS ( 12 FDA reports)
CRANIAL NERVE DISORDER ( 12 FDA reports)
CULTURE WOUND POSITIVE ( 12 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 12 FDA reports)
DUODENOGASTRIC REFLUX ( 12 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 12 FDA reports)
EROSIVE OESOPHAGITIS ( 12 FDA reports)
ERYTHEMA MULTIFORME ( 12 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 12 FDA reports)
EYE ALLERGY ( 12 FDA reports)
FAT NECROSIS ( 12 FDA reports)
FEELINGS OF WORTHLESSNESS ( 12 FDA reports)
FEMORAL ARTERY OCCLUSION ( 12 FDA reports)
FOOD CRAVING ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
GLOBULINS INCREASED ( 12 FDA reports)
HEPATOCELLULAR DAMAGE ( 12 FDA reports)
HYPERPARATHYROIDISM ( 12 FDA reports)
HYPOAESTHESIA FACIAL ( 12 FDA reports)
ILEITIS ( 12 FDA reports)
ILIAC ARTERY THROMBOSIS ( 12 FDA reports)
INCREASED TENDENCY TO BRUISE ( 12 FDA reports)
INTERMITTENT CLAUDICATION ( 12 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 12 FDA reports)
JOINT CREPITATION ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 12 FDA reports)
MENINGIOMA ( 12 FDA reports)
MUMPS ( 12 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 12 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 12 FDA reports)
OPHTHALMOPLEGIA ( 12 FDA reports)
OPTIC NEURITIS ( 12 FDA reports)
ORGANISING PNEUMONIA ( 12 FDA reports)
OVERWEIGHT ( 12 FDA reports)
PANCREATIC MASS ( 12 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 12 FDA reports)
PETIT MAL EPILEPSY ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
PILOERECTION ( 12 FDA reports)
PLEURAL DISORDER ( 12 FDA reports)
POST PROCEDURAL FISTULA ( 12 FDA reports)
PROCTITIS ( 12 FDA reports)
PROSTATE INFECTION ( 12 FDA reports)
PROSTATIC DISORDER ( 12 FDA reports)
PROTEUS INFECTION ( 12 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 12 FDA reports)
PYURIA ( 12 FDA reports)
RENAL CANCER ( 12 FDA reports)
RENAL TUBULAR ACIDOSIS ( 12 FDA reports)
RUBELLA ( 12 FDA reports)
SALPINGO-OOPHORECTOMY ( 12 FDA reports)
SCREAMING ( 12 FDA reports)
SKIN WARM ( 12 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 12 FDA reports)
SOFT TISSUE INFLAMMATION ( 12 FDA reports)
SPINAL CORPECTOMY ( 12 FDA reports)
STREPTOCOCCAL INFECTION ( 12 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 12 FDA reports)
THROAT CANCER ( 12 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
TYPE I HYPERSENSITIVITY ( 12 FDA reports)
ULNA FRACTURE ( 12 FDA reports)
URETHRAL OBSTRUCTION ( 12 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 12 FDA reports)
URINARY TRACT OBSTRUCTION ( 12 FDA reports)
URINE ODOUR ABNORMAL ( 12 FDA reports)
VAGINAL DISCHARGE ( 12 FDA reports)
VASCULAR OPERATION ( 12 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
VITREOUS DETACHMENT ( 12 FDA reports)
VULVITIS ( 12 FDA reports)
RADIATION PNEUMONITIS ( 11 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
RESPIRATORY ACIDOSIS ( 11 FDA reports)
RESUSCITATION ( 11 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 11 FDA reports)
RIGHT ATRIAL DILATATION ( 11 FDA reports)
SACROILIITIS ( 11 FDA reports)
SKELETAL INJURY ( 11 FDA reports)
SKIN EROSION ( 11 FDA reports)
SKIN INFECTION ( 11 FDA reports)
SKIN OEDEMA ( 11 FDA reports)
SKIN SWELLING ( 11 FDA reports)
SPINAL DECOMPRESSION ( 11 FDA reports)
SPLENIC GRANULOMA ( 11 FDA reports)
STRABISMUS ( 11 FDA reports)
STRESS URINARY INCONTINENCE ( 11 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 11 FDA reports)
SYNOVITIS ( 11 FDA reports)
TIBIA FRACTURE ( 11 FDA reports)
TREATMENT FAILURE ( 11 FDA reports)
TUMOUR HAEMORRHAGE ( 11 FDA reports)
UNDERDOSE ( 11 FDA reports)
URGE INCONTINENCE ( 11 FDA reports)
UTERINE ENLARGEMENT ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 11 FDA reports)
WOUND TREATMENT ( 11 FDA reports)
ACCIDENTAL POISONING ( 11 FDA reports)
ACROCHORDON ( 11 FDA reports)
ACTINOMYCES TEST POSITIVE ( 11 FDA reports)
ADHESION ( 11 FDA reports)
ALCOHOL ABUSE ( 11 FDA reports)
AMENORRHOEA ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
ANION GAP INCREASED ( 11 FDA reports)
APPLICATION SITE DISCOLOURATION ( 11 FDA reports)
APPLICATION SITE IRRITATION ( 11 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 11 FDA reports)
ATRIAL TACHYCARDIA ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
BAND SENSATION ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 11 FDA reports)
BLADDER CATHETERISATION ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 11 FDA reports)
BLOOD PRESSURE ABNORMAL ( 11 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 11 FDA reports)
BLOOD URIC ACID INCREASED ( 11 FDA reports)
BONE INFARCTION ( 11 FDA reports)
BRAIN NEOPLASM ( 11 FDA reports)
BREAST NECROSIS ( 11 FDA reports)
BREAST TENDERNESS ( 11 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 11 FDA reports)
CAESAREAN SECTION ( 11 FDA reports)
CARCINOID TUMOUR ( 11 FDA reports)
CENTRAL LINE INFECTION ( 11 FDA reports)
CEREBRAL CYST ( 11 FDA reports)
CERVICITIS ( 11 FDA reports)
COLECTOMY ( 11 FDA reports)
COLONIC OBSTRUCTION ( 11 FDA reports)
CONDUCTION DISORDER ( 11 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 11 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 11 FDA reports)
CORONARY ANGIOPLASTY ( 11 FDA reports)
DERMATOPHYTOSIS ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
DUODENAL POLYP ( 11 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 11 FDA reports)
ENCEPHALITIS HERPES ( 11 FDA reports)
ESCHERICHIA TEST POSITIVE ( 11 FDA reports)
FEBRILE BONE MARROW APLASIA ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 11 FDA reports)
HAEMOPHILUS INFECTION ( 11 FDA reports)
HAEMOTHORAX ( 11 FDA reports)
HEPATIC PAIN ( 11 FDA reports)
HYPERCOAGULATION ( 11 FDA reports)
IMMOBILE ( 11 FDA reports)
INCREASED BRONCHIAL SECRETION ( 11 FDA reports)
INFLAMMATION OF WOUND ( 11 FDA reports)
INJECTION SITE BRUISING ( 11 FDA reports)
INTRAOCULAR MELANOMA ( 11 FDA reports)
INTUSSUSCEPTION ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
LEG AMPUTATION ( 11 FDA reports)
LERICHE SYNDROME ( 11 FDA reports)
LYMPHADENITIS ( 11 FDA reports)
METASTASES TO PERITONEUM ( 11 FDA reports)
MICTURITION DISORDER ( 11 FDA reports)
MITRAL VALVE CALCIFICATION ( 11 FDA reports)
MONOCYTOSIS ( 11 FDA reports)
NEPHROPATHY TOXIC ( 11 FDA reports)
ORAL DISCHARGE ( 11 FDA reports)
OROPHARYNGEAL SWELLING ( 11 FDA reports)
OSTEITIS DEFORMANS ( 11 FDA reports)
OTITIS MEDIA ACUTE ( 11 FDA reports)
PAINFUL DEFAECATION ( 11 FDA reports)
PANCREATIC DISORDER ( 11 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 11 FDA reports)
PERITONEAL ADHESIONS ( 11 FDA reports)
PNEUMONIA KLEBSIELLA ( 11 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 11 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 11 FDA reports)
PNEUMOPERITONEUM ( 11 FDA reports)
PO2 INCREASED ( 11 FDA reports)
POST THROMBOTIC SYNDROME ( 11 FDA reports)
POSTOPERATIVE INFECTION ( 11 FDA reports)
PRIMARY HYPOGONADISM ( 11 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 11 FDA reports)
PROSTHESIS USER ( 11 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 11 FDA reports)
ABDOMINAL ADHESIONS ( 10 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 10 FDA reports)
ANAEMIA POSTOPERATIVE ( 10 FDA reports)
ANTIBODY TEST POSITIVE ( 10 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 10 FDA reports)
ANTISOCIAL BEHAVIOUR ( 10 FDA reports)
APHONIA ( 10 FDA reports)
APTYALISM ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 10 FDA reports)
ATROPHIC VULVOVAGINITIS ( 10 FDA reports)
AUTOIMMUNE THYROIDITIS ( 10 FDA reports)
BACILLUS INFECTION ( 10 FDA reports)
BARTHOLIN'S CYST ( 10 FDA reports)
BIPOLAR I DISORDER ( 10 FDA reports)
BLOOD AMYLASE INCREASED ( 10 FDA reports)
BLOOD LACTIC ACID INCREASED ( 10 FDA reports)
BLOOD URINE ( 10 FDA reports)
BREAST CANCER IN SITU ( 10 FDA reports)
CAROTID ARTERY OCCLUSION ( 10 FDA reports)
CATHETER PLACEMENT ( 10 FDA reports)
CAUDA EQUINA SYNDROME ( 10 FDA reports)
CELLULITIS ORBITAL ( 10 FDA reports)
CHEST TUBE INSERTION ( 10 FDA reports)
COR PULMONALE ( 10 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 10 FDA reports)
CUBITAL TUNNEL SYNDROME ( 10 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 10 FDA reports)
DEMYELINATION ( 10 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 10 FDA reports)
DIABETIC COMA ( 10 FDA reports)
DIABETIC RETINOPATHY ( 10 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 10 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 10 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 10 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 10 FDA reports)
EFFUSION ( 10 FDA reports)
EPIDERMAL NECROSIS ( 10 FDA reports)
ESCHERICHIA BACTERAEMIA ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
EYE LASER SURGERY ( 10 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 10 FDA reports)
FOLATE DEFICIENCY ( 10 FDA reports)
FUNGAL SKIN INFECTION ( 10 FDA reports)
GASTROINTESTINAL ULCER ( 10 FDA reports)
HEARING DISABILITY ( 10 FDA reports)
HEPATITIS CHOLESTATIC ( 10 FDA reports)
HEPATOCELLULAR INJURY ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
HYPOPNOEA ( 10 FDA reports)
IATROGENIC INJURY ( 10 FDA reports)
INJECTION SITE NODULE ( 10 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 10 FDA reports)
KERATOACANTHOMA ( 10 FDA reports)
KIDNEY SMALL ( 10 FDA reports)
LABILE BLOOD PRESSURE ( 10 FDA reports)
LEGAL PROBLEM ( 10 FDA reports)
LEUKODYSTROPHY ( 10 FDA reports)
LEUKOPLAKIA ORAL ( 10 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 10 FDA reports)
LUNG OPERATION ( 10 FDA reports)
MALIGNANT ASCITES ( 10 FDA reports)
MUSCLE SPASTICITY ( 10 FDA reports)
NEURODEGENERATIVE DISORDER ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA ( 10 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 10 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 10 FDA reports)
ONYCHOCLASIS ( 10 FDA reports)
OPERATIVE HAEMORRHAGE ( 10 FDA reports)
ORTHOSIS USER ( 10 FDA reports)
PAPILLOMA ( 10 FDA reports)
PEAU D'ORANGE ( 10 FDA reports)
PELVIC ABSCESS ( 10 FDA reports)
PENILE INFECTION ( 10 FDA reports)
PERIODONTAL INFECTION ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PHAEOCHROMOCYTOMA ( 10 FDA reports)
PITTING OEDEMA ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 10 FDA reports)
POIKILOCYTOSIS ( 10 FDA reports)
POLYARTHRITIS ( 10 FDA reports)
PRESSURE OF SPEECH ( 10 FDA reports)
PROCEDURAL HYPERTENSION ( 10 FDA reports)
PROSTATIC OBSTRUCTION ( 10 FDA reports)
PROSTATISM ( 10 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 10 FDA reports)
PYODERMA GANGRENOSUM ( 10 FDA reports)
RENAL ANEURYSM ( 10 FDA reports)
RENAL COLIC ( 10 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 10 FDA reports)
RHEUMATOID NODULE ( 10 FDA reports)
SCROTAL SWELLING ( 10 FDA reports)
SECRETION DISCHARGE ( 10 FDA reports)
SENSATION OF PRESSURE ( 10 FDA reports)
SIALOADENITIS ( 10 FDA reports)
SINUS ARRHYTHMIA ( 10 FDA reports)
SLEEP WALKING ( 10 FDA reports)
SOFT TISSUE INJURY ( 10 FDA reports)
TESTICULAR FAILURE ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
TONGUE DISCOLOURATION ( 10 FDA reports)
TONSILLITIS ( 10 FDA reports)
TRACHEOBRONCHITIS ( 10 FDA reports)
ULCER HAEMORRHAGE ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 10 FDA reports)
WEGENER'S GRANULOMATOSIS ( 10 FDA reports)
RADIATION FIBROSIS - LUNG ( 9 FDA reports)
RASH VESICULAR ( 9 FDA reports)
RECTAL ABSCESS ( 9 FDA reports)
RETINAL DETACHMENT ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 9 FDA reports)
SELF MUTILATION ( 9 FDA reports)
SKIN CHAPPED ( 9 FDA reports)
SKIN GRAFT ( 9 FDA reports)
SKIN TOXICITY ( 9 FDA reports)
SKULL FRACTURE ( 9 FDA reports)
SKULL MALFORMATION ( 9 FDA reports)
SPLENECTOMY ( 9 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 9 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 9 FDA reports)
TELANGIECTASIA ( 9 FDA reports)
THERAPY CESSATION ( 9 FDA reports)
THYROIDECTOMY ( 9 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 9 FDA reports)
TOURETTE'S DISORDER ( 9 FDA reports)
TRIGGER FINGER ( 9 FDA reports)
TROPONIN I INCREASED ( 9 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 9 FDA reports)
TUMOUR PAIN ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
VASCULAR PSEUDOANEURYSM ( 9 FDA reports)
VENTRICULAR DYSKINESIA ( 9 FDA reports)
X-RAY ( 9 FDA reports)
ABDOMINAL INFECTION ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 9 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
ANAL ULCER ( 9 FDA reports)
AORTIC ATHEROSCLEROSIS ( 9 FDA reports)
APHAKIA ( 9 FDA reports)
APPLICATION SITE SCAR ( 9 FDA reports)
ARTHRITIS INFECTIVE ( 9 FDA reports)
ARTHROPOD STING ( 9 FDA reports)
ASPIRATION BONE MARROW ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
BACTERIA STOOL IDENTIFIED ( 9 FDA reports)
BLADDER DYSFUNCTION ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 9 FDA reports)
BREAST RECONSTRUCTION ( 9 FDA reports)
BUNDLE BRANCH BLOCK ( 9 FDA reports)
CARDIAC FLUTTER ( 9 FDA reports)
CEREBRAL DISORDER ( 9 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 9 FDA reports)
CHAPPED LIPS ( 9 FDA reports)
CHEST WALL PAIN ( 9 FDA reports)
CHOLESTEROSIS ( 9 FDA reports)
CHRONIC HEPATIC FAILURE ( 9 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 9 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 9 FDA reports)
COLON CANCER METASTATIC ( 9 FDA reports)
COMPARTMENT SYNDROME ( 9 FDA reports)
DEMENTIA WITH LEWY BODIES ( 9 FDA reports)
DEVICE RELATED SEPSIS ( 9 FDA reports)
DIABETES INSIPIDUS ( 9 FDA reports)
DIABETIC NEPHROPATHY ( 9 FDA reports)
DIAPHRAGMATIC DISORDER ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 9 FDA reports)
DYSAESTHESIA ( 9 FDA reports)
DYSMENORRHOEA ( 9 FDA reports)
ENTEROBACTER BACTERAEMIA ( 9 FDA reports)
ENTEROCOCCAL SEPSIS ( 9 FDA reports)
EOSINOPHIL COUNT DECREASED ( 9 FDA reports)
EPIDURAL LIPOMATOSIS ( 9 FDA reports)
EYE PRURITUS ( 9 FDA reports)
FACIAL NEURALGIA ( 9 FDA reports)
FEEDING TUBE COMPLICATION ( 9 FDA reports)
FEELING DRUNK ( 9 FDA reports)
FEELING HOT AND COLD ( 9 FDA reports)
FULL BLOOD COUNT DECREASED ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 9 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 9 FDA reports)
GLIOSIS ( 9 FDA reports)
GRANULOCYTOPENIA ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
HALLUCINATIONS, MIXED ( 9 FDA reports)
HAND DEFORMITY ( 9 FDA reports)
HYDROPNEUMOTHORAX ( 9 FDA reports)
HYPERCHLORAEMIA ( 9 FDA reports)
HYPERMAGNESAEMIA ( 9 FDA reports)
IMMUNE SYSTEM DISORDER ( 9 FDA reports)
IMPULSE-CONTROL DISORDER ( 9 FDA reports)
INCISION SITE ERYTHEMA ( 9 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 9 FDA reports)
INJECTION SITE RASH ( 9 FDA reports)
IRON DEFICIENCY ( 9 FDA reports)
JUGULAR VEIN DISTENSION ( 9 FDA reports)
KERATOSIS OBTURANS ( 9 FDA reports)
LIP PAIN ( 9 FDA reports)
LISTLESS ( 9 FDA reports)
LORDOSIS ( 9 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 9 FDA reports)
MASTOCYTOSIS ( 9 FDA reports)
MAXILLOFACIAL OPERATION ( 9 FDA reports)
MENSTRUATION IRREGULAR ( 9 FDA reports)
METASTASES TO BONE MARROW ( 9 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 9 FDA reports)
MOANING ( 9 FDA reports)
MULTIPLE ALLERGIES ( 9 FDA reports)
MYOCARDIAL FIBROSIS ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 9 FDA reports)
OBSTRUCTIVE UROPATHY ( 9 FDA reports)
OLFACTORY NERVE DISORDER ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
OVARIAN ABSCESS ( 9 FDA reports)
PAINFUL RESPIRATION ( 9 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 9 FDA reports)
PAROTITIS ( 9 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 8 FDA reports)
ALVEOLITIS ( 8 FDA reports)
ANGIOMYOLIPOMA ( 8 FDA reports)
ANKYLOSING SPONDYLITIS ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
AORTIC ANEURYSM RUPTURE ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
APPLICATION SITE ULCER ( 8 FDA reports)
APPLICATION SITE VESICLES ( 8 FDA reports)
ARTERIAL THROMBOSIS ( 8 FDA reports)
BASEDOW'S DISEASE ( 8 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 8 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 8 FDA reports)
BLADDER DISCOMFORT ( 8 FDA reports)
BLADDER MASS ( 8 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 8 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 8 FDA reports)
BONE FORMATION INCREASED ( 8 FDA reports)
BOWEL SOUNDS ABNORMAL ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CARDIOPULMONARY FAILURE ( 8 FDA reports)
CARDIOTOXICITY ( 8 FDA reports)
CATHETER SITE ERYTHEMA ( 8 FDA reports)
CATHETER SITE HAEMORRHAGE ( 8 FDA reports)
CEREBRAL THROMBOSIS ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
CULTURE POSITIVE ( 8 FDA reports)
CUSHING'S SYNDROME ( 8 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DEVICE DISLOCATION ( 8 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 8 FDA reports)
DIVERTICULAR PERFORATION ( 8 FDA reports)
DRUG DETOXIFICATION ( 8 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 8 FDA reports)
DYSPAREUNIA ( 8 FDA reports)
DYSPLASIA ( 8 FDA reports)
DYSPNOEA EXACERBATED ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 8 FDA reports)
EOSINOPHILIA ( 8 FDA reports)
EYE DISCHARGE ( 8 FDA reports)
EYE MOVEMENT DISORDER ( 8 FDA reports)
FACIAL NERVE DISORDER ( 8 FDA reports)
FEELING GUILTY ( 8 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 8 FDA reports)
FIBROUS DYSPLASIA OF JAW ( 8 FDA reports)
FIBROUS HISTIOCYTOMA ( 8 FDA reports)
FOAMING AT MOUTH ( 8 FDA reports)
FOOD INTOLERANCE ( 8 FDA reports)
FOOT OPERATION ( 8 FDA reports)
GALLBLADDER OPERATION ( 8 FDA reports)
GALLBLADDER POLYP ( 8 FDA reports)
GROIN ABSCESS ( 8 FDA reports)
HAEMODYNAMIC INSTABILITY ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HANGOVER ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
HETEROTAXIA ( 8 FDA reports)
HISTOPLASMOSIS ( 8 FDA reports)
HYPERALBUMINAEMIA ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
HYPOGONADISM MALE ( 8 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
INCISION SITE INFECTION ( 8 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 8 FDA reports)
INFUSION SITE REACTION ( 8 FDA reports)
INJECTION SITE EXTRAVASATION ( 8 FDA reports)
INJURY ASPHYXIATION ( 8 FDA reports)
INTERTRIGO ( 8 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 8 FDA reports)
KETOACIDOSIS ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LEUKAEMIA ( 8 FDA reports)
LICHENOID KERATOSIS ( 8 FDA reports)
LIP DISORDER ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
LIVEDO RETICULARIS ( 8 FDA reports)
LIVER ABSCESS ( 8 FDA reports)
LOSS OF LIBIDO ( 8 FDA reports)
LYMPH NODE PALPABLE ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
MARFAN'S SYNDROME ( 8 FDA reports)
MEDICAL DEVICE REMOVAL ( 8 FDA reports)
MENINGEAL NEOPLASM ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
MONOPARESIS ( 8 FDA reports)
MYOCARDITIS ( 8 FDA reports)
NASAL POLYPS ( 8 FDA reports)
NASAL TURBINATE ABNORMALITY ( 8 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 8 FDA reports)
NONSPECIFIC REACTION ( 8 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 8 FDA reports)
ORAL NEOPLASM ( 8 FDA reports)
ORAL PRURITUS ( 8 FDA reports)
OSTEOGENESIS IMPERFECTA ( 8 FDA reports)
OSTEOPETROSIS ( 8 FDA reports)
OSTEOSYNTHESIS ( 8 FDA reports)
PANCREATIC PSEUDOCYST ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PERIORBITAL CELLULITIS ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
PITUITARY TUMOUR BENIGN ( 8 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 8 FDA reports)
POSTOPERATIVE ABSCESS ( 8 FDA reports)
POSTURING ( 8 FDA reports)
PYELONEPHRITIS ACUTE ( 8 FDA reports)
RAYNAUD'S PHENOMENON ( 8 FDA reports)
RESPIRATION ABNORMAL ( 8 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 8 FDA reports)
RHEUMATIC FEVER ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
SHOULDER OPERATION ( 8 FDA reports)
SLEEP ATTACKS ( 8 FDA reports)
SPINAL CLAUDICATION ( 8 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
SPLENIC RUPTURE ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
SPONDYLOARTHROPATHY ( 8 FDA reports)
STARING ( 8 FDA reports)
STREPTOCOCCAL SEPSIS ( 8 FDA reports)
SUBILEUS ( 8 FDA reports)
SUICIDAL BEHAVIOUR ( 8 FDA reports)
TENDON PAIN ( 8 FDA reports)
TENSION HEADACHE ( 8 FDA reports)
THORACIC CAVITY DRAINAGE ( 8 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 8 FDA reports)
TINEA CRURIS ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
VAGINAL PAIN ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
VICTIM OF CRIME ( 8 FDA reports)
VITAMIN B12 INCREASED ( 8 FDA reports)
VULVAL DISORDER ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
WOUND DEBRIDEMENT ( 8 FDA reports)
QUADRIPARESIS ( 7 FDA reports)
RADIATION NECROSIS ( 7 FDA reports)
RETICULOCYTE COUNT INCREASED ( 7 FDA reports)
RETINAL MELANOMA ( 7 FDA reports)
SCLERITIS ( 7 FDA reports)
SCROTAL ABSCESS ( 7 FDA reports)
SEPTIC EMBOLUS ( 7 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 7 FDA reports)
SINUS OPERATION ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 7 FDA reports)
SMALL INTESTINE ULCER ( 7 FDA reports)
SMOKER ( 7 FDA reports)
SOLILOQUY ( 7 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
SUBMANDIBULAR MASS ( 7 FDA reports)
SUNBURN ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TINEA INFECTION ( 7 FDA reports)
TONGUE DRY ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TOXOPLASMOSIS ( 7 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
TUMOUR FLARE ( 7 FDA reports)
TUNNEL VISION ( 7 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 7 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 7 FDA reports)
UTERINE CANCER ( 7 FDA reports)
UVEITIS ( 7 FDA reports)
VISCERAL CONGESTION ( 7 FDA reports)
VITAMIN B12 DECREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
XEROSIS ( 7 FDA reports)
ABDOMINAL INJURY ( 7 FDA reports)
ABSCESS LIMB ( 7 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 7 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 7 FDA reports)
APNOEIC ATTACK ( 7 FDA reports)
APPLICATION SITE PUSTULES ( 7 FDA reports)
ARTERIAL INJURY ( 7 FDA reports)
ASEPTIC NECROSIS BONE ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
ASTROCYTOMA ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BENIGN LUNG NEOPLASM ( 7 FDA reports)
BILE DUCT CANCER ( 7 FDA reports)
BILIARY TRACT INFECTION ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BLOOD ETHANOL INCREASED ( 7 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 7 FDA reports)
BLOOD MAGNESIUM INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 7 FDA reports)
BONE FISTULA ( 7 FDA reports)
BRAIN CONTUSION ( 7 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 7 FDA reports)
BURNS THIRD DEGREE ( 7 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 7 FDA reports)
CARCINOMA ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CATHETER SITE INFECTION ( 7 FDA reports)
CATHETER SITE PAIN ( 7 FDA reports)
CEREBELLAR ATROPHY ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
CHONDROPATHY ( 7 FDA reports)
CHRONIC HEPATITIS ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 7 FDA reports)
CNS VENTRICULITIS ( 7 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 7 FDA reports)
COR PULMONALE CHRONIC ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
CYSTITIS NONINFECTIVE ( 7 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 7 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
DETOXIFICATION ( 7 FDA reports)
DIABETIC COMPLICATION ( 7 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 7 FDA reports)
DISORDER OF ORBIT ( 7 FDA reports)
DISSEMINATED TUBERCULOSIS ( 7 FDA reports)
DROWNING ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 7 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
EYE NAEVUS ( 7 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 7 FDA reports)
FAECES HARD ( 7 FDA reports)
FAT TISSUE INCREASED ( 7 FDA reports)
FIBROMA ( 7 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 7 FDA reports)
GALLBLADDER PAIN ( 7 FDA reports)
GASTRITIS HAEMORRHAGIC ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GASTROINTESTINAL PERFORATION ( 7 FDA reports)
HEART INJURY ( 7 FDA reports)
HEPATIC ATROPHY ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HIP DEFORMITY ( 7 FDA reports)
HYPERPHOSPHATAEMIA ( 7 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 7 FDA reports)
HYPERVISCOSITY SYNDROME ( 7 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
ILIAC ARTERY STENOSIS ( 7 FDA reports)
IMPAIRED REASONING ( 7 FDA reports)
INCISIONAL HERNIA ( 7 FDA reports)
INGUINAL HERNIA REPAIR ( 7 FDA reports)
INJECTION SITE BURNING ( 7 FDA reports)
INJECTION SITE OEDEMA ( 7 FDA reports)
INJECTION SITE URTICARIA ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
LAGOPHTHALMOS ( 7 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MIDDLE EAR EFFUSION ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
MYCOSIS FUNGOIDES ( 7 FDA reports)
MYELOID LEUKAEMIA ( 7 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 7 FDA reports)
NAIL DYSTROPHY ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
NIGHT BLINDNESS ( 7 FDA reports)
OCCULT BLOOD ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OOPHORECTOMY ( 7 FDA reports)
ORAL SOFT TISSUE DISORDER ( 7 FDA reports)
OVARIAN DISORDER ( 7 FDA reports)
PALATAL DISORDER ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 7 FDA reports)
PHIMOSIS ( 7 FDA reports)
PHONOPHOBIA ( 7 FDA reports)
PHOTOSENSITIVITY REACTION ( 7 FDA reports)
PHYSICAL ASSAULT ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
POST PROCEDURAL PAIN ( 7 FDA reports)
POSTERIOR CAPSULOTOMY ( 7 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 7 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 7 FDA reports)
POSTNASAL DRIP ( 7 FDA reports)
POSTOPERATIVE ILEUS ( 7 FDA reports)
POSTURE ABNORMAL ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
PULMONARY TOXICITY ( 7 FDA reports)
PULMONARY VASCULAR DISORDER ( 7 FDA reports)
ACARODERMATITIS ( 6 FDA reports)
ADJUSTMENT DISORDER ( 6 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
ALCOHOL INTERACTION ( 6 FDA reports)
ANAL PRURITUS ( 6 FDA reports)
ANDROGEN DEFICIENCY ( 6 FDA reports)
AORTIC VALVE DISEASE ( 6 FDA reports)
APPLICATION SITE EROSION ( 6 FDA reports)
APPLICATION SITE HAEMATOMA ( 6 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ARTHROSCOPY ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
ATROPHY ( 6 FDA reports)
AXILLARY MASS ( 6 FDA reports)
BACTERIAL PYELONEPHRITIS ( 6 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
BLOOD IRON INCREASED ( 6 FDA reports)
BONE FISSURE ( 6 FDA reports)
BREAST ABSCESS ( 6 FDA reports)
BREAST CANCER STAGE I ( 6 FDA reports)
BREAST CYST ( 6 FDA reports)
BREAST DISCHARGE ( 6 FDA reports)
BREAST FIBROSIS ( 6 FDA reports)
BRONCHIOLITIS ( 6 FDA reports)
CALCIFICATION METASTATIC ( 6 FDA reports)
CALCINOSIS ( 6 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CATHETER REMOVAL ( 6 FDA reports)
CENTRAL OBESITY ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
CHEMOTHERAPY ( 6 FDA reports)
CHEST WALL ABSCESS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 6 FDA reports)
COAGULATION TEST ABNORMAL ( 6 FDA reports)
COLORECTAL CANCER METASTATIC ( 6 FDA reports)
COLPOCELE ( 6 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
CULDOPLASTY ( 6 FDA reports)
CULTURE STOOL POSITIVE ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DEPERSONALISATION ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DISLOCATION OF VERTEBRA ( 6 FDA reports)
EAR DEFORMITY ACQUIRED ( 6 FDA reports)
EARLY SATIETY ( 6 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
EPIDIDYMITIS ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 6 FDA reports)
EXTRAVASATION OF URINE ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 6 FDA reports)
GASTROINTESTINAL INJURY ( 6 FDA reports)
GASTROSTOMY TUBE INSERTION ( 6 FDA reports)
GLUCOSE URINE PRESENT ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HAEMOSIDEROSIS ( 6 FDA reports)
HALLUCINATION, TACTILE ( 6 FDA reports)
HEAD AND NECK CANCER ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HEREDITARY ANGIOEDEMA ( 6 FDA reports)
HOMICIDE ( 6 FDA reports)
HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 6 FDA reports)
HYPERACUSIS ( 6 FDA reports)
HYPERMETROPIA ( 6 FDA reports)
HYPERTROPHY ( 6 FDA reports)
HYPOCHROMASIA ( 6 FDA reports)
HYPOTONIC URINARY BLADDER ( 6 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 6 FDA reports)
INCISION SITE OEDEMA ( 6 FDA reports)
INCORRECT STORAGE OF DRUG ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INTERCEPTED MEDICATION ERROR ( 6 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 6 FDA reports)
INTESTINAL POLYP ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 6 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 6 FDA reports)
JOINT SURGERY ( 6 FDA reports)
KLEBSIELLA BACTERAEMIA ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LIMB DEFORMITY ( 6 FDA reports)
LIP BLISTER ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
LOSS OF EMPLOYMENT ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
MOUTH INJURY ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NASAL OBSTRUCTION ( 6 FDA reports)
NASAL VESTIBULITIS ( 6 FDA reports)
NEPHRITIC SYNDROME ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
OBSESSIVE THOUGHTS ( 6 FDA reports)
ODONTOGENIC CYST ( 6 FDA reports)
OESOPHAGEAL POLYP ( 6 FDA reports)
OESOPHAGEAL SPASM ( 6 FDA reports)
ONYCHOLYSIS ( 6 FDA reports)
OPIATES POSITIVE ( 6 FDA reports)
ORAL DYSAESTHESIA ( 6 FDA reports)
ORBITAL OEDEMA ( 6 FDA reports)
OSTEOMALACIA ( 6 FDA reports)
OVARIAN MASS ( 6 FDA reports)
PANCREATIC DUCT STENOSIS ( 6 FDA reports)
PELVIC DISCOMFORT ( 6 FDA reports)
PERIPHERAL EMBOLISM ( 6 FDA reports)
PERIVASCULAR DERMATITIS ( 6 FDA reports)
PHARYNGEAL ABSCESS ( 6 FDA reports)
PHARYNGEAL DISORDER ( 6 FDA reports)
PLEURECTOMY ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYCHROMASIA ( 6 FDA reports)
POTENTIATING DRUG INTERACTION ( 6 FDA reports)
PREMATURE LABOUR ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
PTERYGIUM ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
RADIATION OESOPHAGITIS ( 6 FDA reports)
RADICULITIS ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
RECTOCELE REPAIR ( 6 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 6 FDA reports)
RENAL HAEMORRHAGE ( 6 FDA reports)
RETINITIS ( 6 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 6 FDA reports)
SJOGREN'S SYNDROME ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SPIDER VEIN ( 6 FDA reports)
SPINAL COLUMN INJURY ( 6 FDA reports)
SPINAL PAIN ( 6 FDA reports)
SPLINT APPLICATION ( 6 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
SUBRETINAL FIBROSIS ( 6 FDA reports)
SUTURE RELATED COMPLICATION ( 6 FDA reports)
TEETH BRITTLE ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
THROMBOSIS IN DEVICE ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TONGUE BLISTERING ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOOTH AVULSION ( 6 FDA reports)
TOOTH MALFORMATION ( 6 FDA reports)
TRANSPLANT REJECTION ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
URINE CYTOLOGY ABNORMAL ( 6 FDA reports)
URINE KETONE BODY PRESENT ( 6 FDA reports)
VAGINITIS BACTERIAL ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VASCULAR OCCLUSION ( 6 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 6 FDA reports)
VENOUS STASIS ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
VITREOUS DEGENERATION ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
WALKING DISABILITY ( 6 FDA reports)
PYODERMA ( 5 FDA reports)
RECTAL PROLAPSE ( 5 FDA reports)
RECURRENT CANCER ( 5 FDA reports)
REFLEXES ABNORMAL ( 5 FDA reports)
RENAL CANCER METASTATIC ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RENAL LIPOMATOSIS ( 5 FDA reports)
RENAL NEOPLASM ( 5 FDA reports)
RENAL STONE REMOVAL ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
SARCOMA ( 5 FDA reports)
SCAR EXCISION ( 5 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SERUM SEROTONIN INCREASED ( 5 FDA reports)
SHORT-BOWEL SYNDROME ( 5 FDA reports)
SHOULDER ARTHROPLASTY ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SOFT TISSUE NECROSIS ( 5 FDA reports)
SPLENIC ABSCESS ( 5 FDA reports)
SPLENIC HAEMORRHAGE ( 5 FDA reports)
SPLENIC LESION ( 5 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
TESTIS CANCER ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
TIC ( 5 FDA reports)
TOE AMPUTATION ( 5 FDA reports)
TONGUE EXFOLIATION ( 5 FDA reports)
TONSILLECTOMY ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TROPONIN T INCREASED ( 5 FDA reports)
TUMOUR INVASION ( 5 FDA reports)
TUMOUR NECROSIS ( 5 FDA reports)
UPPER EXTREMITY MASS ( 5 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 5 FDA reports)
URINE OUTPUT INCREASED ( 5 FDA reports)
VENA CAVA INJURY ( 5 FDA reports)
VENOUS INJURY ( 5 FDA reports)
VENOUS STENOSIS ( 5 FDA reports)
VERTEBRAL WEDGING ( 5 FDA reports)
VICTIM OF CHILD ABUSE ( 5 FDA reports)
X-RAY ABNORMAL ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
ABNORMAL WEIGHT GAIN ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC VALVE REPLACEMENT ( 5 FDA reports)
ARM AMPUTATION ( 5 FDA reports)
ASTERIXIS ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BILIARY SEPSIS ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 5 FDA reports)
BLOOD BILIRUBIN ( 5 FDA reports)
BLOOD CREATININE ( 5 FDA reports)
BLOOD FOLATE INCREASED ( 5 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BRACHIAL PLEXOPATHY ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
CALCULUS URETHRAL ( 5 FDA reports)
CARDIAC ASTHMA ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CERVICAL MYELOPATHY ( 5 FDA reports)
CHEST WALL OPERATION ( 5 FDA reports)
CHOREOATHETOSIS ( 5 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
CIRRHOSIS ALCOHOLIC ( 5 FDA reports)
COLONOSCOPY ( 5 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 5 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 5 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 5 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 5 FDA reports)
CUTIS LAXA ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
CYSTOPEXY ( 5 FDA reports)
CYSTOSCOPY ( 5 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 5 FDA reports)
DEAFNESS UNILATERAL ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 5 FDA reports)
DISEASE COMPLICATION ( 5 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
ENAMEL ANOMALY ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
ERYSIPELAS ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYE ABSCESS ( 5 FDA reports)
FACIAL OPERATION ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FISTULA REPAIR ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
FUNGAL TEST POSITIVE ( 5 FDA reports)
GALACTORRHOEA ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GAMMA RADIATION THERAPY TO BRAIN ( 5 FDA reports)
GANGLION ( 5 FDA reports)
GASTRIC PERFORATION ( 5 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 5 FDA reports)
GASTROINTESTINAL OEDEMA ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 5 FDA reports)
HAEMANGIOMA OF SKIN ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 5 FDA reports)
HEART RATE ABNORMAL ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HEPATIC INFECTION BACTERIAL ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATITIS VIRAL ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE DISCOLOURATION ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
JOINT STABILISATION ( 5 FDA reports)
LABORATORY TEST INTERFERENCE ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LEUKOCYTURIA ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIGHT CHAIN ANALYSIS ( 5 FDA reports)
LIVER OPERATION ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYME DISEASE ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MASS EXCISION ( 5 FDA reports)
MASTOID DISORDER ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MECHANICAL ILEUS ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MENINGOCELE ( 5 FDA reports)
METASTASES TO KIDNEY ( 5 FDA reports)
METASTASES TO PANCREAS ( 5 FDA reports)
METASTATIC CARCINOID TUMOUR ( 5 FDA reports)
METHAEMOGLOBINAEMIA ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MICROLITHIASIS ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MURPHY'S SIGN POSITIVE ( 5 FDA reports)
MYELITIS TRANSVERSE ( 5 FDA reports)
NEUROPATHIC ULCER ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 5 FDA reports)
OESOPHAGEAL FISTULA ( 5 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 5 FDA reports)
OPEN ANGLE GLAUCOMA ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
OS TRIGONUM SYNDROME ( 5 FDA reports)
OTITIS MEDIA CHRONIC ( 5 FDA reports)
OVARIAN CYST RUPTURED ( 5 FDA reports)
OXYGEN SATURATION ABNORMAL ( 5 FDA reports)
PANCREATECTOMY ( 5 FDA reports)
PANCREATIC ENZYMES DECREASED ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARATHYROID TUMOUR BENIGN ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PERINEURIAL CYST ( 5 FDA reports)
PERITONEAL HAEMORRHAGE ( 5 FDA reports)
PHANTOM PAIN ( 5 FDA reports)
PIGMENTATION DISORDER ( 5 FDA reports)
PLEURAL ADHESION ( 5 FDA reports)
PLEURAL NEOPLASM ( 5 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 5 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 5 FDA reports)
POLYCYSTIC OVARIES ( 5 FDA reports)
POST LAMINECTOMY SYNDROME ( 5 FDA reports)
POST PROCEDURAL HAEMATOMA ( 5 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROCEDURAL NAUSEA ( 5 FDA reports)
PROTEIN URINE ABSENT ( 5 FDA reports)
PSEUDOPARALYSIS ( 5 FDA reports)
PULMONARY HILUM MASS ( 5 FDA reports)
PULSE ABNORMAL ( 5 FDA reports)
ABDOMINAL NEOPLASM ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ACINETOBACTER INFECTION ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ( 4 FDA reports)
ALCOHOL DETOXIFICATION ( 4 FDA reports)
ALOPECIA AREATA ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
AMPULLA OF VATER STENOSIS ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 4 FDA reports)
ANKLE OPERATION ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APICECTOMY ( 4 FDA reports)
APLASIA ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
AUTOIMMUNE PANCREATITIS ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
AXILLARY PAIN ( 4 FDA reports)
BLADDER NECK OPERATION ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD ALBUMIN ( 4 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD CALCIUM ( 4 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 4 FDA reports)
BLOOD LACTIC ACID DECREASED ( 4 FDA reports)
BLOOD LEAD INCREASED ( 4 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD OSMOLARITY INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS ( 4 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD SODIUM ( 4 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 4 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARCINOID SYNDROME ( 4 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 4 FDA reports)
CARDIAC DEATH ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CATHETER SITE RELATED REACTION ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 4 FDA reports)
CERVIX CARCINOMA RECURRENT ( 4 FDA reports)
CHOLANGITIS SCLEROSING ( 4 FDA reports)
CHOLANGITIS SUPPURATIVE ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COLOSTOMY ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 4 FDA reports)
CORNEAL OPERATION ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 4 FDA reports)
DELAYED ENGRAFTMENT ( 4 FDA reports)
DENTOFACIAL ANOMALY ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 4 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DUODENAL OBSTRUCTION ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ENDOMETRIAL ATROPHY ( 4 FDA reports)
ENDOSCOPY ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTEROBACTER TEST POSITIVE ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ENTEROVESICAL FISTULA ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FOREIGN BODY REACTION ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 4 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 4 FDA reports)
GASTROINTESTINAL FISTULA ( 4 FDA reports)
GASTROSTOMY ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GINGIVAL ATROPHY ( 4 FDA reports)
GINGIVAL BLISTER ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC CANCER METASTATIC ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOPHYSITIS ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
ILEOSTOMY ( 4 FDA reports)
ILEUS SPASTIC ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
IMPRISONMENT ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INCISION SITE ABSCESS ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INGROWN HAIR ( 4 FDA reports)
INJECTION SITE DYSAESTHESIA ( 4 FDA reports)
INJECTION SITE PAPULE ( 4 FDA reports)
INJECTION SITE STINGING ( 4 FDA reports)
INTERNAL HERNIA ( 4 FDA reports)
INTRACRANIAL HAEMATOMA ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
JAW LESION EXCISION ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LACTOBACILLUS INFECTION ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LASER THERAPY ( 4 FDA reports)
LEARNING DISORDER ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIVER TENDERNESS ( 4 FDA reports)
LIVIDITY ( 4 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
LYMPHOCYTE COUNT ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
LYMPHOHISTIOCYTOSIS ( 4 FDA reports)
MACULAR FIBROSIS ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEDIASTINAL MASS ( 4 FDA reports)
MEDIASTINAL SHIFT ( 4 FDA reports)
MEDIASTINUM NEOPLASM ( 4 FDA reports)
MEGAKARYOCYTES INCREASED ( 4 FDA reports)
MEIBOMIANITIS ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO BREAST ( 4 FDA reports)
METASTASES TO CHEST WALL ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTASES TO RETROPERITONEUM ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
METASTASES TO STOMACH ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
MICROANGIOPATHY ( 4 FDA reports)
MONOCYTE COUNT ABNORMAL ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASAL SEPTUM DISORDER ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NASAL SINUS CANCER ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
NO ADVERSE DRUG EFFECT ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OESOPHAGEAL RUPTURE ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PEDAL PULSE DECREASED ( 4 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PELVIC NEOPLASM ( 4 FDA reports)
PENILE HAEMORRHAGE ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PERIDIVERTICULAR ABSCESS ( 4 FDA reports)
PERITONEAL EFFUSION ( 4 FDA reports)
PILONIDAL CYST ( 4 FDA reports)
PINGUECULA ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 4 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PLEURAL CALCIFICATION ( 4 FDA reports)
PLEUROTHOTONUS ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMONITIS CHEMICAL ( 4 FDA reports)
PORPHYRIA ( 4 FDA reports)
PORTAL TRIADITIS ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
POST PROCEDURAL BILE LEAK ( 4 FDA reports)
POST PROCEDURAL DIARRHOEA ( 4 FDA reports)
POSTOPERATIVE ADHESION ( 4 FDA reports)
PRECANCEROUS CELLS PRESENT ( 4 FDA reports)
PREMATURE DELIVERY ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PROCEDURAL VOMITING ( 4 FDA reports)
PRODUCT TAMPERING ( 4 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 4 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
RADICAL HYSTERECTOMY ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
RENAL ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL VEIN THROMBOSIS ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
RETROPERITONEAL CANCER ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
ROULEAUX FORMATION ( 4 FDA reports)
SCLERODERMA RENAL CRISIS ( 4 FDA reports)
SCROTAL CYST ( 4 FDA reports)
SCROTAL DISORDER ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SKIN CANDIDA ( 4 FDA reports)
SKIN DEPIGMENTATION ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SKIN HYPOPIGMENTATION ( 4 FDA reports)
SKIN INJURY ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
SPINAL CORD INJURY ( 4 FDA reports)
SPINAL CORD INJURY CERVICAL ( 4 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 4 FDA reports)
SPOUSAL ABUSE ( 4 FDA reports)
SPUTUM INCREASED ( 4 FDA reports)
STAB WOUND ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STOOL ANALYSIS ABNORMAL ( 4 FDA reports)
STRONGYLOIDIASIS ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
TERMINAL INSOMNIA ( 4 FDA reports)
THEFT ( 4 FDA reports)
THERAPEUTIC EMBOLISATION ( 4 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 4 FDA reports)
THYROID MASS ( 4 FDA reports)
TINEA VERSICOLOUR ( 4 FDA reports)
TOOTH DECALCIFICATION ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
TRACHEAL OPERATION ( 4 FDA reports)
TUMOUR COMPRESSION ( 4 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 4 FDA reports)
URETHRAL STRICTURE ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
URINE SODIUM INCREASED ( 4 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
UVULECTOMY ( 4 FDA reports)
VAGINAL ODOUR ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VESTIBULAR DISORDER ( 4 FDA reports)
VITAMIN K DEFICIENCY ( 4 FDA reports)
WEIGHT ABNORMAL ( 4 FDA reports)
XANTHOPSIA ( 4 FDA reports)
YAWNING ( 4 FDA reports)
RABIES ( 3 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL ADENOMA ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RECTAL STENOSIS ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
REHABILITATION THERAPY ( 3 FDA reports)
RENAL FAILURE NEONATAL ( 3 FDA reports)
RENAL HAEMATOMA ( 3 FDA reports)
RENAL OSTEODYSTROPHY ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETICULOCYTOSIS ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 3 FDA reports)
SALIVA DISCOLOURATION ( 3 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 3 FDA reports)
SCAN ABNORMAL ( 3 FDA reports)
SCAN BONE MARROW ABNORMAL ( 3 FDA reports)
SECONDARY HYPOTHYROIDISM ( 3 FDA reports)
SENILE OSTEOPOROSIS ( 3 FDA reports)
SHIGELLA TEST POSITIVE ( 3 FDA reports)
SICKLE CELL ANAEMIA ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SMALL INTESTINE OPERATION ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL ROD INSERTION ( 3 FDA reports)
SPLENIC VEIN THROMBOSIS ( 3 FDA reports)
SPONDYLOSIS ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
TINEA CAPITIS ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TOXIC OPTIC NEUROPATHY ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
TRANSPLANT ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRAUMATIC RENAL INJURY ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URETERIC CANCER ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
URINE POTASSIUM INCREASED ( 3 FDA reports)
UROBILIN URINE PRESENT ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VAGOTOMY ( 3 FDA reports)
VARICOCELE ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 3 FDA reports)
VICTIM OF SEXUAL ABUSE ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VISCERAL PAIN ( 3 FDA reports)
VITAMIN A DEFICIENCY ( 3 FDA reports)
VITAMIN D ABNORMAL ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
WOUND INFECTION BACTERIAL ( 3 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 3 FDA reports)
ACTINIC ELASTOSIS ( 3 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADRENAL CARCINOMA ( 3 FDA reports)
AGONAL DEATH STRUGGLE ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
AMINO ACID LEVEL INCREASED ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANEURYSM REPAIR ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ARTHROFIBROSIS ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ASPIRATION TRACHEAL ( 3 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
AURA ( 3 FDA reports)
BASE EXCESS DECREASED ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 3 FDA reports)
BEREAVEMENT REACTION ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BITE ( 3 FDA reports)
BLADDER CANCER STAGE III ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLAST CELLS PRESENT ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 3 FDA reports)
BONE MARROW NECROSIS ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN OPERATION ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST OPERATION ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BURN DRESSING ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC SEPTAL DEFECT ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CAROTID ENDARTERECTOMY ( 3 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 3 FDA reports)
CARTILAGE INJURY ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL SARCOIDOSIS ( 3 FDA reports)
CERVICAL SPINE FLATTENING ( 3 FDA reports)
CHEST WALL MASS ( 3 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC TONSILLITIS ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COELIAC ARTERY STENOSIS ( 3 FDA reports)
COLITIS MICROSCOPIC ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 3 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORNEAL REFLEX DECREASED ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CYTOKINE RELEASE SYNDROME ( 3 FDA reports)
DENTAL CARE ( 3 FDA reports)
DENTAL DISCOMFORT ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DENTAL PROSTHESIS USER ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS INFECTED ( 3 FDA reports)
DEVICE EXPULSION ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG THERAPY CHANGED ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
EAR CANAL ERYTHEMA ( 3 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 3 FDA reports)
EATING DISORDER SYMPTOM ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
EJECTION FRACTION ABNORMAL ( 3 FDA reports)
ELBOW OPERATION ( 3 FDA reports)
ELECTRIC SHOCK ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
EMBOLIA CUTIS MEDICAMENTOSA ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
FACTITIOUS DISORDER ( 3 FDA reports)
FAECALITH ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FLAVOBACTERIUM INFECTION ( 3 FDA reports)
FLUID IMBALANCE ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTRIC CANCER RECURRENT ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GENITAL INFECTION BACTERIAL ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GLOBULIN ABNORMAL ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS C RNA POSITIVE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HIP SWELLING ( 3 FDA reports)
HYPERCREATININAEMIA ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 3 FDA reports)
HYPERKINETIC HEART SYNDROME ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPOPITUITARISM ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
ILEOSTOMY CLOSURE ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
IMPLANT SITE INDURATION ( 3 FDA reports)
INCISION SITE COMPLICATION ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INFECTED SEBACEOUS CYST ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 3 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
INTRASPINAL ABSCESS ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
IVTH NERVE PARALYSIS ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LARYNGEAL REPAIR ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIPID METABOLISM DISORDER ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MALIGNANT RENAL HYPERTENSION ( 3 FDA reports)
MAMMARY DUCT ECTASIA ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENISCUS OPERATION ( 3 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 3 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 3 FDA reports)
MILIA ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MONONEUROPATHY MULTIPLEX ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NASAL SEPTAL OPERATION ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NECK SURGERY ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NERVE BLOCK ( 3 FDA reports)
NEUROSURGERY ( 3 FDA reports)
NEUTRALISING ANTIBODIES ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OBTURATOR HERNIA ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
ORTHOSTATIC INTOLERANCE ( 3 FDA reports)
OSTEOARTHROPATHY ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
PACEMAKER GENERATED RHYTHM ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARANOID PERSONALITY DISORDER ( 3 FDA reports)
PARATHYROIDECTOMY ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PELVIC ADHESIONS ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERICARDIAL EXCISION ( 3 FDA reports)
PERINEPHRIC COLLECTION ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PERSEVERATION ( 3 FDA reports)
PHLEBOTHROMBOSIS ( 3 FDA reports)
PLACENTA PRAEVIA ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
PLASTIC SURGERY TO THE FACE ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PNEUMOBILIA ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMOPERICARDIUM ( 3 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
POST PROCEDURAL DISCOMFORT ( 3 FDA reports)
POST PROCEDURAL NAUSEA ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTOPERATIVE THROMBOSIS ( 3 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT COMMINGLING ( 3 FDA reports)
PRODUCT CONTAMINATION ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUPUNCTURE ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADRENALITIS ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
ADVERSE EVENT FOLLOWING IMMUNISATION ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANDROGENS DECREASED ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANION GAP ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
AORTIC BYPASS ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
BASAL GANGLIA INFARCTION ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN GASTRIC NEOPLASM ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD ETHANOL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD OESTROGEN INCREASED ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BODY DYSMORPHIC DISORDER ( 2 FDA reports)
BONE ATROPHY ( 2 FDA reports)
BONE DEFORMITY ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST FEEDING ( 2 FDA reports)
BREAST INDURATION ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARCINOMA IN SITU ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CAT SCRATCH DISEASE ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 2 FDA reports)
CERUMEN REMOVAL ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL ULCER ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYSTITIS BACTERIAL ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISSOCIATIVE FUGUE ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSKINESIA NEONATAL ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
EMOTIONAL DISORDER OF CHILDHOOD ( 2 FDA reports)
EMOTIONAL POVERTY ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTEROSTOMY CLOSURE ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
ERYTHROPHAGOCYTOSIS ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYELID INFECTION ( 2 FDA reports)
FASCIOTOMY ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEMALE STERILISATION ( 2 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLOPPY IRIS SYNDROME ( 2 FDA reports)
FLUID INTAKE RESTRICTION ( 2 FDA reports)
FROSTBITE ( 2 FDA reports)
FUNDOSCOPY ABNORMAL ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 2 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART AND LUNG TRANSPLANT ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATITIS A POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 2 FDA reports)
HIV ANTIBODY POSITIVE ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HORMONE THERAPY ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILLOGICAL THINKING ( 2 FDA reports)
IMPLANT SITE DISCHARGE ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFERIOR VENA CAVA DILATATION ( 2 FDA reports)
INFLAMMATORY PSEUDOTUMOUR ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE FIBROSIS ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERNAL INJURY ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGOSCOPY ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 2 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIMB REDUCTION DEFECT ( 2 FDA reports)
LIPOMA EXCISION ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MALIGNANT MELANOMA STAGE I ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MASTOIDECTOMY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASES TO GALLBLADDER ( 2 FDA reports)
METASTASES TO MOUTH ( 2 FDA reports)
METASTASES TO MUSCLE ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
METASTASES TO THORAX ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MICROVASCULAR ANGINA ( 2 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NAIL AVULSION ( 2 FDA reports)
NAIL HYPERTROPHY ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NEEDLE TRACK MARKS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEONATAL COMPLICATIONS OF SUBSTANCE ABUSE ( 2 FDA reports)
NEONATAL PNEUMONIA ( 2 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NIPPLE SWELLING ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OCULAR TOXICITY ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPIATES ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
OSMOLAR GAP ABNORMAL ( 2 FDA reports)
OVARIAN ADHESION ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PENILE DISCHARGE ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERICARDIAL CYST ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIORBITAL HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PITUITARY ENLARGEMENT ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLEURAL DECORTICATION ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ADVANCED ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POLYCYSTIC LIVER DISEASE ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT PACKAGING ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RADIATION FIBROSIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REOCCLUSION ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RETINAL OPERATION ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 2 FDA reports)
RETROPHARYNGEAL ABSCESS ( 2 FDA reports)
RHABDOMYOSARCOMA ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSATION OF PRESSURE IN EAR ( 2 FDA reports)
SERRATIA TEST POSITIVE ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SINUS ANTROSTOMY ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SKULL X-RAY ABNORMAL ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SNAKE BITE ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE NEOPLASM ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SPERMATOGENESIS ABNORMAL ( 2 FDA reports)
SPINA BIFIDA ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC INFECTION ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TAENIASIS ( 2 FDA reports)
TARSAL TUNNEL DECOMPRESSION ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
THYROIDITIS CHRONIC ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 2 FDA reports)
TUBO-OVARIAN ABSCESS ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC INJURY ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINE AMPHETAMINE POSITIVE ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
URINE OUTPUT ( 2 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARIANT CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VASECTOMY ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VERTEBRAL INJURY ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVAL OEDEMA ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADICULOTOMY ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL TUBE INSERTION ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL AND PANCREAS TRANSPLANT ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CANCER RECURRENT ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY RATE ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHABDOMYOSARCOMA RECURRENT ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SARCOPENIA ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL IRRITATION ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEROCONVERSION TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOPLIFTING ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, HYPERSOMNIA TYPE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL CORD OPERATION ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STENT RELATED INFECTION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SUPPORTIVE CARE ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST DECREASED ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THORACOSTOMY ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONSILLITIS BACTERIAL ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRIGEMINAL NERVE ABLATION ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIGEMINAL PALSY ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TYMPANOMETRY ABNORMAL ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNDERSENSING ( 1 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERIC OPERATION ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE BARBITURATES INCREASED ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VACTERL SYNDROME ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL OEDEMA ( 1 FDA reports)
VAGINITIS GARDNERELLA ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULAR TEST ABNORMAL ( 1 FDA reports)
VENOMOUS BITE ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
VULVOVAGINITIS STREPTOCOCCAL ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 1 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE HIV INFECTION ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL GLAND INJURY ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AIR-BORNE TRANSMISSION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMYLASE ABNORMAL ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APACHE II SCORE ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE ODOUR ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PERSPIRATION ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTHRITIS VIRAL ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROPOD INFESTATION ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL PERICARDITIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BATTERED WIFE ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY BRAIN NORMAL ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER CANCER STAGE II ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CADMIUM INCREASED ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CARBON MONOXIDE ABNORMAL ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES DECREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOOD ZINC INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC PACEMAKER REMOVAL ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIAC VALVE RUPTURE ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHONDROLYSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMA BLISTER ( 1 FDA reports)
COMPLEMENT FACTOR C1 DECREASED ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIVE HOARDING ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE OPERATION ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF SHUNT OPERATION ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEATH OF PET ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUGLAS' ABSCESS ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG IMPLANTATION ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
EAR CANAL INJURY ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EGOBRONCHOPHONY ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMPYEMA DRAINAGE ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCLYSIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
EX-DRUG ABUSER ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EXTRINSIC ILIAC VEIN COMPRESSION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FAMILIAL RISK FACTOR ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FINGER REPAIR OPERATION ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOPERICYTOMA ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPANGINA ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMANS' SIGN POSITIVE ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN VITRO FERTILISATION ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PUSTULE ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL FISTULA INFECTION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTRAOSSEOUS ANGIOMA ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
K-RAS GENE MUTATION ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEAD URINE INCREASED ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBARISATION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS MYOCARDITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 1 FDA reports)
LYMPHANGIOMA ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOMA CUTIS ( 1 FDA reports)
LYMPHOMA TRANSFORMATION ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACRODACTYLY ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MAXILLOFACIAL SINUS NEOPLASM ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELANAEMIA ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENSTRUATION NORMAL ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT RECURRENT ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO DIAPHRAGM ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS I ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL NECROSIS ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MURDER ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOGLOBIN URINE ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
MYXOEDEMA COMA ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NATURAL KILLER-CELL LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEOLOGISM ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 1 FDA reports)
NEOPLASM OF APPENDIX ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NOREPINEPHRINE DECREASED ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL POLYPECTOMY ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
ORBITAL CYST ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN FIBROMA ( 1 FDA reports)
OVARIAN HAEMORRHAGE ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAIN THRESHOLD DECREASED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALINDROMIC RHEUMATISM ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC SPHINCTEROTOMY ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE VEIN THROMBOSIS ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIORBITAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PICA ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY AMYLOIDOSIS ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PRODUCT DISTRIBUTION ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY AIR LEAKAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)