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

RENAL FAILURE ACUTE ( 572 FDA reports)
DRUG INTERACTION ( 536 FDA reports)
DYSPNOEA ( 467 FDA reports)
NAUSEA ( 412 FDA reports)
FATIGUE ( 373 FDA reports)
VOMITING ( 367 FDA reports)
PYREXIA ( 356 FDA reports)
DIARRHOEA ( 349 FDA reports)
MALAISE ( 326 FDA reports)
HYPOTENSION ( 325 FDA reports)
RENAL FAILURE ( 302 FDA reports)
DIZZINESS ( 300 FDA reports)
FALL ( 282 FDA reports)
ASTHENIA ( 281 FDA reports)
ANAEMIA ( 280 FDA reports)
MYOCARDIAL INFARCTION ( 275 FDA reports)
MYALGIA ( 268 FDA reports)
ATRIAL FIBRILLATION ( 254 FDA reports)
RHABDOMYOLYSIS ( 253 FDA reports)
PNEUMONIA ( 251 FDA reports)
PAIN ( 246 FDA reports)
CHEST PAIN ( 237 FDA reports)
HYPERTENSION ( 233 FDA reports)
CONFUSIONAL STATE ( 221 FDA reports)
HEADACHE ( 213 FDA reports)
DEHYDRATION ( 211 FDA reports)
OEDEMA PERIPHERAL ( 197 FDA reports)
CARDIAC ARREST ( 194 FDA reports)
DRUG INEFFECTIVE ( 187 FDA reports)
SEPSIS ( 180 FDA reports)
HAEMOGLOBIN DECREASED ( 177 FDA reports)
URINARY TRACT INFECTION ( 175 FDA reports)
BLOOD CREATININE INCREASED ( 168 FDA reports)
DEATH ( 168 FDA reports)
ABDOMINAL PAIN ( 166 FDA reports)
CARDIAC FAILURE ( 166 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 163 FDA reports)
SYNCOPE ( 159 FDA reports)
WEIGHT DECREASED ( 159 FDA reports)
ARTHRALGIA ( 158 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 158 FDA reports)
CEREBROVASCULAR ACCIDENT ( 156 FDA reports)
DIABETES MELLITUS ( 153 FDA reports)
BACK PAIN ( 150 FDA reports)
CONSTIPATION ( 150 FDA reports)
BLOOD GLUCOSE INCREASED ( 148 FDA reports)
RESPIRATORY FAILURE ( 147 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 145 FDA reports)
DECREASED APPETITE ( 144 FDA reports)
THROMBOCYTOPENIA ( 143 FDA reports)
HYPERKALAEMIA ( 141 FDA reports)
CONDITION AGGRAVATED ( 140 FDA reports)
PAIN IN EXTREMITY ( 140 FDA reports)
PRURITUS ( 139 FDA reports)
LOSS OF CONSCIOUSNESS ( 137 FDA reports)
MULTI-ORGAN FAILURE ( 136 FDA reports)
COUGH ( 135 FDA reports)
HYPERHIDROSIS ( 135 FDA reports)
HYPOGLYCAEMIA ( 133 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 132 FDA reports)
ANXIETY ( 131 FDA reports)
MUSCULAR WEAKNESS ( 129 FDA reports)
DEPRESSION ( 126 FDA reports)
BRADYCARDIA ( 125 FDA reports)
PARAESTHESIA ( 124 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 123 FDA reports)
RENAL IMPAIRMENT ( 123 FDA reports)
SOMNOLENCE ( 122 FDA reports)
WEIGHT INCREASED ( 122 FDA reports)
HYPONATRAEMIA ( 118 FDA reports)
CONVULSION ( 116 FDA reports)
LACTIC ACIDOSIS ( 115 FDA reports)
MUSCLE SPASMS ( 113 FDA reports)
RASH ( 113 FDA reports)
PLEURAL EFFUSION ( 111 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 109 FDA reports)
GAIT DISTURBANCE ( 109 FDA reports)
LETHARGY ( 108 FDA reports)
TACHYCARDIA ( 105 FDA reports)
HALLUCINATION ( 103 FDA reports)
RECTAL HAEMORRHAGE ( 103 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 99 FDA reports)
ANGINA PECTORIS ( 98 FDA reports)
ERYTHEMA ( 98 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 96 FDA reports)
OEDEMA ( 96 FDA reports)
DYSPEPSIA ( 94 FDA reports)
NEUTROPENIA ( 94 FDA reports)
CORONARY ARTERY DISEASE ( 93 FDA reports)
TREMOR ( 93 FDA reports)
HYPOKALAEMIA ( 92 FDA reports)
OVERDOSE ( 91 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 90 FDA reports)
PULMONARY OEDEMA ( 90 FDA reports)
ABDOMINAL PAIN UPPER ( 89 FDA reports)
HAEMORRHAGE ( 88 FDA reports)
CHILLS ( 87 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 86 FDA reports)
PULMONARY EMBOLISM ( 86 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 85 FDA reports)
BLOOD PRESSURE INCREASED ( 83 FDA reports)
MELAENA ( 83 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 82 FDA reports)
AGITATION ( 81 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 81 FDA reports)
PALPITATIONS ( 78 FDA reports)
INSOMNIA ( 77 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 75 FDA reports)
PANCYTOPENIA ( 75 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 75 FDA reports)
ARRHYTHMIA ( 74 FDA reports)
DISORIENTATION ( 74 FDA reports)
VISION BLURRED ( 73 FDA reports)
INTERSTITIAL LUNG DISEASE ( 71 FDA reports)
DYSPHAGIA ( 70 FDA reports)
HYPERGLYCAEMIA ( 70 FDA reports)
MYOCARDIAL ISCHAEMIA ( 70 FDA reports)
RENAL FAILURE CHRONIC ( 70 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 69 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 69 FDA reports)
COMPLETED SUICIDE ( 68 FDA reports)
CONTUSION ( 68 FDA reports)
HAEMATURIA ( 68 FDA reports)
HEART RATE INCREASED ( 67 FDA reports)
CARDIO-RESPIRATORY ARREST ( 66 FDA reports)
DEEP VEIN THROMBOSIS ( 66 FDA reports)
HYPERSENSITIVITY ( 66 FDA reports)
BLOOD PRESSURE DECREASED ( 65 FDA reports)
MENTAL STATUS CHANGES ( 65 FDA reports)
HYPOAESTHESIA ( 64 FDA reports)
MYOPATHY ( 64 FDA reports)
METABOLIC ACIDOSIS ( 63 FDA reports)
CARDIOGENIC SHOCK ( 62 FDA reports)
COMA ( 62 FDA reports)
FEELING ABNORMAL ( 62 FDA reports)
GASTRITIS ( 62 FDA reports)
HEPATIC FAILURE ( 62 FDA reports)
NEUTROPHIL COUNT INCREASED ( 62 FDA reports)
SEPTIC SHOCK ( 61 FDA reports)
PANCREATITIS ( 60 FDA reports)
PLATELET COUNT DECREASED ( 60 FDA reports)
INJURY ( 59 FDA reports)
LEUKOPENIA ( 59 FDA reports)
STAPHYLOCOCCAL INFECTION ( 59 FDA reports)
SUICIDAL IDEATION ( 59 FDA reports)
URINARY RETENTION ( 59 FDA reports)
HAEMATOMA ( 58 FDA reports)
AMNESIA ( 57 FDA reports)
ANGIOEDEMA ( 57 FDA reports)
BURNING SENSATION ( 57 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 57 FDA reports)
HYPOCALCAEMIA ( 57 FDA reports)
PULMONARY FIBROSIS ( 57 FDA reports)
BLOOD BILIRUBIN INCREASED ( 56 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 56 FDA reports)
INFECTION ( 56 FDA reports)
CARDIAC DISORDER ( 55 FDA reports)
DYSARTHRIA ( 55 FDA reports)
HAEMATEMESIS ( 55 FDA reports)
HYPOXIA ( 55 FDA reports)
JAUNDICE ( 55 FDA reports)
PANCREATITIS ACUTE ( 55 FDA reports)
BALANCE DISORDER ( 54 FDA reports)
CYTOLYTIC HEPATITIS ( 54 FDA reports)
DYSKINESIA ( 54 FDA reports)
HEPATITIS ( 54 FDA reports)
RASH ERYTHEMATOUS ( 54 FDA reports)
URTICARIA ( 54 FDA reports)
CARDIAC MURMUR ( 53 FDA reports)
HEPATIC ENZYME INCREASED ( 53 FDA reports)
CELLULITIS ( 52 FDA reports)
EPISTAXIS ( 52 FDA reports)
PALLOR ( 52 FDA reports)
SINUS TACHYCARDIA ( 52 FDA reports)
VENTRICULAR TACHYCARDIA ( 52 FDA reports)
CHEST DISCOMFORT ( 51 FDA reports)
HAEMODIALYSIS ( 51 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 50 FDA reports)
SKIN DISCOLOURATION ( 50 FDA reports)
HYPOTHYROIDISM ( 49 FDA reports)
MEMORY IMPAIRMENT ( 49 FDA reports)
OFF LABEL USE ( 49 FDA reports)
ASTHMA ( 48 FDA reports)
CIRCULATORY COLLAPSE ( 48 FDA reports)
EMOTIONAL DISTRESS ( 48 FDA reports)
DYSPNOEA EXERTIONAL ( 47 FDA reports)
HAEMATOCRIT DECREASED ( 47 FDA reports)
HIATUS HERNIA ( 47 FDA reports)
LEUKOCYTOSIS ( 47 FDA reports)
ANGINA UNSTABLE ( 46 FDA reports)
JOINT SWELLING ( 46 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 46 FDA reports)
HYPOMAGNESAEMIA ( 45 FDA reports)
ABDOMINAL DISTENSION ( 44 FDA reports)
ABORTION SPONTANEOUS ( 44 FDA reports)
BLOOD UREA INCREASED ( 44 FDA reports)
BRONCHITIS ( 44 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 44 FDA reports)
FEAR OF EATING ( 44 FDA reports)
ORTHOSTATIC HYPOTENSION ( 44 FDA reports)
ABDOMINAL TENDERNESS ( 43 FDA reports)
ACUTE CORONARY SYNDROME ( 43 FDA reports)
CHOLESTASIS ( 43 FDA reports)
FEAR ( 43 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 43 FDA reports)
IRON DEFICIENCY ANAEMIA ( 43 FDA reports)
OLIGURIA ( 43 FDA reports)
RESPIRATORY ARREST ( 43 FDA reports)
VERTIGO ( 43 FDA reports)
ALOPECIA ( 42 FDA reports)
LUNG DISORDER ( 42 FDA reports)
MOBILITY DECREASED ( 42 FDA reports)
UNEVALUABLE EVENT ( 42 FDA reports)
DISEASE PROGRESSION ( 41 FDA reports)
HYPERLIPIDAEMIA ( 41 FDA reports)
NEUROPATHY PERIPHERAL ( 41 FDA reports)
SPEECH DISORDER ( 41 FDA reports)
AKATHISIA ( 40 FDA reports)
FEBRILE NEUTROPENIA ( 40 FDA reports)
RASH MACULO-PAPULAR ( 40 FDA reports)
SKIN DISORDER ( 40 FDA reports)
THROMBOCYTOSIS ( 40 FDA reports)
BLOOD POTASSIUM INCREASED ( 39 FDA reports)
LIVER DISORDER ( 39 FDA reports)
MEDICATION ERROR ( 39 FDA reports)
MUSCULOSKELETAL PAIN ( 39 FDA reports)
PHYSICAL ASSAULT ( 39 FDA reports)
WHEEZING ( 39 FDA reports)
ANURIA ( 38 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 38 FDA reports)
HAEMORRHOIDS ( 38 FDA reports)
HYPOPHAGIA ( 38 FDA reports)
INJECTION SITE PAIN ( 38 FDA reports)
LIP SWELLING ( 38 FDA reports)
THROMBOSIS ( 38 FDA reports)
DRUG TOXICITY ( 37 FDA reports)
RESPIRATORY DISTRESS ( 37 FDA reports)
ACUTE HEPATIC FAILURE ( 36 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 36 FDA reports)
CORONARY ARTERY STENOSIS ( 36 FDA reports)
FLUSHING ( 36 FDA reports)
GOUT ( 36 FDA reports)
GRAND MAL CONVULSION ( 36 FDA reports)
NARCOTIC INTOXICATION ( 36 FDA reports)
NASOPHARYNGITIS ( 36 FDA reports)
SWELLING FACE ( 36 FDA reports)
ATRIAL FLUTTER ( 35 FDA reports)
BLOOD ALBUMIN DECREASED ( 35 FDA reports)
COAGULOPATHY ( 35 FDA reports)
DRUG LEVEL INCREASED ( 35 FDA reports)
DRY MOUTH ( 35 FDA reports)
DRY SKIN ( 35 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 35 FDA reports)
RENAL TUBULAR NECROSIS ( 35 FDA reports)
UNRESPONSIVE TO STIMULI ( 35 FDA reports)
AGGRESSION ( 34 FDA reports)
BLOOD GLUCOSE DECREASED ( 34 FDA reports)
BLOOD SODIUM DECREASED ( 34 FDA reports)
BODY MASS INDEX DECREASED ( 34 FDA reports)
HEMIPARESIS ( 34 FDA reports)
MEAN CELL VOLUME DECREASED ( 34 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 34 FDA reports)
SINUS BRADYCARDIA ( 34 FDA reports)
SKIN EXFOLIATION ( 34 FDA reports)
ABASIA ( 33 FDA reports)
ASPIRATION ( 33 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 33 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 33 FDA reports)
GASTRITIS EROSIVE ( 33 FDA reports)
NEPHROLITHIASIS ( 33 FDA reports)
PNEUMONIA ASPIRATION ( 33 FDA reports)
PNEUMONITIS ( 33 FDA reports)
RENAL INJURY ( 33 FDA reports)
ANAPHYLACTIC SHOCK ( 32 FDA reports)
ARTHRITIS ( 32 FDA reports)
BLOOD POTASSIUM DECREASED ( 32 FDA reports)
CEREBRAL HAEMORRHAGE ( 32 FDA reports)
DELIRIUM ( 32 FDA reports)
GASTRIC ULCER ( 32 FDA reports)
GASTROENTERITIS ( 32 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 32 FDA reports)
PROTEINURIA ( 32 FDA reports)
PROTHROMBIN TIME PROLONGED ( 32 FDA reports)
RENAL PAIN ( 32 FDA reports)
SINUSITIS ( 32 FDA reports)
SWOLLEN TONGUE ( 32 FDA reports)
BONE PAIN ( 31 FDA reports)
DYSGEUSIA ( 31 FDA reports)
IMPAIRED HEALING ( 31 FDA reports)
ISCHAEMIC STROKE ( 31 FDA reports)
OESOPHAGITIS ( 31 FDA reports)
ANHEDONIA ( 30 FDA reports)
ANOREXIA ( 30 FDA reports)
APHASIA ( 30 FDA reports)
ENCEPHALOPATHY ( 30 FDA reports)
HEART RATE DECREASED ( 30 FDA reports)
MOUTH ULCERATION ( 30 FDA reports)
SEROTONIN SYNDROME ( 30 FDA reports)
STRESS ( 30 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 30 FDA reports)
TYPE 2 DIABETES MELLITUS ( 30 FDA reports)
BLISTER ( 29 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 29 FDA reports)
CORONARY ARTERY OCCLUSION ( 29 FDA reports)
DUODENAL ULCER ( 29 FDA reports)
MITRAL VALVE INCOMPETENCE ( 29 FDA reports)
MONOCYTE COUNT INCREASED ( 29 FDA reports)
OBESITY ( 29 FDA reports)
PROSTATE CANCER ( 29 FDA reports)
PSYCHOTIC DISORDER ( 29 FDA reports)
RHEUMATOID ARTHRITIS ( 29 FDA reports)
SWELLING ( 29 FDA reports)
TACHYPNOEA ( 29 FDA reports)
TREATMENT NONCOMPLIANCE ( 29 FDA reports)
ANAPHYLACTIC REACTION ( 28 FDA reports)
CATARACT ( 28 FDA reports)
CHROMATURIA ( 28 FDA reports)
COGNITIVE DISORDER ( 28 FDA reports)
DRUG HYPERSENSITIVITY ( 28 FDA reports)
ECCHYMOSIS ( 28 FDA reports)
ERECTILE DYSFUNCTION ( 28 FDA reports)
HYPOTHERMIA ( 28 FDA reports)
INFLUENZA LIKE ILLNESS ( 28 FDA reports)
OROPHARYNGEAL PAIN ( 28 FDA reports)
TRANSAMINASES INCREASED ( 28 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 28 FDA reports)
VENTRICULAR FIBRILLATION ( 28 FDA reports)
ASCITES ( 27 FDA reports)
CORONARY ARTERY THROMBOSIS ( 27 FDA reports)
DISTURBANCE IN ATTENTION ( 27 FDA reports)
INFLAMMATION ( 27 FDA reports)
NEPHROPATHY ( 27 FDA reports)
OSTEOARTHRITIS ( 27 FDA reports)
OSTEONECROSIS ( 27 FDA reports)
VISUAL ACUITY REDUCED ( 27 FDA reports)
ABDOMINAL DISCOMFORT ( 26 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 26 FDA reports)
BRONCHOPNEUMONIA ( 26 FDA reports)
CHOLELITHIASIS ( 26 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 26 FDA reports)
HYPERCHOLESTEROLAEMIA ( 26 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 26 FDA reports)
LUNG NEOPLASM MALIGNANT ( 26 FDA reports)
MIOSIS ( 26 FDA reports)
MYOSITIS ( 26 FDA reports)
PRESYNCOPE ( 26 FDA reports)
URINE OUTPUT DECREASED ( 26 FDA reports)
VASCULITIS ( 26 FDA reports)
APOLIPOPROTEIN A-I DECREASED ( 25 FDA reports)
ARTERIOSCLEROSIS ( 25 FDA reports)
DIPLOPIA ( 25 FDA reports)
EOSINOPHILIA ( 25 FDA reports)
HAEMODYNAMIC INSTABILITY ( 25 FDA reports)
HEAD INJURY ( 25 FDA reports)
HEPATIC STEATOSIS ( 25 FDA reports)
HEPATOCELLULAR INJURY ( 25 FDA reports)
IRRITABILITY ( 25 FDA reports)
NECK PAIN ( 25 FDA reports)
OESOPHAGEAL ULCER ( 25 FDA reports)
PERICARDIAL EFFUSION ( 25 FDA reports)
POST PROCEDURAL COMPLICATION ( 25 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 25 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 25 FDA reports)
WHITE BLOOD CELL DISORDER ( 25 FDA reports)
AGRANULOCYTOSIS ( 24 FDA reports)
BLOOD CALCIUM DECREASED ( 24 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 24 FDA reports)
DEPRESSED MOOD ( 24 FDA reports)
DYSURIA ( 24 FDA reports)
HALLUCINATION, VISUAL ( 24 FDA reports)
INJECTION SITE ERYTHEMA ( 24 FDA reports)
LIVER INJURY ( 24 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 24 FDA reports)
MYASTHENIA GRAVIS ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 24 FDA reports)
PRODUCT QUALITY ISSUE ( 24 FDA reports)
PURPURA ( 24 FDA reports)
RENAL DISORDER ( 24 FDA reports)
SLEEP DISORDER ( 24 FDA reports)
SUICIDE ATTEMPT ( 24 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 24 FDA reports)
VISUAL IMPAIRMENT ( 24 FDA reports)
ABNORMAL BEHAVIOUR ( 23 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 23 FDA reports)
ACUTE PULMONARY OEDEMA ( 23 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 23 FDA reports)
BODY TEMPERATURE INCREASED ( 23 FDA reports)
COLITIS ( 23 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 23 FDA reports)
HAEMOPTYSIS ( 23 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 23 FDA reports)
ILEUS ( 23 FDA reports)
MYOCLONUS ( 23 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 23 FDA reports)
PERIPHERAL ISCHAEMIA ( 23 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 23 FDA reports)
PSORIASIS ( 23 FDA reports)
RESPIRATORY TRACT INFECTION ( 23 FDA reports)
SHOCK ( 23 FDA reports)
SLEEP APNOEA SYNDROME ( 23 FDA reports)
THROMBOSIS IN DEVICE ( 23 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 22 FDA reports)
BASAL CELL CARCINOMA ( 22 FDA reports)
CARDIOMEGALY ( 22 FDA reports)
CEREBRAL HAEMATOMA ( 22 FDA reports)
CREPITATIONS ( 22 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 22 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 22 FDA reports)
EATING DISORDER ( 22 FDA reports)
EJECTION FRACTION DECREASED ( 22 FDA reports)
EPILEPSY ( 22 FDA reports)
FACE OEDEMA ( 22 FDA reports)
FEELING COLD ( 22 FDA reports)
FEELING HOT ( 22 FDA reports)
FLUID RETENTION ( 22 FDA reports)
GASTROINTESTINAL DISORDER ( 22 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 22 FDA reports)
HEPATOMEGALY ( 22 FDA reports)
MYELODYSPLASTIC SYNDROME ( 22 FDA reports)
NERVOUSNESS ( 22 FDA reports)
NIGHTMARE ( 22 FDA reports)
ORAL CANDIDIASIS ( 22 FDA reports)
PULMONARY CONGESTION ( 22 FDA reports)
RASH PRURITIC ( 22 FDA reports)
SHOCK HAEMORRHAGIC ( 22 FDA reports)
SKIN WARM ( 22 FDA reports)
STEVENS-JOHNSON SYNDROME ( 22 FDA reports)
SUDDEN DEATH ( 22 FDA reports)
ACIDOSIS ( 21 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 21 FDA reports)
CARDIAC FAILURE ACUTE ( 21 FDA reports)
DEMENTIA ( 21 FDA reports)
INTENTIONAL DRUG MISUSE ( 21 FDA reports)
MENTAL DISORDER ( 21 FDA reports)
MENTAL IMPAIRMENT ( 21 FDA reports)
MUCOSAL INFLAMMATION ( 21 FDA reports)
MUSCLE DISORDER ( 21 FDA reports)
NEPHROPATHY TOXIC ( 21 FDA reports)
PLATELET COUNT INCREASED ( 21 FDA reports)
RHINORRHOEA ( 21 FDA reports)
ROAD TRAFFIC ACCIDENT ( 21 FDA reports)
SCAR ( 21 FDA reports)
TROPONIN INCREASED ( 21 FDA reports)
URINARY INCONTINENCE ( 21 FDA reports)
WITHDRAWAL SYNDROME ( 21 FDA reports)
ANDROGENETIC ALOPECIA ( 20 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 20 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 20 FDA reports)
EYE SWELLING ( 20 FDA reports)
FLUID OVERLOAD ( 20 FDA reports)
HAEMATOCHEZIA ( 20 FDA reports)
HALLUCINATION, AUDITORY ( 20 FDA reports)
HYPOVOLAEMIC SHOCK ( 20 FDA reports)
INCORRECT DOSE ADMINISTERED ( 20 FDA reports)
INFARCTION ( 20 FDA reports)
LIMB INJURY ( 20 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 20 FDA reports)
NEPHROTIC SYNDROME ( 20 FDA reports)
PERITONITIS ( 20 FDA reports)
RASH GENERALISED ( 20 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 20 FDA reports)
ALVEOLITIS ( 19 FDA reports)
AORTIC ANEURYSM ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 19 FDA reports)
BLOOD MAGNESIUM DECREASED ( 19 FDA reports)
CEREBRAL ISCHAEMIA ( 19 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 19 FDA reports)
COLD SWEAT ( 19 FDA reports)
COLITIS ISCHAEMIC ( 19 FDA reports)
DIVERTICULITIS ( 19 FDA reports)
DRUG DISPENSING ERROR ( 19 FDA reports)
GROIN PAIN ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
INFLUENZA ( 19 FDA reports)
INJECTION SITE HAEMORRHAGE ( 19 FDA reports)
JAUNDICE CHOLESTATIC ( 19 FDA reports)
MUSCLE ATROPHY ( 19 FDA reports)
PANCREATIC CARCINOMA ( 19 FDA reports)
PERIPHERAL COLDNESS ( 19 FDA reports)
PULMONARY HYPERTENSION ( 19 FDA reports)
RESTLESS LEGS SYNDROME ( 19 FDA reports)
SKIN BURNING SENSATION ( 19 FDA reports)
TENDON RUPTURE ( 19 FDA reports)
TINNITUS ( 19 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 18 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 18 FDA reports)
DRUG RESISTANCE ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
FLANK PAIN ( 18 FDA reports)
HOT FLUSH ( 18 FDA reports)
HYPOKINESIA ( 18 FDA reports)
INTENTIONAL OVERDOSE ( 18 FDA reports)
MUSCLE TWITCHING ( 18 FDA reports)
RESPIRATORY RATE INCREASED ( 18 FDA reports)
RIB FRACTURE ( 18 FDA reports)
SKIN HAEMORRHAGE ( 18 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 18 FDA reports)
THIRST ( 18 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 18 FDA reports)
ANGIONEUROTIC OEDEMA ( 17 FDA reports)
BACTERAEMIA ( 17 FDA reports)
CARDIOMYOPATHY ( 17 FDA reports)
COLON CANCER ( 17 FDA reports)
DISCOMFORT ( 17 FDA reports)
DYSPHONIA ( 17 FDA reports)
ELECTROLYTE IMBALANCE ( 17 FDA reports)
FAECES DISCOLOURED ( 17 FDA reports)
FEMUR FRACTURE ( 17 FDA reports)
GENERALISED OEDEMA ( 17 FDA reports)
GLOSSODYNIA ( 17 FDA reports)
GYNAECOMASTIA ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
INJECTION SITE BURNING ( 17 FDA reports)
INTESTINAL OBSTRUCTION ( 17 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 17 FDA reports)
LOCAL SWELLING ( 17 FDA reports)
MALNUTRITION ( 17 FDA reports)
METABOLIC DISORDER ( 17 FDA reports)
MIGRAINE ( 17 FDA reports)
NEUTROPENIC SEPSIS ( 17 FDA reports)
NO THERAPEUTIC RESPONSE ( 17 FDA reports)
OCCULT BLOOD POSITIVE ( 17 FDA reports)
OXYGEN SATURATION DECREASED ( 17 FDA reports)
RENAL ARTERY STENOSIS ( 17 FDA reports)
RESPIRATORY DISORDER ( 17 FDA reports)
SENSORY DISTURBANCE ( 17 FDA reports)
SKIN ULCER ( 17 FDA reports)
TARDIVE DYSKINESIA ( 17 FDA reports)
VIITH NERVE PARALYSIS ( 17 FDA reports)
ANAEMIA MACROCYTIC ( 16 FDA reports)
APLASIA PURE RED CELL ( 16 FDA reports)
ATAXIA ( 16 FDA reports)
ATELECTASIS ( 16 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 16 FDA reports)
BLOOD URINE PRESENT ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
BREAST CANCER ( 16 FDA reports)
CEREBRAL INFARCTION ( 16 FDA reports)
CYANOSIS ( 16 FDA reports)
DYSLIPIDAEMIA ( 16 FDA reports)
ECONOMIC PROBLEM ( 16 FDA reports)
GANGRENE ( 16 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 16 FDA reports)
HEPATITIS CHOLESTATIC ( 16 FDA reports)
HEPATITIS FULMINANT ( 16 FDA reports)
HYPERTENSIVE CRISIS ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
MOUTH HAEMORRHAGE ( 16 FDA reports)
NYSTAGMUS ( 16 FDA reports)
OSTEONECROSIS OF JAW ( 16 FDA reports)
PERITONITIS BACTERIAL ( 16 FDA reports)
PETECHIAE ( 16 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 16 FDA reports)
POLLAKIURIA ( 16 FDA reports)
POLYURIA ( 16 FDA reports)
PREMATURE BABY ( 16 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 16 FDA reports)
PRODUCTIVE COUGH ( 16 FDA reports)
SEDATION ( 16 FDA reports)
SKIN NECROSIS ( 16 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 16 FDA reports)
BLADDER CANCER ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 15 FDA reports)
CARDIAC PACEMAKER INSERTION ( 15 FDA reports)
CARDIAC TAMPONADE ( 15 FDA reports)
CEREBELLAR SYNDROME ( 15 FDA reports)
CEREBRAL ATROPHY ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
DILATATION ATRIAL ( 15 FDA reports)
DRUG EFFECT DECREASED ( 15 FDA reports)
DRUG INTOLERANCE ( 15 FDA reports)
DRUG PRESCRIBING ERROR ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
EXTRASYSTOLES ( 15 FDA reports)
HEART RATE IRREGULAR ( 15 FDA reports)
HIP FRACTURE ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
ISCHAEMIA ( 15 FDA reports)
LARYNGEAL OEDEMA ( 15 FDA reports)
LUNG INFILTRATION ( 15 FDA reports)
MOVEMENT DISORDER ( 15 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 15 FDA reports)
NEUTROPHIL COUNT DECREASED ( 15 FDA reports)
PARALYSIS ( 15 FDA reports)
POLYP ( 15 FDA reports)
RALES ( 15 FDA reports)
RESTLESSNESS ( 15 FDA reports)
SURGERY ( 15 FDA reports)
THINKING ABNORMAL ( 15 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 14 FDA reports)
ANAL HAEMORRHAGE ( 14 FDA reports)
BIPOLAR DISORDER ( 14 FDA reports)
BODY TEMPERATURE DECREASED ( 14 FDA reports)
CYSTITIS ( 14 FDA reports)
DRUG DOSE OMISSION ( 14 FDA reports)
ENTEROCOCCAL INFECTION ( 14 FDA reports)
EXTRADURAL HAEMATOMA ( 14 FDA reports)
EYE DISORDER ( 14 FDA reports)
GASTRIC CANCER ( 14 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 14 FDA reports)
HYPERTHYROIDISM ( 14 FDA reports)
INJECTION SITE PRURITUS ( 14 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
LOBAR PNEUMONIA ( 14 FDA reports)
METABOLIC SYNDROME ( 14 FDA reports)
MUSCLE HAEMORRHAGE ( 14 FDA reports)
MUSCLE RIGIDITY ( 14 FDA reports)
NEOPLASM MALIGNANT ( 14 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 14 FDA reports)
OSTEOMYELITIS ( 14 FDA reports)
REFLUX OESOPHAGITIS ( 14 FDA reports)
SALIVARY HYPERSECRETION ( 14 FDA reports)
SPINAL CORD COMPRESSION ( 14 FDA reports)
SUBDURAL HAEMATOMA ( 14 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 14 FDA reports)
UPPER LIMB FRACTURE ( 14 FDA reports)
UROSEPSIS ( 14 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 13 FDA reports)
ARTHROPATHY ( 13 FDA reports)
BLOOD CHLORIDE INCREASED ( 13 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 13 FDA reports)
BRONCHOSPASM ( 13 FDA reports)
CANDIDIASIS ( 13 FDA reports)
CARPAL TUNNEL SYNDROME ( 13 FDA reports)
CEREBRAL VASOCONSTRICTION ( 13 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
DEVICE RELATED INFECTION ( 13 FDA reports)
DROOLING ( 13 FDA reports)
DRUG ADMINISTRATION ERROR ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
DUODENITIS ( 13 FDA reports)
DYSSTASIA ( 13 FDA reports)
EMOTIONAL DISORDER ( 13 FDA reports)
EXERCISE TOLERANCE DECREASED ( 13 FDA reports)
FLATULENCE ( 13 FDA reports)
HYPERAMMONAEMIA ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 13 FDA reports)
JOINT CONTRACTURE ( 13 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 13 FDA reports)
LEFT VENTRICULAR FAILURE ( 13 FDA reports)
LIVEDO RETICULARIS ( 13 FDA reports)
METASTASES TO BONE ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE ( 13 FDA reports)
NASAL CONGESTION ( 13 FDA reports)
PNEUMOTHORAX ( 13 FDA reports)
POISONING ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
PURULENT DISCHARGE ( 13 FDA reports)
RASH PAPULAR ( 13 FDA reports)
SKIN LESION ( 13 FDA reports)
SKIN REACTION ( 13 FDA reports)
SKIN TIGHTNESS ( 13 FDA reports)
STENT PLACEMENT ( 13 FDA reports)
TENDONITIS ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
VENTRICULAR HYPOKINESIA ( 13 FDA reports)
ACCIDENTAL OVERDOSE ( 12 FDA reports)
ANGER ( 12 FDA reports)
ANKLE FRACTURE ( 12 FDA reports)
BACK INJURY ( 12 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
DIABETIC KETOACIDOSIS ( 12 FDA reports)
DIALYSIS ( 12 FDA reports)
DIASTOLIC DYSFUNCTION ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
DRUG ERUPTION ( 12 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 12 FDA reports)
EPIGASTRIC DISCOMFORT ( 12 FDA reports)
FIBROSIS ( 12 FDA reports)
HEMIPLEGIA ( 12 FDA reports)
HERNIA ( 12 FDA reports)
HYDRONEPHROSIS ( 12 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 12 FDA reports)
LACERATION ( 12 FDA reports)
LIMB DISCOMFORT ( 12 FDA reports)
LYMPHADENOPATHY ( 12 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 12 FDA reports)
MOTOR DYSFUNCTION ( 12 FDA reports)
MULTIPLE MYELOMA ( 12 FDA reports)
NERVOUS SYSTEM DISORDER ( 12 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 12 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 12 FDA reports)
PEMPHIGOID ( 12 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 12 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 12 FDA reports)
RASH MACULAR ( 12 FDA reports)
SPINAL DISORDER ( 12 FDA reports)
STOMATITIS ( 12 FDA reports)
THROMBOCYTHAEMIA ( 12 FDA reports)
TOOTHACHE ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
VASCULITIC RASH ( 12 FDA reports)
VENTRICULAR HYPERTROPHY ( 12 FDA reports)
ADVERSE EVENT ( 11 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 11 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD LACTIC ACID INCREASED ( 11 FDA reports)
CHOLECYSTECTOMY ( 11 FDA reports)
DERMATITIS BULLOUS ( 11 FDA reports)
DERMATITIS EXFOLIATIVE ( 11 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 11 FDA reports)
DYSTONIA ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
EXCORIATION ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GASTRIC DISORDER ( 11 FDA reports)
GINGIVAL BLEEDING ( 11 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 11 FDA reports)
HEPATITIS ACUTE ( 11 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LARGE INTESTINAL ULCER ( 11 FDA reports)
LARGE INTESTINE PERFORATION ( 11 FDA reports)
LUNG INFECTION ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
NEOPLASM PROGRESSION ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
PARKINSON'S DISEASE ( 11 FDA reports)
PHOTOSENSITIVITY REACTION ( 11 FDA reports)
PSEUDOMONAS INFECTION ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
STRIDOR ( 11 FDA reports)
TENDERNESS ( 11 FDA reports)
TENSION HEADACHE ( 11 FDA reports)
THROAT IRRITATION ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
VIRAL INFECTION ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
ACUTE ABDOMEN ( 10 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 10 FDA reports)
AORTIC VALVE INCOMPETENCE ( 10 FDA reports)
BLOOD CREATINE INCREASED ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 10 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 10 FDA reports)
BONE MARROW DEPRESSION ( 10 FDA reports)
BREATH SOUNDS ABNORMAL ( 10 FDA reports)
CARDIOVASCULAR DISORDER ( 10 FDA reports)
CHEST X-RAY ABNORMAL ( 10 FDA reports)
CHOKING ( 10 FDA reports)
DIFFICULTY IN WALKING ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
DRUG DEPENDENCE ( 10 FDA reports)
DUODENAL ULCER PERFORATION ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 10 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
HAEMORRHAGIC ANAEMIA ( 10 FDA reports)
HAEMOTHORAX ( 10 FDA reports)
HEMIANOPIA HOMONYMOUS ( 10 FDA reports)
HEPATIC CIRRHOSIS ( 10 FDA reports)
HEPATIC NECROSIS ( 10 FDA reports)
HICCUPS ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
HYPERTHERMIA ( 10 FDA reports)
HYPOAESTHESIA FACIAL ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 10 FDA reports)
LABORATORY TEST ABNORMAL ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
LOCALISED OEDEMA ( 10 FDA reports)
LOSS OF BLADDER SENSATION ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MALLORY-WEISS SYNDROME ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
NEPHRITIS ( 10 FDA reports)
PARANOIA ( 10 FDA reports)
PARAPARESIS ( 10 FDA reports)
PERICARDITIS ( 10 FDA reports)
PIGMENTATION DISORDER ( 10 FDA reports)
PSORIATIC ARTHROPATHY ( 10 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
SELF-MEDICATION ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
SPINAL COMPRESSION FRACTURE ( 10 FDA reports)
SPINAL FRACTURE ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 10 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 10 FDA reports)
TOOTH DISORDER ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
TRAUMATIC HAEMATOMA ( 10 FDA reports)
TROPONIN I INCREASED ( 10 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
AGEUSIA ( 9 FDA reports)
AREFLEXIA ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 9 FDA reports)
BONE DISORDER ( 9 FDA reports)
BRADYARRHYTHMIA ( 9 FDA reports)
BRADYPHRENIA ( 9 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DEFORMITY ( 9 FDA reports)
DERMATITIS ALLERGIC ( 9 FDA reports)
DEVICE FAILURE ( 9 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 9 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 9 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
ERUCTATION ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FAILURE TO THRIVE ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HEPATIC CONGESTION ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HEPATITIS B ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPERTONIA ( 9 FDA reports)
HYPOPHOSPHATAEMIA ( 9 FDA reports)
HYPOTONIA ( 9 FDA reports)
HYPOVOLAEMIA ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
INFUSION RELATED REACTION ( 9 FDA reports)
INHIBITORY DRUG INTERACTION ( 9 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 9 FDA reports)
JOINT INJURY ( 9 FDA reports)
LEG AMPUTATION ( 9 FDA reports)
LUPUS-LIKE SYNDROME ( 9 FDA reports)
MULTIPLE SCLEROSIS ( 9 FDA reports)
MYOCARDITIS ( 9 FDA reports)
NIGHT SWEATS ( 9 FDA reports)
NO ADVERSE EVENT ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
OVERWEIGHT ( 9 FDA reports)
PANCREATIC MASS ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PHARYNGEAL OEDEMA ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
POLYARTHRITIS ( 9 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 9 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 9 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 9 FDA reports)
RIGHT VENTRICULAR FAILURE ( 9 FDA reports)
SINUS ARRHYTHMIA ( 9 FDA reports)
SPINAL HAEMATOMA ( 9 FDA reports)
SUDDEN CARDIAC DEATH ( 9 FDA reports)
TEARFULNESS ( 9 FDA reports)
TOOTH INFECTION ( 9 FDA reports)
TUBERCULOSIS ( 9 FDA reports)
UNDERDOSE ( 9 FDA reports)
VASCULAR HEADACHE ( 9 FDA reports)
VENTRICULAR DYSFUNCTION ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
ACUTE PRERENAL FAILURE ( 8 FDA reports)
AORTIC STENOSIS ( 8 FDA reports)
ATRIAL SEPTAL DEFECT ( 8 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
CANDIDA OSTEOMYELITIS ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CEREBELLAR HAEMORRHAGE ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
CHOKING SENSATION ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
FOOT DEFORMITY ( 8 FDA reports)
GINGIVAL HYPERPLASIA ( 8 FDA reports)
HAEMARTHROSIS ( 8 FDA reports)
HEART INJURY ( 8 FDA reports)
HELICOBACTER INFECTION ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HEPATITIS TOXIC ( 8 FDA reports)
HYPERPHOSPHATAEMIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
ISCHAEMIC HEPATITIS ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LEFT ATRIAL DILATATION ( 8 FDA reports)
LIPASE INCREASED ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
LOW BIRTH WEIGHT BABY ( 8 FDA reports)
LUNG CONSOLIDATION ( 8 FDA reports)
LYMPHOCELE ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
MASS ( 8 FDA reports)
MYOGLOBINURIA ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NEUTROPHILIA ( 8 FDA reports)
ORAL DISCOMFORT ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
PANCREATIC NEOPLASM ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 8 FDA reports)
PULMONARY HAEMORRHAGE ( 8 FDA reports)
PULSE ABSENT ( 8 FDA reports)
PYELONEPHRITIS ( 8 FDA reports)
RADICULOPATHY ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
RETINAL HAEMORRHAGE ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
SICK SINUS SYNDROME ( 8 FDA reports)
SKIN TURGOR DECREASED ( 8 FDA reports)
SPUTUM DISCOLOURED ( 8 FDA reports)
SUBDURAL HAEMORRHAGE ( 8 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VULVOVAGINAL DISCOMFORT ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ABSCESS ( 7 FDA reports)
ABSCESS LIMB ( 7 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
AFFECTIVE DISORDER ( 7 FDA reports)
AMMONIA INCREASED ( 7 FDA reports)
AMYLASE INCREASED ( 7 FDA reports)
ANAEMIA POSTOPERATIVE ( 7 FDA reports)
ANION GAP INCREASED ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 7 FDA reports)
ASPHYXIA ( 7 FDA reports)
AUTOIMMUNE HEPATITIS ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
BLOOD IRON DECREASED ( 7 FDA reports)
BLOOD PRESSURE ABNORMAL ( 7 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
CALCULUS URETERIC ( 7 FDA reports)
CARDIOPULMONARY FAILURE ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
COLITIS ULCERATIVE ( 7 FDA reports)
COMA SCALE ABNORMAL ( 7 FDA reports)
CONDUCTION DISORDER ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DENTAL OPERATION ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 7 FDA reports)
EMPYEMA ( 7 FDA reports)
ENDOCARDITIS ( 7 FDA reports)
EROSIVE DUODENITIS ( 7 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
GENERALISED ERYTHEMA ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
GRANULOCYTOPENIA ( 7 FDA reports)
HALLUCINATIONS, MIXED ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HEPATIC CYST ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 7 FDA reports)
HYPERPARATHYROIDISM ( 7 FDA reports)
HYPERSEXUALITY ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYPOGLYCAEMIC COMA ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
JAW DISORDER ( 7 FDA reports)
JOINT EFFUSION ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LIBIDO DECREASED ( 7 FDA reports)
LONG QT SYNDROME ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MAJOR DEPRESSION ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MANIA ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
MUSCLE TIGHTNESS ( 7 FDA reports)
NEUROLOGICAL SYMPTOM ( 7 FDA reports)
NODAL ARRHYTHMIA ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PITTING OEDEMA ( 7 FDA reports)
PNEUMOCOCCAL SEPSIS ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
QUALITY OF LIFE DECREASED ( 7 FDA reports)
RADICULAR PAIN ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
RESPIRATORY ACIDOSIS ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
SUICIDAL BEHAVIOUR ( 7 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
THROMBOPHLEBITIS ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
TOXIC ENCEPHALOPATHY ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
ABDOMINAL RIGIDITY ( 6 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 6 FDA reports)
ACUTE LUNG INJURY ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
APATHY ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
ARTERIAL RUPTURE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 6 FDA reports)
BEDRIDDEN ( 6 FDA reports)
BILIARY COLIC ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD CHLORIDE DECREASED ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD OSMOLARITY DECREASED ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CENTRAL OBESITY ( 6 FDA reports)
CEREBRAL DISORDER ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CLEFT PALATE ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
ESCHERICHIA TEST POSITIVE ( 6 FDA reports)
EYE IRRITATION ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 6 FDA reports)
GASTROINTESTINAL CARCINOMA ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GILBERT'S SYNDROME ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
GOITRE ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
HYPOAESTHESIA ORAL ( 6 FDA reports)
IATROGENIC INJURY ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
MALIGNANT TUMOUR EXCISION ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MUSCLE SWELLING ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NEPHRITIS INTERSTITIAL ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
ORAL HERPES ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PAIN OF SKIN ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PELVIC FRACTURE ( 6 FDA reports)
PEMPHIGUS ( 6 FDA reports)
PEPTIC ULCER ( 6 FDA reports)
PERIORBITAL OEDEMA ( 6 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
POISONING DELIBERATE ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PROSTATE CANCER METASTATIC ( 6 FDA reports)
PROTEUS TEST POSITIVE ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RETINAL DETACHMENT ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
SALMONELLOSIS ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SKIN FIBROSIS ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
SPINAL CORD HAEMORRHAGE ( 6 FDA reports)
TERMINAL STATE ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
TROPONIN T INCREASED ( 6 FDA reports)
ULCER ( 6 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 6 FDA reports)
URETERAL NECROSIS ( 6 FDA reports)
URINE FLOW DECREASED ( 6 FDA reports)
VULVOVAGINAL DRYNESS ( 6 FDA reports)
WEIGHT BEARING DIFFICULTY ( 6 FDA reports)
WOUND ( 6 FDA reports)
WOUND INFECTION ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 5 FDA reports)
ACCIDENT ( 5 FDA reports)
ADDISON'S DISEASE ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANGIOPATHY ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
AORTIC DISSECTION ( 5 FDA reports)
AORTIC VALVE DISEASE ( 5 FDA reports)
APALLIC SYNDROME ( 5 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 5 FDA reports)
ASBESTOSIS ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BENIGN GASTRIC NEOPLASM ( 5 FDA reports)
BILE DUCT OBSTRUCTION ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLEPHAROSPASM ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BONE NEOPLASM MALIGNANT ( 5 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BULIMIA NERVOSA ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARDIAC DEATH ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 5 FDA reports)
COLITIS MICROSCOPIC ( 5 FDA reports)
COLON CANCER METASTATIC ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CRYING ( 5 FDA reports)
DENTAL CARIES ( 5 FDA reports)
DEVICE MALFUNCTION ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 5 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
ERYTHRODERMIC PSORIASIS ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
EXOSTOSIS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FOETAL GROWTH RESTRICTION ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HAEMATOMA INFECTION ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HEART TRANSPLANT REJECTION ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPOCOAGULABLE STATE ( 5 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INFECTIOUS PERITONITIS ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
INTESTINAL HAEMORRHAGE ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
KLEBSIELLA SEPSIS ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LIP ULCERATION ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
METASTASES TO SKIN ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MIXED LIVER INJURY ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MUCOSAL HAEMORRHAGE ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
MUTISM ( 5 FDA reports)
MYOCARDIAL STRAIN ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NODULE ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
OESOPHAGEAL RUPTURE ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PATHOLOGICAL FRACTURE ( 5 FDA reports)
PATHOLOGICAL GAMBLING ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 5 FDA reports)
PERITONEAL HAEMORRHAGE ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
PREMATURE DELIVERY ( 5 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
RADIUS FRACTURE ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
REGRESSIVE BEHAVIOUR ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VASCULAR DEMENTIA ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
VOLVULUS ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 4 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ARM AMPUTATION ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BRAIN DEATH ( 4 FDA reports)
BRAIN MALFORMATION ( 4 FDA reports)
BRAIN STEM ISCHAEMIA ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CONTRAST MEDIA REACTION ( 4 FDA reports)
CONUS MEDULLARIS SYNDROME ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
CUTANEOUS VASCULITIS ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DENTURE WEARER ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DROP ATTACKS ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
ESSENTIAL HYPERTENSION ( 4 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
FACTOR VIII DEFICIENCY ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HAEMOGLOBIN ABNORMAL ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPERKERATOSIS ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPOCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOPHYSITIS ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
IMPLANT SITE EXTRAVASATION ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE STINGING ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KNEE DEFORMITY ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LARGE INTESTINE CARCINOMA ( 4 FDA reports)
LIBIDO INCREASED ( 4 FDA reports)
LIMB ASYMMETRY ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 4 FDA reports)
MEDIASTINAL HAEMATOMA ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MENINGOCOCCAL SEPSIS ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
MICROANGIOPATHY ( 4 FDA reports)
MICROCYTIC ANAEMIA ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NASAL NECROSIS ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NEEDLE ISSUE ( 4 FDA reports)
NEPHRITIS ALLERGIC ( 4 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 4 FDA reports)
NEURILEMMOMA ( 4 FDA reports)
NEUROCRYPTOCOCCOSIS ( 4 FDA reports)
NEUROENDOCRINE TUMOUR ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NIPPLE PAIN ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
PALATAL OEDEMA ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PARAPROTEINAEMIA ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PENILE ERYTHEMA ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PSEUDOLYMPHOMA ( 4 FDA reports)
PULSE PRESSURE DECREASED ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
QUADRIPARESIS ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RENAL ISCHAEMIA ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETROPERITONEAL NEOPLASM ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SCROTAL ULCER ( 4 FDA reports)
SEBACEOUS CARCINOMA ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SELF MUTILATION ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SKIN DEPIGMENTATION ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SOMATOFORM DISORDER ( 4 FDA reports)
SPIDER VEIN ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SYSTOLIC HYPERTENSION ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE DISCOLOURATION ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TOXIC SHOCK SYNDROME ( 4 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URETERIC OBSTRUCTION ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 4 FDA reports)
VENOUS RECANALISATION ( 4 FDA reports)
WEIGHT GAIN POOR ( 4 FDA reports)
WOUND SECRETION ( 4 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABDOMINAL WALL INFECTION ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALEXIA ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
AMAUROSIS ( 3 FDA reports)
AMNIOTIC CAVITY INFECTION ( 3 FDA reports)
ANTEROGRADE AMNESIA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
AURA ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 3 FDA reports)
BENIGN COLONIC NEOPLASM ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BILIARY SEPSIS ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CARDIAC ANEURYSM ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL HYPOPERFUSION ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
EPIDIDYMAL INFECTION ( 3 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
FACTOR V LEIDEN MUTATION ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GENITAL CANDIDIASIS ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GLOBAL AMNESIA ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HAEMORRHOID INFECTION ( 3 FDA reports)
HALLUCINATION, TACTILE ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOSPERMIA ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IGA NEPHROPATHY ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INTERCOSTAL NEURALGIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LASER THERAPY ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIGAMENT LAXITY ( 3 FDA reports)
LIP INJURY ( 3 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MASS EXCISION ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENINGIOMA BENIGN ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
METANEPHRINE URINE INCREASED ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MONONEUROPATHY ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MOTOR NEURONE DISEASE ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYCOTIC ANEURYSM ( 3 FDA reports)
NAIL PITTING ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PENILE PAIN ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PLACENTAL DISORDER ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POLYSUBSTANCE ABUSE ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PROCTITIS HERPES ( 3 FDA reports)
PROPOFOL INFUSION SYNDROME ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SERRATIA INFECTION ( 3 FDA reports)
SERUM FERRITIN DECREASED ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SINUS RHYTHM ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STEREOTYPY ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
TENSION ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THORACOSTOMY ( 3 FDA reports)
THROMBOEMBOLECTOMY ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
URETHRAL VALVES ( 3 FDA reports)
URINARY SEDIMENT ABNORMAL ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VASCULAR STENOSIS ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE DECREASED ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ACANTHOSIS NIGRICANS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANALGESIC THERAPY ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC INTRAMURAL HAEMATOMA ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APOLIPOPROTEIN DECREASED ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
AUTOINFLAMMATORY DISEASE ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD TEST ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHITIS MORAXELLA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COLD AGGLUTININS POSITIVE ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONTRACTED BLADDER ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYTOKINE RELEASE SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE DEPOSIT ISSUE ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIET NONCOMPLIANCE ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTERITIS NECROTICANS ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
EXECUTIVE DYSFUNCTION ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRINOLYSIS ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE IV ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIP HAEMATOMA ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MILD MENTAL RETARDATION ( 2 FDA reports)
MITRAL VALVE DISEASE MIXED ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOSCLEROSIS ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OPTIC NERVE INFARCTION ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN ABSCESS ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC FISTULA ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CYST RUPTURED ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL HYPERTENSION ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SCROTAL INFECTION ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN BLEEDING ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TORULOPSIS INFECTION ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINOMA ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
UVULITIS ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACQUIRED PORPHYRIA ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMINO ACID LEVEL DECREASED ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNIOTIC BAND SYNDROME ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANGIOGRAM PULMONARY ( 1 FDA reports)
ANGIOGRAM PULMONARY ABNORMAL ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOPHTHALMOS ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIACETYLCHOLINE RECEPTOR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROSIS MOENCKEBERG-TYPE ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BECKER'S MUSCULAR DYSTROPHY ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CANCER STAGE I, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
C1 ESTERASE INHIBITOR DECREASED ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL DYSGENESIS ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAINDICATION TO SURGERY ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR IRRIGATION ( 1 FDA reports)
ECTOPIC ACTH SYNDROME ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRIEDREICH'S ATAXIA ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS SHIGELLA ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC FEVER ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROMETRA ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INTERCEPTED DRUG PRESCRIBING ERROR ( 1 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ITCHING SCAR ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LARYNGEAL GRANULOMA ( 1 FDA reports)
LARYNGEAL HAEMATOMA ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIMB AMPUTATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULAR PIGMENTATION ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTI-VITAMIN DEFICIENCY ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NITRITOID REACTION ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROLACTIN-PRODUCING PITUITARY TUMOUR ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDOCHOLINESTERASE DEFICIENCY ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADIOISOTOPE SCAN ABNORMAL ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALMONELLA TEST POSITIVE ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCINTIGRAPHY ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLINT APPLICATION ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
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STENT MALFUNCTION ( 1 FDA reports)
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STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCLAVIAN ARTERY EMBOLISM ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUPERFICIAL SIDEROSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOSIS PROPHYLAXIS ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSURETHRAL BLADDER RESECTION ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRAUMATIC ULCER ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC CANCER RECURRENT ( 1 FDA reports)
URETERIC INJURY ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS OXYGEN SATURATION DECREASED ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIIITH NERVE INJURY ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISCERAL OEDEMA ( 1 FDA reports)
VITAMIN A DEFICIENCY ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVAL CANCER STAGE II ( 1 FDA reports)
VULVAL HAEMORRHAGE ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)

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