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

NAUSEA ( 84 FDA reports)
VOMITING ( 84 FDA reports)
DYSPNOEA ( 74 FDA reports)
PAIN ( 71 FDA reports)
ANXIETY ( 63 FDA reports)
DIARRHOEA ( 58 FDA reports)
DIZZINESS ( 56 FDA reports)
HYPERTENSION ( 55 FDA reports)
DEPRESSION ( 52 FDA reports)
FATIGUE ( 47 FDA reports)
HYPOTENSION ( 42 FDA reports)
ASTHENIA ( 41 FDA reports)
FALL ( 40 FDA reports)
PNEUMONIA ( 38 FDA reports)
RENAL FAILURE ACUTE ( 38 FDA reports)
HEADACHE ( 36 FDA reports)
DECREASED APPETITE ( 35 FDA reports)
PYREXIA ( 35 FDA reports)
ATRIAL FIBRILLATION ( 34 FDA reports)
ARTHRALGIA ( 33 FDA reports)
BACK PAIN ( 33 FDA reports)
TREMOR ( 33 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 32 FDA reports)
INJURY ( 32 FDA reports)
RASH ( 32 FDA reports)
CORONARY ARTERY DISEASE ( 31 FDA reports)
ABDOMINAL PAIN ( 30 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 30 FDA reports)
CHEST PAIN ( 30 FDA reports)
ECONOMIC PROBLEM ( 30 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 30 FDA reports)
ABDOMINAL PAIN UPPER ( 29 FDA reports)
ANAEMIA ( 29 FDA reports)
MYOCARDIAL INFARCTION ( 29 FDA reports)
SYNCOPE ( 29 FDA reports)
MENTAL STATUS CHANGES ( 27 FDA reports)
PULMONARY EMBOLISM ( 27 FDA reports)
URINARY TRACT INFECTION ( 27 FDA reports)
ANHEDONIA ( 26 FDA reports)
CHILLS ( 26 FDA reports)
MULTIPLE DRUG OVERDOSE ( 26 FDA reports)
PAIN IN EXTREMITY ( 26 FDA reports)
RENAL FAILURE ( 26 FDA reports)
RESPIRATORY FAILURE ( 26 FDA reports)
CEREBROVASCULAR ACCIDENT ( 25 FDA reports)
CONSTIPATION ( 25 FDA reports)
INFUSION RELATED REACTION ( 25 FDA reports)
COUGH ( 24 FDA reports)
OSTEOARTHRITIS ( 24 FDA reports)
WEIGHT DECREASED ( 24 FDA reports)
HYPERHIDROSIS ( 23 FDA reports)
HYPERLIPIDAEMIA ( 23 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
SOMNOLENCE ( 23 FDA reports)
BLOOD GLUCOSE INCREASED ( 22 FDA reports)
SCAR ( 22 FDA reports)
BRADYCARDIA ( 21 FDA reports)
CONFUSIONAL STATE ( 21 FDA reports)
DEEP VEIN THROMBOSIS ( 21 FDA reports)
EMOTIONAL DISTRESS ( 21 FDA reports)
MALAISE ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
TARDIVE DYSKINESIA ( 21 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
TREATMENT NONCOMPLIANCE ( 20 FDA reports)
UNRESPONSIVE TO STIMULI ( 20 FDA reports)
BLOOD PRESSURE DECREASED ( 19 FDA reports)
EMOTIONAL DISORDER ( 19 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 19 FDA reports)
HAEMOGLOBIN DECREASED ( 19 FDA reports)
INSOMNIA ( 19 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 18 FDA reports)
DEHYDRATION ( 18 FDA reports)
HEART RATE INCREASED ( 18 FDA reports)
LOSS OF CONSCIOUSNESS ( 18 FDA reports)
MITRAL VALVE INCOMPETENCE ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
RECTAL HAEMORRHAGE ( 18 FDA reports)
ASTHMA ( 17 FDA reports)
CHOLELITHIASIS ( 17 FDA reports)
DYSPHAGIA ( 17 FDA reports)
HAEMORRHAGE ( 17 FDA reports)
LETHARGY ( 17 FDA reports)
PANCYTOPENIA ( 17 FDA reports)
CONVULSION ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
HYPERKALAEMIA ( 16 FDA reports)
HYPOAESTHESIA ( 16 FDA reports)
RESPIRATORY DISTRESS ( 16 FDA reports)
STRESS ( 16 FDA reports)
AGITATION ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
BLOOD PRESSURE INCREASED ( 15 FDA reports)
CHEST DISCOMFORT ( 15 FDA reports)
HAEMORRHOIDS ( 15 FDA reports)
MULTIPLE INJURIES ( 15 FDA reports)
MUSCLE SPASMS ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 15 FDA reports)
TYPE 2 DIABETES MELLITUS ( 15 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
DEATH ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
GASTROENTERITIS ( 14 FDA reports)
HYPOVOLAEMIA ( 14 FDA reports)
MENTAL DISORDER ( 14 FDA reports)
OEDEMA ( 14 FDA reports)
SUICIDE ATTEMPT ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
ATELECTASIS ( 13 FDA reports)
COLITIS ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
HYPOXIA ( 13 FDA reports)
OSTEONECROSIS OF JAW ( 13 FDA reports)
OSTEOPENIA ( 13 FDA reports)
OXYGEN SATURATION DECREASED ( 13 FDA reports)
PALLOR ( 13 FDA reports)
PARAESTHESIA ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
BLOOD GLUCOSE DECREASED ( 12 FDA reports)
BRONCHITIS ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
FUNGAL INFECTION ( 12 FDA reports)
GASTRITIS ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HEPATIC LESION ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
HYPOPHAGIA ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
MEMORY IMPAIRMENT ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
PROSTATE CANCER ( 12 FDA reports)
SPINAL OSTEOARTHRITIS ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
VISION BLURRED ( 12 FDA reports)
ANGINA PECTORIS ( 11 FDA reports)
APLASTIC ANAEMIA ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
CANDIDIASIS ( 11 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 11 FDA reports)
COMA ( 11 FDA reports)
DISCOMFORT ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
DYSPNOEA EXERTIONAL ( 11 FDA reports)
DYSTONIA ( 11 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 11 FDA reports)
HERPES ZOSTER ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
NEPHROLITHIASIS ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
OBESITY ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
RENAL CYST ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
BONE PAIN ( 10 FDA reports)
CHOLECYSTITIS CHRONIC ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
COSTOCHONDRITIS ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
DYSKINESIA ( 10 FDA reports)
ELECTROLYTE IMBALANCE ( 10 FDA reports)
FUNGAEMIA ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
INCORRECT DOSE ADMINISTERED ( 10 FDA reports)
LUMBAR SPINAL STENOSIS ( 10 FDA reports)
MENINGIOMA ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
NECK PAIN ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
PULMONARY HYPERTENSION ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RADICULOPATHY ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 9 FDA reports)
AORTIC VALVE INCOMPETENCE ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
COMPRESSION FRACTURE ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DIVERTICULITIS ( 9 FDA reports)
DIVERTICULUM ( 9 FDA reports)
DRUG TOXICITY ( 9 FDA reports)
FEMORAL NECK FRACTURE ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HIATUS HERNIA ( 9 FDA reports)
HYPOCALCAEMIA ( 9 FDA reports)
HYPOPHOSPHATAEMIA ( 9 FDA reports)
LIFE EXPECTANCY SHORTENED ( 9 FDA reports)
OROPHARYNGEAL PAIN ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
PAIN IN JAW ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
PROTHROMBIN TIME PROLONGED ( 9 FDA reports)
RECURRENT CANCER ( 9 FDA reports)
REFLUX OESOPHAGITIS ( 9 FDA reports)
SPLENOMEGALY ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
STRESS URINARY INCONTINENCE ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
TOOTHACHE ( 9 FDA reports)
TYPE 1 DIABETES MELLITUS ( 9 FDA reports)
UMBILICAL HERNIA ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ABASIA ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ATRIAL SEPTAL DEFECT ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BLOOD POTASSIUM DECREASED ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
BONE FRAGMENTATION ( 8 FDA reports)
BONE LESION ( 8 FDA reports)
BREAST CANCER RECURRENT ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
COLONIC POLYP ( 8 FDA reports)
DEVICE RELATED INFECTION ( 8 FDA reports)
DISABILITY ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
EDENTULOUS ( 8 FDA reports)
EJECTION FRACTION DECREASED ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
FISTULA ( 8 FDA reports)
GINGIVAL INFECTION ( 8 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 8 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HEAD INJURY ( 8 FDA reports)
HYPOTHYROIDISM ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
LUNG NEOPLASM MALIGNANT ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
MITRAL VALVE CALCIFICATION ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
NARCOLEPSY ( 8 FDA reports)
NERVE ROOT LESION ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
NODULE ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
OSTEOMYELITIS ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PATHOLOGICAL FRACTURE ( 8 FDA reports)
PERIODONTAL DISEASE ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SACROILIITIS ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
STREPTOCOCCAL SEPSIS ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
SYNOVIAL CYST ( 8 FDA reports)
TOOTH LOSS ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ARTHRITIS ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
BARRETT'S OESOPHAGUS ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CAECITIS ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
ERECTILE DYSFUNCTION ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
FEAR ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PANIC ATTACK ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PNEUMATOSIS INTESTINALIS ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
RENAL TUBULAR NECROSIS ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
VITAMIN D DEFICIENCY ( 7 FDA reports)
AKATHISIA ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
MASS ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
SHOCK ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CAROTID ARTERY STENOSIS ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
DEFORMITY ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GOUT ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
LEFT ATRIAL DILATATION ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
RETCHING ( 5 FDA reports)
SEDATION ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BONE MARROW TRANSPLANT ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
EAR LOBE INFECTION ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
JOINT INJECTION ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SCARLET FEVER ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
UMBILICAL HERNIA REPAIR ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENOPAUSE ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SURGERY ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
WOUND ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBROVASCULAR SPASM ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN CYST TORSION ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PLASMIN INHIBITOR INCREASED ( 2 FDA reports)
PLASMINOGEN ACTIVATOR INHIBITOR ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPIRATION JOINT ABNORMAL ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMMUNOLOGY TEST ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE MASTECTOMY ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use