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

PAIN ( 1492 FDA reports)
NAUSEA ( 1408 FDA reports)
FATIGUE ( 1208 FDA reports)
DYSPNOEA ( 1169 FDA reports)
FALL ( 1087 FDA reports)
DIARRHOEA ( 1038 FDA reports)
ANXIETY ( 977 FDA reports)
HEADACHE ( 974 FDA reports)
DIZZINESS ( 955 FDA reports)
PAIN IN EXTREMITY ( 919 FDA reports)
ASTHENIA ( 904 FDA reports)
ARTHRALGIA ( 887 FDA reports)
VOMITING ( 858 FDA reports)
OEDEMA PERIPHERAL ( 829 FDA reports)
CHEST PAIN ( 809 FDA reports)
ANAEMIA ( 736 FDA reports)
HYPERTENSION ( 707 FDA reports)
PNEUMONIA ( 703 FDA reports)
DRUG INEFFECTIVE ( 702 FDA reports)
DEPRESSION ( 693 FDA reports)
BACK PAIN ( 664 FDA reports)
ABDOMINAL PAIN ( 628 FDA reports)
PYREXIA ( 620 FDA reports)
INSOMNIA ( 602 FDA reports)
INJURY ( 579 FDA reports)
CONSTIPATION ( 566 FDA reports)
COUGH ( 555 FDA reports)
DEEP VEIN THROMBOSIS ( 550 FDA reports)
URINARY TRACT INFECTION ( 550 FDA reports)
PULMONARY EMBOLISM ( 548 FDA reports)
WEIGHT DECREASED ( 546 FDA reports)
RASH ( 524 FDA reports)
OSTEOARTHRITIS ( 513 FDA reports)
PRURITUS ( 509 FDA reports)
FEMUR FRACTURE ( 487 FDA reports)
MUSCLE SPASMS ( 464 FDA reports)
DEHYDRATION ( 458 FDA reports)
FLUSHING ( 458 FDA reports)
HYPOTENSION ( 453 FDA reports)
GAIT DISTURBANCE ( 451 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 442 FDA reports)
MALAISE ( 438 FDA reports)
HYPOAESTHESIA ( 435 FDA reports)
MYOCARDIAL INFARCTION ( 432 FDA reports)
ATRIAL FIBRILLATION ( 426 FDA reports)
ABDOMINAL PAIN UPPER ( 423 FDA reports)
MYALGIA ( 418 FDA reports)
CHOLELITHIASIS ( 414 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 414 FDA reports)
CEREBROVASCULAR ACCIDENT ( 402 FDA reports)
BLOOD GLUCOSE INCREASED ( 398 FDA reports)
FEELING ABNORMAL ( 376 FDA reports)
ERYTHEMA ( 368 FDA reports)
DYSPEPSIA ( 362 FDA reports)
WEIGHT INCREASED ( 361 FDA reports)
OSTEOPOROSIS ( 358 FDA reports)
DECREASED APPETITE ( 353 FDA reports)
RENAL FAILURE ACUTE ( 346 FDA reports)
PARAESTHESIA ( 342 FDA reports)
EMOTIONAL DISTRESS ( 330 FDA reports)
PLEURAL EFFUSION ( 326 FDA reports)
RENAL FAILURE ( 325 FDA reports)
SOMNOLENCE ( 323 FDA reports)
TREMOR ( 316 FDA reports)
CONTUSION ( 308 FDA reports)
CONFUSIONAL STATE ( 306 FDA reports)
SINUSITIS ( 306 FDA reports)
MUSCULAR WEAKNESS ( 301 FDA reports)
CELLULITIS ( 299 FDA reports)
CONVULSION ( 297 FDA reports)
INFECTION ( 294 FDA reports)
OSTEONECROSIS OF JAW ( 290 FDA reports)
HAEMOGLOBIN DECREASED ( 287 FDA reports)
HYPERHIDROSIS ( 283 FDA reports)
SEPSIS ( 283 FDA reports)
CATARACT ( 282 FDA reports)
CONDITION AGGRAVATED ( 280 FDA reports)
THROMBOCYTOPENIA ( 277 FDA reports)
BRONCHITIS ( 276 FDA reports)
ARTHRITIS ( 274 FDA reports)
SPINAL OSTEOARTHRITIS ( 272 FDA reports)
VISION BLURRED ( 271 FDA reports)
PALPITATIONS ( 271 FDA reports)
CHOLECYSTITIS CHRONIC ( 265 FDA reports)
BLOOD PRESSURE INCREASED ( 264 FDA reports)
SYNCOPE ( 263 FDA reports)
ABDOMINAL DISTENSION ( 259 FDA reports)
RESPIRATORY FAILURE ( 256 FDA reports)
ASTHMA ( 253 FDA reports)
DYSPHAGIA ( 250 FDA reports)
MUSCULOSKELETAL PAIN ( 250 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 247 FDA reports)
BALANCE DISORDER ( 245 FDA reports)
CHILLS ( 245 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 243 FDA reports)
JOINT SWELLING ( 243 FDA reports)
HAEMORRHOIDS ( 242 FDA reports)
GALLBLADDER DISORDER ( 241 FDA reports)
MITRAL VALVE INCOMPETENCE ( 241 FDA reports)
LOSS OF CONSCIOUSNESS ( 238 FDA reports)
ABDOMINAL DISCOMFORT ( 233 FDA reports)
CORONARY ARTERY DISEASE ( 233 FDA reports)
HYPOKALAEMIA ( 233 FDA reports)
CHEST DISCOMFORT ( 232 FDA reports)
OSTEOPENIA ( 231 FDA reports)
DEATH ( 229 FDA reports)
LOW TURNOVER OSTEOPATHY ( 229 FDA reports)
THROMBOSIS ( 225 FDA reports)
OSTEOMYELITIS ( 224 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 220 FDA reports)
NEUROPATHY PERIPHERAL ( 220 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 219 FDA reports)
ATELECTASIS ( 215 FDA reports)
BONE DISORDER ( 215 FDA reports)
HYPERLIPIDAEMIA ( 215 FDA reports)
IMPAIRED HEALING ( 211 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 210 FDA reports)
OEDEMA ( 208 FDA reports)
HYPERSENSITIVITY ( 207 FDA reports)
ARTHROPATHY ( 205 FDA reports)
TACHYCARDIA ( 205 FDA reports)
DRY MOUTH ( 204 FDA reports)
NECK PAIN ( 201 FDA reports)
ALOPECIA ( 200 FDA reports)
DIVERTICULUM ( 200 FDA reports)
NASOPHARYNGITIS ( 200 FDA reports)
DYSPNOEA EXERTIONAL ( 199 FDA reports)
INJECTION SITE PAIN ( 196 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 195 FDA reports)
URTICARIA ( 195 FDA reports)
GASTRITIS ( 194 FDA reports)
PANCYTOPENIA ( 192 FDA reports)
TOOTH DISORDER ( 192 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 188 FDA reports)
PAIN IN JAW ( 184 FDA reports)
FEELING HOT ( 181 FDA reports)
FLATULENCE ( 181 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 180 FDA reports)
ANHEDONIA ( 180 FDA reports)
PLATELET COUNT DECREASED ( 180 FDA reports)
HAEMORRHAGE ( 178 FDA reports)
RIB FRACTURE ( 177 FDA reports)
HOT FLUSH ( 175 FDA reports)
MEMORY IMPAIRMENT ( 173 FDA reports)
HIATUS HERNIA ( 170 FDA reports)
VERTIGO ( 169 FDA reports)
RENAL FAILURE CHRONIC ( 167 FDA reports)
CARDIOMEGALY ( 165 FDA reports)
DRUG INTERACTION ( 165 FDA reports)
BONE PAIN ( 164 FDA reports)
HERPES ZOSTER ( 163 FDA reports)
HYPONATRAEMIA ( 163 FDA reports)
DRUG HYPERSENSITIVITY ( 160 FDA reports)
MENTAL STATUS CHANGES ( 160 FDA reports)
NEPHROLITHIASIS ( 160 FDA reports)
OROPHARYNGEAL PAIN ( 160 FDA reports)
SWELLING ( 160 FDA reports)
BLOOD CREATININE INCREASED ( 159 FDA reports)
DYSGEUSIA ( 159 FDA reports)
PULMONARY OEDEMA ( 158 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 158 FDA reports)
DENTAL CARIES ( 155 FDA reports)
DIABETES MELLITUS ( 155 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 155 FDA reports)
CARDIAC DISORDER ( 154 FDA reports)
CARPAL TUNNEL SYNDROME ( 153 FDA reports)
RECTAL HAEMORRHAGE ( 153 FDA reports)
HEART RATE INCREASED ( 151 FDA reports)
EPISTAXIS ( 147 FDA reports)
GASTROINTESTINAL DISORDER ( 147 FDA reports)
AMNESIA ( 145 FDA reports)
BURNING SENSATION ( 145 FDA reports)
CARDIAC ARREST ( 145 FDA reports)
BLOOD PRESSURE DECREASED ( 144 FDA reports)
HAEMATURIA ( 142 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 142 FDA reports)
STAPHYLOCOCCAL INFECTION ( 140 FDA reports)
ROTATOR CUFF SYNDROME ( 139 FDA reports)
ANGINA PECTORIS ( 138 FDA reports)
OSTEONECROSIS ( 138 FDA reports)
PANCREATITIS ( 137 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 137 FDA reports)
STRESS FRACTURE ( 136 FDA reports)
NERVOUSNESS ( 136 FDA reports)
DYSURIA ( 132 FDA reports)
STRESS ( 132 FDA reports)
HYPOTHYROIDISM ( 131 FDA reports)
MIGRAINE ( 131 FDA reports)
ABASIA ( 129 FDA reports)
DRY SKIN ( 129 FDA reports)
HIP FRACTURE ( 129 FDA reports)
LYMPHADENOPATHY ( 129 FDA reports)
ARRHYTHMIA ( 128 FDA reports)
DYSPHONIA ( 128 FDA reports)
INFLUENZA LIKE ILLNESS ( 128 FDA reports)
LETHARGY ( 128 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 128 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 127 FDA reports)
OVERDOSE ( 127 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 126 FDA reports)
URINARY INCONTINENCE ( 125 FDA reports)
SCOLIOSIS ( 125 FDA reports)
ARTERIOSCLEROSIS ( 124 FDA reports)
HALLUCINATION ( 124 FDA reports)
BONE DENSITY DECREASED ( 123 FDA reports)
INFLAMMATION ( 123 FDA reports)
MENTAL DISORDER ( 123 FDA reports)
INCORRECT DOSE ADMINISTERED ( 122 FDA reports)
INJECTION SITE ERYTHEMA ( 122 FDA reports)
COLONIC POLYP ( 121 FDA reports)
LEUKOCYTOSIS ( 121 FDA reports)
RHEUMATOID ARTHRITIS ( 121 FDA reports)
ADVERSE EVENT ( 120 FDA reports)
BURSITIS ( 120 FDA reports)
PULMONARY HYPERTENSION ( 119 FDA reports)
BLOOD POTASSIUM DECREASED ( 118 FDA reports)
IRRITABLE BOWEL SYNDROME ( 117 FDA reports)
RENAL CYST ( 117 FDA reports)
SWELLING FACE ( 117 FDA reports)
HAEMATOCRIT DECREASED ( 116 FDA reports)
RHINORRHOEA ( 116 FDA reports)
EYE PAIN ( 115 FDA reports)
TINNITUS ( 115 FDA reports)
SLEEP DISORDER ( 114 FDA reports)
SEPTIC SHOCK ( 114 FDA reports)
EXOSTOSIS ( 113 FDA reports)
VISUAL ACUITY REDUCED ( 113 FDA reports)
CYSTITIS ( 112 FDA reports)
CARDIO-RESPIRATORY ARREST ( 111 FDA reports)
ADVERSE DRUG REACTION ( 110 FDA reports)
HEPATIC ENZYME INCREASED ( 110 FDA reports)
POLLAKIURIA ( 110 FDA reports)
SKIN ULCER ( 110 FDA reports)
SLEEP APNOEA SYNDROME ( 109 FDA reports)
DISEASE PROGRESSION ( 109 FDA reports)
FOOT FRACTURE ( 109 FDA reports)
HAEMATOMA ( 109 FDA reports)
HYPERGLYCAEMIA ( 109 FDA reports)
IRRITABILITY ( 108 FDA reports)
SPINAL COLUMN STENOSIS ( 108 FDA reports)
SUICIDAL IDEATION ( 108 FDA reports)
TENDONITIS ( 107 FDA reports)
TOOTH ABSCESS ( 107 FDA reports)
CARDIAC FAILURE ( 107 FDA reports)
HAEMATOCHEZIA ( 107 FDA reports)
NEOPLASM MALIGNANT ( 107 FDA reports)
DEVICE FAILURE ( 106 FDA reports)
DISTURBANCE IN ATTENTION ( 106 FDA reports)
FEAR ( 106 FDA reports)
FEBRILE NEUTROPENIA ( 106 FDA reports)
HYPERCHOLESTEROLAEMIA ( 106 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 106 FDA reports)
URINARY RETENTION ( 106 FDA reports)
SINUS DISORDER ( 105 FDA reports)
SPINAL COMPRESSION FRACTURE ( 105 FDA reports)
ANOREXIA ( 105 FDA reports)
BLOOD UREA INCREASED ( 104 FDA reports)
NASAL CONGESTION ( 104 FDA reports)
BLISTER ( 103 FDA reports)
BLOOD GLUCOSE DECREASED ( 103 FDA reports)
OFF LABEL USE ( 102 FDA reports)
VITAMIN D DEFICIENCY ( 102 FDA reports)
SPEECH DISORDER ( 101 FDA reports)
BRADYCARDIA ( 101 FDA reports)
CARDIOMYOPATHY ( 101 FDA reports)
MOUTH ULCERATION ( 101 FDA reports)
MUCOSAL INFLAMMATION ( 101 FDA reports)
CHOLECYSTITIS ( 100 FDA reports)
MENISCUS LESION ( 100 FDA reports)
RESPIRATORY DISTRESS ( 100 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 99 FDA reports)
VISUAL IMPAIRMENT ( 99 FDA reports)
SKIN EXFOLIATION ( 98 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 98 FDA reports)
BONE LESION ( 98 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 98 FDA reports)
HYPOXIA ( 97 FDA reports)
LIMB DISCOMFORT ( 97 FDA reports)
NEUTROPENIA ( 97 FDA reports)
ROAD TRAFFIC ACCIDENT ( 97 FDA reports)
AGITATION ( 96 FDA reports)
BREAST CANCER ( 96 FDA reports)
DRUG DOSE OMISSION ( 96 FDA reports)
HEAD INJURY ( 95 FDA reports)
LIVER DISORDER ( 95 FDA reports)
MASS ( 95 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 94 FDA reports)
TOOTH EXTRACTION ( 94 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 94 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 94 FDA reports)
STOMATITIS ( 93 FDA reports)
FRACTURE NONUNION ( 93 FDA reports)
RENAL IMPAIRMENT ( 93 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 92 FDA reports)
COLITIS ( 92 FDA reports)
SINUS BRADYCARDIA ( 92 FDA reports)
ERECTILE DYSFUNCTION ( 91 FDA reports)
HEART RATE IRREGULAR ( 91 FDA reports)
MULTI-ORGAN FAILURE ( 91 FDA reports)
MULTIPLE MYELOMA ( 91 FDA reports)
DISORIENTATION ( 89 FDA reports)
HEPATIC STEATOSIS ( 89 FDA reports)
JOINT INJURY ( 89 FDA reports)
SPONDYLOLISTHESIS ( 89 FDA reports)
WHEEZING ( 89 FDA reports)
INFLUENZA ( 88 FDA reports)
LUNG NEOPLASM ( 88 FDA reports)
PANIC ATTACK ( 87 FDA reports)
PERICARDIAL EFFUSION ( 87 FDA reports)
PRODUCT QUALITY ISSUE ( 87 FDA reports)
DRUG EFFECT DECREASED ( 86 FDA reports)
ECONOMIC PROBLEM ( 86 FDA reports)
LUNG INFILTRATION ( 86 FDA reports)
MUSCLE STRAIN ( 86 FDA reports)
SINUS TACHYCARDIA ( 86 FDA reports)
WRIST FRACTURE ( 86 FDA reports)
DEFORMITY ( 85 FDA reports)
FOOT DEFORMITY ( 85 FDA reports)
BASAL CELL CARCINOMA ( 84 FDA reports)
DIPLOPIA ( 84 FDA reports)
GASTRIC ULCER ( 84 FDA reports)
LUMBAR SPINAL STENOSIS ( 84 FDA reports)
RASH PRURITIC ( 84 FDA reports)
CANDIDIASIS ( 83 FDA reports)
COGNITIVE DISORDER ( 83 FDA reports)
LIMB INJURY ( 83 FDA reports)
LUNG DISORDER ( 83 FDA reports)
MOBILITY DECREASED ( 83 FDA reports)
POST PROCEDURAL COMPLICATION ( 83 FDA reports)
RASH ERYTHEMATOUS ( 83 FDA reports)
RHINITIS ALLERGIC ( 83 FDA reports)
SCAR ( 83 FDA reports)
HYPERKALAEMIA ( 82 FDA reports)
BLOOD SODIUM DECREASED ( 81 FDA reports)
CHOLECYSTECTOMY ( 80 FDA reports)
DRY EYE ( 80 FDA reports)
MYOCARDIAL ISCHAEMIA ( 80 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 79 FDA reports)
BILIARY DYSKINESIA ( 79 FDA reports)
FIBROMYALGIA ( 79 FDA reports)
HYPOGLYCAEMIA ( 79 FDA reports)
METASTASES TO BONE ( 79 FDA reports)
TOOTHACHE ( 79 FDA reports)
DRUG ADMINISTRATION ERROR ( 78 FDA reports)
PRODUCTIVE COUGH ( 78 FDA reports)
INJECTION SITE HAEMATOMA ( 77 FDA reports)
ORAL PAIN ( 77 FDA reports)
SKIN DISORDER ( 77 FDA reports)
TOOTH FRACTURE ( 77 FDA reports)
EMPHYSEMA ( 76 FDA reports)
HAEMOPTYSIS ( 76 FDA reports)
HYPOPHAGIA ( 76 FDA reports)
OXYGEN SATURATION DECREASED ( 76 FDA reports)
DYSKINESIA ( 75 FDA reports)
HEART RATE DECREASED ( 75 FDA reports)
RENAL DISORDER ( 75 FDA reports)
SKIN DISCOLOURATION ( 75 FDA reports)
TREATMENT NONCOMPLIANCE ( 75 FDA reports)
VIRAL INFECTION ( 75 FDA reports)
UNEVALUABLE EVENT ( 74 FDA reports)
DYSARTHRIA ( 74 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 74 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 74 FDA reports)
MALNUTRITION ( 74 FDA reports)
RASH GENERALISED ( 74 FDA reports)
JOINT STIFFNESS ( 73 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 72 FDA reports)
DIVERTICULITIS ( 72 FDA reports)
THROAT IRRITATION ( 72 FDA reports)
SKIN LESION ( 71 FDA reports)
INJECTION SITE HAEMORRHAGE ( 71 FDA reports)
OBESITY ( 71 FDA reports)
ORAL DISORDER ( 71 FDA reports)
PATHOLOGICAL FRACTURE ( 71 FDA reports)
PRESYNCOPE ( 71 FDA reports)
MELAENA ( 70 FDA reports)
ANKLE FRACTURE ( 69 FDA reports)
CORONARY ARTERY OCCLUSION ( 69 FDA reports)
LACERATION ( 69 FDA reports)
PNEUMOTHORAX ( 69 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 69 FDA reports)
SPINAL DISORDER ( 68 FDA reports)
SPINAL FRACTURE ( 68 FDA reports)
SYNOVIAL CYST ( 68 FDA reports)
BLOOD BILIRUBIN INCREASED ( 68 FDA reports)
CARDIAC MURMUR ( 68 FDA reports)
PNEUMONIA ASPIRATION ( 68 FDA reports)
PNEUMONITIS ( 68 FDA reports)
CEREBRAL HAEMORRHAGE ( 67 FDA reports)
DECUBITUS ULCER ( 67 FDA reports)
DYSLIPIDAEMIA ( 67 FDA reports)
OESOPHAGITIS ( 67 FDA reports)
ABDOMINAL PAIN LOWER ( 66 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 66 FDA reports)
GROIN PAIN ( 66 FDA reports)
JOINT EFFUSION ( 66 FDA reports)
LACUNAR INFARCTION ( 66 FDA reports)
MEDICATION ERROR ( 66 FDA reports)
ORAL CANDIDIASIS ( 66 FDA reports)
PSORIASIS ( 66 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 66 FDA reports)
RHABDOMYOLYSIS ( 66 FDA reports)
SURGERY ( 66 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 66 FDA reports)
TOOTH INFECTION ( 66 FDA reports)
SKIN BURNING SENSATION ( 65 FDA reports)
TOOTH LOSS ( 65 FDA reports)
BLINDNESS ( 65 FDA reports)
DRUG INTOLERANCE ( 65 FDA reports)
FAECES DISCOLOURED ( 65 FDA reports)
GASTRIC DISORDER ( 65 FDA reports)
GOUT ( 65 FDA reports)
HYPERCALCAEMIA ( 65 FDA reports)
JOINT DISLOCATION ( 65 FDA reports)
KNEE ARTHROPLASTY ( 65 FDA reports)
ORTHOSTATIC HYPOTENSION ( 65 FDA reports)
PALLOR ( 65 FDA reports)
ABNORMAL DREAMS ( 64 FDA reports)
BACK DISORDER ( 64 FDA reports)
COAGULOPATHY ( 64 FDA reports)
CYST ( 64 FDA reports)
LOOSE TOOTH ( 64 FDA reports)
NOCTURIA ( 64 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 63 FDA reports)
FEELING COLD ( 63 FDA reports)
INJECTION SITE PRURITUS ( 63 FDA reports)
LEUKOPENIA ( 63 FDA reports)
PULMONARY FIBROSIS ( 63 FDA reports)
FUNGAL INFECTION ( 62 FDA reports)
NEURALGIA ( 62 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 61 FDA reports)
EYE DISORDER ( 61 FDA reports)
FAECAL INCONTINENCE ( 61 FDA reports)
HYPOACUSIS ( 61 FDA reports)
NIGHT SWEATS ( 61 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 61 FDA reports)
PROTHROMBIN TIME PROLONGED ( 61 FDA reports)
RESTLESS LEGS SYNDROME ( 61 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 60 FDA reports)
ASPIRATION ( 60 FDA reports)
CYSTOCELE ( 60 FDA reports)
FLUID OVERLOAD ( 60 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 60 FDA reports)
VENTRICULAR TACHYCARDIA ( 60 FDA reports)
UNRESPONSIVE TO STIMULI ( 59 FDA reports)
HEPATIC FAILURE ( 59 FDA reports)
ILL-DEFINED DISORDER ( 59 FDA reports)
LUNG INFECTION ( 59 FDA reports)
ASCITES ( 58 FDA reports)
CAROTID ARTERY STENOSIS ( 58 FDA reports)
COMA ( 58 FDA reports)
DEAFNESS ( 58 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 58 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 58 FDA reports)
FIBULA FRACTURE ( 58 FDA reports)
IRON DEFICIENCY ANAEMIA ( 58 FDA reports)
OSTEOLYSIS ( 58 FDA reports)
TYPE 2 DIABETES MELLITUS ( 58 FDA reports)
ACUTE RESPIRATORY FAILURE ( 57 FDA reports)
ANAEMIA POSTOPERATIVE ( 57 FDA reports)
FLANK PAIN ( 57 FDA reports)
FLUID RETENTION ( 57 FDA reports)
GINGIVAL PAIN ( 57 FDA reports)
HYPERKERATOSIS ( 57 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 57 FDA reports)
PELVIC FRACTURE ( 57 FDA reports)
POOR QUALITY SLEEP ( 57 FDA reports)
PRURITUS GENERALISED ( 57 FDA reports)
BLOOD CALCIUM DECREASED ( 56 FDA reports)
EXCORIATION ( 56 FDA reports)
GINGIVAL DISORDER ( 56 FDA reports)
HAEMORRHAGIC ANAEMIA ( 56 FDA reports)
HYPERSOMNIA ( 56 FDA reports)
HYPOVOLAEMIA ( 56 FDA reports)
MACULAR DEGENERATION ( 56 FDA reports)
MOVEMENT DISORDER ( 56 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 56 FDA reports)
SWOLLEN TONGUE ( 56 FDA reports)
TIBIA FRACTURE ( 56 FDA reports)
DISCOMFORT ( 55 FDA reports)
HYPOAESTHESIA ORAL ( 55 FDA reports)
INTERSTITIAL LUNG DISEASE ( 55 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 55 FDA reports)
MULTIPLE SCLEROSIS ( 55 FDA reports)
ABSCESS ( 54 FDA reports)
ANGINA UNSTABLE ( 54 FDA reports)
AORTIC VALVE INCOMPETENCE ( 54 FDA reports)
GASTRITIS EROSIVE ( 54 FDA reports)
ORAL INFECTION ( 54 FDA reports)
PARKINSON'S DISEASE ( 54 FDA reports)
RESTLESSNESS ( 54 FDA reports)
VENTRICULAR HYPOKINESIA ( 54 FDA reports)
THROAT TIGHTNESS ( 53 FDA reports)
UPPER LIMB FRACTURE ( 53 FDA reports)
AGEUSIA ( 53 FDA reports)
CARDIOVASCULAR DISORDER ( 53 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 53 FDA reports)
METASTASES TO LIVER ( 53 FDA reports)
NODULE ( 53 FDA reports)
PROCEDURAL PAIN ( 53 FDA reports)
RECTAL POLYP ( 53 FDA reports)
BACTERIAL INFECTION ( 52 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 52 FDA reports)
GASTROENTERITIS ( 52 FDA reports)
HEPATIC CYST ( 52 FDA reports)
INTESTINAL OBSTRUCTION ( 52 FDA reports)
METASTASES TO LUNG ( 52 FDA reports)
VENTRICULAR FIBRILLATION ( 52 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 51 FDA reports)
ACTINIC KERATOSIS ( 51 FDA reports)
ANAPHYLACTIC REACTION ( 51 FDA reports)
ATRIAL FLUTTER ( 51 FDA reports)
CHOLECYSTITIS ACUTE ( 51 FDA reports)
CROHN'S DISEASE ( 51 FDA reports)
ECCHYMOSIS ( 51 FDA reports)
EJECTION FRACTION DECREASED ( 51 FDA reports)
GENERALISED OEDEMA ( 51 FDA reports)
HEPATOMEGALY ( 51 FDA reports)
LARYNGITIS ( 51 FDA reports)
SCIATICA ( 51 FDA reports)
ABNORMAL BEHAVIOUR ( 50 FDA reports)
DELIRIUM ( 50 FDA reports)
DEVICE MALFUNCTION ( 50 FDA reports)
DYSSTASIA ( 50 FDA reports)
EATING DISORDER ( 50 FDA reports)
EYE HAEMORRHAGE ( 50 FDA reports)
GINGIVAL RECESSION ( 50 FDA reports)
GRAND MAL CONVULSION ( 50 FDA reports)
HYPOMAGNESAEMIA ( 50 FDA reports)
INTENTIONAL DRUG MISUSE ( 50 FDA reports)
JAUNDICE ( 50 FDA reports)
LUMBAR RADICULOPATHY ( 50 FDA reports)
MAJOR DEPRESSION ( 50 FDA reports)
THYROID DISORDER ( 50 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 50 FDA reports)
STEVENS-JOHNSON SYNDROME ( 49 FDA reports)
WOUND ( 49 FDA reports)
ANGER ( 49 FDA reports)
BODY HEIGHT DECREASED ( 49 FDA reports)
DEMENTIA ( 49 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 49 FDA reports)
OSTEITIS ( 49 FDA reports)
PREGNANCY ( 49 FDA reports)
ABORTION SPONTANEOUS ( 48 FDA reports)
AGGRESSION ( 48 FDA reports)
APHASIA ( 48 FDA reports)
CEREBRAL ATROPHY ( 48 FDA reports)
COLD SWEAT ( 48 FDA reports)
EMOTIONAL DISORDER ( 48 FDA reports)
HEPATITIS ( 48 FDA reports)
HERNIA ( 48 FDA reports)
JAW DISORDER ( 48 FDA reports)
METABOLIC ACIDOSIS ( 48 FDA reports)
MIDDLE INSOMNIA ( 48 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 48 FDA reports)
PULMONARY CONGESTION ( 48 FDA reports)
TENDERNESS ( 48 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 48 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 47 FDA reports)
COMPRESSION FRACTURE ( 47 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 47 FDA reports)
ENCEPHALOPATHY ( 47 FDA reports)
EYE INFECTION ( 47 FDA reports)
EYE IRRITATION ( 47 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 47 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 47 FDA reports)
INFUSION RELATED REACTION ( 47 FDA reports)
OCULAR HYPERAEMIA ( 47 FDA reports)
PRIMARY SEQUESTRUM ( 47 FDA reports)
RETCHING ( 47 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 46 FDA reports)
CHROMATURIA ( 46 FDA reports)
DERMATITIS ( 46 FDA reports)
HYPERTHYROIDISM ( 46 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 46 FDA reports)
LACRIMATION INCREASED ( 46 FDA reports)
LOCALISED INFECTION ( 46 FDA reports)
PERIPHERAL COLDNESS ( 46 FDA reports)
PERITONITIS ( 46 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 46 FDA reports)
PURULENT DISCHARGE ( 46 FDA reports)
STOMACH DISCOMFORT ( 46 FDA reports)
VAGINAL HAEMORRHAGE ( 45 FDA reports)
ACIDOSIS ( 45 FDA reports)
BLADDER DISORDER ( 45 FDA reports)
BODY TEMPERATURE INCREASED ( 45 FDA reports)
CEREBRAL INFARCTION ( 45 FDA reports)
CEREBRAL ISCHAEMIA ( 45 FDA reports)
ELECTROLYTE IMBALANCE ( 45 FDA reports)
HEMIPARESIS ( 45 FDA reports)
MUSCLE TWITCHING ( 45 FDA reports)
NERVE INJURY ( 45 FDA reports)
NIGHTMARE ( 45 FDA reports)
RADICULOPATHY ( 45 FDA reports)
BILIARY COLIC ( 44 FDA reports)
BLOOD URINE PRESENT ( 44 FDA reports)
DEPRESSED MOOD ( 44 FDA reports)
HAEMATEMESIS ( 44 FDA reports)
HIP ARTHROPLASTY ( 44 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 44 FDA reports)
RENAL TUBULAR NECROSIS ( 44 FDA reports)
WOUND INFECTION ( 44 FDA reports)
ANGIOPATHY ( 43 FDA reports)
AORTIC ANEURYSM ( 43 FDA reports)
BLOOD ALBUMIN DECREASED ( 43 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 43 FDA reports)
DIFFICULTY IN WALKING ( 43 FDA reports)
GINGIVAL SWELLING ( 43 FDA reports)
GINGIVITIS ( 43 FDA reports)
JAW FRACTURE ( 43 FDA reports)
MYOPATHY ( 43 FDA reports)
ORAL HERPES ( 43 FDA reports)
OSTEOSCLEROSIS ( 43 FDA reports)
PROTEINURIA ( 43 FDA reports)
RASH MACULAR ( 43 FDA reports)
DISABILITY ( 42 FDA reports)
ENDODONTIC PROCEDURE ( 42 FDA reports)
EYE SWELLING ( 42 FDA reports)
ILEUS ( 42 FDA reports)
INJECTION SITE SWELLING ( 42 FDA reports)
KYPHOSIS ( 42 FDA reports)
LIP SWELLING ( 42 FDA reports)
LOWER LIMB FRACTURE ( 42 FDA reports)
NO ADVERSE EVENT ( 42 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 42 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 42 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 41 FDA reports)
TONGUE ULCERATION ( 41 FDA reports)
ERUCTATION ( 41 FDA reports)
GLAUCOMA ( 41 FDA reports)
HAND FRACTURE ( 41 FDA reports)
HYPERTONIC BLADDER ( 41 FDA reports)
INCONTINENCE ( 41 FDA reports)
INCREASED TENDENCY TO BRUISE ( 41 FDA reports)
INJECTION SITE REACTION ( 41 FDA reports)
KIDNEY INFECTION ( 41 FDA reports)
MENTAL IMPAIRMENT ( 41 FDA reports)
PEPTIC ULCER ( 41 FDA reports)
PHARYNGEAL OEDEMA ( 41 FDA reports)
RESPIRATORY DISORDER ( 41 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 40 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 40 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 40 FDA reports)
EROSIVE OESOPHAGITIS ( 40 FDA reports)
MOUTH HAEMORRHAGE ( 40 FDA reports)
MULTIPLE INJURIES ( 40 FDA reports)
NEOPLASM PROGRESSION ( 40 FDA reports)
PHOTOSENSITIVITY REACTION ( 40 FDA reports)
POLYP ( 40 FDA reports)
PULMONARY INFARCTION ( 40 FDA reports)
RECTOCELE ( 40 FDA reports)
THIRST ( 40 FDA reports)
VENTRICULAR HYPERTROPHY ( 40 FDA reports)
VISUAL FIELD DEFECT ( 40 FDA reports)
WOUND DEHISCENCE ( 40 FDA reports)
SKIN CANCER ( 39 FDA reports)
STRESS URINARY INCONTINENCE ( 39 FDA reports)
TENDON DISORDER ( 39 FDA reports)
BREAST PAIN ( 39 FDA reports)
EAR PAIN ( 39 FDA reports)
ECZEMA ( 39 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 39 FDA reports)
GOITRE ( 39 FDA reports)
HYPOALBUMINAEMIA ( 39 FDA reports)
LEFT ATRIAL DILATATION ( 39 FDA reports)
MICTURITION URGENCY ( 39 FDA reports)
MUSCLE TIGHTNESS ( 39 FDA reports)
NEUTROPHIL COUNT DECREASED ( 39 FDA reports)
ONYCHOMYCOSIS ( 39 FDA reports)
PHYSICAL DISABILITY ( 39 FDA reports)
PYELONEPHRITIS ( 39 FDA reports)
RESPIRATORY ARREST ( 39 FDA reports)
SENSORY DISTURBANCE ( 39 FDA reports)
SINUS CONGESTION ( 39 FDA reports)
CHONDROMALACIA ( 38 FDA reports)
CYSTITIS INTERSTITIAL ( 38 FDA reports)
DIVERTICULUM INTESTINAL ( 38 FDA reports)
FACIAL PAIN ( 38 FDA reports)
FRACTURE ( 38 FDA reports)
HAEMOLYTIC ANAEMIA ( 38 FDA reports)
LUNG NEOPLASM MALIGNANT ( 38 FDA reports)
PANCREATITIS ACUTE ( 38 FDA reports)
PATHOLOGICAL GAMBLING ( 38 FDA reports)
SOFT TISSUE DISORDER ( 38 FDA reports)
TRANSAMINASES INCREASED ( 38 FDA reports)
VENOUS INSUFFICIENCY ( 38 FDA reports)
SQUAMOUS CELL CARCINOMA ( 37 FDA reports)
SUBCUTANEOUS ABSCESS ( 37 FDA reports)
BONE LOSS ( 37 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 37 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 37 FDA reports)
FISTULA ( 37 FDA reports)
GINGIVAL BLEEDING ( 37 FDA reports)
HERPES SIMPLEX ( 37 FDA reports)
ISCHAEMIA ( 37 FDA reports)
LOBAR PNEUMONIA ( 37 FDA reports)
MOOD SWINGS ( 37 FDA reports)
MYELODYSPLASTIC SYNDROME ( 37 FDA reports)
ACCIDENTAL OVERDOSE ( 36 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 36 FDA reports)
ANGIOEDEMA ( 36 FDA reports)
BUNION ( 36 FDA reports)
DERMATITIS CONTACT ( 36 FDA reports)
HYDRONEPHROSIS ( 36 FDA reports)
INJECTION SITE IRRITATION ( 36 FDA reports)
LYMPHOEDEMA ( 36 FDA reports)
MACULAR OEDEMA ( 36 FDA reports)
ORTHOPNOEA ( 36 FDA reports)
PARANOIA ( 36 FDA reports)
PSYCHOTIC DISORDER ( 36 FDA reports)
THINKING ABNORMAL ( 36 FDA reports)
SNEEZING ( 35 FDA reports)
TEMPORAL ARTERITIS ( 35 FDA reports)
BACK INJURY ( 35 FDA reports)
BLOOD POTASSIUM INCREASED ( 35 FDA reports)
BONE MARROW FAILURE ( 35 FDA reports)
BRAIN OEDEMA ( 35 FDA reports)
CALCULUS URETERIC ( 35 FDA reports)
CARDIOGENIC SHOCK ( 35 FDA reports)
CONJUNCTIVITIS ( 35 FDA reports)
EXPOSED BONE IN JAW ( 35 FDA reports)
GINGIVAL INFECTION ( 35 FDA reports)
GRANULOMA ( 35 FDA reports)
LIPASE INCREASED ( 35 FDA reports)
MUSCLE ATROPHY ( 35 FDA reports)
PERIODONTAL DISEASE ( 35 FDA reports)
PLEURISY ( 35 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 35 FDA reports)
RASH MACULO-PAPULAR ( 35 FDA reports)
BREAST DISORDER ( 34 FDA reports)
CALCIUM DEFICIENCY ( 34 FDA reports)
DECREASED INTEREST ( 34 FDA reports)
DIALYSIS ( 34 FDA reports)
FRACTURE DELAYED UNION ( 34 FDA reports)
GALLBLADDER INJURY ( 34 FDA reports)
HOSPITALISATION ( 34 FDA reports)
INJECTION SITE BRUISING ( 34 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 34 FDA reports)
METASTASES TO LYMPH NODES ( 34 FDA reports)
NO THERAPEUTIC RESPONSE ( 34 FDA reports)
OVARIAN CYST ( 34 FDA reports)
PELVIC PAIN ( 34 FDA reports)
PERIODONTITIS ( 34 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 34 FDA reports)
VISUAL DISTURBANCE ( 34 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 33 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 33 FDA reports)
AORTIC VALVE SCLEROSIS ( 33 FDA reports)
BLOOD CALCIUM INCREASED ( 33 FDA reports)
CHOKING ( 33 FDA reports)
HAEMODIALYSIS ( 33 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 33 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 33 FDA reports)
PARAESTHESIA ORAL ( 33 FDA reports)
PERONEAL NERVE PALSY ( 33 FDA reports)
SENSORY LOSS ( 33 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 32 FDA reports)
CLOSTRIDIAL INFECTION ( 32 FDA reports)
COORDINATION ABNORMAL ( 32 FDA reports)
FEELING JITTERY ( 32 FDA reports)
LIGAMENT SPRAIN ( 32 FDA reports)
METASTASES TO SPINE ( 32 FDA reports)
MITRAL VALVE PROLAPSE ( 32 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 32 FDA reports)
OEDEMA MOUTH ( 32 FDA reports)
SENSATION OF HEAVINESS ( 32 FDA reports)
SPLENOMEGALY ( 32 FDA reports)
SYNOVITIS ( 32 FDA reports)
TRIGGER FINGER ( 32 FDA reports)
VITAMIN D DECREASED ( 32 FDA reports)
WALKING AID USER ( 32 FDA reports)
ULCER ( 31 FDA reports)
ANXIETY DISORDER ( 31 FDA reports)
AORTIC STENOSIS ( 31 FDA reports)
CHRONIC SINUSITIS ( 31 FDA reports)
DRUG TOXICITY ( 31 FDA reports)
EXTRASYSTOLES ( 31 FDA reports)
GLOSSODYNIA ( 31 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 31 FDA reports)
HYPOKINESIA ( 31 FDA reports)
LIGAMENT RUPTURE ( 31 FDA reports)
NASAL SEPTUM DEVIATION ( 31 FDA reports)
ORAL INTAKE REDUCED ( 31 FDA reports)
SHOCK ( 31 FDA reports)
ACUTE SINUSITIS ( 30 FDA reports)
BLEPHARITIS ( 30 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 30 FDA reports)
BRONCHIECTASIS ( 30 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 30 FDA reports)
CERVICAL SPINAL STENOSIS ( 30 FDA reports)
COLLAPSE OF LUNG ( 30 FDA reports)
EXPIRED DRUG ADMINISTERED ( 30 FDA reports)
FACIAL BONES FRACTURE ( 30 FDA reports)
FAMILY STRESS ( 30 FDA reports)
HALLUCINATION, VISUAL ( 30 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
NEURITIS ( 30 FDA reports)
NON-CARDIAC CHEST PAIN ( 30 FDA reports)
PLEURAL FIBROSIS ( 30 FDA reports)
PROSTATE CANCER ( 30 FDA reports)
SINUS HEADACHE ( 30 FDA reports)
ULCER HAEMORRHAGE ( 30 FDA reports)
URINE OUTPUT DECREASED ( 30 FDA reports)
VARICOSE VEIN ( 30 FDA reports)
VASCULITIS ( 30 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 30 FDA reports)
SKIN LACERATION ( 29 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 29 FDA reports)
VIITH NERVE PARALYSIS ( 29 FDA reports)
AORTIC CALCIFICATION ( 29 FDA reports)
BEDRIDDEN ( 29 FDA reports)
BILE DUCT STONE ( 29 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 29 FDA reports)
BONE DEBRIDEMENT ( 29 FDA reports)
BREAST MASS ( 29 FDA reports)
BREATH SOUNDS ABNORMAL ( 29 FDA reports)
CORONARY ARTERY STENOSIS ( 29 FDA reports)
CRYING ( 29 FDA reports)
DIASTOLIC DYSFUNCTION ( 29 FDA reports)
FEMORAL NECK FRACTURE ( 29 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 29 FDA reports)
LIMB DEFORMITY ( 29 FDA reports)
MUSCULOSKELETAL DISORDER ( 29 FDA reports)
OCCULT BLOOD POSITIVE ( 29 FDA reports)
PERICARDITIS ( 29 FDA reports)
PLANTAR FASCIITIS ( 29 FDA reports)
PLATELET COUNT INCREASED ( 29 FDA reports)
RASH PAPULAR ( 29 FDA reports)
SEASONAL ALLERGY ( 29 FDA reports)
SEBORRHOEIC KERATOSIS ( 29 FDA reports)
SICK SINUS SYNDROME ( 29 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 28 FDA reports)
APHAGIA ( 28 FDA reports)
BLOOD CHLORIDE DECREASED ( 28 FDA reports)
COLON CANCER ( 28 FDA reports)
DILATATION VENTRICULAR ( 28 FDA reports)
GASTROENTERITIS VIRAL ( 28 FDA reports)
GENITAL HERPES ( 28 FDA reports)
HYPOAESTHESIA FACIAL ( 28 FDA reports)
INCREASED APPETITE ( 28 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 28 FDA reports)
JOINT SPRAIN ( 28 FDA reports)
NERVOUS SYSTEM DISORDER ( 28 FDA reports)
PROCEDURAL COMPLICATION ( 28 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 28 FDA reports)
RIGHT VENTRICULAR FAILURE ( 28 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 28 FDA reports)
TENDON RUPTURE ( 28 FDA reports)
TONGUE DISCOLOURATION ( 28 FDA reports)
UROSEPSIS ( 28 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 27 FDA reports)
TENOSYNOVITIS ( 27 FDA reports)
THYROID NEOPLASM ( 27 FDA reports)
ADRENAL INSUFFICIENCY ( 27 FDA reports)
ATAXIA ( 27 FDA reports)
ATRIOVENTRICULAR BLOCK ( 27 FDA reports)
BREATH ODOUR ( 27 FDA reports)
CARDIAC FLUTTER ( 27 FDA reports)
CERUMEN IMPACTION ( 27 FDA reports)
DEBRIDEMENT ( 27 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 27 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 27 FDA reports)
HYPERAESTHESIA ( 27 FDA reports)
HYPOMANIA ( 27 FDA reports)
METASTATIC NEOPLASM ( 27 FDA reports)
PARALYSIS ( 27 FDA reports)
PETECHIAE ( 27 FDA reports)
RESPIRATORY TRACT INFECTION ( 27 FDA reports)
ABNORMAL SENSATION IN EYE ( 26 FDA reports)
ACNE ( 26 FDA reports)
APATHY ( 26 FDA reports)
ATRIAL TACHYCARDIA ( 26 FDA reports)
BARRETT'S OESOPHAGUS ( 26 FDA reports)
BLADDER CANCER ( 26 FDA reports)
BLOOD DISORDER ( 26 FDA reports)
BREAST CANCER METASTATIC ( 26 FDA reports)
BREAST CANCER RECURRENT ( 26 FDA reports)
DILATATION ATRIAL ( 26 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 26 FDA reports)
FIBROSIS ( 26 FDA reports)
GLOSSITIS ( 26 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 26 FDA reports)
HEPATIC LESION ( 26 FDA reports)
HYPOCALCAEMIA ( 26 FDA reports)
LACTIC ACIDOSIS ( 26 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 26 FDA reports)
MASTICATION DISORDER ( 26 FDA reports)
REFLUX OESOPHAGITIS ( 26 FDA reports)
RENAL PAIN ( 26 FDA reports)
RESPIRATORY TRACT CONGESTION ( 26 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 26 FDA reports)
TRISMUS ( 26 FDA reports)
SKIN WARM ( 25 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 25 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
UTERINE LEIOMYOMA ( 25 FDA reports)
VITREOUS FLOATERS ( 25 FDA reports)
BLADDER PROLAPSE ( 25 FDA reports)
CATARACT OPERATION ( 25 FDA reports)
COLITIS ISCHAEMIC ( 25 FDA reports)
DIABETIC RETINOPATHY ( 25 FDA reports)
ESCHERICHIA INFECTION ( 25 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 25 FDA reports)
HEPATIC CIRRHOSIS ( 25 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 25 FDA reports)
LYMPHOMA ( 25 FDA reports)
MEDICATION RESIDUE ( 25 FDA reports)
NERVE COMPRESSION ( 25 FDA reports)
PHARYNGITIS ( 25 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 25 FDA reports)
PRE-ECLAMPSIA ( 25 FDA reports)
RHINITIS ( 25 FDA reports)
ROSACEA ( 25 FDA reports)
ABDOMINAL TENDERNESS ( 24 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 24 FDA reports)
ANOSMIA ( 24 FDA reports)
APNOEA ( 24 FDA reports)
APPLICATION SITE ERYTHEMA ( 24 FDA reports)
ARTHROPOD BITE ( 24 FDA reports)
BLINDNESS UNILATERAL ( 24 FDA reports)
BONE SWELLING ( 24 FDA reports)
CEREBROVASCULAR DISORDER ( 24 FDA reports)
DIZZINESS POSTURAL ( 24 FDA reports)
DRUG DEPENDENCE ( 24 FDA reports)
GASTRIC POLYPS ( 24 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 24 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 24 FDA reports)
LUNG HYPERINFLATION ( 24 FDA reports)
MANIA ( 24 FDA reports)
METABOLIC ENCEPHALOPATHY ( 24 FDA reports)
MOOD ALTERED ( 24 FDA reports)
ODYNOPHAGIA ( 24 FDA reports)
OSTEORADIONECROSIS ( 24 FDA reports)
PHOTOPHOBIA ( 24 FDA reports)
SKIN INFECTION ( 24 FDA reports)
TONGUE DISORDER ( 24 FDA reports)
STEM CELL TRANSPLANT ( 23 FDA reports)
SUBDURAL HAEMATOMA ( 23 FDA reports)
ANAPHYLACTIC SHOCK ( 23 FDA reports)
APHONIA ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 23 FDA reports)
AZOTAEMIA ( 23 FDA reports)
BREAST TENDERNESS ( 23 FDA reports)
CARDIAC VALVE DISEASE ( 23 FDA reports)
CAROTID BRUIT ( 23 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 23 FDA reports)
DISEASE RECURRENCE ( 23 FDA reports)
DRUG ERUPTION ( 23 FDA reports)
EARLY SATIETY ( 23 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 23 FDA reports)
EPIGASTRIC DISCOMFORT ( 23 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 23 FDA reports)
GASTROINTESTINAL PAIN ( 23 FDA reports)
HEPATIC NECROSIS ( 23 FDA reports)
HERPES VIRUS INFECTION ( 23 FDA reports)
HUMERUS FRACTURE ( 23 FDA reports)
JOINT CONTRACTURE ( 23 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 23 FDA reports)
MEDICAL DEVICE COMPLICATION ( 23 FDA reports)
MELANOCYTIC NAEVUS ( 23 FDA reports)
METRORRHAGIA ( 23 FDA reports)
MYOSITIS ( 23 FDA reports)
NEUROGENIC BLADDER ( 23 FDA reports)
OPEN WOUND ( 23 FDA reports)
RETINAL HAEMORRHAGE ( 23 FDA reports)
RETINAL TEAR ( 23 FDA reports)
ACCIDENTAL EXPOSURE ( 22 FDA reports)
BLOOD IRON DECREASED ( 22 FDA reports)
BLOOD PRESSURE ABNORMAL ( 22 FDA reports)
BONE ABSCESS ( 22 FDA reports)
BONE DENSITY INCREASED ( 22 FDA reports)
BONE MARROW OEDEMA ( 22 FDA reports)
BREAST CANCER FEMALE ( 22 FDA reports)
DUODENITIS ( 22 FDA reports)
EPILEPSY ( 22 FDA reports)
ESSENTIAL HYPERTENSION ( 22 FDA reports)
FACE OEDEMA ( 22 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 22 FDA reports)
GYNAECOMASTIA ( 22 FDA reports)
HAIR GROWTH ABNORMAL ( 22 FDA reports)
IMPAIRED DRIVING ABILITY ( 22 FDA reports)
JOINT CREPITATION ( 22 FDA reports)
MACROCYTOSIS ( 22 FDA reports)
MUSCLE DISORDER ( 22 FDA reports)
NEOPLASM ( 22 FDA reports)
OESOPHAGEAL ULCER ( 22 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 22 FDA reports)
PLASMACYTOMA ( 22 FDA reports)
SKIN HYPERTROPHY ( 22 FDA reports)
SUICIDE ATTEMPT ( 22 FDA reports)
TENDON INJURY ( 22 FDA reports)
TROPONIN INCREASED ( 22 FDA reports)
VULVOVAGINAL DRYNESS ( 22 FDA reports)
SKIN FISSURES ( 21 FDA reports)
URINARY HESITATION ( 21 FDA reports)
VEIN DISORDER ( 21 FDA reports)
ATRIAL SEPTAL DEFECT ( 21 FDA reports)
BIPOLAR DISORDER ( 21 FDA reports)
BRONCHOSPASM ( 21 FDA reports)
CARDIAC TAMPONADE ( 21 FDA reports)
CATHETER RELATED COMPLICATION ( 21 FDA reports)
CERVICOBRACHIAL SYNDROME ( 21 FDA reports)
CLOSTRIDIUM COLITIS ( 21 FDA reports)
DIABETIC NEUROPATHY ( 21 FDA reports)
FAECALOMA ( 21 FDA reports)
FURUNCLE ( 21 FDA reports)
HAEMANGIOMA ( 21 FDA reports)
HEPATORENAL SYNDROME ( 21 FDA reports)
HEPATOTOXICITY ( 21 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 21 FDA reports)
INJECTION SITE BURNING ( 21 FDA reports)
INJECTION SITE URTICARIA ( 21 FDA reports)
INTESTINAL ISCHAEMIA ( 21 FDA reports)
ISCHAEMIC STROKE ( 21 FDA reports)
LOCAL SWELLING ( 21 FDA reports)
LUNG CONSOLIDATION ( 21 FDA reports)
MALIGNANT MELANOMA ( 21 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 21 FDA reports)
NECROSIS ( 21 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 21 FDA reports)
PLEURITIC PAIN ( 21 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 21 FDA reports)
PULMONARY GRANULOMA ( 21 FDA reports)
RALES ( 21 FDA reports)
SARCOIDOSIS ( 21 FDA reports)
AGRANULOCYTOSIS ( 20 FDA reports)
ANAL SPHINCTER ATONY ( 20 FDA reports)
AORTIC DISORDER ( 20 FDA reports)
AUTONOMIC NEUROPATHY ( 20 FDA reports)
BLOOD COUNT ABNORMAL ( 20 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 20 FDA reports)
BRUXISM ( 20 FDA reports)
CAECITIS ( 20 FDA reports)
CAROTID ARTERY DISEASE ( 20 FDA reports)
CHEST X-RAY ABNORMAL ( 20 FDA reports)
COLITIS ULCERATIVE ( 20 FDA reports)
CYANOSIS ( 20 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 20 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 20 FDA reports)
ERYTHEMA NODOSUM ( 20 FDA reports)
FAILURE TO THRIVE ( 20 FDA reports)
FISTULA DISCHARGE ( 20 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 20 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 20 FDA reports)
HUNGER ( 20 FDA reports)
HYPERPLASIA ( 20 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 20 FDA reports)
LIBIDO DECREASED ( 20 FDA reports)
LUNG CANCER METASTATIC ( 20 FDA reports)
MENOPAUSE ( 20 FDA reports)
MITRAL VALVE CALCIFICATION ( 20 FDA reports)
OESOPHAGEAL PAIN ( 20 FDA reports)
OSTEITIS DEFORMANS ( 20 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 20 FDA reports)
PHLEBITIS ( 20 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 20 FDA reports)
PROCTALGIA ( 20 FDA reports)
PROTEIN TOTAL DECREASED ( 20 FDA reports)
PULMONARY MASS ( 20 FDA reports)
RETINAL VEIN OCCLUSION ( 20 FDA reports)
SCAB ( 20 FDA reports)
SERUM FERRITIN INCREASED ( 20 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 20 FDA reports)
TARDIVE DYSKINESIA ( 20 FDA reports)
TONSILLAR DISORDER ( 20 FDA reports)
TRANSFUSION ( 20 FDA reports)
SKIN INDURATION ( 19 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 19 FDA reports)
URETHRAL STENOSIS ( 19 FDA reports)
VITREOUS DETACHMENT ( 19 FDA reports)
ALCOHOLISM ( 19 FDA reports)
BRONCHIOLITIS ( 19 FDA reports)
COLON ADENOMA ( 19 FDA reports)
DECREASED ACTIVITY ( 19 FDA reports)
DENTAL OPERATION ( 19 FDA reports)
EAR INFECTION ( 19 FDA reports)
HYPERPHAGIA ( 19 FDA reports)
HYPOTHERMIA ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 19 FDA reports)
INTERVERTEBRAL DISCITIS ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
NERVE ROOT COMPRESSION ( 19 FDA reports)
ORAL DISCOMFORT ( 19 FDA reports)
OTITIS MEDIA ( 19 FDA reports)
PANIC DISORDER ( 19 FDA reports)
PATELLA FRACTURE ( 19 FDA reports)
POLYDIPSIA ( 19 FDA reports)
PREMATURE LABOUR ( 19 FDA reports)
RAYNAUD'S PHENOMENON ( 19 FDA reports)
RESORPTION BONE INCREASED ( 19 FDA reports)
SCAPULA FRACTURE ( 19 FDA reports)
ABSCESS JAW ( 18 FDA reports)
ABSCESS ORAL ( 18 FDA reports)
ACETABULUM FRACTURE ( 18 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 18 FDA reports)
ANEURYSM ( 18 FDA reports)
APPLICATION SITE PRURITUS ( 18 FDA reports)
BONE FRAGMENTATION ( 18 FDA reports)
BREAST HYPERPLASIA ( 18 FDA reports)
BRONCHITIS CHRONIC ( 18 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 18 FDA reports)
DELUSION ( 18 FDA reports)
DEVICE DISLOCATION ( 18 FDA reports)
DEVICE RELATED INFECTION ( 18 FDA reports)
DIABETIC FOOT INFECTION ( 18 FDA reports)
EAR DISORDER ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 18 FDA reports)
EMBOLISM ( 18 FDA reports)
EMPYEMA ( 18 FDA reports)
ENTEROCOCCAL INFECTION ( 18 FDA reports)
EXTRASKELETAL OSSIFICATION ( 18 FDA reports)
EYE DISCHARGE ( 18 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 18 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 18 FDA reports)
INGUINAL HERNIA ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 18 FDA reports)
INTESTINAL HAEMORRHAGE ( 18 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 18 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
METABOLIC DISORDER ( 18 FDA reports)
MUSCLE INJURY ( 18 FDA reports)
NAIL DISORDER ( 18 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 18 FDA reports)
OSTEOMYELITIS CHRONIC ( 18 FDA reports)
OVARIAN CANCER ( 18 FDA reports)
PAIN OF SKIN ( 18 FDA reports)
PERIPHERAL ISCHAEMIA ( 18 FDA reports)
PROSTATOMEGALY ( 18 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 18 FDA reports)
PULSE ABSENT ( 18 FDA reports)
SACROILIITIS ( 18 FDA reports)
SEDATION ( 18 FDA reports)
SEQUESTRECTOMY ( 18 FDA reports)
SEXUAL DYSFUNCTION ( 18 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 18 FDA reports)
X-RAY ABNORMAL ( 18 FDA reports)
SKIN HYPERPIGMENTATION ( 17 FDA reports)
TOURETTE'S DISORDER ( 17 FDA reports)
URINARY TRACT DISORDER ( 17 FDA reports)
URINE OUTPUT INCREASED ( 17 FDA reports)
WEIGHT FLUCTUATION ( 17 FDA reports)
ACTINOMYCOSIS ( 17 FDA reports)
AFFECT LABILITY ( 17 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 17 FDA reports)
BASOSQUAMOUS CARCINOMA ( 17 FDA reports)
BLOOD IRON INCREASED ( 17 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 17 FDA reports)
BODY TEMPERATURE DECREASED ( 17 FDA reports)
BONE EROSION ( 17 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 17 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 17 FDA reports)
CHONDROPATHY ( 17 FDA reports)
CLAVICLE FRACTURE ( 17 FDA reports)
CONCUSSION ( 17 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 17 FDA reports)
DENTURE WEARER ( 17 FDA reports)
DERMATOPHYTOSIS ( 17 FDA reports)
DRUG DISPENSING ERROR ( 17 FDA reports)
DYSAESTHESIA ( 17 FDA reports)
DYSPHEMIA ( 17 FDA reports)
EAR DISCOMFORT ( 17 FDA reports)
FACET JOINT SYNDROME ( 17 FDA reports)
GENERALISED ERYTHEMA ( 17 FDA reports)
HEPATITIS C ( 17 FDA reports)
HYPERPARATHYROIDISM ( 17 FDA reports)
INCISIONAL HERNIA ( 17 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 17 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 17 FDA reports)
INITIAL INSOMNIA ( 17 FDA reports)
INJECTION SITE WARMTH ( 17 FDA reports)
INTESTINAL PERFORATION ( 17 FDA reports)
LABYRINTHITIS ( 17 FDA reports)
LACTOSE INTOLERANCE ( 17 FDA reports)
LEG AMPUTATION ( 17 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 17 FDA reports)
LIVER INJURY ( 17 FDA reports)
MENINGIOMA ( 17 FDA reports)
MULTIPLE ALLERGIES ( 17 FDA reports)
PERIORBITAL OEDEMA ( 17 FDA reports)
POOR VENOUS ACCESS ( 17 FDA reports)
POST HERPETIC NEURALGIA ( 17 FDA reports)
PSEUDOMONAS INFECTION ( 17 FDA reports)
PSYCHOLOGICAL TRAUMA ( 17 FDA reports)
RIGHT ATRIAL DILATATION ( 17 FDA reports)
SHOULDER PAIN ( 17 FDA reports)
SINUS ARRHYTHMIA ( 17 FDA reports)
ABDOMINAL ADHESIONS ( 16 FDA reports)
ABNORMAL FAECES ( 16 FDA reports)
ACUTE CORONARY SYNDROME ( 16 FDA reports)
ACUTE PRERENAL FAILURE ( 16 FDA reports)
ARTHRITIS BACTERIAL ( 16 FDA reports)
BLADDER OPERATION ( 16 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 16 FDA reports)
DEMENTIA WITH LEWY BODIES ( 16 FDA reports)
EJECTION FRACTION ABNORMAL ( 16 FDA reports)
ENTEROVESICAL FISTULA ( 16 FDA reports)
EUPHORIC MOOD ( 16 FDA reports)
EYE PRURITUS ( 16 FDA reports)
FRACTURED SACRUM ( 16 FDA reports)
GINGIVAL ULCERATION ( 16 FDA reports)
HAEMARTHROSIS ( 16 FDA reports)
HORMONE LEVEL ABNORMAL ( 16 FDA reports)
HYPERVENTILATION ( 16 FDA reports)
HYPOTONIA ( 16 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 16 FDA reports)
INJECTION SITE RASH ( 16 FDA reports)
INTERMITTENT CLAUDICATION ( 16 FDA reports)
JAW OPERATION ( 16 FDA reports)
LOWER EXTREMITY MASS ( 16 FDA reports)
MULTI-ORGAN DISORDER ( 16 FDA reports)
MUSCLE CRAMP ( 16 FDA reports)
PERFORMANCE STATUS DECREASED ( 16 FDA reports)
PERIRECTAL ABSCESS ( 16 FDA reports)
PHARYNGEAL ERYTHEMA ( 16 FDA reports)
PITTING OEDEMA ( 16 FDA reports)
POLYMYALGIA RHEUMATICA ( 16 FDA reports)
POOR PERIPHERAL CIRCULATION ( 16 FDA reports)
PROSTATE CANCER METASTATIC ( 16 FDA reports)
PYURIA ( 16 FDA reports)
SKIN TIGHTNESS ( 16 FDA reports)
SUDDEN DEATH ( 16 FDA reports)
TOOTH DISCOLOURATION ( 16 FDA reports)
TOXIC ENCEPHALOPATHY ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
UMBILICAL HERNIA ( 16 FDA reports)
UTERINE DISORDER ( 16 FDA reports)
UTERINE POLYP ( 16 FDA reports)
VAGINAL INFECTION ( 16 FDA reports)
WOUND DRAINAGE ( 16 FDA reports)
SKIN IRRITATION ( 15 FDA reports)
SPINAL FUSION SURGERY ( 15 FDA reports)
SPUTUM DISCOLOURED ( 15 FDA reports)
TENOSYNOVITIS STENOSANS ( 15 FDA reports)
THERAPY NON-RESPONDER ( 15 FDA reports)
TOOTH EROSION ( 15 FDA reports)
ULCERATIVE KERATITIS ( 15 FDA reports)
VENOUS OCCLUSION ( 15 FDA reports)
VENOUS THROMBOSIS ( 15 FDA reports)
VENTRICULAR DYSFUNCTION ( 15 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 15 FDA reports)
WRONG DRUG ADMINISTERED ( 15 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 15 FDA reports)
ANAL FISTULA ( 15 FDA reports)
APPENDIX DISORDER ( 15 FDA reports)
BLOOD TEST ABNORMAL ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 15 FDA reports)
BONE MARROW TRANSPLANT ( 15 FDA reports)
BRAIN INJURY ( 15 FDA reports)
CAPILLARY LEAK SYNDROME ( 15 FDA reports)
CARDIAC PACEMAKER INSERTION ( 15 FDA reports)
CAROTID ARTERY OCCLUSION ( 15 FDA reports)
CHEST WALL MASS ( 15 FDA reports)
CHOLESTEROSIS ( 15 FDA reports)
CIRCULATORY COLLAPSE ( 15 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 15 FDA reports)
DEAFNESS NEUROSENSORY ( 15 FDA reports)
DENTAL FISTULA ( 15 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 15 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 15 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 15 FDA reports)
FOOT OPERATION ( 15 FDA reports)
FOREIGN BODY ( 15 FDA reports)
FORMICATION ( 15 FDA reports)
HEARING DISABILITY ( 15 FDA reports)
HEARING IMPAIRED ( 15 FDA reports)
HYPERTENSIVE CRISIS ( 15 FDA reports)
INCISION SITE COMPLICATION ( 15 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 15 FDA reports)
LARGE INTESTINE PERFORATION ( 15 FDA reports)
LIP DRY ( 15 FDA reports)
MARROW HYPERPLASIA ( 15 FDA reports)
MONARTHRITIS ( 15 FDA reports)
MUCOSAL HAEMORRHAGE ( 15 FDA reports)
NEUROGENIC BOWEL ( 15 FDA reports)
OBSTRUCTIVE UROPATHY ( 15 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 15 FDA reports)
OLFACTORY NERVE DISORDER ( 15 FDA reports)
OSTEOGENESIS IMPERFECTA ( 15 FDA reports)
PELVIC VENOUS THROMBOSIS ( 15 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 15 FDA reports)
PIRIFORMIS SYNDROME ( 15 FDA reports)
PLASMACYTOSIS ( 15 FDA reports)
POLYPECTOMY ( 15 FDA reports)
POOR DENTAL CONDITION ( 15 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 15 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 15 FDA reports)
PREMATURE BABY ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
PULMONARY VALVE STENOSIS ( 15 FDA reports)
PURULENCE ( 15 FDA reports)
RADIUS FRACTURE ( 15 FDA reports)
RENAL INJURY ( 15 FDA reports)
RESPIRATORY RATE INCREASED ( 15 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 14 FDA reports)
AMMONIA INCREASED ( 14 FDA reports)
APHTHOUS STOMATITIS ( 14 FDA reports)
BACTERIAL DISEASE CARRIER ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 14 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 14 FDA reports)
BONE DEFORMITY ( 14 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 14 FDA reports)
BRONCHOPNEUMONIA ( 14 FDA reports)
CAESAREAN SECTION ( 14 FDA reports)
CARDIOPULMONARY FAILURE ( 14 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 14 FDA reports)
CEREBRAL THROMBOSIS ( 14 FDA reports)
CHOLESTASIS ( 14 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 14 FDA reports)
COLON NEOPLASM ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 14 FDA reports)
DEVELOPMENTAL DELAY ( 14 FDA reports)
DRUG ABUSE ( 14 FDA reports)
DRUG LEVEL INCREASED ( 14 FDA reports)
ENDOCARDITIS ( 14 FDA reports)
ENTERITIS ( 14 FDA reports)
ENTEROCELE ( 14 FDA reports)
EXOPHTHALMOS ( 14 FDA reports)
FLUID INTAKE REDUCED ( 14 FDA reports)
GINGIVAL ERYTHEMA ( 14 FDA reports)
HEART INJURY ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HYPERSEXUALITY ( 14 FDA reports)
HYPOPHOSPHATAEMIA ( 14 FDA reports)
IMMUNOSUPPRESSION ( 14 FDA reports)
INCOHERENT ( 14 FDA reports)
INGROWING NAIL ( 14 FDA reports)
INJECTION SITE INDURATION ( 14 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 14 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 14 FDA reports)
LENS DISORDER ( 14 FDA reports)
LIFE EXPECTANCY SHORTENED ( 14 FDA reports)
METASTASES TO BONE MARROW ( 14 FDA reports)
NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
OESOPHAGEAL DISORDER ( 14 FDA reports)
OPTIC NEURITIS ( 14 FDA reports)
ORGAN FAILURE ( 14 FDA reports)
OSTEOMA ( 14 FDA reports)
PARAPROTEINAEMIA ( 14 FDA reports)
PAROSMIA ( 14 FDA reports)
PERIORBITAL HAEMATOMA ( 14 FDA reports)
PNEUMATOSIS INTESTINALIS ( 14 FDA reports)
POLYARTHRITIS ( 14 FDA reports)
PROCEDURAL HYPOTENSION ( 14 FDA reports)
PROTEIN URINE PRESENT ( 14 FDA reports)
PSORIATIC ARTHROPATHY ( 14 FDA reports)
PULSE PRESSURE DECREASED ( 14 FDA reports)
RASH MORBILLIFORM ( 14 FDA reports)
RENAL ATROPHY ( 14 FDA reports)
SKIN ODOUR ABNORMAL ( 14 FDA reports)
SPINAL CORD COMPRESSION ( 14 FDA reports)
STREPTOCOCCAL INFECTION ( 14 FDA reports)
SUDDEN CARDIAC DEATH ( 14 FDA reports)
TENSION HEADACHE ( 14 FDA reports)
TONGUE OEDEMA ( 14 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 14 FDA reports)
VERTIGO POSITIONAL ( 14 FDA reports)
YELLOW SKIN ( 14 FDA reports)
SPINAL COLUMN INJURY ( 13 FDA reports)
STREPTOCOCCAL SEPSIS ( 13 FDA reports)
SUPERINFECTION ( 13 FDA reports)
THERMAL BURN ( 13 FDA reports)
THROMBOPHLEBITIS ( 13 FDA reports)
THYROID CANCER ( 13 FDA reports)
VAGINAL DISCHARGE ( 13 FDA reports)
VARICES OESOPHAGEAL ( 13 FDA reports)
VASCULAR CALCIFICATION ( 13 FDA reports)
WEIGHT BEARING DIFFICULTY ( 13 FDA reports)
ABSCESS LIMB ( 13 FDA reports)
ALCOHOL USE ( 13 FDA reports)
ANAL PRURITUS ( 13 FDA reports)
ANGIONEUROTIC OEDEMA ( 13 FDA reports)
APLASIA PURE RED CELL ( 13 FDA reports)
ARTHRITIS INFECTIVE ( 13 FDA reports)
BLOOD CULTURE POSITIVE ( 13 FDA reports)
BLOOD LACTIC ACID INCREASED ( 13 FDA reports)
BLOOD URIC ACID INCREASED ( 13 FDA reports)
BRAIN NEOPLASM ( 13 FDA reports)
CARDIAC FAILURE ACUTE ( 13 FDA reports)
CARTILAGE INJURY ( 13 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 13 FDA reports)
CHANGE OF BOWEL HABIT ( 13 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 13 FDA reports)
COELIAC DISEASE ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
CORONARY ARTERY THROMBOSIS ( 13 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 13 FDA reports)
DEVICE BREAKAGE ( 13 FDA reports)
EJACULATION DISORDER ( 13 FDA reports)
ENTHESOPATHY ( 13 FDA reports)
ENZYME ABNORMALITY ( 13 FDA reports)
EOSINOPHILIA ( 13 FDA reports)
ESCHERICHIA SEPSIS ( 13 FDA reports)
EXTRADURAL ABSCESS ( 13 FDA reports)
EYELID PTOSIS ( 13 FDA reports)
FRUSTRATION ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 13 FDA reports)
GINGIVAL ABSCESS ( 13 FDA reports)
HAIR TEXTURE ABNORMAL ( 13 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 13 FDA reports)
HYPERBILIRUBINAEMIA ( 13 FDA reports)
HYPOGONADISM ( 13 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 13 FDA reports)
IMMUNE SYSTEM DISORDER ( 13 FDA reports)
JUGULAR VEIN DISTENSION ( 13 FDA reports)
KNEE DEFORMITY ( 13 FDA reports)
METASTASES TO LARGE INTESTINE ( 13 FDA reports)
NECK INJURY ( 13 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 13 FDA reports)
NYSTAGMUS ( 13 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 13 FDA reports)
OESOPHAGEAL SPASM ( 13 FDA reports)
ORAL FUNGAL INFECTION ( 13 FDA reports)
ORAL TORUS ( 13 FDA reports)
PAPILLOMA VIRAL INFECTION ( 13 FDA reports)
PELVIC PROLAPSE ( 13 FDA reports)
PHOTOPSIA ( 13 FDA reports)
PNEUMONIA BACTERIAL ( 13 FDA reports)
POLYNEUROPATHY ( 13 FDA reports)
PYOGENIC GRANULOMA ( 13 FDA reports)
RADICULITIS LUMBOSACRAL ( 13 FDA reports)
RADIOTHERAPY ( 13 FDA reports)
RASH VESICULAR ( 13 FDA reports)
RENAL ARTERY STENOSIS ( 13 FDA reports)
RENAL COLIC ( 13 FDA reports)
RESPIRATION ABNORMAL ( 13 FDA reports)
ROTATOR CUFF REPAIR ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SEROSITIS ( 13 FDA reports)
ADJUSTMENT DISORDER ( 12 FDA reports)
ANAEMIA MACROCYTIC ( 12 FDA reports)
APPLICATION SITE IRRITATION ( 12 FDA reports)
ARTERIAL THROMBOSIS ( 12 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 12 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 12 FDA reports)
AUTOIMMUNE DISORDER ( 12 FDA reports)
AUTOIMMUNE THYROIDITIS ( 12 FDA reports)
B-CELL LYMPHOMA ( 12 FDA reports)
BENIGN BONE NEOPLASM ( 12 FDA reports)
BLADDER OBSTRUCTION ( 12 FDA reports)
BLEPHAROSPASM ( 12 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 12 FDA reports)
BONE CYST ( 12 FDA reports)
BONE MARROW DISORDER ( 12 FDA reports)
BREAST FIBROSIS ( 12 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 12 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 12 FDA reports)
COMPLETED SUICIDE ( 12 FDA reports)
CYSTITIS HAEMORRHAGIC ( 12 FDA reports)
DISSOCIATION ( 12 FDA reports)
DRUG PRESCRIBING ERROR ( 12 FDA reports)
DYSTONIA ( 12 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 12 FDA reports)
ENDOTRACHEAL INTUBATION ( 12 FDA reports)
EOSINOPHIL COUNT INCREASED ( 12 FDA reports)
ERYTHEMA MULTIFORME ( 12 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 12 FDA reports)
FOOD POISONING ( 12 FDA reports)
GASTRIC DILATATION ( 12 FDA reports)
GASTROENTERITIS RADIATION ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 12 FDA reports)
HAEMORRHOID OPERATION ( 12 FDA reports)
HALLUCINATIONS, MIXED ( 12 FDA reports)
HEART VALVE INCOMPETENCE ( 12 FDA reports)
HEPATIC FIBROSIS ( 12 FDA reports)
HICCUPS ( 12 FDA reports)
HIP SURGERY ( 12 FDA reports)
HYPERCALCIURIA ( 12 FDA reports)
HYPERNATRAEMIA ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
INCISION SITE HAEMORRHAGE ( 12 FDA reports)
INJECTION SITE INFECTION ( 12 FDA reports)
INJECTION SITE NODULE ( 12 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 12 FDA reports)
INTRAOCULAR LENS IMPLANT ( 12 FDA reports)
KNEE OPERATION ( 12 FDA reports)
KYPHOSCOLIOSIS ( 12 FDA reports)
LEUKOENCEPHALOPATHY ( 12 FDA reports)
MELANOSIS COLI ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
MUMPS ( 12 FDA reports)
NEPHROPATHY ( 12 FDA reports)
ORAL SURGERY ( 12 FDA reports)
OTORRHOEA ( 12 FDA reports)
PAINFUL RESPIRATION ( 12 FDA reports)
PNEUMONIA VIRAL ( 12 FDA reports)
POLYCYTHAEMIA ( 12 FDA reports)
RESPIRATORY DEPRESSION ( 12 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 12 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 12 FDA reports)
SALPINGITIS ( 12 FDA reports)
SENSATION OF FOREIGN BODY ( 12 FDA reports)
SINUS POLYP ( 12 FDA reports)
SJOGREN'S SYNDROME ( 12 FDA reports)
SKIN SWELLING ( 12 FDA reports)
TESTICULAR PAIN ( 12 FDA reports)
TONGUE INJURY ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
URINARY TRACT OBSTRUCTION ( 12 FDA reports)
UVEITIS ( 12 FDA reports)
SOMNAMBULISM ( 11 FDA reports)
SPINAL LAMINECTOMY ( 11 FDA reports)
SPUTUM CULTURE POSITIVE ( 11 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 11 FDA reports)
TOOTH REPAIR ( 11 FDA reports)
TUMOUR LYSIS SYNDROME ( 11 FDA reports)
UNDERDOSE ( 11 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 11 FDA reports)
URINE ODOUR ABNORMAL ( 11 FDA reports)
VASODILATATION ( 11 FDA reports)
VITAMIN C DEFICIENCY ( 11 FDA reports)
VITREOUS HAEMORRHAGE ( 11 FDA reports)
VOCAL CORD DISORDER ( 11 FDA reports)
WITHDRAWAL SYNDROME ( 11 FDA reports)
WOUND SECRETION ( 11 FDA reports)
ACUTE HEPATIC FAILURE ( 11 FDA reports)
ADRENAL MASS ( 11 FDA reports)
AMAUROSIS FUGAX ( 11 FDA reports)
ANOGENITAL WARTS ( 11 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 11 FDA reports)
ANURIA ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 11 FDA reports)
ASPERGILLOSIS ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
ATROPHY ( 11 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BLINDNESS TRANSIENT ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
CALCULUS URINARY ( 11 FDA reports)
CARDIAC OPERATION ( 11 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 11 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 11 FDA reports)
CEREBRAL ARTERY STENOSIS ( 11 FDA reports)
CLUSTER HEADACHE ( 11 FDA reports)
COMMUNICATION DISORDER ( 11 FDA reports)
DENTAL DISCOMFORT ( 11 FDA reports)
DERMAL CYST ( 11 FDA reports)
DRUG ABUSER ( 11 FDA reports)
DRUG SCREEN POSITIVE ( 11 FDA reports)
DUODENAL ULCER ( 11 FDA reports)
EXERCISE TOLERANCE DECREASED ( 11 FDA reports)
EYELID OEDEMA ( 11 FDA reports)
FACIAL PALSY ( 11 FDA reports)
FIBROADENOMA OF BREAST ( 11 FDA reports)
FOOD INTOLERANCE ( 11 FDA reports)
FRACTURED ISCHIUM ( 11 FDA reports)
FULL BLOOD COUNT DECREASED ( 11 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 11 FDA reports)
GASTROINTESTINAL NECROSIS ( 11 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 11 FDA reports)
GLIOSIS ( 11 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 11 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 11 FDA reports)
HAEMORRHAGIC STROKE ( 11 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 11 FDA reports)
HEPATOSPLENOMEGALY ( 11 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 11 FDA reports)
ILEITIS ( 11 FDA reports)
INADEQUATE ANALGESIA ( 11 FDA reports)
INFARCTION ( 11 FDA reports)
INJECTION SITE EXTRAVASATION ( 11 FDA reports)
INTENTIONAL OVERDOSE ( 11 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 11 FDA reports)
INTRACARDIAC THROMBUS ( 11 FDA reports)
LIGAMENT INJURY ( 11 FDA reports)
LIP DISCOLOURATION ( 11 FDA reports)
MENINGITIS ( 11 FDA reports)
METASTASIS ( 11 FDA reports)
MITRAL VALVE SCLEROSIS ( 11 FDA reports)
MYOPIA ( 11 FDA reports)
NODULE ON EXTREMITY ( 11 FDA reports)
OROPHARYNGEAL BLISTERING ( 11 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 11 FDA reports)
PERIARTHRITIS ( 11 FDA reports)
PIGMENTATION DISORDER ( 11 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 11 FDA reports)
POSTNASAL DRIP ( 11 FDA reports)
POSTOPERATIVE ILEUS ( 11 FDA reports)
PRODUCT ADHESION ISSUE ( 11 FDA reports)
PROSTATIC DISORDER ( 11 FDA reports)
PULMONARY TUBERCULOSIS ( 11 FDA reports)
PURPURA ( 11 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 11 FDA reports)
RETINAL ARTERY OCCLUSION ( 11 FDA reports)
RHONCHI ( 11 FDA reports)
SCOTOMA ( 11 FDA reports)
SELF-MEDICATION ( 11 FDA reports)
SHUNT OCCLUSION ( 11 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
ACUTE PULMONARY OEDEMA ( 10 FDA reports)
ADENOMA BENIGN ( 10 FDA reports)
ADHESION ( 10 FDA reports)
ADRENAL SUPPRESSION ( 10 FDA reports)
AFFECTIVE DISORDER ( 10 FDA reports)
AMYLOIDOSIS ( 10 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 10 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 10 FDA reports)
ANAL HAEMORRHAGE ( 10 FDA reports)
ANOXIC ENCEPHALOPATHY ( 10 FDA reports)
APPENDICECTOMY ( 10 FDA reports)
ARTERIOVENOUS MALFORMATION ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
CARCINOID SYNDROME ( 10 FDA reports)
CATARACT NUCLEAR ( 10 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 10 FDA reports)
CONGENITAL ANOMALY ( 10 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 10 FDA reports)
DEAFNESS UNILATERAL ( 10 FDA reports)
DEVICE OCCLUSION ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
DRUG LEVEL DECREASED ( 10 FDA reports)
DYSMENORRHOEA ( 10 FDA reports)
EFFUSION ( 10 FDA reports)
ENCEPHALITIS ( 10 FDA reports)
ENCEPHALOMALACIA ( 10 FDA reports)
EPIDIDYMITIS ( 10 FDA reports)
FOOD CRAVING ( 10 FDA reports)
FUNGAL SKIN INFECTION ( 10 FDA reports)
GALLBLADDER OPERATION ( 10 FDA reports)
GANGRENE ( 10 FDA reports)
GASTROINTESTINAL INFECTION ( 10 FDA reports)
GRIP STRENGTH DECREASED ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
HAND DEFORMITY ( 10 FDA reports)
HANGOVER ( 10 FDA reports)
HYDROPNEUMOTHORAX ( 10 FDA reports)
HYPOPERFUSION ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INJECTION SITE PAPULE ( 10 FDA reports)
INJURY CORNEAL ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 10 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 10 FDA reports)
INTESTINAL STENOSIS ( 10 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 10 FDA reports)
IRON DEFICIENCY ( 10 FDA reports)
JOINT ARTHROPLASTY ( 10 FDA reports)
KLEBSIELLA INFECTION ( 10 FDA reports)
LENTIGO ( 10 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
LYMPHOCYTOSIS ( 10 FDA reports)
MALABSORPTION ( 10 FDA reports)
MECHANICAL VENTILATION ( 10 FDA reports)
MENORRHAGIA ( 10 FDA reports)
MITRAL VALVE DISEASE ( 10 FDA reports)
MOTOR DYSFUNCTION ( 10 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 10 FDA reports)
NAIL DISCOLOURATION ( 10 FDA reports)
NASAL DISCOMFORT ( 10 FDA reports)
NASAL OEDEMA ( 10 FDA reports)
NEPHROTIC SYNDROME ( 10 FDA reports)
NEUROPATHY ( 10 FDA reports)
NEUROTOXICITY ( 10 FDA reports)
OCULAR ICTERUS ( 10 FDA reports)
OESOPHAGEAL STENOSIS ( 10 FDA reports)
ONYCHOCLASIS ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
OSTEOMALACIA ( 10 FDA reports)
PANCREATIC ATROPHY ( 10 FDA reports)
PANCREATIC CARCINOMA ( 10 FDA reports)
PANCREATITIS CHRONIC ( 10 FDA reports)
PAROTITIS ( 10 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 10 FDA reports)
PHAEOCHROMOCYTOMA ( 10 FDA reports)
PULMONARY AIR LEAKAGE ( 10 FDA reports)
PULMONARY TOXICITY ( 10 FDA reports)
PYELOCALIECTASIS ( 10 FDA reports)
RADIATION PNEUMONITIS ( 10 FDA reports)
RENAL TRANSPLANT ( 10 FDA reports)
RETINAL DETACHMENT ( 10 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
RUBELLA ( 10 FDA reports)
SCARLET FEVER ( 10 FDA reports)
SCREAMING ( 10 FDA reports)
SERRATIA INFECTION ( 10 FDA reports)
SKULL FRACTURE ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
SPONDYLITIS ( 10 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 10 FDA reports)
THROMBOCYTOSIS ( 10 FDA reports)
THROMBOTIC STROKE ( 10 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 10 FDA reports)
URINE ANALYSIS ABNORMAL ( 10 FDA reports)
URINE FLOW DECREASED ( 10 FDA reports)
UTERINE CANCER ( 10 FDA reports)
WEGENER'S GRANULOMATOSIS ( 10 FDA reports)
WHEELCHAIR USER ( 10 FDA reports)
SINUS OPERATION ( 9 FDA reports)
SKIN FIBROSIS ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKIN PAPILLOMA ( 9 FDA reports)
SLEEP TERROR ( 9 FDA reports)
SMALL FOR DATES BABY ( 9 FDA reports)
SNORING ( 9 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 9 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 9 FDA reports)
SUBDURAL HAEMORRHAGE ( 9 FDA reports)
TOXIC SHOCK SYNDROME ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
URINE CALCIUM INCREASED ( 9 FDA reports)
UTERINE HAEMORRHAGE ( 9 FDA reports)
UTERINE PROLAPSE ( 9 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 9 FDA reports)
AKATHISIA ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
ANAPHYLACTOID REACTION ( 9 FDA reports)
ANORECTAL DISCOMFORT ( 9 FDA reports)
ANTINUCLEAR ANTIBODY ( 9 FDA reports)
APPENDICITIS ( 9 FDA reports)
APPLICATION SITE RASH ( 9 FDA reports)
APPLICATION SITE REACTION ( 9 FDA reports)
ARTERIAL DISORDER ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
ATROPHIC VULVOVAGINITIS ( 9 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 9 FDA reports)
BACTERAEMIA ( 9 FDA reports)
BLOOD MAGNESIUM DECREASED ( 9 FDA reports)
BLOOD PRESSURE ( 9 FDA reports)
BONE GRAFT ( 9 FDA reports)
BONE METABOLISM DISORDER ( 9 FDA reports)
BRAIN HERNIATION ( 9 FDA reports)
BREAST ENLARGEMENT ( 9 FDA reports)
BRONCHOPLEURAL FISTULA ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CATHETER SITE HAEMORRHAGE ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CHAPPED LIPS ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
CHRONIC FATIGUE SYNDROME ( 9 FDA reports)
CLUMSINESS ( 9 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 9 FDA reports)
CONNECTIVE TISSUE DISORDER ( 9 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 9 FDA reports)
DERMATOMYOSITIS ( 9 FDA reports)
DEVICE RELATED SEPSIS ( 9 FDA reports)
DIPLEGIA ( 9 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 9 FDA reports)
DRUG TOLERANCE ( 9 FDA reports)
DRY THROAT ( 9 FDA reports)
ECLAMPSIA ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
EMBOLIC STROKE ( 9 FDA reports)
EMBOLISM VENOUS ( 9 FDA reports)
ESCHERICHIA TEST POSITIVE ( 9 FDA reports)
EYE INFLAMMATION ( 9 FDA reports)
FACE INJURY ( 9 FDA reports)
FEEDING DISORDER ( 9 FDA reports)
FEELING DRUNK ( 9 FDA reports)
FOETAL HEART RATE ABNORMAL ( 9 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 9 FDA reports)
GASTROINTESTINAL ULCER ( 9 FDA reports)
GENERAL SYMPTOM ( 9 FDA reports)
GRIMACING ( 9 FDA reports)
HELICOBACTER INFECTION ( 9 FDA reports)
HELICOBACTER TEST POSITIVE ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HORNER'S SYNDROME ( 9 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPERTENSIVE HEART DISEASE ( 9 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 9 FDA reports)
HYSTERECTOMY ( 9 FDA reports)
IMMOBILE ( 9 FDA reports)
IMPLANT SITE THROMBOSIS ( 9 FDA reports)
INCISION SITE INFECTION ( 9 FDA reports)
INTERCOSTAL NEURALGIA ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
JUGULAR VEIN THROMBOSIS ( 9 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 9 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 9 FDA reports)
LIMB ASYMMETRY ( 9 FDA reports)
LIPIDS INCREASED ( 9 FDA reports)
LUNG INJURY ( 9 FDA reports)
MOUTH CYST ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
MUSCLE RIGIDITY ( 9 FDA reports)
MUSCLE RUPTURE ( 9 FDA reports)
MUSCLE SPASTICITY ( 9 FDA reports)
NASAL DRYNESS ( 9 FDA reports)
NASAL POLYPS ( 9 FDA reports)
NECK MASS ( 9 FDA reports)
NEOPLASM OF APPENDIX ( 9 FDA reports)
OBSTRUCTION ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
ONYCHALGIA ( 9 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 9 FDA reports)
OSTEOMYELITIS ACUTE ( 9 FDA reports)
PANIC REACTION ( 9 FDA reports)
PERINEAL LACERATION ( 9 FDA reports)
PERITONITIS BACTERIAL ( 9 FDA reports)
PERSONALITY CHANGE ( 9 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 9 FDA reports)
PNEUMONIA HAEMOPHILUS ( 9 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
POSTPARTUM HAEMORRHAGE ( 9 FDA reports)
PROCEDURAL VOMITING ( 9 FDA reports)
PROSTATE CANCER RECURRENT ( 9 FDA reports)
PROTEIN TOTAL INCREASED ( 9 FDA reports)
PSEUDOMYXOMA PERITONEI ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
PULPITIS DENTAL ( 9 FDA reports)
QUALITY OF LIFE DECREASED ( 9 FDA reports)
RADIATION INJURY ( 9 FDA reports)
RASH PUSTULAR ( 9 FDA reports)
RENAL CELL CARCINOMA ( 9 FDA reports)
SEPSIS SYNDROME ( 9 FDA reports)
SIGMOIDITIS ( 9 FDA reports)
ABSCESS DRAINAGE ( 8 FDA reports)
ADMINISTRATION SITE INFECTION ( 8 FDA reports)
ANIMAL BITE ( 8 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
APPLICATION SITE PAIN ( 8 FDA reports)
AREFLEXIA ( 8 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 8 FDA reports)
BIPOLAR I DISORDER ( 8 FDA reports)
BLOOD BICARBONATE DECREASED ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BLOOD SODIUM INCREASED ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 8 FDA reports)
BURNS SECOND DEGREE ( 8 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 8 FDA reports)
CARDIAC VALVE SCLEROSIS ( 8 FDA reports)
CARDITIS ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CHEST INJURY ( 8 FDA reports)
CLAUSTROPHOBIA ( 8 FDA reports)
COMPLICATION OF DELIVERY ( 8 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 8 FDA reports)
CONDUCTION DISORDER ( 8 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 8 FDA reports)
COSTOCHONDRITIS ( 8 FDA reports)
CUBITAL TUNNEL SYNDROME ( 8 FDA reports)
DEPENDENCE ( 8 FDA reports)
DERMATITIS ACNEIFORM ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENERGY INCREASED ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EYE ROLLING ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
FRACTURE DISPLACEMENT ( 8 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 8 FDA reports)
GASTRITIS ATROPHIC ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GLOBULINS INCREASED ( 8 FDA reports)
GRAM STAIN POSITIVE ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HEPATIC PAIN ( 8 FDA reports)
HERNIA REPAIR ( 8 FDA reports)
HYPERCHLORAEMIA ( 8 FDA reports)
HYPEROXALURIA ( 8 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 8 FDA reports)
HYPOSMIA ( 8 FDA reports)
HYPOTRICHOSIS ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INDURATION ( 8 FDA reports)
INFUSION SITE EXTRAVASATION ( 8 FDA reports)
LEUKOPLAKIA ORAL ( 8 FDA reports)
LIVEDO RETICULARIS ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LOOSE BODY IN JOINT ( 8 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
MASTECTOMY ( 8 FDA reports)
MENSTRUAL DISORDER ( 8 FDA reports)
MENSTRUATION IRREGULAR ( 8 FDA reports)
METAPLASIA ( 8 FDA reports)
METASTASES TO THORAX ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
MORTON'S NEUROMA ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
NERVE ROOT LESION ( 8 FDA reports)
NEUROENDOCRINE TUMOUR ( 8 FDA reports)
NEUROSIS ( 8 FDA reports)
NEUTROPENIC COLITIS ( 8 FDA reports)
NEUTROPENIC SEPSIS ( 8 FDA reports)
NODAL RHYTHM ( 8 FDA reports)
OCCIPITAL NEURALGIA ( 8 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 8 FDA reports)
OPTIC ATROPHY ( 8 FDA reports)
OPTIC NERVE DISORDER ( 8 FDA reports)
ORGANISING PNEUMONIA ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PAPILLOEDEMA ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 8 FDA reports)
PHLEBOLITH ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PORTAL VEIN THROMBOSIS ( 8 FDA reports)
POST PROCEDURAL OEDEMA ( 8 FDA reports)
PRESBYOESOPHAGUS ( 8 FDA reports)
PRESBYOPIA ( 8 FDA reports)
PROCEDURAL NAUSEA ( 8 FDA reports)
RADICULITIS ( 8 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 8 FDA reports)
RESPIRATORY ACIDOSIS ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
RHEUMATOID NODULE ( 8 FDA reports)
SALIVARY GLAND ADENOMA ( 8 FDA reports)
SECRETION DISCHARGE ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
SKIN NODULE ( 8 FDA reports)
SKIN WRINKLING ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SMEAR CERVIX ABNORMAL ( 8 FDA reports)
SPINAL DEFORMITY ( 8 FDA reports)
STATUS EPILEPTICUS ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
TEMPERATURE INTOLERANCE ( 8 FDA reports)
TENSION ( 8 FDA reports)
THROMBOCYTHAEMIA ( 8 FDA reports)
TONIC CLONIC MOVEMENTS ( 8 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 8 FDA reports)
TRAUMATIC BRAIN INJURY ( 8 FDA reports)
TRAUMATIC FRACTURE ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
URGE INCONTINENCE ( 8 FDA reports)
VAGINITIS BACTERIAL ( 8 FDA reports)
VERTEBRAL INJURY ( 8 FDA reports)
VITAMIN B12 DEFICIENCY ( 8 FDA reports)
SKIN FRAGILITY ( 7 FDA reports)
SKIN INJURY ( 7 FDA reports)
SLOW RESPONSE TO STIMULI ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPINAL CLAUDICATION ( 7 FDA reports)
STASIS DERMATITIS ( 7 FDA reports)
STENT PLACEMENT ( 7 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 7 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 7 FDA reports)
SYNOVIAL DISORDER ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
THYROID ADENOMA ( 7 FDA reports)
TIC ( 7 FDA reports)
TINEA INFECTION ( 7 FDA reports)
TONGUE COATED ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TRACHEOSTOMY ( 7 FDA reports)
TRIGEMINAL NERVE PARESIS ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
ULNA FRACTURE ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
UROBILINOGEN URINE INCREASED ( 7 FDA reports)
VASCULAR GRAFT ( 7 FDA reports)
VASCULAR INJURY ( 7 FDA reports)
VASCULAR OCCLUSION ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VENOUS THROMBOSIS LIMB ( 7 FDA reports)
VERTEBROPLASTY ( 7 FDA reports)
VULVOVAGINAL PRURITUS ( 7 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ACARODERMATITIS ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ADENOMYOSIS ( 7 FDA reports)
ADRENAL NEOPLASM ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
ANORGASMIA ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 7 FDA reports)
APLASTIC ANAEMIA ( 7 FDA reports)
APTYALISM ( 7 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BACTERIAL TEST POSITIVE ( 7 FDA reports)
BENIGN BREAST NEOPLASM ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BLADDER SPASM ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BONE FISTULA ( 7 FDA reports)
BREAST CYST ( 7 FDA reports)
BREAST SWELLING ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRONCHITIS ACUTE ( 7 FDA reports)
CACHEXIA ( 7 FDA reports)
CANCER PAIN ( 7 FDA reports)
CARDIOVERSION ( 7 FDA reports)
CARTILAGE ATROPHY ( 7 FDA reports)
CATARACT CORTICAL ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
CYANOPSIA ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DENTAL CARE ( 7 FDA reports)
DENTAL PROSTHESIS USER ( 7 FDA reports)
DEPRESSION SUICIDAL ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
DERMATITIS ATOPIC ( 7 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 7 FDA reports)
DYSTHYMIC DISORDER ( 7 FDA reports)
EAR INFECTION VIRAL ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 7 FDA reports)
EYE ALLERGY ( 7 FDA reports)
EYELID DISORDER ( 7 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
FIBROMA ( 7 FDA reports)
FOOD ALLERGY ( 7 FDA reports)
GALLBLADDER PAIN ( 7 FDA reports)
GESTATIONAL HYPERTENSION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
GUN SHOT WOUND ( 7 FDA reports)
HAEMANGIOMA OF LIVER ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HOMOCYSTINAEMIA ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
HYPERALBUMINAEMIA ( 7 FDA reports)
HYPERCHLORHYDRIA ( 7 FDA reports)
HYPERPATHIA ( 7 FDA reports)
HYPERTHERMIA ( 7 FDA reports)
IMMUNODEFICIENCY ( 7 FDA reports)
INCORRECT STORAGE OF DRUG ( 7 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
INTENTIONAL SELF-INJURY ( 7 FDA reports)
INTRA-UTERINE DEATH ( 7 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 7 FDA reports)
IRITIS ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LICHEN SCLEROSUS ( 7 FDA reports)
LIP EXFOLIATION ( 7 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LYMPHOCYTIC INFILTRATION ( 7 FDA reports)
MACROGLOSSIA ( 7 FDA reports)
MALOCCLUSION ( 7 FDA reports)
MAMMOGRAM ABNORMAL ( 7 FDA reports)
MEDIASTINAL HAEMATOMA ( 7 FDA reports)
MENOPAUSAL DISORDER ( 7 FDA reports)
MENOPAUSAL SYMPTOMS ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
MYELITIS TRANSVERSE ( 7 FDA reports)
MYELOMA RECURRENCE ( 7 FDA reports)
MYELOPATHY ( 7 FDA reports)
MYOCARDIAL FIBROSIS ( 7 FDA reports)
NAIL DYSTROPHY ( 7 FDA reports)
NAIL HYPERTROPHY ( 7 FDA reports)
NEUROLOGICAL SYMPTOM ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
NIGHT BLINDNESS ( 7 FDA reports)
NIPPLE PAIN ( 7 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
ORAL CAVITY FISTULA ( 7 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 7 FDA reports)
OSTEOPOROTIC FRACTURE ( 7 FDA reports)
PAROTID GLAND ENLARGEMENT ( 7 FDA reports)
PELVIC ABSCESS ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
PULMONARY VALVE DISEASE ( 7 FDA reports)
REGURGITATION ( 7 FDA reports)
RETINAL DISORDER ( 7 FDA reports)
RETINAL OEDEMA ( 7 FDA reports)
RHINITIS SEASONAL ( 7 FDA reports)
SALIVARY GLAND MASS ( 7 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 7 FDA reports)
SEPSIS NEONATAL ( 7 FDA reports)
SEROMA ( 7 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 6 FDA reports)
ABDOMINAL NEOPLASM ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 6 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 6 FDA reports)
ABORTION INDUCED ( 6 FDA reports)
ACCIDENTAL DEATH ( 6 FDA reports)
ACUTE STRESS DISORDER ( 6 FDA reports)
ALLERGIC SINUSITIS ( 6 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 6 FDA reports)
AMENORRHOEA ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
AORTIC VALVE STENOSIS ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
APPENDICITIS PERFORATED ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
AXILLARY PAIN ( 6 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 6 FDA reports)
BACTERIA URINE ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BLADDER DILATATION ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD CREATININE DECREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 6 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BODY TINEA ( 6 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BREAST CANCER STAGE I ( 6 FDA reports)
BRONCHITIS VIRAL ( 6 FDA reports)
CAMPBELL DE MORGAN SPOTS ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CENTRAL LINE INFECTION ( 6 FDA reports)
CHARLES BONNET SYNDROME ( 6 FDA reports)
CHEMOTHERAPY ( 6 FDA reports)
CITROBACTER INFECTION ( 6 FDA reports)
COARCTATION OF THE AORTA ( 6 FDA reports)
COLITIS MICROSCOPIC ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
COMPLEX PARTIAL SEIZURES ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DISINHIBITION ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
DYSPAREUNIA ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
EAR NEOPLASM ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 6 FDA reports)
FAECES HARD ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FAT NECROSIS ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
GASTRODUODENITIS ( 6 FDA reports)
GASTROINTESTINAL PERFORATION ( 6 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 6 FDA reports)
GLOMERULONEPHRITIS ( 6 FDA reports)
HAEMOGLOBIN ABNORMAL ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEPATIC ADENOMA ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HIP DEFORMITY ( 6 FDA reports)
HYPERADRENALISM ( 6 FDA reports)
HYPERTROPHIC SCAR ( 6 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 6 FDA reports)
ILLUSION ( 6 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 6 FDA reports)
INJECTION SITE CELLULITIS ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
INJECTION SITE MASS ( 6 FDA reports)
INJECTION SITE STINGING ( 6 FDA reports)
INTRACRANIAL HYPOTENSION ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
IRREGULAR SLEEP PHASE ( 6 FDA reports)
KETOACIDOSIS ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LIP INJURY ( 6 FDA reports)
LIP PAIN ( 6 FDA reports)
LIVE BIRTH ( 6 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 6 FDA reports)
LIVER TENDERNESS ( 6 FDA reports)
LUMBAR HERNIA ( 6 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYME DISEASE ( 6 FDA reports)
MANDIBULAR PROSTHESIS USER ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
MEAN CELL VOLUME INCREASED ( 6 FDA reports)
MUCOSAL ULCERATION ( 6 FDA reports)
MULTIPLE LENTIGINES SYNDROME ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NASAL DISORDER ( 6 FDA reports)
NASAL ODOUR ( 6 FDA reports)
NEPHRITIS ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NOCTURNAL DYSPNOEA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER ( 6 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
OPTIC NERVE CUPPING ( 6 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 6 FDA reports)
PARATHYROID TUMOUR BENIGN ( 6 FDA reports)
PERICARDIAL CYST ( 6 FDA reports)
PHARYNGEAL DISORDER ( 6 FDA reports)
PLASMAPHERESIS ( 6 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 6 FDA reports)
POLYP COLORECTAL ( 6 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PSYCHIATRIC SYMPTOM ( 6 FDA reports)
PSYCHOTIC BEHAVIOUR ( 6 FDA reports)
PUBIS FRACTURE ( 6 FDA reports)
PYELONEPHRITIS CHRONIC ( 6 FDA reports)
PYODERMA ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
RECTAL PROLAPSE ( 6 FDA reports)
RED MAN SYNDROME ( 6 FDA reports)
RENAL OSTEODYSTROPHY ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
SCRATCH ( 6 FDA reports)
SEBORRHOEA ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SHOULDER DEFORMITY ( 6 FDA reports)
SHUNT STENOSIS ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SKIN CANDIDA ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
SOFT TISSUE INFECTION ( 6 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 6 FDA reports)
SPIDER VEIN ( 6 FDA reports)
SPLENIC RUPTURE ( 6 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 6 FDA reports)
SPONDYLOSIS ( 6 FDA reports)
STARING ( 6 FDA reports)
STEROID THERAPY ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
STRIDOR ( 6 FDA reports)
SUBACUTE ENDOCARDITIS ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 6 FDA reports)
THYROID CYST ( 6 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 6 FDA reports)
TINEA PEDIS ( 6 FDA reports)
TOOTH IMPACTED ( 6 FDA reports)
TUNNEL VISION ( 6 FDA reports)
URETHRAL CARUNCLE ( 6 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
SKELETAL INJURY ( 5 FDA reports)
SKIN CHAPPED ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SPINAL CORD DISORDER ( 5 FDA reports)
SPONDYLOARTHROPATHY ( 5 FDA reports)
SPUTUM INCREASED ( 5 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TERMINAL STATE ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
THYROIDITIS CHRONIC ( 5 FDA reports)
TOXIC NEUROPATHY ( 5 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 5 FDA reports)
TUMOUR HAEMORRHAGE ( 5 FDA reports)
TUMOUR INVASION ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
URINE ABNORMALITY ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VAGINAL BURNING SENSATION ( 5 FDA reports)
VAGINAL CANDIDIASIS ( 5 FDA reports)
VEIN PAIN ( 5 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VOMITING IN PREGNANCY ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
VULVAL LEUKOPLAKIA ( 5 FDA reports)
VULVAR EROSION ( 5 FDA reports)
WEIGHT GAIN POOR ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
YAWNING ( 5 FDA reports)
ABSCESS NECK ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 5 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 5 FDA reports)
ADRENAL DISORDER ( 5 FDA reports)
ALLERGY TO VACCINE ( 5 FDA reports)
ALLODYNIA ( 5 FDA reports)
ANASTOMOTIC ULCER ( 5 FDA reports)
ANGIODYSPLASIA ( 5 FDA reports)
ANKLE OPERATION ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
APPETITE DISORDER ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
AURA ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
AUTOPHOBIA ( 5 FDA reports)
B-CELL LYMPHOMA STAGE III ( 5 FDA reports)
BASEDOW'S DISEASE ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BINGE EATING ( 5 FDA reports)
BLOOD BLISTER ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BONE OPERATION ( 5 FDA reports)
BONE SARCOMA ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN MASS ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BURNOUT SYNDROME ( 5 FDA reports)
CALCULUS BLADDER ( 5 FDA reports)
CARDIAC DEATH ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CARDIOTOXICITY ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 5 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 5 FDA reports)
CERVICAL INCOMPETENCE ( 5 FDA reports)
CERVICAL POLYP ( 5 FDA reports)
CERVIX INFLAMMATION ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 5 FDA reports)
COMPULSIVE SHOPPING ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CONJUNCTIVAL PALLOR ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CULTURE POSITIVE ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DRESSLER'S SYNDROME ( 5 FDA reports)
DRY GANGRENE ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
DYSPHORIA ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
EAR HAEMORRHAGE ( 5 FDA reports)
EDENTULOUS ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ENDOMETRIAL CANCER ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EXPOSURE TO TOXIC AGENT ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
FAECALURIA ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FINGER DEFORMITY ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
FOLATE DEFICIENCY ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
FOOD INTERACTION ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
HAEMODILUTION ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HALLUCINATION, OLFACTORY ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HERNIA OBSTRUCTIVE ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
HYPOVITAMINOSIS ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INCISION SITE HAEMATOMA ( 5 FDA reports)
INCISIONAL DRAINAGE ( 5 FDA reports)
INCREASED BRONCHIAL SECRETION ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INJECTION SITE INFLAMMATION ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
KELOID SCAR ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 5 FDA reports)
MENISCUS REMOVAL ( 5 FDA reports)
MERALGIA PARAESTHETICA ( 5 FDA reports)
METASTATIC CARCINOID TUMOUR ( 5 FDA reports)
MUSCULAR DYSTROPHY ( 5 FDA reports)
NAIL AVULSION ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NEPHROSCLEROSIS ( 5 FDA reports)
NOCARDIOSIS ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 5 FDA reports)
OBSTRUCTION GASTRIC ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PALMAR ERYTHEMA ( 5 FDA reports)
PANNICULITIS ( 5 FDA reports)
PARAKERATOSIS ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PHYSIOTHERAPY ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
POST THROMBOTIC SYNDROME ( 5 FDA reports)
POSTOPERATIVE ADHESION ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
PRESSURE OF SPEECH ( 5 FDA reports)
PROCTITIS ( 5 FDA reports)
PROPOFOL INFUSION SYNDROME ( 5 FDA reports)
PROSTATIC OPERATION ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PSEUDOMONAL SEPSIS ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PULMONARY CAVITATION ( 5 FDA reports)
PULSE ABNORMAL ( 5 FDA reports)
RADIATION OESOPHAGITIS ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SARCOMA ( 5 FDA reports)
SCLERODACTYLIA ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 4 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
AGRAPHIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALLERGY TO CHEMICALS ( 4 FDA reports)
ALVEOLITIS FIBROSING ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANASTOMOTIC STENOSIS ( 4 FDA reports)
ANGIOLIPOMA ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
ANORECTAL DISORDER ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
APPLICATION SITE DISCOLOURATION ( 4 FDA reports)
APPLICATION SITE EXFOLIATION ( 4 FDA reports)
APPLICATION SITE HAEMATOMA ( 4 FDA reports)
APPLICATION SITE SCAR ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
BENIGN TUMOUR EXCISION ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BIOPSY BONE ABNORMAL ( 4 FDA reports)
BIOPSY BREAST ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD FOLATE INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BONE NEOPLASM ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BRAIN STEM STROKE ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST CELLULITIS ( 4 FDA reports)
BREAST LUMP REMOVAL ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CALCIUM METABOLISM DISORDER ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC VALVE VEGETATION ( 4 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 4 FDA reports)
CAROTID PULSE ABNORMAL ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CERVICAL DYSPLASIA ( 4 FDA reports)
CERVICAL SPINE FLATTENING ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHEYNE-STOKES RESPIRATION ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
COELIAC ARTERY STENOSIS ( 4 FDA reports)
COLECTOMY ( 4 FDA reports)
COLON CANCER STAGE II ( 4 FDA reports)
COLON DYSPLASIA ( 4 FDA reports)
COLPOSCOPY ABNORMAL ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONGENITAL EYE DISORDER ( 4 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 4 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CYSTITIS NONINFECTIVE ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DEVICE INTOLERANCE ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DURAL TEAR ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENDOMETRIOSIS ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
ESCHERICHIA BACTERAEMIA ( 4 FDA reports)
ESSENTIAL TREMOR ( 4 FDA reports)
EXTREMITY CONTRACTURE ( 4 FDA reports)
EYE LASER SURGERY ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FEBRILE CONVULSION ( 4 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FLOPPY IRIS SYNDROME ( 4 FDA reports)
FOREIGN BODY REACTION ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
GAIT SPASTIC ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 4 FDA reports)
GENERAL ANAESTHESIA ( 4 FDA reports)
GINGIVECTOMY ( 4 FDA reports)
GLIOBLASTOMA MULTIFORME ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT ISCHAEMIA ( 4 FDA reports)
GROIN ABSCESS ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HEART VALVE OPERATION ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPATIC ARTERY OCCLUSION ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HERPETIC STOMATITIS ( 4 FDA reports)
HYPERCHROMIC ANAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPERTROPHY ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
ILEOSTOMY ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INSULIN RESISTANT DIABETES ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LAPAROTOMY ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LESION EXCISION ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIP HAEMORRHAGE ( 4 FDA reports)
LIP NEOPLASM BENIGN ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MEDIASTINAL MASS ( 4 FDA reports)
MEDICAL DIET ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METAMORPHOPSIA ( 4 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MONOCYTOSIS ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOCARDIAL STRAIN ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NASAL OBSTRUCTION ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEURODEGENERATIVE DISORDER ( 4 FDA reports)
NEUROGENIC SHOCK ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OESOPHAGEAL PERFORATION ( 4 FDA reports)
OESTROGEN DEFICIENCY ( 4 FDA reports)
OPIATES POSITIVE ( 4 FDA reports)
ORAL PRURITUS ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
ORTHOSIS USER ( 4 FDA reports)
OSTECTOMY ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
OXYGEN SATURATION ABNORMAL ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PAROTIDECTOMY ( 4 FDA reports)
PARVOVIRUS INFECTION ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PENILE OEDEMA ( 4 FDA reports)
PERFORATION BILE DUCT ( 4 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PERIVASCULAR DERMATITIS ( 4 FDA reports)
PHYSICAL ASSAULT ( 4 FDA reports)
PITUITARY ENLARGEMENT ( 4 FDA reports)
PNEUMONITIS CHEMICAL ( 4 FDA reports)
POLYARTERITIS NODOSA ( 4 FDA reports)
POST STROKE DEPRESSION ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 4 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 4 FDA reports)
PSEUDARTHROSIS ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULMONARY CALCIFICATION ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RADICULAR CYST ( 4 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
SCROTAL SWELLING ( 4 FDA reports)
SELF-INDUCED VOMITING ( 4 FDA reports)
SEPTIC PHLEBITIS ( 4 FDA reports)
SHIGELLA INFECTION ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SOMATOFORM DISORDER ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPLEEN PALPABLE ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
STEATORRHOEA ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SUTURE REMOVAL ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TARSAL TUNNEL SYNDROME ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THELITIS ( 4 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 4 FDA reports)
THROMBOSED VARICOSE VEIN ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
TROPONIN ( 4 FDA reports)
TROPONIN I INCREASED ( 4 FDA reports)
UNEMPLOYMENT ( 4 FDA reports)
URTICARIA CHRONIC ( 4 FDA reports)
UTERINE DILATION AND CURETTAGE ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
VAGINAL INFLAMMATION ( 4 FDA reports)
VARICOSE VEIN OPERATION ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
VIROLOGIC FAILURE ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
YERSINIA BACTERAEMIA ( 4 FDA reports)
SKIN GRAFT INFECTION ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SPASTIC DIPLEGIA ( 3 FDA reports)
SPINAL CORD INJURY ( 3 FDA reports)
SPINAL CORD PARALYSIS ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 3 FDA reports)
SPLENIC ABSCESS ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
STENT REMOVAL ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 3 FDA reports)
THYMUS DISORDER ( 3 FDA reports)
THYROID CANCER METASTATIC ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
VAGINAL FISTULA ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASOMOTOR RHINITIS ( 3 FDA reports)
VENA CAVA INJURY ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VENTRICULAR DYSKINESIA ( 3 FDA reports)
VISCERAL PAIN ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
WAGNER'S DISEASE ( 3 FDA reports)
WEIGHT ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
XANTHOPSIA ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ABSCESS BACTERIAL ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
ANASTOMOTIC LEAK ( 3 FDA reports)
ANEURYSM REPAIR ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANTISOCIAL BEHAVIOUR ( 3 FDA reports)
AORTIC BRUIT ( 3 FDA reports)
APICAL GRANULOMA ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BIOPSY BREAST ABNORMAL ( 3 FDA reports)
BIOPSY LIP ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 3 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BREAST RECONSTRUCTION ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHOSPASM PARADOXICAL ( 3 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CALCIPHYLAXIS ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CARDIOLIPIN ANTIBODY ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 3 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL HYPOPERFUSION ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHEST WALL OPERATION ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CIRRHOSIS ALCOHOLIC ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CRANIAL NERVE DISORDER ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 3 FDA reports)
DEJA VU ( 3 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 3 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
DYSPRAXIA ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ELEVATED MOOD ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENCEPHALITIC INFECTION ( 3 FDA reports)
ENDOMETRIAL DISORDER ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPIDIDYMAL DISORDER ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
EPISPADIAS ( 3 FDA reports)
ERYTHROPENIA ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EUSTACHIAN TUBE DISORDER ( 3 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
EXTUBATION ( 3 FDA reports)
EYE INFECTION FUNGAL ( 3 FDA reports)
EYE INFECTION VIRAL ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FEAR OF FALLING ( 3 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 3 FDA reports)
FEMALE STERILISATION ( 3 FDA reports)
FEMORAL HERNIA REPAIR ( 3 FDA reports)
FEMORAL PULSE DECREASED ( 3 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FRACTURE MALUNION ( 3 FDA reports)
FRUCTOSE INTOLERANCE ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GANGLION ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTRIC PH DECREASED ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GLARE ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HEAD AND NECK CANCER ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HELLP SYNDROME ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HEPATITIS B ANTIBODY ( 3 FDA reports)
HILAR LYMPHADENOPATHY ( 3 FDA reports)
HISTAMINE LEVEL INCREASED ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
ILIAC ARTERY THROMBOSIS ( 3 FDA reports)
INCISION SITE ABSCESS ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 3 FDA reports)
INTESTINAL MALROTATION ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 3 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 3 FDA reports)
JAW CYST ( 3 FDA reports)
JOINT ADHESION ( 3 FDA reports)
JOINT LOCK ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 3 FDA reports)
LAGOPHTHALMOS ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LYMPH GLAND INFECTION ( 3 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MACROSOMIA ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MARFAN'S SYNDROME ( 3 FDA reports)
MASTOID DISORDER ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEDICAL DEVICE SITE REACTION ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METASTASES TO EYE ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 3 FDA reports)
METASTASES TO SPLEEN ( 3 FDA reports)
METASTASES TO STOMACH ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYELOID LEUKAEMIA ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEONATAL ASPHYXIA ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROPATHIC ARTHROPATHY ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL NEOPLASM ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
PECTUS CARINATUM ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERINEURIAL CYST ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHARYNGEAL ULCERATION ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POLYHYDRAMNIOS ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PRODUCT FORMULATION ISSUE ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PSEUDODEMENTIA ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY SEQUESTRATION ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RADICULAR PAIN ( 3 FDA reports)
REACTION TO PRESERVATIVES ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL CANCER METASTATIC ( 3 FDA reports)
RENAL CYST HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETROGRADE EJACULATION ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCIATIC NERVE INJURY ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSITISATION ( 3 FDA reports)
SHOULDER ARTHROPLASTY ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINOBRONCHITIS ( 3 FDA reports)
ABDOMINAL EXPLORATION ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACQUIRED PORPHYRIA ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ADNEXA UTERI CYST ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
AEROMONA INFECTION ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANGIOFIBROMA ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANKYLOGLOSSIA ACQUIRED ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARTERIAL SPASM ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPIRATION BIOPSY ( 2 FDA reports)
ATAXIA TELANGIECTASIA ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AUTOIMMUNE ARTHRITIS ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BILE ACID MALABSORPTION ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLADDER CANCER STAGE III ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER NECK SUSPENSION ( 2 FDA reports)
BLADDER PERFORATION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD ARSENIC INCREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CAFFEINE INCREASED ( 2 FDA reports)
BLOOD CALCITONIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CREATINE ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE FORMATION DECREASED ( 2 FDA reports)
BONE MARROW NECROSIS ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CAPILLARITIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID HEART DISEASE ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC IMAGING PROCEDURE NORMAL ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 2 FDA reports)
CAROTID ARTERY STENT INSERTION ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CERVICAL NEURITIS ( 2 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
COGAN'S SYNDROME ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COITAL BLEEDING ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONDYLOMA ACUMINATUM ( 2 FDA reports)
CONGENITAL HIP DEFORMITY ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL OPERATION ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
COW'S MILK INTOLERANCE ( 2 FDA reports)
COXSACKIE VIRUS TEST POSITIVE ( 2 FDA reports)
CRANIAL NEUROPATHY ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATINE URINE ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYCLIC VOMITING SYNDROME ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTIC FIBROSIS LUNG ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE ISSUE ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIAPHRAGMATIC INJURY ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DRUG ADDICT ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER REPAIR ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENTEROBACTER PNEUMONIA ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPIDURAL LIPOMATOSIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FISTULA REPAIR ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FONTANELLE BULGING ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC ILEUS ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL CANDIDIASIS ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
GENITAL INJURY ( 2 FDA reports)
GENITAL SWELLING ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLIOMA ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMOPHILUS SEPSIS ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEAD AND NECK CANCER STAGE III ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC SIDEROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 2 FDA reports)
HYPOPHARYNGEAL NEOPLASM ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INDWELLING CATHETER MANAGEMENT ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE PARAESTHESIA ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INSTILLATION SITE IRRITATION ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERNAL HERNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTUBATION COMPLICATION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER SARCOIDOSIS ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOW TENSION GLAUCOMA ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LUNG INFILTRATION MALIGNANT ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHOCYTOTOXIC ANTIBODY POSITIVE ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT PALATE NEOPLASM ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MEDIASTINAL FIBROSIS ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METATARSUS PRIMUS VARUS ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYCOTIC ALLERGY ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL CAVITY MASS ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESOPHAGOGASTRECTOMY ( 2 FDA reports)
OESTRADIOL DECREASED ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL PETECHIAE ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM ( 2 FDA reports)
OSTEOPETROSIS ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
OXALOSIS ( 2 FDA reports)
PAGET-SCHROETTER SYNDROME ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERFUME SENSITIVITY ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIODONTAL OPERATION ( 2 FDA reports)
PERIORBITAL CELLULITIS ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPROSTHETIC OSTEOLYSIS ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLATELET DESTRUCTION INCREASED ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOCEPHALUS ( 2 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
POST PROCEDURAL SWELLING ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERY ATRESIA ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
PULMONARY MICROEMBOLI ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RADIAL NERVE INJURY ( 2 FDA reports)
RADIATION PROCTOPATHY ( 2 FDA reports)
RAOULTELLA TEST POSITIVE ( 2 FDA reports)
RECTAL SPASM ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFLUX NEPHROPATHY ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY DEPTH DECREASED ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
SALIVARY GLAND OPERATION ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SENSATION OF BLOCK IN EAR ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN WOUND ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SLOW SPEECH ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STICKY SKIN ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STUBBORNNESS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUCROSE INTOLERANCE ( 2 FDA reports)
SUDDEN VISUAL LOSS ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SUPERINFECTION VIRAL ( 2 FDA reports)
SURGICAL VASCULAR SHUNT ( 2 FDA reports)
SWOLLEN TEAR DUCT ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TETANY ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THORACIC HAEMORRHAGE ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRANSVERSE PRESENTATION ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUMOUR LOCAL INVASION ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE PHOSPHATE INCREASED ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
UTERINE MASS ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
SINUS PERFORATION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLE ARTHRITIS ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAG HORN CALCULUS ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE II ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TAKAYASU'S ARTERITIS ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TENDON NECROSIS ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR CYST ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TRIMETHYLAMINURIA ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TYMPANOSCLEROSIS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URETERIC INJURY ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URETHRAL PROLAPSE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CYSTECTOMY ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE BILIRUBIN DECREASED ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE HYPERTONUS ( 1 FDA reports)
UTERINE ISCHAEMIA ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
UTERINE PROLAPSE REPAIR ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
UTEROVAGINAL PROLAPSE ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINISMUS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENOUS LAKE ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VISUAL ACUITY TESTS ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN A DEFICIENCY ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN K INCREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD CYST ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOLIPOMA ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
AMALGAM TATTOO ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE ANAESTHESIA ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOGRAM ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BILE OUTPUT ABNORMAL ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER ADENOCARCINOMA STAGE III ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHAROPACHYNSIS ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HEAVY METAL INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TESTOSTERONE FREE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DENSITOMETRY ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW ISCHAEMIA ( 1 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BOWMAN'S MEMBRANE DISORDER ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CAPSULAR CONTRACTURE ASSOCIATED WITH BREAST IMPLANT ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOROID NEOPLASM ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CITRIC ACID URINE DECREASED ( 1 FDA reports)
CLINICALLY ISOLATED SYNDROME ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON CANCER STAGE 0 ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL EYE NAEVUS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COPPER DEFICIENCY ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
COXSACKIE VIRUS SEROLOGY TEST ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYLINDRURIA ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
DACRYOADENITIS ACQUIRED ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DEPOSIT ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOETOPATHY ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOLICHOCOLON ( 1 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL VARICES ( 1 FDA reports)
DUST INHALATION PNEUMOPATHY ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EGOBRONCHOPHONY ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
EMPYEMA DRAINAGE ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCHONDROMATOSIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC COLITIS ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIPLOIC APPENDAGITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHROID SERIES ABNORMAL ( 1 FDA reports)
ESCHAROTOMY ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXOMPHALOS ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE NAEVUS ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYEGLASSES THERAPY ( 1 FDA reports)
EYELASH DISCOLOURATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMALE SEX HORMONE LEVEL ABNORMAL ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FONTANELLE DEPRESSED ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROSTOMY CLOSURE ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GIANT PAPILLARY CONJUNCTIVITIS ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE III ( 1 FDA reports)
HOFFMANN'S SIGN ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPEROXALAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVITAMINOSIS D ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
ILEAL GANGRENE ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEORECTAL FISTULA ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
IMMINENT ABORTION ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE SCAR ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE PRURITUS ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE JOINT REDNESS ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT RESURFACING SURGERY ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKODERMA ( 1 FDA reports)
LEUKOPLAKIA OESOPHAGEAL ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB PROSTHESIS USER ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MALIGNANT OVARIAN CYST ( 1 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MANGANESE INCREASED ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS ENTEROCOCCAL ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENSTRUATION NORMAL ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROBIOLOGY TEST ABNORMAL ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MINERAL SUPPLEMENTATION ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FLAP OPERATION ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL CANDIDIASIS ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHRITIS HAEMORRHAGIC ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTIPHOBIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
ORTHOSTATIC HEART RATE RESPONSE INCREASED ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN FIBROSIS ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL RESPONSE TO NORMAL STIMULI ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARASITIC TEST POSITIVE ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE PROSTHESIS INSERTION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE VASCULAR DISORDER ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERINEAL INFECTION ( 1 FDA reports)
PERIORBITAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL EXUDATE ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLANTAR FASCIAL FIBROMATOSIS ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL HEADACHE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT EXPIRATION DATE ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDODIVERTICULAR DISEASE ( 1 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYELOPLASTY ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL MICROANEURYSMS ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINOPATHY SICKLE CELL ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
REVISION OF INTERNAL FIXATION ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEBACEOUS NAEVUS ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SELECTIVE IGM IMMUNODEFICIENCY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSORY LEVEL ABNORMAL ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use