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

NAUSEA ( 1785 FDA reports)
PAIN ( 1657 FDA reports)
DYSPNOEA ( 1570 FDA reports)
VOMITING ( 1441 FDA reports)
DIARRHOEA ( 1335 FDA reports)
ANXIETY ( 1321 FDA reports)
FATIGUE ( 1233 FDA reports)
DIZZINESS ( 1114 FDA reports)
PYREXIA ( 1065 FDA reports)
DRUG INEFFECTIVE ( 1052 FDA reports)
CHEST PAIN ( 1003 FDA reports)
HEADACHE ( 993 FDA reports)
ASTHENIA ( 984 FDA reports)
DEPRESSION ( 981 FDA reports)
FALL ( 966 FDA reports)
ANAEMIA ( 920 FDA reports)
HYPERTENSION ( 917 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 894 FDA reports)
BACK PAIN ( 870 FDA reports)
PNEUMONIA ( 870 FDA reports)
ABDOMINAL PAIN ( 866 FDA reports)
WEIGHT DECREASED ( 820 FDA reports)
PAIN IN EXTREMITY ( 768 FDA reports)
ARTHRALGIA ( 759 FDA reports)
INJURY ( 718 FDA reports)
OEDEMA PERIPHERAL ( 711 FDA reports)
INSOMNIA ( 704 FDA reports)
CONSTIPATION ( 694 FDA reports)
ABDOMINAL PAIN UPPER ( 683 FDA reports)
MYOCARDIAL INFARCTION ( 656 FDA reports)
HYPOTENSION ( 642 FDA reports)
MALAISE ( 642 FDA reports)
DYSPEPSIA ( 635 FDA reports)
RASH ( 628 FDA reports)
DEHYDRATION ( 598 FDA reports)
COUGH ( 589 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 558 FDA reports)
HYPOAESTHESIA ( 547 FDA reports)
EMOTIONAL DISTRESS ( 546 FDA reports)
CEREBROVASCULAR ACCIDENT ( 529 FDA reports)
OSTEONECROSIS OF JAW ( 522 FDA reports)
RENAL FAILURE ( 518 FDA reports)
URINARY TRACT INFECTION ( 514 FDA reports)
OSTEOARTHRITIS ( 501 FDA reports)
PRURITUS ( 500 FDA reports)
DECREASED APPETITE ( 494 FDA reports)
OSTEOMYELITIS ( 485 FDA reports)
RENAL FAILURE ACUTE ( 464 FDA reports)
WEIGHT INCREASED ( 460 FDA reports)
BONE DISORDER ( 459 FDA reports)
PLEURAL EFFUSION ( 433 FDA reports)
MUSCLE SPASMS ( 431 FDA reports)
DYSPHAGIA ( 419 FDA reports)
CONVULSION ( 416 FDA reports)
GAIT DISTURBANCE ( 415 FDA reports)
ERYTHEMA ( 411 FDA reports)
CHOLELITHIASIS ( 401 FDA reports)
INFECTION ( 397 FDA reports)
CORONARY ARTERY DISEASE ( 395 FDA reports)
THROMBOCYTOPENIA ( 395 FDA reports)
DEEP VEIN THROMBOSIS ( 390 FDA reports)
SOMNOLENCE ( 389 FDA reports)
PAIN IN JAW ( 387 FDA reports)
MYALGIA ( 386 FDA reports)
PARAESTHESIA ( 385 FDA reports)
ANHEDONIA ( 383 FDA reports)
CONDITION AGGRAVATED ( 379 FDA reports)
CONFUSIONAL STATE ( 378 FDA reports)
DEATH ( 375 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 374 FDA reports)
LOSS OF CONSCIOUSNESS ( 368 FDA reports)
PALPITATIONS ( 368 FDA reports)
RESPIRATORY FAILURE ( 365 FDA reports)
BRONCHITIS ( 356 FDA reports)
SINUSITIS ( 351 FDA reports)
BLOOD GLUCOSE INCREASED ( 348 FDA reports)
DIABETES MELLITUS ( 347 FDA reports)
HYPERSENSITIVITY ( 345 FDA reports)
ATRIAL FIBRILLATION ( 343 FDA reports)
TOOTH EXTRACTION ( 343 FDA reports)
CELLULITIS ( 338 FDA reports)
OSTEONECROSIS ( 337 FDA reports)
FEELING ABNORMAL ( 330 FDA reports)
HAEMOGLOBIN DECREASED ( 327 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 325 FDA reports)
NEUROPATHY PERIPHERAL ( 325 FDA reports)
SEPSIS ( 324 FDA reports)
SPINAL OSTEOARTHRITIS ( 324 FDA reports)
CONTUSION ( 321 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 319 FDA reports)
CHEST DISCOMFORT ( 314 FDA reports)
BLOOD PRESSURE INCREASED ( 313 FDA reports)
HYPERHIDROSIS ( 313 FDA reports)
BLOOD CREATININE INCREASED ( 311 FDA reports)
SYNCOPE ( 311 FDA reports)
INTERSTITIAL LUNG DISEASE ( 309 FDA reports)
VISION BLURRED ( 309 FDA reports)
OSTEOPOROSIS ( 307 FDA reports)
SWELLING ( 307 FDA reports)
HYPERLIPIDAEMIA ( 305 FDA reports)
ABDOMINAL DISCOMFORT ( 304 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 300 FDA reports)
PLATELET COUNT DECREASED ( 299 FDA reports)
GASTRITIS ( 296 FDA reports)
MITRAL VALVE INCOMPETENCE ( 294 FDA reports)
CHILLS ( 292 FDA reports)
MUSCULAR WEAKNESS ( 292 FDA reports)
ASTHMA ( 290 FDA reports)
PULMONARY EMBOLISM ( 290 FDA reports)
TREMOR ( 287 FDA reports)
ABDOMINAL DISTENSION ( 286 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 283 FDA reports)
NEUTROPENIA ( 281 FDA reports)
PANCYTOPENIA ( 281 FDA reports)
URTICARIA ( 278 FDA reports)
BLOOD PRESSURE DECREASED ( 274 FDA reports)
DRY MOUTH ( 273 FDA reports)
STOMATITIS ( 273 FDA reports)
NECK PAIN ( 268 FDA reports)
CARDIAC ARREST ( 267 FDA reports)
ARTHRITIS ( 265 FDA reports)
FLUSHING ( 264 FDA reports)
CHOLECYSTITIS CHRONIC ( 262 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 262 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 261 FDA reports)
BONE LESION ( 257 FDA reports)
HYPOKALAEMIA ( 256 FDA reports)
HEART RATE INCREASED ( 254 FDA reports)
OSTEOPENIA ( 254 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 251 FDA reports)
HIATUS HERNIA ( 251 FDA reports)
HAEMORRHOIDS ( 249 FDA reports)
ATELECTASIS ( 247 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 247 FDA reports)
OEDEMA ( 246 FDA reports)
SWELLING FACE ( 246 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 245 FDA reports)
IMPAIRED HEALING ( 239 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 237 FDA reports)
TACHYCARDIA ( 236 FDA reports)
DRUG DOSE OMISSION ( 229 FDA reports)
FEBRILE NEUTROPENIA ( 227 FDA reports)
RECTAL HAEMORRHAGE ( 222 FDA reports)
BONE PAIN ( 221 FDA reports)
OVERDOSE ( 217 FDA reports)
NEPHROLITHIASIS ( 216 FDA reports)
BALANCE DISORDER ( 215 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 213 FDA reports)
ORAL PAIN ( 208 FDA reports)
ANGINA PECTORIS ( 207 FDA reports)
GALLBLADDER DISORDER ( 207 FDA reports)
MUSCULOSKELETAL PAIN ( 207 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 207 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 205 FDA reports)
AMNESIA ( 204 FDA reports)
EPISTAXIS ( 204 FDA reports)
CARDIOMEGALY ( 201 FDA reports)
ALOPECIA ( 199 FDA reports)
ARRHYTHMIA ( 197 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 196 FDA reports)
JOINT SWELLING ( 196 FDA reports)
ANOREXIA ( 195 FDA reports)
METASTASES TO BONE ( 194 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 194 FDA reports)
PULMONARY OEDEMA ( 194 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 193 FDA reports)
SLEEP APNOEA SYNDROME ( 193 FDA reports)
MENTAL STATUS CHANGES ( 192 FDA reports)
DISEASE PROGRESSION ( 191 FDA reports)
DRUG INTERACTION ( 191 FDA reports)
HERPES ZOSTER ( 191 FDA reports)
DEFORMITY ( 190 FDA reports)
OROPHARYNGEAL PAIN ( 190 FDA reports)
HYPERCHOLESTEROLAEMIA ( 189 FDA reports)
HAEMATURIA ( 186 FDA reports)
CARDIAC DISORDER ( 185 FDA reports)
RENAL IMPAIRMENT ( 184 FDA reports)
ANAPHYLACTIC SHOCK ( 183 FDA reports)
MULTI-ORGAN FAILURE ( 182 FDA reports)
RENAL FAILURE CHRONIC ( 181 FDA reports)
STRESS ( 181 FDA reports)
MEMORY IMPAIRMENT ( 180 FDA reports)
WHEEZING ( 180 FDA reports)
DYSURIA ( 179 FDA reports)
AGITATION ( 176 FDA reports)
HYPOPHAGIA ( 175 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 174 FDA reports)
EXOSTOSIS ( 173 FDA reports)
HYPERGLYCAEMIA ( 173 FDA reports)
SPEECH DISORDER ( 173 FDA reports)
DIVERTICULUM ( 172 FDA reports)
HAEMORRHAGE ( 172 FDA reports)
CARDIAC MURMUR ( 171 FDA reports)
DRUG HYPERSENSITIVITY ( 171 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 171 FDA reports)
PANCREATITIS ( 169 FDA reports)
CATARACT ( 168 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 167 FDA reports)
LETHARGY ( 166 FDA reports)
BLOOD UREA INCREASED ( 165 FDA reports)
CARDIAC FAILURE ( 164 FDA reports)
HAEMATOCRIT DECREASED ( 164 FDA reports)
LIVER DISORDER ( 164 FDA reports)
POLLAKIURIA ( 162 FDA reports)
SUICIDAL IDEATION ( 162 FDA reports)
STAPHYLOCOCCAL INFECTION ( 161 FDA reports)
URINARY INCONTINENCE ( 161 FDA reports)
TOOTHACHE ( 160 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 159 FDA reports)
DYSGEUSIA ( 159 FDA reports)
DYSPNOEA EXERTIONAL ( 159 FDA reports)
MIGRAINE ( 159 FDA reports)
DYSPHONIA ( 157 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 157 FDA reports)
TYPE 2 DIABETES MELLITUS ( 157 FDA reports)
RIB FRACTURE ( 156 FDA reports)
HYPONATRAEMIA ( 155 FDA reports)
MUCOSAL INFLAMMATION ( 155 FDA reports)
COMPRESSION FRACTURE ( 154 FDA reports)
ROAD TRAFFIC ACCIDENT ( 154 FDA reports)
OXYGEN SATURATION DECREASED ( 152 FDA reports)
RESPIRATORY DISTRESS ( 152 FDA reports)
LUNG NEOPLASM ( 151 FDA reports)
NASOPHARYNGITIS ( 151 FDA reports)
DRUG DEPENDENCE ( 150 FDA reports)
LYMPHADENOPATHY ( 150 FDA reports)
ANAPHYLACTIC REACTION ( 148 FDA reports)
DENTAL CARIES ( 148 FDA reports)
DISCOMFORT ( 147 FDA reports)
LUNG DISORDER ( 147 FDA reports)
OSTEITIS ( 147 FDA reports)
BONE DENSITY DECREASED ( 146 FDA reports)
FEAR ( 145 FDA reports)
HEPATIC STEATOSIS ( 145 FDA reports)
JAW DISORDER ( 145 FDA reports)
NEOPLASM MALIGNANT ( 145 FDA reports)
FLATULENCE ( 144 FDA reports)
MEDICATION ERROR ( 144 FDA reports)
GASTROINTESTINAL DISORDER ( 143 FDA reports)
PRIMARY SEQUESTRUM ( 143 FDA reports)
SINUS TACHYCARDIA ( 143 FDA reports)
HEPATIC ENZYME INCREASED ( 142 FDA reports)
HOT FLUSH ( 142 FDA reports)
VISUAL IMPAIRMENT ( 142 FDA reports)
COLITIS ( 141 FDA reports)
HEART RATE IRREGULAR ( 141 FDA reports)
HEPATIC FAILURE ( 140 FDA reports)
HYPOGLYCAEMIA ( 140 FDA reports)
TENDONITIS ( 140 FDA reports)
UNEVALUABLE EVENT ( 140 FDA reports)
HAEMATOCHEZIA ( 139 FDA reports)
BLOOD POTASSIUM DECREASED ( 138 FDA reports)
GASTRIC ULCER ( 138 FDA reports)
HYPOXIA ( 138 FDA reports)
BRADYCARDIA ( 137 FDA reports)
NERVOUSNESS ( 136 FDA reports)
PRODUCTIVE COUGH ( 136 FDA reports)
TOOTH DISORDER ( 136 FDA reports)
TINNITUS ( 135 FDA reports)
TOOTH ABSCESS ( 135 FDA reports)
BURNING SENSATION ( 135 FDA reports)
GINGIVITIS ( 135 FDA reports)
BURSITIS ( 132 FDA reports)
DYSARTHRIA ( 132 FDA reports)
HIP FRACTURE ( 132 FDA reports)
INFLAMMATION ( 132 FDA reports)
MULTIPLE MYELOMA ( 132 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 132 FDA reports)
RHINORRHOEA ( 132 FDA reports)
SLEEP DISORDER ( 132 FDA reports)
THROMBOSIS ( 132 FDA reports)
INFUSION RELATED REACTION ( 131 FDA reports)
PERIODONTAL DISEASE ( 131 FDA reports)
SCOLIOSIS ( 131 FDA reports)
CARPAL TUNNEL SYNDROME ( 130 FDA reports)
HYPOTHYROIDISM ( 130 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 130 FDA reports)
FOOT FRACTURE ( 129 FDA reports)
HALLUCINATION ( 129 FDA reports)
SEPTIC SHOCK ( 129 FDA reports)
TOOTH LOSS ( 129 FDA reports)
HYPERKALAEMIA ( 128 FDA reports)
NEUTROPHIL COUNT DECREASED ( 128 FDA reports)
RHABDOMYOLYSIS ( 127 FDA reports)
SPINAL COMPRESSION FRACTURE ( 127 FDA reports)
VERTIGO ( 126 FDA reports)
SPINAL COLUMN STENOSIS ( 125 FDA reports)
CANDIDIASIS ( 124 FDA reports)
PANIC ATTACK ( 124 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 123 FDA reports)
HAEMATEMESIS ( 123 FDA reports)
LEUKOPENIA ( 123 FDA reports)
ARTERIOSCLEROSIS ( 122 FDA reports)
ASCITES ( 122 FDA reports)
BONE DEBRIDEMENT ( 122 FDA reports)
FEELING HOT ( 122 FDA reports)
PRODUCT QUALITY ISSUE ( 122 FDA reports)
INFLUENZA LIKE ILLNESS ( 121 FDA reports)
IRRITABILITY ( 121 FDA reports)
PULMONARY HYPERTENSION ( 121 FDA reports)
CARDIO-RESPIRATORY ARREST ( 120 FDA reports)
CHOLECYSTITIS ( 120 FDA reports)
JAUNDICE ( 119 FDA reports)
RESPIRATORY DISORDER ( 119 FDA reports)
SHOCK ( 119 FDA reports)
SKIN LESION ( 119 FDA reports)
GINGIVAL BLEEDING ( 118 FDA reports)
OESOPHAGITIS ( 118 FDA reports)
BLOOD BILIRUBIN INCREASED ( 117 FDA reports)
DIVERTICULITIS ( 117 FDA reports)
TENDERNESS ( 117 FDA reports)
MELAENA ( 116 FDA reports)
NASAL CONGESTION ( 116 FDA reports)
CEREBRAL INFARCTION ( 115 FDA reports)
COLONIC POLYP ( 115 FDA reports)
CORONARY ARTERY OCCLUSION ( 115 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 115 FDA reports)
HEAD INJURY ( 115 FDA reports)
JAW OPERATION ( 115 FDA reports)
DRY EYE ( 114 FDA reports)
GOITRE ( 113 FDA reports)
IRRITABLE BOWEL SYNDROME ( 113 FDA reports)
VIRAL INFECTION ( 113 FDA reports)
ULCER ( 112 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 112 FDA reports)
DISABILITY ( 112 FDA reports)
POST PROCEDURAL COMPLICATION ( 112 FDA reports)
SINUS DISORDER ( 112 FDA reports)
DYSKINESIA ( 111 FDA reports)
FISTULA ( 111 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 110 FDA reports)
ECONOMIC PROBLEM ( 110 FDA reports)
MOUTH ULCERATION ( 110 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 109 FDA reports)
INCORRECT DOSE ADMINISTERED ( 109 FDA reports)
MENTAL DISORDER ( 109 FDA reports)
ORAL INFECTION ( 109 FDA reports)
ANGINA UNSTABLE ( 108 FDA reports)
ATRIAL SEPTAL DEFECT ( 108 FDA reports)
CHRONIC SINUSITIS ( 108 FDA reports)
EAR PAIN ( 108 FDA reports)
EJECTION FRACTION DECREASED ( 108 FDA reports)
LUNG INFILTRATION ( 108 FDA reports)
MASS ( 108 FDA reports)
RENAL CYST ( 108 FDA reports)
SCAR ( 108 FDA reports)
VENTRICULAR HYPERTROPHY ( 108 FDA reports)
PNEUMOTHORAX ( 107 FDA reports)
ADVERSE EVENT ( 106 FDA reports)
FACIAL PAIN ( 106 FDA reports)
HAEMOPTYSIS ( 106 FDA reports)
INFLUENZA ( 106 FDA reports)
MASTICATION DISORDER ( 105 FDA reports)
NIGHT SWEATS ( 105 FDA reports)
ROTATOR CUFF SYNDROME ( 105 FDA reports)
CARDIOVASCULAR DISORDER ( 104 FDA reports)
RASH ERYTHEMATOUS ( 104 FDA reports)
RHINITIS ALLERGIC ( 103 FDA reports)
ARTHROPATHY ( 102 FDA reports)
CYANOSIS ( 102 FDA reports)
DEBRIDEMENT ( 102 FDA reports)
DISORIENTATION ( 102 FDA reports)
GASTRIC DISORDER ( 102 FDA reports)
FUNGAL INFECTION ( 101 FDA reports)
DRUG EFFECT DECREASED ( 100 FDA reports)
INJECTION SITE PAIN ( 100 FDA reports)
PNEUMONIA ASPIRATION ( 100 FDA reports)
AGGRESSION ( 99 FDA reports)
TOOTH INFECTION ( 99 FDA reports)
URINARY RETENTION ( 98 FDA reports)
VISUAL ACUITY REDUCED ( 98 FDA reports)
AORTIC VALVE INCOMPETENCE ( 98 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 98 FDA reports)
GOUT ( 97 FDA reports)
RASH GENERALISED ( 96 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 96 FDA reports)
CYST ( 95 FDA reports)
DECREASED INTEREST ( 95 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 95 FDA reports)
FAECES DISCOLOURED ( 95 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 95 FDA reports)
MYOCARDIAL ISCHAEMIA ( 95 FDA reports)
RASH PRURITIC ( 95 FDA reports)
RESPIRATORY ARREST ( 95 FDA reports)
ABASIA ( 94 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 94 FDA reports)
INCONTINENCE ( 94 FDA reports)
OFF LABEL USE ( 94 FDA reports)
GASTROENTERITIS ( 93 FDA reports)
FAILURE TO THRIVE ( 92 FDA reports)
METABOLIC ACIDOSIS ( 92 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 91 FDA reports)
DENTURE WEARER ( 91 FDA reports)
EMPHYSEMA ( 91 FDA reports)
HAEMATOMA ( 91 FDA reports)
MOBILITY DECREASED ( 91 FDA reports)
RENAL INJURY ( 91 FDA reports)
VENTRICULAR FIBRILLATION ( 91 FDA reports)
FEMUR FRACTURE ( 90 FDA reports)
OBESITY ( 90 FDA reports)
HYDRONEPHROSIS ( 89 FDA reports)
THROAT IRRITATION ( 89 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 89 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 88 FDA reports)
CARDIOMYOPATHY ( 88 FDA reports)
PERICARDIAL EFFUSION ( 88 FDA reports)
RENAL DISORDER ( 88 FDA reports)
CYSTITIS ( 87 FDA reports)
DELIRIUM ( 87 FDA reports)
HYPERCALCAEMIA ( 86 FDA reports)
ILL-DEFINED DISORDER ( 86 FDA reports)
SURGERY ( 86 FDA reports)
CIRCULATORY COLLAPSE ( 85 FDA reports)
INTESTINAL OBSTRUCTION ( 85 FDA reports)
MALNUTRITION ( 85 FDA reports)
PHYSICAL DISABILITY ( 85 FDA reports)
RESTLESS LEGS SYNDROME ( 85 FDA reports)
BASAL CELL CARCINOMA ( 84 FDA reports)
BLOOD SODIUM DECREASED ( 84 FDA reports)
BONE MARROW FAILURE ( 84 FDA reports)
COAGULOPATHY ( 84 FDA reports)
CORONARY ARTERY STENOSIS ( 84 FDA reports)
ECZEMA ( 84 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 84 FDA reports)
PALLOR ( 84 FDA reports)
PATHOLOGICAL FRACTURE ( 84 FDA reports)
BLOOD GLUCOSE DECREASED ( 83 FDA reports)
GLAUCOMA ( 83 FDA reports)
GROIN PAIN ( 83 FDA reports)
LOOSE TOOTH ( 83 FDA reports)
LUMBAR SPINAL STENOSIS ( 83 FDA reports)
METASTASES TO LIVER ( 83 FDA reports)
SWOLLEN TONGUE ( 83 FDA reports)
TREATMENT NONCOMPLIANCE ( 83 FDA reports)
GINGIVAL DISORDER ( 82 FDA reports)
HYPOMAGNESAEMIA ( 82 FDA reports)
ACUTE RESPIRATORY FAILURE ( 81 FDA reports)
CEREBRAL ATROPHY ( 81 FDA reports)
CROHN'S DISEASE ( 81 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 81 FDA reports)
DRUG SCREEN POSITIVE ( 81 FDA reports)
INJECTION SITE ERYTHEMA ( 81 FDA reports)
JOINT EFFUSION ( 81 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 81 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 81 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 80 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 80 FDA reports)
LACERATION ( 80 FDA reports)
LIFE EXPECTANCY SHORTENED ( 80 FDA reports)
OSTEOLYSIS ( 80 FDA reports)
RHEUMATOID ARTHRITIS ( 80 FDA reports)
BACTERAEMIA ( 79 FDA reports)
EAR INFECTION ( 79 FDA reports)
EATING DISORDER ( 79 FDA reports)
ENCEPHALOPATHY ( 79 FDA reports)
ERUCTATION ( 79 FDA reports)
JOINT INJURY ( 79 FDA reports)
PHARYNGEAL OEDEMA ( 79 FDA reports)
SINUS CONGESTION ( 79 FDA reports)
SKIN DISORDER ( 79 FDA reports)
SKIN EXFOLIATION ( 79 FDA reports)
VITAMIN D DEFICIENCY ( 79 FDA reports)
DRUG TOXICITY ( 78 FDA reports)
EXCORIATION ( 78 FDA reports)
ANGER ( 77 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 77 FDA reports)
BLOOD CALCIUM DECREASED ( 77 FDA reports)
MUSCLE TWITCHING ( 77 FDA reports)
RADICULOPATHY ( 77 FDA reports)
SCIATICA ( 77 FDA reports)
SINUS BRADYCARDIA ( 77 FDA reports)
SKIN ULCER ( 77 FDA reports)
STEVENS-JOHNSON SYNDROME ( 77 FDA reports)
STOMACH DISCOMFORT ( 77 FDA reports)
CHOKING ( 76 FDA reports)
DIPLOPIA ( 76 FDA reports)
GINGIVAL PAIN ( 76 FDA reports)
ILEUS ( 76 FDA reports)
KYPHOSIS ( 76 FDA reports)
PANCREATITIS ACUTE ( 76 FDA reports)
TARDIVE DYSKINESIA ( 76 FDA reports)
THROAT TIGHTNESS ( 75 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 75 FDA reports)
NERVOUS SYSTEM DISORDER ( 75 FDA reports)
OEDEMA MOUTH ( 75 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 75 FDA reports)
PROTHROMBIN TIME PROLONGED ( 75 FDA reports)
ACTINIC KERATOSIS ( 74 FDA reports)
BLINDNESS ( 74 FDA reports)
CHOLECYSTECTOMY ( 74 FDA reports)
DERMATITIS ( 74 FDA reports)
LEUKOCYTOSIS ( 74 FDA reports)
PLASMACYTOMA ( 74 FDA reports)
RESTLESSNESS ( 74 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 74 FDA reports)
THYROID NEOPLASM ( 73 FDA reports)
WALKING AID USER ( 73 FDA reports)
CAROTID ARTERY STENOSIS ( 73 FDA reports)
DEMENTIA ( 73 FDA reports)
DISTURBANCE IN ATTENTION ( 73 FDA reports)
DRY SKIN ( 73 FDA reports)
FAECAL INCONTINENCE ( 73 FDA reports)
HEPATOMEGALY ( 73 FDA reports)
SEBORRHOEIC KERATOSIS ( 73 FDA reports)
SKIN DISCOLOURATION ( 73 FDA reports)
BLOOD ALBUMIN DECREASED ( 72 FDA reports)
CEREBRAL ISCHAEMIA ( 72 FDA reports)
CRYING ( 72 FDA reports)
EMOTIONAL DISORDER ( 72 FDA reports)
ERECTILE DYSFUNCTION ( 72 FDA reports)
FIBROMYALGIA ( 72 FDA reports)
FLANK PAIN ( 72 FDA reports)
FLUID OVERLOAD ( 72 FDA reports)
MITRAL VALVE PROLAPSE ( 72 FDA reports)
MUSCLE STRAIN ( 72 FDA reports)
NEURALGIA ( 71 FDA reports)
UNRESPONSIVE TO STIMULI ( 71 FDA reports)
VAGINAL HAEMORRHAGE ( 71 FDA reports)
ANKLE FRACTURE ( 70 FDA reports)
APHAGIA ( 70 FDA reports)
JAW FRACTURE ( 70 FDA reports)
METASTASES TO SPINE ( 70 FDA reports)
NOCTURIA ( 70 FDA reports)
RHINITIS ( 70 FDA reports)
BLISTER ( 69 FDA reports)
CHOLECYSTITIS ACUTE ( 69 FDA reports)
ORAL CANDIDIASIS ( 69 FDA reports)
PULMONARY CONGESTION ( 69 FDA reports)
ANGIOEDEMA ( 68 FDA reports)
EYE PAIN ( 68 FDA reports)
PULMONARY FIBROSIS ( 68 FDA reports)
ABDOMINAL PAIN LOWER ( 67 FDA reports)
CEREBRAL HAEMORRHAGE ( 67 FDA reports)
ECCHYMOSIS ( 67 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 67 FDA reports)
SUICIDE ATTEMPT ( 67 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 67 FDA reports)
TOOTH FRACTURE ( 67 FDA reports)
VENTRICULAR TACHYCARDIA ( 66 FDA reports)
ASPIRATION ( 66 FDA reports)
JOINT STIFFNESS ( 66 FDA reports)
ABNORMAL DREAMS ( 65 FDA reports)
DENTAL OPERATION ( 65 FDA reports)
HYPOCALCAEMIA ( 65 FDA reports)
ISCHAEMIA ( 65 FDA reports)
OSTEOSCLEROSIS ( 65 FDA reports)
PNEUMONITIS ( 65 FDA reports)
RESPIRATORY TRACT INFECTION ( 65 FDA reports)
SPINAL FRACTURE ( 65 FDA reports)
BILIARY DYSKINESIA ( 64 FDA reports)
DEAFNESS ( 64 FDA reports)
DRUG ERUPTION ( 64 FDA reports)
FEELING JITTERY ( 64 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 64 FDA reports)
GINGIVAL SWELLING ( 64 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 64 FDA reports)
APHASIA ( 63 FDA reports)
HYPOVOLAEMIA ( 63 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 63 FDA reports)
PEPTIC ULCER ( 63 FDA reports)
ADVERSE DRUG REACTION ( 62 FDA reports)
CARDIOGENIC SHOCK ( 62 FDA reports)
COMA ( 62 FDA reports)
FIBROSIS ( 62 FDA reports)
SPLENOMEGALY ( 62 FDA reports)
CERVICAL SPINAL STENOSIS ( 61 FDA reports)
MOOD ALTERED ( 61 FDA reports)
ORAL DISORDER ( 61 FDA reports)
COLD SWEAT ( 60 FDA reports)
DYSLIPIDAEMIA ( 60 FDA reports)
INJECTION SITE HAEMORRHAGE ( 60 FDA reports)
IRON DEFICIENCY ANAEMIA ( 60 FDA reports)
LYMPHOMA ( 60 FDA reports)
OTITIS MEDIA ( 60 FDA reports)
TONGUE DISORDER ( 60 FDA reports)
URINE OUTPUT DECREASED ( 59 FDA reports)
ABNORMAL BEHAVIOUR ( 59 FDA reports)
ACUTE CORONARY SYNDROME ( 59 FDA reports)
FACE OEDEMA ( 59 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 59 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 59 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 59 FDA reports)
SEDATION ( 59 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 58 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 58 FDA reports)
EXPOSED BONE IN JAW ( 58 FDA reports)
HAEMODIALYSIS ( 58 FDA reports)
RETCHING ( 58 FDA reports)
SPINAL DISORDER ( 58 FDA reports)
ABSCESS JAW ( 57 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 57 FDA reports)
ORAL HERPES ( 57 FDA reports)
PHARYNGITIS ( 57 FDA reports)
PLEURITIC PAIN ( 57 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 57 FDA reports)
PSORIASIS ( 57 FDA reports)
PURULENT DISCHARGE ( 57 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 57 FDA reports)
ACTINOMYCOSIS ( 56 FDA reports)
COLITIS ULCERATIVE ( 56 FDA reports)
DERMAL CYST ( 56 FDA reports)
DIABETIC NEUROPATHY ( 56 FDA reports)
HEPATITIS ( 56 FDA reports)
LUNG NEOPLASM MALIGNANT ( 56 FDA reports)
RESPIRATORY RATE INCREASED ( 56 FDA reports)
THIRST ( 56 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 55 FDA reports)
DIASTOLIC DYSFUNCTION ( 55 FDA reports)
DRUG ADMINISTRATION ERROR ( 55 FDA reports)
LOBAR PNEUMONIA ( 55 FDA reports)
MICTURITION URGENCY ( 55 FDA reports)
MOVEMENT DISORDER ( 55 FDA reports)
ONYCHOMYCOSIS ( 55 FDA reports)
PERIODONTITIS ( 55 FDA reports)
RASH MACULAR ( 55 FDA reports)
BACTERIAL INFECTION ( 54 FDA reports)
BREAST CANCER ( 54 FDA reports)
DISEASE RECURRENCE ( 54 FDA reports)
MOUTH HAEMORRHAGE ( 54 FDA reports)
NEOPLASM PROGRESSION ( 54 FDA reports)
AZOTAEMIA ( 53 FDA reports)
FLUID RETENTION ( 53 FDA reports)
HEART RATE DECREASED ( 53 FDA reports)
HEMIPARESIS ( 53 FDA reports)
LUNG INFECTION ( 53 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 53 FDA reports)
POLYURIA ( 53 FDA reports)
BODY TEMPERATURE INCREASED ( 52 FDA reports)
BREATH ODOUR ( 52 FDA reports)
GASTROENTERITIS VIRAL ( 52 FDA reports)
GINGIVAL RECESSION ( 52 FDA reports)
HYPOACUSIS ( 52 FDA reports)
TACHYPNOEA ( 52 FDA reports)
APNOEA ( 51 FDA reports)
BEDRIDDEN ( 51 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 51 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 51 FDA reports)
FEELING COLD ( 51 FDA reports)
FRACTURE NONUNION ( 51 FDA reports)
GRAND MAL CONVULSION ( 51 FDA reports)
MUSCLE CRAMP ( 51 FDA reports)
OESOPHAGEAL DISORDER ( 51 FDA reports)
ORTHOSTATIC HYPOTENSION ( 51 FDA reports)
PHLEBITIS ( 51 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 51 FDA reports)
BREAST CANCER METASTATIC ( 50 FDA reports)
BRONCHOSPASM ( 50 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 50 FDA reports)
DIALYSIS ( 50 FDA reports)
DIFFICULTY IN WALKING ( 50 FDA reports)
DIVERTICULUM INTESTINAL ( 50 FDA reports)
ELECTROLYTE IMBALANCE ( 50 FDA reports)
HALLUCINATION, VISUAL ( 50 FDA reports)
INADEQUATE ANALGESIA ( 50 FDA reports)
LOCAL SWELLING ( 50 FDA reports)
MAJOR DEPRESSION ( 50 FDA reports)
MULTIPLE INJURIES ( 50 FDA reports)
PREGNANCY ( 50 FDA reports)
PRURITUS GENERALISED ( 50 FDA reports)
PYELONEPHRITIS ( 50 FDA reports)
SPONDYLOLISTHESIS ( 50 FDA reports)
VISUAL DISTURBANCE ( 50 FDA reports)
WOUND DEHISCENCE ( 49 FDA reports)
ACCIDENTAL OVERDOSE ( 49 FDA reports)
COORDINATION ABNORMAL ( 49 FDA reports)
FACET JOINT SYNDROME ( 49 FDA reports)
INTENTIONAL DRUG MISUSE ( 49 FDA reports)
NIGHTMARE ( 49 FDA reports)
OVARIAN CYST ( 49 FDA reports)
BLOOD POTASSIUM INCREASED ( 48 FDA reports)
BONE LOSS ( 48 FDA reports)
EOSINOPHIL COUNT INCREASED ( 48 FDA reports)
FRACTURE ( 48 FDA reports)
HALLUCINATION, AUDITORY ( 48 FDA reports)
HYPOKINESIA ( 48 FDA reports)
LIMB DISCOMFORT ( 48 FDA reports)
METASTASES TO LUNG ( 48 FDA reports)
NON-CARDIAC CHEST PAIN ( 48 FDA reports)
PRESYNCOPE ( 48 FDA reports)
PROCTALGIA ( 48 FDA reports)
PROSTATE CANCER ( 48 FDA reports)
SEASONAL ALLERGY ( 48 FDA reports)
ANGIOPATHY ( 47 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 47 FDA reports)
DIABETIC KETOACIDOSIS ( 47 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 47 FDA reports)
INTESTINAL HAEMORRHAGE ( 47 FDA reports)
NODULE ( 47 FDA reports)
OPEN WOUND ( 47 FDA reports)
REFLUX OESOPHAGITIS ( 47 FDA reports)
ABDOMINAL TENDERNESS ( 46 FDA reports)
DECUBITUS ULCER ( 46 FDA reports)
HERNIA ( 46 FDA reports)
VAGINAL INFECTION ( 46 FDA reports)
BLOOD URINE PRESENT ( 45 FDA reports)
CACHEXIA ( 45 FDA reports)
DEVELOPMENTAL DELAY ( 45 FDA reports)
DUODENAL ULCER ( 45 FDA reports)
ESSENTIAL HYPERTENSION ( 45 FDA reports)
GINGIVAL OEDEMA ( 45 FDA reports)
GINGIVAL ULCERATION ( 45 FDA reports)
MUSCLE TIGHTNESS ( 45 FDA reports)
ORAL INTAKE REDUCED ( 45 FDA reports)
ORAL TORUS ( 45 FDA reports)
AORTIC ANEURYSM ( 44 FDA reports)
BIPOLAR DISORDER ( 44 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 44 FDA reports)
CORONARY ARTERY BYPASS ( 44 FDA reports)
EAR DISCOMFORT ( 44 FDA reports)
ESCHERICHIA INFECTION ( 44 FDA reports)
FACIAL PALSY ( 44 FDA reports)
INGUINAL HERNIA ( 44 FDA reports)
JOINT SPRAIN ( 44 FDA reports)
MOOD SWINGS ( 44 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 44 FDA reports)
RHONCHI ( 44 FDA reports)
STEM CELL TRANSPLANT ( 44 FDA reports)
UTERINE LEIOMYOMA ( 44 FDA reports)
VARICOSE VEIN ( 44 FDA reports)
ABSCESS ( 43 FDA reports)
AORTIC STENOSIS ( 43 FDA reports)
BLADDER DISORDER ( 43 FDA reports)
EDENTULOUS ( 43 FDA reports)
ENDODONTIC PROCEDURE ( 43 FDA reports)
HYPERTHYROIDISM ( 43 FDA reports)
LIP SWELLING ( 43 FDA reports)
MYOPATHY ( 43 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 43 FDA reports)
OSTEOMYELITIS CHRONIC ( 43 FDA reports)
PLEURAL FIBROSIS ( 43 FDA reports)
BRAIN OEDEMA ( 42 FDA reports)
BREAST MASS ( 42 FDA reports)
CAROTID ARTERY DISEASE ( 42 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 42 FDA reports)
CHROMATURIA ( 42 FDA reports)
COGNITIVE DISORDER ( 42 FDA reports)
COLITIS ISCHAEMIC ( 42 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 42 FDA reports)
HYPERSOMNIA ( 42 FDA reports)
MULTIPLE SCLEROSIS ( 42 FDA reports)
PELVIC PAIN ( 42 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 42 FDA reports)
THYROID DISORDER ( 42 FDA reports)
TRANSAMINASES INCREASED ( 42 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 42 FDA reports)
WRIST FRACTURE ( 42 FDA reports)
TRISMUS ( 41 FDA reports)
UPPER LIMB FRACTURE ( 41 FDA reports)
DENTAL FISTULA ( 41 FDA reports)
DEPRESSED MOOD ( 41 FDA reports)
LACUNAR INFARCTION ( 41 FDA reports)
LEFT ATRIAL DILATATION ( 41 FDA reports)
PLATELET COUNT INCREASED ( 41 FDA reports)
PSEUDOMONAS INFECTION ( 41 FDA reports)
SENSORY DISTURBANCE ( 41 FDA reports)
SKIN TIGHTNESS ( 41 FDA reports)
BIOPSY ( 40 FDA reports)
BONE SWELLING ( 40 FDA reports)
CATARACT OPERATION ( 40 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 40 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 40 FDA reports)
DUODENITIS ( 40 FDA reports)
EYE SWELLING ( 40 FDA reports)
GENERALISED OEDEMA ( 40 FDA reports)
GINGIVAL INFECTION ( 40 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 40 FDA reports)
HIP ARTHROPLASTY ( 40 FDA reports)
INJECTION SITE HAEMATOMA ( 40 FDA reports)
INJECTION SITE REACTION ( 40 FDA reports)
JOINT DISLOCATION ( 40 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 40 FDA reports)
LYMPHOEDEMA ( 40 FDA reports)
MYOSITIS ( 40 FDA reports)
NECK INJURY ( 40 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 40 FDA reports)
ORAL SURGERY ( 40 FDA reports)
PARANOIA ( 40 FDA reports)
PROCEDURAL PAIN ( 40 FDA reports)
PSYCHOTIC DISORDER ( 40 FDA reports)
RENAL TUBULAR NECROSIS ( 40 FDA reports)
SEQUESTRECTOMY ( 40 FDA reports)
STENT PLACEMENT ( 40 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 40 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 40 FDA reports)
URINARY HESITATION ( 40 FDA reports)
VIITH NERVE PARALYSIS ( 40 FDA reports)
WEIGHT GAIN POOR ( 40 FDA reports)
TIBIA FRACTURE ( 39 FDA reports)
ATRIAL FLUTTER ( 39 FDA reports)
BRONCHIECTASIS ( 39 FDA reports)
CAESAREAN SECTION ( 39 FDA reports)
COLLAPSE OF LUNG ( 39 FDA reports)
IMPAIRED WORK ABILITY ( 39 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 39 FDA reports)
LIBIDO DECREASED ( 39 FDA reports)
OESOPHAGEAL SPASM ( 39 FDA reports)
SNEEZING ( 39 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 39 FDA reports)
ABORTION SPONTANEOUS ( 38 FDA reports)
ATAXIA ( 38 FDA reports)
BODY HEIGHT DECREASED ( 38 FDA reports)
DELUSION ( 38 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 38 FDA reports)
LUNG HYPERINFLATION ( 38 FDA reports)
OESOPHAGEAL ULCER ( 38 FDA reports)
PANIC DISORDER ( 38 FDA reports)
POLYP ( 38 FDA reports)
RADIATION INJURY ( 38 FDA reports)
SPINAL FUSION SURGERY ( 38 FDA reports)
ADRENAL INSUFFICIENCY ( 37 FDA reports)
GASTRITIS EROSIVE ( 37 FDA reports)
HAEMOLYTIC ANAEMIA ( 37 FDA reports)
HEPATIC LESION ( 37 FDA reports)
LIPIDS INCREASED ( 37 FDA reports)
MELANOCYTIC NAEVUS ( 37 FDA reports)
POOR QUALITY SLEEP ( 37 FDA reports)
TONGUE INJURY ( 37 FDA reports)
WOUND DRAINAGE ( 37 FDA reports)
VENTRICULAR DYSFUNCTION ( 36 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 36 FDA reports)
ATRIAL TACHYCARDIA ( 36 FDA reports)
CARDIAC FLUTTER ( 36 FDA reports)
DRUG DISPENSING ERROR ( 36 FDA reports)
EOSINOPHILIA ( 36 FDA reports)
GLOSSODYNIA ( 36 FDA reports)
HEARING IMPAIRED ( 36 FDA reports)
LACTIC ACIDOSIS ( 36 FDA reports)
MYELODYSPLASTIC SYNDROME ( 36 FDA reports)
PANCREATITIS CHRONIC ( 36 FDA reports)
PERITONITIS ( 36 FDA reports)
SNORING ( 36 FDA reports)
STRESS FRACTURE ( 36 FDA reports)
SUDDEN DEATH ( 36 FDA reports)
BACK INJURY ( 35 FDA reports)
BONE NEOPLASM MALIGNANT ( 35 FDA reports)
BRONCHITIS CHRONIC ( 35 FDA reports)
GINGIVAL ERYTHEMA ( 35 FDA reports)
HEMIPLEGIA ( 35 FDA reports)
HEPATIC CIRRHOSIS ( 35 FDA reports)
HODGKIN'S DISEASE ( 35 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 35 FDA reports)
LARYNGEAL OEDEMA ( 35 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 35 FDA reports)
PARAPLEGIA ( 35 FDA reports)
RECTAL POLYP ( 35 FDA reports)
SIALOADENITIS ( 35 FDA reports)
SJOGREN'S SYNDROME ( 35 FDA reports)
SYNOVIAL CYST ( 35 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 35 FDA reports)
TONGUE DRY ( 35 FDA reports)
WHEELCHAIR USER ( 35 FDA reports)
TONGUE ULCERATION ( 34 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 34 FDA reports)
APHTHOUS STOMATITIS ( 34 FDA reports)
BACK DISORDER ( 34 FDA reports)
BILIARY COLIC ( 34 FDA reports)
BLEPHARITIS ( 34 FDA reports)
BLOOD MAGNESIUM DECREASED ( 34 FDA reports)
BONE OPERATION ( 34 FDA reports)
EYE DISORDER ( 34 FDA reports)
EYE IRRITATION ( 34 FDA reports)
GASTRIC HAEMORRHAGE ( 34 FDA reports)
MENTAL IMPAIRMENT ( 34 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 34 FDA reports)
ODYNOPHAGIA ( 34 FDA reports)
RESORPTION BONE INCREASED ( 34 FDA reports)
AGEUSIA ( 33 FDA reports)
BONE SCAN ABNORMAL ( 33 FDA reports)
CERUMEN IMPACTION ( 33 FDA reports)
COSTOCHONDRITIS ( 33 FDA reports)
DYSPHEMIA ( 33 FDA reports)
DYSSTASIA ( 33 FDA reports)
EPIGASTRIC DISCOMFORT ( 33 FDA reports)
FOLLICULITIS ( 33 FDA reports)
FOOT DEFORMITY ( 33 FDA reports)
GALLBLADDER INJURY ( 33 FDA reports)
HAEMOLYSIS ( 33 FDA reports)
HYPOAESTHESIA ORAL ( 33 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 33 FDA reports)
LOW TURNOVER OSTEOPATHY ( 33 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 33 FDA reports)
MENISCUS LESION ( 33 FDA reports)
ORTHOPNOEA ( 33 FDA reports)
PULMONARY VALVE STENOSIS ( 33 FDA reports)
PURPURA ( 33 FDA reports)
SKIN BURNING SENSATION ( 33 FDA reports)
STREPTOCOCCAL INFECTION ( 33 FDA reports)
BREAST PAIN ( 32 FDA reports)
CATHETER RELATED COMPLICATION ( 32 FDA reports)
DILATATION ATRIAL ( 32 FDA reports)
DIZZINESS POSTURAL ( 32 FDA reports)
DYSTONIA ( 32 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 32 FDA reports)
HEART DISEASE CONGENITAL ( 32 FDA reports)
HEPATIC CYST ( 32 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 32 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 32 FDA reports)
INCREASED TENDENCY TO BRUISE ( 32 FDA reports)
LACRIMATION INCREASED ( 32 FDA reports)
LIMB INJURY ( 32 FDA reports)
LIP DRY ( 32 FDA reports)
LOCALISED INFECTION ( 32 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 32 FDA reports)
MANIA ( 32 FDA reports)
MENORRHAGIA ( 32 FDA reports)
METABOLIC ENCEPHALOPATHY ( 32 FDA reports)
NEUROPATHY ( 32 FDA reports)
PETECHIAE ( 32 FDA reports)
RADICULAR PAIN ( 32 FDA reports)
RALES ( 32 FDA reports)
RASH PAPULAR ( 32 FDA reports)
SKIN HYPERTROPHY ( 32 FDA reports)
ULCER HAEMORRHAGE ( 32 FDA reports)
VITAMIN D DECREASED ( 32 FDA reports)
THERAPY NON-RESPONDER ( 31 FDA reports)
WITHDRAWAL SYNDROME ( 31 FDA reports)
WOUND ( 31 FDA reports)
BLOOD PRESSURE ABNORMAL ( 31 FDA reports)
BRONCHOPNEUMONIA ( 31 FDA reports)
CONJUNCTIVITIS ( 31 FDA reports)
DEVICE MALFUNCTION ( 31 FDA reports)
DRUG ABUSER ( 31 FDA reports)
DRUG INTOLERANCE ( 31 FDA reports)
GASTROINTESTINAL PAIN ( 31 FDA reports)
GENERALISED ANXIETY DISORDER ( 31 FDA reports)
IMMUNODEFICIENCY ( 31 FDA reports)
MUSCLE ATROPHY ( 31 FDA reports)
MUSCLE DISORDER ( 31 FDA reports)
NECK MASS ( 31 FDA reports)
NERVE INJURY ( 31 FDA reports)
OESOPHAGITIS ULCERATIVE ( 31 FDA reports)
PHOTOPHOBIA ( 31 FDA reports)
SKIN ODOUR ABNORMAL ( 31 FDA reports)
SPINAL CORPECTOMY ( 31 FDA reports)
SQUAMOUS CELL CARCINOMA ( 31 FDA reports)
ACIDOSIS ( 30 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 30 FDA reports)
APPENDICITIS ( 30 FDA reports)
BRUXISM ( 30 FDA reports)
CHOLESTASIS ( 30 FDA reports)
CLOSTRIDIAL INFECTION ( 30 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 30 FDA reports)
DYSPAREUNIA ( 30 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 30 FDA reports)
GINGIVAL HYPERPLASIA ( 30 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 30 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 30 FDA reports)
HERPES SIMPLEX ( 30 FDA reports)
HORDEOLUM ( 30 FDA reports)
HOSPITALISATION ( 30 FDA reports)
HUNGER ( 30 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 30 FDA reports)
KIDNEY INFECTION ( 30 FDA reports)
OPTIC NEURITIS ( 30 FDA reports)
PARALYSIS ( 30 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 30 FDA reports)
PLANTAR FASCIITIS ( 30 FDA reports)
PURULENCE ( 30 FDA reports)
RAYNAUD'S PHENOMENON ( 30 FDA reports)
ACNE ( 29 FDA reports)
ANAL FISSURE ( 29 FDA reports)
BODY TEMPERATURE DECREASED ( 29 FDA reports)
BONE MARROW DEPRESSION ( 29 FDA reports)
CERVICAL DYSPLASIA ( 29 FDA reports)
DENTAL DISCOMFORT ( 29 FDA reports)
DILATATION VENTRICULAR ( 29 FDA reports)
FAECALOMA ( 29 FDA reports)
HAND FRACTURE ( 29 FDA reports)
HEPATITIS C ( 29 FDA reports)
HYPERBILIRUBINAEMIA ( 29 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 29 FDA reports)
MACROCYTOSIS ( 29 FDA reports)
MACULAR DEGENERATION ( 29 FDA reports)
MECHANICAL VENTILATION ( 29 FDA reports)
MIDDLE INSOMNIA ( 29 FDA reports)
OLIGURIA ( 29 FDA reports)
ORGAN FAILURE ( 29 FDA reports)
PELVIC FRACTURE ( 29 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 29 FDA reports)
PLASMACYTOSIS ( 29 FDA reports)
PLEURISY ( 29 FDA reports)
PRESCRIBED OVERDOSE ( 29 FDA reports)
PULMONARY MASS ( 29 FDA reports)
QUALITY OF LIFE DECREASED ( 29 FDA reports)
RADIOTHERAPY ( 29 FDA reports)
SUBCUTANEOUS ABSCESS ( 29 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 29 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 29 FDA reports)
TOOTH IMPACTED ( 29 FDA reports)
ACUTE SINUSITIS ( 28 FDA reports)
ANURIA ( 28 FDA reports)
BLADDER CANCER ( 28 FDA reports)
BREAST CANCER RECURRENT ( 28 FDA reports)
CAROTID BRUIT ( 28 FDA reports)
CHEST X-RAY ABNORMAL ( 28 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 28 FDA reports)
CRANIAL NERVE DISORDER ( 28 FDA reports)
ENDOMETRIOSIS ( 28 FDA reports)
ENDOTRACHEAL INTUBATION ( 28 FDA reports)
HAIR TEXTURE ABNORMAL ( 28 FDA reports)
HYPOALBUMINAEMIA ( 28 FDA reports)
INTERMITTENT CLAUDICATION ( 28 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 28 FDA reports)
METASTASIS ( 28 FDA reports)
NEOPLASM ( 28 FDA reports)
OESOPHAGEAL PAIN ( 28 FDA reports)
OSTEOMALACIA ( 28 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 28 FDA reports)
SKIN HYPERPIGMENTATION ( 28 FDA reports)
SPUTUM DISCOLOURED ( 28 FDA reports)
ABDOMINAL HERNIA ( 27 FDA reports)
ANEURYSM ( 27 FDA reports)
AORTIC CALCIFICATION ( 27 FDA reports)
BACTERIAL TEST POSITIVE ( 27 FDA reports)
BREAST TENDERNESS ( 27 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 27 FDA reports)
DECREASED ACTIVITY ( 27 FDA reports)
DEVICE RELATED INFECTION ( 27 FDA reports)
DRUG LEVEL INCREASED ( 27 FDA reports)
EAR HAEMORRHAGE ( 27 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 27 FDA reports)
FOOD POISONING ( 27 FDA reports)
GENERALISED ERYTHEMA ( 27 FDA reports)
INJECTION SITE PRURITUS ( 27 FDA reports)
LEUKOENCEPHALOPATHY ( 27 FDA reports)
LOWER LIMB FRACTURE ( 27 FDA reports)
OSTEOCHONDROSIS ( 27 FDA reports)
OTITIS EXTERNA ( 27 FDA reports)
PROSTATITIS ( 27 FDA reports)
PULSE ABSENT ( 27 FDA reports)
SINUS ARRHYTHMIA ( 27 FDA reports)
SKIN INDURATION ( 27 FDA reports)
SKIN LACERATION ( 27 FDA reports)
SPONDYLITIS ( 27 FDA reports)
TEARFULNESS ( 27 FDA reports)
TUMOUR LYSIS SYNDROME ( 27 FDA reports)
TYPE 1 DIABETES MELLITUS ( 27 FDA reports)
TALIPES ( 26 FDA reports)
VENTRICULAR HYPOKINESIA ( 26 FDA reports)
ABDOMINAL ADHESIONS ( 26 FDA reports)
ABNORMAL FAECES ( 26 FDA reports)
AORTIC VALVE SCLEROSIS ( 26 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 26 FDA reports)
ATRIOVENTRICULAR BLOCK ( 26 FDA reports)
BLINDNESS UNILATERAL ( 26 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 26 FDA reports)
CATHETER PLACEMENT ( 26 FDA reports)
COMPLETED SUICIDE ( 26 FDA reports)
DERMATITIS CONTACT ( 26 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 26 FDA reports)
EYE MOVEMENT DISORDER ( 26 FDA reports)
FIBULA FRACTURE ( 26 FDA reports)
FLAT AFFECT ( 26 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 26 FDA reports)
JUGULAR VEIN THROMBOSIS ( 26 FDA reports)
LIP ULCERATION ( 26 FDA reports)
MEDICAL DEVICE COMPLICATION ( 26 FDA reports)
NODAL OSTEOARTHRITIS ( 26 FDA reports)
OROPHARYNGEAL PLAQUE ( 26 FDA reports)
PARKINSONISM ( 26 FDA reports)
RIGHT ATRIAL DILATATION ( 26 FDA reports)
SEBORRHOEIC DERMATITIS ( 26 FDA reports)
SEROMA ( 26 FDA reports)
ALCOHOLISM ( 25 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 25 FDA reports)
APPENDICITIS PERFORATED ( 25 FDA reports)
APPLICATION SITE PRURITUS ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 25 FDA reports)
BLOOD AMYLASE INCREASED ( 25 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 25 FDA reports)
BONE FORMATION INCREASED ( 25 FDA reports)
BONE MARROW TRANSPLANT ( 25 FDA reports)
BREAST CANCER FEMALE ( 25 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 25 FDA reports)
CULTURE POSITIVE ( 25 FDA reports)
CYSTOCELE ( 25 FDA reports)
EAR DISORDER ( 25 FDA reports)
ERYTHEMA MULTIFORME ( 25 FDA reports)
EYE HAEMORRHAGE ( 25 FDA reports)
FRACTURED SACRUM ( 25 FDA reports)
GINGIVAL EROSION ( 25 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 25 FDA reports)
INJECTION SITE SWELLING ( 25 FDA reports)
LENTIGO ( 25 FDA reports)
MUCOSAL DRYNESS ( 25 FDA reports)
NEUTROPHIL COUNT INCREASED ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 25 FDA reports)
OCULAR HYPERTENSION ( 25 FDA reports)
ORAL CAVITY FISTULA ( 25 FDA reports)
OSTEORADIONECROSIS ( 25 FDA reports)
OVARIAN CANCER ( 25 FDA reports)
PHOTOSENSITIVITY REACTION ( 25 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 25 FDA reports)
PROTEINURIA ( 25 FDA reports)
PULMONARY INFARCTION ( 25 FDA reports)
PYELOCALIECTASIS ( 25 FDA reports)
RETINOPATHY ( 25 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 25 FDA reports)
SHOULDER PAIN ( 25 FDA reports)
THERMAL BURN ( 25 FDA reports)
UMBILICAL CORD ABNORMALITY ( 25 FDA reports)
VISUAL FIELD DEFECT ( 25 FDA reports)
VOMITING PROJECTILE ( 25 FDA reports)
WRONG DRUG ADMINISTERED ( 25 FDA reports)
UTERINE PROLAPSE ( 24 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 24 FDA reports)
ARTERIOSPASM CORONARY ( 24 FDA reports)
BLADDER SPASM ( 24 FDA reports)
BRAIN NEOPLASM ( 24 FDA reports)
BREAST CALCIFICATIONS ( 24 FDA reports)
CLOSTRIDIUM COLITIS ( 24 FDA reports)
DRUG ABUSE ( 24 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 24 FDA reports)
EROSIVE OESOPHAGITIS ( 24 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 24 FDA reports)
GASTROINTESTINAL PERFORATION ( 24 FDA reports)
HYPERURICAEMIA ( 24 FDA reports)
HYPOSPADIAS ( 24 FDA reports)
METRORRHAGIA ( 24 FDA reports)
ORAL DISCOMFORT ( 24 FDA reports)
POLYP COLORECTAL ( 24 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 24 FDA reports)
PREMATURE BABY ( 24 FDA reports)
PROCEDURAL COMPLICATION ( 24 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 24 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 24 FDA reports)
ANAEMIA POSTOPERATIVE ( 23 FDA reports)
ANAPHYLACTOID REACTION ( 23 FDA reports)
BLOOD CALCIUM INCREASED ( 23 FDA reports)
BLOOD CULTURE POSITIVE ( 23 FDA reports)
BONE MARROW OEDEMA ( 23 FDA reports)
CALCIUM DEFICIENCY ( 23 FDA reports)
CARDIAC FAILURE CHRONIC ( 23 FDA reports)
CARDIAC PACEMAKER INSERTION ( 23 FDA reports)
CAROTID ARTERY OCCLUSION ( 23 FDA reports)
DENTAL PROSTHESIS USER ( 23 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 23 FDA reports)
FRACTURE DELAYED UNION ( 23 FDA reports)
HAEMANGIOMA ( 23 FDA reports)
HAEMORRHAGIC ANAEMIA ( 23 FDA reports)
HYPERMETABOLISM ( 23 FDA reports)
IMPAIRED DRIVING ABILITY ( 23 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 23 FDA reports)
KELOID SCAR ( 23 FDA reports)
LIPOMA ( 23 FDA reports)
LUMBAR RADICULOPATHY ( 23 FDA reports)
MICROCYTIC ANAEMIA ( 23 FDA reports)
MYDRIASIS ( 23 FDA reports)
OCULAR HYPERAEMIA ( 23 FDA reports)
PROTEIN TOTAL DECREASED ( 23 FDA reports)
RENAL PAIN ( 23 FDA reports)
RESPIRATORY TRACT CONGESTION ( 23 FDA reports)
SACROILIITIS ( 23 FDA reports)
SENSATION OF FOREIGN BODY ( 23 FDA reports)
SENSORY LOSS ( 23 FDA reports)
SICK SINUS SYNDROME ( 23 FDA reports)
ACETABULUM FRACTURE ( 22 FDA reports)
BASEDOW'S DISEASE ( 22 FDA reports)
BRONCHITIS ACUTE ( 22 FDA reports)
CARDIAC ENZYMES INCREASED ( 22 FDA reports)
CARDIAC VALVE DISEASE ( 22 FDA reports)
CATARACT NUCLEAR ( 22 FDA reports)
CATHETERISATION CARDIAC ( 22 FDA reports)
DEAFNESS NEUROSENSORY ( 22 FDA reports)
DENTAL CARE ( 22 FDA reports)
DRUG PRESCRIBING ERROR ( 22 FDA reports)
DRUG TOLERANCE ( 22 FDA reports)
EMBOLISM ( 22 FDA reports)
ENDOCARDITIS ( 22 FDA reports)
HAIR GROWTH ABNORMAL ( 22 FDA reports)
HELICOBACTER INFECTION ( 22 FDA reports)
HEPATITIS ACUTE ( 22 FDA reports)
HOMICIDAL IDEATION ( 22 FDA reports)
INTENTIONAL OVERDOSE ( 22 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 22 FDA reports)
LABORATORY TEST ABNORMAL ( 22 FDA reports)
MALIGNANT MELANOMA ( 22 FDA reports)
MULTI-ORGAN DISORDER ( 22 FDA reports)
NERVE COMPRESSION ( 22 FDA reports)
NEURITIS ( 22 FDA reports)
NO ADVERSE EVENT ( 22 FDA reports)
NO THERAPEUTIC RESPONSE ( 22 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 22 FDA reports)
PARKINSON'S DISEASE ( 22 FDA reports)
PERIPHERAL COLDNESS ( 22 FDA reports)
POLYPECTOMY ( 22 FDA reports)
POLYTRAUMATISM ( 22 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 22 FDA reports)
RESUSCITATION ( 22 FDA reports)
RETINAL VEIN OCCLUSION ( 22 FDA reports)
SELF-INJURIOUS IDEATION ( 22 FDA reports)
SERUM FERRITIN INCREASED ( 22 FDA reports)
TENDON RUPTURE ( 22 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
THINKING ABNORMAL ( 21 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 21 FDA reports)
WOUND INFECTION ( 21 FDA reports)
ADHESION ( 21 FDA reports)
APLASTIC ANAEMIA ( 21 FDA reports)
BACTERIAL SEPSIS ( 21 FDA reports)
BIOPSY GINGIVAL ( 21 FDA reports)
COLON ADENOMA ( 21 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 21 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 21 FDA reports)
EYELID OEDEMA ( 21 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 21 FDA reports)
GASTROINTESTINAL INFECTION ( 21 FDA reports)
HEPATIC ENCEPHALOPATHY ( 21 FDA reports)
HEPATITIS B ( 21 FDA reports)
HUMERUS FRACTURE ( 21 FDA reports)
HYPERPLASIA ( 21 FDA reports)
INTESTINAL STENOSIS ( 21 FDA reports)
KERATITIS ( 21 FDA reports)
LIGAMENT INJURY ( 21 FDA reports)
LIGAMENT RUPTURE ( 21 FDA reports)
LIPASE INCREASED ( 21 FDA reports)
LOCALISED OEDEMA ( 21 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 21 FDA reports)
MENIERE'S DISEASE ( 21 FDA reports)
MUSCLE INJURY ( 21 FDA reports)
PAINFUL RESPIRATION ( 21 FDA reports)
PERIOSTITIS ( 21 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 21 FDA reports)
PERONEAL NERVE PALSY ( 21 FDA reports)
PREMATURE LABOUR ( 21 FDA reports)
RESPIRATORY DEPRESSION ( 21 FDA reports)
SINUS HEADACHE ( 21 FDA reports)
SKIN PAPILLOMA ( 21 FDA reports)
SPINAL CORD COMPRESSION ( 21 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 21 FDA reports)
ABSCESS DRAINAGE ( 20 FDA reports)
ACCIDENTAL EXPOSURE ( 20 FDA reports)
AMYLOIDOSIS ( 20 FDA reports)
BILE DUCT STONE ( 20 FDA reports)
BLOOD IRON DECREASED ( 20 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 20 FDA reports)
BREATH SOUNDS ABNORMAL ( 20 FDA reports)
CEREBELLAR ATROPHY ( 20 FDA reports)
CHOLECYSTITIS INFECTIVE ( 20 FDA reports)
COLON CANCER ( 20 FDA reports)
CONCUSSION ( 20 FDA reports)
CORONARY ARTERY RESTENOSIS ( 20 FDA reports)
DENTAL IMPLANTATION ( 20 FDA reports)
EAR MALFORMATION ( 20 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 20 FDA reports)
FIBRIN D DIMER INCREASED ( 20 FDA reports)
FOOD INTOLERANCE ( 20 FDA reports)
GRANULOCYTOPENIA ( 20 FDA reports)
HEAD DEFORMITY ( 20 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 20 FDA reports)
HICCUPS ( 20 FDA reports)
HILAR LYMPHADENOPATHY ( 20 FDA reports)
HYPERCHLORHYDRIA ( 20 FDA reports)
HYPOPHOSPHATAEMIA ( 20 FDA reports)
INTESTINAL PERFORATION ( 20 FDA reports)
LARGE INTESTINE PERFORATION ( 20 FDA reports)
LIGAMENT SPRAIN ( 20 FDA reports)
LIVER INJURY ( 20 FDA reports)
MACULAR OEDEMA ( 20 FDA reports)
MASTOCYTOSIS ( 20 FDA reports)
MEDICAL DEVICE REMOVAL ( 20 FDA reports)
MITRAL VALVE DISEASE ( 20 FDA reports)
MUCOSAL HAEMORRHAGE ( 20 FDA reports)
MULTIPLE FRACTURES ( 20 FDA reports)
MUMPS ( 20 FDA reports)
NEUROGENIC BLADDER ( 20 FDA reports)
PALATAL DISORDER ( 20 FDA reports)
PARAESTHESIA ORAL ( 20 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
PERSONALITY CHANGE ( 20 FDA reports)
PROSTATOMEGALY ( 20 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 20 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 20 FDA reports)
SALIVARY HYPERSECRETION ( 20 FDA reports)
SCARLET FEVER ( 20 FDA reports)
SCREAMING ( 20 FDA reports)
SKIN REACTION ( 20 FDA reports)
STASIS DERMATITIS ( 20 FDA reports)
STUPOR ( 20 FDA reports)
UROSEPSIS ( 20 FDA reports)
VITAMIN B12 DEFICIENCY ( 20 FDA reports)
URGE INCONTINENCE ( 19 FDA reports)
VAGINAL DISCHARGE ( 19 FDA reports)
VASCULITIS ( 19 FDA reports)
VERTEBROPLASTY ( 19 FDA reports)
VITREOUS DETACHMENT ( 19 FDA reports)
AFFECTIVE DISORDER ( 19 FDA reports)
ANXIETY DISORDER ( 19 FDA reports)
AORTIC DISORDER ( 19 FDA reports)
APATHY ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 19 FDA reports)
BENIGN BONE NEOPLASM ( 19 FDA reports)
BILE DUCT OBSTRUCTION ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 19 FDA reports)
BURN OESOPHAGEAL ( 19 FDA reports)
CARDIAC ANEURYSM ( 19 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 19 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 19 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 19 FDA reports)
DERMATITIS ACNEIFORM ( 19 FDA reports)
DROOLING ( 19 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 19 FDA reports)
EPICONDYLITIS ( 19 FDA reports)
EPILEPSY ( 19 FDA reports)
FUNGAL SKIN INFECTION ( 19 FDA reports)
GASTRIC POLYPS ( 19 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 19 FDA reports)
GYNAECOMASTIA ( 19 FDA reports)
HEPATIC NECROSIS ( 19 FDA reports)
HYDROCEPHALUS ( 19 FDA reports)
HYPERKERATOSIS ( 19 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
ISCHAEMIC HEPATITIS ( 19 FDA reports)
JAUNDICE NEONATAL ( 19 FDA reports)
MONOCYTE COUNT INCREASED ( 19 FDA reports)
MORTON'S NEUROMA ( 19 FDA reports)
MYOPIA ( 19 FDA reports)
NASAL SEPTUM DEVIATION ( 19 FDA reports)
NASAL ULCER ( 19 FDA reports)
NEUROLOGICAL SYMPTOM ( 19 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 19 FDA reports)
OEDEMA MUCOSAL ( 19 FDA reports)
PERIARTHRITIS ( 19 FDA reports)
POST HERPETIC NEURALGIA ( 19 FDA reports)
RUBELLA ( 19 FDA reports)
SALIVARY GLAND ADENOMA ( 19 FDA reports)
SARCOIDOSIS ( 19 FDA reports)
SENSITIVITY OF TEETH ( 19 FDA reports)
SPINAL CORD DISORDER ( 19 FDA reports)
ALVEOLOPLASTY ( 18 FDA reports)
ANOXIC ENCEPHALOPATHY ( 18 FDA reports)
APLASIA PURE RED CELL ( 18 FDA reports)
CATHETER RELATED INFECTION ( 18 FDA reports)
CATHETER SEPSIS ( 18 FDA reports)
CHEST TUBE INSERTION ( 18 FDA reports)
CHOKING SENSATION ( 18 FDA reports)
DEVICE FAILURE ( 18 FDA reports)
ENTEROCOLITIS ( 18 FDA reports)
EXOPHTHALMOS ( 18 FDA reports)
EXTRASKELETAL OSSIFICATION ( 18 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 18 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 18 FDA reports)
HAEMODYNAMIC INSTABILITY ( 18 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 18 FDA reports)
HYPOMETABOLISM ( 18 FDA reports)
KLEBSIELLA INFECTION ( 18 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
LUNG CONSOLIDATION ( 18 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 18 FDA reports)
MUSCLE RIGIDITY ( 18 FDA reports)
MYELITIS TRANSVERSE ( 18 FDA reports)
NECROSIS ( 18 FDA reports)
NEPHRITIS INTERSTITIAL ( 18 FDA reports)
OSTEOPOROTIC FRACTURE ( 18 FDA reports)
PAIN OF SKIN ( 18 FDA reports)
PARATHYROIDECTOMY ( 18 FDA reports)
PILONIDAL CYST ( 18 FDA reports)
PNEUMONIA BACTERIAL ( 18 FDA reports)
POLYSUBSTANCE ABUSE ( 18 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 18 FDA reports)
PULPITIS DENTAL ( 18 FDA reports)
RECTOCELE ( 18 FDA reports)
REGURGITATION ( 18 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 18 FDA reports)
RETINAL TEAR ( 18 FDA reports)
RIGHT VENTRICULAR FAILURE ( 18 FDA reports)
SHOULDER OPERATION ( 18 FDA reports)
SKIN CANCER ( 18 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 18 FDA reports)
URINE ODOUR ABNORMAL ( 18 FDA reports)
TACHYARRHYTHMIA ( 17 FDA reports)
THROMBOSIS IN DEVICE ( 17 FDA reports)
TRANSPLANT REJECTION ( 17 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 17 FDA reports)
VITAMIN A DEFICIENCY ( 17 FDA reports)
VITREOUS HAEMORRHAGE ( 17 FDA reports)
AFFECT LABILITY ( 17 FDA reports)
AGRANULOCYTOSIS ( 17 FDA reports)
AMENORRHOEA ( 17 FDA reports)
BENIGN NEOPLASM ( 17 FDA reports)
CEREBELLAR INFARCTION ( 17 FDA reports)
CUBITAL TUNNEL SYNDROME ( 17 FDA reports)
CYSTITIS HAEMORRHAGIC ( 17 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 17 FDA reports)
DEVICE OCCLUSION ( 17 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 17 FDA reports)
DYSAESTHESIA ( 17 FDA reports)
FAMILY STRESS ( 17 FDA reports)
HEPATITIS FULMINANT ( 17 FDA reports)
HYPERPHAGIA ( 17 FDA reports)
HYPERPHOSPHATAEMIA ( 17 FDA reports)
HYPOTONIA ( 17 FDA reports)
LARYNGOCELE ( 17 FDA reports)
LARYNGOSPASM ( 17 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 17 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 17 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 17 FDA reports)
MALLORY-WEISS SYNDROME ( 17 FDA reports)
MONOCYTOSIS ( 17 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 17 FDA reports)
OCCULT BLOOD POSITIVE ( 17 FDA reports)
ORAL FUNGAL INFECTION ( 17 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 17 FDA reports)
PHYSICAL ASSAULT ( 17 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 17 FDA reports)
POST LAMINECTOMY SYNDROME ( 17 FDA reports)
PROCTITIS ( 17 FDA reports)
PULMONARY HILUM MASS ( 17 FDA reports)
SKIN FIBROSIS ( 17 FDA reports)
SLUGGISHNESS ( 17 FDA reports)
SOFT TISSUE DISORDER ( 17 FDA reports)
STRESS URINARY INCONTINENCE ( 17 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 16 FDA reports)
ACROCHORDON ( 16 FDA reports)
APPLICATION SITE RASH ( 16 FDA reports)
ASPHYXIA ( 16 FDA reports)
ATHEROSCLEROSIS ( 16 FDA reports)
BARRETT'S OESOPHAGUS ( 16 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 16 FDA reports)
BLADDER DILATATION ( 16 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 16 FDA reports)
BLOOD SODIUM INCREASED ( 16 FDA reports)
BONE TRIMMING ( 16 FDA reports)
BREAST PROSTHESIS USER ( 16 FDA reports)
BUTTOCK PAIN ( 16 FDA reports)
CALCINOSIS ( 16 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 16 FDA reports)
CERVICOBRACHIAL SYNDROME ( 16 FDA reports)
CHRONIC FATIGUE SYNDROME ( 16 FDA reports)
COELIAC DISEASE ( 16 FDA reports)
DEVICE BREAKAGE ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 16 FDA reports)
ENTEROVESICAL FISTULA ( 16 FDA reports)
EYE PRURITUS ( 16 FDA reports)
HAEMORRHAGIC STROKE ( 16 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 16 FDA reports)
HEPATOTOXICITY ( 16 FDA reports)
HYPERCOAGULATION ( 16 FDA reports)
HYPERTONIC BLADDER ( 16 FDA reports)
IMMUNOSUPPRESSION ( 16 FDA reports)
INGROWING NAIL ( 16 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 16 FDA reports)
ISCHAEMIC STROKE ( 16 FDA reports)
JAUNDICE CHOLESTATIC ( 16 FDA reports)
KNEE ARTHROPLASTY ( 16 FDA reports)
MEDICATION RESIDUE ( 16 FDA reports)
PALATAL OEDEMA ( 16 FDA reports)
PANCREATIC CARCINOMA ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
PROTEUS INFECTION ( 16 FDA reports)
SHOCK HAEMORRHAGIC ( 16 FDA reports)
SICCA SYNDROME ( 16 FDA reports)
SKELETAL INJURY ( 16 FDA reports)
SKIN PLAQUE ( 16 FDA reports)
SPINAL DEFORMITY ( 16 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 16 FDA reports)
SYNOVITIS ( 16 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
UVEITIS ( 16 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 16 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 15 FDA reports)
THYROID ADENOMA ( 15 FDA reports)
TRANSFUSION REACTION ( 15 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 15 FDA reports)
VERTIGO POSITIONAL ( 15 FDA reports)
VITAMIN C DEFICIENCY ( 15 FDA reports)
ABSCESS ORAL ( 15 FDA reports)
ANOREXIA NERVOSA ( 15 FDA reports)
AORTIC DILATATION ( 15 FDA reports)
ASEPTIC NECROSIS BONE ( 15 FDA reports)
ATROPHIC VULVOVAGINITIS ( 15 FDA reports)
BLEEDING TIME PROLONGED ( 15 FDA reports)
BLOOD CHLORIDE DECREASED ( 15 FDA reports)
BRADYPHRENIA ( 15 FDA reports)
CARDIAC OPERATION ( 15 FDA reports)
CARDIAC SEPTAL DEFECT ( 15 FDA reports)
CHANGE OF BOWEL HABIT ( 15 FDA reports)
COMPLEX PARTIAL SEIZURES ( 15 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 15 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 15 FDA reports)
DIABETIC RETINOPATHY ( 15 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 15 FDA reports)
DYSPLASIA ( 15 FDA reports)
ENDOCRINE DISORDER ( 15 FDA reports)
ENTEROCELE ( 15 FDA reports)
EYE INFECTION ( 15 FDA reports)
EYE OPERATION ( 15 FDA reports)
FEELING DRUNK ( 15 FDA reports)
FISTULA DISCHARGE ( 15 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 15 FDA reports)
GESTATIONAL DIABETES ( 15 FDA reports)
GLIOBLASTOMA MULTIFORME ( 15 FDA reports)
HAEMORRHAGIC DIATHESIS ( 15 FDA reports)
HYPERALDOSTERONISM ( 15 FDA reports)
HYPERCAPNIA ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 15 FDA reports)
HYPERVISCOSITY SYNDROME ( 15 FDA reports)
ILEUS PARALYTIC ( 15 FDA reports)
INCOHERENT ( 15 FDA reports)
INJECTION SITE RASH ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
JOINT CONTRACTURE ( 15 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 15 FDA reports)
METABOLIC DISORDER ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 15 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 15 FDA reports)
ORTHOPEDIC PROCEDURE ( 15 FDA reports)
PARAPARESIS ( 15 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 15 FDA reports)
PERITONITIS BACTERIAL ( 15 FDA reports)
PIGMENTATION DISORDER ( 15 FDA reports)
PINEAL GLAND CYST ( 15 FDA reports)
PNEUMONIA FUNGAL ( 15 FDA reports)
POOR DENTAL CONDITION ( 15 FDA reports)
POST PROCEDURAL CONSTIPATION ( 15 FDA reports)
PROSTATE CANCER METASTATIC ( 15 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 15 FDA reports)
PULMONARY VASCULAR DISORDER ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
REFLUX LARYNGITIS ( 15 FDA reports)
SENSATION OF HEAVINESS ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 15 FDA reports)
SUPERINFECTION ( 15 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 14 FDA reports)
ANGIONEUROTIC OEDEMA ( 14 FDA reports)
ARTERIAL STENOSIS ( 14 FDA reports)
ASTROCYTOMA ( 14 FDA reports)
B-CELL LYMPHOMA ( 14 FDA reports)
BIPOLAR I DISORDER ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 14 FDA reports)
BLOOD URIC ACID INCREASED ( 14 FDA reports)
BONE CALLUS EXCESSIVE ( 14 FDA reports)
BREAST CYST ( 14 FDA reports)
BRONCHIOLITIS ( 14 FDA reports)
CALCULUS URETERIC ( 14 FDA reports)
CAUDA EQUINA SYNDROME ( 14 FDA reports)
CHOLESTEROSIS ( 14 FDA reports)
CORNEAL OEDEMA ( 14 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 14 FDA reports)
DERMATITIS EXFOLIATIVE ( 14 FDA reports)
DIABETIC FOOT ( 14 FDA reports)
DISORDER OF ORBIT ( 14 FDA reports)
DROP ATTACKS ( 14 FDA reports)
ENTEROCOCCAL INFECTION ( 14 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 14 FDA reports)
ESCHERICHIA SEPSIS ( 14 FDA reports)
EXTREMITY CONTRACTURE ( 14 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
FOREIGN BODY ( 14 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 14 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 14 FDA reports)
HAEMOGLOBIN ABNORMAL ( 14 FDA reports)
HAEMOGLOBIN INCREASED ( 14 FDA reports)
HAIR COLOUR CHANGES ( 14 FDA reports)
HEARING AID USER ( 14 FDA reports)
HELICOBACTER GASTRITIS ( 14 FDA reports)
HEPATOSPLENOMEGALY ( 14 FDA reports)
HIP SURGERY ( 14 FDA reports)
HISTOPLASMOSIS ( 14 FDA reports)
HYPERPARATHYROIDISM ( 14 FDA reports)
HYPERTRANSAMINASAEMIA ( 14 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 14 FDA reports)
INJECTION SITE URTICARIA ( 14 FDA reports)
INTRACRANIAL HYPOTENSION ( 14 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 14 FDA reports)
LARGE INTESTINAL ULCER ( 14 FDA reports)
LEFT VENTRICULAR FAILURE ( 14 FDA reports)
LUNG INJURY ( 14 FDA reports)
MAXILLOFACIAL OPERATION ( 14 FDA reports)
MUSCULOSKELETAL DISORDER ( 14 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 14 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
NEOPLASM RECURRENCE ( 14 FDA reports)
NEUROFIBROMA ( 14 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 14 FDA reports)
ONYCHALGIA ( 14 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 14 FDA reports)
ORAL PRURITUS ( 14 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 14 FDA reports)
PATHOLOGICAL GAMBLING ( 14 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 14 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 14 FDA reports)
POLYDACTYLY ( 14 FDA reports)
POST PROCEDURAL HAEMATOMA ( 14 FDA reports)
PRESBYOPIA ( 14 FDA reports)
PROCEDURAL HYPERTENSION ( 14 FDA reports)
PROSTATISM ( 14 FDA reports)
PSYCHIATRIC SYMPTOM ( 14 FDA reports)
PULMONARY RADIATION INJURY ( 14 FDA reports)
RADIUS FRACTURE ( 14 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 14 FDA reports)
REFLUX GASTRITIS ( 14 FDA reports)
RENAL HAEMORRHAGE ( 14 FDA reports)
ROSACEA ( 14 FDA reports)
SINUS OPERATION ( 14 FDA reports)
SKIN ATROPHY ( 14 FDA reports)
SKULL MALFORMATION ( 14 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 14 FDA reports)
STATUS EPILEPTICUS ( 14 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 14 FDA reports)
TELANGIECTASIA ( 14 FDA reports)
THROMBOPHLEBITIS ( 14 FDA reports)
THYROID CANCER ( 14 FDA reports)
TINEA INFECTION ( 14 FDA reports)
ULCERATIVE KERATITIS ( 14 FDA reports)
ULNA FRACTURE ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
URINE FLOW DECREASED ( 14 FDA reports)
VAGINAL BURNING SENSATION ( 14 FDA reports)
VERTEBRAL WEDGING ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
TENDON DISORDER ( 13 FDA reports)
THORACOTOMY ( 13 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
UMBILICAL HERNIA ( 13 FDA reports)
VASCULAR CALCIFICATION ( 13 FDA reports)
VERBAL ABUSE ( 13 FDA reports)
VULVAL DISORDER ( 13 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 13 FDA reports)
X-RAY ABNORMAL ( 13 FDA reports)
ABDOMINAL ABSCESS ( 13 FDA reports)
ACUTE PRERENAL FAILURE ( 13 FDA reports)
APHONIA ( 13 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 13 FDA reports)
ASTIGMATISM ( 13 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 13 FDA reports)
BUNION ( 13 FDA reports)
CERVICAL CORD COMPRESSION ( 13 FDA reports)
CHOLANGITIS ( 13 FDA reports)
CLAUSTROPHOBIA ( 13 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 13 FDA reports)
DERMATITIS ALLERGIC ( 13 FDA reports)
DERMATITIS BULLOUS ( 13 FDA reports)
DERMATOMYOSITIS ( 13 FDA reports)
DIABETIC GASTROPARESIS ( 13 FDA reports)
DIVERTICULAR PERFORATION ( 13 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 13 FDA reports)
DRY THROAT ( 13 FDA reports)
ENCEPHALOMALACIA ( 13 FDA reports)
EXTRADURAL ABSCESS ( 13 FDA reports)
FOOD ALLERGY ( 13 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 13 FDA reports)
GAZE PALSY ( 13 FDA reports)
GLUCOSE URINE PRESENT ( 13 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 13 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 13 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
IMMOBILE ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
INCREASED BRONCHIAL SECRETION ( 13 FDA reports)
INJECTION SITE NODULE ( 13 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 13 FDA reports)
INTRAOCULAR LENS IMPLANT ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
KIDNEY MALROTATION ( 13 FDA reports)
LENS DISORDER ( 13 FDA reports)
LERICHE SYNDROME ( 13 FDA reports)
LESION EXCISION ( 13 FDA reports)
MENINGEAL NEOPLASM ( 13 FDA reports)
MULTIPLE ALLERGIES ( 13 FDA reports)
MYELOMA RECURRENCE ( 13 FDA reports)
NAIL DYSTROPHY ( 13 FDA reports)
NASAL DISCOMFORT ( 13 FDA reports)
NEONATAL DISORDER ( 13 FDA reports)
NERVE ROOT COMPRESSION ( 13 FDA reports)
NERVE ROOT LESION ( 13 FDA reports)
NEUTROPENIC SEPSIS ( 13 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 13 FDA reports)
OPPORTUNISTIC INFECTION ( 13 FDA reports)
PANCREATIC CYST ( 13 FDA reports)
PAPILLOEDEMA ( 13 FDA reports)
PARONYCHIA ( 13 FDA reports)
PELVIC ABSCESS ( 13 FDA reports)
PERIRECTAL ABSCESS ( 13 FDA reports)
PERSONALITY DISORDER ( 13 FDA reports)
PILONIDAL CYST CONGENITAL ( 13 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 13 FDA reports)
POOR PERSONAL HYGIENE ( 13 FDA reports)
POST PROCEDURAL FISTULA ( 13 FDA reports)
POSTNASAL DRIP ( 13 FDA reports)
PRESBYOESOPHAGUS ( 13 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 13 FDA reports)
QUADRIPLEGIA ( 13 FDA reports)
RENAL COLIC ( 13 FDA reports)
SINUS POLYP ( 13 FDA reports)
SKIN WARM ( 13 FDA reports)
STRIDOR ( 13 FDA reports)
ACCIDENT ( 12 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 12 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 12 FDA reports)
ADJUSTMENT DISORDER ( 12 FDA reports)
ANGIOPLASTY ( 12 FDA reports)
AORTIC VALVE STENOSIS ( 12 FDA reports)
APPLICATION SITE ERYTHEMA ( 12 FDA reports)
AREFLEXIA ( 12 FDA reports)
ARTHRITIS BACTERIAL ( 12 FDA reports)
BLADDER PROLAPSE ( 12 FDA reports)
BLEPHAROSPASM ( 12 FDA reports)
BLOOD CHLORIDE INCREASED ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BLOOD OESTROGEN INCREASED ( 12 FDA reports)
BLOOD PH DECREASED ( 12 FDA reports)
BONE EROSION ( 12 FDA reports)
BREECH PRESENTATION ( 12 FDA reports)
CARDIAC OUTPUT DECREASED ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 12 FDA reports)
CATHETER REMOVAL ( 12 FDA reports)
CATHETER SITE HAEMORRHAGE ( 12 FDA reports)
CHOLANGITIS SCLEROSING ( 12 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 12 FDA reports)
CLAVICLE FRACTURE ( 12 FDA reports)
CLEFT PALATE ( 12 FDA reports)
COLECTOMY ( 12 FDA reports)
CONGENITAL ANOMALY ( 12 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 12 FDA reports)
CORONARY ANGIOPLASTY ( 12 FDA reports)
CULTURE URINE POSITIVE ( 12 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 12 FDA reports)
DYSTHYMIC DISORDER ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 12 FDA reports)
EXPIRED DRUG ADMINISTERED ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
EYELID PTOSIS ( 12 FDA reports)
FIBROMA ( 12 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 12 FDA reports)
GASTRIC BYPASS ( 12 FDA reports)
GASTRIC MUCOSAL LESION ( 12 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 12 FDA reports)
HAEMOSTASIS ( 12 FDA reports)
HIP DEFORMITY ( 12 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 12 FDA reports)
IMPLANT SITE INFECTION ( 12 FDA reports)
INFARCTION ( 12 FDA reports)
INJECTION SITE WARMTH ( 12 FDA reports)
LARYNGITIS ( 12 FDA reports)
LIMB DEFORMITY ( 12 FDA reports)
LISTLESS ( 12 FDA reports)
LYMPHOPENIA ( 12 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 12 FDA reports)
METATARSALGIA ( 12 FDA reports)
MICROANGIOPATHY ( 12 FDA reports)
MOTOR DYSFUNCTION ( 12 FDA reports)
MYOCLONUS ( 12 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 12 FDA reports)
OVERWEIGHT ( 12 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 12 FDA reports)
PERITONSILLITIS ( 12 FDA reports)
PITTING OEDEMA ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 12 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 12 FDA reports)
PROTEIN URINE PRESENT ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
QRS AXIS ABNORMAL ( 12 FDA reports)
RASH MORBILLIFORM ( 12 FDA reports)
RENAL ARTERY STENOSIS ( 12 FDA reports)
RENAL GRAFT LOSS ( 12 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 12 FDA reports)
SIMPLE PARTIAL SEIZURES ( 12 FDA reports)
STATUS ASTHMATICUS ( 12 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 12 FDA reports)
STREPTOCOCCAL SEPSIS ( 12 FDA reports)
SUICIDAL BEHAVIOUR ( 12 FDA reports)
TENOSYNOVITIS STENOSANS ( 12 FDA reports)
THERAPEUTIC PROCEDURE ( 12 FDA reports)
TOBACCO ABUSE ( 12 FDA reports)
TOE DEFORMITY ( 12 FDA reports)
TONGUE DISCOLOURATION ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
TRACHEOBRONCHITIS ( 12 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 12 FDA reports)
VENTRICULAR DYSKINESIA ( 12 FDA reports)
WOUND HAEMORRHAGE ( 12 FDA reports)
THYROID CYST ( 11 FDA reports)
TRIGEMINAL NEURALGIA ( 11 FDA reports)
TRIGGER FINGER ( 11 FDA reports)
TROPONIN INCREASED ( 11 FDA reports)
TUMOUR NECROSIS ( 11 FDA reports)
URETERIC OBSTRUCTION ( 11 FDA reports)
VAGINITIS BACTERIAL ( 11 FDA reports)
VENOUS THROMBOSIS ( 11 FDA reports)
VOCAL CORD PARALYSIS ( 11 FDA reports)
VULVOVAGINAL DRYNESS ( 11 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 11 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 11 FDA reports)
ADRENAL MASS ( 11 FDA reports)
ADRENAL SUPPRESSION ( 11 FDA reports)
AKATHISIA ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
ANAL FISTULA ( 11 FDA reports)
ANDROGENS DECREASED ( 11 FDA reports)
APPLICATION SITE BURN ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 11 FDA reports)
BLOOD TEST ABNORMAL ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 11 FDA reports)
BRADYKINESIA ( 11 FDA reports)
BRAIN HYPOXIA ( 11 FDA reports)
CALCIFICATION METASTATIC ( 11 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 11 FDA reports)
CEREBRAL DISORDER ( 11 FDA reports)
CERVIX CARCINOMA ( 11 FDA reports)
CONVERSION DISORDER ( 11 FDA reports)
CREPITATIONS ( 11 FDA reports)
DENTAL PLAQUE ( 11 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 11 FDA reports)
DYSPNOEA EXACERBATED ( 11 FDA reports)
EBSTEIN'S ANOMALY ( 11 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 11 FDA reports)
EMBOLIC STROKE ( 11 FDA reports)
ENCEPHALITIS ( 11 FDA reports)
FALLOT'S TETRALOGY ( 11 FDA reports)
FEEDING DISORDER ( 11 FDA reports)
FOETAL GROWTH RESTRICTION ( 11 FDA reports)
GASTRIC PH DECREASED ( 11 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 11 FDA reports)
GRANULOCYTE COUNT DECREASED ( 11 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 11 FDA reports)
HAEMOTHORAX ( 11 FDA reports)
HEAD DISCOMFORT ( 11 FDA reports)
HEART INJURY ( 11 FDA reports)
HEART RATE ABNORMAL ( 11 FDA reports)
HEART VALVE INCOMPETENCE ( 11 FDA reports)
HERPES VIRUS INFECTION ( 11 FDA reports)
HOSTILITY ( 11 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 11 FDA reports)
HYPERACUSIS ( 11 FDA reports)
HYPERNATRAEMIA ( 11 FDA reports)
HYPOAESTHESIA FACIAL ( 11 FDA reports)
HYPOPROTEINAEMIA ( 11 FDA reports)
HYPOVENTILATION ( 11 FDA reports)
HYSTERECTOMY ( 11 FDA reports)
IMPULSE-CONTROL DISORDER ( 11 FDA reports)
INCREASED APPETITE ( 11 FDA reports)
INJECTION SITE INDURATION ( 11 FDA reports)
INTERCOSTAL RETRACTION ( 11 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 11 FDA reports)
JOINT INSTABILITY ( 11 FDA reports)
LABYRINTHITIS ( 11 FDA reports)
LAGOPHTHALMOS ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MIOSIS ( 11 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NEPHROSCLEROSIS ( 11 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 11 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 11 FDA reports)
PHONOPHOBIA ( 11 FDA reports)
POSTOPERATIVE ILEUS ( 11 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 11 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 11 FDA reports)
RADIATION ASSOCIATED PAIN ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 11 FDA reports)
RENAL ATROPHY ( 11 FDA reports)
RENAL MASS ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 11 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 11 FDA reports)
SELF-MEDICATION ( 11 FDA reports)
SERUM SICKNESS ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
SKIN CANDIDA ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 11 FDA reports)
SUBDURAL HAEMATOMA ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 10 FDA reports)
ADRENAL ADENOMA ( 10 FDA reports)
ALCOHOL POISONING ( 10 FDA reports)
ALLERGY TO ANIMAL ( 10 FDA reports)
AMMONIA INCREASED ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
AORTIC VALVE DISEASE ( 10 FDA reports)
APPETITE DISORDER ( 10 FDA reports)
ARRESTED LABOUR ( 10 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BEREAVEMENT REACTION ( 10 FDA reports)
BLOOD DISORDER ( 10 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 10 FDA reports)
BONE METABOLISM DISORDER ( 10 FDA reports)
BRAIN ABSCESS ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
CARDIAC FAILURE ACUTE ( 10 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 10 FDA reports)
CHOREA ( 10 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 10 FDA reports)
CONJUNCTIVITIS VIRAL ( 10 FDA reports)
CYSTOPEXY ( 10 FDA reports)
DIABETIC COMPLICATION ( 10 FDA reports)
DIABETIC NEPHROPATHY ( 10 FDA reports)
DIPLEGIA ( 10 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
DUPUYTREN'S CONTRACTURE ( 10 FDA reports)
EJACULATION DISORDER ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 10 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 10 FDA reports)
ENURESIS ( 10 FDA reports)
EXCESSIVE EYE BLINKING ( 10 FDA reports)
EYELID DISORDER ( 10 FDA reports)
FACIAL PARESIS ( 10 FDA reports)
FASCIITIS ( 10 FDA reports)
FAT NECROSIS ( 10 FDA reports)
FISTULA REPAIR ( 10 FDA reports)
FLUID INTAKE REDUCED ( 10 FDA reports)
FORMICATION ( 10 FDA reports)
GASTRIC CANCER ( 10 FDA reports)
GASTRIC PERFORATION ( 10 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 10 FDA reports)
GINGIVAL ATROPHY ( 10 FDA reports)
GRIMACING ( 10 FDA reports)
GRIP STRENGTH DECREASED ( 10 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 10 FDA reports)
HEPATIC MASS ( 10 FDA reports)
HEPATOCELLULAR DAMAGE ( 10 FDA reports)
HYPERAMMONAEMIA ( 10 FDA reports)
HYPERREFLEXIA ( 10 FDA reports)
ILIAC ARTERY THROMBOSIS ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INFUSION SITE ERYTHEMA ( 10 FDA reports)
INITIAL INSOMNIA ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
INTESTINAL ULCER ( 10 FDA reports)
JUVENILE ARTHRITIS ( 10 FDA reports)
LIVEDO RETICULARIS ( 10 FDA reports)
LYMPHADENECTOMY ( 10 FDA reports)
MACULOPATHY ( 10 FDA reports)
MASTECTOMY ( 10 FDA reports)
MEDIASTINAL MASS ( 10 FDA reports)
MEGACOLON ( 10 FDA reports)
MENSTRUATION IRREGULAR ( 10 FDA reports)
MERALGIA PARAESTHETICA ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
MYELOID LEUKAEMIA ( 10 FDA reports)
NARCOLEPSY ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEPHROTIC SYNDROME ( 10 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 10 FDA reports)
PATELLA FRACTURE ( 10 FDA reports)
PERICARDITIS ( 10 FDA reports)
PHOTODERMATOSIS ( 10 FDA reports)
PNEUMOMEDIASTINUM ( 10 FDA reports)
PROTEIN TOTAL INCREASED ( 10 FDA reports)
PULMONARY THROMBOSIS ( 10 FDA reports)
PUPIL FIXED ( 10 FDA reports)
RENAL CANCER ( 10 FDA reports)
RETINAL HAEMORRHAGE ( 10 FDA reports)
RETINOPATHY HYPERTENSIVE ( 10 FDA reports)
SECRETION DISCHARGE ( 10 FDA reports)
SINUSITIS FUNGAL ( 10 FDA reports)
SKIN NODULE ( 10 FDA reports)
STRESS SYMPTOMS ( 10 FDA reports)
TEMPORAL ARTERITIS ( 10 FDA reports)
TEMPORAL LOBE EPILEPSY ( 10 FDA reports)
THORACIC OPERATION ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
TOE AMPUTATION ( 10 FDA reports)
TONSILLITIS ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
VARICES OESOPHAGEAL ( 10 FDA reports)
VENA CAVA THROMBOSIS ( 10 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 10 FDA reports)
VENOUS THROMBOSIS LIMB ( 10 FDA reports)
TACHYPHRENIA ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
TONGUE COATED ( 9 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
VASCULAR OCCLUSION ( 9 FDA reports)
VENOUS OCCLUSION ( 9 FDA reports)
VERTEBRAL INJURY ( 9 FDA reports)
WEIGHT FLUCTUATION ( 9 FDA reports)
ACTINOMYCES TEST POSITIVE ( 9 FDA reports)
ACUTE PSYCHOSIS ( 9 FDA reports)
ADENOMA BENIGN ( 9 FDA reports)
ALCOHOL USE ( 9 FDA reports)
AMPHETAMINES POSITIVE ( 9 FDA reports)
ANTIBODY TEST POSITIVE ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 9 FDA reports)
APPENDICECTOMY ( 9 FDA reports)
ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
ARTHROPOD BITE ( 9 FDA reports)
BENIGN GASTRIC NEOPLASM ( 9 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 9 FDA reports)
BILE DUCT STENOSIS ( 9 FDA reports)
BLINDNESS TRANSIENT ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 9 FDA reports)
BONE FRAGMENTATION ( 9 FDA reports)
BONE GRAFT ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CEREBROVASCULAR DISORDER ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CSF PROTEIN INCREASED ( 9 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 9 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 9 FDA reports)
DIABETIC COMA ( 9 FDA reports)
DRUG LEVEL DECREASED ( 9 FDA reports)
DYSMENORRHOEA ( 9 FDA reports)
EATING DISORDER SYMPTOM ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ENCOPRESIS ( 9 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 9 FDA reports)
EXERCISE TOLERANCE DECREASED ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
EYE INFLAMMATION ( 9 FDA reports)
FACIAL BONES FRACTURE ( 9 FDA reports)
FOETAL GROWTH RETARDATION ( 9 FDA reports)
GALACTORRHOEA ( 9 FDA reports)
GINGIVECTOMY ( 9 FDA reports)
GLOSSITIS ( 9 FDA reports)
GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
HAEMARTHROSIS ( 9 FDA reports)
HEPATIC FIBROSIS ( 9 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 9 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 9 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 9 FDA reports)
IATROGENIC INJURY ( 9 FDA reports)
ILLUSION ( 9 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INGUINAL HERNIA REPAIR ( 9 FDA reports)
INJECTION SITE EXTRAVASATION ( 9 FDA reports)
INTERVERTEBRAL DISCITIS ( 9 FDA reports)
INTRACARDIAC THROMBUS ( 9 FDA reports)
JOINT LOCK ( 9 FDA reports)
KNEE OPERATION ( 9 FDA reports)
LOGORRHOEA ( 9 FDA reports)
LOSS OF LIBIDO ( 9 FDA reports)
LUNG ABSCESS ( 9 FDA reports)
METAPLASIA ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
MITRAL VALVE CALCIFICATION ( 9 FDA reports)
MIXED HYPERLIPIDAEMIA ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
MYASTHENIA GRAVIS ( 9 FDA reports)
NASAL DRYNESS ( 9 FDA reports)
OESOPHAGEAL STENOSIS ( 9 FDA reports)
OPERATIVE HAEMORRHAGE ( 9 FDA reports)
PAIN EXACERBATED ( 9 FDA reports)
PANCREATIC DISORDER ( 9 FDA reports)
PANCREATIC NEOPLASM ( 9 FDA reports)
PERIORBITAL OEDEMA ( 9 FDA reports)
PHARYNGEAL DISORDER ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 9 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 9 FDA reports)
POSTURE ABNORMAL ( 9 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 9 FDA reports)
PRURITUS GENITAL ( 9 FDA reports)
PULMONARY ARTERY STENOSIS ( 9 FDA reports)
PYURIA ( 9 FDA reports)
RADICULITIS ( 9 FDA reports)
RENAL INFARCT ( 9 FDA reports)
RENAL TUBULAR ACIDOSIS ( 9 FDA reports)
RESPIRATORY RATE DECREASED ( 9 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 9 FDA reports)
SCAB ( 9 FDA reports)
SCRATCH ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SINUS ANTROSTOMY ( 9 FDA reports)
SPLENIC GRANULOMA ( 9 FDA reports)
SURGICAL PROCEDURE REPEATED ( 9 FDA reports)
SYNCOPE VASOVAGAL ( 9 FDA reports)
ABDOMINAL SYMPTOM ( 8 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 8 FDA reports)
APPLICATION SITE REACTION ( 8 FDA reports)
ARTERIAL DISORDER ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
AUTISM ( 8 FDA reports)
BASOPHIL COUNT INCREASED ( 8 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 8 FDA reports)
BLOOD IRON ABNORMAL ( 8 FDA reports)
BLOOD IRON INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 8 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BONE LESION EXCISION ( 8 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 8 FDA reports)
BRAIN DEATH ( 8 FDA reports)
BRAIN STEM INFARCTION ( 8 FDA reports)
BREAST DISCHARGE ( 8 FDA reports)
BREAST HYPERPLASIA ( 8 FDA reports)
CATHETER SITE RELATED REACTION ( 8 FDA reports)
CHONDROPATHY ( 8 FDA reports)
CHYLOTHORAX ( 8 FDA reports)
CSF CULTURE POSITIVE ( 8 FDA reports)
CYTOLYTIC HEPATITIS ( 8 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 8 FDA reports)
DEMYELINATION ( 8 FDA reports)
DENTAL PULP DISORDER ( 8 FDA reports)
DEVICE DISLOCATION ( 8 FDA reports)
DIABETIC MICROANGIOPATHY ( 8 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 8 FDA reports)
DRUG EFFECT DELAYED ( 8 FDA reports)
DRUG RESISTANCE ( 8 FDA reports)
DYSPHORIA ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENDOCARDIAL FIBROSIS ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
FALLOPIAN TUBE DISORDER ( 8 FDA reports)
GANGRENE ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GRANULOMA ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HEMIANOPIA HOMONYMOUS ( 8 FDA reports)
HEPATORENAL SYNDROME ( 8 FDA reports)
HIRSUTISM ( 8 FDA reports)
HYDROCELE ( 8 FDA reports)
HYPOPNOEA ( 8 FDA reports)
IMMUNE SYSTEM DISORDER ( 8 FDA reports)
INCISIONAL HERNIA ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
INTESTINAL POLYP ( 8 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 8 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 8 FDA reports)
JOINT ARTHROPLASTY ( 8 FDA reports)
KYPHOSCOLIOSIS ( 8 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 8 FDA reports)
METASTASES TO LYMPH NODES ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NASAL DISORDER ( 8 FDA reports)
NIGHT BLINDNESS ( 8 FDA reports)
OESOPHAGEAL CARCINOMA ( 8 FDA reports)
OROANTRAL FISTULA ( 8 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 8 FDA reports)
PANCREATIC ENLARGEMENT ( 8 FDA reports)
PANIC REACTION ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PNEUMONECTOMY ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
PORPHYRIA ( 8 FDA reports)
PORTAL VEIN THROMBOSIS ( 8 FDA reports)
PREMATURE EJACULATION ( 8 FDA reports)
PROCEDURAL HYPOTENSION ( 8 FDA reports)
PULMONARY GRANULOMA ( 8 FDA reports)
PYODERMA GANGRENOSUM ( 8 FDA reports)
RADICULITIS CERVICAL ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 8 FDA reports)
RESPIRATORY TRACT IRRITATION ( 8 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 8 FDA reports)
RETROPERITONEAL HAEMATOMA ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SELF MUTILATION ( 8 FDA reports)
SENSATION OF PRESSURE ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SKIN OPERATION ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
SPINAL DECOMPRESSION ( 8 FDA reports)
SPINE MALFORMATION ( 8 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 8 FDA reports)
STENT REMOVAL ( 8 FDA reports)
STRABISMUS ( 8 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 8 FDA reports)
SUTURE INSERTION ( 8 FDA reports)
SYSTEMIC SCLEROSIS ( 8 FDA reports)
TESTICULAR PAIN ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 8 FDA reports)
TINEA CRURIS ( 8 FDA reports)
TONSILLAR HYPERTROPHY ( 8 FDA reports)
TRISOMY 21 ( 8 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 8 FDA reports)
URTICARIA GENERALISED ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VESTIBULAR NEURONITIS ( 8 FDA reports)
VULVOVAGINAL DISCOMFORT ( 8 FDA reports)
WEIGHT LOSS POOR ( 8 FDA reports)
TACHYCARDIA FOETAL ( 7 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 7 FDA reports)
TENOSYNOVITIS ( 7 FDA reports)
TONGUE CYST ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TRACHEOSTOMY ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
UTERINE CANCER ( 7 FDA reports)
VASCULAR GRAFT OCCLUSION ( 7 FDA reports)
VENOUS INSUFFICIENCY ( 7 FDA reports)
VERTEBRAL COLUMN MASS ( 7 FDA reports)
VIRAL LABYRINTHITIS ( 7 FDA reports)
VITAMIN B12 DECREASED ( 7 FDA reports)
VULVOVAGINAL PAIN ( 7 FDA reports)
WOUND COMPLICATION ( 7 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ALLERGIC COUGH ( 7 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 7 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 7 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 7 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
AORTA HYPOPLASIA ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
APNOEIC ATTACK ( 7 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 7 FDA reports)
AURICULAR SWELLING ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLOOD BICARBONATE DECREASED ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BRAIN HERNIATION ( 7 FDA reports)
BRAIN SCAN ABNORMAL ( 7 FDA reports)
BREAST CANCER IN SITU ( 7 FDA reports)
BREAST DISORDER ( 7 FDA reports)
BREAST NECROSIS ( 7 FDA reports)
CAECITIS ( 7 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 7 FDA reports)
CARDIAC VALVE SCLEROSIS ( 7 FDA reports)
CARDIOVERSION ( 7 FDA reports)
CAROTID ARTERY ATHEROMA ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
CHORIOAMNIONITIS ( 7 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 7 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
COLORECTAL CANCER ( 7 FDA reports)
CONDUCTION DISORDER ( 7 FDA reports)
CONNECTIVE TISSUE DISORDER ( 7 FDA reports)
COR PULMONALE ( 7 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 7 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 7 FDA reports)
DEAFNESS BILATERAL ( 7 FDA reports)
DEPENDENCE ( 7 FDA reports)
DEPRESSIVE SYMPTOM ( 7 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 7 FDA reports)
DRUG CLEARANCE DECREASED ( 7 FDA reports)
DRUG LEVEL CHANGED ( 7 FDA reports)
EARLY MORNING AWAKENING ( 7 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 7 FDA reports)
ESCHERICHIA BACTERAEMIA ( 7 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 7 FDA reports)
EXCITABILITY ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
FAECES PALE ( 7 FDA reports)
FEAR OF DEATH ( 7 FDA reports)
FEELING OF DESPAIR ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
FRACTURE DISPLACEMENT ( 7 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 7 FDA reports)
FULL BLOOD COUNT DECREASED ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GRIEF REACTION ( 7 FDA reports)
GRUNTING ( 7 FDA reports)
HAEMOCHROMATOSIS ( 7 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 7 FDA reports)
HEPATITIS VIRAL ( 7 FDA reports)
HOARSENESS ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
INCISION SITE INFECTION ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INJECTION SITE ULCER ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
JOINT STABILISATION ( 7 FDA reports)
LARGE INTESTINE CARCINOMA ( 7 FDA reports)
LARYNGEAL CANCER ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LHERMITTE'S SIGN ( 7 FDA reports)
MACULAR SCAR ( 7 FDA reports)
MEAN CELL VOLUME DECREASED ( 7 FDA reports)
METASTASES TO PELVIS ( 7 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 7 FDA reports)
NEPHROBLASTOMA ( 7 FDA reports)
NERVE BLOCK ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 7 FDA reports)
NO ADVERSE EFFECT ( 7 FDA reports)
OESOPHAGEAL PERFORATION ( 7 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 7 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 7 FDA reports)
ORCHITIS ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
ORTHOSIS USER ( 7 FDA reports)
OSTEITIS DEFORMANS ( 7 FDA reports)
OVERGROWTH BACTERIAL ( 7 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 7 FDA reports)
PANCREATIC ENZYMES INCREASED ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 7 FDA reports)
PHARYNGEAL ERYTHEMA ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
POLYMYOSITIS ( 7 FDA reports)
POOR PERIPHERAL CIRCULATION ( 7 FDA reports)
POST PROCEDURAL INFECTION ( 7 FDA reports)
POSTMENOPAUSE ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PRODUCT TASTE ABNORMAL ( 7 FDA reports)
PROSTATECTOMY ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
PULSE PRESSURE DECREASED ( 7 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
PYOGENIC GRANULOMA ( 7 FDA reports)
RADIATION PNEUMONITIS ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RESPIRATORY ACIDOSIS ( 7 FDA reports)
SALIVARY GLAND MASS ( 7 FDA reports)
SARCOMA ( 7 FDA reports)
SCAPULA FRACTURE ( 7 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 7 FDA reports)
SCHIZOPHRENIA ( 7 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 7 FDA reports)
SENSE OF OPPRESSION ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SPINAL X-RAY ABNORMAL ( 7 FDA reports)
SPLENIC LESION ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
STRESS ULCER ( 7 FDA reports)
SUBRETINAL FIBROSIS ( 7 FDA reports)
SWEAT DISCOLOURATION ( 7 FDA reports)
ADRENAL NEOPLASM ( 6 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
ANGIOMYOLIPOMA ( 6 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
AORTIC BRUIT ( 6 FDA reports)
APPLICATION SITE ULCER ( 6 FDA reports)
ARTERIAL BYPASS OPERATION ( 6 FDA reports)
AURICULAR PERICHONDRITIS ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 6 FDA reports)
BILIARY CYST ( 6 FDA reports)
BIOPSY BONE MARROW ( 6 FDA reports)
BLADDER HYPERTROPHY ( 6 FDA reports)
BLADDER OPERATION ( 6 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 6 FDA reports)
BLOOD ALCOHOL INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BRADYPNOEA ( 6 FDA reports)
BRAIN DAMAGE ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BREAST MICROCALCIFICATION ( 6 FDA reports)
BRONCHIAL HYPERACTIVITY ( 6 FDA reports)
BRONCHOSCOPY ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
BURNS SECOND DEGREE ( 6 FDA reports)
CALCULUS BLADDER ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
CARBON DIOXIDE INCREASED ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CENTRAL LINE INFECTION ( 6 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
CEREBRAL PALSY ( 6 FDA reports)
CERVICAL MYELOPATHY ( 6 FDA reports)
CHLAMYDIAL INFECTION ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 6 FDA reports)
COMMINUTED FRACTURE ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
CORONARY ARTERY THROMBOSIS ( 6 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 6 FDA reports)
DEAFNESS UNILATERAL ( 6 FDA reports)
DEATH NEONATAL ( 6 FDA reports)
DENTAL TREATMENT ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 6 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DYSLALIA ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
EJECTION FRACTION ABNORMAL ( 6 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 6 FDA reports)
ENTEROCUTANEOUS FISTULA ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
EXFOLIATIVE RASH ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
FIBROUS HISTIOCYTOMA ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
GRAFT LOSS ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HEPATIC VEIN OCCLUSION ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 6 FDA reports)
ILIAC ARTERY STENOSIS ( 6 FDA reports)
IMPAIRED SELF-CARE ( 6 FDA reports)
INFECTED DERMAL CYST ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INFUSION SITE PAIN ( 6 FDA reports)
INFUSION SITE PRURITUS ( 6 FDA reports)
INJURY ASPHYXIATION ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LARYNGOMALACIA ( 6 FDA reports)
LARYNX IRRITATION ( 6 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 6 FDA reports)
LICHEN PLANUS ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LOOSE STOOLS ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
LUNG CANCER METASTATIC ( 6 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 6 FDA reports)
MASTITIS ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METASTASES TO BLADDER ( 6 FDA reports)
METASTASES TO MENINGES ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MIGRATION OF IMPLANT ( 6 FDA reports)
MITRAL VALVE REPAIR ( 6 FDA reports)
MONOCLONAL GAMMOPATHY ( 6 FDA reports)
MONONEUROPATHY ( 6 FDA reports)
MOTION SICKNESS ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
NEUTROPHILIA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER ( 6 FDA reports)
NUCHAL RIGIDITY ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OPEN ANGLE GLAUCOMA ( 6 FDA reports)
OXYGEN SATURATION ABNORMAL ( 6 FDA reports)
OXYGEN SUPPLEMENTATION ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PARATHYROID TUMOUR BENIGN ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PENIS DISORDER ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PERINEURIAL CYST ( 6 FDA reports)
PERIRENAL HAEMATOMA ( 6 FDA reports)
PIGMENTED NAEVUS ( 6 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
POLYCYSTIC LIVER DISEASE ( 6 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 6 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 6 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 6 FDA reports)
PROSTATIC OBSTRUCTION ( 6 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 6 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 6 FDA reports)
PSEUDOMONAL SEPSIS ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RETROGRADE EJACULATION ( 6 FDA reports)
ROTATOR CUFF REPAIR ( 6 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 6 FDA reports)
SERUM FERRITIN ABNORMAL ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
STRESS CARDIOMYOPATHY ( 6 FDA reports)
SUBCUTANEOUS NODULE ( 6 FDA reports)
SUFFOCATION FEELING ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
TARSAL TUNNEL SYNDROME ( 6 FDA reports)
TENDON INJURY ( 6 FDA reports)
THROAT CANCER ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
TIC ( 6 FDA reports)
TOBACCO USER ( 6 FDA reports)
TONGUE HAEMORRHAGE ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 6 FDA reports)
TYPE I HYPERSENSITIVITY ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 6 FDA reports)
UTERINE ENLARGEMENT ( 6 FDA reports)
VASCULAR INJURY ( 6 FDA reports)
VASOCONSTRICTION ( 6 FDA reports)
VESICOURETERIC REFLUX ( 6 FDA reports)
VITREOUS DEGENERATION ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
WOUND DEBRIDEMENT ( 6 FDA reports)
WOUND SECRETION ( 6 FDA reports)
TETANY ( 5 FDA reports)
THOUGHT INSERTION ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TONIC CLONIC MOVEMENTS ( 5 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
ULNAR NERVE INJURY ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 5 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 5 FDA reports)
URINE AMPHETAMINE POSITIVE ( 5 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 5 FDA reports)
URINE OUTPUT INCREASED ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
VASCULAR ACCESS COMPLICATION ( 5 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 5 FDA reports)
VASOSPASM ( 5 FDA reports)
VIRAL LOAD INCREASED ( 5 FDA reports)
VOLVULUS ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
ACCIDENTAL NEEDLE STICK ( 5 FDA reports)
ACUTE ABDOMEN ( 5 FDA reports)
ADIPOSIS DOLOROSA ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 5 FDA reports)
AMBLYOPIA ( 5 FDA reports)
ANAPHYLACTOID SHOCK ( 5 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 5 FDA reports)
ANASTOMOTIC ULCER ( 5 FDA reports)
ANORECTAL DISCOMFORT ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 5 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
AORTIC VALVE REPLACEMENT ( 5 FDA reports)
APTYALISM ( 5 FDA reports)
ARTERIOVENOUS FISTULA ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
AXILLARY MASS ( 5 FDA reports)
BACTERIURIA ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BLADDER CANCER RECURRENT ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLAST CELL COUNT INCREASED ( 5 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
BLOOD PH INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 5 FDA reports)
BREAKTHROUGH PAIN ( 5 FDA reports)
BREAST CANCER STAGE I ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BREAST FIBROSIS ( 5 FDA reports)
BRONCHIAL OBSTRUCTION ( 5 FDA reports)
CATARACT CORTICAL ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CEREBRAL ARTERY STENOSIS ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
CHOLELITHOTOMY ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
CLEFT LIP ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
COARCTATION OF THE AORTA ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
COLONOSCOPY ABNORMAL ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CORNEAL NEOVASCULARISATION ( 5 FDA reports)
CORNEAL OPACITY ( 5 FDA reports)
CORONARY ARTERY REOCCLUSION ( 5 FDA reports)
CRANIAL NEUROPATHY ( 5 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
CYTOGENETIC ABNORMALITY ( 5 FDA reports)
DARK CIRCLES UNDER EYES ( 5 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
DEVICE LEAKAGE ( 5 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 5 FDA reports)
DRUG TOLERANCE DECREASED ( 5 FDA reports)
DYSTROPHIC CALCIFICATION ( 5 FDA reports)
EAR CANAL ERYTHEMA ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 5 FDA reports)
ENCEPHALITIS HERPES ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FAT INTOLERANCE ( 5 FDA reports)
FEBRILE BONE MARROW APLASIA ( 5 FDA reports)
FEMALE STERILISATION ( 5 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 5 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 5 FDA reports)
FUNGAL OESOPHAGITIS ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GALLBLADDER POLYP ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GASTRODUODENITIS ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROSTOMY TUBE INSERTION ( 5 FDA reports)
GLIOBLASTOMA ( 5 FDA reports)
GLOBULINS DECREASED ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
GRIP STRENGTH ( 5 FDA reports)
GROIN ABSCESS ( 5 FDA reports)
GROWTH RETARDATION ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
HAEMORRHAGE URINARY TRACT ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERTENSIVE EMERGENCY ( 5 FDA reports)
HYPERTHERMIA MALIGNANT ( 5 FDA reports)
HYPERTROPHY BREAST ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 5 FDA reports)
INCORRECT STORAGE OF DRUG ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INFUSION SITE REACTION ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE DISCOMFORT ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INJECTION SITE VESICLES ( 5 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
INTESTINAL PROLAPSE ( 5 FDA reports)
INTESTINAL RESECTION ( 5 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 5 FDA reports)
IUCD COMPLICATION ( 5 FDA reports)
JOINT CREPITATION ( 5 FDA reports)
KERATITIS INTERSTITIAL ( 5 FDA reports)
KETOACIDOSIS ( 5 FDA reports)
KLEBSIELLA TEST POSITIVE ( 5 FDA reports)
LUNG NEOPLASM SURGERY ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 5 FDA reports)
LYMPHOCYTOSIS ( 5 FDA reports)
MAMMOGRAM ABNORMAL ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
METABOLIC SYNDROME ( 5 FDA reports)
METASTASES TO ADRENALS ( 5 FDA reports)
METASTASES TO SPLEEN ( 5 FDA reports)
METATARSAL EXCISION ( 5 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 5 FDA reports)
MIDDLE EAR EFFUSION ( 5 FDA reports)
MIGRAINE WITH AURA ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
NAIL HYPERTROPHY ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
NEURODERMATITIS ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 5 FDA reports)
OROPHARYNGEAL BLISTERING ( 5 FDA reports)
OSTEOCHONDRITIS ( 5 FDA reports)
OTITIS MEDIA CHRONIC ( 5 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 5 FDA reports)
PANCREATIC ABSCESS ( 5 FDA reports)
PANCREATIC MASS ( 5 FDA reports)
PANNICULITIS ( 5 FDA reports)
PAPILLARY THYROID CANCER ( 5 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 5 FDA reports)
PARESIS ( 5 FDA reports)
PAROSMIA ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PERINEAL ABSCESS ( 5 FDA reports)
PERNICIOUS ANAEMIA ( 5 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PNEUMONIA ESCHERICHIA ( 5 FDA reports)
PNEUMONITIS CHEMICAL ( 5 FDA reports)
POLYCYSTIC OVARIES ( 5 FDA reports)
POLYCYTHAEMIA VERA ( 5 FDA reports)
POLYMYALGIA RHEUMATICA ( 5 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 5 FDA reports)
POST PROCEDURAL DIARRHOEA ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
PRE-ECLAMPSIA ( 5 FDA reports)
PREMENSTRUAL SYNDROME ( 5 FDA reports)
PRODUCT ADHESION ISSUE ( 5 FDA reports)
PROLAPSE REPAIR ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
PYODERMA ( 5 FDA reports)
PYOTHORAX ( 5 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 5 FDA reports)
RASH SCARLATINIFORM ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
REFRACTION DISORDER ( 5 FDA reports)
REFRACTORY ANAEMIA ( 5 FDA reports)
REGURGITATION OF FOOD ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RENAL VESSEL DISORDER ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RETINAL SCAR ( 5 FDA reports)
SCIATIC NERVE INJURY ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SHUNT MALFUNCTION ( 5 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
SOCIAL PHOBIA ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
SPERMATOCELE ( 5 FDA reports)
SPINAL CORD INFARCTION ( 5 FDA reports)
SPINAL LAMINECTOMY ( 5 FDA reports)
SPLENIC ARTERY ANEURYSM ( 5 FDA reports)
SPONDYLOSIS ( 5 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
ADENOIDECTOMY ( 4 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMINO ACID LEVEL INCREASED ( 4 FDA reports)
ANAL SKIN TAGS ( 4 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 4 FDA reports)
ANASTOMOTIC STENOSIS ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APPARENT DEATH ( 4 FDA reports)
APPLICATION SITE IRRITATION ( 4 FDA reports)
APPLICATION SITE VESICLES ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BENIGN BILIARY NEOPLASM ( 4 FDA reports)
BENIGN COLONIC POLYP ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BILIARY TRACT INFECTION ( 4 FDA reports)
BILOMA ( 4 FDA reports)
BINGE EATING ( 4 FDA reports)
BIOPSY COLON ABNORMAL ( 4 FDA reports)
BLADDER DISCOMFORT ( 4 FDA reports)
BLADDER NECK OPERATION ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLAST CELLS ABSENT ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN DECREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW NECROSIS ( 4 FDA reports)
BONE MARROW TOXICITY ( 4 FDA reports)
BRAIN CONTUSION ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BRAIN STEM STROKE ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CERVIX INFLAMMATION ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CLEFT UVULA ( 4 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
COGWHEEL RIGIDITY ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COLONIC STENOSIS ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CUTANEOUS TUBERCULOSIS ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
CYSTITIS RADIATION ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 4 FDA reports)
CYTOTOXIC OEDEMA ( 4 FDA reports)
DACRYOCYSTITIS ( 4 FDA reports)
DANDRUFF ( 4 FDA reports)
DAYDREAMING ( 4 FDA reports)
DELAYED FONTANELLE CLOSURE ( 4 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 4 FDA reports)
DERMATITIS HERPETIFORMIS ( 4 FDA reports)
DEVICE RELATED SEPSIS ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DIABETIC ULCER ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 4 FDA reports)
DISSEMINATED TUBERCULOSIS ( 4 FDA reports)
DISSOCIATIVE DISORDER ( 4 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
EAR TUBE INSERTION ( 4 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ENDOSCOPY ( 4 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 4 FDA reports)
ENEMA ADMINISTRATION ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
ENTEROCOLONIC FISTULA ( 4 FDA reports)
EPIDERMAL NAEVUS ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FAILURE OF IMPLANT ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FOOT OPERATION ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTRIC OPERATION ( 4 FDA reports)
GASTROENTERITIS NOROVIRUS ( 4 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
GASTROINTESTINAL EROSION ( 4 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GIARDIASIS ( 4 FDA reports)
GLIOSIS ( 4 FDA reports)
GOUTY TOPHUS ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMORRHOID OPERATION ( 4 FDA reports)
HAEMOSIDEROSIS ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HETEROPHORIA ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HYDROTHORAX ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPERTONIA NEONATAL ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
ILEOCOLECTOMY ( 4 FDA reports)
ILIUM FRACTURE ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INHALATION THERAPY ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE SCAR ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERTRIGO CANDIDA ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LDL/HDL RATIO ( 4 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LICHEN SCLEROSUS ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MAMMARY DUCT ECTASIA ( 4 FDA reports)
MARASMUS ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MUCOSAL ULCERATION ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MYCOBACTERIAL INFECTION ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 4 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 4 FDA reports)
MYELOMALACIA ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 4 FDA reports)
NEONATAL ASPIRATION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NEUTROPENIC COLITIS ( 4 FDA reports)
NIKOLSKY'S SIGN ( 4 FDA reports)
NIPPLE EXUDATE BLOODY ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PELVIC DISCOMFORT ( 4 FDA reports)
PERFORATED ULCER ( 4 FDA reports)
PERIORBITAL CELLULITIS ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 4 FDA reports)
PERITONEAL INFECTION ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PNEUMATOSIS ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMATURIA ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PRESBYACUSIS ( 4 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 4 FDA reports)
PSEUDOMENINGOCELE ( 4 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 4 FDA reports)
PULMONARY VALVE DISEASE ( 4 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
RADIATION SKIN INJURY ( 4 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 4 FDA reports)
RECTAL ULCER ( 4 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
RHEUMATIC HEART DISEASE ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
SCAN ABDOMEN ABNORMAL ( 4 FDA reports)
SCHOOL REFUSAL ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SCROTAL CYST ( 4 FDA reports)
SCROTAL SWELLING ( 4 FDA reports)
SENSATION OF BLOOD FLOW ( 4 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 4 FDA reports)
SIGMOIDECTOMY ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SKIN DESQUAMATION ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SLEEP TALKING ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
SOFT TISSUE INFLAMMATION ( 4 FDA reports)
SOLILOQUY ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SPLENIC CYST ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STARING ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
SWEAT GLAND DISORDER ( 4 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
TETANUS ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THROMBOLYSIS ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYMUS DISORDER ( 4 FDA reports)
THYROID MASS ( 4 FDA reports)
THYROXINE FREE DECREASED ( 4 FDA reports)
THYROXINE INCREASED ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TOOTH DISCOLOURATION ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TOXIC SHOCK SYNDROME ( 4 FDA reports)
TRACHEITIS ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRICHOMONIASIS ( 4 FDA reports)
TRICHOTILLOMANIA ( 4 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 4 FDA reports)
URETHRAL DILATATION ( 4 FDA reports)
URETHRAL FISTULA ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINARY TRACT OPERATION ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UROBILIN URINE PRESENT ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VASCULAR HEADACHE ( 4 FDA reports)
VASCULAR INSUFFICIENCY ( 4 FDA reports)
VASCULAR OPERATION ( 4 FDA reports)
VOCAL CORD PARESIS ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
WEIGHT DECREASE NEONATAL ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
WOUND TREATMENT ( 4 FDA reports)
T-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
TEETH BRITTLE ( 3 FDA reports)
TENDON GRAFT ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
THYROXINE DECREASED ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
TONGUE BLACK HAIRY ( 3 FDA reports)
TONGUE SPASM ( 3 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRANSAMINASES DECREASED ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URETHRAL DISCHARGE ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
URTICARIA PAPULAR ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
UTERINE SPASM ( 3 FDA reports)
VAGINAL INFLAMMATION ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VALVULOPLASTY CARDIAC ( 3 FDA reports)
VARICOCELE ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENA CAVA INJURY ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VIRAL RHINITIS ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WEANING FAILURE ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
YAWNING ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ZINC DEFICIENCY ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE FATTY LIVER OF PREGNANCY ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ADENOIDAL DISORDER ( 3 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
ALCOHOLIC PANCREATITIS ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 3 FDA reports)
ALVEOLAR OSTEITIS ( 3 FDA reports)
ALVEOLAR SOFT PART SARCOMA ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANAL CANDIDIASIS ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANASTOMOTIC LEAK ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTISOCIAL BEHAVIOUR ( 3 FDA reports)
ANTITHROMBIN III DECREASED ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 3 FDA reports)
ASPIRATION BONE MARROW ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
ATLANTOAXIAL INSTABILITY ( 3 FDA reports)
AUTISM SPECTRUM DISORDER ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
AVERSION ( 3 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 3 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BEREAVEMENT ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILIARY ADENOMA ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BIOPSY SKIN ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER NECK SUSPENSION ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLAST CELL COUNT DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
BRADYCARDIA NEONATAL ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BREAST CELLULITIS ( 3 FDA reports)
BREAST FIBROMA ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL CYST ( 3 FDA reports)
CERVICAL NEURITIS ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHEMICAL BURN OF SKIN ( 3 FDA reports)
CHONDRODYSTROPHY ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COLITIS MICROSCOPIC ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
CONGENITAL INTESTINAL MALFORMATION ( 3 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 3 FDA reports)
CONJUNCTIVAL PALLOR ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
COOMBS TEST POSITIVE ( 3 FDA reports)
CORONARY BYPASS THROMBOSIS ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CUTANEOUS SARCOIDOSIS ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DERMATOPHYTOSIS ( 3 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DISINHIBITION ( 3 FDA reports)
DIVERTICULUM DUODENAL ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG INTERACTION POTENTIATION ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
EMBOLISM VENOUS ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
EVANS SYNDROME ( 3 FDA reports)
EXPLORATIVE LAPAROTOMY ( 3 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FIBROADENOMA OF BREAST ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GALLBLADDER OEDEMA ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GASTRIC PH INCREASED ( 3 FDA reports)
GASTRIC ULCER HELICOBACTER ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GLIOMA ( 3 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 3 FDA reports)
GONORRHOEA ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 3 FDA reports)
HBV DNA INCREASED ( 3 FDA reports)
HEAD AND NECK CANCER ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEPATIC ADENOMA ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HERPES PHARYNGITIS ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HOMANS' SIGN ( 3 FDA reports)
HYPERALBUMINAEMIA ( 3 FDA reports)
HYPEREMESIS GRAVIDARUM ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERKINETIC HEART SYNDROME ( 3 FDA reports)
HYPERLIPASAEMIA ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMPLANT SITE PAIN ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INFANTILE SPITTING UP ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
INJECTION SITE OEDEMA ( 3 FDA reports)
INJECTION SITE STREAKING ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 3 FDA reports)
INTESTINAL ANASTOMOSIS ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
LACRIMATION DECREASED ( 3 FDA reports)
LASER THERAPY ( 3 FDA reports)
LEGAL PROBLEM ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LIMB OPERATION ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MARCUS GUNN SYNDROME ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METASTASES TO EYE ( 3 FDA reports)
METASTASES TO STOMACH ( 3 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 3 FDA reports)
MILIA ( 3 FDA reports)
MILK ALLERGY ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MUNCHAUSEN'S SYNDROME ( 3 FDA reports)
MURPHY'S SIGN POSITIVE ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYOGLOBINURIA ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OMENTECTOMY ( 3 FDA reports)
ONYCHOGRYPHOSIS ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
PACEMAKER COMPLICATION ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PLANTAR ERYTHEMA ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMOCONIOSIS ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
PO2 ABNORMAL ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYCHONDRITIS ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL VOMITING ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
POSTPARTUM HAEMORRHAGE ( 3 FDA reports)
POUCHITIS ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PRODUCT LABEL ISSUE ( 3 FDA reports)
PROPOFOL INFUSION SYNDROME ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATIC OPERATION ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
RADIAL PULSE ABNORMAL ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL CANCER STAGE IV ( 3 FDA reports)
REPERFUSION ARRHYTHMIA ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
RHINITIS SEASONAL ( 3 FDA reports)
ROSAI-DORFMAN SYNDROME ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SEBORRHOEA ( 3 FDA reports)
SECONDARY SEQUESTRUM ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
SINOBRONCHITIS ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN FRAGILITY ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN LESION EXCISION ( 3 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACHLORHYDRIA ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGITATION NEONATAL ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 2 FDA reports)
ALVEOLAR PROTEINOSIS ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANDROGENS ABNORMAL ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CYST EXCISION ( 2 FDA reports)
BREAST INFLAMMATION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 2 FDA reports)
BRONCHOMALACIA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CAPSULE PHYSICAL ISSUE ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 2 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR HAEMATOMA ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL CONISATION ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLANGITIS SUPPURATIVE ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMA URAEMIC ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL CYSTIC DISEASE OF LIVER ( 2 FDA reports)
CONGENITAL HYDROCEPHALUS ( 2 FDA reports)
CONGENITAL PNEUMONIA ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CONVULSIONS LOCAL ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYTOKINE STORM ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEMENTIA WITH LEWY BODIES ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE ADHESION ISSUE ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DEVICE STIMULATION ISSUE ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DIPHTHERIA ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DISUSE SYNDROME ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG LABEL CONFUSION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTROCARDIOGRAM ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
ENTERECTOMY ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOETAL MACROSOMIA ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FUNDOPLICATION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GENITAL DISORDER MALE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLUCOSE URINE ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 2 FDA reports)
HAEMODILUTION ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HERPES SIMPLEX OTITIS EXTERNA ( 2 FDA reports)
HIGH ARCHED PALATE ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HIV TEST POSITIVE ( 2 FDA reports)
HOMANS' SIGN POSITIVE ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HUMORAL IMMUNE DEFECT ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPOALDOSTERONISM ( 2 FDA reports)
HYPOFIBRINOGENAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOTHERMIA NEONATAL ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INFANTILE COLIC ( 2 FDA reports)
INFECTED EPIDERMAL CYST ( 2 FDA reports)
INFECTED SEBACEOUS CYST ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFERTILITY MALE ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE VASCULITIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
ISCHAEMIC LIMB PAIN ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT SURGERY ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LABOUR INDUCTION ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGOPHARYNGITIS ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LAXATIVE ABUSE ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPOPROTEIN (A) ABNORMAL ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METASTATIC LYMPHOMA ( 2 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MYCOTIC ALLERGY ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCARDIAC ABSCESS ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NIPPLE SWELLING ( 2 FDA reports)
NITRITE URINE ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR DYSMETRIA ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESOPHAGOSCOPY ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSTEOCHONDROMA ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE ADHESION ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL NERVE INJURY ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POSTICTAL HEADACHE ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT DEPOSIT ( 2 FDA reports)
PRODUCT DROPPER ISSUE ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN TIME RATIO ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL PAPILLARY NECROSIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENOVASCULAR HYPERTENSION ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 2 FDA reports)
REYE'S SYNDROME ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCIATIC NERVE NEUROPATHY ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SELF ESTEEM INFLATED ( 2 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPINA BIFIDA ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAG HORN CALCULUS ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
STENT MALFUNCTION ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
SUBMANDIBULAR MASS ( 2 FDA reports)
SUPPRESSED LACTATION ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TENSION ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UNEQUAL LIMB LENGTH ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URETERIC INJURY ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRAL SPASM ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINE BARBITURATES ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URTICARIA CHRONIC ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VAGUS NERVE DISORDER ( 2 FDA reports)
VASCULAR CAUTERISATION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VENTRICULAR HYPOPLASIA ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VOCAL CORD CYST ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VON WILLEBRAND'S DISEASE ( 2 FDA reports)
VULVAL LEUKOPLAKIA ( 2 FDA reports)
VULVOVAGINITIS ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC CAVITY DRAINAGE TEST ABNORMAL ( 1 FDA reports)
THREATENED LABOUR ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THYMOMA MALIGNANT ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TOOTH ANKYLOSIS ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TRUANCY ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY ANASTOMOTIC LEAK ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA AQUAGENIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE HYPERTONUS ( 1 FDA reports)
UTERINE MALPOSITION ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE POLYPECTOMY ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULAR TEST ABNORMAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIITH NERVE INJURY ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VULVOVAGINAL ULCERATION ( 1 FDA reports)
VULVOVAGINITIS GONOCOCCAL ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)
17-HYDROXYPROGESTERONE DECREASED ( 1 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACROKERATOSIS PARANEOPLASTICA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADENOSINE DEAMINASE DEFICIENCY ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA SCARRING ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNIOCENTESIS ABNORMAL ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL ( 1 FDA reports)
ANALGESIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANKYLOGLOSSIA ACQUIRED ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS MOENCKEBERG-TYPE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
ASYMPTOMATIC HIV INFECTION ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BIOPSY LARYNX ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLAST CELLS ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALUMINIUM INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE CYST EXCISION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST MALFORMATION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BUCCAL CAVITY PAPILLOMA ( 1 FDA reports)
BUCCOGLOSSAL SYNDROME ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURN DRESSING ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY NAIL REFILL TEST ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBELLAR HYPOPLASIA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROSPINAL FISTULA ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEST WALL NECROSIS ( 1 FDA reports)
CHEST X-RAY ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHOANAL ATRESIA ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONGENITAL ACROCHORDON ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTACT LENS COMPLICATION ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS DUODENITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DACRYOCYSTORHINOSTOMY ( 1 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEHYDROEPIANDROSTERONE DECREASED ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA NEONATAL ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DISLOCATION OF STERNUM ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DRUG CLEARANCE INCREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR NEOPLASM MALIGNANT ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EATON-LAMBERT SYNDROME ( 1 FDA reports)
ECHOENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA INFANTILE ( 1 FDA reports)
EGOBRONCHOPHONY ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC PNEUMONIA ( 1 FDA reports)
EMERGENCY CARE EXAMINATION ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
EMPHYSEMATOUS CHOLECYSTITIS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCRINE TEST ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTERNAL EAR LESION EXCISION ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACE LIFT ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FATTY ACID DEFICIENCY ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROADENOMA ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FINGER HYPOPLASIA ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL INFECTION ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLUCOCORTICOIDS DECREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GYNAECOLOGICAL CHLAMYDIA INFECTION ( 1 FDA reports)
HAEMANGIOMA REMOVAL ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART BLOCK CONGENITAL ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS NON-A NON-B ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOBILIARY INFECTION ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HEPATOBLASTOMA ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 1 FDA reports)
HORSESHOE KIDNEY ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCHROMASIA ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOTELORISM OF ORBIT ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOZINCAEMIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCREASED ANTEROPOSTERIOR CHEST DIAMETER ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED INSECT BITE ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRANASAL NUMBNESS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATITIS SCLEROSING ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP OPERATION ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULE ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASTOCYTOMA ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS ENTEROVIRAL ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINERAL SUPPLEMENTATION ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORAXELLA TEST POSITIVE ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOBLAST COUNT INCREASED ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPLASTY ( 1 FDA reports)
MYXOEDEMA COMA ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEEDLE BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO DECREASED ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL MUCOSA ATROPHY ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEITIS CONDENSANS ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANASAL SINUS HAEMATOMA ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARASITIC INFECTION INTESTINAL ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC ORGAN INJURY ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE CURVATURE ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERINEAL LACERATION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL EROSION ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCHROMIC RED BLOOD CELLS PRESENT ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POSTURING ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULMONARY VEIN OCCLUSION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYOPNEUMOTHORAX ( 1 FDA reports)
RABIES ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RASH PSORIAFORM ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
REBOUND TACHYCARDIA ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL OBSTRUCTION ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL GLYCOSURIA ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOENDOTHELIAL SYSTEM STIMULATED ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINITIS PERENNIAL ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC RASH ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINA BIFIDA OCCULTA ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STRUCK BY LIGHTNING ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)