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

PAIN ( 2017 FDA reports)
NAUSEA ( 1969 FDA reports)
ANAEMIA ( 1870 FDA reports)
PYREXIA ( 1858 FDA reports)
DIARRHOEA ( 1745 FDA reports)
DYSPNOEA ( 1690 FDA reports)
PNEUMONIA ( 1608 FDA reports)
ANXIETY ( 1597 FDA reports)
FATIGUE ( 1597 FDA reports)
VOMITING ( 1509 FDA reports)
ASTHENIA ( 1392 FDA reports)
OSTEONECROSIS OF JAW ( 1379 FDA reports)
BACK PAIN ( 1305 FDA reports)
BONE DISORDER ( 1245 FDA reports)
CONSTIPATION ( 1091 FDA reports)
NEUROPATHY PERIPHERAL ( 1089 FDA reports)
DEHYDRATION ( 1088 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1065 FDA reports)
HEADACHE ( 1031 FDA reports)
OSTEOMYELITIS ( 1026 FDA reports)
OEDEMA PERIPHERAL ( 1023 FDA reports)
PAIN IN JAW ( 976 FDA reports)
PLATELET COUNT DECREASED ( 969 FDA reports)
HAEMOGLOBIN DECREASED ( 959 FDA reports)
DEEP VEIN THROMBOSIS ( 944 FDA reports)
TOOTH EXTRACTION ( 938 FDA reports)
INJURY ( 928 FDA reports)
HYPOTENSION ( 926 FDA reports)
NEUTROPENIA ( 921 FDA reports)
WEIGHT DECREASED ( 909 FDA reports)
PLEURAL EFFUSION ( 899 FDA reports)
THROMBOCYTOPENIA ( 880 FDA reports)
DECREASED APPETITE ( 878 FDA reports)
OSTEONECROSIS ( 866 FDA reports)
ARTHRALGIA ( 856 FDA reports)
INTERSTITIAL LUNG DISEASE ( 834 FDA reports)
HYPOAESTHESIA ( 823 FDA reports)
INFECTION ( 814 FDA reports)
DEATH ( 806 FDA reports)
ABDOMINAL PAIN ( 797 FDA reports)
FALL ( 795 FDA reports)
PANCYTOPENIA ( 794 FDA reports)
MULTIPLE MYELOMA ( 793 FDA reports)
DIZZINESS ( 791 FDA reports)
RASH ( 765 FDA reports)
CHEST PAIN ( 759 FDA reports)
PAIN IN EXTREMITY ( 741 FDA reports)
HYPERTENSION ( 737 FDA reports)
PULMONARY EMBOLISM ( 737 FDA reports)
SEPSIS ( 732 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 725 FDA reports)
OSTEOARTHRITIS ( 703 FDA reports)
DISEASE PROGRESSION ( 674 FDA reports)
CONFUSIONAL STATE ( 670 FDA reports)
FEBRILE NEUTROPENIA ( 662 FDA reports)
DEPRESSION ( 651 FDA reports)
MALAISE ( 648 FDA reports)
OSTEOPENIA ( 640 FDA reports)
SWELLING ( 628 FDA reports)
RENAL FAILURE ( 622 FDA reports)
SPINAL OSTEOARTHRITIS ( 613 FDA reports)
BRONCHITIS ( 610 FDA reports)
COUGH ( 608 FDA reports)
NEUTROPHIL COUNT DECREASED ( 602 FDA reports)
HYPOKALAEMIA ( 599 FDA reports)
DYSPHAGIA ( 598 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 593 FDA reports)
STOMATITIS ( 590 FDA reports)
PARAESTHESIA ( 581 FDA reports)
SINUSITIS ( 577 FDA reports)
METASTASES TO BONE ( 572 FDA reports)
CONVULSION ( 571 FDA reports)
RENAL FAILURE ACUTE ( 556 FDA reports)
BONE PAIN ( 547 FDA reports)
ERYTHEMA ( 543 FDA reports)
EMOTIONAL DISTRESS ( 540 FDA reports)
ATELECTASIS ( 539 FDA reports)
IMPAIRED HEALING ( 532 FDA reports)
URINARY TRACT INFECTION ( 525 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 524 FDA reports)
RESPIRATORY FAILURE ( 524 FDA reports)
CELLULITIS ( 514 FDA reports)
ANHEDONIA ( 512 FDA reports)
GAIT DISTURBANCE ( 507 FDA reports)
INSOMNIA ( 501 FDA reports)
MUSCULAR WEAKNESS ( 496 FDA reports)
BONE LESION ( 492 FDA reports)
DEFORMITY ( 479 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 474 FDA reports)
LEUKOPENIA ( 472 FDA reports)
DENTAL CARIES ( 465 FDA reports)
ATRIAL FIBRILLATION ( 464 FDA reports)
HYPERGLYCAEMIA ( 456 FDA reports)
MENTAL STATUS CHANGES ( 449 FDA reports)
NEOPLASM MALIGNANT ( 447 FDA reports)
HYPONATRAEMIA ( 438 FDA reports)
HERPES ZOSTER ( 436 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 419 FDA reports)
CHILLS ( 419 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 406 FDA reports)
BLOOD CREATININE INCREASED ( 398 FDA reports)
SYNCOPE ( 397 FDA reports)
TOOTH DISORDER ( 394 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 385 FDA reports)
HAEMATOCRIT DECREASED ( 381 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 380 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 377 FDA reports)
BLOOD GLUCOSE INCREASED ( 373 FDA reports)
PRURITUS ( 370 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 369 FDA reports)
OEDEMA ( 368 FDA reports)
DECREASED INTEREST ( 364 FDA reports)
TACHYCARDIA ( 363 FDA reports)
TOOTHACHE ( 363 FDA reports)
HYPOPHAGIA ( 362 FDA reports)
SPINAL COMPRESSION FRACTURE ( 362 FDA reports)
SWELLING FACE ( 362 FDA reports)
RIB FRACTURE ( 354 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 351 FDA reports)
SOMNOLENCE ( 350 FDA reports)
HAEMORRHOIDS ( 348 FDA reports)
VISION BLURRED ( 347 FDA reports)
DRUG INEFFECTIVE ( 342 FDA reports)
CATARACT ( 340 FDA reports)
MUSCLE SPASMS ( 338 FDA reports)
OSTEOPOROSIS ( 336 FDA reports)
HYPOXIA ( 329 FDA reports)
LYMPHADENOPATHY ( 321 FDA reports)
PRIMARY SEQUESTRUM ( 321 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 319 FDA reports)
CARDIOMEGALY ( 319 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 317 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 317 FDA reports)
OSTEOLYSIS ( 316 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 315 FDA reports)
RECTAL HAEMORRHAGE ( 314 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 311 FDA reports)
MUSCULOSKELETAL PAIN ( 311 FDA reports)
MYALGIA ( 307 FDA reports)
NECK PAIN ( 306 FDA reports)
INFLAMMATION ( 305 FDA reports)
CHEST DISCOMFORT ( 303 FDA reports)
COMPRESSION FRACTURE ( 303 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 300 FDA reports)
LOSS OF CONSCIOUSNESS ( 299 FDA reports)
MUCOSAL INFLAMMATION ( 295 FDA reports)
BLOOD PRESSURE DECREASED ( 294 FDA reports)
EXOSTOSIS ( 294 FDA reports)
JAW OPERATION ( 290 FDA reports)
METASTASES TO LIVER ( 290 FDA reports)
ANOREXIA ( 288 FDA reports)
DIABETES MELLITUS ( 288 FDA reports)
HIATUS HERNIA ( 287 FDA reports)
TOOTH ABSCESS ( 282 FDA reports)
DEBRIDEMENT ( 280 FDA reports)
INFUSION RELATED REACTION ( 280 FDA reports)
ORAL PAIN ( 280 FDA reports)
EPISTAXIS ( 277 FDA reports)
FLUSHING ( 276 FDA reports)
RENAL IMPAIRMENT ( 275 FDA reports)
DISABILITY ( 274 FDA reports)
DIVERTICULUM ( 271 FDA reports)
ARTHRITIS ( 270 FDA reports)
GASTRITIS ( 266 FDA reports)
ABDOMINAL PAIN UPPER ( 264 FDA reports)
STAPHYLOCOCCAL INFECTION ( 264 FDA reports)
METASTASES TO LUNG ( 259 FDA reports)
MOUTH ULCERATION ( 259 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 258 FDA reports)
HAEMATURIA ( 257 FDA reports)
ABDOMINAL DISTENSION ( 256 FDA reports)
LUNG NEOPLASM ( 256 FDA reports)
HYPERSENSITIVITY ( 255 FDA reports)
SEPTIC SHOCK ( 250 FDA reports)
TREMOR ( 250 FDA reports)
ENDODONTIC PROCEDURE ( 249 FDA reports)
BONE MARROW FAILURE ( 248 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 245 FDA reports)
DYSPNOEA EXERTIONAL ( 243 FDA reports)
LUNG INFILTRATION ( 242 FDA reports)
ALOPECIA ( 241 FDA reports)
DYSPEPSIA ( 241 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 238 FDA reports)
LUNG DISORDER ( 237 FDA reports)
RENAL FAILURE CHRONIC ( 233 FDA reports)
BONE DEBRIDEMENT ( 232 FDA reports)
LETHARGY ( 231 FDA reports)
CARDIAC ARREST ( 230 FDA reports)
EMPHYSEMA ( 229 FDA reports)
METASTASES TO SPINE ( 229 FDA reports)
SINUS TACHYCARDIA ( 229 FDA reports)
BLOOD UREA INCREASED ( 228 FDA reports)
PATHOLOGICAL FRACTURE ( 228 FDA reports)
RENAL CYST ( 225 FDA reports)
BLOOD PRESSURE INCREASED ( 224 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 224 FDA reports)
LIFE EXPECTANCY SHORTENED ( 224 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 223 FDA reports)
EAR PAIN ( 223 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 223 FDA reports)
ABSCESS ( 222 FDA reports)
CHOLELITHIASIS ( 222 FDA reports)
MITRAL VALVE INCOMPETENCE ( 222 FDA reports)
BURSITIS ( 221 FDA reports)
ORAL DISORDER ( 220 FDA reports)
CONDITION AGGRAVATED ( 218 FDA reports)
NEPHROLITHIASIS ( 218 FDA reports)
PURULENT DISCHARGE ( 213 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 213 FDA reports)
LOOSE TOOTH ( 212 FDA reports)
ASCITES ( 211 FDA reports)
WEIGHT INCREASED ( 211 FDA reports)
SINUS DISORDER ( 209 FDA reports)
ASTHMA ( 208 FDA reports)
PULMONARY OEDEMA ( 208 FDA reports)
CANDIDIASIS ( 207 FDA reports)
TOOTH LOSS ( 207 FDA reports)
HAEMORRHAGE ( 206 FDA reports)
MULTI-ORGAN FAILURE ( 206 FDA reports)
MYOCARDIAL INFARCTION ( 205 FDA reports)
SEQUESTRECTOMY ( 205 FDA reports)
DYSGEUSIA ( 203 FDA reports)
FISTULA ( 203 FDA reports)
SLEEP APNOEA SYNDROME ( 203 FDA reports)
OROPHARYNGEAL PAIN ( 202 FDA reports)
DYSURIA ( 200 FDA reports)
GINGIVITIS ( 199 FDA reports)
ORAL CANDIDIASIS ( 199 FDA reports)
PHYSICAL DISABILITY ( 199 FDA reports)
CONTUSION ( 196 FDA reports)
OESOPHAGITIS ( 195 FDA reports)
DECUBITUS ULCER ( 194 FDA reports)
PRODUCTIVE COUGH ( 194 FDA reports)
EXPOSED BONE IN JAW ( 192 FDA reports)
GINGIVAL SWELLING ( 192 FDA reports)
SCOLIOSIS ( 192 FDA reports)
BALANCE DISORDER ( 191 FDA reports)
CORONARY ARTERY DISEASE ( 190 FDA reports)
OSTEITIS ( 190 FDA reports)
CEREBROVASCULAR ACCIDENT ( 187 FDA reports)
HEPATIC STEATOSIS ( 187 FDA reports)
HYPERHIDROSIS ( 187 FDA reports)
GINGIVAL INFECTION ( 186 FDA reports)
DISCOMFORT ( 183 FDA reports)
HYPERLIPIDAEMIA ( 181 FDA reports)
TOOTH FRACTURE ( 181 FDA reports)
GINGIVAL BLEEDING ( 180 FDA reports)
ACTINOMYCOSIS ( 179 FDA reports)
ILEUS ( 179 FDA reports)
PERIODONTAL DISEASE ( 179 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 179 FDA reports)
ROTATOR CUFF SYNDROME ( 179 FDA reports)
CEREBRAL INFARCTION ( 177 FDA reports)
ANAPHYLACTIC SHOCK ( 175 FDA reports)
MALNUTRITION ( 175 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 174 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 174 FDA reports)
OSTEOSCLEROSIS ( 174 FDA reports)
URTICARIA ( 174 FDA reports)
COLITIS ( 173 FDA reports)
HAEMATOCHEZIA ( 173 FDA reports)
PALPITATIONS ( 173 FDA reports)
LUMBAR SPINAL STENOSIS ( 172 FDA reports)
OXYGEN SATURATION DECREASED ( 172 FDA reports)
PNEUMOTHORAX ( 172 FDA reports)
ABDOMINAL DISCOMFORT ( 171 FDA reports)
HYPOMAGNESAEMIA ( 171 FDA reports)
SHOCK ( 171 FDA reports)
DENTAL OPERATION ( 170 FDA reports)
HAEMOPTYSIS ( 169 FDA reports)
HYPERKALAEMIA ( 168 FDA reports)
SURGERY ( 168 FDA reports)
WHEEZING ( 168 FDA reports)
HYPERCALCAEMIA ( 167 FDA reports)
NEOPLASM PROGRESSION ( 167 FDA reports)
CARDIO-RESPIRATORY ARREST ( 166 FDA reports)
CARDIOMYOPATHY ( 166 FDA reports)
LIVER DISORDER ( 166 FDA reports)
URINARY INCONTINENCE ( 166 FDA reports)
URINARY RETENTION ( 166 FDA reports)
FEELING ABNORMAL ( 165 FDA reports)
HIP FRACTURE ( 165 FDA reports)
HOT FLUSH ( 165 FDA reports)
MASS ( 165 FDA reports)
EATING DISORDER ( 164 FDA reports)
KYPHOSIS ( 164 FDA reports)
RASH ERYTHEMATOUS ( 164 FDA reports)
GINGIVAL PAIN ( 163 FDA reports)
RESPIRATORY DISTRESS ( 163 FDA reports)
MASTICATION DISORDER ( 162 FDA reports)
BLOOD SODIUM DECREASED ( 161 FDA reports)
DYSARTHRIA ( 161 FDA reports)
GINGIVAL DISORDER ( 161 FDA reports)
JAW DISORDER ( 161 FDA reports)
DERMATITIS ACNEIFORM ( 160 FDA reports)
HYPERCHOLESTEROLAEMIA ( 159 FDA reports)
PERICARDIAL EFFUSION ( 159 FDA reports)
TENDERNESS ( 159 FDA reports)
CHRONIC SINUSITIS ( 158 FDA reports)
CEREBRAL HAEMORRHAGE ( 157 FDA reports)
TOOTH INFECTION ( 157 FDA reports)
HYPOAESTHESIA ORAL ( 156 FDA reports)
BRAIN OEDEMA ( 155 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 155 FDA reports)
STEM CELL TRANSPLANT ( 155 FDA reports)
JAW FRACTURE ( 154 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 153 FDA reports)
DRY MOUTH ( 153 FDA reports)
PROTHROMBIN TIME PROLONGED ( 153 FDA reports)
RESPIRATORY DISORDER ( 153 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 151 FDA reports)
PNEUMONITIS ( 151 FDA reports)
EJECTION FRACTION DECREASED ( 150 FDA reports)
RASH PRURITIC ( 149 FDA reports)
WALKING AID USER ( 149 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 148 FDA reports)
HEART RATE INCREASED ( 148 FDA reports)
SPINAL DISORDER ( 147 FDA reports)
THROMBOSIS ( 147 FDA reports)
DEAFNESS ( 146 FDA reports)
HYPOALBUMINAEMIA ( 146 FDA reports)
JOINT SWELLING ( 145 FDA reports)
LUNG NEOPLASM MALIGNANT ( 145 FDA reports)
ORAL INFECTION ( 145 FDA reports)
GASTRIC ULCER ( 144 FDA reports)
HEPATIC FAILURE ( 144 FDA reports)
RADIOTHERAPY ( 144 FDA reports)
BLOOD BILIRUBIN INCREASED ( 143 FDA reports)
FUNGAL INFECTION ( 143 FDA reports)
NEURALGIA ( 143 FDA reports)
SPINAL COLUMN STENOSIS ( 143 FDA reports)
SCAR ( 142 FDA reports)
CARDIAC DISORDER ( 141 FDA reports)
HALLUCINATION ( 141 FDA reports)
HYPOTHYROIDISM ( 141 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 141 FDA reports)
METASTASES TO LYMPH NODES ( 141 FDA reports)
PERIODONTITIS ( 141 FDA reports)
BONE DENSITY DECREASED ( 140 FDA reports)
HYPOCALCAEMIA ( 140 FDA reports)
BACTERIAL INFECTION ( 139 FDA reports)
DYSPHONIA ( 139 FDA reports)
POLLAKIURIA ( 139 FDA reports)
VERTEBROPLASTY ( 139 FDA reports)
OBESITY ( 138 FDA reports)
PLATELET COUNT INCREASED ( 138 FDA reports)
SKIN ULCER ( 138 FDA reports)
ABSCESS DRAINAGE ( 136 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 136 FDA reports)
HEPATIC LESION ( 136 FDA reports)
OVARIAN CANCER RECURRENT ( 136 FDA reports)
BREAST CANCER METASTATIC ( 135 FDA reports)
SKIN LESION ( 135 FDA reports)
SPINAL CORD COMPRESSION ( 135 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 134 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 134 FDA reports)
ADRENAL INSUFFICIENCY ( 133 FDA reports)
DELIRIUM ( 133 FDA reports)
DENTURE WEARER ( 133 FDA reports)
MELAENA ( 133 FDA reports)
ARRHYTHMIA ( 132 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 132 FDA reports)
LEUKOCYTOSIS ( 132 FDA reports)
PNEUMONIA ASPIRATION ( 132 FDA reports)
DRUG HYPERSENSITIVITY ( 131 FDA reports)
VERTIGO ( 131 FDA reports)
PURULENCE ( 129 FDA reports)
AMNESIA ( 128 FDA reports)
ARTERIOSCLEROSIS ( 128 FDA reports)
NASAL CONGESTION ( 128 FDA reports)
RHINORRHOEA ( 128 FDA reports)
DIVERTICULUM INTESTINAL ( 127 FDA reports)
CARDIAC FAILURE ( 126 FDA reports)
HEPATIC CYST ( 126 FDA reports)
ONYCHOMYCOSIS ( 126 FDA reports)
ALVEOLOPLASTY ( 125 FDA reports)
COMA ( 125 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 125 FDA reports)
INTESTINAL OBSTRUCTION ( 124 FDA reports)
ORTHOSTATIC HYPOTENSION ( 124 FDA reports)
DERMATITIS ( 123 FDA reports)
METASTATIC NEOPLASM ( 123 FDA reports)
SPEECH DISORDER ( 123 FDA reports)
DRY SKIN ( 122 FDA reports)
GENERALISED OEDEMA ( 122 FDA reports)
AGITATION ( 120 FDA reports)
BLOOD CALCIUM DECREASED ( 120 FDA reports)
HYPOGLYCAEMIA ( 120 FDA reports)
OVARIAN CANCER ( 120 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 119 FDA reports)
BLOOD ALBUMIN DECREASED ( 119 FDA reports)
BODY TEMPERATURE INCREASED ( 118 FDA reports)
DRUG TOXICITY ( 118 FDA reports)
ENCEPHALOPATHY ( 118 FDA reports)
OVERDOSE ( 118 FDA reports)
CYST ( 117 FDA reports)
STEVENS-JOHNSON SYNDROME ( 117 FDA reports)
VISUAL IMPAIRMENT ( 116 FDA reports)
BRADYCARDIA ( 115 FDA reports)
FAILURE TO THRIVE ( 115 FDA reports)
ORAL HERPES ( 115 FDA reports)
BREATH ODOUR ( 114 FDA reports)
COAGULOPATHY ( 113 FDA reports)
DYSKINESIA ( 113 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 113 FDA reports)
PHARYNGITIS ( 113 FDA reports)
PULMONARY HYPERTENSION ( 113 FDA reports)
SUICIDAL IDEATION ( 113 FDA reports)
SYNOVIAL CYST ( 113 FDA reports)
BONE MARROW TRANSPLANT ( 112 FDA reports)
PERITONITIS ( 112 FDA reports)
PULMONARY FIBROSIS ( 112 FDA reports)
RENAL DISORDER ( 112 FDA reports)
SOFT TISSUE INFLAMMATION ( 112 FDA reports)
CONJUNCTIVITIS ( 111 FDA reports)
TRISMUS ( 110 FDA reports)
UNRESPONSIVE TO STIMULI ( 109 FDA reports)
ANAPHYLACTIC REACTION ( 108 FDA reports)
BLOOD POTASSIUM DECREASED ( 108 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 108 FDA reports)
AORTIC VALVE INCOMPETENCE ( 106 FDA reports)
FLUID RETENTION ( 106 FDA reports)
UTERINE LEIOMYOMA ( 106 FDA reports)
DIVERTICULITIS ( 105 FDA reports)
DRUG INTERACTION ( 105 FDA reports)
GASTROINTESTINAL PERFORATION ( 105 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 105 FDA reports)
HEPATITIS ( 104 FDA reports)
METABOLIC ACIDOSIS ( 104 FDA reports)
BONE FRAGMENTATION ( 103 FDA reports)
BONE OPERATION ( 103 FDA reports)
HEMIPARESIS ( 103 FDA reports)
NIGHT SWEATS ( 103 FDA reports)
SPLENOMEGALY ( 102 FDA reports)
ABSCESS JAW ( 101 FDA reports)
ACUTE RESPIRATORY FAILURE ( 101 FDA reports)
HYDRONEPHROSIS ( 101 FDA reports)
PLASMACYTOMA ( 101 FDA reports)
PULMONARY CONGESTION ( 101 FDA reports)
HEPATOMEGALY ( 99 FDA reports)
JAUNDICE ( 99 FDA reports)
MEMORY IMPAIRMENT ( 99 FDA reports)
SQUAMOUS CELL CARCINOMA ( 99 FDA reports)
COLITIS ULCERATIVE ( 98 FDA reports)
IMMUNODEFICIENCY ( 98 FDA reports)
JOINT DISLOCATION ( 98 FDA reports)
PROSTATE CANCER ( 98 FDA reports)
COLONIC POLYP ( 97 FDA reports)
GOITRE ( 97 FDA reports)
MOBILITY DECREASED ( 97 FDA reports)
MYOPATHY ( 97 FDA reports)
PROTEINURIA ( 97 FDA reports)
VISUAL ACUITY REDUCED ( 97 FDA reports)
DIPLOPIA ( 96 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 96 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 95 FDA reports)
ERECTILE DYSFUNCTION ( 95 FDA reports)
FACIAL PAIN ( 95 FDA reports)
HEPATIC ENZYME INCREASED ( 95 FDA reports)
INTESTINAL PERFORATION ( 95 FDA reports)
RESTLESSNESS ( 95 FDA reports)
ARTHROPATHY ( 94 FDA reports)
BASAL CELL CARCINOMA ( 94 FDA reports)
CEREBRAL ATROPHY ( 94 FDA reports)
DEVICE RELATED INFECTION ( 94 FDA reports)
HYPOPHOSPHATAEMIA ( 94 FDA reports)
DISORIENTATION ( 93 FDA reports)
SKIN EXFOLIATION ( 93 FDA reports)
SPONDYLOLISTHESIS ( 93 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 93 FDA reports)
CYSTITIS ( 92 FDA reports)
GASTROINTESTINAL DISORDER ( 92 FDA reports)
HYPOVOLAEMIA ( 92 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 92 FDA reports)
MIGRAINE ( 92 FDA reports)
NEUTROPHIL COUNT INCREASED ( 92 FDA reports)
RESPIRATORY ARREST ( 92 FDA reports)
BLOOD POTASSIUM INCREASED ( 91 FDA reports)
BREAST CANCER ( 91 FDA reports)
SOFT TISSUE DISORDER ( 91 FDA reports)
INCISIONAL DRAINAGE ( 90 FDA reports)
PNEUMONIA BACTERIAL ( 90 FDA reports)
ABASIA ( 89 FDA reports)
ANGINA PECTORIS ( 89 FDA reports)
BACTERAEMIA ( 89 FDA reports)
ELECTROLYTE IMBALANCE ( 89 FDA reports)
NASOPHARYNGITIS ( 89 FDA reports)
BONE EROSION ( 88 FDA reports)
CHOLECYSTECTOMY ( 88 FDA reports)
NOCTURIA ( 88 FDA reports)
ORAL SURGERY ( 88 FDA reports)
CANCER PAIN ( 87 FDA reports)
LYMPHOPENIA ( 87 FDA reports)
POST PROCEDURAL COMPLICATION ( 87 FDA reports)
FOOT FRACTURE ( 86 FDA reports)
MYELOMA RECURRENCE ( 86 FDA reports)
OSTEORADIONECROSIS ( 86 FDA reports)
STRESS ( 86 FDA reports)
HERPES SIMPLEX ( 85 FDA reports)
BLINDNESS ( 84 FDA reports)
CEREBRAL ISCHAEMIA ( 84 FDA reports)
PALLOR ( 84 FDA reports)
PETECHIAE ( 84 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 84 FDA reports)
ESCHERICHIA INFECTION ( 83 FDA reports)
OPEN REDUCTION OF FRACTURE ( 83 FDA reports)
PLEURAL FIBROSIS ( 83 FDA reports)
PRESYNCOPE ( 83 FDA reports)
RASH MACULO-PAPULAR ( 83 FDA reports)
SERUM FERRITIN INCREASED ( 83 FDA reports)
WOUND DEHISCENCE ( 83 FDA reports)
ACNE ( 82 FDA reports)
COLORECTAL CANCER ( 82 FDA reports)
PELVIC FRACTURE ( 82 FDA reports)
GYNAECOMASTIA ( 81 FDA reports)
PARONYCHIA ( 81 FDA reports)
RADICULOPATHY ( 81 FDA reports)
SLEEP DISORDER ( 81 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 80 FDA reports)
SINUS BRADYCARDIA ( 80 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 79 FDA reports)
GLIOBLASTOMA MULTIFORME ( 79 FDA reports)
INFLUENZA ( 79 FDA reports)
PSYCHOTIC DISORDER ( 79 FDA reports)
DIALYSIS ( 78 FDA reports)
DRY EYE ( 78 FDA reports)
IRON DEFICIENCY ANAEMIA ( 78 FDA reports)
ORAL CAVITY FISTULA ( 78 FDA reports)
PANCREATITIS ( 78 FDA reports)
PSEUDOMONAS INFECTION ( 78 FDA reports)
SENSITIVITY OF TEETH ( 78 FDA reports)
GLAUCOMA ( 77 FDA reports)
HAEMATEMESIS ( 77 FDA reports)
OPEN WOUND ( 77 FDA reports)
ULCER ( 77 FDA reports)
VIITH NERVE PARALYSIS ( 77 FDA reports)
CERVICAL SPINAL STENOSIS ( 76 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 76 FDA reports)
AGRANULOCYTOSIS ( 75 FDA reports)
SCIATICA ( 75 FDA reports)
TONGUE ULCERATION ( 75 FDA reports)
TUMOUR LYSIS SYNDROME ( 75 FDA reports)
CYANOSIS ( 74 FDA reports)
DIABETIC KETOACIDOSIS ( 74 FDA reports)
PAROTITIS ( 74 FDA reports)
RHINITIS ALLERGIC ( 74 FDA reports)
TENDONITIS ( 74 FDA reports)
EDENTULOUS ( 73 FDA reports)
GINGIVAL ULCERATION ( 73 FDA reports)
HUMERUS FRACTURE ( 73 FDA reports)
JOINT STIFFNESS ( 73 FDA reports)
APHASIA ( 72 FDA reports)
BREAST MASS ( 72 FDA reports)
EAR DISCOMFORT ( 72 FDA reports)
FEELING HOT ( 72 FDA reports)
IRRITABLE BOWEL SYNDROME ( 72 FDA reports)
LOBAR PNEUMONIA ( 72 FDA reports)
NAIL DISORDER ( 72 FDA reports)
ROAD TRAFFIC ACCIDENT ( 72 FDA reports)
DEMENTIA ( 71 FDA reports)
TINNITUS ( 71 FDA reports)
FAECAL INCONTINENCE ( 70 FDA reports)
FEMUR FRACTURE ( 70 FDA reports)
RASH GENERALISED ( 70 FDA reports)
BRONCHOPNEUMONIA ( 69 FDA reports)
DUODENAL ULCER ( 69 FDA reports)
HAEMANGIOMA ( 69 FDA reports)
LOCAL SWELLING ( 69 FDA reports)
OSTEITIS DEFORMANS ( 69 FDA reports)
PERSONALITY CHANGE ( 69 FDA reports)
PLASMACYTOSIS ( 69 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 68 FDA reports)
BONE LOSS ( 68 FDA reports)
CHOLECYSTITIS ( 68 FDA reports)
ECCHYMOSIS ( 68 FDA reports)
EYE SWELLING ( 68 FDA reports)
FLUID OVERLOAD ( 68 FDA reports)
FOOT DEFORMITY ( 68 FDA reports)
IRRITABILITY ( 68 FDA reports)
JOINT EFFUSION ( 68 FDA reports)
PANCREATITIS ACUTE ( 68 FDA reports)
RASH MACULAR ( 68 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 68 FDA reports)
COSTOCHONDRITIS ( 67 FDA reports)
ENTEROCOCCAL INFECTION ( 67 FDA reports)
ORAL INTAKE REDUCED ( 67 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 66 FDA reports)
GRAND MAL CONVULSION ( 66 FDA reports)
NEOPLASM ( 66 FDA reports)
BONE NEOPLASM MALIGNANT ( 65 FDA reports)
LYMPHOEDEMA ( 65 FDA reports)
OCULAR HYPERAEMIA ( 65 FDA reports)
SKIN HYPERPIGMENTATION ( 65 FDA reports)
SPINAL LAMINECTOMY ( 65 FDA reports)
ATAXIA ( 64 FDA reports)
HICCUPS ( 64 FDA reports)
MUSCLE STRAIN ( 64 FDA reports)
OLIGURIA ( 64 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 64 FDA reports)
TOOTH DEPOSIT ( 64 FDA reports)
IMMUNOSUPPRESSION ( 63 FDA reports)
LEFT ATRIAL DILATATION ( 63 FDA reports)
MOUTH HAEMORRHAGE ( 63 FDA reports)
MYELODYSPLASTIC SYNDROME ( 63 FDA reports)
NEUROGENIC BLADDER ( 63 FDA reports)
POLYP ( 63 FDA reports)
SKIN DISCOLOURATION ( 63 FDA reports)
UNEVALUABLE EVENT ( 63 FDA reports)
WOUND DRAINAGE ( 63 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 62 FDA reports)
CATARACT OPERATION ( 62 FDA reports)
EYE PAIN ( 62 FDA reports)
HAEMATOMA ( 62 FDA reports)
PAROTID GLAND ENLARGEMENT ( 62 FDA reports)
SUDDEN DEATH ( 62 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 61 FDA reports)
ENDOTRACHEAL INTUBATION ( 61 FDA reports)
ENTEROCOLITIS ( 61 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 61 FDA reports)
OSTEOMYELITIS CHRONIC ( 61 FDA reports)
RESPIRATORY RATE INCREASED ( 61 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 60 FDA reports)
FACET JOINT SYNDROME ( 60 FDA reports)
FISTULA DISCHARGE ( 60 FDA reports)
GASTROENTERITIS ( 60 FDA reports)
INFLUENZA LIKE ILLNESS ( 60 FDA reports)
RALES ( 60 FDA reports)
RHABDOMYOLYSIS ( 60 FDA reports)
SEBORRHOEIC KERATOSIS ( 60 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 60 FDA reports)
TYPE 2 DIABETES MELLITUS ( 60 FDA reports)
COGNITIVE DISORDER ( 59 FDA reports)
EARLY SATIETY ( 59 FDA reports)
EPICONDYLITIS ( 59 FDA reports)
EYE MOVEMENT DISORDER ( 59 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 59 FDA reports)
ABSCESS ORAL ( 58 FDA reports)
FACE OEDEMA ( 58 FDA reports)
FLANK PAIN ( 58 FDA reports)
INTRAOCULAR LENS IMPLANT ( 58 FDA reports)
LACRIMATION INCREASED ( 58 FDA reports)
METASTASIS ( 58 FDA reports)
NO THERAPEUTIC RESPONSE ( 58 FDA reports)
PIGMENTATION DISORDER ( 58 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 58 FDA reports)
RENAL ATROPHY ( 58 FDA reports)
RESPIRATORY TRACT INFECTION ( 58 FDA reports)
TREATMENT NONCOMPLIANCE ( 58 FDA reports)
WOUND DEBRIDEMENT ( 58 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 57 FDA reports)
GROIN PAIN ( 57 FDA reports)
HEPATITIS B ( 57 FDA reports)
MITRAL VALVE CALCIFICATION ( 57 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 57 FDA reports)
REFLUX OESOPHAGITIS ( 57 FDA reports)
RESTLESS LEGS SYNDROME ( 57 FDA reports)
BONE SCAN ABNORMAL ( 56 FDA reports)
CARPAL TUNNEL SYNDROME ( 56 FDA reports)
GASTRITIS EROSIVE ( 56 FDA reports)
MEDICATION ERROR ( 56 FDA reports)
NERVOUSNESS ( 56 FDA reports)
RHEUMATOID ARTHRITIS ( 56 FDA reports)
SENSORY LOSS ( 56 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 56 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 56 FDA reports)
VISUAL DISTURBANCE ( 56 FDA reports)
CARDIAC MURMUR ( 55 FDA reports)
DYSSTASIA ( 55 FDA reports)
EOSINOPHIL COUNT INCREASED ( 55 FDA reports)
HYPERKERATOSIS ( 55 FDA reports)
KLEBSIELLA INFECTION ( 55 FDA reports)
LARGE INTESTINE PERFORATION ( 55 FDA reports)
ORAL DISCOMFORT ( 55 FDA reports)
OVARIAN CYST ( 55 FDA reports)
ASPIRATION PLEURAL CAVITY ( 54 FDA reports)
CHOLANGITIS ( 54 FDA reports)
GASTROENTERITIS VIRAL ( 54 FDA reports)
GINGIVAL ERYTHEMA ( 54 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 54 FDA reports)
MUSCLE TWITCHING ( 54 FDA reports)
MYELOPATHY ( 54 FDA reports)
ODYNOPHAGIA ( 54 FDA reports)
OEDEMA MOUTH ( 54 FDA reports)
OTITIS MEDIA ( 54 FDA reports)
SPINAL FRACTURE ( 54 FDA reports)
VAGINAL HAEMORRHAGE ( 54 FDA reports)
BLOOD CREATININE DECREASED ( 53 FDA reports)
FIBROSIS ( 53 FDA reports)
GOUT ( 53 FDA reports)
HYPERPLASIA ( 53 FDA reports)
MASTECTOMY ( 53 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 53 FDA reports)
SINUS HEADACHE ( 53 FDA reports)
VAGINAL INFECTION ( 53 FDA reports)
ACIDOSIS ( 52 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 52 FDA reports)
BLISTER ( 52 FDA reports)
BREAST PAIN ( 52 FDA reports)
CYSTITIS HAEMORRHAGIC ( 52 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 52 FDA reports)
ENTERITIS ( 52 FDA reports)
NECROSIS ( 52 FDA reports)
PYELONEPHRITIS ( 52 FDA reports)
SPONDYLOLYSIS ( 52 FDA reports)
STREPTOCOCCAL SEPSIS ( 52 FDA reports)
URINE OUTPUT DECREASED ( 52 FDA reports)
VENTRICULAR TACHYCARDIA ( 52 FDA reports)
AZOTAEMIA ( 51 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 51 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 51 FDA reports)
BRONCHOSPASM ( 51 FDA reports)
CATHETERISATION CARDIAC ( 51 FDA reports)
CLOSTRIDIAL INFECTION ( 51 FDA reports)
COLLAPSE OF LUNG ( 51 FDA reports)
ECZEMA ( 51 FDA reports)
HYPERBILIRUBINAEMIA ( 51 FDA reports)
INCONTINENCE ( 51 FDA reports)
PERONEAL NERVE PALSY ( 51 FDA reports)
THROAT TIGHTNESS ( 51 FDA reports)
TOOTH IMPACTED ( 51 FDA reports)
VENTRICULAR HYPERTROPHY ( 51 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 50 FDA reports)
COLD SWEAT ( 50 FDA reports)
FEAR ( 50 FDA reports)
HYDROCEPHALUS ( 50 FDA reports)
LACERATION ( 50 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 50 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 50 FDA reports)
OESOPHAGEAL ULCER ( 50 FDA reports)
PEPTIC ULCER ( 50 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 50 FDA reports)
THERAPY NON-RESPONDER ( 50 FDA reports)
VASCULITIS ( 50 FDA reports)
WHEELCHAIR USER ( 50 FDA reports)
ABDOMINAL HERNIA ( 49 FDA reports)
ACUTE SINUSITIS ( 49 FDA reports)
BONE NEOPLASM ( 49 FDA reports)
CACHEXIA ( 49 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 49 FDA reports)
CERUMEN IMPACTION ( 49 FDA reports)
DISEASE RECURRENCE ( 49 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 49 FDA reports)
MYOSITIS ( 49 FDA reports)
PHLEBITIS ( 49 FDA reports)
PROSTATOMEGALY ( 49 FDA reports)
PULMONARY MASS ( 49 FDA reports)
SKIN DISORDER ( 49 FDA reports)
SPINAL FUSION SURGERY ( 49 FDA reports)
COLON CANCER ( 48 FDA reports)
FLATULENCE ( 48 FDA reports)
GALLBLADDER DISORDER ( 48 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 48 FDA reports)
PURPURA ( 48 FDA reports)
THROMBOCYTOSIS ( 48 FDA reports)
UMBILICAL HERNIA ( 48 FDA reports)
APPENDICITIS ( 47 FDA reports)
BLOOD MAGNESIUM DECREASED ( 47 FDA reports)
CARDIOVASCULAR DISORDER ( 47 FDA reports)
MELANOCYTIC NAEVUS ( 47 FDA reports)
NERVOUS SYSTEM DISORDER ( 47 FDA reports)
NEUROPATHY ( 47 FDA reports)
PLEURITIC PAIN ( 47 FDA reports)
POOR DENTAL CONDITION ( 47 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 47 FDA reports)
RADICULAR PAIN ( 47 FDA reports)
X-RAY ABNORMAL ( 47 FDA reports)
APNOEA ( 46 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 46 FDA reports)
BRONCHIECTASIS ( 46 FDA reports)
DEAFNESS NEUROSENSORY ( 46 FDA reports)
HEMIPLEGIA ( 46 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 46 FDA reports)
MECHANICAL VENTILATION ( 46 FDA reports)
MENINGITIS ( 46 FDA reports)
PARAESTHESIA ORAL ( 46 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 46 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 46 FDA reports)
PROTEIN TOTAL DECREASED ( 46 FDA reports)
SUBDURAL HAEMATOMA ( 46 FDA reports)
VENOUS THROMBOSIS LIMB ( 46 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 45 FDA reports)
AORTIC STENOSIS ( 45 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 45 FDA reports)
BREAST CANCER RECURRENT ( 45 FDA reports)
BURNING SENSATION ( 45 FDA reports)
DILATATION VENTRICULAR ( 45 FDA reports)
DISTURBANCE IN ATTENTION ( 45 FDA reports)
FRACTURE ( 45 FDA reports)
HAEMODIALYSIS ( 45 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 45 FDA reports)
LUNG HYPERINFLATION ( 45 FDA reports)
LUNG INFECTION ( 45 FDA reports)
LYMPHOMA ( 45 FDA reports)
MYOCLONUS ( 45 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 45 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 44 FDA reports)
ASEPTIC NECROSIS BONE ( 44 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 44 FDA reports)
CHOLECYSTITIS CHRONIC ( 44 FDA reports)
DEPRESSED MOOD ( 44 FDA reports)
DRUG DEPENDENCE ( 44 FDA reports)
HAEMANGIOMA OF LIVER ( 44 FDA reports)
HYPERPARATHYROIDISM ( 44 FDA reports)
NERVE INJURY ( 44 FDA reports)
NEURITIS ( 44 FDA reports)
OFF LABEL USE ( 44 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 44 FDA reports)
PELVIC PAIN ( 44 FDA reports)
PROCTALGIA ( 44 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 44 FDA reports)
SEDATION ( 44 FDA reports)
BIOPSY BONE ABNORMAL ( 43 FDA reports)
BLOOD GLUCOSE DECREASED ( 43 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 43 FDA reports)
DYSLIPIDAEMIA ( 43 FDA reports)
FEMORAL NECK FRACTURE ( 43 FDA reports)
GASTROINTESTINAL PAIN ( 43 FDA reports)
MUCOSAL ULCERATION ( 43 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 43 FDA reports)
TRANSAMINASES INCREASED ( 43 FDA reports)
TRANSFUSION ( 43 FDA reports)
VASCULAR CALCIFICATION ( 43 FDA reports)
ABNORMAL BEHAVIOUR ( 42 FDA reports)
ATRIOVENTRICULAR BLOCK ( 42 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 42 FDA reports)
DECREASED ACTIVITY ( 42 FDA reports)
DENTAL CARE ( 42 FDA reports)
DENTAL PROSTHESIS USER ( 42 FDA reports)
HORDEOLUM ( 42 FDA reports)
ILEUS PARALYTIC ( 42 FDA reports)
PERIODONTAL OPERATION ( 42 FDA reports)
POLYURIA ( 42 FDA reports)
PULSE ABSENT ( 42 FDA reports)
RENAL CELL CARCINOMA ( 42 FDA reports)
SINUS CONGESTION ( 42 FDA reports)
SKIN PAPILLOMA ( 42 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 42 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 42 FDA reports)
THROMBOPHLEBITIS ( 42 FDA reports)
VIRAL INFECTION ( 42 FDA reports)
ARTHRITIS BACTERIAL ( 41 FDA reports)
CEREBELLAR INFARCTION ( 41 FDA reports)
CIRCULATORY COLLAPSE ( 41 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 41 FDA reports)
DERMATITIS CONTACT ( 41 FDA reports)
DIVERTICULAR PERFORATION ( 41 FDA reports)
DRUG ERUPTION ( 41 FDA reports)
DUODENITIS ( 41 FDA reports)
JOINT SPRAIN ( 41 FDA reports)
MACULAR DEGENERATION ( 41 FDA reports)
MALIGNANT ASCITES ( 41 FDA reports)
MASS EXCISION ( 41 FDA reports)
MENISCUS LESION ( 41 FDA reports)
MYOCARDIAL ISCHAEMIA ( 41 FDA reports)
OESOPHAGEAL STENOSIS ( 41 FDA reports)
PLEURISY ( 41 FDA reports)
PROSTATE CANCER METASTATIC ( 41 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 41 FDA reports)
ACTINIC KERATOSIS ( 40 FDA reports)
BRAIN MASS ( 40 FDA reports)
CERVICAL DYSPLASIA ( 40 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 40 FDA reports)
GASTRODUODENITIS ( 40 FDA reports)
GINGIVAL EROSION ( 40 FDA reports)
GRANULOMA ( 40 FDA reports)
HEAD INJURY ( 40 FDA reports)
HYPOACUSIS ( 40 FDA reports)
ISCHAEMIA ( 40 FDA reports)
LISTERIA SEPSIS ( 40 FDA reports)
RHINITIS ( 40 FDA reports)
TONGUE DISCOLOURATION ( 40 FDA reports)
ANAPHYLACTOID REACTION ( 39 FDA reports)
AORTIC CALCIFICATION ( 39 FDA reports)
ASPIRATION ( 39 FDA reports)
BACK DISORDER ( 39 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 39 FDA reports)
CAROTID ARTERY STENOSIS ( 39 FDA reports)
DRUG INTOLERANCE ( 39 FDA reports)
NEUTROPENIC SEPSIS ( 39 FDA reports)
POST HERPETIC NEURALGIA ( 39 FDA reports)
ABDOMINAL PAIN LOWER ( 38 FDA reports)
ATRIAL FLUTTER ( 38 FDA reports)
AXILLARY PAIN ( 38 FDA reports)
BLADDER CANCER ( 38 FDA reports)
BLOOD AMYLASE INCREASED ( 38 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 38 FDA reports)
COORDINATION ABNORMAL ( 38 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 38 FDA reports)
HEART RATE IRREGULAR ( 38 FDA reports)
HEPATIC ENCEPHALOPATHY ( 38 FDA reports)
HYPOPROTEINAEMIA ( 38 FDA reports)
INGROWING NAIL ( 38 FDA reports)
IRITIS ( 38 FDA reports)
MAXILLOFACIAL OPERATION ( 38 FDA reports)
NODULE ( 38 FDA reports)
POOR PERSONAL HYGIENE ( 38 FDA reports)
PULMONARY GRANULOMA ( 38 FDA reports)
PULPITIS DENTAL ( 38 FDA reports)
RESPIRATORY TRACT CONGESTION ( 38 FDA reports)
SKIN INFECTION ( 38 FDA reports)
SYNOVITIS ( 38 FDA reports)
TENDON DISORDER ( 38 FDA reports)
TENOSYNOVITIS ( 38 FDA reports)
VITREOUS FLOATERS ( 38 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 37 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 37 FDA reports)
BEDRIDDEN ( 37 FDA reports)
BLEPHARITIS ( 37 FDA reports)
BLOOD CHLORIDE DECREASED ( 37 FDA reports)
BLOOD CULTURE POSITIVE ( 37 FDA reports)
BONE TRIMMING ( 37 FDA reports)
CHEST X-RAY ABNORMAL ( 37 FDA reports)
EMBOLISM ( 37 FDA reports)
FOLLICULITIS ( 37 FDA reports)
HYPOAESTHESIA FACIAL ( 37 FDA reports)
INTESTINAL ISCHAEMIA ( 37 FDA reports)
LARYNGITIS ( 37 FDA reports)
LUMBAR RADICULOPATHY ( 37 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 37 FDA reports)
OCCULT BLOOD POSITIVE ( 37 FDA reports)
PRURITUS GENERALISED ( 37 FDA reports)
RENAL INJURY ( 37 FDA reports)
RENAL PAIN ( 37 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 37 FDA reports)
ADENOCARCINOMA ( 36 FDA reports)
BLOOD URINE PRESENT ( 36 FDA reports)
CUSHING'S SYNDROME ( 36 FDA reports)
EAR INFECTION ( 36 FDA reports)
FAECES DISCOLOURED ( 36 FDA reports)
FEELING JITTERY ( 36 FDA reports)
GASTRIC POLYPS ( 36 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 36 FDA reports)
HEARING IMPAIRED ( 36 FDA reports)
IMPAIRED WORK ABILITY ( 36 FDA reports)
NEOPLASM RECURRENCE ( 36 FDA reports)
PROSTATE CANCER STAGE IV ( 36 FDA reports)
RENAL TUBULAR NECROSIS ( 36 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 36 FDA reports)
SENSORY DISTURBANCE ( 36 FDA reports)
SWOLLEN TONGUE ( 36 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 36 FDA reports)
THROMBOSIS IN DEVICE ( 36 FDA reports)
TOOTH REPAIR ( 36 FDA reports)
VENOUS INSUFFICIENCY ( 36 FDA reports)
VENTRICULAR FIBRILLATION ( 36 FDA reports)
WOUND ( 36 FDA reports)
BLOOD UREA DECREASED ( 35 FDA reports)
BRUXISM ( 35 FDA reports)
DELUSION ( 35 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 35 FDA reports)
EXCORIATION ( 35 FDA reports)
HAEMATOCRIT INCREASED ( 35 FDA reports)
HEAD DISCOMFORT ( 35 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 35 FDA reports)
INGUINAL HERNIA ( 35 FDA reports)
INJECTION SITE PAIN ( 35 FDA reports)
LIGAMENT RUPTURE ( 35 FDA reports)
MENTAL DISORDER ( 35 FDA reports)
MONOCLONAL GAMMOPATHY ( 35 FDA reports)
OEDEMA MUCOSAL ( 35 FDA reports)
PARKINSON'S DISEASE ( 35 FDA reports)
PRESBYOPIA ( 35 FDA reports)
SACROILIITIS ( 35 FDA reports)
SINUS ARRHYTHMIA ( 35 FDA reports)
SKIN CANCER ( 35 FDA reports)
VENTRICULAR HYPOKINESIA ( 35 FDA reports)
BONE MARROW DEPRESSION ( 34 FDA reports)
CROHN'S DISEASE ( 34 FDA reports)
DENTAL FISTULA ( 34 FDA reports)
HYPOVENTILATION ( 34 FDA reports)
INTERMITTENT CLAUDICATION ( 34 FDA reports)
ONYCHALGIA ( 34 FDA reports)
ORAL DISCHARGE ( 34 FDA reports)
OTITIS EXTERNA ( 34 FDA reports)
RESPIRATORY DEPRESSION ( 34 FDA reports)
SMALL FOR DATES BABY ( 34 FDA reports)
STRESS URINARY INCONTINENCE ( 34 FDA reports)
THYROIDECTOMY ( 34 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 34 FDA reports)
ADVERSE EVENT ( 33 FDA reports)
ANGIOPATHY ( 33 FDA reports)
ANURIA ( 33 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 33 FDA reports)
CALCULUS URETERIC ( 33 FDA reports)
CHOLECYSTITIS ACUTE ( 33 FDA reports)
CULTURE URINE POSITIVE ( 33 FDA reports)
DIASTOLIC DYSFUNCTION ( 33 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 33 FDA reports)
INCREASED TENDENCY TO BRUISE ( 33 FDA reports)
LUNG CANCER METASTATIC ( 33 FDA reports)
MALIGNANT MELANOMA ( 33 FDA reports)
METAPLASIA ( 33 FDA reports)
NASAL MUCOSAL DISORDER ( 33 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 33 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 33 FDA reports)
SCAB ( 33 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 33 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 33 FDA reports)
ADRENAL MASS ( 32 FDA reports)
AORTIC VALVE DISEASE ( 32 FDA reports)
BARRETT'S OESOPHAGUS ( 32 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 32 FDA reports)
BLOOD PRESSURE ABNORMAL ( 32 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 32 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 32 FDA reports)
DERMAL CYST ( 32 FDA reports)
ECONOMIC PROBLEM ( 32 FDA reports)
EPILEPSY ( 32 FDA reports)
GRANULOCYTOPENIA ( 32 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 32 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 32 FDA reports)
LIP DRY ( 32 FDA reports)
LUNG CONSOLIDATION ( 32 FDA reports)
MACULAR OEDEMA ( 32 FDA reports)
MICTURITION URGENCY ( 32 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 32 FDA reports)
OXYGEN SUPPLEMENTATION ( 32 FDA reports)
PHOTOPHOBIA ( 32 FDA reports)
SKIN LACERATION ( 32 FDA reports)
SPUTUM DISCOLOURED ( 32 FDA reports)
AGGRESSION ( 31 FDA reports)
APLASTIC ANAEMIA ( 31 FDA reports)
APTYALISM ( 31 FDA reports)
BLOOD CALCIUM INCREASED ( 31 FDA reports)
BONE GRAFT ( 31 FDA reports)
COLITIS ISCHAEMIC ( 31 FDA reports)
COLON ADENOMA ( 31 FDA reports)
ENCEPHALITIS HERPES ( 31 FDA reports)
FACIAL BONES FRACTURE ( 31 FDA reports)
HYPERMETROPIA ( 31 FDA reports)
LIMB DISCOMFORT ( 31 FDA reports)
MEAN CELL VOLUME INCREASED ( 31 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 31 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 31 FDA reports)
MOVEMENT DISORDER ( 31 FDA reports)
MUSCLE INJURY ( 31 FDA reports)
PROTEIN URINE ( 31 FDA reports)
SKIN NEOPLASM EXCISION ( 31 FDA reports)
SKIN REACTION ( 31 FDA reports)
STRESS FRACTURE ( 31 FDA reports)
UROSEPSIS ( 31 FDA reports)
ANGINA UNSTABLE ( 30 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 30 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 30 FDA reports)
BONE SWELLING ( 30 FDA reports)
BRAIN NEOPLASM ( 30 FDA reports)
CATHETER PLACEMENT ( 30 FDA reports)
CATHETER RELATED INFECTION ( 30 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 30 FDA reports)
ERYTHEMA MULTIFORME ( 30 FDA reports)
EXTRAVASATION ( 30 FDA reports)
FEELING COLD ( 30 FDA reports)
HEART RATE DECREASED ( 30 FDA reports)
HYPERAMMONAEMIA ( 30 FDA reports)
HYPERNATRAEMIA ( 30 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 30 FDA reports)
LOCALISED INFECTION ( 30 FDA reports)
MOOD SWINGS ( 30 FDA reports)
NEURODERMATITIS ( 30 FDA reports)
PARAPROTEINAEMIA ( 30 FDA reports)
PROTEIN URINE PRESENT ( 30 FDA reports)
PYURIA ( 30 FDA reports)
RETINAL DISORDER ( 30 FDA reports)
SCLERODERMA ( 30 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 30 FDA reports)
TACHYPNOEA ( 30 FDA reports)
THYROID NEOPLASM ( 30 FDA reports)
TOOTH EROSION ( 30 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 30 FDA reports)
VITAMIN B12 DEFICIENCY ( 30 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 30 FDA reports)
VITREOUS DETACHMENT ( 30 FDA reports)
COLON CANCER METASTATIC ( 29 FDA reports)
DENTAL PLAQUE ( 29 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 29 FDA reports)
EYELID OEDEMA ( 29 FDA reports)
GRAFT VERSUS HOST DISEASE ( 29 FDA reports)
HYPERTONIC BLADDER ( 29 FDA reports)
MULTIPLE INJURIES ( 29 FDA reports)
NECROTISING FASCIITIS ( 29 FDA reports)
NON-SMALL CELL LUNG CANCER ( 29 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 29 FDA reports)
OESOPHAGEAL PAIN ( 29 FDA reports)
ORTHOPNOEA ( 29 FDA reports)
ORTHOSIS USER ( 29 FDA reports)
RESUSCITATION ( 29 FDA reports)
SENSATION OF HEAVINESS ( 29 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 29 FDA reports)
STOMACH DISCOMFORT ( 29 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 29 FDA reports)
TENDON RUPTURE ( 29 FDA reports)
BACTERIAL TEST POSITIVE ( 28 FDA reports)
BLOOD COUNT ABNORMAL ( 28 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 28 FDA reports)
BREAST TENDERNESS ( 28 FDA reports)
EXTRADURAL ABSCESS ( 28 FDA reports)
LACTIC ACIDOSIS ( 28 FDA reports)
PANCREATIC CARCINOMA ( 28 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 28 FDA reports)
PREMATURE BABY ( 28 FDA reports)
PROCTITIS ( 28 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 28 FDA reports)
THROAT IRRITATION ( 28 FDA reports)
TUMOUR HAEMORRHAGE ( 28 FDA reports)
BACTERIAL SEPSIS ( 27 FDA reports)
CERVIX CARCINOMA ( 27 FDA reports)
CHORIORETINAL DISORDER ( 27 FDA reports)
CHORIORETINOPATHY ( 27 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 27 FDA reports)
DYSTONIA ( 27 FDA reports)
EMOTIONAL DISORDER ( 27 FDA reports)
EMPYEMA ( 27 FDA reports)
EYE LASER SURGERY ( 27 FDA reports)
FACIAL NEURALGIA ( 27 FDA reports)
HAEMORRHAGIC DIATHESIS ( 27 FDA reports)
HEPATIC CIRRHOSIS ( 27 FDA reports)
HERPES ZOSTER OTICUS ( 27 FDA reports)
HYPOKINESIA ( 27 FDA reports)
INFECTED SKIN ULCER ( 27 FDA reports)
MALLORY-WEISS SYNDROME ( 27 FDA reports)
MALOCCLUSION ( 27 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 27 FDA reports)
PERIODONTAL INFECTION ( 27 FDA reports)
PULMONARY HAEMORRHAGE ( 27 FDA reports)
RADIATION ASSOCIATED PAIN ( 27 FDA reports)
SICK SINUS SYNDROME ( 27 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 27 FDA reports)
SUBCUTANEOUS ABSCESS ( 27 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 27 FDA reports)
TOOTH INJURY ( 27 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 27 FDA reports)
WEGENER'S GRANULOMATOSIS ( 27 FDA reports)
WOUND TREATMENT ( 27 FDA reports)
WOUND SECRETION ( 27 FDA reports)
WOUND COMPLICATION ( 27 FDA reports)
VITAMIN D DEFICIENCY ( 27 FDA reports)
ASPERGILLOSIS ( 26 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 26 FDA reports)
BODY TEMPERATURE DECREASED ( 26 FDA reports)
CUSHINGOID ( 26 FDA reports)
DIFFICULTY IN WALKING ( 26 FDA reports)
DILATATION ATRIAL ( 26 FDA reports)
DUODENAL PERFORATION ( 26 FDA reports)
EJECTION FRACTION ABNORMAL ( 26 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 26 FDA reports)
HYPERURICAEMIA ( 26 FDA reports)
ILEAL PERFORATION ( 26 FDA reports)
INJECTION SITE ERYTHEMA ( 26 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 26 FDA reports)
LIPOMA ( 26 FDA reports)
MENINGIOMA ( 26 FDA reports)
MITRAL VALVE DISEASE ( 26 FDA reports)
ORAL SOFT TISSUE DISORDER ( 26 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 26 FDA reports)
POLYPECTOMY ( 26 FDA reports)
PSORIASIS ( 26 FDA reports)
SEASONAL ALLERGY ( 26 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 26 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 26 FDA reports)
ABSCESS NECK ( 25 FDA reports)
ADENOMA BENIGN ( 25 FDA reports)
ADVERSE DRUG REACTION ( 25 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 25 FDA reports)
BONE MARROW DISORDER ( 25 FDA reports)
BRAIN SCAN ABNORMAL ( 25 FDA reports)
CHEILITIS ( 25 FDA reports)
CHROMATURIA ( 25 FDA reports)
DYSPLASIA ( 25 FDA reports)
EAR CONGESTION ( 25 FDA reports)
EOSINOPHILIA ( 25 FDA reports)
EYE IRRITATION ( 25 FDA reports)
GLOSSODYNIA ( 25 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 25 FDA reports)
IMPLANT SITE INFECTION ( 25 FDA reports)
LEUKOENCEPHALOPATHY ( 25 FDA reports)
LIBIDO DECREASED ( 25 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 25 FDA reports)
MACULOPATHY ( 25 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 25 FDA reports)
RASH PAPULAR ( 25 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 25 FDA reports)
SPINAL COLUMN INJURY ( 25 FDA reports)
STRONGYLOIDIASIS ( 25 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 25 FDA reports)
THIRST ( 25 FDA reports)
ZYGOMYCOSIS ( 25 FDA reports)
WRIST FRACTURE ( 25 FDA reports)
WOUND INFECTION ( 24 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 24 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 24 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 24 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 24 FDA reports)
CHEST TUBE INSERTION ( 24 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 24 FDA reports)
DYSAESTHESIA ( 24 FDA reports)
FOREIGN BODY ( 24 FDA reports)
GASTRIC HAEMORRHAGE ( 24 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 24 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 24 FDA reports)
METABOLIC ENCEPHALOPATHY ( 24 FDA reports)
METASTASES TO MENINGES ( 24 FDA reports)
NON-CARDIAC CHEST PAIN ( 24 FDA reports)
OVERWEIGHT ( 24 FDA reports)
PAIN OF SKIN ( 24 FDA reports)
PERIRECTAL ABSCESS ( 24 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 24 FDA reports)
RASH PUSTULAR ( 24 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 24 FDA reports)
SKIN BURNING SENSATION ( 24 FDA reports)
TUMOUR MARKER INCREASED ( 24 FDA reports)
TUMOUR NECROSIS ( 24 FDA reports)
VARICOSE VEIN ( 24 FDA reports)
ABDOMINAL ABSCESS ( 23 FDA reports)
ADDISON'S DISEASE ( 23 FDA reports)
ADRENAL NEOPLASM ( 23 FDA reports)
AFFECTIVE DISORDER ( 23 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 23 FDA reports)
CAROTID BRUIT ( 23 FDA reports)
CORONARY ARTERY BYPASS ( 23 FDA reports)
CRANIOTOMY ( 23 FDA reports)
DEVICE FAILURE ( 23 FDA reports)
DRUG ADMINISTRATION ERROR ( 23 FDA reports)
DRUG EFFECT DECREASED ( 23 FDA reports)
EXTUBATION ( 23 FDA reports)
EYE INFECTION ( 23 FDA reports)
HAEMOLYSIS ( 23 FDA reports)
HEART VALVE INCOMPETENCE ( 23 FDA reports)
HEPATIC FIBROSIS ( 23 FDA reports)
HYPERSOMNIA ( 23 FDA reports)
HYPERTHERMIA ( 23 FDA reports)
ILEAL ULCER ( 23 FDA reports)
INFARCTION ( 23 FDA reports)
KNEE ARTHROPLASTY ( 23 FDA reports)
KYPHOSCOLIOSIS ( 23 FDA reports)
LEUKAEMIA ( 23 FDA reports)
LIP SWELLING ( 23 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 23 FDA reports)
MALIGNANT TUMOUR EXCISION ( 23 FDA reports)
METASTASES TO SKIN ( 23 FDA reports)
MONOCYTE COUNT INCREASED ( 23 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 23 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 23 FDA reports)
PERIPHERAL COLDNESS ( 23 FDA reports)
PNEUMATOSIS INTESTINALIS ( 23 FDA reports)
POLYNEUROPATHY ( 23 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 23 FDA reports)
RECTAL ULCER ( 23 FDA reports)
RENAL TUBULAR ACIDOSIS ( 23 FDA reports)
SKIN NECROSIS ( 23 FDA reports)
SOFT TISSUE INFECTION ( 23 FDA reports)
TENDON INJURY ( 23 FDA reports)
THORACOTOMY ( 23 FDA reports)
THYROID CANCER ( 23 FDA reports)
UPPER LIMB FRACTURE ( 23 FDA reports)
UVEITIS ( 23 FDA reports)
AORTIC VALVE SCLEROSIS ( 22 FDA reports)
APHTHOUS STOMATITIS ( 22 FDA reports)
APPETITE DISORDER ( 22 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 22 FDA reports)
BLOOD URIC ACID INCREASED ( 22 FDA reports)
BLOODY DISCHARGE ( 22 FDA reports)
BREAST DISCHARGE ( 22 FDA reports)
BUNDLE BRANCH BLOCK ( 22 FDA reports)
CARDIAC VALVE DISEASE ( 22 FDA reports)
COLONIC OBSTRUCTION ( 22 FDA reports)
CONJUNCTIVITIS VIRAL ( 22 FDA reports)
CRYING ( 22 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 22 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 22 FDA reports)
DRUG DOSE OMISSION ( 22 FDA reports)
ENDOCARDITIS ( 22 FDA reports)
FISTULA REPAIR ( 22 FDA reports)
GASTRIC DISORDER ( 22 FDA reports)
GLIOBLASTOMA ( 22 FDA reports)
HAEMOLYTIC ANAEMIA ( 22 FDA reports)
HODGKIN'S DISEASE ( 22 FDA reports)
INJECTION SITE REACTION ( 22 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 22 FDA reports)
JOINT CREPITATION ( 22 FDA reports)
JOINT INJURY ( 22 FDA reports)
LYMPHADENECTOMY ( 22 FDA reports)
PATHOGEN RESISTANCE ( 22 FDA reports)
REFLUX LARYNGITIS ( 22 FDA reports)
RHONCHI ( 22 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 22 FDA reports)
ROSACEA ( 22 FDA reports)
SENSATION OF FOREIGN BODY ( 22 FDA reports)
SINUS OPERATION ( 22 FDA reports)
TRISOMY 21 ( 22 FDA reports)
VENTRICULAR DYSFUNCTION ( 22 FDA reports)
VISUAL FIELD DEFECT ( 22 FDA reports)
VOCAL CORD PARALYSIS ( 22 FDA reports)
ABDOMEN CRUSHING ( 21 FDA reports)
ACUTE PRERENAL FAILURE ( 21 FDA reports)
AMYLOIDOSIS ( 21 FDA reports)
ANKLE FRACTURE ( 21 FDA reports)
APPENDICECTOMY ( 21 FDA reports)
ATROPHIC VULVOVAGINITIS ( 21 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 21 FDA reports)
BIOPSY LYMPH GLAND ( 21 FDA reports)
BLADDER CATHETERISATION ( 21 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 21 FDA reports)
BREATH SOUNDS ABNORMAL ( 21 FDA reports)
BULLOUS LUNG DISEASE ( 21 FDA reports)
CYST RUPTURE ( 21 FDA reports)
FAT NECROSIS ( 21 FDA reports)
GASTRIC PERFORATION ( 21 FDA reports)
GLOMERULOSCLEROSIS ( 21 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 21 FDA reports)
HYDROPNEUMOTHORAX ( 21 FDA reports)
HYPERAESTHESIA ( 21 FDA reports)
NECK MASS ( 21 FDA reports)
NERVE ROOT COMPRESSION ( 21 FDA reports)
PANIC ATTACK ( 21 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 21 FDA reports)
PULMONARY INFARCTION ( 21 FDA reports)
RECTOCELE ( 21 FDA reports)
SENSATION OF PRESSURE ( 21 FDA reports)
SINUS POLYP ( 21 FDA reports)
SKIN EROSION ( 21 FDA reports)
STRIDOR ( 21 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 21 FDA reports)
TRACHEOBRONCHITIS ( 21 FDA reports)
VENOUS THROMBOSIS ( 21 FDA reports)
ANAL FISTULA ( 20 FDA reports)
ANGER ( 20 FDA reports)
APHAGIA ( 20 FDA reports)
APHONIA ( 20 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 20 FDA reports)
BLADDER DISORDER ( 20 FDA reports)
BREAKTHROUGH PAIN ( 20 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 20 FDA reports)
CAESAREAN SECTION ( 20 FDA reports)
EROSIVE OESOPHAGITIS ( 20 FDA reports)
EXTREMITY NECROSIS ( 20 FDA reports)
FRACTURED SACRUM ( 20 FDA reports)
GASTRIC CANCER ( 20 FDA reports)
GINGIVAL OEDEMA ( 20 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 20 FDA reports)
LEUKAEMIA PLASMACYTIC ( 20 FDA reports)
LICHEN PLANUS ( 20 FDA reports)
MENOPAUSE ( 20 FDA reports)
METASTASES TO ADRENALS ( 20 FDA reports)
METASTASES TO PERITONEUM ( 20 FDA reports)
MULTIPLE FRACTURES ( 20 FDA reports)
MUSCLE ATROPHY ( 20 FDA reports)
NEPHROSCLEROSIS ( 20 FDA reports)
NEUROTOXICITY ( 20 FDA reports)
OTITIS MEDIA CHRONIC ( 20 FDA reports)
PARAPARESIS ( 20 FDA reports)
PLANTAR FASCIITIS ( 20 FDA reports)
PNEUMONIA FUNGAL ( 20 FDA reports)
POLYDIPSIA ( 20 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 20 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 20 FDA reports)
PYOTHORAX ( 20 FDA reports)
RADIATION OESOPHAGITIS ( 20 FDA reports)
RADIATION SKIN INJURY ( 20 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 20 FDA reports)
RETCHING ( 20 FDA reports)
SIALOADENITIS ( 20 FDA reports)
SKIN ODOUR ABNORMAL ( 20 FDA reports)
SPINAL CORPECTOMY ( 20 FDA reports)
STOMATOCYTES PRESENT ( 20 FDA reports)
TRIGGER FINGER ( 20 FDA reports)
URINARY HESITATION ( 20 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 20 FDA reports)
ABDOMINAL NEOPLASM ( 19 FDA reports)
ANORECTAL DISORDER ( 19 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 19 FDA reports)
BLINDNESS TRANSIENT ( 19 FDA reports)
BLOOD BICARBONATE DECREASED ( 19 FDA reports)
BLOOD DISORDER ( 19 FDA reports)
CARDIAC PACEMAKER INSERTION ( 19 FDA reports)
CATHETER SITE INFECTION ( 19 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 19 FDA reports)
ENCEPHALOMALACIA ( 19 FDA reports)
EPIGASTRIC DISCOMFORT ( 19 FDA reports)
ESCHERICHIA TEST POSITIVE ( 19 FDA reports)
EXTERNAL EAR DISORDER ( 19 FDA reports)
FACIAL PALSY ( 19 FDA reports)
GINGIVAL ABSCESS ( 19 FDA reports)
HAEMOGLOBIN ABNORMAL ( 19 FDA reports)
HERPES VIRUS INFECTION ( 19 FDA reports)
HIP ARTHROPLASTY ( 19 FDA reports)
HYPERCAPNIA ( 19 FDA reports)
HYPEROXALURIA ( 19 FDA reports)
INCOHERENT ( 19 FDA reports)
INFECTIOUS PERITONITIS ( 19 FDA reports)
INJECTION SITE EXTRAVASATION ( 19 FDA reports)
INTESTINAL HAEMORRHAGE ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
LARYNGOSPASM ( 19 FDA reports)
LIGAMENT SPRAIN ( 19 FDA reports)
LIPASE INCREASED ( 19 FDA reports)
MACROGLOSSIA ( 19 FDA reports)
METASTASES TO PLEURA ( 19 FDA reports)
MOOD ALTERED ( 19 FDA reports)
NASAL DISCOMFORT ( 19 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 19 FDA reports)
PAPILLOEDEMA ( 19 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 19 FDA reports)
PERFORMANCE STATUS DECREASED ( 19 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 19 FDA reports)
SARCOIDOSIS ( 19 FDA reports)
SYSTEMIC CANDIDA ( 19 FDA reports)
TOXIC ENCEPHALOPATHY ( 19 FDA reports)
UTERINE PROLAPSE ( 19 FDA reports)
VENA CAVA THROMBOSIS ( 19 FDA reports)
ATROPHY ( 18 FDA reports)
BLOOD MAGNESIUM INCREASED ( 18 FDA reports)
BLOOD PH DECREASED ( 18 FDA reports)
BLOOD SODIUM INCREASED ( 18 FDA reports)
BONE FISTULA ( 18 FDA reports)
BONE INFARCTION ( 18 FDA reports)
CARDIAC FAILURE ACUTE ( 18 FDA reports)
CARDIOPULMONARY FAILURE ( 18 FDA reports)
CHEYNE-STOKES RESPIRATION ( 18 FDA reports)
DEFAECATION URGENCY ( 18 FDA reports)
DENTAL TREATMENT ( 18 FDA reports)
DYSTHYMIC DISORDER ( 18 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 18 FDA reports)
EYELID PTOSIS ( 18 FDA reports)
GENERALISED ERYTHEMA ( 18 FDA reports)
HYPERTENSIVE HEART DISEASE ( 18 FDA reports)
ILIAC ARTERY STENOSIS ( 18 FDA reports)
ILL-DEFINED DISORDER ( 18 FDA reports)
IRON DEFICIENCY ( 18 FDA reports)
LOWER LIMB FRACTURE ( 18 FDA reports)
LYMPHADENITIS ( 18 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 18 FDA reports)
MEAN CELL HAEMOGLOBIN ( 18 FDA reports)
MEDIASTINAL MASS ( 18 FDA reports)
MEDICAL DEVICE REMOVAL ( 18 FDA reports)
METASTASES TO THE MEDIASTINUM ( 18 FDA reports)
MONOPLEGIA ( 18 FDA reports)
NASAL DISORDER ( 18 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 18 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 18 FDA reports)
OESOPHAGEAL SPASM ( 18 FDA reports)
PANCREATIC MASS ( 18 FDA reports)
PERICARDITIS ( 18 FDA reports)
PHOTOPSIA ( 18 FDA reports)
PROTEIN TOTAL INCREASED ( 18 FDA reports)
RADIATION INJURY ( 18 FDA reports)
RENAL STONE REMOVAL ( 18 FDA reports)
RETINAL DETACHMENT ( 18 FDA reports)
SEBORRHOEIC DERMATITIS ( 18 FDA reports)
SNORING ( 18 FDA reports)
STASIS DERMATITIS ( 18 FDA reports)
TEETH BRITTLE ( 18 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 18 FDA reports)
THYROID CYST ( 18 FDA reports)
TROPONIN INCREASED ( 18 FDA reports)
ULCERATIVE KERATITIS ( 18 FDA reports)
URINE ANALYSIS ABNORMAL ( 18 FDA reports)
VENOUS OCCLUSION ( 18 FDA reports)
ALVEOLAR OSTEITIS ( 17 FDA reports)
ALVEOLITIS ALLERGIC ( 17 FDA reports)
AORTIC ANEURYSM ( 17 FDA reports)
BIOPSY GINGIVAL ( 17 FDA reports)
BLINDNESS UNILATERAL ( 17 FDA reports)
BREAST CALCIFICATIONS ( 17 FDA reports)
BREAST CANCER FEMALE ( 17 FDA reports)
COMPLETED SUICIDE ( 17 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 17 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 17 FDA reports)
DIABETIC NEUROPATHY ( 17 FDA reports)
DUODENAL ULCER PERFORATION ( 17 FDA reports)
EAR DISORDER ( 17 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 17 FDA reports)
EYE DISCHARGE ( 17 FDA reports)
EYE DISORDER ( 17 FDA reports)
FANCONI SYNDROME ( 17 FDA reports)
FULL BLOOD COUNT DECREASED ( 17 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 17 FDA reports)
HEPATIC MASS ( 17 FDA reports)
HEPATIC PAIN ( 17 FDA reports)
HYPERREFLEXIA ( 17 FDA reports)
INTRACRANIAL ANEURYSM ( 17 FDA reports)
JUGULAR VEIN THROMBOSIS ( 17 FDA reports)
MASTOIDITIS ( 17 FDA reports)
MONOPARESIS ( 17 FDA reports)
MYOPATHY STEROID ( 17 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 17 FDA reports)
PANCREATIC CYST ( 17 FDA reports)
PARALYSIS ( 17 FDA reports)
PARANOIA ( 17 FDA reports)
PARAPLEGIA ( 17 FDA reports)
PHYSIOTHERAPY ( 17 FDA reports)
POLYARTHRITIS ( 17 FDA reports)
PSEUDOMONAL SEPSIS ( 17 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 17 FDA reports)
QRS AXIS ABNORMAL ( 17 FDA reports)
RECTAL PERFORATION ( 17 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 17 FDA reports)
SCAN BONE MARROW ABNORMAL ( 17 FDA reports)
SKELETAL INJURY ( 17 FDA reports)
SKIN CANDIDA ( 17 FDA reports)
SPLENIC INFARCTION ( 17 FDA reports)
STARING ( 17 FDA reports)
TONGUE INJURY ( 17 FDA reports)
URETERIC OBSTRUCTION ( 17 FDA reports)
URINARY TRACT OBSTRUCTION ( 17 FDA reports)
ACCIDENT AT WORK ( 16 FDA reports)
ACCIDENTAL OVERDOSE ( 16 FDA reports)
ADRENAL ADENOMA ( 16 FDA reports)
AGEUSIA ( 16 FDA reports)
AMMONIA INCREASED ( 16 FDA reports)
ANAL ULCER ( 16 FDA reports)
ANIMAL BITE ( 16 FDA reports)
ATRIAL TACHYCARDIA ( 16 FDA reports)
BILIARY DILATATION ( 16 FDA reports)
BIOPSY BONE ( 16 FDA reports)
BLADDER OBSTRUCTION ( 16 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 16 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 16 FDA reports)
BRAIN HERNIATION ( 16 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 16 FDA reports)
CARDIAC TAMPONADE ( 16 FDA reports)
CARDIOGENIC SHOCK ( 16 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 16 FDA reports)
CLAVICLE FRACTURE ( 16 FDA reports)
CSF TEST ABNORMAL ( 16 FDA reports)
CYSTOCELE ( 16 FDA reports)
DEVICE MALFUNCTION ( 16 FDA reports)
DIABETIC FOOT ( 16 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 16 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 16 FDA reports)
ENTERITIS INFECTIOUS ( 16 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 16 FDA reports)
GAMMOPATHY ( 16 FDA reports)
GASTROINTESTINAL NECROSIS ( 16 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 16 FDA reports)
GLOMERULONEPHRITIS ( 16 FDA reports)
HEPATITIS FULMINANT ( 16 FDA reports)
HERNIA REPAIR ( 16 FDA reports)
HILAR LYMPHADENOPATHY ( 16 FDA reports)
HYSTERECTOMY ( 16 FDA reports)
INTRACRANIAL HYPOTENSION ( 16 FDA reports)
ISCHAEMIC STROKE ( 16 FDA reports)
LARGE INTESTINAL ULCER ( 16 FDA reports)
MANIA ( 16 FDA reports)
MARROW HYPERPLASIA ( 16 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 16 FDA reports)
NASAL SEPTUM DEVIATION ( 16 FDA reports)
NEPHROTIC SYNDROME ( 16 FDA reports)
NEUROLOGICAL SYMPTOM ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 16 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 16 FDA reports)
OPPORTUNISTIC INFECTION ( 16 FDA reports)
PARATHYROID TUMOUR BENIGN ( 16 FDA reports)
PNEUMONIA KLEBSIELLA ( 16 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 16 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 16 FDA reports)
RADIATION PNEUMONITIS ( 16 FDA reports)
SHOCK HAEMORRHAGIC ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 16 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 16 FDA reports)
STOMATITIS NECROTISING ( 16 FDA reports)
THERMAL BURN ( 16 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 16 FDA reports)
UTERINE ENLARGEMENT ( 16 FDA reports)
ACCIDENT ( 15 FDA reports)
ADNEXA UTERI MASS ( 15 FDA reports)
AXILLARY MASS ( 15 FDA reports)
BIOPSY BONE MARROW ( 15 FDA reports)
BLOOD CHLORIDE INCREASED ( 15 FDA reports)
CAPILLARY LEAK SYNDROME ( 15 FDA reports)
CEREBROVASCULAR DISORDER ( 15 FDA reports)
CHONDROMALACIA ( 15 FDA reports)
COLON POLYPECTOMY ( 15 FDA reports)
COMMINUTED FRACTURE ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
DIPLEGIA ( 15 FDA reports)
DUODENAL POLYP ( 15 FDA reports)
ECHOCARDIOGRAM ( 15 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 15 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 15 FDA reports)
EMBOLISM VENOUS ( 15 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 15 FDA reports)
ESCHERICHIA SEPSIS ( 15 FDA reports)
FLUID INTAKE REDUCED ( 15 FDA reports)
FOOD INTOLERANCE ( 15 FDA reports)
FUNGAEMIA ( 15 FDA reports)
GANGRENE ( 15 FDA reports)
HAEMORRHAGIC STROKE ( 15 FDA reports)
HAIR GROWTH ABNORMAL ( 15 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 15 FDA reports)
HOSPITALISATION ( 15 FDA reports)
INJECTION SITE INDURATION ( 15 FDA reports)
JOINT ARTHROPLASTY ( 15 FDA reports)
LARYNGEAL OEDEMA ( 15 FDA reports)
MAMMOGRAM ( 15 FDA reports)
MENTAL IMPAIRMENT ( 15 FDA reports)
MUCORMYCOSIS ( 15 FDA reports)
NAIL INFECTION ( 15 FDA reports)
NEPHROPATHY ( 15 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 15 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 15 FDA reports)
OSTEOCHONDROSIS ( 15 FDA reports)
OSTEOMA ( 15 FDA reports)
PERIARTHRITIS ( 15 FDA reports)
PHARYNGEAL OEDEMA ( 15 FDA reports)
PLATELET COUNT ABNORMAL ( 15 FDA reports)
POOR PERIPHERAL CIRCULATION ( 15 FDA reports)
POST PROCEDURAL INFECTION ( 15 FDA reports)
PROCEDURAL HYPERTENSION ( 15 FDA reports)
PULMONARY HILUM MASS ( 15 FDA reports)
QUALITY OF LIFE DECREASED ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
RESPIRATORY ACIDOSIS ( 15 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 15 FDA reports)
SPONDYLITIC MYELOPATHY ( 15 FDA reports)
SUPERINFECTION ( 15 FDA reports)
TACHYARRHYTHMIA ( 15 FDA reports)
VENOOCCLUSIVE DISEASE ( 15 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 14 FDA reports)
ANGIOEDEMA ( 14 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 14 FDA reports)
ARTHROSCOPIC SURGERY ( 14 FDA reports)
ASTIGMATISM ( 14 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 14 FDA reports)
BIOPSY BREAST ABNORMAL ( 14 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
BRAIN CANCER METASTATIC ( 14 FDA reports)
CAECITIS ( 14 FDA reports)
CALCINOSIS ( 14 FDA reports)
CATHETER RELATED COMPLICATION ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
CHOLESTASIS ( 14 FDA reports)
COLECTOMY ( 14 FDA reports)
COLOSTOMY ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
CROUP INFECTIOUS ( 14 FDA reports)
DROOLING ( 14 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 14 FDA reports)
ERYTHEMA OF EYELID ( 14 FDA reports)
EXTRADURAL HAEMATOMA ( 14 FDA reports)
EYE HAEMORRHAGE ( 14 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 14 FDA reports)
GINGIVAL OPERATION ( 14 FDA reports)
GINGIVAL RECESSION ( 14 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 14 FDA reports)
HAEMORRHAGIC ANAEMIA ( 14 FDA reports)
HELICOBACTER TEST POSITIVE ( 14 FDA reports)
HEPATOTOXICITY ( 14 FDA reports)
HIDRADENITIS ( 14 FDA reports)
HYPERCOAGULATION ( 14 FDA reports)
HYPOTHERMIA ( 14 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 14 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 14 FDA reports)
JAUNDICE CHOLESTATIC ( 14 FDA reports)
KIDNEY SMALL ( 14 FDA reports)
LEUKOPLAKIA ORAL ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
METASTASES TO BONE MARROW ( 14 FDA reports)
MOTOR DYSFUNCTION ( 14 FDA reports)
NEURODEGENERATIVE DISORDER ( 14 FDA reports)
NEUROFIBROMA ( 14 FDA reports)
NEUROMYOPATHY ( 14 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 14 FDA reports)
OBSTRUCTIVE UROPATHY ( 14 FDA reports)
OCCIPITAL NEURALGIA ( 14 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 14 FDA reports)
OVARIAN MASS ( 14 FDA reports)
PAINFUL RESPIRATION ( 14 FDA reports)
PARTIAL SEIZURES ( 14 FDA reports)
PHARYNGEAL ABSCESS ( 14 FDA reports)
PHLEBITIS SUPERFICIAL ( 14 FDA reports)
PLEURODESIS ( 14 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 14 FDA reports)
PREGNANCY TEST POSITIVE ( 14 FDA reports)
PROCEDURAL COMPLICATION ( 14 FDA reports)
PROCTITIS ULCERATIVE ( 14 FDA reports)
PUPILS UNEQUAL ( 14 FDA reports)
RECTAL CANCER ( 14 FDA reports)
RENAL CANCER METASTATIC ( 14 FDA reports)
RENAL COLIC ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SMALL INTESTINAL PERFORATION ( 14 FDA reports)
SNEEZING ( 14 FDA reports)
SPINAL DECOMPRESSION ( 14 FDA reports)
STREPTOCOCCAL INFECTION ( 14 FDA reports)
TONGUE DISORDER ( 14 FDA reports)
TOOTH AVULSION ( 14 FDA reports)
TUBERCULOSIS ( 14 FDA reports)
TUMOUR EMBOLISM ( 14 FDA reports)
TUMOUR INVASION ( 14 FDA reports)
URETHRAL STENOSIS ( 14 FDA reports)
URGE INCONTINENCE ( 14 FDA reports)
URINARY TRACT DISORDER ( 14 FDA reports)
VAGINAL DISCHARGE ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VASCULAR PSEUDOANEURYSM ( 14 FDA reports)
VULVOVAGINAL DRYNESS ( 14 FDA reports)
WRONG DRUG ADMINISTERED ( 13 FDA reports)
ABDOMINAL TENDERNESS ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ADHESION ( 13 FDA reports)
ANAL CANDIDIASIS ( 13 FDA reports)
ARTHROSCOPY ( 13 FDA reports)
ASTEATOSIS ( 13 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 13 FDA reports)
BACK INJURY ( 13 FDA reports)
BACTERIA STOOL IDENTIFIED ( 13 FDA reports)
BACTERIAL DISEASE CARRIER ( 13 FDA reports)
BILE DUCT OBSTRUCTION ( 13 FDA reports)
BLOOD CREATINE INCREASED ( 13 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 13 FDA reports)
BRAIN ABSCESS ( 13 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 13 FDA reports)
BRONCHOPLEURAL FISTULA ( 13 FDA reports)
BRONCHOSTENOSIS ( 13 FDA reports)
CARDIAC FAILURE CHRONIC ( 13 FDA reports)
CATHETER SITE PAIN ( 13 FDA reports)
CLOSTRIDIUM COLITIS ( 13 FDA reports)
CONGENITAL ANOMALY ( 13 FDA reports)
CRANIAL NERVE DISORDER ( 13 FDA reports)
CREPITATIONS ( 13 FDA reports)
CYSTOSCOPY ( 13 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
DERMOID CYST ( 13 FDA reports)
DRUG LEVEL INCREASED ( 13 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 13 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 13 FDA reports)
ENGRAFTMENT SYNDROME ( 13 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 13 FDA reports)
ENTEROVESICAL FISTULA ( 13 FDA reports)
FIBROMYALGIA ( 13 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 13 FDA reports)
HALLUCINATION, VISUAL ( 13 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 13 FDA reports)
HEPATIC CANCER METASTATIC ( 13 FDA reports)
HYPERAMYLASAEMIA ( 13 FDA reports)
ISCHAEMIC HEPATITIS ( 13 FDA reports)
LABYRINTHITIS ( 13 FDA reports)
METABOLIC ALKALOSIS ( 13 FDA reports)
MICTURITION FREQUENCY DECREASED ( 13 FDA reports)
MITRAL VALVE REPLACEMENT ( 13 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 13 FDA reports)
MUCOUS MEMBRANE DISORDER ( 13 FDA reports)
MULTIPLE SCLEROSIS ( 13 FDA reports)
MUSCULOSKELETAL DISORDER ( 13 FDA reports)
MYDRIASIS ( 13 FDA reports)
ORAL FUNGAL INFECTION ( 13 FDA reports)
PANCREATIC CALCIFICATION ( 13 FDA reports)
PERIORBITAL OEDEMA ( 13 FDA reports)
PHOTOSENSITIVITY REACTION ( 13 FDA reports)
PITTING OEDEMA ( 13 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 13 FDA reports)
PULMONARY TOXICITY ( 13 FDA reports)
RADIUS FRACTURE ( 13 FDA reports)
RASH MORBILLIFORM ( 13 FDA reports)
RECURRENT CANCER ( 13 FDA reports)
REFLUX GASTRITIS ( 13 FDA reports)
RESPIRATORY RATE DECREASED ( 13 FDA reports)
RETINOPATHY ( 13 FDA reports)
SEXUAL DYSFUNCTION ( 13 FDA reports)
SKIN ATROPHY ( 13 FDA reports)
SMALL INTESTINE OPERATION ( 13 FDA reports)
SPINAL OPERATION ( 13 FDA reports)
SPUTUM CULTURE POSITIVE ( 13 FDA reports)
SYNOVIAL RUPTURE ( 13 FDA reports)
TELANGIECTASIA ( 13 FDA reports)
THORACOSTOMY ( 13 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 13 FDA reports)
TOBACCO ABUSE ( 13 FDA reports)
TRACHEOSTOMY ( 13 FDA reports)
TREATMENT FAILURE ( 13 FDA reports)
UMBILICAL HERNIA REPAIR ( 13 FDA reports)
URINE FLOW DECREASED ( 13 FDA reports)
UTERINE CANCER ( 13 FDA reports)
VEIN DISORDER ( 13 FDA reports)
ABSCESS MANAGEMENT ( 12 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 12 FDA reports)
ADENOVIRAL HEPATITIS ( 12 FDA reports)
AORTIC DILATATION ( 12 FDA reports)
APATHY ( 12 FDA reports)
BIOPSY ( 12 FDA reports)
BLADDER DYSFUNCTION ( 12 FDA reports)
BLADDER OPERATION ( 12 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 12 FDA reports)
BRACHIAL PLEXOPATHY ( 12 FDA reports)
BREAST NEOPLASM ( 12 FDA reports)
BREAST PROSTHESIS REMOVAL ( 12 FDA reports)
BREAST RECONSTRUCTION ( 12 FDA reports)
BRONCHIOLITIS ( 12 FDA reports)
CAROTID ARTERY DISEASE ( 12 FDA reports)
CAROTID BODY TUMOUR ( 12 FDA reports)
CHEST WALL ABSCESS ( 12 FDA reports)
CHEST WALL MASS ( 12 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 12 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 12 FDA reports)
COLON OPERATION ( 12 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 12 FDA reports)
DIABETIC RETINOPATHY ( 12 FDA reports)
DYSPHEMIA ( 12 FDA reports)
ENTEROBACTER INFECTION ( 12 FDA reports)
EPIDERMOLYSIS ( 12 FDA reports)
EPIDIDYMITIS ( 12 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
FAECALOMA ( 12 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 12 FDA reports)
FIBROUS HISTIOCYTOMA ( 12 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 12 FDA reports)
GALLBLADDER ENLARGEMENT ( 12 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 12 FDA reports)
GASTROENTERITIS BACTERIAL ( 12 FDA reports)
GASTROINTESTINAL TOXICITY ( 12 FDA reports)
GINGIVAL ATROPHY ( 12 FDA reports)
GLYCOSURIA ( 12 FDA reports)
GOUTY ARTHRITIS ( 12 FDA reports)
HAEMATOTOXICITY ( 12 FDA reports)
HEPATIC ENZYME ABNORMAL ( 12 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 12 FDA reports)
IMPETIGO ( 12 FDA reports)
INCORRECT DOSE ADMINISTERED ( 12 FDA reports)
LHERMITTE'S SIGN ( 12 FDA reports)
MENORRHAGIA ( 12 FDA reports)
MESOTHELIOMA ( 12 FDA reports)
METASTASES TO NASAL SINUSES ( 12 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 12 FDA reports)
MITRAL VALVE PROLAPSE ( 12 FDA reports)
MORGANELLA INFECTION ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
MYELITIS TRANSVERSE ( 12 FDA reports)
NASAL POLYPS ( 12 FDA reports)
NECK INJURY ( 12 FDA reports)
NEONATAL DISORDER ( 12 FDA reports)
NERVE BLOCK ( 12 FDA reports)
NYSTAGMUS ( 12 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 12 FDA reports)
OESOPHAGITIS ULCERATIVE ( 12 FDA reports)
OSTEOMYELITIS ACUTE ( 12 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 12 FDA reports)
PERIORBITAL HAEMATOMA ( 12 FDA reports)
PERITONSILLITIS ( 12 FDA reports)
PERSONALITY DISORDER ( 12 FDA reports)
PHAEOCHROMOCYTOMA CRISIS ( 12 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 12 FDA reports)
RADICAL HYSTERECTOMY ( 12 FDA reports)
RADIOTHERAPY TO BRAIN ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 12 FDA reports)
SALIVARY GLAND DISORDER ( 12 FDA reports)
SCAPULA FRACTURE ( 12 FDA reports)
SEPSIS SYNDROME ( 12 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 12 FDA reports)
SUICIDE ATTEMPT ( 12 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 12 FDA reports)
TEMPERATURE INTOLERANCE ( 12 FDA reports)
TENDON GRAFT ( 12 FDA reports)
THYROID DISORDER ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
URETHRAL CARUNCLE ( 12 FDA reports)
VENA CAVA FILTER INSERTION ( 12 FDA reports)
VENTRICULAR ARRHYTHMIA ( 12 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 12 FDA reports)
VIRAL PHARYNGITIS ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 11 FDA reports)
VIRAEMIA ( 11 FDA reports)
ABDOMINAL ADHESIONS ( 11 FDA reports)
ACROCHORDON ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 11 FDA reports)
ADRENAL SUPPRESSION ( 11 FDA reports)
AMBLYOPIA ( 11 FDA reports)
ANGIOPLASTY ( 11 FDA reports)
ASBESTOSIS ( 11 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 11 FDA reports)
BACTERIAL TEST NEGATIVE ( 11 FDA reports)
BARTHOLIN'S CYST ( 11 FDA reports)
BEHCET'S SYNDROME ( 11 FDA reports)
BLADDER CYST ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 11 FDA reports)
BLOOD OSMOLARITY DECREASED ( 11 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BONE GIANT CELL TUMOUR ( 11 FDA reports)
CATHETER SITE HAEMATOMA ( 11 FDA reports)
CELLULITIS ORBITAL ( 11 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 11 FDA reports)
CERVICOBRACHIAL SYNDROME ( 11 FDA reports)
CHOKING ( 11 FDA reports)
CHOKING SENSATION ( 11 FDA reports)
COLONIC STENOSIS ( 11 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 11 FDA reports)
CORNEAL ABRASION ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 11 FDA reports)
DEPRESSIVE SYMPTOM ( 11 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 11 FDA reports)
DIZZINESS POSTURAL ( 11 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 11 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 11 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 11 FDA reports)
ESCHERICHIA BACTERAEMIA ( 11 FDA reports)
EYE ROLLING ( 11 FDA reports)
FEEDING TUBE COMPLICATION ( 11 FDA reports)
FIBROMA ( 11 FDA reports)
GLARE ( 11 FDA reports)
GLIOSIS ( 11 FDA reports)
GRANULOCYTE COUNT DECREASED ( 11 FDA reports)
HEPATORENAL SYNDROME ( 11 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
HYPERTROPHY ( 11 FDA reports)
INFECTIVE TENOSYNOVITIS ( 11 FDA reports)
INGUINAL HERNIA REPAIR ( 11 FDA reports)
INGUINAL MASS ( 11 FDA reports)
INJECTION SITE PHLEBITIS ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
KERATOACANTHOMA ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LUNG ADENOCARCINOMA ( 11 FDA reports)
MACROCYTOSIS ( 11 FDA reports)
MACROPHAGES INCREASED ( 11 FDA reports)
MEGACOLON ( 11 FDA reports)
MENSTRUAL DISORDER ( 11 FDA reports)
MUSCLE SWELLING ( 11 FDA reports)
MUSCLE TIGHTNESS ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
NEUTROPENIC INFECTION ( 11 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 11 FDA reports)
OPTIC NEUROPATHY ( 11 FDA reports)
ORAL FIBROMA ( 11 FDA reports)
OTITIS MEDIA ACUTE ( 11 FDA reports)
PANCOAST'S TUMOUR ( 11 FDA reports)
PCO2 DECREASED ( 11 FDA reports)
PERITONEAL DISORDER ( 11 FDA reports)
PO2 DECREASED ( 11 FDA reports)
POLYP COLORECTAL ( 11 FDA reports)
POOR VENOUS ACCESS ( 11 FDA reports)
PROSTATECTOMY ( 11 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 11 FDA reports)
PROTEUS INFECTION ( 11 FDA reports)
PULMONARY THROMBOSIS ( 11 FDA reports)
RASH VESICULAR ( 11 FDA reports)
RECTAL TENESMUS ( 11 FDA reports)
RED BLOOD CELL ABNORMALITY ( 11 FDA reports)
RENAL CANCER ( 11 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 11 FDA reports)
RESORPTION BONE INCREASED ( 11 FDA reports)
RETINAL ISCHAEMIA ( 11 FDA reports)
RIGHT ATRIAL DILATATION ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SPINAL X-RAY ABNORMAL ( 11 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 11 FDA reports)
THYROID MASS ( 11 FDA reports)
TONGUE COATED ( 11 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 11 FDA reports)
TYPE 1 DIABETES MELLITUS ( 11 FDA reports)
URINE ANALYSIS ( 11 FDA reports)
VAGINITIS BACTERIAL ( 11 FDA reports)
VARICELLA ( 11 FDA reports)
VENOUS STENOSIS ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
ABDOMINAL SEPSIS ( 10 FDA reports)
ABSCESS LIMB ( 10 FDA reports)
ACUTE LEUKAEMIA ( 10 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 10 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 10 FDA reports)
ARTHROPOD BITE ( 10 FDA reports)
ASPHYXIA ( 10 FDA reports)
ASTERIXIS ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BACTEROIDES TEST POSITIVE ( 10 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 10 FDA reports)
BONE DENSITY INCREASED ( 10 FDA reports)
BONE MARROW OEDEMA ( 10 FDA reports)
BONE SARCOMA ( 10 FDA reports)
BREAST CYST ( 10 FDA reports)
CANDIDA PNEUMONIA ( 10 FDA reports)
CARDIAC ENZYMES INCREASED ( 10 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 10 FDA reports)
CAUDA EQUINA SYNDROME ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 10 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 10 FDA reports)
CHARLES BONNET SYNDROME ( 10 FDA reports)
CHROMATOPSIA ( 10 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 10 FDA reports)
CULTURE POSITIVE ( 10 FDA reports)
CYST ASPIRATION ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 10 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 10 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 10 FDA reports)
DYSPHASIA ( 10 FDA reports)
DYSTROPHIC CALCIFICATION ( 10 FDA reports)
EAR HAEMORRHAGE ( 10 FDA reports)
EAR NEOPLASM ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
ERYTHEMA NODOSUM ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
EXTRASKELETAL OSSIFICATION ( 10 FDA reports)
EYE INFLAMMATION ( 10 FDA reports)
FACIAL OPERATION ( 10 FDA reports)
FASCIITIS ( 10 FDA reports)
FOETAL GROWTH RETARDATION ( 10 FDA reports)
FOOD CRAVING ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
GASTROINTESTINAL INFECTION ( 10 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 10 FDA reports)
GRIEF REACTION ( 10 FDA reports)
HAEMOGLOBINURIA ( 10 FDA reports)
HAEMOPHILUS INFECTION ( 10 FDA reports)
HAND FRACTURE ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 10 FDA reports)
HEPATIC CONGESTION ( 10 FDA reports)
HEPATIC HAEMORRHAGE ( 10 FDA reports)
HEPATIC NEOPLASM ( 10 FDA reports)
HYDROCELE ( 10 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 10 FDA reports)
HYPERTENSIVE CRISIS ( 10 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 10 FDA reports)
INTESTINAL ULCER ( 10 FDA reports)
LIMB INJURY ( 10 FDA reports)
LOCALISED OEDEMA ( 10 FDA reports)
LOSS OF PROPRIOCEPTION ( 10 FDA reports)
LUDWIG ANGINA ( 10 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 10 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
MACULE ( 10 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 10 FDA reports)
MANTLE CELL LYMPHOMA ( 10 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 10 FDA reports)
MICROCYTOSIS ( 10 FDA reports)
MITRAL VALVE SCLEROSIS ( 10 FDA reports)
MIXED DEAFNESS ( 10 FDA reports)
MONOCYTE COUNT DECREASED ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
MYOCARDITIS ( 10 FDA reports)
NEOPLASM SKIN ( 10 FDA reports)
NEPHRITIC SYNDROME ( 10 FDA reports)
NEPHRITIS INTERSTITIAL ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEUTROPHILIA ( 10 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 10 FDA reports)
OESOPHAGEAL DILATATION ( 10 FDA reports)
OESOPHAGEAL POLYP ( 10 FDA reports)
OLIGOHYDRAMNIOS ( 10 FDA reports)
OPTIC NEURITIS ( 10 FDA reports)
OROPHARYNGEAL BLISTERING ( 10 FDA reports)
OVARIAN FAILURE ( 10 FDA reports)
PARAPSORIASIS ( 10 FDA reports)
PARTNER STRESS ( 10 FDA reports)
PELVIC ABSCESS ( 10 FDA reports)
PERINEPHRIC ABSCESS ( 10 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 10 FDA reports)
PNEUMOPERITONEUM ( 10 FDA reports)
PULMONARY NECROSIS ( 10 FDA reports)
PUPIL FIXED ( 10 FDA reports)
RADICULAR SYNDROME ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RESPIRATORY TRACT OEDEMA ( 10 FDA reports)
SHOULDER OPERATION ( 10 FDA reports)
SKIN FRAGILITY ( 10 FDA reports)
SKIN SWELLING ( 10 FDA reports)
SPINAL DEFORMITY ( 10 FDA reports)
SUBACUTE ENDOCARDITIS ( 10 FDA reports)
THROMBECTOMY ( 10 FDA reports)
TONGUE PARALYSIS ( 10 FDA reports)
TONSILLAR DISORDER ( 10 FDA reports)
TOXIC SKIN ERUPTION ( 10 FDA reports)
TRAUMATIC HAEMATOMA ( 10 FDA reports)
URINE KETONE BODY PRESENT ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
VERTEBRAL COLUMN MASS ( 10 FDA reports)
VOLVULUS ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
VITAMIN B12 INCREASED ( 9 FDA reports)
VITH NERVE PARALYSIS ( 9 FDA reports)
VITREOUS HAEMORRHAGE ( 9 FDA reports)
WEIGHT BEARING DIFFICULTY ( 9 FDA reports)
ABDOMINAL INFECTION ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
ANAL HAEMORRHAGE ( 9 FDA reports)
ANASTOMOTIC LEAK ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANGIOMYOLIPOMA ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 9 FDA reports)
ATRIAL SEPTAL DEFECT ( 9 FDA reports)
BACTERIA URINE IDENTIFIED ( 9 FDA reports)
BASOPHIL COUNT DECREASED ( 9 FDA reports)
BENIGN GASTRIC NEOPLASM ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 9 FDA reports)
BLOOD IRON INCREASED ( 9 FDA reports)
BLOOD PH INCREASED ( 9 FDA reports)
BLOOD TEST ABNORMAL ( 9 FDA reports)
BREAST LUMP REMOVAL ( 9 FDA reports)
BRONCHITIS CHRONIC ( 9 FDA reports)
CARBON DIOXIDE DECREASED ( 9 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 9 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CHONDROCALCINOSIS ( 9 FDA reports)
COLON CANCER RECURRENT ( 9 FDA reports)
COLONOSCOPY ABNORMAL ( 9 FDA reports)
COMMUNICATION DISORDER ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CONJUNCTIVAL OEDEMA ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CSF CULTURE POSITIVE ( 9 FDA reports)
CYST DRAINAGE ( 9 FDA reports)
CYSTOPEXY ( 9 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 9 FDA reports)
DRUG PRESCRIBING ERROR ( 9 FDA reports)
DYSPONESIS ( 9 FDA reports)
EATING DISORDER SYMPTOM ( 9 FDA reports)
EFFUSION ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 9 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 9 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 9 FDA reports)
FIBULA FRACTURE ( 9 FDA reports)
FLAT AFFECT ( 9 FDA reports)
FOETAL DISORDER ( 9 FDA reports)
FOOD POISONING ( 9 FDA reports)
GASTRIC CANCER RECURRENT ( 9 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 9 FDA reports)
GASTROSTOMY TUBE INSERTION ( 9 FDA reports)
GAZE PALSY ( 9 FDA reports)
GENITAL HERPES ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HEPATIC NECROSIS ( 9 FDA reports)
HEPATOSPLENOMEGALY ( 9 FDA reports)
HOSPICE CARE ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
HYPERPROTEINAEMIA ( 9 FDA reports)
HYPERVENTILATION ( 9 FDA reports)
HYPOPNOEA ( 9 FDA reports)
ILLUSION ( 9 FDA reports)
IMMUNE SYSTEM DISORDER ( 9 FDA reports)
INJECTION SITE SWELLING ( 9 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 9 FDA reports)
KERATITIS ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LEARNING DISABILITY ( 9 FDA reports)
LIP ULCERATION ( 9 FDA reports)
LITHOTRIPSY ( 9 FDA reports)
LIVER TRANSPLANT ( 9 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 9 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
MEASLES ( 9 FDA reports)
MEDIASTINAL DISORDER ( 9 FDA reports)
MEDICAL DEVICE COMPLICATION ( 9 FDA reports)
MEGAKARYOCYTES DECREASED ( 9 FDA reports)
MENINGITIS ASEPTIC ( 9 FDA reports)
METASTASES TO HEART ( 9 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 9 FDA reports)
MONONUCLEOSIS SYNDROME ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
MYELOFIBROSIS ( 9 FDA reports)
NAIL DYSTROPHY ( 9 FDA reports)
NEUROGENIC BOWEL ( 9 FDA reports)
NEUTROPENIC COLITIS ( 9 FDA reports)
NEUTROPHIL COUNT ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 9 FDA reports)
OBSTRUCTION ( 9 FDA reports)
OBSTRUCTION GASTRIC ( 9 FDA reports)
OSTECTOMY ( 9 FDA reports)
PANCREATIC NEOPLASM ( 9 FDA reports)
PATELLA FRACTURE ( 9 FDA reports)
PELVIC HAEMATOMA ( 9 FDA reports)
PERICARDIAL CYST ( 9 FDA reports)
PERINEURIAL CYST ( 9 FDA reports)
PERIPHERAL ISCHAEMIA ( 9 FDA reports)
POIKILOCYTOSIS ( 9 FDA reports)
POLYMYALGIA RHEUMATICA ( 9 FDA reports)
POSTURE ABNORMAL ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 9 FDA reports)
RADICULITIS LUMBOSACRAL ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SECONDARY SEQUESTRUM ( 9 FDA reports)
SKIN CHAPPED ( 9 FDA reports)
SKIN INDURATION ( 9 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 9 FDA reports)
STENT PLACEMENT ( 9 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 9 FDA reports)
STRABISMUS ( 9 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 9 FDA reports)
TESTICULAR ATROPHY ( 9 FDA reports)
THROAT CANCER ( 9 FDA reports)
THYROID ADENOMA ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
TORTICOLLIS ( 9 FDA reports)
URATE NEPHROPATHY ( 9 FDA reports)
URINE ABNORMALITY ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
VASCULAR CAUTERISATION ( 9 FDA reports)
VASCULAR COMPRESSION ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANAPHYLACTOID SHOCK ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 8 FDA reports)
ANXIETY DISORDER ( 8 FDA reports)
APLASIA PURE RED CELL ( 8 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 8 FDA reports)
ARTERIOVENOUS MALFORMATION ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BALANOPOSTHITIS ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BIOPSY BLADDER ABNORMAL ( 8 FDA reports)
BIOPSY SKIN ABNORMAL ( 8 FDA reports)
BLADDER SPASM ( 8 FDA reports)
BLEEDING TIME PROLONGED ( 8 FDA reports)
BLEPHAROSPASM ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 8 FDA reports)
BRONCHIAL HAEMORRHAGE ( 8 FDA reports)
CALCULUS URINARY ( 8 FDA reports)
CARDIAC OPERATION ( 8 FDA reports)
CEREBRAL DISORDER ( 8 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 8 FDA reports)
CLAUSTROPHOBIA ( 8 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
CUBITAL TUNNEL SYNDROME ( 8 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 8 FDA reports)
DEMYELINATION ( 8 FDA reports)
DENTOFACIAL ANOMALY ( 8 FDA reports)
DISSEMINATED TUBERCULOSIS ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
DRY SOCKET ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
EPIDIDYMAL CYST ( 8 FDA reports)
EPIDURAL LIPOMATOSIS ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
EYE INJURY ( 8 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 8 FDA reports)
GASTRITIS HAEMORRHAGIC ( 8 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GENITAL CANDIDIASIS ( 8 FDA reports)
H1N1 INFLUENZA ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INCISION SITE COMPLICATION ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
INFUSION SITE REACTION ( 8 FDA reports)
JOINT CONTRACTURE ( 8 FDA reports)
JOINT DESTRUCTION ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 8 FDA reports)
LEUKOPLAKIA ( 8 FDA reports)
LIP PAIN ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
LYMPHOCYTOSIS ( 8 FDA reports)
MEDICAL DEVICE CHANGE ( 8 FDA reports)
MENISCUS REMOVAL ( 8 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 8 FDA reports)
MULTI-ORGAN DISORDER ( 8 FDA reports)
NARCOLEPSY ( 8 FDA reports)
NASAL SEPTUM PERFORATION ( 8 FDA reports)
NASAL ULCER ( 8 FDA reports)
NEPHRECTOMY ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
NERVE ROOT LESION ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OROANTRAL FISTULA ( 8 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 8 FDA reports)
PAINFUL DEFAECATION ( 8 FDA reports)
PALATAL DISORDER ( 8 FDA reports)
PANCREATIC DUCT DILATATION ( 8 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PELVIC DISCOMFORT ( 8 FDA reports)
PERICARDITIS MALIGNANT ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PEYRONIE'S DISEASE ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
PLEURAL DECORTICATION ( 8 FDA reports)
PLEURAL HAEMORRHAGE ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 8 FDA reports)
PO2 INCREASED ( 8 FDA reports)
POLYDACTYLY ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
PORTAL HYPERTENSION ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
PULSE PRESSURE DECREASED ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
REHABILITATION THERAPY ( 8 FDA reports)
RETINAL SCAR ( 8 FDA reports)
RETINAL TEAR ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
RIGHT VENTRICULAR FAILURE ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SCROTAL ABSCESS ( 8 FDA reports)
SCROTAL INFECTION ( 8 FDA reports)
SENILE OSTEOPOROSIS ( 8 FDA reports)
SEROSITIS ( 8 FDA reports)
SIMPLE PARTIAL SEIZURES ( 8 FDA reports)
SJOGREN'S SYNDROME ( 8 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 8 FDA reports)
STRESS ULCER ( 8 FDA reports)
SUBDURAL HAEMORRHAGE ( 8 FDA reports)
SUBMANDIBULAR MASS ( 8 FDA reports)
SYNCOPE VASOVAGAL ( 8 FDA reports)
SYRINGOMYELIA ( 8 FDA reports)
TENDON PAIN ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
THORACIC OPERATION ( 8 FDA reports)
TINEA PEDIS ( 8 FDA reports)
TONGUE NEOPLASM ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 8 FDA reports)
VOCAL CORD POLYP ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 7 FDA reports)
VIRAL LABYRINTHITIS ( 7 FDA reports)
VITAMIN K DEFICIENCY ( 7 FDA reports)
WOUND CLOSURE ( 7 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 7 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
ANOGENITAL WARTS ( 7 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 7 FDA reports)
ATRIAL THROMBOSIS ( 7 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 7 FDA reports)
BILIARY TRACT DISORDER ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 7 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 7 FDA reports)
BLUNTED AFFECT ( 7 FDA reports)
BODY DYSMORPHIC DISORDER ( 7 FDA reports)
BONE FORMATION INCREASED ( 7 FDA reports)
BRAIN DAMAGE ( 7 FDA reports)
BRAIN INJURY ( 7 FDA reports)
BRAIN OPERATION ( 7 FDA reports)
BRAIN STEM INFARCTION ( 7 FDA reports)
BREAST NECROSIS ( 7 FDA reports)
CALCULUS BLADDER ( 7 FDA reports)
CANDIDA SEPSIS ( 7 FDA reports)
CARDIAC AMYLOIDOSIS ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHRONIC HEPATIC FAILURE ( 7 FDA reports)
CLOSED FRACTURE MANIPULATION ( 7 FDA reports)
CONDUCTION DISORDER ( 7 FDA reports)
COR PULMONALE ( 7 FDA reports)
CORONARY ANGIOPLASTY ( 7 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 7 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
DISEASE COMPLICATION ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
DYSPAREUNIA ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 7 FDA reports)
ERUCTATION ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
FLUID REPLACEMENT ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
FOREIGN BODY IN EYE ( 7 FDA reports)
GASTRECTOMY ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
GRIP STRENGTH DECREASED ( 7 FDA reports)
HAEMORRHAGE URINARY TRACT ( 7 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYDROPS FOETALIS ( 7 FDA reports)
HYPOGONADISM ( 7 FDA reports)
HYPOVITAMINOSIS ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
INFUSION SITE EXTRAVASATION ( 7 FDA reports)
INFUSION SITE HAEMORRHAGE ( 7 FDA reports)
INJECTION SITE PRURITUS ( 7 FDA reports)
INTRA-UTERINE DEATH ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 7 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
JOINT INJECTION ( 7 FDA reports)
KLEBSIELLA TEST POSITIVE ( 7 FDA reports)
LENS DISORDER ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
LIMB OPERATION ( 7 FDA reports)
LIVER ABSCESS ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
LUNG OPERATION ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 7 FDA reports)
MAMMARY DUCT ECTASIA ( 7 FDA reports)
MENINGEAL DISORDER ( 7 FDA reports)
MERALGIA PARAESTHETICA ( 7 FDA reports)
METASTATIC LYMPHOMA ( 7 FDA reports)
MUSCLE ABSCESS ( 7 FDA reports)
MYOPIA ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
ONYCHOCLASIS ( 7 FDA reports)
ONYCHOLYSIS ( 7 FDA reports)
OPHTHALMOPLEGIA ( 7 FDA reports)
ORAL TORUS ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
PANCREATIC ENLARGEMENT ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PHAEOCHROMOCYTOMA ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PLATELET TRANSFUSION ( 7 FDA reports)
PNEUMOMEDIASTINUM ( 7 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 7 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 7 FDA reports)
PREGNANCY ( 7 FDA reports)
PRIMARY HYPOGONADISM ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PRINZMETAL ANGINA ( 7 FDA reports)
PROSTATISM ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
RED MAN SYNDROME ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
RESPIRATION ABNORMAL ( 7 FDA reports)
RETINAL VEIN OCCLUSION ( 7 FDA reports)
SKIN PLAQUE ( 7 FDA reports)
SKIN ULCER HAEMORRHAGE ( 7 FDA reports)
SOFT TISSUE MASS ( 7 FDA reports)
SPINAL CORD DISORDER ( 7 FDA reports)
SPUTUM INCREASED ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
STERNAL FRACTURE ( 7 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
THALASSAEMIA BETA ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
TONGUE DRY ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TONIC CONVULSION ( 7 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 7 FDA reports)
TOXIC NODULAR GOITRE ( 7 FDA reports)
TROPONIN I INCREASED ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
UTERINE ATONY ( 7 FDA reports)
UTERINE POLYP ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VASCULAR OPERATION ( 7 FDA reports)
ABDOMINAL OPERATION ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ALOPECIA AREATA ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
ARTERITIS ( 6 FDA reports)
ATONIC SEIZURES ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
AVULSION FRACTURE ( 6 FDA reports)
AXONAL NEUROPATHY ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BASOPHIL COUNT INCREASED ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BLADDER PERFORATION ( 6 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 6 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 6 FDA reports)
BREATH SOUNDS DECREASED ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CATHETER REMOVAL ( 6 FDA reports)
CATHETER SITE HAEMORRHAGE ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
CHAPPED LIPS ( 6 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 6 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CLUSTER HEADACHE ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
CORNEAL DYSTROPHY ( 6 FDA reports)
CRYOGLOBULINAEMIA ( 6 FDA reports)
CULTURE WOUND POSITIVE ( 6 FDA reports)
CYST REMOVAL ( 6 FDA reports)
DERMATITIS ALLERGIC ( 6 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 6 FDA reports)
DYSCHEZIA ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
EAR IRRIGATION ( 6 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ENCEPHALITIS VIRAL ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
ENTEROCUTANEOUS FISTULA ( 6 FDA reports)
EOSINOPHIL COUNT DECREASED ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GRIMACING ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 6 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HAEMODILUTION ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEPATIC INFARCTION ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HERPES ZOSTER DISSEMINATED ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
HYPERVISCOSITY SYNDROME ( 6 FDA reports)
HYPOCHLORAEMIA ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
HYPOTONIA ( 6 FDA reports)
IMMUNOGLOBULINS DECREASED ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
IMPAIRED SELF-CARE ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
JOINT SURGERY ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LESION EXCISION ( 6 FDA reports)
LIGAMENT INJURY ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 6 FDA reports)
LYMPH NODE PAIN ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MENIERE'S DISEASE ( 6 FDA reports)
MENINGITIS TUBERCULOUS ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
METASTASES TO SPLEEN ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NOCARDIOSIS ( 6 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
PAIN EXACERBATED ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 6 FDA reports)
PELVIC PROLAPSE ( 6 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 6 FDA reports)
PERIPHERAL EMBOLISM ( 6 FDA reports)
PNEUMATOSIS ( 6 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 6 FDA reports)
POST PROCEDURAL DISCHARGE ( 6 FDA reports)
POSTICTAL STATE ( 6 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 6 FDA reports)
POSTNASAL DRIP ( 6 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 6 FDA reports)
PRODUCT QUALITY ISSUE ( 6 FDA reports)
PSEUDOMENINGOCELE ( 6 FDA reports)
PSYCHIATRIC SYMPTOM ( 6 FDA reports)
PULMONARY CALCIFICATION ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
QUADRIPARESIS ( 6 FDA reports)
QUADRIPLEGIA ( 6 FDA reports)
RENAL ARTERIOSCLEROSIS ( 6 FDA reports)
RENIN DECREASED ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
ROTATOR CUFF REPAIR ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SHUNT MALFUNCTION ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SKIN LESION EXCISION ( 6 FDA reports)
SKIN NODULE ( 6 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
SPINAL CORD INFARCTION ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
SUBCUTANEOUS NODULE ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
SUDDEN CARDIAC DEATH ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
TESTICULAR PAIN ( 6 FDA reports)
TOOTH DISCOLOURATION ( 6 FDA reports)
TRANSFERRIN DECREASED ( 6 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TUMOUR PAIN ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
WISDOM TEETH REMOVAL ( 5 FDA reports)
17-HYDROXYPROGESTERONE INCREASED ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
ANGIOSARCOMA ( 5 FDA reports)
ANGIOSCLEROSIS ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
ANTI-INSULIN ANTIBODY DECREASED ( 5 FDA reports)
APHERESIS ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 5 FDA reports)
BIPOLAR I DISORDER ( 5 FDA reports)
BLADDER DIVERTICULUM ( 5 FDA reports)
BLISTER INFECTED ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD SELENIUM INCREASED ( 5 FDA reports)
BLOOD UREA ABNORMAL ( 5 FDA reports)
BODY HEIGHT DECREASED ( 5 FDA reports)
BONE ABSCESS ( 5 FDA reports)
BONE FORMATION DECREASED ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST DISORDER ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 5 FDA reports)
CATHETER SITE RELATED REACTION ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
CEREBRAL ARTERY STENOSIS ( 5 FDA reports)
CEREBRAL CYST ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CORNEAL OPACITY ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DERMATOMYOSITIS ( 5 FDA reports)
DETOXIFICATION ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
DYSPHORIA ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
EMBOLISM ARTERIAL ( 5 FDA reports)
ENTEROCOCCAL SEPSIS ( 5 FDA reports)
ENTEROCOLITIS VIRAL ( 5 FDA reports)
EPIPLOIC APPENDAGITIS ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
ERYSIPELAS ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
EYE INFECTION VIRAL ( 5 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 5 FDA reports)
FLASHBACK ( 5 FDA reports)
FOAMING AT MOUTH ( 5 FDA reports)
GALLBLADDER PERFORATION ( 5 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 5 FDA reports)
GASTROENTERITIS RADIATION ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMOGLOBIN ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HAEMOSIDEROSIS ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HIGH FREQUENCY ABLATION ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HYPERCHLORAEMIA ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
HYPERVITAMINOSIS ( 5 FDA reports)
HYPOCHROMASIA ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
HYPOPHYSITIS ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
INCISION SITE PAIN ( 5 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
JAW LESION EXCISION ( 5 FDA reports)
JOINT LOCK ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LARYNGEAL STENOSIS ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LIGHT CHAIN DISEASE ( 5 FDA reports)
LIP EROSION ( 5 FDA reports)
LIP HAEMORRHAGE ( 5 FDA reports)
LIP INJURY ( 5 FDA reports)
LIP NEOPLASM BENIGN ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
LYMPHOHISTIOCYTOSIS ( 5 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 5 FDA reports)
METASTATIC PAIN ( 5 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
MILIA ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MIXED LIVER INJURY ( 5 FDA reports)
MOANING ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MYRINGOTOMY ( 5 FDA reports)
NARCOTIC INTOXICATION ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 5 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 5 FDA reports)
OPTIC NERVE DISORDER ( 5 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PACHYMENINGITIS ( 5 FDA reports)
PARALYSIS FLACCID ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 5 FDA reports)
PHARYNX DISCOMFORT ( 5 FDA reports)
PIRIFORMIS SYNDROME ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PLEURAL NEOPLASM ( 5 FDA reports)
PLEURECTOMY ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
POST PROCEDURAL VOMITING ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
PROCEDURAL NAUSEA ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROTEIN TOTAL ABNORMAL ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RADICULAR CYST ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
RECALL PHENOMENON ( 5 FDA reports)
RECTAL STENOSIS ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SARCOMA ( 5 FDA reports)
SEPSIS NEONATAL ( 5 FDA reports)
SHOCK HYPOGLYCAEMIC ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SKIN GRAFT ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
SPLENIC CYST ( 5 FDA reports)
SPUTUM ABNORMAL ( 5 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 5 FDA reports)
SUBDURAL HYGROMA ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SUTURE REMOVAL ( 5 FDA reports)
SWEAT GLAND INFECTION ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
TERMINAL STATE ( 5 FDA reports)
THORACIC OUTLET SYNDROME ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TINEL'S SIGN ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 5 FDA reports)
TUMOUR EXCISION ( 5 FDA reports)
ULNA FRACTURE ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
URETHRAL OBSTRUCTION ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ACANTHOSIS ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ADENOIDAL HYPERTROPHY ( 4 FDA reports)
ADRENAL ATROPHY ( 4 FDA reports)
ADRENAL HAEMORRHAGE ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 4 FDA reports)
ALPHA GLOBULIN INCREASED ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 4 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
AORTITIS ( 4 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 4 FDA reports)
ASTROCYTOMA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
AUTISM ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BACTERIAL CULTURE POSITIVE ( 4 FDA reports)
BACTERIURIA ( 4 FDA reports)
BALLISMUS ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BENIGN CARDIAC NEOPLASM ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BILIARY SEPSIS ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN DECREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 4 FDA reports)
BLOOD SODIUM ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
BONE LESION EXCISION ( 4 FDA reports)
BONE MARROW NECROSIS ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BREAST CANCER STAGE IV ( 4 FDA reports)
BREAST HAEMATOMA ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BURN INFECTION ( 4 FDA reports)
BURSITIS INFECTIVE ( 4 FDA reports)
CANDIDA TEST POSITIVE ( 4 FDA reports)
CARDIAC FIBROMA ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CAUSTIC INJURY ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL ASPERGILLOSIS ( 4 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHRONIC TONSILLITIS ( 4 FDA reports)
COAGULATION TIME ABNORMAL ( 4 FDA reports)
COLPORRHAPHY ( 4 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
CRANIAL NEUROPATHY ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRUG THERAPY CHANGED ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FOETAL HEART RATE INCREASED ( 4 FDA reports)
GASTROINTESTINAL EROSION ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL OEDEMA ( 4 FDA reports)
GASTROSTOMY ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GLIOMA ( 4 FDA reports)
GROWTH RETARDATION ( 4 FDA reports)
HAEMATOCRIT ABNORMAL ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC HAEMATOMA ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERCHLORHYDRIA ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INFECTED EPIDERMAL CYST ( 4 FDA reports)
INFECTION MASKED ( 4 FDA reports)
INFUSION SITE PHLEBITIS ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE PUSTULE ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 4 FDA reports)
INTRACRANIAL HAEMATOMA ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LABOUR COMPLICATION ( 4 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 4 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
LARGE INTESTINE CARCINOMA ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LEUKAEMOID REACTION ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOSS OF CONTROL OF LEGS ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 4 FDA reports)
MEGAKARYOCYTES INCREASED ( 4 FDA reports)
MENINGEAL NEOPLASM ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 4 FDA reports)
MENOPAUSAL SYMPTOMS ( 4 FDA reports)
MESENTERITIS ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METASTASES TO BLADDER ( 4 FDA reports)
METASTASES TO CHEST WALL ( 4 FDA reports)
METASTASES TO KIDNEY ( 4 FDA reports)
METASTASES TO MUSCLE ( 4 FDA reports)
METASTASES TO OVARY ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 4 FDA reports)
MIGRATION OF IMPLANT ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 4 FDA reports)
MYOTONIA ( 4 FDA reports)
NEUROMA ( 4 FDA reports)
NO ADVERSE EFFECT ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 4 FDA reports)
OCULAR HYPERTENSION ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OSTEOARTHROPATHY ( 4 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PAPULE ( 4 FDA reports)
PARESIS CRANIAL NERVE ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PENILE PROSTHESIS INSERTION ( 4 FDA reports)
PERIANAL ABSCESS ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL CARCINOMA ( 4 FDA reports)
PHLEBOTHROMBOSIS ( 4 FDA reports)
PINGUECULITIS ( 4 FDA reports)
PLATELET DESTRUCTION INCREASED ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 4 FDA reports)
PNEUMONIA HERPES VIRAL ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
PORCELAIN GALLBLADDER ( 4 FDA reports)
PORTAL VENOUS GAS ( 4 FDA reports)
POST PROCEDURAL NAUSEA ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PROCEDURAL VOMITING ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
PULMONARY VEIN OCCLUSION ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PYELONEPHRITIS FUNGAL ( 4 FDA reports)
REACTIVE PSYCHOSIS ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
SALMONELLA BACTERAEMIA ( 4 FDA reports)
SALMONELLOSIS ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SMALL INTESTINE ULCER ( 4 FDA reports)
SPINAL CORD HAEMORRHAGE ( 4 FDA reports)
SPINAL HAEMANGIOMA ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
STATUS ASTHMATICUS ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
TAENIASIS ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THORACIC CAVITY DRAINAGE ( 4 FDA reports)
THYROID ATROPHY ( 4 FDA reports)
THYROTOXIC CRISIS ( 4 FDA reports)
TONSIL CANCER ( 4 FDA reports)
TONSILLECTOMY ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URETERIC RUPTURE ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VAGINOPLASTY ( 4 FDA reports)
VEIN DISCOLOURATION ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VULVAL CANCER ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VITAMIN B12 DECREASED ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WOUND ABSCESS ( 4 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
WOUND DECOMPOSITION ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ABULIA ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE TONSILLITIS ( 3 FDA reports)
ADENOCARCINOMA PANCREAS ( 3 FDA reports)
ADNEXA UTERI CYST ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAESTHESIA DOLOROSA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARTERIOENTERIC FISTULA ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 3 FDA reports)
ASPIRATION BRONCHIAL ( 3 FDA reports)
ATONIC URINARY BLADDER ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 3 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 3 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 3 FDA reports)
BLOOD CORTISOL ABNORMAL ( 3 FDA reports)
BLOOD CORTISOL INCREASED ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ( 3 FDA reports)
BLOOD VISCOSITY INCREASED ( 3 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC VALVE SCLEROSIS ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST WALL CYST ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHONDROSARCOMA ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLOSTRIDIUM TEST ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CYSTIC LYMPHANGIOMA ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DENTAL CLEANING ( 3 FDA reports)
DENTAL FLUORIDE THERAPY ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 3 FDA reports)
DIAPHRAGMATIC HERNIA ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 3 FDA reports)
DIVERTICULAR HERNIA ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
ECHOGRAPHY ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENCEPHALOMYELITIS ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTEROCOLITIS BACTERIAL ( 3 FDA reports)
ENTHESOPATHY ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EPENDYMOMA ( 3 FDA reports)
EVANS SYNDROME ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EYE NAEVUS ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FLUCTUANCE ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GAS GANGRENE ( 3 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROENTERITIS BACILLUS ( 3 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GINGIVAL DISCOLOURATION ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 3 FDA reports)
GRAM STAIN POSITIVE ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMATOMA INFECTION ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEART VALVE INSUFFICIENCY ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HORNER'S SYNDROME ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 3 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MALFORMATION VENOUS ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MANDIBULECTOMY ( 3 FDA reports)
MECHANICAL ILEUS ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MEDIASTINUM NEOPLASM ( 3 FDA reports)
MENINGITIS HAEMOPHILUS ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
METASTASES TO MOUTH ( 3 FDA reports)
METASTASES TO OESOPHAGUS ( 3 FDA reports)
METASTASES TO PANCREAS ( 3 FDA reports)
METASTASES TO SMALL INTESTINE ( 3 FDA reports)
MICROALBUMINURIA ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
ORTHOPEDIC PROCEDURE ( 3 FDA reports)
OSTEODYSTROPHY ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERFORATION BILE DUCT ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PLASMABLASTIC LYMPHOMA ( 3 FDA reports)
PNEUMOCONIOSIS ( 3 FDA reports)
PNEUMONIA INFLUENZAL ( 3 FDA reports)
PNEUMORETROPERITONEUM ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PROSTHESIS USER ( 3 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
RADICULITIS ( 3 FDA reports)
RECTAL CANCER METASTATIC ( 3 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL CORTICAL NECROSIS ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SHUNT OCCLUSION ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SOFT TISSUE NECROSIS ( 3 FDA reports)
SPINAL CORD INJURY ( 3 FDA reports)
SPINAL CORD OPERATION ( 3 FDA reports)
SPLENIC LESION ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
SUTURE RELATED COMPLICATION ( 3 FDA reports)
SYMPTOM MASKED ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THREATENED LABOUR ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TRICHOSPORON INFECTION ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
URETERAL STENT INSERTION ( 3 FDA reports)
URETERIC OPERATION ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
UROGENITAL HAEMORRHAGE ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINAL ULCERATION ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR ANOMALY ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASOCONSTRICTION ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
AGONAL DEATH STRUGGLE ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMOEBIC COLITIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
APICECTOMY ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BASAL GANGLIA INFARCTION ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BILE OUTPUT ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLAST CELLS ( 2 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 2 FDA reports)
BLOOD CALCITONIN INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD GLUCAGON INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD STEM CELL HARVEST ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CALCULUS URETHRAL ( 2 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CELLULITIS PHARYNGEAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEPHALHAEMATOMA ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 2 FDA reports)
CEREBROSPINAL FISTULA ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVIX CARCINOMA RECURRENT ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONGENITAL CEREBRAL CYST ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DUODENAL STENOSIS ( 2 FDA reports)
DURAL ABSCESS ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ELLIPTOCYTOSIS ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FIBRIN D DIMER ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FLAVOBACTERIUM INFECTION ( 2 FDA reports)
FOLLICULAR MUCINOSIS ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FORCEPS DELIVERY ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUNGAL PARONYCHIA ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLUCOCORTICOIDS DECREASED ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATITIS INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERADRENALISM ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPATHIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
IATROGENIC INFECTION ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILEOSTOMY CLOSURE ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFLAMMATORY PAIN ( 2 FDA reports)
INFUSION SITE BURNING ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MALIGNANT GLIOMA ( 2 FDA reports)
MANIPULATION ( 2 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 2 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 2 FDA reports)
MECONIUM PLUG SYNDROME ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENINGIOMA MALIGNANT ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTASES TO NECK ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
METASTASES TO THORAX ( 2 FDA reports)
METASTASES TO TRACHEA ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL NECROSIS ( 2 FDA reports)
NECROLYTIC MIGRATORY ERYTHEMA ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OSTEITIS CONDENSANS ( 2 FDA reports)
OSTEOSARCOMA METASTATIC ( 2 FDA reports)
OVARIAN EPITHELIAL CANCER ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PLATELET AGGREGATION ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET COUNT ( 2 FDA reports)
PLEURAL MESOTHELIOMA ( 2 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ADVANCED ( 2 FDA reports)
PNEUMOCEPHALUS ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
POSTURING ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY ARTERY ANEURYSM ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RADIATION DYSPHAGIA ( 2 FDA reports)
RADIATION FIBROSIS ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RADIATION NECROSIS ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY RATE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHISTOSOMIASIS ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SECONDARY AMYLOIDOSIS ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERRATIA SEPSIS ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SYMBLEPHARON ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENOSYNOVITIS STENOSANS ( 2 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 2 FDA reports)
TIC ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
UROGENITAL ATROPHY ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WATERHOUSE-FRIDERICHSEN SYNDROME ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT NORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ACTIVATED PROTEIN C RESISTANCE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENOGENITAL SYNDROME ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA RECURRENT ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM PULMONARY ABNORMAL ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANOVULVAR FISTULA ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE ANAESTHESIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTROCYTOMA MALIGNANT ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD FOLATE ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BONE FRAGMENTATION AROUND IMPLANT ( 1 FDA reports)
BONE GRAFT LYSIS ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM THROMBOSIS ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE NECROSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SALT-WASTING SYNDROME ( 1 FDA reports)
CEREBRAL SARCOIDOSIS ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHEST WALL NECROSIS ( 1 FDA reports)
CHOLANGIOGRAM ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONGENITAL AORTIC ATRESIA ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CORTISOL FREE URINE INCREASED ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIFFUSE AXONAL INJURY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
EMPHYSEMATOUS CHOLECYSTITIS ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENDOCARDIAL FIBROELASTOSIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROCOLITIS FUNGAL ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXERESIS ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR IX INHIBITION ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GERSTMANN'S SYNDROME ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GUM NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCOELE ( 1 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMOPHILUS SEPSIS ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS POST TRANSFUSION ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAUTERINE INFECTION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAW INFLAMMATION ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
KARNOFSKY SCALE WORSENED ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATITIS INTERSTITIAL ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE ABSCESS ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE HYPOPLASIA ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MORAXELLA TEST POSITIVE ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE FLAP OPERATION ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NAIL DISCOMFORT ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NATURAL KILLER-CELL LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEISSERIA TEST POSITIVE ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANEOPLASTIC CEREBELLAR DEGENERATION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROXYSMAL CHOREOATHETOSIS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA MORAXELLA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMIC RED BLOOD CELLS PRESENT ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORENCEPHALY ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
PRECURSOR B-LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE MUSCULAR ATROPHY ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION MYELOPATHY ( 1 FDA reports)
RADIATION PERICARDITIS ( 1 FDA reports)
RADIOTHERAPY TO BONE ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY DEPTH DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SEPTIC ARTHRITIS STREPTOCOCCAL ( 1 FDA reports)
SEPTUM PELLUCIDUM AGENESIS ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHOULDER DEFORMITY ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS CANCER METASTATIC ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBDURAL EFFUSION ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYNOVIAL SARCOMA METASTATIC ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR OPERATION ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VANILLYL MANDELIC ACID URINE INCREASED ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)