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

PAIN ( 5968 FDA reports)
OSTEONECROSIS ( 5262 FDA reports)
ANXIETY ( 4949 FDA reports)
BONE DISORDER ( 4682 FDA reports)
OSTEONECROSIS OF JAW ( 4504 FDA reports)
TOOTH EXTRACTION ( 3842 FDA reports)
OSTEOMYELITIS ( 3752 FDA reports)
INJURY ( 3143 FDA reports)
PAIN IN JAW ( 3006 FDA reports)
ANAEMIA ( 2992 FDA reports)
BACK PAIN ( 2726 FDA reports)
IMPAIRED HEALING ( 2371 FDA reports)
ARTHRALGIA ( 2257 FDA reports)
DYSPNOEA ( 2257 FDA reports)
INFECTION ( 2250 FDA reports)
OSTEOARTHRITIS ( 2242 FDA reports)
FATIGUE ( 2122 FDA reports)
NAUSEA ( 1971 FDA reports)
DEPRESSION ( 1960 FDA reports)
FALL ( 1952 FDA reports)
ANHEDONIA ( 1868 FDA reports)
SPINAL OSTEOARTHRITIS ( 1867 FDA reports)
NEUROPATHY PERIPHERAL ( 1864 FDA reports)
OEDEMA PERIPHERAL ( 1802 FDA reports)
WEIGHT DECREASED ( 1780 FDA reports)
PYREXIA ( 1777 FDA reports)
OSTEOPENIA ( 1754 FDA reports)
SWELLING ( 1752 FDA reports)
DIARRHOEA ( 1673 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1658 FDA reports)
PLEURAL EFFUSION ( 1652 FDA reports)
ASTHENIA ( 1644 FDA reports)
EMOTIONAL DISTRESS ( 1628 FDA reports)
PNEUMONIA ( 1599 FDA reports)
HYPOAESTHESIA ( 1574 FDA reports)
DEFORMITY ( 1530 FDA reports)
PAIN IN EXTREMITY ( 1528 FDA reports)
HEADACHE ( 1509 FDA reports)
ATELECTASIS ( 1503 FDA reports)
HYPERTENSION ( 1494 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1468 FDA reports)
VOMITING ( 1462 FDA reports)
METASTASES TO BONE ( 1457 FDA reports)
CHEST PAIN ( 1438 FDA reports)
PRIMARY SEQUESTRUM ( 1435 FDA reports)
DECREASED INTEREST ( 1413 FDA reports)
CONSTIPATION ( 1400 FDA reports)
BONE PAIN ( 1379 FDA reports)
SINUSITIS ( 1378 FDA reports)
DENTAL CARIES ( 1345 FDA reports)
OSTEOPOROSIS ( 1345 FDA reports)
BONE LESION ( 1335 FDA reports)
DIZZINESS ( 1332 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1299 FDA reports)
DYSPHAGIA ( 1297 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1290 FDA reports)
CELLULITIS ( 1259 FDA reports)
TOOTH DISORDER ( 1222 FDA reports)
COUGH ( 1169 FDA reports)
URINARY TRACT INFECTION ( 1148 FDA reports)
INSOMNIA ( 1147 FDA reports)
BRONCHITIS ( 1138 FDA reports)
ABDOMINAL PAIN ( 1136 FDA reports)
DISABILITY ( 1107 FDA reports)
MULTIPLE MYELOMA ( 1105 FDA reports)
TOOTHACHE ( 1102 FDA reports)
PARAESTHESIA ( 1087 FDA reports)
DECREASED APPETITE ( 1082 FDA reports)
BONE DEBRIDEMENT ( 1065 FDA reports)
CATARACT ( 1048 FDA reports)
ORAL PAIN ( 1027 FDA reports)
TOOTH ABSCESS ( 1024 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1018 FDA reports)
RIB FRACTURE ( 1014 FDA reports)
ERYTHEMA ( 1004 FDA reports)
NEOPLASM MALIGNANT ( 983 FDA reports)
DEEP VEIN THROMBOSIS ( 969 FDA reports)
TOOTH LOSS ( 967 FDA reports)
GAIT DISTURBANCE ( 966 FDA reports)
INFLAMMATION ( 942 FDA reports)
CARDIOMEGALY ( 936 FDA reports)
PANCYTOPENIA ( 936 FDA reports)
FISTULA ( 929 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 928 FDA reports)
HIATUS HERNIA ( 928 FDA reports)
LYMPHADENOPATHY ( 925 FDA reports)
COMPRESSION FRACTURE ( 923 FDA reports)
DEATH ( 910 FDA reports)
RENAL FAILURE ( 906 FDA reports)
HERPES ZOSTER ( 898 FDA reports)
NECK PAIN ( 894 FDA reports)
THROMBOCYTOPENIA ( 892 FDA reports)
PURULENT DISCHARGE ( 863 FDA reports)
MUSCULOSKELETAL PAIN ( 846 FDA reports)
OSTEOLYSIS ( 844 FDA reports)
DEHYDRATION ( 836 FDA reports)
HAEMORRHOIDS ( 832 FDA reports)
JAW DISORDER ( 830 FDA reports)
DIVERTICULUM ( 821 FDA reports)
ARTHRITIS ( 813 FDA reports)
MOUTH ULCERATION ( 807 FDA reports)
GINGIVITIS ( 791 FDA reports)
OSTEITIS ( 779 FDA reports)
EXOSTOSIS ( 778 FDA reports)
VISION BLURRED ( 777 FDA reports)
MITRAL VALVE INCOMPETENCE ( 776 FDA reports)
RENAL CYST ( 771 FDA reports)
HYPERLIPIDAEMIA ( 768 FDA reports)
MUSCLE SPASMS ( 767 FDA reports)
SEQUESTRECTOMY ( 763 FDA reports)
RASH ( 755 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 753 FDA reports)
PATHOLOGICAL FRACTURE ( 748 FDA reports)
ENDODONTIC PROCEDURE ( 742 FDA reports)
HYPOKALAEMIA ( 742 FDA reports)
GINGIVAL SWELLING ( 739 FDA reports)
MUSCULAR WEAKNESS ( 732 FDA reports)
CONFUSIONAL STATE ( 721 FDA reports)
BLOOD CREATININE INCREASED ( 720 FDA reports)
MASTICATION DISORDER ( 715 FDA reports)
RENAL FAILURE CHRONIC ( 705 FDA reports)
SCOLIOSIS ( 702 FDA reports)
PHYSICAL DISABILITY ( 700 FDA reports)
SYNCOPE ( 695 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 694 FDA reports)
JAW OPERATION ( 683 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 683 FDA reports)
LOOSE TOOTH ( 680 FDA reports)
HYPOPHAGIA ( 669 FDA reports)
ACTINOMYCOSIS ( 667 FDA reports)
SWELLING FACE ( 666 FDA reports)
TOOTH FRACTURE ( 664 FDA reports)
PERIODONTAL DISEASE ( 655 FDA reports)
LUNG NEOPLASM ( 654 FDA reports)
DEBRIDEMENT ( 651 FDA reports)
ATRIAL FIBRILLATION ( 649 FDA reports)
ARTERIOSCLEROSIS ( 647 FDA reports)
STOMATITIS ( 633 FDA reports)
ORAL DISORDER ( 618 FDA reports)
CHOLELITHIASIS ( 617 FDA reports)
EXPOSED BONE IN JAW ( 617 FDA reports)
MYALGIA ( 604 FDA reports)
HYPOTENSION ( 602 FDA reports)
OSTEOSCLEROSIS ( 598 FDA reports)
TENDERNESS ( 596 FDA reports)
METASTASES TO LIVER ( 594 FDA reports)
GINGIVAL BLEEDING ( 593 FDA reports)
DYSPEPSIA ( 592 FDA reports)
NEUTROPENIA ( 588 FDA reports)
ORAL SURGERY ( 580 FDA reports)
EAR PAIN ( 578 FDA reports)
METASTASES TO SPINE ( 575 FDA reports)
BURSITIS ( 565 FDA reports)
CORONARY ARTERY DISEASE ( 565 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 564 FDA reports)
GASTRITIS ( 562 FDA reports)
LIFE EXPECTANCY SHORTENED ( 561 FDA reports)
SPINAL COMPRESSION FRACTURE ( 559 FDA reports)
DYSPNOEA EXERTIONAL ( 554 FDA reports)
SINUS DISORDER ( 543 FDA reports)
LUNG INFILTRATION ( 538 FDA reports)
RENAL FAILURE ACUTE ( 529 FDA reports)
CONTUSION ( 525 FDA reports)
GINGIVAL PAIN ( 522 FDA reports)
MALAISE ( 521 FDA reports)
KYPHOSIS ( 517 FDA reports)
CEREBROVASCULAR ACCIDENT ( 512 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 512 FDA reports)
PERIODONTITIS ( 511 FDA reports)
TOOTH INFECTION ( 508 FDA reports)
VERTIGO ( 506 FDA reports)
OEDEMA ( 504 FDA reports)
ABSCESS ( 503 FDA reports)
SURGERY ( 503 FDA reports)
SEPSIS ( 501 FDA reports)
LEUKOPENIA ( 499 FDA reports)
ROTATOR CUFF SYNDROME ( 499 FDA reports)
MASS ( 496 FDA reports)
GINGIVAL DISORDER ( 495 FDA reports)
JAW FRACTURE ( 493 FDA reports)
HAEMOGLOBIN DECREASED ( 492 FDA reports)
BONE DENSITY DECREASED ( 491 FDA reports)
GINGIVAL INFECTION ( 491 FDA reports)
LUMBAR SPINAL STENOSIS ( 487 FDA reports)
HYPERCHOLESTEROLAEMIA ( 484 FDA reports)
HEPATIC STEATOSIS ( 475 FDA reports)
NEPHROLITHIASIS ( 475 FDA reports)
DENTURE WEARER ( 473 FDA reports)
RECTAL HAEMORRHAGE ( 473 FDA reports)
DIABETES MELLITUS ( 471 FDA reports)
ASTHMA ( 469 FDA reports)
DYSURIA ( 469 FDA reports)
HAEMATURIA ( 468 FDA reports)
ABDOMINAL PAIN UPPER ( 461 FDA reports)
TACHYCARDIA ( 460 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 457 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 456 FDA reports)
BLOOD GLUCOSE INCREASED ( 453 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 445 FDA reports)
HIP FRACTURE ( 442 FDA reports)
ORAL INFECTION ( 441 FDA reports)
RESPIRATORY FAILURE ( 441 FDA reports)
MENTAL STATUS CHANGES ( 440 FDA reports)
OROPHARYNGEAL PAIN ( 436 FDA reports)
MUCOSAL INFLAMMATION ( 435 FDA reports)
METASTASES TO LUNG ( 429 FDA reports)
CHRONIC SINUSITIS ( 428 FDA reports)
DIVERTICULUM INTESTINAL ( 427 FDA reports)
FOOT FRACTURE ( 427 FDA reports)
SLEEP APNOEA SYNDROME ( 423 FDA reports)
DENTAL OPERATION ( 422 FDA reports)
COLONIC POLYP ( 418 FDA reports)
EMPHYSEMA ( 416 FDA reports)
PULMONARY EMBOLISM ( 416 FDA reports)
STAPHYLOCOCCAL INFECTION ( 416 FDA reports)
ABSCESS JAW ( 415 FDA reports)
SKIN LESION ( 412 FDA reports)
HYPOXIA ( 406 FDA reports)
HYPERCALCAEMIA ( 405 FDA reports)
VISUAL IMPAIRMENT ( 403 FDA reports)
DISCOMFORT ( 402 FDA reports)
HOT FLUSH ( 396 FDA reports)
CEREBRAL ATROPHY ( 394 FDA reports)
WEIGHT INCREASED ( 391 FDA reports)
EPISTAXIS ( 388 FDA reports)
ARTHROPATHY ( 387 FDA reports)
ALOPECIA ( 386 FDA reports)
SPONDYLOLISTHESIS ( 386 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 382 FDA reports)
BASAL CELL CARCINOMA ( 379 FDA reports)
ORAL CANDIDIASIS ( 375 FDA reports)
DISEASE PROGRESSION ( 374 FDA reports)
DEAFNESS ( 372 FDA reports)
ABSCESS DRAINAGE ( 371 FDA reports)
BONE SCAN ABNORMAL ( 371 FDA reports)
STEM CELL TRANSPLANT ( 371 FDA reports)
HAEMORRHAGE ( 370 FDA reports)
CYST ( 369 FDA reports)
PRURITUS ( 368 FDA reports)
SOFT TISSUE DISORDER ( 365 FDA reports)
CHILLS ( 363 FDA reports)
HYPOTHYROIDISM ( 362 FDA reports)
BLOOD CALCIUM DECREASED ( 360 FDA reports)
DYSGEUSIA ( 360 FDA reports)
HEPATIC CYST ( 360 FDA reports)
WOUND DEBRIDEMENT ( 359 FDA reports)
NEURALGIA ( 350 FDA reports)
ORAL DISCOMFORT ( 350 FDA reports)
PULMONARY HYPERTENSION ( 349 FDA reports)
TREMOR ( 349 FDA reports)
AMNESIA ( 348 FDA reports)
HYPONATRAEMIA ( 347 FDA reports)
HYPERGLYCAEMIA ( 345 FDA reports)
MYOCARDIAL INFARCTION ( 345 FDA reports)
HYPOAESTHESIA ORAL ( 341 FDA reports)
NASAL CONGESTION ( 341 FDA reports)
DENTAL FISTULA ( 340 FDA reports)
GINGIVAL ULCERATION ( 339 FDA reports)
PALPITATIONS ( 339 FDA reports)
CERVICAL SPINAL STENOSIS ( 337 FDA reports)
JOINT SWELLING ( 336 FDA reports)
ASEPTIC NECROSIS BONE ( 335 FDA reports)
DRY MOUTH ( 332 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 332 FDA reports)
JOINT EFFUSION ( 329 FDA reports)
GINGIVAL RECESSION ( 328 FDA reports)
OESOPHAGITIS ( 328 FDA reports)
HYDRONEPHROSIS ( 327 FDA reports)
HAEMATOCHEZIA ( 325 FDA reports)
TENDONITIS ( 325 FDA reports)
SYNOVIAL CYST ( 324 FDA reports)
SPINAL COLUMN STENOSIS ( 323 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 322 FDA reports)
SENSITIVITY OF TEETH ( 321 FDA reports)
SCAR ( 318 FDA reports)
NEOPLASM PROGRESSION ( 317 FDA reports)
DIPLOPIA ( 316 FDA reports)
FEMUR FRACTURE ( 316 FDA reports)
ORAL CAVITY FISTULA ( 315 FDA reports)
CANDIDIASIS ( 314 FDA reports)
CARDIOMYOPATHY ( 314 FDA reports)
SINUS TACHYCARDIA ( 311 FDA reports)
CARPAL TUNNEL SYNDROME ( 310 FDA reports)
IRON DEFICIENCY ANAEMIA ( 308 FDA reports)
CHEST DISCOMFORT ( 307 FDA reports)
BACTERIAL INFECTION ( 306 FDA reports)
ERECTILE DYSFUNCTION ( 303 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 301 FDA reports)
FACIAL PAIN ( 300 FDA reports)
EATING DISORDER ( 297 FDA reports)
HEPATIC LESION ( 290 FDA reports)
BONE OPERATION ( 286 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 286 FDA reports)
TYPE 2 DIABETES MELLITUS ( 286 FDA reports)
VISUAL ACUITY REDUCED ( 286 FDA reports)
ONYCHOMYCOSIS ( 285 FDA reports)
PULMONARY OEDEMA ( 285 FDA reports)
CONVULSION ( 284 FDA reports)
ACTINIC KERATOSIS ( 282 FDA reports)
DECUBITUS ULCER ( 282 FDA reports)
MIGRAINE ( 282 FDA reports)
URINARY RETENTION ( 282 FDA reports)
HYPERKALAEMIA ( 281 FDA reports)
ABDOMINAL DISCOMFORT ( 279 FDA reports)
BREAST CANCER METASTATIC ( 278 FDA reports)
NIGHT SWEATS ( 278 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 277 FDA reports)
EJECTION FRACTION DECREASED ( 276 FDA reports)
PURULENCE ( 276 FDA reports)
RADICULOPATHY ( 276 FDA reports)
URINARY INCONTINENCE ( 276 FDA reports)
WOUND DEHISCENCE ( 276 FDA reports)
SKIN ULCER ( 274 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 274 FDA reports)
GLAUCOMA ( 273 FDA reports)
BONE SWELLING ( 272 FDA reports)
SEBORRHOEIC KERATOSIS ( 272 FDA reports)
PULMONARY FIBROSIS ( 271 FDA reports)
BREATH ODOUR ( 269 FDA reports)
HAEMOPTYSIS ( 269 FDA reports)
RADIOTHERAPY ( 269 FDA reports)
PULMONARY CONGESTION ( 267 FDA reports)
ASCITES ( 266 FDA reports)
WHEEZING ( 266 FDA reports)
POLLAKIURIA ( 265 FDA reports)
METASTATIC NEOPLASM ( 264 FDA reports)
PERICARDIAL EFFUSION ( 264 FDA reports)
OPEN WOUND ( 263 FDA reports)
DRY EYE ( 262 FDA reports)
DYSPHONIA ( 262 FDA reports)
OBESITY ( 261 FDA reports)
FUNGAL INFECTION ( 260 FDA reports)
GOITRE ( 258 FDA reports)
MEMORY IMPAIRMENT ( 258 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 254 FDA reports)
SQUAMOUS CELL CARCINOMA ( 254 FDA reports)
WOUND DRAINAGE ( 252 FDA reports)
FEBRILE NEUTROPENIA ( 249 FDA reports)
FOOT DEFORMITY ( 249 FDA reports)
HAEMATOCRIT DECREASED ( 249 FDA reports)
HYPERHIDROSIS ( 248 FDA reports)
ABSCESS ORAL ( 247 FDA reports)
BLOOD UREA INCREASED ( 247 FDA reports)
OSTEORADIONECROSIS ( 247 FDA reports)
PRODUCTIVE COUGH ( 247 FDA reports)
BONE NEOPLASM MALIGNANT ( 246 FDA reports)
LUNG DISORDER ( 245 FDA reports)
CARDIAC ARREST ( 240 FDA reports)
THROMBOSIS ( 240 FDA reports)
PLATELET COUNT DECREASED ( 239 FDA reports)
PLEURAL FIBROSIS ( 239 FDA reports)
RHINORRHOEA ( 239 FDA reports)
SOMNOLENCE ( 238 FDA reports)
LEUKOCYTOSIS ( 237 FDA reports)
BLOOD PRESSURE INCREASED ( 236 FDA reports)
BONE LOSS ( 236 FDA reports)
LOSS OF CONSCIOUSNESS ( 236 FDA reports)
MUSCLE STRAIN ( 236 FDA reports)
ARRHYTHMIA ( 235 FDA reports)
LEFT ATRIAL DILATATION ( 235 FDA reports)
SPINAL FRACTURE ( 235 FDA reports)
INTERSTITIAL LUNG DISEASE ( 234 FDA reports)
ANGINA PECTORIS ( 233 FDA reports)
CARDIAC MURMUR ( 233 FDA reports)
IRRITABLE BOWEL SYNDROME ( 233 FDA reports)
SPINAL DISORDER ( 233 FDA reports)
AZOTAEMIA ( 230 FDA reports)
LYMPHOEDEMA ( 229 FDA reports)
BONE EROSION ( 227 FDA reports)
DEVICE RELATED INFECTION ( 226 FDA reports)
PLASMACYTOMA ( 225 FDA reports)
SCIATICA ( 225 FDA reports)
VITREOUS FLOATERS ( 224 FDA reports)
UTERINE LEIOMYOMA ( 223 FDA reports)
GINGIVAL EROSION ( 222 FDA reports)
HYPOACUSIS ( 221 FDA reports)
AORTIC VALVE INCOMPETENCE ( 219 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 219 FDA reports)
EDENTULOUS ( 218 FDA reports)
PLASMACYTOSIS ( 218 FDA reports)
ABDOMINAL DISTENSION ( 217 FDA reports)
HALLUCINATION ( 217 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 217 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 217 FDA reports)
HYPOCALCAEMIA ( 216 FDA reports)
NOCTURIA ( 216 FDA reports)
BALANCE DISORDER ( 214 FDA reports)
MALNUTRITION ( 214 FDA reports)
ROAD TRAFFIC ACCIDENT ( 214 FDA reports)
BIOPSY ( 212 FDA reports)
OSTEOMYELITIS CHRONIC ( 211 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 210 FDA reports)
GASTRIC ULCER ( 210 FDA reports)
X-RAY ABNORMAL ( 210 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 209 FDA reports)
CARDIAC DISORDER ( 208 FDA reports)
FIBROSIS ( 207 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 207 FDA reports)
ALVEOLOPLASTY ( 206 FDA reports)
MYELOMA RECURRENCE ( 206 FDA reports)
ORTHOSTATIC HYPOTENSION ( 206 FDA reports)
RHINITIS ALLERGIC ( 206 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 206 FDA reports)
TINNITUS ( 205 FDA reports)
WALKING AID USER ( 205 FDA reports)
FACET JOINT SYNDROME ( 201 FDA reports)
GOUT ( 201 FDA reports)
OEDEMA MOUTH ( 197 FDA reports)
CEREBRAL ISCHAEMIA ( 196 FDA reports)
INCISIONAL DRAINAGE ( 196 FDA reports)
NASAL SEPTUM DEVIATION ( 196 FDA reports)
BONE FRAGMENTATION ( 195 FDA reports)
PROTEINURIA ( 194 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 193 FDA reports)
CATARACT OPERATION ( 193 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 193 FDA reports)
BONE MARROW TRANSPLANT ( 192 FDA reports)
SPINAL CORD COMPRESSION ( 192 FDA reports)
SPLENOMEGALY ( 192 FDA reports)
TRISMUS ( 192 FDA reports)
PROTHROMBIN TIME PROLONGED ( 191 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 190 FDA reports)
HAEMATOMA ( 190 FDA reports)
GRANULOMA ( 188 FDA reports)
RENAL IMPAIRMENT ( 185 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 183 FDA reports)
GINGIVAL ERYTHEMA ( 183 FDA reports)
LUMBAR RADICULOPATHY ( 182 FDA reports)
NEURITIS ( 182 FDA reports)
BREAST CANCER ( 181 FDA reports)
LETHARGY ( 181 FDA reports)
INFLUENZA LIKE ILLNESS ( 180 FDA reports)
URTICARIA ( 180 FDA reports)
SINUS BRADYCARDIA ( 179 FDA reports)
ULCER ( 179 FDA reports)
HYPERPLASIA ( 178 FDA reports)
MENISCUS LESION ( 178 FDA reports)
ANKLE FRACTURE ( 177 FDA reports)
METASTASIS ( 177 FDA reports)
RESORPTION BONE INCREASED ( 177 FDA reports)
RESPIRATORY DISTRESS ( 177 FDA reports)
EYE PAIN ( 175 FDA reports)
GROIN PAIN ( 174 FDA reports)
DIVERTICULITIS ( 173 FDA reports)
DRUG HYPERSENSITIVITY ( 173 FDA reports)
JOINT DISLOCATION ( 173 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 173 FDA reports)
AORTIC ANEURYSM ( 172 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 172 FDA reports)
RENAL DISORDER ( 172 FDA reports)
DENTAL TREATMENT ( 171 FDA reports)
HYPERKERATOSIS ( 171 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 171 FDA reports)
SOFT TISSUE INFECTION ( 170 FDA reports)
ODYNOPHAGIA ( 169 FDA reports)
PNEUMOTHORAX ( 169 FDA reports)
PULMONARY MASS ( 169 FDA reports)
VERTEBROPLASTY ( 169 FDA reports)
BREAST CANCER RECURRENT ( 168 FDA reports)
CONDITION AGGRAVATED ( 168 FDA reports)
MOUTH HAEMORRHAGE ( 168 FDA reports)
POLYP ( 167 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 166 FDA reports)
RESTLESS LEGS SYNDROME ( 166 FDA reports)
CAROTID ARTERY STENOSIS ( 165 FDA reports)
RHINITIS ( 165 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 165 FDA reports)
THYROID NEOPLASM ( 165 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 164 FDA reports)
GINGIVAL OEDEMA ( 164 FDA reports)
DERMATITIS ( 163 FDA reports)
FIBROMYALGIA ( 163 FDA reports)
CHOLECYSTITIS ( 162 FDA reports)
GASTROINTESTINAL DISORDER ( 161 FDA reports)
BRUXISM ( 160 FDA reports)
CERUMEN IMPACTION ( 160 FDA reports)
TONGUE ULCERATION ( 160 FDA reports)
MOBILITY DECREASED ( 159 FDA reports)
NODULE ( 159 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 158 FDA reports)
CYSTITIS ( 157 FDA reports)
PRESYNCOPE ( 156 FDA reports)
DYSLIPIDAEMIA ( 155 FDA reports)
SOFT TISSUE INFLAMMATION ( 155 FDA reports)
ESSENTIAL HYPERTENSION ( 154 FDA reports)
METABOLIC ACIDOSIS ( 154 FDA reports)
GALLBLADDER DISORDER ( 153 FDA reports)
OVERDOSE ( 153 FDA reports)
CHOLECYSTECTOMY ( 152 FDA reports)
DEMENTIA ( 152 FDA reports)
FEELING ABNORMAL ( 152 FDA reports)
LIMB INJURY ( 152 FDA reports)
PELVIC PAIN ( 152 FDA reports)
PERONEAL NERVE PALSY ( 152 FDA reports)
DERMAL CYST ( 151 FDA reports)
FRACTURE ( 151 FDA reports)
HEPATOMEGALY ( 151 FDA reports)
PELVIC FRACTURE ( 151 FDA reports)
ORAL DISCHARGE ( 150 FDA reports)
POOR PERSONAL HYGIENE ( 150 FDA reports)
METASTASES TO LYMPH NODES ( 149 FDA reports)
ECCHYMOSIS ( 147 FDA reports)
HYPERPARATHYROIDISM ( 147 FDA reports)
CEREBRAL INFARCTION ( 146 FDA reports)
LIBIDO DECREASED ( 145 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 144 FDA reports)
BACK DISORDER ( 143 FDA reports)
HYPOMAGNESAEMIA ( 143 FDA reports)
LACERATION ( 143 FDA reports)
ILEUS ( 142 FDA reports)
BONE TRIMMING ( 141 FDA reports)
COLITIS ( 141 FDA reports)
FRACTURED SACRUM ( 141 FDA reports)
GYNAECOMASTIA ( 141 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 141 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 141 FDA reports)
RADIATION INJURY ( 140 FDA reports)
VENOUS INSUFFICIENCY ( 140 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 140 FDA reports)
HYPOPHOSPHATAEMIA ( 139 FDA reports)
SINUS HEADACHE ( 139 FDA reports)
VAGINAL INFECTION ( 139 FDA reports)
WHEELCHAIR USER ( 139 FDA reports)
ALVEOLAR OSTEITIS ( 138 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 138 FDA reports)
BONE MARROW FAILURE ( 138 FDA reports)
CATHETERISATION CARDIAC ( 138 FDA reports)
ATRIAL FLUTTER ( 137 FDA reports)
ECZEMA ( 137 FDA reports)
HIP ARTHROPLASTY ( 137 FDA reports)
SLEEP DISORDER ( 137 FDA reports)
DEVICE FAILURE ( 136 FDA reports)
FLUID OVERLOAD ( 136 FDA reports)
DEPRESSED MOOD ( 135 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 134 FDA reports)
FLANK PAIN ( 134 FDA reports)
PHARYNGITIS ( 134 FDA reports)
POLYURIA ( 134 FDA reports)
POOR DENTAL CONDITION ( 134 FDA reports)
BIOPSY BONE ABNORMAL ( 132 FDA reports)
ENCEPHALOPATHY ( 132 FDA reports)
SEPTIC SHOCK ( 132 FDA reports)
SUBCUTANEOUS ABSCESS ( 132 FDA reports)
TENDON DISORDER ( 132 FDA reports)
VASCULAR CALCIFICATION ( 132 FDA reports)
BLINDNESS ( 131 FDA reports)
LOCALISED INFECTION ( 131 FDA reports)
PROSTATOMEGALY ( 131 FDA reports)
UNRESPONSIVE TO STIMULI ( 131 FDA reports)
ORAL SOFT TISSUE DISORDER ( 130 FDA reports)
PHLEBITIS ( 130 FDA reports)
RHEUMATOID ARTHRITIS ( 130 FDA reports)
VENOUS THROMBOSIS ( 130 FDA reports)
FACE OEDEMA ( 129 FDA reports)
FAILURE TO THRIVE ( 129 FDA reports)
HAEMATEMESIS ( 129 FDA reports)
OTITIS EXTERNA ( 129 FDA reports)
ABDOMINAL HERNIA ( 128 FDA reports)
SKIN PAPILLOMA ( 128 FDA reports)
DILATATION VENTRICULAR ( 127 FDA reports)
FAECAL INCONTINENCE ( 127 FDA reports)
GASTROENTERITIS ( 127 FDA reports)
LUNG HYPERINFLATION ( 127 FDA reports)
OPEN REDUCTION OF FRACTURE ( 127 FDA reports)
ORAL HERPES ( 127 FDA reports)
OTITIS MEDIA ( 127 FDA reports)
SEASONAL ALLERGY ( 127 FDA reports)
ESCHERICHIA INFECTION ( 126 FDA reports)
LUNG NEOPLASM MALIGNANT ( 126 FDA reports)
MELAENA ( 125 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 125 FDA reports)
DYSAESTHESIA ( 124 FDA reports)
FISTULA REPAIR ( 124 FDA reports)
GINGIVAL ABSCESS ( 124 FDA reports)
HYPOGLYCAEMIA ( 124 FDA reports)
JOINT STIFFNESS ( 124 FDA reports)
MYELODYSPLASTIC SYNDROME ( 124 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 123 FDA reports)
OVARIAN CYST ( 123 FDA reports)
POLYPECTOMY ( 123 FDA reports)
SKIN DISORDER ( 123 FDA reports)
COSTOCHONDRITIS ( 122 FDA reports)
INFLUENZA ( 122 FDA reports)
KYPHOSCOLIOSIS ( 122 FDA reports)
VAGINAL HAEMORRHAGE ( 122 FDA reports)
ADRENAL INSUFFICIENCY ( 121 FDA reports)
CATHETER PLACEMENT ( 121 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 121 FDA reports)
DENTAL CARE ( 121 FDA reports)
HAEMANGIOMA ( 121 FDA reports)
NERVOUSNESS ( 121 FDA reports)
PULPITIS DENTAL ( 121 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 121 FDA reports)
TOOTH DEPOSIT ( 121 FDA reports)
DYSARTHRIA ( 120 FDA reports)
OEDEMA MUCOSAL ( 120 FDA reports)
POST HERPETIC NEURALGIA ( 120 FDA reports)
PYELONEPHRITIS ( 120 FDA reports)
AORTIC CALCIFICATION ( 119 FDA reports)
ENDOTRACHEAL INTUBATION ( 119 FDA reports)
FLUID RETENTION ( 119 FDA reports)
JOINT INJURY ( 119 FDA reports)
VIRAL INFECTION ( 119 FDA reports)
BLEPHARITIS ( 118 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 118 FDA reports)
ASTIGMATISM ( 117 FDA reports)
BONE NEOPLASM ( 117 FDA reports)
CONJUNCTIVITIS ( 117 FDA reports)
INTRAOCULAR LENS IMPLANT ( 117 FDA reports)
MAXILLOFACIAL OPERATION ( 117 FDA reports)
PARAPROTEINAEMIA ( 117 FDA reports)
RASH PRURITIC ( 117 FDA reports)
SINUS CONGESTION ( 117 FDA reports)
SINUS POLYP ( 117 FDA reports)
ACUTE SINUSITIS ( 116 FDA reports)
BARRETT'S OESOPHAGUS ( 116 FDA reports)
FACIAL BONES FRACTURE ( 116 FDA reports)
HYPOALBUMINAEMIA ( 116 FDA reports)
MITRAL VALVE CALCIFICATION ( 116 FDA reports)
SPEECH DISORDER ( 116 FDA reports)
SPINAL LAMINECTOMY ( 116 FDA reports)
MACULAR DEGENERATION ( 115 FDA reports)
TOOTH IMPACTED ( 115 FDA reports)
ANGINA UNSTABLE ( 114 FDA reports)
HEAD INJURY ( 114 FDA reports)
JOINT SPRAIN ( 114 FDA reports)
KLEBSIELLA INFECTION ( 114 FDA reports)
VENTRICULAR HYPERTROPHY ( 114 FDA reports)
BACTERAEMIA ( 113 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 113 FDA reports)
BONE FORMATION INCREASED ( 113 FDA reports)
BRONCHIECTASIS ( 113 FDA reports)
DENTAL PROSTHESIS USER ( 113 FDA reports)
PARAESTHESIA ORAL ( 113 FDA reports)
THROMBOCYTOSIS ( 113 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 112 FDA reports)
MUSCLE TWITCHING ( 112 FDA reports)
PRESBYOPIA ( 112 FDA reports)
PSORIASIS ( 112 FDA reports)
BONE GRAFT ( 111 FDA reports)
SENSORY LOSS ( 111 FDA reports)
SUICIDAL IDEATION ( 111 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 110 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 110 FDA reports)
DENTAL DISCOMFORT ( 110 FDA reports)
LACUNAR INFARCTION ( 110 FDA reports)
PEPTIC ULCER ( 110 FDA reports)
POLYNEUROPATHY ( 110 FDA reports)
ATAXIA ( 109 FDA reports)
HYPOVOLAEMIA ( 109 FDA reports)
SWOLLEN TONGUE ( 109 FDA reports)
HEPATITIS ( 108 FDA reports)
PLATELET COUNT INCREASED ( 108 FDA reports)
SKIN EXFOLIATION ( 108 FDA reports)
VITAMIN D DEFICIENCY ( 108 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 107 FDA reports)
CAROTID ARTERY DISEASE ( 107 FDA reports)
DEAFNESS NEUROSENSORY ( 107 FDA reports)
NEPHROSCLEROSIS ( 107 FDA reports)
BLOOD POTASSIUM DECREASED ( 106 FDA reports)
COORDINATION ABNORMAL ( 106 FDA reports)
HEPATIC MASS ( 106 FDA reports)
INCONTINENCE ( 106 FDA reports)
AORTIC STENOSIS ( 105 FDA reports)
MASTECTOMY ( 105 FDA reports)
SINUS OPERATION ( 105 FDA reports)
SPINAL DEFORMITY ( 105 FDA reports)
ATROPHIC VULVOVAGINITIS ( 104 FDA reports)
DENTAL PLAQUE ( 104 FDA reports)
ORAL INTAKE REDUCED ( 104 FDA reports)
BURNING SENSATION ( 103 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 103 FDA reports)
HUMERUS FRACTURE ( 103 FDA reports)
LARYNGITIS ( 103 FDA reports)
LIPOMA ( 103 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 103 FDA reports)
RASH ERYTHEMATOUS ( 103 FDA reports)
FIBULA FRACTURE ( 102 FDA reports)
LYMPHOMA ( 102 FDA reports)
VOCAL CORD PARALYSIS ( 102 FDA reports)
COLON ADENOMA ( 101 FDA reports)
INCREASED TENDENCY TO BRUISE ( 101 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 101 FDA reports)
MYOSITIS ( 101 FDA reports)
PSEUDOMONAS INFECTION ( 101 FDA reports)
WOUND INFECTION ( 101 FDA reports)
ADRENAL MASS ( 100 FDA reports)
PLANTAR FASCIITIS ( 100 FDA reports)
BLOOD CALCIUM INCREASED ( 99 FDA reports)
HEART RATE INCREASED ( 99 FDA reports)
INGROWING NAIL ( 99 FDA reports)
OSTEITIS DEFORMANS ( 99 FDA reports)
STRESS ( 99 FDA reports)
STRESS FRACTURE ( 99 FDA reports)
DISORIENTATION ( 98 FDA reports)
WOUND SECRETION ( 98 FDA reports)
BLOOD ALBUMIN DECREASED ( 97 FDA reports)
CERVICAL DYSPLASIA ( 97 FDA reports)
FOLLICULITIS ( 97 FDA reports)
LIGAMENT SPRAIN ( 97 FDA reports)
PNEUMONITIS ( 97 FDA reports)
THROMBOPHLEBITIS ( 97 FDA reports)
ABSCESS NECK ( 96 FDA reports)
COAGULOPATHY ( 96 FDA reports)
DIALYSIS ( 96 FDA reports)
NECK MASS ( 96 FDA reports)
PALATAL DISORDER ( 96 FDA reports)
PLEURITIC PAIN ( 96 FDA reports)
TENDON INJURY ( 96 FDA reports)
VIITH NERVE PARALYSIS ( 96 FDA reports)
AGRANULOCYTOSIS ( 95 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 95 FDA reports)
ANGIOEDEMA ( 95 FDA reports)
APHASIA ( 95 FDA reports)
ASPIRATION PLEURAL CAVITY ( 95 FDA reports)
CERVICOBRACHIAL SYNDROME ( 95 FDA reports)
HAND FRACTURE ( 95 FDA reports)
HILAR LYMPHADENOPATHY ( 95 FDA reports)
SUBDURAL HAEMATOMA ( 95 FDA reports)
UPPER LIMB FRACTURE ( 95 FDA reports)
VENTRICULAR TACHYCARDIA ( 95 FDA reports)
CATHETER REMOVAL ( 94 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 94 FDA reports)
LOCAL SWELLING ( 94 FDA reports)
MARROW HYPERPLASIA ( 94 FDA reports)
DILATATION ATRIAL ( 93 FDA reports)
DRY SKIN ( 93 FDA reports)
MICTURITION URGENCY ( 93 FDA reports)
MONOCLONAL GAMMOPATHY ( 93 FDA reports)
PNEUMONIA ASPIRATION ( 93 FDA reports)
BREAST MASS ( 92 FDA reports)
GASTRIC POLYPS ( 92 FDA reports)
GENERALISED OEDEMA ( 92 FDA reports)
NEURODERMATITIS ( 92 FDA reports)
THORACOTOMY ( 92 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 91 FDA reports)
DELIRIUM ( 91 FDA reports)
FEMORAL NECK FRACTURE ( 91 FDA reports)
RENAL ATROPHY ( 91 FDA reports)
UMBILICAL HERNIA ( 91 FDA reports)
VARICOSE VEIN ( 91 FDA reports)
ANOREXIA ( 90 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 90 FDA reports)
MELANOCYTIC NAEVUS ( 90 FDA reports)
MYOCLONUS ( 90 FDA reports)
RESPIRATORY TRACT INFECTION ( 90 FDA reports)
TOOTH REPAIR ( 89 FDA reports)
WOUND TREATMENT ( 89 FDA reports)
BLADDER CANCER ( 88 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 88 FDA reports)
EPICONDYLITIS ( 88 FDA reports)
FAECES DISCOLOURED ( 88 FDA reports)
NECROSIS ( 88 FDA reports)
OCULAR HYPERAEMIA ( 88 FDA reports)
SARCOIDOSIS ( 88 FDA reports)
SYNOVITIS ( 88 FDA reports)
TRANSFUSION ( 88 FDA reports)
TUMOUR MARKER INCREASED ( 88 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 88 FDA reports)
HYPOAESTHESIA FACIAL ( 87 FDA reports)
RESPIRATORY DISORDER ( 87 FDA reports)
TONGUE DISCOLOURATION ( 87 FDA reports)
CAROTID BRUIT ( 86 FDA reports)
ELECTROLYTE IMBALANCE ( 86 FDA reports)
HAEMANGIOMA OF LIVER ( 86 FDA reports)
LACRIMATION INCREASED ( 86 FDA reports)
LOBAR PNEUMONIA ( 86 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 86 FDA reports)
STREPTOCOCCAL SEPSIS ( 86 FDA reports)
CARDIOVASCULAR DISORDER ( 85 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 85 FDA reports)
MECHANICAL VENTILATION ( 85 FDA reports)
OESOPHAGEAL DISORDER ( 85 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 85 FDA reports)
WOUND ( 85 FDA reports)
AGITATION ( 84 FDA reports)
FLATULENCE ( 84 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 84 FDA reports)
MYOCARDIAL ISCHAEMIA ( 84 FDA reports)
MYOPIA ( 84 FDA reports)
PERIODONTAL OPERATION ( 84 FDA reports)
SKIN CANCER ( 84 FDA reports)
VISUAL FIELD DEFECT ( 84 FDA reports)
CALCULUS URETERIC ( 83 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 83 FDA reports)
ENCEPHALOMALACIA ( 83 FDA reports)
FRACTURE NONUNION ( 83 FDA reports)
INTESTINAL OBSTRUCTION ( 83 FDA reports)
IRRITABILITY ( 83 FDA reports)
MASS EXCISION ( 83 FDA reports)
MENINGIOMA ( 83 FDA reports)
MENTAL DISORDER ( 83 FDA reports)
RADIUS FRACTURE ( 83 FDA reports)
SPINAL HAEMANGIOMA ( 83 FDA reports)
ANEURYSM ( 82 FDA reports)
BLISTER ( 82 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 82 FDA reports)
BRADYCARDIA ( 82 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 82 FDA reports)
ATROPHY ( 81 FDA reports)
HEART RATE IRREGULAR ( 81 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 81 FDA reports)
LIVER DISORDER ( 81 FDA reports)
MITRAL VALVE PROLAPSE ( 81 FDA reports)
MYELOPATHY ( 81 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 81 FDA reports)
TONGUE DISORDER ( 81 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 80 FDA reports)
CORONARY ARTERY BYPASS ( 80 FDA reports)
DIASTOLIC DYSFUNCTION ( 80 FDA reports)
LUNG CONSOLIDATION ( 80 FDA reports)
AORTIC VALVE SCLEROSIS ( 79 FDA reports)
DRUG ABUSE ( 79 FDA reports)
ISCHAEMIA ( 79 FDA reports)
MALIGNANT MELANOMA ( 79 FDA reports)
OSTEOMYELITIS ACUTE ( 79 FDA reports)
SPINAL FUSION SURGERY ( 79 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 79 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 78 FDA reports)
HYPERMETROPIA ( 78 FDA reports)
HYPERTONIC BLADDER ( 78 FDA reports)
METAPLASIA ( 78 FDA reports)
OESOPHAGEAL STENOSIS ( 78 FDA reports)
PERIODONTAL INFECTION ( 78 FDA reports)
RASH MACULO-PAPULAR ( 78 FDA reports)
ROSACEA ( 78 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 78 FDA reports)
THYROID DISORDER ( 78 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 77 FDA reports)
MEDICAL DEVICE REMOVAL ( 77 FDA reports)
OESOPHAGEAL ULCER ( 77 FDA reports)
OROANTRAL FISTULA ( 77 FDA reports)
STRESS URINARY INCONTINENCE ( 77 FDA reports)
ADENOMA BENIGN ( 76 FDA reports)
CACHEXIA ( 76 FDA reports)
DRUG DEPENDENCE ( 76 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 76 FDA reports)
PROTEIN URINE PRESENT ( 76 FDA reports)
RADICULAR PAIN ( 76 FDA reports)
TENDON RUPTURE ( 76 FDA reports)
IMMUNODEFICIENCY ( 75 FDA reports)
CIRCULATORY COLLAPSE ( 74 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 74 FDA reports)
EAR INFECTION ( 74 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 74 FDA reports)
FISTULA DISCHARGE ( 74 FDA reports)
INTERMITTENT CLAUDICATION ( 74 FDA reports)
PETECHIAE ( 74 FDA reports)
PULMONARY GRANULOMA ( 74 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 74 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 73 FDA reports)
DISTURBANCE IN ATTENTION ( 73 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 73 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 73 FDA reports)
TOOTH INJURY ( 73 FDA reports)
UROSEPSIS ( 73 FDA reports)
VITREOUS DETACHMENT ( 73 FDA reports)
MANDIBULECTOMY ( 72 FDA reports)
OSTEOMALACIA ( 72 FDA reports)
PHOTOPSIA ( 72 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 72 FDA reports)
TACHYPNOEA ( 72 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 71 FDA reports)
EYE SWELLING ( 71 FDA reports)
HAEMODIALYSIS ( 71 FDA reports)
JOINT CREPITATION ( 71 FDA reports)
PARKINSON'S DISEASE ( 71 FDA reports)
PERIARTHRITIS ( 71 FDA reports)
RASH MACULAR ( 71 FDA reports)
BRONCHITIS CHRONIC ( 70 FDA reports)
CHONDROMALACIA ( 70 FDA reports)
GASTRITIS EROSIVE ( 70 FDA reports)
NASOPHARYNGITIS ( 70 FDA reports)
SPONDYLOLYSIS ( 70 FDA reports)
TONGUE INJURY ( 70 FDA reports)
DYSKINESIA ( 69 FDA reports)
GLIOSIS ( 69 FDA reports)
HEARING IMPAIRED ( 69 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 69 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 69 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 69 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 69 FDA reports)
APLASTIC ANAEMIA ( 68 FDA reports)
CARDIAC PACEMAKER INSERTION ( 68 FDA reports)
COLONOSCOPY ABNORMAL ( 68 FDA reports)
EROSIVE OESOPHAGITIS ( 68 FDA reports)
HYPERTHYROIDISM ( 68 FDA reports)
IMMUNOSUPPRESSION ( 68 FDA reports)
LIMB DISCOMFORT ( 68 FDA reports)
NEOPLASM ( 68 FDA reports)
PANCREATITIS ( 68 FDA reports)
STREPTOCOCCAL INFECTION ( 68 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 67 FDA reports)
BRONCHOSPASM ( 67 FDA reports)
COGNITIVE DISORDER ( 67 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 67 FDA reports)
MASTOIDITIS ( 67 FDA reports)
NERVOUS SYSTEM DISORDER ( 67 FDA reports)
OCCULT BLOOD POSITIVE ( 67 FDA reports)
PALATAL OEDEMA ( 67 FDA reports)
PAROTID GLAND ENLARGEMENT ( 67 FDA reports)
PROSTATE CANCER METASTATIC ( 67 FDA reports)
APPENDICITIS ( 66 FDA reports)
BACTERIAL TEST POSITIVE ( 66 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 66 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 66 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 66 FDA reports)
SECONDARY SEQUESTRUM ( 66 FDA reports)
SICK SINUS SYNDROME ( 66 FDA reports)
VENTRICULAR HYPOKINESIA ( 66 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 65 FDA reports)
ADENOCARCINOMA ( 65 FDA reports)
BREAST PAIN ( 65 FDA reports)
COLITIS ULCERATIVE ( 65 FDA reports)
DIABETIC NEUROPATHY ( 65 FDA reports)
ENDOCARDITIS ( 65 FDA reports)
FURUNCLE ( 65 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 65 FDA reports)
TELANGIECTASIA ( 65 FDA reports)
THYROID CANCER ( 65 FDA reports)
TOOTH EROSION ( 65 FDA reports)
VASCULITIS ( 65 FDA reports)
DERMATITIS CONTACT ( 64 FDA reports)
HYSTERECTOMY ( 64 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 64 FDA reports)
MASTOCYTOSIS ( 64 FDA reports)
POOR PERIPHERAL CIRCULATION ( 64 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 64 FDA reports)
SINUS ANTROSTOMY ( 64 FDA reports)
SUBCUTANEOUS NODULE ( 64 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 63 FDA reports)
BACK INJURY ( 63 FDA reports)
BASEDOW'S DISEASE ( 63 FDA reports)
BLOOD GLUCOSE DECREASED ( 63 FDA reports)
BODY TEMPERATURE INCREASED ( 63 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 63 FDA reports)
LYMPHADENITIS ( 63 FDA reports)
ORAL PRURITUS ( 63 FDA reports)
PARAPLEGIA ( 63 FDA reports)
POOR QUALITY SLEEP ( 63 FDA reports)
UTERINE POLYP ( 63 FDA reports)
VENOUS OCCLUSION ( 63 FDA reports)
CYSTOCELE ( 62 FDA reports)
GLOSSODYNIA ( 62 FDA reports)
HEMIPARESIS ( 62 FDA reports)
HERNIA ( 62 FDA reports)
METASTASES TO BONE MARROW ( 62 FDA reports)
MUSCLE INJURY ( 62 FDA reports)
NAIL DISORDER ( 62 FDA reports)
NEUTROPHIL COUNT INCREASED ( 62 FDA reports)
RECTOCELE ( 62 FDA reports)
ADRENAL ADENOMA ( 61 FDA reports)
AORTIC DISORDER ( 61 FDA reports)
DENTAL IMPLANTATION ( 61 FDA reports)
FAECALOMA ( 61 FDA reports)
HYDROCEPHALUS ( 61 FDA reports)
HYPERAESTHESIA ( 61 FDA reports)
METASTATIC PAIN ( 61 FDA reports)
ORAL TORUS ( 61 FDA reports)
RALES ( 61 FDA reports)
REFLUX OESOPHAGITIS ( 61 FDA reports)
RHONCHI ( 61 FDA reports)
SKIN ATROPHY ( 61 FDA reports)
SPUTUM DISCOLOURED ( 61 FDA reports)
APPENDICECTOMY ( 60 FDA reports)
BILIARY DILATATION ( 60 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 60 FDA reports)
DUODENITIS ( 60 FDA reports)
EXCORIATION ( 60 FDA reports)
GASTROINTESTINAL PAIN ( 60 FDA reports)
GRAFT VERSUS HOST DISEASE ( 60 FDA reports)
HYPERURICAEMIA ( 60 FDA reports)
HYPOGONADISM ( 60 FDA reports)
INGUINAL HERNIA ( 60 FDA reports)
LACTOSE INTOLERANCE ( 60 FDA reports)
PALLOR ( 60 FDA reports)
PANCREATIC CYST ( 60 FDA reports)
PANIC DISORDER ( 60 FDA reports)
THROMBOSIS IN DEVICE ( 60 FDA reports)
VISUAL DISTURBANCE ( 60 FDA reports)
WOUND COMPLICATION ( 60 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 59 FDA reports)
BREAST HYPERPLASIA ( 59 FDA reports)
CARDIAC FAILURE ( 59 FDA reports)
CLAVICLE FRACTURE ( 59 FDA reports)
EYELID PTOSIS ( 59 FDA reports)
PYURIA ( 59 FDA reports)
VOCAL CORD THICKENING ( 59 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 58 FDA reports)
BLOOD PRESSURE DECREASED ( 58 FDA reports)
CERVICAL CORD COMPRESSION ( 58 FDA reports)
EXOPHTHALMOS ( 58 FDA reports)
HALLUCINATION, VISUAL ( 58 FDA reports)
MONOCYTE COUNT INCREASED ( 58 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 58 FDA reports)
URETHRAL STENOSIS ( 58 FDA reports)
URINARY HESITATION ( 58 FDA reports)
VAGINAL DISCHARGE ( 58 FDA reports)
ATRIOVENTRICULAR BLOCK ( 57 FDA reports)
BLOOD BILIRUBIN INCREASED ( 57 FDA reports)
BRONCHOPNEUMONIA ( 57 FDA reports)
DUODENAL ULCER ( 57 FDA reports)
HEPATITIS C ( 57 FDA reports)
MULTIPLE SCLEROSIS ( 57 FDA reports)
MYOPATHY ( 57 FDA reports)
NASAL MUCOSAL DISORDER ( 57 FDA reports)
NASAL POLYPS ( 57 FDA reports)
PANCREATITIS ACUTE ( 57 FDA reports)
SUBMANDIBULAR MASS ( 57 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 56 FDA reports)
AORTIC DILATATION ( 56 FDA reports)
CERVICITIS ( 56 FDA reports)
MUCOSAL ULCERATION ( 56 FDA reports)
OPTIC NERVE CUPPING ( 56 FDA reports)
RECTAL POLYP ( 56 FDA reports)
THYROID CYST ( 56 FDA reports)
ADDISON'S DISEASE ( 55 FDA reports)
ANOGENITAL WARTS ( 55 FDA reports)
BACTERIAL DISEASE CARRIER ( 55 FDA reports)
BIOPSY BONE ( 55 FDA reports)
COLON CANCER ( 55 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 55 FDA reports)
DYSPHEMIA ( 55 FDA reports)
NEPHROPATHY ( 55 FDA reports)
ANAPHYLACTIC REACTION ( 54 FDA reports)
APNOEA ( 54 FDA reports)
BLOOD SODIUM DECREASED ( 54 FDA reports)
BLOOD URINE PRESENT ( 54 FDA reports)
BONE FISTULA ( 54 FDA reports)
BONE MARROW OEDEMA ( 54 FDA reports)
EATING DISORDER SYMPTOM ( 54 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 54 FDA reports)
FACIAL PALSY ( 54 FDA reports)
HYDROCELE ( 54 FDA reports)
KERATITIS ( 54 FDA reports)
MAJOR DEPRESSION ( 54 FDA reports)
ABASIA ( 53 FDA reports)
ANIMAL BITE ( 53 FDA reports)
APICAL GRANULOMA ( 53 FDA reports)
HYPERMETABOLISM ( 53 FDA reports)
NEPHROGENIC ANAEMIA ( 53 FDA reports)
PARANOIA ( 53 FDA reports)
BREAST CALCIFICATIONS ( 52 FDA reports)
BULLOUS LUNG DISEASE ( 52 FDA reports)
DERMATOPHYTOSIS ( 52 FDA reports)
DEVICE MALFUNCTION ( 52 FDA reports)
DISORDER OF ORBIT ( 52 FDA reports)
ENTEROCOCCAL INFECTION ( 52 FDA reports)
HEPATIC ENZYME INCREASED ( 52 FDA reports)
HYPERSENSITIVITY ( 52 FDA reports)
MULTI-ORGAN FAILURE ( 52 FDA reports)
MUSCLE ATROPHY ( 52 FDA reports)
PROCTALGIA ( 52 FDA reports)
ASTROCYTOMA ( 51 FDA reports)
BLADDER DISORDER ( 51 FDA reports)
BUNION ( 51 FDA reports)
COLON POLYPECTOMY ( 51 FDA reports)
CORONARY ANGIOPLASTY ( 51 FDA reports)
GASTROENTERITIS VIRAL ( 51 FDA reports)
HERNIA REPAIR ( 51 FDA reports)
KNEE ARTHROPLASTY ( 51 FDA reports)
LOWER LIMB FRACTURE ( 51 FDA reports)
NEPHROTIC SYNDROME ( 51 FDA reports)
NERVE ROOT LESION ( 51 FDA reports)
OESOPHAGEAL PAIN ( 51 FDA reports)
ORTHOSIS USER ( 51 FDA reports)
OTITIS MEDIA CHRONIC ( 51 FDA reports)
PHOTOPHOBIA ( 51 FDA reports)
PROSTATE CANCER ( 51 FDA reports)
PROSTHESIS IMPLANTATION ( 51 FDA reports)
RIGHT ATRIAL DILATATION ( 51 FDA reports)
EAR DISCOMFORT ( 50 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 50 FDA reports)
EMPYEMA ( 50 FDA reports)
GASTRODUODENITIS ( 50 FDA reports)
HISTOPLASMOSIS ( 50 FDA reports)
IMPAIRED WORK ABILITY ( 50 FDA reports)
INDURATION ( 50 FDA reports)
MULTIPLE FRACTURES ( 50 FDA reports)
MULTIPLE INJURIES ( 50 FDA reports)
NEOPLASM SKIN ( 50 FDA reports)
ORTHOPNOEA ( 50 FDA reports)
SKIN LACERATION ( 50 FDA reports)
STASIS DERMATITIS ( 50 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 50 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 50 FDA reports)
TRANSAMINASES INCREASED ( 50 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 49 FDA reports)
ENTERITIS ( 49 FDA reports)
FOREIGN BODY ( 49 FDA reports)
MENINGITIS ( 49 FDA reports)
NEUTROPHIL COUNT DECREASED ( 49 FDA reports)
PERINEURIAL CYST ( 49 FDA reports)
PUBIS FRACTURE ( 49 FDA reports)
RESTLESSNESS ( 49 FDA reports)
SERUM FERRITIN INCREASED ( 49 FDA reports)
AMAUROSIS FUGAX ( 48 FDA reports)
APHTHOUS STOMATITIS ( 48 FDA reports)
ASPIRATION ( 48 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 48 FDA reports)
EJECTION FRACTION ABNORMAL ( 48 FDA reports)
HIP SURGERY ( 48 FDA reports)
ILEUS PARALYTIC ( 48 FDA reports)
METASTASES TO MENINGES ( 48 FDA reports)
METASTASES TO PELVIS ( 48 FDA reports)
MORGANELLA INFECTION ( 48 FDA reports)
OBSTRUCTIVE UROPATHY ( 48 FDA reports)
PARATHYROID TUMOUR BENIGN ( 48 FDA reports)
VITAMIN B12 DEFICIENCY ( 48 FDA reports)
AORTIC VALVE DISEASE ( 47 FDA reports)
COMA ( 47 FDA reports)
DIABETIC RETINOPATHY ( 47 FDA reports)
EYE LASER SURGERY ( 47 FDA reports)
EYELID OEDEMA ( 47 FDA reports)
HAEMORRHAGIC DIATHESIS ( 47 FDA reports)
LABYRINTHITIS ( 47 FDA reports)
MENTAL IMPAIRMENT ( 47 FDA reports)
OCULAR HYPERTENSION ( 47 FDA reports)
POLYP COLORECTAL ( 47 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 47 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 47 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 47 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 47 FDA reports)
WRIST FRACTURE ( 47 FDA reports)
ACUTE RESPIRATORY FAILURE ( 46 FDA reports)
AFFECTIVE DISORDER ( 46 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 46 FDA reports)
BLINDNESS UNILATERAL ( 46 FDA reports)
BLOOD IRON DECREASED ( 46 FDA reports)
CARDIAC VALVE SCLEROSIS ( 46 FDA reports)
DRUG INTOLERANCE ( 46 FDA reports)
HYPERSOMNIA ( 46 FDA reports)
MENOPAUSE ( 46 FDA reports)
MUSCLE DISORDER ( 46 FDA reports)
NEUROGENIC BLADDER ( 46 FDA reports)
OLIGURIA ( 46 FDA reports)
OSTECTOMY ( 46 FDA reports)
PANCREATIC ATROPHY ( 46 FDA reports)
PROCEDURAL PAIN ( 46 FDA reports)
PROSTATITIS ( 46 FDA reports)
RENAL MASS ( 46 FDA reports)
SIALOADENITIS ( 46 FDA reports)
TRIGEMINAL NEURALGIA ( 46 FDA reports)
ADNEXA UTERI MASS ( 45 FDA reports)
BENIGN COLONIC NEOPLASM ( 45 FDA reports)
BLADDER OBSTRUCTION ( 45 FDA reports)
BLOOD POTASSIUM INCREASED ( 45 FDA reports)
CALCINOSIS ( 45 FDA reports)
CEREBROVASCULAR DISORDER ( 45 FDA reports)
DRUG TOXICITY ( 45 FDA reports)
DYSTHYMIC DISORDER ( 45 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 45 FDA reports)
PLEURISY ( 45 FDA reports)
PYELOCALIECTASIS ( 45 FDA reports)
RENAL OSTEODYSTROPHY ( 45 FDA reports)
SALIVARY GLAND DISORDER ( 45 FDA reports)
SNORING ( 45 FDA reports)
SPINAL DECOMPRESSION ( 45 FDA reports)
URGE INCONTINENCE ( 45 FDA reports)
AGGRESSION ( 44 FDA reports)
ARTHRITIS BACTERIAL ( 44 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 44 FDA reports)
BLOODY DISCHARGE ( 44 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 44 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 44 FDA reports)
EARLY SATIETY ( 44 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 44 FDA reports)
GLOSSITIS ( 44 FDA reports)
HYPERCOAGULATION ( 44 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 44 FDA reports)
LENTIGO ( 44 FDA reports)
MANDIBULAR PROSTHESIS USER ( 44 FDA reports)
MOUTH CYST ( 44 FDA reports)
OVARIAN MASS ( 44 FDA reports)
PANCREATIC CARCINOMA ( 44 FDA reports)
PHARYNGEAL OEDEMA ( 44 FDA reports)
POLYMYALGIA RHEUMATICA ( 44 FDA reports)
SEPSIS SYNDROME ( 44 FDA reports)
TOBACCO USER ( 44 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 44 FDA reports)
VEIN DISORDER ( 44 FDA reports)
ACCIDENTAL OVERDOSE ( 43 FDA reports)
ADRENAL NEOPLASM ( 43 FDA reports)
ASPIRATION JOINT ( 43 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 43 FDA reports)
EYE INFECTION ( 43 FDA reports)
GLARE ( 43 FDA reports)
HYPERTENSIVE HEART DISEASE ( 43 FDA reports)
HYPERTROPHY ( 43 FDA reports)
LIGAMENT RUPTURE ( 43 FDA reports)
MEAN CELL VOLUME INCREASED ( 43 FDA reports)
MENORRHAGIA ( 43 FDA reports)
ONYCHALGIA ( 43 FDA reports)
PSYCHOTIC DISORDER ( 43 FDA reports)
SEBORRHOEIC DERMATITIS ( 43 FDA reports)
THIRST ( 43 FDA reports)
TONSILLAR DISORDER ( 43 FDA reports)
TUBERCULOSIS ( 43 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 43 FDA reports)
VENA CAVA FILTER INSERTION ( 43 FDA reports)
VENOUS THROMBOSIS LIMB ( 43 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 42 FDA reports)
ADRENAL DISORDER ( 42 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 42 FDA reports)
BONE DENSITY INCREASED ( 42 FDA reports)
BREAST RECONSTRUCTION ( 42 FDA reports)
CARDIAC FAILURE CHRONIC ( 42 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 42 FDA reports)
GENITAL HERPES ( 42 FDA reports)
GINGIVAL ATROPHY ( 42 FDA reports)
LEUKOENCEPHALOPATHY ( 42 FDA reports)
LYMPHADENECTOMY ( 42 FDA reports)
MENIERE'S DISEASE ( 42 FDA reports)
OXYGEN SATURATION DECREASED ( 42 FDA reports)
PANIC ATTACK ( 42 FDA reports)
PAPILLOMA ( 42 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 42 FDA reports)
RETCHING ( 42 FDA reports)
SKIN DISCOLOURATION ( 42 FDA reports)
SMEAR CERVIX ABNORMAL ( 42 FDA reports)
TINEA PEDIS ( 42 FDA reports)
TOOTH DISCOLOURATION ( 42 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 42 FDA reports)
BONE CYST ( 41 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 41 FDA reports)
COLLAPSE OF LUNG ( 41 FDA reports)
CYSTITIS INTERSTITIAL ( 41 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 41 FDA reports)
FIBROMA ( 41 FDA reports)
HYPOVENTILATION ( 41 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 41 FDA reports)
LEUKAEMIA ( 41 FDA reports)
MITRAL VALVE DISEASE ( 41 FDA reports)
OROPHARYNGEAL BLISTERING ( 41 FDA reports)
OTORRHOEA ( 41 FDA reports)
PAROTITIS ( 41 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 41 FDA reports)
POLYDIPSIA ( 41 FDA reports)
RETINAL HAEMORRHAGE ( 41 FDA reports)
SKIN NEOPLASM EXCISION ( 41 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 41 FDA reports)
TENOSYNOVITIS ( 41 FDA reports)
THYROIDECTOMY ( 41 FDA reports)
ACROCHORDON ( 40 FDA reports)
ANGER ( 40 FDA reports)
CHANGE OF BOWEL HABIT ( 40 FDA reports)
DIABETIC KETOACIDOSIS ( 40 FDA reports)
FOREIGN BODY IN EYE ( 40 FDA reports)
HERPES SIMPLEX ( 40 FDA reports)
HYPERNATRAEMIA ( 40 FDA reports)
LESION EXCISION ( 40 FDA reports)
MUSCULOSKELETAL DISORDER ( 40 FDA reports)
ORAL FIBROMA ( 40 FDA reports)
OSTEOCHONDROSIS ( 40 FDA reports)
PATELLA FRACTURE ( 40 FDA reports)
TEMPERATURE INTOLERANCE ( 40 FDA reports)
THYROID MASS ( 40 FDA reports)
ULNA FRACTURE ( 40 FDA reports)
VULVOVAGINAL DRYNESS ( 40 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 39 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 39 FDA reports)
CEREBRAL ARTERY STENOSIS ( 39 FDA reports)
EXTRASYSTOLES ( 39 FDA reports)
EYE OPERATION ( 39 FDA reports)
HERPES VIRUS INFECTION ( 39 FDA reports)
HYPOGEUSIA ( 39 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 39 FDA reports)
JOINT SURGERY ( 39 FDA reports)
MACROCYTOSIS ( 39 FDA reports)
MACROGLOSSIA ( 39 FDA reports)
PARALYSIS ( 39 FDA reports)
PHYSIOTHERAPY ( 39 FDA reports)
RETINOPATHY ( 39 FDA reports)
SEDATION ( 39 FDA reports)
SKELETAL INJURY ( 39 FDA reports)
SOFT TISSUE MASS ( 39 FDA reports)
ABSCESS MANAGEMENT ( 38 FDA reports)
ACNE ( 38 FDA reports)
AGEUSIA ( 38 FDA reports)
AUTONOMIC NEUROPATHY ( 38 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 38 FDA reports)
BILIARY COLIC ( 38 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 38 FDA reports)
BONE MARROW DISORDER ( 38 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 38 FDA reports)
CHOLECYSTITIS CHRONIC ( 38 FDA reports)
DEMENTIA WITH LEWY BODIES ( 38 FDA reports)
DENTAL PULP DISORDER ( 38 FDA reports)
DEVICE OCCLUSION ( 38 FDA reports)
DRUG INEFFECTIVE ( 38 FDA reports)
GALLBLADDER POLYP ( 38 FDA reports)
GANGRENE ( 38 FDA reports)
HEART VALVE INCOMPETENCE ( 38 FDA reports)
MOOD SWINGS ( 38 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 38 FDA reports)
OLFACTORY NERVE DISORDER ( 38 FDA reports)
PARESIS ( 38 FDA reports)
PLASTIC SURGERY ( 38 FDA reports)
POST PROCEDURAL FISTULA ( 38 FDA reports)
PYOGENIC GRANULOMA ( 38 FDA reports)
SACROILIITIS ( 38 FDA reports)
SEXUAL DYSFUNCTION ( 38 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 38 FDA reports)
STOMATITIS NECROTISING ( 38 FDA reports)
TUMOUR INVASION ( 38 FDA reports)
BEDRIDDEN ( 37 FDA reports)
BLADDER CATHETERISATION ( 37 FDA reports)
BREAST CYST ( 37 FDA reports)
EYE NAEVUS ( 37 FDA reports)
HYPERPHOSPHATAEMIA ( 37 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 37 FDA reports)
JUGULAR VEIN THROMBOSIS ( 37 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 37 FDA reports)
MALOCCLUSION ( 37 FDA reports)
MELANOSIS COLI ( 37 FDA reports)
MOVEMENT DISORDER ( 37 FDA reports)
OPTIC NEURITIS ( 37 FDA reports)
SKIN HYPERPIGMENTATION ( 37 FDA reports)
VASCULAR PSEUDOANEURYSM ( 37 FDA reports)
BIPOLAR DISORDER ( 36 FDA reports)
BLINDNESS TRANSIENT ( 36 FDA reports)
BLOOD BICARBONATE DECREASED ( 36 FDA reports)
BONE GIANT CELL TUMOUR ( 36 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 36 FDA reports)
CARDIAC OPERATION ( 36 FDA reports)
CELLULITIS ORBITAL ( 36 FDA reports)
CRANIAL NERVE DISORDER ( 36 FDA reports)
CYSTITIS HAEMORRHAGIC ( 36 FDA reports)
DECREASED ACTIVITY ( 36 FDA reports)
DYSSTASIA ( 36 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 36 FDA reports)
ERUCTATION ( 36 FDA reports)
FACIAL NEURALGIA ( 36 FDA reports)
FANCONI SYNDROME ( 36 FDA reports)
HEPATIC FAILURE ( 36 FDA reports)
HYPERREFLEXIA ( 36 FDA reports)
JAUNDICE ( 36 FDA reports)
LHERMITTE'S SIGN ( 36 FDA reports)
LIP ULCERATION ( 36 FDA reports)
NEUTROPENIC SEPSIS ( 36 FDA reports)
POSTNASAL DRIP ( 36 FDA reports)
PULMONARY RADIATION INJURY ( 36 FDA reports)
SECRETION DISCHARGE ( 36 FDA reports)
SHOULDER OPERATION ( 36 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 36 FDA reports)
TEMPORAL ARTERITIS ( 36 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 36 FDA reports)
TOURETTE'S DISORDER ( 36 FDA reports)
ARTHROSCOPIC SURGERY ( 35 FDA reports)
BREAST CANCER STAGE IV ( 35 FDA reports)
DENTAL CLEANING ( 35 FDA reports)
DERMATITIS ATOPIC ( 35 FDA reports)
DISEASE RECURRENCE ( 35 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 35 FDA reports)
ENTEROCOLITIS ( 35 FDA reports)
EPIDIDYMITIS ( 35 FDA reports)
HAEMOLYTIC ANAEMIA ( 35 FDA reports)
HAIR GROWTH ABNORMAL ( 35 FDA reports)
HEPATIC CIRRHOSIS ( 35 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 35 FDA reports)
INTESTINAL ULCER ( 35 FDA reports)
NASAL ULCER ( 35 FDA reports)
PAPULE ( 35 FDA reports)
PERIOSTITIS ( 35 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 35 FDA reports)
SALIVARY GLAND PAIN ( 35 FDA reports)
SENSATION OF FOREIGN BODY ( 35 FDA reports)
SINUS ARRHYTHMIA ( 35 FDA reports)
ULCERATIVE KERATITIS ( 35 FDA reports)
UTERINE CANCER ( 35 FDA reports)
APTYALISM ( 34 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 34 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 34 FDA reports)
EXTREMITY NECROSIS ( 34 FDA reports)
GOUTY ARTHRITIS ( 34 FDA reports)
HEARING AID USER ( 34 FDA reports)
HEARING DISABILITY ( 34 FDA reports)
HYPERCAPNIA ( 34 FDA reports)
MUCOSAL HAEMORRHAGE ( 34 FDA reports)
NEOPLASM RECURRENCE ( 34 FDA reports)
ORAL FUNGAL INFECTION ( 34 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 34 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 34 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 34 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 34 FDA reports)
RENAL CANCER ( 34 FDA reports)
SCAN ABNORMAL ( 34 FDA reports)
SUTURE INSERTION ( 34 FDA reports)
TYPE 1 DIABETES MELLITUS ( 34 FDA reports)
UTERINE HAEMORRHAGE ( 34 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 34 FDA reports)
X-RAY DENTAL ( 34 FDA reports)
ANXIETY DISORDER ( 33 FDA reports)
AORTIC VALVE CALCIFICATION ( 33 FDA reports)
BIOPSY SKIN ABNORMAL ( 33 FDA reports)
CARDIAC VALVE DISEASE ( 33 FDA reports)
DEPRESSIVE SYMPTOM ( 33 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 33 FDA reports)
EYE HAEMORRHAGE ( 33 FDA reports)
EYE IRRITATION ( 33 FDA reports)
GALLBLADDER ENLARGEMENT ( 33 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 33 FDA reports)
HEAT EXHAUSTION ( 33 FDA reports)
LIP SWELLING ( 33 FDA reports)
NASAL ODOUR ( 33 FDA reports)
NERVE INJURY ( 33 FDA reports)
NON-SMALL CELL LUNG CANCER ( 33 FDA reports)
OESOPHAGITIS ULCERATIVE ( 33 FDA reports)
OPEN ANGLE GLAUCOMA ( 33 FDA reports)
ORAL NEOPLASM ( 33 FDA reports)
PERSONALITY CHANGE ( 33 FDA reports)
POST PROCEDURAL COMPLICATION ( 33 FDA reports)
RADICULITIS ( 33 FDA reports)
RASH VESICULAR ( 33 FDA reports)
RETINAL TEAR ( 33 FDA reports)
SCAPULA FRACTURE ( 33 FDA reports)
SCLEROMALACIA ( 33 FDA reports)
SPINAL COLUMN INJURY ( 33 FDA reports)
SPINAL X-RAY ABNORMAL ( 33 FDA reports)
SPLENIC CYST ( 33 FDA reports)
SPONDYLITIS ( 33 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 33 FDA reports)
STENT PLACEMENT ( 33 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 33 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 33 FDA reports)
TACHYARRHYTHMIA ( 33 FDA reports)
THERAPEUTIC PROCEDURE ( 33 FDA reports)
TREATMENT NONCOMPLIANCE ( 33 FDA reports)
ABDOMINAL PAIN LOWER ( 32 FDA reports)
BASOSQUAMOUS CARCINOMA ( 32 FDA reports)
BLADDER DIVERTICULUM ( 32 FDA reports)
BODY DYSMORPHIC DISORDER ( 32 FDA reports)
BONE LESION EXCISION ( 32 FDA reports)
BRAIN NEOPLASM ( 32 FDA reports)
BREAST CANCER IN SITU ( 32 FDA reports)
CATHETERISATION VENOUS ( 32 FDA reports)
CONJUNCTIVITIS VIRAL ( 32 FDA reports)
CRYOTHERAPY ( 32 FDA reports)
CYST RUPTURE ( 32 FDA reports)
CYSTOSCOPY ( 32 FDA reports)
DIABETIC NEPHROPATHY ( 32 FDA reports)
DROP ATTACKS ( 32 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 32 FDA reports)
GINGIVECTOMY ( 32 FDA reports)
HEART RATE DECREASED ( 32 FDA reports)
INTRACRANIAL ANEURYSM ( 32 FDA reports)
INTRACRANIAL HYPOTENSION ( 32 FDA reports)
JAW LESION EXCISION ( 32 FDA reports)
METABOLIC SYNDROME ( 32 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 32 FDA reports)
OSTEOSYNTHESIS ( 32 FDA reports)
POLYARTHRITIS ( 32 FDA reports)
RETINAL INFARCTION ( 32 FDA reports)
SPLENIC LESION ( 32 FDA reports)
ANGIOMYOLIPOMA ( 31 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 31 FDA reports)
BIOPSY GINGIVAL ( 31 FDA reports)
BONE ABSCESS ( 31 FDA reports)
BREATH SOUNDS ABNORMAL ( 31 FDA reports)
DEVICE RELATED SEPSIS ( 31 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 31 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 31 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 31 FDA reports)
GINGIVAL OPERATION ( 31 FDA reports)
INCREASED APPETITE ( 31 FDA reports)
LOWER EXTREMITY MASS ( 31 FDA reports)
MACULOPATHY ( 31 FDA reports)
MIDDLE INSOMNIA ( 31 FDA reports)
OSTEOTOMY ( 31 FDA reports)
OVARIAN CANCER ( 31 FDA reports)
PARONYCHIA ( 31 FDA reports)
PERIPHERAL COLDNESS ( 31 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 31 FDA reports)
ABDOMINAL MASS ( 30 FDA reports)
ACETABULUM FRACTURE ( 30 FDA reports)
APHONIA ( 30 FDA reports)
ARTHROSCOPY ( 30 FDA reports)
BIOPSY BLADDER ABNORMAL ( 30 FDA reports)
BLADDER NEOPLASM ( 30 FDA reports)
BLADDER OPERATION ( 30 FDA reports)
BREAST TENDERNESS ( 30 FDA reports)
BRONCHIAL SECRETION RETENTION ( 30 FDA reports)
CARDIAC SEPTAL DEFECT ( 30 FDA reports)
CEREBELLAR ATROPHY ( 30 FDA reports)
CHEST WALL MASS ( 30 FDA reports)
COLD SWEAT ( 30 FDA reports)
COLITIS ISCHAEMIC ( 30 FDA reports)
CUTIS LAXA ( 30 FDA reports)
EMBOLISM ( 30 FDA reports)
FLUID REPLACEMENT ( 30 FDA reports)
GASTRIC DISORDER ( 30 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 30 FDA reports)
HYPOPNOEA ( 30 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 30 FDA reports)
METASTASES TO SKIN ( 30 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 30 FDA reports)
OSTEOPETROSIS ( 30 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 30 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 30 FDA reports)
PROTEIN TOTAL DECREASED ( 30 FDA reports)
RENAL TUBULAR NECROSIS ( 30 FDA reports)
RESPIRATORY ARREST ( 30 FDA reports)
SCLERODERMA ( 30 FDA reports)
SKIN BURNING SENSATION ( 30 FDA reports)
SKIN EROSION ( 30 FDA reports)
SPINAL OPERATION ( 30 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 30 FDA reports)
TRACHEAL DEVIATION ( 30 FDA reports)
TRACHEOSTOMY ( 30 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 30 FDA reports)
BIPOLAR I DISORDER ( 29 FDA reports)
CARBON DIOXIDE INCREASED ( 29 FDA reports)
CEREBELLAR INFARCTION ( 29 FDA reports)
CYSTITIS NONINFECTIVE ( 29 FDA reports)
EPIDURAL LIPOMATOSIS ( 29 FDA reports)
GRAM STAIN POSITIVE ( 29 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 29 FDA reports)
LYMPH NODE CALCIFICATION ( 29 FDA reports)
MASTITIS ( 29 FDA reports)
MONONEURITIS ( 29 FDA reports)
NERVE COMPRESSION ( 29 FDA reports)
PAINFUL RESPIRATION ( 29 FDA reports)
PERICARDITIS ( 29 FDA reports)
QRS AXIS ABNORMAL ( 29 FDA reports)
SCAB ( 29 FDA reports)
SENSATION OF PRESSURE ( 29 FDA reports)
SKIN REACTION ( 29 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 29 FDA reports)
SYNOVIAL RUPTURE ( 29 FDA reports)
TENOSYNOVITIS STENOSANS ( 29 FDA reports)
UTERINE PROLAPSE ( 29 FDA reports)
VASCULAR OPERATION ( 29 FDA reports)
ALKALOSIS ( 28 FDA reports)
ANGIOPATHY ( 28 FDA reports)
APICECTOMY ( 28 FDA reports)
AUTOIMMUNE DISORDER ( 28 FDA reports)
BLADDER SPASM ( 28 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 28 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 28 FDA reports)
BOWEN'S DISEASE ( 28 FDA reports)
BRAIN INJURY ( 28 FDA reports)
BREAST NECROSIS ( 28 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 28 FDA reports)
BUNION OPERATION ( 28 FDA reports)
CLOSTRIDIAL INFECTION ( 28 FDA reports)
CREPITATIONS ( 28 FDA reports)
DYSHIDROSIS ( 28 FDA reports)
EOSINOPHILIA ( 28 FDA reports)
EPIDIDYMAL CYST ( 28 FDA reports)
EXTRASKELETAL OSSIFICATION ( 28 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 28 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 28 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 28 FDA reports)
HEPATOSPLENOMEGALY ( 28 FDA reports)
INFECTED SKIN ULCER ( 28 FDA reports)
KIDNEY INFECTION ( 28 FDA reports)
LEUKAEMIA PLASMACYTIC ( 28 FDA reports)
METASTASES TO PLEURA ( 28 FDA reports)
MICROCYTIC ANAEMIA ( 28 FDA reports)
MUCOSAL EROSION ( 28 FDA reports)
NEUROPATHY ( 28 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 28 FDA reports)
OCCULT BLOOD ( 28 FDA reports)
PROCTITIS ( 28 FDA reports)
PULMONARY ARTERY DILATATION ( 28 FDA reports)
PULMONARY HILUM MASS ( 28 FDA reports)
SENSORY DISTURBANCE ( 28 FDA reports)
SINUS POLYP DEGENERATION ( 28 FDA reports)
SMALL INTESTINE OPERATION ( 28 FDA reports)
TONGUE OEDEMA ( 28 FDA reports)
TOOTH RESORPTION ( 28 FDA reports)
TUMOUR EXCISION ( 28 FDA reports)
UTERINE ENLARGEMENT ( 28 FDA reports)
WEGENER'S GRANULOMATOSIS ( 28 FDA reports)
ACUTE CORONARY SYNDROME ( 27 FDA reports)
ADVERSE DRUG REACTION ( 27 FDA reports)
ANAEMIA MACROCYTIC ( 27 FDA reports)
ARTERIAL STENOSIS ( 27 FDA reports)
ARTERIOVENOUS FISTULA ( 27 FDA reports)
BLOOD MAGNESIUM DECREASED ( 27 FDA reports)
CARDIAC FLUTTER ( 27 FDA reports)
COLECTOMY ( 27 FDA reports)
CORNEAL DYSTROPHY ( 27 FDA reports)
FAILURE OF IMPLANT ( 27 FDA reports)
GRAVITATIONAL OEDEMA ( 27 FDA reports)
HYPOKINESIA ( 27 FDA reports)
IMMUNOGLOBULINS DECREASED ( 27 FDA reports)
IMPETIGO ( 27 FDA reports)
JOINT ARTHROPLASTY ( 27 FDA reports)
KNEE OPERATION ( 27 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 27 FDA reports)
ORTHOPEDIC PROCEDURE ( 27 FDA reports)
OSTEOGENESIS IMPERFECTA ( 27 FDA reports)
OTITIS MEDIA ACUTE ( 27 FDA reports)
PLASTIC SURGERY TO THE FACE ( 27 FDA reports)
PLATELET TRANSFUSION ( 27 FDA reports)
RESPIRATORY TRACT CONGESTION ( 27 FDA reports)
RHABDOMYOLYSIS ( 27 FDA reports)
SKIN IRRITATION ( 27 FDA reports)
SPINAL CORPECTOMY ( 27 FDA reports)
THROAT CANCER ( 27 FDA reports)
THROMBECTOMY ( 27 FDA reports)
VAGINITIS BACTERIAL ( 27 FDA reports)
VERTEBRAL WEDGING ( 27 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 27 FDA reports)
ABNORMAL SENSATION IN EYE ( 26 FDA reports)
ANGIOPLASTY ( 26 FDA reports)
AORTIC VALVE STENOSIS ( 26 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 26 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 26 FDA reports)
BLOOD CREATININE DECREASED ( 26 FDA reports)
BRAIN OEDEMA ( 26 FDA reports)
CONTRAST MEDIA REACTION ( 26 FDA reports)
COR PULMONALE CHRONIC ( 26 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 26 FDA reports)
DENTAL NECROSIS ( 26 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 26 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 26 FDA reports)
EAR HAEMORRHAGE ( 26 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 26 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 26 FDA reports)
HYDROURETER ( 26 FDA reports)
ILIAC ARTERY STENOSIS ( 26 FDA reports)
LUDWIG ANGINA ( 26 FDA reports)
METASTASES TO OVARY ( 26 FDA reports)
MITRAL VALVE REPLACEMENT ( 26 FDA reports)
OVARIAN FAILURE ( 26 FDA reports)
PLEURODESIS ( 26 FDA reports)
POSTURE ABNORMAL ( 26 FDA reports)
RADICULITIS CERVICAL ( 26 FDA reports)
RADICULITIS LUMBOSACRAL ( 26 FDA reports)
RASH PAPULAR ( 26 FDA reports)
SPINAL CORD DISORDER ( 26 FDA reports)
SPONDYLOARTHROPATHY ( 26 FDA reports)
TESTICULAR PAIN ( 26 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 26 FDA reports)
WEIGHT FLUCTUATION ( 26 FDA reports)
ALCOHOLIC LIVER DISEASE ( 25 FDA reports)
ANORECTAL DISORDER ( 25 FDA reports)
APHAGIA ( 25 FDA reports)
AXILLARY MASS ( 25 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 25 FDA reports)
BRAIN OPERATION ( 25 FDA reports)
CANCER PAIN ( 25 FDA reports)
CAPILLARY LEAK SYNDROME ( 25 FDA reports)
CARDIAC ANEURYSM ( 25 FDA reports)
CATARACT NUCLEAR ( 25 FDA reports)
CHOLESTEATOMA ( 25 FDA reports)
CYST REMOVAL ( 25 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 25 FDA reports)
DRUG ADMINISTRATION ERROR ( 25 FDA reports)
EPIGASTRIC DISCOMFORT ( 25 FDA reports)
ERYTHEMA OF EYELID ( 25 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 25 FDA reports)
HYPOMANIA ( 25 FDA reports)
LARGE INTESTINAL ULCER ( 25 FDA reports)
LIGHT CHAIN DISEASE ( 25 FDA reports)
LORDOSIS ( 25 FDA reports)
MEDICAL DEVICE COMPLICATION ( 25 FDA reports)
METASTASES TO ADRENALS ( 25 FDA reports)
METASTASES TO SPLEEN ( 25 FDA reports)
METASTASES TO THE MEDIASTINUM ( 25 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 25 FDA reports)
OESOPHAGEAL SPASM ( 25 FDA reports)
PROCEDURAL COMPLICATION ( 25 FDA reports)
PROTEIN URINE ( 25 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 25 FDA reports)
RECURRENT CANCER ( 25 FDA reports)
REFLUX LARYNGITIS ( 25 FDA reports)
RESPIRATORY ACIDOSIS ( 25 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 25 FDA reports)
URETHRAL CARUNCLE ( 25 FDA reports)
VESICAL FISTULA ( 25 FDA reports)
VITREOUS HAEMORRHAGE ( 25 FDA reports)
ACIDOSIS ( 24 FDA reports)
AMYLOIDOSIS ( 24 FDA reports)
ANDROGENS DECREASED ( 24 FDA reports)
ARTHROPOD BITE ( 24 FDA reports)
BLOOD COUNT ABNORMAL ( 24 FDA reports)
BLOOD OSMOLARITY DECREASED ( 24 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 24 FDA reports)
BODY TINEA ( 24 FDA reports)
BONE INFARCTION ( 24 FDA reports)
CARDIAC ASTHMA ( 24 FDA reports)
CEREBROSCLEROSIS ( 24 FDA reports)
CHONDROCALCINOSIS ( 24 FDA reports)
CHROMATURIA ( 24 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 24 FDA reports)
CONNECTIVE TISSUE DISORDER ( 24 FDA reports)
CUBITAL TUNNEL SYNDROME ( 24 FDA reports)
DIAPHRAGMATIC HERNIA ( 24 FDA reports)
DUODENAL POLYP ( 24 FDA reports)
DUODENOGASTRIC REFLUX ( 24 FDA reports)
ENDOMETRIAL ATROPHY ( 24 FDA reports)
EXTERNAL EAR DISORDER ( 24 FDA reports)
EXTRADURAL ABSCESS ( 24 FDA reports)
EYE ALLERGY ( 24 FDA reports)
FAMILY STRESS ( 24 FDA reports)
FIBROADENOMA OF BREAST ( 24 FDA reports)
FIBROUS HISTIOCYTOMA ( 24 FDA reports)
GALLBLADDER OPERATION ( 24 FDA reports)
GRANULOCYTOPENIA ( 24 FDA reports)
HIDRADENITIS ( 24 FDA reports)
HORDEOLUM ( 24 FDA reports)
METASTASES TO EYE ( 24 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 24 FDA reports)
MITRAL VALVE SCLEROSIS ( 24 FDA reports)
NAIL DYSTROPHY ( 24 FDA reports)
NASAL SEPTAL OPERATION ( 24 FDA reports)
NERVE BLOCK ( 24 FDA reports)
NERVE ROOT COMPRESSION ( 24 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 24 FDA reports)
ORAL PUSTULE ( 24 FDA reports)
PHARYNGEAL ERYTHEMA ( 24 FDA reports)
PIGMENTATION DISORDER ( 24 FDA reports)
PLASMAPHERESIS ( 24 FDA reports)
PROTEIN TOTAL INCREASED ( 24 FDA reports)
PURPURA ( 24 FDA reports)
SCAN BONE MARROW ABNORMAL ( 24 FDA reports)
SEROSITIS ( 24 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 24 FDA reports)
SPINAL FUSION ACQUIRED ( 24 FDA reports)
VENTRICULAR DYSFUNCTION ( 24 FDA reports)
VERTEBRAL COLUMN MASS ( 24 FDA reports)
ADJUSTMENT DISORDER ( 23 FDA reports)
ANAL FISTULA ( 23 FDA reports)
ANISOCYTOSIS ( 23 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 23 FDA reports)
B-CELL LYMPHOMA ( 23 FDA reports)
BLADDER MASS ( 23 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 23 FDA reports)
BREAST OPERATION ( 23 FDA reports)
CALCIUM METABOLISM DISORDER ( 23 FDA reports)
CATHETER RELATED COMPLICATION ( 23 FDA reports)
COMMINUTED FRACTURE ( 23 FDA reports)
CSF PROTEIN INCREASED ( 23 FDA reports)
EAR DISORDER ( 23 FDA reports)
ENDOMETRIOSIS ( 23 FDA reports)
ENTEROVESICAL FISTULA ( 23 FDA reports)
EOSINOPHIL COUNT INCREASED ( 23 FDA reports)
EPILEPSY ( 23 FDA reports)
HEPATIC ENZYME ABNORMAL ( 23 FDA reports)
HEPATIC NEOPLASM ( 23 FDA reports)
HYPOTHERMIA ( 23 FDA reports)
LAPAROTOMY ( 23 FDA reports)
LIGAMENT DISORDER ( 23 FDA reports)
LIMB OPERATION ( 23 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 23 FDA reports)
NIGHTMARE ( 23 FDA reports)
NYSTAGMUS ( 23 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 23 FDA reports)
OOPHORECTOMY ( 23 FDA reports)
PARATHYROIDECTOMY ( 23 FDA reports)
PELVIC HAEMATOMA ( 23 FDA reports)
PELVIC MASS ( 23 FDA reports)
PHLEBOLITH ( 23 FDA reports)
RAYNAUD'S PHENOMENON ( 23 FDA reports)
RETINOPATHY HYPERTENSIVE ( 23 FDA reports)
STEAL SYNDROME ( 23 FDA reports)
TENSION ( 23 FDA reports)
TINEA CRURIS ( 23 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 23 FDA reports)
VASODILATATION ( 23 FDA reports)
ABSCESS LIMB ( 22 FDA reports)
APATHY ( 22 FDA reports)
BICYTOPENIA ( 22 FDA reports)
BONE CALLUS EXCESSIVE ( 22 FDA reports)
BONE INFECTION ( 22 FDA reports)
BRAIN CANCER METASTATIC ( 22 FDA reports)
BREAST DISCHARGE ( 22 FDA reports)
COLONIC OBSTRUCTION ( 22 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 22 FDA reports)
DENTOFACIAL ANOMALY ( 22 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 22 FDA reports)
DRUG INTERACTION ( 22 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 22 FDA reports)
EMBOLISM ARTERIAL ( 22 FDA reports)
EXERCISE TOLERANCE DECREASED ( 22 FDA reports)
EYE DISORDER ( 22 FDA reports)
EYE INJURY ( 22 FDA reports)
FEELING HOT ( 22 FDA reports)
FOOT OPERATION ( 22 FDA reports)
GRAND MAL CONVULSION ( 22 FDA reports)
HEPATIC CANCER METASTATIC ( 22 FDA reports)
LOCAL ANAESTHESIA ( 22 FDA reports)
MERALGIA PARAESTHETICA ( 22 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 22 FDA reports)
NAIL DISCOLOURATION ( 22 FDA reports)
NAIL HYPERTROPHY ( 22 FDA reports)
NASAL DISORDER ( 22 FDA reports)
NEPHRITIC SYNDROME ( 22 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 22 FDA reports)
ONYCHOCLASIS ( 22 FDA reports)
PNEUMONIA VIRAL ( 22 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 22 FDA reports)
PROSTHESIS USER ( 22 FDA reports)
RADIATION OESOPHAGITIS ( 22 FDA reports)
RECTAL PROLAPSE ( 22 FDA reports)
REHABILITATION THERAPY ( 22 FDA reports)
RENAL LIPOMATOSIS ( 22 FDA reports)
RENAL TUBULAR ACIDOSIS ( 22 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 22 FDA reports)
SCROTAL SWELLING ( 22 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 22 FDA reports)
STRABISMUS ( 22 FDA reports)
TIBIA FRACTURE ( 22 FDA reports)
URETHRAL OBSTRUCTION ( 22 FDA reports)
VENTRICULAR FIBRILLATION ( 22 FDA reports)
VERTIGO POSITIONAL ( 22 FDA reports)
WEIGHT BEARING DIFFICULTY ( 22 FDA reports)
X-RAY ( 22 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
ANOSMIA ( 21 FDA reports)
BLADDER CANCER RECURRENT ( 21 FDA reports)
BREAST LUMP REMOVAL ( 21 FDA reports)
CHARLES BONNET SYNDROME ( 21 FDA reports)
CLOSED FRACTURE MANIPULATION ( 21 FDA reports)
CRYING ( 21 FDA reports)
CUSHINGOID ( 21 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 21 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 21 FDA reports)
GLOMERULONEPHRITIS ( 21 FDA reports)
INFARCTION ( 21 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 21 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 21 FDA reports)
LARYNGEAL CYST ( 21 FDA reports)
LIGAMENT INJURY ( 21 FDA reports)
LIP HAEMORRHAGE ( 21 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
MENINGEAL NEOPLASM ( 21 FDA reports)
METATARSALGIA ( 21 FDA reports)
MORTON'S NEUROMA ( 21 FDA reports)
MYASTHENIA GRAVIS ( 21 FDA reports)
NEUROMA ( 21 FDA reports)
ONYCHOLYSIS ( 21 FDA reports)
ORAL NEOPLASM BENIGN ( 21 FDA reports)
OSTEOMYELITIS DRAINAGE ( 21 FDA reports)
OVARIAN DISORDER ( 21 FDA reports)
PANCREATIC NEOPLASM ( 21 FDA reports)
PAPILLOEDEMA ( 21 FDA reports)
PERITONEAL DISORDER ( 21 FDA reports)
QUADRIPLEGIA ( 21 FDA reports)
RED BLOOD CELL ABNORMALITY ( 21 FDA reports)
SEROMA ( 21 FDA reports)
SICCA SYNDROME ( 21 FDA reports)
STOMATOCYTES PRESENT ( 21 FDA reports)
THORACOSTOMY ( 21 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 21 FDA reports)
TRACHEOBRONCHITIS ( 21 FDA reports)
VAGINAL PROLAPSE ( 21 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 21 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 20 FDA reports)
ADENOMYOSIS ( 20 FDA reports)
AEROMONA INFECTION ( 20 FDA reports)
ALLERGIC COUGH ( 20 FDA reports)
AORTIC VALVE REPLACEMENT ( 20 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 20 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 20 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 20 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 20 FDA reports)
CORNEAL ABRASION ( 20 FDA reports)
CULTURE URINE POSITIVE ( 20 FDA reports)
DRY SOCKET ( 20 FDA reports)
ENCOPRESIS ( 20 FDA reports)
ENTEROCELE ( 20 FDA reports)
FASCIITIS ( 20 FDA reports)
FAT NECROSIS ( 20 FDA reports)
FEELING COLD ( 20 FDA reports)
GINGIVAL HYPERTROPHY ( 20 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 20 FDA reports)
INTESTINAL MASS ( 20 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 20 FDA reports)
LIPIDS INCREASED ( 20 FDA reports)
MALIGNANT MELANOMA IN SITU ( 20 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 20 FDA reports)
MONOPARESIS ( 20 FDA reports)
MOOD ALTERED ( 20 FDA reports)
NASAL VESTIBULITIS ( 20 FDA reports)
OBSTRUCTION GASTRIC ( 20 FDA reports)
OSTEOSARCOMA METASTATIC ( 20 FDA reports)
OVERWEIGHT ( 20 FDA reports)
PAIN OF SKIN ( 20 FDA reports)
PANCREATIC MASS ( 20 FDA reports)
PELVIC ADHESIONS ( 20 FDA reports)
PERIORBITAL CELLULITIS ( 20 FDA reports)
POST PROCEDURAL INFECTION ( 20 FDA reports)
POSTMENOPAUSE ( 20 FDA reports)
PROCEDURAL HYPERTENSION ( 20 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 20 FDA reports)
RASH PUSTULAR ( 20 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 20 FDA reports)
SCHAMBERG'S DISEASE ( 20 FDA reports)
SPUTUM PURULENT ( 20 FDA reports)
SUICIDE ATTEMPT ( 20 FDA reports)
THERMAL BURN ( 20 FDA reports)
VOCAL CORD DISORDER ( 20 FDA reports)
WOUND DECOMPOSITION ( 20 FDA reports)
ACCIDENT AT WORK ( 19 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 19 FDA reports)
ASBESTOSIS ( 19 FDA reports)
ATRIAL TACHYCARDIA ( 19 FDA reports)
BARTHOLIN'S CYST ( 19 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 19 FDA reports)
CARDIAC TAMPONADE ( 19 FDA reports)
CARDIORENAL SYNDROME ( 19 FDA reports)
CEREBRAL HAEMORRHAGE ( 19 FDA reports)
CHEILITIS ( 19 FDA reports)
CLAUSTROPHOBIA ( 19 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 19 FDA reports)
CYANOSIS ( 19 FDA reports)
CYST ASPIRATION ( 19 FDA reports)
ECONOMIC PROBLEM ( 19 FDA reports)
EMOTIONAL DISORDER ( 19 FDA reports)
ENTHESOPATHY ( 19 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 19 FDA reports)
FEMALE STERILISATION ( 19 FDA reports)
FLUSHING ( 19 FDA reports)
GAMMOPATHY ( 19 FDA reports)
GASTRIC HAEMORRHAGE ( 19 FDA reports)
GASTRINOMA ( 19 FDA reports)
HYPERVISCOSITY SYNDROME ( 19 FDA reports)
INJECTION SITE PAIN ( 19 FDA reports)
IRITIS ( 19 FDA reports)
JAUNDICE CHOLESTATIC ( 19 FDA reports)
KIDNEY SMALL ( 19 FDA reports)
LUNG CANCER METASTATIC ( 19 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 19 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 19 FDA reports)
MONARTHRITIS ( 19 FDA reports)
OCCIPITAL NEURALGIA ( 19 FDA reports)
PARTIAL SEIZURES ( 19 FDA reports)
PERICARDIAL DISEASE ( 19 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 19 FDA reports)
PERIPHERAL EMBOLISM ( 19 FDA reports)
PERIVASCULAR DERMATITIS ( 19 FDA reports)
RADICAL MASTECTOMY ( 19 FDA reports)
RADICULAR CYST ( 19 FDA reports)
RADICULAR SYNDROME ( 19 FDA reports)
RENAL ISCHAEMIA ( 19 FDA reports)
SALIVARY GLAND MASS ( 19 FDA reports)
SKIN CANDIDA ( 19 FDA reports)
SKIN LESION EXCISION ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
SUPERINFECTION ( 19 FDA reports)
TESTICULAR SWELLING ( 19 FDA reports)
TOE OPERATION ( 19 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 19 FDA reports)
ULCER HAEMORRHAGE ( 19 FDA reports)
UVEITIS ( 19 FDA reports)
VULVOVAGINITIS ( 19 FDA reports)
WOUND CLOSURE ( 19 FDA reports)
ANAL FISSURE ( 18 FDA reports)
AORTIC BRUIT ( 18 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 18 FDA reports)
AUTOIMMUNE THYROIDITIS ( 18 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 18 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 18 FDA reports)
BRACHIAL PLEXOPATHY ( 18 FDA reports)
BRAIN MASS ( 18 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 18 FDA reports)
BREAST OEDEMA ( 18 FDA reports)
CALCIFICATION METASTATIC ( 18 FDA reports)
CARDIAC VALVE ABSCESS ( 18 FDA reports)
CARTILAGE ATROPHY ( 18 FDA reports)
DYSPLASIA ( 18 FDA reports)
EAR NEOPLASM ( 18 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 18 FDA reports)
ENGRAFTMENT SYNDROME ( 18 FDA reports)
EYE ABSCESS ( 18 FDA reports)
EYE MOVEMENT DISORDER ( 18 FDA reports)
FACET JOINT BLOCK ( 18 FDA reports)
FACIAL OPERATION ( 18 FDA reports)
FEELING JITTERY ( 18 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 18 FDA reports)
GASTROINTESTINAL TOXICITY ( 18 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 18 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 18 FDA reports)
HYPERPATHIA ( 18 FDA reports)
INTESTINAL ISCHAEMIA ( 18 FDA reports)
LERICHE SYNDROME ( 18 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 18 FDA reports)
MANIA ( 18 FDA reports)
MEAN CELL HAEMOGLOBIN ( 18 FDA reports)
METASTASES TO SOFT TISSUE ( 18 FDA reports)
NEPHROPATHY TOXIC ( 18 FDA reports)
OPHTHALMOPLEGIA ( 18 FDA reports)
PANCREATIC CALCIFICATION ( 18 FDA reports)
PARANASAL SINUS DISCOMFORT ( 18 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 18 FDA reports)
PATHOGEN RESISTANCE ( 18 FDA reports)
PERIRECTAL ABSCESS ( 18 FDA reports)
PITUITARY ENLARGEMENT ( 18 FDA reports)
POST CONCUSSION SYNDROME ( 18 FDA reports)
REFLUX GASTRITIS ( 18 FDA reports)
RENAL CELL CARCINOMA ( 18 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 18 FDA reports)
RHINALGIA ( 18 FDA reports)
RIB DEFORMITY ( 18 FDA reports)
SKIN ODOUR ABNORMAL ( 18 FDA reports)
SPINAL CORD INJURY THORACIC ( 18 FDA reports)
STAG HORN CALCULUS ( 18 FDA reports)
THROAT TIGHTNESS ( 18 FDA reports)
TOE AMPUTATION ( 18 FDA reports)
TRANSFUSION REACTION ( 18 FDA reports)
URETERIC OBSTRUCTION ( 18 FDA reports)
VARICOCELE ( 18 FDA reports)
VENOUS STENOSIS ( 18 FDA reports)
VULVITIS ( 18 FDA reports)
WITHDRAWAL SYNDROME ( 18 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 17 FDA reports)
ANEURYSM REPAIR ( 17 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 17 FDA reports)
BENIGN GASTRIC NEOPLASM ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 17 FDA reports)
BUNDLE BRANCH BLOCK ( 17 FDA reports)
CALCIUM IONISED INCREASED ( 17 FDA reports)
CHEST TUBE INSERTION ( 17 FDA reports)
CULTURE POSITIVE ( 17 FDA reports)
DERMATITIS ALLERGIC ( 17 FDA reports)
DERMOID CYST ( 17 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 17 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 17 FDA reports)
ERB'S PALSY ( 17 FDA reports)
ETHMOID SINUS SURGERY ( 17 FDA reports)
FAT TISSUE INCREASED ( 17 FDA reports)
FEAR ( 17 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 17 FDA reports)
FOREIGN BODY REACTION ( 17 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 17 FDA reports)
HEMIPLEGIA ( 17 FDA reports)
HYPERMAGNESAEMIA ( 17 FDA reports)
INCISION SITE ERYTHEMA ( 17 FDA reports)
INCISION SITE OEDEMA ( 17 FDA reports)
INFUSION RELATED REACTION ( 17 FDA reports)
JAW CYST ( 17 FDA reports)
LIP PAIN ( 17 FDA reports)
LYMPHOCYTIC INFILTRATION ( 17 FDA reports)
MALIGNANT TUMOUR EXCISION ( 17 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 17 FDA reports)
MENISCUS REMOVAL ( 17 FDA reports)
MONONEUROPATHY MULTIPLEX ( 17 FDA reports)
NASAL OBSTRUCTION ( 17 FDA reports)
NEPHRITIS INTERSTITIAL ( 17 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 17 FDA reports)
ORAL DYSAESTHESIA ( 17 FDA reports)
OROPHARYNGEAL PLAQUE ( 17 FDA reports)
PARACENTESIS ( 17 FDA reports)
PERINEAL PAIN ( 17 FDA reports)
PERSONALITY DISORDER ( 17 FDA reports)
RETINAL ISCHAEMIA ( 17 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 17 FDA reports)
SALIVARY HYPERSECRETION ( 17 FDA reports)
SCINTIGRAPHY ( 17 FDA reports)
SCOTOMA ( 17 FDA reports)
SCROTAL CYST ( 17 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 17 FDA reports)
SJOGREN'S SYNDROME ( 17 FDA reports)
SPINAL CORD OEDEMA ( 17 FDA reports)
STOMACH DISCOMFORT ( 17 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 17 FDA reports)
TOBACCO ABUSE ( 17 FDA reports)
TONGUE PARALYSIS ( 17 FDA reports)
TOXIC NODULAR GOITRE ( 17 FDA reports)
URINE ANALYSIS ABNORMAL ( 17 FDA reports)
URINE ODOUR ABNORMAL ( 17 FDA reports)
VESTIBULAR DISORDER ( 17 FDA reports)
VIRAL LABYRINTHITIS ( 17 FDA reports)
ABDOMINAL TENDERNESS ( 16 FDA reports)
BLADDER PROLAPSE ( 16 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 16 FDA reports)
BONE FISSURE ( 16 FDA reports)
BRAIN SCAN ABNORMAL ( 16 FDA reports)
BREAST INDURATION ( 16 FDA reports)
COR PULMONALE ( 16 FDA reports)
CRANIOTOMY ( 16 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 16 FDA reports)
DYSTROPHIC CALCIFICATION ( 16 FDA reports)
EAR CONGESTION ( 16 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 16 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 16 FDA reports)
EOSINOPHIL COUNT DECREASED ( 16 FDA reports)
ESCHERICHIA BACTERAEMIA ( 16 FDA reports)
ESSENTIAL TREMOR ( 16 FDA reports)
EYELID MARGIN CRUSTING ( 16 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 16 FDA reports)
GENERALISED ANXIETY DISORDER ( 16 FDA reports)
GLOBULINS INCREASED ( 16 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 16 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 16 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 16 FDA reports)
LUNG OPERATION ( 16 FDA reports)
MAMMARY DUCT ECTASIA ( 16 FDA reports)
MONOCYTE COUNT DECREASED ( 16 FDA reports)
NEURECTOMY ( 16 FDA reports)
NEURODEGENERATIVE DISORDER ( 16 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 16 FDA reports)
OSTEOMA ( 16 FDA reports)
OXYGEN SUPPLEMENTATION ( 16 FDA reports)
PARAPARESIS ( 16 FDA reports)
PHLEBITIS SUPERFICIAL ( 16 FDA reports)
PULMONARY THROMBOSIS ( 16 FDA reports)
PULMONARY VALVE STENOSIS ( 16 FDA reports)
RADIOTHERAPY TO BONE ( 16 FDA reports)
SALIVA ALTERED ( 16 FDA reports)
SENSATION OF HEAVINESS ( 16 FDA reports)
SEPTIC EMBOLUS ( 16 FDA reports)
SKELETAL SURVEY ABNORMAL ( 16 FDA reports)
SKIN GRAFT ( 16 FDA reports)
SKIN NECROSIS ( 16 FDA reports)
SPLENIC ARTERY ANEURYSM ( 16 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 16 FDA reports)
TONGUE DRY ( 16 FDA reports)
TRIGGER FINGER ( 16 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 16 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 16 FDA reports)
URINE ABNORMALITY ( 16 FDA reports)
VASOCONSTRICTION ( 16 FDA reports)
VENOOCCLUSIVE DISEASE ( 16 FDA reports)
VOCAL CORD POLYP ( 16 FDA reports)
VOMITING PROJECTILE ( 16 FDA reports)
ABSCESS INTESTINAL ( 15 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 15 FDA reports)
ACUTE LEUKAEMIA ( 15 FDA reports)
ALOPECIA AREATA ( 15 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 15 FDA reports)
ASTERIXIS ( 15 FDA reports)
BENIGN BREAST NEOPLASM ( 15 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 15 FDA reports)
BENIGN OVARIAN TUMOUR ( 15 FDA reports)
BIOPSY BONE MARROW ( 15 FDA reports)
BIOPSY TONGUE ABNORMAL ( 15 FDA reports)
BLADDER CYST ( 15 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 15 FDA reports)
CARDIOTOXICITY ( 15 FDA reports)
CERVICAL SPINE FLATTENING ( 15 FDA reports)
CHOLECYSTITIS ACUTE ( 15 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 15 FDA reports)
CYTOREDUCTIVE SURGERY ( 15 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 15 FDA reports)
DEMYELINATION ( 15 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 15 FDA reports)
DIABETIC GASTROPARESIS ( 15 FDA reports)
ECHOCARDIOGRAM ( 15 FDA reports)
EJECTION FRACTION ( 15 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 15 FDA reports)
ENTEROBACTER INFECTION ( 15 FDA reports)
FOOD POISONING ( 15 FDA reports)
GASTRIC BYPASS ( 15 FDA reports)
GRANULOCYTE COUNT DECREASED ( 15 FDA reports)
HAEMOPHILUS INFECTION ( 15 FDA reports)
HALLUCINATION, AUDITORY ( 15 FDA reports)
HIGH FREQUENCY ABLATION ( 15 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 15 FDA reports)
IMPULSIVE BEHAVIOUR ( 15 FDA reports)
IRIS ADHESIONS ( 15 FDA reports)
KERATOACANTHOMA ( 15 FDA reports)
LARYNGEAL OEDEMA ( 15 FDA reports)
LARYNGEAL REPAIR ( 15 FDA reports)
LEUKODYSTROPHY ( 15 FDA reports)
LIGHT CHAIN ANALYSIS ( 15 FDA reports)
LIP DISORDER ( 15 FDA reports)
MAMMOGRAM ( 15 FDA reports)
MEDIASTINAL DISORDER ( 15 FDA reports)
MENOPAUSAL SYMPTOMS ( 15 FDA reports)
METASTASES TO LARGE INTESTINE ( 15 FDA reports)
MONOCYTOSIS ( 15 FDA reports)
NO THERAPEUTIC RESPONSE ( 15 FDA reports)
OESOPHAGEAL DILATATION ( 15 FDA reports)
PECTUS EXCAVATUM ( 15 FDA reports)
PELVIC DISCOMFORT ( 15 FDA reports)
PELVIC PROLAPSE ( 15 FDA reports)
PNEUMATOSIS INTESTINALIS ( 15 FDA reports)
POST THROMBOTIC SYNDROME ( 15 FDA reports)
PRIMARY HYPOGONADISM ( 15 FDA reports)
PROSTATE TENDERNESS ( 15 FDA reports)
PROTEIN URINE ABSENT ( 15 FDA reports)
PULMONARY CALCIFICATION ( 15 FDA reports)
REACTIVE PSYCHOSIS ( 15 FDA reports)
RETINAL MELANOMA ( 15 FDA reports)
ROTATOR CUFF REPAIR ( 15 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 15 FDA reports)
SINUS TARSI SYNDROME ( 15 FDA reports)
TEETH BRITTLE ( 15 FDA reports)
TESTICULAR FAILURE ( 15 FDA reports)
TIC ( 15 FDA reports)
TRANSPLANT ( 15 FDA reports)
UMBILICAL HERNIA REPAIR ( 15 FDA reports)
UNEVALUABLE EVENT ( 15 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 15 FDA reports)
URINARY TRACT OBSTRUCTION ( 15 FDA reports)
VENA CAVA THROMBOSIS ( 15 FDA reports)
ANAPHYLACTIC SHOCK ( 14 FDA reports)
ANGIOLIPOMA ( 14 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
BASAL GANGLIA INFARCTION ( 14 FDA reports)
BETA GLOBULIN INCREASED ( 14 FDA reports)
BILE DUCT STONE ( 14 FDA reports)
BIOPSY CHEST WALL ABNORMAL ( 14 FDA reports)
BONE ATROPHY ( 14 FDA reports)
BREAKTHROUGH PAIN ( 14 FDA reports)
BREAST ATROPHY ( 14 FDA reports)
BREAST INFECTION ( 14 FDA reports)
CARDIAC ENZYMES INCREASED ( 14 FDA reports)
CAROTID BODY TUMOUR ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
CHEST WALL OPERATION ( 14 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 14 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
CYSTOPEXY ( 14 FDA reports)
DRUG ERUPTION ( 14 FDA reports)
DYSPLASTIC NAEVUS ( 14 FDA reports)
ESCHERICHIA SEPSIS ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 14 FDA reports)
HAEMORRHOID OPERATION ( 14 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 14 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 14 FDA reports)
HYPOTONIA ( 14 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 14 FDA reports)
LABILE HYPERTENSION ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
LICHENOID KERATOSIS ( 14 FDA reports)
LYMPH NODE PALPABLE ( 14 FDA reports)
METASTASES TO CHEST WALL ( 14 FDA reports)
METASTASES TO NASAL SINUSES ( 14 FDA reports)
MICROANGIOPATHY ( 14 FDA reports)
MONONUCLEOSIS SYNDROME ( 14 FDA reports)
NON-CARDIAC CHEST PAIN ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
ORAL MUCOSAL DISORDER ( 14 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
PERCUSSION TEST ABNORMAL ( 14 FDA reports)
PERITONITIS ( 14 FDA reports)
PERNICIOUS ANAEMIA ( 14 FDA reports)
PHOTOSENSITIVITY REACTION ( 14 FDA reports)
POLYARTERITIS NODOSA ( 14 FDA reports)
RENAL ANEURYSM ( 14 FDA reports)
RHINITIS SEASONAL ( 14 FDA reports)
SCRATCH ( 14 FDA reports)
SHOULDER ARTHROPLASTY ( 14 FDA reports)
SINUS RHYTHM ( 14 FDA reports)
SPINAL MYELOGRAM ( 14 FDA reports)
SPUTUM INCREASED ( 14 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 14 FDA reports)
SUTURE REMOVAL ( 14 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 14 FDA reports)
URINE OUTPUT DECREASED ( 14 FDA reports)
UROGRAM ( 14 FDA reports)
WOUND ABSCESS ( 14 FDA reports)
ACANTHOMA ( 13 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 13 FDA reports)
ANAL HAEMORRHAGE ( 13 FDA reports)
ANURIA ( 13 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 13 FDA reports)
ATRIAL SEPTAL DEFECT ( 13 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 13 FDA reports)
BLOOD CHLORIDE DECREASED ( 13 FDA reports)
BLOOD DISORDER ( 13 FDA reports)
BODY HEIGHT DECREASED ( 13 FDA reports)
CALCULUS URINARY ( 13 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 13 FDA reports)
CATHETER RELATED INFECTION ( 13 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 13 FDA reports)
CHEST X-RAY ABNORMAL ( 13 FDA reports)
CHOROIDAL DETACHMENT ( 13 FDA reports)
COLON OPERATION ( 13 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 13 FDA reports)
CYSTITIS KLEBSIELLA ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
ESCHAR ( 13 FDA reports)
FACE INJURY ( 13 FDA reports)
FLAT AFFECT ( 13 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 13 FDA reports)
FRONTAL SINUS OPERATION ( 13 FDA reports)
FUNGAEMIA ( 13 FDA reports)
GLYCOSURIA ( 13 FDA reports)
HAEMORRHAGIC ANAEMIA ( 13 FDA reports)
HEPATIC CALCIFICATION ( 13 FDA reports)
HERNIA PAIN ( 13 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 13 FDA reports)
INCISION SITE INFECTION ( 13 FDA reports)
LARYNGOSPASM ( 13 FDA reports)
METASTASES TO MOUTH ( 13 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 13 FDA reports)
MYOFASCITIS ( 13 FDA reports)
NAIL AVULSION ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 13 FDA reports)
OPEN FRACTURE ( 13 FDA reports)
ORCHITIS ( 13 FDA reports)
PERIORBITAL HAEMATOMA ( 13 FDA reports)
PNEUMOCEPHALUS ( 13 FDA reports)
POIKILOCYTOSIS ( 13 FDA reports)
QUALITY OF LIFE DECREASED ( 13 FDA reports)
RADIATION SKIN INJURY ( 13 FDA reports)
RECTAL PROLAPSE REPAIR ( 13 FDA reports)
RESUSCITATION ( 13 FDA reports)
RHEUMATIC FEVER ( 13 FDA reports)
SINUSITIS FUNGAL ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SPONDYLITIC MYELOPATHY ( 13 FDA reports)
SYNOVIAL DISORDER ( 13 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 13 FDA reports)
THYROID ADENOMA ( 13 FDA reports)
TINEA INFECTION ( 13 FDA reports)
TRYPTASE INCREASED ( 13 FDA reports)
URINE FLOW DECREASED ( 13 FDA reports)
VARICELLA ( 13 FDA reports)
VENTRICULAR DYSKINESIA ( 13 FDA reports)
WOUND HAEMORRHAGE ( 13 FDA reports)
ABNORMAL BEHAVIOUR ( 12 FDA reports)
ALVEOLITIS ( 12 FDA reports)
ANAEMIA POSTOPERATIVE ( 12 FDA reports)
BACTERIAL TEST ( 12 FDA reports)
BACTERIAL TEST NEGATIVE ( 12 FDA reports)
BALANITIS ( 12 FDA reports)
BENCE JONES PROTEINURIA ( 12 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 12 FDA reports)
BREAST CANCER FEMALE ( 12 FDA reports)
BRONCHIOLITIS ( 12 FDA reports)
BURNS THIRD DEGREE ( 12 FDA reports)
CALCULUS BLADDER ( 12 FDA reports)
CENTRAL OBESITY ( 12 FDA reports)
CERVICAL MYELOPATHY ( 12 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 12 FDA reports)
CHONDROPATHY ( 12 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CORNEAL OEDEMA ( 12 FDA reports)
DYSTONIA ( 12 FDA reports)
EAR IRRIGATION ( 12 FDA reports)
ECTROPION ( 12 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 12 FDA reports)
EXPLORATORY OPERATION ( 12 FDA reports)
EYELID OPERATION ( 12 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 12 FDA reports)
GASTROSTOMY TUBE INSERTION ( 12 FDA reports)
GENITAL CANDIDIASIS ( 12 FDA reports)
GENITAL RASH ( 12 FDA reports)
GINGIVAL HYPERPLASIA ( 12 FDA reports)
GLOMERULOSCLEROSIS ( 12 FDA reports)
HORMONE LEVEL ABNORMAL ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 12 FDA reports)
INJECTION SITE HAEMATOMA ( 12 FDA reports)
INTESTINAL POLYP ( 12 FDA reports)
JOINT DESTRUCTION ( 12 FDA reports)
LUMBAR SPINE FLATTENING ( 12 FDA reports)
MALABSORPTION ( 12 FDA reports)
MALLORY-WEISS SYNDROME ( 12 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 12 FDA reports)
OESOPHAGEAL RUPTURE ( 12 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 12 FDA reports)
OVARIAN ADHESION ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PANCREATIC DUCT DILATATION ( 12 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 12 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 12 FDA reports)
PEAU D'ORANGE ( 12 FDA reports)
PITUITARY TUMOUR BENIGN ( 12 FDA reports)
PLASMA CELLS INCREASED ( 12 FDA reports)
PRESBYOESOPHAGUS ( 12 FDA reports)
PROSTATECTOMY ( 12 FDA reports)
PROSTATIC OBSTRUCTION ( 12 FDA reports)
RADICULITIS BRACHIAL ( 12 FDA reports)
RASH MORBILLIFORM ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
REGURGITATION ( 12 FDA reports)
RENAL STONE REMOVAL ( 12 FDA reports)
SHOULDER DEFORMITY ( 12 FDA reports)
SINUS CANCER METASTATIC ( 12 FDA reports)
SKIN OPERATION ( 12 FDA reports)
SKIN PLAQUE ( 12 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
THERAPY NON-RESPONDER ( 12 FDA reports)
THYROGLOBULIN INCREASED ( 12 FDA reports)
TOOTH DECALCIFICATION ( 12 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
WISDOM TEETH REMOVAL ( 12 FDA reports)
ACTINIC ELASTOSIS ( 11 FDA reports)
ACUTE PSYCHOSIS ( 11 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 11 FDA reports)
ADHESIOLYSIS ( 11 FDA reports)
ADNEXA UTERI CYST ( 11 FDA reports)
ADRENAL SUPPRESSION ( 11 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 11 FDA reports)
AMENORRHOEA ( 11 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 11 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 11 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 11 FDA reports)
BIOPSY BREAST ABNORMAL ( 11 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 11 FDA reports)
BLOOD CULTURE POSITIVE ( 11 FDA reports)
BLOOD FOLATE INCREASED ( 11 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 11 FDA reports)
BODY TEMPERATURE DECREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BONE CANCER METASTATIC ( 11 FDA reports)
CAECUM OPERATION ( 11 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
COMPUTERISED TOMOGRAM ( 11 FDA reports)
CYST DRAINAGE ( 11 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 11 FDA reports)
DIAPHRAGMATIC DISORDER ( 11 FDA reports)
EFFUSION ( 11 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 11 FDA reports)
EMPTY SELLA SYNDROME ( 11 FDA reports)
ENDARTERECTOMY ( 11 FDA reports)
ENTEROCUTANEOUS FISTULA ( 11 FDA reports)
EPIDERMAL NECROSIS ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
GENERAL ANAESTHESIA ( 11 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 11 FDA reports)
HAEMATOCRIT ABNORMAL ( 11 FDA reports)
HAND DEFORMITY ( 11 FDA reports)
HYPERKINESIA ( 11 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 11 FDA reports)
HYPOPROTEINAEMIA ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
IMPLANT SITE SWELLING ( 11 FDA reports)
INFECTIOUS PERITONITIS ( 11 FDA reports)
INFECTIVE TENOSYNOVITIS ( 11 FDA reports)
INFUSION SITE HAEMORRHAGE ( 11 FDA reports)
INFUSION SITE SWELLING ( 11 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 11 FDA reports)
INTUBATION ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
LAGOPHTHALMOS ( 11 FDA reports)
LIMB CRUSHING INJURY ( 11 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 11 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 11 FDA reports)
MACULE ( 11 FDA reports)
MAMMOGRAM ABNORMAL ( 11 FDA reports)
MAMMOPLASTY ( 11 FDA reports)
MEDICATION ERROR ( 11 FDA reports)
METASTASES TO HEART ( 11 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 11 FDA reports)
MIXED DEAFNESS ( 11 FDA reports)
MIXED HYPERLIPIDAEMIA ( 11 FDA reports)
NEPHROCALCINOSIS ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
NEUROSENSORY HYPOACUSIS ( 11 FDA reports)
NODULE ON EXTREMITY ( 11 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 11 FDA reports)
PAROSMIA ( 11 FDA reports)
PERICARDITIS CONSTRICTIVE ( 11 FDA reports)
PHARYNGEAL MASS ( 11 FDA reports)
PHLEBOSCLEROSIS ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 11 FDA reports)
PROSTATIC CALCIFICATION ( 11 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 11 FDA reports)
RESIDUAL URINE ( 11 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SKIN HAEMORRHAGE ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
THROAT LESION ( 11 FDA reports)
TUMOUR LYSIS SYNDROME ( 11 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
UTERINE MALPOSITION ( 11 FDA reports)
UTEROVAGINAL PROLAPSE ( 11 FDA reports)
VAGINAL ULCERATION ( 11 FDA reports)
VENA CAVA INJURY ( 11 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 11 FDA reports)
VITAMIN B12 INCREASED ( 11 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 11 FDA reports)
ACTINOMYCES TEST POSITIVE ( 10 FDA reports)
ALCOHOL ABUSE ( 10 FDA reports)
AMBLYOPIA ( 10 FDA reports)
ANAESTHESIA ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ANAL ULCER ( 10 FDA reports)
ANGIOSARCOMA ( 10 FDA reports)
ARTERIOSPASM CORONARY ( 10 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BACTEROIDES TEST POSITIVE ( 10 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 10 FDA reports)
BLOOD CHLORIDE INCREASED ( 10 FDA reports)
BLOOD URINE ( 10 FDA reports)
BONE SARCOMA ( 10 FDA reports)
BREAST HAEMATOMA ( 10 FDA reports)
BREAST SWELLING ( 10 FDA reports)
BULIMIA NERVOSA ( 10 FDA reports)
CARBUNCLE ( 10 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 10 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 10 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 10 FDA reports)
CATHETER SITE HAEMATOMA ( 10 FDA reports)
CATHETER SITE INFECTION ( 10 FDA reports)
CERVICAL POLYP ( 10 FDA reports)
CHOLANGIOGRAM ( 10 FDA reports)
COITAL BLEEDING ( 10 FDA reports)
COLITIS MICROSCOPIC ( 10 FDA reports)
COLON CANCER RECURRENT ( 10 FDA reports)
COLONOSCOPY ( 10 FDA reports)
CONJUNCTIVAL PALLOR ( 10 FDA reports)
CORONARY ARTERY STENOSIS ( 10 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 10 FDA reports)
DIABETIC FOOT ( 10 FDA reports)
DIPLEGIA ( 10 FDA reports)
DYSPAREUNIA ( 10 FDA reports)
EJACULATION DISORDER ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
ENDOSCOPY ( 10 FDA reports)
EROSIVE DUODENITIS ( 10 FDA reports)
FUSOBACTERIUM INFECTION ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 10 FDA reports)
HAEMANGIOMA OF SPLEEN ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HAEMOTHORAX ( 10 FDA reports)
HELICOBACTER GASTRITIS ( 10 FDA reports)
ILIAC ARTERY THROMBOSIS ( 10 FDA reports)
IMPLANT SITE THROMBOSIS ( 10 FDA reports)
INCREASED BRONCHIAL SECRETION ( 10 FDA reports)
INFECTED SEBACEOUS CYST ( 10 FDA reports)
INGUINAL HERNIA REPAIR ( 10 FDA reports)
INTERTRIGO ( 10 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 10 FDA reports)
LABORATORY TEST ABNORMAL ( 10 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 10 FDA reports)
LIP OEDEMA ( 10 FDA reports)
MACULAR OEDEMA ( 10 FDA reports)
MASTOID DISORDER ( 10 FDA reports)
MEIBOMIANITIS ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MITRAL VALVE STENOSIS ( 10 FDA reports)
MUCOSAL ATROPHY ( 10 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA ( 10 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 10 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 10 FDA reports)
OESOPHAGEAL POLYP ( 10 FDA reports)
OSTEOCHONDROMA ( 10 FDA reports)
PARACENTESIS ABDOMEN ( 10 FDA reports)
PCO2 DECREASED ( 10 FDA reports)
PELVIC NEOPLASM ( 10 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 10 FDA reports)
PILONIDAL CYST ( 10 FDA reports)
PLATELET DISORDER ( 10 FDA reports)
PLEURAL CALCIFICATION ( 10 FDA reports)
PLEURAL DISORDER ( 10 FDA reports)
POSTOPERATIVE ABSCESS ( 10 FDA reports)
PRURITUS GENERALISED ( 10 FDA reports)
RADIAL NERVE PALSY ( 10 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 10 FDA reports)
RESPIRATORY TRACT OEDEMA ( 10 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 10 FDA reports)
RETINAL VEIN OCCLUSION ( 10 FDA reports)
SCROTAL ABSCESS ( 10 FDA reports)
SCROTAL INFECTION ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
SKIN FRAGILITY ( 10 FDA reports)
SKIN NODULE ( 10 FDA reports)
SKIN OEDEMA ( 10 FDA reports)
SKIN SWELLING ( 10 FDA reports)
SOFT TISSUE INJURY ( 10 FDA reports)
SPHENOID SINUS OPERATION ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
TETANY ( 10 FDA reports)
THROAT IRRITATION ( 10 FDA reports)
THROMBOSED VARICOSE VEIN ( 10 FDA reports)
TOOTH AVULSION ( 10 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 10 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
VASCULAR INSUFFICIENCY ( 10 FDA reports)
VIRAL PERICARDITIS ( 10 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 9 FDA reports)
ACCELERATED HYPERTENSION ( 9 FDA reports)
ACUTE STRESS DISORDER ( 9 FDA reports)
ADRENALECTOMY ( 9 FDA reports)
ANAL INFLAMMATION ( 9 FDA reports)
ANAL SPHINCTER ATONY ( 9 FDA reports)
ANIMAL SCRATCH ( 9 FDA reports)
AURICULAR SWELLING ( 9 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
BIOPSY LUNG ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLADDER TRABECULATION ( 9 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
BONE MARROW GRANULOMA ( 9 FDA reports)
CATHETER SITE RELATED REACTION ( 9 FDA reports)
CHOKING ( 9 FDA reports)
CHORIORETINAL DISORDER ( 9 FDA reports)
CHORIORETINOPATHY ( 9 FDA reports)
CHROMATOPSIA ( 9 FDA reports)
COLON CANCER METASTATIC ( 9 FDA reports)
COLONIC STENOSIS ( 9 FDA reports)
COLOSTOMY ( 9 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 9 FDA reports)
CONJUNCTIVAL OEDEMA ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CUSHING'S SYNDROME ( 9 FDA reports)
CYCLOTHYMIC DISORDER ( 9 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
DUPUYTREN'S CONTRACTURE ( 9 FDA reports)
ERYTHEMA NODOSUM ( 9 FDA reports)
FOLATE DEFICIENCY ( 9 FDA reports)
FOOD ALLERGY ( 9 FDA reports)
GASTRIC VARICES ( 9 FDA reports)
GASTRITIS HAEMORRHAGIC ( 9 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
GRAFT COMPLICATION ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
GRIEF REACTION ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HELICOBACTER INFECTION ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HIP DEFORMITY ( 9 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 9 FDA reports)
INGROWN HAIR ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
JOINT ANKYLOSIS ( 9 FDA reports)
JOINT CONTRACTURE ( 9 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 9 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 9 FDA reports)
LIP BLISTER ( 9 FDA reports)
LIP NEOPLASM BENIGN ( 9 FDA reports)
LOCALISED OEDEMA ( 9 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 9 FDA reports)
LYMPH NODE PAIN ( 9 FDA reports)
LYMPHOPENIA ( 9 FDA reports)
MEGAKARYOCYTES DECREASED ( 9 FDA reports)
MENSTRUAL DISORDER ( 9 FDA reports)
METABOLIC ALKALOSIS ( 9 FDA reports)
METASTASES TO KIDNEY ( 9 FDA reports)
METASTASES TO PANCREAS ( 9 FDA reports)
METASTASES TO STOMACH ( 9 FDA reports)
MUSCLE TIGHTNESS ( 9 FDA reports)
NODAL OSTEOARTHRITIS ( 9 FDA reports)
ONYCHOGRYPHOSIS ( 9 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 9 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 9 FDA reports)
PERFORMANCE STATUS DECREASED ( 9 FDA reports)
PHOTODERMATOSIS ( 9 FDA reports)
PINGUECULA ( 9 FDA reports)
PLEURAL NEOPLASM ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
POST PROCEDURAL HAEMATOMA ( 9 FDA reports)
PROSTATE INFECTION ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
RECTAL CANCER ( 9 FDA reports)
RETICULOCYTE COUNT INCREASED ( 9 FDA reports)
RETINAL DETACHMENT ( 9 FDA reports)
RETINAL DISORDER ( 9 FDA reports)
RHEUMATIC HEART DISEASE ( 9 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SMALL INTESTINE CARCINOMA ( 9 FDA reports)
SUBDURAL HAEMORRHAGE ( 9 FDA reports)
SYMBOLIC DYSFUNCTION ( 9 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
TENDON SHEATH INCISION ( 9 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 9 FDA reports)
URACHAL ABNORMALITY ( 9 FDA reports)
URETHRAL DISORDER ( 9 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 9 FDA reports)
WHITE BLOOD CELL DISORDER ( 9 FDA reports)
ABDOMINAL WALL DISORDER ( 8 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
AMPUTATION ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 8 FDA reports)
ARTERIAL INSUFFICIENCY ( 8 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 8 FDA reports)
AXILLARY PAIN ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BACTERIAL TOXAEMIA ( 8 FDA reports)
BALANOPOSTHITIS ( 8 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 8 FDA reports)
BENIGN BONE NEOPLASM ( 8 FDA reports)
BIFASCICULAR BLOCK ( 8 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
BLADDER PAIN ( 8 FDA reports)
BLINDNESS CORTICAL ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
CARDIAC PSEUDOANEURYSM ( 8 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 8 FDA reports)
CERVIX CARCINOMA ( 8 FDA reports)
CERVIX INFLAMMATION ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
COLLATERAL CIRCULATION ( 8 FDA reports)
COMPLEX PARTIAL SEIZURES ( 8 FDA reports)
CONCUSSION ( 8 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 8 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 8 FDA reports)
CSF TEST ABNORMAL ( 8 FDA reports)
DEAFNESS UNILATERAL ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DIFFICULTY IN WALKING ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENDOMETRIAL CANCER ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
FRACTURE DISPLACEMENT ( 8 FDA reports)
FULL BLOOD COUNT DECREASED ( 8 FDA reports)
FUNGAL SKIN INFECTION ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTRIC PH DECREASED ( 8 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 8 FDA reports)
GINGIVAL CANCER ( 8 FDA reports)
HAEMOPHILIA ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
HOMOCYSTINAEMIA ( 8 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 8 FDA reports)
HYPERTRANSAMINASAEMIA ( 8 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 8 FDA reports)
ILEAL STENOSIS ( 8 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 8 FDA reports)
INTERCOSTAL NEURALGIA ( 8 FDA reports)
INTERVERTEBRAL DISCITIS ( 8 FDA reports)
INTESTINAL PERFORATION ( 8 FDA reports)
JOINT INJECTION ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
JOINT STABILISATION ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
LIVEDO RETICULARIS ( 8 FDA reports)
LIVER INJURY ( 8 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
METASTATIC LYMPHOMA ( 8 FDA reports)
MICROALBUMINURIA ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
MYELOMALACIA ( 8 FDA reports)
NARCOLEPSY ( 8 FDA reports)
NEPHRECTOMY ( 8 FDA reports)
NERVE ROOT INJURY LUMBAR ( 8 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
OMENTUM NEOPLASM ( 8 FDA reports)
OPTIC NEUROPATHY ( 8 FDA reports)
ORGAN FAILURE ( 8 FDA reports)
OVARIAN ATROPHY ( 8 FDA reports)
PAPILLOMA VIRAL INFECTION ( 8 FDA reports)
PELVIC ABSCESS ( 8 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 8 FDA reports)
PERICORONITIS ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PHIMOSIS ( 8 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 8 FDA reports)
PNEUMONIA HAEMOPHILUS ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
POLYCYSTIC OVARIES ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
POST PROCEDURAL PAIN ( 8 FDA reports)
PROSTATISM ( 8 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
RADIATION NEUROPATHY ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
RECTAL ULCER ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
RENAL CYST HAEMORRHAGE ( 8 FDA reports)
RENAL PAIN ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SKIN MASS ( 8 FDA reports)
SPEECH REHABILITATION ( 8 FDA reports)
SPINAL CLAUDICATION ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 8 FDA reports)
SUFFOCATION FEELING ( 8 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 8 FDA reports)
TESTICULAR ATROPHY ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
TUMOUR NECROSIS ( 8 FDA reports)
URETHRAL PAIN ( 8 FDA reports)
VASOMOTOR RHINITIS ( 8 FDA reports)
VESTIBULITIS ( 8 FDA reports)
VITAMIN D DECREASED ( 8 FDA reports)
VULVOVAGINAL PAIN ( 8 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 8 FDA reports)
XANTHOGRANULOMA ( 8 FDA reports)
XEROSIS ( 8 FDA reports)
ABDOMINAL SYMPTOM ( 7 FDA reports)
ABSCESS SOFT TISSUE ( 7 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ANION GAP DECREASED ( 7 FDA reports)
ANION GAP INCREASED ( 7 FDA reports)
ANKYLOSING SPONDYLITIS ( 7 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ASTHENOPIA ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLEEDING TIME PROLONGED ( 7 FDA reports)
BLEPHAROSPASM ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 7 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 7 FDA reports)
BLOOD LACTIC ACID INCREASED ( 7 FDA reports)
BLOOD PROLACTIN INCREASED ( 7 FDA reports)
BONE FORMATION DECREASED ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
CAECITIS ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CARDIOPULMONARY FAILURE ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CLUSTER HEADACHE ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 7 FDA reports)
DUODENAL STENOSIS ( 7 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 7 FDA reports)
ENANTHEMA ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EYELID DISORDER ( 7 FDA reports)
FLUID INTAKE REDUCED ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
GAMMA RADIATION THERAPY TO BRAIN ( 7 FDA reports)
GASTRECTOMY ( 7 FDA reports)
GASTROINTESTINAL ULCER ( 7 FDA reports)
GENERAL NUTRITION DISORDER ( 7 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 7 FDA reports)
HERPES ZOSTER DISSEMINATED ( 7 FDA reports)
HISTOLOGY ABNORMAL ( 7 FDA reports)
HIV INFECTION ( 7 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 7 FDA reports)
HYPOPHOSPHATASIA ( 7 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INFECTED DERMAL CYST ( 7 FDA reports)
INFUSION SITE REACTION ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INTESTINAL RESECTION ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
LABIA ENLARGED ( 7 FDA reports)
LEUKOPLAKIA ( 7 FDA reports)
LIMB DEFORMITY ( 7 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 7 FDA reports)
LIP EROSION ( 7 FDA reports)
LIPOATROPHY ( 7 FDA reports)
LIPOMA EXCISION ( 7 FDA reports)
LUNG LOBECTOMY ( 7 FDA reports)
LYMPH GLAND INFECTION ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 7 FDA reports)
MYELITIS ( 7 FDA reports)
NAIL OPERATION ( 7 FDA reports)
NASAL SEPTUM PERFORATION ( 7 FDA reports)
NASAL SINUS DRAINAGE ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
NICOTINE DEPENDENCE ( 7 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 7 FDA reports)
OOPHORECTOMY BILATERAL ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PENILE PROSTHESIS INSERTION ( 7 FDA reports)
PERIORBITAL OEDEMA ( 7 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 7 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 7 FDA reports)
PINEAL GLAND CYST ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
POST LAMINECTOMY SYNDROME ( 7 FDA reports)
PRESBYACUSIS ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 7 FDA reports)
SCLERITIS ( 7 FDA reports)
SIGMOIDECTOMY ( 7 FDA reports)
SKIN CYST EXCISION ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SKIN INJURY ( 7 FDA reports)
SPIROMETRY ABNORMAL ( 7 FDA reports)
SPLENIC GRANULOMA ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
STRESS SYMPTOMS ( 7 FDA reports)
STUPOR ( 7 FDA reports)
SUBACUTE ENDOCARDITIS ( 7 FDA reports)
SUBRETINAL FIBROSIS ( 7 FDA reports)
SURGICAL FAILURE ( 7 FDA reports)
TENDON CALCIFICATION ( 7 FDA reports)
THROMBOLYSIS ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
TRANSFERRIN DECREASED ( 7 FDA reports)
TRAUMATIC HAEMATOMA ( 7 FDA reports)
TREATMENT FAILURE ( 7 FDA reports)
TUMOUR ULCERATION ( 7 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 7 FDA reports)
URETHRAL STENT INSERTION ( 7 FDA reports)
UTERINE ATONY ( 7 FDA reports)
VAGINAL EROSION ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VITAMIN K DEFICIENCY ( 7 FDA reports)
VULVAL DISORDER ( 7 FDA reports)
ABDOMINAL NEOPLASM ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
APHERESIS ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
APPLICATION SITE BURN ( 6 FDA reports)
ARTIFICIAL MENOPAUSE ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BLADDER DISCOMFORT ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 6 FDA reports)
CARDIAC VALVE VEGETATION ( 6 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CATHETER SITE HAEMORRHAGE ( 6 FDA reports)
CEREBRAL CALCIFICATION ( 6 FDA reports)
CEREBRAL CYST ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 6 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 6 FDA reports)
CHRONIC TONSILLITIS ( 6 FDA reports)
CLONUS ( 6 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 6 FDA reports)
COCCIDIOIDOMYCOSIS ( 6 FDA reports)
CORNEAL OPACITY ( 6 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 6 FDA reports)
CYSTITIS BACTERIAL ( 6 FDA reports)
DACRYOCYSTORHINOSTOMY ( 6 FDA reports)
DEAFNESS BILATERAL ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
ELECTROPHORESIS ABNORMAL ( 6 FDA reports)
ENCHONDROMA ( 6 FDA reports)
EPIGLOTTIC OEDEMA ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
EYE INFECTION VIRAL ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
FLOPPY IRIS SYNDROME ( 6 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 6 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 6 FDA reports)
GASTROENTERITIS RADIATION ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GRANULOCYTES MATURATION ARREST ( 6 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 6 FDA reports)
HAEMODILUTION ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HEAD AND NECK CANCER ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
HEREDITARY ANGIOEDEMA ( 6 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
IMPLANT SITE DISCHARGE ( 6 FDA reports)
IMPLANT SITE PAIN ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
IRON DEFICIENCY ( 6 FDA reports)
ISCHIORECTAL HERNIA ( 6 FDA reports)
LENS DISORDER ( 6 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
LYMPHOCYTOSIS ( 6 FDA reports)
MAGNESIUM DEFICIENCY ( 6 FDA reports)
MEDIASTINAL SHIFT ( 6 FDA reports)
MENINGITIS VIRAL ( 6 FDA reports)
MENOMETRORRHAGIA ( 6 FDA reports)
METASTASES TO PERITONEUM ( 6 FDA reports)
MITRAL VALVE REPAIR ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MYRINGOTOMY ( 6 FDA reports)
NASAL SEPTUM DISORDER ( 6 FDA reports)
NECK INJURY ( 6 FDA reports)
NEUROGENIC BOWEL ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 6 FDA reports)
PANCREATIC ENLARGEMENT ( 6 FDA reports)
PARAKERATOSIS ( 6 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PERITONSILLAR ABSCESS ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PITUITARY TUMOUR ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
POST PROCEDURAL DISCHARGE ( 6 FDA reports)
POSTERIOR CAPSULOTOMY ( 6 FDA reports)
PREAURICULAR CYST ( 6 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RETINAL DEGENERATION ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 6 FDA reports)
SOFT TISSUE NEOPLASM ( 6 FDA reports)
SPINAL PAIN ( 6 FDA reports)
STERNAL FRACTURE ( 6 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 6 FDA reports)
SUTURE RELATED COMPLICATION ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
THORACIC OUTLET SYNDROME ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
UTERINE FIBROSIS ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VULVAL ABSCESS ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
AURICULAR PERICHONDRITIS ( 5 FDA reports)
BACTERIAL CULTURE ( 5 FDA reports)
BILIARY CIRRHOSIS ( 5 FDA reports)
BIOPSY BREAST ( 5 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 5 FDA reports)
BLEPHAROPLASTY ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD PH INCREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BURNS FIRST DEGREE ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CHOKING SENSATION ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CHYLOTHORAX ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 5 FDA reports)
DEVICE BREAKAGE ( 5 FDA reports)
DIASTOLIC HYPERTENSION ( 5 FDA reports)
EAR CANAL ERYTHEMA ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EPIPLOIC APPENDAGITIS ( 5 FDA reports)
EPISCLERITIS ( 5 FDA reports)
ERYTHROPLASIA ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
EXPLORATIVE LAPAROTOMY ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
FLASHBACK ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FRACTURE TREATMENT ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
GINGIVAL DISCOLOURATION ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 5 FDA reports)
HIRSUTISM ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYDROMYELIA ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
IMPLANT SITE INFLAMMATION ( 5 FDA reports)
INCISIONAL HERNIA ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INGUINAL HERNIA STRANGULATED ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
KETONURIA ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
LACRIMAL DUCT PROCEDURE ( 5 FDA reports)
LIFE SUPPORT ( 5 FDA reports)
LIGAMENT LAXITY ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 5 FDA reports)
MEDIASTINAL MASS ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENINGOCELE ( 5 FDA reports)
METASTASES TO MUSCLE ( 5 FDA reports)
NAIL DISCOMFORT ( 5 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 5 FDA reports)
NIGHT BLINDNESS ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
PAPILLARY THYROID CANCER ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIHEPATIC ABSCESS ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
PNEUMONITIS CHEMICAL ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 5 FDA reports)
RECTAL ADENOMA ( 5 FDA reports)
RENAL HYPERTROPHY ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SEPTOPLASTY ( 5 FDA reports)
SKIN DISCOMFORT ( 5 FDA reports)
SKIN INFLAMMATION ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
STENT REMOVAL ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SWEAT GLAND INFECTION ( 5 FDA reports)
THERAPEUTIC EMBOLISATION ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TOXIC NEUROPATHY ( 5 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
VAGINAL OPERATION ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACANTHOSIS ( 4 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ALPHA GLOBULIN INCREASED ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 4 FDA reports)
ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BIOPSY LIP ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER PAPILLOMA ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST MICROCALCIFICATION ( 4 FDA reports)
BREAST NEOPLASM ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CAROTID ENDARTERECTOMY ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLPORRHAPHY ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CONJUNCTIVAL ABRASION ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DIABETIC FOOT INFECTION ( 4 FDA reports)
DRUG CLEARANCE DECREASED ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
EAR OPERATION ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GILBERT'S SYNDROME ( 4 FDA reports)
GINGIVAL INJURY ( 4 FDA reports)
HALITOSIS ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEMIPLEGIA TRANSIENT ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HYDROCHOLECYSTIS ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERGLOBULINAEMIA ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
IMPLANT SITE EROSION ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INSULINOMA ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
JEJUNECTOMY ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIPOHYPERTROPHY ( 4 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 4 FDA reports)
MASTOID EFFUSION ( 4 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 4 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 4 FDA reports)
MOLE EXCISION ( 4 FDA reports)
MUMPS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCLE FLAP OPERATION ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
NEISSERIA INFECTION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUROLYSIS SURGICAL ( 4 FDA reports)
NEUROPATHIC ARTHROPATHY ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 4 FDA reports)
OESTROGEN DEFICIENCY ( 4 FDA reports)
ORBITAL OEDEMA ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
PANCREATICODUODENECTOMY ( 4 FDA reports)
PERITONEAL CARCINOMA ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PHRENIC NERVE PARALYSIS ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POST PROCEDURAL SWELLING ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
RADIATION NECROSIS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RENAL SURGERY ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RETINAL DYSTROPHY ( 4 FDA reports)
RETROPERITONEAL CANCER ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
SALIVARY GLAND RESECTION ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TONGUE AMYLOIDOSIS ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETHRAL OPERATION ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
VAGINOPLASTY ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VOCAL CORD PARESIS ( 4 FDA reports)
WEIGHT LOSS DIET ( 4 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 4 FDA reports)
XANTHOMA ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ANAL POLYP ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
ARTERIAL CATHETERISATION ( 3 FDA reports)
ARTERIAL SPASM ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BIOPSY STOMACH ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BREAST CELLULITIS ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CEREBELLOPONTINE ANGLE TUMOUR ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CHEST WALL CYST ( 3 FDA reports)
CHEST WALL NECROSIS ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
DACRYOCYSTITIS ( 3 FDA reports)
DEVICE MATERIAL ISSUE ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ECZEMA NUMMULAR ( 3 FDA reports)
ENDOCERVICAL CURETTAGE ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EYE MUSCLE OPERATION ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOLLICULAR THYROID CANCER ( 3 FDA reports)
FRACTURE REDUCTION ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTROSTOMY FAILURE ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOAESTHESIA TEETH ( 3 FDA reports)
HYPOLIPIDAEMIA ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFLAMMATION OF WOUND ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
INFUSION SITE WARMTH ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
LARGE INTESTINE FIBROMA ( 3 FDA reports)
LEVATOR SYNDROME ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MACULAR FIBROSIS ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MASTOIDECTOMY ( 3 FDA reports)
MEDICAL OBSERVATION ( 3 FDA reports)
MENINGIOMA SURGERY ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MILIA ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NECROSIS ISCHAEMIC ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
OESOPHAGEAL MASS ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OSTEOMYELITIS BACTERIAL ( 3 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 3 FDA reports)
PANNICULITIS LOBULAR ( 3 FDA reports)
PARKINSONIAN GAIT ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POSTOPERATIVE FEVER ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PYELOGRAM RETROGRADE ( 3 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SINOBRONCHITIS ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKULL X-RAY ABNORMAL ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUDDEN VISUAL LOSS ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THYMIC CANCER METASTATIC ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 3 FDA reports)
TRICHIASIS ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
VAGINAL PAIN ( 3 FDA reports)
VARICOSE VEIN OPERATION ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VULVAL LEUKOPLAKIA ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUPUNCTURE ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA STAGE IV ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BANDAEMIA ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY EYELID ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 2 FDA reports)
BIOPSY PERIPHERAL NERVE ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLAST CELLS ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BURSA REMOVAL ( 2 FDA reports)
CALCIUM IONISED ABNORMAL ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CHEST WALL ABSCESS ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
COCHLEA IMPLANT ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYTOKINE STORM ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DESQUAMATION GINGIVAL ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EAR MALFORMATION ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLISM INFECTIVE ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EUTHANASIA ( 2 FDA reports)
EXERESIS ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FRACTURE MALUNION ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FRONTAL SINUS OPERATIONS ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GRAM STAIN NEGATIVE ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATOTYMPANUM ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCALCIURIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMMUNISATION ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTRA-NASAL ANTROSTOMY ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LAPAROSCOPY ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
MACROGNATHIA ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MAXILLARY ANTRUM OPERATION ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESENTERITIS ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 2 FDA reports)
MUCOSAL EXCORIATION ( 2 FDA reports)
MUCOSAL EXFOLIATION ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL BED TENDERNESS ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NEUROLYSIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OCULAR CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL PAPILLOMA ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERIODONTAL DESTRUCTION ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PEUTZ-JEGHERS SYNDROME ( 2 FDA reports)
PLASMA CELL DISORDER ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA ASPERGILLUS ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIOTHERAPY TO BRAIN ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL GLYCOSURIA ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SPLEEN SCAN ABNORMAL ( 2 FDA reports)
SUPERINFECTION ORAL ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENOLYSIS ( 2 FDA reports)
TESTICULAR MASS ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUBO-OVARIAN ABSCESS ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPHOID FEVER ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS LAKE ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WRIST DEFORMITY ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE PHASE REACTION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPERGILLOSIS ORAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BIOPSY PALATE ABNORMAL ( 1 FDA reports)
BIOPSY THYROID GLAND ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE FRAGMENTATION AROUND IMPLANT ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST PROSTHESIS REMOVAL ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CANALITH REPOSITIONING PROCEDURE ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHONDROMA ( 1 FDA reports)
CHOROID NEOPLASM ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE THERAPY ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISORDER OF GLOBE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCHONDROMATOSIS ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPULIS ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION TOXOPLASMAL ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FULL BLOOD COUNT ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GINGIVAL HYPERPIGMENTATION ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLYCOGEN STORAGE DISORDER ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMOBILIZATION PROLONGED ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE IRRITATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PUSTULE ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE PIGMENTATION CHANGES ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW OSTEITIS ( 1 FDA reports)
JOINT IRRIGATION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPID PROTEINOSIS ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MAXIMAL VOLUNTARY VENTILATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MENINGITIS HERPES ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOCUTANEOUS FLAP OPERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROTISING ULCERATIVE PERIODONTITIS ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 1 FDA reports)
OTOSCOPY ABNORMAL ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROMOTION OF WOUND HEALING ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSOAS SIGN ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RETINAL IMPLANT ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SELECTIVE IGA IMMUNODEFICIENCY ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLINT APPLICATION ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VITAMIN A DEFICIENCY ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL HAEMATOMA ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)

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