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

DIARRHOEA ( 1758 FDA reports)
NEUROPATHY PERIPHERAL ( 1641 FDA reports)
PNEUMONIA ( 1572 FDA reports)
THROMBOCYTOPENIA ( 1495 FDA reports)
MULTIPLE MYELOMA ( 1480 FDA reports)
PYREXIA ( 1406 FDA reports)
DEATH ( 1360 FDA reports)
DISEASE PROGRESSION ( 1314 FDA reports)
PLATELET COUNT DECREASED ( 1205 FDA reports)
ANAEMIA ( 1192 FDA reports)
PAIN ( 1123 FDA reports)
DYSPNOEA ( 1120 FDA reports)
NAUSEA ( 1105 FDA reports)
ASTHENIA ( 1063 FDA reports)
FATIGUE ( 1054 FDA reports)
HYPOTENSION ( 950 FDA reports)
CONSTIPATION ( 848 FDA reports)
VOMITING ( 830 FDA reports)
RENAL FAILURE ACUTE ( 764 FDA reports)
PANCYTOPENIA ( 754 FDA reports)
DEHYDRATION ( 749 FDA reports)
HAEMOGLOBIN DECREASED ( 734 FDA reports)
PLEURAL EFFUSION ( 729 FDA reports)
SEPSIS ( 704 FDA reports)
INFECTION ( 670 FDA reports)
ANXIETY ( 657 FDA reports)
RENAL FAILURE ( 641 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 620 FDA reports)
BACK PAIN ( 607 FDA reports)
FALL ( 599 FDA reports)
HYPOAESTHESIA ( 590 FDA reports)
OEDEMA PERIPHERAL ( 581 FDA reports)
OSTEONECROSIS OF JAW ( 578 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 567 FDA reports)
NEUTROPENIA ( 566 FDA reports)
BONE DISORDER ( 549 FDA reports)
ABDOMINAL PAIN ( 528 FDA reports)
ATRIAL FIBRILLATION ( 525 FDA reports)
HERPES ZOSTER ( 525 FDA reports)
DIZZINESS ( 519 FDA reports)
CHEST PAIN ( 504 FDA reports)
DECREASED APPETITE ( 501 FDA reports)
PAIN IN EXTREMITY ( 497 FDA reports)
RESPIRATORY FAILURE ( 489 FDA reports)
OSTEONECROSIS ( 457 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 449 FDA reports)
RASH ( 449 FDA reports)
FEBRILE NEUTROPENIA ( 446 FDA reports)
ARTHRALGIA ( 439 FDA reports)
HYPONATRAEMIA ( 436 FDA reports)
HYPERTENSION ( 432 FDA reports)
DEEP VEIN THROMBOSIS ( 431 FDA reports)
BLOOD CREATININE INCREASED ( 429 FDA reports)
WEIGHT DECREASED ( 427 FDA reports)
CONFUSIONAL STATE ( 423 FDA reports)
URINARY TRACT INFECTION ( 415 FDA reports)
PARAESTHESIA ( 414 FDA reports)
HYPOKALAEMIA ( 397 FDA reports)
INJURY ( 388 FDA reports)
DRUG INEFFECTIVE ( 375 FDA reports)
CARDIAC FAILURE ( 372 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 372 FDA reports)
CELLULITIS ( 370 FDA reports)
COUGH ( 369 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 368 FDA reports)
ATELECTASIS ( 361 FDA reports)
ORTHOSTATIC HYPOTENSION ( 361 FDA reports)
SYNCOPE ( 359 FDA reports)
HYPOXIA ( 358 FDA reports)
HEADACHE ( 355 FDA reports)
LEUKOPENIA ( 350 FDA reports)
PAIN IN JAW ( 350 FDA reports)
BRONCHITIS ( 345 FDA reports)
TOOTH EXTRACTION ( 340 FDA reports)
MALAISE ( 339 FDA reports)
SEPTIC SHOCK ( 339 FDA reports)
OSTEOMYELITIS ( 335 FDA reports)
PULMONARY OEDEMA ( 323 FDA reports)
TUMOUR LYSIS SYNDROME ( 318 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 317 FDA reports)
PULMONARY EMBOLISM ( 310 FDA reports)
MUSCULAR WEAKNESS ( 308 FDA reports)
DEPRESSION ( 301 FDA reports)
LUNG DISORDER ( 299 FDA reports)
IMPAIRED HEALING ( 297 FDA reports)
CHILLS ( 294 FDA reports)
SPINAL OSTEOARTHRITIS ( 294 FDA reports)
INTERSTITIAL LUNG DISEASE ( 284 FDA reports)
CONDITION AGGRAVATED ( 282 FDA reports)
HYPERCALCAEMIA ( 280 FDA reports)
TACHYCARDIA ( 274 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 272 FDA reports)
OSTEOARTHRITIS ( 269 FDA reports)
DYSPHAGIA ( 267 FDA reports)
OEDEMA ( 267 FDA reports)
MUCOSAL INFLAMMATION ( 261 FDA reports)
HYPERGLYCAEMIA ( 259 FDA reports)
NEUTROPHIL COUNT DECREASED ( 257 FDA reports)
CARDIOMEGALY ( 254 FDA reports)
MULTI-ORGAN FAILURE ( 252 FDA reports)
BONE PAIN ( 249 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 247 FDA reports)
STAPHYLOCOCCAL INFECTION ( 245 FDA reports)
SOMNOLENCE ( 243 FDA reports)
BONE LESION ( 231 FDA reports)
ERYTHEMA ( 231 FDA reports)
INSOMNIA ( 230 FDA reports)
LUNG INFILTRATION ( 230 FDA reports)
OSTEOPOROSIS ( 228 FDA reports)
MYOCARDIAL INFARCTION ( 227 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 226 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 221 FDA reports)
HAEMATOCRIT DECREASED ( 219 FDA reports)
SWELLING ( 219 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 218 FDA reports)
PLASMACYTOMA ( 214 FDA reports)
STEM CELL TRANSPLANT ( 213 FDA reports)
EMOTIONAL DISTRESS ( 212 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 212 FDA reports)
MENTAL STATUS CHANGES ( 211 FDA reports)
RENAL FAILURE CHRONIC ( 211 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 210 FDA reports)
SINUSITIS ( 209 FDA reports)
VISION BLURRED ( 209 FDA reports)
MYALGIA ( 208 FDA reports)
BLOOD UREA INCREASED ( 203 FDA reports)
CATARACT ( 203 FDA reports)
ABDOMINAL DISTENSION ( 201 FDA reports)
RENAL IMPAIRMENT ( 199 FDA reports)
HYPOCALCAEMIA ( 198 FDA reports)
LOSS OF CONSCIOUSNESS ( 198 FDA reports)
OSTEOPENIA ( 194 FDA reports)
COLITIS ( 193 FDA reports)
CONVULSION ( 193 FDA reports)
HYPERKALAEMIA ( 192 FDA reports)
NEOPLASM MALIGNANT ( 189 FDA reports)
ANOREXIA ( 188 FDA reports)
CARDIAC ARREST ( 188 FDA reports)
POLYNEUROPATHY ( 188 FDA reports)
ANHEDONIA ( 186 FDA reports)
PULMONARY HYPERTENSION ( 185 FDA reports)
DEFORMITY ( 184 FDA reports)
TREMOR ( 184 FDA reports)
GAIT DISTURBANCE ( 181 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 178 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 174 FDA reports)
COMPRESSION FRACTURE ( 172 FDA reports)
DYSPEPSIA ( 172 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 170 FDA reports)
BONE MARROW FAILURE ( 169 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 168 FDA reports)
EPISTAXIS ( 168 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 168 FDA reports)
RESPIRATORY DISTRESS ( 167 FDA reports)
GASTRITIS ( 165 FDA reports)
INFLAMMATION ( 165 FDA reports)
MITRAL VALVE INCOMPETENCE ( 164 FDA reports)
DYSPNOEA EXERTIONAL ( 163 FDA reports)
CORONARY ARTERY DISEASE ( 162 FDA reports)
NEURALGIA ( 162 FDA reports)
NEUROPATHY ( 162 FDA reports)
RIB FRACTURE ( 162 FDA reports)
MUSCULOSKELETAL PAIN ( 159 FDA reports)
ILEUS ( 157 FDA reports)
SPINAL COMPRESSION FRACTURE ( 157 FDA reports)
URINARY RETENTION ( 157 FDA reports)
CEREBRAL HAEMORRHAGE ( 156 FDA reports)
DENTAL CARIES ( 156 FDA reports)
DECREASED INTEREST ( 155 FDA reports)
ABDOMINAL PAIN UPPER ( 153 FDA reports)
ASTHMA ( 153 FDA reports)
OSTEOLYSIS ( 151 FDA reports)
PNEUMONITIS ( 151 FDA reports)
DIABETES MELLITUS ( 149 FDA reports)
HAEMORRHAGE ( 148 FDA reports)
HYPOPHOSPHATAEMIA ( 147 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 147 FDA reports)
BLOOD CALCIUM DECREASED ( 146 FDA reports)
EJECTION FRACTION DECREASED ( 145 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 145 FDA reports)
HAEMATURIA ( 143 FDA reports)
MUSCLE SPASMS ( 143 FDA reports)
DIVERTICULUM ( 142 FDA reports)
CEREBROVASCULAR ACCIDENT ( 141 FDA reports)
OFF LABEL USE ( 141 FDA reports)
HYPOPHAGIA ( 139 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 138 FDA reports)
NO THERAPEUTIC RESPONSE ( 138 FDA reports)
SWELLING FACE ( 138 FDA reports)
EXOSTOSIS ( 137 FDA reports)
HIATUS HERNIA ( 137 FDA reports)
LIVER DISORDER ( 137 FDA reports)
CARDIOMYOPATHY ( 136 FDA reports)
DIALYSIS ( 135 FDA reports)
RECTAL HAEMORRHAGE ( 135 FDA reports)
BLOOD SODIUM DECREASED ( 134 FDA reports)
ILEUS PARALYTIC ( 133 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 133 FDA reports)
WEIGHT INCREASED ( 133 FDA reports)
BLOOD GLUCOSE INCREASED ( 132 FDA reports)
DRUG TOXICITY ( 132 FDA reports)
BLOOD POTASSIUM DECREASED ( 131 FDA reports)
HYPOALBUMINAEMIA ( 131 FDA reports)
PRODUCTIVE COUGH ( 131 FDA reports)
FLUID OVERLOAD ( 128 FDA reports)
THROMBOSIS ( 128 FDA reports)
ARRHYTHMIA ( 126 FDA reports)
HAEMORRHOIDS ( 126 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 126 FDA reports)
PATHOLOGICAL FRACTURE ( 125 FDA reports)
BURSITIS ( 124 FDA reports)
RENAL CYST ( 124 FDA reports)
BACTERIAL INFECTION ( 123 FDA reports)
TOOTHACHE ( 122 FDA reports)
BLOOD PRESSURE INCREASED ( 121 FDA reports)
HAEMOPTYSIS ( 119 FDA reports)
SINUS TACHYCARDIA ( 119 FDA reports)
DISABILITY ( 118 FDA reports)
STOMATITIS ( 118 FDA reports)
BLOOD PRESSURE DECREASED ( 117 FDA reports)
ELECTROLYTE IMBALANCE ( 117 FDA reports)
ENCEPHALOPATHY ( 117 FDA reports)
BACTERAEMIA ( 116 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 116 FDA reports)
LETHARGY ( 116 FDA reports)
PERICARDIAL EFFUSION ( 116 FDA reports)
BLOOD BILIRUBIN INCREASED ( 115 FDA reports)
CARDIAC DISORDER ( 115 FDA reports)
LYMPHADENOPATHY ( 115 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 115 FDA reports)
LUMBAR SPINAL STENOSIS ( 114 FDA reports)
PRURITUS ( 114 FDA reports)
HYPOGLYCAEMIA ( 113 FDA reports)
LYMPHOPENIA ( 113 FDA reports)
SCAR ( 113 FDA reports)
CARDIO-RESPIRATORY ARREST ( 112 FDA reports)
CHEST DISCOMFORT ( 112 FDA reports)
OESOPHAGITIS ( 112 FDA reports)
ORAL CANDIDIASIS ( 111 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 109 FDA reports)
HYPERHIDROSIS ( 107 FDA reports)
INFLUENZA ( 107 FDA reports)
LUNG INFECTION ( 107 FDA reports)
DYSURIA ( 106 FDA reports)
PULMONARY FIBROSIS ( 106 FDA reports)
ARTHRITIS ( 105 FDA reports)
ASCITES ( 104 FDA reports)
CONTUSION ( 103 FDA reports)
DIVERTICULITIS ( 103 FDA reports)
PROTHROMBIN TIME PROLONGED ( 103 FDA reports)
HAEMODIALYSIS ( 102 FDA reports)
HEPATIC FAILURE ( 102 FDA reports)
BRONCHOPNEUMONIA ( 101 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 101 FDA reports)
METABOLIC ACIDOSIS ( 100 FDA reports)
NEPHROLITHIASIS ( 100 FDA reports)
ORAL PAIN ( 100 FDA reports)
OXYGEN SATURATION DECREASED ( 100 FDA reports)
ARTERIOSCLEROSIS ( 99 FDA reports)
OVERDOSE ( 99 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 98 FDA reports)
ROTATOR CUFF SYNDROME ( 98 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 97 FDA reports)
MASTICATION DISORDER ( 97 FDA reports)
MYELODYSPLASTIC SYNDROME ( 97 FDA reports)
VISUAL ACUITY REDUCED ( 97 FDA reports)
MASS ( 95 FDA reports)
METASTASES TO BONE ( 95 FDA reports)
COMA ( 94 FDA reports)
HAEMATOMA ( 94 FDA reports)
HYPERLIPIDAEMIA ( 94 FDA reports)
JAW DISORDER ( 94 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 93 FDA reports)
LOOSE TOOTH ( 93 FDA reports)
EXPOSED BONE IN JAW ( 92 FDA reports)
HALLUCINATION ( 92 FDA reports)
NEUROTOXICITY ( 92 FDA reports)
PRIMARY SEQUESTRUM ( 92 FDA reports)
BLOOD ALBUMIN DECREASED ( 91 FDA reports)
DYSGEUSIA ( 91 FDA reports)
EMPHYSEMA ( 91 FDA reports)
MYELOMA RECURRENCE ( 91 FDA reports)
DELIRIUM ( 90 FDA reports)
HEART RATE INCREASED ( 90 FDA reports)
NECK PAIN ( 90 FDA reports)
SKIN LESION ( 90 FDA reports)
SPINAL CORD COMPRESSION ( 90 FDA reports)
BALANCE DISORDER ( 89 FDA reports)
MOUTH ULCERATION ( 89 FDA reports)
OSTEITIS ( 89 FDA reports)
ANGINA PECTORIS ( 88 FDA reports)
DECUBITUS ULCER ( 88 FDA reports)
LEUKAEMIA PLASMACYTIC ( 88 FDA reports)
TOOTH DISORDER ( 88 FDA reports)
ENDODONTIC PROCEDURE ( 87 FDA reports)
SHOCK ( 87 FDA reports)
SPLENOMEGALY ( 87 FDA reports)
HYPOMAGNESAEMIA ( 86 FDA reports)
NEOPLASM PROGRESSION ( 86 FDA reports)
OROPHARYNGEAL PAIN ( 86 FDA reports)
PROTEINURIA ( 86 FDA reports)
VIRAL INFECTION ( 86 FDA reports)
ABDOMINAL DISCOMFORT ( 85 FDA reports)
TOOTH LOSS ( 85 FDA reports)
AUTONOMIC NEUROPATHY ( 84 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 84 FDA reports)
PLASMACYTOSIS ( 84 FDA reports)
RESPIRATORY DISORDER ( 84 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 84 FDA reports)
BLOOD CULTURE POSITIVE ( 83 FDA reports)
DISORIENTATION ( 83 FDA reports)
LEUKOCYTOSIS ( 83 FDA reports)
JOINT SWELLING ( 82 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 82 FDA reports)
PNEUMONIA ASPIRATION ( 82 FDA reports)
SUDDEN DEATH ( 82 FDA reports)
CHOLELITHIASIS ( 81 FDA reports)
URTICARIA ( 81 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 80 FDA reports)
BLOOD POTASSIUM INCREASED ( 80 FDA reports)
HAEMATEMESIS ( 80 FDA reports)
HERPES SIMPLEX ( 80 FDA reports)
NEUROGENIC BLADDER ( 80 FDA reports)
PROTEIN TOTAL INCREASED ( 80 FDA reports)
SPINAL DISORDER ( 80 FDA reports)
WHEEZING ( 80 FDA reports)
RENAL DISORDER ( 79 FDA reports)
SPINAL COLUMN STENOSIS ( 79 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 78 FDA reports)
BRADYCARDIA ( 78 FDA reports)
DEBRIDEMENT ( 78 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 78 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 78 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 77 FDA reports)
BLINDNESS ( 77 FDA reports)
BONE MARROW TRANSPLANT ( 77 FDA reports)
CANDIDIASIS ( 77 FDA reports)
FUNGAL INFECTION ( 77 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 77 FDA reports)
URINARY INCONTINENCE ( 77 FDA reports)
DISCOMFORT ( 76 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 76 FDA reports)
INTESTINAL OBSTRUCTION ( 76 FDA reports)
PULMONARY CONGESTION ( 76 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 75 FDA reports)
HYPOVOLAEMIA ( 75 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 75 FDA reports)
PHYSICAL DISABILITY ( 75 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 74 FDA reports)
CARDIAC AMYLOIDOSIS ( 74 FDA reports)
DEAFNESS ( 74 FDA reports)
GRAFT VERSUS HOST DISEASE ( 74 FDA reports)
PALPITATIONS ( 74 FDA reports)
TENDERNESS ( 74 FDA reports)
TOOTH FRACTURE ( 74 FDA reports)
ACUTE RESPIRATORY FAILURE ( 73 FDA reports)
ATRIAL FLUTTER ( 73 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 73 FDA reports)
TRANSAMINASES INCREASED ( 73 FDA reports)
CIRCULATORY COLLAPSE ( 72 FDA reports)
CONJUNCTIVITIS ( 72 FDA reports)
MYOCARDIAL ISCHAEMIA ( 72 FDA reports)
PERFORMANCE STATUS DECREASED ( 72 FDA reports)
VERTIGO ( 72 FDA reports)
WOUND DEHISCENCE ( 72 FDA reports)
ABASIA ( 71 FDA reports)
CHOLECYSTITIS ( 71 FDA reports)
DYSPHONIA ( 71 FDA reports)
HEPATITIS B ( 71 FDA reports)
MYOCLONUS ( 71 FDA reports)
PSEUDOMONAS INFECTION ( 71 FDA reports)
SKIN ULCER ( 71 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 71 FDA reports)
ACIDOSIS ( 70 FDA reports)
CLOSTRIDIAL INFECTION ( 70 FDA reports)
EAR PAIN ( 70 FDA reports)
FAILURE TO THRIVE ( 70 FDA reports)
GENERALISED OEDEMA ( 70 FDA reports)
SCOLIOSIS ( 70 FDA reports)
VISUAL IMPAIRMENT ( 70 FDA reports)
GINGIVAL BLEEDING ( 69 FDA reports)
PERIODONTAL DISEASE ( 69 FDA reports)
CEREBRAL INFARCTION ( 68 FDA reports)
MALNUTRITION ( 68 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 68 FDA reports)
BLOOD CREATINE INCREASED ( 67 FDA reports)
EYE PAIN ( 67 FDA reports)
MELAENA ( 67 FDA reports)
ULCER ( 67 FDA reports)
COAGULOPATHY ( 66 FDA reports)
COLONIC POLYP ( 66 FDA reports)
DIVERTICULUM INTESTINAL ( 66 FDA reports)
KYPHOSIS ( 66 FDA reports)
NERVOUS SYSTEM DISORDER ( 66 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 66 FDA reports)
RASH ERYTHEMATOUS ( 66 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 66 FDA reports)
BLEPHARITIS ( 65 FDA reports)
PERONEAL NERVE PALSY ( 65 FDA reports)
RHABDOMYOLYSIS ( 65 FDA reports)
SINUS DISORDER ( 65 FDA reports)
TINNITUS ( 65 FDA reports)
UROSEPSIS ( 65 FDA reports)
ACTINOMYCOSIS ( 64 FDA reports)
FEELING ABNORMAL ( 64 FDA reports)
TOOTH ABSCESS ( 64 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 63 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 63 FDA reports)
BLOOD URIC ACID INCREASED ( 63 FDA reports)
DRY MOUTH ( 63 FDA reports)
GASTROINTESTINAL DISORDER ( 63 FDA reports)
GINGIVAL PAIN ( 63 FDA reports)
HEPATOMEGALY ( 63 FDA reports)
OSTEOSCLEROSIS ( 63 FDA reports)
PURPURA ( 63 FDA reports)
SQUAMOUS CELL CARCINOMA ( 63 FDA reports)
TENDONITIS ( 63 FDA reports)
TOOTH INFECTION ( 63 FDA reports)
BODY TEMPERATURE INCREASED ( 62 FDA reports)
GINGIVITIS ( 62 FDA reports)
HYDRONEPHROSIS ( 62 FDA reports)
JOINT EFFUSION ( 62 FDA reports)
HYPERSENSITIVITY ( 61 FDA reports)
RASH PRURITIC ( 61 FDA reports)
URINE OUTPUT DECREASED ( 61 FDA reports)
HOSPITALISATION ( 60 FDA reports)
PROTEIN URINE PRESENT ( 60 FDA reports)
UNRESPONSIVE TO STIMULI ( 60 FDA reports)
ACUTE PULMONARY OEDEMA ( 59 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 59 FDA reports)
CEREBRAL ISCHAEMIA ( 59 FDA reports)
DEVICE RELATED INFECTION ( 59 FDA reports)
FISTULA ( 59 FDA reports)
INTESTINAL ISCHAEMIA ( 59 FDA reports)
LIFE EXPECTANCY SHORTENED ( 59 FDA reports)
OBESITY ( 59 FDA reports)
ORAL CAVITY FISTULA ( 59 FDA reports)
AGITATION ( 58 FDA reports)
AZOTAEMIA ( 58 FDA reports)
HYPERCHOLESTEROLAEMIA ( 58 FDA reports)
LEUKOENCEPHALOPATHY ( 58 FDA reports)
LUNG NEOPLASM ( 58 FDA reports)
PURULENT DISCHARGE ( 58 FDA reports)
ROAD TRAFFIC ACCIDENT ( 58 FDA reports)
SENSORY LOSS ( 58 FDA reports)
TYPE 2 DIABETES MELLITUS ( 58 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 57 FDA reports)
DISEASE RECURRENCE ( 57 FDA reports)
DRUG INTERACTION ( 57 FDA reports)
PULMONARY HAEMORRHAGE ( 57 FDA reports)
RASH MACULO-PAPULAR ( 57 FDA reports)
RESPIRATORY TRACT INFECTION ( 57 FDA reports)
SPINAL FRACTURE ( 57 FDA reports)
ENTEROCOCCAL INFECTION ( 56 FDA reports)
FLUID RETENTION ( 56 FDA reports)
GINGIVAL INFECTION ( 56 FDA reports)
GINGIVAL SWELLING ( 56 FDA reports)
IMMUNODEFICIENCY ( 56 FDA reports)
SKIN EXFOLIATION ( 56 FDA reports)
BLOOD CALCIUM INCREASED ( 55 FDA reports)
ENTEROCOLITIS ( 55 FDA reports)
ERYTHEMA MULTIFORME ( 55 FDA reports)
HAEMATOCHEZIA ( 55 FDA reports)
HEPATIC CYST ( 55 FDA reports)
INFLUENZA LIKE ILLNESS ( 55 FDA reports)
PETECHIAE ( 55 FDA reports)
SPONDYLOLISTHESIS ( 55 FDA reports)
VENTRICULAR HYPERTROPHY ( 55 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 54 FDA reports)
ENDOCARDITIS ( 54 FDA reports)
GLAUCOMA ( 54 FDA reports)
HEAD INJURY ( 54 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 54 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 54 FDA reports)
PANCREATITIS ACUTE ( 54 FDA reports)
THERAPY NON-RESPONDER ( 54 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 53 FDA reports)
GASTRIC ULCER ( 53 FDA reports)
HYPERVISCOSITY SYNDROME ( 53 FDA reports)
HYPOACUSIS ( 53 FDA reports)
JAW FRACTURE ( 53 FDA reports)
JAW OPERATION ( 53 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 53 FDA reports)
AMNESIA ( 52 FDA reports)
AORTIC ANEURYSM ( 52 FDA reports)
ASPERGILLOSIS ( 52 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 52 FDA reports)
BONE DEBRIDEMENT ( 52 FDA reports)
CAPILLARY LEAK SYNDROME ( 52 FDA reports)
NASOPHARYNGITIS ( 52 FDA reports)
OLIGURIA ( 52 FDA reports)
PNEUMOTHORAX ( 52 FDA reports)
RENAL TUBULAR NECROSIS ( 52 FDA reports)
SURGERY ( 52 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 51 FDA reports)
CYSTITIS ( 51 FDA reports)
GYNAECOMASTIA ( 51 FDA reports)
IMMUNOSUPPRESSION ( 51 FDA reports)
MIGRAINE ( 51 FDA reports)
ORAL DISORDER ( 51 FDA reports)
ORAL HERPES ( 51 FDA reports)
PAPILLOEDEMA ( 51 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 51 FDA reports)
SLEEP APNOEA SYNDROME ( 51 FDA reports)
CYST ( 50 FDA reports)
FAECAL INCONTINENCE ( 50 FDA reports)
HERPES ZOSTER DISSEMINATED ( 50 FDA reports)
NERVOUSNESS ( 50 FDA reports)
RESPIRATORY ARREST ( 50 FDA reports)
SPEECH DISORDER ( 50 FDA reports)
CAECITIS ( 49 FDA reports)
DERMATITIS ( 49 FDA reports)
DIPLOPIA ( 49 FDA reports)
ERECTILE DYSFUNCTION ( 49 FDA reports)
HIP FRACTURE ( 49 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 49 FDA reports)
HYPOTHYROIDISM ( 49 FDA reports)
LOCALISED INFECTION ( 49 FDA reports)
ORAL INTAKE REDUCED ( 49 FDA reports)
PANCREATITIS ( 49 FDA reports)
PARAPLEGIA ( 49 FDA reports)
VASCULITIS ( 49 FDA reports)
BLOOD CHLORIDE DECREASED ( 48 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 48 FDA reports)
CATHETER RELATED INFECTION ( 48 FDA reports)
CHEST X-RAY ABNORMAL ( 48 FDA reports)
COGNITIVE DISORDER ( 48 FDA reports)
EATING DISORDER ( 48 FDA reports)
ESCHERICHIA INFECTION ( 48 FDA reports)
GOUT ( 48 FDA reports)
POLLAKIURIA ( 48 FDA reports)
PYELONEPHRITIS ( 48 FDA reports)
ASPIRATION ( 47 FDA reports)
GUILLAIN-BARRE SYNDROME ( 47 FDA reports)
HEPATIC STEATOSIS ( 47 FDA reports)
HYPOAESTHESIA ORAL ( 47 FDA reports)
MEMORY IMPAIRMENT ( 47 FDA reports)
NEUTROPENIC SEPSIS ( 47 FDA reports)
PNEUMONIA BACTERIAL ( 47 FDA reports)
PSYCHOTIC DISORDER ( 47 FDA reports)
PURULENCE ( 47 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 47 FDA reports)
RESPIRATORY RATE INCREASED ( 47 FDA reports)
BASAL CELL CARCINOMA ( 46 FDA reports)
BONE EROSION ( 46 FDA reports)
BRONCHIECTASIS ( 46 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 46 FDA reports)
COORDINATION ABNORMAL ( 46 FDA reports)
ENCEPHALITIS ( 46 FDA reports)
GINGIVAL DISORDER ( 46 FDA reports)
NERVE INJURY ( 46 FDA reports)
RASH GENERALISED ( 46 FDA reports)
VARICELLA ( 46 FDA reports)
WRONG DRUG ADMINISTERED ( 46 FDA reports)
ABSCESS ( 45 FDA reports)
ADVERSE EVENT ( 45 FDA reports)
CEREBRAL ATROPHY ( 45 FDA reports)
ESCHERICHIA SEPSIS ( 45 FDA reports)
FIBROSIS ( 45 FDA reports)
GASTRITIS EROSIVE ( 45 FDA reports)
LIMB DISCOMFORT ( 45 FDA reports)
MOBILITY DECREASED ( 45 FDA reports)
MYOPATHY ( 45 FDA reports)
NOCTURIA ( 45 FDA reports)
ORAL DISCOMFORT ( 45 FDA reports)
PALLOR ( 45 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 45 FDA reports)
SOFT TISSUE DISORDER ( 45 FDA reports)
DILATATION VENTRICULAR ( 44 FDA reports)
DYSARTHRIA ( 44 FDA reports)
INGUINAL HERNIA ( 44 FDA reports)
LACTIC ACIDOSIS ( 44 FDA reports)
LUNG CONSOLIDATION ( 44 FDA reports)
NEOPLASM ( 44 FDA reports)
OSTEORADIONECROSIS ( 44 FDA reports)
PERIODONTITIS ( 44 FDA reports)
PHLEBITIS ( 44 FDA reports)
VASCULAR CALCIFICATION ( 44 FDA reports)
WOUND DRAINAGE ( 44 FDA reports)
ABSCESS JAW ( 43 FDA reports)
AMYLOIDOSIS ( 43 FDA reports)
BONE NEOPLASM ( 43 FDA reports)
BRONCHOSPASM ( 43 FDA reports)
CARDIOVASCULAR DISORDER ( 43 FDA reports)
EMBOLISM ( 43 FDA reports)
EMPYEMA ( 43 FDA reports)
PHARYNGITIS ( 43 FDA reports)
SEQUESTRECTOMY ( 43 FDA reports)
SPUTUM CULTURE POSITIVE ( 43 FDA reports)
VENTRICULAR DYSFUNCTION ( 43 FDA reports)
AORTIC VALVE INCOMPETENCE ( 42 FDA reports)
BLADDER CANCER ( 42 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 42 FDA reports)
BREATH ODOUR ( 42 FDA reports)
DYSSTASIA ( 42 FDA reports)
FLANK PAIN ( 42 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 42 FDA reports)
NEPHROPATHY ( 42 FDA reports)
OPTIC NEURITIS ( 42 FDA reports)
PANIC ATTACK ( 42 FDA reports)
TOXIC SKIN ERUPTION ( 42 FDA reports)
VENTRICULAR HYPOKINESIA ( 42 FDA reports)
ANGIOPATHY ( 41 FDA reports)
BLINDNESS UNILATERAL ( 41 FDA reports)
EPILEPSY ( 41 FDA reports)
INTRAOCULAR LENS IMPLANT ( 41 FDA reports)
LABORATORY TEST ABNORMAL ( 41 FDA reports)
LOBAR PNEUMONIA ( 41 FDA reports)
PARESIS ( 41 FDA reports)
RASH MACULAR ( 41 FDA reports)
RHINITIS ALLERGIC ( 41 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 41 FDA reports)
ACUTE PRERENAL FAILURE ( 40 FDA reports)
ANURIA ( 40 FDA reports)
BONE DENSITY DECREASED ( 40 FDA reports)
DENTAL OPERATION ( 40 FDA reports)
DENTAL TREATMENT ( 40 FDA reports)
FACIAL PAIN ( 40 FDA reports)
GASTROENTERITIS ( 40 FDA reports)
GROIN PAIN ( 40 FDA reports)
MOTOR DYSFUNCTION ( 40 FDA reports)
MUSCLE STRAIN ( 40 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 40 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 40 FDA reports)
PULMONARY TOXICITY ( 40 FDA reports)
RHINORRHOEA ( 40 FDA reports)
WALKING AID USER ( 40 FDA reports)
ARTHROPATHY ( 39 FDA reports)
ASTIGMATISM ( 39 FDA reports)
BONE OPERATION ( 39 FDA reports)
DEMENTIA ( 39 FDA reports)
DIZZINESS POSTURAL ( 39 FDA reports)
DRY EYE ( 39 FDA reports)
HYPERURICAEMIA ( 39 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 39 FDA reports)
LYMPHOMA ( 39 FDA reports)
PERICARDITIS ( 39 FDA reports)
PNEUMONIA FUNGAL ( 39 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 39 FDA reports)
ACCIDENTAL OVERDOSE ( 38 FDA reports)
ACTINIC KERATOSIS ( 38 FDA reports)
APHASIA ( 38 FDA reports)
ATAXIA ( 38 FDA reports)
BLOOD COUNT ABNORMAL ( 38 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 38 FDA reports)
DERMAL CYST ( 38 FDA reports)
ECCHYMOSIS ( 38 FDA reports)
H1N1 INFLUENZA ( 38 FDA reports)
HOT FLUSH ( 38 FDA reports)
HYPERTHERMIA ( 38 FDA reports)
INFUSION RELATED REACTION ( 38 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 38 FDA reports)
ONYCHOMYCOSIS ( 38 FDA reports)
PROSTATE CANCER ( 38 FDA reports)
SPINAL FUSION SURGERY ( 38 FDA reports)
SUICIDE ATTEMPT ( 38 FDA reports)
VERTEBROPLASTY ( 38 FDA reports)
CHEYNE-STOKES RESPIRATION ( 37 FDA reports)
DERMATITIS EXFOLIATIVE ( 37 FDA reports)
DRUG HYPERSENSITIVITY ( 37 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 37 FDA reports)
FEBRILE BONE MARROW APLASIA ( 37 FDA reports)
HEPATITIS C ( 37 FDA reports)
HYPERKERATOSIS ( 37 FDA reports)
INFECTIOUS PERITONITIS ( 37 FDA reports)
PROTEIN TOTAL DECREASED ( 37 FDA reports)
AORTIC STENOSIS ( 36 FDA reports)
CARDIOTOXICITY ( 36 FDA reports)
CAROTID ARTERY STENOSIS ( 36 FDA reports)
EAR INFECTION ( 36 FDA reports)
HEPATIC ENZYME INCREASED ( 36 FDA reports)
INTERMITTENT CLAUDICATION ( 36 FDA reports)
MEDICATION ERROR ( 36 FDA reports)
OEDEMA MOUTH ( 36 FDA reports)
STEVENS-JOHNSON SYNDROME ( 36 FDA reports)
CYTOLYTIC HEPATITIS ( 35 FDA reports)
DIASTOLIC DYSFUNCTION ( 35 FDA reports)
EYE INFLAMMATION ( 35 FDA reports)
FOOT FRACTURE ( 35 FDA reports)
FRACTURE ( 35 FDA reports)
GASTRIC HAEMORRHAGE ( 35 FDA reports)
HAEMATOTOXICITY ( 35 FDA reports)
HEPATITIS ( 35 FDA reports)
LEFT ATRIAL DILATATION ( 35 FDA reports)
METASTASES TO LIVER ( 35 FDA reports)
ORTHOPNOEA ( 35 FDA reports)
PLEURAL FIBROSIS ( 35 FDA reports)
PLEURITIC PAIN ( 35 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 35 FDA reports)
SKIN DISORDER ( 35 FDA reports)
TROPONIN INCREASED ( 35 FDA reports)
VENTRICULAR TACHYCARDIA ( 35 FDA reports)
ANGINA UNSTABLE ( 34 FDA reports)
CATARACT OPERATION ( 34 FDA reports)
DILATATION ATRIAL ( 34 FDA reports)
DYSAESTHESIA ( 34 FDA reports)
GRANULOMA ( 34 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 34 FDA reports)
HAEMORRHAGIC DIATHESIS ( 34 FDA reports)
HYPERMETROPIA ( 34 FDA reports)
IRON DEFICIENCY ANAEMIA ( 34 FDA reports)
LOCAL SWELLING ( 34 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 34 FDA reports)
NEUTROPHIL COUNT INCREASED ( 34 FDA reports)
ORAL SOFT TISSUE DISORDER ( 34 FDA reports)
PELVIC FRACTURE ( 34 FDA reports)
PLEURISY ( 34 FDA reports)
RALES ( 34 FDA reports)
TACHYARRHYTHMIA ( 34 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 34 FDA reports)
TREATMENT NONCOMPLIANCE ( 34 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 33 FDA reports)
ALOPECIA ( 33 FDA reports)
BRONCHIOLITIS ( 33 FDA reports)
DIABETIC KETOACIDOSIS ( 33 FDA reports)
ENTEROCOCCAL SEPSIS ( 33 FDA reports)
FAECALOMA ( 33 FDA reports)
GINGIVAL RECESSION ( 33 FDA reports)
GOITRE ( 33 FDA reports)
GRAND MAL CONVULSION ( 33 FDA reports)
HALLUCINATION, VISUAL ( 33 FDA reports)
INTERCOSTAL NEURALGIA ( 33 FDA reports)
INTESTINAL PERFORATION ( 33 FDA reports)
MENTAL DISORDER ( 33 FDA reports)
SUBDURAL HAEMATOMA ( 33 FDA reports)
ACUTE SINUSITIS ( 32 FDA reports)
AORTIC CALCIFICATION ( 32 FDA reports)
BONE LOSS ( 32 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 32 FDA reports)
DEMYELINATION ( 32 FDA reports)
HICCUPS ( 32 FDA reports)
HYPERPARATHYROIDISM ( 32 FDA reports)
JAUNDICE ( 32 FDA reports)
JOINT DISLOCATION ( 32 FDA reports)
LEUKAEMIA ( 32 FDA reports)
MOUTH HAEMORRHAGE ( 32 FDA reports)
PRESYNCOPE ( 32 FDA reports)
PSORIASIS ( 32 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 32 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 32 FDA reports)
ABNORMAL BEHAVIOUR ( 31 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 31 FDA reports)
BACTERIAL SEPSIS ( 31 FDA reports)
BLISTER ( 31 FDA reports)
BRAIN OEDEMA ( 31 FDA reports)
DENTAL FISTULA ( 31 FDA reports)
DIVERTICULAR PERFORATION ( 31 FDA reports)
DRUG ERUPTION ( 31 FDA reports)
ECZEMA ( 31 FDA reports)
ENTERITIS ( 31 FDA reports)
MALIGNANT MELANOMA ( 31 FDA reports)
ORAL SURGERY ( 31 FDA reports)
SUICIDAL IDEATION ( 31 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 31 FDA reports)
TOOTH IMPACTED ( 31 FDA reports)
ABSCESS LIMB ( 30 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 30 FDA reports)
ASEPTIC NECROSIS BONE ( 30 FDA reports)
BLOOD AMYLASE INCREASED ( 30 FDA reports)
BLOOD MAGNESIUM DECREASED ( 30 FDA reports)
BOWEN'S DISEASE ( 30 FDA reports)
BURNING SENSATION ( 30 FDA reports)
COLITIS ISCHAEMIC ( 30 FDA reports)
EJECTION FRACTION ABNORMAL ( 30 FDA reports)
FLUSHING ( 30 FDA reports)
GASTROINTESTINAL TOXICITY ( 30 FDA reports)
HEPATOTOXICITY ( 30 FDA reports)
NECK INJURY ( 30 FDA reports)
PARALYSIS ( 30 FDA reports)
PERITONITIS ( 30 FDA reports)
SINUS BRADYCARDIA ( 30 FDA reports)
SKIN HYPERPIGMENTATION ( 30 FDA reports)
SKIN NODULE ( 30 FDA reports)
VOCAL CORD PARALYSIS ( 30 FDA reports)
DEVICE RELATED SEPSIS ( 29 FDA reports)
DISTURBANCE IN ATTENTION ( 29 FDA reports)
DRUG INTOLERANCE ( 29 FDA reports)
INCREASED TENDENCY TO BRUISE ( 29 FDA reports)
MYOCARDITIS ( 29 FDA reports)
ORAL INFECTION ( 29 FDA reports)
RESTLESSNESS ( 29 FDA reports)
SCIATICA ( 29 FDA reports)
VITREOUS FLOATERS ( 29 FDA reports)
ABNORMAL SENSATION IN EYE ( 28 FDA reports)
ADRENAL INSUFFICIENCY ( 28 FDA reports)
APLASIA ( 28 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 28 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 28 FDA reports)
BONE FRAGMENTATION ( 28 FDA reports)
EAR DISCOMFORT ( 28 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 28 FDA reports)
FLATULENCE ( 28 FDA reports)
HEPATIC LESION ( 28 FDA reports)
LEFT VENTRICULAR FAILURE ( 28 FDA reports)
MENISCUS LESION ( 28 FDA reports)
METASTASES TO SPINE ( 28 FDA reports)
PCO2 DECREASED ( 28 FDA reports)
TACHYPNOEA ( 28 FDA reports)
VISUAL DISTURBANCE ( 28 FDA reports)
ABSCESS DRAINAGE ( 27 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 27 FDA reports)
BLINDNESS TRANSIENT ( 27 FDA reports)
BLOOD BICARBONATE DECREASED ( 27 FDA reports)
CHOLECYSTECTOMY ( 27 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 27 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 27 FDA reports)
DRY SKIN ( 27 FDA reports)
EAR DISORDER ( 27 FDA reports)
EOSINOPHILIA ( 27 FDA reports)
FACET JOINT SYNDROME ( 27 FDA reports)
HERPES VIRUS INFECTION ( 27 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 27 FDA reports)
HYPOTONIA ( 27 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 27 FDA reports)
NASAL CONGESTION ( 27 FDA reports)
NEUROLOGICAL SYMPTOM ( 27 FDA reports)
NIGHT SWEATS ( 27 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 27 FDA reports)
PARAPARESIS ( 27 FDA reports)
POLYURIA ( 27 FDA reports)
RETCHING ( 27 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 27 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 27 FDA reports)
TROPONIN I INCREASED ( 27 FDA reports)
VENOUS THROMBOSIS LIMB ( 27 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 27 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 26 FDA reports)
CACHEXIA ( 26 FDA reports)
CATHETER RELATED COMPLICATION ( 26 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 26 FDA reports)
EYELID PTOSIS ( 26 FDA reports)
FACE OEDEMA ( 26 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 26 FDA reports)
HUMERUS FRACTURE ( 26 FDA reports)
LUNG NEOPLASM MALIGNANT ( 26 FDA reports)
PELVIC PAIN ( 26 FDA reports)
PERIORBITAL OEDEMA ( 26 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 26 FDA reports)
PORTAL HYPERTENSION ( 26 FDA reports)
RADIOTHERAPY ( 26 FDA reports)
RASH PAPULAR ( 26 FDA reports)
RESTLESS LEGS SYNDROME ( 26 FDA reports)
SEXUAL DYSFUNCTION ( 26 FDA reports)
STREPTOCOCCAL SEPSIS ( 26 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 26 FDA reports)
UNEVALUABLE EVENT ( 26 FDA reports)
ACUTE ABDOMEN ( 25 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 25 FDA reports)
APNOEA ( 25 FDA reports)
CHOLESTASIS ( 25 FDA reports)
DERMATITIS CONTACT ( 25 FDA reports)
ENTEROVESICAL FISTULA ( 25 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 25 FDA reports)
EYE NAEVUS ( 25 FDA reports)
FOOT DEFORMITY ( 25 FDA reports)
HAEMODYNAMIC INSTABILITY ( 25 FDA reports)
HYPERBILIRUBINAEMIA ( 25 FDA reports)
INJECTION SITE ERYTHEMA ( 25 FDA reports)
LARGE INTESTINE PERFORATION ( 25 FDA reports)
OPTIC NERVE CUPPING ( 25 FDA reports)
OTITIS MEDIA ( 25 FDA reports)
PLATELET COUNT INCREASED ( 25 FDA reports)
PO2 DECREASED ( 25 FDA reports)
POST HERPETIC NEURALGIA ( 25 FDA reports)
PROCTALGIA ( 25 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 25 FDA reports)
RADICULOPATHY ( 25 FDA reports)
RENAL ATROPHY ( 25 FDA reports)
RETINAL HAEMORRHAGE ( 25 FDA reports)
SEBORRHOEIC KERATOSIS ( 25 FDA reports)
SEPSIS SYNDROME ( 25 FDA reports)
SKIN TOXICITY ( 25 FDA reports)
SOFT TISSUE INFECTION ( 25 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 25 FDA reports)
VESICAL FISTULA ( 25 FDA reports)
VITAMIN B12 DEFICIENCY ( 25 FDA reports)
AFFECTIVE DISORDER ( 24 FDA reports)
BLOOD MAGNESIUM INCREASED ( 24 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 24 FDA reports)
CLOSTRIDIUM COLITIS ( 24 FDA reports)
COSTOCHONDRITIS ( 24 FDA reports)
DENTAL CARE ( 24 FDA reports)
DIABETIC RETINOPATHY ( 24 FDA reports)
DRUG EFFECT DECREASED ( 24 FDA reports)
DUODENITIS ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 24 FDA reports)
HAEMANGIOMA ( 24 FDA reports)
LIGAMENT SPRAIN ( 24 FDA reports)
MITRAL VALVE DISEASE ( 24 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 24 FDA reports)
PARAESTHESIA ORAL ( 24 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 24 FDA reports)
PSEUDOMONAL SEPSIS ( 24 FDA reports)
SLEEP DISORDER ( 24 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 24 FDA reports)
UTERINE LEIOMYOMA ( 24 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 24 FDA reports)
VENTRICULAR FIBRILLATION ( 24 FDA reports)
WOUND ( 24 FDA reports)
AORTIC DISORDER ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK ( 23 FDA reports)
ATROPHY ( 23 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 23 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 23 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 23 FDA reports)
CARDIOGENIC SHOCK ( 23 FDA reports)
CHALAZION ( 23 FDA reports)
COLON CANCER ( 23 FDA reports)
CREPITATIONS ( 23 FDA reports)
CYTOKINE RELEASE SYNDROME ( 23 FDA reports)
DISEASE COMPLICATION ( 23 FDA reports)
FACIAL PALSY ( 23 FDA reports)
FAT NECROSIS ( 23 FDA reports)
FURUNCLE ( 23 FDA reports)
GINGIVAL ULCERATION ( 23 FDA reports)
HAEMOLYTIC ANAEMIA ( 23 FDA reports)
HYPERAMMONAEMIA ( 23 FDA reports)
HYPOPROTEINAEMIA ( 23 FDA reports)
KLEBSIELLA INFECTION ( 23 FDA reports)
MUSCLE INJURY ( 23 FDA reports)
NECK MASS ( 23 FDA reports)
NECROSIS ( 23 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 23 FDA reports)
OCULAR HYPERAEMIA ( 23 FDA reports)
OSTEOMYELITIS CHRONIC ( 23 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 23 FDA reports)
PROSTATOMEGALY ( 23 FDA reports)
ROSACEA ( 23 FDA reports)
SENSITIVITY OF TEETH ( 23 FDA reports)
SENSORY DISTURBANCE ( 23 FDA reports)
STATUS EPILEPTICUS ( 23 FDA reports)
SUBILEUS ( 23 FDA reports)
SYNOVIAL CYST ( 23 FDA reports)
TONGUE ULCERATION ( 23 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 23 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 22 FDA reports)
HALLUCINATION, AUDITORY ( 22 FDA reports)
HEPATIC NEOPLASM ( 22 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 22 FDA reports)
HORDEOLUM ( 22 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 22 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 22 FDA reports)
MANTLE CELL LYMPHOMA ( 22 FDA reports)
MENINGITIS ( 22 FDA reports)
MONOCLONAL GAMMOPATHY ( 22 FDA reports)
MUSCLE TWITCHING ( 22 FDA reports)
NERVE ROOT COMPRESSION ( 22 FDA reports)
PAIN OF SKIN ( 22 FDA reports)
PARAPROTEINAEMIA ( 22 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 22 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 22 FDA reports)
RENAL MASS ( 22 FDA reports)
SEDATION ( 22 FDA reports)
SLEEP TALKING ( 22 FDA reports)
STREPTOCOCCAL INFECTION ( 22 FDA reports)
TRANSPLANT ( 22 FDA reports)
WOUND DEBRIDEMENT ( 22 FDA reports)
ANORECTAL DISORDER ( 21 FDA reports)
ARTHROPOD BITE ( 21 FDA reports)
BLOOD GLUCOSE DECREASED ( 21 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 21 FDA reports)
CARDIAC FAILURE ACUTE ( 21 FDA reports)
CARPAL TUNNEL SYNDROME ( 21 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 21 FDA reports)
FEELING COLD ( 21 FDA reports)
FIBROUS HISTIOCYTOMA ( 21 FDA reports)
GASTRIC CANCER ( 21 FDA reports)
GASTRITIS HAEMORRHAGIC ( 21 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 21 FDA reports)
GINGIVAL ERYTHEMA ( 21 FDA reports)
HAEMOGLOBIN ABNORMAL ( 21 FDA reports)
HIP ARTHROPLASTY ( 21 FDA reports)
HYPERTHYROIDISM ( 21 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 21 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 21 FDA reports)
LIVEDO RETICULARIS ( 21 FDA reports)
METABOLIC ENCEPHALOPATHY ( 21 FDA reports)
METASTATIC NEOPLASM ( 21 FDA reports)
NODULE ( 21 FDA reports)
OESOPHAGEAL ULCER ( 21 FDA reports)
OPEN WOUND ( 21 FDA reports)
PNEUMONIA KLEBSIELLA ( 21 FDA reports)
POST PROCEDURAL COMPLICATION ( 21 FDA reports)
PROTEUS INFECTION ( 21 FDA reports)
PULMONARY GRANULOMA ( 21 FDA reports)
QUADRIPLEGIA ( 21 FDA reports)
RECTAL POLYP ( 21 FDA reports)
SEPTIC EMBOLUS ( 21 FDA reports)
SERUM FERRITIN INCREASED ( 21 FDA reports)
SKIN NEOPLASM EXCISION ( 21 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 21 FDA reports)
WOUND INFECTION ( 21 FDA reports)
ABDOMINAL TENDERNESS ( 20 FDA reports)
AEROMONA INFECTION ( 20 FDA reports)
BRONCHITIS CHRONIC ( 20 FDA reports)
CARDIAC ENZYMES INCREASED ( 20 FDA reports)
CENTRAL LINE INFECTION ( 20 FDA reports)
CHOLECYSTITIS ACUTE ( 20 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 20 FDA reports)
DIFFICULTY IN WALKING ( 20 FDA reports)
EMBOLISM VENOUS ( 20 FDA reports)
ERYSIPELAS ( 20 FDA reports)
EYE INFECTION ( 20 FDA reports)
FEELING HOT ( 20 FDA reports)
FIBRIN D DIMER INCREASED ( 20 FDA reports)
HAEMOLYSIS ( 20 FDA reports)
HAEMOPHILUS INFECTION ( 20 FDA reports)
HEPATOSPLENOMEGALY ( 20 FDA reports)
HYPERAESTHESIA ( 20 FDA reports)
HYPERPLASIA ( 20 FDA reports)
HYPOVENTILATION ( 20 FDA reports)
INCORRECT DOSE ADMINISTERED ( 20 FDA reports)
LARGE INTESTINAL ULCER ( 20 FDA reports)
MONOCYTOSIS ( 20 FDA reports)
MUSCLE ATROPHY ( 20 FDA reports)
NASAL SEPTUM DEVIATION ( 20 FDA reports)
NEPHROPATHY TOXIC ( 20 FDA reports)
NEPHROSCLEROSIS ( 20 FDA reports)
OPPORTUNISTIC INFECTION ( 20 FDA reports)
PEPTIC ULCER ( 20 FDA reports)
PERIRECTAL ABSCESS ( 20 FDA reports)
PROCEDURAL COMPLICATION ( 20 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 20 FDA reports)
PULMONARY MASS ( 20 FDA reports)
RESUSCITATION ( 20 FDA reports)
RIGHT VENTRICULAR FAILURE ( 20 FDA reports)
SICK SINUS SYNDROME ( 20 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 20 FDA reports)
WOUND DECOMPOSITION ( 20 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 19 FDA reports)
ALVEOLOPLASTY ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 19 FDA reports)
BEDRIDDEN ( 19 FDA reports)
BIOPSY ( 19 FDA reports)
BLOOD CHLORIDE INCREASED ( 19 FDA reports)
BODY TEMPERATURE DECREASED ( 19 FDA reports)
BREAST MASS ( 19 FDA reports)
CATHETER SITE INFECTION ( 19 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 19 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 19 FDA reports)
DEAFNESS UNILATERAL ( 19 FDA reports)
DECREASED ACTIVITY ( 19 FDA reports)
DRUG DISPENSING ERROR ( 19 FDA reports)
DYSPLASTIC NAEVUS ( 19 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 19 FDA reports)
EYELID OEDEMA ( 19 FDA reports)
FISTULA REPAIR ( 19 FDA reports)
FLUID INTAKE REDUCED ( 19 FDA reports)
GALLBLADDER POLYP ( 19 FDA reports)
GAMMOPATHY ( 19 FDA reports)
GASTRIC POLYPS ( 19 FDA reports)
GASTROINTESTINAL PAIN ( 19 FDA reports)
HAEMANGIOMA OF SPLEEN ( 19 FDA reports)
HEARING IMPAIRED ( 19 FDA reports)
HYPOAESTHESIA FACIAL ( 19 FDA reports)
INJECTION SITE REACTION ( 19 FDA reports)
ISCHAEMIC STROKE ( 19 FDA reports)
LACRIMATION INCREASED ( 19 FDA reports)
LOWER LIMB FRACTURE ( 19 FDA reports)
LYMPHOEDEMA ( 19 FDA reports)
MELANOCYTIC NAEVUS ( 19 FDA reports)
MONOPLEGIA ( 19 FDA reports)
NECROTISING FASCIITIS ( 19 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 19 FDA reports)
RETINAL DETACHMENT ( 19 FDA reports)
SEROMA ( 19 FDA reports)
SKIN FIBROSIS ( 19 FDA reports)
SOFT TISSUE INFLAMMATION ( 19 FDA reports)
SPINAL LAMINECTOMY ( 19 FDA reports)
SPLENIC INFARCTION ( 19 FDA reports)
THROMBOSIS IN DEVICE ( 19 FDA reports)
TOE AMPUTATION ( 19 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 19 FDA reports)
UVEITIS ( 19 FDA reports)
VIITH NERVE PARALYSIS ( 19 FDA reports)
APHTHOUS STOMATITIS ( 18 FDA reports)
AREFLEXIA ( 18 FDA reports)
ARTHRITIS BACTERIAL ( 18 FDA reports)
ASPIRATION PLEURAL CAVITY ( 18 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 18 FDA reports)
BENCE JONES PROTEINURIA ( 18 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 18 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 18 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 18 FDA reports)
CARDIAC MURMUR ( 18 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 18 FDA reports)
CHEST TUBE INSERTION ( 18 FDA reports)
DYSPHEMIA ( 18 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 18 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 18 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 18 FDA reports)
EYE SWELLING ( 18 FDA reports)
HEART RATE DECREASED ( 18 FDA reports)
HYPERAMYLASAEMIA ( 18 FDA reports)
HYPERPHOSPHATAEMIA ( 18 FDA reports)
HYPERSOMNIA ( 18 FDA reports)
LACERATION ( 18 FDA reports)
MITRAL VALVE PROLAPSE ( 18 FDA reports)
MYOSITIS ( 18 FDA reports)
ODYNOPHAGIA ( 18 FDA reports)
PAROTITIS ( 18 FDA reports)
PRESBYOPIA ( 18 FDA reports)
PSYCHOMOTOR RETARDATION ( 18 FDA reports)
RASH PUSTULAR ( 18 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 18 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 18 FDA reports)
SINUS HEADACHE ( 18 FDA reports)
SKIN REACTION ( 18 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 18 FDA reports)
TONGUE COATED ( 18 FDA reports)
AGRANULOCYTOSIS ( 17 FDA reports)
BLOOD PH INCREASED ( 17 FDA reports)
BUNDLE BRANCH BLOCK ( 17 FDA reports)
CARBON DIOXIDE DECREASED ( 17 FDA reports)
CARDIAC TAMPONADE ( 17 FDA reports)
CULTURE STOOL POSITIVE ( 17 FDA reports)
CYSTITIS HAEMORRHAGIC ( 17 FDA reports)
CYSTOCELE ( 17 FDA reports)
DENTAL PLAQUE ( 17 FDA reports)
DENTAL PROSTHESIS USER ( 17 FDA reports)
DEPRESSED MOOD ( 17 FDA reports)
DRUG ABUSE ( 17 FDA reports)
DRUG ADMINISTRATION ERROR ( 17 FDA reports)
DRUG DEPENDENCE ( 17 FDA reports)
DUODENAL ULCER ( 17 FDA reports)
FAECES DISCOLOURED ( 17 FDA reports)
FEMUR FRACTURE ( 17 FDA reports)
FIBULA FRACTURE ( 17 FDA reports)
FRACTURED SACRUM ( 17 FDA reports)
GLARE ( 17 FDA reports)
GRAFT LOSS ( 17 FDA reports)
HEPATIC CIRRHOSIS ( 17 FDA reports)
ICHTHYOSIS ( 17 FDA reports)
INCONTINENCE ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 17 FDA reports)
INTESTINAL INFARCTION ( 17 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 17 FDA reports)
JUGULAR VEIN THROMBOSIS ( 17 FDA reports)
MOOD SWINGS ( 17 FDA reports)
MORGANELLA INFECTION ( 17 FDA reports)
OPTIC NEUROPATHY ( 17 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 17 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 17 FDA reports)
PNEUMONIA VIRAL ( 17 FDA reports)
POOR PERSONAL HYGIENE ( 17 FDA reports)
PULMONARY INFARCTION ( 17 FDA reports)
QRS AXIS ABNORMAL ( 17 FDA reports)
SKIN CANCER ( 17 FDA reports)
SUBDURAL HAEMORRHAGE ( 17 FDA reports)
SUDDEN CARDIAC DEATH ( 17 FDA reports)
SUPERINFECTION ( 17 FDA reports)
TENDON RUPTURE ( 17 FDA reports)
THIRST ( 17 FDA reports)
THROMBOPHLEBITIS ( 17 FDA reports)
TRANSFUSION ( 17 FDA reports)
X-RAY ABNORMAL ( 17 FDA reports)
ABDOMINAL PAIN LOWER ( 16 FDA reports)
ACUTE HEPATIC FAILURE ( 16 FDA reports)
BLOOD PH DECREASED ( 16 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 16 FDA reports)
BONE FISTULA ( 16 FDA reports)
BREAST CANCER ( 16 FDA reports)
CALCULUS URETERIC ( 16 FDA reports)
CARDIAC PACEMAKER INSERTION ( 16 FDA reports)
CARDIOPULMONARY FAILURE ( 16 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 16 FDA reports)
CERUMEN IMPACTION ( 16 FDA reports)
CULTURE URINE POSITIVE ( 16 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 16 FDA reports)
DIPLEGIA ( 16 FDA reports)
EDENTULOUS ( 16 FDA reports)
EPIGASTRIC DISCOMFORT ( 16 FDA reports)
FEMORAL NECK FRACTURE ( 16 FDA reports)
FISTULA DISCHARGE ( 16 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 16 FDA reports)
HEPATIC NECROSIS ( 16 FDA reports)
HYPERPYREXIA ( 16 FDA reports)
HYPOTHERMIA ( 16 FDA reports)
ILIAC ARTERY STENOSIS ( 16 FDA reports)
INCOHERENT ( 16 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 16 FDA reports)
LERICHE SYNDROME ( 16 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 16 FDA reports)
NAIL DYSTROPHY ( 16 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 16 FDA reports)
ONYCHALGIA ( 16 FDA reports)
PANCREATIC CARCINOMA ( 16 FDA reports)
POOR DENTAL CONDITION ( 16 FDA reports)
PULSE ABSENT ( 16 FDA reports)
RADIAL NERVE PALSY ( 16 FDA reports)
RADICULITIS LUMBOSACRAL ( 16 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 16 FDA reports)
SHOCK HAEMORRHAGIC ( 16 FDA reports)
SKIN DISCOLOURATION ( 16 FDA reports)
SKIN INDURATION ( 16 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 16 FDA reports)
TENDON DISORDER ( 16 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 16 FDA reports)
TOXIC ENCEPHALOPATHY ( 16 FDA reports)
TRANSPLANT REJECTION ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
ACCIDENTAL EXPOSURE ( 15 FDA reports)
ADVERSE DRUG REACTION ( 15 FDA reports)
ALVEOLAR OSTEITIS ( 15 FDA reports)
AORTIC DILATATION ( 15 FDA reports)
ATRIAL SEPTAL DEFECT ( 15 FDA reports)
BIOPSY BONE MARROW ( 15 FDA reports)
BLOOD LACTIC ACID INCREASED ( 15 FDA reports)
BODY TINEA ( 15 FDA reports)
CARBUNCLE ( 15 FDA reports)
CATHETER PLACEMENT ( 15 FDA reports)
CEREBRAL ASPERGILLOSIS ( 15 FDA reports)
CERVICAL SPINAL STENOSIS ( 15 FDA reports)
CYANOSIS ( 15 FDA reports)
CYSTITIS NONINFECTIVE ( 15 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 15 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 15 FDA reports)
DRUG DOSE OMISSION ( 15 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 15 FDA reports)
ECZEMA ASTEATOTIC ( 15 FDA reports)
ENCEPHALITIS HERPES ( 15 FDA reports)
ENCEPHALITIS VIRAL ( 15 FDA reports)
ESCHERICHIA BACTERAEMIA ( 15 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 15 FDA reports)
FOLLICULITIS ( 15 FDA reports)
GANGRENE ( 15 FDA reports)
GLYCOSURIA ( 15 FDA reports)
HAND FRACTURE ( 15 FDA reports)
HIDRADENITIS ( 15 FDA reports)
HYPERCOAGULATION ( 15 FDA reports)
HYPOVOLAEMIC SHOCK ( 15 FDA reports)
IRRITABILITY ( 15 FDA reports)
JOINT INJURY ( 15 FDA reports)
LIPASE INCREASED ( 15 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 15 FDA reports)
NEPHROTIC SYNDROME ( 15 FDA reports)
OESOPHAGEAL DISORDER ( 15 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 15 FDA reports)
ORAL FIBROMA ( 15 FDA reports)
ORAL MUCOSA ATROPHY ( 15 FDA reports)
ORTHODONTIC APPLIANCE USER ( 15 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 15 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 15 FDA reports)
PULMONARY VALVE STENOSIS ( 15 FDA reports)
RADIATION OESOPHAGITIS ( 15 FDA reports)
RASH MORBILLIFORM ( 15 FDA reports)
REFLUX OESOPHAGITIS ( 15 FDA reports)
RESPIRATORY ACIDOSIS ( 15 FDA reports)
RESPIRATORY TRACT CONGESTION ( 15 FDA reports)
RHONCHI ( 15 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 15 FDA reports)
SKIN HYPERTROPHY ( 15 FDA reports)
SKIN TIGHTNESS ( 15 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 15 FDA reports)
TOOTH DISCOLOURATION ( 15 FDA reports)
ACUTE CORONARY SYNDROME ( 14 FDA reports)
ALANINE AMINOTRANSFERASE ( 14 FDA reports)
ANAL FISTULA ( 14 FDA reports)
ANGIOEDEMA ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
B-CELL LYMPHOMA ( 14 FDA reports)
BACILLUS INFECTION ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
BENIGN BREAST NEOPLASM ( 14 FDA reports)
BLADDER SPASM ( 14 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 14 FDA reports)
BONE MARROW DISORDER ( 14 FDA reports)
COLLAPSE OF LUNG ( 14 FDA reports)
COLONIC OBSTRUCTION ( 14 FDA reports)
COR PULMONALE ( 14 FDA reports)
CSF PROTEIN INCREASED ( 14 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 14 FDA reports)
DYSKINESIA ( 14 FDA reports)
ELECTROLYTE DEPLETION ( 14 FDA reports)
EROSIVE DUODENITIS ( 14 FDA reports)
EXCORIATION ( 14 FDA reports)
GASTROINTESTINAL NECROSIS ( 14 FDA reports)
HYPERCAPNIA ( 14 FDA reports)
HYPERVENTILATION ( 14 FDA reports)
HYPOPNOEA ( 14 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 14 FDA reports)
JOINT SPRAIN ( 14 FDA reports)
KERATITIS ( 14 FDA reports)
LIP SWELLING ( 14 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
LUMBAR RADICULOPATHY ( 14 FDA reports)
MALLORY-WEISS SYNDROME ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
MOUTH CYST ( 14 FDA reports)
MOVEMENT DISORDER ( 14 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 14 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 14 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 14 FDA reports)
OSTEOMYELITIS DRAINAGE ( 14 FDA reports)
PELVIC DISCOMFORT ( 14 FDA reports)
PELVIC PROLAPSE ( 14 FDA reports)
PERIPHERAL COLDNESS ( 14 FDA reports)
POOR QUALITY SLEEP ( 14 FDA reports)
PULMONARY SEPSIS ( 14 FDA reports)
PUPIL FIXED ( 14 FDA reports)
QUALITY OF LIFE DECREASED ( 14 FDA reports)
RADIATION PNEUMONITIS ( 14 FDA reports)
VASCULAR PSEUDOANEURYSM ( 14 FDA reports)
VENOUS INSUFFICIENCY ( 14 FDA reports)
ZYGOMYCOSIS ( 14 FDA reports)
ACROCHORDON ( 13 FDA reports)
ALKALOSIS ( 13 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 13 FDA reports)
ANAL FISSURE ( 13 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 13 FDA reports)
BACTERIA STOOL IDENTIFIED ( 13 FDA reports)
BONE NEOPLASM MALIGNANT ( 13 FDA reports)
BREATH SOUNDS ABNORMAL ( 13 FDA reports)
CHONDROCALCINOSIS ( 13 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 13 FDA reports)
DELUSION ( 13 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 13 FDA reports)
ESSENTIAL HYPERTENSION ( 13 FDA reports)
GOUTY ARTHRITIS ( 13 FDA reports)
HAEMANGIOMA OF LIVER ( 13 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
INGROWING NAIL ( 13 FDA reports)
INGUINAL HERNIA REPAIR ( 13 FDA reports)
ISCHAEMIA ( 13 FDA reports)
JOINT STIFFNESS ( 13 FDA reports)
LIPOMA ( 13 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 13 FDA reports)
MENINGIOMA ( 13 FDA reports)
MICTURITION URGENCY ( 13 FDA reports)
MITRAL VALVE CALCIFICATION ( 13 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NEUTROPENIC INFECTION ( 13 FDA reports)
ORCHITIS ( 13 FDA reports)
ORGANISING PNEUMONIA ( 13 FDA reports)
OROANTRAL FISTULA ( 13 FDA reports)
OTITIS MEDIA ACUTE ( 13 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 13 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 13 FDA reports)
PERINEURIAL CYST ( 13 FDA reports)
PERIORBITAL HAEMATOMA ( 13 FDA reports)
PO2 INCREASED ( 13 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 13 FDA reports)
RADICULAR PAIN ( 13 FDA reports)
SINUS ARRHYTHMIA ( 13 FDA reports)
SKIN LACERATION ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
STRESS URINARY INCONTINENCE ( 13 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 13 FDA reports)
TESTICULAR PAIN ( 13 FDA reports)
THROMBOCYTOSIS ( 13 FDA reports)
TORSADE DE POINTES ( 13 FDA reports)
TRACHEOBRONCHITIS ( 13 FDA reports)
TREATMENT FAILURE ( 13 FDA reports)
VOLVULUS ( 13 FDA reports)
ACCIDENT ( 12 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 12 FDA reports)
AGGRESSION ( 12 FDA reports)
ALOPECIA AREATA ( 12 FDA reports)
ANGIOMYOLIPOMA ( 12 FDA reports)
AORTIC VALVE CALCIFICATION ( 12 FDA reports)
AORTIC VALVE DISEASE ( 12 FDA reports)
APATHY ( 12 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 12 FDA reports)
BETA GLOBULIN INCREASED ( 12 FDA reports)
BLADDER CYST ( 12 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 12 FDA reports)
BONE INFARCTION ( 12 FDA reports)
BONE SCAN ABNORMAL ( 12 FDA reports)
BULLOUS LUNG DISEASE ( 12 FDA reports)
CARDIAC ANEURYSM ( 12 FDA reports)
CARDIAC FAILURE CHRONIC ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
CHOROIDAL EFFUSION ( 12 FDA reports)
COLD SWEAT ( 12 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 12 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 12 FDA reports)
DIURETIC THERAPY ( 12 FDA reports)
DRY SOCKET ( 12 FDA reports)
EAR CONGESTION ( 12 FDA reports)
EPICONDYLITIS ( 12 FDA reports)
FOOD INTOLERANCE ( 12 FDA reports)
GASTROENTERITIS VIRAL ( 12 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 12 FDA reports)
GINGIVAL GRAFT ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HYPERTENSIVE CRISIS ( 12 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 12 FDA reports)
IIIRD NERVE PARALYSIS ( 12 FDA reports)
IMMUNE SYSTEM DISORDER ( 12 FDA reports)
INJECTION SITE PAIN ( 12 FDA reports)
LACUNAR INFARCTION ( 12 FDA reports)
LYMPHADENITIS ( 12 FDA reports)
MACULAR DEGENERATION ( 12 FDA reports)
MUCOSAL HAEMORRHAGE ( 12 FDA reports)
MYELOPATHY ( 12 FDA reports)
NEUROPATHIC PAIN ( 12 FDA reports)
OESOPHAGEAL STENOSIS ( 12 FDA reports)
ORTHOPEDIC PROCEDURE ( 12 FDA reports)
PANCREATIC MASS ( 12 FDA reports)
PARKINSON'S DISEASE ( 12 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 12 FDA reports)
PITTING OEDEMA ( 12 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 12 FDA reports)
POOR PERIPHERAL CIRCULATION ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PUBIS FRACTURE ( 12 FDA reports)
PULMONARY HILUM MASS ( 12 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 12 FDA reports)
RECTOCELE ( 12 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 12 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 12 FDA reports)
SCLEROMALACIA ( 12 FDA reports)
SKIN PLAQUE ( 12 FDA reports)
SPINAL CORPECTOMY ( 12 FDA reports)
SPONDYLOLYSIS ( 12 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 12 FDA reports)
TEETH BRITTLE ( 12 FDA reports)
TOOTH EROSION ( 12 FDA reports)
TRIGGER FINGER ( 12 FDA reports)
UMBILICAL HERNIA ( 12 FDA reports)
VENTRICULAR DYSKINESIA ( 12 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
VITAMIN D DEFICIENCY ( 12 FDA reports)
ABDOMINAL ABSCESS ( 11 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 11 FDA reports)
ADRENAL SUPPRESSION ( 11 FDA reports)
ANAPHYLACTIC REACTION ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 11 FDA reports)
BACK DISORDER ( 11 FDA reports)
BASOPHIL COUNT DECREASED ( 11 FDA reports)
BLADDER DISORDER ( 11 FDA reports)
BLINDNESS CORTICAL ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 11 FDA reports)
BLOOD BILIRUBIN ( 11 FDA reports)
BLOOD CREATININE DECREASED ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 11 FDA reports)
BLOOD UREA DECREASED ( 11 FDA reports)
BLOOD VISCOSITY INCREASED ( 11 FDA reports)
CATHETER REMOVAL ( 11 FDA reports)
COLON ADENOMA ( 11 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 11 FDA reports)
CORONARY ARTERY BYPASS ( 11 FDA reports)
CORONARY ARTERY STENOSIS ( 11 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 11 FDA reports)
EFFUSION ( 11 FDA reports)
ENTEROBACTER INFECTION ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
FOREIGN BODY IN EYE ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
FULL BLOOD COUNT DECREASED ( 11 FDA reports)
FUNGAL DNA TEST POSITIVE ( 11 FDA reports)
GALLBLADDER DISORDER ( 11 FDA reports)
GINGIVAL ABSCESS ( 11 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 11 FDA reports)
HAEMORRHAGIC STROKE ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
HODGKIN'S DISEASE ( 11 FDA reports)
HYPOCHLORAEMIA ( 11 FDA reports)
HYPOGONADISM ( 11 FDA reports)
ILIAC ARTERY THROMBOSIS ( 11 FDA reports)
IMMUNOGLOBULINS INCREASED ( 11 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 11 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 11 FDA reports)
INTERVERTEBRAL DISCITIS ( 11 FDA reports)
KLEBSIELLA SEPSIS ( 11 FDA reports)
LIMB CRUSHING INJURY ( 11 FDA reports)
MACULOPATHY ( 11 FDA reports)
MASS EXCISION ( 11 FDA reports)
MEGAKARYOCYTES DECREASED ( 11 FDA reports)
METASTASES TO MENINGES ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
MUSCLE TIGHTNESS ( 11 FDA reports)
OESOPHAGEAL RUPTURE ( 11 FDA reports)
ORAL DISCHARGE ( 11 FDA reports)
OVARIAN FAILURE ( 11 FDA reports)
PANCREATIC CYST ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
PHARYNGEAL OEDEMA ( 11 FDA reports)
PLATELET COUNT ABNORMAL ( 11 FDA reports)
PNEUMONIA LEGIONELLA ( 11 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 11 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 11 FDA reports)
PROSTATIC CALCIFICATION ( 11 FDA reports)
PROTEIN URINE ( 11 FDA reports)
PYURIA ( 11 FDA reports)
RECURRENT CANCER ( 11 FDA reports)
RENAL STONE REMOVAL ( 11 FDA reports)
RIGHT ATRIAL DILATATION ( 11 FDA reports)
SCAB ( 11 FDA reports)
SENSATION OF PRESSURE ( 11 FDA reports)
SHOULDER PAIN ( 11 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 11 FDA reports)
SUBMANDIBULAR MASS ( 11 FDA reports)
SYNOVIAL DISORDER ( 11 FDA reports)
TONGUE DISORDER ( 11 FDA reports)
TOXIC NEUROPATHY ( 11 FDA reports)
TUMOUR NECROSIS ( 11 FDA reports)
URINARY HESITATION ( 11 FDA reports)
UTEROVAGINAL PROLAPSE ( 11 FDA reports)
VENOUS THROMBOSIS ( 11 FDA reports)
VITH NERVE PARALYSIS ( 11 FDA reports)
WOUND SECRETION ( 11 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BILE DUCT OBSTRUCTION ( 10 FDA reports)
BLOOD ALBUMIN INCREASED ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BRAIN DEATH ( 10 FDA reports)
BREAST HYPERPLASIA ( 10 FDA reports)
BRONCHIAL WALL THICKENING ( 10 FDA reports)
CATHETER SITE HAEMORRHAGE ( 10 FDA reports)
COLITIS ULCERATIVE ( 10 FDA reports)
CONDUCTION DISORDER ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 10 FDA reports)
DYSGRAPHIA ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 10 FDA reports)
FASCIITIS ( 10 FDA reports)
FUNGAEMIA ( 10 FDA reports)
GASTROINTESTINAL PERFORATION ( 10 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 10 FDA reports)
HEPATIC MASS ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
LIGAMENT RUPTURE ( 10 FDA reports)
MARROW HYPERPLASIA ( 10 FDA reports)
MASTOCYTOSIS ( 10 FDA reports)
MEIBOMIANITIS ( 10 FDA reports)
METAPLASIA ( 10 FDA reports)
METASTASES TO BONE MARROW ( 10 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 10 FDA reports)
NAIL DISCOLOURATION ( 10 FDA reports)
NEPHROGENIC ANAEMIA ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
ORGAN FAILURE ( 10 FDA reports)
OVARIAN MASS ( 10 FDA reports)
OXYGEN SUPPLEMENTATION ( 10 FDA reports)
PAROTID GLAND ENLARGEMENT ( 10 FDA reports)
PATHOGEN RESISTANCE ( 10 FDA reports)
PHARYNGEAL INFLAMMATION ( 10 FDA reports)
PNEUMOCONIOSIS ( 10 FDA reports)
PNEUMONIA HAEMOPHILUS ( 10 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 10 FDA reports)
PYODERMA GANGRENOSUM ( 10 FDA reports)
RED BLOOD CELL ABNORMALITY ( 10 FDA reports)
RENAL TUBULAR DISORDER ( 10 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 10 FDA reports)
SARCOIDOSIS ( 10 FDA reports)
SCOTOMA ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
SINUS POLYP ( 10 FDA reports)
SKIN CHAPPED ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SYNCOPE VASOVAGAL ( 10 FDA reports)
SYNOVIAL RUPTURE ( 10 FDA reports)
TEMPORAL ARTERITIS ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
TESTICULAR SWELLING ( 10 FDA reports)
TYPE 1 DIABETES MELLITUS ( 10 FDA reports)
URETERAL STENT INSERTION ( 10 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 10 FDA reports)
ABSCESS INTESTINAL ( 9 FDA reports)
ABSCESS ORAL ( 9 FDA reports)
ADENOCARCINOMA ( 9 FDA reports)
ADRENAL DISORDER ( 9 FDA reports)
ALVEOLITIS ALLERGIC ( 9 FDA reports)
AMYLASE INCREASED ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANKLE FRACTURE ( 9 FDA reports)
ANTIBODY TEST POSITIVE ( 9 FDA reports)
APHAGIA ( 9 FDA reports)
ASBESTOSIS ( 9 FDA reports)
ASTERIXIS ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BLOOD DISORDER ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BLOOD SODIUM INCREASED ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BREAST PAIN ( 9 FDA reports)
CALCULUS BLADDER ( 9 FDA reports)
CATHETER SITE CELLULITIS ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CEREBELLAR SYNDROME ( 9 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 9 FDA reports)
CHOROIDAL DETACHMENT ( 9 FDA reports)
CLAVICLE FRACTURE ( 9 FDA reports)
CUTANEOUS VASCULITIS ( 9 FDA reports)
CYST RUPTURE ( 9 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 9 FDA reports)
DERMOID CYST ( 9 FDA reports)
DRUG PRESCRIBING ERROR ( 9 FDA reports)
EJECTION FRACTION ( 9 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 9 FDA reports)
ERUCTATION ( 9 FDA reports)
EXTRADURAL HAEMATOMA ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
EYE MOVEMENT DISORDER ( 9 FDA reports)
FOREIGN BODY REACTION ( 9 FDA reports)
GASTRIC DISORDER ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
GINGIVAL EROSION ( 9 FDA reports)
GRIP STRENGTH DECREASED ( 9 FDA reports)
HAEMOGLOBIN INCREASED ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HAIR GROWTH ABNORMAL ( 9 FDA reports)
HYPERPROTEINAEMIA ( 9 FDA reports)
HYPOKINESIA ( 9 FDA reports)
HYPOREFLEXIA ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 9 FDA reports)
JOINT ARTHROPLASTY ( 9 FDA reports)
JOINT CREPITATION ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 9 FDA reports)
LIBIDO DECREASED ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
LYMPHOCYTIC INFILTRATION ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
MECHANICAL VENTILATION ( 9 FDA reports)
MICROANGIOPATHY ( 9 FDA reports)
MONOPARESIS ( 9 FDA reports)
MUSCLE DISORDER ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
NAIL HYPERTROPHY ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
NON-CARDIAC CHEST PAIN ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER ( 9 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 9 FDA reports)
OOPHORECTOMY ( 9 FDA reports)
OSTEOARTHROPATHY ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
PANCREATIC DUCT DILATATION ( 9 FDA reports)
PLATELET DISORDER ( 9 FDA reports)
PNEUMOCOCCAL SEPSIS ( 9 FDA reports)
POOR VENOUS ACCESS ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
RENAL ARTERY STENOSIS ( 9 FDA reports)
RENAL COLIC ( 9 FDA reports)
RENAL PAIN ( 9 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SWOLLEN TONGUE ( 9 FDA reports)
SYSTEMIC CANDIDA ( 9 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 9 FDA reports)
TOOTH REPAIR ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
URETHRAL HAEMORRHAGE ( 9 FDA reports)
URINARY TRACT DISORDER ( 9 FDA reports)
URINE ANALYSIS ABNORMAL ( 9 FDA reports)
VASCULAR INSUFFICIENCY ( 9 FDA reports)
VITREOUS HAEMORRHAGE ( 9 FDA reports)
ACUTE LEUKAEMIA ( 8 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 8 FDA reports)
ADHESION ( 8 FDA reports)
ADNEXA UTERI MASS ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
AMMONIA INCREASED ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
AORTIC VALVE STENOSIS ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
ARTHROSCOPIC SURGERY ( 8 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 8 FDA reports)
BIOPSY GINGIVAL ( 8 FDA reports)
BLOOD BICARBONATE INCREASED ( 8 FDA reports)
BLOOD CREATININE ABNORMAL ( 8 FDA reports)
BRAIN HERNIATION ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BRAIN OPERATION ( 8 FDA reports)
BREAST DISCHARGE ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BULIMIA NERVOSA ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CANCER PAIN ( 8 FDA reports)
CARDIAC ASTHMA ( 8 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 8 FDA reports)
CATHETER SEPSIS ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CHOLECYSTITIS CHRONIC ( 8 FDA reports)
CLAUSTROPHOBIA ( 8 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 8 FDA reports)
COMMINUTED FRACTURE ( 8 FDA reports)
CUTIS LAXA ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 8 FDA reports)
DENTOFACIAL ANOMALY ( 8 FDA reports)
DUODENAL ULCER PERFORATION ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
DYSPLASIA ( 8 FDA reports)
DYSTHYMIC DISORDER ( 8 FDA reports)
EOSINOPHIL COUNT INCREASED ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
EYE HAEMORRHAGE ( 8 FDA reports)
EYE LASER SURGERY ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
GALLBLADDER ENLARGEMENT ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HEPATIC CONGESTION ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HEPATIC INFARCTION ( 8 FDA reports)
HERNIA ( 8 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
HYSTERECTOMY ( 8 FDA reports)
INJECTION SITE RASH ( 8 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 8 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 8 FDA reports)
IRRITABLE BOWEL SYNDROME ( 8 FDA reports)
LABORATORY TEST INTERFERENCE ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LIP PAIN ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
LONG QT SYNDROME ( 8 FDA reports)
LUNG INJURY ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 8 FDA reports)
METASTASES TO LUNG ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 8 FDA reports)
MUCORMYCOSIS ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OPEN ANGLE GLAUCOMA ( 8 FDA reports)
OVERWEIGHT ( 8 FDA reports)
PAPILLOMA ( 8 FDA reports)
PERICARDIAL DISEASE ( 8 FDA reports)
PERICORONITIS ( 8 FDA reports)
PINGUECULA ( 8 FDA reports)
PNEUMOCOCCAL INFECTION ( 8 FDA reports)
PNEUMONIA MYCOPLASMAL ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
PNEUMONITIS CHEMICAL ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
PSOAS ABSCESS ( 8 FDA reports)
PTERYGIUM ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RESPIRATORY ALKALOSIS ( 8 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 8 FDA reports)
RETINAL VEIN THROMBOSIS ( 8 FDA reports)
ROTATOR CUFF REPAIR ( 8 FDA reports)
SCROTAL SWELLING ( 8 FDA reports)
SEBORRHOEIC DERMATITIS ( 8 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 8 FDA reports)
SEROSITIS ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SKIN INFECTION ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SKIN WARM ( 8 FDA reports)
SOFT TISSUE MASS ( 8 FDA reports)
SPLEEN CONGESTION ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
STOMATITIS NECROTISING ( 8 FDA reports)
TINEA PEDIS ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 8 FDA reports)
TUMOUR INVASION ( 8 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 8 FDA reports)
URINE ABNORMALITY ( 8 FDA reports)
VASCULAR COMPRESSION ( 8 FDA reports)
VITAMIN K DEFICIENCY ( 8 FDA reports)
WHITE BLOOD CELL DISORDER ( 8 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ACINETOBACTER INFECTION ( 7 FDA reports)
ACUTE POLYNEUROPATHY ( 7 FDA reports)
ADRENAL CARCINOMA ( 7 FDA reports)
ARTERIAL DISORDER ( 7 FDA reports)
ARTHRITIS INFECTIVE ( 7 FDA reports)
BACTERIAL TEST POSITIVE ( 7 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 7 FDA reports)
BLOOD CALCIUM ABNORMAL ( 7 FDA reports)
BLOODY DISCHARGE ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
BRAIN ABSCESS ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CALCINOSIS ( 7 FDA reports)
CARDIAC VALVE DISEASE ( 7 FDA reports)
CEREBELLAR HAEMORRHAGE ( 7 FDA reports)
CEREBRAL CALCIFICATION ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 7 FDA reports)
COLON POLYPECTOMY ( 7 FDA reports)
COMMUNICATION DISORDER ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
CRANIAL NERVE DISORDER ( 7 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 7 FDA reports)
CULTURE POSITIVE ( 7 FDA reports)
CULTURE WOUND POSITIVE ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
CYST REMOVAL ( 7 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 7 FDA reports)
DENTURE WEARER ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 7 FDA reports)
DYSPNOEA AT REST ( 7 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 7 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 7 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 7 FDA reports)
FACIAL PARESIS ( 7 FDA reports)
FEBRILE INFECTION ( 7 FDA reports)
FEEDING DISORDER ( 7 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 7 FDA reports)
FRACTURE DISPLACEMENT ( 7 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 7 FDA reports)
HAEMOSIDEROSIS ( 7 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 7 FDA reports)
HEPATITIS VIRAL ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
IMMOBILE ( 7 FDA reports)
INADEQUATE ANALGESIA ( 7 FDA reports)
INTESTINAL HAEMORRHAGE ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
LIPOATROPHY ( 7 FDA reports)
MACROCYTOSIS ( 7 FDA reports)
MALIGNANT HYPERTENSION ( 7 FDA reports)
MANIA ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
MIOSIS ( 7 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 7 FDA reports)
MORAXELLA INFECTION ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
NEURODERMATITIS ( 7 FDA reports)
NEUTROPENIC COLITIS ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
OEDEMA MUCOSAL ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OPTIC NERVE DISORDER ( 7 FDA reports)
OSTEOSYNTHESIS ( 7 FDA reports)
PALATAL DISORDER ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PCO2 INCREASED ( 7 FDA reports)
PELVIC ABSCESS ( 7 FDA reports)
PERFORATED ULCER ( 7 FDA reports)
PERIDIVERTICULAR ABSCESS ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PHRENIC NERVE PARALYSIS ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
POLYP ( 7 FDA reports)
PROCTITIS ( 7 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
RADIATION INJURY ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
RENAL HAEMORRHAGE ( 7 FDA reports)
RHEUMATOID ARTHRITIS ( 7 FDA reports)
RHINITIS ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SALMONELLOSIS ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN ATROPHY ( 7 FDA reports)
SPUTUM INCREASED ( 7 FDA reports)
STRESS ( 7 FDA reports)
SUBACUTE ENDOCARDITIS ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
SUBRETINAL FIBROSIS ( 7 FDA reports)
THORACOTOMY ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
THYROID MASS ( 7 FDA reports)
THYROIDECTOMY ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
VASCULAR ENCEPHALOPATHY ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
WEST NILE VIRAL INFECTION ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
ADDISON'S DISEASE ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
BLADDER DISTENSION ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 6 FDA reports)
BONE INFECTION ( 6 FDA reports)
BONE LESION EXCISION ( 6 FDA reports)
BONE SWELLING ( 6 FDA reports)
BRAIN SCAN ABNORMAL ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
CARDIAC HYPERTROPHY ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COLOUR BLINDNESS ( 6 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CYSTITIS INTERSTITIAL ( 6 FDA reports)
DEMENTIA WITH LEWY BODIES ( 6 FDA reports)
DERMATOPHYTOSIS ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DRUG RESISTANCE ( 6 FDA reports)
DYSLIPIDAEMIA ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENGRAFT FAILURE ( 6 FDA reports)
EPIDIDYMITIS ( 6 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
EYE INFECTION VIRAL ( 6 FDA reports)
EYE IRRITATION ( 6 FDA reports)
FACIAL BONES FRACTURE ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEARING DISABILITY ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPERMAGNESAEMIA ( 6 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 6 FDA reports)
HYPOGEUSIA ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTESTINAL DILATATION ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
KLEBSIELLA BACTERAEMIA ( 6 FDA reports)
KYPHOSCOLIOSIS ( 6 FDA reports)
LENS DISORDER ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 6 FDA reports)
MEAN CELL VOLUME INCREASED ( 6 FDA reports)
MEDULLOBLASTOMA ( 6 FDA reports)
MEGACOLON ( 6 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 6 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 6 FDA reports)
METASTASES TO MUSCLE ( 6 FDA reports)
METASTASES TO SKIN ( 6 FDA reports)
MONOCYTE COUNT DECREASED ( 6 FDA reports)
MUCOSAL INFECTION ( 6 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 6 FDA reports)
MUSCLE NECROSIS ( 6 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 6 FDA reports)
NEOPLASM RECURRENCE ( 6 FDA reports)
NEURITIS ( 6 FDA reports)
NODAL ARRHYTHMIA ( 6 FDA reports)
OESOPHAGEAL CARCINOMA ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
OLFACTORY NERVE DISORDER ( 6 FDA reports)
OSTEOMALACIA ( 6 FDA reports)
PANNICULITIS ( 6 FDA reports)
PEPTIC ULCER PERFORATION ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PERIODONTAL INFECTION ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PLATELET TRANSFUSION ( 6 FDA reports)
PNEUMONIA INFLUENZAL ( 6 FDA reports)
POLYPECTOMY ( 6 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
QUADRIPARESIS ( 6 FDA reports)
RASH VESICULAR ( 6 FDA reports)
RECALL PHENOMENON ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
SNORING ( 6 FDA reports)
SPINAL CORD DISORDER ( 6 FDA reports)
SPLENIC RUPTURE ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 6 FDA reports)
SUBDURAL EMPYEMA ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 6 FDA reports)
TONGUE DRY ( 6 FDA reports)
TONGUE INJURY ( 6 FDA reports)
TOURETTE'S DISORDER ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TROPONIN T INCREASED ( 6 FDA reports)
URINARY TRACT OBSTRUCTION ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VASCULITIC RASH ( 6 FDA reports)
VULVAL ULCERATION ( 6 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 5 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 5 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
AMAUROSIS ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANGER ( 5 FDA reports)
AORTIC VALVE REPLACEMENT ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 5 FDA reports)
ATRIAL THROMBOSIS ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BACTERIA URINE IDENTIFIED ( 5 FDA reports)
BACTERIAL DISEASE CARRIER ( 5 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BONE GRAFT ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BREAST OEDEMA ( 5 FDA reports)
BRONCHIAL HAEMORRHAGE ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
COMA HEPATIC ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CSF TEST ABNORMAL ( 5 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 5 FDA reports)
DENGUE FEVER ( 5 FDA reports)
DEPRESSION SUICIDAL ( 5 FDA reports)
DERMATITIS PSORIASIFORM ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EXOPHTHALMOS ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTROINTESTINAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HUNGER ( 5 FDA reports)
HYDROCELE ( 5 FDA reports)
HYPERMETABOLISM ( 5 FDA reports)
HYPERPHOSPHATASAEMIA ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMPETIGO ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
INNER EAR DISORDER ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
IRITIS ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LAPAROTOMY ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LIGHT CHAIN DISEASE ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENINGEAL DISORDER ( 5 FDA reports)
MENINGITIS BACTERIAL ( 5 FDA reports)
MIDDLE EAR EFFUSION ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MUCOCUTANEOUS RASH ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
MYELOCYTOSIS ( 5 FDA reports)
MYOPATHY STEROID ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
NO ADVERSE DRUG EFFECT ( 5 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OTORRHOEA ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PARALYSIS FLACCID ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PERIORBITAL CELLULITIS ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PLEURAL CALCIFICATION ( 5 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
RENAL INJURY ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
SCAN BONE MARROW ABNORMAL ( 5 FDA reports)
SCROTAL PAIN ( 5 FDA reports)
SERRATIA BACTERAEMIA ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
SINUS CONGESTION ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SKIN GRAFT ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SOPOR ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
SPLENIC GRANULOMA ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STERNAL FRACTURE ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
STUPOR ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
TESTICULAR FAILURE ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TINEA CRURIS ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TRACHEITIS ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
URETERIC RUPTURE ( 5 FDA reports)
URETHRAL STENOSIS ( 5 FDA reports)
VAGINAL OPERATION ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
VASCULITIS NECROTISING ( 5 FDA reports)
VENOOCCLUSIVE DISEASE ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
VITAL CAPACITY DECREASED ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
WOUND TREATMENT ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ADRENAL HAEMORRHAGE ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
APHERESIS ( 4 FDA reports)
APICAL GRANULOMA ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ARTERIAL HAEMORRHAGE ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ARTHRITIS REACTIVE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ATONIC URINARY BLADDER ( 4 FDA reports)
ATROPHIC VULVOVAGINITIS ( 4 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD URIC ACID ABNORMAL ( 4 FDA reports)
BONE DEFORMITY ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BRONCHOPNEUMOPATHY ( 4 FDA reports)
BRONCHOSTENOSIS ( 4 FDA reports)
BUDD-CHIARI SYNDROME ( 4 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 4 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CATHETER SITE ERYTHEMA ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 4 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 4 FDA reports)
COAGULATION TEST ABNORMAL ( 4 FDA reports)
COLONIC STENOSIS ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
COOMBS TEST POSITIVE ( 4 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 4 FDA reports)
CRANIAL NEUROPATHY ( 4 FDA reports)
CRYOGLOBULINAEMIA ( 4 FDA reports)
CYANOSIS CENTRAL ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 4 FDA reports)
ENCEPHALITIC INFECTION ( 4 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
ENTEROCOLITIS BACTERIAL ( 4 FDA reports)
ENTEROVIRUS INFECTION ( 4 FDA reports)
EPIGLOTTITIS ( 4 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
EYE ROLLING ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 4 FDA reports)
GASTROENTERITIS SALMONELLA ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GRAM STAIN POSITIVE ( 4 FDA reports)
GRANULOCYTES ABNORMAL ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 4 FDA reports)
HAEMOPHILUS SEPSIS ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HIV INFECTION ( 4 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPOCAPNIA ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INFESTATION ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
INJECTION SITE STREAKING ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
INTESTINAL MASS ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JESSNER'S LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEUKOARAIOSIS ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
MALOCCLUSION ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 4 FDA reports)
MEDIASTINAL SHIFT ( 4 FDA reports)
MEDICAL DEVICE REMOVAL ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOSITIS OSSIFICANS ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ORAL NEOPLASM ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
PANCREATIC NEOPLASM ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PERITONEAL EFFUSION ( 4 FDA reports)
PERONEAL NERVE INJURY ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PLASMA CELLS INCREASED ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY VASCULITIS ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RECTAL ABSCESS ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
REFLUX GASTRITIS ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
ROTAVIRUS INFECTION ( 4 FDA reports)
SALIVARY GLAND CANCER ( 4 FDA reports)
SARCOMA ( 4 FDA reports)
SCAPULA FRACTURE ( 4 FDA reports)
SENSORIMOTOR DISORDER ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
SPINAL CORD HAEMORRHAGE ( 4 FDA reports)
SPLENIC HAEMORRHAGE ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 4 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VASCULAR OPERATION ( 4 FDA reports)
VEIN DISCOLOURATION ( 4 FDA reports)
VIRAL RASH ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 3 FDA reports)
AMNESTIC DISORDER ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAL POLYP ( 3 FDA reports)
ANHIDROSIS ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE NECROSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
BACTERIAL TOXAEMIA ( 3 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BIOPSY LUNG ABNORMAL ( 3 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLAST CELLS PRESENT ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD STEM CELL HARVEST ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 3 FDA reports)
BONE TRIMMING ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETER SITE INFLAMMATION ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
CHOREOATHETOSIS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CHROMOSOME ABNORMALITY ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLON CANCER RECURRENT ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CRYOGLOBULINS ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
CSF GLUCOSE DECREASED ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DENTAL IMPLANTATION ( 3 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 3 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 3 FDA reports)
DIAPHRAGMATIC HERNIA ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 3 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
EPIDERMOLYSIS BULLOSA ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ERYTHEMA ELEVATUM DIUTINUM ( 3 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FIBRINOUS BRONCHITIS ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 3 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 3 FDA reports)
HYDROTHORAX ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERCREATININAEMIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INFUSION SITE DERMATITIS ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE PIGMENTATION CHANGES ( 3 FDA reports)
INJECTION SITE VASCULITIS ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LACTATE DEHYDROGENASE URINE INCREASED ( 3 FDA reports)
LARYNGEAL OBSTRUCTION ( 3 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIPASE ABNORMAL ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG INFILTRATION MALIGNANT ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 3 FDA reports)
MANTLE CELL LYMPHOMA REFRACTORY ( 3 FDA reports)
MEDIASTINAL FIBROSIS ( 3 FDA reports)
MENINGEAL NEOPLASM ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NERVE BLOCK ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEURALGIC AMYOTROPHY ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
ORAL DYSAESTHESIA ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
OSTECTOMY ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PANCREATIC CALCIFICATION ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHARYNGEAL ABSCESS ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLASTIC SURGERY TO THE FACE ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PLEURAL ADHESION ( 3 FDA reports)
PNEUMATURIA ( 3 FDA reports)
PNEUMONIA ESCHERICHIA ( 3 FDA reports)
PNEUMONIA NECROTISING ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POSTERIOR CAPSULOTOMY ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RADIATION SKIN INJURY ( 3 FDA reports)
RADICULITIS ( 3 FDA reports)
RECTAL PERFORATION ( 3 FDA reports)
RENAL AMYLOIDOSIS ( 3 FDA reports)
RENAL CANCER ( 3 FDA reports)
RENAL CYST INFECTION ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPONTANEOUS HAEMATOMA ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 3 FDA reports)
UMBILICAL HERNIA REPAIR ( 3 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URATE NEPHROPATHY ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR STENOSIS ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VASCULITIS GASTROINTESTINAL ( 3 FDA reports)
VENTRICULAR ASYSTOLE ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VERTEBRAL WEDGING ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VISCERAL LEISHMANIASIS ( 3 FDA reports)
VOLUME BLOOD DECREASED ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
5Q MINUS SYNDROME ( 2 FDA reports)
ABDOMINAL BRUIT ( 2 FDA reports)
ABDOMINAL WALL MASS ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ACANTHAMOEBA INFECTION ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACNE ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC ELONGATION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AUTOIMMUNE NEUROPATHY ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACILLUS TEST POSITIVE ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLASTOCYSTIS INFECTION ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHEST WALL ABSCESS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHYLOTHORAX ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
COXSACKIE VIRAL INFECTION ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CSF IMMUNOGLOBULIN DECREASED ( 2 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DYSGLOBULINAEMIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 2 FDA reports)
ECTROPION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELECTROPHORESIS ABNORMAL ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
EMBOLISM INFECTIVE ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURITIS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FIBRIN ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FRONTAL SINUS OPERATIONS ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
FUNGUS CULTURE POSITIVE ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GINGIVAL OEDEMA ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOGLOBIN S DECREASED ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPONATRAEMIC SYNDROME ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
IATROGENIC INFECTION ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL ADENOCARCINOMA ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOMA TRANSFORMATION ( 2 FDA reports)
MACROPHAGES INCREASED ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MASTOID DISORDER ( 2 FDA reports)
MAXILLOFACIAL OPERATION ( 2 FDA reports)
MEDIAN NERVE INJURY ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGITIS STREPTOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL BED INFLAMMATION ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NEUROBORRELIOSIS ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL NECROSIS ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLASMABLASTIC LYMPHOMA ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLATELET TOXICITY ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL OPERATION ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHINITIS ATROPHIC ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 2 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SECONDARY HYPERTHYROIDISM ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SERRATIA SEPSIS ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SPINAL CORD HERNIATION ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
STRANGURY ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDON SHEATH INCISION ( 2 FDA reports)
TENOLYSIS ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
THROMBOSIS PROPHYLAXIS ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TRACHEAL INFLAMMATION ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
UTERINE INFLAMMATION ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENOUS PRESSURE JUGULAR DECREASED ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
YAWNING ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCESSORY SPLEEN ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALBUMIN CSF INCREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALPHA 1 GLOBULIN DECREASED ( 1 FDA reports)
ALVEOLITIS NECROTISING ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
AMYLOIDOMA ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANTI FACTOR VII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTHROPOD INFESTATION ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENIGN DUODENAL NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN D DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN D INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE ABSENT ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CARCINOID TUMOUR OF THE CAECUM ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL VARICELLA INFECTION ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
COW POX ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE INFECTION INTRAOCULAR ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID INJURY ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPATIC CYST INFECTION ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HYALURONIC ACID ABNORMAL ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION REACTIVATION ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT DISLOCATION PATHOLOGICAL ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC HAEMORRHAGE ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASES TO TESTICLE ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MILIA ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NATURAL KILLER-CELL LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
NEEDLE BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTOSCOPY ABNORMAL ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARAESTHESIA EAR ( 1 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIORBITAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLASMA CELLS DECREASED ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA SALMONELLA ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYMERASE CHAIN REACTION ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE MUSCULAR ATROPHY ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROPHYLAXIS OF NAUSEA AND VOMITING ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RETROPERITONEAL MASS ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIB DEFORMITY ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SARCOMA UTERUS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCINTIGRAPHY ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SELECTIVE IGA IMMUNODEFICIENCY ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHIGELLA INFECTION ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLENIC CANDIDIASIS ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STARING ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
T-CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH AVULSION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URAEMIC NEUROPATHY ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT CARCINOMA IN SITU ( 1 FDA reports)
URINE ALANINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIIITH NERVE INJURY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITAMIN B6 INCREASED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELL SCAN ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)