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

DYSPNOEA ( 45 FDA reports)
ASTHENIA ( 44 FDA reports)
PAIN ( 42 FDA reports)
DRUG INEFFECTIVE ( 41 FDA reports)
WEIGHT DECREASED ( 40 FDA reports)
CONDITION AGGRAVATED ( 39 FDA reports)
DIZZINESS ( 38 FDA reports)
MYOCARDIAL INFARCTION ( 38 FDA reports)
CHOLELITHIASIS ( 34 FDA reports)
PNEUMONIA ( 34 FDA reports)
ATRIAL FIBRILLATION ( 31 FDA reports)
FEELING ABNORMAL ( 30 FDA reports)
NAUSEA ( 30 FDA reports)
DIARRHOEA ( 29 FDA reports)
PAIN IN EXTREMITY ( 29 FDA reports)
PYREXIA ( 29 FDA reports)
FALL ( 28 FDA reports)
VOMITING ( 28 FDA reports)
CHEST PAIN ( 27 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 26 FDA reports)
ARTHRALGIA ( 26 FDA reports)
HYPERTENSION ( 26 FDA reports)
RENAL FAILURE ACUTE ( 26 FDA reports)
DRUG INTERACTION ( 25 FDA reports)
CEREBROVASCULAR ACCIDENT ( 23 FDA reports)
MYALGIA ( 23 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
DEHYDRATION ( 22 FDA reports)
DISEASE RECURRENCE ( 22 FDA reports)
BLOOD GLUCOSE INCREASED ( 21 FDA reports)
FATIGUE ( 21 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
POST PROCEDURAL COMPLICATION ( 21 FDA reports)
RENAL FAILURE ( 21 FDA reports)
SYNCOPE ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
HEADACHE ( 20 FDA reports)
OEDEMA PERIPHERAL ( 20 FDA reports)
TREATMENT NONCOMPLIANCE ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
CONFUSIONAL STATE ( 19 FDA reports)
PARAESTHESIA ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
LOSS OF CONSCIOUSNESS ( 18 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
BACK PAIN ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 17 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 17 FDA reports)
BLOOD PRESSURE INCREASED ( 17 FDA reports)
DEPRESSION ( 17 FDA reports)
DIFFICULTY IN WALKING ( 17 FDA reports)
ANGINA PECTORIS ( 16 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
DRUG EFFECT DECREASED ( 16 FDA reports)
HYPOAESTHESIA ( 16 FDA reports)
CIRCULATORY COLLAPSE ( 15 FDA reports)
GAIT DISTURBANCE ( 15 FDA reports)
HAEMATURIA ( 15 FDA reports)
HYPOTENSION ( 15 FDA reports)
MALAISE ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 14 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
CORONARY ARTERY OCCLUSION ( 14 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 14 FDA reports)
PANCREATITIS ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
ANOREXIA ( 13 FDA reports)
ANXIETY ( 13 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
MEDICATION ERROR ( 13 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 13 FDA reports)
PULMONARY OEDEMA ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
ARTHRITIS ( 12 FDA reports)
DIVERTICULITIS ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
JAUNDICE ( 12 FDA reports)
PROSTATE CANCER ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 11 FDA reports)
CARDIOMEGALY ( 11 FDA reports)
CHILLS ( 11 FDA reports)
COUGH ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
VISION BLURRED ( 11 FDA reports)
ABASIA ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
HERPES ZOSTER ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
RASH ( 10 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 10 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
AORTIC ANEURYSM ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
METASTASES TO LIVER ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CORONARY ARTERY THROMBOSIS ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
MYOPATHY ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
PULMONARY FIBROSIS ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 7 FDA reports)
ANGINA UNSTABLE ( 7 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CHOLANGITIS ( 7 FDA reports)
COMA ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
DUODENAL ULCER ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MYOSITIS ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CATARACT ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
FEAR ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INTESTINAL ISCHAEMIA ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LOCALISED OSTEOARTHRITIS ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
POSTOPERATIVE ILEUS ( 5 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SKIN TEST POSITIVE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
GOUT ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INCISIONAL HERNIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERNICIOUS ANAEMIA ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OPEN FRACTURE ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SWELLING ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THORACIC OUTLET SYNDROME ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BENIGN COLONIC POLYP ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BLADDER CANCER STAGE II ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY CALCIFICATION ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STARING ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOXIC DILATATION OF COLON ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTIACETYLCHOLINE RECEPTOR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CATHETER REPLACEMENT ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GUM NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOPHILIA A WITH ANTI FACTOR VIII ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROCTALGIA FUGAX ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SPERM COUNT ZERO ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B1 DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WORD SALAD ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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