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

DEATH ( 2011 FDA reports)
DIARRHOEA ( 1485 FDA reports)
NAUSEA ( 1440 FDA reports)
DISEASE PROGRESSION ( 1417 FDA reports)
VOMITING ( 1285 FDA reports)
PYREXIA ( 1000 FDA reports)
HYPERTENSION ( 958 FDA reports)
DEHYDRATION ( 939 FDA reports)
DYSPNOEA ( 866 FDA reports)
FATIGUE ( 848 FDA reports)
ANAEMIA ( 788 FDA reports)
ABDOMINAL PAIN ( 787 FDA reports)
PAIN ( 783 FDA reports)
DECREASED APPETITE ( 734 FDA reports)
ASTHENIA ( 689 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 602 FDA reports)
PNEUMONIA ( 597 FDA reports)
PULMONARY EMBOLISM ( 596 FDA reports)
PLEURAL EFFUSION ( 578 FDA reports)
EPISTAXIS ( 564 FDA reports)
OSTEONECROSIS OF JAW ( 522 FDA reports)
HAEMOGLOBIN DECREASED ( 517 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 516 FDA reports)
BACK PAIN ( 512 FDA reports)
CONSTIPATION ( 510 FDA reports)
RENAL FAILURE ACUTE ( 495 FDA reports)
THROMBOCYTOPENIA ( 485 FDA reports)
WEIGHT DECREASED ( 483 FDA reports)
NEUTROPENIA ( 479 FDA reports)
HEADACHE ( 477 FDA reports)
GASTROINTESTINAL PERFORATION ( 468 FDA reports)
PLATELET COUNT DECREASED ( 467 FDA reports)
NEUROPATHY PERIPHERAL ( 466 FDA reports)
DEEP VEIN THROMBOSIS ( 465 FDA reports)
ANXIETY ( 450 FDA reports)
STOMATITIS ( 444 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 440 FDA reports)
SEPSIS ( 439 FDA reports)
CONFUSIONAL STATE ( 430 FDA reports)
INTERSTITIAL LUNG DISEASE ( 425 FDA reports)
CHEST PAIN ( 409 FDA reports)
CONVULSION ( 401 FDA reports)
DIZZINESS ( 396 FDA reports)
FEBRILE NEUTROPENIA ( 381 FDA reports)
OSTEONECROSIS ( 374 FDA reports)
RASH ( 371 FDA reports)
HYPOTENSION ( 363 FDA reports)
INFECTION ( 361 FDA reports)
FALL ( 355 FDA reports)
NEUTROPHIL COUNT DECREASED ( 353 FDA reports)
RENAL FAILURE ( 352 FDA reports)
BONE DISORDER ( 347 FDA reports)
ENDOPHTHALMITIS ( 347 FDA reports)
METASTASES TO LIVER ( 346 FDA reports)
ARTHRALGIA ( 336 FDA reports)
CEREBROVASCULAR ACCIDENT ( 327 FDA reports)
NEOPLASM MALIGNANT ( 326 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 325 FDA reports)
ASCITES ( 317 FDA reports)
METASTASES TO BONE ( 317 FDA reports)
MUCOSAL INFLAMMATION ( 317 FDA reports)
PAIN IN EXTREMITY ( 317 FDA reports)
MALAISE ( 316 FDA reports)
PROTEINURIA ( 313 FDA reports)
HYPOAESTHESIA ( 307 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 300 FDA reports)
DYSPHAGIA ( 299 FDA reports)
BLOOD PRESSURE INCREASED ( 298 FDA reports)
IMPAIRED HEALING ( 297 FDA reports)
PERITONITIS ( 292 FDA reports)
VISUAL ACUITY REDUCED ( 291 FDA reports)
PAIN IN JAW ( 290 FDA reports)
RESPIRATORY FAILURE ( 280 FDA reports)
BLOOD CREATININE INCREASED ( 274 FDA reports)
CHILLS ( 273 FDA reports)
DEPRESSION ( 272 FDA reports)
MYOCARDIAL INFARCTION ( 272 FDA reports)
HAEMOPTYSIS ( 270 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 269 FDA reports)
OEDEMA PERIPHERAL ( 263 FDA reports)
URINARY TRACT INFECTION ( 259 FDA reports)
LARGE INTESTINE PERFORATION ( 253 FDA reports)
INTESTINAL PERFORATION ( 245 FDA reports)
HYPOKALAEMIA ( 244 FDA reports)
INJURY ( 244 FDA reports)
BLINDNESS ( 241 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 235 FDA reports)
PARAESTHESIA ( 229 FDA reports)
TACHYCARDIA ( 227 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 226 FDA reports)
CARDIAC ARREST ( 223 FDA reports)
ABDOMINAL PAIN UPPER ( 222 FDA reports)
INTESTINAL OBSTRUCTION ( 222 FDA reports)
COUGH ( 214 FDA reports)
WOUND DEHISCENCE ( 214 FDA reports)
ATELECTASIS ( 212 FDA reports)
HAEMORRHAGE ( 212 FDA reports)
ATRIAL FIBRILLATION ( 210 FDA reports)
ALOPECIA ( 208 FDA reports)
LUNG DISORDER ( 206 FDA reports)
ANHEDONIA ( 203 FDA reports)
ERYTHEMA ( 203 FDA reports)
TOOTH EXTRACTION ( 202 FDA reports)
PANCYTOPENIA ( 201 FDA reports)
LEUKOPENIA ( 200 FDA reports)
DRUG INEFFECTIVE ( 199 FDA reports)
OSTEOMYELITIS ( 199 FDA reports)
PNEUMOTHORAX ( 197 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 197 FDA reports)
HAEMATOCRIT DECREASED ( 194 FDA reports)
ILEUS ( 193 FDA reports)
THROMBOSIS ( 192 FDA reports)
LOSS OF CONSCIOUSNESS ( 190 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 190 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 189 FDA reports)
HAEMATURIA ( 189 FDA reports)
PRODUCT QUALITY ISSUE ( 189 FDA reports)
METASTASES TO LUNG ( 188 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 186 FDA reports)
RECTAL HAEMORRHAGE ( 185 FDA reports)
CARDIAC FAILURE ( 184 FDA reports)
SYNCOPE ( 181 FDA reports)
BLOOD GLUCOSE INCREASED ( 180 FDA reports)
HYPONATRAEMIA ( 180 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 178 FDA reports)
SEPTIC SHOCK ( 174 FDA reports)
VISION BLURRED ( 174 FDA reports)
BLOOD BILIRUBIN INCREASED ( 173 FDA reports)
ANOREXIA ( 171 FDA reports)
GAIT DISTURBANCE ( 169 FDA reports)
VISUAL IMPAIRMENT ( 169 FDA reports)
ABDOMINAL DISTENSION ( 168 FDA reports)
HEPATIC FAILURE ( 164 FDA reports)
NEOPLASM PROGRESSION ( 164 FDA reports)
MUSCULOSKELETAL PAIN ( 163 FDA reports)
RENAL IMPAIRMENT ( 163 FDA reports)
CARDIO-RESPIRATORY ARREST ( 162 FDA reports)
OSTEOARTHRITIS ( 162 FDA reports)
EJECTION FRACTION DECREASED ( 161 FDA reports)
BONE PAIN ( 160 FDA reports)
HYPERSENSITIVITY ( 160 FDA reports)
DEFORMITY ( 158 FDA reports)
EYE PAIN ( 158 FDA reports)
INSOMNIA ( 158 FDA reports)
LYMPHADENOPATHY ( 157 FDA reports)
METASTASES TO SPINE ( 157 FDA reports)
CEREBRAL HAEMORRHAGE ( 153 FDA reports)
UVEITIS ( 152 FDA reports)
MENTAL STATUS CHANGES ( 151 FDA reports)
SHOCK ( 150 FDA reports)
BLOOD SODIUM DECREASED ( 149 FDA reports)
EYE INFLAMMATION ( 149 FDA reports)
SPINAL OSTEOARTHRITIS ( 149 FDA reports)
MULTI-ORGAN FAILURE ( 148 FDA reports)
TREMOR ( 148 FDA reports)
BLOOD POTASSIUM DECREASED ( 147 FDA reports)
OESOPHAGITIS ( 147 FDA reports)
CEREBRAL INFARCTION ( 146 FDA reports)
BONE MARROW FAILURE ( 143 FDA reports)
BRONCHITIS ( 143 FDA reports)
TOOTHACHE ( 143 FDA reports)
CARDIOMYOPATHY ( 141 FDA reports)
PANCREATITIS ( 140 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 139 FDA reports)
PERICARDIAL EFFUSION ( 139 FDA reports)
SWELLING ( 138 FDA reports)
DYSPEPSIA ( 136 FDA reports)
GASTRITIS ( 135 FDA reports)
RETINAL HAEMORRHAGE ( 135 FDA reports)
HEART RATE INCREASED ( 134 FDA reports)
BONE LESION ( 133 FDA reports)
HAEMORRHOIDS ( 133 FDA reports)
JAUNDICE ( 132 FDA reports)
GASTRIC ULCER ( 131 FDA reports)
MUSCLE SPASMS ( 130 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 129 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 127 FDA reports)
HYPOMAGNESAEMIA ( 127 FDA reports)
SOMNOLENCE ( 127 FDA reports)
HYPOXIA ( 126 FDA reports)
OEDEMA ( 126 FDA reports)
SMALL INTESTINAL PERFORATION ( 125 FDA reports)
APHASIA ( 124 FDA reports)
FISTULA ( 123 FDA reports)
CHEST DISCOMFORT ( 122 FDA reports)
MUSCULAR WEAKNESS ( 122 FDA reports)
PULMONARY OEDEMA ( 121 FDA reports)
LOOSE TOOTH ( 120 FDA reports)
METASTASES TO LYMPH NODES ( 120 FDA reports)
CONDITION AGGRAVATED ( 118 FDA reports)
DENTAL CARIES ( 118 FDA reports)
EMBOLISM ( 118 FDA reports)
OSTEOPENIA ( 118 FDA reports)
ABSCESS ( 116 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 116 FDA reports)
PULMONARY HYPERTENSION ( 115 FDA reports)
SINUSITIS ( 115 FDA reports)
SKIN EXFOLIATION ( 113 FDA reports)
COLITIS ( 111 FDA reports)
HYPOCALCAEMIA ( 111 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 111 FDA reports)
LUNG INFILTRATION ( 111 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 111 FDA reports)
BLOOD PRESSURE DECREASED ( 110 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 110 FDA reports)
BLOOD UREA INCREASED ( 108 FDA reports)
CELLULITIS ( 108 FDA reports)
DIVERTICULITIS ( 108 FDA reports)
ORAL PAIN ( 108 FDA reports)
CARDIAC DISORDER ( 107 FDA reports)
CATARACT ( 107 FDA reports)
DRUG TOXICITY ( 107 FDA reports)
MYALGIA ( 107 FDA reports)
HAEMATEMESIS ( 106 FDA reports)
BLOOD ALBUMIN DECREASED ( 105 FDA reports)
BREAST CANCER METASTATIC ( 105 FDA reports)
DRUG HYPERSENSITIVITY ( 105 FDA reports)
ILEAL PERFORATION ( 105 FDA reports)
INFUSION RELATED REACTION ( 105 FDA reports)
LACRIMATION INCREASED ( 105 FDA reports)
PNEUMONITIS ( 105 FDA reports)
PRURITUS ( 105 FDA reports)
DYSPHONIA ( 103 FDA reports)
INFLAMMATION ( 102 FDA reports)
DECREASED INTEREST ( 101 FDA reports)
LEUKOENCEPHALOPATHY ( 101 FDA reports)
BLINDNESS UNILATERAL ( 100 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 100 FDA reports)
CARDIOMEGALY ( 100 FDA reports)
HYPOPHAGIA ( 100 FDA reports)
NEPHROTIC SYNDROME ( 100 FDA reports)
PNEUMONIA ASPIRATION ( 100 FDA reports)
RECTAL PERFORATION ( 100 FDA reports)
SUDDEN DEATH ( 100 FDA reports)
URTICARIA ( 100 FDA reports)
NEPHROLITHIASIS ( 99 FDA reports)
RETINAL DETACHMENT ( 99 FDA reports)
ABDOMINAL DISCOMFORT ( 97 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 96 FDA reports)
URINARY RETENTION ( 96 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 96 FDA reports)
EMOTIONAL DISTRESS ( 95 FDA reports)
INFECTIOUS PERITONITIS ( 94 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 94 FDA reports)
STAPHYLOCOCCAL INFECTION ( 94 FDA reports)
DERMATITIS ACNEIFORM ( 93 FDA reports)
HYDRONEPHROSIS ( 93 FDA reports)
ANAPHYLACTIC SHOCK ( 92 FDA reports)
DEVICE RELATED INFECTION ( 92 FDA reports)
ENCEPHALOPATHY ( 92 FDA reports)
FLUSHING ( 92 FDA reports)
HIATUS HERNIA ( 91 FDA reports)
LUNG NEOPLASM ( 91 FDA reports)
ARRHYTHMIA ( 90 FDA reports)
DYSURIA ( 90 FDA reports)
MELAENA ( 90 FDA reports)
ORAL INTAKE REDUCED ( 90 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 90 FDA reports)
COLITIS ISCHAEMIC ( 89 FDA reports)
NECROSIS ( 89 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 89 FDA reports)
VITRITIS ( 89 FDA reports)
DRUG INTOLERANCE ( 88 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 88 FDA reports)
DISABILITY ( 87 FDA reports)
EYE HAEMORRHAGE ( 87 FDA reports)
HEPATIC STEATOSIS ( 87 FDA reports)
OXYGEN SATURATION DECREASED ( 87 FDA reports)
EMPHYSEMA ( 86 FDA reports)
GINGIVITIS ( 86 FDA reports)
HAEMATOCHEZIA ( 86 FDA reports)
HEPATIC LESION ( 86 FDA reports)
PULMONARY HAEMORRHAGE ( 86 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 85 FDA reports)
BALANCE DISORDER ( 85 FDA reports)
HYPERGLYCAEMIA ( 85 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 85 FDA reports)
SKIN ULCER ( 85 FDA reports)
TOOTH ABSCESS ( 85 FDA reports)
VENTRICULAR FIBRILLATION ( 85 FDA reports)
HAEMOLYTIC ANAEMIA ( 84 FDA reports)
PURULENT DISCHARGE ( 84 FDA reports)
CHOLELITHIASIS ( 83 FDA reports)
COLON CANCER METASTATIC ( 83 FDA reports)
OCULAR HYPERAEMIA ( 83 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 82 FDA reports)
MITRAL VALVE INCOMPETENCE ( 81 FDA reports)
DYSARTHRIA ( 80 FDA reports)
NECK PAIN ( 80 FDA reports)
PRIMARY SEQUESTRUM ( 80 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 79 FDA reports)
HYPOPHOSPHATAEMIA ( 79 FDA reports)
INTESTINAL ISCHAEMIA ( 79 FDA reports)
MOUTH ULCERATION ( 79 FDA reports)
SPEECH DISORDER ( 79 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 79 FDA reports)
ARTHRITIS ( 78 FDA reports)
FLANK PAIN ( 78 FDA reports)
TOOTH DISORDER ( 78 FDA reports)
BLOOD CALCIUM DECREASED ( 77 FDA reports)
BODY TEMPERATURE INCREASED ( 77 FDA reports)
DYSPNOEA EXERTIONAL ( 76 FDA reports)
HEMIPARESIS ( 76 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 74 FDA reports)
DISORIENTATION ( 74 FDA reports)
HEPATIC CYST ( 74 FDA reports)
UNEVALUABLE EVENT ( 74 FDA reports)
GINGIVAL BLEEDING ( 73 FDA reports)
HYPERHIDROSIS ( 73 FDA reports)
HYPOALBUMINAEMIA ( 73 FDA reports)
LIVER DISORDER ( 73 FDA reports)
AORTIC DISSECTION ( 72 FDA reports)
COMA ( 72 FDA reports)
EXPOSED BONE IN JAW ( 72 FDA reports)
LUMBAR SPINAL STENOSIS ( 72 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 71 FDA reports)
HAEMATOMA ( 71 FDA reports)
HEPATIC CIRRHOSIS ( 71 FDA reports)
LUNG INFECTION ( 71 FDA reports)
RESPIRATORY DISTRESS ( 71 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 71 FDA reports)
DIPLOPIA ( 70 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 70 FDA reports)
AMNESIA ( 69 FDA reports)
DEAFNESS ( 69 FDA reports)
EPILEPSY ( 69 FDA reports)
HYPERAMMONAEMIA ( 69 FDA reports)
METASTASES TO MENINGES ( 69 FDA reports)
SPLENOMEGALY ( 69 FDA reports)
VENOUS THROMBOSIS ( 69 FDA reports)
APHAGIA ( 68 FDA reports)
GASTROINTESTINAL DISORDER ( 68 FDA reports)
HYPOTHYROIDISM ( 68 FDA reports)
COMPRESSION FRACTURE ( 67 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 67 FDA reports)
RENAL CYST ( 67 FDA reports)
TOOTH LOSS ( 67 FDA reports)
VERTIGO ( 67 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 66 FDA reports)
CEREBRAL ISCHAEMIA ( 66 FDA reports)
HERPES ZOSTER ( 66 FDA reports)
JOINT SWELLING ( 66 FDA reports)
PERIODONTAL DISEASE ( 66 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 66 FDA reports)
CORONARY ARTERY DISEASE ( 65 FDA reports)
DUODENAL ULCER PERFORATION ( 65 FDA reports)
ENTERITIS ( 65 FDA reports)
GRAND MAL CONVULSION ( 65 FDA reports)
SHOCK HAEMORRHAGIC ( 65 FDA reports)
DELIRIUM ( 64 FDA reports)
DIABETES MELLITUS ( 64 FDA reports)
MALNUTRITION ( 64 FDA reports)
MYOCARDIAL ISCHAEMIA ( 64 FDA reports)
ORAL CANDIDIASIS ( 64 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 64 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 64 FDA reports)
WOUND INFECTION ( 64 FDA reports)
ABASIA ( 63 FDA reports)
DEBRIDEMENT ( 63 FDA reports)
SINUS TACHYCARDIA ( 63 FDA reports)
TUMOUR HAEMORRHAGE ( 63 FDA reports)
BRONCHOSPASM ( 62 FDA reports)
JAW DISORDER ( 62 FDA reports)
LETHARGY ( 62 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 61 FDA reports)
BURSITIS ( 61 FDA reports)
FAILURE TO THRIVE ( 61 FDA reports)
SINUS DISORDER ( 61 FDA reports)
CEREBRAL ATROPHY ( 60 FDA reports)
DUODENAL ULCER ( 60 FDA reports)
EYE DISORDER ( 60 FDA reports)
HYPERLIPIDAEMIA ( 60 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 60 FDA reports)
MENINGITIS ( 60 FDA reports)
OPEN WOUND ( 60 FDA reports)
PALPITATIONS ( 60 FDA reports)
POST PROCEDURAL COMPLICATION ( 60 FDA reports)
GASTROENTERITIS ( 59 FDA reports)
GASTROINTESTINAL NECROSIS ( 59 FDA reports)
LUNG NEOPLASM MALIGNANT ( 59 FDA reports)
MASTICATION DISORDER ( 59 FDA reports)
PLATELET COUNT INCREASED ( 59 FDA reports)
POLYNEUROPATHY ( 59 FDA reports)
SEQUESTRECTOMY ( 58 FDA reports)
URINARY INCONTINENCE ( 58 FDA reports)
ABDOMINAL ABSCESS ( 57 FDA reports)
CONTUSION ( 57 FDA reports)
DRUG INTERACTION ( 57 FDA reports)
METASTATIC NEOPLASM ( 57 FDA reports)
ORAL DISORDER ( 57 FDA reports)
PETECHIAE ( 57 FDA reports)
ANAL FISTULA ( 56 FDA reports)
BRADYCARDIA ( 56 FDA reports)
ISCHAEMIC STROKE ( 56 FDA reports)
WEIGHT INCREASED ( 56 FDA reports)
NERVOUS SYSTEM DISORDER ( 55 FDA reports)
PERIODONTITIS ( 55 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 55 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 55 FDA reports)
ANAL ABSCESS ( 54 FDA reports)
ANAL FISSURE ( 54 FDA reports)
ANGINA PECTORIS ( 54 FDA reports)
EAR PAIN ( 54 FDA reports)
NEURALGIA ( 54 FDA reports)
RESPIRATORY ARREST ( 54 FDA reports)
ACUTE CORONARY SYNDROME ( 53 FDA reports)
DYSKINESIA ( 53 FDA reports)
GLAUCOMA ( 53 FDA reports)
HEPATIC ENZYME INCREASED ( 53 FDA reports)
HICCUPS ( 53 FDA reports)
ILL-DEFINED DISORDER ( 53 FDA reports)
VENTRICULAR TACHYCARDIA ( 53 FDA reports)
CANDIDIASIS ( 52 FDA reports)
EYE IRRITATION ( 52 FDA reports)
JAW FRACTURE ( 52 FDA reports)
OSTEITIS ( 52 FDA reports)
ACUTE RESPIRATORY FAILURE ( 51 FDA reports)
ANAPHYLACTIC REACTION ( 51 FDA reports)
BLOOD URINE PRESENT ( 51 FDA reports)
IRITIS ( 51 FDA reports)
NIGHT SWEATS ( 51 FDA reports)
PROTHROMBIN TIME PROLONGED ( 51 FDA reports)
PULMONARY FIBROSIS ( 51 FDA reports)
CYANOSIS ( 50 FDA reports)
CYST ( 50 FDA reports)
LEUKOCYTOSIS ( 50 FDA reports)
MEMORY IMPAIRMENT ( 50 FDA reports)
PATHOLOGICAL FRACTURE ( 50 FDA reports)
SKIN LESION ( 50 FDA reports)
SKIN NECROSIS ( 50 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 50 FDA reports)
CHOLECYSTITIS ( 49 FDA reports)
CHRONIC SINUSITIS ( 49 FDA reports)
COAGULOPATHY ( 49 FDA reports)
DIVERTICULUM ( 49 FDA reports)
HYPOGLYCAEMIA ( 49 FDA reports)
NASAL SEPTUM PERFORATION ( 49 FDA reports)
NECROTISING FASCIITIS ( 49 FDA reports)
OROPHARYNGEAL PAIN ( 49 FDA reports)
PANCREATITIS ACUTE ( 49 FDA reports)
SKIN DISORDER ( 49 FDA reports)
CARDIAC MURMUR ( 48 FDA reports)
COLON CANCER ( 48 FDA reports)
GASTRIC PERFORATION ( 48 FDA reports)
GINGIVAL PAIN ( 48 FDA reports)
HYPERKALAEMIA ( 48 FDA reports)
MACULAR DEGENERATION ( 48 FDA reports)
MIGRAINE ( 48 FDA reports)
NEOPLASM ( 48 FDA reports)
ODYNOPHAGIA ( 48 FDA reports)
PULMONARY CONGESTION ( 48 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 47 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 47 FDA reports)
DECUBITUS ULCER ( 47 FDA reports)
FEELING ABNORMAL ( 47 FDA reports)
HALLUCINATION ( 47 FDA reports)
METASTASES TO PERITONEUM ( 47 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 47 FDA reports)
PRODUCTIVE COUGH ( 47 FDA reports)
TRANSAMINASES INCREASED ( 47 FDA reports)
VITREOUS FLOATERS ( 47 FDA reports)
VITREOUS HAEMORRHAGE ( 47 FDA reports)
ANAPHYLACTOID REACTION ( 46 FDA reports)
ARTERIOSCLEROSIS ( 46 FDA reports)
CACHEXIA ( 46 FDA reports)
DENTAL OPERATION ( 46 FDA reports)
EYE INFECTION ( 46 FDA reports)
FUNGAL INFECTION ( 46 FDA reports)
HEPATIC MASS ( 46 FDA reports)
HYPERTENSIVE CRISIS ( 46 FDA reports)
METABOLIC ACIDOSIS ( 46 FDA reports)
TOOTH FRACTURE ( 46 FDA reports)
BREAST CANCER ( 45 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 45 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 45 FDA reports)
OSTEORADIONECROSIS ( 45 FDA reports)
POLLAKIURIA ( 45 FDA reports)
ROTATOR CUFF SYNDROME ( 45 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 44 FDA reports)
DUODENAL PERFORATION ( 44 FDA reports)
FEBRILE BONE MARROW APLASIA ( 44 FDA reports)
PELVIC ABSCESS ( 44 FDA reports)
RENAL DISORDER ( 44 FDA reports)
BRAIN OEDEMA ( 43 FDA reports)
CARDIOPULMONARY FAILURE ( 43 FDA reports)
LIPASE INCREASED ( 43 FDA reports)
MACULAR OEDEMA ( 43 FDA reports)
METASTASIS ( 43 FDA reports)
PROCTALGIA ( 43 FDA reports)
RASH ERYTHEMATOUS ( 43 FDA reports)
RESPIRATORY DISORDER ( 43 FDA reports)
BACTERIAL INFECTION ( 42 FDA reports)
CYSTITIS ( 42 FDA reports)
ESCHERICHIA INFECTION ( 42 FDA reports)
ILEAL ULCER ( 42 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 42 FDA reports)
MASS ( 42 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 42 FDA reports)
SUICIDAL IDEATION ( 42 FDA reports)
VARICES OESOPHAGEAL ( 42 FDA reports)
ARTHROPATHY ( 41 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 41 FDA reports)
DISCOMFORT ( 41 FDA reports)
DRY EYE ( 41 FDA reports)
ENTEROCOLITIS ( 41 FDA reports)
HYPERCHOLESTEROLAEMIA ( 41 FDA reports)
NEUTROPHIL COUNT INCREASED ( 41 FDA reports)
OFF LABEL USE ( 41 FDA reports)
OSTEOLYSIS ( 41 FDA reports)
OSTEOPOROSIS ( 41 FDA reports)
PORTAL HYPERTENSION ( 41 FDA reports)
SPONDYLOLISTHESIS ( 41 FDA reports)
BONE FRAGMENTATION ( 40 FDA reports)
DILATATION ATRIAL ( 40 FDA reports)
EYE SWELLING ( 40 FDA reports)
HEPATITIS ( 40 FDA reports)
HERPES SIMPLEX ( 40 FDA reports)
RHABDOMYOLYSIS ( 40 FDA reports)
SPINAL COMPRESSION FRACTURE ( 40 FDA reports)
ULCER ( 40 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 39 FDA reports)
BLOOD CULTURE POSITIVE ( 39 FDA reports)
DIVERTICULAR PERFORATION ( 39 FDA reports)
DRY MOUTH ( 39 FDA reports)
LYMPHOEDEMA ( 39 FDA reports)
NEUROTOXICITY ( 39 FDA reports)
OSTEOSCLEROSIS ( 39 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 39 FDA reports)
RADICULOPATHY ( 39 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 39 FDA reports)
VASCULITIS ( 39 FDA reports)
WHEELCHAIR USER ( 39 FDA reports)
CHOLESTASIS ( 38 FDA reports)
EMBOLISM ARTERIAL ( 38 FDA reports)
ENDODONTIC PROCEDURE ( 38 FDA reports)
HIP FRACTURE ( 38 FDA reports)
HYPOVOLAEMIA ( 38 FDA reports)
IMPETIGO ( 38 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 38 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 38 FDA reports)
AORTIC VALVE INCOMPETENCE ( 37 FDA reports)
ARTERIOSPASM CORONARY ( 37 FDA reports)
ASPHYXIA ( 37 FDA reports)
BLOOD CALCIUM INCREASED ( 37 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 37 FDA reports)
CIRCULATORY COLLAPSE ( 37 FDA reports)
CORNEAL OEDEMA ( 37 FDA reports)
CYTOKINE STORM ( 37 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 37 FDA reports)
PHOTOPHOBIA ( 37 FDA reports)
RESPIRATORY RATE INCREASED ( 37 FDA reports)
SPINAL COLUMN STENOSIS ( 37 FDA reports)
SPINAL CORD COMPRESSION ( 37 FDA reports)
WHEEZING ( 37 FDA reports)
ABDOMINAL PAIN LOWER ( 36 FDA reports)
BACTERAEMIA ( 36 FDA reports)
DYSGEUSIA ( 36 FDA reports)
LARYNGITIS ( 36 FDA reports)
LOCAL SWELLING ( 36 FDA reports)
NEUTROPENIC SEPSIS ( 36 FDA reports)
OESOPHAGEAL ULCER ( 36 FDA reports)
RASH PRURITIC ( 36 FDA reports)
RECTAL ULCER ( 36 FDA reports)
SWELLING FACE ( 36 FDA reports)
TOOTH INFECTION ( 36 FDA reports)
UNRESPONSIVE TO STIMULI ( 36 FDA reports)
ASPIRATION ( 35 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 35 FDA reports)
CATHETER RELATED INFECTION ( 35 FDA reports)
COLONIC OBSTRUCTION ( 35 FDA reports)
DYSSTASIA ( 35 FDA reports)
GINGIVAL SWELLING ( 35 FDA reports)
INFLUENZA LIKE ILLNESS ( 35 FDA reports)
IRIDOCYCLITIS ( 35 FDA reports)
LIVER ABSCESS ( 35 FDA reports)
METABOLIC DISORDER ( 35 FDA reports)
ORAL INFECTION ( 35 FDA reports)
SUBCUTANEOUS ABSCESS ( 35 FDA reports)
VISUAL DISTURBANCE ( 35 FDA reports)
VOCAL CORD PARALYSIS ( 35 FDA reports)
ASPIRATION PLEURAL CAVITY ( 34 FDA reports)
BONE DEBRIDEMENT ( 34 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 34 FDA reports)
HEPATIC ENCEPHALOPATHY ( 34 FDA reports)
NASOPHARYNGITIS ( 34 FDA reports)
PERFORMANCE STATUS DECREASED ( 34 FDA reports)
SYNOVIAL CYST ( 34 FDA reports)
ARTERIAL THROMBOSIS ( 33 FDA reports)
BONE DENSITY DECREASED ( 33 FDA reports)
CHOLANGITIS ( 33 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 33 FDA reports)
DISEASE RECURRENCE ( 33 FDA reports)
EATING DISORDER ( 33 FDA reports)
HILAR LYMPHADENOPATHY ( 33 FDA reports)
HYPERBILIRUBINAEMIA ( 33 FDA reports)
IRON DEFICIENCY ANAEMIA ( 33 FDA reports)
JOINT EFFUSION ( 33 FDA reports)
JUGULAR VEIN THROMBOSIS ( 33 FDA reports)
LOBAR PNEUMONIA ( 33 FDA reports)
METASTASES TO THE MEDIASTINUM ( 33 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 33 FDA reports)
NON-SMALL CELL LUNG CANCER ( 33 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 33 FDA reports)
RIB FRACTURE ( 33 FDA reports)
THERAPY NON-RESPONDER ( 33 FDA reports)
THROAT IRRITATION ( 33 FDA reports)
TOOTH IMPACTED ( 33 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 32 FDA reports)
ATAXIA ( 32 FDA reports)
CARDIOVASCULAR DISORDER ( 32 FDA reports)
GLIOBLASTOMA ( 32 FDA reports)
HAEMATOTOXICITY ( 32 FDA reports)
HOT FLUSH ( 32 FDA reports)
HYPOAESTHESIA ORAL ( 32 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 32 FDA reports)
MOBILITY DECREASED ( 32 FDA reports)
RESTLESS LEGS SYNDROME ( 32 FDA reports)
SINUS BRADYCARDIA ( 32 FDA reports)
SUBDURAL HAEMATOMA ( 32 FDA reports)
SURGERY ( 32 FDA reports)
ACTINOMYCOSIS ( 31 FDA reports)
AORTIC ANEURYSM ( 31 FDA reports)
CARDIOTOXICITY ( 31 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 31 FDA reports)
COGNITIVE DISORDER ( 31 FDA reports)
DERMATITIS ALLERGIC ( 31 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 31 FDA reports)
ELECTROLYTE IMBALANCE ( 31 FDA reports)
HYDROCEPHALUS ( 31 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 31 FDA reports)
MENTAL DISORDER ( 31 FDA reports)
NASAL CONGESTION ( 31 FDA reports)
PEPTIC ULCER ( 31 FDA reports)
PERICARDITIS ( 31 FDA reports)
PROTEIN URINE PRESENT ( 31 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 31 FDA reports)
ABDOMINAL HERNIA ( 30 FDA reports)
BLOOD CHLORIDE DECREASED ( 30 FDA reports)
CATARACT OPERATION ( 30 FDA reports)
CATHETER RELATED COMPLICATION ( 30 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 30 FDA reports)
COLONIC FISTULA ( 30 FDA reports)
COLONIC POLYP ( 30 FDA reports)
ERECTILE DYSFUNCTION ( 30 FDA reports)
FACE OEDEMA ( 30 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 30 FDA reports)
ISCHAEMIA ( 30 FDA reports)
LIMB DEFORMITY ( 30 FDA reports)
LUNG CONSOLIDATION ( 30 FDA reports)
MALIGNANT ASCITES ( 30 FDA reports)
MOUTH HAEMORRHAGE ( 30 FDA reports)
MYOSITIS ( 30 FDA reports)
OCULAR HYPERTENSION ( 30 FDA reports)
PALLOR ( 30 FDA reports)
PHLEBITIS ( 30 FDA reports)
PNEUMATOSIS INTESTINALIS ( 30 FDA reports)
SKIN IRRITATION ( 30 FDA reports)
SLEEP DISORDER ( 30 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 30 FDA reports)
TENDERNESS ( 30 FDA reports)
THROAT TIGHTNESS ( 30 FDA reports)
TYPE 2 DIABETES MELLITUS ( 30 FDA reports)
VAGINAL HAEMORRHAGE ( 30 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 29 FDA reports)
BLOOD GLUCOSE DECREASED ( 29 FDA reports)
COLORECTAL CANCER METASTATIC ( 29 FDA reports)
CULTURE URINE POSITIVE ( 29 FDA reports)
DRY SKIN ( 29 FDA reports)
ENTEROCUTANEOUS FISTULA ( 29 FDA reports)
FEELING HOT ( 29 FDA reports)
GINGIVAL INFECTION ( 29 FDA reports)
HEPATOMEGALY ( 29 FDA reports)
HYPERURICAEMIA ( 29 FDA reports)
INCORRECT DOSE ADMINISTERED ( 29 FDA reports)
LYMPHOPENIA ( 29 FDA reports)
MENISCUS LESION ( 29 FDA reports)
PSEUDOENDOPHTHALMITIS ( 29 FDA reports)
PULSE ABSENT ( 29 FDA reports)
TUMOUR LYSIS SYNDROME ( 29 FDA reports)
ABSCESS DRAINAGE ( 28 FDA reports)
AGITATION ( 28 FDA reports)
BLOOD POTASSIUM INCREASED ( 28 FDA reports)
COLON CANCER RECURRENT ( 28 FDA reports)
DEPRESSED MOOD ( 28 FDA reports)
DERMATITIS ( 28 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 28 FDA reports)
EXTRAVASATION ( 28 FDA reports)
FAECALOMA ( 28 FDA reports)
FIBRIN D DIMER INCREASED ( 28 FDA reports)
FIBROMYALGIA ( 28 FDA reports)
GASTROINTESTINAL TOXICITY ( 28 FDA reports)
GLIOBLASTOMA MULTIFORME ( 28 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 28 FDA reports)
INJECTION SITE REACTION ( 28 FDA reports)
MASTECTOMY ( 28 FDA reports)
NEOPLASM RECURRENCE ( 28 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 28 FDA reports)
RENAL FAILURE CHRONIC ( 28 FDA reports)
RENAL TUBULAR NECROSIS ( 28 FDA reports)
SCAR ( 28 FDA reports)
SKIN INFECTION ( 28 FDA reports)
SUBILEUS ( 28 FDA reports)
TUMOUR MARKER INCREASED ( 28 FDA reports)
VENTRICULAR HYPOKINESIA ( 28 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 28 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 27 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 27 FDA reports)
BRAIN NEOPLASM ( 27 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 27 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 27 FDA reports)
CONJUNCTIVITIS ( 27 FDA reports)
CYSTITIS HAEMORRHAGIC ( 27 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 27 FDA reports)
EXCORIATION ( 27 FDA reports)
HAEMOLYSIS ( 27 FDA reports)
HYPERCALCAEMIA ( 27 FDA reports)
HYPERTHERMIA ( 27 FDA reports)
HYPOPYON ( 27 FDA reports)
JAW OPERATION ( 27 FDA reports)
PERIPHERAL COLDNESS ( 27 FDA reports)
PHARYNGITIS ( 27 FDA reports)
PROTEIN TOTAL DECREASED ( 27 FDA reports)
RETINAL TEAR ( 27 FDA reports)
RHINORRHOEA ( 27 FDA reports)
SENSORY DISTURBANCE ( 27 FDA reports)
STREPTOCOCCAL INFECTION ( 27 FDA reports)
TINNITUS ( 27 FDA reports)
URINE OUTPUT DECREASED ( 27 FDA reports)
ANGINA UNSTABLE ( 26 FDA reports)
ANGIOEDEMA ( 26 FDA reports)
ANGIOPATHY ( 26 FDA reports)
BLISTER ( 26 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 26 FDA reports)
CHOLECYSTITIS ACUTE ( 26 FDA reports)
COLORECTAL CANCER ( 26 FDA reports)
DILATATION VENTRICULAR ( 26 FDA reports)
DUODENITIS ( 26 FDA reports)
ECZEMA ( 26 FDA reports)
EDENTULOUS ( 26 FDA reports)
ENTEROCOCCAL INFECTION ( 26 FDA reports)
FLUID RETENTION ( 26 FDA reports)
HUMERUS FRACTURE ( 26 FDA reports)
ILEUS PARALYTIC ( 26 FDA reports)
MACULAR HOLE ( 26 FDA reports)
MICTURITION URGENCY ( 26 FDA reports)
NEUROGENIC BLADDER ( 26 FDA reports)
ONYCHOMYCOSIS ( 26 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 26 FDA reports)
RESTLESSNESS ( 26 FDA reports)
TUMOUR NECROSIS ( 26 FDA reports)
AGEUSIA ( 25 FDA reports)
BREAST CANCER RECURRENT ( 25 FDA reports)
CARDIAC FAILURE ACUTE ( 25 FDA reports)
COORDINATION ABNORMAL ( 25 FDA reports)
GINGIVAL ULCERATION ( 25 FDA reports)
HEART RATE DECREASED ( 25 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 25 FDA reports)
MEDICATION ERROR ( 25 FDA reports)
ORTHOSTATIC HYPOTENSION ( 25 FDA reports)
PARAESTHESIA ORAL ( 25 FDA reports)
POLYCYTHAEMIA ( 25 FDA reports)
REFLUX OESOPHAGITIS ( 25 FDA reports)
RETCHING ( 25 FDA reports)
ROAD TRAFFIC ACCIDENT ( 25 FDA reports)
STRESS ( 25 FDA reports)
VENA CAVA THROMBOSIS ( 25 FDA reports)
APHONIA ( 24 FDA reports)
CARDIAC TAMPONADE ( 24 FDA reports)
CERUMEN IMPACTION ( 24 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 24 FDA reports)
DIALYSIS ( 24 FDA reports)
EXOSTOSIS ( 24 FDA reports)
EYELID PTOSIS ( 24 FDA reports)
FACIAL PAIN ( 24 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 24 FDA reports)
FLATULENCE ( 24 FDA reports)
HAEMATOCRIT INCREASED ( 24 FDA reports)
LUNG ABSCESS ( 24 FDA reports)
NO THERAPEUTIC RESPONSE ( 24 FDA reports)
OBESITY ( 24 FDA reports)
OESOPHAGEAL STENOSIS ( 24 FDA reports)
PARTIAL SEIZURES ( 24 FDA reports)
PROTEIN URINE ( 24 FDA reports)
SKIN DISCOLOURATION ( 24 FDA reports)
SKIN LACERATION ( 24 FDA reports)
SKIN TOXICITY ( 24 FDA reports)
SQUAMOUS CELL CARCINOMA ( 24 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 24 FDA reports)
ACUTE PULMONARY OEDEMA ( 23 FDA reports)
APHTHOUS STOMATITIS ( 23 FDA reports)
BREAST CALCIFICATIONS ( 23 FDA reports)
CAROTID BRUIT ( 23 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 23 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 23 FDA reports)
CORONARY ARTERY OCCLUSION ( 23 FDA reports)
CORONARY ARTERY STENOSIS ( 23 FDA reports)
FEELING COLD ( 23 FDA reports)
GASTRIC HAEMORRHAGE ( 23 FDA reports)
GENERALISED OEDEMA ( 23 FDA reports)
INJECTION SITE PAIN ( 23 FDA reports)
KERATITIS ( 23 FDA reports)
LABORATORY TEST ABNORMAL ( 23 FDA reports)
MELANOCYTIC NAEVUS ( 23 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 23 FDA reports)
OVARIAN CYST ( 23 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 23 FDA reports)
PERIRECTAL ABSCESS ( 23 FDA reports)
PNEUMOPERITONEUM ( 23 FDA reports)
SEBORRHOEIC KERATOSIS ( 23 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
TESTICULAR PAIN ( 23 FDA reports)
VAGINAL INFECTION ( 23 FDA reports)
VENTRICULAR DYSFUNCTION ( 23 FDA reports)
ARTERIAL HAEMORRHAGE ( 22 FDA reports)
ASTHMA ( 22 FDA reports)
BLADDER DISORDER ( 22 FDA reports)
BLOOD AMYLASE INCREASED ( 22 FDA reports)
BREATH ODOUR ( 22 FDA reports)
CANDIDA TEST POSITIVE ( 22 FDA reports)
CLOSTRIDIAL INFECTION ( 22 FDA reports)
EAR CONGESTION ( 22 FDA reports)
EXTREMITY NECROSIS ( 22 FDA reports)
HEMIPLEGIA ( 22 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 22 FDA reports)
LYMPHOMA ( 22 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 22 FDA reports)
NODULE ( 22 FDA reports)
ONYCHOLYSIS ( 22 FDA reports)
OSTEOCHONDROSIS ( 22 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 22 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 22 FDA reports)
RASH PUSTULAR ( 22 FDA reports)
RETINAL ARTERY OCCLUSION ( 22 FDA reports)
SCOLIOSIS ( 22 FDA reports)
SOFT TISSUE DISORDER ( 22 FDA reports)
THROMBOPHLEBITIS ( 22 FDA reports)
WOUND SECRETION ( 22 FDA reports)
ANASTOMOTIC COMPLICATION ( 21 FDA reports)
BLOOD MAGNESIUM DECREASED ( 21 FDA reports)
BONE CYST ( 21 FDA reports)
BONE NEOPLASM MALIGNANT ( 21 FDA reports)
DERMATITIS EXFOLIATIVE ( 21 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 21 FDA reports)
GALLBLADDER DISORDER ( 21 FDA reports)
HAEMOTHORAX ( 21 FDA reports)
IRRITABLE BOWEL SYNDROME ( 21 FDA reports)
JAUNDICE CHOLESTATIC ( 21 FDA reports)
LARGE INTESTINAL ULCER ( 21 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
LUNG ADENOCARCINOMA ( 21 FDA reports)
LUNG CANCER METASTATIC ( 21 FDA reports)
MENTAL IMPAIRMENT ( 21 FDA reports)
METASTASES TO THORAX ( 21 FDA reports)
MYOPATHY ( 21 FDA reports)
NASAL DISORDER ( 21 FDA reports)
OROANTRAL FISTULA ( 21 FDA reports)
PHARYNGEAL OEDEMA ( 21 FDA reports)
PLEURISY ( 21 FDA reports)
PRODUCT COUNTERFEIT ( 21 FDA reports)
PSEUDOMONAS INFECTION ( 21 FDA reports)
PULMONARY THROMBOSIS ( 21 FDA reports)
SEROMA ( 21 FDA reports)
TORSADE DE POINTES ( 21 FDA reports)
VASCULAR ANOMALY ( 21 FDA reports)
ACIDOSIS ( 20 FDA reports)
AGRANULOCYTOSIS ( 20 FDA reports)
ANKLE FRACTURE ( 20 FDA reports)
ATRIAL FLUTTER ( 20 FDA reports)
BLOOD BICARBONATE DECREASED ( 20 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 20 FDA reports)
CARDIOGENIC SHOCK ( 20 FDA reports)
DYSTHYMIC DISORDER ( 20 FDA reports)
ENCEPHALOMALACIA ( 20 FDA reports)
FAECES DISCOLOURED ( 20 FDA reports)
FIBROADENOMA OF BREAST ( 20 FDA reports)
FOOT FRACTURE ( 20 FDA reports)
GINGIVAL DISORDER ( 20 FDA reports)
IMMUNOSUPPRESSION ( 20 FDA reports)
INGROWING NAIL ( 20 FDA reports)
INTESTINAL DILATATION ( 20 FDA reports)
KLEBSIELLA INFECTION ( 20 FDA reports)
LEFT ATRIAL DILATATION ( 20 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 20 FDA reports)
MAMMOGRAM ABNORMAL ( 20 FDA reports)
METASTASES TO SKIN ( 20 FDA reports)
MITRAL VALVE CALCIFICATION ( 20 FDA reports)
MOVEMENT DISORDER ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
PORTAL VEIN THROMBOSIS ( 20 FDA reports)
PROCEDURAL COMPLICATION ( 20 FDA reports)
TONGUE ULCERATION ( 20 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 20 FDA reports)
TROPONIN INCREASED ( 20 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 20 FDA reports)
WOUND COMPLICATION ( 20 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 20 FDA reports)
ABSCESS INTESTINAL ( 19 FDA reports)
ACUTE PRERENAL FAILURE ( 19 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 19 FDA reports)
BLINDNESS TRANSIENT ( 19 FDA reports)
BODY TEMPERATURE DECREASED ( 19 FDA reports)
DERMAL CYST ( 19 FDA reports)
ECCHYMOSIS ( 19 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 19 FDA reports)
EMBOLISM VENOUS ( 19 FDA reports)
EYE PRURITUS ( 19 FDA reports)
EYELID OEDEMA ( 19 FDA reports)
FOLLICULITIS ( 19 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 19 FDA reports)
GINGIVAL RECESSION ( 19 FDA reports)
HAEMORRHAGIC STROKE ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
HIGH FREQUENCY ABLATION ( 19 FDA reports)
LARYNGOSPASM ( 19 FDA reports)
MUSCLE TWITCHING ( 19 FDA reports)
OSTEOMYELITIS CHRONIC ( 19 FDA reports)
OTITIS MEDIA ( 19 FDA reports)
OVERDOSE ( 19 FDA reports)
PARALYSIS ( 19 FDA reports)
PERIPHERAL ISCHAEMIA ( 19 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 19 FDA reports)
PULMONARY INFARCTION ( 19 FDA reports)
PURULENCE ( 19 FDA reports)
PYOTHORAX ( 19 FDA reports)
SKIN PAPILLOMA ( 19 FDA reports)
STATUS EPILEPTICUS ( 19 FDA reports)
SWOLLEN TONGUE ( 19 FDA reports)
THYROID NEOPLASM ( 19 FDA reports)
TROPONIN I INCREASED ( 19 FDA reports)
UTERINE LEIOMYOMA ( 19 FDA reports)
VENOUS THROMBOSIS LIMB ( 19 FDA reports)
VENTRICULAR HYPERTROPHY ( 19 FDA reports)
VIRAL INFECTION ( 19 FDA reports)
ABDOMINAL ADHESIONS ( 18 FDA reports)
ABDOMINAL SEPSIS ( 18 FDA reports)
ADJUSTMENT DISORDER ( 18 FDA reports)
BLOOD DISORDER ( 18 FDA reports)
BLOOD UREA DECREASED ( 18 FDA reports)
CAPILLARY LEAK SYNDROME ( 18 FDA reports)
CERVICAL DYSPLASIA ( 18 FDA reports)
CYTOLYTIC HEPATITIS ( 18 FDA reports)
DIVERTICULUM INTESTINAL ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
GASTROINTESTINAL OEDEMA ( 18 FDA reports)
HEART RATE IRREGULAR ( 18 FDA reports)
HYDROPNEUMOTHORAX ( 18 FDA reports)
HYPOVOLAEMIC SHOCK ( 18 FDA reports)
ILEITIS ( 18 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 18 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 18 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 18 FDA reports)
MENINGISM ( 18 FDA reports)
MENORRHAGIA ( 18 FDA reports)
MYELODYSPLASTIC SYNDROME ( 18 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 18 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 18 FDA reports)
ORAL CAVITY FISTULA ( 18 FDA reports)
PARKINSON'S DISEASE ( 18 FDA reports)
PARONYCHIA ( 18 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 18 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 18 FDA reports)
SCOTOMA ( 18 FDA reports)
SINUS HEADACHE ( 18 FDA reports)
THROMBOSIS IN DEVICE ( 18 FDA reports)
TRISMUS ( 18 FDA reports)
APLASIA ( 17 FDA reports)
APPENDICITIS ( 17 FDA reports)
AZOTAEMIA ( 17 FDA reports)
BILE DUCT STONE ( 17 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 17 FDA reports)
BURNING SENSATION ( 17 FDA reports)
CALCINOSIS ( 17 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 17 FDA reports)
DEMENTIA ( 17 FDA reports)
ENTEROVESICAL FISTULA ( 17 FDA reports)
EOSINOPHIL COUNT INCREASED ( 17 FDA reports)
FACIAL PALSY ( 17 FDA reports)
FLUID INTAKE REDUCED ( 17 FDA reports)
FLUID OVERLOAD ( 17 FDA reports)
GALLBLADDER PERFORATION ( 17 FDA reports)
GASTROENTERITIS VIRAL ( 17 FDA reports)
HAND FRACTURE ( 17 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 17 FDA reports)
INTESTINAL FISTULA ( 17 FDA reports)
LACERATION ( 17 FDA reports)
LARYNGEAL OEDEMA ( 17 FDA reports)
LEFT VENTRICULAR FAILURE ( 17 FDA reports)
LIBIDO DECREASED ( 17 FDA reports)
LOCALISED INFECTION ( 17 FDA reports)
MUSCLE STRAIN ( 17 FDA reports)
NAIL DISORDER ( 17 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 17 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 17 FDA reports)
OPTIC ATROPHY ( 17 FDA reports)
OTITIS EXTERNA ( 17 FDA reports)
PHYSICAL DISABILITY ( 17 FDA reports)
PSYCHOTIC DISORDER ( 17 FDA reports)
PURPURA ( 17 FDA reports)
RASH GENERALISED ( 17 FDA reports)
SCLERODERMA ( 17 FDA reports)
SERUM FERRITIN INCREASED ( 17 FDA reports)
TACHYARRHYTHMIA ( 17 FDA reports)
TENDONITIS ( 17 FDA reports)
TUMOUR PERFORATION ( 17 FDA reports)
URETERIC OBSTRUCTION ( 17 FDA reports)
VARICOSE VEIN ( 17 FDA reports)
VITREOUS DETACHMENT ( 17 FDA reports)
ACTINIC KERATOSIS ( 16 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 16 FDA reports)
ANASTOMOTIC LEAK ( 16 FDA reports)
ANEURYSM ( 16 FDA reports)
APPENDICITIS PERFORATED ( 16 FDA reports)
BASAL CELL CARCINOMA ( 16 FDA reports)
BILE DUCT OBSTRUCTION ( 16 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 16 FDA reports)
BRONCHIAL FISTULA ( 16 FDA reports)
BRUXISM ( 16 FDA reports)
CALCULUS URINARY ( 16 FDA reports)
CHEST X-RAY ABNORMAL ( 16 FDA reports)
CHOLECYSTITIS CHRONIC ( 16 FDA reports)
DRUG ERUPTION ( 16 FDA reports)
DYSLALIA ( 16 FDA reports)
ERUCTATION ( 16 FDA reports)
HAEMANGIOMA ( 16 FDA reports)
HAEMODIALYSIS ( 16 FDA reports)
HAEMORRHAGIC DIATHESIS ( 16 FDA reports)
HAPTOGLOBIN DECREASED ( 16 FDA reports)
HEAD INJURY ( 16 FDA reports)
HEART VALVE INCOMPETENCE ( 16 FDA reports)
HEPATITIS TOXIC ( 16 FDA reports)
INCONTINENCE ( 16 FDA reports)
JOINT INJURY ( 16 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 16 FDA reports)
LACTIC ACIDOSIS ( 16 FDA reports)
LACUNAR INFARCTION ( 16 FDA reports)
MALIGNANT MELANOMA ( 16 FDA reports)
MALOCCLUSION ( 16 FDA reports)
MEDIASTINAL MASS ( 16 FDA reports)
MENISCUS REMOVAL ( 16 FDA reports)
NEURITIS ( 16 FDA reports)
NEUROPATHY ( 16 FDA reports)
PAIN OF SKIN ( 16 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 16 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 16 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 16 FDA reports)
PULMONARY CAVITATION ( 16 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 16 FDA reports)
RADIATION PNEUMONITIS ( 16 FDA reports)
RECURRENT CANCER ( 16 FDA reports)
RETINAL DISORDER ( 16 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 16 FDA reports)
SKIN FISSURES ( 16 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 16 FDA reports)
TEMPERATURE INTOLERANCE ( 16 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 16 FDA reports)
VULVOVAGINAL DRYNESS ( 16 FDA reports)
ABDOMINAL INFECTION ( 15 FDA reports)
ABSCESS ORAL ( 15 FDA reports)
ACUTE SINUSITIS ( 15 FDA reports)
ANEURYSM RUPTURED ( 15 FDA reports)
BILE DUCT STENOSIS ( 15 FDA reports)
BONE OPERATION ( 15 FDA reports)
CAECITIS ( 15 FDA reports)
CATHETER SITE PAIN ( 15 FDA reports)
CENTRAL LINE INFECTION ( 15 FDA reports)
CEREBRAL DISORDER ( 15 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 15 FDA reports)
CROHN'S DISEASE ( 15 FDA reports)
DECREASED ACTIVITY ( 15 FDA reports)
DENTAL CARE ( 15 FDA reports)
DIZZINESS POSTURAL ( 15 FDA reports)
DYSAESTHESIA ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
FEMUR FRACTURE ( 15 FDA reports)
GANGRENE ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
HYPOKINESIA ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 15 FDA reports)
JOINT STIFFNESS ( 15 FDA reports)
KNEE OPERATION ( 15 FDA reports)
LIPOMA ( 15 FDA reports)
LYMPHANGITIS ( 15 FDA reports)
MYDRIASIS ( 15 FDA reports)
NEUROLOGICAL SYMPTOM ( 15 FDA reports)
NO ADVERSE EVENT ( 15 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 15 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 15 FDA reports)
ORAL HERPES ( 15 FDA reports)
PANCREATIC CARCINOMA ( 15 FDA reports)
PCO2 DECREASED ( 15 FDA reports)
PHOTOSENSITIVITY REACTION ( 15 FDA reports)
POLYMYOSITIS ( 15 FDA reports)
RADIOTHERAPY ( 15 FDA reports)
RHINITIS ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
SMALL INTESTINE ULCER ( 15 FDA reports)
SPINAL FRACTURE ( 15 FDA reports)
SPLENIC INFARCTION ( 15 FDA reports)
SUDDEN CARDIAC DEATH ( 15 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 15 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 15 FDA reports)
WOUND ( 15 FDA reports)
ABDOMINAL MASS ( 14 FDA reports)
AMENORRHOEA ( 14 FDA reports)
ANIMAL BITE ( 14 FDA reports)
ANION GAP INCREASED ( 14 FDA reports)
BACTERIAL TEST POSITIVE ( 14 FDA reports)
BILE DUCT CANCER ( 14 FDA reports)
BIOPSY BONE ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 14 FDA reports)
CATHETER SITE INFECTION ( 14 FDA reports)
CHROMATURIA ( 14 FDA reports)
COLONIC STENOSIS ( 14 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 14 FDA reports)
EFFUSION ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 14 FDA reports)
FAECAL INCONTINENCE ( 14 FDA reports)
FEMORAL NECK FRACTURE ( 14 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 14 FDA reports)
GASTRIC DISORDER ( 14 FDA reports)
GASTROINTESTINAL FISTULA ( 14 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 14 FDA reports)
GASTROINTESTINAL ULCER ( 14 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 14 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 14 FDA reports)
INFARCTION ( 14 FDA reports)
INTESTINAL INFARCTION ( 14 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 14 FDA reports)
LIVER INJURY ( 14 FDA reports)
MAJOR DEPRESSION ( 14 FDA reports)
MALIGNANT HYPERTENSION ( 14 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 14 FDA reports)
MONOCYTE COUNT DECREASED ( 14 FDA reports)
MUCOUS MEMBRANE DISORDER ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
PRESYNCOPE ( 14 FDA reports)
PROSTATE CANCER ( 14 FDA reports)
RENAL ATROPHY ( 14 FDA reports)
RETINAL OEDEMA ( 14 FDA reports)
RETINAL VEIN OCCLUSION ( 14 FDA reports)
SPLENIC RUPTURE ( 14 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 14 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 14 FDA reports)
THYROID CYST ( 14 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 14 FDA reports)
UROSEPSIS ( 14 FDA reports)
UTERINE HAEMORRHAGE ( 14 FDA reports)
VERTEBROPLASTY ( 14 FDA reports)
WRIST FRACTURE ( 14 FDA reports)
ABDOMINAL WALL ABSCESS ( 13 FDA reports)
ABSCESS JAW ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ACNE ( 13 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 13 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 13 FDA reports)
ADVERSE DRUG REACTION ( 13 FDA reports)
AORTIC DILATATION ( 13 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 13 FDA reports)
BLADDER PERFORATION ( 13 FDA reports)
BLOOD CHLORIDE INCREASED ( 13 FDA reports)
BREAST PAIN ( 13 FDA reports)
CEREBELLAR INFARCTION ( 13 FDA reports)
CEREBRAL HAEMATOMA ( 13 FDA reports)
CLOSTRIDIUM COLITIS ( 13 FDA reports)
COLITIS ULCERATIVE ( 13 FDA reports)
DIABETIC KETOACIDOSIS ( 13 FDA reports)
DRUG EFFECT DECREASED ( 13 FDA reports)
DYSCHEZIA ( 13 FDA reports)
ENCEPHALITIS ( 13 FDA reports)
FRACTURE ( 13 FDA reports)
GINGIVAL EROSION ( 13 FDA reports)
GOITRE ( 13 FDA reports)
HAEMOGLOBIN INCREASED ( 13 FDA reports)
ILEAL FISTULA ( 13 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 13 FDA reports)
INTRACARDIAC THROMBUS ( 13 FDA reports)
METAMORPHOPSIA ( 13 FDA reports)
MYOPIA ( 13 FDA reports)
NASAL MUCOSAL DISORDER ( 13 FDA reports)
NEPHROPATHY TOXIC ( 13 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 13 FDA reports)
NON-CARDIAC CHEST PAIN ( 13 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 13 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 13 FDA reports)
PANCREATIC ENZYMES INCREASED ( 13 FDA reports)
PANCREATIC NEOPLASM ( 13 FDA reports)
PANIC ATTACK ( 13 FDA reports)
PELVIC PAIN ( 13 FDA reports)
PERIANAL ABSCESS ( 13 FDA reports)
PORCELAIN GALLBLADDER ( 13 FDA reports)
POSTURE ABNORMAL ( 13 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 13 FDA reports)
PULMONARY MASS ( 13 FDA reports)
RADIATION MUCOSITIS ( 13 FDA reports)
RESPIRATORY TRACT INFECTION ( 13 FDA reports)
SINUS CONGESTION ( 13 FDA reports)
SPUTUM CULTURE POSITIVE ( 13 FDA reports)
STENT OCCLUSION ( 13 FDA reports)
STUPOR ( 13 FDA reports)
SUBRETINAL FIBROSIS ( 13 FDA reports)
TACHYPNOEA ( 13 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 13 FDA reports)
VISUAL FIELD DEFECT ( 13 FDA reports)
ACETABULUM FRACTURE ( 12 FDA reports)
ACUTE HEPATIC FAILURE ( 12 FDA reports)
ANAL HAEMORRHAGE ( 12 FDA reports)
ANASTOMOTIC ULCER ( 12 FDA reports)
ANGER ( 12 FDA reports)
AORTIC ANEURYSM RUPTURE ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
AXILLARY MASS ( 12 FDA reports)
BEDRIDDEN ( 12 FDA reports)
BLOOD ALBUMIN INCREASED ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BLOOD SODIUM INCREASED ( 12 FDA reports)
BONE TRIMMING ( 12 FDA reports)
CATHETER SITE DISCHARGE ( 12 FDA reports)
COLD SWEAT ( 12 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 12 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
ERYTHROSIS ( 12 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
GASTRITIS HAEMORRHAGIC ( 12 FDA reports)
GASTROENTERITIS RADIATION ( 12 FDA reports)
GLIOSIS ( 12 FDA reports)
GLOMERULONEPHRITIS ( 12 FDA reports)
GLOSSITIS ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
GROIN ABSCESS ( 12 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 12 FDA reports)
HALLUCINATION, VISUAL ( 12 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 12 FDA reports)
HYPERCOAGULATION ( 12 FDA reports)
HYPERTHYROIDISM ( 12 FDA reports)
HYPOCOAGULABLE STATE ( 12 FDA reports)
HYPOREFLEXIA ( 12 FDA reports)
INTERMITTENT CLAUDICATION ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 12 FDA reports)
LIFE EXPECTANCY SHORTENED ( 12 FDA reports)
LUNG HYPERINFLATION ( 12 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 12 FDA reports)
MALLORY-WEISS SYNDROME ( 12 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 12 FDA reports)
MENOPAUSE ( 12 FDA reports)
METASTASES TO HEART ( 12 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 12 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 12 FDA reports)
OESOPHAGITIS ULCERATIVE ( 12 FDA reports)
ONYCHOMADESIS ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
ORAL DISCOMFORT ( 12 FDA reports)
OSTEOMYELITIS ACUTE ( 12 FDA reports)
PERINEAL ABSCESS ( 12 FDA reports)
PERIODONTAL INFECTION ( 12 FDA reports)
PIGMENTATION DISORDER ( 12 FDA reports)
POLYMYALGIA RHEUMATICA ( 12 FDA reports)
PRURITUS GENERALISED ( 12 FDA reports)
RADICULITIS BRACHIAL ( 12 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 12 FDA reports)
RETINAL SCAR ( 12 FDA reports)
SCIATICA ( 12 FDA reports)
SCROTAL OEDEMA ( 12 FDA reports)
SEASONAL ALLERGY ( 12 FDA reports)
SNEEZING ( 12 FDA reports)
TOOTH REPAIR ( 12 FDA reports)
VARICELLA ( 12 FDA reports)
VENTRICULAR ARRHYTHMIA ( 12 FDA reports)
ACUTE ABDOMEN ( 11 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 11 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 11 FDA reports)
ALVEOLITIS ( 11 FDA reports)
ANURIA ( 11 FDA reports)
AORTIC THROMBOSIS ( 11 FDA reports)
APPETITE DISORDER ( 11 FDA reports)
ARTERIAL RUPTURE ( 11 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 11 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 11 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BRAIN INJURY ( 11 FDA reports)
BRONCHOPNEUMONIA ( 11 FDA reports)
CATHETER SITE ERYTHEMA ( 11 FDA reports)
CATHETER SITE HAEMATOMA ( 11 FDA reports)
DEFAECATION URGENCY ( 11 FDA reports)
DEMYELINATION ( 11 FDA reports)
DYSLIPIDAEMIA ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 11 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 11 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
EROSIVE DUODENITIS ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
FUNGAL SEPSIS ( 11 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 11 FDA reports)
GINGIVAL ERYTHEMA ( 11 FDA reports)
HAEMORRHAGIC ASCITES ( 11 FDA reports)
HEPATIC NEOPLASM ( 11 FDA reports)
HEPATOCELLULAR INJURY ( 11 FDA reports)
HYPERSOMNIA ( 11 FDA reports)
HYPERTENSIVE EMERGENCY ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
HYPOTHERMIA ( 11 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 11 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 11 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 11 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 11 FDA reports)
LOSS OF PROPRIOCEPTION ( 11 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 11 FDA reports)
METASTASES TO ADRENALS ( 11 FDA reports)
METASTASES TO SOFT TISSUE ( 11 FDA reports)
MYOCLONUS ( 11 FDA reports)
NASAL SEPTUM DEVIATION ( 11 FDA reports)
NEUTROPENIC INFECTION ( 11 FDA reports)
NOSOCOMIAL INFECTION ( 11 FDA reports)
OBSTRUCTION ( 11 FDA reports)
OCULAR VASCULAR DISORDER ( 11 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 11 FDA reports)
OMENTUM NEOPLASM ( 11 FDA reports)
OPEN REDUCTION OF FRACTURE ( 11 FDA reports)
ORTHOPNOEA ( 11 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 11 FDA reports)
PERICARDIAL DRAINAGE ( 11 FDA reports)
PEYRONIE'S DISEASE ( 11 FDA reports)
PLEURAL FIBROSIS ( 11 FDA reports)
PLEURECTOMY ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 11 FDA reports)
POLYP ( 11 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 11 FDA reports)
PULMONARY TOXICITY ( 11 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
RASH MACULAR ( 11 FDA reports)
RECTAL CANCER ( 11 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 11 FDA reports)
RENAL CANCER ( 11 FDA reports)
RENAL CANCER METASTATIC ( 11 FDA reports)
RESUSCITATION ( 11 FDA reports)
RETROPERITONEAL ABSCESS ( 11 FDA reports)
SALIVARY GLAND MASS ( 11 FDA reports)
SPLENIC CYST ( 11 FDA reports)
STRIDOR ( 11 FDA reports)
TUMOUR PAIN ( 11 FDA reports)
ULCER HAEMORRHAGE ( 11 FDA reports)
VASCULAR CALCIFICATION ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 11 FDA reports)
ABSCESS NECK ( 10 FDA reports)
AMMONIA INCREASED ( 10 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 10 FDA reports)
ATRIAL THROMBOSIS ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 10 FDA reports)
BLOOD TEST ABNORMAL ( 10 FDA reports)
BRAIN MASS ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
CEREBROVASCULAR DISORDER ( 10 FDA reports)
CERVICAL SPINAL STENOSIS ( 10 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 10 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
CONTRAST MEDIA ALLERGY ( 10 FDA reports)
CRANIAL NERVE DISORDER ( 10 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 10 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 10 FDA reports)
CULTURE WOUND POSITIVE ( 10 FDA reports)
CYST ASPIRATION ( 10 FDA reports)
DENTAL PLAQUE ( 10 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 10 FDA reports)
DYSTONIA ( 10 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
ENDOTRACHEAL INTUBATION ( 10 FDA reports)
EPICONDYLITIS ( 10 FDA reports)
EROSIVE OESOPHAGITIS ( 10 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 10 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 10 FDA reports)
EYE INJURY ( 10 FDA reports)
FACIAL PARESIS ( 10 FDA reports)
FIBROSIS ( 10 FDA reports)
FUNGAL OESOPHAGITIS ( 10 FDA reports)
GASTRIC VARICES ( 10 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 10 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 10 FDA reports)
GOUT ( 10 FDA reports)
GRANULOCYTE COUNT DECREASED ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HEPATIC PAIN ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HOSPITALISATION ( 10 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 10 FDA reports)
HYPERKERATOSIS ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
HYPERTRANSAMINASAEMIA ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
MACROPHAGES INCREASED ( 10 FDA reports)
MACULE ( 10 FDA reports)
MAXILLOFACIAL OPERATION ( 10 FDA reports)
MEAN CELL VOLUME INCREASED ( 10 FDA reports)
MENISCAL DEGENERATION ( 10 FDA reports)
METASTASES TO CHEST WALL ( 10 FDA reports)
METASTASES TO PLEURA ( 10 FDA reports)
MICROANGIOPATHY ( 10 FDA reports)
MITRAL VALVE PROLAPSE ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
OESOPHAGEAL PAIN ( 10 FDA reports)
ORAL SOFT TISSUE DISORDER ( 10 FDA reports)
OTITIS MEDIA ACUTE ( 10 FDA reports)
OVARIAN MASS ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PANCREATITIS CHRONIC ( 10 FDA reports)
PERIODONTAL OPERATION ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PLEURITIC PAIN ( 10 FDA reports)
POSTOPERATIVE INFECTION ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
PROCEDURAL SITE REACTION ( 10 FDA reports)
PULMONARY HILUM MASS ( 10 FDA reports)
PULPITIS DENTAL ( 10 FDA reports)
PYELONEPHRITIS ( 10 FDA reports)
RADIATION INJURY ( 10 FDA reports)
RADIATION OESOPHAGITIS ( 10 FDA reports)
RADICULAR SYNDROME ( 10 FDA reports)
RASH MACULO-PAPULAR ( 10 FDA reports)
RASH PAPULAR ( 10 FDA reports)
RECTAL CANCER METASTATIC ( 10 FDA reports)
RETINAL ISCHAEMIA ( 10 FDA reports)
RETINAL VASCULAR DISORDER ( 10 FDA reports)
RETINOPATHY HYPERTENSIVE ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
SCLERODERMA RENAL CRISIS ( 10 FDA reports)
SENSORY LOSS ( 10 FDA reports)
SHORT-BOWEL SYNDROME ( 10 FDA reports)
SPINAL CLAUDICATION ( 10 FDA reports)
SPLENIC GRANULOMA ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
STENT PLACEMENT ( 10 FDA reports)
SUTURE RUPTURE ( 10 FDA reports)
SYNOVITIS ( 10 FDA reports)
THERAPY REGIMEN CHANGED ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
TOXIC ENCEPHALOPATHY ( 10 FDA reports)
TOXIC SKIN ERUPTION ( 10 FDA reports)
URINE ANALYSIS ABNORMAL ( 10 FDA reports)
URINE KETONE BODY PRESENT ( 10 FDA reports)
VENOUS OCCLUSION ( 10 FDA reports)
VITRECTOMY ( 10 FDA reports)
WOUND NECROSIS ( 10 FDA reports)
ABDOMINAL RIGIDITY ( 9 FDA reports)
ACANTHOLYSIS ( 9 FDA reports)
ADRENAL DISORDER ( 9 FDA reports)
ADVERSE REACTION ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ALVEOLOPLASTY ( 9 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 9 FDA reports)
ANAL ULCER ( 9 FDA reports)
ARTIFICIAL MENOPAUSE ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 9 FDA reports)
ASTHENOPIA ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 9 FDA reports)
BACTERIA URINE IDENTIFIED ( 9 FDA reports)
BACTERIAL SEPSIS ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
BRONCHITIS VIRAL ( 9 FDA reports)
CARDIAC DEATH ( 9 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DELUSION ( 9 FDA reports)
DENTAL FISTULA ( 9 FDA reports)
DIASTOLIC DYSFUNCTION ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 9 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 9 FDA reports)
FOREIGN BODY ( 9 FDA reports)
FORMICATION ( 9 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HYPERAESTHESIA ( 9 FDA reports)
HYPERMAGNESAEMIA ( 9 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 9 FDA reports)
INCISIONAL HERNIA ( 9 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 9 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
INJECTION SITE INFECTION ( 9 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 9 FDA reports)
JEJUNAL PERFORATION ( 9 FDA reports)
LIGAMENT SPRAIN ( 9 FDA reports)
LIP BLISTER ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MACULAR ISCHAEMIA ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
METASTASES TO ABDOMINAL WALL ( 9 FDA reports)
METASTASES TO SPLEEN ( 9 FDA reports)
MONONEURITIS ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
MUCOSAL HAEMORRHAGE ( 9 FDA reports)
NECROTISING COLITIS ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
NIPPLE PAIN ( 9 FDA reports)
OPTIC NERVE DISORDER ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
PERINEURIAL CYST ( 9 FDA reports)
PERIORBITAL OEDEMA ( 9 FDA reports)
PHARYNGEAL ERYTHEMA ( 9 FDA reports)
PHLEBOLITH ( 9 FDA reports)
PNEUMOMEDIASTINUM ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POST PROCEDURAL BILE LEAK ( 9 FDA reports)
PRESBYOPIA ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 9 FDA reports)
QRS AXIS ABNORMAL ( 9 FDA reports)
RADICAL MASTECTOMY ( 9 FDA reports)
RADICULITIS ( 9 FDA reports)
RECTAL ABSCESS ( 9 FDA reports)
RENAL HAEMORRHAGE ( 9 FDA reports)
RENAL SALT-WASTING SYNDROME ( 9 FDA reports)
SKIN CHAPPED ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SOFT TISSUE NECROSIS ( 9 FDA reports)
THERMAL BURN ( 9 FDA reports)
TONGUE OEDEMA ( 9 FDA reports)
TONGUE PARALYSIS ( 9 FDA reports)
TOOTH DEPOSIT ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
URINARY TRACT OBSTRUCTION ( 9 FDA reports)
VITREOUS DISORDER ( 9 FDA reports)
VITREOUS OPACITIES ( 9 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 9 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ADHESION ( 8 FDA reports)
ADNEXA UTERI MASS ( 8 FDA reports)
ALVEOLITIS ALLERGIC ( 8 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 8 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 8 FDA reports)
BACK INJURY ( 8 FDA reports)
BACTEROIDES INFECTION ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BLOOD CREATININE DECREASED ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 8 FDA reports)
BONE GRAFT ( 8 FDA reports)
BREAST MASS ( 8 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 8 FDA reports)
CALCULUS URETERIC ( 8 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CATHETER SITE HAEMORRHAGE ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
CHOLANGITIS SCLEROSING ( 8 FDA reports)
CHOLECYSTITIS INFECTIVE ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DUODENAL STENOSIS ( 8 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 8 FDA reports)
EAR INFECTION ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
ESSENTIAL HYPERTENSION ( 8 FDA reports)
EXTRAVASATION OF URINE ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
GASTRIC CANCER ( 8 FDA reports)
GASTRITIS EROSIVE ( 8 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HEPATIC ARTERY OCCLUSION ( 8 FDA reports)
HEPATIC HAEMORRHAGE ( 8 FDA reports)
HERNIA ( 8 FDA reports)
HIP ARTHROPLASTY ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
IATROGENIC INJURY ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
INJECTION SITE EXTRAVASATION ( 8 FDA reports)
INTESTINAL STOMA SITE BLEEDING ( 8 FDA reports)
INTRACRANIAL ANEURYSM ( 8 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 8 FDA reports)
JOINT SPRAIN ( 8 FDA reports)
LATEX ALLERGY ( 8 FDA reports)
LIGAMENT RUPTURE ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 8 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 8 FDA reports)
METABOLIC SYNDROME ( 8 FDA reports)
METRORRHAGIA ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
MOTOR DYSFUNCTION ( 8 FDA reports)
MOUTH CYST ( 8 FDA reports)
MUCOSAL ATROPHY ( 8 FDA reports)
MUCOSAL ULCERATION ( 8 FDA reports)
MULTIPLE MYELOMA ( 8 FDA reports)
NEUTROPENIC COLITIS ( 8 FDA reports)
NYSTAGMUS ( 8 FDA reports)
OBSTRUCTION GASTRIC ( 8 FDA reports)
OESOPHAGEAL PERFORATION ( 8 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 8 FDA reports)
OROPHARYNGEAL BLISTERING ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PAINFUL RESPIRATION ( 8 FDA reports)
PALATAL DISORDER ( 8 FDA reports)
PALMAR ERYTHEMA ( 8 FDA reports)
PERICARDIAL DISEASE ( 8 FDA reports)
PERINEAL PAIN ( 8 FDA reports)
PERIPHERAL EMBOLISM ( 8 FDA reports)
PERITONEAL ADHESIONS ( 8 FDA reports)
PITTING OEDEMA ( 8 FDA reports)
PLATELET COUNT ABNORMAL ( 8 FDA reports)
POLYPECTOMY ( 8 FDA reports)
PROCTITIS ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PULMONARY FISTULA ( 8 FDA reports)
RADIATION SKIN INJURY ( 8 FDA reports)
RADICULAR CYST ( 8 FDA reports)
RALES ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 8 FDA reports)
SCAB ( 8 FDA reports)
SEBORRHOEIC DERMATITIS ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SKIN HYPERPIGMENTATION ( 8 FDA reports)
SOFT TISSUE INFECTION ( 8 FDA reports)
SPINAL DISORDER ( 8 FDA reports)
SPLENIC CALCIFICATION ( 8 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 8 FDA reports)
STRESS CARDIOMYOPATHY ( 8 FDA reports)
SUTURE RELATED COMPLICATION ( 8 FDA reports)
TACHYPHYLAXIS ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
THYROXINE FREE DECREASED ( 8 FDA reports)
TRACHEAL FISTULA ( 8 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 8 FDA reports)
ULCERATIVE KERATITIS ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
UTERINE POLYP ( 8 FDA reports)
VASCULAR OCCLUSION ( 8 FDA reports)
VULVOVAGINAL DISCOMFORT ( 8 FDA reports)
WALKING AID USER ( 8 FDA reports)
WHITE BLOOD CELL COUNT ( 8 FDA reports)
WOUND DEBRIDEMENT ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 7 FDA reports)
ANAL INFECTION ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
APNOEA ( 7 FDA reports)
ATROPHY ( 7 FDA reports)
BILIARY DYSKINESIA ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD PRESSURE ABNORMAL ( 7 FDA reports)
BONE EROSION ( 7 FDA reports)
BONE LOSS ( 7 FDA reports)
BRAIN HERNIATION ( 7 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 7 FDA reports)
BREAST OPERATION ( 7 FDA reports)
BREATH SOUNDS ABNORMAL ( 7 FDA reports)
BRONCHIAL OBSTRUCTION ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
CANDIDA SEPSIS ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
CORNEAL ABRASION ( 7 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 7 FDA reports)
CULTURE POSITIVE ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DEVICE FAILURE ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
EATING DISORDER SYMPTOM ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 7 FDA reports)
ESCHERICHIA SEPSIS ( 7 FDA reports)
FISTULA DISCHARGE ( 7 FDA reports)
GASTRIC ULCER PERFORATION ( 7 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 7 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 7 FDA reports)
GASTROSTOMY TUBE INSERTION ( 7 FDA reports)
HEMIANOPIA ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HYDROURETER ( 7 FDA reports)
HYPERCREATININAEMIA ( 7 FDA reports)
HYPOPERFUSION ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
IMMUNODEFICIENCY ( 7 FDA reports)
INCOHERENT ( 7 FDA reports)
INFUSION SITE PAIN ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 7 FDA reports)
INTESTINAL ULCER ( 7 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LIVEDO RETICULARIS ( 7 FDA reports)
LIVER SCAN ABNORMAL ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 7 FDA reports)
MASTOID DISORDER ( 7 FDA reports)
METAPLASIA ( 7 FDA reports)
METASTASES TO EYE ( 7 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 7 FDA reports)
METASTASES TO OVARY ( 7 FDA reports)
METASTASES TO PELVIS ( 7 FDA reports)
MYOCARDITIS ( 7 FDA reports)
MYOSCLEROSIS ( 7 FDA reports)
NAIL TOXICITY ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
NERVE ROOT COMPRESSION ( 7 FDA reports)
OCCULT BLOOD POSITIVE ( 7 FDA reports)
OESOPHAGEAL CARCINOMA ( 7 FDA reports)
OPHTHALMOPLEGIA ( 7 FDA reports)
PANCREATIC CYST ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PARAPLEGIA ( 7 FDA reports)
PELVIC INFECTION ( 7 FDA reports)
PERICARDIAL CALCIFICATION ( 7 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 7 FDA reports)
PNEUMOPERICARDIUM ( 7 FDA reports)
RECTAL OBSTRUCTION ( 7 FDA reports)
REFLUX LARYNGITIS ( 7 FDA reports)
RETINAL DEGENERATION ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
RIGHT ATRIAL DILATATION ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SKIN NODULE ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
TELANGIECTASIA ( 7 FDA reports)
TENOSYNOVITIS STENOSANS ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
TRACHEAL DISORDER ( 7 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 7 FDA reports)
VASCULAR PSEUDOANEURYSM ( 7 FDA reports)
VESICAL FISTULA ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VITH NERVE PARALYSIS ( 7 FDA reports)
VULVITIS ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
ACUTE LUNG INJURY ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
AMYLOIDOSIS ( 6 FDA reports)
ANAL DISCOMFORT ( 6 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
APRAXIA ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
ATRIAL TACHYCARDIA ( 6 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 6 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILIARY FISTULA ( 6 FDA reports)
BLADDER HYPERTROPHY ( 6 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 6 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 6 FDA reports)
BREAST RECONSTRUCTION ( 6 FDA reports)
BULLOUS LUNG DISEASE ( 6 FDA reports)
CAMPYLOBACTER INFECTION ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARBON DIOXIDE DECREASED ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CEREBELLAR HAEMORRHAGE ( 6 FDA reports)
CEREBELLAR SYNDROME ( 6 FDA reports)
CERVICAL ROOT PAIN ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
CHARLES BONNET SYNDROME ( 6 FDA reports)
CHOKING ( 6 FDA reports)
CHOLINERGIC SYNDROME ( 6 FDA reports)
CHOROIDAL DETACHMENT ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
CORNEAL STRIAE ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CORYNEBACTERIUM INFECTION ( 6 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
DYSTROPHIC CALCIFICATION ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 6 FDA reports)
ENTERITIS INFECTIOUS ( 6 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
GRANULOCYTOPENIA ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 6 FDA reports)
HAEMOSIDEROSIS ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEPATIC ATROPHY ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
HYPOCHROMASIA ( 6 FDA reports)
HYPOGEUSIA ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
ICHTHYOSIS ACQUIRED ( 6 FDA reports)
IMMOBILE ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
INTENTION TREMOR ( 6 FDA reports)
KERATOSIS OBTURANS ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
LACTOBACILLUS INFECTION ( 6 FDA reports)
LIMB INJURY ( 6 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 6 FDA reports)
MECHANICAL ILEUS ( 6 FDA reports)
MEDICAL DEVICE REMOVAL ( 6 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
MICTURITION FREQUENCY DECREASED ( 6 FDA reports)
MUCOSAL EXFOLIATION ( 6 FDA reports)
MUSCLE ATROPHY ( 6 FDA reports)
MUSCLE CONTRACTURE ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NASAL ODOUR ( 6 FDA reports)
NEOPLASM SKIN ( 6 FDA reports)
NEPHRECTOMY ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NEUTROPHIL COUNT ( 6 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 6 FDA reports)
OCULAR DISCOMFORT ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
ONYCHOCLASIS ( 6 FDA reports)
OPTIC NEURITIS ( 6 FDA reports)
OVARIAN HAEMORRHAGE ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PARAPSORIASIS ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PATHOGEN RESISTANCE ( 6 FDA reports)
PCO2 INCREASED ( 6 FDA reports)
PELVIC HAEMATOMA ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 6 FDA reports)
PERITONEAL DISORDER ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POST THROMBOTIC SYNDROME ( 6 FDA reports)
POSTOPERATIVE ABSCESS ( 6 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 6 FDA reports)
PRODUCT STERILITY LACKING ( 6 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 6 FDA reports)
PSOAS ABSCESS ( 6 FDA reports)
PULMONARY NECROSIS ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
RENAL INFARCT ( 6 FDA reports)
RENAL TUBULAR ACIDOSIS ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
RESPIRATORY ALKALOSIS ( 6 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
RETINAL ARTERY THROMBOSIS ( 6 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
RETROPERITONEAL FIBROSIS ( 6 FDA reports)
SALIVARY GLAND PAIN ( 6 FDA reports)
SCROTAL INFECTION ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SINUS OPERATION ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 6 FDA reports)
TENDON INJURY ( 6 FDA reports)
THYROID ATROPHY ( 6 FDA reports)
TOBACCO ABUSE ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
URINARY FISTULA ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
VAGINAL FISTULA ( 6 FDA reports)
VAGINAL LACERATION ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VITAMIN B12 INCREASED ( 6 FDA reports)
VITREAL CELLS ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 5 FDA reports)
ACCIDENT ( 5 FDA reports)
ADNEXA UTERI CYST ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 5 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 5 FDA reports)
AORTIC RUPTURE ( 5 FDA reports)
APPENDIX DISORDER ( 5 FDA reports)
ARTERIOENTERIC FISTULA ( 5 FDA reports)
ASCITES INFECTION ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
BACTERIA STOOL IDENTIFIED ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
BONE SWELLING ( 5 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
BREAST CANCER STAGE IV ( 5 FDA reports)
BREAST FIBROMA ( 5 FDA reports)
BREAST NECROSIS ( 5 FDA reports)
BRONCHIAL CARCINOMA ( 5 FDA reports)
BUNDLE BRANCH BLOCK ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CERVICOBRACHIAL SYNDROME ( 5 FDA reports)
CHEST WALL MASS ( 5 FDA reports)
CHEST WALL NECROSIS ( 5 FDA reports)
CHEYNE-STOKES RESPIRATION ( 5 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 5 FDA reports)
CONJUNCTIVAL DISORDER ( 5 FDA reports)
CONJUNCTIVAL IRRITATION ( 5 FDA reports)
CORONARY ARTERY BYPASS ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DENTURE WEARER ( 5 FDA reports)
DEVICE MALFUNCTION ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
EAR HAEMORRHAGE ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
EPISCLERITIS ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
ETHMOID SINUS SURGERY ( 5 FDA reports)
EXERCISE TOLERANCE DECREASED ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
EYE INFECTION BACTERIAL ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
FAECES PALE ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FIBROMA ( 5 FDA reports)
FRONTAL SINUS OPERATION ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GALLBLADDER OBSTRUCTION ( 5 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 5 FDA reports)
GASTRODUODENAL ULCER ( 5 FDA reports)
GASTROINTESTINAL CARCINOMA ( 5 FDA reports)
HAEMORRHAGIC INFARCTION ( 5 FDA reports)
HEMIANOPIA HOMONYMOUS ( 5 FDA reports)
HEPATIC FIBROSIS ( 5 FDA reports)
HEPATIC HAEMATOMA ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HYPERCREATINAEMIA ( 5 FDA reports)
HYPERSPLENISM ( 5 FDA reports)
HYPHAEMA ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
IGA NEPHROPATHY ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJURY ASPHYXIATION ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
INTESTINAL STOMA COMPLICATION ( 5 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LUNG INFILTRATION MALIGNANT ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
METASTATIC PAIN ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYELITIS TRANSVERSE ( 5 FDA reports)
MYELOID LEUKAEMIA ( 5 FDA reports)
NASAL SEPTAL OPERATION ( 5 FDA reports)
NASAL SEPTUM DISORDER ( 5 FDA reports)
NEPHRITIS INTERSTITIAL ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NOCTURIA ( 5 FDA reports)
OEDEMA MUCOSAL ( 5 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 5 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
OSTEOSARCOMA METASTATIC ( 5 FDA reports)
OVARIAN ENLARGEMENT ( 5 FDA reports)
PANCREATIC ATROPHY ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PERFORATED ULCER ( 5 FDA reports)
PERICARDIAL EXCISION ( 5 FDA reports)
PLICATED TONGUE ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POOR PERIPHERAL CIRCULATION ( 5 FDA reports)
POST PROCEDURAL DIARRHOEA ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 5 FDA reports)
REACTIVE PSYCHOSIS ( 5 FDA reports)
RECALL PHENOMENON ( 5 FDA reports)
RECTAL NEOPLASM ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RENAL INJURY ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
RETINAL CYST ( 5 FDA reports)
RETINAL EXUDATES ( 5 FDA reports)
RETINAL MELANOMA ( 5 FDA reports)
SENSE OF OPPRESSION ( 5 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SINUS ANTROSTOMY ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SOFT TISSUE INFLAMMATION ( 5 FDA reports)
SPHENOID SINUS OPERATION ( 5 FDA reports)
SPINAL CORD INFARCTION ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
SPLENIC ARTERY ANEURYSM ( 5 FDA reports)
SPLENIC NECROSIS ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 5 FDA reports)
SURGICAL PROCEDURE REPEATED ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TOOTH DISCOLOURATION ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
VOLVULUS OF SMALL BOWEL ( 5 FDA reports)
WISDOM TEETH REMOVAL ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL WALL DISORDER ( 4 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC DISSECTION RUPTURE ( 4 FDA reports)
AORTIC INJURY ( 4 FDA reports)
AORTO-OESOPHAGEAL FISTULA ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ATROPHY OF GLOBE ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD CREATININE ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE DENSITY ABNORMAL ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN DEATH ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
BRONCHOSCOPY ABNORMAL ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CATHETER SITE OEDEMA ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 4 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 4 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBRAL VASOCONSTRICTION ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHEST INJURY ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHORIORETINAL ATROPHY ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
COLOSTOMY ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 4 FDA reports)
CORNEAL INFILTRATES ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CRYING ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 4 FDA reports)
DENTAL TREATMENT ( 4 FDA reports)
DEPOSIT EYE ( 4 FDA reports)
DERMATOSIS ( 4 FDA reports)
DETACHMENT OF MACULAR RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
DEVICE DAMAGE ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DROWNING ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEBRILE INFECTION ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GAMMA RADIATION THERAPY ( 4 FDA reports)
GASTRIC FISTULA ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
GRIP STRENGTH DECREASED ( 4 FDA reports)
HAEMATOMA INFECTION ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEPATIC CANCER METASTATIC ( 4 FDA reports)
HEPATIC ISCHAEMIA ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERPLASIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
HYPOTONY OF EYE ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCISION SITE ABSCESS ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INFUSION SITE EXTRAVASATION ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
JEJUNAL ULCER ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
KERATITIS INTERSTITIAL ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LEUKODYSTROPHY ( 4 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 4 FDA reports)
LYMPHATIC DISORDER ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
METASTASES TO BLADDER ( 4 FDA reports)
METASTASES TO PANCREAS ( 4 FDA reports)
METASTASES TO SMALL INTESTINE ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
NAIL DYSTROPHY ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
OESOPHAGEAL FISTULA ( 4 FDA reports)
OESOPHAGEAL INFECTION ( 4 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
OVARIAN CANCER METASTATIC ( 4 FDA reports)
OVARIAN TORSION ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 4 FDA reports)
PARAPARESIS ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PCO2 ABNORMAL ( 4 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERCUSSION TEST ABNORMAL ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERINEAL FISTULA ( 4 FDA reports)
PERITONEAL CARCINOMA ( 4 FDA reports)
PINEAL GLAND CYST ( 4 FDA reports)
PLANTAR ERYTHEMA ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PNEUMOCEPHALUS ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 4 FDA reports)
PORTAL VENOUS GAS ( 4 FDA reports)
POUCHITIS ( 4 FDA reports)
PREMATURE DELIVERY ( 4 FDA reports)
PROTEIN TOTAL ABNORMAL ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 4 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 4 FDA reports)
RENAL HYPERTENSION ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RESPIRATORY PARALYSIS ( 4 FDA reports)
RETINAL ANEURYSM ( 4 FDA reports)
RETROPERITONEAL INFECTION ( 4 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCAN ABDOMEN ABNORMAL ( 4 FDA reports)
SCRATCH ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SKIN ULCER HAEMORRHAGE ( 4 FDA reports)
SPLENIC LESION ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
TENOSYNOVITIS ( 4 FDA reports)
THIRST ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRACHEAL HAEMORRHAGE ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TUMOUR INVASION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
UROGENITAL FISTULA ( 4 FDA reports)
VASCULITIS CEREBRAL ( 4 FDA reports)
VASOCONSTRICTION ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
WHITE BLOOD CELLS URINE ( 4 FDA reports)
WOUND DECOMPOSITION ( 4 FDA reports)
WOUND DRAINAGE ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACARODERMATITIS ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALVEOLAR SOFT PART SARCOMA ( 3 FDA reports)
AMOEBIASIS ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANTERIOR CHAMBER DISORDER ( 3 FDA reports)
ANTERIOR CHAMBER FLARE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
ARTERIAL CATHETERISATION ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL SPASM ( 3 FDA reports)
ASPERMIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BASILAR ARTERY OCCLUSION ( 3 FDA reports)
BILE DUCT NECROSIS ( 3 FDA reports)
BLADDER NECROSIS ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
CAECOPEXY ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 3 FDA reports)
CARCINOID TUMOUR PULMONARY ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDITIS ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CATHETER SITE EROSION ( 3 FDA reports)
CATHETER SITE PRURITUS ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CERVICAL CORD COMPRESSION ( 3 FDA reports)
CHEMICAL INJURY ( 3 FDA reports)
CHEMICAL PERITONITIS ( 3 FDA reports)
CHOROIDAL HAEMORRHAGE ( 3 FDA reports)
CHOROIDITIS ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLON CANCER STAGE IV ( 3 FDA reports)
COLON GANGRENE ( 3 FDA reports)
COMMINUTED FRACTURE ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONJUNCTIVAL VASCULAR DISORDER ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DEMENTIA WITH LEWY BODIES ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETIC GANGRENE ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIAPHRAGMATIC DISORDER ( 3 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DURAL FISTULA ( 3 FDA reports)
ECTROPION ( 3 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ENCEPHALOMYELITIS ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE OPERATION COMPLICATION ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
EYELID PAIN ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FIXED ERUPTION ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 3 FDA reports)
FULL BLOOD COUNT INCREASED ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GASTROSTOMY FAILURE ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
GLIOMA ( 3 FDA reports)
GLIOMATOSIS CEREBRI ( 3 FDA reports)
GLUCOSE URINE ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HEPATIC ENZYME DECREASED ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPOPHYSITIS ( 3 FDA reports)
IIIRD NERVE DISORDER ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPLANT SITE EFFUSION ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTESTINAL ULCER PERFORATION ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JEJUNITIS ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LACRIMAL DISORDER ( 3 FDA reports)
LENS DISORDER ( 3 FDA reports)
LESION EXCISION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LIVIDITY ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LUNG INJURY ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
MACULAR SCAR ( 3 FDA reports)
MARCHIAFAVA-BIGNAMI DISEASE ( 3 FDA reports)
MENINGORRHAGIA ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTASES TO LARGE INTESTINE ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL ULCER ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 3 FDA reports)
OCULAR SURFACE DISEASE ( 3 FDA reports)
OMENTAL INFARCTION ( 3 FDA reports)
OOPHORECTOMY ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
OPPORTUNISTIC INFECTION PROPHYLAXIS ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PELVIC SEPSIS ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PERFORATION BILE DUCT ( 3 FDA reports)
PERINEAL INFECTION ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERITONEAL NEOPLASM ( 3 FDA reports)
PERITONEAL PERFORATION ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHLEBITIS INFECTIVE ( 3 FDA reports)
PHLEBOTHROMBOSIS ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMORETROPERITONEUM ( 3 FDA reports)
PORTAL VEIN OCCLUSION ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POST PROCEDURAL VOMITING ( 3 FDA reports)
POSTOPERATIVE HERNIA ( 3 FDA reports)
POVERTY OF SPEECH ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PUTAMEN HAEMORRHAGE ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
RADIATION NECROSIS ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RECTAL STENOSIS ( 3 FDA reports)
RENAL ARTERY THROMBOSIS ( 3 FDA reports)
RENAL ISCHAEMIA ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
RETINAL FIBROSIS ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SCLERAL HAEMORRHAGE ( 3 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SNORING ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TRACHEAL INJURY ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TUMOUR COMPRESSION ( 3 FDA reports)
TUMOUR EMBOLISM ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
URETHRAL OBSTRUCTION ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VARICOSE VEIN RUPTURED ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND INFECTION BACTERIAL ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ABDOMINAL WALL CYST ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APOLIPOPROTEIN B INCREASED ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
AURICULAR PERICHONDRITIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BILIARY CANCER METASTATIC ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER TAMPONADE ( 2 FDA reports)
BLAST CELLS ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CAROTID ANEURYSM RUPTURE ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETER SITE NECROSIS ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CELLS IN URINE ( 2 FDA reports)
CEMENT EMBOLISM ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 2 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 2 FDA reports)
CHLOASMA ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHOROIDAL INFARCTION ( 2 FDA reports)
CHOROIDAL RUPTURE ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON INJURY ( 2 FDA reports)
COLORECTAL CANCER STAGE IV ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIAL NEUROPATHY ( 2 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYTOLOGY ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIAPHRAGMATIC RUPTURE ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ENDOCRINE NEOPLASM ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPIPLOIC APPENDAGITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA INDURATUM ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EXPLORATORY OPERATION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYEBALL AVULSION ( 2 FDA reports)
EYELASH THICKENING ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GENITAL ABSCESS ( 2 FDA reports)
GENITAL HERPES ZOSTER ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HERPETIC GINGIVOSTOMATITIS ( 2 FDA reports)
HYPERCATABOLISM ( 2 FDA reports)
HYPERCHROMIC ANAEMIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTESTINAL HAEMATOMA ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT SURGERY ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
LAGOPHTHALMOS ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPH GLAND INFECTION ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHATIC OBSTRUCTION ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGOCELE ( 2 FDA reports)
MESENTERIC FIBROSIS ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTASES TO STOMACH ( 2 FDA reports)
METASTASES TO THYROID ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MURDER ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOPERICARDITIS ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NAIL BED INFECTION BACTERIAL ( 2 FDA reports)
NAIL BED INFLAMMATION ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL SEPTUM ULCERATION ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NECROTISING RETINITIS ( 2 FDA reports)
NEOVASCULARISATION ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR CANCER METASTATIC ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPSOCLONUS MYOCLONUS ( 2 FDA reports)
OPTIC NERVE NEOPLASM ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PARANEOPLASTIC CEREBELLAR DEGENERATION ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYCHROMIC RED BLOOD CELLS PRESENT ( 2 FDA reports)
POLYPOIDAL CHOROIDAL VASCULOPATHY ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
PORTAL VEIN STENOSIS ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PRODUCT DROPPER ISSUE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUNCTURE SITE PAIN ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PURPURA FULMINANS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RADIATION MYELOPATHY ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RECTAL CANCER RECURRENT ( 2 FDA reports)
RECTAL CANCER STAGE IV ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL SPASM ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINAL ARTERY SPASM ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SALIVARY GLAND RESECTION ( 2 FDA reports)
SCLERAL HYPERAEMIA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN FLAP NECROSIS ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP STUDY ABNORMAL ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SPIGELIAN HERNIA ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPINAL CORD ISCHAEMIA ( 2 FDA reports)
SPORTS INJURY ( 2 FDA reports)
STARING ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STOMA SITE REACTION ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SYMPATHETIC OPHTHALMIA ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TORUS FRACTURE ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSIENT PSYCHOSIS ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TROPONIN I ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC RUPTURE ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL CANCER ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASCULAR NEOPLASM ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULAR SHUNT ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENOUS STENT INSERTION ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVAL ERYTHEMA ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
YERSINIA INFECTION ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN DECREASED ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL EXAMINATION ABNORMAL ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL CATHETERISATION NORMAL ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ASTRINGENT THERAPY ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CANCER IN REMISSION ( 1 FDA reports)
CAPILLARY PERMEABILITY ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBROSPINAL FISTULA ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLANGITIS SUPPURATIVE ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLONY STIMULATING FACTOR THERAPY ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL DECOMPENSATION ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE NORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSCOPY LARGE BOWEL ABNORMAL ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO CAPTURE ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRIN ABNORMAL ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTROENTERITIS AEROBACTER ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCOELE ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
ILEOCOLECTOMY ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTED LYMPHOCELE ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERNAL HERNIA ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JEJUNAL FISTULA ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE CELL LUNG CANCER METASTATIC ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
LARYNGOSCOPY ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LESION OF SCIATIC NERVE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELANAEMIA ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METASTASES TO DIAPHRAGM ( 1 FDA reports)
METASTASES TO MOUTH ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO RECTUM ( 1 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOCUTANEOUS FLAP OPERATION ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCOAST'S TUMOUR ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC LEAK ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PARTIAL LUNG RESECTION ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PENILE VASCULAR DISORDER ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICORONITIS ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHLEBITIS ( 1 FDA reports)
PERITONEAL CARCINOMA METASTATIC ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL FISTULA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRETERNATURAL ANUS ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
PYURIA ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECTOURETHRAL FISTULA ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL PELVIS FISTULA ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VEIN EMBOLISM ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL GANGRENE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMALL INTESTINE CARCINOMA RECURRENT ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENON'S CYST ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR INFARCTION ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THALASSAEMIA TRAIT ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOPHLEBITIS PELVIC VEIN ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TOOTH AVULSION ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TRACHEAL CANCER ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY ANASTOMOTIC LEAK ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRAL UVEITIS ( 1 FDA reports)
VITAMIN B12 ABNORMAL ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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