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

MYOCARDIAL INFARCTION ( 8297 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5338 FDA reports)
PAIN ( 4429 FDA reports)
ANXIETY ( 3046 FDA reports)
DRUG INEFFECTIVE ( 3042 FDA reports)
DEPRESSION ( 2979 FDA reports)
DYSPNOEA ( 2921 FDA reports)
NAUSEA ( 2852 FDA reports)
CARDIOVASCULAR DISORDER ( 2847 FDA reports)
ARTHRALGIA ( 2683 FDA reports)
HYPERTENSION ( 2414 FDA reports)
CHEST PAIN ( 2379 FDA reports)
DIZZINESS ( 2296 FDA reports)
HEADACHE ( 2294 FDA reports)
FATIGUE ( 2292 FDA reports)
PAIN IN EXTREMITY ( 2233 FDA reports)
FALL ( 2131 FDA reports)
BACK PAIN ( 2080 FDA reports)
OEDEMA PERIPHERAL ( 2060 FDA reports)
DIARRHOEA ( 1967 FDA reports)
ASTHENIA ( 1850 FDA reports)
VOMITING ( 1740 FDA reports)
ANAEMIA ( 1655 FDA reports)
INJURY ( 1651 FDA reports)
INSOMNIA ( 1612 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1539 FDA reports)
WEIGHT DECREASED ( 1521 FDA reports)
ARTHRITIS ( 1500 FDA reports)
RASH ( 1446 FDA reports)
OSTEOARTHRITIS ( 1423 FDA reports)
PNEUMONIA ( 1365 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1363 FDA reports)
HYPOAESTHESIA ( 1291 FDA reports)
CARDIAC DISORDER ( 1288 FDA reports)
CONSTIPATION ( 1261 FDA reports)
PYREXIA ( 1242 FDA reports)
WEIGHT INCREASED ( 1189 FDA reports)
CORONARY ARTERY DISEASE ( 1189 FDA reports)
DEEP VEIN THROMBOSIS ( 1159 FDA reports)
ABDOMINAL PAIN ( 1134 FDA reports)
PULMONARY EMBOLISM ( 1134 FDA reports)
DEATH ( 1131 FDA reports)
OSTEONECROSIS OF JAW ( 1130 FDA reports)
MALAISE ( 1113 FDA reports)
THROMBOSIS ( 1110 FDA reports)
ABDOMINAL PAIN UPPER ( 1094 FDA reports)
RENAL FAILURE ( 1089 FDA reports)
COUGH ( 1061 FDA reports)
BONE DISORDER ( 1051 FDA reports)
PRURITUS ( 1038 FDA reports)
MUSCLE SPASMS ( 1001 FDA reports)
EMOTIONAL DISTRESS ( 999 FDA reports)
GAIT DISTURBANCE ( 981 FDA reports)
FEELING ABNORMAL ( 955 FDA reports)
PARAESTHESIA ( 945 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 926 FDA reports)
URINARY TRACT INFECTION ( 888 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 883 FDA reports)
CONDITION AGGRAVATED ( 883 FDA reports)
OSTEOMYELITIS ( 882 FDA reports)
TREMOR ( 871 FDA reports)
SINUSITIS ( 853 FDA reports)
MYALGIA ( 853 FDA reports)
ATRIAL FIBRILLATION ( 852 FDA reports)
DIABETES MELLITUS ( 832 FDA reports)
DYSPEPSIA ( 831 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 825 FDA reports)
BLOOD PRESSURE INCREASED ( 813 FDA reports)
DEHYDRATION ( 809 FDA reports)
SPINAL OSTEOARTHRITIS ( 806 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 796 FDA reports)
SWELLING ( 794 FDA reports)
HYPERHIDROSIS ( 784 FDA reports)
HYPOTENSION ( 781 FDA reports)
DYSPHAGIA ( 772 FDA reports)
OSTEONECROSIS ( 772 FDA reports)
SOMNOLENCE ( 771 FDA reports)
ERYTHEMA ( 767 FDA reports)
IMPAIRED HEALING ( 753 FDA reports)
VISION BLURRED ( 753 FDA reports)
BRONCHITIS ( 748 FDA reports)
CONFUSIONAL STATE ( 742 FDA reports)
AMNESIA ( 739 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 738 FDA reports)
ARTHROPATHY ( 729 FDA reports)
NEUROPATHY PERIPHERAL ( 726 FDA reports)
HYPERSENSITIVITY ( 725 FDA reports)
OSTEOPOROSIS ( 698 FDA reports)
PALPITATIONS ( 686 FDA reports)
INFECTION ( 684 FDA reports)
PLEURAL EFFUSION ( 678 FDA reports)
CELLULITIS ( 675 FDA reports)
ANHEDONIA ( 674 FDA reports)
HAEMORRHAGE ( 674 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 674 FDA reports)
NECK PAIN ( 674 FDA reports)
LOSS OF CONSCIOUSNESS ( 664 FDA reports)
PAIN IN JAW ( 658 FDA reports)
RENAL FAILURE ACUTE ( 650 FDA reports)
TOOTH EXTRACTION ( 646 FDA reports)
GASTRITIS ( 635 FDA reports)
ABDOMINAL DISCOMFORT ( 632 FDA reports)
MUSCULAR WEAKNESS ( 626 FDA reports)
CATARACT ( 596 FDA reports)
CONTUSION ( 595 FDA reports)
URTICARIA ( 583 FDA reports)
BLOOD GLUCOSE INCREASED ( 579 FDA reports)
DECREASED APPETITE ( 577 FDA reports)
RHEUMATOID ARTHRITIS ( 576 FDA reports)
SYNCOPE ( 571 FDA reports)
MEMORY IMPAIRMENT ( 571 FDA reports)
ASTHMA ( 568 FDA reports)
BONE PAIN ( 565 FDA reports)
CONVULSION ( 563 FDA reports)
JOINT SWELLING ( 560 FDA reports)
OSTEOPENIA ( 557 FDA reports)
DRUG INTERACTION ( 554 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 552 FDA reports)
ANGINA PECTORIS ( 549 FDA reports)
MITRAL VALVE INCOMPETENCE ( 547 FDA reports)
ARRHYTHMIA ( 538 FDA reports)
DRUG HYPERSENSITIVITY ( 534 FDA reports)
ATELECTASIS ( 532 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 529 FDA reports)
MUSCULOSKELETAL PAIN ( 527 FDA reports)
CHEST DISCOMFORT ( 501 FDA reports)
HIATUS HERNIA ( 500 FDA reports)
BALANCE DISORDER ( 497 FDA reports)
CARDIOMEGALY ( 493 FDA reports)
CARDIAC ARREST ( 484 FDA reports)
METASTASES TO BONE ( 480 FDA reports)
RECTAL HAEMORRHAGE ( 478 FDA reports)
HAEMORRHOIDS ( 477 FDA reports)
HYPERLIPIDAEMIA ( 474 FDA reports)
RESPIRATORY FAILURE ( 472 FDA reports)
NERVOUSNESS ( 470 FDA reports)
DRUG EFFECT DECREASED ( 469 FDA reports)
HAEMOGLOBIN DECREASED ( 465 FDA reports)
CHOLELITHIASIS ( 462 FDA reports)
CHILLS ( 459 FDA reports)
RIB FRACTURE ( 454 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 450 FDA reports)
GASTRIC DISORDER ( 443 FDA reports)
RENAL DISORDER ( 442 FDA reports)
FIBROMYALGIA ( 438 FDA reports)
HAEMATOCHEZIA ( 435 FDA reports)
EXOSTOSIS ( 434 FDA reports)
DYSURIA ( 428 FDA reports)
HEART RATE INCREASED ( 418 FDA reports)
NEOPLASM MALIGNANT ( 417 FDA reports)
DRY MOUTH ( 415 FDA reports)
DIVERTICULUM ( 409 FDA reports)
HERPES ZOSTER ( 409 FDA reports)
CORONARY ARTERY OCCLUSION ( 407 FDA reports)
STRESS ( 406 FDA reports)
ABASIA ( 403 FDA reports)
CARDIAC FAILURE ( 401 FDA reports)
INFLAMMATION ( 400 FDA reports)
SURGERY ( 400 FDA reports)
THROMBOCYTOPENIA ( 400 FDA reports)
BURSITIS ( 397 FDA reports)
ABDOMINAL DISTENSION ( 396 FDA reports)
SWELLING FACE ( 396 FDA reports)
ROTATOR CUFF SYNDROME ( 394 FDA reports)
ISCHAEMIC STROKE ( 394 FDA reports)
OEDEMA ( 394 FDA reports)
TACHYCARDIA ( 393 FDA reports)
TREATMENT NONCOMPLIANCE ( 391 FDA reports)
DENTAL CARIES ( 391 FDA reports)
NEPHROLITHIASIS ( 389 FDA reports)
ORAL PAIN ( 383 FDA reports)
SLEEP APNOEA SYNDROME ( 381 FDA reports)
CEREBROVASCULAR DISORDER ( 379 FDA reports)
TOOTH DISORDER ( 378 FDA reports)
TOOTHACHE ( 377 FDA reports)
HYPOKALAEMIA ( 375 FDA reports)
ARTERIOSCLEROSIS ( 374 FDA reports)
SPINAL COLUMN STENOSIS ( 374 FDA reports)
SEPSIS ( 370 FDA reports)
KNEE ARTHROPLASTY ( 370 FDA reports)
LYMPHADENOPATHY ( 370 FDA reports)
TINNITUS ( 368 FDA reports)
HOT FLUSH ( 366 FDA reports)
MIGRAINE ( 365 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 363 FDA reports)
ROAD TRAFFIC ACCIDENT ( 361 FDA reports)
DEFORMITY ( 357 FDA reports)
NASOPHARYNGITIS ( 357 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 353 FDA reports)
ULCER ( 353 FDA reports)
RENAL IMPAIRMENT ( 352 FDA reports)
STAPHYLOCOCCAL INFECTION ( 350 FDA reports)
ALOPECIA ( 346 FDA reports)
BLOOD CREATININE INCREASED ( 345 FDA reports)
BURNING SENSATION ( 340 FDA reports)
DECREASED INTEREST ( 335 FDA reports)
PULMONARY OEDEMA ( 334 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 333 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 329 FDA reports)
HYPERCHOLESTEROLAEMIA ( 326 FDA reports)
HEART RATE IRREGULAR ( 324 FDA reports)
DISABILITY ( 323 FDA reports)
SUICIDAL IDEATION ( 319 FDA reports)
VERTIGO ( 319 FDA reports)
FLUSHING ( 317 FDA reports)
GASTROINTESTINAL DISORDER ( 316 FDA reports)
RENAL FAILURE CHRONIC ( 316 FDA reports)
DYSGEUSIA ( 314 FDA reports)
URINARY INCONTINENCE ( 313 FDA reports)
BONE LESION ( 311 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 308 FDA reports)
CARPAL TUNNEL SYNDROME ( 308 FDA reports)
INJECTION SITE PAIN ( 306 FDA reports)
MYOCARDIAL ISCHAEMIA ( 306 FDA reports)
DRUG DEPENDENCE ( 305 FDA reports)
PRIMARY SEQUESTRUM ( 305 FDA reports)
POLLAKIURIA ( 302 FDA reports)
DISTURBANCE IN ATTENTION ( 300 FDA reports)
ERECTILE DYSFUNCTION ( 300 FDA reports)
IRRITABILITY ( 300 FDA reports)
STEVENS-JOHNSON SYNDROME ( 300 FDA reports)
ANGINA UNSTABLE ( 299 FDA reports)
OVERDOSE ( 296 FDA reports)
TOOTH ABSCESS ( 296 FDA reports)
SPEECH DISORDER ( 293 FDA reports)
FEAR ( 293 FDA reports)
CARDIOMYOPATHY ( 292 FDA reports)
LUNG DISORDER ( 292 FDA reports)
SCOLIOSIS ( 291 FDA reports)
HAEMATURIA ( 289 FDA reports)
BONE DENSITY DECREASED ( 282 FDA reports)
DIFFICULTY IN WALKING ( 282 FDA reports)
MENTAL STATUS CHANGES ( 282 FDA reports)
UNEVALUABLE EVENT ( 282 FDA reports)
RENAL CYST ( 280 FDA reports)
FOOT FRACTURE ( 279 FDA reports)
BLINDNESS ( 278 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 278 FDA reports)
TOOTH LOSS ( 277 FDA reports)
TYPE 2 DIABETES MELLITUS ( 277 FDA reports)
VISUAL ACUITY REDUCED ( 276 FDA reports)
AGITATION ( 276 FDA reports)
FLUID RETENTION ( 275 FDA reports)
TOOTH INFECTION ( 275 FDA reports)
INFLUENZA LIKE ILLNESS ( 274 FDA reports)
DYSPHONIA ( 273 FDA reports)
BODY HEIGHT DECREASED ( 272 FDA reports)
EPISTAXIS ( 272 FDA reports)
SLEEP DISORDER ( 272 FDA reports)
GASTRIC ULCER ( 271 FDA reports)
BREAST CANCER ( 270 FDA reports)
HYPONATRAEMIA ( 270 FDA reports)
VISUAL IMPAIRMENT ( 270 FDA reports)
BACK DISORDER ( 269 FDA reports)
HYPOTHYROIDISM ( 268 FDA reports)
FLATULENCE ( 265 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 265 FDA reports)
NASAL CONGESTION ( 265 FDA reports)
SCIATICA ( 264 FDA reports)
STOMACH DISCOMFORT ( 264 FDA reports)
BASAL CELL CARCINOMA ( 262 FDA reports)
DIVERTICULITIS ( 262 FDA reports)
LETHARGY ( 261 FDA reports)
LOOSE TOOTH ( 259 FDA reports)
BLOOD PRESSURE DECREASED ( 258 FDA reports)
CAROTID ARTERY STENOSIS ( 258 FDA reports)
EAR PAIN ( 258 FDA reports)
LUNG NEOPLASM ( 258 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 257 FDA reports)
FEMUR FRACTURE ( 256 FDA reports)
DYSARTHRIA ( 254 FDA reports)
PULMONARY HYPERTENSION ( 254 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 252 FDA reports)
ECONOMIC PROBLEM ( 252 FDA reports)
DRUG DOSE OMISSION ( 251 FDA reports)
HALLUCINATION ( 251 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 250 FDA reports)
MOUTH ULCERATION ( 249 FDA reports)
HIP FRACTURE ( 247 FDA reports)
PANCYTOPENIA ( 247 FDA reports)
PANCREATITIS ( 246 FDA reports)
PLATELET COUNT DECREASED ( 246 FDA reports)
NIGHT SWEATS ( 245 FDA reports)
CYSTITIS ( 243 FDA reports)
ENDODONTIC PROCEDURE ( 243 FDA reports)
OROPHARYNGEAL PAIN ( 243 FDA reports)
HEPATIC STEATOSIS ( 242 FDA reports)
HIP ARTHROPLASTY ( 242 FDA reports)
LUMBAR SPINAL STENOSIS ( 242 FDA reports)
POST PROCEDURAL COMPLICATION ( 241 FDA reports)
BLISTER ( 238 FDA reports)
ANOREXIA ( 237 FDA reports)
JOINT INJURY ( 237 FDA reports)
STOMATITIS ( 237 FDA reports)
TOOTH FRACTURE ( 236 FDA reports)
NEUTROPENIA ( 236 FDA reports)
DEBRIDEMENT ( 235 FDA reports)
BRADYCARDIA ( 234 FDA reports)
GLAUCOMA ( 232 FDA reports)
DYSPNOEA EXERTIONAL ( 231 FDA reports)
DRY SKIN ( 230 FDA reports)
MULTIPLE MYELOMA ( 230 FDA reports)
RHINORRHOEA ( 229 FDA reports)
BONE DEBRIDEMENT ( 228 FDA reports)
FEELING HOT ( 228 FDA reports)
JAW DISORDER ( 228 FDA reports)
NEURALGIA ( 227 FDA reports)
TENDONITIS ( 227 FDA reports)
PANIC ATTACK ( 225 FDA reports)
ADVERSE EVENT ( 224 FDA reports)
WHEEZING ( 224 FDA reports)
SCAR ( 223 FDA reports)
PATHOLOGICAL FRACTURE ( 221 FDA reports)
SWOLLEN TONGUE ( 220 FDA reports)
ORAL DISORDER ( 219 FDA reports)
COMPRESSION FRACTURE ( 217 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 216 FDA reports)
CARDIAC MURMUR ( 215 FDA reports)
DISEASE PROGRESSION ( 215 FDA reports)
JOINT EFFUSION ( 215 FDA reports)
MOBILITY DECREASED ( 215 FDA reports)
GINGIVAL BLEEDING ( 214 FDA reports)
SKIN DISCOLOURATION ( 214 FDA reports)
SPINAL FRACTURE ( 214 FDA reports)
HAEMATOCRIT DECREASED ( 213 FDA reports)
EMBOLISM ( 211 FDA reports)
FISTULA ( 211 FDA reports)
HYPOXIA ( 211 FDA reports)
JAW OPERATION ( 210 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 210 FDA reports)
BLOOD UREA INCREASED ( 209 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 208 FDA reports)
LUNG INFILTRATION ( 208 FDA reports)
MEDICATION ERROR ( 208 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 208 FDA reports)
SINUS DISORDER ( 208 FDA reports)
OBESITY ( 207 FDA reports)
TENDERNESS ( 206 FDA reports)
ABSCESS ( 205 FDA reports)
MASTICATION DISORDER ( 205 FDA reports)
RASH PRURITIC ( 204 FDA reports)
SKIN ULCER ( 203 FDA reports)
HEPATIC CYST ( 203 FDA reports)
COLONIC POLYP ( 202 FDA reports)
GINGIVAL ULCERATION ( 202 FDA reports)
HYPOPHAGIA ( 202 FDA reports)
MENTAL DISORDER ( 202 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 202 FDA reports)
RASH GENERALISED ( 202 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 202 FDA reports)
CORONARY ARTERY STENOSIS ( 201 FDA reports)
AORTIC VALVE INCOMPETENCE ( 200 FDA reports)
OSTEOSCLEROSIS ( 200 FDA reports)
SKIN LESION ( 200 FDA reports)
URINARY RETENTION ( 197 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 197 FDA reports)
BACK INJURY ( 197 FDA reports)
HAEMATEMESIS ( 196 FDA reports)
JOINT STIFFNESS ( 196 FDA reports)
PERICARDIAL EFFUSION ( 196 FDA reports)
CYST ( 195 FDA reports)
SPINAL COMPRESSION FRACTURE ( 195 FDA reports)
CARDIAC VALVE DISEASE ( 194 FDA reports)
DRY EYE ( 194 FDA reports)
INJECTION SITE ERYTHEMA ( 193 FDA reports)
LEUKOPENIA ( 193 FDA reports)
COMA ( 192 FDA reports)
DYSSTASIA ( 192 FDA reports)
PURULENT DISCHARGE ( 192 FDA reports)
SPINAL DISORDER ( 192 FDA reports)
DISORIENTATION ( 190 FDA reports)
OSTEITIS ( 190 FDA reports)
HAEMOPTYSIS ( 189 FDA reports)
INCORRECT DOSE ADMINISTERED ( 189 FDA reports)
MICTURITION URGENCY ( 188 FDA reports)
ANAPHYLACTIC REACTION ( 186 FDA reports)
HYPERKALAEMIA ( 186 FDA reports)
ANGER ( 184 FDA reports)
DISCOMFORT ( 184 FDA reports)
INFLUENZA ( 184 FDA reports)
GINGIVAL SWELLING ( 183 FDA reports)
MASS ( 183 FDA reports)
WOUND DEHISCENCE ( 182 FDA reports)
VIRAL INFECTION ( 181 FDA reports)
IRRITABLE BOWEL SYNDROME ( 181 FDA reports)
LIVER DISORDER ( 181 FDA reports)
MUSCLE STRAIN ( 181 FDA reports)
HEAD INJURY ( 180 FDA reports)
SYNOVIAL CYST ( 180 FDA reports)
GASTRIC HAEMORRHAGE ( 179 FDA reports)
HYPERGLYCAEMIA ( 179 FDA reports)
MOVEMENT DISORDER ( 179 FDA reports)
VISUAL DISTURBANCE ( 178 FDA reports)
PULMONARY FIBROSIS ( 176 FDA reports)
CARDIO-RESPIRATORY ARREST ( 175 FDA reports)
CEREBRAL INFARCTION ( 175 FDA reports)
EMPHYSEMA ( 175 FDA reports)
EXPOSED BONE IN JAW ( 175 FDA reports)
MENISCUS LESION ( 175 FDA reports)
GOUT ( 174 FDA reports)
SKIN DISORDER ( 174 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 173 FDA reports)
EMOTIONAL DISORDER ( 172 FDA reports)
ILL-DEFINED DISORDER ( 172 FDA reports)
KYPHOSIS ( 172 FDA reports)
HAEMATOMA ( 171 FDA reports)
COLITIS ( 170 FDA reports)
DEAFNESS ( 170 FDA reports)
EATING DISORDER ( 170 FDA reports)
METASTASES TO LIVER ( 170 FDA reports)
EJECTION FRACTION DECREASED ( 169 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 169 FDA reports)
VENTRICULAR HYPERTROPHY ( 169 FDA reports)
RESTLESS LEGS SYNDROME ( 168 FDA reports)
JAW FRACTURE ( 168 FDA reports)
LIMB INJURY ( 168 FDA reports)
MUCOSAL INFLAMMATION ( 168 FDA reports)
DIPLOPIA ( 167 FDA reports)
RHINITIS ( 167 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 166 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 166 FDA reports)
SKIN EXFOLIATION ( 165 FDA reports)
SPONDYLOLISTHESIS ( 165 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 164 FDA reports)
DYSKINESIA ( 163 FDA reports)
HEPATIC ENZYME INCREASED ( 163 FDA reports)
IRON DEFICIENCY ANAEMIA ( 163 FDA reports)
PHYSICAL DISABILITY ( 163 FDA reports)
RENAL INJURY ( 163 FDA reports)
PRODUCTIVE COUGH ( 162 FDA reports)
METASTASES TO SPINE ( 162 FDA reports)
ABNORMAL DREAMS ( 161 FDA reports)
DRUG INTOLERANCE ( 161 FDA reports)
GINGIVAL PAIN ( 161 FDA reports)
INJECTION SITE HAEMORRHAGE ( 161 FDA reports)
RADICULOPATHY ( 161 FDA reports)
GINGIVITIS ( 160 FDA reports)
NOCTURIA ( 160 FDA reports)
GINGIVAL DISORDER ( 159 FDA reports)
GINGIVAL RECESSION ( 159 FDA reports)
RASH ERYTHEMATOUS ( 159 FDA reports)
RESPIRATORY DISTRESS ( 159 FDA reports)
PSORIASIS ( 157 FDA reports)
FAECES DISCOLOURED ( 157 FDA reports)
GALLBLADDER DISORDER ( 157 FDA reports)
HYPOACUSIS ( 157 FDA reports)
FUNGAL INFECTION ( 156 FDA reports)
HYPOAESTHESIA ORAL ( 156 FDA reports)
NERVOUS SYSTEM DISORDER ( 156 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 155 FDA reports)
BLOOD GLUCOSE DECREASED ( 154 FDA reports)
HEART RATE DECREASED ( 154 FDA reports)
COGNITIVE DISORDER ( 153 FDA reports)
GASTROENTERITIS ( 153 FDA reports)
ANGIOPATHY ( 152 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 152 FDA reports)
EYE PAIN ( 151 FDA reports)
PERIODONTAL DISEASE ( 151 FDA reports)
IMPAIRED WORK ABILITY ( 150 FDA reports)
LEUKOCYTOSIS ( 150 FDA reports)
MELAENA ( 150 FDA reports)
BLOOD POTASSIUM DECREASED ( 149 FDA reports)
HEPATITIS ( 149 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 149 FDA reports)
SINUS TACHYCARDIA ( 148 FDA reports)
DEPRESSED MOOD ( 148 FDA reports)
HEART INJURY ( 148 FDA reports)
CHRONIC SINUSITIS ( 147 FDA reports)
LUNG NEOPLASM MALIGNANT ( 147 FDA reports)
SINUS BRADYCARDIA ( 147 FDA reports)
CRYING ( 146 FDA reports)
MULTI-ORGAN FAILURE ( 146 FDA reports)
PHARYNGEAL OEDEMA ( 146 FDA reports)
ORAL CANDIDIASIS ( 145 FDA reports)
THYROID DISORDER ( 145 FDA reports)
SEQUESTRECTOMY ( 144 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 144 FDA reports)
HERNIA ( 144 FDA reports)
DERMAL CYST ( 143 FDA reports)
HYPOGLYCAEMIA ( 143 FDA reports)
PULMONARY CONGESTION ( 143 FDA reports)
UPPER LIMB FRACTURE ( 143 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 142 FDA reports)
MACULAR DEGENERATION ( 142 FDA reports)
CEREBRAL ISCHAEMIA ( 141 FDA reports)
DIABETIC NEUROPATHY ( 141 FDA reports)
EYE DISORDER ( 141 FDA reports)
HEARING IMPAIRED ( 141 FDA reports)
PNEUMOTHORAX ( 141 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 141 FDA reports)
THROAT IRRITATION ( 140 FDA reports)
HEPATOCELLULAR DAMAGE ( 139 FDA reports)
APHASIA ( 138 FDA reports)
LUMBAR RADICULOPATHY ( 138 FDA reports)
METASTASES TO LUNG ( 137 FDA reports)
ACTINIC KERATOSIS ( 136 FDA reports)
CEREBRAL ATROPHY ( 136 FDA reports)
ECCHYMOSIS ( 136 FDA reports)
FACE OEDEMA ( 136 FDA reports)
SEBORRHOEIC KERATOSIS ( 136 FDA reports)
THROAT TIGHTNESS ( 136 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 136 FDA reports)
PRODUCT QUALITY ISSUE ( 135 FDA reports)
PRURITUS GENERALISED ( 135 FDA reports)
AGGRESSION ( 135 FDA reports)
HEMIPARESIS ( 135 FDA reports)
JOINT DISLOCATION ( 135 FDA reports)
LIBIDO DECREASED ( 135 FDA reports)
ORAL CAVITY FISTULA ( 135 FDA reports)
OSTEOLYSIS ( 135 FDA reports)
FRACTURE ( 134 FDA reports)
INTERSTITIAL LUNG DISEASE ( 134 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 133 FDA reports)
PARANOIA ( 133 FDA reports)
ANAPHYLACTIC SHOCK ( 132 FDA reports)
AORTIC ANEURYSM ( 132 FDA reports)
PERIODONTITIS ( 132 FDA reports)
PRESYNCOPE ( 132 FDA reports)
VENTRICULAR TACHYCARDIA ( 132 FDA reports)
PROSTATE CANCER ( 131 FDA reports)
CEREBRAL HAEMORRHAGE ( 131 FDA reports)
GINGIVAL INFECTION ( 131 FDA reports)
KNEE OPERATION ( 131 FDA reports)
MULTIPLE INJURIES ( 131 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 130 FDA reports)
DERMATITIS ( 130 FDA reports)
GASTRITIS EROSIVE ( 130 FDA reports)
LIMB DISCOMFORT ( 130 FDA reports)
CERVICAL SPINAL STENOSIS ( 128 FDA reports)
MUSCLE TWITCHING ( 128 FDA reports)
ORAL INFECTION ( 128 FDA reports)
GYNAECOMASTIA ( 127 FDA reports)
ISCHAEMIA ( 127 FDA reports)
MAJOR DEPRESSION ( 127 FDA reports)
CANDIDIASIS ( 126 FDA reports)
DYSLIPIDAEMIA ( 126 FDA reports)
ECZEMA ( 126 FDA reports)
INFUSION RELATED REACTION ( 126 FDA reports)
RHABDOMYOLYSIS ( 126 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 125 FDA reports)
VAGINAL HAEMORRHAGE ( 125 FDA reports)
BLOOD SODIUM DECREASED ( 125 FDA reports)
DRUG TOXICITY ( 125 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 125 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 125 FDA reports)
PALLOR ( 125 FDA reports)
ADVERSE DRUG REACTION ( 124 FDA reports)
COAGULOPATHY ( 124 FDA reports)
LACUNAR INFARCTION ( 124 FDA reports)
LIFE EXPECTANCY SHORTENED ( 124 FDA reports)
HEPATIC LESION ( 123 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 123 FDA reports)
MULTIPLE SCLEROSIS ( 123 FDA reports)
ORGAN FAILURE ( 123 FDA reports)
POLYP ( 123 FDA reports)
JOINT SPRAIN ( 122 FDA reports)
OFF LABEL USE ( 122 FDA reports)
EYE SWELLING ( 121 FDA reports)
MUSCLE TIGHTNESS ( 121 FDA reports)
BLOOD CALCIUM DECREASED ( 120 FDA reports)
DIVERTICULUM INTESTINAL ( 120 FDA reports)
DEMENTIA ( 119 FDA reports)
INADEQUATE ANALGESIA ( 119 FDA reports)
INJECTION SITE HAEMATOMA ( 119 FDA reports)
OESOPHAGITIS ( 119 FDA reports)
ABNORMAL BEHAVIOUR ( 118 FDA reports)
COORDINATION ABNORMAL ( 118 FDA reports)
ONYCHOMYCOSIS ( 118 FDA reports)
RESTLESSNESS ( 118 FDA reports)
SINUS CONGESTION ( 117 FDA reports)
BLOOD URINE PRESENT ( 117 FDA reports)
FOOT DEFORMITY ( 117 FDA reports)
BACTERIAL INFECTION ( 116 FDA reports)
SUICIDE ATTEMPT ( 116 FDA reports)
VARICOSE VEIN ( 116 FDA reports)
VENOUS INSUFFICIENCY ( 115 FDA reports)
ANGIOEDEMA ( 115 FDA reports)
BREAST CANCER FEMALE ( 115 FDA reports)
DEVICE RELATED INFECTION ( 115 FDA reports)
HYDRONEPHROSIS ( 115 FDA reports)
HYPERSOMNIA ( 115 FDA reports)
PEPTIC ULCER ( 115 FDA reports)
PLANTAR FASCIITIS ( 115 FDA reports)
MELANOCYTIC NAEVUS ( 114 FDA reports)
MENTAL IMPAIRMENT ( 114 FDA reports)
ORTHOSTATIC HYPOTENSION ( 114 FDA reports)
ANKLE FRACTURE ( 113 FDA reports)
CATARACT OPERATION ( 113 FDA reports)
ENCEPHALOPATHY ( 113 FDA reports)
EYE IRRITATION ( 113 FDA reports)
INTESTINAL OBSTRUCTION ( 113 FDA reports)
MITRAL VALVE PROLAPSE ( 113 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 113 FDA reports)
TENDON DISORDER ( 113 FDA reports)
BLADDER DISORDER ( 112 FDA reports)
PELVIC PAIN ( 112 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 111 FDA reports)
NERVE INJURY ( 111 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 111 FDA reports)
FEELING COLD ( 110 FDA reports)
HYPERCALCAEMIA ( 110 FDA reports)
ORAL SURGERY ( 110 FDA reports)
PARAESTHESIA ORAL ( 110 FDA reports)
RASH MACULAR ( 110 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 109 FDA reports)
MUSCLE CRAMP ( 109 FDA reports)
NERVE COMPRESSION ( 109 FDA reports)
ABDOMINAL PAIN LOWER ( 108 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 108 FDA reports)
DEVICE FAILURE ( 108 FDA reports)
NIGHTMARE ( 108 FDA reports)
PHARYNGITIS ( 108 FDA reports)
SENSITIVITY OF TEETH ( 108 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 107 FDA reports)
ASCITES ( 107 FDA reports)
MALNUTRITION ( 107 FDA reports)
MUSCULOSKELETAL DISORDER ( 107 FDA reports)
OEDEMA MOUTH ( 107 FDA reports)
PNEUMONIA ASPIRATION ( 107 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 106 FDA reports)
NEOPLASM PROGRESSION ( 106 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 106 FDA reports)
THINKING ABNORMAL ( 106 FDA reports)
THYROID NEOPLASM ( 105 FDA reports)
UNRESPONSIVE TO STIMULI ( 105 FDA reports)
UTERINE LEIOMYOMA ( 105 FDA reports)
CHOLECYSTITIS CHRONIC ( 105 FDA reports)
GROIN PAIN ( 105 FDA reports)
LYMPHOEDEMA ( 105 FDA reports)
ANEURYSM ( 104 FDA reports)
FEBRILE NEUTROPENIA ( 104 FDA reports)
HYPOVOLAEMIA ( 104 FDA reports)
PANCREATITIS ACUTE ( 104 FDA reports)
RETCHING ( 104 FDA reports)
STEM CELL TRANSPLANT ( 104 FDA reports)
TENDON RUPTURE ( 104 FDA reports)
CROHN'S DISEASE ( 103 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 103 FDA reports)
LARYNGITIS ( 103 FDA reports)
LOCALISED INFECTION ( 103 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 102 FDA reports)
FACIAL PAIN ( 102 FDA reports)
HYPOKINESIA ( 102 FDA reports)
PROTHROMBIN TIME PROLONGED ( 102 FDA reports)
RADIOTHERAPY ( 101 FDA reports)
RHINITIS ALLERGIC ( 101 FDA reports)
STRESS FRACTURE ( 101 FDA reports)
ACUTE CORONARY SYNDROME ( 101 FDA reports)
DRUG ABUSER ( 101 FDA reports)
FAECAL INCONTINENCE ( 101 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 101 FDA reports)
MIDDLE INSOMNIA ( 101 FDA reports)
BREAST MASS ( 100 FDA reports)
EXCORIATION ( 100 FDA reports)
FACIAL PALSY ( 100 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 100 FDA reports)
LOBAR PNEUMONIA ( 100 FDA reports)
METASTATIC NEOPLASM ( 100 FDA reports)
SEPTIC SHOCK ( 100 FDA reports)
RASH PAPULAR ( 99 FDA reports)
ATRIAL FLUTTER ( 99 FDA reports)
BLOOD PRESSURE ABNORMAL ( 99 FDA reports)
PARALYSIS ( 99 FDA reports)
POLYTRAUMATISM ( 99 FDA reports)
ABDOMINAL HERNIA ( 98 FDA reports)
BRUXISM ( 98 FDA reports)
CHOLECYSTITIS ( 98 FDA reports)
KIDNEY INFECTION ( 98 FDA reports)
LOWER LIMB FRACTURE ( 98 FDA reports)
SOFT TISSUE DISORDER ( 98 FDA reports)
WALKING AID USER ( 98 FDA reports)
RESPIRATORY DISORDER ( 97 FDA reports)
SHOCK ( 97 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 97 FDA reports)
CHOLECYSTECTOMY ( 97 FDA reports)
DUODENAL ULCER ( 97 FDA reports)
HAEMANGIOMA ( 97 FDA reports)
HAND FRACTURE ( 97 FDA reports)
HELICOBACTER INFECTION ( 97 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 96 FDA reports)
LACERATION ( 96 FDA reports)
BLOOD BILIRUBIN INCREASED ( 95 FDA reports)
GENERALISED OEDEMA ( 95 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 95 FDA reports)
ORAL HERPES ( 95 FDA reports)
RESPIRATORY ARREST ( 95 FDA reports)
SPINAL CORD COMPRESSION ( 95 FDA reports)
SKIN CANCER ( 94 FDA reports)
AZOTAEMIA ( 94 FDA reports)
EYE HAEMORRHAGE ( 94 FDA reports)
ILEUS ( 94 FDA reports)
IMPAIRED DRIVING ABILITY ( 94 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 94 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 93 FDA reports)
DISEASE RECURRENCE ( 93 FDA reports)
FACET JOINT SYNDROME ( 93 FDA reports)
HEPATIC FAILURE ( 93 FDA reports)
AGRANULOCYTOSIS ( 92 FDA reports)
BLINDNESS UNILATERAL ( 92 FDA reports)
INTENTIONAL DRUG MISUSE ( 92 FDA reports)
MOOD SWINGS ( 92 FDA reports)
SKIN PAPILLOMA ( 92 FDA reports)
STENT PLACEMENT ( 92 FDA reports)
SKIN INJURY ( 91 FDA reports)
THERAPY NON-RESPONDER ( 91 FDA reports)
AORTIC STENOSIS ( 91 FDA reports)
EAR INFECTION ( 91 FDA reports)
OESOPHAGEAL DISORDER ( 90 FDA reports)
PSORIATIC ARTHROPATHY ( 90 FDA reports)
PROCEDURAL COMPLICATION ( 89 FDA reports)
SKIN LACERATION ( 89 FDA reports)
TARDIVE DYSKINESIA ( 89 FDA reports)
WRIST FRACTURE ( 89 FDA reports)
FLANK PAIN ( 89 FDA reports)
PARKINSON'S DISEASE ( 89 FDA reports)
ACTINOMYCOSIS ( 88 FDA reports)
CARDIAC PACEMAKER INSERTION ( 88 FDA reports)
NECK INJURY ( 88 FDA reports)
NODULE ( 88 FDA reports)
PLATELET COUNT INCREASED ( 88 FDA reports)
ULCER HAEMORRHAGE ( 88 FDA reports)
VENTRICULAR DYSFUNCTION ( 87 FDA reports)
HYPERKERATOSIS ( 87 FDA reports)
INTRACRANIAL ANEURYSM ( 87 FDA reports)
PHLEBITIS ( 87 FDA reports)
DECUBITUS ULCER ( 86 FDA reports)
DILATATION ATRIAL ( 86 FDA reports)
LOCAL SWELLING ( 86 FDA reports)
OCULAR HYPERAEMIA ( 86 FDA reports)
SYNOVITIS ( 86 FDA reports)
RAYNAUD'S PHENOMENON ( 85 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 85 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 85 FDA reports)
BLOOD POTASSIUM INCREASED ( 84 FDA reports)
COLON CANCER ( 84 FDA reports)
DIALYSIS ( 84 FDA reports)
DILATATION VENTRICULAR ( 84 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 84 FDA reports)
ERUCTATION ( 84 FDA reports)
GLOSSODYNIA ( 84 FDA reports)
HEMIPLEGIA ( 84 FDA reports)
INJECTION SITE REACTION ( 84 FDA reports)
PNEUMONITIS ( 84 FDA reports)
SEDATION ( 84 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 83 FDA reports)
TONGUE ULCERATION ( 83 FDA reports)
WITHDRAWAL SYNDROME ( 83 FDA reports)
BONE SCAN ABNORMAL ( 83 FDA reports)
COLD SWEAT ( 83 FDA reports)
DELIRIUM ( 83 FDA reports)
HALLUCINATION, VISUAL ( 83 FDA reports)
LACRIMATION INCREASED ( 83 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 83 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 83 FDA reports)
PERIPHERAL COLDNESS ( 83 FDA reports)
POOR QUALITY SLEEP ( 83 FDA reports)
ABSCESS JAW ( 82 FDA reports)
ACUTE RESPIRATORY FAILURE ( 82 FDA reports)
ACUTE SINUSITIS ( 82 FDA reports)
BONE NEOPLASM MALIGNANT ( 82 FDA reports)
EPICONDYLITIS ( 82 FDA reports)
METABOLIC ACIDOSIS ( 82 FDA reports)
OVARIAN CYST ( 82 FDA reports)
PANIC DISORDER ( 82 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 82 FDA reports)
VITREOUS FLOATERS ( 82 FDA reports)
SHOULDER PAIN ( 81 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 81 FDA reports)
WOUND INFECTION ( 81 FDA reports)
APHTHOUS STOMATITIS ( 81 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 81 FDA reports)
COLITIS ULCERATIVE ( 81 FDA reports)
FLUID OVERLOAD ( 81 FDA reports)
HYPERPLASIA ( 81 FDA reports)
BRONCHOSPASM ( 80 FDA reports)
CIRCULATORY COLLAPSE ( 80 FDA reports)
COSTOCHONDRITIS ( 80 FDA reports)
DRUG ADMINISTRATION ERROR ( 80 FDA reports)
FIBROSIS ( 80 FDA reports)
GASTROENTERITIS VIRAL ( 80 FDA reports)
INCREASED APPETITE ( 80 FDA reports)
OXYGEN SATURATION DECREASED ( 80 FDA reports)
ANXIETY DISORDER ( 79 FDA reports)
BACTERAEMIA ( 79 FDA reports)
BARRETT'S OESOPHAGUS ( 79 FDA reports)
DIASTOLIC DYSFUNCTION ( 79 FDA reports)
MUSCLE ATROPHY ( 79 FDA reports)
SKIN BURNING SENSATION ( 79 FDA reports)
THIRST ( 79 FDA reports)
WOUND DRAINAGE ( 78 FDA reports)
CHROMATURIA ( 78 FDA reports)
LUNG INFECTION ( 77 FDA reports)
NASAL SEPTUM DEVIATION ( 77 FDA reports)
PYELONEPHRITIS ( 77 FDA reports)
SPINAL FUSION SURGERY ( 76 FDA reports)
SPLENOMEGALY ( 76 FDA reports)
TONGUE DISCOLOURATION ( 76 FDA reports)
CAROTID ARTERY DISEASE ( 76 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 76 FDA reports)
GRANULOMA ( 76 FDA reports)
JAUNDICE ( 76 FDA reports)
NEURITIS ( 76 FDA reports)
PERONEAL NERVE PALSY ( 76 FDA reports)
BLINDNESS TRANSIENT ( 75 FDA reports)
BREAST CANCER METASTATIC ( 75 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 75 FDA reports)
HEPATOMEGALY ( 75 FDA reports)
INCONTINENCE ( 75 FDA reports)
PHOTOPHOBIA ( 75 FDA reports)
PSYCHOTIC DISORDER ( 75 FDA reports)
SICK SINUS SYNDROME ( 75 FDA reports)
VENTRICULAR FIBRILLATION ( 75 FDA reports)
PURPURA ( 74 FDA reports)
RECTAL POLYP ( 74 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 74 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 74 FDA reports)
COMPLETED SUICIDE ( 74 FDA reports)
DENTAL OPERATION ( 74 FDA reports)
DRUG ERUPTION ( 74 FDA reports)
GINGIVAL ERYTHEMA ( 74 FDA reports)
OPEN WOUND ( 74 FDA reports)
ABSCESS ORAL ( 73 FDA reports)
ATHEROSCLEROSIS ( 73 FDA reports)
DEAFNESS NEUROSENSORY ( 73 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 73 FDA reports)
FOOT OPERATION ( 73 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 73 FDA reports)
ORAL DISCOMFORT ( 73 FDA reports)
POLYURIA ( 73 FDA reports)
VISUAL FIELD DEFECT ( 73 FDA reports)
SUDDEN DEATH ( 72 FDA reports)
BEDRIDDEN ( 72 FDA reports)
FAILURE TO THRIVE ( 72 FDA reports)
INCREASED TENDENCY TO BRUISE ( 72 FDA reports)
INJECTION SITE PRURITUS ( 72 FDA reports)
LIP SWELLING ( 72 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 72 FDA reports)
ODYNOPHAGIA ( 72 FDA reports)
PERICARDITIS ( 72 FDA reports)
BONE FRAGMENTATION ( 71 FDA reports)
ELECTROLYTE IMBALANCE ( 71 FDA reports)
FOLLICULITIS ( 71 FDA reports)
PURULENCE ( 71 FDA reports)
SQUAMOUS CELL CARCINOMA ( 71 FDA reports)
VENTRICULAR HYPOKINESIA ( 71 FDA reports)
ABSCESS DRAINAGE ( 70 FDA reports)
AGEUSIA ( 70 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 70 FDA reports)
BREAST PAIN ( 70 FDA reports)
BUNION ( 70 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 70 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 70 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 70 FDA reports)
ESSENTIAL HYPERTENSION ( 70 FDA reports)
FRACTURE NONUNION ( 70 FDA reports)
GRAND MAL CONVULSION ( 70 FDA reports)
HERPES SIMPLEX ( 70 FDA reports)
NEOPLASM ( 70 FDA reports)
AFFECTIVE DISORDER ( 69 FDA reports)
CARDIAC OPERATION ( 69 FDA reports)
GOITRE ( 69 FDA reports)
UROSEPSIS ( 69 FDA reports)
TENDON INJURY ( 68 FDA reports)
TRISMUS ( 68 FDA reports)
VITAMIN B12 DEFICIENCY ( 68 FDA reports)
FACIAL BONES FRACTURE ( 68 FDA reports)
METASTASES TO LYMPH NODES ( 68 FDA reports)
MOOD ALTERED ( 68 FDA reports)
MUSCLE INJURY ( 68 FDA reports)
OTITIS MEDIA ( 68 FDA reports)
ATRIOVENTRICULAR BLOCK ( 67 FDA reports)
BIPOLAR DISORDER ( 67 FDA reports)
CERVICOBRACHIAL SYNDROME ( 67 FDA reports)
DEVICE MALFUNCTION ( 67 FDA reports)
EXTRASYSTOLES ( 67 FDA reports)
HYPOMAGNESAEMIA ( 67 FDA reports)
INTRACARDIAC THROMBUS ( 67 FDA reports)
PRESCRIBED OVERDOSE ( 67 FDA reports)
PULMONARY MASS ( 67 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 66 FDA reports)
SENSORY DISTURBANCE ( 66 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 66 FDA reports)
TONGUE DISORDER ( 66 FDA reports)
UMBILICAL HERNIA ( 66 FDA reports)
CARDIAC FLUTTER ( 66 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 66 FDA reports)
CONJUNCTIVITIS ( 66 FDA reports)
DENTURE WEARER ( 66 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 66 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 66 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 66 FDA reports)
LEFT ATRIAL DILATATION ( 66 FDA reports)
FURUNCLE ( 65 FDA reports)
HYSTERECTOMY ( 65 FDA reports)
INGUINAL HERNIA ( 65 FDA reports)
NON-CARDIAC CHEST PAIN ( 65 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 65 FDA reports)
OESOPHAGEAL STENOSIS ( 65 FDA reports)
SKIN REACTION ( 65 FDA reports)
SNEEZING ( 65 FDA reports)
VITAMIN D DEFICIENCY ( 65 FDA reports)
X-RAY ABNORMAL ( 65 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 64 FDA reports)
SEXUAL DYSFUNCTION ( 64 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 64 FDA reports)
CLAVICLE FRACTURE ( 64 FDA reports)
LABORATORY TEST ABNORMAL ( 64 FDA reports)
ORAL INTAKE REDUCED ( 64 FDA reports)
APHAGIA ( 63 FDA reports)
APPENDICITIS ( 63 FDA reports)
BLOOD ALBUMIN DECREASED ( 63 FDA reports)
DELUSION ( 63 FDA reports)
HYPOALBUMINAEMIA ( 63 FDA reports)
LIGAMENT SPRAIN ( 63 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 63 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 63 FDA reports)
WOUND ( 63 FDA reports)
SINUS OPERATION ( 62 FDA reports)
SPONDYLITIS ( 62 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 62 FDA reports)
ATROPHIC VULVOVAGINITIS ( 62 FDA reports)
BLOOD IRON DECREASED ( 62 FDA reports)
BODY TEMPERATURE INCREASED ( 62 FDA reports)
CORONARY ARTERY BYPASS ( 62 FDA reports)
FIBULA FRACTURE ( 62 FDA reports)
HYPERTENSIVE HEART DISEASE ( 62 FDA reports)
MEDICAL DEVICE COMPLICATION ( 62 FDA reports)
MUSCLE DISORDER ( 62 FDA reports)
LYMPHOMA ( 61 FDA reports)
PETECHIAE ( 61 FDA reports)
PREGNANCY ( 61 FDA reports)
PROCEDURAL PAIN ( 60 FDA reports)
PROSTATITIS ( 60 FDA reports)
SKIN INFECTION ( 60 FDA reports)
STRESS SYMPTOMS ( 60 FDA reports)
ADNEXA UTERI MASS ( 60 FDA reports)
ARTHROPOD BITE ( 60 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 60 FDA reports)
DENTAL FISTULA ( 60 FDA reports)
DERMATITIS CONTACT ( 60 FDA reports)
FEELING JITTERY ( 60 FDA reports)
INTERMITTENT CLAUDICATION ( 60 FDA reports)
MYOSITIS ( 60 FDA reports)
OVARIAN CANCER ( 60 FDA reports)
PLASMACYTOMA ( 60 FDA reports)
PLEURISY ( 60 FDA reports)
AFFECT LABILITY ( 59 FDA reports)
BLADDER CANCER ( 59 FDA reports)
BLOOD DISORDER ( 59 FDA reports)
BONE MARROW FAILURE ( 59 FDA reports)
CHOKING ( 59 FDA reports)
CHONDROMALACIA ( 59 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 59 FDA reports)
DECREASED ACTIVITY ( 59 FDA reports)
FISTULA DISCHARGE ( 59 FDA reports)
HEPATITIS C ( 59 FDA reports)
HYPERPARATHYROIDISM ( 59 FDA reports)
PLEURAL FIBROSIS ( 59 FDA reports)
PROTEINURIA ( 59 FDA reports)
RASH MACULO-PAPULAR ( 59 FDA reports)
STREPTOCOCCAL INFECTION ( 59 FDA reports)
PULMONARY THROMBOSIS ( 58 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 58 FDA reports)
STRESS URINARY INCONTINENCE ( 58 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 58 FDA reports)
CYANOSIS ( 58 FDA reports)
FAMILY STRESS ( 58 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 58 FDA reports)
HEPATIC CIRRHOSIS ( 58 FDA reports)
HYPERTONIC BLADDER ( 58 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 58 FDA reports)
METASTASIS ( 58 FDA reports)
NEUROPATHY ( 58 FDA reports)
OCCULT BLOOD POSITIVE ( 58 FDA reports)
ACCIDENT ( 57 FDA reports)
BLOOD CALCIUM INCREASED ( 57 FDA reports)
BONE LOSS ( 57 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 57 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 57 FDA reports)
LOW TURNOVER OSTEOPATHY ( 57 FDA reports)
PERITONITIS ( 57 FDA reports)
RENAL PAIN ( 57 FDA reports)
SCAB ( 57 FDA reports)
WHEELCHAIR USER ( 57 FDA reports)
REFLUX OESOPHAGITIS ( 56 FDA reports)
SEBORRHOEIC DERMATITIS ( 56 FDA reports)
SKIN IRRITATION ( 56 FDA reports)
VASCULITIS ( 56 FDA reports)
WEIGHT FLUCTUATION ( 56 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 56 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 56 FDA reports)
CEREBRAL THROMBOSIS ( 56 FDA reports)
CORONARY ARTERY THROMBOSIS ( 56 FDA reports)
INJECTION SITE SWELLING ( 56 FDA reports)
MENINGIOMA ( 56 FDA reports)
ANGIONEUROTIC OEDEMA ( 55 FDA reports)
ARTERIAL DISORDER ( 55 FDA reports)
CHEST X-RAY ABNORMAL ( 55 FDA reports)
DRUG TOLERANCE ( 55 FDA reports)
GANGRENE ( 55 FDA reports)
NO ADVERSE EVENT ( 55 FDA reports)
PELVIC FRACTURE ( 55 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 55 FDA reports)
SENSATION OF HEAVINESS ( 54 FDA reports)
VAGINAL DISCHARGE ( 54 FDA reports)
ACCIDENTAL OVERDOSE ( 54 FDA reports)
ADRENAL INSUFFICIENCY ( 54 FDA reports)
ASPIRATION ( 54 FDA reports)
BONE SWELLING ( 54 FDA reports)
GASTROINTESTINAL PAIN ( 54 FDA reports)
JOINT CREPITATION ( 54 FDA reports)
ACNE ( 53 FDA reports)
BEHCET'S SYNDROME ( 53 FDA reports)
BLEPHARITIS ( 53 FDA reports)
BRAIN DAMAGE ( 53 FDA reports)
CHONDROPATHY ( 53 FDA reports)
HALLUCINATION, AUDITORY ( 53 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 53 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 53 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 53 FDA reports)
POOR PERIPHERAL CIRCULATION ( 53 FDA reports)
RESPIRATORY TRACT INFECTION ( 53 FDA reports)
SUBDURAL HAEMATOMA ( 53 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 53 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 53 FDA reports)
PULMONARY GRANULOMA ( 52 FDA reports)
SEROMA ( 52 FDA reports)
SHOULDER OPERATION ( 52 FDA reports)
SKIN ATROPHY ( 52 FDA reports)
ANIMAL BITE ( 52 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 52 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 52 FDA reports)
DYSPHEMIA ( 52 FDA reports)
HIP SURGERY ( 52 FDA reports)
HYPOCALCAEMIA ( 52 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 52 FDA reports)
ATAXIA ( 51 FDA reports)
BONE EROSION ( 51 FDA reports)
CARTILAGE INJURY ( 51 FDA reports)
EAR DISORDER ( 51 FDA reports)
EDENTULOUS ( 51 FDA reports)
EOSINOPHILIA ( 51 FDA reports)
EYELID PTOSIS ( 51 FDA reports)
MULTIPLE FRACTURES ( 51 FDA reports)
NAIL DISORDER ( 51 FDA reports)
NECROSIS ( 51 FDA reports)
PLEURITIC PAIN ( 51 FDA reports)
POSTOPERATIVE INFECTION ( 51 FDA reports)
PROSTATOMEGALY ( 51 FDA reports)
TEMPERATURE INTOLERANCE ( 51 FDA reports)
VERTEBROPLASTY ( 51 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 50 FDA reports)
POSTNASAL DRIP ( 50 FDA reports)
RADIUS FRACTURE ( 50 FDA reports)
RESPIRATORY TRACT CONGESTION ( 50 FDA reports)
RETINAL HAEMORRHAGE ( 50 FDA reports)
SINUS HEADACHE ( 50 FDA reports)
SKIN TIGHTNESS ( 50 FDA reports)
SUBCUTANEOUS ABSCESS ( 50 FDA reports)
VITREOUS DETACHMENT ( 50 FDA reports)
ABDOMINAL TENDERNESS ( 50 FDA reports)
ACCIDENT AT WORK ( 50 FDA reports)
APPENDICECTOMY ( 50 FDA reports)
FRACTURED SACRUM ( 50 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 50 FDA reports)
INGROWING NAIL ( 50 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 50 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 50 FDA reports)
MALIGNANT MELANOMA ( 50 FDA reports)
MENOPAUSE ( 50 FDA reports)
MENORRHAGIA ( 50 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 50 FDA reports)
ORAL TORUS ( 50 FDA reports)
PHOTOSENSITIVITY REACTION ( 50 FDA reports)
ATRIAL TACHYCARDIA ( 49 FDA reports)
CATHETERISATION CARDIAC ( 49 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 49 FDA reports)
HERPES VIRUS INFECTION ( 49 FDA reports)
HUMERUS FRACTURE ( 49 FDA reports)
LIPOMA ( 49 FDA reports)
OEDEMA MUCOSAL ( 49 FDA reports)
OSTEITIS DEFORMANS ( 49 FDA reports)
OSTEORADIONECROSIS ( 49 FDA reports)
PROCTALGIA ( 49 FDA reports)
QUALITY OF LIFE DECREASED ( 49 FDA reports)
RESPIRATORY RATE INCREASED ( 49 FDA reports)
TIBIA FRACTURE ( 49 FDA reports)
TYPE 1 DIABETES MELLITUS ( 49 FDA reports)
SENSORY LOSS ( 48 FDA reports)
THERMAL BURN ( 48 FDA reports)
VASCULAR INJURY ( 48 FDA reports)
VEIN DISORDER ( 48 FDA reports)
BONE OPERATION ( 48 FDA reports)
COLITIS ISCHAEMIC ( 48 FDA reports)
DERMATITIS ALLERGIC ( 48 FDA reports)
DIVERTICULAR PERFORATION ( 48 FDA reports)
DRY THROAT ( 48 FDA reports)
EYE PRURITUS ( 48 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 48 FDA reports)
LUPUS-LIKE SYNDROME ( 48 FDA reports)
MANIA ( 48 FDA reports)
PANCREATITIS CHRONIC ( 48 FDA reports)
ADENOCARCINOMA ( 47 FDA reports)
CONCUSSION ( 47 FDA reports)
CYSTOCELE ( 47 FDA reports)
DRUG DISPENSING ERROR ( 47 FDA reports)
INTRAOCULAR LENS IMPLANT ( 47 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 47 FDA reports)
LIGAMENT INJURY ( 47 FDA reports)
MONOCLONAL GAMMOPATHY ( 47 FDA reports)
NEURODERMATITIS ( 47 FDA reports)
RENAL ATROPHY ( 47 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 47 FDA reports)
TUBERCULOSIS ( 47 FDA reports)
SEASONAL ALLERGY ( 46 FDA reports)
TENOSYNOVITIS ( 46 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 46 FDA reports)
URINE OUTPUT DECREASED ( 46 FDA reports)
ABORTION SPONTANEOUS ( 46 FDA reports)
ACROCHORDON ( 46 FDA reports)
ALVEOLOPLASTY ( 46 FDA reports)
ANGIOPLASTY ( 46 FDA reports)
BREAST CANCER RECURRENT ( 46 FDA reports)
HAEMORRHAGIC STROKE ( 46 FDA reports)
LIMB OPERATION ( 46 FDA reports)
LIVER INJURY ( 46 FDA reports)
NEUTROPHIL COUNT DECREASED ( 46 FDA reports)
BRONCHIECTASIS ( 45 FDA reports)
CHRONIC FATIGUE SYNDROME ( 45 FDA reports)
HYPERCOAGULATION ( 45 FDA reports)
HYPOGONADISM ( 45 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 45 FDA reports)
INTESTINAL PERFORATION ( 45 FDA reports)
MACROCYTOSIS ( 45 FDA reports)
MYELODYSPLASTIC SYNDROME ( 45 FDA reports)
NEUTROPHIL COUNT INCREASED ( 45 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 45 FDA reports)
TENSION ( 44 FDA reports)
TRANSAMINASES INCREASED ( 44 FDA reports)
ADJUSTMENT DISORDER ( 44 FDA reports)
ANAEMIA MACROCYTIC ( 44 FDA reports)
AORTIC CALCIFICATION ( 44 FDA reports)
AORTIC VALVE SCLEROSIS ( 44 FDA reports)
BONE GRAFT ( 44 FDA reports)
BRAIN OEDEMA ( 44 FDA reports)
CAROTID ARTERY OCCLUSION ( 44 FDA reports)
CEREBELLAR INFARCTION ( 44 FDA reports)
CHEST WALL PAIN ( 44 FDA reports)
CHOLECYSTITIS ACUTE ( 44 FDA reports)
CLOSTRIDIAL INFECTION ( 44 FDA reports)
COLON ADENOMA ( 44 FDA reports)
LACTOSE INTOLERANCE ( 44 FDA reports)
PATHOLOGICAL GAMBLING ( 44 FDA reports)
PERSONALITY CHANGE ( 44 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 43 FDA reports)
CALCULUS URETERIC ( 43 FDA reports)
DEAFNESS UNILATERAL ( 43 FDA reports)
DEPENDENCE ( 43 FDA reports)
DRUG ABUSE ( 43 FDA reports)
FACE INJURY ( 43 FDA reports)
GOUTY ARTHRITIS ( 43 FDA reports)
HOSPITALISATION ( 43 FDA reports)
JOINT ARTHROPLASTY ( 43 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 43 FDA reports)
ORTHOPNOEA ( 43 FDA reports)
POLYNEUROPATHY ( 43 FDA reports)
PULPITIS DENTAL ( 43 FDA reports)
SKIN HYPERPIGMENTATION ( 43 FDA reports)
SUDDEN CARDIAC DEATH ( 43 FDA reports)
TROPONIN INCREASED ( 43 FDA reports)
UTERINE HAEMORRHAGE ( 43 FDA reports)
POSTURE ABNORMAL ( 42 FDA reports)
RECTOCELE ( 42 FDA reports)
SOFT TISSUE INFLAMMATION ( 42 FDA reports)
TOXIC SKIN ERUPTION ( 42 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 42 FDA reports)
BODY TEMPERATURE DECREASED ( 42 FDA reports)
DIABETIC KETOACIDOSIS ( 42 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 42 FDA reports)
DRUG SCREEN POSITIVE ( 42 FDA reports)
ERYTHEMA MULTIFORME ( 42 FDA reports)
FRUSTRATION ( 42 FDA reports)
GASTRIC POLYPS ( 42 FDA reports)
IMMUNOSUPPRESSION ( 42 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 42 FDA reports)
OSTEOMYELITIS CHRONIC ( 42 FDA reports)
APNOEA ( 41 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 41 FDA reports)
ESCHERICHIA INFECTION ( 41 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 41 FDA reports)
GENERALISED ERYTHEMA ( 41 FDA reports)
IMMUNE SYSTEM DISORDER ( 41 FDA reports)
INTENTIONAL OVERDOSE ( 41 FDA reports)
MYOPATHY ( 41 FDA reports)
PANCREATIC CARCINOMA ( 41 FDA reports)
RHONCHI ( 41 FDA reports)
ROSACEA ( 41 FDA reports)
SARCOIDOSIS ( 41 FDA reports)
SENSATION OF FOREIGN BODY ( 41 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 41 FDA reports)
UTERINE POLYP ( 41 FDA reports)
SJOGREN'S SYNDROME ( 40 FDA reports)
SOFT TISSUE INFECTION ( 40 FDA reports)
SPONDYLOLYSIS ( 40 FDA reports)
TOOTH DEPOSIT ( 40 FDA reports)
URINARY HESITATION ( 40 FDA reports)
VERTIGO POSITIONAL ( 40 FDA reports)
VIITH NERVE PARALYSIS ( 40 FDA reports)
DRUG LEVEL INCREASED ( 40 FDA reports)
DUODENITIS ( 40 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 40 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 40 FDA reports)
EXPIRED DRUG ADMINISTERED ( 40 FDA reports)
GALLBLADDER OPERATION ( 40 FDA reports)
GASTROINTESTINAL ULCER ( 40 FDA reports)
GINGIVAL OEDEMA ( 40 FDA reports)
GLOSSITIS ( 40 FDA reports)
HEART VALVE INCOMPETENCE ( 40 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 40 FDA reports)
PAIN OF SKIN ( 40 FDA reports)
PAPILLOMA ( 40 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 40 FDA reports)
ABDOMINAL ADHESIONS ( 39 FDA reports)
ANAEMIA POSTOPERATIVE ( 39 FDA reports)
ATROPHY ( 39 FDA reports)
BREAST TENDERNESS ( 39 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 39 FDA reports)
CORONARY ARTERY RESTENOSIS ( 39 FDA reports)
EROSIVE OESOPHAGITIS ( 39 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 39 FDA reports)
MOUTH HAEMORRHAGE ( 39 FDA reports)
NEUROMA ( 39 FDA reports)
RADICULAR PAIN ( 39 FDA reports)
RASH PUSTULAR ( 39 FDA reports)
SACROILIITIS ( 39 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 39 FDA reports)
VASCULAR CALCIFICATION ( 39 FDA reports)
POST PROCEDURAL PAIN ( 38 FDA reports)
SKIN HYPERTROPHY ( 38 FDA reports)
SNORING ( 38 FDA reports)
SPINAL LAMINECTOMY ( 38 FDA reports)
THYROID CANCER ( 38 FDA reports)
ANOXIC ENCEPHALOPATHY ( 38 FDA reports)
APPLICATION SITE ERYTHEMA ( 38 FDA reports)
BRONCHITIS ACUTE ( 38 FDA reports)
CARDIOGENIC SHOCK ( 38 FDA reports)
EMPYEMA ( 38 FDA reports)
EPIGASTRIC DISCOMFORT ( 38 FDA reports)
EYELID OEDEMA ( 38 FDA reports)
HAEMORRHAGIC ANAEMIA ( 38 FDA reports)
HEPATOTOXICITY ( 38 FDA reports)
HYPERVENTILATION ( 38 FDA reports)
INTESTINAL POLYP ( 38 FDA reports)
MOTOR DYSFUNCTION ( 38 FDA reports)
POLYARTHRITIS ( 38 FDA reports)
ACUTE PRERENAL FAILURE ( 37 FDA reports)
ACUTE PULMONARY OEDEMA ( 37 FDA reports)
ADHESION ( 37 FDA reports)
ALCOHOLISM ( 37 FDA reports)
APATHY ( 37 FDA reports)
APHONIA ( 37 FDA reports)
AREFLEXIA ( 37 FDA reports)
ARTHRITIS INFECTIVE ( 37 FDA reports)
BONE MARROW OEDEMA ( 37 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 37 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 37 FDA reports)
CATHETER RELATED COMPLICATION ( 37 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 37 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 37 FDA reports)
INJECTION SITE IRRITATION ( 37 FDA reports)
LIGAMENT RUPTURE ( 37 FDA reports)
METABOLIC SYNDROME ( 37 FDA reports)
MITRAL VALVE CALCIFICATION ( 37 FDA reports)
ORAL DISCHARGE ( 37 FDA reports)
POLYDIPSIA ( 37 FDA reports)
POLYMYALGIA RHEUMATICA ( 37 FDA reports)
POOR DENTAL CONDITION ( 37 FDA reports)
RETINAL VEIN OCCLUSION ( 37 FDA reports)
SELF-MEDICATION ( 37 FDA reports)
SKIN INDURATION ( 37 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 37 FDA reports)
VAGINAL INFECTION ( 37 FDA reports)
VASCULAR OCCLUSION ( 37 FDA reports)
RALES ( 36 FDA reports)
TEMPORAL ARTERITIS ( 36 FDA reports)
TINEA PEDIS ( 36 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 36 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 36 FDA reports)
BLOOD CHLORIDE DECREASED ( 36 FDA reports)
BLOOD TEST ABNORMAL ( 36 FDA reports)
BREAST CALCIFICATIONS ( 36 FDA reports)
DYSAESTHESIA ( 36 FDA reports)
DYSGRAPHIA ( 36 FDA reports)
FAECALOMA ( 36 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 36 FDA reports)
GINGIVAL ABSCESS ( 36 FDA reports)
HYPERTHYROIDISM ( 36 FDA reports)
ILEUS PARALYTIC ( 36 FDA reports)
INITIAL INSOMNIA ( 36 FDA reports)
PERIARTHRITIS ( 36 FDA reports)
PHOTOPSIA ( 36 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 35 FDA reports)
APPENDICITIS PERFORATED ( 35 FDA reports)
BREAST RECONSTRUCTION ( 35 FDA reports)
CARDIAC ANEURYSM ( 35 FDA reports)
CORONARY ARTERY SURGERY ( 35 FDA reports)
DENTAL CARE ( 35 FDA reports)
DERMATITIS EXFOLIATIVE ( 35 FDA reports)
EAR DISCOMFORT ( 35 FDA reports)
EPILEPSY ( 35 FDA reports)
EXERCISE TOLERANCE DECREASED ( 35 FDA reports)
FEELING DRUNK ( 35 FDA reports)
FISTULA REPAIR ( 35 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 35 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 35 FDA reports)
INJECTION SITE WARMTH ( 35 FDA reports)
MORTON'S NEUROMA ( 35 FDA reports)
NEUROLOGICAL SYMPTOM ( 35 FDA reports)
OCULAR VASCULAR DISORDER ( 35 FDA reports)
PULMONARY TUBERCULOSIS ( 35 FDA reports)
RECTAL FISSURE ( 35 FDA reports)
RETINAL DETACHMENT ( 35 FDA reports)
SKIN FIBROSIS ( 35 FDA reports)
SPINAL DEFORMITY ( 35 FDA reports)
SPUTUM DISCOLOURED ( 35 FDA reports)
PROTEIN URINE PRESENT ( 34 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 34 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 34 FDA reports)
TOBACCO ABUSE ( 34 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 34 FDA reports)
WOUND SECRETION ( 34 FDA reports)
ANURIA ( 34 FDA reports)
AUTOIMMUNE DISORDER ( 34 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 34 FDA reports)
BREAST CANCER IN SITU ( 34 FDA reports)
BUNION OPERATION ( 34 FDA reports)
CERUMEN IMPACTION ( 34 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 34 FDA reports)
COELIAC DISEASE ( 34 FDA reports)
GASTRIC BYPASS ( 34 FDA reports)
HUNGER ( 34 FDA reports)
HYPERAESTHESIA ( 34 FDA reports)
LARYNGEAL OEDEMA ( 34 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 34 FDA reports)
LOCALISED OSTEOARTHRITIS ( 34 FDA reports)
OPEN REDUCTION OF FRACTURE ( 34 FDA reports)
PHARYNGEAL ERYTHEMA ( 34 FDA reports)
POLYP COLORECTAL ( 34 FDA reports)
ANAL FISSURE ( 33 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 33 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 33 FDA reports)
CULTURE URINE POSITIVE ( 33 FDA reports)
EMBOLIC STROKE ( 33 FDA reports)
ENCEPHALOMALACIA ( 33 FDA reports)
FORMICATION ( 33 FDA reports)
HYPOAESTHESIA FACIAL ( 33 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 33 FDA reports)
NASAL DISORDER ( 33 FDA reports)
OESOPHAGEAL ULCER ( 33 FDA reports)
PATELLA FRACTURE ( 33 FDA reports)
RENAL TUBULAR NECROSIS ( 33 FDA reports)
ROTATOR CUFF REPAIR ( 33 FDA reports)
SPONDYLOSIS ( 33 FDA reports)
VITAMIN D DECREASED ( 33 FDA reports)
RENAL MASS ( 32 FDA reports)
SCRATCH ( 32 FDA reports)
SINUS ARRHYTHMIA ( 32 FDA reports)
SOMNAMBULISM ( 32 FDA reports)
TACHYPNOEA ( 32 FDA reports)
TRIGEMINAL NEURALGIA ( 32 FDA reports)
URINE ODOUR ABNORMAL ( 32 FDA reports)
WALKING DISABILITY ( 32 FDA reports)
ABNORMAL FAECES ( 32 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 32 FDA reports)
CATARACT NUCLEAR ( 32 FDA reports)
DIABETIC RETINOPATHY ( 32 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 32 FDA reports)
DUODENAL ULCER PERFORATION ( 32 FDA reports)
DYSTONIA ( 32 FDA reports)
EYE DISCHARGE ( 32 FDA reports)
GASTRIC CANCER ( 32 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 32 FDA reports)
HAEMARTHROSIS ( 32 FDA reports)
HYPERURICAEMIA ( 32 FDA reports)
IMMOBILE ( 32 FDA reports)
JOINT CONTRACTURE ( 32 FDA reports)
LYMPHADENITIS ( 32 FDA reports)
METABOLIC ENCEPHALOPATHY ( 32 FDA reports)
METRORRHAGIA ( 32 FDA reports)
ORAL NEOPLASM ( 32 FDA reports)
ABSCESS LIMB ( 31 FDA reports)
ABSCESS NECK ( 31 FDA reports)
ANOGENITAL WARTS ( 31 FDA reports)
APLASTIC ANAEMIA ( 31 FDA reports)
ASPIRATION PLEURAL CAVITY ( 31 FDA reports)
BILIARY DILATATION ( 31 FDA reports)
BRAIN INJURY ( 31 FDA reports)
BUNDLE BRANCH BLOCK ( 31 FDA reports)
CEREBRAL DISORDER ( 31 FDA reports)
CHOLESTASIS ( 31 FDA reports)
EJACULATION DISORDER ( 31 FDA reports)
FAT TISSUE INCREASED ( 31 FDA reports)
FOREIGN BODY ( 31 FDA reports)
HAEMANGIOMA OF LIVER ( 31 FDA reports)
INFARCTION ( 31 FDA reports)
LUNG CANCER METASTATIC ( 31 FDA reports)
MONOPLEGIA ( 31 FDA reports)
NO THERAPEUTIC RESPONSE ( 31 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 31 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 31 FDA reports)
SCHIZOPHRENIA ( 31 FDA reports)
SKIN FISSURES ( 31 FDA reports)
TELANGIECTASIA ( 31 FDA reports)
THROMBOPHLEBITIS ( 31 FDA reports)
TRIGGER FINGER ( 31 FDA reports)
PULSE ABSENT ( 30 FDA reports)
SHOULDER ARTHROPLASTY ( 30 FDA reports)
SKIN NEOPLASM EXCISION ( 30 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 30 FDA reports)
UTERINE ENLARGEMENT ( 30 FDA reports)
VENOUS THROMBOSIS ( 30 FDA reports)
WOUND TREATMENT ( 30 FDA reports)
ADRENAL MASS ( 30 FDA reports)
BREATH ODOUR ( 30 FDA reports)
BRONCHIOLITIS ( 30 FDA reports)
BRONCHITIS CHRONIC ( 30 FDA reports)
BUTTOCK PAIN ( 30 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 30 FDA reports)
DERMATITIS ATOPIC ( 30 FDA reports)
EFFUSION ( 30 FDA reports)
FEMORAL NECK FRACTURE ( 30 FDA reports)
HEPATIC NECROSIS ( 30 FDA reports)
HILAR LYMPHADENOPATHY ( 30 FDA reports)
IMPULSIVE BEHAVIOUR ( 30 FDA reports)
INJECTION SITE NODULE ( 30 FDA reports)
INJECTION SITE RASH ( 30 FDA reports)
MUCOSAL ULCERATION ( 30 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 30 FDA reports)
ORAL FUNGAL INFECTION ( 30 FDA reports)
OVARIAN MASS ( 30 FDA reports)
APPLICATION SITE PRURITUS ( 29 FDA reports)
AUTONOMIC NEUROPATHY ( 29 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 29 FDA reports)
BREAST HYPERPLASIA ( 29 FDA reports)
CERVICITIS ( 29 FDA reports)
CHEST TUBE INSERTION ( 29 FDA reports)
COLLAPSE OF LUNG ( 29 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 29 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 29 FDA reports)
HEPATIC MASS ( 29 FDA reports)
HYPERPHAGIA ( 29 FDA reports)
INCISION SITE INFECTION ( 29 FDA reports)
INCOHERENT ( 29 FDA reports)
LEG AMPUTATION ( 29 FDA reports)
LIP DISORDER ( 29 FDA reports)
LUNG CONSOLIDATION ( 29 FDA reports)
MASTECTOMY ( 29 FDA reports)
MASTOIDITIS ( 29 FDA reports)
MULTIPLE DRUG OVERDOSE ( 29 FDA reports)
MYELOPATHY ( 29 FDA reports)
MYOCLONUS ( 29 FDA reports)
NECK MASS ( 29 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 29 FDA reports)
SKIN WARM ( 29 FDA reports)
SPONDYLOARTHROPATHY ( 29 FDA reports)
THYROIDECTOMY ( 29 FDA reports)
TOBACCO USER ( 29 FDA reports)
TOOTH REPAIR ( 29 FDA reports)
VENOUS THROMBOSIS LIMB ( 29 FDA reports)
PULMONARY INFARCTION ( 28 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 28 FDA reports)
SURGICAL PROCEDURE REPEATED ( 28 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 28 FDA reports)
WOUND DEBRIDEMENT ( 28 FDA reports)
ABDOMINAL MASS ( 28 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 28 FDA reports)
ALCOHOL USE ( 28 FDA reports)
ANOSMIA ( 28 FDA reports)
BIOPSY TONGUE ABNORMAL ( 28 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 28 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 28 FDA reports)
CYTOLYTIC HEPATITIS ( 28 FDA reports)
DIABETIC NEPHROPATHY ( 28 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 28 FDA reports)
EUPHORIC MOOD ( 28 FDA reports)
FACIAL PARESIS ( 28 FDA reports)
FLAT AFFECT ( 28 FDA reports)
HAEMODIALYSIS ( 28 FDA reports)
HAND DEFORMITY ( 28 FDA reports)
HEPATOSPLENOMEGALY ( 28 FDA reports)
HYPERMETABOLISM ( 28 FDA reports)
HYPERTHERMIA ( 28 FDA reports)
INJECTION SITE BRUISING ( 28 FDA reports)
INTESTINAL HAEMORRHAGE ( 28 FDA reports)
LYMPHOPENIA ( 28 FDA reports)
MACULAR OEDEMA ( 28 FDA reports)
MENINGITIS ( 28 FDA reports)
MONOCYTE COUNT INCREASED ( 28 FDA reports)
OBSTRUCTION ( 28 FDA reports)
PNEUMONIA BACTERIAL ( 28 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 27 FDA reports)
ANKYLOSING SPONDYLITIS ( 27 FDA reports)
AORTIC ATHEROSCLEROSIS ( 27 FDA reports)
ARTERIAL STENOSIS ( 27 FDA reports)
ASTIGMATISM ( 27 FDA reports)
BLADDER SPASM ( 27 FDA reports)
BRAIN STEM INFARCTION ( 27 FDA reports)
CARDIAC ENZYMES INCREASED ( 27 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 27 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 27 FDA reports)
ENCEPHALITIS ( 27 FDA reports)
EYE OEDEMA ( 27 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 27 FDA reports)
GLIOSIS ( 27 FDA reports)
HORDEOLUM ( 27 FDA reports)
HYPOVENTILATION ( 27 FDA reports)
INJECTION SITE URTICARIA ( 27 FDA reports)
LABYRINTHITIS ( 27 FDA reports)
LARGE INTESTINE PERFORATION ( 27 FDA reports)
LOCALISED OEDEMA ( 27 FDA reports)
MENIERE'S DISEASE ( 27 FDA reports)
NEPHRITIS INTERSTITIAL ( 27 FDA reports)
OESOPHAGEAL PAIN ( 27 FDA reports)
OESOPHAGEAL RUPTURE ( 27 FDA reports)
OVERWEIGHT ( 27 FDA reports)
PAPILLOEDEMA ( 27 FDA reports)
PUPIL FIXED ( 27 FDA reports)
RESUSCITATION ( 27 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 27 FDA reports)
TOOTH INJURY ( 27 FDA reports)
URINARY TRACT DISORDER ( 27 FDA reports)
WOUND COMPLICATION ( 27 FDA reports)
WRONG DRUG ADMINISTERED ( 27 FDA reports)
PROTEIN TOTAL DECREASED ( 26 FDA reports)
RESORPTION BONE INCREASED ( 26 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 26 FDA reports)
RHINALGIA ( 26 FDA reports)
SEROTONIN SYNDROME ( 26 FDA reports)
SKIN HAEMORRHAGE ( 26 FDA reports)
STENT OCCLUSION ( 26 FDA reports)
TENDON PAIN ( 26 FDA reports)
UTERINE DISORDER ( 26 FDA reports)
APPETITE DISORDER ( 26 FDA reports)
ARACHNOID CYST ( 26 FDA reports)
BLOOD COUNT ABNORMAL ( 26 FDA reports)
BONE DENSITY INCREASED ( 26 FDA reports)
DEPRESSIVE SYMPTOM ( 26 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 26 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 26 FDA reports)
ENDOCARDITIS ( 26 FDA reports)
EYE OPERATION ( 26 FDA reports)
GASTRIC PERFORATION ( 26 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 26 FDA reports)
HERNIA REPAIR ( 26 FDA reports)
HODGKIN'S DISEASE ( 26 FDA reports)
HYPERTENSIVE CRISIS ( 26 FDA reports)
IATROGENIC INJURY ( 26 FDA reports)
LARGE INTESTINAL ULCER ( 26 FDA reports)
MACULAR HOLE ( 26 FDA reports)
MALLORY-WEISS SYNDROME ( 26 FDA reports)
MULTIPLE ALLERGIES ( 26 FDA reports)
OSTEOTOMY ( 26 FDA reports)
PARATHYROID TUMOUR BENIGN ( 26 FDA reports)
PAROSMIA ( 26 FDA reports)
PLASTIC SURGERY ( 26 FDA reports)
ABDOMINAL ABSCESS ( 25 FDA reports)
BONE NEOPLASM ( 25 FDA reports)
CATHETER PLACEMENT ( 25 FDA reports)
CHEILITIS ( 25 FDA reports)
DEMENTIA WITH LEWY BODIES ( 25 FDA reports)
DENTAL IMPLANTATION ( 25 FDA reports)
DIZZINESS POSTURAL ( 25 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 25 FDA reports)
EOSINOPHIL COUNT INCREASED ( 25 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 25 FDA reports)
HEART RATE ABNORMAL ( 25 FDA reports)
MACROGLOSSIA ( 25 FDA reports)
METASTASES TO SKIN ( 25 FDA reports)
MYELOMA RECURRENCE ( 25 FDA reports)
NODAL OSTEOARTHRITIS ( 25 FDA reports)
OCULAR ICTERUS ( 25 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 25 FDA reports)
OPTIC NEURITIS ( 25 FDA reports)
OROANTRAL FISTULA ( 25 FDA reports)
OSTEOCHONDROSIS ( 25 FDA reports)
PAINFUL RESPIRATION ( 25 FDA reports)
PARKINSONISM ( 25 FDA reports)
PARONYCHIA ( 25 FDA reports)
POST HERPETIC NEURALGIA ( 25 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 25 FDA reports)
RENAL CELL CARCINOMA ( 25 FDA reports)
SKELETAL INJURY ( 25 FDA reports)
SPINAL CORPECTOMY ( 25 FDA reports)
VASCULAR GRAFT OCCLUSION ( 25 FDA reports)
PROSTATE INFECTION ( 24 FDA reports)
SKIN ODOUR ABNORMAL ( 24 FDA reports)
SPINAL OPERATION ( 24 FDA reports)
SPUTUM CULTURE POSITIVE ( 24 FDA reports)
STREPTOCOCCAL SEPSIS ( 24 FDA reports)
TOE AMPUTATION ( 24 FDA reports)
TONSILLAR DISORDER ( 24 FDA reports)
TOURETTE'S DISORDER ( 24 FDA reports)
TRAUMATIC BRAIN INJURY ( 24 FDA reports)
UMBILICAL HERNIA REPAIR ( 24 FDA reports)
URINE ANALYSIS ABNORMAL ( 24 FDA reports)
URINE FLOW DECREASED ( 24 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 24 FDA reports)
ADENOMA BENIGN ( 24 FDA reports)
AKATHISIA ( 24 FDA reports)
ARACHNOIDITIS ( 24 FDA reports)
BLADDER OBSTRUCTION ( 24 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 24 FDA reports)
BRAIN NEOPLASM ( 24 FDA reports)
BREAST DISORDER ( 24 FDA reports)
CACHEXIA ( 24 FDA reports)
CALCINOSIS ( 24 FDA reports)
CAPILLARY LEAK SYNDROME ( 24 FDA reports)
CLAUSTROPHOBIA ( 24 FDA reports)
DISSEMINATED TUBERCULOSIS ( 24 FDA reports)
EYE MOVEMENT DISORDER ( 24 FDA reports)
FEELING OF DESPAIR ( 24 FDA reports)
HEAD DISCOMFORT ( 24 FDA reports)
HEARING DISABILITY ( 24 FDA reports)
HEPATIC FIBROSIS ( 24 FDA reports)
IMPETIGO ( 24 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 24 FDA reports)
LENTIGO ( 24 FDA reports)
LICHENOID KERATOSIS ( 24 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 24 FDA reports)
MACULOPATHY ( 24 FDA reports)
MASTITIS ( 24 FDA reports)
MONONUCLEOSIS SYNDROME ( 24 FDA reports)
NEPHROPATHY ( 24 FDA reports)
OLFACTORY NERVE DISORDER ( 24 FDA reports)
OTITIS EXTERNA ( 24 FDA reports)
PARAPROTEINAEMIA ( 24 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 24 FDA reports)
POLYSUBSTANCE ABUSE ( 24 FDA reports)
ARTHRITIS BACTERIAL ( 23 FDA reports)
ARTHROSCOPY ( 23 FDA reports)
BREAST CANCER STAGE IV ( 23 FDA reports)
BREAST CYST ( 23 FDA reports)
BRONCHOPNEUMONIA ( 23 FDA reports)
CALCULUS BLADDER ( 23 FDA reports)
CLUMSINESS ( 23 FDA reports)
COLECTOMY ( 23 FDA reports)
COLITIS MICROSCOPIC ( 23 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 23 FDA reports)
DENTAL DISCOMFORT ( 23 FDA reports)
DERMATITIS BULLOUS ( 23 FDA reports)
DEVICE DISLOCATION ( 23 FDA reports)
DIABETIC COMA ( 23 FDA reports)
GALLBLADDER POLYP ( 23 FDA reports)
GASTRITIS HAEMORRHAGIC ( 23 FDA reports)
HAEMATOCRIT ABNORMAL ( 23 FDA reports)
HYPERNATRAEMIA ( 23 FDA reports)
MALABSORPTION ( 23 FDA reports)
MASS EXCISION ( 23 FDA reports)
MICTURITION DISORDER ( 23 FDA reports)
PAIN EXACERBATED ( 23 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 23 FDA reports)
PROSTATIC DISORDER ( 23 FDA reports)
PSEUDOMONAS INFECTION ( 23 FDA reports)
RASH VESICULAR ( 23 FDA reports)
RENAL CANCER ( 23 FDA reports)
RENAL TUBULAR ACIDOSIS ( 23 FDA reports)
SALIVARY GLAND ADENOMA ( 23 FDA reports)
SINUS ANTROSTOMY ( 23 FDA reports)
SINUS POLYP DEGENERATION ( 23 FDA reports)
SPLENIC LESION ( 23 FDA reports)
TESTICULAR PAIN ( 23 FDA reports)
THROMBOCYTOSIS ( 23 FDA reports)
VENTRICULAR ARRHYTHMIA ( 23 FDA reports)
VITREOUS HAEMORRHAGE ( 23 FDA reports)
PRESBYOPIA ( 22 FDA reports)
RADICULITIS LUMBOSACRAL ( 22 FDA reports)
RED BLOOD CELL ABNORMALITY ( 22 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 22 FDA reports)
SCLERODERMA ( 22 FDA reports)
SLUGGISHNESS ( 22 FDA reports)
SOCIAL PROBLEM ( 22 FDA reports)
TIC ( 22 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 22 FDA reports)
TUMOUR LYSIS SYNDROME ( 22 FDA reports)
ACCIDENTAL EXPOSURE ( 22 FDA reports)
AMAUROSIS FUGAX ( 22 FDA reports)
AORTIC DISORDER ( 22 FDA reports)
AORTIC VALVE DISEASE ( 22 FDA reports)
APPLICATION SITE RASH ( 22 FDA reports)
ATRIAL SEPTAL DEFECT ( 22 FDA reports)
AUTOIMMUNE THYROIDITIS ( 22 FDA reports)
BACTERIAL DISEASE CARRIER ( 22 FDA reports)
BILIARY COLIC ( 22 FDA reports)
BIPOLAR I DISORDER ( 22 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 22 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 22 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 22 FDA reports)
CATHETER REMOVAL ( 22 FDA reports)
CEREBRAL CYST ( 22 FDA reports)
CERVICAL CORD COMPRESSION ( 22 FDA reports)
CERVICAL SPINE FLATTENING ( 22 FDA reports)
CHOLECYSTITIS INFECTIVE ( 22 FDA reports)
CORNEAL DYSTROPHY ( 22 FDA reports)
DERMATOPHYTOSIS ( 22 FDA reports)
DRUG PRESCRIBING ERROR ( 22 FDA reports)
ENTHESOPATHY ( 22 FDA reports)
HEPATITIS ACUTE ( 22 FDA reports)
INCISIONAL DRAINAGE ( 22 FDA reports)
KIDNEY SMALL ( 22 FDA reports)
LESION EXCISION ( 22 FDA reports)
LEUKAEMIA ( 22 FDA reports)
LIP DRY ( 22 FDA reports)
LIPASE INCREASED ( 22 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 22 FDA reports)
MITRAL VALVE DISEASE ( 22 FDA reports)
OESOPHAGEAL CARCINOMA ( 22 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 22 FDA reports)
PHLEBITIS SUPERFICIAL ( 22 FDA reports)
PITTING OEDEMA ( 22 FDA reports)
PNEUMONIA VIRAL ( 22 FDA reports)
POOR PERSONAL HYGIENE ( 22 FDA reports)
ANAPHYLACTOID REACTION ( 21 FDA reports)
BALANITIS ( 21 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 21 FDA reports)
BONE ABSCESS ( 21 FDA reports)
BRONCHOPLEURAL FISTULA ( 21 FDA reports)
CAROTID BRUIT ( 21 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 21 FDA reports)
CHANGE OF BOWEL HABIT ( 21 FDA reports)
CHARLES BONNET SYNDROME ( 21 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 21 FDA reports)
CORNEAL ABRASION ( 21 FDA reports)
DENTAL PLAQUE ( 21 FDA reports)
DEVICE BREAKAGE ( 21 FDA reports)
DRUG EFFECT INCREASED ( 21 FDA reports)
DRUG TOLERANCE INCREASED ( 21 FDA reports)
DYSPLASTIC NAEVUS ( 21 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 21 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 21 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 21 FDA reports)
FAT NECROSIS ( 21 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 21 FDA reports)
HYPOTHERMIA ( 21 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 21 FDA reports)
LIP BLISTER ( 21 FDA reports)
LIP DISCOLOURATION ( 21 FDA reports)
LIP ULCERATION ( 21 FDA reports)
LYMPHADENECTOMY ( 21 FDA reports)
MECHANICAL VENTILATION ( 21 FDA reports)
METASTASES TO PLEURA ( 21 FDA reports)
METASTATIC PAIN ( 21 FDA reports)
NECROTISING FASCIITIS ( 21 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 21 FDA reports)
OLIGURIA ( 21 FDA reports)
ORAL FIBROMA ( 21 FDA reports)
OTITIS MEDIA ACUTE ( 21 FDA reports)
PANIC REACTION ( 21 FDA reports)
QRS AXIS ABNORMAL ( 21 FDA reports)
RECTAL ABSCESS ( 21 FDA reports)
RENAL CANCER METASTATIC ( 21 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 21 FDA reports)
SENSATION OF PRESSURE ( 21 FDA reports)
SERUM FERRITIN INCREASED ( 21 FDA reports)
SPINAL CORD DISORDER ( 21 FDA reports)
THYROID MASS ( 21 FDA reports)
TINEA CRURIS ( 21 FDA reports)
TOE OPERATION ( 21 FDA reports)
URINE ABNORMALITY ( 21 FDA reports)
VOCAL CORD DISORDER ( 21 FDA reports)
VULVOVAGINAL DRYNESS ( 21 FDA reports)
PORTAL HYPERTENSION ( 20 FDA reports)
PSYCHIATRIC SYMPTOM ( 20 FDA reports)
PULMONARY AIR LEAKAGE ( 20 FDA reports)
RHINITIS SEASONAL ( 20 FDA reports)
SALIVARY HYPERSECRETION ( 20 FDA reports)
SUNBURN ( 20 FDA reports)
TENOSYNOVITIS STENOSANS ( 20 FDA reports)
TENSION HEADACHE ( 20 FDA reports)
TOOTH IMPACTED ( 20 FDA reports)
ULNA FRACTURE ( 20 FDA reports)
VENOUS OCCLUSION ( 20 FDA reports)
VULVOVAGINITIS ( 20 FDA reports)
ADRENAL DISORDER ( 20 FDA reports)
ANGIODYSPLASIA ( 20 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 20 FDA reports)
ARTERIAL THROMBOSIS ( 20 FDA reports)
BILE DUCT STONE ( 20 FDA reports)
BLADDER PROLAPSE ( 20 FDA reports)
BONE FORMATION DECREASED ( 20 FDA reports)
BONE FORMATION INCREASED ( 20 FDA reports)
BONE TRIMMING ( 20 FDA reports)
CENTRAL LINE INFECTION ( 20 FDA reports)
CERVICAL MYELOPATHY ( 20 FDA reports)
COITAL BLEEDING ( 20 FDA reports)
COMMUNICATION DISORDER ( 20 FDA reports)
DIABETIC FOOT ( 20 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 20 FDA reports)
DROOLING ( 20 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 20 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 20 FDA reports)
ERYTHEMA NODOSUM ( 20 FDA reports)
EXTRASKELETAL OSSIFICATION ( 20 FDA reports)
FEELING GUILTY ( 20 FDA reports)
FOREIGN BODY IN EYE ( 20 FDA reports)
HELICOBACTER GASTRITIS ( 20 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 20 FDA reports)
HEPATIC PAIN ( 20 FDA reports)
HISTOPLASMOSIS ( 20 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 20 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 20 FDA reports)
LEFT VENTRICULAR FAILURE ( 20 FDA reports)
MALIGNANT MELANOMA IN SITU ( 20 FDA reports)
NICOTINE DEPENDENCE ( 20 FDA reports)
NYSTAGMUS ( 20 FDA reports)
ORTHOSIS USER ( 20 FDA reports)
PATHOGEN RESISTANCE ( 20 FDA reports)
PHOTODERMATOSIS ( 20 FDA reports)
POLYPECTOMY ( 20 FDA reports)
ABNORMAL SENSATION IN EYE ( 19 FDA reports)
ACTINIC ELASTOSIS ( 19 FDA reports)
ANAL HAEMORRHAGE ( 19 FDA reports)
APPARENT DEATH ( 19 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 19 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 19 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 19 FDA reports)
BLOOD CULTURE POSITIVE ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 19 FDA reports)
BLOOD MAGNESIUM DECREASED ( 19 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 19 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 19 FDA reports)
CONDUCTION DISORDER ( 19 FDA reports)
CORNEAL DISORDER ( 19 FDA reports)
CYSTITIS INTERSTITIAL ( 19 FDA reports)
DISSOCIATION ( 19 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 19 FDA reports)
DRUG LEVEL DECREASED ( 19 FDA reports)
DYSPNOEA EXACERBATED ( 19 FDA reports)
ECZEMA ASTEATOTIC ( 19 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 19 FDA reports)
EYE INFLAMMATION ( 19 FDA reports)
EYE LASER SURGERY ( 19 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 19 FDA reports)
FOOD ALLERGY ( 19 FDA reports)
FOREIGN BODY TRAUMA ( 19 FDA reports)
FRACTURE DISPLACEMENT ( 19 FDA reports)
GAMMOPATHY ( 19 FDA reports)
GASTROINTESTINAL INFECTION ( 19 FDA reports)
GENERAL SYMPTOM ( 19 FDA reports)
GENERALISED ANXIETY DISORDER ( 19 FDA reports)
HEPATITIS CHOLESTATIC ( 19 FDA reports)
ILIAC ARTERY STENOSIS ( 19 FDA reports)
INFECTED SKIN ULCER ( 19 FDA reports)
IRITIS ( 19 FDA reports)
JAUNDICE CHOLESTATIC ( 19 FDA reports)
JOINT LOCK ( 19 FDA reports)
LIVEDO RETICULARIS ( 19 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 19 FDA reports)
METASTASES TO THE MEDIASTINUM ( 19 FDA reports)
MITRAL VALVE SCLEROSIS ( 19 FDA reports)
NEPHROTIC SYNDROME ( 19 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 19 FDA reports)
ODONTOGENIC CYST ( 19 FDA reports)
OESOPHAGEAL DILATATION ( 19 FDA reports)
OVARIAN DISORDER ( 19 FDA reports)
PANCREATIC DISORDER ( 19 FDA reports)
PERFORATED ULCER ( 19 FDA reports)
PERINEAL PAIN ( 19 FDA reports)
PERSONALITY DISORDER ( 19 FDA reports)
PLASMACYTOSIS ( 19 FDA reports)
POST PROCEDURAL INFECTION ( 19 FDA reports)
POSTOPERATIVE ILEUS ( 19 FDA reports)
RADICULITIS ( 19 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 19 FDA reports)
SKIN WRINKLING ( 19 FDA reports)
STASIS DERMATITIS ( 19 FDA reports)
STOMATOCYTES PRESENT ( 19 FDA reports)
STRESS INCONTINENCE ( 19 FDA reports)
TRANSFUSION ( 19 FDA reports)
VENA CAVA FILTER INSERTION ( 19 FDA reports)
WEIGHT BEARING DIFFICULTY ( 19 FDA reports)
POST CONCUSSION SYNDROME ( 18 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 18 FDA reports)
PROTEIN URINE ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RADIATION INJURY ( 18 FDA reports)
REFLUX GASTRITIS ( 18 FDA reports)
RETINAL ISCHAEMIA ( 18 FDA reports)
SCOTOMA ( 18 FDA reports)
SINUS POLYP ( 18 FDA reports)
SMOKER ( 18 FDA reports)
SOFT TISSUE MASS ( 18 FDA reports)
SPINAL CLAUDICATION ( 18 FDA reports)
SPINAL CORD OEDEMA ( 18 FDA reports)
TEARFULNESS ( 18 FDA reports)
TONGUE COATED ( 18 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 18 FDA reports)
VAGINAL PROLAPSE ( 18 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 18 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 18 FDA reports)
ALCOHOL POISONING ( 18 FDA reports)
ALVEOLAR OSTEITIS ( 18 FDA reports)
AUTOIMMUNE HEPATITIS ( 18 FDA reports)
BLOOD URIC ACID INCREASED ( 18 FDA reports)
BONE ATROPHY ( 18 FDA reports)
BREATH SOUNDS ABNORMAL ( 18 FDA reports)
DEVICE OCCLUSION ( 18 FDA reports)
DYSPHORIA ( 18 FDA reports)
EAR NEOPLASM ( 18 FDA reports)
ENTEROVESICAL FISTULA ( 18 FDA reports)
FEELING HOT AND COLD ( 18 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 18 FDA reports)
FEELINGS OF WORTHLESSNESS ( 18 FDA reports)
FULL BLOOD COUNT DECREASED ( 18 FDA reports)
GASTRITIS ATROPHIC ( 18 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 18 FDA reports)
HOARSENESS ( 18 FDA reports)
HYDROPNEUMOTHORAX ( 18 FDA reports)
HYPOPHOSPHATAEMIA ( 18 FDA reports)
HYPOTONIA ( 18 FDA reports)
KNEE DEFORMITY ( 18 FDA reports)
LIP PAIN ( 18 FDA reports)
MEDICAL DEVICE REMOVAL ( 18 FDA reports)
MENINGITIS ASEPTIC ( 18 FDA reports)
MOUTH CYST ( 18 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 18 FDA reports)
OESOPHAGEAL SPASM ( 18 FDA reports)
OROPHARYNGEAL SWELLING ( 18 FDA reports)
OSTEOMYELITIS ACUTE ( 18 FDA reports)
PERIPHERAL ISCHAEMIA ( 18 FDA reports)
AORTIC VALVE REPLACEMENT ( 17 FDA reports)
ASEPTIC NECROSIS BONE ( 17 FDA reports)
BENIGN BREAST NEOPLASM ( 17 FDA reports)
BLOOD BLISTER ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 17 FDA reports)
BLOOD PH INCREASED ( 17 FDA reports)
BLOOD URINE ( 17 FDA reports)
BODY TINEA ( 17 FDA reports)
BONE MARROW TRANSPLANT ( 17 FDA reports)
BRAIN SCAN ABNORMAL ( 17 FDA reports)
BREAST ENLARGEMENT ( 17 FDA reports)
COCCIDIOIDOMYCOSIS ( 17 FDA reports)
CONNECTIVE TISSUE DISORDER ( 17 FDA reports)
DEMYELINATION ( 17 FDA reports)
ENDOMETRIOSIS ( 17 FDA reports)
FIBRIN D DIMER INCREASED ( 17 FDA reports)
FOOD INTOLERANCE ( 17 FDA reports)
GENITAL RASH ( 17 FDA reports)
GRAFT INFECTION ( 17 FDA reports)
GRIP STRENGTH DECREASED ( 17 FDA reports)
HAIR GROWTH ABNORMAL ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
INCISION SITE HAEMORRHAGE ( 17 FDA reports)
INJECTION SITE DISCOLOURATION ( 17 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 17 FDA reports)
KERATITIS ( 17 FDA reports)
LARYNGOSPASM ( 17 FDA reports)
LUNG ADENOCARCINOMA ( 17 FDA reports)
MYOCARDITIS ( 17 FDA reports)
NASAL DISCOMFORT ( 17 FDA reports)
ORAL MUCOSAL BLISTERING ( 17 FDA reports)
ORAL PUSTULE ( 17 FDA reports)
OSTEOMA ( 17 FDA reports)
PCO2 DECREASED ( 17 FDA reports)
PIRIFORMIS SYNDROME ( 17 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 17 FDA reports)
POISONING ( 17 FDA reports)
PRODUCT ADHESION ISSUE ( 17 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 17 FDA reports)
PROSTATE CANCER METASTATIC ( 17 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 17 FDA reports)
PULMONARY HILUM MASS ( 17 FDA reports)
PYOGENIC GRANULOMA ( 17 FDA reports)
RADIATION OESOPHAGITIS ( 17 FDA reports)
RENAL ARTERY STENOSIS ( 17 FDA reports)
RETROPERITONEAL HAEMATOMA ( 17 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 17 FDA reports)
SMEAR CERVIX ABNORMAL ( 17 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 17 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 17 FDA reports)
SUBCUTANEOUS NODULE ( 17 FDA reports)
RADICULITIS CERVICAL ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
RETINAL TEAR ( 16 FDA reports)
SKELETAL SURVEY ABNORMAL ( 16 FDA reports)
SKIN NODULE ( 16 FDA reports)
SPINAL CORD INJURY ( 16 FDA reports)
SUBMANDIBULAR MASS ( 16 FDA reports)
TACHYARRHYTHMIA ( 16 FDA reports)
TOXIC ENCEPHALOPATHY ( 16 FDA reports)
TRACHEOBRONCHITIS ( 16 FDA reports)
TRAUMATIC HAEMATOMA ( 16 FDA reports)
UNDERDOSE ( 16 FDA reports)
VASCULAR BYPASS GRAFT ( 16 FDA reports)
ACIDOSIS ( 16 FDA reports)
AMYLOIDOSIS ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
APPLICATION SITE REACTION ( 16 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 16 FDA reports)
BLADDER MASS ( 16 FDA reports)
BONE LESION EXCISION ( 16 FDA reports)
BONE MARROW DEPRESSION ( 16 FDA reports)
BRAIN CONTUSION ( 16 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 16 FDA reports)
BREAST CANCER STAGE I ( 16 FDA reports)
BREAST PROSTHESIS USER ( 16 FDA reports)
CAECITIS ( 16 FDA reports)
CARDIAC FIBRILLATION ( 16 FDA reports)
CARDIAC TAMPONADE ( 16 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 16 FDA reports)
CHEST WALL MASS ( 16 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 16 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 16 FDA reports)
CONVERSION DISORDER ( 16 FDA reports)
CORONARY ANGIOPLASTY ( 16 FDA reports)
DIABETIC GASTROPARESIS ( 16 FDA reports)
DIAPHRAGMATIC DISORDER ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
EJECTION FRACTION ABNORMAL ( 16 FDA reports)
ENTERITIS ( 16 FDA reports)
ENTEROCOCCAL INFECTION ( 16 FDA reports)
ESCHERICHIA SEPSIS ( 16 FDA reports)
FRACTURE DELAYED UNION ( 16 FDA reports)
HAEMOLYTIC ANAEMIA ( 16 FDA reports)
HAEMORRHAGIC DIATHESIS ( 16 FDA reports)
HYPERCAPNIA ( 16 FDA reports)
HYPERCHLORHYDRIA ( 16 FDA reports)
HYPOCHROMIC ANAEMIA ( 16 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 16 FDA reports)
HYPOREFLEXIA ( 16 FDA reports)
ICHTHYOSIS ( 16 FDA reports)
IMMUNODEFICIENCY ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
INTESTINAL ULCER ( 16 FDA reports)
LERICHE SYNDROME ( 16 FDA reports)
LYMPH NODE CALCIFICATION ( 16 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 16 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 16 FDA reports)
MEDICATION RESIDUE ( 16 FDA reports)
METAPLASIA ( 16 FDA reports)
MICROCYTIC ANAEMIA ( 16 FDA reports)
MUSCLE RIGIDITY ( 16 FDA reports)
NIPPLE PAIN ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 16 FDA reports)
ONYCHALGIA ( 16 FDA reports)
OSTEOPOROTIC FRACTURE ( 16 FDA reports)
PERIODONTAL INFECTION ( 16 FDA reports)
PERIORBITAL OEDEMA ( 16 FDA reports)
PERNICIOUS ANAEMIA ( 16 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 16 FDA reports)
PNEUMONIA KLEBSIELLA ( 16 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 16 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 15 FDA reports)
AMENORRHOEA ( 15 FDA reports)
APPLICATION SITE VESICLES ( 15 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 15 FDA reports)
BENIGN OVARIAN TUMOUR ( 15 FDA reports)
BILE DUCT OBSTRUCTION ( 15 FDA reports)
BLOOD CHOLESTEROL ( 15 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 15 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 15 FDA reports)
BRAIN HERNIATION ( 15 FDA reports)
BRAIN OPERATION ( 15 FDA reports)
CERVICAL DYSPLASIA ( 15 FDA reports)
COAGULATION TIME PROLONGED ( 15 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 15 FDA reports)
DEFAECATION URGENCY ( 15 FDA reports)
DENTAL PROSTHESIS USER ( 15 FDA reports)
DYSPHASIA ( 15 FDA reports)
DYSTHYMIC DISORDER ( 15 FDA reports)
EAR CONGESTION ( 15 FDA reports)
ECHOCARDIOGRAM ( 15 FDA reports)
FEMORAL ARTERY OCCLUSION ( 15 FDA reports)
FIBROMA ( 15 FDA reports)
FIBROUS HISTIOCYTOMA ( 15 FDA reports)
FINGER DEFORMITY ( 15 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 15 FDA reports)
GRIEF REACTION ( 15 FDA reports)
GRIMACING ( 15 FDA reports)
HOMICIDAL IDEATION ( 15 FDA reports)
HYDROCELE ( 15 FDA reports)
HYPERMETROPIA ( 15 FDA reports)
HYPOVOLAEMIC SHOCK ( 15 FDA reports)
IMPULSE-CONTROL DISORDER ( 15 FDA reports)
INJECTION SITE INDURATION ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 15 FDA reports)
JOINT INSTABILITY ( 15 FDA reports)
LISTLESS ( 15 FDA reports)
MAMMOGRAM ( 15 FDA reports)
METABOLIC DISORDER ( 15 FDA reports)
MUCOUS MEMBRANE DISORDER ( 15 FDA reports)
MUSCLE RUPTURE ( 15 FDA reports)
MUSCLE SPASTICITY ( 15 FDA reports)
MYASTHENIA GRAVIS ( 15 FDA reports)
NERVE ROOT LESION ( 15 FDA reports)
NEUROENDOCRINE CARCINOMA ( 15 FDA reports)
NEUROGENIC BLADDER ( 15 FDA reports)
NODULE ON EXTREMITY ( 15 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 15 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 15 FDA reports)
PIGMENTATION DISORDER ( 15 FDA reports)
PLEURECTOMY ( 15 FDA reports)
PROSTATE TENDERNESS ( 15 FDA reports)
PSYCHOMOTOR RETARDATION ( 15 FDA reports)
PULSE ABNORMAL ( 15 FDA reports)
PYURIA ( 15 FDA reports)
RADIATION PNEUMONITIS ( 15 FDA reports)
RENAL STONE REMOVAL ( 15 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 15 FDA reports)
SOMATISATION DISORDER ( 15 FDA reports)
SPINAL HAEMANGIOMA ( 15 FDA reports)
SPINAL MYELOGRAM ( 15 FDA reports)
THROMBOCYTHAEMIA ( 15 FDA reports)
THYROIDITIS ( 15 FDA reports)
TOOTH EROSION ( 15 FDA reports)
WEIGHT LOSS POOR ( 15 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 14 FDA reports)
PROSTATE CANCER RECURRENT ( 14 FDA reports)
PROTEIN TOTAL INCREASED ( 14 FDA reports)
PULMONARY VALVE STENOSIS ( 14 FDA reports)
RADICAL MASTECTOMY ( 14 FDA reports)
READING DISORDER ( 14 FDA reports)
RECTAL PROLAPSE ( 14 FDA reports)
REITER'S SYNDROME ( 14 FDA reports)
RETINAL ARTERY OCCLUSION ( 14 FDA reports)
RETINAL VEIN THROMBOSIS ( 14 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SELF-INJURIOUS IDEATION ( 14 FDA reports)
SKIN SWELLING ( 14 FDA reports)
SLEEP TALKING ( 14 FDA reports)
SPINAL COLUMN INJURY ( 14 FDA reports)
SPINAL DECOMPRESSION ( 14 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 14 FDA reports)
TUMOUR EXCISION ( 14 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
YELLOW SKIN ( 14 FDA reports)
ABDOMINAL INFECTION ( 14 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 14 FDA reports)
AORTIC VALVE STENOSIS ( 14 FDA reports)
ASPHYXIA ( 14 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 14 FDA reports)
B-CELL LYMPHOMA ( 14 FDA reports)
BLEPHAROSPASM ( 14 FDA reports)
BLOOD BICARBONATE DECREASED ( 14 FDA reports)
BLOOD CREATINE INCREASED ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
BONE GIANT CELL TUMOUR ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
CYSTITIS NONINFECTIVE ( 14 FDA reports)
CYSTOSCOPY ( 14 FDA reports)
DERMATITIS ACNEIFORM ( 14 FDA reports)
DIABETIC COMPLICATION ( 14 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 14 FDA reports)
DRUG TOLERANCE DECREASED ( 14 FDA reports)
ENDOTRACHEAL INTUBATION ( 14 FDA reports)
ENTEROCOLITIS ( 14 FDA reports)
EPIDIDYMITIS ( 14 FDA reports)
FEEDING DISORDER ( 14 FDA reports)
FLUID INTAKE REDUCED ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
FRACTURED COCCYX ( 14 FDA reports)
GALLBLADDER ENLARGEMENT ( 14 FDA reports)
GASTROINTESTINAL NECROSIS ( 14 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 14 FDA reports)
GINGIVAL EROSION ( 14 FDA reports)
GROIN ABSCESS ( 14 FDA reports)
H1N1 INFLUENZA ( 14 FDA reports)
HAIR COLOUR CHANGES ( 14 FDA reports)
HALLUCINATIONS, MIXED ( 14 FDA reports)
HEAT STROKE ( 14 FDA reports)
HICCUPS ( 14 FDA reports)
HYPERTROPHY ( 14 FDA reports)
IMPAIRED SELF-CARE ( 14 FDA reports)
INCORRECT STORAGE OF DRUG ( 14 FDA reports)
INTENTIONAL MISUSE ( 14 FDA reports)
INTERVERTEBRAL DISC INJURY ( 14 FDA reports)
INTESTINAL RESECTION ( 14 FDA reports)
IRON DEFICIENCY ( 14 FDA reports)
JOINT DESTRUCTION ( 14 FDA reports)
JOINT SURGERY ( 14 FDA reports)
KERATOMILEUSIS ( 14 FDA reports)
KLEBSIELLA INFECTION ( 14 FDA reports)
LICHEN PLANUS ( 14 FDA reports)
LIPIDS ABNORMAL ( 14 FDA reports)
LOOSE STOOLS ( 14 FDA reports)
MAMMOGRAM ABNORMAL ( 14 FDA reports)
MARROW HYPERPLASIA ( 14 FDA reports)
MENSTRUATION IRREGULAR ( 14 FDA reports)
MIGRAINE WITH AURA ( 14 FDA reports)
MONOCYTOSIS ( 14 FDA reports)
MOUTH INJURY ( 14 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 14 FDA reports)
MYELITIS TRANSVERSE ( 14 FDA reports)
NARCOLEPSY ( 14 FDA reports)
NEOPLASM RECURRENCE ( 14 FDA reports)
NEPHRECTOMY ( 14 FDA reports)
NEPHROSCLEROSIS ( 14 FDA reports)
NERVE ROOT COMPRESSION ( 14 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 14 FDA reports)
ONYCHOMADESIS ( 14 FDA reports)
ORAL MUCOSA ATROPHY ( 14 FDA reports)
ORTHODONTIC APPLIANCE USER ( 14 FDA reports)
OSTEOMALACIA ( 14 FDA reports)
OVARIAN CANCER STAGE I ( 14 FDA reports)
PANCREATIC CYST ( 14 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 14 FDA reports)
PARAPSORIASIS ( 14 FDA reports)
PAROTID GLAND ENLARGEMENT ( 14 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 14 FDA reports)
PERFORMANCE STATUS DECREASED ( 14 FDA reports)
PERICARDIAL HAEMORRHAGE ( 14 FDA reports)
ANORECTAL DISORDER ( 13 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 13 FDA reports)
ARTHROSCOPIC SURGERY ( 13 FDA reports)
ASPIRATION JOINT ( 13 FDA reports)
BACTERIAL SEPSIS ( 13 FDA reports)
BENIGN BONE NEOPLASM ( 13 FDA reports)
BIOPSY BONE ABNORMAL ( 13 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 13 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 13 FDA reports)
BREAST OPERATION ( 13 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
CARDIOPULMONARY FAILURE ( 13 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 13 FDA reports)
CEREBRAL ARTERY STENOSIS ( 13 FDA reports)
CHOKING SENSATION ( 13 FDA reports)
CHOLANGITIS SCLEROSING ( 13 FDA reports)
CHOLESTEATOMA ( 13 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 13 FDA reports)
CLUSTER HEADACHE ( 13 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 13 FDA reports)
CUBITAL TUNNEL SYNDROME ( 13 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 13 FDA reports)
DROWNING ( 13 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 13 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 13 FDA reports)
DYSMENORRHOEA ( 13 FDA reports)
ESSENTIAL TREMOR ( 13 FDA reports)
ETHMOID SINUS SURGERY ( 13 FDA reports)
EYELID DISORDER ( 13 FDA reports)
FINGER AMPUTATION ( 13 FDA reports)
FOOD POISONING ( 13 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 13 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 13 FDA reports)
GUILLAIN-BARRE SYNDROME ( 13 FDA reports)
HAEMOLYSIS ( 13 FDA reports)
HEPATITIS B ( 13 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 13 FDA reports)
HORMONE LEVEL ABNORMAL ( 13 FDA reports)
HYDROCEPHALUS ( 13 FDA reports)
HYPOTRICHOSIS ( 13 FDA reports)
INJECTION SITE INFLAMMATION ( 13 FDA reports)
INNER EAR DISORDER ( 13 FDA reports)
INTESTINAL ISCHAEMIA ( 13 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 13 FDA reports)
LACTIC ACIDOSIS ( 13 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 13 FDA reports)
LIMB DEFORMITY ( 13 FDA reports)
LYMPH GLAND INFECTION ( 13 FDA reports)
MAXILLOFACIAL OPERATION ( 13 FDA reports)
METASTASES TO BONE MARROW ( 13 FDA reports)
MICROANGIOPATHY ( 13 FDA reports)
MICTURITION FREQUENCY DECREASED ( 13 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 13 FDA reports)
MUSCLE CONTRACTURE ( 13 FDA reports)
MYOFASCITIS ( 13 FDA reports)
NASAL ODOUR ( 13 FDA reports)
NASAL POLYPS ( 13 FDA reports)
OBSTRUCTIVE UROPATHY ( 13 FDA reports)
OCULAR HYPERTENSION ( 13 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 13 FDA reports)
OOPHORECTOMY ( 13 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 13 FDA reports)
OROPHARYNGEAL BLISTERING ( 13 FDA reports)
PARAPARESIS ( 13 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 13 FDA reports)
PERIODONTAL DESTRUCTION ( 13 FDA reports)
PERIORBITAL HAEMATOMA ( 13 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 13 FDA reports)
PLATELET AGGREGATION INCREASED ( 13 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 13 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 13 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
RADICULAR CYST ( 13 FDA reports)
REFLUX LARYNGITIS ( 13 FDA reports)
RESPIRATORY DEPRESSION ( 13 FDA reports)
RETINAL DISORDER ( 13 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SECRETION DISCHARGE ( 13 FDA reports)
SERUM SICKNESS ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SPINAL PAIN ( 13 FDA reports)
STATUS EPILEPTICUS ( 13 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 13 FDA reports)
TEETH BRITTLE ( 13 FDA reports)
THORACOTOMY ( 13 FDA reports)
TREATMENT FAILURE ( 13 FDA reports)
URETERIC OBSTRUCTION ( 13 FDA reports)
URETHRITIS ( 13 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 13 FDA reports)
VESTIBULAR NEURONITIS ( 13 FDA reports)
VICTIM OF CRIME ( 13 FDA reports)
VITAMIN B1 DEFICIENCY ( 13 FDA reports)
WOUND HAEMORRHAGE ( 13 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 12 FDA reports)
PROCEDURAL HYPOTENSION ( 12 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 12 FDA reports)
PSEUDOCYST ( 12 FDA reports)
REACTIVE PSYCHOSIS ( 12 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 12 FDA reports)
RENAL HAEMORRHAGE ( 12 FDA reports)
RETINAL VASCULAR OCCLUSION ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SCLERAL OPERATION ( 12 FDA reports)
SEBORRHOEA ( 12 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 12 FDA reports)
SHOCK HAEMORRHAGIC ( 12 FDA reports)
SIMPLE PARTIAL SEIZURES ( 12 FDA reports)
SKIN CANDIDA ( 12 FDA reports)
SKULL FRACTURE ( 12 FDA reports)
STERNAL FRACTURE ( 12 FDA reports)
SUTURE REMOVAL ( 12 FDA reports)
SYNCOPE VASOVAGAL ( 12 FDA reports)
THORACIC OUTLET SYNDROME ( 12 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 12 FDA reports)
TONGUE OEDEMA ( 12 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 12 FDA reports)
UTERINE DILATION AND CURETTAGE ( 12 FDA reports)
VASCULAR PSEUDOANEURYSM ( 12 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 12 FDA reports)
VIRAL PERICARDITIS ( 12 FDA reports)
VULVOVAGINAL PRURITUS ( 12 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 12 FDA reports)
AKINESIA ( 12 FDA reports)
AMBLYOPIA ( 12 FDA reports)
ANAL CANDIDIASIS ( 12 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 12 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
APPENDIX DISORDER ( 12 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 12 FDA reports)
BEREAVEMENT REACTION ( 12 FDA reports)
BILE DUCT CANCER ( 12 FDA reports)
BIOPSY ( 12 FDA reports)
BLADDER DIVERTICULUM ( 12 FDA reports)
BRADYPHRENIA ( 12 FDA reports)
BRAIN STEM SYNDROME ( 12 FDA reports)
CARCINOMA ( 12 FDA reports)
CHAPPED LIPS ( 12 FDA reports)
CHEST WALL OPERATION ( 12 FDA reports)
CHRONIC HEPATITIS ( 12 FDA reports)
COLONOSCOPY ( 12 FDA reports)
CREPITATIONS ( 12 FDA reports)
CSF PROTEIN INCREASED ( 12 FDA reports)
DANDRUFF ( 12 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 12 FDA reports)
DIPLEGIA ( 12 FDA reports)
DRESSLER'S SYNDROME ( 12 FDA reports)
DRUG LEVEL CHANGED ( 12 FDA reports)
ENDOMETRIAL ATROPHY ( 12 FDA reports)
ENTEROBACTER INFECTION ( 12 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 12 FDA reports)
EROSIVE DUODENITIS ( 12 FDA reports)
EYE INJURY ( 12 FDA reports)
EYELID OPERATION ( 12 FDA reports)
GASTRODUODENITIS ( 12 FDA reports)
HAEMODYNAMIC INSTABILITY ( 12 FDA reports)
HAEMOPHILUS INFECTION ( 12 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 12 FDA reports)
HEART VALVE INSUFFICIENCY ( 12 FDA reports)
HEAT EXHAUSTION ( 12 FDA reports)
HOSTILITY ( 12 FDA reports)
IMPLANT SITE INFECTION ( 12 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 12 FDA reports)
INCISIONAL HERNIA ( 12 FDA reports)
JAW CYST ( 12 FDA reports)
KERATOSIS PILARIS ( 12 FDA reports)
LOSS OF EMPLOYMENT ( 12 FDA reports)
LOSS OF PROPRIOCEPTION ( 12 FDA reports)
LUNG INJURY ( 12 FDA reports)
LUNG OPERATION ( 12 FDA reports)
MEDIASTINUM NEOPLASM ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
MERALGIA PARAESTHETICA ( 12 FDA reports)
METASTASES TO MENINGES ( 12 FDA reports)
MONONEURITIS ( 12 FDA reports)
MOTION SICKNESS ( 12 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 12 FDA reports)
MYOPIA ( 12 FDA reports)
NASAL DRYNESS ( 12 FDA reports)
NEOPLASM SKIN ( 12 FDA reports)
NO ADVERSE EFFECT ( 12 FDA reports)
NON-SMALL CELL LUNG CANCER ( 12 FDA reports)
ONYCHOCLASIS ( 12 FDA reports)
OPTIC ATROPHY ( 12 FDA reports)
OTORRHOEA ( 12 FDA reports)
PALATAL DISORDER ( 12 FDA reports)
PANCREATIC INSUFFICIENCY ( 12 FDA reports)
PANCREATITIS NECROTISING ( 12 FDA reports)
PEMPHIGOID ( 12 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 12 FDA reports)
PERICARDIAL DISEASE ( 12 FDA reports)
PEYRONIE'S DISEASE ( 12 FDA reports)
POLYCYTHAEMIA ( 12 FDA reports)
ABDOMINAL SEPSIS ( 11 FDA reports)
ACUTE PSYCHOSIS ( 11 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 11 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 11 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 11 FDA reports)
AGORAPHOBIA ( 11 FDA reports)
ALLERGY TO CHEMICALS ( 11 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 11 FDA reports)
ARTERIOSPASM CORONARY ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BIOPSY BONE MARROW ( 11 FDA reports)
BLADDER DISCOMFORT ( 11 FDA reports)
BLOOD AMYLASE INCREASED ( 11 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 11 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BULLOUS LUNG DISEASE ( 11 FDA reports)
CARDIORENAL SYNDROME ( 11 FDA reports)
CAROTID ARTERY ATHEROMA ( 11 FDA reports)
CATHETER SITE HAEMORRHAGE ( 11 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 11 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 11 FDA reports)
CHOREA ( 11 FDA reports)
CLOSED HEAD INJURY ( 11 FDA reports)
COGWHEEL RIGIDITY ( 11 FDA reports)
COLITIS COLLAGENOUS ( 11 FDA reports)
COR PULMONALE ( 11 FDA reports)
CRANIOCEREBRAL INJURY ( 11 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 11 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 11 FDA reports)
CYSTOPEXY ( 11 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 11 FDA reports)
DIURETIC THERAPY ( 11 FDA reports)
DYSHIDROSIS ( 11 FDA reports)
EAR HAEMORRHAGE ( 11 FDA reports)
EMBOLISM VENOUS ( 11 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 11 FDA reports)
EXOPHTHALMOS ( 11 FDA reports)
EXPLORATORY OPERATION ( 11 FDA reports)
EYE INFECTION ( 11 FDA reports)
GASTROENTERITIS HELICOBACTER ( 11 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 11 FDA reports)
GINGIVAL GRAFT ( 11 FDA reports)
GUN SHOT WOUND ( 11 FDA reports)
HEPATITIS FULMINANT ( 11 FDA reports)
HYPERAEMIA ( 11 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 11 FDA reports)
HYPOGEUSIA ( 11 FDA reports)
ILIAC ARTERY THROMBOSIS ( 11 FDA reports)
IMMUNOGLOBULINS INCREASED ( 11 FDA reports)
IMPRISONMENT ( 11 FDA reports)
INCISION SITE COMPLICATION ( 11 FDA reports)
INFUSION SITE SWELLING ( 11 FDA reports)
INJECTION SITE MASS ( 11 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 11 FDA reports)
LENS DISORDER ( 11 FDA reports)
LIPIDS INCREASED ( 11 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 11 FDA reports)
MEDIASTINAL DISORDER ( 11 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 11 FDA reports)
MICROALBUMINURIA ( 11 FDA reports)
MITRAL VALVE REPAIR ( 11 FDA reports)
MONARTHRITIS ( 11 FDA reports)
MULTI-ORGAN DISORDER ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
MYOCARDIAL FIBROSIS ( 11 FDA reports)
NASAL SEPTAL OPERATION ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 11 FDA reports)
NIGHT BLINDNESS ( 11 FDA reports)
NO ADVERSE DRUG EFFECT ( 11 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 11 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 11 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 11 FDA reports)
ORAL SOFT TISSUE DISORDER ( 11 FDA reports)
PALATAL OEDEMA ( 11 FDA reports)
PERSECUTORY DELUSION ( 11 FDA reports)
PHARYNGEAL DISORDER ( 11 FDA reports)
PHYSICAL ASSAULT ( 11 FDA reports)
PITUITARY TUMOUR BENIGN ( 11 FDA reports)
PLASTIC SURGERY TO THE FACE ( 11 FDA reports)
PNEUMATOSIS INTESTINALIS ( 11 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PROSTATIC OBSTRUCTION ( 11 FDA reports)
PROTEUS INFECTION ( 11 FDA reports)
PSEUDOMONAL SEPSIS ( 11 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 11 FDA reports)
RENAL ARTERY OCCLUSION ( 11 FDA reports)
RENAL COLIC ( 11 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 11 FDA reports)
RIGHT VENTRICULAR FAILURE ( 11 FDA reports)
SALPINGO-OOPHORECTOMY ( 11 FDA reports)
SINUS ARREST ( 11 FDA reports)
SKIN MASS ( 11 FDA reports)
SKIN NECROSIS ( 11 FDA reports)
SKIN TOXICITY ( 11 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 11 FDA reports)
SUPRAPUBIC PAIN ( 11 FDA reports)
ULCERATIVE KERATITIS ( 11 FDA reports)
ULNAR NERVE INJURY ( 11 FDA reports)
URETHRAL PAIN ( 11 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 11 FDA reports)
UTERINE PROLAPSE REPAIR ( 11 FDA reports)
VAGINITIS BACTERIAL ( 11 FDA reports)
VARICOSE ULCERATION ( 11 FDA reports)
VASCULAR PURPURA ( 11 FDA reports)
VENTRICULAR DYSKINESIA ( 11 FDA reports)
VERTEBRAL WEDGING ( 11 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 10 FDA reports)
PULSE PRESSURE DECREASED ( 10 FDA reports)
PYELOCALIECTASIS ( 10 FDA reports)
RASH MORBILLIFORM ( 10 FDA reports)
RECURRENT CANCER ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RENAL SURGERY ( 10 FDA reports)
RETINOPATHY ( 10 FDA reports)
RHEUMATOID FACTOR INCREASED ( 10 FDA reports)
SCIATIC NERVE INJURY ( 10 FDA reports)
SICCA SYNDROME ( 10 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 10 FDA reports)
SKIN FRAGILITY ( 10 FDA reports)
SKIN GRAFT ( 10 FDA reports)
SPLENIC RUPTURE ( 10 FDA reports)
STARING ( 10 FDA reports)
STEATORRHOEA ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 10 FDA reports)
THIRST DECREASED ( 10 FDA reports)
TINEL'S SIGN ( 10 FDA reports)
TOE DEFORMITY ( 10 FDA reports)
TONGUE BITING ( 10 FDA reports)
TRAUMATIC ARTHRITIS ( 10 FDA reports)
TRAUMATIC FRACTURE ( 10 FDA reports)
URETHRAL DISORDER ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
UTERINE PROLAPSE ( 10 FDA reports)
UVEITIS ( 10 FDA reports)
VITH NERVE PARALYSIS ( 10 FDA reports)
ACCELERATED HYPERTENSION ( 10 FDA reports)
ADRENAL NEOPLASM ( 10 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 10 FDA reports)
ALCOHOLIC LIVER DISEASE ( 10 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 10 FDA reports)
AORTIC VALVE CALCIFICATION ( 10 FDA reports)
APPLICATION SITE IRRITATION ( 10 FDA reports)
ASTHMATIC CRISIS ( 10 FDA reports)
AXILLARY MASS ( 10 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 10 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 10 FDA reports)
BLOOD CHLORIDE INCREASED ( 10 FDA reports)
BLOOD CREATININE ABNORMAL ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 10 FDA reports)
BLOOD PROLACTIN INCREASED ( 10 FDA reports)
BRAIN CANCER METASTATIC ( 10 FDA reports)
BREAST ABSCESS ( 10 FDA reports)
BURNS SECOND DEGREE ( 10 FDA reports)
CARDIAC ASTHMA ( 10 FDA reports)
CARDIAC HYPERTROPHY ( 10 FDA reports)
CAUDA EQUINA SYNDROME ( 10 FDA reports)
CHEMOTHERAPY ( 10 FDA reports)
CHOLANGIOGRAM ( 10 FDA reports)
COELIAC ARTERY COMPRESSION SYNDROME ( 10 FDA reports)
CONGENITAL ANOMALY ( 10 FDA reports)
CULTURE POSITIVE ( 10 FDA reports)
DENTAL TREATMENT ( 10 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 10 FDA reports)
DUODENAL POLYP ( 10 FDA reports)
ENDOSCOPY ( 10 FDA reports)
ERECTION INCREASED ( 10 FDA reports)
ESCHERICHIA BACTERAEMIA ( 10 FDA reports)
FAILURE OF IMPLANT ( 10 FDA reports)
FEAR OF DEATH ( 10 FDA reports)
GASTROINTESTINAL TOXICITY ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GINGIVECTOMY ( 10 FDA reports)
GLOBULINS INCREASED ( 10 FDA reports)
HAIR DISORDER ( 10 FDA reports)
HAIR TEXTURE ABNORMAL ( 10 FDA reports)
HEART VALVE REPLACEMENT ( 10 FDA reports)
HEPATIC ENCEPHALOPATHY ( 10 FDA reports)
HEPATIC ENZYME ABNORMAL ( 10 FDA reports)
HEPATITIS TOXIC ( 10 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 10 FDA reports)
HYPERREFLEXIA ( 10 FDA reports)
HYPOPROTEINAEMIA ( 10 FDA reports)
IMPAIRED FASTING GLUCOSE ( 10 FDA reports)
IMPLANT SITE THROMBOSIS ( 10 FDA reports)
INFECTIOUS PERITONITIS ( 10 FDA reports)
INGUINAL HERNIA REPAIR ( 10 FDA reports)
INJECTION SITE EXTRAVASATION ( 10 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 10 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 10 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 10 FDA reports)
KETOACIDOSIS ( 10 FDA reports)
LUNG ABSCESS ( 10 FDA reports)
LUNG HYPERINFLATION ( 10 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 10 FDA reports)
LYMPHANGIOMA ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
MACROPHAGES INCREASED ( 10 FDA reports)
MEAN CELL VOLUME INCREASED ( 10 FDA reports)
METASTASES TO ADRENALS ( 10 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
METATARSALGIA ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MITRAL VALVE STENOSIS ( 10 FDA reports)
MONOCYTE COUNT DECREASED ( 10 FDA reports)
MUCOSAL ATROPHY ( 10 FDA reports)
NAIL DISCOLOURATION ( 10 FDA reports)
NASAL ULCER ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEURECTOMY ( 10 FDA reports)
NONSPECIFIC REACTION ( 10 FDA reports)
OESOPHAGITIS ULCERATIVE ( 10 FDA reports)
OPTIC NERVE INJURY ( 10 FDA reports)
PARAPLEGIA ( 10 FDA reports)
PERIPHERAL EMBOLISM ( 10 FDA reports)
PHLEBOTHROMBOSIS ( 10 FDA reports)
PLEURODESIS ( 10 FDA reports)
ADVERSE REACTION ( 9 FDA reports)
ALLERGY TO METALS ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
AORTIC BYPASS ( 9 FDA reports)
BASAL GANGLIA INFARCTION ( 9 FDA reports)
BILE DUCT STENOSIS ( 9 FDA reports)
BILIARY DYSKINESIA ( 9 FDA reports)
BIOPSY BONE ( 9 FDA reports)
BLADDER DILATATION ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLADDER PAIN ( 9 FDA reports)
BLOOD CREATININE DECREASED ( 9 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 9 FDA reports)
BLOOD IRON INCREASED ( 9 FDA reports)
BLOOD PRESSURE ( 9 FDA reports)
BLOOD UREA DECREASED ( 9 FDA reports)
BONE DEFORMITY ( 9 FDA reports)
BRACHIAL PLEXOPATHY ( 9 FDA reports)
BRAIN DEATH ( 9 FDA reports)
BREAST SWELLING ( 9 FDA reports)
BREATH SOUNDS DECREASED ( 9 FDA reports)
BRONCHIAL CARCINOMA ( 9 FDA reports)
BRONCHIAL OBSTRUCTION ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATHETER RELATED INFECTION ( 9 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
COLON POLYPECTOMY ( 9 FDA reports)
COLONIC OBSTRUCTION ( 9 FDA reports)
COMMINUTED FRACTURE ( 9 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 9 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
DELIRIUM TREMENS ( 9 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 9 FDA reports)
EARLY SATIETY ( 9 FDA reports)
EJACULATION FAILURE ( 9 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 9 FDA reports)
EMBOLISM ARTERIAL ( 9 FDA reports)
EPIDURAL LIPOMATOSIS ( 9 FDA reports)
ERYTHEMA OF EYELID ( 9 FDA reports)
EXTREMITY CONTRACTURE ( 9 FDA reports)
EYE NAEVUS ( 9 FDA reports)
FAECES HARD ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
FRACTURE MALUNION ( 9 FDA reports)
FRONTAL SINUS OPERATION ( 9 FDA reports)
FUNGAEMIA ( 9 FDA reports)
GASTRIC INFECTION ( 9 FDA reports)
GASTROINTESTINAL PERFORATION ( 9 FDA reports)
GASTROSTOMY TUBE INSERTION ( 9 FDA reports)
GINGIVAL HYPERPLASIA ( 9 FDA reports)
GLYCOSURIA ( 9 FDA reports)
HAEMATOSPERMIA ( 9 FDA reports)
HANGOVER ( 9 FDA reports)
HEAD AND NECK CANCER ( 9 FDA reports)
HEART DISEASE CONGENITAL ( 9 FDA reports)
HEMIANOPIA ( 9 FDA reports)
HEMIANOPIA HOMONYMOUS ( 9 FDA reports)
HEPATOCELLULAR INJURY ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
HIGH FREQUENCY ABLATION ( 9 FDA reports)
HYPERMAGNESAEMIA ( 9 FDA reports)
HYPERPROTEINAEMIA ( 9 FDA reports)
INDURATION ( 9 FDA reports)
INGROWN HAIR ( 9 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 9 FDA reports)
INJECTION SITE NECROSIS ( 9 FDA reports)
INJECTION SITE VESICLES ( 9 FDA reports)
INJURY ASPHYXIATION ( 9 FDA reports)
INTERNAL HERNIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 9 FDA reports)
INTERVERTEBRAL DISCITIS ( 9 FDA reports)
INTESTINAL STENOSIS ( 9 FDA reports)
IRIS ADHESIONS ( 9 FDA reports)
KYPHOSCOLIOSIS ( 9 FDA reports)
LEUKOPLAKIA ( 9 FDA reports)
LIMB CRUSHING INJURY ( 9 FDA reports)
LIP NEOPLASM BENIGN ( 9 FDA reports)
LOSS OF LIBIDO ( 9 FDA reports)
LYME DISEASE ( 9 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 9 FDA reports)
MENISCUS REMOVAL ( 9 FDA reports)
MENSTRUAL DISORDER ( 9 FDA reports)
METABOLIC ALKALOSIS ( 9 FDA reports)
METASTASES TO MOUTH ( 9 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 9 FDA reports)
MIOSIS ( 9 FDA reports)
MUCOSAL DISCOLOURATION ( 9 FDA reports)
MUCOUS STOOLS ( 9 FDA reports)
MYCOBACTERIAL INFECTION ( 9 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 9 FDA reports)
NAIL OPERATION ( 9 FDA reports)
NASAL OEDEMA ( 9 FDA reports)
NEGATIVE THOUGHTS ( 9 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 9 FDA reports)
NOCTURNAL DYSPNOEA ( 9 FDA reports)
OPEN ANGLE GLAUCOMA ( 9 FDA reports)
PARESIS ( 9 FDA reports)
PARTNER STRESS ( 9 FDA reports)
PELVIC ADHESIONS ( 9 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 9 FDA reports)
PENIS DISORDER ( 9 FDA reports)
PHARYNGEAL ULCERATION ( 9 FDA reports)
PILONIDAL CYST ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POST PROCEDURAL NAUSEA ( 9 FDA reports)
POSTOPERATIVE ADHESION ( 9 FDA reports)
POSTOPERATIVE FEVER ( 9 FDA reports)
PRESSURE OF SPEECH ( 9 FDA reports)
PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
PRODUCT COUNTERFEIT ( 9 FDA reports)
PSEUDODEMENTIA ( 9 FDA reports)
PSEUDOMONAS BRONCHITIS ( 9 FDA reports)
PULMONARY TOXICITY ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 9 FDA reports)
RADIAL NERVE PALSY ( 9 FDA reports)
RECTAL ULCER ( 9 FDA reports)
RIB DEFORMITY ( 9 FDA reports)
SALIVARY GLAND PAIN ( 9 FDA reports)
SARCOMA ( 9 FDA reports)
SCHAMBERG'S DISEASE ( 9 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 9 FDA reports)
SELF ESTEEM DECREASED ( 9 FDA reports)
SEROSITIS ( 9 FDA reports)
SLEEP WALKING ( 9 FDA reports)
SMALL INTESTINE ULCER ( 9 FDA reports)
SPHENOID SINUS OPERATION ( 9 FDA reports)
SPINAL CORD INJURY THORACIC ( 9 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 9 FDA reports)
STAG HORN CALCULUS ( 9 FDA reports)
STRABISMUS ( 9 FDA reports)
STRESS ULCER ( 9 FDA reports)
STUPOR ( 9 FDA reports)
SUDDEN HEARING LOSS ( 9 FDA reports)
SUICIDAL BEHAVIOUR ( 9 FDA reports)
TONGUE BLISTERING ( 9 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 9 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 9 FDA reports)
URAEMIC ENCEPHALOPATHY ( 9 FDA reports)
URGE INCONTINENCE ( 9 FDA reports)
URINE COLOUR ABNORMAL ( 9 FDA reports)
VAGINAL CANDIDIASIS ( 9 FDA reports)
VARICOCELE ( 9 FDA reports)
VASCULAR DEMENTIA ( 9 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 9 FDA reports)
VOCAL CORD PARALYSIS ( 9 FDA reports)
WHIPLASH INJURY ( 9 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 8 FDA reports)
POSTURING ( 8 FDA reports)
PROCTITIS ULCERATIVE ( 8 FDA reports)
PROSTATIC OPERATION ( 8 FDA reports)
PSEUDOPHAKIA ( 8 FDA reports)
RADIATION EXPOSURE ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
RESIDUAL URINE ( 8 FDA reports)
RESPIRATORY ALKALOSIS ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 8 FDA reports)
RETINAL VASCULAR DISORDER ( 8 FDA reports)
RHEUMATOID LUNG ( 8 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 8 FDA reports)
SCROTAL SWELLING ( 8 FDA reports)
SERRATIA INFECTION ( 8 FDA reports)
SINUSITIS FUNGAL ( 8 FDA reports)
SKIN TURGOR DECREASED ( 8 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 8 FDA reports)
STOMATITIS NECROTISING ( 8 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 8 FDA reports)
SUBDURAL HAEMORRHAGE ( 8 FDA reports)
SUPERINFECTION BACTERIAL ( 8 FDA reports)
TENDON SHEATH INCISION ( 8 FDA reports)
THALAMIC INFARCTION ( 8 FDA reports)
THORACOSTOMY ( 8 FDA reports)
THYROXINE DECREASED ( 8 FDA reports)
TONGUE HAEMORRHAGE ( 8 FDA reports)
TUMOUR MARKER INCREASED ( 8 FDA reports)
TUNNEL VISION ( 8 FDA reports)
URETHRAL STENOSIS ( 8 FDA reports)
URTICARIA GENERALISED ( 8 FDA reports)
VAGINAL ULCERATION ( 8 FDA reports)
VENOUS STASIS ( 8 FDA reports)
VENOUS STENOSIS ( 8 FDA reports)
VOCAL CORD INFLAMMATION ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
ABSCESS INTESTINAL ( 8 FDA reports)
ACANTHOSIS ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ALCOHOL ABUSE ( 8 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 8 FDA reports)
ANKLE OPERATION ( 8 FDA reports)
ANORECTAL DISCOMFORT ( 8 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 8 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 8 FDA reports)
ARTERIAL RUPTURE ( 8 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BACTERIAL TEST POSITIVE ( 8 FDA reports)
BENIGN GASTRIC NEOPLASM ( 8 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 8 FDA reports)
BILIARY NEOPLASM ( 8 FDA reports)
BIOPSY BREAST ABNORMAL ( 8 FDA reports)
BLEEDING TIME PROLONGED ( 8 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BONE CYST ( 8 FDA reports)
BORDERLINE GLAUCOMA ( 8 FDA reports)
BREAST MICROCALCIFICATION ( 8 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 8 FDA reports)
CARDIOTOXICITY ( 8 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CEREBRAL HAEMATOMA ( 8 FDA reports)
COLONIC FISTULA ( 8 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 8 FDA reports)
CORONARY OSTIAL STENOSIS ( 8 FDA reports)
CORRECTIVE LENS USER ( 8 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 8 FDA reports)
CRYOGLOBULINAEMIA ( 8 FDA reports)
DENTAL CLEANING ( 8 FDA reports)
DEPRESSION SUICIDAL ( 8 FDA reports)
DIAPHRAGMATIC HERNIA ( 8 FDA reports)
DRUG INTERACTION POTENTIATION ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
DYSPAREUNIA ( 8 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENERGY INCREASED ( 8 FDA reports)
ENZYME ABNORMALITY ( 8 FDA reports)
EPIDIDYMAL CYST ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EYE ROLLING ( 8 FDA reports)
EYELID INFECTION ( 8 FDA reports)
FACIAL SPASM ( 8 FDA reports)
FALLOPIAN TUBE DISORDER ( 8 FDA reports)
FOOD CRAVING ( 8 FDA reports)
FOOD INTERACTION ( 8 FDA reports)
GALACTORRHOEA ( 8 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 8 FDA reports)
GENITAL PRURITUS FEMALE ( 8 FDA reports)
GRANULOCYTOPENIA ( 8 FDA reports)
HAEMOGLOBIN INCREASED ( 8 FDA reports)
HEART SOUNDS ABNORMAL ( 8 FDA reports)
HEART VALVE CALCIFICATION ( 8 FDA reports)
HYPERACUSIS ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 8 FDA reports)
HYPOPERFUSION ( 8 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 8 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 8 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INCREASED BRONCHIAL SECRETION ( 8 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
INTRAOCULAR HAEMATOMA ( 8 FDA reports)
IRIDOCYCLITIS ( 8 FDA reports)
IVTH NERVE PARALYSIS ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LABILE HYPERTENSION ( 8 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 8 FDA reports)
LARYNGITIS ALLERGIC ( 8 FDA reports)
LEGAL PROBLEM ( 8 FDA reports)
LIBIDO INCREASED ( 8 FDA reports)
LIP INJURY ( 8 FDA reports)
LIVER ABSCESS ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LOOSE BODY IN JOINT ( 8 FDA reports)
LYMPH NODE PAIN ( 8 FDA reports)
LYMPHOCYTOSIS ( 8 FDA reports)
MAMMOPLASTY ( 8 FDA reports)
MEDIASTINITIS ( 8 FDA reports)
MENOMETRORRHAGIA ( 8 FDA reports)
MESENTERIC OCCLUSION ( 8 FDA reports)
MONOPARESIS ( 8 FDA reports)
NASAL OBSTRUCTION ( 8 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 8 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 8 FDA reports)
OESOPHAGEAL DISCOMFORT ( 8 FDA reports)
OPPORTUNISTIC INFECTION ( 8 FDA reports)
OPTIC NERVE DISORDER ( 8 FDA reports)
ORCHITIS ( 8 FDA reports)
OVARIAN ABSCESS ( 8 FDA reports)
OVARIAN CANCER METASTATIC ( 8 FDA reports)
PACEMAKER COMPLICATION ( 8 FDA reports)
PELVIC HAEMATOMA ( 8 FDA reports)
PHARYNGEAL ABSCESS ( 8 FDA reports)
PNEUMONIA HAEMOPHILUS ( 8 FDA reports)
ABDOMINAL HERNIA REPAIR ( 7 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 7 FDA reports)
ABDOMINOPLASTY ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
ADENOMYOSIS ( 7 FDA reports)
ADENOTONSILLECTOMY ( 7 FDA reports)
ALLODYNIA ( 7 FDA reports)
ANAESTHETIC COMPLICATION ( 7 FDA reports)
ANAL FISTULA ( 7 FDA reports)
AORTIC DILATATION ( 7 FDA reports)
APPLICATION SITE BURN ( 7 FDA reports)
APPLICATION SITE PAIN ( 7 FDA reports)
AURICULOTEMPORAL SYNDROME ( 7 FDA reports)
BIOPSY BREAST ( 7 FDA reports)
BLEEDING ANOVULATORY ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BREAST CELLULITIS ( 7 FDA reports)
BREAST OEDEMA ( 7 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 7 FDA reports)
CARDIAC DISCOMFORT ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CAUSTIC INJURY ( 7 FDA reports)
CEREBELLAR HAEMORRHAGE ( 7 FDA reports)
CEREBELLAR SYNDROME ( 7 FDA reports)
CEREBRAL HAEMANGIOMA ( 7 FDA reports)
CHEST EXPANSION DECREASED ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHOLESTEROSIS ( 7 FDA reports)
CITROBACTER INFECTION ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
COLOSTOMY ( 7 FDA reports)
COMPARTMENT SYNDROME ( 7 FDA reports)
CONDUCTIVE DEAFNESS ( 7 FDA reports)
CORONARY ARTERY ANEURYSM ( 7 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 7 FDA reports)
CORONARY ARTERY REOCCLUSION ( 7 FDA reports)
CRYSTAL ARTHROPATHY ( 7 FDA reports)
DERMOID CYST ( 7 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 7 FDA reports)
DIABETIC ULCER ( 7 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DRUG SCREEN NEGATIVE ( 7 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 7 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 7 FDA reports)
ENDOMETRIAL CANCER ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EXCITABILITY ( 7 FDA reports)
EXERCISE LACK OF ( 7 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 7 FDA reports)
FASCIITIS ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
GALLOP RHYTHM PRESENT ( 7 FDA reports)
GASTRIC ULCER PERFORATION ( 7 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 7 FDA reports)
GLIOBLASTOMA MULTIFORME ( 7 FDA reports)
HAEMATOCRIT INCREASED ( 7 FDA reports)
HEAT RASH ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HEPATIC CONGESTION ( 7 FDA reports)
HEPATIC NEOPLASM ( 7 FDA reports)
HYPOMETABOLISM ( 7 FDA reports)
IMPLANT SITE EFFUSION ( 7 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
INJECTION SITE ULCER ( 7 FDA reports)
INTENTIONAL SELF-INJURY ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 7 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 7 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
IRON OVERLOAD ( 7 FDA reports)
JOINT INJECTION ( 7 FDA reports)
JOINT WARMTH ( 7 FDA reports)
JUDGEMENT IMPAIRED ( 7 FDA reports)
KIDNEY MALROTATION ( 7 FDA reports)
LIGAMENT DISORDER ( 7 FDA reports)
LIGAMENT LAXITY ( 7 FDA reports)
MARFAN'S SYNDROME ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 7 FDA reports)
METASTASES TO MUSCLE ( 7 FDA reports)
MIDDLE EAR EFFUSION ( 7 FDA reports)
MUCOSAL DRYNESS ( 7 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 7 FDA reports)
NASAL MUCOSAL DISORDER ( 7 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 7 FDA reports)
NEPHROCALCINOSIS ( 7 FDA reports)
NEUROPATHIC PAIN ( 7 FDA reports)
NIPPLE DISORDER ( 7 FDA reports)
NODAL ARRHYTHMIA ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
OLIGOMENORRHOEA ( 7 FDA reports)
ORAL MUCOSAL ERUPTION ( 7 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 7 FDA reports)
OROPHARYNGEAL SPASM ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PALMAR ERYTHEMA ( 7 FDA reports)
PANCREATIC ATROPHY ( 7 FDA reports)
PANCREATIC MASS ( 7 FDA reports)
PANCREATIC NECROSIS ( 7 FDA reports)
PAROTID ABSCESS ( 7 FDA reports)
PENILE PROSTHESIS INSERTION ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 7 FDA reports)
PHIMOSIS ( 7 FDA reports)
PHONOPHOBIA ( 7 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 7 FDA reports)
PNEUMOPERITONEUM ( 7 FDA reports)
PO2 INCREASED ( 7 FDA reports)
POLYCHONDRITIS ( 7 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PROTRUSION TONGUE ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PUBIS FRACTURE ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PYODERMA GANGRENOSUM ( 7 FDA reports)
RADICULITIS BRACHIAL ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 7 FDA reports)
RENAL INFARCT ( 7 FDA reports)
RENAL PAPILLARY NECROSIS ( 7 FDA reports)
RETICULOCYTE COUNT INCREASED ( 7 FDA reports)
RETINOPATHY HYPERTENSIVE ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
SCROTAL DISORDER ( 7 FDA reports)
SEMEN VOLUME DECREASED ( 7 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 7 FDA reports)
SERUM FERRITIN DECREASED ( 7 FDA reports)
SERUM SEROTONIN DECREASED ( 7 FDA reports)
SIGHT DISABILITY ( 7 FDA reports)
SKIN DEPIGMENTATION ( 7 FDA reports)
SKIN OPERATION ( 7 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 7 FDA reports)
SPINAL CORD INJURY CERVICAL ( 7 FDA reports)
SPINAL FUSION ACQUIRED ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SPLENIC CYST ( 7 FDA reports)
SPONDYLITIC MYELOPATHY ( 7 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 7 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
SYPHILIS ( 7 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
THROAT CANCER ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
TONGUE GEOGRAPHIC ( 7 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
URINARY TRACT PAIN ( 7 FDA reports)
VAGINAL LEUKOPLAKIA ( 7 FDA reports)
VAGINAL PAIN ( 7 FDA reports)
VASODILATATION ( 7 FDA reports)
VEIN PAIN ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
VITAMIN B12 DECREASED ( 7 FDA reports)
VOCAL CORD PARESIS ( 7 FDA reports)
VULVAL DISORDER ( 7 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 7 FDA reports)
WEIGHT ABNORMAL ( 7 FDA reports)
WISDOM TEETH REMOVAL ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
POST LAMINECTOMY SYNDROME ( 6 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 6 FDA reports)
POST THROMBOTIC SYNDROME ( 6 FDA reports)
POSTOPERATIVE THROMBOSIS ( 6 FDA reports)
PRECANCEROUS CELLS PRESENT ( 6 FDA reports)
PRECANCEROUS SKIN LESION ( 6 FDA reports)
PRESBYACUSIS ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PROSTHESIS IMPLANTATION ( 6 FDA reports)
PSOAS ABSCESS ( 6 FDA reports)
PSYCHOLOGICAL TRAUMA ( 6 FDA reports)
PULMONARY CALCIFICATION ( 6 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 6 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 6 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 6 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
SCLERODACTYLIA ( 6 FDA reports)
SKIN CHAPPED ( 6 FDA reports)
SKIN EROSION ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STOOL ANALYSIS ABNORMAL ( 6 FDA reports)
SUPERINFECTION ( 6 FDA reports)
TARSAL TUNNEL SYNDROME ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
THERAPEUTIC PROCEDURE ( 6 FDA reports)
THROMBOEMBOLIC STROKE ( 6 FDA reports)
THYROGLOBULIN INCREASED ( 6 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 6 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
URINARY BLADDER POLYP ( 6 FDA reports)
UTERINE NEOPLASM ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VASCULAR OPERATION ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 6 FDA reports)
VESTIBULITIS ( 6 FDA reports)
VIRAL LABYRINTHITIS ( 6 FDA reports)
VIRAL PHARYNGITIS ( 6 FDA reports)
VITILIGO ( 6 FDA reports)
VOCAL CORD ATROPHY ( 6 FDA reports)
VOLUME BLOOD DECREASED ( 6 FDA reports)
WHITE BLOOD CELL DISORDER ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
YAWNING ( 6 FDA reports)
ABDOMINAL BRUIT ( 6 FDA reports)
ACARODERMATITIS ( 6 FDA reports)
ACCOMMODATION DISORDER ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ANGIOGRAM ABNORMAL ( 6 FDA reports)
ANTICOAGULANT THERAPY ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 6 FDA reports)
AORTIC ANEURYSM RUPTURE ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
AORTIC OCCLUSION ( 6 FDA reports)
APPLICATION SITE DERMATITIS ( 6 FDA reports)
ARTERIAL INSUFFICIENCY ( 6 FDA reports)
ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
BENIGN DUODENAL NEOPLASM ( 6 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 6 FDA reports)
BLADDER OPERATION ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 6 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 6 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD OESTROGEN DECREASED ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BLOOD VISCOSITY INCREASED ( 6 FDA reports)
BLOODY DISCHARGE ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BREAST LUMP REMOVAL ( 6 FDA reports)
BURNING MOUTH SYNDROME ( 6 FDA reports)
CALCIPHYLAXIS ( 6 FDA reports)
CALCIUM DEFICIENCY ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARBON DIOXIDE DECREASED ( 6 FDA reports)
CATATONIA ( 6 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 6 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 6 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 6 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 6 FDA reports)
CERVIX DISORDER ( 6 FDA reports)
CHEST INJURY ( 6 FDA reports)
CHROMATOPSIA ( 6 FDA reports)
COELIAC ARTERY STENOSIS ( 6 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 6 FDA reports)
COMPLEX PARTIAL SEIZURES ( 6 FDA reports)
COMPULSIVE SHOPPING ( 6 FDA reports)
CONJUNCTIVITIS VIRAL ( 6 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 6 FDA reports)
CORNEAL SCAR ( 6 FDA reports)
COXSACKIE VIRAL INFECTION ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DEATH OF RELATIVE ( 6 FDA reports)
DEPERSONALISATION ( 6 FDA reports)
DEVICE RELATED SEPSIS ( 6 FDA reports)
DISSOCIATIVE DISORDER ( 6 FDA reports)
DRUG EFFECT DELAYED ( 6 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
DYSPLASIA ( 6 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 6 FDA reports)
ENANTHEMA ( 6 FDA reports)
ENTEROCELE ( 6 FDA reports)
EPIDERMAL NECROSIS ( 6 FDA reports)
EPIGLOTTITIS ( 6 FDA reports)
EUSTACHIAN TUBE PATULOUS ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FEAR OF DISEASE ( 6 FDA reports)
FELTY'S SYNDROME ( 6 FDA reports)
FIBROADENOMA OF BREAST ( 6 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 6 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 6 FDA reports)
GASTRIC OPERATION ( 6 FDA reports)
GASTRODUODENAL ULCER ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
GINGIVAL OPERATION ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
HAEMOGLOBIN ABNORMAL ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HALLUCINATION, OLFACTORY ( 6 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 6 FDA reports)
HEAD TITUBATION ( 6 FDA reports)
HEMICEPHALALGIA ( 6 FDA reports)
HEPATIC CALCIFICATION ( 6 FDA reports)
HEPATITIS A ( 6 FDA reports)
HEPATITIS ALCOHOLIC ( 6 FDA reports)
HERPES OESOPHAGITIS ( 6 FDA reports)
HORMONE THERAPY ( 6 FDA reports)
HYPERAMYLASAEMIA ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOPNOEA ( 6 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
INJECTION SITE PAPULE ( 6 FDA reports)
INJECTION SITE STINGING ( 6 FDA reports)
INTESTINAL DILATATION ( 6 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
JUVENILE ARTHRITIS ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 6 FDA reports)
LEUKOENCEPHALOPATHY ( 6 FDA reports)
LEUKOPLAKIA ORAL ( 6 FDA reports)
LIMB ASYMMETRY ( 6 FDA reports)
LIPOATROPHY ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUPUS NEPHRITIS ( 6 FDA reports)
MANDIBULAR PROSTHESIS USER ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 6 FDA reports)
METAMORPHOPSIA ( 6 FDA reports)
METASTASES TO SPLEEN ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCLE HAEMORRHAGE ( 6 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 6 FDA reports)
MYELITIS ( 6 FDA reports)
MYOCARDIAL RUPTURE ( 6 FDA reports)
NEUROGENIC BOWEL ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
OVARIAN ENLARGEMENT ( 6 FDA reports)
PANCREATIC PSEUDOCYST ( 6 FDA reports)
PANNICULITIS LOBULAR ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PARATHYROID DISORDER ( 6 FDA reports)
PAROPHTHALMIA ( 6 FDA reports)
PAROTITIS ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PERIANAL ABSCESS ( 6 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 6 FDA reports)
PERIPHERAL NERVE LESION ( 6 FDA reports)
PERIRECTAL ABSCESS ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHLEBOLITH ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PITUITARY TUMOUR ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 6 FDA reports)
POLYCYTHAEMIA VERA ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POOR SUCKING REFLEX ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 5 FDA reports)
ABDOMINAL WALL DISORDER ( 5 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 5 FDA reports)
ABNORMAL WEIGHT GAIN ( 5 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ALDOLASE INCREASED ( 5 FDA reports)
ALVEOLITIS ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
ANAL POLYP ( 5 FDA reports)
ANAL PRURITUS ( 5 FDA reports)
ANDROGEN DEFICIENCY ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 5 FDA reports)
ANTITHROMBIN III DECREASED ( 5 FDA reports)
APPLICATION SITE SWELLING ( 5 FDA reports)
APTYALISM ( 5 FDA reports)
ARM AMPUTATION ( 5 FDA reports)
ARTERIAL BYPASS OPERATION ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
ARTHROPOD STING ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 5 FDA reports)
BASEDOW'S DISEASE ( 5 FDA reports)
BED REST ( 5 FDA reports)
BENIGN COLONIC NEOPLASM ( 5 FDA reports)
BENIGN NEOPLASM OF SKIN ( 5 FDA reports)
BICUSPID AORTIC VALVE ( 5 FDA reports)
BILIARY CYST ( 5 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 5 FDA reports)
BLOOD LACTIC ACID INCREASED ( 5 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BLOOD SODIUM ABNORMAL ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES ( 5 FDA reports)
BONE DENSITY ABNORMAL ( 5 FDA reports)
BONE GRAFT LYSIS ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BOVINE TUBERCULOSIS ( 5 FDA reports)
BREAKTHROUGH PAIN ( 5 FDA reports)
BREAST DISCOMFORT ( 5 FDA reports)
BREAST NECROSIS ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
CANDIDA SEPSIS ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CAPILLARY DISORDER ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 5 FDA reports)
CARDIOVERSION ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CERVIX CARCINOMA ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
COCCYDYNIA ( 5 FDA reports)
COLONIC HAEMORRHAGE ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 5 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 5 FDA reports)
CONTRAST MEDIA REACTION ( 5 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
CSF TEST ABNORMAL ( 5 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELUSIONS ( 5 FDA reports)
DENTOFACIAL ANOMALY ( 5 FDA reports)
DERMATITIS PSORIASIFORM ( 5 FDA reports)
DERMATOMYOSITIS ( 5 FDA reports)
DIABETIC FOOT INFECTION ( 5 FDA reports)
DISLOCATION OF VERTEBRA ( 5 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 5 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 5 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 5 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 5 FDA reports)
DUODENOGASTRIC REFLUX ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOCARDITIS BACTERIAL ( 5 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 5 FDA reports)
ENTEROCOCCAL SEPSIS ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EPIPLOIC APPENDAGITIS ( 5 FDA reports)
ERYSIPELAS ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
EXTRAVASATION ( 5 FDA reports)
FACIAL NERVE DISORDER ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOAMING AT MOUTH ( 5 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 5 FDA reports)
FUNGAL SKIN INFECTION ( 5 FDA reports)
GALLBLADDER CANCER ( 5 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 5 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 5 FDA reports)
GASTROINTESTINAL NEOPLASM ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
GRAFT THROMBOSIS ( 5 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 5 FDA reports)
HEPATIC CANCER METASTATIC ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 5 FDA reports)
HIDRADENITIS ( 5 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 5 FDA reports)
HYPOCOAGULABLE STATE ( 5 FDA reports)
HYPOVITAMINOSIS ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
ILIUM FRACTURE ( 5 FDA reports)
IMPATIENCE ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INFUSION SITE REACTION ( 5 FDA reports)
INJECTION SITE ABSCESS ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 5 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 5 FDA reports)
INTUBATION COMPLICATION ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 5 FDA reports)
LIBIDO DISORDER ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LOWER LIMB DEFORMITY ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MARITAL PROBLEM ( 5 FDA reports)
MENINGITIS TUBERCULOUS ( 5 FDA reports)
MENINGITIS VIRAL ( 5 FDA reports)
MENINGOCELE ( 5 FDA reports)
MENOPAUSAL DISORDER ( 5 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 5 FDA reports)
MITRAL VALVE REPLACEMENT ( 5 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
MOANING ( 5 FDA reports)
MOUTH BREATHING ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MUSCLE SWELLING ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
NAIL GROWTH ABNORMAL ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
NO ADVERSE REACTION ( 5 FDA reports)
NODAL RHYTHM ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 5 FDA reports)
OESOPHAGEAL ACHALASIA ( 5 FDA reports)
OESOPHAGEAL PERFORATION ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
OSTEOARTHROPATHY ( 5 FDA reports)
OVARIAN NEOPLASM ( 5 FDA reports)
OXYGEN SUPPLEMENTATION ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PELVIC PROLAPSE ( 5 FDA reports)
PERITONEAL DISORDER ( 5 FDA reports)
PERTUSSIS ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
PNEUMONIA LEGIONELLA ( 5 FDA reports)
POLYARTERITIS NODOSA ( 5 FDA reports)
POST PROCEDURAL CELLULITIS ( 5 FDA reports)
POST PROCEDURAL DISCHARGE ( 5 FDA reports)
POST PROCEDURAL FISTULA ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROPIONIBACTERIUM INFECTION ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PRURIGO ( 5 FDA reports)
PSYCHOSOMATIC DISEASE ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
RECTAL ADENOMA ( 5 FDA reports)
RECTAL DISCHARGE ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
REGURGITATION OF FOOD ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RENAL NEOPLASM ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RETINAL ARTERY THROMBOSIS ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
SALMONELLOSIS ( 5 FDA reports)
SALPINGITIS ( 5 FDA reports)
SCAPULA FRACTURE ( 5 FDA reports)
SEBACEOUS HYPERPLASIA ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
SKIN DESQUAMATION ( 5 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 5 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
SPINAL CORD OPERATION ( 5 FDA reports)
SPLENIC INFARCTION ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
SUBSTANCE ABUSE ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
TESTICULAR ATROPHY ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
THOUGHT BLOCKING ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
THYROID ADENOMA ( 5 FDA reports)
TINEA INFECTION ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
TRICUSPID VALVE DISEASE ( 5 FDA reports)
TRISOMY 21 ( 5 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
URETHRAL POLYP ( 5 FDA reports)
VAGINAL DISORDER ( 5 FDA reports)
VAGINAL DYSPLASIA ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VASECTOMY ( 5 FDA reports)
VENOUS INJURY ( 5 FDA reports)
VENTRICULAR FAILURE ( 5 FDA reports)
VITAMIN D ABNORMAL ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
WANDERING PACEMAKER ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WOUND CLOSURE ( 5 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 4 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 4 FDA reports)
POST PROCEDURAL VOMITING ( 4 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PROCEDURAL NAUSEA ( 4 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PYELONEPHRITIS CHRONIC ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
RADIATION SKIN INJURY ( 4 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 4 FDA reports)
RASH SCALY ( 4 FDA reports)
RECTAL CANCER METASTATIC ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 4 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 4 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 4 FDA reports)
SALIVARY GLAND DISORDER ( 4 FDA reports)
SARCOMA OF SKIN ( 4 FDA reports)
SCLERAL HAEMORRHAGE ( 4 FDA reports)
SEPTOPLASTY ( 4 FDA reports)
SERUM SEROTONIN INCREASED ( 4 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 4 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SOMATIC DELUSION ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL CORD HERNIATION ( 4 FDA reports)
SPINAL HAEMATOMA ( 4 FDA reports)
STIFF-MAN SYNDROME ( 4 FDA reports)
STITCH ABSCESS ( 4 FDA reports)
STRESS AT WORK ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 4 FDA reports)
TENDON OPERATION ( 4 FDA reports)
TESTICULAR CYST ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
THYROID CYST ( 4 FDA reports)
THYROID OPERATION ( 4 FDA reports)
TOLOSA-HUNT SYNDROME ( 4 FDA reports)
TONGUE INJURY ( 4 FDA reports)
TONIC CLONIC MOVEMENTS ( 4 FDA reports)
TONSILLECTOMY ( 4 FDA reports)
TOOTH CROWDING ( 4 FDA reports)
TORTICOLLIS ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
TRIGEMINAL NERVE DISORDER ( 4 FDA reports)
TUBERCULIN TEST POSITIVE ( 4 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 4 FDA reports)
URETHRAL CARUNCLE ( 4 FDA reports)
URETHRAL DISCHARGE ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
VAGINAL LESION ( 4 FDA reports)
VAGINITIS ATROPHIC ( 4 FDA reports)
VARICOSE VEIN RUPTURED ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VIRAEMIA ( 4 FDA reports)
VIRAL SINUSITIS ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
X-RAY DENTAL ( 4 FDA reports)
XERODERMA ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 4 FDA reports)
ACUTE STRESS DISORDER ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
AIR EMBOLISM ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANAL CANCER METASTATIC ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
ANEURYSM RUPTURED ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANTISOCIAL BEHAVIOUR ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APLASIA ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
APPLICATION SITE INFLAMMATION ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 4 FDA reports)
ARTERY DISSECTION ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
ATRIAL THROMBOSIS ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BASILAR MIGRAINE ( 4 FDA reports)
BENCE JONES PROTEINURIA ( 4 FDA reports)
BILIARY CIRRHOSIS ( 4 FDA reports)
BIOPSY LIP ( 4 FDA reports)
BIPOLAR II DISORDER ( 4 FDA reports)
BLADDER DISTENSION ( 4 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE INFECTION ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BREAST CANCER STAGE III ( 4 FDA reports)
BREAST HAEMORRHAGE ( 4 FDA reports)
CANDIDA TEST POSITIVE ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 4 FDA reports)
CARCINOID TUMOUR ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC INFECTION ( 4 FDA reports)
CARDIAC PERFORATION ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CAROTID ARTERY ANEURYSM ( 4 FDA reports)
CATHETER SITE PHLEBITIS ( 4 FDA reports)
CELLS IN URINE ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CERVICAL POLYP ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
CHLORACNE ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 4 FDA reports)
CHONDRITIS ( 4 FDA reports)
CHONDROPLASTY ( 4 FDA reports)
CHONDROSIS ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 4 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 4 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 4 FDA reports)
CORONARY ARTERY DISSECTION ( 4 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DEAFNESS TRANSITORY ( 4 FDA reports)
DEATH OF PARENT ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DENTAL NECROSIS ( 4 FDA reports)
DERMATITIS INFECTED ( 4 FDA reports)
DERMOGRAPHISM ( 4 FDA reports)
DEVICE INEFFECTIVE ( 4 FDA reports)
DIABETIC ENTEROPATHY ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 4 FDA reports)
ENDOSCOPY ABNORMAL ( 4 FDA reports)
EOSINOPHIL COUNT DECREASED ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
ESCHERICHIA TEST POSITIVE ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
FAT EMBOLISM ( 4 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOLLICULAR THYROID CANCER ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
GASTRECTOMY ( 4 FDA reports)
GASTRIC BANDING ( 4 FDA reports)
GASTRIC NEOPLASM ( 4 FDA reports)
GASTRIC PH DECREASED ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GENERAL ANAESTHESIA ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GLOBULINS DECREASED ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 4 FDA reports)
GLOMERULOSCLEROSIS ( 4 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAEMORRHOID OPERATION ( 4 FDA reports)
HEART TRANSPLANT ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC INFARCTION ( 4 FDA reports)
HEPATIC INFECTION ( 4 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HIP DEFORMITY ( 4 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HOMELESS ( 4 FDA reports)
HYDROMYELIA ( 4 FDA reports)
HYPERADRENALISM ( 4 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
IMPLANT SITE PAIN ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INGUINAL MASS ( 4 FDA reports)
INJECTION SITE COLDNESS ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE DRYNESS ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTESTINAL MASS ( 4 FDA reports)
INTESTINAL PROLAPSE ( 4 FDA reports)
INVESTIGATION ABNORMAL ( 4 FDA reports)
JOINT ANKYLOSIS ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 4 FDA reports)
LACRIMAL DISORDER ( 4 FDA reports)
LAGOPHTHALMOS ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LITHOTRIPSY ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LOCKED-IN SYNDROME ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 4 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MALOCCLUSION ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 4 FDA reports)
MOLE EXCISION ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MUSCLE GRAFT ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYOPATHY TOXIC ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NAIL INJURY ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NEOVASCULARISATION ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OSTECTOMY ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
OSTEOGENESIS IMPERFECTA ( 4 FDA reports)
OSTEOMYELITIS FUNGAL ( 4 FDA reports)
OVARIAN INFECTION ( 4 FDA reports)
PANCREATIC ENLARGEMENT ( 4 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PERICARDITIS CONSTRICTIVE ( 4 FDA reports)
PERIDIVERTICULAR ABSCESS ( 4 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PHAEOCHROMOCYTOMA ( 4 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 4 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POLYMYALGIA ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABNORMAL LABOUR ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ABSCESS SOFT TISSUE ( 3 FDA reports)
ACCIDENT AT HOME ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACID BASE BALANCE ABNORMAL ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ADENOIDECTOMY ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALCOHOL INTOLERANCE ( 3 FDA reports)
ALCOHOLIC ( 3 FDA reports)
ALLERGIC SINUSITIS ( 3 FDA reports)
ALVEOLAR PROTEINOSIS ( 3 FDA reports)
AMNESTIC DISORDER ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAEMIA MEGALOBLASTIC ( 3 FDA reports)
ANAL DISCOMFORT ( 3 FDA reports)
ANAPHYLACTOID SYNDROME OF PREGNANCY ( 3 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 3 FDA reports)
ANDROGENS DECREASED ( 3 FDA reports)
ANGIOSARCOMA ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTIBODY TEST ABNORMAL ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APICAL GRANULOMA ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
APPLICATION SITE PAPULES ( 3 FDA reports)
APPLICATION SITE ULCER ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL STENT INSERTION ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
AURA ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
AXILLARY VEIN THROMBOSIS ( 3 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA LOW GRADE ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BASILAR ARTERY STENOSIS ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BENIGN RENAL NEOPLASM ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BENIGN UTERINE NEOPLASM ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 3 FDA reports)
BITE ( 3 FDA reports)
BLADDER DYSFUNCTION ( 3 FDA reports)
BLADDER HYPERTROPHY ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER STENOSIS ( 3 FDA reports)
BLASTOMYCOSIS ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD AMYLASE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 3 FDA reports)
BLOOD KETONE BODY INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD URIC ACID ABNORMAL ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRAIN STEM ISCHAEMIA ( 3 FDA reports)
BRAIN STEM THROMBOSIS ( 3 FDA reports)
BREAST CANCER MALE ( 3 FDA reports)
BREAST DISCHARGE ( 3 FDA reports)
BREAST INFECTION ( 3 FDA reports)
BREAST NEOPLASM ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
BURNOUT SYNDROME ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOMA IN SITU OF SKIN ( 3 FDA reports)
CARDIAC ABLATION ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CAROTID ARTERY THROMBOSIS ( 3 FDA reports)
CAROTID ENDARTERECTOMY ( 3 FDA reports)
CARTILAGE GRAFT ( 3 FDA reports)
CATARACT OPERATION COMPLICATION ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CHEMICAL INJURY ( 3 FDA reports)
CHEST WALL CYST ( 3 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLON CANCER RECURRENT ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL REFLEX DECREASED ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CRANIAL NERVE DISORDER ( 3 FDA reports)
CRANIAL NERVE PARALYSIS ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 3 FDA reports)
CRUSH SYNDROME ( 3 FDA reports)
DEATH OF SPOUSE ( 3 FDA reports)
DEGENERATION OF UTERINE FIBROID ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC MICROANGIOPATHY ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DNA ANTIBODY POSITIVE ( 3 FDA reports)
DRUG EFFECT PROLONGED ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
EJECTION FRACTION ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
EMBOLIA CUTIS MEDICAMENTOSA ( 3 FDA reports)
ENCHONDROMATOSIS ( 3 FDA reports)
ENDOCRINE DISORDER ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EYE ALLERGY ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
EYELID MARGIN CRUSTING ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
FACIAL NEURALGIA ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FRACTURED ISCHIUM ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
FUNGATING WOUND ( 3 FDA reports)
GAS GANGRENE ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTROENTERITIS RADIATION ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GLIOMA ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 3 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRUNTING ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HYPERANDROGENISM ( 3 FDA reports)
HYPERLIPASAEMIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTROPHY BREAST ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INFECTED BITES ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
INFLAMMATION LOCALISED ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE OEDEMA ( 3 FDA reports)
INJECTION SITE SCAR ( 3 FDA reports)
INSULIN RESISTANCE SYNDROME ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERNAL INJURY ( 3 FDA reports)
INTERTRIGO ( 3 FDA reports)
INTESTINAL GANGRENE ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
IRIS DISORDER ( 3 FDA reports)
IRREGULAR SLEEP PHASE ( 3 FDA reports)
ITCHING SCAR ( 3 FDA reports)
JOINT ABSCESS ( 3 FDA reports)
JOINT LIGAMENT RUPTURE ( 3 FDA reports)
KETOSIS ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 3 FDA reports)
LIGAMENT OPERATION ( 3 FDA reports)
LIGAMENT PAIN ( 3 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LIPID METABOLISM DISORDER ( 3 FDA reports)
LIPOMA EXCISION ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG LOBECTOMY ( 3 FDA reports)
LYMPH NODE CANCER METASTATIC ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
MACULAR CYST ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MALE SEXUAL DYSFUNCTION ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MENINGEAL NEOPLASM ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
METASTASES TO GALLBLADDER ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MONONEUROPATHY ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MYASTHENIC SYNDROME ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NASAL SEPTUM PERFORATION ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NECK SURGERY ( 3 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 3 FDA reports)
NOSE DEFORMITY ( 3 FDA reports)
OBESITY SURGERY ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OBTURATOR HERNIA ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
ONYCHORRHEXIS ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPIATES POSITIVE ( 3 FDA reports)
OPTIC DISC HAEMORRHAGE ( 3 FDA reports)
ORAL LICHEN PLANUS ( 3 FDA reports)
OSTEOSARCOMA METASTATIC ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
OXYGEN SATURATION ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PELVIC CONGESTION ( 3 FDA reports)
PENILE SWELLING ( 3 FDA reports)
PEPTIC ULCER PERFORATION ( 3 FDA reports)
PERICARDITIS TUBERCULOUS ( 3 FDA reports)
PERINEAL ABSCESS ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL CARCINOMA ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
PHARYNGEAL CYST ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PHOBIA ( 3 FDA reports)
PICA ( 3 FDA reports)
PINGUECULA ( 3 FDA reports)
PLASMA CELLS INCREASED ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYMENORRHOEA ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
POST PROCEDURAL OEDEMA ( 3 FDA reports)
POSTICTAL PARALYSIS ( 3 FDA reports)
POSTMENOPAUSE ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PREMATURE MENOPAUSE ( 3 FDA reports)
PREMENSTRUAL SYNDROME ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 3 FDA reports)
PRODUCT PACKAGING ISSUE ( 3 FDA reports)
PRODUCT TAMPERING ( 3 FDA reports)
PROSTATECTOMY ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 3 FDA reports)
PROTEIN C DEFICIENCY ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RADIAL NERVE INJURY ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
REBOUND HYPERTENSION ( 3 FDA reports)
RECALL PHENOMENON ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 3 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
REHABILITATION THERAPY ( 3 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
REPERFUSION ARRHYTHMIA ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY TRACT OEDEMA ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 3 FDA reports)
RHEUMATOID VASCULITIS ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 3 FDA reports)
SCAN ABDOMEN ABNORMAL ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SKIN GRAFT FAILURE ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SLEEP TERROR ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SOCIAL PHOBIA ( 3 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 3 FDA reports)
SPINAL CORD INFARCTION ( 3 FDA reports)
SPLENIC VEIN THROMBOSIS ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
STREPTOCOCCAL ABSCESS ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 3 FDA reports)
SUCROSE INTOLERANCE ( 3 FDA reports)
SUTURE INSERTION ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
TABLET ISSUE ( 3 FDA reports)
TETANY ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOLYSIS ( 3 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 3 FDA reports)
THYMUS DISORDER ( 3 FDA reports)
THYROID GLAND CANCER ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TRAUMATIC ARTHROPATHY ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINE CALCIUM INCREASED ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
UTEROVAGINAL PROLAPSE ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VAGINITIS ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR GRAFT COMPLICATION ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VENTRICULAR ASYSTOLE ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
VOLVULUS OF BOWEL ( 3 FDA reports)
VULVA CYST ( 3 FDA reports)
VULVAL CANCER STAGE I ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WHOLE BLOOD TRANSFUSION ( 3 FDA reports)
WRIST SURGERY ( 3 FDA reports)
X-RAY LIMB ABNORMAL ( 3 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PROSTATIC HAEMORRHAGE ( 2 FDA reports)
PROSTHESIS USER ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN S INCREASED ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY ANEURYSM ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RADIOTHERAPY TO BRAIN ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETROSTERNAL INFECTION ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RIB HYPOPLASIA ( 2 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 2 FDA reports)
ROSEOLA ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVA DISCOLOURATION ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SECONDARY SYPHILIS ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SENILE OSTEOPOROSIS ( 2 FDA reports)
SENSATION OF BLOCK IN EAR ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SICK RELATIVE ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SINUS CANCER METASTATIC ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SKIN WOUND ( 2 FDA reports)
SLOW SPEECH ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPERM CONCENTRATION ZERO ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINA BIFIDA ( 2 FDA reports)
SPINDLE CELL SARCOMA ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
SPOUSAL ABUSE ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TAENIASIS ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TENDINOUS CONTRACTURE ( 2 FDA reports)
TERMINAL DRIBBLING ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR MASS ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THROMBIN TIME SHORTENED ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TONGUE AMYLOIDOSIS ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOTAL HYSTERECTOMY ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUBEROUS SCLEROSIS ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPE II HYPERSENSITIVITY ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETHRAL STRICTURE ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE ATONY ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UTERINE PAIN ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR FRAGILITY ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENTRICULAR WALL THICKENING ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VIRAL LOAD DECREASED ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 2 FDA reports)
VITAMIN C DECREASED ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITREOUS DEGENERATION ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 2 FDA reports)
WEIGHT ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABORTION EARLY ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 2 FDA reports)
ACQUIRED PHIMOSIS ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 2 FDA reports)
ADENOIDAL DISORDER ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ADRENALECTOMY ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AGONAL DEATH STRUGGLE ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMMONIA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIDEPRESSANT THERAPY ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARTERIAL SPASM ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
B-CELL LYMPHOMA STAGE I ( 2 FDA reports)
B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BASE EXCESS DECREASED ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BILE OUTPUT ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE CANCER METASTATIC ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW EOSINOPHILIC LEUKOCYTE COUNT INCREASED ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST DISORDER FEMALE ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCIUM IONISED ABNORMAL ( 2 FDA reports)
CALCIUM METABOLISM DISORDER ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CAPSULE ISSUE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARDIAC VALVE SCLEROSIS ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CARDITIS ( 2 FDA reports)
CATARACT CONGENITAL ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHOROIDAL HAEMORRHAGE ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 2 ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COLD-STIMULUS HEADACHE ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLONIC ATONY ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMA ACIDOTIC ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 2 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONJUNCTIVAL IRRITATION ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
CRANIAL NERVE OPERATION ( 2 FDA reports)
CRANIAL NEUROPATHY ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CULTURE URINE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYSTITIS GLANDULARIS ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYTOLOGY ABNORMAL ( 2 FDA reports)
DEATH OF CHILD ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DELUSIONAL DISORDER, SOMATIC TYPE ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DEVICE CONNECTION ISSUE ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DOUBLE VESSEL BYPASS GRAFT ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG NAME CONFUSION ( 2 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
EAR TUBERCULOSIS ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 2 FDA reports)
ELECTROCONVULSIVE THERAPY ( 2 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
EUSTACHIAN TUBE DISORDER ( 2 FDA reports)
EXTERNAL EAR INFLAMMATION ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELID EXFOLIATION ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
FALLOPIAN TUBE ABSCESS ( 2 FDA reports)
FALLOPIAN TUBE CANCER METASTATIC ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEAR OF NEEDLES ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEMORAL BRUIT ( 2 FDA reports)
FEMORAL NERVE INJURY ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FOREIGN BODY REACTION ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
GAIT DEVIATION ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GAMMA RADIATION THERAPY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC FISTULA ( 2 FDA reports)
GASTRIC STENOSIS ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 2 FDA reports)
GENITAL ABSCESS ( 2 FDA reports)
GENITAL INFECTION ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 2 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HEAT OEDEMA ( 2 FDA reports)
HELMINTHIC INFECTION ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOTONIC URINARY BLADDER ( 2 FDA reports)
HYPOURICAEMIA ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILIAC VEIN THROMBOSIS ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANT SITE INFLAMMATION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCISION SITE HYPOAESTHESIA ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFERTILITY FEMALE ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFUSION SITE BRUISING ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INJECTION SITE EXFOLIATION ( 2 FDA reports)
INJECTION SITE SCAB ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INTESTINAL ULCER PERFORATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 2 FDA reports)
IODINE ALLERGY ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
JAW LESION EXCISION ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 2 FDA reports)
KELOID SCAR ( 2 FDA reports)
KIDNEY ABLATION ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LABOUR COMPLICATION ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LICHEN MYXOEDEMATOSUS ( 2 FDA reports)
LIMB IMMOBILISATION ( 2 FDA reports)
LIMB REDUCTION DEFECT ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPASE ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LOCAL ANAESTHESIA ( 2 FDA reports)
LOW TENSION GLAUCOMA ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MALE ORGASMIC DISORDER ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEDICAL DEVICE CHANGE ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MELANODERMIA ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MILIA ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOSIS FUNGOIDES STAGE I ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYRINGITIS ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL ABSCESS ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL TURBINATE ABNORMALITY ( 2 FDA reports)
NASOPHARYNGEAL CANCER STAGE IV ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NERVE ROOT INJURY CERVICAL ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NITRITOID CRISIS ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-CONSUMMATION ( 2 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OCCIPITAL NEURALGIA ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL DYSPLASIA ( 2 FDA reports)
OESOPHAGEAL OPERATION ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORBITAL INFECTION ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN EPITHELIAL CANCER ( 2 FDA reports)
OVARIAN FAILURE ( 2 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PAPILLARY MUSCLE DISORDER ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARADOXICAL EMBOLISM ( 2 FDA reports)
PARAESTHESIA MUCOSAL ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARASITE STOOL TEST POSITIVE ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC INFECTION ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERIPHERAL NERVE TRANSPOSITION ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PLASMA CELL DISORDER ( 2 FDA reports)
PLASMA VISCOSITY DECREASED ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL DECORTICATION ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION OF ECTOPIC PREGNANCY ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACOUSTIC NEURITIS ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACRODYNIA ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADENOID CYSTIC CARCINOMA ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 1 FDA reports)
ANAL CANCER STAGE II ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANKLE DEFORMITY ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APPLICATION SITE ANAESTHESIA ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE MASS ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PERSPIRATION ( 1 FDA reports)
APPLICATION SITE PHOTOSENSITIVITY REACTION ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
AQUAGENIC PRURITUS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTICULAR DISC DISORDER ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPERGER'S DISORDER ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATROPHIC GLOSSITIS ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAKER'S CYST EXCISION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BAND SENSATION ( 1 FDA reports)
BANKRUPTCY ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN MESOTHELIOMA ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY ARTERY ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIOPSY STOMACH ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CYST EXCISION ( 1 FDA reports)
BONE DENSITOMETRY ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BOTULISM ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
BURN DRESSING ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CAPSULAR CONTRACTURE ASSOCIATED WITH BREAST IMPLANT ( 1 FDA reports)
CAPUT MEDUSAE ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC MONITORING ABNORMAL ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAREGIVER ( 1 FDA reports)
CARNITINE DECREASED ( 1 FDA reports)
CAROTID ANEURYSM RUPTURE ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEMENTOPLASTY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL DISCHARGE ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 1 FDA reports)
CERVIX CARCINOMA RECURRENT ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL INCREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 INCREASED ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL HEPATOMEGALY ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL DECOMPENSATION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOPLASTY ( 1 FDA reports)
CREATINE URINE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS MYOCARDITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DESQUAMATION GINGIVAL ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE SIGNAL DETECTION ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATIVE AMNESIA ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DONOR SITE COMPLICATION ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR ABRASION ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EARLY RETIREMENT ( 1 FDA reports)
ECHOCARDIOGRAM NORMAL ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EHLERS-DANLOS SYNDROME ( 1 FDA reports)
ELDERLY ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPOPLASIA ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC CYSTITIS ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EOSINOPHILS URINE ( 1 FDA reports)
EPIDEMIC PLEURODYNIA ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDURITIS ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INFECTION TOXOPLASMAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FALSE LABOUR ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FASCIECTOMY ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
FEMALE GENITAL OPERATION ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FINGER CRUSHING ( 1 FDA reports)
FINGER REPAIR OPERATION ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL TUBE REMOVAL ( 1 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL INFECTION MALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GENITOURINARY CHLAMYDIA INFECTION ( 1 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOPHILIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HAMARTOMA VASCULAR ( 1 FDA reports)
HAND REPAIR OPERATION ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEADACHE POSTOPERATIVE ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE STAGE II ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCREASED VENTRICULAR PRELOAD ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTED LYMPHOCELE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE ECZEMA ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRA-NASAL ANTROSTOMY ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS HAEMORRHAGE ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL ABNORMAL ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
IVTH NERVE PARESIS ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS SCLEROSING ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE II ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LDL/HDL RATIO INCREASED ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEG CRUSHING ( 1 FDA reports)
LESION OF SCIATIC NERVE ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOCYTE VACUOLISATION ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIPAEMIA RETINALIS ( 1 FDA reports)
LIPASE URINE INCREASED ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOID TISSUE OPERATION ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MAXILLOFACIAL SINUS NEOPLASM ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MENISCUS OPERATION ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC CARCINOID TUMOUR ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED HEPATOCELLULAR CHOLANGIOCARCINOMA ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MUCOSAL NECROSIS ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME UNCLASSIFIABLE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDITIS SEPTIC ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFECTION FUNGAL ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NOCTIPHOBIA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL CARCINOMA RECURRENT ( 1 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTRADIOL ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIVOPONTOCEREBELLAR ATROPHY ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPHTHALMIC FLUID DRAINAGE ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 1 FDA reports)
ORAL VIRAL INFECTION ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
OSLER'S NODES ( 1 FDA reports)
OSSICLE DISORDER ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVERWORK ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA CIRCUMORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PATHOLOGY TEST ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC ORGAN INJURY ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENETRATING ABDOMINAL TRAUMA ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENILE VASCULAR DISORDER ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERFORMANCE FEAR ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PILONIDAL SINUS REPAIR ( 1 FDA reports)
PINEAL GLAND CYST ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PLATELET ADHESIVENESS ABNORMAL ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
PODIATRIC EXAMINATION ABNORMAL ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTAL SHUNT ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL COUNTERFEIT ( 1 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PTERYGIUM ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION DYSPHAGIA ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RADIOTHERAPY TO PROSTATE ( 1 FDA reports)
RASH PSORIAFORM ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT CARCINOMA IN SITU ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
RETINAL FIBROSIS ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL INFECTION ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
REVISION OF INTERNAL FIXATION ( 1 FDA reports)
RHEUMATOID FACTOR DECREASED ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SARCOMA UTERUS ( 1 FDA reports)
SCAN BRAIN ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SCROTAL CYST ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SEBACEOUS ADENOMA ( 1 FDA reports)
SEBACEOUS NAEVUS ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEMEN VOLUME INCREASED ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHOULDER DEFORMITY ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIALOMETAPLASIA ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS TARSI SYNDROME ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPERMATORRHOEA ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBACUTE COMBINED CORD DEGENERATION ( 1 FDA reports)
SUBCLAVIAN ARTERY EMBOLISM ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPERINFECTION ORAL ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOSTOSIS ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
SYNOVIAL FLUID RED BLOOD CELLS POSITIVE ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON REPAIR ( 1 FDA reports)
TERATOSPERMIA ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 1 FDA reports)
THORACOPLASTY ( 1 FDA reports)
THROMBOENDARTERECTOMY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE CARCINOMA STAGE I ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE PIGMENTATION ( 1 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE DECREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TUBERCULOSIS OF INTRATHORACIC LYMPH NODES ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL DILATATION ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL PROLAPSE ( 1 FDA reports)
URINARY CYSTECTOMY ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE BARBITURATES INCREASED ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE PHOSPHATE ABNORMAL ( 1 FDA reports)
URINE POTASSIUM ABNORMAL ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UROGRAPHY ABNORMAL ( 1 FDA reports)
URTICARIA PRESSURE ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UVEITIS-GLAUCOMA-HYPHAEMA SYNDROME ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR TEST ABNORMAL ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENIPUNCTURE SITE BRUISE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VENTRICULOGRAM ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 1 FDA reports)
VIITH NERVE INJURY ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL ACUITY TESTS NORMAL ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVAL CANCER STAGE 0 ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINITIS GONOCOCCAL ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
XITH NERVE PARALYSIS ( 1 FDA reports)