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

DRUG INTERACTION ( 814 FDA reports)
DYSPNOEA ( 691 FDA reports)
NAUSEA ( 673 FDA reports)
RENAL FAILURE ACUTE ( 666 FDA reports)
MYALGIA ( 568 FDA reports)
DIZZINESS ( 557 FDA reports)
MYOCARDIAL INFARCTION ( 552 FDA reports)
DIARRHOEA ( 546 FDA reports)
DRUG INEFFECTIVE ( 541 FDA reports)
ASTHENIA ( 537 FDA reports)
HYPOTENSION ( 480 FDA reports)
FATIGUE ( 478 FDA reports)
VOMITING ( 472 FDA reports)
RHABDOMYOLYSIS ( 455 FDA reports)
MALAISE ( 452 FDA reports)
RENAL FAILURE ( 450 FDA reports)
PYREXIA ( 449 FDA reports)
CHEST PAIN ( 446 FDA reports)
ANAEMIA ( 429 FDA reports)
ARTHRALGIA ( 391 FDA reports)
FALL ( 388 FDA reports)
HEADACHE ( 366 FDA reports)
OEDEMA PERIPHERAL ( 363 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 345 FDA reports)
PNEUMONIA ( 342 FDA reports)
PRURITUS ( 335 FDA reports)
HYPERTENSION ( 327 FDA reports)
PAIN ( 325 FDA reports)
CONFUSIONAL STATE ( 316 FDA reports)
INSOMNIA ( 310 FDA reports)
CONDITION AGGRAVATED ( 303 FDA reports)
ATRIAL FIBRILLATION ( 298 FDA reports)
PAIN IN EXTREMITY ( 291 FDA reports)
HAEMOGLOBIN DECREASED ( 289 FDA reports)
BLOOD CREATININE INCREASED ( 285 FDA reports)
BLOOD GLUCOSE INCREASED ( 272 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 269 FDA reports)
DEHYDRATION ( 265 FDA reports)
WEIGHT DECREASED ( 256 FDA reports)
CEREBROVASCULAR ACCIDENT ( 254 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 250 FDA reports)
RASH ( 248 FDA reports)
THROMBOCYTOPENIA ( 248 FDA reports)
MUSCLE SPASMS ( 245 FDA reports)
BRADYCARDIA ( 241 FDA reports)
ABDOMINAL PAIN ( 238 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 236 FDA reports)
LOSS OF CONSCIOUSNESS ( 225 FDA reports)
HYPERHIDROSIS ( 222 FDA reports)
SYNCOPE ( 221 FDA reports)
MUSCULAR WEAKNESS ( 212 FDA reports)
ERYTHEMA ( 210 FDA reports)
DEPRESSION ( 209 FDA reports)
DYSGEUSIA ( 209 FDA reports)
ANGINA PECTORIS ( 208 FDA reports)
CORONARY ARTERY DISEASE ( 208 FDA reports)
FLUSHING ( 208 FDA reports)
URINARY TRACT INFECTION ( 207 FDA reports)
CARDIAC ARREST ( 205 FDA reports)
BACK PAIN ( 195 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 195 FDA reports)
DEATH ( 193 FDA reports)
CARDIAC FAILURE ( 192 FDA reports)
TREMOR ( 192 FDA reports)
GAIT DISTURBANCE ( 191 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 191 FDA reports)
RENAL IMPAIRMENT ( 189 FDA reports)
PARAESTHESIA ( 188 FDA reports)
SOMNOLENCE ( 188 FDA reports)
ANXIETY ( 184 FDA reports)
HYPERKALAEMIA ( 182 FDA reports)
ABDOMINAL PAIN UPPER ( 181 FDA reports)
BLOOD PRESSURE INCREASED ( 181 FDA reports)
PULMONARY OEDEMA ( 179 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 178 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 176 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 173 FDA reports)
SEPSIS ( 172 FDA reports)
COUGH ( 171 FDA reports)
CONSTIPATION ( 170 FDA reports)
RESPIRATORY FAILURE ( 162 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 161 FDA reports)
HYPONATRAEMIA ( 160 FDA reports)
HYPERSENSITIVITY ( 158 FDA reports)
FEELING ABNORMAL ( 152 FDA reports)
DIABETES MELLITUS ( 150 FDA reports)
HYPOKALAEMIA ( 147 FDA reports)
DECREASED APPETITE ( 146 FDA reports)
HYPOGLYCAEMIA ( 141 FDA reports)
MULTI-ORGAN FAILURE ( 140 FDA reports)
WEIGHT INCREASED ( 140 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 139 FDA reports)
MYOCARDIAL ISCHAEMIA ( 139 FDA reports)
CONVULSION ( 138 FDA reports)
CHILLS ( 135 FDA reports)
OVERDOSE ( 135 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 133 FDA reports)
PALPITATIONS ( 132 FDA reports)
HEPATIC FAILURE ( 131 FDA reports)
HYPOAESTHESIA ( 130 FDA reports)
HAEMODIALYSIS ( 128 FDA reports)
TACHYCARDIA ( 128 FDA reports)
INTERSTITIAL LUNG DISEASE ( 122 FDA reports)
PULMONARY EMBOLISM ( 122 FDA reports)
ANOREXIA ( 121 FDA reports)
CORONARY ARTERY STENOSIS ( 119 FDA reports)
DYSPEPSIA ( 119 FDA reports)
HEPATITIS ( 116 FDA reports)
URTICARIA ( 116 FDA reports)
AMNESIA ( 114 FDA reports)
BLOOD UREA INCREASED ( 114 FDA reports)
CHEST DISCOMFORT ( 114 FDA reports)
EPISTAXIS ( 114 FDA reports)
LETHARGY ( 114 FDA reports)
INCORRECT DOSE ADMINISTERED ( 113 FDA reports)
PLATELET COUNT DECREASED ( 111 FDA reports)
CYTOLYTIC HEPATITIS ( 110 FDA reports)
MYOPATHY ( 110 FDA reports)
BALANCE DISORDER ( 108 FDA reports)
DYSPHAGIA ( 107 FDA reports)
PLEURAL EFFUSION ( 107 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 107 FDA reports)
AGITATION ( 105 FDA reports)
HALLUCINATION ( 105 FDA reports)
OEDEMA ( 105 FDA reports)
CHOLELITHIASIS ( 104 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 104 FDA reports)
MEMORY IMPAIRMENT ( 104 FDA reports)
CHOLESTASIS ( 103 FDA reports)
HYPERGLYCAEMIA ( 103 FDA reports)
HAEMATEMESIS ( 102 FDA reports)
JAUNDICE ( 100 FDA reports)
BLOOD PRESSURE DECREASED ( 99 FDA reports)
CARDIAC DISORDER ( 99 FDA reports)
GASTRIC ULCER ( 99 FDA reports)
PANCREATITIS ACUTE ( 99 FDA reports)
VISION BLURRED ( 98 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 97 FDA reports)
HAEMORRHAGE ( 97 FDA reports)
INFECTION ( 97 FDA reports)
JOINT SWELLING ( 96 FDA reports)
RENAL FAILURE CHRONIC ( 96 FDA reports)
HEPATIC ENZYME INCREASED ( 95 FDA reports)
PANCYTOPENIA ( 95 FDA reports)
VERTIGO ( 94 FDA reports)
CORONARY ARTERY OCCLUSION ( 92 FDA reports)
LACTIC ACIDOSIS ( 92 FDA reports)
BLOOD BILIRUBIN INCREASED ( 91 FDA reports)
HEART RATE INCREASED ( 91 FDA reports)
INJECTION SITE PAIN ( 91 FDA reports)
MITRAL VALVE INCOMPETENCE ( 90 FDA reports)
ABDOMINAL DISCOMFORT ( 89 FDA reports)
CONTUSION ( 89 FDA reports)
DYSARTHRIA ( 89 FDA reports)
BURNING SENSATION ( 88 FDA reports)
MELAENA ( 88 FDA reports)
RECTAL HAEMORRHAGE ( 88 FDA reports)
SEPTIC SHOCK ( 88 FDA reports)
ARRHYTHMIA ( 86 FDA reports)
HAEMATOMA ( 86 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 85 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 85 FDA reports)
COMPLETED SUICIDE ( 85 FDA reports)
LEUKOPENIA ( 85 FDA reports)
MIDDLE INSOMNIA ( 85 FDA reports)
NEUTROPENIA ( 85 FDA reports)
DISORIENTATION ( 83 FDA reports)
VENTRICULAR FIBRILLATION ( 83 FDA reports)
VENTRICULAR TACHYCARDIA ( 82 FDA reports)
ANGINA UNSTABLE ( 82 FDA reports)
BLOOD POTASSIUM INCREASED ( 82 FDA reports)
MUSCULOSKELETAL PAIN ( 81 FDA reports)
ACUTE CORONARY SYNDROME ( 80 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 80 FDA reports)
COMA ( 79 FDA reports)
ANGIOEDEMA ( 78 FDA reports)
GASTRITIS ( 78 FDA reports)
HAEMATOCRIT DECREASED ( 78 FDA reports)
HEPATIC STEATOSIS ( 78 FDA reports)
LIVER DISORDER ( 78 FDA reports)
CARDIO-RESPIRATORY ARREST ( 77 FDA reports)
DRUG TOXICITY ( 76 FDA reports)
PANCREATITIS ( 76 FDA reports)
FEELING HOT ( 75 FDA reports)
ABDOMINAL DISTENSION ( 74 FDA reports)
DEEP VEIN THROMBOSIS ( 74 FDA reports)
HAEMATURIA ( 74 FDA reports)
DRUG EFFECT DECREASED ( 73 FDA reports)
DRY MOUTH ( 73 FDA reports)
EOSINOPHILIA ( 73 FDA reports)
HYPOXIA ( 73 FDA reports)
ALOPECIA ( 72 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 72 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 72 FDA reports)
NASOPHARYNGITIS ( 72 FDA reports)
SWELLING FACE ( 72 FDA reports)
ANURIA ( 71 FDA reports)
CEREBRAL INFARCTION ( 71 FDA reports)
DYSPNOEA EXERTIONAL ( 71 FDA reports)
CELLULITIS ( 70 FDA reports)
ORTHOSTATIC HYPOTENSION ( 70 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 69 FDA reports)
HYPOMAGNESAEMIA ( 69 FDA reports)
MENTAL STATUS CHANGES ( 69 FDA reports)
GASTROENTERITIS ( 68 FDA reports)
RHEUMATOID ARTHRITIS ( 68 FDA reports)
CARDIOMEGALY ( 67 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 67 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 67 FDA reports)
NECK PAIN ( 67 FDA reports)
TRANSAMINASES INCREASED ( 67 FDA reports)
TENDON RUPTURE ( 66 FDA reports)
ASTHMA ( 66 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 66 FDA reports)
DELIRIUM ( 66 FDA reports)
STAPHYLOCOCCAL INFECTION ( 66 FDA reports)
CARDIOGENIC SHOCK ( 65 FDA reports)
AGGRESSION ( 64 FDA reports)
BRONCHITIS ( 64 FDA reports)
METABOLIC ACIDOSIS ( 64 FDA reports)
VENTRICULAR HYPERTROPHY ( 64 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 63 FDA reports)
ECZEMA ( 63 FDA reports)
CIRCULATORY COLLAPSE ( 62 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 62 FDA reports)
HYPOCALCAEMIA ( 62 FDA reports)
POST PROCEDURAL COMPLICATION ( 62 FDA reports)
BLOOD SODIUM DECREASED ( 61 FDA reports)
SWOLLEN TONGUE ( 61 FDA reports)
THROMBOSIS ( 61 FDA reports)
DIALYSIS ( 60 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 60 FDA reports)
FLATULENCE ( 60 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 60 FDA reports)
INFLAMMATION ( 60 FDA reports)
INITIAL INSOMNIA ( 60 FDA reports)
MUSCLE ATROPHY ( 60 FDA reports)
PROTEINURIA ( 60 FDA reports)
ABASIA ( 59 FDA reports)
CARDIAC MURMUR ( 59 FDA reports)
DISTURBANCE IN ATTENTION ( 59 FDA reports)
INFLUENZA LIKE ILLNESS ( 59 FDA reports)
MEDICATION ERROR ( 59 FDA reports)
NEUROPATHY PERIPHERAL ( 59 FDA reports)
ACCIDENTAL EXPOSURE ( 58 FDA reports)
COLON CANCER ( 58 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 57 FDA reports)
FEBRILE NEUTROPENIA ( 57 FDA reports)
MYOSITIS ( 57 FDA reports)
PNEUMONITIS ( 57 FDA reports)
CEREBRAL HAEMORRHAGE ( 56 FDA reports)
RASH ERYTHEMATOUS ( 56 FDA reports)
TREATMENT NONCOMPLIANCE ( 56 FDA reports)
UNEVALUABLE EVENT ( 56 FDA reports)
URINARY RETENTION ( 55 FDA reports)
CATARACT ( 55 FDA reports)
DRUG HYPERSENSITIVITY ( 55 FDA reports)
DRUG LEVEL INCREASED ( 55 FDA reports)
DYSURIA ( 55 FDA reports)
OSTEOARTHRITIS ( 55 FDA reports)
PRURITUS GENERALISED ( 55 FDA reports)
SLEEP DISORDER ( 55 FDA reports)
SPEECH DISORDER ( 55 FDA reports)
LUNG DISORDER ( 54 FDA reports)
SINUSITIS ( 54 FDA reports)
SUDDEN DEATH ( 54 FDA reports)
SWELLING ( 54 FDA reports)
APHASIA ( 53 FDA reports)
ARTHRITIS ( 53 FDA reports)
BLISTER ( 53 FDA reports)
DUODENAL ULCER ( 53 FDA reports)
LEUKOCYTOSIS ( 53 FDA reports)
PULMONARY HYPERTENSION ( 53 FDA reports)
SHOCK ( 53 FDA reports)
HIATUS HERNIA ( 52 FDA reports)
INJECTION SITE ERYTHEMA ( 52 FDA reports)
TINNITUS ( 52 FDA reports)
ARTERIOSCLEROSIS ( 51 FDA reports)
ERECTILE DYSFUNCTION ( 51 FDA reports)
STEVENS-JOHNSON SYNDROME ( 51 FDA reports)
GASTROINTESTINAL DISORDER ( 50 FDA reports)
HEPATITIS CHOLESTATIC ( 50 FDA reports)
LUNG NEOPLASM MALIGNANT ( 50 FDA reports)
ANGIONEUROTIC OEDEMA ( 49 FDA reports)
COAGULOPATHY ( 49 FDA reports)
HEART RATE IRREGULAR ( 49 FDA reports)
INTESTINAL OBSTRUCTION ( 49 FDA reports)
OSTEONECROSIS ( 49 FDA reports)
PALLOR ( 49 FDA reports)
ATRIAL FLUTTER ( 48 FDA reports)
HEART RATE DECREASED ( 48 FDA reports)
IMPAIRED HEALING ( 48 FDA reports)
RENAL DISORDER ( 48 FDA reports)
SINUS TACHYCARDIA ( 48 FDA reports)
THERAPY NON-RESPONDER ( 48 FDA reports)
VISUAL ACUITY REDUCED ( 48 FDA reports)
HEPATOCELLULAR DAMAGE ( 47 FDA reports)
HEPATORENAL SYNDROME ( 47 FDA reports)
HYPOVOLAEMIA ( 47 FDA reports)
IRRITABILITY ( 47 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 47 FDA reports)
RASH PRURITIC ( 47 FDA reports)
RESTLESSNESS ( 47 FDA reports)
SKIN DISCOLOURATION ( 47 FDA reports)
ACUTE HEPATIC FAILURE ( 46 FDA reports)
ENCEPHALOPATHY ( 46 FDA reports)
LABORATORY TEST ABNORMAL ( 46 FDA reports)
NEUTROPHIL COUNT INCREASED ( 46 FDA reports)
POLLAKIURIA ( 46 FDA reports)
SKIN EXFOLIATION ( 46 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 46 FDA reports)
CARDIOMYOPATHY ( 45 FDA reports)
HEMIPARESIS ( 45 FDA reports)
NEPHROTIC SYNDROME ( 45 FDA reports)
OESOPHAGITIS ( 45 FDA reports)
ROAD TRAFFIC ACCIDENT ( 45 FDA reports)
SKIN ULCER ( 45 FDA reports)
DRUG ERUPTION ( 44 FDA reports)
MYOCLONUS ( 44 FDA reports)
PERITONITIS ( 44 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 44 FDA reports)
PULMONARY FIBROSIS ( 44 FDA reports)
RASH GENERALISED ( 44 FDA reports)
AGRANULOCYTOSIS ( 43 FDA reports)
DYSKINESIA ( 43 FDA reports)
HERPES ZOSTER ( 43 FDA reports)
INJURY ( 43 FDA reports)
OFF LABEL USE ( 43 FDA reports)
OXYGEN SATURATION DECREASED ( 43 FDA reports)
RESPIRATORY DISTRESS ( 43 FDA reports)
ASCITES ( 42 FDA reports)
HEPATITIS ACUTE ( 42 FDA reports)
LABILE BLOOD PRESSURE ( 42 FDA reports)
PROTHROMBIN TIME PROLONGED ( 42 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 42 FDA reports)
WHEEZING ( 42 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 41 FDA reports)
ATRIOVENTRICULAR BLOCK ( 41 FDA reports)
BLOOD ALBUMIN DECREASED ( 41 FDA reports)
BLOOD POTASSIUM DECREASED ( 41 FDA reports)
BRONCHOPNEUMONIA ( 41 FDA reports)
COLITIS ( 41 FDA reports)
DISEASE PROGRESSION ( 41 FDA reports)
FAECES DISCOLOURED ( 41 FDA reports)
MENTAL DISORDER ( 41 FDA reports)
NIGHTMARE ( 41 FDA reports)
PROCEDURAL COMPLICATION ( 41 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 40 FDA reports)
CEREBRAL ISCHAEMIA ( 40 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 40 FDA reports)
GRAND MAL CONVULSION ( 40 FDA reports)
HAEMOPTYSIS ( 40 FDA reports)
HEPATIC NECROSIS ( 40 FDA reports)
HYPERCHOLESTEROLAEMIA ( 40 FDA reports)
MUSCLE INJURY ( 40 FDA reports)
RENAL TUBULAR NECROSIS ( 40 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 40 FDA reports)
URINARY INCONTINENCE ( 40 FDA reports)
VENTRICULAR DYSFUNCTION ( 40 FDA reports)
SUICIDAL IDEATION ( 39 FDA reports)
BLOOD GLUCOSE DECREASED ( 39 FDA reports)
DIFFICULTY IN WALKING ( 39 FDA reports)
DRY SKIN ( 39 FDA reports)
GASTRIC DISORDER ( 39 FDA reports)
HEAD INJURY ( 39 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 39 FDA reports)
LYMPHADENOPATHY ( 39 FDA reports)
PURPURA ( 39 FDA reports)
RESPIRATORY DISORDER ( 39 FDA reports)
SLEEP APNOEA SYNDROME ( 39 FDA reports)
ANAPHYLACTIC REACTION ( 38 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 38 FDA reports)
HALLUCINATION, VISUAL ( 38 FDA reports)
HEPATOTOXICITY ( 38 FDA reports)
LARYNGEAL OEDEMA ( 38 FDA reports)
SINUS BRADYCARDIA ( 38 FDA reports)
ANAPHYLACTIC SHOCK ( 37 FDA reports)
CARDIOVASCULAR DISORDER ( 37 FDA reports)
FLUID RETENTION ( 37 FDA reports)
HAEMOLYTIC ANAEMIA ( 37 FDA reports)
ISCHAEMIC STROKE ( 37 FDA reports)
LUNG INFILTRATION ( 37 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 37 FDA reports)
RASH MACULO-PAPULAR ( 37 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 37 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 36 FDA reports)
BLOOD CREATINE INCREASED ( 36 FDA reports)
HAEMATOCHEZIA ( 36 FDA reports)
HOT FLUSH ( 36 FDA reports)
MESOTHELIOMA ( 36 FDA reports)
MUSCLE DISORDER ( 36 FDA reports)
POLYNEUROPATHY ( 36 FDA reports)
RHINORRHOEA ( 36 FDA reports)
SKIN DISORDER ( 36 FDA reports)
CEREBRAL ATROPHY ( 35 FDA reports)
CHROMATURIA ( 35 FDA reports)
DEMENTIA ( 35 FDA reports)
DEPRESSED MOOD ( 35 FDA reports)
HEPATOMEGALY ( 35 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 35 FDA reports)
TENDONITIS ( 35 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 35 FDA reports)
TROPONIN INCREASED ( 34 FDA reports)
VISUAL IMPAIRMENT ( 34 FDA reports)
AUTOIMMUNE HEPATITIS ( 34 FDA reports)
BONE PAIN ( 34 FDA reports)
HAEMORRHAGIC STROKE ( 34 FDA reports)
HAEMORRHOIDS ( 34 FDA reports)
HYPOTHYROIDISM ( 34 FDA reports)
INJECTION SITE IRRITATION ( 34 FDA reports)
LIPASE INCREASED ( 34 FDA reports)
LYMPHOMA ( 34 FDA reports)
NERVOUSNESS ( 34 FDA reports)
OSTEOMYELITIS ( 34 FDA reports)
PSORIASIS ( 34 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 34 FDA reports)
RESPIRATORY TRACT INFECTION ( 34 FDA reports)
ACCIDENTAL OVERDOSE ( 33 FDA reports)
AORTIC STENOSIS ( 33 FDA reports)
ARTHROPATHY ( 33 FDA reports)
IRON DEFICIENCY ANAEMIA ( 33 FDA reports)
MYELODYSPLASTIC SYNDROME ( 33 FDA reports)
PETECHIAE ( 33 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 33 FDA reports)
SEROTONIN SYNDROME ( 33 FDA reports)
COGNITIVE DISORDER ( 32 FDA reports)
GOUT ( 32 FDA reports)
HEPATITIS FULMINANT ( 32 FDA reports)
LARYNGOSPASM ( 32 FDA reports)
OBESITY ( 32 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 32 FDA reports)
RASH PAPULAR ( 32 FDA reports)
RESTLESS LEGS SYNDROME ( 32 FDA reports)
RIB FRACTURE ( 32 FDA reports)
SKIN LESION ( 32 FDA reports)
UNRESPONSIVE TO STIMULI ( 32 FDA reports)
VASCULITIS ( 32 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 32 FDA reports)
TOXIC SKIN ERUPTION ( 31 FDA reports)
ACUTE PULMONARY OEDEMA ( 31 FDA reports)
BONE MARROW FAILURE ( 31 FDA reports)
CHOLECYSTITIS ( 31 FDA reports)
CYANOSIS ( 31 FDA reports)
DISCOMFORT ( 31 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 31 FDA reports)
EJECTION FRACTION DECREASED ( 31 FDA reports)
ELECTROLYTE IMBALANCE ( 31 FDA reports)
EMOTIONAL DISTRESS ( 31 FDA reports)
EPILEPSY ( 31 FDA reports)
FACE OEDEMA ( 31 FDA reports)
GRANULOCYTOPENIA ( 31 FDA reports)
ILL-DEFINED DISORDER ( 31 FDA reports)
LIP SWELLING ( 31 FDA reports)
MOBILITY DECREASED ( 31 FDA reports)
NERVOUS SYSTEM DISORDER ( 31 FDA reports)
PERICARDIAL EFFUSION ( 31 FDA reports)
PULMONARY CONGESTION ( 31 FDA reports)
ABNORMAL BEHAVIOUR ( 30 FDA reports)
ACIDOSIS ( 30 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 30 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 30 FDA reports)
BLOOD CALCIUM DECREASED ( 30 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 30 FDA reports)
DYSPHONIA ( 30 FDA reports)
FUNGAL INFECTION ( 30 FDA reports)
HEPATITIS TOXIC ( 30 FDA reports)
HYPERBILIRUBINAEMIA ( 30 FDA reports)
HYPERLIPIDAEMIA ( 30 FDA reports)
IMMUNOSUPPRESSION ( 30 FDA reports)
INFARCTION ( 30 FDA reports)
MEAN CELL VOLUME DECREASED ( 30 FDA reports)
OSTEOPOROSIS ( 30 FDA reports)
PERIPHERAL COLDNESS ( 30 FDA reports)
PERIPHERAL ISCHAEMIA ( 30 FDA reports)
PLATELET COUNT INCREASED ( 30 FDA reports)
RESPIRATORY ARREST ( 30 FDA reports)
STRIDOR ( 30 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 30 FDA reports)
SUBDURAL HAEMATOMA ( 29 FDA reports)
VISUAL DISTURBANCE ( 29 FDA reports)
VITREOUS DETACHMENT ( 29 FDA reports)
ABDOMINAL TENDERNESS ( 29 FDA reports)
DRUG INTOLERANCE ( 29 FDA reports)
DYSSTASIA ( 29 FDA reports)
FEMUR FRACTURE ( 29 FDA reports)
HYPOTHERMIA ( 29 FDA reports)
INJECTION SITE PRURITUS ( 29 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 29 FDA reports)
MOVEMENT DISORDER ( 29 FDA reports)
PHARYNGEAL OEDEMA ( 29 FDA reports)
PNEUMONIA ASPIRATION ( 29 FDA reports)
PRESYNCOPE ( 29 FDA reports)
RALES ( 29 FDA reports)
RETINAL DETACHMENT ( 29 FDA reports)
ABNORMAL DREAMS ( 28 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 28 FDA reports)
ACUTE RESPIRATORY FAILURE ( 28 FDA reports)
COLD SWEAT ( 28 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 28 FDA reports)
HYPERTENSIVE CRISIS ( 28 FDA reports)
STOMATITIS ( 28 FDA reports)
BACTERIAL INFECTION ( 27 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 27 FDA reports)
DIPLOPIA ( 27 FDA reports)
GANGRENE ( 27 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 27 FDA reports)
NEOPLASM MALIGNANT ( 27 FDA reports)
PANIC ATTACK ( 27 FDA reports)
PSYCHOTIC DISORDER ( 27 FDA reports)
RASH MACULAR ( 27 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 27 FDA reports)
UVEITIS ( 27 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 26 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 26 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 26 FDA reports)
CARPAL TUNNEL SYNDROME ( 26 FDA reports)
CEREBRAL HAEMATOMA ( 26 FDA reports)
DILATATION ATRIAL ( 26 FDA reports)
DISEASE RECURRENCE ( 26 FDA reports)
ERYTHEMA MULTIFORME ( 26 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 26 FDA reports)
GENERALISED OEDEMA ( 26 FDA reports)
HEPATIC CIRRHOSIS ( 26 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 26 FDA reports)
ILEUS PARALYTIC ( 26 FDA reports)
INTENTIONAL OVERDOSE ( 26 FDA reports)
LEFT VENTRICULAR FAILURE ( 26 FDA reports)
LIVER INJURY ( 26 FDA reports)
MIOSIS ( 26 FDA reports)
SENSORY DISTURBANCE ( 26 FDA reports)
SERUM FERRITIN INCREASED ( 26 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 25 FDA reports)
AGEUSIA ( 25 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 25 FDA reports)
BLOOD URINE PRESENT ( 25 FDA reports)
CANDIDIASIS ( 25 FDA reports)
COLONIC POLYP ( 25 FDA reports)
CYSTITIS ( 25 FDA reports)
DERMATITIS EXFOLIATIVE ( 25 FDA reports)
DIABETIC NEPHROPATHY ( 25 FDA reports)
DIVERTICULITIS ( 25 FDA reports)
EYE SWELLING ( 25 FDA reports)
FLUID OVERLOAD ( 25 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 25 FDA reports)
HYPOKINESIA ( 25 FDA reports)
INFUSION RELATED REACTION ( 25 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 25 FDA reports)
MUSCLE HAEMORRHAGE ( 25 FDA reports)
MYASTHENIA GRAVIS ( 25 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 25 FDA reports)
ORAL INTAKE REDUCED ( 25 FDA reports)
OROPHARYNGEAL PAIN ( 25 FDA reports)
RENAL CYST ( 25 FDA reports)
RESPIRATORY RATE INCREASED ( 25 FDA reports)
RETINAL TEAR ( 25 FDA reports)
SKIN BURNING SENSATION ( 25 FDA reports)
TOOTH DISORDER ( 25 FDA reports)
VIRAL INFECTION ( 25 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 24 FDA reports)
BODY TEMPERATURE INCREASED ( 24 FDA reports)
DUODENITIS ( 24 FDA reports)
HAEMODYNAMIC INSTABILITY ( 24 FDA reports)
HYPOTONIA ( 24 FDA reports)
INJECTION SITE HAEMORRHAGE ( 24 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 24 FDA reports)
ISCHAEMIA ( 24 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 24 FDA reports)
METASTASES TO LIVER ( 24 FDA reports)
NEPHROPATHY ( 24 FDA reports)
PULSE ABSENT ( 24 FDA reports)
AORTIC VALVE INCOMPETENCE ( 23 FDA reports)
ASPIRATION ( 23 FDA reports)
ATELECTASIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 23 FDA reports)
BASAL CELL CARCINOMA ( 23 FDA reports)
BLOOD AMYLASE INCREASED ( 23 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 23 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 23 FDA reports)
DYSTONIA ( 23 FDA reports)
ERUCTATION ( 23 FDA reports)
FEELING COLD ( 23 FDA reports)
GENERALISED ERYTHEMA ( 23 FDA reports)
INJECTION SITE SWELLING ( 23 FDA reports)
MENTAL IMPAIRMENT ( 23 FDA reports)
MUSCLE TWITCHING ( 23 FDA reports)
ORAL CANDIDIASIS ( 23 FDA reports)
PHOTOSENSITIVITY REACTION ( 23 FDA reports)
PRURIGO ( 23 FDA reports)
SALIVARY HYPERSECRETION ( 23 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 23 FDA reports)
TORSADE DE POINTES ( 22 FDA reports)
BREAST CANCER ( 22 FDA reports)
CORONARY ARTERY THROMBOSIS ( 22 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 22 FDA reports)
DERMAL CYST ( 22 FDA reports)
DIVERTICULUM ( 22 FDA reports)
FUNGAL SKIN INFECTION ( 22 FDA reports)
HYPOPHAGIA ( 22 FDA reports)
INTESTINAL ISCHAEMIA ( 22 FDA reports)
JOINT INJURY ( 22 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 22 FDA reports)
LUNG INFECTION ( 22 FDA reports)
METASTASES TO BONE ( 22 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 22 FDA reports)
NEPHROLITHIASIS ( 22 FDA reports)
NEURALGIA ( 22 FDA reports)
NIGHT SWEATS ( 22 FDA reports)
NO THERAPEUTIC RESPONSE ( 22 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 22 FDA reports)
PARALYSIS ( 22 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 22 FDA reports)
SARCOIDOSIS ( 22 FDA reports)
ABDOMINAL PAIN LOWER ( 21 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 21 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 21 FDA reports)
CARDIAC TAMPONADE ( 21 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 21 FDA reports)
COORDINATION ABNORMAL ( 21 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 21 FDA reports)
GASTRITIS EROSIVE ( 21 FDA reports)
HEPATOCELLULAR INJURY ( 21 FDA reports)
HYPOACUSIS ( 21 FDA reports)
INFLUENZA ( 21 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 21 FDA reports)
LEG AMPUTATION ( 21 FDA reports)
MUSCLE RUPTURE ( 21 FDA reports)
NEPHRITIS INTERSTITIAL ( 21 FDA reports)
REFLUX OESOPHAGITIS ( 21 FDA reports)
SCIATICA ( 21 FDA reports)
SENSATION OF HEAVINESS ( 21 FDA reports)
STRESS ( 21 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 21 FDA reports)
THIRST ( 21 FDA reports)
THROMBOSIS IN DEVICE ( 20 FDA reports)
TYPE 2 DIABETES MELLITUS ( 20 FDA reports)
ALCOHOL USE ( 20 FDA reports)
ANGIOPLASTY ( 20 FDA reports)
BLINDNESS ( 20 FDA reports)
BLOOD LACTIC ACID INCREASED ( 20 FDA reports)
BONE DISORDER ( 20 FDA reports)
CHOLANGITIS ( 20 FDA reports)
CORONARY ARTERY BYPASS ( 20 FDA reports)
DEAFNESS ( 20 FDA reports)
DERMATITIS BULLOUS ( 20 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 20 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 20 FDA reports)
EYE DISORDER ( 20 FDA reports)
FEAR ( 20 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 20 FDA reports)
HEPATIC ENCEPHALOPATHY ( 20 FDA reports)
HYPERAESTHESIA ( 20 FDA reports)
HYPERSOMNIA ( 20 FDA reports)
HYPOALBUMINAEMIA ( 20 FDA reports)
MOUTH ULCERATION ( 20 FDA reports)
MUCOSAL INFLAMMATION ( 20 FDA reports)
NEUTROPENIC SEPSIS ( 20 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 20 FDA reports)
POLYURIA ( 20 FDA reports)
PRODUCTIVE COUGH ( 20 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 19 FDA reports)
ATAXIA ( 19 FDA reports)
AZOTAEMIA ( 19 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 19 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 19 FDA reports)
BLOOD URIC ACID INCREASED ( 19 FDA reports)
BODY TEMPERATURE DECREASED ( 19 FDA reports)
DYSLIPIDAEMIA ( 19 FDA reports)
FAECAL INCONTINENCE ( 19 FDA reports)
FIBROMYALGIA ( 19 FDA reports)
HOSPITALISATION ( 19 FDA reports)
ILEUS ( 19 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
LYMPHOPENIA ( 19 FDA reports)
METASTASES TO LUNG ( 19 FDA reports)
MIGRAINE ( 19 FDA reports)
MONOCYTE COUNT INCREASED ( 19 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 19 FDA reports)
MULTIPLE SCLEROSIS ( 19 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 19 FDA reports)
NASAL CONGESTION ( 19 FDA reports)
NEPHROPATHY TOXIC ( 19 FDA reports)
RENAL ARTERY STENOSIS ( 19 FDA reports)
SEBORRHOEIC DERMATITIS ( 19 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
TENDON DISORDER ( 18 FDA reports)
URINE OUTPUT DECREASED ( 18 FDA reports)
VENTRICULAR ARRHYTHMIA ( 18 FDA reports)
ADVERSE EVENT ( 18 FDA reports)
BILE DUCT STONE ( 18 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 18 FDA reports)
CAROTID ARTERY STENOSIS ( 18 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 18 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 18 FDA reports)
GASTROINTESTINAL PAIN ( 18 FDA reports)
GLAUCOMA ( 18 FDA reports)
HYPERCALCAEMIA ( 18 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 18 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 18 FDA reports)
LUNG NEOPLASM ( 18 FDA reports)
OEDEMA MOUTH ( 18 FDA reports)
OLIGURIA ( 18 FDA reports)
PEMPHIGUS ( 18 FDA reports)
POLYP ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
PYELONEPHRITIS ( 18 FDA reports)
SKIN NECROSIS ( 18 FDA reports)
ANAEMIA MACROCYTIC ( 17 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 17 FDA reports)
APNOEA ( 17 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 17 FDA reports)
BODY MASS INDEX DECREASED ( 17 FDA reports)
CARDIAC PACEMAKER INSERTION ( 17 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 17 FDA reports)
DRY EYE ( 17 FDA reports)
ECCHYMOSIS ( 17 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 17 FDA reports)
ESCHERICHIA INFECTION ( 17 FDA reports)
EYELID OEDEMA ( 17 FDA reports)
FACIAL PALSY ( 17 FDA reports)
HAEMORRHAGIC ANAEMIA ( 17 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 17 FDA reports)
HYPOPHOSPHATAEMIA ( 17 FDA reports)
INJECTION SITE RASH ( 17 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 17 FDA reports)
INTESTINAL PERFORATION ( 17 FDA reports)
INTRACARDIAC THROMBUS ( 17 FDA reports)
LOCAL SWELLING ( 17 FDA reports)
MUSCLE RIGIDITY ( 17 FDA reports)
NO ADVERSE EVENT ( 17 FDA reports)
NOCTURIA ( 17 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 17 FDA reports)
ORTHOPNOEA ( 17 FDA reports)
PANCREATIC CARCINOMA ( 17 FDA reports)
PARKINSONISM ( 17 FDA reports)
PHYSICAL ASSAULT ( 17 FDA reports)
POLYMYOSITIS ( 17 FDA reports)
PRODUCT QUALITY ISSUE ( 17 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 17 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 17 FDA reports)
SPINAL COMPRESSION FRACTURE ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA ( 17 FDA reports)
STENT PLACEMENT ( 17 FDA reports)
STREPTOCOCCAL SEPSIS ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
TENDERNESS ( 17 FDA reports)
THINKING ABNORMAL ( 17 FDA reports)
UROSEPSIS ( 17 FDA reports)
VENTRICULAR HYPOKINESIA ( 17 FDA reports)
WHITE BLOOD CELL DISORDER ( 17 FDA reports)
SYNCOPE VASOVAGAL ( 16 FDA reports)
THROAT IRRITATION ( 16 FDA reports)
TOE AMPUTATION ( 16 FDA reports)
TRANSPLANT REJECTION ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
VIITH NERVE PARALYSIS ( 16 FDA reports)
ABORTION SPONTANEOUS ( 16 FDA reports)
ACNE ( 16 FDA reports)
ACUTE PRERENAL FAILURE ( 16 FDA reports)
ALVEOLITIS FIBROSING ( 16 FDA reports)
APLASIA PURE RED CELL ( 16 FDA reports)
BLADDER CANCER ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 16 FDA reports)
CHEST X-RAY ABNORMAL ( 16 FDA reports)
COLITIS ISCHAEMIC ( 16 FDA reports)
CONJUNCTIVITIS ( 16 FDA reports)
DIVERTICULUM INTESTINAL ( 16 FDA reports)
DRUG ADMINISTRATION ERROR ( 16 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 16 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 16 FDA reports)
EYE PAIN ( 16 FDA reports)
EYELID PTOSIS ( 16 FDA reports)
FORMICATION ( 16 FDA reports)
GLUCOSE URINE PRESENT ( 16 FDA reports)
HIP FRACTURE ( 16 FDA reports)
INJECTION SITE HAEMATOMA ( 16 FDA reports)
INJECTION SITE NODULE ( 16 FDA reports)
MALNUTRITION ( 16 FDA reports)
MOOD ALTERED ( 16 FDA reports)
NARCOTIC INTOXICATION ( 16 FDA reports)
NEUTROPHILIA ( 16 FDA reports)
OCULAR HYPERAEMIA ( 16 FDA reports)
OESOPHAGEAL ULCER ( 16 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 16 FDA reports)
PROSTATE CANCER ( 16 FDA reports)
SCAR ( 16 FDA reports)
STOMACH DISCOMFORT ( 16 FDA reports)
ABDOMINAL RIGIDITY ( 15 FDA reports)
ANGER ( 15 FDA reports)
ANGIOPATHY ( 15 FDA reports)
ARTHRITIS BACTERIAL ( 15 FDA reports)
BEDRIDDEN ( 15 FDA reports)
BLINDNESS UNILATERAL ( 15 FDA reports)
BLOOD BICARBONATE DECREASED ( 15 FDA reports)
BLOOD CULTURE POSITIVE ( 15 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 15 FDA reports)
BRADYPHRENIA ( 15 FDA reports)
BRAIN STEM INFARCTION ( 15 FDA reports)
BREAST CANCER FEMALE ( 15 FDA reports)
BRONCHOSPASM ( 15 FDA reports)
CARDIAC DEATH ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
CARDIAC OUTPUT DECREASED ( 15 FDA reports)
CARDIAC VALVE DISEASE ( 15 FDA reports)
CARDIOPULMONARY FAILURE ( 15 FDA reports)
CAROTID ARTERY OCCLUSION ( 15 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 15 FDA reports)
CORONARY ARTERY RESTENOSIS ( 15 FDA reports)
DELUSION ( 15 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 15 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 15 FDA reports)
EWING'S SARCOMA ( 15 FDA reports)
EXTRASYSTOLES ( 15 FDA reports)
GLOMERULONEPHRITIS ( 15 FDA reports)
HEPATIC FIBROSIS ( 15 FDA reports)
HIP ARTHROPLASTY ( 15 FDA reports)
JAUNDICE CHOLESTATIC ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 15 FDA reports)
LIMB DISCOMFORT ( 15 FDA reports)
MULTIPLE DRUG OVERDOSE ( 15 FDA reports)
MUSCLE CRAMP ( 15 FDA reports)
MUSCLE STRAIN ( 15 FDA reports)
PARANOIA ( 15 FDA reports)
PITTING OEDEMA ( 15 FDA reports)
SHOCK HAEMORRHAGIC ( 15 FDA reports)
SPINAL OSTEOARTHRITIS ( 15 FDA reports)
STENT OCCLUSION ( 15 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
SURGERY ( 15 FDA reports)
TARDIVE DYSKINESIA ( 15 FDA reports)
THROAT TIGHTNESS ( 15 FDA reports)
THROMBOCYTOSIS ( 15 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 15 FDA reports)
TOOTH EXTRACTION ( 15 FDA reports)
ULCER ( 15 FDA reports)
WOUND INFECTION ( 15 FDA reports)
TENDON PAIN ( 14 FDA reports)
THROMBOCYTHAEMIA ( 14 FDA reports)
VISUAL FIELD DEFECT ( 14 FDA reports)
ACTINIC KERATOSIS ( 14 FDA reports)
ANKLE FRACTURE ( 14 FDA reports)
BACK INJURY ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
BLOOD CHLORIDE DECREASED ( 14 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 14 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 14 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 14 FDA reports)
CREPITATIONS ( 14 FDA reports)
CRYING ( 14 FDA reports)
DEVICE FAILURE ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
DROOLING ( 14 FDA reports)
DRUG DOSE OMISSION ( 14 FDA reports)
ECONOMIC PROBLEM ( 14 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 14 FDA reports)
EMPHYSEMA ( 14 FDA reports)
EXERCISE TOLERANCE DECREASED ( 14 FDA reports)
FISTULA ( 14 FDA reports)
HAEMOLYSIS ( 14 FDA reports)
HEMIANOPIA HOMONYMOUS ( 14 FDA reports)
HEPATIC INFARCTION ( 14 FDA reports)
HYPOAESTHESIA ORAL ( 14 FDA reports)
INJECTION SITE WARMTH ( 14 FDA reports)
LIP BLISTER ( 14 FDA reports)
LIP ULCERATION ( 14 FDA reports)
MEDICATION RESIDUE ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
PARESIS ( 14 FDA reports)
PNEUMONIA BACTERIAL ( 14 FDA reports)
POLYMYALGIA RHEUMATICA ( 14 FDA reports)
PSEUDOMONAS INFECTION ( 14 FDA reports)
PSORIATIC ARTHROPATHY ( 14 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 14 FDA reports)
PULMONARY TUBERCULOSIS ( 14 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 14 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 14 FDA reports)
SPINAL COLUMN STENOSIS ( 14 FDA reports)
ACCIDENTAL NEEDLE STICK ( 13 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 13 FDA reports)
AUTOIMMUNE DISORDER ( 13 FDA reports)
BLOOD SODIUM INCREASED ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 13 FDA reports)
CHOLECYSTITIS ACUTE ( 13 FDA reports)
COLITIS ULCERATIVE ( 13 FDA reports)
CORNEAL ABRASION ( 13 FDA reports)
DEAFNESS UNILATERAL ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
GASTRIC CANCER ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
GROIN PAIN ( 13 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 13 FDA reports)
HEARING IMPAIRED ( 13 FDA reports)
HEPATIC CONGESTION ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
HEPATOBILIARY DISEASE ( 13 FDA reports)
INJECTION SITE BURNING ( 13 FDA reports)
INJECTION SITE EXTRAVASATION ( 13 FDA reports)
INJECTION SITE REACTION ( 13 FDA reports)
KLEBSIELLA INFECTION ( 13 FDA reports)
LACRIMATION INCREASED ( 13 FDA reports)
LICHENOID KERATOSIS ( 13 FDA reports)
LIPIDS INCREASED ( 13 FDA reports)
LOBAR PNEUMONIA ( 13 FDA reports)
LYMPHOCELE ( 13 FDA reports)
MACULAR OEDEMA ( 13 FDA reports)
MALIGNANT MELANOMA ( 13 FDA reports)
MOTOR DYSFUNCTION ( 13 FDA reports)
NECROSIS ( 13 FDA reports)
NEOPLASM PROGRESSION ( 13 FDA reports)
NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
ORAL PAIN ( 13 FDA reports)
PHOTOPHOBIA ( 13 FDA reports)
POISONING ( 13 FDA reports)
POLYARTHRITIS ( 13 FDA reports)
PROTEIN URINE PRESENT ( 13 FDA reports)
RENAL COLIC ( 13 FDA reports)
RIGHT VENTRICULAR FAILURE ( 13 FDA reports)
SENSORY LOSS ( 13 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 13 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 13 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 13 FDA reports)
TOXIC SHOCK SYNDROME ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
TRISMUS ( 12 FDA reports)
AKINESIA ( 12 FDA reports)
ANDROGENETIC ALOPECIA ( 12 FDA reports)
ANOSMIA ( 12 FDA reports)
AORTIC ANEURYSM ( 12 FDA reports)
AORTIC VALVE STENOSIS ( 12 FDA reports)
APHTHOUS STOMATITIS ( 12 FDA reports)
ARTERIAL DISORDER ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BLOOD DISORDER ( 12 FDA reports)
BRAIN DAMAGE ( 12 FDA reports)
CHOLECYSTECTOMY ( 12 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 12 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 12 FDA reports)
CROHN'S DISEASE ( 12 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 12 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 12 FDA reports)
DERMATITIS ALLERGIC ( 12 FDA reports)
DEVICE RELATED INFECTION ( 12 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 12 FDA reports)
FIBROSIS ( 12 FDA reports)
FURUNCLE ( 12 FDA reports)
GINGIVITIS ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
GYNAECOMASTIA ( 12 FDA reports)
HAEMORRHAGIC DIATHESIS ( 12 FDA reports)
HELICOBACTER INFECTION ( 12 FDA reports)
HYDROCEPHALUS ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
INCOHERENT ( 12 FDA reports)
INTENTIONAL MISUSE ( 12 FDA reports)
LIVER TRANSPLANT ( 12 FDA reports)
LOCALISED INFECTION ( 12 FDA reports)
LUMBAR SPINAL STENOSIS ( 12 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 12 FDA reports)
MANIA ( 12 FDA reports)
MEAN CELL VOLUME INCREASED ( 12 FDA reports)
MUSCLE TIGHTNESS ( 12 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 12 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 12 FDA reports)
NEUROMUSCULAR BLOCKADE ( 12 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 12 FDA reports)
NYSTAGMUS ( 12 FDA reports)
OEDEMA GENITAL ( 12 FDA reports)
OESOPHAGEAL CARCINOMA ( 12 FDA reports)
OSTEITIS ( 12 FDA reports)
PARADOXICAL DRUG REACTION ( 12 FDA reports)
PARKINSON'S DISEASE ( 12 FDA reports)
PERICARDITIS ( 12 FDA reports)
PHARYNGITIS ( 12 FDA reports)
PLEURISY ( 12 FDA reports)
RENAL INJURY ( 12 FDA reports)
RENAL NEOPLASM ( 12 FDA reports)
RHINITIS ( 12 FDA reports)
SEDATION ( 12 FDA reports)
SELF-MEDICATION ( 12 FDA reports)
SKIN IRRITATION ( 12 FDA reports)
SKIN REACTION ( 12 FDA reports)
ABDOMINAL HERNIA ( 11 FDA reports)
ADVERSE DRUG REACTION ( 11 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 11 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 11 FDA reports)
APLASTIC ANAEMIA ( 11 FDA reports)
AREFLEXIA ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BLINDNESS TRANSIENT ( 11 FDA reports)
BLOOD CALCIUM INCREASED ( 11 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 11 FDA reports)
BLOOD PRESSURE ABNORMAL ( 11 FDA reports)
BRADYKINESIA ( 11 FDA reports)
CARDIAC FAILURE CHRONIC ( 11 FDA reports)
CATHETER RELATED COMPLICATION ( 11 FDA reports)
CATHETER RELATED INFECTION ( 11 FDA reports)
DIASTOLIC DYSFUNCTION ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
EATING DISORDER ( 11 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 11 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 11 FDA reports)
EMBOLISM ( 11 FDA reports)
ERYSIPELAS ( 11 FDA reports)
FACIAL BONES FRACTURE ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
FOOD POISONING ( 11 FDA reports)
GASTROINTESTINAL NECROSIS ( 11 FDA reports)
GOITRE ( 11 FDA reports)
HALLUCINATIONS, MIXED ( 11 FDA reports)
HELICOBACTER GASTRITIS ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
HYPERTHYROIDISM ( 11 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 11 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 11 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 11 FDA reports)
INGUINAL HERNIA ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
LACUNAR INFARCTION ( 11 FDA reports)
LIVEDO RETICULARIS ( 11 FDA reports)
LUNG CANCER METASTATIC ( 11 FDA reports)
LUPUS-LIKE SYNDROME ( 11 FDA reports)
MASS ( 11 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 11 FDA reports)
MUSCLE FATIGUE ( 11 FDA reports)
MUSCLE NECROSIS ( 11 FDA reports)
OPPORTUNISTIC INFECTION ( 11 FDA reports)
ORAL DISCOMFORT ( 11 FDA reports)
ORGANISING PNEUMONIA ( 11 FDA reports)
OVERWEIGHT ( 11 FDA reports)
PAPILLOEDEMA ( 11 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
PROTHROMBIN TIME SHORTENED ( 11 FDA reports)
PULMONARY HAEMORRHAGE ( 11 FDA reports)
RESPIRATORY DEPRESSION ( 11 FDA reports)
SKIN LACERATION ( 11 FDA reports)
SPINAL DISORDER ( 11 FDA reports)
TOOTHACHE ( 11 FDA reports)
UNDERDOSE ( 11 FDA reports)
VENOUS INSUFFICIENCY ( 11 FDA reports)
VENOUS THROMBOSIS ( 11 FDA reports)
VIRAL LOAD INCREASED ( 11 FDA reports)
WOUND ( 11 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 10 FDA reports)
TACHYARRHYTHMIA ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
TOOTH LOSS ( 10 FDA reports)
VAGINAL HAEMORRHAGE ( 10 FDA reports)
WOUND SECRETION ( 10 FDA reports)
ABSCESS ( 10 FDA reports)
ABSCESS LIMB ( 10 FDA reports)
ANHEDONIA ( 10 FDA reports)
ARM AMPUTATION ( 10 FDA reports)
ASPHYXIA ( 10 FDA reports)
BLEPHARITIS ( 10 FDA reports)
BLOOD ALBUMIN INCREASED ( 10 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 10 FDA reports)
BRAIN OEDEMA ( 10 FDA reports)
BREATH SOUNDS ABNORMAL ( 10 FDA reports)
CARDIAC ANEURYSM ( 10 FDA reports)
CARDIAC OPERATION ( 10 FDA reports)
CEREBROVASCULAR DISORDER ( 10 FDA reports)
CHOKING ( 10 FDA reports)
CLOSTRIDIAL INFECTION ( 10 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 10 FDA reports)
CYST ( 10 FDA reports)
DECREASED ACTIVITY ( 10 FDA reports)
DERMATOMYOSITIS ( 10 FDA reports)
DIABETIC RETINOPATHY ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DROP ATTACKS ( 10 FDA reports)
ENTEROCOCCAL INFECTION ( 10 FDA reports)
ENTEROCOLITIS ( 10 FDA reports)
FAECALOMA ( 10 FDA reports)
FINGER DEFORMITY ( 10 FDA reports)
FRACTURE ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
HAEMOGLOBIN INCREASED ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
IATROGENIC INJURY ( 10 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 10 FDA reports)
KNEE ARTHROPLASTY ( 10 FDA reports)
LIMB INJURY ( 10 FDA reports)
LIPOMA ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
MICROALBUMINURIA ( 10 FDA reports)
MITRAL VALVE DISEASE ( 10 FDA reports)
MOUTH HAEMORRHAGE ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
NASAL POLYPS ( 10 FDA reports)
NEUROMYOPATHY ( 10 FDA reports)
NODAL ARRHYTHMIA ( 10 FDA reports)
NODULE ( 10 FDA reports)
ORAL HERPES ( 10 FDA reports)
OSTEONECROSIS OF JAW ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
PANCREATIC PSEUDOCYST ( 10 FDA reports)
PERIORBITAL OEDEMA ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
PLEURITIC PAIN ( 10 FDA reports)
POOR QUALITY SLEEP ( 10 FDA reports)
PRESCRIBED OVERDOSE ( 10 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 10 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
RASH PUSTULAR ( 10 FDA reports)
RESPIRATORY ACIDOSIS ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
SKIN HYPERTROPHY ( 10 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 10 FDA reports)
SPINAL FRACTURE ( 10 FDA reports)
ABDOMINAL ABSCESS ( 9 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 9 FDA reports)
APATHY ( 9 FDA reports)
ATROPHY ( 9 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 9 FDA reports)
BLOOD CHLORIDE INCREASED ( 9 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 9 FDA reports)
BLOOD PH DECREASED ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 9 FDA reports)
BODY HEIGHT DECREASED ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CARDIAC HYPERTROPHY ( 9 FDA reports)
CELL DEATH ( 9 FDA reports)
CEREBELLAR SYNDROME ( 9 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 9 FDA reports)
DEPRESSIVE SYMPTOM ( 9 FDA reports)
DERMATITIS ( 9 FDA reports)
DUODENAL ULCER PERFORATION ( 9 FDA reports)
EMOTIONAL DISORDER ( 9 FDA reports)
ENDOCARDITIS ( 9 FDA reports)
ENTERITIS ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
EPIGASTRIC DISCOMFORT ( 9 FDA reports)
ERYTHRASMA ( 9 FDA reports)
EXCORIATION ( 9 FDA reports)
EYE HAEMORRHAGE ( 9 FDA reports)
FEELING DRUNK ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
FOOT DEFORMITY ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
HAEMATOMA INFECTION ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HEPATIC PAIN ( 9 FDA reports)
HERNIA ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
HYPERKERATOSIS ( 9 FDA reports)
HYPOMANIA ( 9 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 9 FDA reports)
INJURY ASPHYXIATION ( 9 FDA reports)
INTESTINAL HAEMORRHAGE ( 9 FDA reports)
IRON DEFICIENCY ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
JOINT EFFUSION ( 9 FDA reports)
LACERATION ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
LYSOZYME INCREASED ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
MOOD SWINGS ( 9 FDA reports)
MULTIPLE MYELOMA ( 9 FDA reports)
MUSCLE SPASTICITY ( 9 FDA reports)
NASAL SEPTUM DEVIATION ( 9 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
NON-CARDIAC CHEST PAIN ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER ( 9 FDA reports)
OCULAR ICTERUS ( 9 FDA reports)
PANCREATIC ENZYMES INCREASED ( 9 FDA reports)
PAROSMIA ( 9 FDA reports)
PROCTOCOLITIS ( 9 FDA reports)
RASH MORBILLIFORM ( 9 FDA reports)
RENAL TUBULAR DISORDER ( 9 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 9 FDA reports)
SICK SINUS SYNDROME ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKIN TEST POSITIVE ( 9 FDA reports)
SKIN TIGHTNESS ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 9 FDA reports)
TONGUE DISCOLOURATION ( 9 FDA reports)
TOOTH ABSCESS ( 9 FDA reports)
TRANSPLANT FAILURE ( 9 FDA reports)
TROPONIN I INCREASED ( 9 FDA reports)
TROPONIN T INCREASED ( 9 FDA reports)
VARICES OESOPHAGEAL ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
VASCULAR OCCLUSION ( 9 FDA reports)
VEIN DISORDER ( 9 FDA reports)
WOUND HAEMORRHAGE ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUBILEUS ( 8 FDA reports)
SUICIDAL BEHAVIOUR ( 8 FDA reports)
SURGICAL PROCEDURE REPEATED ( 8 FDA reports)
SYNOVITIS ( 8 FDA reports)
TEARFULNESS ( 8 FDA reports)
TONGUE OEDEMA ( 8 FDA reports)
TRAUMATIC HAEMATOMA ( 8 FDA reports)
TUBERCULOSIS ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
ULCER HAEMORRHAGE ( 8 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
VITAMIN D DEFICIENCY ( 8 FDA reports)
VITREOUS HAEMORRHAGE ( 8 FDA reports)
WEGENER'S GRANULOMATOSIS ( 8 FDA reports)
WITHDRAWAL SYNDROME ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 8 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 8 FDA reports)
AMYOTROPHY ( 8 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 8 FDA reports)
AORTIC VALVE DISEASE ( 8 FDA reports)
APOLIPOPROTEIN A-I DECREASED ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM DECREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BREAST MASS ( 8 FDA reports)
CORONARY ARTERY SURGERY ( 8 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 8 FDA reports)
DEPENDENCE ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DIABETIC NEUROPATHY ( 8 FDA reports)
DRUG DISPENSING ERROR ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
DYSAESTHESIA ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
FEAR OF EATING ( 8 FDA reports)
FRACTURE DELAYED UNION ( 8 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 8 FDA reports)
HAEMANGIOMA ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 8 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 8 FDA reports)
HEPATIC ENZYME ABNORMAL ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPERPARATHYROIDISM ( 8 FDA reports)
HYPERPYREXIA ( 8 FDA reports)
HYPERVENTILATION ( 8 FDA reports)
IMPAIRED WORK ABILITY ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
LARGE INTESTINE PERFORATION ( 8 FDA reports)
LIP HAEMORRHAGE ( 8 FDA reports)
LISTLESS ( 8 FDA reports)
LYMPHOEDEMA ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
MENISCUS LESION ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
MICROCYTIC ANAEMIA ( 8 FDA reports)
MITRAL VALVE CALCIFICATION ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
NEUROPATHY ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
ODYNOPHAGIA ( 8 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 8 FDA reports)
OESOPHAGEAL RUPTURE ( 8 FDA reports)
OSTEOPENIA ( 8 FDA reports)
PANCREATIC NEOPLASM ( 8 FDA reports)
PARAESTHESIA ORAL ( 8 FDA reports)
PERITONEAL HAEMORRHAGE ( 8 FDA reports)
PNEUMONIA FUNGAL ( 8 FDA reports)
PO2 DECREASED ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POST PROCEDURAL HAEMATOMA ( 8 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 8 FDA reports)
POSTOPERATIVE INFECTION ( 8 FDA reports)
PULMONARY THROMBOSIS ( 8 FDA reports)
QUADRIPARESIS ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
RHEUMATOID NODULE ( 8 FDA reports)
SKIN WARM ( 8 FDA reports)
SOFT TISSUE DISORDER ( 8 FDA reports)
SPLEEN DISORDER ( 8 FDA reports)
SPUTUM DISCOLOURED ( 8 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 7 FDA reports)
AMAUROSIS ( 7 FDA reports)
AMMONIA INCREASED ( 7 FDA reports)
ANEURYSM ( 7 FDA reports)
AORTIC DILATATION ( 7 FDA reports)
APPLICATION SITE ERYTHEMA ( 7 FDA reports)
ARTERIAL STENOSIS ( 7 FDA reports)
ASPERGILLOSIS ( 7 FDA reports)
ATRIAL SEPTAL DEFECT ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 7 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 7 FDA reports)
BLOOD IRON DECREASED ( 7 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 7 FDA reports)
BONE DENSITY DECREASED ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CALCIPHYLAXIS ( 7 FDA reports)
CARDIAC FLUTTER ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
CHRONIC SINUSITIS ( 7 FDA reports)
COLLAPSE OF LUNG ( 7 FDA reports)
CONVERSION DISORDER ( 7 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
CUTANEOUS VASCULITIS ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG PRESCRIBING ERROR ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
EYELID DISORDER ( 7 FDA reports)
FEELING JITTERY ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
FOOT FRACTURE ( 7 FDA reports)
GALLBLADDER DISORDER ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GASTROINTESTINAL PERFORATION ( 7 FDA reports)
GOUTY ARTHRITIS ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
HUMERUS FRACTURE ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 7 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 7 FDA reports)
HYPOVENTILATION ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
INADEQUATE ANALGESIA ( 7 FDA reports)
INTENTIONAL SELF-INJURY ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
LIPIDS ABNORMAL ( 7 FDA reports)
LIPODYSTROPHY ACQUIRED ( 7 FDA reports)
LISTERIOSIS ( 7 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
MIXED LIVER INJURY ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MUSCLE SWELLING ( 7 FDA reports)
MUSCULAR DYSTROPHY ( 7 FDA reports)
NEOPLASM ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NEURITIS ( 7 FDA reports)
ORAL MUCOSAL BLISTERING ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
PANCREATIC CYST ( 7 FDA reports)
PARANEOPLASTIC SYNDROME ( 7 FDA reports)
PEMPHIGOID ( 7 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
PLATELET COUNT ABNORMAL ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
PO2 INCREASED ( 7 FDA reports)
POST PROCEDURAL PAIN ( 7 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 7 FDA reports)
PROSTATITIS ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
RENAL PAIN ( 7 FDA reports)
RENAL TRANSPLANT ( 7 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
RETCHING ( 7 FDA reports)
RETINAL HAEMORRHAGE ( 7 FDA reports)
ROTATOR CUFF SYNDROME ( 7 FDA reports)
SINUS DISORDER ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SOMNAMBULISM ( 7 FDA reports)
SUBDURAL HAEMORRHAGE ( 7 FDA reports)
SUDDEN HEARING LOSS ( 7 FDA reports)
TETANY ( 7 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
TOOTH INFECTION ( 7 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 7 FDA reports)
VAGINAL INFECTION ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VITAMIN B12 DEFICIENCY ( 7 FDA reports)
WALKING AID USER ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 6 FDA reports)
SUPERINFECTION ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
THROMBOPHLEBITIS ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
TONGUE DISORDER ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VASCULAR PURPURA ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 6 FDA reports)
ABNORMAL SENSATION IN EYE ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
ADVERSE REACTION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
AMYLASE INCREASED ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANAL SPHINCTER ATONY ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ATHEROSCLEROSIS ( 6 FDA reports)
ATRIAL TACHYCARDIA ( 6 FDA reports)
BEZOAR ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BONE MARROW DISORDER ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 6 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 6 FDA reports)
CATHETER SITE HAEMORRHAGE ( 6 FDA reports)
CATHETERISATION CARDIAC ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 6 FDA reports)
CEREBRAL DISORDER ( 6 FDA reports)
CERVIX CARCINOMA ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
COMPLEX PARTIAL SEIZURES ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 6 FDA reports)
CORONARY ANGIOPLASTY ( 6 FDA reports)
CORONARY ARTERY EMBOLISM ( 6 FDA reports)
CORONARY ARTERY REOCCLUSION ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DEVICE INTERACTION ( 6 FDA reports)
DIABETIC COMPLICATION ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
DRUG CLEARANCE DECREASED ( 6 FDA reports)
DRUG INTERACTION POTENTIATION ( 6 FDA reports)
DRUG RESISTANCE ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 6 FDA reports)
ERYTHEMA NODOSUM ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
FACIAL PAIN ( 6 FDA reports)
FEELING OF DESPAIR ( 6 FDA reports)
FOOD AVERSION ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
GRAFT LOSS ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HALO VISION ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEART TRANSPLANT REJECTION ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HEPATOJUGULAR REFLUX ( 6 FDA reports)
HERPES OPHTHALMIC ( 6 FDA reports)
HYPERLACTACIDAEMIA ( 6 FDA reports)
HYPERPLASIA ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOCHLORAEMIA ( 6 FDA reports)
HYPOGLYCAEMIC COMA ( 6 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 6 FDA reports)
INJECTION SITE BRUISING ( 6 FDA reports)
INJECTION SITE STINGING ( 6 FDA reports)
INSULIN RESISTANCE ( 6 FDA reports)
INTRACRANIAL ANEURYSM ( 6 FDA reports)
JOINT DESTRUCTION ( 6 FDA reports)
JOINT STIFFNESS ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LIBIDO DECREASED ( 6 FDA reports)
LIPOPROTEIN (A) INCREASED ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 6 FDA reports)
LOWER LIMB FRACTURE ( 6 FDA reports)
LUNG CONSOLIDATION ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
MALLORY-WEISS SYNDROME ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 6 FDA reports)
MUCOSAL EXFOLIATION ( 6 FDA reports)
NAIL DISORDER ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NEOPLASM SKIN ( 6 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 6 FDA reports)
NEURILEMMOMA BENIGN ( 6 FDA reports)
NOCTURNAL DYSPNOEA ( 6 FDA reports)
OESOPHAGEAL PAIN ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PAROTITIS ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 6 FDA reports)
PNEUMATOSIS INTESTINALIS ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
PULMONARY MASS ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
RENAL TUBULAR ACIDOSIS ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SCROTAL SWELLING ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SERRATIA BACTERAEMIA ( 6 FDA reports)
SEXUAL DYSFUNCTION ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN BLEEDING ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 6 FDA reports)
SNORING ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
ABORTION INDUCED ( 5 FDA reports)
ABSCESS JAW ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANAESTHETIC COMPLICATION ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 5 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
AORTIC DISORDER ( 5 FDA reports)
AORTIC VALVE REPLACEMENT ( 5 FDA reports)
APPLICATION SITE VESICLES ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
AUTOIMMUNE THYROIDITIS ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BENIGN GASTRIC NEOPLASM ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD MAGNESIUM INCREASED ( 5 FDA reports)
BRAIN ABSCESS ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
CAESAREAN SECTION ( 5 FDA reports)
CARBON DIOXIDE DECREASED ( 5 FDA reports)
CARDIOVERSION ( 5 FDA reports)
CAROTID ARTERY ATHEROMA ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 5 FDA reports)
CHRONIC FATIGUE SYNDROME ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CLONIC CONVULSION ( 5 FDA reports)
COLITIS COLLAGENOUS ( 5 FDA reports)
CONTRAST MEDIA REACTION ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 5 FDA reports)
ENTEROVESICAL FISTULA ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXSANGUINATION ( 5 FDA reports)
FAILURE TO THRIVE ( 5 FDA reports)
FEBRILE BONE MARROW APLASIA ( 5 FDA reports)
FIBULA FRACTURE ( 5 FDA reports)
FINE MOTOR DELAY ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
FOOD INTERACTION ( 5 FDA reports)
FOOT AMPUTATION ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GAMMOPATHY ( 5 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 5 FDA reports)
GASTRIC POLYPS ( 5 FDA reports)
GASTROINTESTINAL CARCINOMA ( 5 FDA reports)
GASTROINTESTINAL INFECTION ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GRANULOMA ANNULARE ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMATOTOXICITY ( 5 FDA reports)
HAEMOGLOBINURIA ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HAPTOGLOBIN DECREASED ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HEPATIC ISCHAEMIA ( 5 FDA reports)
HEPATORENAL FAILURE ( 5 FDA reports)
HOMICIDE ( 5 FDA reports)
HOSTILITY ( 5 FDA reports)
HYPERTRANSAMINASAEMIA ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOCHOLESTEROLAEMIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
IMPATIENCE ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INHIBITORY DRUG INTERACTION ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
IRIS DISORDER ( 5 FDA reports)
ISCHAEMIC HEPATITIS ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KLEBSIELLA SEPSIS ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LARYNGEAL DISORDER ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
MENOPAUSAL SYMPTOMS ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METASTASES TO BONE MARROW ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MICTURITION URGENCY ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MULTI-ORGAN DISORDER ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
MYOPATHY TOXIC ( 5 FDA reports)
NASAL DISORDER ( 5 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 5 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 5 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NODAL RHYTHM ( 5 FDA reports)
NOSOCOMIAL INFECTION ( 5 FDA reports)
OBSTRUCTION ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
PALMAR ERYTHEMA ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PHARYNGEAL ABSCESS ( 5 FDA reports)
PHLEBITIS SUPERFICIAL ( 5 FDA reports)
PNEUMONIA HAEMOPHILUS ( 5 FDA reports)
POOR PERIPHERAL CIRCULATION ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PROSTATE CANCER RECURRENT ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
READING DISORDER ( 5 FDA reports)
REBOUND EFFECT ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
RETROPERITONEAL FIBROSIS ( 5 FDA reports)
SCAB ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SENSE OF OPPRESSION ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SHUNT OCCLUSION ( 5 FDA reports)
SHUNT THROMBOSIS ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SKIN DESQUAMATION ( 5 FDA reports)
SKIN FIBROSIS ( 5 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPLENIC INFARCTION ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
STEATORRHOEA ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
TERMINAL INSOMNIA ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TONGUE DRY ( 5 FDA reports)
TRANSAMINASES ABNORMAL ( 5 FDA reports)
URETHRAL HAEMORRHAGE ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
VASCULAR GRAFT COMPLICATION ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VOCAL CORD POLYPECTOMY ( 5 FDA reports)
VULVITIS ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
STRESS SYMPTOMS ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TOXIC OPTIC NEUROPATHY ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 4 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URINOMA ( 4 FDA reports)
VANISHING BILE DUCT SYNDROME ( 4 FDA reports)
VASCULAR DEMENTIA ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VASCULITIC RASH ( 4 FDA reports)
VASCULITIS NECROTISING ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 4 FDA reports)
VULVAL CANCER ( 4 FDA reports)
VULVOVAGINAL DRYNESS ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
XANTHOPSIA ( 4 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ADHESION ( 4 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC VALVE CALCIFICATION ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APOLIPOPROTEIN A-I INCREASED ( 4 FDA reports)
APPLICATION SITE DISCOLOURATION ( 4 FDA reports)
APPLICATION SITE HAEMATOMA ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASPIRATION BONE MARROW ( 4 FDA reports)
AUTISM ( 4 FDA reports)
BACTEROIDES INFECTION ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BILE DUCT NECROSIS ( 4 FDA reports)
BIOPSY BONE MARROW ( 4 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE EROSION ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRAIN SCAN ABNORMAL ( 4 FDA reports)
BREAST CANCER MALE ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CALCULUS URINARY ( 4 FDA reports)
CARBON DIOXIDE ABNORMAL ( 4 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
CLUBBING ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COGWHEEL RIGIDITY ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLLAGEN DISORDER ( 4 FDA reports)
COLON ADENOMA ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
CONGENITAL HEPATOMEGALY ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CONJUNCTIVAL OEDEMA ( 4 FDA reports)
COOMBS TEST POSITIVE ( 4 FDA reports)
CORONARY BYPASS THROMBOSIS ( 4 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DEVICE OCCLUSION ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC MICROANGIOPATHY ( 4 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENDOMETRIAL CANCER ( 4 FDA reports)
ENDOMETRIAL DISORDER ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ENTEROCOLITIS VIRAL ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
EOSINOPHILIC FASCIITIS ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
FABRY'S DISEASE ( 4 FDA reports)
FACE INJURY ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 4 FDA reports)
GASTROINTESTINAL OEDEMA ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GINGIVAL PAIN ( 4 FDA reports)
GINGIVITIS ULCERATIVE ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HEPATITIS C POSITIVE ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFECTIVE TENOSYNOVITIS ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
INTENTION TREMOR ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
INTRAPERICARDIAL THROMBOSIS ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRON METABOLISM DISORDER ( 4 FDA reports)
IRON OVERLOAD ( 4 FDA reports)
ITCHING SCAR ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LACRIMAL DISORDER ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LICHEN PLANUS ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MASTITIS ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METASTASES TO ADRENALS ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
METASTASES TO SKIN ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NITRITOID REACTION ( 4 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
OVARIAN NEOPLASM ( 4 FDA reports)
PAIN EXACERBATED ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATIC ATROPHY ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PENIS DISORDER ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL TUBERCULOSIS ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PLASMACYTOMA ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POSTOPERATIVE ABSCESS ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
PYURIA ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
REITER'S SYNDROME ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETROGRADE AMNESIA ( 4 FDA reports)
SALIVARY GLAND NEOPLASM ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SPIDER VEIN ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
ALVEOLAR SOFT PART SARCOMA ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BASOPHIL COUNT DECREASED ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIARY FIBROSIS ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLADDER CANCER RECURRENT ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARNITINE DECREASED ( 3 FDA reports)
CAROTID BRUIT ( 3 FDA reports)
CATAPLEXY ( 3 FDA reports)
CATARACT OPERATION COMPLICATION ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL HYPOPERFUSION ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DENGUE FEVER ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG INTERACTION INHIBITION ( 3 FDA reports)
DRUG LEVEL CHANGED ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
EJECTION FRACTION ABNORMAL ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ERECTION INCREASED ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERNIA PAIN ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
ILIAC VEIN OCCLUSION ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 3 FDA reports)
INTERCOSTAL NEURALGIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTUBATION COMPLICATION ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JOINT LOCK ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LEUKOENCEPHALOMYELITIS ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
MACROSOMIA ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 3 FDA reports)
MEGAKARYOCYTES INCREASED ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTASES TO OVARY ( 3 FDA reports)
MITRAL VALVE DISEASE MIXED ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
NAIL PITTING ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
NITRITOID CRISIS ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PENILE OEDEMA ( 3 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 3 FDA reports)
PERIANAL ABSCESS ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
PERIPROSTHETIC FRACTURE ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PEYRONIE'S DISEASE ( 3 FDA reports)
PHAEOCHROMOCYTOMA ( 3 FDA reports)
PHOBIA ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PLEURAL DECORTICATION ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PNEUMONIA CHLAMYDIAL ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTINFARCTION ANGINA ( 3 FDA reports)
POSTOPERATIVE FEVER ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PRURITUS ANI ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RENAL ISCHAEMIA ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
RINNE TUNING FORK TEST ABNORMAL ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCROTAL HAEMATOMA ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SERONEGATIVE ARTHRITIS ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKIN TEST NEGATIVE ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STAB WOUND ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
TENSION ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOEMBOLECTOMY ( 3 FDA reports)
THYROID CYST ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TONSILLAR INFLAMMATION ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TROPONIN ( 3 FDA reports)
TROUSSEAU'S SYNDROME ( 3 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 3 FDA reports)
URETERAL NECROSIS ( 3 FDA reports)
URINARY ANASTOMOTIC LEAK ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VASCULAR ANOMALY ( 3 FDA reports)
VASCULAR ENCEPHALOPATHY ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIIITH NERVE INJURY ( 3 FDA reports)
VITAL CAPACITY DECREASED ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TERATOMA ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THORACOSTOMY ( 2 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TYPHOID FEVER ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULTRASOUND BILIARY TRACT ( 2 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY FISTULA ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VACCINATION FAILURE ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VASCULAR NEOPLASM ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VESSEL PERFORATION ( 2 FDA reports)
VESTIBULAR ATAXIA ( 2 FDA reports)
VIRAL TEST POSITIVE ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WEST NILE VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID DECREASED ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABORTED PREGNANCY ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADMINISTRATION SITE REACTION ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALOPECIA UNIVERSALIS ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMNIOTIC BAND SYNDROME ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL NEOPLASM ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANENCEPHALY ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGIOGRAM PULMONARY ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTICHOLINERGIC SYNDROME ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTERITIS OBLITERANS ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ATRIAL PRESSURE INCREASED ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACILLARY ANGIOMATOSIS ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BASE EXCESS DECREASED ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BENIGN PERITONEAL NEOPLASM ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BLADDER CONSTRICTION ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER GRANULOMA ( 2 FDA reports)
BLADDER SPHINCTER ATONY ( 2 FDA reports)
BLADDER STENOSIS ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BORRELIA INFECTION ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOMA IN SITU OF BLADDER ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CATECHOLAMINES URINE INCREASED ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR HAEMATOMA ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBRAL VASOCONSTRICTION ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLESTEROL GRANULOMA ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHROMOSOMAL MUTATION ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
COPPER DEFICIENCY ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
CRANIOPHARYNGIOMA ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DECREASED VIBRATORY SENSE ( 2 FDA reports)
DEFICIENCY OF BILE SECRETION ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISORDER OF GLOBE ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
EPIDIDYMAL INFECTION ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
ERYTHROBLASTOSIS ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAT ATROPHY ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBRINOLYSIS ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL OEDEMA ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHAGIC FEVER ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEARING DISABILITY ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYDROCHOLECYSTIS ( 2 FDA reports)
HYDROMETRA ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTERMEDIATE UVEITIS ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL FISTULA INFECTION ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRIDOCELE ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JEALOUS DELUSION ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARGE INTESTINAL STRICTURE ( 2 FDA reports)
LARYNGEAL OPERATION ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIGAMENT LAXITY ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIVER INDURATION ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MICROSCOPIC POLYANGIITIS ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOSCLEROSIS ( 2 FDA reports)
NAIL BED TENDERNESS ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEPHROANGIOSCLEROSIS ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROSYPHILIS ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NOSE DEFORMITY ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OSTEOARTHROPATHY ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN ATROPHY ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 2 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 2 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RECTAL CANCER STAGE I ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REGRESSIVE BEHAVIOUR ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SELECTIVE MUTISM ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SINGLE UMBILICAL ARTERY ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STARING ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCESSORY SPLEEN ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACQUIRED PORPHYRIA ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALEXIA ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALPHA 1 GLOBULIN ABNORMAL ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC CAVITY DISORDER ( 1 FDA reports)
AMNIOTIC CAVITY INFECTION ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANEURYSM ARTERIOVENOUS ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOKERATOMA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST SENSITIVE ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC WALL HYPERTROPHY ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BECKER'S MUSCULAR DYSTROPHY ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY PROSTATE ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CANCER STAGE II ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PROINSULIN INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAST ADENOMA ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ANEURYSM RUPTURE ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE ABNORMAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL CONISATION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVIX CARCINOMA STAGE I ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLEDOCHAL CYST ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR C1 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONJUNCTIVAL BLEB ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL STAINING ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY NO-REFLOW PHENOMENON ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
COXSACKIE VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIORACHISCHISIS ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DECREASED INSULIN REQUIREMENT ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DEPRESSIVE DELUSION ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC DERMOPATHY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC MACROANGIOPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOMETRIAL ADENOMA ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENDOMETRIAL DYSPLASIA ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIOMA ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FREE THYROXINE INDEX INCREASED ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL PARONYCHIA ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC DYSPLASIA ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOTTIS CARCINOMA ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAM STAIN NEGATIVE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMODYNAMIC REBOUND ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HERNIA GANGRENOUS ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAUNDICE HEPATOCELLULAR ( 1 FDA reports)
JESSNER'S LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT LIGAMENT RUPTURE ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
JUVENILE MELANOMA BENIGN ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEG CRUSHING ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MALIGNANT NEOPLASM OF CORNEA ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENISCUS REMOVAL ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO FALLOPIAN TUBE ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE LENTIGINES SYNDROME ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOBLAST COUNT INCREASED ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESTROGENIC EFFECT ( 1 FDA reports)
OLFACTORY TEST ABNORMAL ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARASITE BLOOD TEST POSITIVE ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID REIMPLANTATION ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC KIDNEY ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERINEAL INDURATION ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONEAL CANDIDIASIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PITUITARY HYPOPLASIA ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTPARTUM HYPOPITUITARISM ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
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PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
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PROSTATIC MASS ( 1 FDA reports)
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PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
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PROTRUSION TONGUE ( 1 FDA reports)
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PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
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PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
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PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
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RADIATION MUCOSITIS ( 1 FDA reports)
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RADIOISOTOPE SCAN ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
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RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
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REACTION TO COLOURING ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL AGENESIS ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
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RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
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RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
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RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
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RETROPERITONEAL OEDEMA ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
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RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID NODULE REMOVAL ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
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SALMONELLOSIS ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
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SCINTIGRAPHY ( 1 FDA reports)
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SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
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SECONDARY SYPHILIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
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SKIN TURGOR DECREASED ( 1 FDA reports)
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SKULL FRACTURE ( 1 FDA reports)
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SPINA BIFIDA ( 1 FDA reports)
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SPINAL CORD INJURY CAUDA EQUINA ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
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SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
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TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
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TUBERCULOSIS BLADDER ( 1 FDA reports)
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TYPE I HYPERSENSITIVITY ( 1 FDA reports)
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