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

PAIN ( 924 FDA reports)
PYREXIA ( 912 FDA reports)
NAUSEA ( 813 FDA reports)
DIARRHOEA ( 806 FDA reports)
ANAEMIA ( 778 FDA reports)
PNEUMONIA ( 752 FDA reports)
ANXIETY ( 637 FDA reports)
VOMITING ( 627 FDA reports)
DYSPNOEA ( 620 FDA reports)
FATIGUE ( 587 FDA reports)
OEDEMA PERIPHERAL ( 541 FDA reports)
SEPSIS ( 525 FDA reports)
ASTHENIA ( 510 FDA reports)
HEADACHE ( 489 FDA reports)
THROMBOCYTOPENIA ( 482 FDA reports)
BACK PAIN ( 460 FDA reports)
PLATELET COUNT DECREASED ( 460 FDA reports)
ABDOMINAL PAIN ( 453 FDA reports)
ARTHRALGIA ( 452 FDA reports)
RASH ( 452 FDA reports)
HYPOTENSION ( 432 FDA reports)
RENAL FAILURE ACUTE ( 422 FDA reports)
PAIN IN EXTREMITY ( 419 FDA reports)
OSTEONECROSIS OF JAW ( 418 FDA reports)
INJURY ( 412 FDA reports)
DEHYDRATION ( 411 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 402 FDA reports)
CHEST PAIN ( 392 FDA reports)
WEIGHT DECREASED ( 392 FDA reports)
FEBRILE NEUTROPENIA ( 386 FDA reports)
PANCYTOPENIA ( 385 FDA reports)
RENAL FAILURE ( 384 FDA reports)
HYPERTENSION ( 381 FDA reports)
DEPRESSION ( 380 FDA reports)
DIZZINESS ( 378 FDA reports)
INFECTION ( 374 FDA reports)
PLEURAL EFFUSION ( 360 FDA reports)
DEEP VEIN THROMBOSIS ( 352 FDA reports)
BONE DISORDER ( 340 FDA reports)
HAEMOGLOBIN DECREASED ( 335 FDA reports)
OSTEOARTHRITIS ( 334 FDA reports)
NEUROPATHY PERIPHERAL ( 332 FDA reports)
OSTEOMYELITIS ( 318 FDA reports)
FALL ( 314 FDA reports)
DECREASED APPETITE ( 313 FDA reports)
HYPOKALAEMIA ( 311 FDA reports)
NEUTROPENIA ( 311 FDA reports)
CONSTIPATION ( 309 FDA reports)
DRUG INEFFECTIVE ( 305 FDA reports)
HYPOAESTHESIA ( 302 FDA reports)
RESPIRATORY FAILURE ( 299 FDA reports)
URINARY TRACT INFECTION ( 297 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 291 FDA reports)
COUGH ( 280 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 275 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 273 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 265 FDA reports)
SINUSITIS ( 264 FDA reports)
BRONCHITIS ( 263 FDA reports)
CELLULITIS ( 261 FDA reports)
PAIN IN JAW ( 261 FDA reports)
EMOTIONAL DISTRESS ( 259 FDA reports)
GAIT DISTURBANCE ( 255 FDA reports)
DYSPHAGIA ( 252 FDA reports)
BLOOD CREATININE INCREASED ( 251 FDA reports)
TOOTH EXTRACTION ( 250 FDA reports)
MALAISE ( 248 FDA reports)
IMPAIRED HEALING ( 242 FDA reports)
CONVULSION ( 240 FDA reports)
MULTI-ORGAN FAILURE ( 231 FDA reports)
PULMONARY EMBOLISM ( 230 FDA reports)
SWELLING ( 225 FDA reports)
RENAL IMPAIRMENT ( 219 FDA reports)
STAPHYLOCOCCAL INFECTION ( 219 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 218 FDA reports)
CONDITION AGGRAVATED ( 218 FDA reports)
INSOMNIA ( 217 FDA reports)
ATELECTASIS ( 215 FDA reports)
DIABETES MELLITUS ( 213 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 212 FDA reports)
DEATH ( 212 FDA reports)
ERYTHEMA ( 211 FDA reports)
OSTEONECROSIS ( 208 FDA reports)
PRURITUS ( 207 FDA reports)
DISEASE PROGRESSION ( 205 FDA reports)
ABDOMINAL PAIN UPPER ( 204 FDA reports)
BONE PAIN ( 203 FDA reports)
FUNGAL INFECTION ( 201 FDA reports)
HYPONATRAEMIA ( 200 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 199 FDA reports)
HYPERGLYCAEMIA ( 198 FDA reports)
MYALGIA ( 198 FDA reports)
ANHEDONIA ( 197 FDA reports)
CHILLS ( 197 FDA reports)
DRUG INTERACTION ( 197 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 197 FDA reports)
OSTEOPENIA ( 197 FDA reports)
STOMATITIS ( 197 FDA reports)
ATRIAL FIBRILLATION ( 196 FDA reports)
MUSCULAR WEAKNESS ( 196 FDA reports)
BLOOD BILIRUBIN INCREASED ( 188 FDA reports)
SPINAL OSTEOARTHRITIS ( 184 FDA reports)
PULMONARY OEDEMA ( 182 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 181 FDA reports)
CANDIDIASIS ( 181 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 181 FDA reports)
OSTEOPOROSIS ( 180 FDA reports)
WEIGHT INCREASED ( 179 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 178 FDA reports)
CONFUSIONAL STATE ( 175 FDA reports)
LOSS OF CONSCIOUSNESS ( 173 FDA reports)
ORAL CANDIDIASIS ( 172 FDA reports)
SEPTIC SHOCK ( 172 FDA reports)
CEREBROVASCULAR ACCIDENT ( 171 FDA reports)
LYMPHADENOPATHY ( 171 FDA reports)
PARAESTHESIA ( 170 FDA reports)
MUCOSAL INFLAMMATION ( 169 FDA reports)
DYSPEPSIA ( 168 FDA reports)
HERPES ZOSTER ( 168 FDA reports)
NEUTROPHIL COUNT DECREASED ( 166 FDA reports)
VISION BLURRED ( 163 FDA reports)
BLOOD UREA INCREASED ( 160 FDA reports)
CHOLELITHIASIS ( 159 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 158 FDA reports)
SOMNOLENCE ( 158 FDA reports)
HAEMORRHAGE ( 156 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 154 FDA reports)
BONE MARROW FAILURE ( 154 FDA reports)
HYPOXIA ( 153 FDA reports)
MYOCARDIAL INFARCTION ( 153 FDA reports)
SYNCOPE ( 153 FDA reports)
CARDIOMEGALY ( 152 FDA reports)
TREMOR ( 152 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 151 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 151 FDA reports)
LEUKOPENIA ( 151 FDA reports)
BLOOD GLUCOSE INCREASED ( 150 FDA reports)
TACHYCARDIA ( 148 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 146 FDA reports)
METASTASES TO BONE ( 145 FDA reports)
GASTRITIS ( 144 FDA reports)
MUSCLE SPASMS ( 144 FDA reports)
RENAL FAILURE CHRONIC ( 144 FDA reports)
ASTHMA ( 143 FDA reports)
CARDIAC FAILURE ( 143 FDA reports)
PNEUMOTHORAX ( 143 FDA reports)
ALOPECIA ( 141 FDA reports)
INFLAMMATION ( 141 FDA reports)
BONE LESION ( 138 FDA reports)
HAEMATOCRIT DECREASED ( 138 FDA reports)
HYPERSENSITIVITY ( 136 FDA reports)
OEDEMA ( 136 FDA reports)
CARDIAC ARREST ( 135 FDA reports)
EXOSTOSIS ( 135 FDA reports)
LIVER DISORDER ( 135 FDA reports)
RIB FRACTURE ( 135 FDA reports)
DENTAL CARIES ( 134 FDA reports)
INTERSTITIAL LUNG DISEASE ( 134 FDA reports)
BLOOD PRESSURE DECREASED ( 133 FDA reports)
CORONARY ARTERY DISEASE ( 132 FDA reports)
HYPERKALAEMIA ( 132 FDA reports)
DYSURIA ( 131 FDA reports)
MENTAL STATUS CHANGES ( 131 FDA reports)
MOUTH ULCERATION ( 131 FDA reports)
HYPERLIPIDAEMIA ( 130 FDA reports)
SWELLING FACE ( 130 FDA reports)
TOOTH DISORDER ( 129 FDA reports)
HIATUS HERNIA ( 128 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 126 FDA reports)
LUNG INFILTRATION ( 123 FDA reports)
NEOPLASM MALIGNANT ( 123 FDA reports)
EATING DISORDER ( 122 FDA reports)
HAEMORRHOIDS ( 122 FDA reports)
NECK PAIN ( 122 FDA reports)
RENAL DISORDER ( 122 FDA reports)
ABDOMINAL DISTENSION ( 120 FDA reports)
NEPHROLITHIASIS ( 120 FDA reports)
DEBRIDEMENT ( 118 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 118 FDA reports)
MULTIPLE MYELOMA ( 116 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 115 FDA reports)
TOOTH ABSCESS ( 115 FDA reports)
PANCREATITIS ( 113 FDA reports)
ARTHRITIS ( 112 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 112 FDA reports)
ANOREXIA ( 111 FDA reports)
DRY MOUTH ( 110 FDA reports)
MUSCULOSKELETAL PAIN ( 110 FDA reports)
ENDODONTIC PROCEDURE ( 109 FDA reports)
STEVENS-JOHNSON SYNDROME ( 109 FDA reports)
HAEMATURIA ( 108 FDA reports)
BURSITIS ( 106 FDA reports)
CATARACT ( 106 FDA reports)
MITRAL VALVE INCOMPETENCE ( 106 FDA reports)
PALPITATIONS ( 106 FDA reports)
BLOOD PRESSURE INCREASED ( 105 FDA reports)
DEFORMITY ( 104 FDA reports)
EMPHYSEMA ( 103 FDA reports)
HYPERHIDROSIS ( 102 FDA reports)
JAUNDICE ( 102 FDA reports)
MALNUTRITION ( 102 FDA reports)
RECTAL HAEMORRHAGE ( 102 FDA reports)
AGRANULOCYTOSIS ( 101 FDA reports)
AMNESIA ( 101 FDA reports)
CARDIAC DISORDER ( 101 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 101 FDA reports)
FOOT FRACTURE ( 100 FDA reports)
ARRHYTHMIA ( 99 FDA reports)
HEPATIC FAILURE ( 99 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 99 FDA reports)
ORAL PAIN ( 99 FDA reports)
SURGERY ( 99 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 98 FDA reports)
LUNG DISORDER ( 98 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 97 FDA reports)
GINGIVAL BLEEDING ( 97 FDA reports)
OSTEOSCLEROSIS ( 97 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 97 FDA reports)
LEUKOCYTOSIS ( 96 FDA reports)
SINUS TACHYCARDIA ( 96 FDA reports)
TYPE 2 DIABETES MELLITUS ( 96 FDA reports)
ASCITES ( 95 FDA reports)
JAW OPERATION ( 95 FDA reports)
MIGRAINE ( 95 FDA reports)
PULMONARY HYPERTENSION ( 95 FDA reports)
ABSCESS ( 94 FDA reports)
BONE DEBRIDEMENT ( 94 FDA reports)
CONTUSION ( 93 FDA reports)
HAEMODIALYSIS ( 93 FDA reports)
BLOOD CALCIUM DECREASED ( 92 FDA reports)
DECREASED INTEREST ( 92 FDA reports)
HAEMATOCHEZIA ( 92 FDA reports)
SINUS DISORDER ( 92 FDA reports)
BALANCE DISORDER ( 91 FDA reports)
HYPOPHAGIA ( 90 FDA reports)
STEM CELL TRANSPLANT ( 90 FDA reports)
ACUTE RESPIRATORY FAILURE ( 89 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 88 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 88 FDA reports)
NIGHT SWEATS ( 88 FDA reports)
PROTHROMBIN TIME PROLONGED ( 88 FDA reports)
COAGULOPATHY ( 87 FDA reports)
DIVERTICULUM ( 87 FDA reports)
CHEST DISCOMFORT ( 86 FDA reports)
DYSPNOEA EXERTIONAL ( 86 FDA reports)
GRAFT VERSUS HOST DISEASE ( 86 FDA reports)
OSTEOLYSIS ( 85 FDA reports)
URINARY INCONTINENCE ( 85 FDA reports)
HEART RATE INCREASED ( 84 FDA reports)
BLOOD POTASSIUM DECREASED ( 83 FDA reports)
METABOLIC ACIDOSIS ( 83 FDA reports)
RESPIRATORY ARREST ( 83 FDA reports)
TOOTHACHE ( 83 FDA reports)
URTICARIA ( 83 FDA reports)
CARDIO-RESPIRATORY ARREST ( 82 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 82 FDA reports)
SHOCK ( 82 FDA reports)
GALLBLADDER DISORDER ( 81 FDA reports)
HEPATIC STEATOSIS ( 81 FDA reports)
PRODUCTIVE COUGH ( 81 FDA reports)
PULMONARY CONGESTION ( 81 FDA reports)
SPINAL COMPRESSION FRACTURE ( 81 FDA reports)
COLITIS ( 80 FDA reports)
SCAR ( 80 FDA reports)
TENDERNESS ( 80 FDA reports)
DYSGEUSIA ( 78 FDA reports)
EPISTAXIS ( 78 FDA reports)
GENERALISED OEDEMA ( 78 FDA reports)
PHARYNGITIS ( 78 FDA reports)
ARTHROPATHY ( 77 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 77 FDA reports)
RESPIRATORY DISTRESS ( 77 FDA reports)
DRUG HYPERSENSITIVITY ( 76 FDA reports)
HYPOALBUMINAEMIA ( 76 FDA reports)
LUNG NEOPLASM ( 76 FDA reports)
BACTERAEMIA ( 75 FDA reports)
PNEUMONITIS ( 75 FDA reports)
PRIMARY SEQUESTRUM ( 75 FDA reports)
WHEEZING ( 75 FDA reports)
CHOLECYSTITIS CHRONIC ( 74 FDA reports)
FAILURE TO THRIVE ( 74 FDA reports)
FEELING ABNORMAL ( 74 FDA reports)
GINGIVAL INFECTION ( 74 FDA reports)
SKIN LESION ( 74 FDA reports)
THROMBOSIS ( 74 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 73 FDA reports)
BACTERIAL INFECTION ( 73 FDA reports)
ENCEPHALOPATHY ( 73 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 73 FDA reports)
VAGINAL INFECTION ( 73 FDA reports)
BLOOD SODIUM DECREASED ( 72 FDA reports)
CYST ( 72 FDA reports)
GINGIVITIS ( 72 FDA reports)
LUMBAR SPINAL STENOSIS ( 72 FDA reports)
PURULENT DISCHARGE ( 72 FDA reports)
TOOTH FRACTURE ( 72 FDA reports)
ARTERIOSCLEROSIS ( 71 FDA reports)
CARDIAC MURMUR ( 71 FDA reports)
DIALYSIS ( 71 FDA reports)
EAR PAIN ( 71 FDA reports)
LUNG NEOPLASM MALIGNANT ( 71 FDA reports)
SKIN EXFOLIATION ( 71 FDA reports)
BLOOD ALBUMIN DECREASED ( 70 FDA reports)
ENTEROCOCCAL INFECTION ( 70 FDA reports)
ILEUS PARALYTIC ( 70 FDA reports)
OSTEITIS ( 70 FDA reports)
GINGIVAL PAIN ( 69 FDA reports)
SLEEP DISORDER ( 69 FDA reports)
VISUAL IMPAIRMENT ( 69 FDA reports)
DISCOMFORT ( 68 FDA reports)
JOINT SWELLING ( 68 FDA reports)
MASTICATION DISORDER ( 68 FDA reports)
CROHN'S DISEASE ( 67 FDA reports)
GASTROINTESTINAL DISORDER ( 67 FDA reports)
LETHARGY ( 67 FDA reports)
COMA ( 66 FDA reports)
DRY SKIN ( 66 FDA reports)
HAEMATEMESIS ( 66 FDA reports)
HYPOGLYCAEMIA ( 66 FDA reports)
METASTASES TO LIVER ( 66 FDA reports)
ROTATOR CUFF SYNDROME ( 66 FDA reports)
SLEEP APNOEA SYNDROME ( 66 FDA reports)
DRUG TOXICITY ( 65 FDA reports)
GASTROENTERITIS ( 65 FDA reports)
INFLUENZA ( 65 FDA reports)
OBESITY ( 65 FDA reports)
ORAL DISORDER ( 65 FDA reports)
SOFT TISSUE DISORDER ( 65 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 65 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 65 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 64 FDA reports)
DEVICE RELATED INFECTION ( 64 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 64 FDA reports)
OROPHARYNGEAL PAIN ( 64 FDA reports)
VASCULITIS ( 64 FDA reports)
CARPAL TUNNEL SYNDROME ( 63 FDA reports)
CYSTITIS ( 63 FDA reports)
DISABILITY ( 63 FDA reports)
GINGIVAL SWELLING ( 63 FDA reports)
HYPERCALCAEMIA ( 63 FDA reports)
NASAL CONGESTION ( 63 FDA reports)
POLLAKIURIA ( 63 FDA reports)
TENDONITIS ( 63 FDA reports)
TOOTH INFECTION ( 63 FDA reports)
EJECTION FRACTION DECREASED ( 62 FDA reports)
FISTULA ( 62 FDA reports)
VENTRICULAR TACHYCARDIA ( 62 FDA reports)
BRADYCARDIA ( 61 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 61 FDA reports)
HERPES SIMPLEX ( 61 FDA reports)
HIP FRACTURE ( 61 FDA reports)
LOOSE TOOTH ( 61 FDA reports)
PERICARDIAL EFFUSION ( 61 FDA reports)
SCOLIOSIS ( 61 FDA reports)
STRESS ( 61 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 60 FDA reports)
HEPATIC CYST ( 60 FDA reports)
LIFE EXPECTANCY SHORTENED ( 60 FDA reports)
ORTHOSTATIC HYPOTENSION ( 60 FDA reports)
RHABDOMYOLYSIS ( 60 FDA reports)
SCIATICA ( 60 FDA reports)
CARDIOVASCULAR DISORDER ( 59 FDA reports)
MYELOMA RECURRENCE ( 59 FDA reports)
OESOPHAGITIS ( 59 FDA reports)
ADRENAL INSUFFICIENCY ( 58 FDA reports)
HEPATIC ENZYME INCREASED ( 58 FDA reports)
HUMERUS FRACTURE ( 58 FDA reports)
PERIODONTAL DISEASE ( 58 FDA reports)
RASH PRURITIC ( 58 FDA reports)
BLINDNESS ( 57 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 57 FDA reports)
ENCEPHALITIS ( 57 FDA reports)
FLUID OVERLOAD ( 57 FDA reports)
HEPATOMEGALY ( 57 FDA reports)
HYPOTHYROIDISM ( 57 FDA reports)
JAW FRACTURE ( 57 FDA reports)
MELAENA ( 57 FDA reports)
RHINITIS ALLERGIC ( 57 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 57 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 57 FDA reports)
ABDOMINAL DISCOMFORT ( 56 FDA reports)
ESCHERICHIA INFECTION ( 56 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 56 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 56 FDA reports)
MOBILITY DECREASED ( 56 FDA reports)
OLIGURIA ( 56 FDA reports)
OXYGEN SATURATION DECREASED ( 56 FDA reports)
BLISTER ( 55 FDA reports)
COLONIC POLYP ( 55 FDA reports)
DELIRIUM ( 55 FDA reports)
DEVICE FAILURE ( 55 FDA reports)
HAEMOPTYSIS ( 55 FDA reports)
INFLUENZA LIKE ILLNESS ( 55 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 55 FDA reports)
MASS ( 55 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 55 FDA reports)
PETECHIAE ( 55 FDA reports)
SUICIDAL IDEATION ( 55 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 55 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 54 FDA reports)
CHRONIC SINUSITIS ( 54 FDA reports)
DIVERTICULITIS ( 54 FDA reports)
DRY EYE ( 54 FDA reports)
JOINT CREPITATION ( 54 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 54 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 54 FDA reports)
TRANSAMINASES INCREASED ( 54 FDA reports)
UNEVALUABLE EVENT ( 54 FDA reports)
BLOOD POTASSIUM INCREASED ( 53 FDA reports)
DYSPHONIA ( 53 FDA reports)
ECONOMIC PROBLEM ( 53 FDA reports)
JOINT DISLOCATION ( 53 FDA reports)
LACRIMATION INCREASED ( 53 FDA reports)
MEMORY IMPAIRMENT ( 53 FDA reports)
METASTATIC NEOPLASM ( 53 FDA reports)
ASPERGILLOSIS ( 52 FDA reports)
FEAR ( 52 FDA reports)
HYPERCHOLESTEROLAEMIA ( 52 FDA reports)
PLATELET COUNT INCREASED ( 52 FDA reports)
TREATMENT NONCOMPLIANCE ( 52 FDA reports)
TUMOUR LYSIS SYNDROME ( 52 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 52 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 51 FDA reports)
CACHEXIA ( 51 FDA reports)
CERVICAL SPINAL STENOSIS ( 51 FDA reports)
GASTRIC ULCER ( 51 FDA reports)
HAEMANGIOMA ( 51 FDA reports)
IRRITABLE BOWEL SYNDROME ( 51 FDA reports)
UTERINE LEIOMYOMA ( 51 FDA reports)
VERTIGO ( 51 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 50 FDA reports)
CONJUNCTIVITIS ( 50 FDA reports)
EOSINOPHIL COUNT INCREASED ( 50 FDA reports)
FLUID RETENTION ( 50 FDA reports)
HOT FLUSH ( 50 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 50 FDA reports)
ONYCHOMYCOSIS ( 50 FDA reports)
ORAL HERPES ( 50 FDA reports)
PSEUDOMONAS INFECTION ( 50 FDA reports)
PULMONARY FIBROSIS ( 50 FDA reports)
SEQUESTRECTOMY ( 50 FDA reports)
SYNOVIAL CYST ( 50 FDA reports)
VENTRICULAR FIBRILLATION ( 50 FDA reports)
ANGINA PECTORIS ( 49 FDA reports)
BONE DENSITY DECREASED ( 49 FDA reports)
BONE MARROW TRANSPLANT ( 49 FDA reports)
CEREBRAL HAEMORRHAGE ( 49 FDA reports)
DEAFNESS ( 49 FDA reports)
DISORIENTATION ( 49 FDA reports)
DYSKINESIA ( 49 FDA reports)
RASH GENERALISED ( 49 FDA reports)
STREPTOCOCCAL INFECTION ( 49 FDA reports)
AORTIC VALVE INCOMPETENCE ( 48 FDA reports)
BLOOD GLUCOSE DECREASED ( 48 FDA reports)
CEREBRAL INFARCTION ( 48 FDA reports)
COLITIS ULCERATIVE ( 48 FDA reports)
DECUBITUS ULCER ( 48 FDA reports)
HYPOCALCAEMIA ( 48 FDA reports)
INFUSION RELATED REACTION ( 48 FDA reports)
KLEBSIELLA INFECTION ( 48 FDA reports)
PERIODONTITIS ( 48 FDA reports)
RHINITIS ( 48 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 47 FDA reports)
DIPLOPIA ( 47 FDA reports)
DYSARTHRIA ( 47 FDA reports)
MYOPATHY ( 47 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 47 FDA reports)
PHYSICAL DISABILITY ( 47 FDA reports)
ACTINOMYCOSIS ( 46 FDA reports)
DIABETIC NEUROPATHY ( 46 FDA reports)
ELECTROLYTE IMBALANCE ( 46 FDA reports)
FACIAL PAIN ( 46 FDA reports)
FLANK PAIN ( 46 FDA reports)
ILEUS ( 46 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 46 FDA reports)
PROTEINURIA ( 46 FDA reports)
RHINORRHOEA ( 46 FDA reports)
SPINAL FRACTURE ( 46 FDA reports)
URINARY RETENTION ( 46 FDA reports)
OCULAR HYPERAEMIA ( 45 FDA reports)
PELVIC FRACTURE ( 45 FDA reports)
PNEUMONIA ASPIRATION ( 45 FDA reports)
RASH ERYTHEMATOUS ( 45 FDA reports)
ABASIA ( 44 FDA reports)
ABNORMAL BEHAVIOUR ( 44 FDA reports)
BURNING SENSATION ( 44 FDA reports)
DISTURBANCE IN ATTENTION ( 44 FDA reports)
DIVERTICULUM INTESTINAL ( 44 FDA reports)
HALLUCINATION ( 44 FDA reports)
HEAD INJURY ( 44 FDA reports)
HYPERTHERMIA ( 44 FDA reports)
LOCALISED INFECTION ( 44 FDA reports)
NEOPLASM ( 44 FDA reports)
SPEECH DISORDER ( 44 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 44 FDA reports)
APHASIA ( 43 FDA reports)
ATRIAL SEPTAL DEFECT ( 43 FDA reports)
BODY TEMPERATURE INCREASED ( 43 FDA reports)
ECCHYMOSIS ( 43 FDA reports)
FAECAL INCONTINENCE ( 43 FDA reports)
HAEMATOMA ( 43 FDA reports)
LUNG INFECTION ( 43 FDA reports)
MYOCLONUS ( 43 FDA reports)
NASOPHARYNGITIS ( 43 FDA reports)
SPLENOMEGALY ( 43 FDA reports)
BONE OPERATION ( 42 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 42 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 42 FDA reports)
HYPOMAGNESAEMIA ( 42 FDA reports)
MENISCUS LESION ( 42 FDA reports)
METASTASES TO SPINE ( 42 FDA reports)
PATHOLOGICAL FRACTURE ( 42 FDA reports)
RADIOTHERAPY ( 42 FDA reports)
RHEUMATOID ARTHRITIS ( 42 FDA reports)
SUBCUTANEOUS ABSCESS ( 42 FDA reports)
TINNITUS ( 42 FDA reports)
ULCER ( 42 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 42 FDA reports)
ABSCESS DRAINAGE ( 41 FDA reports)
BACK DISORDER ( 41 FDA reports)
DENTAL OPERATION ( 41 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 41 FDA reports)
GLAUCOMA ( 41 FDA reports)
ILL-DEFINED DISORDER ( 41 FDA reports)
JAW DISORDER ( 41 FDA reports)
PANIC ATTACK ( 41 FDA reports)
SENSITIVITY OF TEETH ( 41 FDA reports)
UNRESPONSIVE TO STIMULI ( 41 FDA reports)
APPENDICITIS ( 40 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 40 FDA reports)
COMPRESSION FRACTURE ( 40 FDA reports)
FLATULENCE ( 40 FDA reports)
GINGIVAL RECESSION ( 40 FDA reports)
LEFT ATRIAL DILATATION ( 40 FDA reports)
MENTAL DISORDER ( 40 FDA reports)
SKIN ULCER ( 40 FDA reports)
TORSADE DE POINTES ( 40 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 40 FDA reports)
WALKING AID USER ( 40 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 39 FDA reports)
DISEASE RECURRENCE ( 39 FDA reports)
DRUG ERUPTION ( 39 FDA reports)
FIBROMYALGIA ( 39 FDA reports)
FIBROSIS ( 39 FDA reports)
HEPATITIS ( 39 FDA reports)
JOINT STIFFNESS ( 39 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 39 FDA reports)
PNEUMONIA FUNGAL ( 39 FDA reports)
SPINAL COLUMN STENOSIS ( 39 FDA reports)
VIRAL INFECTION ( 39 FDA reports)
BLOOD CULTURE POSITIVE ( 38 FDA reports)
CATHETER RELATED INFECTION ( 38 FDA reports)
EYE PAIN ( 38 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 38 FDA reports)
NEUROGENIC BLADDER ( 38 FDA reports)
RENAL CYST ( 38 FDA reports)
SCAB ( 38 FDA reports)
SKIN DISCOLOURATION ( 38 FDA reports)
SKIN DISORDER ( 38 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 38 FDA reports)
VAGINAL HAEMORRHAGE ( 38 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 37 FDA reports)
AGITATION ( 37 FDA reports)
APLASTIC ANAEMIA ( 37 FDA reports)
CARDIOMYOPATHY ( 37 FDA reports)
CHOLECYSTITIS ( 37 FDA reports)
CYANOSIS ( 37 FDA reports)
DRUG LEVEL INCREASED ( 37 FDA reports)
HEPATITIS C ( 37 FDA reports)
PLEURAL FIBROSIS ( 37 FDA reports)
SQUAMOUS CELL CARCINOMA ( 37 FDA reports)
BREAST CANCER ( 36 FDA reports)
BREAST CANCER METASTATIC ( 36 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 36 FDA reports)
FOOT DEFORMITY ( 36 FDA reports)
HYPOVOLAEMIA ( 36 FDA reports)
LYMPHOMA ( 36 FDA reports)
MULTIPLE INJURIES ( 36 FDA reports)
PANCREATITIS ACUTE ( 36 FDA reports)
PROCTALGIA ( 36 FDA reports)
PROTEIN TOTAL DECREASED ( 36 FDA reports)
URINE OUTPUT DECREASED ( 36 FDA reports)
VENTRICULAR HYPERTROPHY ( 36 FDA reports)
BLOOD CALCIUM INCREASED ( 35 FDA reports)
BONE EROSION ( 35 FDA reports)
CHOLECYSTECTOMY ( 35 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 35 FDA reports)
NEOPLASM PROGRESSION ( 35 FDA reports)
PARAESTHESIA ORAL ( 35 FDA reports)
PATHOLOGICAL GAMBLING ( 35 FDA reports)
PULPITIS DENTAL ( 35 FDA reports)
PURPURA ( 35 FDA reports)
THROMBOPHLEBITIS ( 35 FDA reports)
TOOTH LOSS ( 35 FDA reports)
ALVEOLAR OSTEITIS ( 34 FDA reports)
BASAL CELL CARCINOMA ( 34 FDA reports)
BLOOD URINE PRESENT ( 34 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 34 FDA reports)
EDENTULOUS ( 34 FDA reports)
HYPOAESTHESIA ORAL ( 34 FDA reports)
INJECTION SITE PAIN ( 34 FDA reports)
MEDICATION ERROR ( 34 FDA reports)
METASTASES TO LYMPH NODES ( 34 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 34 FDA reports)
NERVOUS SYSTEM DISORDER ( 34 FDA reports)
ORAL INTAKE REDUCED ( 34 FDA reports)
RENAL TUBULAR NECROSIS ( 34 FDA reports)
SKIN INDURATION ( 34 FDA reports)
SPINAL DISORDER ( 34 FDA reports)
TACHYPNOEA ( 34 FDA reports)
X-RAY ABNORMAL ( 34 FDA reports)
ANURIA ( 33 FDA reports)
BRONCHOPNEUMONIA ( 33 FDA reports)
CEREBRAL ATROPHY ( 33 FDA reports)
COGNITIVE DISORDER ( 33 FDA reports)
CYSTITIS HAEMORRHAGIC ( 33 FDA reports)
EAR CONGESTION ( 33 FDA reports)
ENTERITIS ( 33 FDA reports)
HYPERPARATHYROIDISM ( 33 FDA reports)
HYPOPHOSPHATAEMIA ( 33 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 33 FDA reports)
NO THERAPEUTIC RESPONSE ( 33 FDA reports)
OVERDOSE ( 33 FDA reports)
RESPIRATORY DISORDER ( 33 FDA reports)
STREPTOCOCCAL SEPSIS ( 33 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 33 FDA reports)
THORACOTOMY ( 33 FDA reports)
ADVERSE EVENT ( 32 FDA reports)
BIOPSY BONE ABNORMAL ( 32 FDA reports)
BREAST PAIN ( 32 FDA reports)
BREATH ODOUR ( 32 FDA reports)
DILATATION VENTRICULAR ( 32 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 32 FDA reports)
LIP SWELLING ( 32 FDA reports)
NERVOUSNESS ( 32 FDA reports)
OSTEITIS DEFORMANS ( 32 FDA reports)
PSYCHIATRIC SYMPTOM ( 32 FDA reports)
RADICULAR PAIN ( 32 FDA reports)
STRESS FRACTURE ( 32 FDA reports)
SUBDURAL HAEMATOMA ( 32 FDA reports)
TUBERCULOSIS ( 32 FDA reports)
UROSEPSIS ( 32 FDA reports)
WHEELCHAIR USER ( 32 FDA reports)
ABDOMINAL PAIN LOWER ( 31 FDA reports)
AGGRESSION ( 31 FDA reports)
APPENDICECTOMY ( 31 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 31 FDA reports)
COORDINATION ABNORMAL ( 31 FDA reports)
ERECTILE DYSFUNCTION ( 31 FDA reports)
GASTRIC DISORDER ( 31 FDA reports)
HEPATIC LESION ( 31 FDA reports)
HEPATITIS B ( 31 FDA reports)
HYDROCEPHALUS ( 31 FDA reports)
HYPERBILIRUBINAEMIA ( 31 FDA reports)
HYPERURICAEMIA ( 31 FDA reports)
LYMPHOEDEMA ( 31 FDA reports)
MOUTH HAEMORRHAGE ( 31 FDA reports)
MULTIPLE SCLEROSIS ( 31 FDA reports)
ORAL SURGERY ( 31 FDA reports)
OSTEORADIONECROSIS ( 31 FDA reports)
PRESYNCOPE ( 31 FDA reports)
RENAL INJURY ( 31 FDA reports)
SENSORY LOSS ( 31 FDA reports)
SINUS BRADYCARDIA ( 31 FDA reports)
SKIN PAPILLOMA ( 31 FDA reports)
TOOTH IMPACTED ( 31 FDA reports)
TOOTH INJURY ( 31 FDA reports)
WOUND SECRETION ( 31 FDA reports)
ACUTE CORONARY SYNDROME ( 30 FDA reports)
ANGINA UNSTABLE ( 30 FDA reports)
GASTRITIS EROSIVE ( 30 FDA reports)
GRANULOMA ( 30 FDA reports)
HYPOACUSIS ( 30 FDA reports)
MENINGITIS ( 30 FDA reports)
MYOSITIS ( 30 FDA reports)
ODYNOPHAGIA ( 30 FDA reports)
OTITIS EXTERNA ( 30 FDA reports)
OTITIS MEDIA ( 30 FDA reports)
PURULENCE ( 30 FDA reports)
SKIN BURNING SENSATION ( 30 FDA reports)
SKIN HYPERTROPHY ( 30 FDA reports)
SYNOVITIS ( 30 FDA reports)
BLOOD CHLORIDE DECREASED ( 29 FDA reports)
BONE SCAN ABNORMAL ( 29 FDA reports)
CLOSTRIDIAL INFECTION ( 29 FDA reports)
ECZEMA ( 29 FDA reports)
EMPYEMA ( 29 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 29 FDA reports)
HEMIPARESIS ( 29 FDA reports)
ILEITIS ( 29 FDA reports)
INJECTION SITE REACTION ( 29 FDA reports)
LIBIDO DECREASED ( 29 FDA reports)
LIGAMENT RUPTURE ( 29 FDA reports)
MALOCCLUSION ( 29 FDA reports)
NODULE ( 29 FDA reports)
PERITONITIS ( 29 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 29 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 29 FDA reports)
TONGUE ULCERATION ( 29 FDA reports)
VISUAL ACUITY REDUCED ( 29 FDA reports)
VITREOUS DETACHMENT ( 29 FDA reports)
ABSCESS ORAL ( 28 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 28 FDA reports)
DRUG EFFECT DECREASED ( 28 FDA reports)
FEMUR FRACTURE ( 28 FDA reports)
FUNGAEMIA ( 28 FDA reports)
GOITRE ( 28 FDA reports)
INJECTION SITE HAEMORRHAGE ( 28 FDA reports)
LIPASE INCREASED ( 28 FDA reports)
LYMPHOPENIA ( 28 FDA reports)
MAJOR DEPRESSION ( 28 FDA reports)
PARANOIA ( 28 FDA reports)
POOR DENTAL CONDITION ( 28 FDA reports)
PULMONARY VALVE STENOSIS ( 28 FDA reports)
SENSORY DISTURBANCE ( 28 FDA reports)
TONGUE DISCOLOURATION ( 28 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 28 FDA reports)
TRACHEITIS ( 28 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 28 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 28 FDA reports)
ATAXIA ( 27 FDA reports)
BLOOD CHLORIDE INCREASED ( 27 FDA reports)
BLOOD MAGNESIUM DECREASED ( 27 FDA reports)
BONE FRAGMENTATION ( 27 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 27 FDA reports)
DIABETIC KETOACIDOSIS ( 27 FDA reports)
DRUG DEPENDENCE ( 27 FDA reports)
EPICONDYLITIS ( 27 FDA reports)
FAECES DISCOLOURED ( 27 FDA reports)
GASTRIC POLYPS ( 27 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 27 FDA reports)
LACTIC ACIDOSIS ( 27 FDA reports)
MUSCLE TWITCHING ( 27 FDA reports)
MYELODYSPLASTIC SYNDROME ( 27 FDA reports)
NASAL SEPTUM DEVIATION ( 27 FDA reports)
NEURODERMATITIS ( 27 FDA reports)
POLYNEUROPATHY ( 27 FDA reports)
POST PROCEDURAL COMPLICATION ( 27 FDA reports)
RADICULOPATHY ( 27 FDA reports)
SKIN TIGHTNESS ( 27 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 27 FDA reports)
THERAPY NON-RESPONDER ( 27 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 26 FDA reports)
ANAPHYLACTIC REACTION ( 26 FDA reports)
ANGER ( 26 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 26 FDA reports)
ASPIRATION ( 26 FDA reports)
BLOOD AMYLASE INCREASED ( 26 FDA reports)
BREAST CANCER RECURRENT ( 26 FDA reports)
BRONCHOSPASM ( 26 FDA reports)
CEREBRAL ISCHAEMIA ( 26 FDA reports)
ENTEROCOLITIS ( 26 FDA reports)
FLUSHING ( 26 FDA reports)
GINGIVAL OEDEMA ( 26 FDA reports)
HYPERNATRAEMIA ( 26 FDA reports)
JOINT EFFUSION ( 26 FDA reports)
LOBAR PNEUMONIA ( 26 FDA reports)
NEPHROTIC SYNDROME ( 26 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 26 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 26 FDA reports)
POLYP ( 26 FDA reports)
PSORIASIS ( 26 FDA reports)
RECTAL POLYP ( 26 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 26 FDA reports)
SARCOIDOSIS ( 26 FDA reports)
SCLERODERMA ( 26 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 26 FDA reports)
THROMBOCYTOSIS ( 26 FDA reports)
THYROID NEOPLASM ( 26 FDA reports)
VARICOSE VEIN ( 26 FDA reports)
VISUAL DISTURBANCE ( 26 FDA reports)
APHTHOUS STOMATITIS ( 25 FDA reports)
APTYALISM ( 25 FDA reports)
BLOOD PRESSURE ABNORMAL ( 25 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 25 FDA reports)
CHOLESTASIS ( 25 FDA reports)
CIRCULATORY COLLAPSE ( 25 FDA reports)
DYSTHYMIC DISORDER ( 25 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 25 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 25 FDA reports)
EYE IRRITATION ( 25 FDA reports)
FACE OEDEMA ( 25 FDA reports)
FACIAL NEURALGIA ( 25 FDA reports)
HEPATOCELLULAR DAMAGE ( 25 FDA reports)
HERNIA ( 25 FDA reports)
JOINT INJURY ( 25 FDA reports)
LIVER INJURY ( 25 FDA reports)
MYOCARDIAL ISCHAEMIA ( 25 FDA reports)
OFF LABEL USE ( 25 FDA reports)
OTITIS MEDIA ACUTE ( 25 FDA reports)
OVARIAN CYST ( 25 FDA reports)
PALLOR ( 25 FDA reports)
PERFORMANCE STATUS DECREASED ( 25 FDA reports)
PREGNANCY ( 25 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 25 FDA reports)
SEBORRHOEIC KERATOSIS ( 25 FDA reports)
SEPSIS SYNDROME ( 25 FDA reports)
SERUM FERRITIN INCREASED ( 25 FDA reports)
SPINAL CORD COMPRESSION ( 25 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 25 FDA reports)
WEGENER'S GRANULOMATOSIS ( 25 FDA reports)
WOUND DEHISCENCE ( 25 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 24 FDA reports)
ANAL HAEMORRHAGE ( 24 FDA reports)
ASPIRATION PLEURAL CAVITY ( 24 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 24 FDA reports)
CHEST X-RAY ABNORMAL ( 24 FDA reports)
DENTAL PROSTHESIS USER ( 24 FDA reports)
GINGIVAL ABSCESS ( 24 FDA reports)
HYPERCOAGULATION ( 24 FDA reports)
LOCAL SWELLING ( 24 FDA reports)
LUNG CONSOLIDATION ( 24 FDA reports)
METASTASES TO THORAX ( 24 FDA reports)
PULMONARY INFARCTION ( 24 FDA reports)
RASH MACULAR ( 24 FDA reports)
SKIN LACERATION ( 24 FDA reports)
SPUTUM CULTURE POSITIVE ( 24 FDA reports)
THYROID CYST ( 24 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 23 FDA reports)
BACK INJURY ( 23 FDA reports)
BARRETT'S OESOPHAGUS ( 23 FDA reports)
BLOOD BICARBONATE DECREASED ( 23 FDA reports)
BREAST MASS ( 23 FDA reports)
BREATH SOUNDS ABNORMAL ( 23 FDA reports)
BRONCHIECTASIS ( 23 FDA reports)
CHAPPED LIPS ( 23 FDA reports)
CHOLECYSTITIS ACUTE ( 23 FDA reports)
DECREASED ACTIVITY ( 23 FDA reports)
DIFFICULTY IN WALKING ( 23 FDA reports)
HAEMORRHAGIC DIATHESIS ( 23 FDA reports)
HEART RATE IRREGULAR ( 23 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 23 FDA reports)
HEPATIC NECROSIS ( 23 FDA reports)
HEPATOTOXICITY ( 23 FDA reports)
HYDRONEPHROSIS ( 23 FDA reports)
INGUINAL HERNIA ( 23 FDA reports)
JOINT SPRAIN ( 23 FDA reports)
LIMB DISCOMFORT ( 23 FDA reports)
MASTECTOMY ( 23 FDA reports)
MENISCUS REMOVAL ( 23 FDA reports)
MICTURITION URGENCY ( 23 FDA reports)
NEUROPATHY ( 23 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 23 FDA reports)
OVARIAN CANCER ( 23 FDA reports)
RADIOTHERAPY TO BRAIN ( 23 FDA reports)
THIRST ( 23 FDA reports)
VASCULAR ANOMALY ( 23 FDA reports)
ACIDOSIS ( 22 FDA reports)
ACTINIC KERATOSIS ( 22 FDA reports)
AMENORRHOEA ( 22 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 22 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 22 FDA reports)
CATHETER REMOVAL ( 22 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 22 FDA reports)
CHONDROMALACIA ( 22 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 22 FDA reports)
EMOTIONAL DISORDER ( 22 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 22 FDA reports)
HEPATITIS ACUTE ( 22 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 22 FDA reports)
INCORRECT DOSE ADMINISTERED ( 22 FDA reports)
LACERATION ( 22 FDA reports)
LIMB INJURY ( 22 FDA reports)
MECHANICAL VENTILATION ( 22 FDA reports)
MENOPAUSE ( 22 FDA reports)
NEUTROPHIL COUNT INCREASED ( 22 FDA reports)
OEDEMA MUCOSAL ( 22 FDA reports)
PEPTIC ULCER ( 22 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 22 FDA reports)
RESPIRATORY ACIDOSIS ( 22 FDA reports)
RETINAL HAEMORRHAGE ( 22 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 22 FDA reports)
SYSTEMIC CANDIDA ( 22 FDA reports)
WOUND INFECTION ( 22 FDA reports)
ACUTE SINUSITIS ( 21 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 21 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 21 FDA reports)
AZOTAEMIA ( 21 FDA reports)
BACTERIAL DISEASE CARRIER ( 21 FDA reports)
BACTERIAL SEPSIS ( 21 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 21 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 21 FDA reports)
CATHETERISATION CARDIAC ( 21 FDA reports)
CHOLANGITIS ( 21 FDA reports)
CHROMATURIA ( 21 FDA reports)
DERMATITIS CONTACT ( 21 FDA reports)
DIASTOLIC DYSFUNCTION ( 21 FDA reports)
DYSPHEMIA ( 21 FDA reports)
DYSSTASIA ( 21 FDA reports)
ENTEROVESICAL FISTULA ( 21 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 21 FDA reports)
GINGIVAL DISORDER ( 21 FDA reports)
GLOSSODYNIA ( 21 FDA reports)
HEPATIC CIRRHOSIS ( 21 FDA reports)
HYPERPLASIA ( 21 FDA reports)
HYPOPROTEINAEMIA ( 21 FDA reports)
LARYNGITIS ( 21 FDA reports)
LIVER TRANSPLANT REJECTION ( 21 FDA reports)
MUSCLE DISORDER ( 21 FDA reports)
NOCTURIA ( 21 FDA reports)
ORAL CAVITY FISTULA ( 21 FDA reports)
ORTHOPNOEA ( 21 FDA reports)
PHLEBITIS ( 21 FDA reports)
PNEUMONIA BACTERIAL ( 21 FDA reports)
PROSTATE CANCER ( 21 FDA reports)
PROTEIN URINE PRESENT ( 21 FDA reports)
PULMONARY HAEMORRHAGE ( 21 FDA reports)
SWOLLEN TONGUE ( 21 FDA reports)
TARDIVE DYSKINESIA ( 21 FDA reports)
TENDON DISORDER ( 21 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 21 FDA reports)
VAGINAL DISCHARGE ( 21 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 20 FDA reports)
ADDISON'S DISEASE ( 20 FDA reports)
ADJUSTMENT DISORDER ( 20 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 20 FDA reports)
ASTIGMATISM ( 20 FDA reports)
BIOPSY ( 20 FDA reports)
BLINDNESS UNILATERAL ( 20 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
BODY HEIGHT DECREASED ( 20 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 20 FDA reports)
CATHETER PLACEMENT ( 20 FDA reports)
COLON ADENOMA ( 20 FDA reports)
COLON CANCER ( 20 FDA reports)
CULTURE URINE POSITIVE ( 20 FDA reports)
DEPRESSIVE SYMPTOM ( 20 FDA reports)
EAR INFECTION ( 20 FDA reports)
EROSIVE OESOPHAGITIS ( 20 FDA reports)
EXPOSED BONE IN JAW ( 20 FDA reports)
FOREIGN BODY ( 20 FDA reports)
GANGRENE ( 20 FDA reports)
HAEMATOCRIT INCREASED ( 20 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 20 FDA reports)
INTESTINAL ISCHAEMIA ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 20 FDA reports)
KNEE OPERATION ( 20 FDA reports)
LIP PAIN ( 20 FDA reports)
MACULOPATHY ( 20 FDA reports)
MELANOCYTIC NAEVUS ( 20 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 20 FDA reports)
NEURALGIA ( 20 FDA reports)
NIGHT BLINDNESS ( 20 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 20 FDA reports)
PCO2 DECREASED ( 20 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 20 FDA reports)
PROTEIN TOTAL INCREASED ( 20 FDA reports)
RADIATION INJURY ( 20 FDA reports)
RETCHING ( 20 FDA reports)
TIBIA FRACTURE ( 20 FDA reports)
TRANSPLANT REJECTION ( 20 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 19 FDA reports)
ATROPHY ( 19 FDA reports)
AUTOIMMUNE HEPATITIS ( 19 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 19 FDA reports)
BRONCHIOLITIS ( 19 FDA reports)
BUNION ( 19 FDA reports)
CORONARY ARTERY STENOSIS ( 19 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 19 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 19 FDA reports)
DERMATITIS ( 19 FDA reports)
DRUG ABUSE ( 19 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 19 FDA reports)
EPIGASTRIC DISCOMFORT ( 19 FDA reports)
EXCORIATION ( 19 FDA reports)
EYE DISORDER ( 19 FDA reports)
EYE LASER SURGERY ( 19 FDA reports)
FEELING HOT ( 19 FDA reports)
FURUNCLE ( 19 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 19 FDA reports)
HEART VALVE INCOMPETENCE ( 19 FDA reports)
HERNIA REPAIR ( 19 FDA reports)
HYPERPHOSPHATAEMIA ( 19 FDA reports)
LUMBAR RADICULOPATHY ( 19 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 19 FDA reports)
MUSCLE ATROPHY ( 19 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 19 FDA reports)
PAIN OF SKIN ( 19 FDA reports)
PROSTATOMEGALY ( 19 FDA reports)
ROAD TRAFFIC ACCIDENT ( 19 FDA reports)
SKIN FISSURES ( 19 FDA reports)
SKIN REACTION ( 19 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 19 FDA reports)
ALVEOLITIS ALLERGIC ( 18 FDA reports)
ALVEOLOPLASTY ( 18 FDA reports)
BLOOD URIC ACID INCREASED ( 18 FDA reports)
BRAIN OEDEMA ( 18 FDA reports)
CANDIDURIA ( 18 FDA reports)
DIABETIC FOOT ( 18 FDA reports)
DUODENITIS ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
EYE SWELLING ( 18 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 18 FDA reports)
GASTROINTESTINAL PERFORATION ( 18 FDA reports)
GINGIVAL EROSION ( 18 FDA reports)
GINGIVAL ULCERATION ( 18 FDA reports)
GRAND MAL CONVULSION ( 18 FDA reports)
GROIN PAIN ( 18 FDA reports)
HAEMOLYTIC ANAEMIA ( 18 FDA reports)
HEPATOSPLENOMEGALY ( 18 FDA reports)
HIP ARTHROPLASTY ( 18 FDA reports)
HYSTERECTOMY ( 18 FDA reports)
KAPOSI'S SARCOMA ( 18 FDA reports)
LIGAMENT SPRAIN ( 18 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 18 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 18 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 18 FDA reports)
POLYP COLORECTAL ( 18 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 18 FDA reports)
PRURITUS GENERALISED ( 18 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 18 FDA reports)
PULMONARY VASCULAR DISORDER ( 18 FDA reports)
PYELONEPHRITIS ( 18 FDA reports)
QUALITY OF LIFE DECREASED ( 18 FDA reports)
RADIATION SKIN INJURY ( 18 FDA reports)
RADIUS FRACTURE ( 18 FDA reports)
RASH MACULO-PAPULAR ( 18 FDA reports)
RASH PAPULAR ( 18 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 18 FDA reports)
REFLUX OESOPHAGITIS ( 18 FDA reports)
RESPIRATORY RATE INCREASED ( 18 FDA reports)
SEDATION ( 18 FDA reports)
SOFT TISSUE INFLAMMATION ( 18 FDA reports)
STOMATOCYTES PRESENT ( 18 FDA reports)
SUDDEN DEATH ( 18 FDA reports)
THROMBOSIS IN DEVICE ( 18 FDA reports)
ACCIDENT AT WORK ( 17 FDA reports)
ACUTE HEPATIC FAILURE ( 17 FDA reports)
ALKALOSIS ( 17 FDA reports)
CAROTID ARTERY STENOSIS ( 17 FDA reports)
CEREBROVASCULAR DISORDER ( 17 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
DYSLIPIDAEMIA ( 17 FDA reports)
EAR DISCOMFORT ( 17 FDA reports)
EXTREMITY NECROSIS ( 17 FDA reports)
EYELID PTOSIS ( 17 FDA reports)
FALLOT'S TETRALOGY ( 17 FDA reports)
FANCONI SYNDROME ( 17 FDA reports)
FRACTURE ( 17 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 17 FDA reports)
HAND FRACTURE ( 17 FDA reports)
HEART DISEASE CONGENITAL ( 17 FDA reports)
HEART TRANSPLANT REJECTION ( 17 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 17 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 17 FDA reports)
LABORATORY TEST ABNORMAL ( 17 FDA reports)
MASS EXCISION ( 17 FDA reports)
MULTI-ORGAN DISORDER ( 17 FDA reports)
NEURITIS ( 17 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 17 FDA reports)
OPEN WOUND ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 17 FDA reports)
PHARYNGEAL OEDEMA ( 17 FDA reports)
PLEURISY ( 17 FDA reports)
PNEUMONIA KLEBSIELLA ( 17 FDA reports)
POLYURIA ( 17 FDA reports)
PSYCHOTIC DISORDER ( 17 FDA reports)
RESPIRATORY TRACT INFECTION ( 17 FDA reports)
RESTLESSNESS ( 17 FDA reports)
SCAN BONE MARROW ABNORMAL ( 17 FDA reports)
SECRETION DISCHARGE ( 17 FDA reports)
SEXUAL DYSFUNCTION ( 17 FDA reports)
SKIN HYPERPIGMENTATION ( 17 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 17 FDA reports)
SPINAL CORD DISORDER ( 17 FDA reports)
SPINAL FUSION SURGERY ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 17 FDA reports)
VAGINITIS BACTERIAL ( 17 FDA reports)
VASCULAR OPERATION ( 17 FDA reports)
VENOUS INSUFFICIENCY ( 17 FDA reports)
VITAMIN B12 DEFICIENCY ( 17 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 17 FDA reports)
WOUND ( 17 FDA reports)
WOUND TREATMENT ( 17 FDA reports)
ALLERGY TO CHEMICALS ( 16 FDA reports)
AORTIC ANEURYSM ( 16 FDA reports)
ARTHROPOD BITE ( 16 FDA reports)
ATROPHIC VULVOVAGINITIS ( 16 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 16 FDA reports)
BLOOD CREATINE INCREASED ( 16 FDA reports)
BONE NEOPLASM MALIGNANT ( 16 FDA reports)
CARDIAC ENZYMES INCREASED ( 16 FDA reports)
CARDIAC VALVE DISEASE ( 16 FDA reports)
CERVICAL DYSPLASIA ( 16 FDA reports)
COR PULMONALE CHRONIC ( 16 FDA reports)
DENTURE WEARER ( 16 FDA reports)
DIZZINESS POSTURAL ( 16 FDA reports)
ENDOTRACHEAL INTUBATION ( 16 FDA reports)
ENTEROCOCCAL SEPSIS ( 16 FDA reports)
EYE PRURITUS ( 16 FDA reports)
GASTRODUODENITIS ( 16 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 16 FDA reports)
IMPETIGO ( 16 FDA reports)
INCISION SITE INFECTION ( 16 FDA reports)
INCISIONAL DRAINAGE ( 16 FDA reports)
INJECTION SITE HAEMATOMA ( 16 FDA reports)
INTESTINAL OBSTRUCTION ( 16 FDA reports)
ISCHAEMIA ( 16 FDA reports)
MALIGNANT TUMOUR EXCISION ( 16 FDA reports)
MENORRHAGIA ( 16 FDA reports)
MULTIPLE FRACTURES ( 16 FDA reports)
MYELOPATHY ( 16 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 16 FDA reports)
ORAL DISCOMFORT ( 16 FDA reports)
PAPILLOEDEMA ( 16 FDA reports)
PELVIC PAIN ( 16 FDA reports)
PERIODONTAL OPERATION ( 16 FDA reports)
PERIPHERAL COLDNESS ( 16 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 16 FDA reports)
PLASMACYTOMA ( 16 FDA reports)
PRESBYOPIA ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
PSEUDOMONAL SEPSIS ( 16 FDA reports)
RESTLESS LEGS SYNDROME ( 16 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 16 FDA reports)
SINUS OPERATION ( 16 FDA reports)
SKIN PLAQUE ( 16 FDA reports)
SUBCUTANEOUS NODULE ( 16 FDA reports)
TENOSYNOVITIS ( 16 FDA reports)
TONGUE DISORDER ( 16 FDA reports)
TONGUE INJURY ( 16 FDA reports)
TOOTH DEPOSIT ( 16 FDA reports)
ABORTION SPONTANEOUS ( 15 FDA reports)
ANGIOEDEMA ( 15 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 15 FDA reports)
ARTHROSCOPY ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 15 FDA reports)
BLADDER DISORDER ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BONE CYST ( 15 FDA reports)
BONE GRAFT ( 15 FDA reports)
BONE LOSS ( 15 FDA reports)
BONE MARROW DEPRESSION ( 15 FDA reports)
CATARACT OPERATION ( 15 FDA reports)
CENTRAL LINE INFECTION ( 15 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 15 FDA reports)
CHEILITIS ( 15 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 15 FDA reports)
DRUG INTOLERANCE ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 15 FDA reports)
EPILEPSY ( 15 FDA reports)
EXANTHEM ( 15 FDA reports)
EYE DISCHARGE ( 15 FDA reports)
GRANULOCYTOPENIA ( 15 FDA reports)
HALLUCINATION, AUDITORY ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
INTESTINAL PERFORATION ( 15 FDA reports)
KYPHOSCOLIOSIS ( 15 FDA reports)
LUNG TRANSPLANT REJECTION ( 15 FDA reports)
MARROW HYPERPLASIA ( 15 FDA reports)
MENINGISM ( 15 FDA reports)
METASTASIS ( 15 FDA reports)
MOOD SWINGS ( 15 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 15 FDA reports)
NEPHRITIS INTERSTITIAL ( 15 FDA reports)
NEPHROPATHY TOXIC ( 15 FDA reports)
PANCREATITIS CHRONIC ( 15 FDA reports)
PEAU D'ORANGE ( 15 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
PHOTOSENSITIVITY REACTION ( 15 FDA reports)
PLASMACYTOSIS ( 15 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 15 FDA reports)
PO2 DECREASED ( 15 FDA reports)
POOR PERIPHERAL CIRCULATION ( 15 FDA reports)
RENAL TUBULAR DISORDER ( 15 FDA reports)
RESPIRATORY TRACT CONGESTION ( 15 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 15 FDA reports)
SKIN ODOUR ABNORMAL ( 15 FDA reports)
SPINAL LAMINECTOMY ( 15 FDA reports)
SPLENIC INFARCTION ( 15 FDA reports)
SUBILEUS ( 15 FDA reports)
TOOTH REPAIR ( 15 FDA reports)
TYPE 1 DIABETES MELLITUS ( 15 FDA reports)
URETERIC RUPTURE ( 15 FDA reports)
UTERINE ENLARGEMENT ( 15 FDA reports)
VENA CAVA FILTER INSERTION ( 15 FDA reports)
VERTIGO POSITIONAL ( 15 FDA reports)
VULVOVAGINAL DRYNESS ( 15 FDA reports)
ABDOMINAL HERNIA ( 14 FDA reports)
ABDOMINAL TENDERNESS ( 14 FDA reports)
ABSCESS NECK ( 14 FDA reports)
ACNE ( 14 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 14 FDA reports)
APATHY ( 14 FDA reports)
ARTHRITIS BACTERIAL ( 14 FDA reports)
ATRIAL FLUTTER ( 14 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 14 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 14 FDA reports)
BLADDER CANCER ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BONE MARROW DISORDER ( 14 FDA reports)
BREAST RECONSTRUCTION ( 14 FDA reports)
CAECITIS ( 14 FDA reports)
CARDIAC FAILURE ACUTE ( 14 FDA reports)
DIABETIC RETINOPATHY ( 14 FDA reports)
DRUG DISPENSING ERROR ( 14 FDA reports)
ENCEPHALITIS HERPES ( 14 FDA reports)
ENCEPHALITIS VIRAL ( 14 FDA reports)
ENURESIS ( 14 FDA reports)
EXTRASYSTOLES ( 14 FDA reports)
FIBRIN D DIMER INCREASED ( 14 FDA reports)
FIBULA FRACTURE ( 14 FDA reports)
FOOD CRAVING ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
HAEMODYNAMIC INSTABILITY ( 14 FDA reports)
HAEMOLYSIS ( 14 FDA reports)
HAEMORRHAGIC ANAEMIA ( 14 FDA reports)
HEART RATE DECREASED ( 14 FDA reports)
HEPATIC ENCEPHALOPATHY ( 14 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 14 FDA reports)
HYPERKERATOSIS ( 14 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 14 FDA reports)
INJECTION SITE ERYTHEMA ( 14 FDA reports)
LARGE INTESTINE PERFORATION ( 14 FDA reports)
LESION EXCISION ( 14 FDA reports)
LEUKOENCEPHALOPATHY ( 14 FDA reports)
LEUKOPLAKIA ORAL ( 14 FDA reports)
LICHEN PLANUS ( 14 FDA reports)
LIP DISCOLOURATION ( 14 FDA reports)
MENINGIOMA ( 14 FDA reports)
MUSCLE STRAIN ( 14 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 14 FDA reports)
NEOPLASM RECURRENCE ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 14 FDA reports)
OESOPHAGITIS ULCERATIVE ( 14 FDA reports)
ONYCHALGIA ( 14 FDA reports)
POOR PERSONAL HYGIENE ( 14 FDA reports)
PREMATURE BABY ( 14 FDA reports)
PULMONARY ARTERY DILATATION ( 14 FDA reports)
PULSE ABSENT ( 14 FDA reports)
RADICULAR CYST ( 14 FDA reports)
RASH MORBILLIFORM ( 14 FDA reports)
RENAL ATROPHY ( 14 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 14 FDA reports)
SKIN ATROPHY ( 14 FDA reports)
SKIN NODULE ( 14 FDA reports)
SPINAL DEFORMITY ( 14 FDA reports)
SPONDYLOLISTHESIS ( 14 FDA reports)
STRIDOR ( 14 FDA reports)
TENDON RUPTURE ( 14 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 14 FDA reports)
TONGUE COATED ( 14 FDA reports)
VENOUS THROMBOSIS ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
VOCAL CORD THICKENING ( 14 FDA reports)
WOUND DEBRIDEMENT ( 14 FDA reports)
ABDOMINAL NEOPLASM ( 13 FDA reports)
ACUTE PRERENAL FAILURE ( 13 FDA reports)
ANEURYSM ( 13 FDA reports)
ANOGENITAL WARTS ( 13 FDA reports)
AORTIC VALVE SCLEROSIS ( 13 FDA reports)
APNOEA ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
AURICULAR SWELLING ( 13 FDA reports)
BONE DENSITY INCREASED ( 13 FDA reports)
BRONCHOPLEURAL FISTULA ( 13 FDA reports)
CAESAREAN SECTION ( 13 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
CANCER PAIN ( 13 FDA reports)
CAPILLARY LEAK SYNDROME ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
CORONARY ARTERY OCCLUSION ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
DEMENTIA ( 13 FDA reports)
DENTAL IMPLANTATION ( 13 FDA reports)
DERMAL CYST ( 13 FDA reports)
DEVELOPMENTAL DELAY ( 13 FDA reports)
DIABETIC EYE DISEASE ( 13 FDA reports)
ENTEROCUTANEOUS FISTULA ( 13 FDA reports)
ERUCTATION ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
EYE MOVEMENT DISORDER ( 13 FDA reports)
GLUCOSE URINE PRESENT ( 13 FDA reports)
GYNAECOMASTIA ( 13 FDA reports)
HYDROPNEUMOTHORAX ( 13 FDA reports)
HYPOTONIA ( 13 FDA reports)
IMMUNE SYSTEM DISORDER ( 13 FDA reports)
IMPAIRED DRIVING ABILITY ( 13 FDA reports)
INCOHERENT ( 13 FDA reports)
INJURY CORNEAL ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 13 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 13 FDA reports)
INTRAOCULAR LENS IMPLANT ( 13 FDA reports)
IRON DEFICIENCY ANAEMIA ( 13 FDA reports)
JAUNDICE CHOLESTATIC ( 13 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 13 FDA reports)
LUNG OPERATION ( 13 FDA reports)
MOVEMENT DISORDER ( 13 FDA reports)
MUCOUS MEMBRANE DISORDER ( 13 FDA reports)
NECK MASS ( 13 FDA reports)
NEUROLOGICAL SYMPTOM ( 13 FDA reports)
ORAL FUNGAL INFECTION ( 13 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 13 FDA reports)
POLYPECTOMY ( 13 FDA reports)
PROCEDURAL PAIN ( 13 FDA reports)
PULMONARY AIR LEAKAGE ( 13 FDA reports)
PYELOCALIECTASIS ( 13 FDA reports)
RETROPERITONEAL HAEMATOMA ( 13 FDA reports)
SEPTIC EMBOLUS ( 13 FDA reports)
SINUS ARRHYTHMIA ( 13 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 13 FDA reports)
THROAT TIGHTNESS ( 13 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 13 FDA reports)
UPPER LIMB FRACTURE ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
WRIST FRACTURE ( 13 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 13 FDA reports)
ACANTHOMA ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
ANAPHYLACTIC SHOCK ( 12 FDA reports)
AORTIC STENOSIS ( 12 FDA reports)
BLAST CELL COUNT INCREASED ( 12 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 12 FDA reports)
BLOOD UREA DECREASED ( 12 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 12 FDA reports)
BONE ATROPHY ( 12 FDA reports)
BULLOUS LUNG DISEASE ( 12 FDA reports)
CARBON DIOXIDE INCREASED ( 12 FDA reports)
CARDIOGENIC SHOCK ( 12 FDA reports)
CERUMEN IMPACTION ( 12 FDA reports)
CERVICITIS ( 12 FDA reports)
CLOSTRIDIUM COLITIS ( 12 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
DRUG RESISTANCE ( 12 FDA reports)
ENTEROBACTER INFECTION ( 12 FDA reports)
EPIDURAL LIPOMATOSIS ( 12 FDA reports)
ESCHERICHIA SEPSIS ( 12 FDA reports)
ESSENTIAL HYPERTENSION ( 12 FDA reports)
FLAT AFFECT ( 12 FDA reports)
FRUSTRATION ( 12 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 12 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 12 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 12 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 12 FDA reports)
GLOSSITIS ( 12 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 12 FDA reports)
HEPATITIS FULMINANT ( 12 FDA reports)
HIP SURGERY ( 12 FDA reports)
HIV INFECTION ( 12 FDA reports)
HYPERCAPNIA ( 12 FDA reports)
HYPERSOMNIA ( 12 FDA reports)
HYPERTHYROIDISM ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
INTERCOSTAL NEURALGIA ( 12 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 12 FDA reports)
JOINT SURGERY ( 12 FDA reports)
MEGACOLON ( 12 FDA reports)
MITRAL VALVE REPLACEMENT ( 12 FDA reports)
MYOCARDITIS ( 12 FDA reports)
NASAL DISORDER ( 12 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 12 FDA reports)
NECROSIS ( 12 FDA reports)
NERVE INJURY ( 12 FDA reports)
NON-CARDIAC CHEST PAIN ( 12 FDA reports)
NYSTAGMUS ( 12 FDA reports)
OESOPHAGEAL INFECTION ( 12 FDA reports)
OESOPHAGEAL STENOSIS ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
PARTIAL SEIZURES ( 12 FDA reports)
PATHOGEN RESISTANCE ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 12 FDA reports)
PORTAL VEIN THROMBOSIS ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 12 FDA reports)
PYOGENIC GRANULOMA ( 12 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 12 FDA reports)
RENAL TUBULAR ACIDOSIS ( 12 FDA reports)
RETINAL INFARCTION ( 12 FDA reports)
TAKAYASU'S ARTERITIS ( 12 FDA reports)
TELANGIECTASIA ( 12 FDA reports)
TEMPERATURE INTOLERANCE ( 12 FDA reports)
TRACHEOSTOMY ( 12 FDA reports)
TRANSFUSION ( 12 FDA reports)
VENTRICULAR HYPOKINESIA ( 12 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 12 FDA reports)
VITREOUS HAEMORRHAGE ( 12 FDA reports)
WOUND COMPLICATION ( 12 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 11 FDA reports)
AGEUSIA ( 11 FDA reports)
APLASIA PURE RED CELL ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BIPOLAR DISORDER ( 11 FDA reports)
BLOOD DISORDER ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 11 FDA reports)
BLOOD OSMOLARITY DECREASED ( 11 FDA reports)
BLOOD SODIUM INCREASED ( 11 FDA reports)
BODY TEMPERATURE DECREASED ( 11 FDA reports)
BREAST CALCIFICATIONS ( 11 FDA reports)
CALCULUS URETERIC ( 11 FDA reports)
CARDIAC OPERATION ( 11 FDA reports)
CEREBELLAR INFARCTION ( 11 FDA reports)
COCCIDIOIDOMYCOSIS ( 11 FDA reports)
COLECTOMY ( 11 FDA reports)
COLOUR BLINDNESS ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 11 FDA reports)
CSF PROTEIN INCREASED ( 11 FDA reports)
DEPRESSED MOOD ( 11 FDA reports)
DEVICE RELATED SEPSIS ( 11 FDA reports)
DIABETIC NEPHROPATHY ( 11 FDA reports)
DILATATION ATRIAL ( 11 FDA reports)
DRUG DOSE OMISSION ( 11 FDA reports)
FEELING COLD ( 11 FDA reports)
FOREIGN BODY REACTION ( 11 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 11 FDA reports)
GLIOSIS ( 11 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
HEMIPLEGIA ( 11 FDA reports)
HODGKIN'S DISEASE ( 11 FDA reports)
HOSPITALISATION ( 11 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 11 FDA reports)
HYPOAESTHESIA FACIAL ( 11 FDA reports)
HYPOTHERMIA ( 11 FDA reports)
HYPOVOLAEMIC SHOCK ( 11 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 11 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 11 FDA reports)
INTENTIONAL DRUG MISUSE ( 11 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 11 FDA reports)
KYPHOSIS ( 11 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 11 FDA reports)
LIPOMA ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
MECONIUM STAIN ( 11 FDA reports)
METASTASES TO PLEURA ( 11 FDA reports)
MITRAL VALVE PROLAPSE ( 11 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 11 FDA reports)
OBSTRUCTION GASTRIC ( 11 FDA reports)
ONYCHOLYSIS ( 11 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 11 FDA reports)
OVARIAN DISORDER ( 11 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 11 FDA reports)
PERITONEAL HAEMORRHAGE ( 11 FDA reports)
PHOTOPHOBIA ( 11 FDA reports)
PLEURITIC PAIN ( 11 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 11 FDA reports)
PRODUCT QUALITY ISSUE ( 11 FDA reports)
RALES ( 11 FDA reports)
RECURRENT CANCER ( 11 FDA reports)
RESPIRATORY DEPRESSION ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 11 FDA reports)
STATUS EPILEPTICUS ( 11 FDA reports)
STUPOR ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
THYROID DISORDER ( 11 FDA reports)
TOBACCO ABUSE ( 11 FDA reports)
TROPONIN INCREASED ( 11 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
VAGINAL CANDIDIASIS ( 11 FDA reports)
VASCULAR CALCIFICATION ( 11 FDA reports)
VERTEBROPLASTY ( 11 FDA reports)
VOCAL CORD DISORDER ( 11 FDA reports)
WOUND DRAINAGE ( 11 FDA reports)
ACCIDENTAL OVERDOSE ( 10 FDA reports)
ADRENAL SUPPRESSION ( 10 FDA reports)
AFFECTIVE DISORDER ( 10 FDA reports)
AMMONIA INCREASED ( 10 FDA reports)
ANAL FISSURE ( 10 FDA reports)
ANAL FISTULA ( 10 FDA reports)
AORTIC DISORDER ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BILIARY DYSKINESIA ( 10 FDA reports)
BIOPSY GINGIVAL ( 10 FDA reports)
BODY TINEA ( 10 FDA reports)
CANDIDA PNEUMONIA ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CHEST WALL PAIN ( 10 FDA reports)
CITROBACTER INFECTION ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 10 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 10 FDA reports)
DELUSION ( 10 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 10 FDA reports)
DEMYELINATION ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
DEVICE MALFUNCTION ( 10 FDA reports)
DIVERTICULAR PERFORATION ( 10 FDA reports)
DROOLING ( 10 FDA reports)
DRUG EFFECT INCREASED ( 10 FDA reports)
EMBOLISM VENOUS ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
FACIAL PALSY ( 10 FDA reports)
FAT TISSUE INCREASED ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
GASTROENTERITIS VIRAL ( 10 FDA reports)
GUILLAIN-BARRE SYNDROME ( 10 FDA reports)
HAIR GROWTH ABNORMAL ( 10 FDA reports)
HEARING IMPAIRED ( 10 FDA reports)
HEPATIC ENZYME ABNORMAL ( 10 FDA reports)
HEPATIC ISCHAEMIA ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERVENTILATION ( 10 FDA reports)
HYPOKINESIA ( 10 FDA reports)
INJECTION SITE SWELLING ( 10 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 10 FDA reports)
INTRACRANIAL HYPOTENSION ( 10 FDA reports)
ISCHAEMIC HEPATITIS ( 10 FDA reports)
KNEE ARTHROPLASTY ( 10 FDA reports)
LIP EROSION ( 10 FDA reports)
LIVE BIRTH ( 10 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
MACULE ( 10 FDA reports)
MAMMOPLASTY ( 10 FDA reports)
MANIA ( 10 FDA reports)
METASTASES TO LUNG ( 10 FDA reports)
MICTURITION FREQUENCY DECREASED ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
NERVE ROOT COMPRESSION ( 10 FDA reports)
NEUTROPENIC SEPSIS ( 10 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 10 FDA reports)
NO ADVERSE EVENT ( 10 FDA reports)
OCCULT BLOOD POSITIVE ( 10 FDA reports)
ODONTOGENIC CYST ( 10 FDA reports)
ORAL PUSTULE ( 10 FDA reports)
OSTEOMYELITIS CHRONIC ( 10 FDA reports)
OTITIS MEDIA CHRONIC ( 10 FDA reports)
PARALYSIS ( 10 FDA reports)
PAROSMIA ( 10 FDA reports)
PULMONARY MYCOSIS ( 10 FDA reports)
RADICULITIS ( 10 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 10 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 10 FDA reports)
RHONCHI ( 10 FDA reports)
SJOGREN'S SYNDROME ( 10 FDA reports)
SKIN CANDIDA ( 10 FDA reports)
SKIN FIBROSIS ( 10 FDA reports)
SPINAL CORD OEDEMA ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 10 FDA reports)
THROMBECTOMY ( 10 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 10 FDA reports)
VISUAL FIELD DEFECT ( 10 FDA reports)
VITAMIN D DEFICIENCY ( 10 FDA reports)
VULVOVAGINAL PAIN ( 10 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 10 FDA reports)
ABNORMAL DREAMS ( 9 FDA reports)
ADHESION ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ANGIOPLASTY ( 9 FDA reports)
AORTIC THROMBOSIS ( 9 FDA reports)
BACTERIAL DIARRHOEA ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 9 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 9 FDA reports)
BRUXISM ( 9 FDA reports)
CANDIDA SEPSIS ( 9 FDA reports)
CARDIAC PACEMAKER INSERTION ( 9 FDA reports)
CATHETER SITE HAEMATOMA ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CHEST TUBE INSERTION ( 9 FDA reports)
CUSHING'S SYNDROME ( 9 FDA reports)
DENTAL FISTULA ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
DYSAESTHESIA ( 9 FDA reports)
DYSPAREUNIA ( 9 FDA reports)
EARLY SATIETY ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 9 FDA reports)
EXFOLIATIVE RASH ( 9 FDA reports)
FOLLICULITIS ( 9 FDA reports)
GENITAL CANDIDIASIS ( 9 FDA reports)
GENITAL HERPES ( 9 FDA reports)
HAEMOTHORAX ( 9 FDA reports)
HALLUCINATIONS, MIXED ( 9 FDA reports)
HEPATIC NEOPLASM ( 9 FDA reports)
HEPATOBLASTOMA ( 9 FDA reports)
HEPATORENAL SYNDROME ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 9 FDA reports)
HORDEOLUM ( 9 FDA reports)
HYPERPROTEINAEMIA ( 9 FDA reports)
IMPAIRED WORK ABILITY ( 9 FDA reports)
INFECTIVE TENOSYNOVITIS ( 9 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 9 FDA reports)
JOINT INSTABILITY ( 9 FDA reports)
KERATITIS ( 9 FDA reports)
LARGE INTESTINAL ULCER ( 9 FDA reports)
LEUKAEMIA ( 9 FDA reports)
LIP HAEMORRHAGE ( 9 FDA reports)
LIP NEOPLASM BENIGN ( 9 FDA reports)
LIPOATROPHY ( 9 FDA reports)
LIVEDO RETICULARIS ( 9 FDA reports)
LIVER ABSCESS ( 9 FDA reports)
LYMPHADENECTOMY ( 9 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 9 FDA reports)
MEDICAL DEVICE COMPLICATION ( 9 FDA reports)
METASTASES TO ADRENALS ( 9 FDA reports)
METASTASES TO BONE MARROW ( 9 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MYOFASCITIS ( 9 FDA reports)
NASAL POLYPS ( 9 FDA reports)
NECK INJURY ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NEUROTOXICITY ( 9 FDA reports)
NIKOLSKY'S SIGN ( 9 FDA reports)
OCULAR ICTERUS ( 9 FDA reports)
OSTEOMYELITIS ACUTE ( 9 FDA reports)
OXYGEN SUPPLEMENTATION ( 9 FDA reports)
PALATAL DISORDER ( 9 FDA reports)
PARAPSORIASIS ( 9 FDA reports)
PERICARDIAL CYST ( 9 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 9 FDA reports)
PNEUMONIA HAEMOPHILUS ( 9 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
PROCTITIS ULCERATIVE ( 9 FDA reports)
RED MAN SYNDROME ( 9 FDA reports)
RENAL PAIN ( 9 FDA reports)
RETINAL ANOMALY CONGENITAL ( 9 FDA reports)
RETINAL TEAR ( 9 FDA reports)
RETINITIS PIGMENTOSA ( 9 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 9 FDA reports)
ROTAVIRUS INFECTION ( 9 FDA reports)
SCHAMBERG'S DISEASE ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SKELETAL INJURY ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SNORING ( 9 FDA reports)
SPLEEN DISORDER ( 9 FDA reports)
SPLENIC ABSCESS ( 9 FDA reports)
SUICIDAL BEHAVIOUR ( 9 FDA reports)
SUPERINFECTION ( 9 FDA reports)
SUTURE REMOVAL ( 9 FDA reports)
THERMAL BURN ( 9 FDA reports)
THYROID ADENOMA ( 9 FDA reports)
TINEA CRURIS ( 9 FDA reports)
VENOUS THROMBOSIS LIMB ( 9 FDA reports)
VITAMIN D DECREASED ( 9 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 9 FDA reports)
WRONG DRUG ADMINISTERED ( 9 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ACUTE PSYCHOSIS ( 8 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
ADENOVIRUS INFECTION ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ALLERGY TO ANIMAL ( 8 FDA reports)
ANGIOPATHY ( 8 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 8 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 8 FDA reports)
APGAR SCORE LOW ( 8 FDA reports)
ASBESTOSIS ( 8 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BLOOD COUNT ABNORMAL ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BONE FISTULA ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
CARDIAC FAILURE CHRONIC ( 8 FDA reports)
CARDIAC HYPERTROPHY ( 8 FDA reports)
CARDIAC OUTPUT DECREASED ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CATHETER SITE HAEMORRHAGE ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
COLLAPSE OF LUNG ( 8 FDA reports)
COMMUNICATION DISORDER ( 8 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 8 FDA reports)
CORNEAL DYSTROPHY ( 8 FDA reports)
CRYING ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
DEPENDENCE ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 8 FDA reports)
EMBOLISM ( 8 FDA reports)
END STAGE AIDS ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
EYELID OEDEMA ( 8 FDA reports)
FACET JOINT SYNDROME ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FLUID INTAKE REDUCED ( 8 FDA reports)
FUNGAL SKIN INFECTION ( 8 FDA reports)
GALLBLADDER INJURY ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTRIC HAEMORRHAGE ( 8 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 8 FDA reports)
HEPATECTOMY ( 8 FDA reports)
HEPATIC CONGESTION ( 8 FDA reports)
HERPES VIRUS INFECTION ( 8 FDA reports)
HICCUPS ( 8 FDA reports)
IMMUNODEFICIENCY ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 8 FDA reports)
INTESTINAL ADENOCARCINOMA ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LIGAMENT INJURY ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 8 FDA reports)
LOWER LIMB FRACTURE ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LYMPHATIC DISORDER ( 8 FDA reports)
MENSTRUATION IRREGULAR ( 8 FDA reports)
METASTATIC PAIN ( 8 FDA reports)
METATARSUS PRIMUS VARUS ( 8 FDA reports)
MIDDLE INSOMNIA ( 8 FDA reports)
MOUTH BREATHING ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
MUSCLE TIGHTNESS ( 8 FDA reports)
MYELITIS TRANSVERSE ( 8 FDA reports)
NEPHROPATHY ( 8 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
OROPHARYNGEAL BLISTERING ( 8 FDA reports)
PERICARDIAL DRAINAGE ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 8 FDA reports)
POST LAMINECTOMY SYNDROME ( 8 FDA reports)
PREMATURE LABOUR ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
PYURIA ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
SCROTAL IRRITATION ( 8 FDA reports)
SEASONAL ALLERGY ( 8 FDA reports)
SINUS HEADACHE ( 8 FDA reports)
SINUS RHYTHM ( 8 FDA reports)
SKIN GRAFT ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
TESTICULAR ATROPHY ( 8 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 8 FDA reports)
TRANSPLANT ( 8 FDA reports)
TUMOUR INVASION ( 8 FDA reports)
URETHRAL DISORDER ( 8 FDA reports)
URINE ANALYSIS ABNORMAL ( 8 FDA reports)
VAGINAL MYCOSIS ( 8 FDA reports)
VULVOVAGINAL DISCOMFORT ( 8 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ACTINOMYCES TEST POSITIVE ( 7 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 7 FDA reports)
ALLODYNIA ( 7 FDA reports)
ANAEMIA NEONATAL ( 7 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 7 FDA reports)
ARTHROSCOPIC SURGERY ( 7 FDA reports)
ASTERIXIS ( 7 FDA reports)
AUTOIMMUNE DISORDER ( 7 FDA reports)
BACILLUS INFECTION ( 7 FDA reports)
BACTERIA URINE ( 7 FDA reports)
BALANOPOSTHITIS ( 7 FDA reports)
BILIARY TRACT DISORDER ( 7 FDA reports)
BLADDER OPERATION ( 7 FDA reports)
BLINDNESS CORTICAL ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BREAST CANCER FEMALE ( 7 FDA reports)
BRONCHITIS CHRONIC ( 7 FDA reports)
CANDIDA TEST POSITIVE ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 7 FDA reports)
CATARACT NUCLEAR ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CLEFT UVULA ( 7 FDA reports)
COLD SWEAT ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 7 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 7 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 7 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 7 FDA reports)
DENTAL CARE ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
DIABETES INSIPIDUS ( 7 FDA reports)
DIABETIC COMPLICATION ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
DUODENAL STENOSIS ( 7 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 7 FDA reports)
EJECTION FRACTION ( 7 FDA reports)
ENTHESOPATHY ( 7 FDA reports)
EOSINOPHIL COUNT DECREASED ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
EPIDIDYMAL CYST ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
FEELING JITTERY ( 7 FDA reports)
GASTRECTOMY ( 7 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 7 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 7 FDA reports)
GENITAL PRURITUS FEMALE ( 7 FDA reports)
GINGIVAL ERYTHEMA ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
GLIOBLASTOMA MULTIFORME ( 7 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 7 FDA reports)
HAEMOGLOBIN ABNORMAL ( 7 FDA reports)
HAEMORRHAGIC DISORDER ( 7 FDA reports)
HELICOBACTER INFECTION ( 7 FDA reports)
HEPATIC CANCER METASTATIC ( 7 FDA reports)
HEPATITIS TOXIC ( 7 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
IMMUNOSUPPRESSION ( 7 FDA reports)
INCISIONAL HERNIA ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INFECTIOUS DISEASE CARRIER ( 7 FDA reports)
INTENTION TREMOR ( 7 FDA reports)
INTESTINAL HAEMORRHAGE ( 7 FDA reports)
INTESTINAL RESECTION ( 7 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 7 FDA reports)
ISCHAEMIC STROKE ( 7 FDA reports)
JOINT ARTHROPLASTY ( 7 FDA reports)
KELOID SCAR ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
LIMB OPERATION ( 7 FDA reports)
LISTLESS ( 7 FDA reports)
LOWER EXTREMITY MASS ( 7 FDA reports)
MALIGNANT MELANOMA ( 7 FDA reports)
MASTOIDITIS ( 7 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
MAXILLOFACIAL OPERATION ( 7 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 7 FDA reports)
MENIERE'S DISEASE ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
MYCOPLASMA INFECTION ( 7 FDA reports)
MYOPIA ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
NEUTROPENIC INFECTION ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
OEDEMA MOUTH ( 7 FDA reports)
OESOPHAGEAL PAIN ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
PAINFUL RESPIRATION ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PARAPROTEINAEMIA ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PERIPHERAL ISCHAEMIA ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
PLACENTAL DISORDER ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PULMONARY SEPSIS ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RENAL ANEURYSM ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 7 FDA reports)
RETINOPATHY ( 7 FDA reports)
RIB DEFORMITY ( 7 FDA reports)
SCROTAL ABSCESS ( 7 FDA reports)
SCROTAL INFECTION ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
SINUS POLYP ( 7 FDA reports)
SKIN FRAGILITY ( 7 FDA reports)
SKIN HAEMORRHAGE ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SKIN LESION EXCISION ( 7 FDA reports)
SLEEP TERROR ( 7 FDA reports)
SOFT TISSUE INFECTION ( 7 FDA reports)
SPINAL DECOMPRESSION ( 7 FDA reports)
SPONDYLITIS ( 7 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
STOMACH DISCOMFORT ( 7 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 7 FDA reports)
SYSTEMIC MYCOSIS ( 7 FDA reports)
TENDON INJURY ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
THALASSAEMIA ALPHA ( 7 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 7 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 7 FDA reports)
TINEA PEDIS ( 7 FDA reports)
TONSILLITIS ( 7 FDA reports)
TRIGGER FINGER ( 7 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VENTRICULAR DYSFUNCTION ( 7 FDA reports)
VOCAL CORD CYST ( 7 FDA reports)
VULVAL DISORDER ( 7 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ACUTE LEUKAEMIA ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
ADENOIDITIS ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
ANION GAP DECREASED ( 6 FDA reports)
ANISOCYTOSIS ( 6 FDA reports)
ANTITHROMBIN III DECREASED ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPENDICITIS PERFORATED ( 6 FDA reports)
ASCITES INFECTION ( 6 FDA reports)
ATHEROSCLEROSIS ( 6 FDA reports)
B-CELL LYMPHOMA ( 6 FDA reports)
BIOPSY LIP ( 6 FDA reports)
BLADDER DILATATION ( 6 FDA reports)
BLADDER PROLAPSE ( 6 FDA reports)
BLAST CELLS PRESENT ( 6 FDA reports)
BLOOD CORTISOL DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BONE NEOPLASM ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
CARBON DIOXIDE DECREASED ( 6 FDA reports)
CHEMOTHERAPY ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
CONGENITAL HEPATOMEGALY ( 6 FDA reports)
CRANIOTOMY ( 6 FDA reports)
CREATININE URINE DECREASED ( 6 FDA reports)
CULTURE WOUND POSITIVE ( 6 FDA reports)
CYSTITIS INTERSTITIAL ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
EAR DISORDER ( 6 FDA reports)
ELECTROPHORESIS ABNORMAL ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 6 FDA reports)
EROSIVE DUODENITIS ( 6 FDA reports)
EYE INFECTION FUNGAL ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
FAT NECROSIS ( 6 FDA reports)
FEMORAL NECK FRACTURE ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
FUNGAL PERITONITIS ( 6 FDA reports)
FUNGAL SEPSIS ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GASTRIC BYPASS ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GOUT ( 6 FDA reports)
GRIMACING ( 6 FDA reports)
HAEMODILUTION ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 6 FDA reports)
HIV WASTING SYNDROME ( 6 FDA reports)
HOMICIDAL IDEATION ( 6 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 6 FDA reports)
HYPERCHLORHYDRIA ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERPHAGIA ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 6 FDA reports)
HYPERTRICHOSIS ( 6 FDA reports)
HYPOGONADISM ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
IRON DEFICIENCY ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LARYNGOCELE ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
LIPOMATOSIS ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
MAMMARY DUCT ECTASIA ( 6 FDA reports)
MANDIBULECTOMY ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
METAPLASIA ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 6 FDA reports)
MOTION SICKNESS ( 6 FDA reports)
MUMPS ( 6 FDA reports)
MUSCLE SPASTICITY ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NASAL SEPTUM PERFORATION ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 6 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
OROANTRAL FISTULA ( 6 FDA reports)
OSTEOPOROTIC FRACTURE ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
PNEUMONIA INFLUENZAL ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYCYSTIC OVARIES ( 6 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 6 FDA reports)
POSTOPERATIVE INFECTION ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
PROCEDURAL HYPERTENSION ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
RADIATION OESOPHAGITIS ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
REFLUX LARYNGITIS ( 6 FDA reports)
RESPIRATORY ALKALOSIS ( 6 FDA reports)
RESPIRATORY DEPTH DECREASED ( 6 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 6 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 6 FDA reports)
SERUM SICKNESS ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SMALL INTESTINAL RESECTION ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
TRACHEOBRONCHITIS ( 6 FDA reports)
TRANSPLANT FAILURE ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRIGONITIS ( 6 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 6 FDA reports)
URINE OSMOLARITY DECREASED ( 6 FDA reports)
URINE OUTPUT INCREASED ( 6 FDA reports)
URINE URIC ACID DECREASED ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
VITH NERVE PARALYSIS ( 6 FDA reports)
VULVOVAGINAL PRURITUS ( 6 FDA reports)
WEIGHT GAIN POOR ( 6 FDA reports)
WHITE CLOT SYNDROME ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ACETABULUM FRACTURE ( 5 FDA reports)
ACINETOBACTER INFECTION ( 5 FDA reports)
ACROCHORDON ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 5 FDA reports)
AEROPHAGIA ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ANAEMIA OF PREGNANCY ( 5 FDA reports)
ANAL ULCER ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
AUTOIMMUNE THYROIDITIS ( 5 FDA reports)
AXILLARY MASS ( 5 FDA reports)
BACTERIA URINE IDENTIFIED ( 5 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 5 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 5 FDA reports)
BIPOLAR II DISORDER ( 5 FDA reports)
BLADDER CANCER RECURRENT ( 5 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD GASES ABNORMAL ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BUNION OPERATION ( 5 FDA reports)
CALCIUM METABOLISM DISORDER ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIORENAL SYNDROME ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CHOKING ( 5 FDA reports)
CHOREA ( 5 FDA reports)
CHROMOSOMAL DELETION ( 5 FDA reports)
CHYLOTHORAX ( 5 FDA reports)
CLEFT PALATE ( 5 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 5 FDA reports)
COMA HEPATIC ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
COR PULMONALE ( 5 FDA reports)
CORNEAL ABRASION ( 5 FDA reports)
CRYPTOCOCCOSIS ( 5 FDA reports)
CYTOGENETIC ABNORMALITY ( 5 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 5 FDA reports)
CYTOMEGALOVIRUS TEST ( 5 FDA reports)
DERMOID CYST ( 5 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DUODENAL POLYP ( 5 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 5 FDA reports)
DYSMENORRHOEA ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
EJACULATION DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
EPIDERMOLYSIS BULLOSA ( 5 FDA reports)
EPIPLOIC APPENDAGITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 5 FDA reports)
ERYTHEMA MIGRANS ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
EYE NAEVUS ( 5 FDA reports)
EYELID PTOSIS CONGENITAL ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
HAEMOGLOBIN C TRAIT ( 5 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HEPATIC MASS ( 5 FDA reports)
HEPATIC VEIN OCCLUSION ( 5 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 5 FDA reports)
HETEROTAXIA ( 5 FDA reports)
HISTONE ANTIBODY POSITIVE ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HYPERADRENOCORTICISM ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPERAMYLASAEMIA ( 5 FDA reports)
HYPERLACTACIDAEMIA ( 5 FDA reports)
HYPERMETABOLISM ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
INCREASED APPETITE ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INFECTIOUS PERITONITIS ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE PRURITUS ( 5 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 5 FDA reports)
KERATITIS HERPETIC ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LIP DISORDER ( 5 FDA reports)
LOCKED-IN SYNDROME ( 5 FDA reports)
LOSS OF EMPLOYMENT ( 5 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
LYMPHATIC DUCT RUPTURE ( 5 FDA reports)
MACROCEPHALY ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MEDIASTINITIS ( 5 FDA reports)
MENINGEAL NEOPLASM ( 5 FDA reports)
MENINGITIS ENTEROCOCCAL ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
MOEBIUS II SYNDROME ( 5 FDA reports)
MULTIPLE ALLERGIES ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
MUSCLE FLAP OPERATION ( 5 FDA reports)
MUSCLE MASS ( 5 FDA reports)
MUSCLE NECROSIS ( 5 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NARCOLEPSY ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
NODAL RHYTHM ( 5 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 5 FDA reports)
OESOPHAGEAL PERFORATION ( 5 FDA reports)
OESOPHAGEAL SPASM ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PANCREATIC NEOPLASM ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PLACENTA PRAEVIA ( 5 FDA reports)
PLANTAR FASCIITIS ( 5 FDA reports)
PNEUMONIA NECROTISING ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 5 FDA reports)
PNEUMOPERITONEUM ( 5 FDA reports)
POISONING ( 5 FDA reports)
POST HERPETIC NEURALGIA ( 5 FDA reports)
PRECOCIOUS PUBERTY ( 5 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 5 FDA reports)
PSORIATIC ARTHROPATHY ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RENAL STONE REMOVAL ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
ROTATOR CUFF REPAIR ( 5 FDA reports)
RUBELLA ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SCARLET FEVER ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SIGMOIDECTOMY ( 5 FDA reports)
SINUSITIS FUNGAL ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SPEECH REHABILITATION ( 5 FDA reports)
SPLENECTOMY ( 5 FDA reports)
STEATORRHOEA ( 5 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
SUPRANUCLEAR PALSY ( 5 FDA reports)
TACHYPHRENIA ( 5 FDA reports)
TEETH BRITTLE ( 5 FDA reports)
TOOTH EROSION ( 5 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 5 FDA reports)
TRANSFERRIN INCREASED ( 5 FDA reports)
TREATMENT FAILURE ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
URETHRITIS ( 5 FDA reports)
VAGINAL BURNING SENSATION ( 5 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 5 FDA reports)
VENOOCCLUSIVE DISEASE ( 5 FDA reports)
VULVAL ULCERATION ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
WHITE BLOOD CELL DISORDER ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ABSCESS JAW ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
AIDS ENCEPHALOPATHY ( 4 FDA reports)
AIDS RELATED COMPLICATION ( 4 FDA reports)
ALLERGY TEST POSITIVE ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
ANAL SKIN TAGS ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ASPERGILLOSIS ORAL ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BONE INFARCTION ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CANDIDA ENDOPHTHALMITIS ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CATHETER SEPSIS ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 4 FDA reports)
CLEFT LIP AND PALATE ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 4 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CORNEAL EROSION ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORYNEBACTERIUM INFECTION ( 4 FDA reports)
CRANIOSYNOSTOSIS ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DIABETIC ULCER ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENGRAFTMENT SYNDROME ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENTEROCOLITIS VIRAL ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
ERYTHROPENIA ( 4 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 4 FDA reports)
EXTRAVASATION ( 4 FDA reports)
EYELID BLEEDING ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL INJURY ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GENERAL NUTRITION DISORDER ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT DYSFUNCTION ( 4 FDA reports)
GRAFT THROMBOSIS ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAPTOGLOBIN DECREASED ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC ARTERY STENOSIS ( 4 FDA reports)
HEPATIC INFARCTION ( 4 FDA reports)
HEPATIC SIDEROSIS ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPERVISCOSITY SYNDROME ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INGROWING NAIL ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LICHENOID KERATOSIS ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIVER OPERATION ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LUNG LOBECTOMY ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYME DISEASE ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MASTOID EFFUSION ( 4 FDA reports)
MEGAKARYOCYTES INCREASED ( 4 FDA reports)
MEIBOMIANITIS ( 4 FDA reports)
MENOPAUSAL SYMPTOMS ( 4 FDA reports)
MENSTRUATION DELAYED ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METASTASES TO KIDNEY ( 4 FDA reports)
METASTASES TO MENINGES ( 4 FDA reports)
METASTASES TO THE MEDIASTINUM ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONOCYTE COUNT ABNORMAL ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 4 FDA reports)
MYOGLOBINAEMIA ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEURODEGENERATIVE DISORDER ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OESOPHAGEAL RUPTURE ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
OOPHORECTOMY ( 4 FDA reports)
OPEN ANGLE GLAUCOMA ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
OSTEOARTHROPATHY ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PERFORATED ULCER ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGEAL CANDIDIASIS ( 4 FDA reports)
PINGUECULA ( 4 FDA reports)
PNEUMONIA ASPERGILLUS ( 4 FDA reports)
POIKILOCYTOSIS ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POST PROCEDURAL BILE LEAK ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
POST-TRAUMATIC HEADACHE ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
PUS IN STOOL ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETICULOCYTOSIS ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
REYE'S SYNDROME ( 4 FDA reports)
RIGHT ATRIAL DILATATION ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SCAR EXCISION ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
SPUTUM PURULENT ( 4 FDA reports)
STARING ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STERNAL FRACTURE ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SWEAT GLAND INFECTION ( 4 FDA reports)
T-CELL LYMPHOMA STAGE III ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TENOSYNOVITIS STENOSANS ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THYROIDECTOMY ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
TRANSFUSION MICROCHIMERISM ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
TUMOUR MARKER INCREASED ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
UTERINE RUPTURE ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VAGINAL PAIN ( 4 FDA reports)
VAGINAL SWELLING ( 4 FDA reports)
VAGINITIS ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VENOUS STENT INSERTION ( 4 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
ZINC DEFICIENCY ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE STRESS DISORDER ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
AMMONIA DECREASED ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAL CANDIDIASIS ( 3 FDA reports)
ANAL EROSION ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 3 FDA reports)
BASE EXCESS INCREASED ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 3 FDA reports)
BLOOD URIC ACID DECREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BOWEN'S DISEASE ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST HAEMATOMA ( 3 FDA reports)
BREAST NEOPLASM ( 3 FDA reports)
BRONCHITIS FUNGAL ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CERVICAL CORD COMPRESSION ( 3 FDA reports)
CHEMICAL BURN OF SKIN ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
COMMINUTED FRACTURE ( 3 FDA reports)
CONJUNCTIVITIS VIRAL ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DIABETIC GASTROPARESIS ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DISSOCIATIVE DISORDER ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EVANS SYNDROME ( 3 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOETAL MOVEMENTS DECREASED ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGAL TEST POSITIVE ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
GLYCOGEN STORAGE DISORDER ( 3 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 3 FDA reports)
HAEMANGIOMA OF SKIN ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAIRY CELL LEUKAEMIA ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HELICOBACTER SEPSIS ( 3 FDA reports)
HEPATOBILIARY DISEASE ( 3 FDA reports)
HERPES DERMATITIS ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INCISION SITE COMPLICATION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 3 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTERTRIGO CANDIDA ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LACTOBACILLUS INFECTION ( 3 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 3 FDA reports)
LEUKAEMOID REACTION ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENINGIOMA SURGERY ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS FUNGAL ( 3 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 3 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
MICROALBUMINURIA ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MIDDLE EAR DISORDER ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MOANING ( 3 FDA reports)
MOUTH CYST ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 3 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NERVE ROOT LESION ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL POLYP ( 3 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL MUCOSAL DISORDER ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 3 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMONIA ESCHERICHIA ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST PROCEDURAL CONSTIPATION ( 3 FDA reports)
POSTMENOPAUSE ( 3 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 3 FDA reports)
POSTRENAL FAILURE ( 3 FDA reports)
PREGNANCY TEST POSITIVE ( 3 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY COCCIDIOIDES ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PULSE PRESSURE INCREASED ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
PYOMYOSITIS ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RADICULITIS LUMBOSACRAL ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL OSTEODYSTROPHY ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RESPIRATORY MONILIASIS ( 3 FDA reports)
RETICULIN INCREASED ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SALIVARY GLAND CANCER ( 3 FDA reports)
SALPINGO-OOPHORECTOMY ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SERUM SEROTONIN DECREASED ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SHUNT OCCLUSION ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPLENIC INJURY ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STRESS INCONTINENCE ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 3 FDA reports)
SUBMANDIBULAR MASS ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TENSION ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TIC ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONGUE NEOPLASM ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URETHRAL CARUNCLE ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
WOUND INFECTION BACTERIAL ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AIDS CHOLANGIOPATHY ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
ALOPECIA TOTALIS ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
ALVEOLAR PROTEINOSIS ( 2 FDA reports)
AMMONIA ABNORMAL ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE OEDEMA ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTIFICIAL ANUS ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASOPHIL COUNT DECREASED ( 2 FDA reports)
BASOPHILIA ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD INSULIN DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BONE CANCER METASTATIC ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST HYPERPLASIA ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COLITIS VIRAL ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
CONGENITAL NAEVUS ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
COXSACKIE VIRAL INFECTION ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
ENCEPHALITIS FUNGAL ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
ENZYME INHIBITION ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTERNAL EAR CELLULITIS ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FOETAL HEART RATE INCREASED ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HBV DNA INCREASED ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATITIS B VIRUS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERPHOSPHATASAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPERURICOSURIA ( 2 FDA reports)
HYPHAEMA ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KERATITIS FUNGAL ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LAPAROSCOPIC STERILISATION ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 2 FDA reports)
LEUKOENCEPHALOMYELITIS ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL DUCT ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENINGITIS COCCIDIOIDES ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
MYOCARDIAL DEPRESSION ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NOSE DEFORMITY ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
ORTHODONTIC PROCEDURE ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PAINFUL RESPONSE TO NORMAL STIMULI ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL LESION ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PILONIDAL CYST CONGENITAL ( 2 FDA reports)
PINEAL NEOPLASM ( 2 FDA reports)
PLAGUE ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL NEOPLASM ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PREMATURE AGEING ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 2 FDA reports)
PROTEIN S INCREASED ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTEUS TEST POSITIVE ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY HAEMATOMA ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PYONEPHROSIS ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RADICULITIS CERVICAL ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RETICULOCYTOPENIA ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
ROULEAUX FORMATION ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL CELL CARCINOMA ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENIC CALCIFICATION ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
SUBDURAL EFFUSION ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THORACIC HAEMORRHAGE ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRISOMY 21 ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
UMBILICAL CORD COMPRESSION ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VASCULAR CAUTERISATION ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULITIS GASTROINTESTINAL ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR DRAINAGE ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WEST NILE VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABORTION COMPLETE ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID DECREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANENCEPHALY ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BARTHOLIN'S ABSCESS ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE OUTPUT ( 1 FDA reports)
BILIARY ANASTOMOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLINDNESS CONGENITAL ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST FIBROSIS ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATARACT CONGENITAL ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 1 FDA reports)
CERVICAL DISCHARGE ( 1 FDA reports)
CHEMICAL CYSTITIS ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL NEGATIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS MYOCARDITIS ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EROSIVE BALANITIS ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHROPLASIA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR IX DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL FAT INCREASED ( 1 FDA reports)
FALLOPIAN TUBE OPERATION ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 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 INTERACTION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 1 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 1 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPANGINA ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HIV INFECTION CDC GROUP IV SUBGROUP A ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPLASTIC ANAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRANASAL NUMBNESS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ISOIMMUNISATION ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JAUNDICE HEPATOCELLULAR ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOBLAST COUNT INCREASED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROPHAGES DECREASED ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIFOCAL MICRONODULAR PNEUMOCYTE HYPERPLASIA ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE FIBROSIS ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOTIC CORNEAL ULCER ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOBLAST COUNT INCREASED ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL CARDIAC FAILURE ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OTOSALPINGITIS ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLASMA CELLS DECREASED ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE WAVEFORM ( 1 FDA reports)
PULSE WAVEFORM ABNORMAL ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RADIATION EXPOSURE IN UTERO ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKIN WOUND ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOBACILLUS INFECTION ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYMPATHOMIMETIC EFFECT ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALASSAEMIA TRAIT ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC OPERATION ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TIBIAL TORSION ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR CYST ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URETHRAL SYNDROME ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR DISSECTION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEILLONELLA INFECTION ( 1 FDA reports)
VELO-CARDIO-FACIAL SYNDROME ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)