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

NAUSEA ( 805 FDA reports)
PAIN ( 768 FDA reports)
MYOCARDIAL INFARCTION ( 724 FDA reports)
ANXIETY ( 708 FDA reports)
DIZZINESS ( 700 FDA reports)
DYSPNOEA ( 696 FDA reports)
FATIGUE ( 660 FDA reports)
CHEST PAIN ( 648 FDA reports)
ASTHENIA ( 589 FDA reports)
PAIN IN EXTREMITY ( 586 FDA reports)
MYALGIA ( 527 FDA reports)
HYPERTENSION ( 525 FDA reports)
CORONARY ARTERY DISEASE ( 517 FDA reports)
FALL ( 517 FDA reports)
DEPRESSION ( 507 FDA reports)
ARTHRALGIA ( 500 FDA reports)
DRUG INEFFECTIVE ( 490 FDA reports)
DIARRHOEA ( 480 FDA reports)
OEDEMA PERIPHERAL ( 480 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 474 FDA reports)
BACK PAIN ( 454 FDA reports)
HEADACHE ( 440 FDA reports)
CEREBROVASCULAR ACCIDENT ( 432 FDA reports)
INJURY ( 431 FDA reports)
VOMITING ( 407 FDA reports)
ANAEMIA ( 401 FDA reports)
WEIGHT DECREASED ( 372 FDA reports)
RENAL FAILURE ( 358 FDA reports)
PNEUMONIA ( 349 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 344 FDA reports)
INSOMNIA ( 335 FDA reports)
ABDOMINAL PAIN ( 333 FDA reports)
HYPOTENSION ( 318 FDA reports)
PYREXIA ( 310 FDA reports)
EMOTIONAL DISTRESS ( 300 FDA reports)
HYPOAESTHESIA ( 298 FDA reports)
CONSTIPATION ( 295 FDA reports)
MUSCLE SPASMS ( 289 FDA reports)
OSTEOARTHRITIS ( 289 FDA reports)
DEATH ( 286 FDA reports)
BLOOD GLUCOSE INCREASED ( 280 FDA reports)
URINARY TRACT INFECTION ( 277 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 270 FDA reports)
ATRIAL FIBRILLATION ( 269 FDA reports)
WEIGHT INCREASED ( 265 FDA reports)
COUGH ( 263 FDA reports)
DEHYDRATION ( 259 FDA reports)
MALAISE ( 258 FDA reports)
RENAL FAILURE ACUTE ( 240 FDA reports)
NEUROPATHY PERIPHERAL ( 238 FDA reports)
RASH ( 231 FDA reports)
ANHEDONIA ( 230 FDA reports)
CELLULITIS ( 227 FDA reports)
GAIT DISTURBANCE ( 224 FDA reports)
PARAESTHESIA ( 221 FDA reports)
HYPERLIPIDAEMIA ( 220 FDA reports)
DIABETES MELLITUS ( 219 FDA reports)
ANGINA PECTORIS ( 218 FDA reports)
BLOOD PRESSURE INCREASED ( 218 FDA reports)
CARDIAC DISORDER ( 218 FDA reports)
BONE DISORDER ( 215 FDA reports)
PLEURAL EFFUSION ( 215 FDA reports)
CONFUSIONAL STATE ( 208 FDA reports)
DYSPEPSIA ( 206 FDA reports)
FEELING ABNORMAL ( 204 FDA reports)
SPINAL OSTEOARTHRITIS ( 201 FDA reports)
MUSCULAR WEAKNESS ( 194 FDA reports)
PRURITUS ( 193 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 190 FDA reports)
PALPITATIONS ( 188 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 188 FDA reports)
ABDOMINAL PAIN UPPER ( 186 FDA reports)
OSTEONECROSIS OF JAW ( 186 FDA reports)
DECREASED APPETITE ( 185 FDA reports)
SYNCOPE ( 184 FDA reports)
ROTATOR CUFF SYNDROME ( 181 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 179 FDA reports)
MITRAL VALVE INCOMPETENCE ( 179 FDA reports)
SOMNOLENCE ( 176 FDA reports)
CONDITION AGGRAVATED ( 175 FDA reports)
LOSS OF CONSCIOUSNESS ( 173 FDA reports)
PAIN IN JAW ( 170 FDA reports)
CONVULSION ( 168 FDA reports)
OSTEOMYELITIS ( 168 FDA reports)
OSTEOPOROSIS ( 168 FDA reports)
TREMOR ( 167 FDA reports)
VISION BLURRED ( 163 FDA reports)
DRY MOUTH ( 161 FDA reports)
DYSPHAGIA ( 161 FDA reports)
CONTUSION ( 159 FDA reports)
HYPERHIDROSIS ( 159 FDA reports)
SINUSITIS ( 159 FDA reports)
CATARACT ( 153 FDA reports)
GASTRITIS ( 153 FDA reports)
BRONCHITIS ( 152 FDA reports)
ARTHRITIS ( 149 FDA reports)
ERYTHEMA ( 149 FDA reports)
HAEMOGLOBIN DECREASED ( 149 FDA reports)
BLOOD CREATININE INCREASED ( 148 FDA reports)
OSTEOPENIA ( 147 FDA reports)
ABDOMINAL DISTENSION ( 146 FDA reports)
ASTHMA ( 145 FDA reports)
BRADYCARDIA ( 145 FDA reports)
UNEVALUABLE EVENT ( 144 FDA reports)
HIATUS HERNIA ( 143 FDA reports)
MUSCULOSKELETAL PAIN ( 143 FDA reports)
DEEP VEIN THROMBOSIS ( 141 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 141 FDA reports)
AMNESIA ( 140 FDA reports)
CHEST DISCOMFORT ( 140 FDA reports)
HYPERCHOLESTEROLAEMIA ( 140 FDA reports)
OSTEONECROSIS ( 140 FDA reports)
OEDEMA ( 137 FDA reports)
SWELLING FACE ( 134 FDA reports)
HAEMORRHOIDS ( 133 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 133 FDA reports)
ATELECTASIS ( 132 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 130 FDA reports)
FLUSHING ( 127 FDA reports)
SWELLING ( 126 FDA reports)
HEART RATE INCREASED ( 125 FDA reports)
STRESS ( 125 FDA reports)
CHILLS ( 122 FDA reports)
NECK PAIN ( 121 FDA reports)
SEPSIS ( 121 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 120 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 119 FDA reports)
INFECTION ( 119 FDA reports)
MYOCARDIAL ISCHAEMIA ( 119 FDA reports)
VERTIGO ( 119 FDA reports)
ALOPECIA ( 117 FDA reports)
BURSITIS ( 116 FDA reports)
RECTAL HAEMORRHAGE ( 116 FDA reports)
CORONARY ARTERY OCCLUSION ( 115 FDA reports)
RENAL IMPAIRMENT ( 115 FDA reports)
DYSPHONIA ( 113 FDA reports)
POLLAKIURIA ( 112 FDA reports)
BONE PAIN ( 111 FDA reports)
HYPERGLYCAEMIA ( 111 FDA reports)
MEMORY IMPAIRMENT ( 110 FDA reports)
PANCREATITIS ( 110 FDA reports)
RESPIRATORY FAILURE ( 110 FDA reports)
THROMBOCYTOPENIA ( 110 FDA reports)
ARRHYTHMIA ( 109 FDA reports)
CHOLELITHIASIS ( 109 FDA reports)
DYSPNOEA EXERTIONAL ( 109 FDA reports)
BALANCE DISORDER ( 108 FDA reports)
FEAR ( 108 FDA reports)
HYPERSENSITIVITY ( 108 FDA reports)
MENTAL STATUS CHANGES ( 108 FDA reports)
TOOTH EXTRACTION ( 108 FDA reports)
ANGINA UNSTABLE ( 106 FDA reports)
TOOTH DISORDER ( 106 FDA reports)
SCAR ( 105 FDA reports)
DENTAL CARIES ( 104 FDA reports)
PULMONARY EMBOLISM ( 103 FDA reports)
CARDIOMEGALY ( 102 FDA reports)
DIVERTICULUM ( 102 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 101 FDA reports)
HYPOKALAEMIA ( 101 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 101 FDA reports)
RENAL FAILURE CHRONIC ( 101 FDA reports)
SLEEP APNOEA SYNDROME ( 101 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 99 FDA reports)
CARDIAC ARREST ( 99 FDA reports)
RENAL DISORDER ( 99 FDA reports)
DYSARTHRIA ( 98 FDA reports)
FOOT FRACTURE ( 98 FDA reports)
HERPES ZOSTER ( 98 FDA reports)
LETHARGY ( 98 FDA reports)
ARTERIOSCLEROSIS ( 97 FDA reports)
DYSGEUSIA ( 97 FDA reports)
STOMATITIS ( 97 FDA reports)
ARTHROPATHY ( 96 FDA reports)
RENAL INJURY ( 96 FDA reports)
DRUG HYPERSENSITIVITY ( 95 FDA reports)
HEART RATE IRREGULAR ( 95 FDA reports)
LUMBAR SPINAL STENOSIS ( 95 FDA reports)
LUNG DISORDER ( 95 FDA reports)
ADVERSE EVENT ( 94 FDA reports)
CARDIAC MURMUR ( 94 FDA reports)
INFLUENZA ( 94 FDA reports)
NASAL CONGESTION ( 94 FDA reports)
BURNING SENSATION ( 93 FDA reports)
TYPE 2 DIABETES MELLITUS ( 93 FDA reports)
HEPATIC ENZYME INCREASED ( 92 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 92 FDA reports)
NERVOUSNESS ( 92 FDA reports)
OSTEOLYSIS ( 92 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 91 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 90 FDA reports)
BLOOD GLUCOSE DECREASED ( 89 FDA reports)
DRUG INTERACTION ( 89 FDA reports)
EXOSTOSIS ( 89 FDA reports)
GINGIVITIS ( 89 FDA reports)
JOINT SWELLING ( 89 FDA reports)
HAEMATOCRIT DECREASED ( 88 FDA reports)
NEPHROLITHIASIS ( 88 FDA reports)
CARPAL TUNNEL SYNDROME ( 87 FDA reports)
ERECTILE DYSFUNCTION ( 87 FDA reports)
PULMONARY OEDEMA ( 87 FDA reports)
PULMONARY HYPERTENSION ( 86 FDA reports)
SLEEP DISORDER ( 86 FDA reports)
BLOOD PRESSURE DECREASED ( 85 FDA reports)
RHINITIS ALLERGIC ( 85 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 84 FDA reports)
ECONOMIC PROBLEM ( 83 FDA reports)
THROMBOSIS ( 83 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 82 FDA reports)
HYPONATRAEMIA ( 82 FDA reports)
CARDIAC FAILURE ( 81 FDA reports)
NASOPHARYNGITIS ( 81 FDA reports)
BREAST CANCER ( 80 FDA reports)
FACIAL PAIN ( 80 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 80 FDA reports)
TACHYCARDIA ( 80 FDA reports)
TINNITUS ( 80 FDA reports)
TOOTH ABSCESS ( 80 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 79 FDA reports)
BLOOD UREA INCREASED ( 79 FDA reports)
ANOREXIA ( 78 FDA reports)
RIB FRACTURE ( 78 FDA reports)
GINGIVAL BLEEDING ( 77 FDA reports)
NEUTROPENIA ( 77 FDA reports)
MULTIPLE MYELOMA ( 76 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 76 FDA reports)
EMPHYSEMA ( 75 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 75 FDA reports)
HAEMORRHAGE ( 75 FDA reports)
URINARY INCONTINENCE ( 75 FDA reports)
HAEMATURIA ( 74 FDA reports)
MOUTH ULCERATION ( 74 FDA reports)
RHABDOMYOLYSIS ( 74 FDA reports)
TOOTHACHE ( 74 FDA reports)
CARDIOMYOPATHY ( 73 FDA reports)
FEELING HOT ( 73 FDA reports)
HUMERUS FRACTURE ( 73 FDA reports)
HYPOGLYCAEMIA ( 73 FDA reports)
OVERDOSE ( 73 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 72 FDA reports)
FEMUR FRACTURE ( 72 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 72 FDA reports)
FOOT DEFORMITY ( 71 FDA reports)
PANCYTOPENIA ( 71 FDA reports)
SKIN EXFOLIATION ( 71 FDA reports)
URTICARIA ( 71 FDA reports)
HYPOPHAGIA ( 70 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 70 FDA reports)
OESOPHAGITIS ( 70 FDA reports)
ROAD TRAFFIC ACCIDENT ( 70 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 70 FDA reports)
LUNG NEOPLASM ( 69 FDA reports)
SINUS BRADYCARDIA ( 69 FDA reports)
AGITATION ( 68 FDA reports)
CARDIOVASCULAR DISORDER ( 68 FDA reports)
FLATULENCE ( 68 FDA reports)
MOBILITY DECREASED ( 68 FDA reports)
WHEEZING ( 68 FDA reports)
EPISTAXIS ( 67 FDA reports)
SPEECH DISORDER ( 67 FDA reports)
DEFORMITY ( 66 FDA reports)
DIVERTICULITIS ( 66 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 66 FDA reports)
RENAL CYST ( 66 FDA reports)
MULTI-ORGAN FAILURE ( 65 FDA reports)
MULTIPLE INJURIES ( 65 FDA reports)
PERIODONTITIS ( 65 FDA reports)
RASH PRURITIC ( 65 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 65 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 64 FDA reports)
GENERALISED OEDEMA ( 64 FDA reports)
GOUT ( 64 FDA reports)
PULPITIS DENTAL ( 64 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 63 FDA reports)
HAEMOPTYSIS ( 63 FDA reports)
HYPOXIA ( 63 FDA reports)
VISUAL ACUITY REDUCED ( 63 FDA reports)
DIVERTICULUM INTESTINAL ( 62 FDA reports)
GROIN PAIN ( 62 FDA reports)
MEDICATION ERROR ( 62 FDA reports)
NEOPLASM MALIGNANT ( 62 FDA reports)
SURGERY ( 62 FDA reports)
OBESITY ( 61 FDA reports)
PERIODONTAL DISEASE ( 61 FDA reports)
SPINAL COLUMN STENOSIS ( 61 FDA reports)
CAROTID ARTERY STENOSIS ( 60 FDA reports)
DISORIENTATION ( 60 FDA reports)
DYSURIA ( 60 FDA reports)
IMPAIRED HEALING ( 60 FDA reports)
SUICIDAL IDEATION ( 60 FDA reports)
ACUTE SINUSITIS ( 59 FDA reports)
ESCHERICHIA INFECTION ( 59 FDA reports)
FLUID RETENTION ( 59 FDA reports)
LEUKOCYTOSIS ( 59 FDA reports)
PLATELET COUNT DECREASED ( 59 FDA reports)
URINARY RETENTION ( 59 FDA reports)
VENTRICULAR TACHYCARDIA ( 59 FDA reports)
ABDOMINAL DISCOMFORT ( 58 FDA reports)
HAEMATOMA ( 58 FDA reports)
HYPOTHYROIDISM ( 58 FDA reports)
SKIN TIGHTNESS ( 58 FDA reports)
TREATMENT NONCOMPLIANCE ( 58 FDA reports)
VIRAL INFECTION ( 58 FDA reports)
BONE DEBRIDEMENT ( 57 FDA reports)
DRY SKIN ( 57 FDA reports)
HALLUCINATION ( 57 FDA reports)
LEUKOPENIA ( 57 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 57 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 56 FDA reports)
GINGIVAL PAIN ( 56 FDA reports)
HIP FRACTURE ( 56 FDA reports)
SPLENOMEGALY ( 56 FDA reports)
COLONIC POLYP ( 55 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 55 FDA reports)
FIBROSIS ( 55 FDA reports)
HAEMATOCHEZIA ( 55 FDA reports)
HOT FLUSH ( 55 FDA reports)
INJECTION SITE PAIN ( 55 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 55 FDA reports)
LACERATION ( 55 FDA reports)
UTERINE LEIOMYOMA ( 55 FDA reports)
DYSKINESIA ( 54 FDA reports)
ILL-DEFINED DISORDER ( 54 FDA reports)
RASH GENERALISED ( 54 FDA reports)
SKIN INDURATION ( 54 FDA reports)
ULCER ( 54 FDA reports)
ACUTE CORONARY SYNDROME ( 53 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 53 FDA reports)
GASTRIC ULCER ( 53 FDA reports)
INFLUENZA LIKE ILLNESS ( 53 FDA reports)
TENDONITIS ( 53 FDA reports)
VISUAL DISTURBANCE ( 53 FDA reports)
ABASIA ( 52 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 52 FDA reports)
AORTIC VALVE INCOMPETENCE ( 52 FDA reports)
CORONARY ARTERY STENOSIS ( 52 FDA reports)
JOINT STIFFNESS ( 52 FDA reports)
RESPIRATORY DISTRESS ( 52 FDA reports)
ABDOMINAL PAIN LOWER ( 51 FDA reports)
BONE EROSION ( 51 FDA reports)
GINGIVAL INFECTION ( 51 FDA reports)
GOITRE ( 51 FDA reports)
INTERSTITIAL LUNG DISEASE ( 51 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 51 FDA reports)
NOCTURIA ( 51 FDA reports)
OROPHARYNGEAL PAIN ( 51 FDA reports)
PRESYNCOPE ( 51 FDA reports)
SEDATION ( 51 FDA reports)
STOMACH DISCOMFORT ( 51 FDA reports)
VITREOUS DETACHMENT ( 51 FDA reports)
BLINDNESS ( 50 FDA reports)
DIPLOPIA ( 50 FDA reports)
GLAUCOMA ( 50 FDA reports)
HYPERKALAEMIA ( 50 FDA reports)
INJECTION SITE HAEMORRHAGE ( 50 FDA reports)
IRON DEFICIENCY ANAEMIA ( 50 FDA reports)
IRRITABILITY ( 50 FDA reports)
LIMB INJURY ( 50 FDA reports)
OSTEITIS DEFORMANS ( 50 FDA reports)
PELVIC FRACTURE ( 50 FDA reports)
RADICULOPATHY ( 50 FDA reports)
SKIN DISCOLOURATION ( 50 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 49 FDA reports)
DISTURBANCE IN ATTENTION ( 49 FDA reports)
JOINT DISLOCATION ( 49 FDA reports)
PANCREATITIS ACUTE ( 49 FDA reports)
CYSTITIS ( 48 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 48 FDA reports)
ENTEROCOCCAL INFECTION ( 48 FDA reports)
HAEMANGIOMA ( 48 FDA reports)
OSTEITIS ( 48 FDA reports)
PULMONARY FIBROSIS ( 48 FDA reports)
SKIN HYPERTROPHY ( 48 FDA reports)
VASCULITIS ( 48 FDA reports)
ANGIOPATHY ( 47 FDA reports)
CEREBRAL ATROPHY ( 47 FDA reports)
COLITIS ULCERATIVE ( 47 FDA reports)
FAECES DISCOLOURED ( 47 FDA reports)
GINGIVAL SWELLING ( 47 FDA reports)
JAW DISORDER ( 47 FDA reports)
RHINORRHOEA ( 47 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 46 FDA reports)
CEREBRAL INFARCTION ( 46 FDA reports)
DEVICE FAILURE ( 46 FDA reports)
EAR PAIN ( 46 FDA reports)
LUNG NEOPLASM MALIGNANT ( 46 FDA reports)
ORAL CANDIDIASIS ( 46 FDA reports)
SPINAL COMPRESSION FRACTURE ( 46 FDA reports)
DIABETIC NEUROPATHY ( 45 FDA reports)
DISCOMFORT ( 45 FDA reports)
EJECTION FRACTION DECREASED ( 45 FDA reports)
ENTERITIS ( 45 FDA reports)
GINGIVAL DISORDER ( 45 FDA reports)
MYOPATHY ( 45 FDA reports)
OLIGURIA ( 45 FDA reports)
PEPTIC ULCER ( 45 FDA reports)
PLATELET COUNT INCREASED ( 45 FDA reports)
SKIN ULCER ( 45 FDA reports)
VENTRICULAR HYPERTROPHY ( 45 FDA reports)
BODY HEIGHT DECREASED ( 44 FDA reports)
FACIAL NEURALGIA ( 44 FDA reports)
GASTROINTESTINAL DISORDER ( 44 FDA reports)
SINUS TACHYCARDIA ( 44 FDA reports)
WALKING AID USER ( 44 FDA reports)
BLOOD SODIUM DECREASED ( 43 FDA reports)
CARDIO-RESPIRATORY ARREST ( 43 FDA reports)
CHRONIC SINUSITIS ( 43 FDA reports)
ENDODONTIC PROCEDURE ( 43 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 43 FDA reports)
METASTATIC NEOPLASM ( 43 FDA reports)
STAPHYLOCOCCAL INFECTION ( 43 FDA reports)
APPENDICITIS ( 42 FDA reports)
BLOOD URINE PRESENT ( 42 FDA reports)
BONE FRAGMENTATION ( 42 FDA reports)
BRONCHOPNEUMONIA ( 42 FDA reports)
GASTRIC DISORDER ( 42 FDA reports)
LYMPHADENOPATHY ( 42 FDA reports)
MALOCCLUSION ( 42 FDA reports)
MASS ( 42 FDA reports)
MUSCLE CRAMP ( 42 FDA reports)
SCLERODERMA ( 42 FDA reports)
SCOLIOSIS ( 42 FDA reports)
STRESS FRACTURE ( 42 FDA reports)
TOOTH LOSS ( 42 FDA reports)
WEGENER'S GRANULOMATOSIS ( 42 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 42 FDA reports)
APTYALISM ( 41 FDA reports)
BLOOD POTASSIUM DECREASED ( 41 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 41 FDA reports)
FAECAL INCONTINENCE ( 41 FDA reports)
GALLBLADDER DISORDER ( 41 FDA reports)
HEPATITIS ( 41 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 41 FDA reports)
PHYSICAL DISABILITY ( 41 FDA reports)
POOR DENTAL CONDITION ( 41 FDA reports)
SKIN LESION ( 41 FDA reports)
THROMBOCYTOSIS ( 41 FDA reports)
TOOTH FRACTURE ( 41 FDA reports)
TOOTH INJURY ( 41 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 41 FDA reports)
ABSCESS ( 40 FDA reports)
BASAL CELL CARCINOMA ( 40 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 40 FDA reports)
CERVICAL SPINAL STENOSIS ( 40 FDA reports)
DIFFICULTY IN WALKING ( 40 FDA reports)
DRUG EFFECT DECREASED ( 40 FDA reports)
ISCHAEMIA ( 40 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 40 FDA reports)
LOW TURNOVER OSTEOPATHY ( 40 FDA reports)
MELAENA ( 40 FDA reports)
MUSCLE STRAIN ( 40 FDA reports)
OTITIS EXTERNA ( 40 FDA reports)
SCAB ( 40 FDA reports)
SEBORRHOEIC KERATOSIS ( 40 FDA reports)
VENTRICULAR DYSFUNCTION ( 40 FDA reports)
AGGRESSION ( 39 FDA reports)
APPENDICECTOMY ( 39 FDA reports)
DISABILITY ( 39 FDA reports)
EXCORIATION ( 39 FDA reports)
FEELING JITTERY ( 39 FDA reports)
MAJOR DEPRESSION ( 39 FDA reports)
MIGRAINE ( 39 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 39 FDA reports)
PRODUCTIVE COUGH ( 39 FDA reports)
RASH ERYTHEMATOUS ( 39 FDA reports)
RESTLESS LEGS SYNDROME ( 39 FDA reports)
SKIN HYPERPIGMENTATION ( 39 FDA reports)
BONE OPERATION ( 38 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 38 FDA reports)
DEPRESSED MOOD ( 38 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 38 FDA reports)
DRY EYE ( 38 FDA reports)
EYE DISORDER ( 38 FDA reports)
HAEMATEMESIS ( 38 FDA reports)
HYPOVOLAEMIA ( 38 FDA reports)
MENISCUS LESION ( 38 FDA reports)
MOOD SWINGS ( 38 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 38 FDA reports)
NODULE ( 38 FDA reports)
RESPIRATORY DISORDER ( 38 FDA reports)
BONE DENSITY DECREASED ( 37 FDA reports)
CYST ( 37 FDA reports)
DEVICE MALFUNCTION ( 37 FDA reports)
HEART RATE DECREASED ( 37 FDA reports)
INCORRECT DOSE ADMINISTERED ( 37 FDA reports)
MENTAL DISORDER ( 37 FDA reports)
PROTHROMBIN TIME PROLONGED ( 37 FDA reports)
RHEUMATOID ARTHRITIS ( 37 FDA reports)
ABNORMAL DREAMS ( 36 FDA reports)
BACK DISORDER ( 36 FDA reports)
BLOOD CALCIUM DECREASED ( 36 FDA reports)
CEREBRAL ISCHAEMIA ( 36 FDA reports)
ECZEMA ( 36 FDA reports)
FIBROMYALGIA ( 36 FDA reports)
FISTULA ( 36 FDA reports)
HEPATIC STEATOSIS ( 36 FDA reports)
MIDDLE INSOMNIA ( 36 FDA reports)
OFF LABEL USE ( 36 FDA reports)
SCIATICA ( 36 FDA reports)
SPONDYLOLISTHESIS ( 36 FDA reports)
BLISTER ( 35 FDA reports)
BREAST CANCER FEMALE ( 35 FDA reports)
CEREBROVASCULAR DISORDER ( 35 FDA reports)
DENTAL OPERATION ( 35 FDA reports)
DISEASE PROGRESSION ( 35 FDA reports)
DRUG DOSE OMISSION ( 35 FDA reports)
DYSLIPIDAEMIA ( 35 FDA reports)
INFLAMMATION ( 35 FDA reports)
IRRITABLE BOWEL SYNDROME ( 35 FDA reports)
JOINT INJURY ( 35 FDA reports)
LIMB DISCOMFORT ( 35 FDA reports)
PERIPHERAL COLDNESS ( 35 FDA reports)
TENDON RUPTURE ( 35 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 35 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 34 FDA reports)
FLUID OVERLOAD ( 34 FDA reports)
HEAD INJURY ( 34 FDA reports)
LUMBAR RADICULOPATHY ( 34 FDA reports)
LUNG INFILTRATION ( 34 FDA reports)
METABOLIC ACIDOSIS ( 34 FDA reports)
METASTASES TO BONE ( 34 FDA reports)
OXYGEN SATURATION DECREASED ( 34 FDA reports)
PERICARDIAL EFFUSION ( 34 FDA reports)
PNEUMONITIS ( 34 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 34 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 34 FDA reports)
SJOGREN'S SYNDROME ( 34 FDA reports)
ACTINIC KERATOSIS ( 33 FDA reports)
ATRIAL FLUTTER ( 33 FDA reports)
BONE LOSS ( 33 FDA reports)
DERMATITIS CONTACT ( 33 FDA reports)
DIASTOLIC DYSFUNCTION ( 33 FDA reports)
EYE LASER SURGERY ( 33 FDA reports)
GASTROENTERITIS ( 33 FDA reports)
LOWER LIMB FRACTURE ( 33 FDA reports)
ORTHOSTATIC HYPOTENSION ( 33 FDA reports)
PANIC ATTACK ( 33 FDA reports)
POST PROCEDURAL COMPLICATION ( 33 FDA reports)
PROSTATE CANCER ( 33 FDA reports)
SWOLLEN TONGUE ( 33 FDA reports)
ADVERSE DRUG REACTION ( 32 FDA reports)
DRUG INTOLERANCE ( 32 FDA reports)
INGUINAL HERNIA ( 32 FDA reports)
METASTASES TO SPINE ( 32 FDA reports)
MUCOSAL INFLAMMATION ( 32 FDA reports)
NERVOUS SYSTEM DISORDER ( 32 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 32 FDA reports)
RENAL PAIN ( 32 FDA reports)
RESPIRATORY RATE INCREASED ( 32 FDA reports)
SHOULDER PAIN ( 32 FDA reports)
SPINAL DISORDER ( 32 FDA reports)
THROAT TIGHTNESS ( 32 FDA reports)
THYROID NEOPLASM ( 32 FDA reports)
COAGULOPATHY ( 31 FDA reports)
DEAFNESS ( 31 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 31 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 31 FDA reports)
HEPATIC FAILURE ( 31 FDA reports)
HYPERTENSIVE HEART DISEASE ( 31 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 31 FDA reports)
SCAN BONE MARROW ABNORMAL ( 31 FDA reports)
SUICIDE ATTEMPT ( 31 FDA reports)
VITREOUS HAEMORRHAGE ( 31 FDA reports)
ANGER ( 30 FDA reports)
COLITIS ( 30 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 30 FDA reports)
DIABETIC RETINOPATHY ( 30 FDA reports)
DYSSTASIA ( 30 FDA reports)
EMOTIONAL DISORDER ( 30 FDA reports)
EYE HAEMORRHAGE ( 30 FDA reports)
HERNIA ( 30 FDA reports)
INJECTION SITE ERYTHEMA ( 30 FDA reports)
MUSCLE ATROPHY ( 30 FDA reports)
NECK INJURY ( 30 FDA reports)
NEUROPATHY ( 30 FDA reports)
ORAL PAIN ( 30 FDA reports)
PNEUMOTHORAX ( 30 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 30 FDA reports)
TOOTH INFECTION ( 30 FDA reports)
BONE LESION ( 29 FDA reports)
COGNITIVE DISORDER ( 29 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 29 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 29 FDA reports)
EYE PAIN ( 29 FDA reports)
FLANK PAIN ( 29 FDA reports)
HEARING IMPAIRED ( 29 FDA reports)
HEMIPARESIS ( 29 FDA reports)
INJECTION SITE HAEMATOMA ( 29 FDA reports)
JOINT SPRAIN ( 29 FDA reports)
MACULAR DEGENERATION ( 29 FDA reports)
MALNUTRITION ( 29 FDA reports)
NEURALGIA ( 29 FDA reports)
NIGHTMARE ( 29 FDA reports)
RENAL TUBULAR NECROSIS ( 29 FDA reports)
TOOTH IMPACTED ( 29 FDA reports)
UPPER LIMB FRACTURE ( 29 FDA reports)
APHASIA ( 28 FDA reports)
ATAXIA ( 28 FDA reports)
BLOOD BILIRUBIN INCREASED ( 28 FDA reports)
DECREASED INTEREST ( 28 FDA reports)
DEMENTIA ( 28 FDA reports)
DENTURE WEARER ( 28 FDA reports)
INCREASED TENDENCY TO BRUISE ( 28 FDA reports)
JOINT EFFUSION ( 28 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 28 FDA reports)
NEPHROPATHY ( 28 FDA reports)
PLASMACYTOMA ( 28 FDA reports)
SKIN FIBROSIS ( 28 FDA reports)
SPINAL FRACTURE ( 28 FDA reports)
DERMATITIS ( 27 FDA reports)
DRUG TOXICITY ( 27 FDA reports)
ESSENTIAL HYPERTENSION ( 27 FDA reports)
FRACTURED SACRUM ( 27 FDA reports)
FUNGAL INFECTION ( 27 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 27 FDA reports)
INCREASED APPETITE ( 27 FDA reports)
MELANOCYTIC NAEVUS ( 27 FDA reports)
MYELODYSPLASTIC SYNDROME ( 27 FDA reports)
PNEUMONIA ASPIRATION ( 27 FDA reports)
REFLUX OESOPHAGITIS ( 27 FDA reports)
RESPIRATORY ARREST ( 27 FDA reports)
SENSORY LOSS ( 27 FDA reports)
SKIN PLAQUE ( 27 FDA reports)
TENDON DISORDER ( 27 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 27 FDA reports)
COLD SWEAT ( 26 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 26 FDA reports)
DIABETIC KETOACIDOSIS ( 26 FDA reports)
FRACTURE ( 26 FDA reports)
GINGIVAL HYPERPLASIA ( 26 FDA reports)
GLOSSODYNIA ( 26 FDA reports)
HEART INJURY ( 26 FDA reports)
HYPERCALCAEMIA ( 26 FDA reports)
LIFE EXPECTANCY SHORTENED ( 26 FDA reports)
ORAL HERPES ( 26 FDA reports)
PAIN OF SKIN ( 26 FDA reports)
PLEURAL FIBROSIS ( 26 FDA reports)
RETCHING ( 26 FDA reports)
SKIN LACERATION ( 26 FDA reports)
URINARY TRACT DISORDER ( 26 FDA reports)
ACUTE RESPIRATORY FAILURE ( 25 FDA reports)
BRONCHITIS ACUTE ( 25 FDA reports)
CAROTID ARTERY OCCLUSION ( 25 FDA reports)
COMA ( 25 FDA reports)
DRUG DEPENDENCE ( 25 FDA reports)
ERUCTATION ( 25 FDA reports)
JAUNDICE ( 25 FDA reports)
LIPIDS INCREASED ( 25 FDA reports)
LIPOMA ( 25 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 25 FDA reports)
MICTURITION URGENCY ( 25 FDA reports)
MOVEMENT DISORDER ( 25 FDA reports)
OCULAR HYPERAEMIA ( 25 FDA reports)
POLYP ( 25 FDA reports)
RETINAL HAEMORRHAGE ( 25 FDA reports)
RHINITIS ( 25 FDA reports)
SHOCK ( 25 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 25 FDA reports)
THINKING ABNORMAL ( 25 FDA reports)
TIBIA FRACTURE ( 25 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
ANEURYSM ( 24 FDA reports)
BLINDNESS UNILATERAL ( 24 FDA reports)
CARDIAC VALVE DISEASE ( 24 FDA reports)
COORDINATION ABNORMAL ( 24 FDA reports)
DEAFNESS NEUROSENSORY ( 24 FDA reports)
GASTROENTERITIS VIRAL ( 24 FDA reports)
INNER EAR DISORDER ( 24 FDA reports)
INTERMITTENT CLAUDICATION ( 24 FDA reports)
LEFT ATRIAL DILATATION ( 24 FDA reports)
LOCALISED INFECTION ( 24 FDA reports)
MUCOSAL DRYNESS ( 24 FDA reports)
NON-CARDIAC CHEST PAIN ( 24 FDA reports)
PARANOIA ( 24 FDA reports)
PSORIASIS ( 24 FDA reports)
RADICULAR PAIN ( 24 FDA reports)
SKIN BURNING SENSATION ( 24 FDA reports)
SKIN DISORDER ( 24 FDA reports)
TENDERNESS ( 24 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 24 FDA reports)
AGEUSIA ( 23 FDA reports)
BACTERIAL INFECTION ( 23 FDA reports)
CHOLECYSTITIS ( 23 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 23 FDA reports)
CORONARY ARTERY BYPASS ( 23 FDA reports)
GASTRODUODENITIS ( 23 FDA reports)
GINGIVAL RECESSION ( 23 FDA reports)
HYDRONEPHROSIS ( 23 FDA reports)
LABORATORY TEST ABNORMAL ( 23 FDA reports)
LUNG INFECTION ( 23 FDA reports)
MASTICATION DISORDER ( 23 FDA reports)
NEUROMA ( 23 FDA reports)
QUALITY OF LIFE DECREASED ( 23 FDA reports)
RESTLESSNESS ( 23 FDA reports)
SKIN CANCER ( 23 FDA reports)
SPINAL CORD COMPRESSION ( 23 FDA reports)
STENT PLACEMENT ( 23 FDA reports)
TENOSYNOVITIS ( 23 FDA reports)
THYROID DISORDER ( 23 FDA reports)
TRIGGER FINGER ( 23 FDA reports)
UNRESPONSIVE TO STIMULI ( 23 FDA reports)
WRIST FRACTURE ( 23 FDA reports)
ANAEMIA POSTOPERATIVE ( 22 FDA reports)
ANGIOEDEMA ( 22 FDA reports)
AORTIC ANEURYSM ( 22 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 22 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 22 FDA reports)
CHEST WALL PAIN ( 22 FDA reports)
COMPRESSION FRACTURE ( 22 FDA reports)
DRUG ADMINISTRATION ERROR ( 22 FDA reports)
EYE DISCHARGE ( 22 FDA reports)
FEELING COLD ( 22 FDA reports)
GINGIVAL OEDEMA ( 22 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 22 FDA reports)
HYPERSOMNIA ( 22 FDA reports)
INJECTION SITE REACTION ( 22 FDA reports)
LIVER DISORDER ( 22 FDA reports)
LOBAR PNEUMONIA ( 22 FDA reports)
PALLOR ( 22 FDA reports)
PATHOLOGICAL FRACTURE ( 22 FDA reports)
PRODUCT QUALITY ISSUE ( 22 FDA reports)
STRESS INCONTINENCE ( 22 FDA reports)
TACHYPNOEA ( 22 FDA reports)
TARDIVE DYSKINESIA ( 22 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 22 FDA reports)
VENOUS INSUFFICIENCY ( 22 FDA reports)
VIITH NERVE PARALYSIS ( 22 FDA reports)
VISUAL IMPAIRMENT ( 22 FDA reports)
ARTERIAL DISORDER ( 21 FDA reports)
ATHEROSCLEROSIS ( 21 FDA reports)
BACK INJURY ( 21 FDA reports)
BARRETT'S OESOPHAGUS ( 21 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 21 FDA reports)
BODY TEMPERATURE INCREASED ( 21 FDA reports)
BONE MARROW TRANSPLANT ( 21 FDA reports)
CHEST TUBE INSERTION ( 21 FDA reports)
CHONDROMALACIA ( 21 FDA reports)
CRYING ( 21 FDA reports)
EYE IRRITATION ( 21 FDA reports)
FIBULA FRACTURE ( 21 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 21 FDA reports)
INADEQUATE ANALGESIA ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MENTAL IMPAIRMENT ( 21 FDA reports)
MULTIPLE SCLEROSIS ( 21 FDA reports)
MUSCLE TIGHTNESS ( 21 FDA reports)
OROPHARYNGEAL PLAQUE ( 21 FDA reports)
OSTEORADIONECROSIS ( 21 FDA reports)
RASH PAPULAR ( 21 FDA reports)
RESPIRATORY TRACT INFECTION ( 21 FDA reports)
THIRST ( 21 FDA reports)
BLOOD POTASSIUM INCREASED ( 20 FDA reports)
COMPLETED SUICIDE ( 20 FDA reports)
COR PULMONALE CHRONIC ( 20 FDA reports)
DERMATITIS ATOPIC ( 20 FDA reports)
DIABETIC COMA ( 20 FDA reports)
FACIAL PALSY ( 20 FDA reports)
LABYRINTHITIS ( 20 FDA reports)
LACRIMATION INCREASED ( 20 FDA reports)
LACUNAR INFARCTION ( 20 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 20 FDA reports)
MITRAL VALVE PROLAPSE ( 20 FDA reports)
ONYCHOMYCOSIS ( 20 FDA reports)
PHARYNGEAL OEDEMA ( 20 FDA reports)
PLANTAR FASCIITIS ( 20 FDA reports)
SEPTIC SHOCK ( 20 FDA reports)
SINUS DISORDER ( 20 FDA reports)
SUBCUTANEOUS ABSCESS ( 20 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 20 FDA reports)
TYPE 1 DIABETES MELLITUS ( 20 FDA reports)
UMBILICAL HERNIA ( 20 FDA reports)
UTERINE ENLARGEMENT ( 20 FDA reports)
ARTERIAL STENOSIS ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK ( 19 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 19 FDA reports)
BRONCHOSPASM ( 19 FDA reports)
CAROTID BRUIT ( 19 FDA reports)
CHROMATURIA ( 19 FDA reports)
DIALYSIS ( 19 FDA reports)
DILATATION ATRIAL ( 19 FDA reports)
EAR HAEMORRHAGE ( 19 FDA reports)
EAR INFECTION ( 19 FDA reports)
EATING DISORDER ( 19 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 19 FDA reports)
NEOPLASM PROGRESSION ( 19 FDA reports)
NERVE COMPRESSION ( 19 FDA reports)
OESOPHAGEAL STENOSIS ( 19 FDA reports)
PELVIC PAIN ( 19 FDA reports)
PLEURISY ( 19 FDA reports)
POLYMYALGIA RHEUMATICA ( 19 FDA reports)
PROSTATITIS ( 19 FDA reports)
RETINAL DETACHMENT ( 19 FDA reports)
RHONCHI ( 19 FDA reports)
TONGUE ULCERATION ( 19 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 19 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 19 FDA reports)
ABNORMAL BEHAVIOUR ( 18 FDA reports)
ANAPHYLACTIC REACTION ( 18 FDA reports)
BLOOD CALCIUM INCREASED ( 18 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 18 FDA reports)
CONJUNCTIVITIS ( 18 FDA reports)
DELUSION ( 18 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 18 FDA reports)
DRUG ERUPTION ( 18 FDA reports)
DUODENAL ULCER ( 18 FDA reports)
EMPYEMA ( 18 FDA reports)
EYE SWELLING ( 18 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 18 FDA reports)
HIP ARTHROPLASTY ( 18 FDA reports)
HYPOACUSIS ( 18 FDA reports)
INFUSION RELATED REACTION ( 18 FDA reports)
INTENTIONAL DRUG MISUSE ( 18 FDA reports)
JAW OPERATION ( 18 FDA reports)
KNEE ARTHROPLASTY ( 18 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 18 FDA reports)
LIP DISCOLOURATION ( 18 FDA reports)
METASTASES TO LYMPH NODES ( 18 FDA reports)
MUSCLE DISORDER ( 18 FDA reports)
MUSCLE TWITCHING ( 18 FDA reports)
OPEN WOUND ( 18 FDA reports)
POST PROCEDURAL HAEMATOMA ( 18 FDA reports)
RADIOTHERAPY ( 18 FDA reports)
RALES ( 18 FDA reports)
RASH MACULAR ( 18 FDA reports)
RENAL ABSCESS ( 18 FDA reports)
SICCA SYNDROME ( 18 FDA reports)
SINUS HEADACHE ( 18 FDA reports)
THERMAL BURN ( 18 FDA reports)
AORTIC STENOSIS ( 17 FDA reports)
AORTIC VALVE SCLEROSIS ( 17 FDA reports)
APHTHOUS STOMATITIS ( 17 FDA reports)
ASCITES ( 17 FDA reports)
BACTERIAL DISEASE CARRIER ( 17 FDA reports)
BLADDER CANCER ( 17 FDA reports)
BONE MARROW FAILURE ( 17 FDA reports)
BRONCHOPLEURAL FISTULA ( 17 FDA reports)
CANDIDIASIS ( 17 FDA reports)
CARDIAC PACEMAKER INSERTION ( 17 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 17 FDA reports)
CHOLECYSTECTOMY ( 17 FDA reports)
CORONARY ARTERY RESTENOSIS ( 17 FDA reports)
CROHN'S DISEASE ( 17 FDA reports)
DERMAL CYST ( 17 FDA reports)
DIABETIC NEPHROPATHY ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
DYSTONIA ( 17 FDA reports)
ECCHYMOSIS ( 17 FDA reports)
FRACTURE DELAYED UNION ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
HEMIPLEGIA ( 17 FDA reports)
HOSPITALISATION ( 17 FDA reports)
HYDROCEPHALUS ( 17 FDA reports)
HYDROPNEUMOTHORAX ( 17 FDA reports)
HYPOMAGNESAEMIA ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 17 FDA reports)
LARYNGEAL OEDEMA ( 17 FDA reports)
LOOSE TOOTH ( 17 FDA reports)
MITRAL VALVE CALCIFICATION ( 17 FDA reports)
NEURITIS ( 17 FDA reports)
ORTHOPNOEA ( 17 FDA reports)
PARKINSON'S DISEASE ( 17 FDA reports)
PERITONITIS ( 17 FDA reports)
PHARYNGITIS ( 17 FDA reports)
PHOTOSENSITIVITY REACTION ( 17 FDA reports)
PULMONARY MASS ( 17 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 17 FDA reports)
RESUSCITATION ( 17 FDA reports)
SEQUESTRECTOMY ( 17 FDA reports)
SKIN FISSURES ( 17 FDA reports)
SPONDYLITIS ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
TOBACCO ABUSE ( 17 FDA reports)
VENTRICULAR FIBRILLATION ( 17 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
ANKLE FRACTURE ( 16 FDA reports)
AZOTAEMIA ( 16 FDA reports)
BLADDER DISORDER ( 16 FDA reports)
BREAST MASS ( 16 FDA reports)
BREATH SOUNDS ABNORMAL ( 16 FDA reports)
CARDIAC FLUTTER ( 16 FDA reports)
CEREBRAL HAEMORRHAGE ( 16 FDA reports)
CHEILITIS ( 16 FDA reports)
DUODENITIS ( 16 FDA reports)
EDENTULOUS ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 16 FDA reports)
HYPOAESTHESIA FACIAL ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
LIBIDO DECREASED ( 16 FDA reports)
MOUTH HAEMORRHAGE ( 16 FDA reports)
MYOSITIS ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
ORAL SURGERY ( 16 FDA reports)
OROPHARYNGEAL BLISTERING ( 16 FDA reports)
POOR QUALITY SLEEP ( 16 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 16 FDA reports)
PYELOCALIECTASIS ( 16 FDA reports)
ROTATOR CUFF REPAIR ( 16 FDA reports)
SALIVARY GLAND ADENOMA ( 16 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 16 FDA reports)
VITAMIN B12 DEFICIENCY ( 16 FDA reports)
WOUND ( 16 FDA reports)
ABDOMINAL TENDERNESS ( 15 FDA reports)
ANOSMIA ( 15 FDA reports)
BLOOD ALBUMIN DECREASED ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 15 FDA reports)
CATARACT OPERATION ( 15 FDA reports)
COLITIS ISCHAEMIC ( 15 FDA reports)
DECUBITUS ULCER ( 15 FDA reports)
DILATATION VENTRICULAR ( 15 FDA reports)
DISEASE RECURRENCE ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
HAEMOTHORAX ( 15 FDA reports)
HYPERTONIC BLADDER ( 15 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 15 FDA reports)
INITIAL INSOMNIA ( 15 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 15 FDA reports)
ISCHAEMIC STROKE ( 15 FDA reports)
LISTLESS ( 15 FDA reports)
LOCAL SWELLING ( 15 FDA reports)
METASTASES TO LIVER ( 15 FDA reports)
MOOD ALTERED ( 15 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 15 FDA reports)
ORAL INTAKE REDUCED ( 15 FDA reports)
ORAL TORUS ( 15 FDA reports)
PARAESTHESIA ORAL ( 15 FDA reports)
PERICARDITIS ( 15 FDA reports)
PHOTOPSIA ( 15 FDA reports)
PLASMACYTOSIS ( 15 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 15 FDA reports)
PRURITUS GENERALISED ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
RENAL MASS ( 15 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 15 FDA reports)
SKELETAL SURVEY ABNORMAL ( 15 FDA reports)
SPINAL CORPECTOMY ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA ( 15 FDA reports)
STEVENS-JOHNSON SYNDROME ( 15 FDA reports)
TEARFULNESS ( 15 FDA reports)
TENSION HEADACHE ( 15 FDA reports)
THYROID ADENOMA ( 15 FDA reports)
UROSEPSIS ( 15 FDA reports)
BLOODY DISCHARGE ( 14 FDA reports)
BONE CYST ( 14 FDA reports)
BRAIN OEDEMA ( 14 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 14 FDA reports)
CAROTID ARTERY DISEASE ( 14 FDA reports)
CERVIX CARCINOMA ( 14 FDA reports)
CLOSTRIDIUM COLITIS ( 14 FDA reports)
COLON CANCER ( 14 FDA reports)
DERMATITIS ALLERGIC ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 14 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 14 FDA reports)
EYE PRURITUS ( 14 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 14 FDA reports)
GASTROINTESTINAL ULCER ( 14 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 14 FDA reports)
HAND FRACTURE ( 14 FDA reports)
HEPATIC CYST ( 14 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 14 FDA reports)
HYPERTENSIVE EMERGENCY ( 14 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 14 FDA reports)
LIGAMENT SPRAIN ( 14 FDA reports)
LYMPHOMA ( 14 FDA reports)
MULTIPLE FRACTURES ( 14 FDA reports)
OEDEMA MUCOSAL ( 14 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 14 FDA reports)
ORGAN FAILURE ( 14 FDA reports)
PNEUMONIA VIRAL ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
PULMONARY CONGESTION ( 14 FDA reports)
RESPIRATORY DEPRESSION ( 14 FDA reports)
SICK SINUS SYNDROME ( 14 FDA reports)
SPINAL MYELOGRAM ( 14 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 14 FDA reports)
TESTICULAR PAIN ( 14 FDA reports)
THERAPY NON-RESPONDER ( 14 FDA reports)
TRISMUS ( 14 FDA reports)
URINE OUTPUT DECREASED ( 14 FDA reports)
VAGINAL HAEMORRHAGE ( 14 FDA reports)
VARICOSE VEIN ( 14 FDA reports)
VERTEBROPLASTY ( 14 FDA reports)
VISUAL FIELD DEFECT ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
ACCIDENTAL OVERDOSE ( 13 FDA reports)
ADENOCARCINOMA ( 13 FDA reports)
ADRENAL INSUFFICIENCY ( 13 FDA reports)
AGRANULOCYTOSIS ( 13 FDA reports)
ANGIONEUROTIC OEDEMA ( 13 FDA reports)
BLOOD DISORDER ( 13 FDA reports)
BREAST CALCIFICATIONS ( 13 FDA reports)
BUTTOCK PAIN ( 13 FDA reports)
CARDIOGENIC SHOCK ( 13 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 13 FDA reports)
CERVICAL DYSPLASIA ( 13 FDA reports)
CHOLECYSTITIS CHRONIC ( 13 FDA reports)
CLOSTRIDIAL INFECTION ( 13 FDA reports)
DELIRIUM ( 13 FDA reports)
DEMYELINATION ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FOREIGN BODY TRAUMA ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
HEPATITIS C ( 13 FDA reports)
HEPATOMEGALY ( 13 FDA reports)
HORDEOLUM ( 13 FDA reports)
HUNGER ( 13 FDA reports)
HYPOPHOSPHATAEMIA ( 13 FDA reports)
IMPAIRED DRIVING ABILITY ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
IMPLANT SITE INFECTION ( 13 FDA reports)
INCONTINENCE ( 13 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 13 FDA reports)
INTRACARDIAC THROMBUS ( 13 FDA reports)
JOINT CONTRACTURE ( 13 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
LUNG ABSCESS ( 13 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 13 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 13 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 13 FDA reports)
NERVE INJURY ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
OESOPHAGEAL DISORDER ( 13 FDA reports)
OPTIC NEURITIS ( 13 FDA reports)
POLYDIPSIA ( 13 FDA reports)
POLYTRAUMATISM ( 13 FDA reports)
PROCEDURAL COMPLICATION ( 13 FDA reports)
PULMONARY HILUM MASS ( 13 FDA reports)
PULSE ABSENT ( 13 FDA reports)
PURPURA ( 13 FDA reports)
RADIATION ASSOCIATED PAIN ( 13 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 13 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 13 FDA reports)
SNORING ( 13 FDA reports)
SPINAL FUSION SURGERY ( 13 FDA reports)
STASIS DERMATITIS ( 13 FDA reports)
STEM CELL TRANSPLANT ( 13 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 13 FDA reports)
TOE DEFORMITY ( 13 FDA reports)
TRACHEOBRONCHITIS ( 13 FDA reports)
ABSCESS NECK ( 12 FDA reports)
AMYLOIDOSIS ( 12 FDA reports)
ANAPHYLACTIC SHOCK ( 12 FDA reports)
ANASTOMOTIC ULCER ( 12 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 12 FDA reports)
AORTIC DILATATION ( 12 FDA reports)
ARTHROPOD BITE ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 12 FDA reports)
BENIGN BONE NEOPLASM ( 12 FDA reports)
BLEPHARITIS ( 12 FDA reports)
BLOOD CULTURE POSITIVE ( 12 FDA reports)
BRAIN STEM INFARCTION ( 12 FDA reports)
BRONCHIECTASIS ( 12 FDA reports)
CATHETERISATION CARDIAC ( 12 FDA reports)
CERVICOBRACHIAL SYNDROME ( 12 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 12 FDA reports)
COMMUNICATION DISORDER ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
CORONARY ARTERY THROMBOSIS ( 12 FDA reports)
DEBRIDEMENT ( 12 FDA reports)
DENTAL IMPLANTATION ( 12 FDA reports)
DRUG DISPENSING ERROR ( 12 FDA reports)
DYSPHEMIA ( 12 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 12 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
FAILURE TO THRIVE ( 12 FDA reports)
FEMORAL NECK FRACTURE ( 12 FDA reports)
GRAND MAL CONVULSION ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HEPATOCELLULAR DAMAGE ( 12 FDA reports)
HODGKIN'S DISEASE ( 12 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 12 FDA reports)
INTESTINAL OBSTRUCTION ( 12 FDA reports)
MALIGNANT MELANOMA ( 12 FDA reports)
MEDICAL DEVICE REMOVAL ( 12 FDA reports)
MOTOR DYSFUNCTION ( 12 FDA reports)
NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
NIGHT SWEATS ( 12 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
ONYCHALGIA ( 12 FDA reports)
PARALYSIS ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
RENAL ARTERY STENOSIS ( 12 FDA reports)
RESPIRATORY TRACT CONGESTION ( 12 FDA reports)
RETINAL VASCULAR DISORDER ( 12 FDA reports)
SACROILIITIS ( 12 FDA reports)
SALIVARY GLAND CANCER ( 12 FDA reports)
SCRATCH ( 12 FDA reports)
SENSORY DISTURBANCE ( 12 FDA reports)
SEROMA ( 12 FDA reports)
SINUS ARRHYTHMIA ( 12 FDA reports)
SPINAL CORD DISORDER ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
SUDDEN DEATH ( 12 FDA reports)
SYNCOPE VASOVAGAL ( 12 FDA reports)
ULCER HAEMORRHAGE ( 12 FDA reports)
VERTIGO POSITIONAL ( 12 FDA reports)
ADRENAL ADENOMA ( 11 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 11 FDA reports)
ALVEOLOPLASTY ( 11 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 11 FDA reports)
BLINDNESS TRANSIENT ( 11 FDA reports)
BLOOD MAGNESIUM DECREASED ( 11 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BONE SARCOMA ( 11 FDA reports)
CANCER PAIN ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
CONCUSSION ( 11 FDA reports)
CYSTOCELE ( 11 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 11 FDA reports)
DIABETIC COMPLICATION ( 11 FDA reports)
DIVERTICULAR PERFORATION ( 11 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 11 FDA reports)
EMBOLIC STROKE ( 11 FDA reports)
EXPLORATORY OPERATION ( 11 FDA reports)
FACE INJURY ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 11 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 11 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 11 FDA reports)
GENITAL CANDIDIASIS ( 11 FDA reports)
GRAFT VERSUS HOST DISEASE ( 11 FDA reports)
HAEMORRHAGE URINARY TRACT ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HERPES VIRUS INFECTION ( 11 FDA reports)
HYPERAESTHESIA ( 11 FDA reports)
HYPOAESTHESIA ORAL ( 11 FDA reports)
HYPOPARATHYROIDISM ( 11 FDA reports)
ILEUS ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 11 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 11 FDA reports)
LIP SWELLING ( 11 FDA reports)
MAMMOPLASTY ( 11 FDA reports)
METABOLIC DISORDER ( 11 FDA reports)
METABOLIC ENCEPHALOPATHY ( 11 FDA reports)
METASTASES TO LUNG ( 11 FDA reports)
MYELOPATHY ( 11 FDA reports)
OSTEOMYELITIS ACUTE ( 11 FDA reports)
PANIC DISORDER ( 11 FDA reports)
PERIARTHRITIS ( 11 FDA reports)
PERIPHERAL ISCHAEMIA ( 11 FDA reports)
POLYNEUROPATHY ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
RENAL CANCER METASTATIC ( 11 FDA reports)
SINUS CONGESTION ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
SYNOVIAL RUPTURE ( 11 FDA reports)
TINEA PEDIS ( 11 FDA reports)
ULNA FRACTURE ( 11 FDA reports)
VESTIBULAR DISORDER ( 11 FDA reports)
ABDOMINAL HERNIA ( 10 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 10 FDA reports)
ABSCESS LIMB ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 10 FDA reports)
ADNEXA UTERI CYST ( 10 FDA reports)
ADRENAL MASS ( 10 FDA reports)
ANGIOLIPOMA ( 10 FDA reports)
AREFLEXIA ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
ATRIAL SEPTAL DEFECT ( 10 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BIPOLAR DISORDER ( 10 FDA reports)
BLADDER NEOPLASM ( 10 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
CHEST X-RAY ABNORMAL ( 10 FDA reports)
CHRONIC FATIGUE SYNDROME ( 10 FDA reports)
COAGULATION TIME PROLONGED ( 10 FDA reports)
COMMINUTED FRACTURE ( 10 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 10 FDA reports)
DECREASED ACTIVITY ( 10 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 10 FDA reports)
DIZZINESS POSTURAL ( 10 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 10 FDA reports)
DRY THROAT ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 10 FDA reports)
EPIDIDYMAL CYST ( 10 FDA reports)
ESCHERICHIA BACTERAEMIA ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
FEELING OF RELAXATION ( 10 FDA reports)
FISTULA DISCHARGE ( 10 FDA reports)
FLAT AFFECT ( 10 FDA reports)
GASTRIC POLYPS ( 10 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 10 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 10 FDA reports)
HEART DISEASE CONGENITAL ( 10 FDA reports)
HEPATIC LESION ( 10 FDA reports)
HYPOCALCAEMIA ( 10 FDA reports)
INJECTION SITE PRURITUS ( 10 FDA reports)
LIPASE INCREASED ( 10 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
MANIA ( 10 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 10 FDA reports)
MORTON'S NEUROMA ( 10 FDA reports)
MUSCLE HAEMORRHAGE ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
NASAL SEPTUM DEVIATION ( 10 FDA reports)
NEUROSIS ( 10 FDA reports)
OCCULT BLOOD POSITIVE ( 10 FDA reports)
OPTIC NERVE INJURY ( 10 FDA reports)
ORTHOPEDIC PROCEDURE ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
PAROTID GLAND ENLARGEMENT ( 10 FDA reports)
PARTIAL SEIZURES ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
PIRIFORMIS SYNDROME ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
POLYSUBSTANCE ABUSE ( 10 FDA reports)
POSTNASAL DRIP ( 10 FDA reports)
PRESCRIBED OVERDOSE ( 10 FDA reports)
PROTEIN URINE PRESENT ( 10 FDA reports)
PSEUDOMONAS INFECTION ( 10 FDA reports)
RIB DEFORMITY ( 10 FDA reports)
ROSACEA ( 10 FDA reports)
SCLERODACTYLIA ( 10 FDA reports)
SCROTAL ABSCESS ( 10 FDA reports)
SCROTAL INFECTION ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
SENSITIVITY OF TEETH ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 10 FDA reports)
SUBCUTANEOUS NODULE ( 10 FDA reports)
SUPRAPUBIC PAIN ( 10 FDA reports)
TENSION ( 10 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 10 FDA reports)
THORACOTOMY ( 10 FDA reports)
TINEL'S SIGN ( 10 FDA reports)
TONGUE DISORDER ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
TROPONIN INCREASED ( 10 FDA reports)
URINE ODOUR ABNORMAL ( 10 FDA reports)
VENOUS STASIS ( 10 FDA reports)
VENTRICULAR ARRHYTHMIA ( 10 FDA reports)
VENTRICULAR HYPOKINESIA ( 10 FDA reports)
VULVOVAGINAL DRYNESS ( 10 FDA reports)
WHEELCHAIR USER ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 9 FDA reports)
ALCOHOL POISONING ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
ANXIETY DISORDER ( 9 FDA reports)
AORTIC VALVE STENOSIS ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BILIARY DILATATION ( 9 FDA reports)
BLOOD CHLORIDE INCREASED ( 9 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 9 FDA reports)
BRADYPHRENIA ( 9 FDA reports)
BREAST PAIN ( 9 FDA reports)
CEREBRAL CYST ( 9 FDA reports)
CERUMEN IMPACTION ( 9 FDA reports)
CHOKING ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
CLAUSTROPHOBIA ( 9 FDA reports)
COSTOCHONDRITIS ( 9 FDA reports)
CYSTITIS GLANDULARIS ( 9 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 9 FDA reports)
DRUG PRESCRIBING ERROR ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
ELECTROLYTE IMBALANCE ( 9 FDA reports)
EMBOLISM ( 9 FDA reports)
EXPOSED BONE IN JAW ( 9 FDA reports)
EXTREMITY CONTRACTURE ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FACIAL BONES FRACTURE ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
GYNAECOMASTIA ( 9 FDA reports)
HAEMORRHAGIC ANAEMIA ( 9 FDA reports)
HALLUCINATION, VISUAL ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HERPES SIMPLEX ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
INCOHERENT ( 9 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 9 FDA reports)
LABILE BLOOD PRESSURE ( 9 FDA reports)
LARYNGITIS ( 9 FDA reports)
LUNG HYPERINFLATION ( 9 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 9 FDA reports)
NODULE ON EXTREMITY ( 9 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
OTITIS MEDIA ( 9 FDA reports)
PARKINSONISM ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PEAU D'ORANGE ( 9 FDA reports)
PERSONALITY CHANGE ( 9 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 9 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 9 FDA reports)
PROTEUS INFECTION ( 9 FDA reports)
RECTAL CANCER ( 9 FDA reports)
RESPIRATORY RATE DECREASED ( 9 FDA reports)
RETINAL TEAR ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
SEXUAL DYSFUNCTION ( 9 FDA reports)
SHOULDER OPERATION ( 9 FDA reports)
SLEEP WALKING ( 9 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 9 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
URETHRAL CARUNCLE ( 9 FDA reports)
URINARY HESITATION ( 9 FDA reports)
VAGINAL DISCHARGE ( 9 FDA reports)
VARICES OESOPHAGEAL ( 9 FDA reports)
VITAMIN D DEFICIENCY ( 9 FDA reports)
ACROCHORDON ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
ANURIA ( 8 FDA reports)
ARTHRITIS BACTERIAL ( 8 FDA reports)
AUTONOMIC NEUROPATHY ( 8 FDA reports)
BALANOPOSTHITIS ( 8 FDA reports)
BASAL GANGLIA INFARCTION ( 8 FDA reports)
BEDRIDDEN ( 8 FDA reports)
BIFASCICULAR BLOCK ( 8 FDA reports)
BLADDER PERFORATION ( 8 FDA reports)
BLADDER PROLAPSE ( 8 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
BLOOD CHLORIDE DECREASED ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BODY TEMPERATURE DECREASED ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BREAST CANCER IN SITU ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BREATH ODOUR ( 8 FDA reports)
BRONCHITIS CHRONIC ( 8 FDA reports)
CALCINOSIS ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DEVELOPMENTAL DELAY ( 8 FDA reports)
DEVICE RELATED INFECTION ( 8 FDA reports)
DIABETIC GASTROPARESIS ( 8 FDA reports)
ENDOCARDITIS ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
GASTRITIS EROSIVE ( 8 FDA reports)
GLIOSIS ( 8 FDA reports)
GRANULOMA ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HAIR COLOUR CHANGES ( 8 FDA reports)
HANGOVER ( 8 FDA reports)
HEART TRANSPLANT REJECTION ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
INGUINAL HERNIA REPAIR ( 8 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 8 FDA reports)
KLEBSIELLA INFECTION ( 8 FDA reports)
KYPHOSIS ( 8 FDA reports)
LARGE INTESTINE PERFORATION ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MASTOIDITIS ( 8 FDA reports)
MENIERE'S DISEASE ( 8 FDA reports)
METAPLASIA ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MONOCYTE COUNT INCREASED ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE ( 8 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NODAL RHYTHM ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 8 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 8 FDA reports)
ORAL DISORDER ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PENIS DISORDER ( 8 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 8 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 8 FDA reports)
RENAL HAEMORRHAGE ( 8 FDA reports)
SARCOMA ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
THROMBOSIS IN DEVICE ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
TRANSPLANT REJECTION ( 8 FDA reports)
TROPONIN I INCREASED ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
WEIGHT BEARING DIFFICULTY ( 8 FDA reports)
WITHDRAWAL SYNDROME ( 8 FDA reports)
WOUND DEHISCENCE ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
ABSCESS ORAL ( 7 FDA reports)
ALCOHOL USE ( 7 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 7 FDA reports)
ANAL HAEMORRHAGE ( 7 FDA reports)
AORTIC VALVE CALCIFICATION ( 7 FDA reports)
APHAGIA ( 7 FDA reports)
ARACHNOID CYST ( 7 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 7 FDA reports)
ATRIAL TACHYCARDIA ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 7 FDA reports)
BILIARY DYSKINESIA ( 7 FDA reports)
BINGE EATING ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 7 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 7 FDA reports)
BONE FORMATION INCREASED ( 7 FDA reports)
BRAIN MASS ( 7 FDA reports)
BREAST FIBROSIS ( 7 FDA reports)
BURNOUT SYNDROME ( 7 FDA reports)
CARDIAC ENZYMES INCREASED ( 7 FDA reports)
CARDIAC FIBRILLATION ( 7 FDA reports)
CARDIAC OPERATION ( 7 FDA reports)
CERVICAL CYST ( 7 FDA reports)
CHAPPED LIPS ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
CLOSED HEAD INJURY ( 7 FDA reports)
CLUMSINESS ( 7 FDA reports)
COLON ADENOMA ( 7 FDA reports)
CORNEAL ABRASION ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DIABETIC GASTROPATHY ( 7 FDA reports)
DIAPHRAGMATIC DISORDER ( 7 FDA reports)
DRUG ABUSER ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
FASCIITIS ( 7 FDA reports)
GENERALISED ANXIETY DISORDER ( 7 FDA reports)
GENITAL HERPES ( 7 FDA reports)
GENITAL INFECTION FEMALE ( 7 FDA reports)
GINGIVAL ABSCESS ( 7 FDA reports)
GLOBAL AMNESIA ( 7 FDA reports)
GRAFT THROMBOSIS ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
HAEMOGLOBIN INCREASED ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HEPATITIS C POSITIVE ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HYPERNATRAEMIA ( 7 FDA reports)
HYPERTHYROIDISM ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
INJECTION SITE RASH ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 7 FDA reports)
INTRACRANIAL ANEURYSM ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
JOINT LOCK ( 7 FDA reports)
LATEX ALLERGY ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LORDOSIS ( 7 FDA reports)
LUNG OPERATION ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
METASTASES TO PANCREAS ( 7 FDA reports)
METASTASES TO SPLEEN ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
NAIL DYSTROPHY ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
ODYNOPHAGIA ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
ORAL FUNGAL INFECTION ( 7 FDA reports)
OSTEOMYELITIS CHRONIC ( 7 FDA reports)
OVERGROWTH BACTERIAL ( 7 FDA reports)
OVERWEIGHT ( 7 FDA reports)
PAPILLARY THYROID CANCER ( 7 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
PHLEBOSCLEROSIS ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PLEURITIC PAIN ( 7 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 7 FDA reports)
PREGNANCY ( 7 FDA reports)
PSEUDOPHAKIA ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 7 FDA reports)
RENAL ATROPHY ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 7 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 7 FDA reports)
SCOTOMA ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SKULL FRACTURE ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SOFT TISSUE DISORDER ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SYNOVITIS ( 7 FDA reports)
THROMBOEMBOLIC STROKE ( 7 FDA reports)
TINEA INFECTION ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
URINE ABNORMALITY ( 7 FDA reports)
VENOUS OCCLUSION ( 7 FDA reports)
VITH NERVE PARALYSIS ( 7 FDA reports)
VOCAL CORD PARESIS ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ACCIDENT ( 6 FDA reports)
ACNE ( 6 FDA reports)
ACOUSTIC NEUROMA ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ALCOHOL ABUSE ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
AORTIC ATHEROSCLEROSIS ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
ATROPHODERMA OF PASINI AND PIERINI ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 6 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
BREAST ENLARGEMENT ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CAECITIS ( 6 FDA reports)
CAROTID ARTERY ANEURYSM ( 6 FDA reports)
CHONDROSARCOMA ( 6 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CONTRAST MEDIA REACTION ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
DEAFNESS BILATERAL ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
EAR PRURITUS ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
EROSIVE OESOPHAGITIS ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FACE LIFT ( 6 FDA reports)
FEELING OF DESPAIR ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
GAMMOPATHY ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
GUN SHOT WOUND ( 6 FDA reports)
HAEMANGIOMA OF LIVER ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HAND DEFORMITY ( 6 FDA reports)
HEART VALVE CALCIFICATION ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
INGROWING NAIL ( 6 FDA reports)
INJECTION SITE CALCIFICATION ( 6 FDA reports)
INJECTION SITE URTICARIA ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 6 FDA reports)
INTRAOCULAR LENS IMPLANT ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
LEUKOPLAKIA ( 6 FDA reports)
LIP INJURY ( 6 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
LIP PAIN ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LUNG CONSOLIDATION ( 6 FDA reports)
LYMPHOEDEMA ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MASTOCYTOSIS ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MENSTRUATION IRREGULAR ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MITRAL VALVE DISEASE ( 6 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 6 FDA reports)
MUSCLE CONTRACTURE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
NEPHRITIS INTERSTITIAL ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NEUROPATHIC ARTHROPATHY ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NYSTAGMUS ( 6 FDA reports)
OPTIC NEUROPATHY ( 6 FDA reports)
OROPHARYNGEAL SPASM ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PERITONITIS BACTERIAL ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PILONIDAL CYST ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POST POLIO SYNDROME ( 6 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 6 FDA reports)
PROSTATIC DISORDER ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PULSE ABNORMAL ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RECTOCELE ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
RETROGRADE EJACULATION ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SERUM SICKNESS ( 6 FDA reports)
SHOULDER ARTHROPLASTY ( 6 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SPINAL ANAESTHESIA ( 6 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
STRESS URINARY INCONTINENCE ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SYNOVIAL CYST ( 6 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
THOUGHT INSERTION ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 6 FDA reports)
URTICARIA GENERALISED ( 6 FDA reports)
UTERINE DISORDER ( 6 FDA reports)
VAGINAL INFECTION ( 6 FDA reports)
VITAMIN D DECREASED ( 6 FDA reports)
VULVOVAGINAL PRURITUS ( 6 FDA reports)
WOUND INFECTION BACTERIAL ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ABDOMINAL HERNIA REPAIR ( 5 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AGITATION POSTOPERATIVE ( 5 FDA reports)
AKINESIA ( 5 FDA reports)
ALCOHOLISM ( 5 FDA reports)
AORTIC VALVE DISEASE ( 5 FDA reports)
APATHY ( 5 FDA reports)
APPLICATION SITE RASH ( 5 FDA reports)
APPLICATION SITE VESICLES ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BACTERIAL TEST POSITIVE ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD MAGNESIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BODY FAT DISORDER ( 5 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BREAST SWELLING ( 5 FDA reports)
BREAST TENDERNESS ( 5 FDA reports)
BRONCHOMALACIA ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
CARDIOVERSION ( 5 FDA reports)
CAROTID ARTERY THROMBOSIS ( 5 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 5 FDA reports)
CARTILAGE INJURY ( 5 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
CHANGE OF BOWEL HABIT ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 5 FDA reports)
COLON CANCER STAGE III ( 5 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
DEATH OF RELATIVE ( 5 FDA reports)
DERMOID CYST ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
DRUG TOLERANCE ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FOAMING AT MOUTH ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
FRACTURE NONUNION ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GASTRIC PERFORATION ( 5 FDA reports)
GASTRIC PH DECREASED ( 5 FDA reports)
GASTROENTERITIS RADIATION ( 5 FDA reports)
GLYCOSURIA ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
GRIP STRENGTH DECREASED ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
IMPAIRED FASTING GLUCOSE ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
LYMPHOCYTOSIS ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MARFAN'S SYNDROME ( 5 FDA reports)
METABOLIC SYNDROME ( 5 FDA reports)
NASAL DRYNESS ( 5 FDA reports)
NASAL SEPTUM DISORDER ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NEUTROPENIC COLITIS ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 5 FDA reports)
OBSTRUCTIVE UROPATHY ( 5 FDA reports)
OPEN REDUCTION OF FRACTURE ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
PACEMAKER COMPLICATION ( 5 FDA reports)
PAINFUL RESPIRATION ( 5 FDA reports)
PANIC REACTION ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 5 FDA reports)
PERNICIOUS ANAEMIA ( 5 FDA reports)
PNEUMONIA LEGIONELLA ( 5 FDA reports)
POLYCYTHAEMIA ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PROCTITIS ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
PUPIL FIXED ( 5 FDA reports)
RADIUS FRACTURE ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RETINAL ARTERY OCCLUSION ( 5 FDA reports)
RHEUMATIC HEART DISEASE ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 5 FDA reports)
SHUNT INFECTION ( 5 FDA reports)
SHUNT OCCLUSION ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SLUGGISHNESS ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
SPINAL HAEMANGIOMA ( 5 FDA reports)
SPINAL LAMINECTOMY ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
TESTICULAR SWELLING ( 5 FDA reports)
THALAMIC INFARCTION ( 5 FDA reports)
THROMBOPHLEBITIS ( 5 FDA reports)
THYROID CANCER METASTATIC ( 5 FDA reports)
TRIGEMINAL NEURALGIA ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 5 FDA reports)
VARICOSE ULCERATION ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
VASCULAR INSUFFICIENCY ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ANGIODYSPLASIA ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANION GAP INCREASED ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AORTIC BRUIT ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APNOEA ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 4 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREAST CYST ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
BURKITT'S LYMPHOMA ( 4 FDA reports)
CARBON DIOXIDE DECREASED ( 4 FDA reports)
CARDIAC ABLATION ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CAROTID ARTERY DISSECTION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CERVIX DISORDER ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 4 FDA reports)
CONFUSION POSTOPERATIVE ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CREST SYNDROME ( 4 FDA reports)
CULTURE WOUND POSITIVE ( 4 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 4 FDA reports)
DENTAL CLEANING ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DENTAL PROSTHESIS USER ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIZZINESS EXERTIONAL ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DUODENAL ULCER PERFORATION ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ECZEMA NUMMULAR ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
EXCESSIVE MASTURBATION ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
FAT TISSUE INCREASED ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FINGER DEFORMITY ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GAMBLING ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMORRHOID OPERATION ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEART TRANSPLANT ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATORENAL FAILURE ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERCHROMIC ANAEMIA ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPERTROPHY ( 4 FDA reports)
HYPOTRICHOSIS ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 4 FDA reports)
JOINT HYPEREXTENSION ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
KIDNEY ENLARGEMENT ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MICTURITION DISORDER ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NAIL DISORDER ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NASAL CYST ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEOPLASM PROSTATE ( 4 FDA reports)
NIPPLE PAIN ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORAL CAVITY FISTULA ( 4 FDA reports)
OVERLAP SYNDROME ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PHAGOPHOBIA ( 4 FDA reports)
PINGUECULA ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PRESBYOESOPHAGUS ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
RECTAL CANCER STAGE III ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RED BLOOD CELL ABNORMALITY ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SEMEN VOLUME DECREASED ( 4 FDA reports)
SKIN INFECTION ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SPINAL CORD HERNIATION ( 4 FDA reports)
SPINDLE CELL SARCOMA ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
STRESS SYMPTOMS ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE DISCOLOURATION ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TRACHEAL HAEMORRHAGE ( 4 FDA reports)
TRICHOTILLOMANIA ( 4 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VENA CAVA FILTER INSERTION ( 4 FDA reports)
VISCERAL OEDEMA ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
WHITE CLOT SYNDROME ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACNE CONGLOBATA ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADENOVIRUS INFECTION ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTHROPOD STING ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRAIN CANCER METASTATIC ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST DISORDER FEMALE ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BRONCHITIS FUNGAL ( 3 FDA reports)
BUNION ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIAC ANEURYSM ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CATARACT CORTICAL ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 3 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
COGNITIVE DETERIORATION ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
COMPULSIONS ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CRANIAL NERVE DISORDER ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CYSTITIS KLEBSIELLA ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DENTAL DISCOMFORT ( 3 FDA reports)
DENTAL FISTULA ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EYE BURNS ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE OPERATION COMPLICATION ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMPLANTABLE PLEURAL CATHETER INSERTION ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 3 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LERICHE SYNDROME ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIMB RECONSTRUCTIVE SURGERY ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LIVER SCAN ABNORMAL ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
MACROCEPHALY ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MITRAL VALVE SCLEROSIS ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOTOR NEURONE DISEASE ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NASAL ULCER ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NERVE ROOT COMPRESSION ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROSTATE INFECTION ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RETICULOCYTE COUNT INCREASED ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SECONDARY SEQUESTRUM ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SEPTOPLASTY ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPLENIC INJURY ( 3 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
TEETH BRITTLE ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TENOSYNOVITIS STENOSANS ( 3 FDA reports)
TESTICULAR ATROPHY ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TRICUSPID VALVE REPAIR ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URETHRAL STENOSIS ( 3 FDA reports)
URINARY BLADDER POLYP ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENTRICULAR DYSKINESIA ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
WEANING FAILURE ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALLERGY TO VACCINE ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMAUROSIS FUGAX ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTOMATIC BLADDER ( 2 FDA reports)
BACTERIAL TEST ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BIOPSY HEART ABNORMAL ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
BLADDER CANCER STAGE IV ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER DYSPLASIA ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST HYPERPLASIA ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
CALCIUM DEFICIENCY ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 2 FDA reports)
CAROTID ARTERY STENT INSERTION ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLON INJURY ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONJUNCTIVAL CYST ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIABETIC GASTROENTEROPATHY ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSAESTHESIA PHARYNX ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURAL LIPOMATOSIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXCESSIVE EXERCISE ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HISTAMINE LEVEL INCREASED ( 2 FDA reports)
HOMELESS ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE CELLULITIS ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTIVE TENOSYNOVITIS ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
IODINE UPTAKE DECREASED ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARYNX IRRITATION ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEGACOLON ACQUIRED ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MOANING ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NECK SURGERY ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PRESENILE DEMENTIA ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADIATION NEUROPATHY ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHABDOMYOMA ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCROTAL DISORDER ( 2 FDA reports)
SCROTAL HAEMATOCOELE ( 2 FDA reports)
SCROTAL VARICOSE VEINS ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SHOULDER DEFORMITY ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STARING ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SWEAT GLAND TUMOUR ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TIC ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VERTEBRAL INJURY ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL LOAD DECREASED ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVAR DYSPLASIA ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALLERGIC COUGH ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANENCEPHALY ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATOPY ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY BONE MARROW ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARTILAGE ATROPHY ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHLOASMA ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSALPINGIOSIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTERNAL EAR PAIN ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT MELANOMA STAGE II ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINERAL SUPPLEMENTATION ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE ENZYME ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OCHLOPHOBIA ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGY TEST ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REDUCED BLADDER CAPACITY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL MICROANEURYSMS ( 1 FDA reports)
RETINAL MIGRAINE ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETROPERITONEAL EFFUSION ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TAENIASIS ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETHRAL CANCER METASTATIC ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL PROLAPSE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL HYSTERECTOMY ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)