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

PAIN ( 3228 FDA reports)
NAUSEA ( 3056 FDA reports)
FATIGUE ( 3001 FDA reports)
FALL ( 2726 FDA reports)
DYSPNOEA ( 2373 FDA reports)
ARTHRALGIA ( 2359 FDA reports)
HEADACHE ( 2333 FDA reports)
DIARRHOEA ( 2277 FDA reports)
ASTHENIA ( 2247 FDA reports)
DIZZINESS ( 2246 FDA reports)
PAIN IN EXTREMITY ( 2056 FDA reports)
BACK PAIN ( 1963 FDA reports)
VOMITING ( 1715 FDA reports)
OEDEMA PERIPHERAL ( 1514 FDA reports)
DRUG INEFFECTIVE ( 1479 FDA reports)
WEIGHT DECREASED ( 1464 FDA reports)
MALAISE ( 1443 FDA reports)
PNEUMONIA ( 1431 FDA reports)
PYREXIA ( 1421 FDA reports)
ANXIETY ( 1399 FDA reports)
ANAEMIA ( 1396 FDA reports)
CHEST PAIN ( 1296 FDA reports)
GAIT DISTURBANCE ( 1287 FDA reports)
PRURITUS ( 1253 FDA reports)
CONSTIPATION ( 1158 FDA reports)
MUSCLE SPASMS ( 1148 FDA reports)
INSOMNIA ( 1138 FDA reports)
DEPRESSION ( 1133 FDA reports)
COUGH ( 1084 FDA reports)
FEELING ABNORMAL ( 1064 FDA reports)
MYALGIA ( 1063 FDA reports)
HYPERTENSION ( 1028 FDA reports)
URINARY TRACT INFECTION ( 1006 FDA reports)
HYPOAESTHESIA ( 999 FDA reports)
RASH ( 984 FDA reports)
DEHYDRATION ( 976 FDA reports)
FLUSHING ( 970 FDA reports)
PARAESTHESIA ( 965 FDA reports)
ABDOMINAL PAIN ( 940 FDA reports)
INJECTION SITE PAIN ( 921 FDA reports)
MUSCULAR WEAKNESS ( 869 FDA reports)
DECREASED APPETITE ( 864 FDA reports)
ERYTHEMA ( 849 FDA reports)
BONE PAIN ( 825 FDA reports)
TREMOR ( 802 FDA reports)
WEIGHT INCREASED ( 797 FDA reports)
DEATH ( 769 FDA reports)
HYPOTENSION ( 760 FDA reports)
CONTUSION ( 752 FDA reports)
ATRIAL FIBRILLATION ( 751 FDA reports)
BLOOD PRESSURE INCREASED ( 736 FDA reports)
OSTEOARTHRITIS ( 732 FDA reports)
CHILLS ( 722 FDA reports)
ABDOMINAL PAIN UPPER ( 717 FDA reports)
CONFUSIONAL STATE ( 699 FDA reports)
BLOOD GLUCOSE INCREASED ( 679 FDA reports)
OSTEOPOROSIS ( 660 FDA reports)
SOMNOLENCE ( 656 FDA reports)
VISION BLURRED ( 648 FDA reports)
BONE DISORDER ( 648 FDA reports)
OSTEONECROSIS OF JAW ( 638 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 622 FDA reports)
BALANCE DISORDER ( 620 FDA reports)
OSTEONECROSIS ( 611 FDA reports)
SINUSITIS ( 606 FDA reports)
PALPITATIONS ( 604 FDA reports)
HYPERHIDROSIS ( 603 FDA reports)
INJURY ( 598 FDA reports)
MUSCULOSKELETAL PAIN ( 585 FDA reports)
ABDOMINAL DISCOMFORT ( 583 FDA reports)
CEREBROVASCULAR ACCIDENT ( 575 FDA reports)
PAIN IN JAW ( 569 FDA reports)
CONVULSION ( 564 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 561 FDA reports)
INJECTION SITE ERYTHEMA ( 561 FDA reports)
RENAL FAILURE ACUTE ( 553 FDA reports)
LOSS OF CONSCIOUSNESS ( 552 FDA reports)
MEMORY IMPAIRMENT ( 551 FDA reports)
INFECTION ( 549 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 548 FDA reports)
PULMONARY EMBOLISM ( 548 FDA reports)
CHEST DISCOMFORT ( 542 FDA reports)
DYSPEPSIA ( 542 FDA reports)
DYSPHAGIA ( 532 FDA reports)
DRUG DOSE OMISSION ( 529 FDA reports)
JOINT SWELLING ( 526 FDA reports)
HAEMOGLOBIN DECREASED ( 523 FDA reports)
CONDITION AGGRAVATED ( 518 FDA reports)
SWELLING ( 515 FDA reports)
BRONCHITIS ( 512 FDA reports)
ARTHRITIS ( 507 FDA reports)
INFLUENZA LIKE ILLNESS ( 507 FDA reports)
DEEP VEIN THROMBOSIS ( 502 FDA reports)
NASOPHARYNGITIS ( 501 FDA reports)
RENAL FAILURE ( 501 FDA reports)
FEELING HOT ( 494 FDA reports)
MYOCARDIAL INFARCTION ( 487 FDA reports)
NECK PAIN ( 485 FDA reports)
PLEURAL EFFUSION ( 482 FDA reports)
SYNCOPE ( 482 FDA reports)
ALOPECIA ( 477 FDA reports)
HEART RATE INCREASED ( 474 FDA reports)
OSTEOMYELITIS ( 464 FDA reports)
INJECTION SITE HAEMATOMA ( 459 FDA reports)
VISUAL IMPAIRMENT ( 456 FDA reports)
URTICARIA ( 449 FDA reports)
CATARACT ( 449 FDA reports)
OROPHARYNGEAL PAIN ( 447 FDA reports)
NEUROPATHY PERIPHERAL ( 440 FDA reports)
TOOTH EXTRACTION ( 439 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 438 FDA reports)
SEPSIS ( 432 FDA reports)
RIB FRACTURE ( 428 FDA reports)
ABDOMINAL DISTENSION ( 413 FDA reports)
CELLULITIS ( 413 FDA reports)
BLOOD CREATININE INCREASED ( 412 FDA reports)
FEMUR FRACTURE ( 410 FDA reports)
HIP FRACTURE ( 410 FDA reports)
HOT FLUSH ( 404 FDA reports)
HYPERSENSITIVITY ( 403 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 401 FDA reports)
SPINAL OSTEOARTHRITIS ( 401 FDA reports)
IMPAIRED HEALING ( 396 FDA reports)
CHOLELITHIASIS ( 394 FDA reports)
THROMBOCYTOPENIA ( 390 FDA reports)
AMNESIA ( 378 FDA reports)
ASTHMA ( 374 FDA reports)
OSTEOPENIA ( 370 FDA reports)
DRY MOUTH ( 369 FDA reports)
ATELECTASIS ( 365 FDA reports)
HAEMORRHAGE ( 360 FDA reports)
BREAST CANCER ( 358 FDA reports)
DYSGEUSIA ( 357 FDA reports)
BURNING SENSATION ( 351 FDA reports)
INJECTION SITE HAEMORRHAGE ( 351 FDA reports)
MIGRAINE ( 350 FDA reports)
RHEUMATOID ARTHRITIS ( 344 FDA reports)
BONE DENSITY DECREASED ( 340 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 340 FDA reports)
RESPIRATORY FAILURE ( 336 FDA reports)
DRUG INTERACTION ( 335 FDA reports)
ABASIA ( 331 FDA reports)
DYSURIA ( 328 FDA reports)
HERPES ZOSTER ( 323 FDA reports)
BLOOD PRESSURE DECREASED ( 322 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 322 FDA reports)
OFF LABEL USE ( 320 FDA reports)
NEPHROLITHIASIS ( 319 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 318 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 317 FDA reports)
VERTIGO ( 316 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 313 FDA reports)
CARDIAC DISORDER ( 308 FDA reports)
NEOPLASM MALIGNANT ( 308 FDA reports)
POLLAKIURIA ( 308 FDA reports)
ANHEDONIA ( 306 FDA reports)
MOBILITY DECREASED ( 306 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 305 FDA reports)
HYPOKALAEMIA ( 303 FDA reports)
HYPONATRAEMIA ( 301 FDA reports)
RECTAL HAEMORRHAGE ( 299 FDA reports)
DENTAL CARIES ( 295 FDA reports)
OEDEMA ( 293 FDA reports)
RENAL FAILURE CHRONIC ( 291 FDA reports)
THROMBOSIS ( 291 FDA reports)
EMOTIONAL DISTRESS ( 289 FDA reports)
HAEMORRHOIDS ( 286 FDA reports)
TACHYCARDIA ( 286 FDA reports)
BLOOD POTASSIUM DECREASED ( 285 FDA reports)
GASTRITIS ( 284 FDA reports)
DYSPHONIA ( 283 FDA reports)
EPISTAXIS ( 282 FDA reports)
PANCYTOPENIA ( 281 FDA reports)
PLATELET COUNT DECREASED ( 281 FDA reports)
SWELLING FACE ( 278 FDA reports)
CORONARY ARTERY DISEASE ( 276 FDA reports)
CROHN'S DISEASE ( 274 FDA reports)
DIVERTICULUM ( 274 FDA reports)
INFLUENZA ( 274 FDA reports)
BLOOD CALCIUM INCREASED ( 271 FDA reports)
NEUTROPENIA ( 270 FDA reports)
DIABETES MELLITUS ( 267 FDA reports)
NERVOUSNESS ( 266 FDA reports)
TOOTHACHE ( 266 FDA reports)
SPINAL COMPRESSION FRACTURE ( 262 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 261 FDA reports)
HAEMATOCHEZIA ( 261 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 260 FDA reports)
HYPOPHAGIA ( 260 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 260 FDA reports)
RHINORRHOEA ( 259 FDA reports)
SLEEP DISORDER ( 259 FDA reports)
HEPATIC ENZYME INCREASED ( 259 FDA reports)
VISUAL ACUITY REDUCED ( 257 FDA reports)
FLATULENCE ( 256 FDA reports)
ARTHROPATHY ( 255 FDA reports)
SPINAL FRACTURE ( 254 FDA reports)
MULTIPLE MYELOMA ( 249 FDA reports)
STRESS ( 248 FDA reports)
URINARY INCONTINENCE ( 246 FDA reports)
RENAL IMPAIRMENT ( 244 FDA reports)
TOOTH DISORDER ( 244 FDA reports)
DYSPNOEA EXERTIONAL ( 244 FDA reports)
HAEMATOCRIT DECREASED ( 240 FDA reports)
LUNG DISORDER ( 239 FDA reports)
MITRAL VALVE INCOMPETENCE ( 239 FDA reports)
PANCREATITIS ( 239 FDA reports)
LYMPHADENOPATHY ( 237 FDA reports)
HYPOCALCAEMIA ( 235 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 235 FDA reports)
DRUG HYPERSENSITIVITY ( 234 FDA reports)
SURGERY ( 233 FDA reports)
WHEEZING ( 232 FDA reports)
EYE PAIN ( 231 FDA reports)
INFLAMMATION ( 229 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 229 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 229 FDA reports)
SPEECH DISORDER ( 228 FDA reports)
TOOTH LOSS ( 228 FDA reports)
BLOOD GLUCOSE DECREASED ( 228 FDA reports)
LETHARGY ( 226 FDA reports)
STAPHYLOCOCCAL INFECTION ( 225 FDA reports)
FIBROMYALGIA ( 224 FDA reports)
HYPERLIPIDAEMIA ( 224 FDA reports)
CYSTITIS ( 223 FDA reports)
VITAMIN D DECREASED ( 223 FDA reports)
RASH PRURITIC ( 222 FDA reports)
BONE LESION ( 222 FDA reports)
DRY SKIN ( 222 FDA reports)
GASTROINTESTINAL DISORDER ( 221 FDA reports)
PRODUCT QUALITY ISSUE ( 220 FDA reports)
INCORRECT DOSE ADMINISTERED ( 219 FDA reports)
MOVEMENT DISORDER ( 219 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 217 FDA reports)
SUICIDAL IDEATION ( 217 FDA reports)
AGITATION ( 216 FDA reports)
FOOT FRACTURE ( 216 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 215 FDA reports)
URINARY RETENTION ( 214 FDA reports)
UPPER LIMB FRACTURE ( 213 FDA reports)
DISTURBANCE IN ATTENTION ( 212 FDA reports)
MENTAL STATUS CHANGES ( 212 FDA reports)
VITAMIN D DEFICIENCY ( 211 FDA reports)
CARDIOMEGALY ( 210 FDA reports)
ARTERIOSCLEROSIS ( 208 FDA reports)
CARDIAC ARREST ( 208 FDA reports)
ARRHYTHMIA ( 207 FDA reports)
BLOOD CALCIUM DECREASED ( 207 FDA reports)
FEELING COLD ( 207 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 207 FDA reports)
HEART RATE IRREGULAR ( 205 FDA reports)
DRY EYE ( 204 FDA reports)
HIATUS HERNIA ( 204 FDA reports)
METASTASES TO BONE ( 203 FDA reports)
ORAL PAIN ( 202 FDA reports)
TOOTH ABSCESS ( 202 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 200 FDA reports)
PULMONARY HYPERTENSION ( 198 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 198 FDA reports)
DYSARTHRIA ( 196 FDA reports)
NASAL CONGESTION ( 195 FDA reports)
HEART RATE DECREASED ( 194 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 194 FDA reports)
STOMATITIS ( 194 FDA reports)
DEFORMITY ( 192 FDA reports)
BRADYCARDIA ( 191 FDA reports)
PSORIASIS ( 191 FDA reports)
HAEMATURIA ( 190 FDA reports)
HOSPITALISATION ( 189 FDA reports)
WRIST FRACTURE ( 189 FDA reports)
DIVERTICULITIS ( 187 FDA reports)
SKIN BURNING SENSATION ( 186 FDA reports)
PRURITUS GENERALISED ( 185 FDA reports)
TINNITUS ( 185 FDA reports)
JOINT STIFFNESS ( 184 FDA reports)
BLISTER ( 182 FDA reports)
DISCOMFORT ( 182 FDA reports)
NIGHT SWEATS ( 182 FDA reports)
DYSKINESIA ( 181 FDA reports)
BLOOD UREA INCREASED ( 180 FDA reports)
HALLUCINATION ( 180 FDA reports)
NEURALGIA ( 180 FDA reports)
OVERDOSE ( 180 FDA reports)
ANGINA PECTORIS ( 179 FDA reports)
CARDIAC FAILURE ( 179 FDA reports)
HYPOTHYROIDISM ( 179 FDA reports)
MULTIPLE SCLEROSIS ( 178 FDA reports)
FLUID RETENTION ( 177 FDA reports)
HEAD INJURY ( 176 FDA reports)
DYSSTASIA ( 174 FDA reports)
EXOSTOSIS ( 174 FDA reports)
RENAL CYST ( 174 FDA reports)
SKIN ULCER ( 173 FDA reports)
INJECTION SITE PRURITUS ( 173 FDA reports)
LEUKOPENIA ( 173 FDA reports)
EAR PAIN ( 172 FDA reports)
PULMONARY OEDEMA ( 172 FDA reports)
SKIN DISCOLOURATION ( 171 FDA reports)
COMPRESSION FRACTURE ( 171 FDA reports)
PRODUCTIVE COUGH ( 170 FDA reports)
ROAD TRAFFIC ACCIDENT ( 170 FDA reports)
DISEASE PROGRESSION ( 169 FDA reports)
JOINT INJURY ( 169 FDA reports)
JAW DISORDER ( 168 FDA reports)
DISORIENTATION ( 167 FDA reports)
IRRITABILITY ( 166 FDA reports)
PULMONARY FIBROSIS ( 166 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 165 FDA reports)
VIRAL INFECTION ( 164 FDA reports)
DIPLOPIA ( 164 FDA reports)
DRUG EFFECT DECREASED ( 164 FDA reports)
BODY HEIGHT DECREASED ( 163 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 163 FDA reports)
INJECTION SITE REACTION ( 162 FDA reports)
OXYGEN SATURATION DECREASED ( 162 FDA reports)
ABNORMAL DREAMS ( 161 FDA reports)
HIP ARTHROPLASTY ( 161 FDA reports)
HYPERCHOLESTEROLAEMIA ( 161 FDA reports)
HEPATIC STEATOSIS ( 160 FDA reports)
SPINAL COLUMN STENOSIS ( 160 FDA reports)
SKIN EXFOLIATION ( 159 FDA reports)
INTESTINAL OBSTRUCTION ( 159 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 158 FDA reports)
COGNITIVE DISORDER ( 157 FDA reports)
LOOSE TOOTH ( 157 FDA reports)
LIMB INJURY ( 155 FDA reports)
ROTATOR CUFF SYNDROME ( 155 FDA reports)
GALLBLADDER DISORDER ( 154 FDA reports)
HYPERCALCAEMIA ( 154 FDA reports)
INFUSION RELATED REACTION ( 154 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 153 FDA reports)
BASAL CELL CARCINOMA ( 152 FDA reports)
PRESYNCOPE ( 152 FDA reports)
SLEEP APNOEA SYNDROME ( 152 FDA reports)
PELVIC FRACTURE ( 150 FDA reports)
NOCTURIA ( 149 FDA reports)
PRIMARY SEQUESTRUM ( 149 FDA reports)
RASH ERYTHEMATOUS ( 149 FDA reports)
RENAL DISORDER ( 149 FDA reports)
SCOLIOSIS ( 148 FDA reports)
EYE SWELLING ( 148 FDA reports)
KYPHOSIS ( 148 FDA reports)
MEDICATION ERROR ( 148 FDA reports)
FISTULA ( 147 FDA reports)
CANDIDIASIS ( 146 FDA reports)
FUNGAL INFECTION ( 146 FDA reports)
SINUS DISORDER ( 146 FDA reports)
GLAUCOMA ( 145 FDA reports)
HAEMOPTYSIS ( 145 FDA reports)
LIMB DISCOMFORT ( 145 FDA reports)
PATHOLOGICAL FRACTURE ( 145 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 144 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 143 FDA reports)
DEAFNESS ( 142 FDA reports)
DECREASED INTEREST ( 141 FDA reports)
EXCORIATION ( 141 FDA reports)
EYE DISORDER ( 141 FDA reports)
RASH GENERALISED ( 141 FDA reports)
ANKLE FRACTURE ( 140 FDA reports)
BURSITIS ( 140 FDA reports)
CARPAL TUNNEL SYNDROME ( 140 FDA reports)
DISABILITY ( 139 FDA reports)
INJECTION SITE SWELLING ( 139 FDA reports)
IRRITABLE BOWEL SYNDROME ( 139 FDA reports)
TOOTH INFECTION ( 139 FDA reports)
FEAR ( 138 FDA reports)
INTENTIONAL DRUG MISUSE ( 138 FDA reports)
BLINDNESS ( 137 FDA reports)
BLOOD SODIUM DECREASED ( 137 FDA reports)
COLITIS ( 137 FDA reports)
RASH MACULAR ( 137 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 136 FDA reports)
APHASIA ( 136 FDA reports)
ILL-DEFINED DISORDER ( 136 FDA reports)
LUNG NEOPLASM ( 136 FDA reports)
ORTHOSTATIC HYPOTENSION ( 136 FDA reports)
CRYING ( 135 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 135 FDA reports)
HYPOXIA ( 134 FDA reports)
LEUKOCYTOSIS ( 133 FDA reports)
MENTAL DISORDER ( 133 FDA reports)
NODULE ( 133 FDA reports)
TENDONITIS ( 133 FDA reports)
THROAT IRRITATION ( 133 FDA reports)
PALLOR ( 132 FDA reports)
CYST ( 131 FDA reports)
LOWER LIMB FRACTURE ( 131 FDA reports)
LUMBAR SPINAL STENOSIS ( 130 FDA reports)
UNRESPONSIVE TO STIMULI ( 129 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 129 FDA reports)
SEPTIC SHOCK ( 128 FDA reports)
COLONIC POLYP ( 128 FDA reports)
ECONOMIC PROBLEM ( 126 FDA reports)
FRACTURE ( 126 FDA reports)
LACERATION ( 126 FDA reports)
SKIN LESION ( 126 FDA reports)
FEBRILE NEUTROPENIA ( 125 FDA reports)
HYPERGLYCAEMIA ( 124 FDA reports)
OESOPHAGITIS ( 124 FDA reports)
EATING DISORDER ( 123 FDA reports)
HYPERSOMNIA ( 123 FDA reports)
HYPOGLYCAEMIA ( 123 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 123 FDA reports)
MOUTH ULCERATION ( 123 FDA reports)
SCAR ( 123 FDA reports)
DEBRIDEMENT ( 122 FDA reports)
DEPRESSED MOOD ( 122 FDA reports)
KNEE ARTHROPLASTY ( 122 FDA reports)
MASS ( 122 FDA reports)
EMPHYSEMA ( 121 FDA reports)
FLANK PAIN ( 121 FDA reports)
ORAL CANDIDIASIS ( 121 FDA reports)
ADVERSE DRUG REACTION ( 120 FDA reports)
ORAL DISORDER ( 120 FDA reports)
PURULENT DISCHARGE ( 120 FDA reports)
SKIN DISORDER ( 120 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 120 FDA reports)
TYPE 2 DIABETES MELLITUS ( 119 FDA reports)
JAW FRACTURE ( 119 FDA reports)
OSTEITIS ( 119 FDA reports)
DEMENTIA ( 118 FDA reports)
GASTRIC ULCER ( 118 FDA reports)
HYPERKALAEMIA ( 118 FDA reports)
SINUS BRADYCARDIA ( 118 FDA reports)
VAGINAL HAEMORRHAGE ( 118 FDA reports)
WALKING AID USER ( 117 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 117 FDA reports)
HAEMATOMA ( 117 FDA reports)
LUNG NEOPLASM MALIGNANT ( 116 FDA reports)
OCULAR HYPERAEMIA ( 116 FDA reports)
TOOTH FRACTURE ( 116 FDA reports)
CARDIAC MURMUR ( 115 FDA reports)
PANIC ATTACK ( 115 FDA reports)
CORONARY ARTERY OCCLUSION ( 114 FDA reports)
PROSTATE CANCER ( 114 FDA reports)
UNEVALUABLE EVENT ( 113 FDA reports)
MASTICATION DISORDER ( 113 FDA reports)
ANGER ( 112 FDA reports)
HYPOACUSIS ( 112 FDA reports)
MICTURITION URGENCY ( 112 FDA reports)
SYNOVIAL CYST ( 112 FDA reports)
GINGIVITIS ( 111 FDA reports)
ENDODONTIC PROCEDURE ( 110 FDA reports)
PHYSICAL DISABILITY ( 110 FDA reports)
SCIATICA ( 110 FDA reports)
SPINAL DISORDER ( 110 FDA reports)
SWOLLEN TONGUE ( 110 FDA reports)
THYROID DISORDER ( 110 FDA reports)
HEMIPARESIS ( 109 FDA reports)
LIP SWELLING ( 109 FDA reports)
BACTERIAL INFECTION ( 107 FDA reports)
MUSCLE TWITCHING ( 107 FDA reports)
TREATMENT NONCOMPLIANCE ( 107 FDA reports)
ANOREXIA ( 106 FDA reports)
CHRONIC SINUSITIS ( 106 FDA reports)
GASTRIC DISORDER ( 106 FDA reports)
GOUT ( 106 FDA reports)
POOR QUALITY SLEEP ( 106 FDA reports)
ABSCESS ( 105 FDA reports)
METASTASES TO LIVER ( 105 FDA reports)
AORTIC ANEURYSM ( 104 FDA reports)
BREAST MASS ( 104 FDA reports)
DERMATITIS ( 103 FDA reports)
LOCALISED INFECTION ( 103 FDA reports)
RESTLESS LEGS SYNDROME ( 103 FDA reports)
SINUS TACHYCARDIA ( 103 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 102 FDA reports)
CARDIOMYOPATHY ( 102 FDA reports)
GYNAECOMASTIA ( 102 FDA reports)
BACK DISORDER ( 101 FDA reports)
IRON DEFICIENCY ANAEMIA ( 101 FDA reports)
JOINT DISLOCATION ( 101 FDA reports)
PNEUMOTHORAX ( 101 FDA reports)
TENDERNESS ( 101 FDA reports)
RASH PAPULAR ( 100 FDA reports)
RESPIRATORY DISORDER ( 100 FDA reports)
SINUS CONGESTION ( 100 FDA reports)
THROAT TIGHTNESS ( 100 FDA reports)
LIVER DISORDER ( 100 FDA reports)
HYDRONEPHROSIS ( 99 FDA reports)
MALNUTRITION ( 99 FDA reports)
PNEUMONIA ASPIRATION ( 99 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 98 FDA reports)
DEVICE MALFUNCTION ( 98 FDA reports)
EMOTIONAL DISORDER ( 98 FDA reports)
GASTROENTERITIS ( 98 FDA reports)
GOITRE ( 98 FDA reports)
GROIN PAIN ( 98 FDA reports)
LACRIMATION INCREASED ( 98 FDA reports)
MUSCLE TIGHTNESS ( 98 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 98 FDA reports)
SENSORY DISTURBANCE ( 97 FDA reports)
BLOOD ALBUMIN DECREASED ( 97 FDA reports)
NERVOUS SYSTEM DISORDER ( 97 FDA reports)
PERIODONTAL DISEASE ( 97 FDA reports)
ABNORMAL BEHAVIOUR ( 96 FDA reports)
ACTINOMYCOSIS ( 96 FDA reports)
BLOOD URINE PRESENT ( 96 FDA reports)
BODY TEMPERATURE INCREASED ( 96 FDA reports)
PARKINSON'S DISEASE ( 96 FDA reports)
PERIODONTITIS ( 96 FDA reports)
PULMONARY CONGESTION ( 96 FDA reports)
STRESS FRACTURE ( 96 FDA reports)
RESTLESSNESS ( 95 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 95 FDA reports)
DRUG INTOLERANCE ( 95 FDA reports)
EXPOSED BONE IN JAW ( 95 FDA reports)
EYE IRRITATION ( 95 FDA reports)
GLOSSODYNIA ( 95 FDA reports)
HAEMATEMESIS ( 95 FDA reports)
INCREASED APPETITE ( 95 FDA reports)
JAW OPERATION ( 95 FDA reports)
PERICARDIAL EFFUSION ( 95 FDA reports)
BLOOD POTASSIUM INCREASED ( 94 FDA reports)
CLOSTRIDIAL INFECTION ( 94 FDA reports)
DIVERTICULUM INTESTINAL ( 94 FDA reports)
FAECES DISCOLOURED ( 94 FDA reports)
GINGIVAL SWELLING ( 94 FDA reports)
AORTIC VALVE INCOMPETENCE ( 93 FDA reports)
CATARACT OPERATION ( 93 FDA reports)
ECCHYMOSIS ( 93 FDA reports)
HYPOMAGNESAEMIA ( 93 FDA reports)
LUNG INFILTRATION ( 93 FDA reports)
NEOPLASM PROGRESSION ( 93 FDA reports)
OSTEOSCLEROSIS ( 93 FDA reports)
RETCHING ( 93 FDA reports)
RESPIRATORY DISTRESS ( 92 FDA reports)
SPONDYLOLISTHESIS ( 92 FDA reports)
DELIRIUM ( 92 FDA reports)
MUSCLE STRAIN ( 92 FDA reports)
OSTEOLYSIS ( 92 FDA reports)
POST PROCEDURAL COMPLICATION ( 92 FDA reports)
ADVERSE EVENT ( 91 FDA reports)
BLOOD MAGNESIUM DECREASED ( 91 FDA reports)
DRUG ADMINISTRATION ERROR ( 91 FDA reports)
GINGIVAL BLEEDING ( 91 FDA reports)
GINGIVAL INFECTION ( 91 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 91 FDA reports)
LUNG INFECTION ( 90 FDA reports)
MIDDLE INSOMNIA ( 90 FDA reports)
ABDOMINAL PAIN LOWER ( 89 FDA reports)
AGGRESSION ( 89 FDA reports)
CHOLECYSTECTOMY ( 89 FDA reports)
FEMORAL NECK FRACTURE ( 89 FDA reports)
GINGIVAL RECESSION ( 89 FDA reports)
MULTI-ORGAN FAILURE ( 89 FDA reports)
ATRIAL FLUTTER ( 88 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 88 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 88 FDA reports)
CHOLECYSTITIS ( 88 FDA reports)
CHOLECYSTITIS CHRONIC ( 88 FDA reports)
DEVICE RELATED INFECTION ( 88 FDA reports)
MACULAR DEGENERATION ( 88 FDA reports)
OVARIAN CYST ( 88 FDA reports)
COLD SWEAT ( 87 FDA reports)
KIDNEY INFECTION ( 87 FDA reports)
MUSCLE DISORDER ( 87 FDA reports)
NO ADVERSE EVENT ( 87 FDA reports)
PROCEDURAL PAIN ( 87 FDA reports)
ANAPHYLACTIC REACTION ( 86 FDA reports)
DECUBITUS ULCER ( 86 FDA reports)
HEPATIC FAILURE ( 86 FDA reports)
LYMPHOMA ( 86 FDA reports)
MYELODYSPLASTIC SYNDROME ( 86 FDA reports)
BEDRIDDEN ( 85 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 85 FDA reports)
TIBIA FRACTURE ( 85 FDA reports)
BACK INJURY ( 84 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 84 FDA reports)
ERECTILE DYSFUNCTION ( 84 FDA reports)
HYPOPHOSPHATAEMIA ( 84 FDA reports)
JOINT EFFUSION ( 84 FDA reports)
LYMPHOEDEMA ( 84 FDA reports)
METASTASES TO LUNG ( 84 FDA reports)
METASTASES TO SPINE ( 84 FDA reports)
METASTATIC NEOPLASM ( 84 FDA reports)
PHARYNGEAL OEDEMA ( 84 FDA reports)
ABDOMINAL HERNIA ( 83 FDA reports)
CARDIO-RESPIRATORY ARREST ( 83 FDA reports)
COMA ( 83 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 83 FDA reports)
HYPOKINESIA ( 83 FDA reports)
INTERSTITIAL LUNG DISEASE ( 83 FDA reports)
LEFT ATRIAL DILATATION ( 83 FDA reports)
CERVICAL SPINAL STENOSIS ( 82 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 82 FDA reports)
DENTURE WEARER ( 82 FDA reports)
ECZEMA ( 82 FDA reports)
FEELING JITTERY ( 82 FDA reports)
GINGIVAL DISORDER ( 82 FDA reports)
HERNIA ( 82 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 82 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 81 FDA reports)
AORTIC STENOSIS ( 81 FDA reports)
CEREBRAL ATROPHY ( 81 FDA reports)
CHROMATURIA ( 81 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 81 FDA reports)
ATAXIA ( 80 FDA reports)
FACIAL PAIN ( 80 FDA reports)
HEPATITIS ( 80 FDA reports)
HEPATOMEGALY ( 80 FDA reports)
HYPERKERATOSIS ( 80 FDA reports)
MENTAL IMPAIRMENT ( 80 FDA reports)
RESPIRATORY TRACT INFECTION ( 80 FDA reports)
SKIN CANCER ( 80 FDA reports)
ULCER ( 80 FDA reports)
STENT PLACEMENT ( 79 FDA reports)
ASCITES ( 79 FDA reports)
CEREBRAL HAEMORRHAGE ( 79 FDA reports)
NIGHTMARE ( 79 FDA reports)
PNEUMONITIS ( 79 FDA reports)
ERUCTATION ( 78 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 78 FDA reports)
BLOOD BILIRUBIN INCREASED ( 77 FDA reports)
GINGIVAL PAIN ( 77 FDA reports)
JAUNDICE ( 77 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 77 FDA reports)
ONYCHOMYCOSIS ( 77 FDA reports)
AGEUSIA ( 76 FDA reports)
BONE DEBRIDEMENT ( 76 FDA reports)
GASTROENTERITIS VIRAL ( 76 FDA reports)
GENERALISED OEDEMA ( 76 FDA reports)
GRAND MAL CONVULSION ( 76 FDA reports)
HALLUCINATION, VISUAL ( 76 FDA reports)
MENISCUS LESION ( 76 FDA reports)
MUCOSAL INFLAMMATION ( 76 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 75 FDA reports)
CEREBRAL INFARCTION ( 75 FDA reports)
FAECAL INCONTINENCE ( 75 FDA reports)
NEUTROPHIL COUNT DECREASED ( 75 FDA reports)
PARALYSIS ( 75 FDA reports)
ACNE ( 74 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 74 FDA reports)
MOOD SWINGS ( 74 FDA reports)
NASAL SEPTUM DEVIATION ( 74 FDA reports)
RHABDOMYOLYSIS ( 74 FDA reports)
PROTHROMBIN TIME PROLONGED ( 73 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 73 FDA reports)
BREAST PAIN ( 73 FDA reports)
EJECTION FRACTION DECREASED ( 73 FDA reports)
FLUID OVERLOAD ( 73 FDA reports)
LOCAL SWELLING ( 73 FDA reports)
COAGULOPATHY ( 72 FDA reports)
COORDINATION ABNORMAL ( 72 FDA reports)
EYE HAEMORRHAGE ( 72 FDA reports)
HEARING IMPAIRED ( 72 FDA reports)
PERIPHERAL COLDNESS ( 72 FDA reports)
SENSATION OF HEAVINESS ( 72 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 71 FDA reports)
VITAMIN B12 DEFICIENCY ( 71 FDA reports)
HUMERUS FRACTURE ( 71 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 71 FDA reports)
ORAL HERPES ( 71 FDA reports)
CHOKING ( 70 FDA reports)
DIZZINESS POSTURAL ( 70 FDA reports)
ENCEPHALOPATHY ( 70 FDA reports)
HYPOAESTHESIA ORAL ( 70 FDA reports)
MOOD ALTERED ( 70 FDA reports)
NERVE COMPRESSION ( 70 FDA reports)
ACUTE RESPIRATORY FAILURE ( 69 FDA reports)
DECREASED ACTIVITY ( 69 FDA reports)
FIBROSIS ( 69 FDA reports)
ILEUS ( 69 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 69 FDA reports)
LIGAMENT SPRAIN ( 69 FDA reports)
MULTIPLE INJURIES ( 69 FDA reports)
PERONEAL NERVE PALSY ( 69 FDA reports)
WOUND ( 69 FDA reports)
THIRST ( 68 FDA reports)
APHAGIA ( 68 FDA reports)
BLADDER DISORDER ( 68 FDA reports)
CONJUNCTIVITIS ( 68 FDA reports)
DEVICE FAILURE ( 68 FDA reports)
LABORATORY TEST ABNORMAL ( 68 FDA reports)
ORAL DISCOMFORT ( 68 FDA reports)
FACE OEDEMA ( 67 FDA reports)
HEPATIC CYST ( 67 FDA reports)
HYPOVOLAEMIA ( 67 FDA reports)
SEQUESTRECTOMY ( 67 FDA reports)
THYROID NEOPLASM ( 67 FDA reports)
TONGUE DISCOLOURATION ( 67 FDA reports)
UROSEPSIS ( 67 FDA reports)
RHINITIS ALLERGIC ( 66 FDA reports)
SKIN LACERATION ( 66 FDA reports)
SUBDURAL HAEMATOMA ( 66 FDA reports)
ELECTROLYTE IMBALANCE ( 66 FDA reports)
MYOCARDIAL ISCHAEMIA ( 66 FDA reports)
ANGIOEDEMA ( 65 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 65 FDA reports)
FRACTURE NONUNION ( 65 FDA reports)
RADIUS FRACTURE ( 65 FDA reports)
SEDATION ( 65 FDA reports)
THINKING ABNORMAL ( 65 FDA reports)
PREGNANCY ( 64 FDA reports)
PULMONARY MASS ( 64 FDA reports)
THYROID CANCER ( 64 FDA reports)
ADRENAL INSUFFICIENCY ( 64 FDA reports)
CARDIOVASCULAR DISORDER ( 64 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 64 FDA reports)
INJECTION SITE MASS ( 64 FDA reports)
OEDEMA MOUTH ( 64 FDA reports)
ACCIDENT ( 63 FDA reports)
CAROTID ARTERY STENOSIS ( 63 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 63 FDA reports)
EYE PRURITUS ( 63 FDA reports)
FAILURE TO THRIVE ( 63 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 63 FDA reports)
LOW TURNOVER OSTEOPATHY ( 63 FDA reports)
NEUTROPHIL COUNT INCREASED ( 63 FDA reports)
TENDON RUPTURE ( 63 FDA reports)
WITHDRAWAL SYNDROME ( 63 FDA reports)
RASH MACULO-PAPULAR ( 62 FDA reports)
SPLENOMEGALY ( 62 FDA reports)
APHONIA ( 62 FDA reports)
ASPIRATION ( 62 FDA reports)
CERUMEN IMPACTION ( 62 FDA reports)
HEPATIC CIRRHOSIS ( 62 FDA reports)
JOINT CREPITATION ( 62 FDA reports)
MELAENA ( 62 FDA reports)
MUSCLE ATROPHY ( 62 FDA reports)
PARAESTHESIA ORAL ( 62 FDA reports)
DIALYSIS ( 61 FDA reports)
ESSENTIAL HYPERTENSION ( 61 FDA reports)
MANIA ( 61 FDA reports)
ABDOMINAL TENDERNESS ( 60 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 60 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 60 FDA reports)
SENSITIVITY OF TEETH ( 60 FDA reports)
SERUM FERRITIN INCREASED ( 60 FDA reports)
VIITH NERVE PARALYSIS ( 59 FDA reports)
ABSCESS JAW ( 59 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 59 FDA reports)
PHOTOPHOBIA ( 59 FDA reports)
BLOOD COUNT ABNORMAL ( 58 FDA reports)
BONE SCAN ABNORMAL ( 58 FDA reports)
FOOT DEFORMITY ( 58 FDA reports)
HYPOALBUMINAEMIA ( 58 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 58 FDA reports)
NO THERAPEUTIC RESPONSE ( 58 FDA reports)
PLATELET COUNT INCREASED ( 58 FDA reports)
TARDIVE DYSKINESIA ( 58 FDA reports)
RESPIRATORY TRACT CONGESTION ( 57 FDA reports)
URINE OUTPUT DECREASED ( 57 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 57 FDA reports)
BREATH ODOUR ( 57 FDA reports)
MAJOR DEPRESSION ( 57 FDA reports)
ABORTION SPONTANEOUS ( 56 FDA reports)
BREAST CANCER METASTATIC ( 56 FDA reports)
DENTAL OPERATION ( 56 FDA reports)
GASTROINTESTINAL PAIN ( 56 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 56 FDA reports)
IMPAIRED WORK ABILITY ( 56 FDA reports)
INJECTION SITE RASH ( 56 FDA reports)
PETECHIAE ( 56 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 56 FDA reports)
SPINAL FUSION SURGERY ( 56 FDA reports)
PYELONEPHRITIS ( 55 FDA reports)
SEASONAL ALLERGY ( 55 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 55 FDA reports)
BLOOD IRON DECREASED ( 55 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 55 FDA reports)
BONE MARROW FAILURE ( 55 FDA reports)
FACIAL BONES FRACTURE ( 55 FDA reports)
INCREASED TENDENCY TO BRUISE ( 55 FDA reports)
INJECTION SITE NODULE ( 55 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 55 FDA reports)
NAIL DISORDER ( 55 FDA reports)
NERVE INJURY ( 55 FDA reports)
ODYNOPHAGIA ( 55 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 55 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 54 FDA reports)
HEPATIC LESION ( 54 FDA reports)
INJECTION SITE DISCOLOURATION ( 54 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 54 FDA reports)
METABOLIC ACIDOSIS ( 54 FDA reports)
ORAL CAVITY FISTULA ( 54 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 54 FDA reports)
PHOTOSENSITIVITY REACTION ( 54 FDA reports)
RESPIRATORY ARREST ( 54 FDA reports)
SNEEZING ( 54 FDA reports)
PROTEINURIA ( 53 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 53 FDA reports)
VENTRICULAR HYPERTROPHY ( 53 FDA reports)
COELIAC DISEASE ( 53 FDA reports)
COLITIS ISCHAEMIC ( 53 FDA reports)
EAR DISCOMFORT ( 53 FDA reports)
EDENTULOUS ( 53 FDA reports)
ORAL INFECTION ( 53 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 52 FDA reports)
EAR INFECTION ( 52 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 52 FDA reports)
OPEN WOUND ( 52 FDA reports)
PROTEIN TOTAL DECREASED ( 52 FDA reports)
WOUND DEHISCENCE ( 52 FDA reports)
SENSORY LOSS ( 51 FDA reports)
SQUAMOUS CELL CARCINOMA ( 51 FDA reports)
TEMPORAL ARTERITIS ( 51 FDA reports)
TONGUE DISORDER ( 51 FDA reports)
UTERINE LEIOMYOMA ( 51 FDA reports)
WOUND INFECTION ( 51 FDA reports)
ARTHROPOD BITE ( 51 FDA reports)
AZOTAEMIA ( 51 FDA reports)
BLADDER CANCER ( 51 FDA reports)
EYELID OEDEMA ( 51 FDA reports)
MALIGNANT MELANOMA ( 51 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 51 FDA reports)
MEDICAL DEVICE COMPLICATION ( 51 FDA reports)
OBESITY ( 51 FDA reports)
COLITIS ULCERATIVE ( 50 FDA reports)
DRUG PRESCRIBING ERROR ( 50 FDA reports)
DRUG TOXICITY ( 50 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 50 FDA reports)
NEOPLASM ( 50 FDA reports)
PELVIC PAIN ( 50 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 50 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 50 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 50 FDA reports)
WEIGHT BEARING DIFFICULTY ( 50 FDA reports)
PROCTALGIA ( 49 FDA reports)
SYNOVITIS ( 49 FDA reports)
TROPONIN INCREASED ( 49 FDA reports)
ANIMAL BITE ( 49 FDA reports)
DERMAL CYST ( 49 FDA reports)
DEVICE BREAKAGE ( 49 FDA reports)
DRUG DEPENDENCE ( 49 FDA reports)
IMMUNOSUPPRESSION ( 49 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 49 FDA reports)
INJECTION SITE WARMTH ( 49 FDA reports)
LACUNAR INFARCTION ( 49 FDA reports)
MULTIPLE FRACTURES ( 49 FDA reports)
NEURODERMATITIS ( 49 FDA reports)
PANCREATITIS ACUTE ( 49 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 49 FDA reports)
AORTIC CALCIFICATION ( 48 FDA reports)
BLOOD TEST ABNORMAL ( 48 FDA reports)
DRUG ABUSE ( 48 FDA reports)
DYSLIPIDAEMIA ( 48 FDA reports)
INCONTINENCE ( 48 FDA reports)
OCULAR ICTERUS ( 48 FDA reports)
PSEUDOMONAS INFECTION ( 48 FDA reports)
SENSATION OF FOREIGN BODY ( 48 FDA reports)
WOUND DRAINAGE ( 48 FDA reports)
RADICULOPATHY ( 47 FDA reports)
ABSCESS DRAINAGE ( 47 FDA reports)
ACTINIC KERATOSIS ( 47 FDA reports)
BONE CYST ( 47 FDA reports)
BRUXISM ( 47 FDA reports)
CARDIAC PACEMAKER INSERTION ( 47 FDA reports)
CEREBRAL ISCHAEMIA ( 47 FDA reports)
DENTAL FISTULA ( 47 FDA reports)
DILATATION VENTRICULAR ( 47 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 47 FDA reports)
HYPOAESTHESIA FACIAL ( 47 FDA reports)
LARYNGITIS ( 47 FDA reports)
MUSCLE CRAMP ( 47 FDA reports)
MUSCULOSKELETAL DISORDER ( 47 FDA reports)
NON-CARDIAC CHEST PAIN ( 47 FDA reports)
APPENDICITIS ( 46 FDA reports)
BLOOD CHLORIDE DECREASED ( 46 FDA reports)
BREAST CANCER IN SITU ( 46 FDA reports)
DERMATITIS CONTACT ( 46 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 46 FDA reports)
PHARYNGITIS ( 46 FDA reports)
SPINAL CORD COMPRESSION ( 46 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 45 FDA reports)
SKIN TIGHTNESS ( 45 FDA reports)
WHEELCHAIR USER ( 45 FDA reports)
ACCIDENTAL OVERDOSE ( 45 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 45 FDA reports)
BACTERAEMIA ( 45 FDA reports)
BODY TEMPERATURE DECREASED ( 45 FDA reports)
BREAST CANCER FEMALE ( 45 FDA reports)
CALCINOSIS ( 45 FDA reports)
CATHETERISATION CARDIAC ( 45 FDA reports)
CONCUSSION ( 45 FDA reports)
DIASTOLIC DYSFUNCTION ( 45 FDA reports)
LUMBAR RADICULOPATHY ( 45 FDA reports)
MEDICATION RESIDUE ( 45 FDA reports)
MOTOR DYSFUNCTION ( 45 FDA reports)
MYOPATHY ( 45 FDA reports)
MYOPIA ( 45 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 45 FDA reports)
ABSCESS ORAL ( 44 FDA reports)
APPLICATION SITE ERYTHEMA ( 44 FDA reports)
BONE LOSS ( 44 FDA reports)
BUNION ( 44 FDA reports)
CYANOSIS ( 44 FDA reports)
EYELID PTOSIS ( 44 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 44 FDA reports)
FIBULA FRACTURE ( 44 FDA reports)
ONYCHOCLASIS ( 44 FDA reports)
PAIN OF SKIN ( 44 FDA reports)
POST PROCEDURAL INFECTION ( 44 FDA reports)
STEM CELL TRANSPLANT ( 44 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 44 FDA reports)
VENTRICULAR TACHYCARDIA ( 44 FDA reports)
SKIN HYPERTROPHY ( 43 FDA reports)
SOFT TISSUE INFECTION ( 43 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 43 FDA reports)
VARICOSE VEIN ( 43 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 43 FDA reports)
APPLICATION SITE PRURITUS ( 43 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 43 FDA reports)
BREATH SOUNDS ABNORMAL ( 43 FDA reports)
DIFFICULTY IN WALKING ( 43 FDA reports)
HYPERPARATHYROIDISM ( 43 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 43 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 43 FDA reports)
MENINGIOMA ( 43 FDA reports)
MENORRHAGIA ( 43 FDA reports)
PHLEBITIS ( 43 FDA reports)
BLOOD DISORDER ( 42 FDA reports)
BLOOD PRESSURE ABNORMAL ( 42 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 42 FDA reports)
COLON CANCER ( 42 FDA reports)
HEAD DISCOMFORT ( 42 FDA reports)
HYPERTONIC BLADDER ( 42 FDA reports)
HYSTERECTOMY ( 42 FDA reports)
INCOHERENT ( 42 FDA reports)
MAXILLOFACIAL OPERATION ( 42 FDA reports)
MOUTH HAEMORRHAGE ( 42 FDA reports)
PERICARDITIS ( 42 FDA reports)
POLYMYALGIA RHEUMATICA ( 42 FDA reports)
STRESS URINARY INCONTINENCE ( 42 FDA reports)
TEMPERATURE INTOLERANCE ( 42 FDA reports)
TRANSAMINASES INCREASED ( 42 FDA reports)
UVEITIS ( 42 FDA reports)
VITREOUS FLOATERS ( 42 FDA reports)
PSYCHOTIC DISORDER ( 41 FDA reports)
RENAL TUBULAR NECROSIS ( 41 FDA reports)
SKIN PAPILLOMA ( 41 FDA reports)
SOFT TISSUE DISORDER ( 41 FDA reports)
SPINAL DEFORMITY ( 41 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 41 FDA reports)
BLOOD URIC ACID INCREASED ( 41 FDA reports)
CAROTID BRUIT ( 41 FDA reports)
CLAVICLE FRACTURE ( 41 FDA reports)
DENTAL DISCOMFORT ( 41 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 41 FDA reports)
FRUSTRATION ( 41 FDA reports)
INJECTION SITE IRRITATION ( 41 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 41 FDA reports)
ACUTE SINUSITIS ( 40 FDA reports)
ANORECTAL DISCOMFORT ( 40 FDA reports)
BIPOLAR DISORDER ( 40 FDA reports)
GASTRITIS EROSIVE ( 40 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 40 FDA reports)
HEART VALVE INCOMPETENCE ( 40 FDA reports)
HERNIA REPAIR ( 40 FDA reports)
HYPOTONIA ( 40 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 40 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 40 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 40 FDA reports)
INTESTINAL ISCHAEMIA ( 40 FDA reports)
INTESTINAL PERFORATION ( 40 FDA reports)
JOINT SPRAIN ( 40 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 40 FDA reports)
OPTIC NEURITIS ( 40 FDA reports)
PLEURISY ( 40 FDA reports)
RENAL PAIN ( 40 FDA reports)
SEBORRHOEIC KERATOSIS ( 40 FDA reports)
SINUS POLYP ( 40 FDA reports)
TENDON INJURY ( 40 FDA reports)
URINE FLOW DECREASED ( 40 FDA reports)
VAGINAL INFECTION ( 40 FDA reports)
VERTEBROPLASTY ( 40 FDA reports)
WEIGHT FLUCTUATION ( 40 FDA reports)
SCAB ( 39 FDA reports)
SKIN ATROPHY ( 39 FDA reports)
STOMACH DISCOMFORT ( 39 FDA reports)
TENDON DISORDER ( 39 FDA reports)
VISUAL FIELD DEFECT ( 39 FDA reports)
ACUTE CORONARY SYNDROME ( 39 FDA reports)
ATRIOVENTRICULAR BLOCK ( 39 FDA reports)
BLINDNESS UNILATERAL ( 39 FDA reports)
DIABETIC NEUROPATHY ( 39 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 39 FDA reports)
DYSAESTHESIA ( 39 FDA reports)
ESCHERICHIA INFECTION ( 39 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 39 FDA reports)
HYPERTHYROIDISM ( 39 FDA reports)
HYPOGONADISM ( 39 FDA reports)
INJECTION SITE URTICARIA ( 39 FDA reports)
LYMPHOPENIA ( 39 FDA reports)
METASTASES TO LYMPH NODES ( 39 FDA reports)
MYOSITIS ( 39 FDA reports)
POLYP ( 39 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 39 FDA reports)
ABDOMINAL MASS ( 38 FDA reports)
APNOEA ( 38 FDA reports)
BLADDER PROLAPSE ( 38 FDA reports)
BLEPHARITIS ( 38 FDA reports)
BRONCHOSPASM ( 38 FDA reports)
CAROTID ARTERY DISEASE ( 38 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 38 FDA reports)
DISEASE RECURRENCE ( 38 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 38 FDA reports)
EXTRASYSTOLES ( 38 FDA reports)
EYE MOVEMENT DISORDER ( 38 FDA reports)
GASTROINTESTINAL INFECTION ( 38 FDA reports)
HAEMORRHAGIC ANAEMIA ( 38 FDA reports)
INGUINAL HERNIA ( 38 FDA reports)
INITIAL INSOMNIA ( 38 FDA reports)
INJECTION SITE INDURATION ( 38 FDA reports)
MACULAR OEDEMA ( 38 FDA reports)
PATELLA FRACTURE ( 38 FDA reports)
RALES ( 38 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 38 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 38 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 38 FDA reports)
RECTAL POLYP ( 37 FDA reports)
RESORPTION BONE INCREASED ( 37 FDA reports)
SARCOIDOSIS ( 37 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 37 FDA reports)
TRISMUS ( 37 FDA reports)
URINE OUTPUT INCREASED ( 37 FDA reports)
VASCULITIS ( 37 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 37 FDA reports)
ANAEMIA POSTOPERATIVE ( 37 FDA reports)
ANOSMIA ( 37 FDA reports)
APPETITE DISORDER ( 37 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 37 FDA reports)
BONE FRAGMENTATION ( 37 FDA reports)
CEREBROVASCULAR DISORDER ( 37 FDA reports)
EXPIRED DRUG ADMINISTERED ( 37 FDA reports)
HAEMOLYTIC ANAEMIA ( 37 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 37 FDA reports)
LUNG CONSOLIDATION ( 37 FDA reports)
NODAL OSTEOARTHRITIS ( 37 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 37 FDA reports)
ABNORMAL FAECES ( 36 FDA reports)
ANGINA UNSTABLE ( 36 FDA reports)
BILE DUCT STONE ( 36 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 36 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 36 FDA reports)
BRAIN NEOPLASM ( 36 FDA reports)
COSTOCHONDRITIS ( 36 FDA reports)
DENTAL PROSTHESIS USER ( 36 FDA reports)
DILATATION ATRIAL ( 36 FDA reports)
EAR DISORDER ( 36 FDA reports)
FRACTURED SACRUM ( 36 FDA reports)
GRANULOMA ( 36 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 36 FDA reports)
HEPATIC MASS ( 36 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 36 FDA reports)
HERPES SIMPLEX ( 36 FDA reports)
IMPAIRED DRIVING ABILITY ( 36 FDA reports)
MACROCYTOSIS ( 36 FDA reports)
MASTECTOMY ( 36 FDA reports)
SICK SINUS SYNDROME ( 36 FDA reports)
SKIN INJURY ( 36 FDA reports)
SKIN IRRITATION ( 36 FDA reports)
URINE ANALYSIS ABNORMAL ( 36 FDA reports)
UTERINE POLYP ( 36 FDA reports)
PSORIATIC ARTHROPATHY ( 35 FDA reports)
SACROILIITIS ( 35 FDA reports)
SCREAMING ( 35 FDA reports)
SINUS HEADACHE ( 35 FDA reports)
SKIN INDURATION ( 35 FDA reports)
TOOTH INJURY ( 35 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 35 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 35 FDA reports)
APATHY ( 35 FDA reports)
APPENDICITIS PERFORATED ( 35 FDA reports)
BLINDNESS TRANSIENT ( 35 FDA reports)
CHOLECYSTITIS ACUTE ( 35 FDA reports)
DERMATOPHYTOSIS ( 35 FDA reports)
DRY THROAT ( 35 FDA reports)
DYSGRAPHIA ( 35 FDA reports)
GASTRIC POLYPS ( 35 FDA reports)
IMMUNE SYSTEM DISORDER ( 35 FDA reports)
LIBIDO DECREASED ( 35 FDA reports)
MALABSORPTION ( 35 FDA reports)
MELANOCYTIC NAEVUS ( 35 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 35 FDA reports)
PEPTIC ULCER ( 35 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 34 FDA reports)
BRONCHIECTASIS ( 34 FDA reports)
CREPITATIONS ( 34 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 34 FDA reports)
EYE INFECTION ( 34 FDA reports)
HAND FRACTURE ( 34 FDA reports)
INGROWING NAIL ( 34 FDA reports)
METAPLASIA ( 34 FDA reports)
OESOPHAGEAL SPASM ( 34 FDA reports)
ORAL SURGERY ( 34 FDA reports)
OVARIAN CANCER ( 34 FDA reports)
POLYDIPSIA ( 34 FDA reports)
POSTURE ABNORMAL ( 34 FDA reports)
PURULENCE ( 34 FDA reports)
QUALITY OF LIFE DECREASED ( 34 FDA reports)
RECTOCELE ( 34 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 34 FDA reports)
SUDDEN DEATH ( 34 FDA reports)
RENAL MASS ( 33 FDA reports)
RIGHT VENTRICULAR FAILURE ( 33 FDA reports)
SUBCUTANEOUS ABSCESS ( 33 FDA reports)
APPENDICECTOMY ( 33 FDA reports)
ASTIGMATISM ( 33 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 33 FDA reports)
CARDIAC VALVE DISEASE ( 33 FDA reports)
COLON ADENOMA ( 33 FDA reports)
FEELING DRUNK ( 33 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 33 FDA reports)
HYPERAESTHESIA ( 33 FDA reports)
HYPERPLASIA ( 33 FDA reports)
MULTIPLE ALLERGIES ( 33 FDA reports)
NECROSIS ( 33 FDA reports)
OESOPHAGEAL STENOSIS ( 33 FDA reports)
OPEN REDUCTION OF FRACTURE ( 33 FDA reports)
PERITONITIS ( 33 FDA reports)
ANXIETY DISORDER ( 32 FDA reports)
AUTONOMIC NEUROPATHY ( 32 FDA reports)
BONE MARROW OEDEMA ( 32 FDA reports)
BONE NEOPLASM MALIGNANT ( 32 FDA reports)
CERVICAL DYSPLASIA ( 32 FDA reports)
CHEILITIS ( 32 FDA reports)
CIRCULATORY COLLAPSE ( 32 FDA reports)
COMPLETED SUICIDE ( 32 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 32 FDA reports)
EMPYEMA ( 32 FDA reports)
GASTRIC HAEMORRHAGE ( 32 FDA reports)
HAEMODIALYSIS ( 32 FDA reports)
INJECTION SITE PAPULE ( 32 FDA reports)
MUSCLE SPASTICITY ( 32 FDA reports)
MYOCLONUS ( 32 FDA reports)
NEPHROPATHY ( 32 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 32 FDA reports)
PAINFUL RESPIRATION ( 32 FDA reports)
PAPILLOMA ( 32 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 32 FDA reports)
PARANOIA ( 32 FDA reports)
PERIODONTAL OPERATION ( 32 FDA reports)
POLYURIA ( 32 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 32 FDA reports)
PULSE ABSENT ( 32 FDA reports)
SKIN PLAQUE ( 32 FDA reports)
SPINAL LAMINECTOMY ( 32 FDA reports)
SPUTUM DISCOLOURED ( 32 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 32 FDA reports)
TOOTH IMPACTED ( 32 FDA reports)
ULCER HAEMORRHAGE ( 32 FDA reports)
URINE ODOUR ABNORMAL ( 32 FDA reports)
PROSTATE CANCER METASTATIC ( 31 FDA reports)
STREPTOCOCCAL INFECTION ( 31 FDA reports)
TRANSFUSION ( 31 FDA reports)
VAGINAL DISCHARGE ( 31 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 31 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 31 FDA reports)
BONE OPERATION ( 31 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 31 FDA reports)
CHEST X-RAY ABNORMAL ( 31 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 31 FDA reports)
DEAFNESS NEUROSENSORY ( 31 FDA reports)
ENTEROVESICAL FISTULA ( 31 FDA reports)
EUPHORIC MOOD ( 31 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 31 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 31 FDA reports)
LIMB OPERATION ( 31 FDA reports)
LIPASE INCREASED ( 31 FDA reports)
LUNG HYPERINFLATION ( 31 FDA reports)
MENIERE'S DISEASE ( 31 FDA reports)
MITRAL VALVE PROLAPSE ( 31 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 31 FDA reports)
NECK MASS ( 31 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 31 FDA reports)
PANCREATIC CYST ( 31 FDA reports)
ADRENAL DISORDER ( 30 FDA reports)
BLOOD BLISTER ( 30 FDA reports)
BLOOD CHLORIDE INCREASED ( 30 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 30 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 30 FDA reports)
BONE GRAFT ( 30 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 30 FDA reports)
BREAST CALCIFICATIONS ( 30 FDA reports)
BREAST CANCER STAGE I ( 30 FDA reports)
CORONARY ARTERY STENOSIS ( 30 FDA reports)
DUODENAL ULCER ( 30 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 30 FDA reports)
HIP SURGERY ( 30 FDA reports)
HUNGER ( 30 FDA reports)
HYPERTENSIVE CRISIS ( 30 FDA reports)
HYPOTHERMIA ( 30 FDA reports)
INTRAOCULAR LENS IMPLANT ( 30 FDA reports)
METASTASIS ( 30 FDA reports)
MYELOPATHY ( 30 FDA reports)
NASAL MUCOSAL DISORDER ( 30 FDA reports)
OCCULT BLOOD POSITIVE ( 30 FDA reports)
OESOPHAGEAL DISORDER ( 30 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 30 FDA reports)
RESPIRATORY RATE INCREASED ( 30 FDA reports)
TETANY ( 30 FDA reports)
ULNA FRACTURE ( 30 FDA reports)
URINARY TRACT OBSTRUCTION ( 30 FDA reports)
VENOUS INSUFFICIENCY ( 30 FDA reports)
WOUND COMPLICATION ( 30 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 29 FDA reports)
RAYNAUD'S PHENOMENON ( 29 FDA reports)
SPINAL OPERATION ( 29 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 29 FDA reports)
VEIN DISORDER ( 29 FDA reports)
VITREOUS DETACHMENT ( 29 FDA reports)
ANAPHYLACTIC SHOCK ( 29 FDA reports)
BONE SWELLING ( 29 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 29 FDA reports)
BRONCHOPNEUMONIA ( 29 FDA reports)
CERVICOBRACHIAL SYNDROME ( 29 FDA reports)
CHOLESTASIS ( 29 FDA reports)
CORONARY ARTERY BYPASS ( 29 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 29 FDA reports)
DEMYELINATION ( 29 FDA reports)
ENTEROCOCCAL INFECTION ( 29 FDA reports)
EOSINOPHILIA ( 29 FDA reports)
FOREIGN BODY ( 29 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 29 FDA reports)
HAIR TEXTURE ABNORMAL ( 29 FDA reports)
INJECTION SITE EXTRAVASATION ( 29 FDA reports)
ISCHAEMIA ( 29 FDA reports)
JOINT CONTRACTURE ( 29 FDA reports)
LARGE INTESTINAL ULCER ( 29 FDA reports)
LYME DISEASE ( 29 FDA reports)
OESOPHAGEAL ULCER ( 29 FDA reports)
ORTHOPNOEA ( 29 FDA reports)
PAPILLOEDEMA ( 29 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 29 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 28 FDA reports)
ARTHRITIS INFECTIVE ( 28 FDA reports)
ASPIRATION PLEURAL CAVITY ( 28 FDA reports)
BILIARY DYSKINESIA ( 28 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 28 FDA reports)
BRAIN OEDEMA ( 28 FDA reports)
CHOKING SENSATION ( 28 FDA reports)
FACET JOINT SYNDROME ( 28 FDA reports)
FACIAL PALSY ( 28 FDA reports)
GENERALISED ERYTHEMA ( 28 FDA reports)
HAIR GROWTH ABNORMAL ( 28 FDA reports)
INCORRECT STORAGE OF DRUG ( 28 FDA reports)
LIFE EXPECTANCY SHORTENED ( 28 FDA reports)
LOSS OF CONTROL OF LEGS ( 28 FDA reports)
NASAL POLYPS ( 28 FDA reports)
NYSTAGMUS ( 28 FDA reports)
OTITIS EXTERNA ( 28 FDA reports)
PANCREATIC CARCINOMA ( 28 FDA reports)
PARONYCHIA ( 28 FDA reports)
PIGMENTATION DISORDER ( 28 FDA reports)
PROCEDURAL COMPLICATION ( 28 FDA reports)
PROSTATOMEGALY ( 28 FDA reports)
RHINITIS ( 28 FDA reports)
SEROMA ( 28 FDA reports)
SHOULDER ARTHROPLASTY ( 28 FDA reports)
SKELETAL INJURY ( 28 FDA reports)
SNORING ( 28 FDA reports)
SUICIDE ATTEMPT ( 28 FDA reports)
THERMAL BURN ( 28 FDA reports)
TONGUE ULCERATION ( 28 FDA reports)
TOOTH DEPOSIT ( 28 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 28 FDA reports)
WRONG DRUG ADMINISTERED ( 28 FDA reports)
X-RAY ABNORMAL ( 28 FDA reports)
RENAL CANCER ( 27 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 27 FDA reports)
SKIN INFECTION ( 27 FDA reports)
SKIN REACTION ( 27 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 27 FDA reports)
TYPE 1 DIABETES MELLITUS ( 27 FDA reports)
VASCULAR OCCLUSION ( 27 FDA reports)
VULVOVAGINAL DRYNESS ( 27 FDA reports)
WOUND SECRETION ( 27 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 27 FDA reports)
ATRIAL SEPTAL DEFECT ( 27 FDA reports)
BLEPHAROSPASM ( 27 FDA reports)
BREAST CYST ( 27 FDA reports)
BREAST NECROSIS ( 27 FDA reports)
CACHEXIA ( 27 FDA reports)
DYSTONIA ( 27 FDA reports)
EMBOLISM ( 27 FDA reports)
EYE DISCHARGE ( 27 FDA reports)
HAEMANGIOMA OF LIVER ( 27 FDA reports)
HERPES VIRUS INFECTION ( 27 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 27 FDA reports)
KLEBSIELLA INFECTION ( 27 FDA reports)
KNEE OPERATION ( 27 FDA reports)
MONOCYTE COUNT INCREASED ( 27 FDA reports)
OESOPHAGEAL PAIN ( 27 FDA reports)
PLEURAL FIBROSIS ( 27 FDA reports)
APLASTIC ANAEMIA ( 26 FDA reports)
BLOOD CREATININE DECREASED ( 26 FDA reports)
BRAIN INJURY ( 26 FDA reports)
CHONDROPATHY ( 26 FDA reports)
CYSTOCELE ( 26 FDA reports)
EAR HAEMORRHAGE ( 26 FDA reports)
ENTERITIS ( 26 FDA reports)
EPILEPSY ( 26 FDA reports)
FACIAL NERVE DISORDER ( 26 FDA reports)
FACIAL PARESIS ( 26 FDA reports)
FRACTURE DELAYED UNION ( 26 FDA reports)
GALLBLADDER OPERATION ( 26 FDA reports)
HAEMOLYSIS ( 26 FDA reports)
HYDROCEPHALUS ( 26 FDA reports)
IRON DEFICIENCY ( 26 FDA reports)
JUGULAR VEIN THROMBOSIS ( 26 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 26 FDA reports)
LABYRINTHITIS ( 26 FDA reports)
LISTLESS ( 26 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 26 FDA reports)
ORAL DISCHARGE ( 26 FDA reports)
OTITIS MEDIA ( 26 FDA reports)
PAROSMIA ( 26 FDA reports)
PERSONALITY CHANGE ( 26 FDA reports)
PLANTAR FASCIITIS ( 26 FDA reports)
PLASMACYTOMA ( 26 FDA reports)
RASH VESICULAR ( 26 FDA reports)
RENAL CELL CARCINOMA ( 26 FDA reports)
SECRETION DISCHARGE ( 26 FDA reports)
SLUGGISHNESS ( 26 FDA reports)
THYROID CYST ( 26 FDA reports)
THYROIDECTOMY ( 26 FDA reports)
URINARY TRACT DISORDER ( 26 FDA reports)
VASCULAR CALCIFICATION ( 26 FDA reports)
POSTOPERATIVE ILEUS ( 25 FDA reports)
SHOCK ( 25 FDA reports)
SKIN HAEMORRHAGE ( 25 FDA reports)
SKIN NEOPLASM EXCISION ( 25 FDA reports)
SKIN WARM ( 25 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 25 FDA reports)
THROMBOPHLEBITIS ( 25 FDA reports)
TONGUE INJURY ( 25 FDA reports)
TREATMENT FAILURE ( 25 FDA reports)
ABNORMAL SENSATION IN EYE ( 25 FDA reports)
ANEURYSM ( 25 FDA reports)
ATRIAL TACHYCARDIA ( 25 FDA reports)
AUTOIMMUNE HEPATITIS ( 25 FDA reports)
CALCULUS URETERIC ( 25 FDA reports)
CARTILAGE INJURY ( 25 FDA reports)
DERMATITIS ALLERGIC ( 25 FDA reports)
DIVERTICULAR PERFORATION ( 25 FDA reports)
DRUG DISPENSING ERROR ( 25 FDA reports)
ENDOMETRIOSIS ( 25 FDA reports)
EYE INFLAMMATION ( 25 FDA reports)
FOOT OPERATION ( 25 FDA reports)
HAEMANGIOMA ( 25 FDA reports)
INTERMITTENT CLAUDICATION ( 25 FDA reports)
ISCHAEMIC STROKE ( 25 FDA reports)
LOCALISED OEDEMA ( 25 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
MUSCLE INJURY ( 25 FDA reports)
OESOPHAGITIS ULCERATIVE ( 25 FDA reports)
PLASMACYTOSIS ( 25 FDA reports)
AORTIC VALVE SCLEROSIS ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 24 FDA reports)
B-CELL LYMPHOMA ( 24 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 24 FDA reports)
BONE DENSITY ABNORMAL ( 24 FDA reports)
BONE EROSION ( 24 FDA reports)
BREAST CANCER RECURRENT ( 24 FDA reports)
CALCULUS URINARY ( 24 FDA reports)
CARDIAC FLUTTER ( 24 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 24 FDA reports)
DEAFNESS UNILATERAL ( 24 FDA reports)
FLUID INTAKE REDUCED ( 24 FDA reports)
H1N1 INFLUENZA ( 24 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 24 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 24 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 24 FDA reports)
INTRACRANIAL ANEURYSM ( 24 FDA reports)
LEUKAEMIA ( 24 FDA reports)
MENSTRUAL DISORDER ( 24 FDA reports)
MUSCLE RIGIDITY ( 24 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 24 FDA reports)
ORTHOSIS USER ( 24 FDA reports)
OSTEOMALACIA ( 24 FDA reports)
PHOTOPSIA ( 24 FDA reports)
POLYNEUROPATHY ( 24 FDA reports)
POOR DENTAL CONDITION ( 24 FDA reports)
RASH PUSTULAR ( 24 FDA reports)
RECTAL ABSCESS ( 24 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 24 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 24 FDA reports)
STERNAL FRACTURE ( 24 FDA reports)
TENSION ( 24 FDA reports)
THROMBOCYTOSIS ( 24 FDA reports)
TOBACCO ABUSE ( 24 FDA reports)
VISUAL DISTURBANCE ( 24 FDA reports)
PREMATURE BABY ( 23 FDA reports)
SHOULDER OPERATION ( 23 FDA reports)
SUNBURN ( 23 FDA reports)
TENDON PAIN ( 23 FDA reports)
URINE COLOUR ABNORMAL ( 23 FDA reports)
YELLOW SKIN ( 23 FDA reports)
ACCIDENT AT WORK ( 23 FDA reports)
ACIDOSIS ( 23 FDA reports)
ACROCHORDON ( 23 FDA reports)
ACUTE PULMONARY OEDEMA ( 23 FDA reports)
ADNEXA UTERI MASS ( 23 FDA reports)
APHTHOUS STOMATITIS ( 23 FDA reports)
APLASIA PURE RED CELL ( 23 FDA reports)
BARRETT'S OESOPHAGUS ( 23 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 23 FDA reports)
BLOOD UREA DECREASED ( 23 FDA reports)
BREAST RECONSTRUCTION ( 23 FDA reports)
CARDIAC ENZYMES INCREASED ( 23 FDA reports)
CUBITAL TUNNEL SYNDROME ( 23 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 23 FDA reports)
ENDOMETRIAL CANCER ( 23 FDA reports)
EXERCISE TOLERANCE DECREASED ( 23 FDA reports)
FAECALOMA ( 23 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 23 FDA reports)
FOOD CRAVING ( 23 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 23 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 23 FDA reports)
HYPERMETROPIA ( 23 FDA reports)
IMMOBILE ( 23 FDA reports)
INADEQUATE ANALGESIA ( 23 FDA reports)
INTENTIONAL OVERDOSE ( 23 FDA reports)
LACTIC ACIDOSIS ( 23 FDA reports)
LOBAR PNEUMONIA ( 23 FDA reports)
MONOCYTE COUNT DECREASED ( 23 FDA reports)
MUCOSAL HAEMORRHAGE ( 23 FDA reports)
NERVE ROOT LESION ( 23 FDA reports)
OPTIC NERVE DISORDER ( 23 FDA reports)
PERIODONTAL INFECTION ( 23 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 23 FDA reports)
PERIPHERAL ISCHAEMIA ( 23 FDA reports)
POOR VENOUS ACCESS ( 23 FDA reports)
APPLICATION SITE RASH ( 22 FDA reports)
AUTOIMMUNE THYROIDITIS ( 22 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 22 FDA reports)
BREAST HYPERPLASIA ( 22 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 22 FDA reports)
DEMENTIA WITH LEWY BODIES ( 22 FDA reports)
DEVICE MISUSE ( 22 FDA reports)
DRUG ERUPTION ( 22 FDA reports)
DYSPHEMIA ( 22 FDA reports)
HAEMORRHAGIC DIATHESIS ( 22 FDA reports)
JOINT LOCK ( 22 FDA reports)
LEG AMPUTATION ( 22 FDA reports)
LEUKOENCEPHALOPATHY ( 22 FDA reports)
LUNG ADENOCARCINOMA ( 22 FDA reports)
LYMPHADENECTOMY ( 22 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 22 FDA reports)
MEAN CELL VOLUME INCREASED ( 22 FDA reports)
MUCOSAL ULCERATION ( 22 FDA reports)
NARCOLEPSY ( 22 FDA reports)
OVERWEIGHT ( 22 FDA reports)
PANCREATITIS CHRONIC ( 22 FDA reports)
PARAPLEGIA ( 22 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 22 FDA reports)
PERITONITIS BACTERIAL ( 22 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 22 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 22 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 22 FDA reports)
RENAL INJURY ( 22 FDA reports)
RETINAL DISORDER ( 22 FDA reports)
RETINOPATHY ( 22 FDA reports)
SOFT TISSUE MASS ( 22 FDA reports)
TERMINAL STATE ( 22 FDA reports)
VENTRICULAR HYPOKINESIA ( 22 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 22 FDA reports)
PREMATURE LABOUR ( 21 FDA reports)
PULMONARY GRANULOMA ( 21 FDA reports)
PURPURA ( 21 FDA reports)
QUADRIPLEGIA ( 21 FDA reports)
RENAL ATROPHY ( 21 FDA reports)
SCRATCH ( 21 FDA reports)
SKIN NECROSIS ( 21 FDA reports)
SKIN WRINKLING ( 21 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 21 FDA reports)
TRIGGER FINGER ( 21 FDA reports)
UMBILICAL HERNIA ( 21 FDA reports)
UNDERDOSE ( 21 FDA reports)
ACUTE PRERENAL FAILURE ( 21 FDA reports)
ADHESION ( 21 FDA reports)
AFFECTIVE DISORDER ( 21 FDA reports)
AORTIC DISORDER ( 21 FDA reports)
APPARENT DEATH ( 21 FDA reports)
ATROPHIC VULVOVAGINITIS ( 21 FDA reports)
AUTOIMMUNE DISORDER ( 21 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 21 FDA reports)
BLADDER PAIN ( 21 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 21 FDA reports)
BREAKTHROUGH PAIN ( 21 FDA reports)
CAESAREAN SECTION ( 21 FDA reports)
CALCIUM DEFICIENCY ( 21 FDA reports)
CARDIOGENIC SHOCK ( 21 FDA reports)
CAROTID ARTERY OCCLUSION ( 21 FDA reports)
CATARACT NUCLEAR ( 21 FDA reports)
CEREBELLAR INFARCTION ( 21 FDA reports)
CHAPPED LIPS ( 21 FDA reports)
DEVICE DISLOCATION ( 21 FDA reports)
DRUG LEVEL INCREASED ( 21 FDA reports)
FAT TISSUE INCREASED ( 21 FDA reports)
FINGER DEFORMITY ( 21 FDA reports)
GINGIVAL ULCERATION ( 21 FDA reports)
HEPATIC PAIN ( 21 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 21 FDA reports)
INTESTINAL RESECTION ( 21 FDA reports)
LACTOSE INTOLERANCE ( 21 FDA reports)
LIMB ASYMMETRY ( 21 FDA reports)
MITRAL VALVE STENOSIS ( 21 FDA reports)
OSTEOCHONDROSIS ( 21 FDA reports)
PARATHYROID TUMOUR BENIGN ( 21 FDA reports)
PLEURITIC PAIN ( 21 FDA reports)
ABDOMINAL ABSCESS ( 20 FDA reports)
ADRENAL MASS ( 20 FDA reports)
ANOGENITAL WARTS ( 20 FDA reports)
BIPOLAR I DISORDER ( 20 FDA reports)
BLOOD AMYLASE INCREASED ( 20 FDA reports)
BONE CALLUS EXCESSIVE ( 20 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 20 FDA reports)
CHOLANGITIS ( 20 FDA reports)
CYSTITIS INTERSTITIAL ( 20 FDA reports)
DEFAECATION URGENCY ( 20 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 20 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 20 FDA reports)
ESCHERICHIA SEPSIS ( 20 FDA reports)
FACE INJURY ( 20 FDA reports)
FAMILY STRESS ( 20 FDA reports)
FIBRIN D DIMER INCREASED ( 20 FDA reports)
FRACTURE DISPLACEMENT ( 20 FDA reports)
GINGIVAL ERYTHEMA ( 20 FDA reports)
GLOBULINS INCREASED ( 20 FDA reports)
GRANULOCYTOPENIA ( 20 FDA reports)
HEARING DISABILITY ( 20 FDA reports)
HEMIPLEGIA ( 20 FDA reports)
HEPATIC FIBROSIS ( 20 FDA reports)
HEPATOTOXICITY ( 20 FDA reports)
HYPERVENTILATION ( 20 FDA reports)
HYPOREFLEXIA ( 20 FDA reports)
INTESTINAL STENOSIS ( 20 FDA reports)
JOINT ARTHROPLASTY ( 20 FDA reports)
KYPHOSCOLIOSIS ( 20 FDA reports)
LARGE INTESTINE PERFORATION ( 20 FDA reports)
METABOLIC ENCEPHALOPATHY ( 20 FDA reports)
METASTASES TO THE MEDIASTINUM ( 20 FDA reports)
MITRAL VALVE CALCIFICATION ( 20 FDA reports)
NEOPLASM RECURRENCE ( 20 FDA reports)
OLFACTORY NERVE DISORDER ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
ORAL FUNGAL INFECTION ( 20 FDA reports)
PERIARTHRITIS ( 20 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 20 FDA reports)
PROTEIN TOTAL INCREASED ( 20 FDA reports)
PROTEIN URINE PRESENT ( 20 FDA reports)
PUBIS FRACTURE ( 20 FDA reports)
SALIVARY HYPERSECRETION ( 20 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 20 FDA reports)
STRABISMUS ( 20 FDA reports)
SUDDEN CARDIAC DEATH ( 20 FDA reports)
THROAT CANCER ( 20 FDA reports)
TONGUE OEDEMA ( 20 FDA reports)
TOURETTE'S DISORDER ( 20 FDA reports)
VULVOVAGINAL DISCOMFORT ( 20 FDA reports)
PRODUCT TASTE ABNORMAL ( 19 FDA reports)
PYODERMA GANGRENOSUM ( 19 FDA reports)
RADICULAR SYNDROME ( 19 FDA reports)
RADIOTHERAPY ( 19 FDA reports)
RECTAL PROLAPSE ( 19 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 19 FDA reports)
SEXUAL DYSFUNCTION ( 19 FDA reports)
SPLENIC LESION ( 19 FDA reports)
SPONDYLOLYSIS ( 19 FDA reports)
STATUS EPILEPTICUS ( 19 FDA reports)
STEVENS-JOHNSON SYNDROME ( 19 FDA reports)
TUBERCULOSIS ( 19 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 19 FDA reports)
VENTRICULAR FIBRILLATION ( 19 FDA reports)
VITAMIN B12 DECREASED ( 19 FDA reports)
VITAMIN D INCREASED ( 19 FDA reports)
ABDOMINAL ADHESIONS ( 19 FDA reports)
ADRENAL NEOPLASM ( 19 FDA reports)
AMENORRHOEA ( 19 FDA reports)
AMMONIA INCREASED ( 19 FDA reports)
AORTIC VALVE STENOSIS ( 19 FDA reports)
BLOOD CREATINE INCREASED ( 19 FDA reports)
BREAST TENDERNESS ( 19 FDA reports)
COMMINUTED FRACTURE ( 19 FDA reports)
EPIGASTRIC DISCOMFORT ( 19 FDA reports)
FAECES HARD ( 19 FDA reports)
FOLLICULITIS ( 19 FDA reports)
FORMICATION ( 19 FDA reports)
FUNGAL SKIN INFECTION ( 19 FDA reports)
FURUNCLE ( 19 FDA reports)
GANGRENE ( 19 FDA reports)
HELICOBACTER INFECTION ( 19 FDA reports)
HEPATIC ENCEPHALOPATHY ( 19 FDA reports)
HEPATIC ENZYME ABNORMAL ( 19 FDA reports)
HEPATIC NEOPLASM ( 19 FDA reports)
HEPATITIS B ( 19 FDA reports)
HYPERCHLORHYDRIA ( 19 FDA reports)
INCISION SITE INFECTION ( 19 FDA reports)
INJECTION SITE CYST ( 19 FDA reports)
INJECTION SITE DISCOMFORT ( 19 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 19 FDA reports)
IRITIS ( 19 FDA reports)
KERATITIS ( 19 FDA reports)
LIP PAIN ( 19 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 19 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 19 FDA reports)
MONOCLONAL GAMMOPATHY ( 19 FDA reports)
MUCOUS STOOLS ( 19 FDA reports)
NEPHROTIC SYNDROME ( 19 FDA reports)
NEUROLOGICAL SYMPTOM ( 19 FDA reports)
NEUROMA ( 19 FDA reports)
PARATHYROID DISORDER ( 19 FDA reports)
POLYP COLORECTAL ( 19 FDA reports)
POST HERPETIC NEURALGIA ( 19 FDA reports)
ADENOCARCINOMA ( 18 FDA reports)
ALVEOLITIS ( 18 FDA reports)
ANGIOPATHY ( 18 FDA reports)
ARTHRITIS BACTERIAL ( 18 FDA reports)
ASTHENOPIA ( 18 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 18 FDA reports)
BLADDER CATHETERISATION ( 18 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 18 FDA reports)
BRONCHITIS CHRONIC ( 18 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 18 FDA reports)
COMMUNICATION DISORDER ( 18 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 18 FDA reports)
CRANIAL NERVE DISORDER ( 18 FDA reports)
CYST ASPIRATION ( 18 FDA reports)
DIABETIC KETOACIDOSIS ( 18 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 18 FDA reports)
ENDOTRACHEAL INTUBATION ( 18 FDA reports)
EOSINOPHIL COUNT DECREASED ( 18 FDA reports)
EOSINOPHIL COUNT INCREASED ( 18 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 18 FDA reports)
GASTROINTESTINAL ULCER ( 18 FDA reports)
GENERALISED ANXIETY DISORDER ( 18 FDA reports)
HORDEOLUM ( 18 FDA reports)
HYPERTENSIVE HEART DISEASE ( 18 FDA reports)
ILIAC ARTERY STENOSIS ( 18 FDA reports)
INFUSION SITE SWELLING ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 18 FDA reports)
INTRACARDIAC THROMBUS ( 18 FDA reports)
LENTIGO ( 18 FDA reports)
LIP DISORDER ( 18 FDA reports)
LIVER INJURY ( 18 FDA reports)
LYMPH NODE PAIN ( 18 FDA reports)
MADAROSIS ( 18 FDA reports)
MENSTRUATION IRREGULAR ( 18 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 18 FDA reports)
MUSCLE RUPTURE ( 18 FDA reports)
NEURITIS ( 18 FDA reports)
NEUROGENIC BLADDER ( 18 FDA reports)
OCULAR HYPERTENSION ( 18 FDA reports)
ORAL INTAKE REDUCED ( 18 FDA reports)
ORAL PUSTULE ( 18 FDA reports)
OSTEOSARCOMA METASTATIC ( 18 FDA reports)
PANCREATIC DISORDER ( 18 FDA reports)
PERIORBITAL OEDEMA ( 18 FDA reports)
PNEUMONIA BACTERIAL ( 18 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 18 FDA reports)
POOR PERIPHERAL CIRCULATION ( 18 FDA reports)
POST PROCEDURAL FISTULA ( 18 FDA reports)
PULMONARY INFARCTION ( 18 FDA reports)
ROTATOR CUFF REPAIR ( 18 FDA reports)
SCLERAL DISCOLOURATION ( 18 FDA reports)
SKIN FIBROSIS ( 18 FDA reports)
SOMNAMBULISM ( 18 FDA reports)
SPONDYLITIS ( 18 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 18 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 18 FDA reports)
URGE INCONTINENCE ( 18 FDA reports)
UTERINE CANCER ( 18 FDA reports)
VITAMIN D ABNORMAL ( 18 FDA reports)
VITH NERVE PARALYSIS ( 18 FDA reports)
PROSTHESIS USER ( 17 FDA reports)
PULMONARY THROMBOSIS ( 17 FDA reports)
RADIATION INJURY ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
RETINAL TEAR ( 17 FDA reports)
SCOTOMA ( 17 FDA reports)
SINUS ARRHYTHMIA ( 17 FDA reports)
SJOGREN'S SYNDROME ( 17 FDA reports)
SPINAL COLUMN INJURY ( 17 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 17 FDA reports)
VERTIGO POSITIONAL ( 17 FDA reports)
ABSCESS INTESTINAL ( 17 FDA reports)
ACUTE HEPATIC FAILURE ( 17 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 17 FDA reports)
ANURIA ( 17 FDA reports)
BASEDOW'S DISEASE ( 17 FDA reports)
BIOPSY BREAST ABNORMAL ( 17 FDA reports)
BLADDER SPASM ( 17 FDA reports)
BONE MARROW DISORDER ( 17 FDA reports)
CARDIAC VALVE SCLEROSIS ( 17 FDA reports)
CATHETER PLACEMENT ( 17 FDA reports)
CEREBELLAR SYNDROME ( 17 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 17 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 17 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 17 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 17 FDA reports)
ENCEPHALITIS HERPES ( 17 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 17 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 17 FDA reports)
EROSIVE OESOPHAGITIS ( 17 FDA reports)
EYE INJURY ( 17 FDA reports)
FACIAL OPERATION ( 17 FDA reports)
FISTULA REPAIR ( 17 FDA reports)
GRAFT VERSUS HOST DISEASE ( 17 FDA reports)
HILAR LYMPHADENOPATHY ( 17 FDA reports)
HYPOVITAMINOSIS ( 17 FDA reports)
IMMUNODEFICIENCY ( 17 FDA reports)
INFUSION SITE PAIN ( 17 FDA reports)
INJECTION SITE OEDEMA ( 17 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 17 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 17 FDA reports)
METABOLIC DISORDER ( 17 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 17 FDA reports)
METRORRHAGIA ( 17 FDA reports)
MIGRAINE WITH AURA ( 17 FDA reports)
MITRAL VALVE DISEASE ( 17 FDA reports)
MYDRIASIS ( 17 FDA reports)
MYELOMA RECURRENCE ( 17 FDA reports)
NASAL DRYNESS ( 17 FDA reports)
NEPHROGENIC ANAEMIA ( 17 FDA reports)
NEPHROPATHY TOXIC ( 17 FDA reports)
NON-SMALL CELL LUNG CANCER ( 17 FDA reports)
ORAL PRURITUS ( 17 FDA reports)
OSTEOMYELITIS CHRONIC ( 17 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 17 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 17 FDA reports)
ACCIDENTAL EXPOSURE ( 16 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 16 FDA reports)
ANAL FISSURE ( 16 FDA reports)
ARTHROSCOPY ( 16 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 16 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 16 FDA reports)
BRADYPHRENIA ( 16 FDA reports)
CALCIPHYLAXIS ( 16 FDA reports)
CARDIAC TAMPONADE ( 16 FDA reports)
CUSHINGOID ( 16 FDA reports)
DIABETIC RETINOPATHY ( 16 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 16 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 16 FDA reports)
EPICONDYLITIS ( 16 FDA reports)
EXOPHTHALMOS ( 16 FDA reports)
HALLUCINATION, AUDITORY ( 16 FDA reports)
HEPATITIS ACUTE ( 16 FDA reports)
HEPATITIS C ( 16 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 16 FDA reports)
HORMONE LEVEL ABNORMAL ( 16 FDA reports)
HYPERMETABOLISM ( 16 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 16 FDA reports)
INJECTION SITE VESICLES ( 16 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 16 FDA reports)
MONOPLEGIA ( 16 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 16 FDA reports)
ONYCHALGIA ( 16 FDA reports)
OVARIAN ENLARGEMENT ( 16 FDA reports)
PHARYNGEAL ERYTHEMA ( 16 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 16 FDA reports)
POLYARTHRITIS ( 16 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 16 FDA reports)
PRECANCEROUS SKIN LESION ( 16 FDA reports)
PROCEDURAL HYPERTENSION ( 16 FDA reports)
PRODUCT ADHESION ISSUE ( 16 FDA reports)
RIGHT ATRIAL DILATATION ( 16 FDA reports)
SKIN MASS ( 16 FDA reports)
SKIN ODOUR ABNORMAL ( 16 FDA reports)
SOCIAL PROBLEM ( 16 FDA reports)
SPINAL CORD OEDEMA ( 16 FDA reports)
STASIS DERMATITIS ( 16 FDA reports)
TACHYPNOEA ( 16 FDA reports)
TESTICULAR SWELLING ( 16 FDA reports)
TRACHEOBRONCHITIS ( 16 FDA reports)
VASCULAR PSEUDOANEURYSM ( 16 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 16 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 16 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 15 FDA reports)
PRESBYOPIA ( 15 FDA reports)
RETINAL VEIN OCCLUSION ( 15 FDA reports)
SENSATION OF PRESSURE ( 15 FDA reports)
SKIN FISSURES ( 15 FDA reports)
SKULL FRACTURE ( 15 FDA reports)
SPLEEN DISORDER ( 15 FDA reports)
STRESS CARDIOMYOPATHY ( 15 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 15 FDA reports)
TONGUE COATED ( 15 FDA reports)
TUMOUR LYSIS SYNDROME ( 15 FDA reports)
UTERINE DILATION AND CURETTAGE ( 15 FDA reports)
VASCULAR GRAFT ( 15 FDA reports)
VASODILATATION ( 15 FDA reports)
ADNEXA UTERI CYST ( 15 FDA reports)
ANAEMIA MACROCYTIC ( 15 FDA reports)
APPLICATION SITE IRRITATION ( 15 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 15 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 15 FDA reports)
AXILLARY PAIN ( 15 FDA reports)
BACTERIAL TEST POSITIVE ( 15 FDA reports)
BENIGN OVARIAN TUMOUR ( 15 FDA reports)
BILE DUCT OBSTRUCTION ( 15 FDA reports)
BILIARY COLIC ( 15 FDA reports)
BLOOD CULTURE POSITIVE ( 15 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 15 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 15 FDA reports)
BONE FORMATION INCREASED ( 15 FDA reports)
BONE MARROW TRANSPLANT ( 15 FDA reports)
BONE NEOPLASM ( 15 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 15 FDA reports)
BREAST ENLARGEMENT ( 15 FDA reports)
BREAST PROSTHESIS USER ( 15 FDA reports)
BUNION OPERATION ( 15 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 15 FDA reports)
CONJUNCTIVAL OEDEMA ( 15 FDA reports)
ENCEPHALOMALACIA ( 15 FDA reports)
EYELID DISORDER ( 15 FDA reports)
FOOD INTOLERANCE ( 15 FDA reports)
GASTRIC CANCER ( 15 FDA reports)
HAND DEFORMITY ( 15 FDA reports)
HIDRADENITIS ( 15 FDA reports)
HYDROURETER ( 15 FDA reports)
HYPERTHERMIA ( 15 FDA reports)
JAUNDICE CHOLESTATIC ( 15 FDA reports)
KNEE DEFORMITY ( 15 FDA reports)
LIP DRY ( 15 FDA reports)
LUPUS-LIKE SYNDROME ( 15 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 15 FDA reports)
MEDICAL DEVICE REMOVAL ( 15 FDA reports)
NAIL DISCOLOURATION ( 15 FDA reports)
OBSTRUCTIVE UROPATHY ( 15 FDA reports)
OROPHARYNGEAL BLISTERING ( 15 FDA reports)
OSTEITIS DEFORMANS ( 15 FDA reports)
ABDOMINAL INFECTION ( 14 FDA reports)
AFFECT LABILITY ( 14 FDA reports)
ALVEOLOPLASTY ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 14 FDA reports)
APPLICATION SITE PAIN ( 14 FDA reports)
ASPERGILLOSIS ( 14 FDA reports)
ATROPHY ( 14 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 14 FDA reports)
BLADDER DYSFUNCTION ( 14 FDA reports)
BLOOD IRON INCREASED ( 14 FDA reports)
BLOOD MAGNESIUM INCREASED ( 14 FDA reports)
BONE METABOLISM DISORDER ( 14 FDA reports)
CARDIAC FIBRILLATION ( 14 FDA reports)
CEREBELLAR ATROPHY ( 14 FDA reports)
CHANGE OF BOWEL HABIT ( 14 FDA reports)
COLECTOMY ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
DELUSION ( 14 FDA reports)
DERMATITIS EXFOLIATIVE ( 14 FDA reports)
DUODENITIS ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 14 FDA reports)
EMBOLISM ARTERIAL ( 14 FDA reports)
FEEDING DISORDER ( 14 FDA reports)
FOREARM FRACTURE ( 14 FDA reports)
FULL BLOOD COUNT DECREASED ( 14 FDA reports)
GLIOSIS ( 14 FDA reports)
HAEMOGLOBIN ABNORMAL ( 14 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 14 FDA reports)
HAIR DISORDER ( 14 FDA reports)
HYPERBILIRUBINAEMIA ( 14 FDA reports)
IMPETIGO ( 14 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 14 FDA reports)
INCISION SITE HAEMORRHAGE ( 14 FDA reports)
INFUSION SITE ERYTHEMA ( 14 FDA reports)
INJECTION SITE INFECTION ( 14 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 14 FDA reports)
LEUKODYSTROPHY ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
MECHANICAL VENTILATION ( 14 FDA reports)
MENINGITIS ( 14 FDA reports)
NEUROENDOCRINE CARCINOMA ( 14 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 14 FDA reports)
OSTEOPOROTIC FRACTURE ( 14 FDA reports)
PARKINSONISM ( 14 FDA reports)
PCO2 DECREASED ( 14 FDA reports)
PHARYNGEAL DISORDER ( 14 FDA reports)
PRESBYOESOPHAGUS ( 14 FDA reports)
READING DISORDER ( 14 FDA reports)
RETINAL ISCHAEMIA ( 14 FDA reports)
SCAPULA FRACTURE ( 14 FDA reports)
SCAR EXCISION ( 14 FDA reports)
SEROTONIN SYNDROME ( 14 FDA reports)
SKIN EROSION ( 14 FDA reports)
SKIN SWELLING ( 14 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 14 FDA reports)
THERAPY NON-RESPONDER ( 14 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 14 FDA reports)
TRANSPLANT REJECTION ( 14 FDA reports)
VENOUS INJURY ( 14 FDA reports)
VENOUS OCCLUSION ( 14 FDA reports)
VOCAL CORD DISORDER ( 14 FDA reports)
PULMONARY TUBERCULOSIS ( 13 FDA reports)
PYELONEPHRITIS ACUTE ( 13 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 13 FDA reports)
RENAL ARTERY STENOSIS ( 13 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 13 FDA reports)
RENAL TRANSPLANT ( 13 FDA reports)
RENAL TUBULAR DISORDER ( 13 FDA reports)
RETINAL MELANOMA ( 13 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 13 FDA reports)
SINUS ARREST ( 13 FDA reports)
SMALL INTESTINE OPERATION ( 13 FDA reports)
SPIDER VEIN ( 13 FDA reports)
SPINAL PAIN ( 13 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 13 FDA reports)
TOBACCO USER ( 13 FDA reports)
TOXIC ENCEPHALOPATHY ( 13 FDA reports)
TRAUMATIC FRACTURE ( 13 FDA reports)
URINARY HESITATION ( 13 FDA reports)
URINE ABNORMALITY ( 13 FDA reports)
VASCULAR INJURY ( 13 FDA reports)
VERBAL ABUSE ( 13 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
VULVOVAGINITIS ( 13 FDA reports)
AKATHISIA ( 13 FDA reports)
ARTERIAL BYPASS OPERATION ( 13 FDA reports)
ARTERIAL DISORDER ( 13 FDA reports)
ARTERIOSPASM CORONARY ( 13 FDA reports)
BACTERIAL SEPSIS ( 13 FDA reports)
BILIARY DILATATION ( 13 FDA reports)
BLADDER OBSTRUCTION ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 13 FDA reports)
BRAIN SCAN ABNORMAL ( 13 FDA reports)
BREAST DISCHARGE ( 13 FDA reports)
BREAST OPERATION ( 13 FDA reports)
BREAST SWELLING ( 13 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 13 FDA reports)
CHOREA ( 13 FDA reports)
COLLAPSE OF LUNG ( 13 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 13 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 13 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 13 FDA reports)
DENTAL NECROSIS ( 13 FDA reports)
DENTAL TREATMENT ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
EAR CONGESTION ( 13 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 13 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 13 FDA reports)
ENERGY INCREASED ( 13 FDA reports)
ERYTHEMA MULTIFORME ( 13 FDA reports)
ERYTHEMA OF EYELID ( 13 FDA reports)
EXFOLIATIVE RASH ( 13 FDA reports)
FEELING GUILTY ( 13 FDA reports)
FOOD ALLERGY ( 13 FDA reports)
FOOD POISONING ( 13 FDA reports)
FRACTURED COCCYX ( 13 FDA reports)
GLOSSITIS ( 13 FDA reports)
HAEMORRHAGIC STROKE ( 13 FDA reports)
HEART RATE ABNORMAL ( 13 FDA reports)
HIGH FREQUENCY ABLATION ( 13 FDA reports)
HIP DEFORMITY ( 13 FDA reports)
HODGKIN'S DISEASE ( 13 FDA reports)
HOSTILITY ( 13 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 13 FDA reports)
HYPERTONIA ( 13 FDA reports)
HYPOCOAGULABLE STATE ( 13 FDA reports)
ILEOSTOMY ( 13 FDA reports)
INCISIONAL HERNIA ( 13 FDA reports)
INCREASED BRONCHIAL SECRETION ( 13 FDA reports)
INFECTIOUS PERITONITIS ( 13 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 13 FDA reports)
LESION EXCISION ( 13 FDA reports)
LIGAMENT INJURY ( 13 FDA reports)
LIP BLISTER ( 13 FDA reports)
METABOLIC SYNDROME ( 13 FDA reports)
MICTURITION DISORDER ( 13 FDA reports)
NASAL DISCOMFORT ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NEPHROCALCINOSIS ( 13 FDA reports)
NEPHROSCLEROSIS ( 13 FDA reports)
NEUTROPENIC SEPSIS ( 13 FDA reports)
NONSPECIFIC REACTION ( 13 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 13 FDA reports)
ONYCHOMADESIS ( 13 FDA reports)
OSTEORADIONECROSIS ( 13 FDA reports)
PALATAL DISORDER ( 13 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 13 FDA reports)
PANCREATIC INSUFFICIENCY ( 13 FDA reports)
PHOTODERMATOSIS ( 13 FDA reports)
PILOERECTION ( 13 FDA reports)
PNEUMONIA FUNGAL ( 13 FDA reports)
ABDOMINAL RIGIDITY ( 12 FDA reports)
ABSCESS LIMB ( 12 FDA reports)
ADRENAL HAEMORRHAGE ( 12 FDA reports)
ADVERSE REACTION ( 12 FDA reports)
AGRANULOCYTOSIS ( 12 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 12 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 12 FDA reports)
ANAL FISTULA ( 12 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 12 FDA reports)
ASEPTIC NECROSIS BONE ( 12 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 12 FDA reports)
BIOPSY BONE MARROW ( 12 FDA reports)
BLADDER OPERATION ( 12 FDA reports)
BONE FISTULA ( 12 FDA reports)
CALCIFICATION METASTATIC ( 12 FDA reports)
CARDIAC OPERATION ( 12 FDA reports)
CHEST INJURY ( 12 FDA reports)
CHOLECYSTITIS INFECTIVE ( 12 FDA reports)
CHOLESTEATOMA ( 12 FDA reports)
CHONDROMALACIA ( 12 FDA reports)
COLONOSCOPY ( 12 FDA reports)
COMPARTMENT SYNDROME ( 12 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 12 FDA reports)
CYSTITIS NONINFECTIVE ( 12 FDA reports)
DEPENDENCE ( 12 FDA reports)
DIAPHRAGMATIC HERNIA ( 12 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 12 FDA reports)
DISLOCATION OF VERTEBRA ( 12 FDA reports)
DISSOCIATION ( 12 FDA reports)
DROOLING ( 12 FDA reports)
DRUG EFFECT INCREASED ( 12 FDA reports)
EFFUSION ( 12 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 12 FDA reports)
ERYSIPELAS ( 12 FDA reports)
EYE ALLERGY ( 12 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 12 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 12 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 12 FDA reports)
GASTRIC BYPASS ( 12 FDA reports)
HAEMARTHROSIS ( 12 FDA reports)
HAIR COLOUR CHANGES ( 12 FDA reports)
HELICOBACTER GASTRITIS ( 12 FDA reports)
HICCUPS ( 12 FDA reports)
HISTOPLASMOSIS ( 12 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 12 FDA reports)
HYPOVENTILATION ( 12 FDA reports)
INJECTION SITE BRUISING ( 12 FDA reports)
LAGOPHTHALMOS ( 12 FDA reports)
LIGAMENT RUPTURE ( 12 FDA reports)
LYMPH NODE PALPABLE ( 12 FDA reports)
MAMMOGRAM ABNORMAL ( 12 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 12 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 12 FDA reports)
NEGATIVE THOUGHTS ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 12 FDA reports)
PARTIAL SEIZURES ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PITTING OEDEMA ( 12 FDA reports)
PLATELET COUNT ABNORMAL ( 12 FDA reports)
POOR PERSONAL HYGIENE ( 12 FDA reports)
PROSTHESIS IMPLANTATION ( 12 FDA reports)
PRURITUS GENITAL ( 12 FDA reports)
PSEUDODEMENTIA ( 12 FDA reports)
PYURIA ( 12 FDA reports)
RENAL COLIC ( 12 FDA reports)
RESPIRATORY TRACT OEDEMA ( 12 FDA reports)
RHONCHI ( 12 FDA reports)
ROSACEA ( 12 FDA reports)
SINUS OPERATION ( 12 FDA reports)
SOFT TISSUE INFLAMMATION ( 12 FDA reports)
SPLENIC RUPTURE ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
SYSTEMIC SCLEROSIS ( 12 FDA reports)
TINEA CRURIS ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
TUMOUR MARKER INCREASED ( 12 FDA reports)
UNDERWEIGHT ( 12 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 12 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 12 FDA reports)
VULVAL DISORDER ( 12 FDA reports)
VULVOVAGINAL PRURITUS ( 12 FDA reports)
PULMONARY HAEMORRHAGE ( 11 FDA reports)
PULMONARY VALVE STENOSIS ( 11 FDA reports)
PULSE ABNORMAL ( 11 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 11 FDA reports)
RECTAL CANCER ( 11 FDA reports)
SCIATIC NERVE INJURY ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SEPSIS SYNDROME ( 11 FDA reports)
SHOCK HAEMORRHAGIC ( 11 FDA reports)
SKIN HYPERPIGMENTATION ( 11 FDA reports)
SPINAL CORD DISORDER ( 11 FDA reports)
STEATORRHOEA ( 11 FDA reports)
STREPTOCOCCAL SEPSIS ( 11 FDA reports)
SUFFOCATION FEELING ( 11 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 11 FDA reports)
TENSION HEADACHE ( 11 FDA reports)
TOOTH EROSION ( 11 FDA reports)
TRANSPLANT FAILURE ( 11 FDA reports)
URETERIC OBSTRUCTION ( 11 FDA reports)
VAGINITIS BACTERIAL ( 11 FDA reports)
VENOUS THROMBOSIS LIMB ( 11 FDA reports)
VENTRICULAR DYSFUNCTION ( 11 FDA reports)
WHITE BLOOD CELL DISORDER ( 11 FDA reports)
XEROSIS ( 11 FDA reports)
ADDISON'S DISEASE ( 11 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 11 FDA reports)
ANAL ABSCESS ( 11 FDA reports)
ANKLE OPERATION ( 11 FDA reports)
ANKYLOSING SPONDYLITIS ( 11 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 11 FDA reports)
AORTIC VALVE CALCIFICATION ( 11 FDA reports)
APPENDIX DISORDER ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
ARTERIAL THROMBOSIS ( 11 FDA reports)
BLADDER DILATATION ( 11 FDA reports)
BLADDER DISCOMFORT ( 11 FDA reports)
BLOOD CALCIUM ABNORMAL ( 11 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BREAST CANCER STAGE III ( 11 FDA reports)
BREAST FIBROSIS ( 11 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 11 FDA reports)
CAECITIS ( 11 FDA reports)
CATHETER RELATED COMPLICATION ( 11 FDA reports)
CATHETER RELATED INFECTION ( 11 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 11 FDA reports)
COCCIDIOIDOMYCOSIS ( 11 FDA reports)
COLONIC OBSTRUCTION ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
CONDUCTION DISORDER ( 11 FDA reports)
CONNECTIVE TISSUE DISORDER ( 11 FDA reports)
CONTRAST MEDIA REACTION ( 11 FDA reports)
CORONARY ANGIOPLASTY ( 11 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
EAR PRURITUS ( 11 FDA reports)
ENTEROCUTANEOUS FISTULA ( 11 FDA reports)
EYE OEDEMA ( 11 FDA reports)
GINGIVAL ABSCESS ( 11 FDA reports)
GRIP STRENGTH DECREASED ( 11 FDA reports)
HEAT RASH ( 11 FDA reports)
HYPERVITAMINOSIS ( 11 FDA reports)
IMMUNOGLOBULINS DECREASED ( 11 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 11 FDA reports)
INTENTIONAL SELF-INJURY ( 11 FDA reports)
INTESTINAL HAEMORRHAGE ( 11 FDA reports)
INVESTIGATION ( 11 FDA reports)
LIGAMENT DISORDER ( 11 FDA reports)
LIP OEDEMA ( 11 FDA reports)
LUNG ABSCESS ( 11 FDA reports)
LUNG CANCER METASTATIC ( 11 FDA reports)
MAMMOPLASTY ( 11 FDA reports)
MENISCAL DEGENERATION ( 11 FDA reports)
METASTASES TO PANCREAS ( 11 FDA reports)
MIXED DEAFNESS ( 11 FDA reports)
MYOFASCITIS ( 11 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 11 FDA reports)
NASAL OEDEMA ( 11 FDA reports)
NODAL RHYTHM ( 11 FDA reports)
PANIC DISORDER ( 11 FDA reports)
PANIC REACTION ( 11 FDA reports)
PERICARDIAL DISEASE ( 11 FDA reports)
PERIORBITAL HAEMATOMA ( 11 FDA reports)
PERSONALITY DISORDER ( 11 FDA reports)
PHYSICAL ASSAULT ( 11 FDA reports)
PLASTIC SURGERY TO THE FACE ( 11 FDA reports)
PNEUMONIA LEGIONELLA ( 11 FDA reports)
PO2 DECREASED ( 11 FDA reports)
POLYPECTOMY ( 11 FDA reports)
PORTAL VEIN THROMBOSIS ( 11 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 11 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 10 FDA reports)
ADRENAL ADENOMA ( 10 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 10 FDA reports)
ALCOHOL ABUSE ( 10 FDA reports)
AMAUROSIS FUGAX ( 10 FDA reports)
ANAL SPHINCTER ATONY ( 10 FDA reports)
ANEURYSM REPAIR ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 10 FDA reports)
AORTIC DILATATION ( 10 FDA reports)
APPLICATION SITE EROSION ( 10 FDA reports)
BACTEROIDES TEST POSITIVE ( 10 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 10 FDA reports)
BLADDER NEOPLASM ( 10 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BLOOD CREATININE ABNORMAL ( 10 FDA reports)
BLOOD PH DECREASED ( 10 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 10 FDA reports)
BRAIN CONTUSION ( 10 FDA reports)
BREAST LUMP REMOVAL ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
BUNDLE BRANCH BLOCK ( 10 FDA reports)
BURNS SECOND DEGREE ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CELLULITIS ORBITAL ( 10 FDA reports)
CEREBRAL HAEMATOMA ( 10 FDA reports)
CEREBRAL THROMBOSIS ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 10 FDA reports)
COLONIC STENOSIS ( 10 FDA reports)
COLOSTOMY ( 10 FDA reports)
CSF PROTEIN INCREASED ( 10 FDA reports)
CUSHING'S SYNDROME ( 10 FDA reports)
CYTOLYTIC HEPATITIS ( 10 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 10 FDA reports)
DENTAL CARE ( 10 FDA reports)
DERMATITIS ACNEIFORM ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DIABETIC MICROANGIOPATHY ( 10 FDA reports)
DISORDER OF ORBIT ( 10 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 10 FDA reports)
EMBOLIC STROKE ( 10 FDA reports)
ENCEPHALITIS ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
FACIAL SPASM ( 10 FDA reports)
FEAR OF DISEASE ( 10 FDA reports)
FISTULA DISCHARGE ( 10 FDA reports)
FLAT AFFECT ( 10 FDA reports)
FOOD AVERSION ( 10 FDA reports)
FOREIGN BODY REACTION ( 10 FDA reports)
GASTROINTESTINAL NECROSIS ( 10 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 10 FDA reports)
GINGIVAL OEDEMA ( 10 FDA reports)
GINGIVECTOMY ( 10 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 10 FDA reports)
GUILLAIN-BARRE SYNDROME ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HEPATIC CONGESTION ( 10 FDA reports)
HEPATITIS CHOLESTATIC ( 10 FDA reports)
HYPERACUSIS ( 10 FDA reports)
HYPERPHAGIA ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
ILEITIS ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INCISIONAL DRAINAGE ( 10 FDA reports)
INFECTED CYST ( 10 FDA reports)
INTESTINAL POLYP ( 10 FDA reports)
JOINT DESTRUCTION ( 10 FDA reports)
KERATOACANTHOMA ( 10 FDA reports)
LABILE BLOOD PRESSURE ( 10 FDA reports)
LIVEDO RETICULARIS ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
LOWER EXTREMITY MASS ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 10 FDA reports)
METAMORPHOPSIA ( 10 FDA reports)
METASTASES TO KIDNEY ( 10 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 10 FDA reports)
MUSCLE CONTRACTURE ( 10 FDA reports)
MUSCLE FATIGUE ( 10 FDA reports)
MYASTHENIA GRAVIS ( 10 FDA reports)
NERVE ROOT COMPRESSION ( 10 FDA reports)
NODULE ON EXTREMITY ( 10 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 10 FDA reports)
OOPHORECTOMY ( 10 FDA reports)
OPTIC ATROPHY ( 10 FDA reports)
OVARIAN MASS ( 10 FDA reports)
PLEURODESIS ( 10 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 10 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 10 FDA reports)
PROSTATIC CALCIFICATION ( 10 FDA reports)
RADIATION PNEUMONITIS ( 10 FDA reports)
REGURGITATION ( 10 FDA reports)
RESPIRATORY DEPRESSION ( 10 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 10 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
SINUSITIS FUNGAL ( 10 FDA reports)
SKIN CHAPPED ( 10 FDA reports)
SKIN LESION EXCISION ( 10 FDA reports)
SKIN OEDEMA ( 10 FDA reports)
SPONDYLITIC MYELOPATHY ( 10 FDA reports)
STENT REMOVAL ( 10 FDA reports)
SURGICAL FAILURE ( 10 FDA reports)
SYNCOPE VASOVAGAL ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
THROMBOSIS IN DEVICE ( 10 FDA reports)
TINEA PEDIS ( 10 FDA reports)
TOOTH DISCOLOURATION ( 10 FDA reports)
TRACHEOSTOMY ( 10 FDA reports)
URINE CALCIUM DECREASED ( 10 FDA reports)
URINE CALCIUM INCREASED ( 10 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
UTERINE PROLAPSE ( 10 FDA reports)
VENOOCCLUSIVE DISEASE ( 10 FDA reports)
WEIGHT LOSS POOR ( 10 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 10 FDA reports)
WRIST SURGERY ( 10 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 9 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 9 FDA reports)
RECTAL TENESMUS ( 9 FDA reports)
RESPIRATION ABNORMAL ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
RHEUMATOID FACTOR INCREASED ( 9 FDA reports)
SCHIZOPHRENIA ( 9 FDA reports)
SERUM FERRITIN DECREASED ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 9 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 9 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 9 FDA reports)
TACHYARRHYTHMIA ( 9 FDA reports)
TEARFULNESS ( 9 FDA reports)
TEMPORAL LOBE EPILEPSY ( 9 FDA reports)
TESTICULAR PAIN ( 9 FDA reports)
THALAMIC INFARCTION ( 9 FDA reports)
TONSILLAR DISORDER ( 9 FDA reports)
TONSILLAR HYPERTROPHY ( 9 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 9 FDA reports)
TRANSPLANT ( 9 FDA reports)
TROPONIN I INCREASED ( 9 FDA reports)
VARICELLA ( 9 FDA reports)
VOLVULUS ( 9 FDA reports)
WOUND HAEMORRHAGE ( 9 FDA reports)
ANAL PRURITUS ( 9 FDA reports)
ANGIOMYOLIPOMA ( 9 FDA reports)
AORTIC VALVE REPLACEMENT ( 9 FDA reports)
APPLICATION SITE REACTION ( 9 FDA reports)
APPLICATION SITE VESICLES ( 9 FDA reports)
ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
ASBESTOSIS ( 9 FDA reports)
AURA ( 9 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 9 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
BODY TINEA ( 9 FDA reports)
BRADYKINESIA ( 9 FDA reports)
BRAIN OPERATION ( 9 FDA reports)
CALCULUS BLADDER ( 9 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 9 FDA reports)
CARBON DIOXIDE DECREASED ( 9 FDA reports)
CARDIAC FAILURE CHRONIC ( 9 FDA reports)
CATHETERISATION VENOUS ( 9 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 9 FDA reports)
CEREBROSCLEROSIS ( 9 FDA reports)
CHONDROCALCINOSIS ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CYST REMOVAL ( 9 FDA reports)
CYSTITIS HAEMORRHAGIC ( 9 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 9 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 9 FDA reports)
DERMATITIS PSORIASIFORM ( 9 FDA reports)
DEVICE OCCLUSION ( 9 FDA reports)
DIPLEGIA ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
DUODENAL ULCER PERFORATION ( 9 FDA reports)
EARLY SATIETY ( 9 FDA reports)
ENDOMETRIAL DISORDER ( 9 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 9 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 9 FDA reports)
EXCESSIVE EYE BLINKING ( 9 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 9 FDA reports)
FOLATE DEFICIENCY ( 9 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 9 FDA reports)
GASTRODUODENITIS ( 9 FDA reports)
GASTROINTESTINAL OEDEMA ( 9 FDA reports)
GENITAL HERPES ( 9 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 9 FDA reports)
GRAM STAIN ( 9 FDA reports)
HAEMOCHROMATOSIS ( 9 FDA reports)
HAEMOGLOBIN INCREASED ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPERREFLEXIA ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
IMPAIRED SELF-CARE ( 9 FDA reports)
INHALATION THERAPY ( 9 FDA reports)
INTESTINAL OPERATION ( 9 FDA reports)
INTESTINAL ULCER ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
ITCHING SCAR ( 9 FDA reports)
LIPIDS INCREASED ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 9 FDA reports)
MARROW HYPERPLASIA ( 9 FDA reports)
MASTOCYTOSIS ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 9 FDA reports)
MEAN CELL VOLUME DECREASED ( 9 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 9 FDA reports)
MENOPAUSE ( 9 FDA reports)
METASTASES TO PERITONEUM ( 9 FDA reports)
METASTATIC PAIN ( 9 FDA reports)
MOANING ( 9 FDA reports)
MONARTHRITIS ( 9 FDA reports)
MOUTH INJURY ( 9 FDA reports)
MUSCLE HAEMORRHAGE ( 9 FDA reports)
MYELOFIBROSIS ( 9 FDA reports)
MYOCARDITIS ( 9 FDA reports)
NASAL TURBINATE ABNORMALITY ( 9 FDA reports)
NEUROPATHY ( 9 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 9 FDA reports)
NIGHT BLINDNESS ( 9 FDA reports)
OCULAR DISCOMFORT ( 9 FDA reports)
OESOPHAGEAL CARCINOMA ( 9 FDA reports)
OESOPHAGEAL IRRITATION ( 9 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
ONYCHOLYSIS ( 9 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 9 FDA reports)
OROANTRAL FISTULA ( 9 FDA reports)
PAINFUL DEFAECATION ( 9 FDA reports)
PCO2 INCREASED ( 9 FDA reports)
PELVIC ABSCESS ( 9 FDA reports)
PEMPHIGOID ( 9 FDA reports)
PERFORMANCE STATUS DECREASED ( 9 FDA reports)
PERINEURIAL CYST ( 9 FDA reports)
PERIPHERAL EMBOLISM ( 9 FDA reports)
PHLEBOSCLEROSIS ( 9 FDA reports)
POLYCYSTIC OVARIES ( 9 FDA reports)
POLYMYOSITIS ( 9 FDA reports)
POST PROCEDURAL HAEMATOMA ( 9 FDA reports)
ABDOMINAL WALL ABSCESS ( 8 FDA reports)
ACANTHOSIS ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 8 FDA reports)
AGORAPHOBIA ( 8 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 8 FDA reports)
ANAESTHETIC COMPLICATION ( 8 FDA reports)
ANAL HAEMORRHAGE ( 8 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 8 FDA reports)
APPLICATION SITE URTICARIA ( 8 FDA reports)
AREFLEXIA ( 8 FDA reports)
ASTROCYTOMA ( 8 FDA reports)
ATRIAL THROMBOSIS ( 8 FDA reports)
ATYPICAL FEMUR FRACTURE ( 8 FDA reports)
BACTERIURIA ( 8 FDA reports)
BLOOD BICARBONATE DECREASED ( 8 FDA reports)
BLOOD CORTISOL DECREASED ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 8 FDA reports)
BLOOD SODIUM INCREASED ( 8 FDA reports)
BONE TRIMMING ( 8 FDA reports)
BRAIN COMPRESSION ( 8 FDA reports)
BREAST CELLULITIS ( 8 FDA reports)
BREAST DISCOMFORT ( 8 FDA reports)
BREAST HAEMATOMA ( 8 FDA reports)
BRONCHIAL DISORDER ( 8 FDA reports)
BRONCHIAL OBSTRUCTION ( 8 FDA reports)
BRONCHITIS VIRAL ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CARDIAC ANEURYSM ( 8 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 8 FDA reports)
CAROTID ARTERY ANEURYSM ( 8 FDA reports)
CAROTIDYNIA ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CERULOPLASMIN DECREASED ( 8 FDA reports)
CERVICAL SPINE FLATTENING ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COAGULATION TIME PROLONGED ( 8 FDA reports)
COLON OPERATION ( 8 FDA reports)
COLON POLYPECTOMY ( 8 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 8 FDA reports)
CORNEAL DYSTROPHY ( 8 FDA reports)
CYANOPSIA ( 8 FDA reports)
DARK CIRCLES UNDER EYES ( 8 FDA reports)
DEAFNESS BILATERAL ( 8 FDA reports)
DEVICE COMPONENT ISSUE ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 8 FDA reports)
DIABETIC COMPLICATION ( 8 FDA reports)
DIAPHRAGMATIC DISORDER ( 8 FDA reports)
DRUG TOLERANCE ( 8 FDA reports)
DRY GANGRENE ( 8 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
EXTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
EXTRASKELETAL OSSIFICATION ( 8 FDA reports)
EYE OPERATION ( 8 FDA reports)
FAT NECROSIS ( 8 FDA reports)
FOAMING AT MOUTH ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
FUNGAEMIA ( 8 FDA reports)
GALLBLADDER PAIN ( 8 FDA reports)
GALLBLADDER POLYP ( 8 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 8 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 8 FDA reports)
GESTATIONAL DIABETES ( 8 FDA reports)
GINGIVAL BLISTER ( 8 FDA reports)
GINGIVAL EROSION ( 8 FDA reports)
HEMICEPHALALGIA ( 8 FDA reports)
HYPERNATRAEMIA ( 8 FDA reports)
HYPERTRANSAMINASAEMIA ( 8 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 8 FDA reports)
INCISION SITE PAIN ( 8 FDA reports)
INGROWN HAIR ( 8 FDA reports)
INGUINAL HERNIA REPAIR ( 8 FDA reports)
INJECTION SITE ANAESTHESIA ( 8 FDA reports)
INJECTION SITE INFLAMMATION ( 8 FDA reports)
INJECTION SITE STINGING ( 8 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 8 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 8 FDA reports)
JOINT INJECTION ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LABILE HYPERTENSION ( 8 FDA reports)
LEUKOCYTURIA ( 8 FDA reports)
LIBIDO INCREASED ( 8 FDA reports)
LICHEN PLANUS ( 8 FDA reports)
LIMB CRUSHING INJURY ( 8 FDA reports)
LIVER ABSCESS ( 8 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
MIDDLE EAR EFFUSION ( 8 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 8 FDA reports)
NASAL SEPTUM DISORDER ( 8 FDA reports)
NEUROSENSORY HYPOACUSIS ( 8 FDA reports)
NOSOCOMIAL INFECTION ( 8 FDA reports)
OBSTRUCTION ( 8 FDA reports)
OPERATIVE HAEMORRHAGE ( 8 FDA reports)
OSTEOGENESIS IMPERFECTA ( 8 FDA reports)
OXYGEN SUPPLEMENTATION ( 8 FDA reports)
PALATAL OEDEMA ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 8 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 8 FDA reports)
PERNICIOUS ANAEMIA ( 8 FDA reports)
PETIT MAL EPILEPSY ( 8 FDA reports)
PNEUMATOSIS INTESTINALIS ( 8 FDA reports)
PNEUMONIA HAEMOPHILUS ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 8 FDA reports)
POISONING ( 8 FDA reports)
POST PROCEDURAL CELLULITIS ( 8 FDA reports)
POSTICTAL STATE ( 8 FDA reports)
PROCEDURAL HAEMORRHAGE ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
RECTAL DISCHARGE ( 8 FDA reports)
REFLUX LARYNGITIS ( 8 FDA reports)
REFLUX OESOPHAGITIS ( 8 FDA reports)
REFRACTORY ANAEMIA ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RHINALGIA ( 8 FDA reports)
SARCOMA ( 8 FDA reports)
SELF-INJURIOUS IDEATION ( 8 FDA reports)
SELF-MEDICATION ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SKIN GRAFT ( 8 FDA reports)
SLOW RESPONSE TO STIMULI ( 8 FDA reports)
SOFT TISSUE INJURY ( 8 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 8 FDA reports)
STENT OCCLUSION ( 8 FDA reports)
SUTURE INSERTION ( 8 FDA reports)
TEETH BRITTLE ( 8 FDA reports)
TEMPERATURE REGULATION DISORDER ( 8 FDA reports)
TENOSYNOVITIS STENOSANS ( 8 FDA reports)
TERMINAL INSOMNIA ( 8 FDA reports)
THORACOSTOMY ( 8 FDA reports)
THORACOTOMY ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
TOOTH REPAIR ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
UTERINE INFECTION ( 8 FDA reports)
VENOUS STENOSIS ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VOMITING PROJECTILE ( 8 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 8 FDA reports)
WALKING DISABILITY ( 8 FDA reports)
POTENTIATING DRUG INTERACTION ( 7 FDA reports)
PREMATURE DELIVERY ( 7 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
RASH MORBILLIFORM ( 7 FDA reports)
RENAL NEOPLASM ( 7 FDA reports)
RESPIRATORY ACIDOSIS ( 7 FDA reports)
RESPIRATORY RATE DECREASED ( 7 FDA reports)
RETINAL EXUDATES ( 7 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
SHUNT OCCLUSION ( 7 FDA reports)
SKIN DISCOMFORT ( 7 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 7 FDA reports)
SMALL INTESTINAL RESECTION ( 7 FDA reports)
SPUTUM PURULENT ( 7 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 7 FDA reports)
SUDDEN HEARING LOSS ( 7 FDA reports)
THERAPY CESSATION ( 7 FDA reports)
THROMBOCYTHAEMIA ( 7 FDA reports)
TIC ( 7 FDA reports)
TOE AMPUTATION ( 7 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 7 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 7 FDA reports)
TRAUMATIC HAEMATOMA ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
URETHRAL STENOSIS ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
UTERINE DISORDER ( 7 FDA reports)
VAGINAL DISORDER ( 7 FDA reports)
VAGINAL PROLAPSE ( 7 FDA reports)
VARICES OESOPHAGEAL ( 7 FDA reports)
VENOUS THROMBOSIS ( 7 FDA reports)
VULVAL CANCER ( 7 FDA reports)
VULVOVAGINAL PAIN ( 7 FDA reports)
WEIGHT GAIN POOR ( 7 FDA reports)
ABDOMINAL SEPSIS ( 7 FDA reports)
ABDOMINAL WALL DISORDER ( 7 FDA reports)
ABSCESS MANAGEMENT ( 7 FDA reports)
ACETABULUM FRACTURE ( 7 FDA reports)
AKINESIA ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 7 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 7 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
AORTIC ANEURYSM REPAIR ( 7 FDA reports)
APTYALISM ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
ARTICULAR CALCIFICATION ( 7 FDA reports)
ASTERIXIS ( 7 FDA reports)
AXILLARY MASS ( 7 FDA reports)
AXILLARY VEIN THROMBOSIS ( 7 FDA reports)
BEHCET'S SYNDROME ( 7 FDA reports)
BENIGN BREAST NEOPLASM ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 7 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 7 FDA reports)
BLOOD PH INCREASED ( 7 FDA reports)
BONE GIANT CELL TUMOUR ( 7 FDA reports)
BREAST DISORDER ( 7 FDA reports)
BREAST INFECTION ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 7 FDA reports)
CARCINOID TUMOUR ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CARDIAC SEPTAL DEFECT ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 7 FDA reports)
CARDIOVERSION ( 7 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 7 FDA reports)
CARTILAGE ATROPHY ( 7 FDA reports)
CENTRAL OBESITY ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
CERVICAL POLYP ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CLONUS ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 7 FDA reports)
COLITIS MICROSCOPIC ( 7 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 7 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 7 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 7 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 7 FDA reports)
DEVICE ISSUE ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DRUG LEVEL FLUCTUATING ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DUODENAL PERFORATION ( 7 FDA reports)
EAR INFECTION FUNGAL ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 7 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EXTREMITY CONTRACTURE ( 7 FDA reports)
EYE BURNS ( 7 FDA reports)
EYELIDS PRURITUS ( 7 FDA reports)
FAECES PALE ( 7 FDA reports)
FEELING OF DESPAIR ( 7 FDA reports)
FLASHBACK ( 7 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
FRACTURE TREATMENT ( 7 FDA reports)
FUNGAL OESOPHAGITIS ( 7 FDA reports)
GALLBLADDER CANCER ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 7 FDA reports)
GINGIVAL ATROPHY ( 7 FDA reports)
GOUTY ARTHRITIS ( 7 FDA reports)
GRIMACING ( 7 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
HIRSUTISM ( 7 FDA reports)
HYPERCALCIURIA ( 7 FDA reports)
HYPERCOAGULATION ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
HYPOPROTEINAEMIA ( 7 FDA reports)
HYPOSMIA ( 7 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 7 FDA reports)
IMPATIENCE ( 7 FDA reports)
INDURATION ( 7 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 7 FDA reports)
INTESTINAL PROLAPSE ( 7 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 7 FDA reports)
IRIDOCYCLITIS ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
JOINT WARMTH ( 7 FDA reports)
JUDGEMENT IMPAIRED ( 7 FDA reports)
LIMB DEFORMITY ( 7 FDA reports)
LIP HAEMORRHAGE ( 7 FDA reports)
LIPIDS ABNORMAL ( 7 FDA reports)
LITHOTRIPSY ( 7 FDA reports)
LYMPH NODE CANCER METASTATIC ( 7 FDA reports)
MEDIASTINAL MASS ( 7 FDA reports)
MENINGORADICULITIS ( 7 FDA reports)
MENOPAUSAL SYMPTOMS ( 7 FDA reports)
METASTASES TO ADRENALS ( 7 FDA reports)
MOTION SICKNESS ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
MUNCHAUSEN'S SYNDROME ( 7 FDA reports)
NEOPLASM SKIN ( 7 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 7 FDA reports)
ORAL MUCOSAL BLISTERING ( 7 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 7 FDA reports)
OSTEOCALCIN INCREASED ( 7 FDA reports)
OSTEOSYNTHESIS ( 7 FDA reports)
OTITIS MEDIA CHRONIC ( 7 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 7 FDA reports)
PALMAR ERYTHEMA ( 7 FDA reports)
PANCREATIC DUCT DILATATION ( 7 FDA reports)
PANCREATIC ENZYMES INCREASED ( 7 FDA reports)
PARVOVIRUS INFECTION ( 7 FDA reports)
PATHOLOGICAL GAMBLING ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PHARYNGEAL INFLAMMATION ( 7 FDA reports)
PIRIFORMIS SYNDROME ( 7 FDA reports)
PITUITARY TUMOUR ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
POLYMEDICATION ( 7 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 7 FDA reports)
POST THROMBOTIC SYNDROME ( 7 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ACUTE PHASE REACTION ( 6 FDA reports)
ALCOHOL POISONING ( 6 FDA reports)
ALCOHOLISM ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 6 FDA reports)
ANORECTAL OPERATION ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
ANTIBODY TEST POSITIVE ( 6 FDA reports)
AORTIC ANEURYSM RUPTURE ( 6 FDA reports)
AORTIC VALVE DISEASE ( 6 FDA reports)
ARTERIAL RUPTURE ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
AURICULAR SWELLING ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BIOPSY BREAST ( 6 FDA reports)
BLADDER MASS ( 6 FDA reports)
BLEEDING TIME PROLONGED ( 6 FDA reports)
BLISTER INFECTED ( 6 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 6 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 6 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 6 FDA reports)
BONE INFARCTION ( 6 FDA reports)
BONE MARROW NECROSIS ( 6 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BREAST CANCER STAGE II ( 6 FDA reports)
BUTTERFLY RASH ( 6 FDA reports)
CALCIUM IONISED DECREASED ( 6 FDA reports)
CANDIDA SEPSIS ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CAPILLARY FRAGILITY ( 6 FDA reports)
CARDIAC DISCOMFORT ( 6 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 6 FDA reports)
CEREBELLAR ATAXIA ( 6 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 6 FDA reports)
CEREBRAL CALCIFICATION ( 6 FDA reports)
CERVIX CARCINOMA ( 6 FDA reports)
CHEMICAL INJURY ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CLAUSTROPHOBIA ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
COMPLICATION OF DELIVERY ( 6 FDA reports)
CONTRAST MEDIA ALLERGY ( 6 FDA reports)
COR PULMONALE ( 6 FDA reports)
CORONARY ARTERY THROMBOSIS ( 6 FDA reports)
CORRECTIVE LENS USER ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
CYTOREDUCTIVE SURGERY ( 6 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 6 FDA reports)
DRUG EFFECT DELAYED ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
DYSPAREUNIA ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
DYSPHORIA ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
ECTOPIC PREGNANCY ( 6 FDA reports)
EMBOLISM VENOUS ( 6 FDA reports)
ENDOCRINE DISORDER ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
ENURESIS ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EXTRADURAL ABSCESS ( 6 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
EYELID INFECTION ( 6 FDA reports)
EYELID MARGIN CRUSTING ( 6 FDA reports)
FACTITIOUS DISORDER ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FEEDING DISORDER NEONATAL ( 6 FDA reports)
FRACTURE REDUCTION ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTRIC MUCOSAL LESION ( 6 FDA reports)
GASTRIC OPERATION ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GASTROINTESTINAL CARCINOMA ( 6 FDA reports)
GASTROINTESTINAL INJURY ( 6 FDA reports)
GENITAL RASH ( 6 FDA reports)
GLIOBLASTOMA MULTIFORME ( 6 FDA reports)
GRIEF REACTION ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HAEMATOCRIT INCREASED ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HALO VISION ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERCHLORAEMIA ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
HYPOCHROMIC ANAEMIA ( 6 FDA reports)
HYPOMETABOLISM ( 6 FDA reports)
HYPOPITUITARISM ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 6 FDA reports)
INCORRECT PRODUCT STORAGE ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
INFLAMMATORY MARKER INCREASED ( 6 FDA reports)
INFUSION SITE HAEMORRHAGE ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 6 FDA reports)
INTESTINAL FISTULA ( 6 FDA reports)
IRON OVERLOAD ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
LAZINESS ( 6 FDA reports)
LEFT VENTRICULAR FAILURE ( 6 FDA reports)
LIP EXFOLIATION ( 6 FDA reports)
LIP INJURY ( 6 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
LUMBAR HERNIA ( 6 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 6 FDA reports)
MACULAR HOLE ( 6 FDA reports)
MACULOPATHY ( 6 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
MICROCYTIC ANAEMIA ( 6 FDA reports)
MONOCYTOSIS ( 6 FDA reports)
MORGANELLA INFECTION ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
NAIL BED BLEEDING ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEEDLE ISSUE ( 6 FDA reports)
NEUROPATHIC ARTHROPATHY ( 6 FDA reports)
OBSESSIVE THOUGHTS ( 6 FDA reports)
OEDEMA GENITAL ( 6 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 6 FDA reports)
OPIATES POSITIVE ( 6 FDA reports)
ORAL NEOPLASM ( 6 FDA reports)
OROPHARYNGEAL PLAQUE ( 6 FDA reports)
OVARIAN NEOPLASM ( 6 FDA reports)
PANNICULITIS ( 6 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 6 FDA reports)
PENIS DISORDER ( 6 FDA reports)
PNEUMONIA NECROTISING ( 6 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POLYCYTHAEMIA VERA ( 6 FDA reports)
POSITIVE ROMBERGISM ( 6 FDA reports)
POST PROCEDURAL HAEMATURIA ( 6 FDA reports)
POSTMENOPAUSE ( 6 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 6 FDA reports)
PROCEDURAL NAUSEA ( 6 FDA reports)
PRODUCT PACKAGING ISSUE ( 6 FDA reports)
PROSTATIC DISORDER ( 6 FDA reports)
PROTEIN URINE ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PSYCHOLOGICAL TRAUMA ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PUPILLARY DISORDER ( 6 FDA reports)
PUPILS UNEQUAL ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RADIATION OESOPHAGITIS ( 6 FDA reports)
RADIATION SKIN INJURY ( 6 FDA reports)
RADICAL MASTECTOMY ( 6 FDA reports)
RECTAL ULCER ( 6 FDA reports)
RED BLOOD CELL ABNORMALITY ( 6 FDA reports)
REHABILITATION THERAPY ( 6 FDA reports)
RENAL HAEMORRHAGE ( 6 FDA reports)
RENAL TUBULAR ACIDOSIS ( 6 FDA reports)
RHINOVIRUS INFECTION ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SCLERODERMA ( 6 FDA reports)
SKIN FRAGILITY ( 6 FDA reports)
SMALL INTESTINAL STENOSIS ( 6 FDA reports)
SPINAL ROD INSERTION ( 6 FDA reports)
SPONDYLOARTHROPATHY ( 6 FDA reports)
TACHYPHRENIA ( 6 FDA reports)
THYROID CANCER METASTATIC ( 6 FDA reports)
TINEA INFECTION ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRANSFUSION REACTION ( 6 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 6 FDA reports)
TROPONIN T INCREASED ( 6 FDA reports)
TUBERCULIN TEST POSITIVE ( 6 FDA reports)
TUNNEL VISION ( 6 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 6 FDA reports)
URINE LEUKOCYTE ESTERASE ( 6 FDA reports)
VESICAL TENESMUS ( 6 FDA reports)
VISUAL BRIGHTNESS ( 6 FDA reports)
VITAMIN K DEFICIENCY ( 6 FDA reports)
WEGENER'S GRANULOMATOSIS ( 6 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 5 FDA reports)
PREMATURE MENOPAUSE ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PRODUCT ODOUR ABNORMAL ( 5 FDA reports)
PRODUCT TAMPERING ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PROTRUSION TONGUE ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PUBIC RAMI FRACTURE ( 5 FDA reports)
PULSE PRESSURE DECREASED ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RETICULOCYTE COUNT INCREASED ( 5 FDA reports)
RETROPERITONEAL ABSCESS ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SEBORRHOEIC DERMATITIS ( 5 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
SEPSIS NEONATAL ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SHORT-BOWEL SYNDROME ( 5 FDA reports)
SHOULDER DEFORMITY ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
SKIN CANDIDA ( 5 FDA reports)
SKIN DEPIGMENTATION ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SKULL FRACTURED BASE ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SPLENIC VEIN THROMBOSIS ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
STARING ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
STUPOR ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 5 FDA reports)
TESTICULAR ATROPHY ( 5 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 5 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 5 FDA reports)
THYROIDITIS ( 5 FDA reports)
TOE OPERATION ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TRAUMATIC LIVER INJURY ( 5 FDA reports)
TRICHORRHEXIS ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
URINE CALCIUM ( 5 FDA reports)
URINE POTASSIUM INCREASED ( 5 FDA reports)
VAGINAL BURNING SENSATION ( 5 FDA reports)
VAGINAL CANCER ( 5 FDA reports)
VAGINAL MYCOSIS ( 5 FDA reports)
VASCULAR DEMENTIA ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VASECTOMY ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
VULVAL ULCERATION ( 5 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 5 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 5 FDA reports)
WOUND CLOSURE ( 5 FDA reports)
WOUND INFECTION BACTERIAL ( 5 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 5 FDA reports)
WOUND TREATMENT ( 5 FDA reports)
ACINETOBACTER BACTERAEMIA ( 5 FDA reports)
ACINETOBACTER INFECTION ( 5 FDA reports)
ACOUSTIC NEUROMA ( 5 FDA reports)
ADJUSTMENT DISORDER ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ALLERGIC BRONCHITIS ( 5 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 5 FDA reports)
AMYLASE INCREASED ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 5 FDA reports)
ANGIODYSPLASIA ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 5 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 5 FDA reports)
APPLICATION SITE EXFOLIATION ( 5 FDA reports)
APPLICATION SITE HAEMATOMA ( 5 FDA reports)
ARACHNOIDITIS ( 5 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 5 FDA reports)
ATONIC SEIZURES ( 5 FDA reports)
BED REST ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BENIGN LUNG NEOPLASM ( 5 FDA reports)
BENIGN NEOPLASM OF SKIN ( 5 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BIOPSY BONE ( 5 FDA reports)
BIOPSY BONE ABNORMAL ( 5 FDA reports)
BITE ( 5 FDA reports)
BLADDER CANCER STAGE III ( 5 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD CREATINE ABNORMAL ( 5 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 5 FDA reports)
BLOOD UREA ABNORMAL ( 5 FDA reports)
BLOOD VISCOSITY INCREASED ( 5 FDA reports)
BLOOD ZINC DECREASED ( 5 FDA reports)
BODY MASS INDEX INCREASED ( 5 FDA reports)
BONE LESION EXCISION ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BRAIN ABSCESS ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BRAIN MIDLINE SHIFT ( 5 FDA reports)
BREECH PRESENTATION ( 5 FDA reports)
BURN INFECTION ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
CARDIAC ABLATION ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CAST APPLICATION ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 5 FDA reports)
CHRONIC FATIGUE SYNDROME ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
COLON CANCER METASTATIC ( 5 FDA reports)
COLON CANCER STAGE II ( 5 FDA reports)
COLON CANCER STAGE III ( 5 FDA reports)
COLON CANCER STAGE IV ( 5 FDA reports)
COMPLICATED MIGRAINE ( 5 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 5 FDA reports)
COOMBS TEST POSITIVE ( 5 FDA reports)
CORNEAL DISORDER ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CRYSTAL URINE PRESENT ( 5 FDA reports)
CULTURE POSITIVE ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CYSTOPEXY ( 5 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 5 FDA reports)
DERMOID CYST ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DISEASE COMPLICATION ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 5 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 5 FDA reports)
DUPUYTREN'S CONTRACTURE ( 5 FDA reports)
DYSENTERY ( 5 FDA reports)
EAR NEOPLASM MALIGNANT ( 5 FDA reports)
EARLY MORNING AWAKENING ( 5 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 5 FDA reports)
ELECTROLYTE DEPLETION ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
ENTEROVIRUS INFECTION ( 5 FDA reports)
ENZYME ABNORMALITY ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
EUSTACHIAN TUBE DISORDER ( 5 FDA reports)
EYE LASER SURGERY ( 5 FDA reports)
EYELID FUNCTION DISORDER ( 5 FDA reports)
FEBRILE INFECTION ( 5 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
FOOD INTERACTION ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GALLBLADDER OBSTRUCTION ( 5 FDA reports)
GASTRIC PH DECREASED ( 5 FDA reports)
GASTRIC ULCER PERFORATION ( 5 FDA reports)
GASTROENTERITIS NOROVIRUS ( 5 FDA reports)
GASTROENTERITIS RADIATION ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
GAZE PALSY ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GRUNTING ( 5 FDA reports)
HAEMORRHAGE URINARY TRACT ( 5 FDA reports)
HALLUCINATION, TACTILE ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEART DISEASE CONGENITAL ( 5 FDA reports)
HEPATIC CALCIFICATION ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HERNIA HIATUS REPAIR ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HORMONE THERAPY ( 5 FDA reports)
HUNGRY BONE SYNDROME ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPERTROPHY BREAST ( 5 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
ILIUM FRACTURE ( 5 FDA reports)
ILLUSION ( 5 FDA reports)
IMPAIRED FASTING GLUCOSE ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INJECTION SITE BURNING ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE INJURY ( 5 FDA reports)
INJECTION SITE MACULE ( 5 FDA reports)
INJECTION SITE SCAR ( 5 FDA reports)
INNER EAR DISORDER ( 5 FDA reports)
INTENTION TREMOR ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
INTESTINAL MASS ( 5 FDA reports)
INTRAOCULAR MELANOMA ( 5 FDA reports)
JOINT INSTABILITY ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LEARNING DISORDER ( 5 FDA reports)
LENTICULAR OPACITIES ( 5 FDA reports)
LIPOMATOSIS ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
LOSS OF LIBIDO ( 5 FDA reports)
LUPUS PNEUMONITIS ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
MACULE ( 5 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUCOSAL DRYNESS ( 5 FDA reports)
MUSCLE FIBROSIS ( 5 FDA reports)
MUSCLE SWELLING ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 5 FDA reports)
OESOPHAGEAL PERFORATION ( 5 FDA reports)
OOPHORECTOMY BILATERAL ( 5 FDA reports)
OPHTHALMOPLEGIA ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
OPTIC NERVE CUPPING ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
OSTEOMYELITIS ACUTE ( 5 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 5 FDA reports)
OTITIS MEDIA ACUTE ( 5 FDA reports)
OVARIAN LOW MALIGNANT POTENTIAL TUMOUR ( 5 FDA reports)
PAPILLOMA VIRAL INFECTION ( 5 FDA reports)
PARACENTESIS ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARAPARESIS ( 5 FDA reports)
PARATHYROID TUMOUR ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
PEAU D'ORANGE ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PEMPHIGUS ( 5 FDA reports)
PENILE PROSTHESIS INSERTION ( 5 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 5 FDA reports)
PHLEBITIS SUPERFICIAL ( 5 FDA reports)
PLEURAL DECORTICATION ( 5 FDA reports)
PNEUMATOSIS ( 5 FDA reports)
PNEUMOCEPHALUS ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 5 FDA reports)
POST LAMINECTOMY SYNDROME ( 5 FDA reports)
POST-TRAUMATIC PAIN ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACCIDENTAL NEEDLE STICK ( 4 FDA reports)
ACNE CYSTIC ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ADENOTONSILLECTOMY ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
ALLERGY TO CHEMICALS ( 4 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 4 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 4 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC RUPTURE ( 4 FDA reports)
ARRESTED LABOUR ( 4 FDA reports)
ARTERY DISSECTION ( 4 FDA reports)
ARTHROPOD STING ( 4 FDA reports)
ARTHROSCOPIC SURGERY ( 4 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 4 FDA reports)
BAND SENSATION ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BEZOAR ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 4 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 4 FDA reports)
BLOODY DISCHARGE ( 4 FDA reports)
BLUE TOE SYNDROME ( 4 FDA reports)
BODY FAT DISORDER ( 4 FDA reports)
BONE DENSITOMETRY ( 4 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 4 FDA reports)
BRAIN CANCER METASTATIC ( 4 FDA reports)
CALCIUM METABOLISM DISORDER ( 4 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 4 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 4 FDA reports)
CATARACT CORTICAL ( 4 FDA reports)
CEREBELLAR HAEMATOMA ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CERVICAL CYST ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHORIOAMNIONITIS ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 4 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
COR PULMONALE ACUTE ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CORNEAL EROSION ( 4 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 4 FDA reports)
COXSACKIE VIRUS TEST POSITIVE ( 4 FDA reports)
CRANIOPHARYNGIOMA ( 4 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
CYSTOID MACULAR OEDEMA ( 4 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DERMATOFIBROSARCOMA ( 4 FDA reports)
DEVICE LEAKAGE ( 4 FDA reports)
DIET REFUSAL ( 4 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 4 FDA reports)
DYSLEXIA ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENDOMETRIAL ATROPHY ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 4 FDA reports)
ENTROPION ( 4 FDA reports)
EPIDURAL ANAESTHESIA ( 4 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
FACIAL ASYMMETRY ( 4 FDA reports)
FACTOR XI DEFICIENCY ( 4 FDA reports)
FAECAL VOLUME DECREASED ( 4 FDA reports)
FALLOPIAN TUBE DISORDER ( 4 FDA reports)
FANCONI SYNDROME ACQUIRED ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FAT EMBOLISM ( 4 FDA reports)
FEBRILE CONVULSION ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FEELING OF RELAXATION ( 4 FDA reports)
FRACTURE MALUNION ( 4 FDA reports)
FROSTBITE ( 4 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 4 FDA reports)
GASTRECTOMY ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GLOMUS TUMOUR ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMOGLOBIN ( 4 FDA reports)
HAEMORRHAGIC CYST ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAEMORRHOID INFECTION ( 4 FDA reports)
HAEMORRHOID OPERATION ( 4 FDA reports)
HEART VALVE CALCIFICATION ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HIP SWELLING ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HYPERADRENALISM ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPERVIGILANCE ( 4 FDA reports)
HYPERVITAMINOSIS D ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOMENORRHOEA ( 4 FDA reports)
HYPOPARATHYROIDISM ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
INCISION SITE CELLULITIS ( 4 FDA reports)
INDIFFERENCE ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INFESTATION ( 4 FDA reports)
INFUSION SITE EXTRAVASATION ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INFUSION SITE PRURITUS ( 4 FDA reports)
INFUSION SITE RASH ( 4 FDA reports)
INJECTION ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
INTRASPINAL ABSCESS ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRIS ADHESIONS ( 4 FDA reports)
JARISCH-HERXHEIMER REACTION ( 4 FDA reports)
JOINT STABILISATION ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
KELOID SCAR ( 4 FDA reports)
KERATECTOMY ( 4 FDA reports)
KERATOCONUS ( 4 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 4 FDA reports)
LASER THERAPY ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
MALIGNANT MELANOMA IN SITU ( 4 FDA reports)
MALIGNANT TUMOUR EXCISION ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MAMMOGRAM ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
MASTOIDITIS ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MENOPAUSE DELAYED ( 4 FDA reports)
METASTASES TO BONE MARROW ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MORPHOEA ( 4 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 4 FDA reports)
MOUTH BREATHING ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 4 FDA reports)
NIPPLE DISORDER ( 4 FDA reports)
NIPPLE PAIN ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
NONINFECTIOUS PERITONITIS ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 4 FDA reports)
NOSE DEFORMITY ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OESOPHAGEAL OEDEMA ( 4 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
OSTEOPETROSIS ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
OVARIAN DISORDER ( 4 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 4 FDA reports)
PANCREATIC NEOPLASM ( 4 FDA reports)
PANCREATITIS RELAPSING ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PARANASAL CYST ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PENILE SIZE REDUCED ( 4 FDA reports)
PERICARDITIS LUPUS ( 4 FDA reports)
PERIPHERAL NERVE OPERATION ( 4 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 4 FDA reports)
PHANTOM PAIN ( 4 FDA reports)
PLATELET TRANSFUSION ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
PORPHYRIA NON-ACUTE ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 4 FDA reports)
POST PROCEDURAL DISCOMFORT ( 4 FDA reports)
POST PROCEDURAL DRAINAGE ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
POSTURING ( 4 FDA reports)
POUCHITIS ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 4 FDA reports)
PROCEDURAL VOMITING ( 4 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 4 FDA reports)
PRODUCT FORMULATION ISSUE ( 4 FDA reports)
PRODUCT LABEL ISSUE ( 4 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 4 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 4 FDA reports)
PROSTATE CANCER RECURRENT ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
RADIATION NEUROPATHY ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RECTAL FISSURE ( 4 FDA reports)
REFLUX GASTRITIS ( 4 FDA reports)
RELAPSING FEVER ( 4 FDA reports)
REPETITIVE STRAIN INJURY ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 4 FDA reports)
RHEUMATIC FEVER ( 4 FDA reports)
RHEUMATOID NODULE ( 4 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
SALMONELLOSIS ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SEMEN VOLUME DECREASED ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SERUM SEROTONIN INCREASED ( 4 FDA reports)
SHUNT MALFUNCTION ( 4 FDA reports)
SKIN DESQUAMATION ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
SPINAL CLAUDICATION ( 4 FDA reports)
SPINAL CORD NEOPLASM ( 4 FDA reports)
SPINAL HAEMANGIOMA ( 4 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 4 FDA reports)
STOMACH MASS ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
TABLET PHYSICAL ISSUE ( 4 FDA reports)
TALIPES ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
THERMOHYPERAESTHESIA ( 4 FDA reports)
THOUGHT BLOCKING ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
THYROXINE FREE INCREASED ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE EXFOLIATION ( 4 FDA reports)
TONIC CLONIC MOVEMENTS ( 4 FDA reports)
TRACHEITIS ( 4 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TRANSVERSE PRESENTATION ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TRIGEMINAL NERVE DISORDER ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
URETHRAL CARUNCLE ( 4 FDA reports)
URETHRAL DILATATION ( 4 FDA reports)
URINARY BLADDER POLYP ( 4 FDA reports)
UTERINE CYST ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
UTERINE NEOPLASM ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VASCULAR PURPURA ( 4 FDA reports)
VENOGRAM ( 4 FDA reports)
VESSEL PERFORATION ( 4 FDA reports)
VIRAL PERICARDITIS ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
VITRECTOMY ( 4 FDA reports)
VULVAL ABSCESS ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PRODUCT COLOUR ISSUE ( 3 FDA reports)
PROLONGED LABOUR ( 3 FDA reports)
PROSTATIC HAEMORRHAGE ( 3 FDA reports)
PROSTRATION ( 3 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULPITIS DENTAL ( 3 FDA reports)
PUS IN STOOL ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
PYONEPHROSIS ( 3 FDA reports)
RADICULITIS ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL PERFORATION ( 3 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
RENAL AMYLOIDOSIS ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL STONE REMOVAL ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
RETICULIN INCREASED ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETINAL INFARCTION ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETROGRADE EJACULATION ( 3 FDA reports)
RHODOCOCCUS INFECTION ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
RICKETS ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SALPINGITIS ( 3 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SEBACEOUS CARCINOMA ( 3 FDA reports)
SHORTENED CERVIX ( 3 FDA reports)
SHUNT STENOSIS ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SKIN SENSITISATION ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC GRANULOMA ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
STENT MALFUNCTION ( 3 FDA reports)
STICKY SKIN ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
SUCROSE INTOLERANCE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TESTICULAR CYST ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID ADENOMA ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TONSILLAR INFLAMMATION ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TOXIC NODULAR GOITRE ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRANSFERRIN DECREASED ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
TUMOUR INVASION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 3 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 3 FDA reports)
UNEQUAL LIMB LENGTH ( 3 FDA reports)
UPPER MOTOR NEURONE LESION ( 3 FDA reports)
URETERAL STENT INSERTION ( 3 FDA reports)
URETERITIS ( 3 FDA reports)
URETHRAL CANCER METASTATIC ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 3 FDA reports)
UTERINE CERVIX STENOSIS ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
UTERINE MASS ( 3 FDA reports)
VAGINAL ULCERATION ( 3 FDA reports)
VAGUS NERVE DISORDER ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR GRAFT COMPLICATION ( 3 FDA reports)
VASCULAR STENOSIS ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VEILLONELLA INFECTION ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENA CAVA FILTER INSERTION ( 3 FDA reports)
VENTRICULAR HYPOPLASIA ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VISUAL PATHWAY DISORDER ( 3 FDA reports)
VITILIGO ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
VULVAL CANCER STAGE 0 ( 3 FDA reports)
VULVAR DYSPLASIA ( 3 FDA reports)
WRIST DEFORMITY ( 3 FDA reports)
YAWNING ( 3 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABDOMINAL OPERATION ( 3 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 3 FDA reports)
ABSCESS BACTERIAL ( 3 FDA reports)
ABSCESS RUPTURE ( 3 FDA reports)
ACCOMMODATION DISORDER ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACROMEGALY ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
AGRAPHIA ( 3 FDA reports)
ALBUMINURIA ( 3 FDA reports)
ANAL STENOSIS ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPLICATION SITE ATROPHY ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
APPLICATION SITE INFLAMMATION ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BENIGN BONE NEOPLASM ( 3 FDA reports)
BENIGN COLONIC NEOPLASM ( 3 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILE OUTPUT ABNORMAL ( 3 FDA reports)
BIOPSY BREAST NORMAL ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BIOPSY PROSTATE ( 3 FDA reports)
BIOPSY STOMACH ( 3 FDA reports)
BLADDER CANCER RECURRENT ( 3 FDA reports)
BLADDER TAMPONADE ( 3 FDA reports)
BLAST CELL CRISIS ( 3 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 3 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL INCREASED ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD ARSENIC INCREASED ( 3 FDA reports)
BLOOD CORTISOL INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 3 FDA reports)
BLOOD FOLATE INCREASED ( 3 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BODY TEMPERATURE ( 3 FDA reports)
BONE DEFORMITY ( 3 FDA reports)
BONE FORMATION DECREASED ( 3 FDA reports)
BONE MARROW PLASMACYTE COUNT INCREASED ( 3 FDA reports)
BONE SARCOMA ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN NEOPLASM BENIGN ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BURN OESOPHAGEAL ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
CALCIUM IONISED INCREASED ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 3 FDA reports)
CARCINOID HEART DISEASE ( 3 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CARDIAC SIDEROSIS ( 3 FDA reports)
CARDIAC STRESS TEST ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CARDITIS ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 3 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CERVICAL CORD COMPRESSION ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHEST WALL ABSCESS ( 3 FDA reports)
CHOLANGIOGRAM ( 3 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 3 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 3 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 3 FDA reports)
CHYLOTHORAX ( 3 FDA reports)
CIRRHOSIS ALCOHOLIC ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLONAL EVOLUTION ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COELIAC ARTERY STENOSIS ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 3 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 3 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
COPPER DEFICIENCY ( 3 FDA reports)
CRANIOSYNOSTOSIS ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DACRYOCYSTORHINOSTOMY ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATITIS INFECTED ( 3 FDA reports)
DEVICE DEPOSIT ISSUE ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 3 FDA reports)
DISBACTERIOSIS ( 3 FDA reports)
DISINHIBITION ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DROP ATTACKS ( 3 FDA reports)
DRUG CLEARANCE DECREASED ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG NAME CONFUSION ( 3 FDA reports)
DRUG SCREEN NEGATIVE ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DUODENAL ULCER REPAIR ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSPLASTIC NAEVUS ( 3 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 3 FDA reports)
EAR OPERATION ( 3 FDA reports)
EJECTION FRACTION ABNORMAL ( 3 FDA reports)
ELBOW OPERATION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOMETRIAL NEOPLASM ( 3 FDA reports)
ENDOSCOPY ( 3 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 3 FDA reports)
ENTHESOPATHY ( 3 FDA reports)
EPHELIDES ( 3 FDA reports)
EPIDURITIS ( 3 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 3 FDA reports)
ERECTION INCREASED ( 3 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 3 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EYE EXCISION ( 3 FDA reports)
EYE NAEVUS ( 3 FDA reports)
EYELID EXFOLIATION ( 3 FDA reports)
FACIAL NEURALGIA ( 3 FDA reports)
FIBROUS HISTIOCYTOMA ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FUNDOSCOPY ABNORMAL ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
FUNISITIS ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRIC INFECTION ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 3 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 3 FDA reports)
GASTROINTESTINAL MALFORMATION ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENITAL ULCERATION ( 3 FDA reports)
GLARE ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
HAEMATOCRIT ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HANGNAIL ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERPES ZOSTER OTICUS ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 3 FDA reports)
HOFFMANN'S SIGN ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYALOSIS ASTEROID ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPEROXALURIA ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPHYSITIS ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
IMPLANT SITE INFLAMMATION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INABILITY TO CRAWL ( 3 FDA reports)
INFECTED BITES ( 3 FDA reports)
INFECTED SEBACEOUS CYST ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 3 FDA reports)
INFUSION SITE URTICARIA ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE DERMATITIS ( 3 FDA reports)
INJECTION SITE DYSAESTHESIA ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE STREAKING ( 3 FDA reports)
INJECTION SITE THROMBOSIS ( 3 FDA reports)
INJURY CORNEAL ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTENSIVE CARE ( 3 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
INTESTINAL STRANGULATION ( 3 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 3 FDA reports)
IRREGULAR SLEEP PHASE ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
JOINT HYPEREXTENSION ( 3 FDA reports)
KERATITIS BACTERIAL ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARGE INTESTINAL STRICTURE ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGEAL GRANULOMA ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LENS DISORDER ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LIGHT CHAIN DISEASE ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LUDWIG ANGINA ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
MACULAR CYST ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 3 FDA reports)
MASS EXCISION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN ( 3 FDA reports)
MEDICAL DEVICE PAIN ( 3 FDA reports)
MENISCUS OPERATION ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 3 FDA reports)
METASTASES TO HEART ( 3 FDA reports)
MICROALBUMINURIA ( 3 FDA reports)
MILK-ALKALI SYNDROME ( 3 FDA reports)
MULTIMORBIDITY ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYELITIS TRANSVERSE ( 3 FDA reports)
MYELOID LEUKAEMIA ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
MYXOEDEMA COMA ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEONATAL RESPIRATORY ARREST ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 3 FDA reports)
NEUTROPHIL COUNT ( 3 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NON-HIGH-DENSITY LIPOPROTEIN CHOLESTEROL INCREASED ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESTROGEN DEFICIENCY ( 3 FDA reports)
ONYCHOGRYPHOSIS ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL LICHEN PLANUS ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
OVARIAN FAILURE ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PAINFUL ERECTION ( 3 FDA reports)
PALLANAESTHESIA ( 3 FDA reports)
PANCREATIC CALCIFICATION ( 3 FDA reports)
PANCREATIC ENLARGEMENT ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PARASPINAL ABSCESS ( 3 FDA reports)
PARATHYROIDECTOMY ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PELVIC NEOPLASM ( 3 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 3 FDA reports)
PERIANAL ABSCESS ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERIPROSTHETIC FRACTURE ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERITONEAL ABSCESS ( 3 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERONEAL NERVE INJURY ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PHARYNGEAL NEOPLASM ( 3 FDA reports)
PINEAL GLAND CYST ( 3 FDA reports)
PLACENTAL DISORDER ( 3 FDA reports)
PLATELET COUNT ( 3 FDA reports)
PLEURAL FLUID ANALYSIS ( 3 FDA reports)
POLYCHROMASIA ( 3 FDA reports)
POST PROCEDURAL OEDEMA ( 3 FDA reports)
POST PROCEDURAL SWELLING ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
ABDOMEN SCAN ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOSIS NIGRICANS ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACQUIRED CLAW TOE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACROCHORDON EXCISION ( 2 FDA reports)
ACTINOMYCES TEST POSITIVE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 2 FDA reports)
ADMINISTRATION SITE PAIN ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
ALLOIMMUNISATION ( 2 FDA reports)
ALOPECIA UNIVERSALIS ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMOEBIASIS ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANORECTAL STENOSIS ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBODY TEST NEGATIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC VALVE DISEASE MIXED ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
ARTHRITIS ENTEROPATHIC ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASPIRATION JOINT ( 2 FDA reports)
ATELECTASIS NEONATAL ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA LOW GRADE ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 2 FDA reports)
BENIGN EAR NEOPLASM ( 2 FDA reports)
BEREAVEMENT ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BILIARY DRAINAGE ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER NECK SUSPENSION ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLEPHAROPLASTY ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CALCITONIN INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD OESTROGEN INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLOOD UREA ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 2 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BOREDOM ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CANCER STAGE IV ( 2 FDA reports)
BREAST INDURATION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST PROSTHESIS REMOVAL ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALCIUM IONISED ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOPLEGIA ( 2 FDA reports)
CARDIOPULMONARY BYPASS ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CAROTID PULSE ABNORMAL ( 2 FDA reports)
CARTILAGE NEOPLASM ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE EROSION ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEPHALHAEMATOMA ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHEMICAL BURN OF SKIN ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHOLELITHOTOMY ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 2 FDA reports)
COAGULATION FACTOR X LEVEL ABNORMAL ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COCHLEA IMPLANT ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL DEGENERATION ( 2 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 2 FDA reports)
CORNEAL EXFOLIATION ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CRANIAL NERVE INFECTION ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CRYSTAL ARTHROPATHY ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTIC FIBROSIS LUNG ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
EAR LOBE INFECTION ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
EJACULATION DELAYED ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELBOW DEFORMITY ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENCEPHALITIS BRAIN STEM ( 2 FDA reports)
ENCHONDROMATOSIS ( 2 FDA reports)
ENDOMETRIAL ABLATION ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ENTEROBIASIS ( 2 FDA reports)
ENTEROCELE ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPIGLOTTIC CARCINOMA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 2 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 2 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 2 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE INFECTION TOXOPLASMAL ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYELASH DISCOLOURATION ( 2 FDA reports)
EYELASH THICKENING ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEAR OF NEEDLES ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FEMORAL HERNIA ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FLAVOBACTERIUM INFECTION ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GASTRIC ATONY ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL HYPOAESTHESIA ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL GRAFT ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HUMAN EHRLICHIOSIS ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYDROMETRA ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCHROMIC ANAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERMOBILITY SYNDROME ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVITAMINOSIS A ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPHOSPHATASIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
ICHTHYOSIS ACQUIRED ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILLOGICAL THINKING ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCISION SITE PRURITUS ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INDWELLING CATHETER MANAGEMENT ( 2 FDA reports)
INFECTED BUNION ( 2 FDA reports)
INFECTED VARICOSE VEIN ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFERTILITY FEMALE ( 2 FDA reports)
INFILTRATION ANAESTHESIA ( 2 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INJECTION SITE PARAESTHESIA ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INSTILLATION SITE PAIN ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
INTESTINAL ADENOCARCINOMA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRACARDIAC MASS ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRIS HYPOPIGMENTATION ( 2 FDA reports)
JAW LESION EXCISION ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL POLYP ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOOSE BODY IN JOINT ( 2 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 2 FDA reports)
MEDIAN NERVE INJURY ( 2 FDA reports)
MEDIASTINAL FIBROSIS ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDICAL DEVICE SITE REACTION ( 2 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGEAL NEOPLASM ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METASTASES TO EYE ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
METASTATIC CARCINOID TUMOUR ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
METASTATIC LYMPHOMA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MILIA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MINERAL DEFICIENCY ( 2 FDA reports)
MINERAL SUPPLEMENTATION ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOMECTOMY ( 2 FDA reports)
N-TELOPEPTIDE URINE INCREASED ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NAIL PSORIASIS ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NASAL SEPTUM ULCERATION ( 2 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEONATAL TACHYCARDIA ( 2 FDA reports)
NEOVASCULARISATION ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEPHROSTOMY ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEURALGIC AMYOTROPHY ( 2 FDA reports)
NEUROMYELITIS OPTICA ( 2 FDA reports)
NEUROPATHIC ULCER ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 2 FDA reports)
OCULAR DYSMETRIA ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORBITAL PSEUDOTUMOUR ( 2 FDA reports)
ORCHITIS NONINFECTIVE ( 2 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOCHONDRITIS ( 2 FDA reports)
OTITIS MEDIA VIRAL ( 2 FDA reports)
OTOSCLEROSIS ( 2 FDA reports)
OVARIAN HAEMATOMA ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PAIN THRESHOLD DECREASED ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANOPHTHALMITIS ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARASITE STOOL TEST POSITIVE ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PARKINSONIAN CRISIS ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC INFECTION ( 2 FDA reports)
PELVIC PROLAPSE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERFUME SENSITIVITY ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL LESION ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHOBIA OF DRIVING ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PITUITARY ENLARGEMENT ( 2 FDA reports)
PITYRIASIS ROSEA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POLYPOIDAL CHOROIDAL VASCULOPATHY ( 2 FDA reports)
PORCELAIN GALLBLADDER ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POSTMATURE BABY ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTEIN C DEFICIENCY ( 2 FDA reports)
PROTEIN S DEFICIENCY ( 2 FDA reports)
PROTEIN TOTAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY SARCOIDOSIS ( 2 FDA reports)
RADIAL NERVE INJURY ( 2 FDA reports)
RADICULAR CYST ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL CYST RUPTURED ( 2 FDA reports)
RENAL FUNCTION TEST ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESECTION OF RECTUM ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL TOXICITY ( 2 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SACCADIC EYE MOVEMENT ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SALMONELLA BACTERAEMIA ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCINTIGRAPHY ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SEBACEOUS GLANDS OVERACTIVITY ( 2 FDA reports)
SEIZURE LIKE PHENOMENA ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENILE OSTEOPOROSIS ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SINUS PAIN ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN WOUND ( 2 FDA reports)
SLOW SPEECH ( 2 FDA reports)
SMALL CELL LUNG CANCER LIMITED STAGE ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SOCIAL FEAR ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPLENIC HAEMATOMA ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STATUS MIGRAINOSUS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STERNOTOMY ( 2 FDA reports)
STITCH ABSCESS ( 2 FDA reports)
STREPTOBACILLUS INFECTION ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBACUTE COMBINED CORD DEGENERATION ( 2 FDA reports)
SUBCHORIONIC HAEMORRHAGE ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 2 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBMANDIBULAR MASS ( 2 FDA reports)
SUPERINFECTION VIRAL ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENOTOMY ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TONGUE CANCER METASTATIC ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TONSILLOLITH ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND LIVER ( 2 FDA reports)
ULTRASOUND SCAN ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
URINE URIC ACID ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
UVULITIS ( 2 FDA reports)
VAGINAL DYSPLASIA ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VARICOSE VEIN RUPTURED ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR DISSECTION ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENOUS PRESSURE JUGULAR DECREASED ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBRAL WEDGING ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN E DECREASED ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VOCAL CORD NEOPLASM ( 2 FDA reports)
VULVAL HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL RASH ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
WART EXCISION ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
YERSINIA INFECTION ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
POSTERIOR CAPSULOTOMY ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
PROCOLLAGEN TYPE I C-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PROCTOSCOPY ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATE CANCER STAGE 0 ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTATE KERATOSIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELOGRAM RETROGRADE ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RADIOTHERAPY TO BREAST ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL CANCER RECURRENT ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL TUBE INSERTION ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TUBERCULOSIS ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CARCINOMA IN SITU ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL MICROANEURYSMS ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SALIVARY GLAND ADENOMA ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND OPERATION ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCIATIC NERVE PALSY ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SEBACEOUS GLAND INFECTION ( 1 FDA reports)
SEBACEOUS HYPERPLASIA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SELECTIVE IGM IMMUNODEFICIENCY ( 1 FDA reports)
SELENIUM DEFICIENCY ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SEXUAL INHIBITION ( 1 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 1 FDA reports)
SI QIII TIII PATTERN ( 1 FDA reports)
SICK BUILDING SYNDROME ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL INTESTINAL BACTERIAL OVERGROWTH ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD DRAINAGE ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL MENINGEAL CYST ( 1 FDA reports)
SPINAL SUPPORT ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPINOCEREBELLAR ATAXIA ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOMA ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUCCINYLACETONE INCREASED ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYMPATHETIC OPHTHALMIA ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TAENIASIS ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TANNING ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TENDON SHEATH LESION EXCISION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TETANUS IMMUNISATION ( 1 FDA reports)
THALASSAEMIA ALPHA ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THOUGHT BROADCASTING ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID C-CELL HYPERPLASIA ( 1 FDA reports)
THYROID CANCER STAGE IV ( 1 FDA reports)
THYROID FUNCTION TEST NORMAL ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONSILLITIS BACTERIAL ( 1 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACTION ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LUMBAR PUNCTURE ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPHUS ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL MALFORMATION ( 1 FDA reports)
UNEVALUABLE INVESTIGATION ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URETERAL SPASM ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY ANASTOMOTIC LEAK ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE CALCIUM/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
URINE URIC ACID ABNORMAL ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
UTERINE CARCINOMA IN SITU ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
UTERINE POLYPECTOMY ( 1 FDA reports)
UTEROVAGINAL PROLAPSE ( 1 FDA reports)
UVEITIS-GLAUCOMA-HYPHAEMA SYNDROME ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VAGINITIS ATROPHIC ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 1 FDA reports)
VERTEBRAL ARTERY DISSECTION ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL RHINITIS ( 1 FDA reports)
VIRAL TITRE INCREASED ( 1 FDA reports)
VISCERAL PAIN ( 1 FDA reports)
VITAMIN A DECREASED ( 1 FDA reports)
VITAMIN B1 INCREASED ( 1 FDA reports)
VITAMIN B2 DECREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VITAMIN D ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVAL CANCER RECURRENT ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACARIASIS ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACNE CONGLOBATA ( 1 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACTINIC ELASTOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALKAPTONURIA ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANKLE DEFORMITY ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRITIS SALMONELLA ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVERSION ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILE OUTPUT INCREASED ( 1 FDA reports)
BILEVEL POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY CERVIX ( 1 FDA reports)
BIOPSY LYMPH GLAND ( 1 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD COPPER DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE ABNORMAL ( 1 FDA reports)
BLOOD HEAVY METAL INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TESTOSTERONE ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE CYST EXCISION ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FORMATION TEST ABNORMAL ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW DONATION ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE OEDEMA ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BONE SCAN NORMAL ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRACHIAL PULSE ABNORMAL ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST DYSPLASIA ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CAMPTOCORMIA ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PACEMAKER REMOVAL ( 1 FDA reports)
CARDIAC VALVE RUPTURE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEMENTOPLASTY ( 1 FDA reports)
CENTRAL AUDITORY PROCESSING DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHLOASMA ( 1 FDA reports)
CHOLELITHIASIS MIGRATION ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOCARCINOMA ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CHRYSIASIS ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLUMSY CHILD SYNDROME ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLD-STIMULUS HEADACHE ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN ANTIGEN TYPE 1 ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER STAGE 0 ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON DYSPLASIA ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONFLUENT AND RETICULATE PAPILLOMATOSIS ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL HEPATOMEGALY ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAINDICATION TO VACCINATION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL OPERATION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUPULOLITHIASIS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
DACRYOADENITIS ACQUIRED ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEHYDROEPIANDROSTERONE DECREASED ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL CLEANING ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETES MELLITUS MANAGEMENT ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIPHTHERIA IMMUNISATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ECTOPIC KIDNEY ( 1 FDA reports)
ECTROPION OF CERVIX ( 1 FDA reports)
ECZEMA EYELIDS ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
EMOTIONAL POVERTY ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOLYMPHATIC HYDROPS ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCHROMAFFIN CELL HYPERPLASIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EPIDIDYMAL INFECTION ( 1 FDA reports)
EPIDURAL INJECTION ( 1 FDA reports)
EPIPHYSEAL DISORDER ( 1 FDA reports)
EPIPHYSEAL FRACTURE ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYSIPELOID ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ( 1 FDA reports)
EXPANDED DISABILITY STATUS SCALE SCORE INCREASED ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALLOPIAN TUBE CANCER METASTATIC ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALLOPIAN TUBE OPERATION ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
FEMALE SEX HORMONE LEVEL ABNORMAL ( 1 FDA reports)
FEMORAL HERNIA REPAIR ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL MALPRESENTATION ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FRACTURED ZYGOMATIC ARCH ELEVATION ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRO-JEJUNOSTOMY ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GRADENIGO'S SYNDROME ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
HAEMANGIOBLASTOMA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD AND NECK CANCER STAGE III ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
HEPATITIS A IMMUNISATION ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 1 FDA reports)
HYDROXYPROLINE INCREASED ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOAESTHESIA TEETH ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOPHARYNGEAL NEOPLASM ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILEOCOLECTOMY ( 1 FDA reports)
ILEORECTAL FISTULA ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMPLANT SITE CALCIFICATION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IN VITRO FERTILISATION ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE CYST ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE EROSION ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERMEDIATE UVEITIS ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KERATOSIS PILARIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LACRIMAL PASSAGE GRANULOMA ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIPOEDEMA ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUPUS HEPATITIS ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR FIBROSIS ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT MELANOMA STAGE II ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MALIGNANT MIDDLE EAR NEOPLASM ( 1 FDA reports)
MALIGNANT MUSCLE NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOID ABSCESS ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MEDULLARY THYROID CANCER ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGIOMA MALIGNANT ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENOPAUSAL DEPRESSION ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTASES TO TRACHEA ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
METATARSUS PRIMUS VARUS ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MIKULICZ'S DISEASE ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED HEPATOCELLULAR CHOLANGIOCARCINOMA ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL BED INFECTION FUNGAL ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NAIL RIDGING ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASOPHARYNGEAL REFLUX ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEISSERIA TEST POSITIVE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NICOTINAMIDE DECREASED ( 1 FDA reports)
NIPPLE NEOPLASM ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NON-SECRETORY ADENOMA OF PITUITARY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BREAST ABNORMAL ( 1 FDA reports)
NUTRITIONAL SUPPORT ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOCALCIN ( 1 FDA reports)
OSTEOCALCIN DECREASED ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOMYELITIS DRAINAGE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS ISLET CELL TRANSPLANT ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATIC PSEUDOCYST DRAINAGE ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA MUCOSAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN ABNORMAL ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PENIS CARCINOMA METASTATIC ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL INFECTION ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PERTUSSIS IMMUNISATION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL CYST ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLAGUE ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)