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

PAIN ( 109 FDA reports)
DYSPNOEA ( 106 FDA reports)
NAUSEA ( 99 FDA reports)
DIZZINESS ( 92 FDA reports)
ANXIETY ( 83 FDA reports)
BACK PAIN ( 83 FDA reports)
DEPRESSION ( 74 FDA reports)
PYREXIA ( 73 FDA reports)
FATIGUE ( 68 FDA reports)
CHEST PAIN ( 64 FDA reports)
HEADACHE ( 64 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 63 FDA reports)
ARTHRALGIA ( 60 FDA reports)
ABDOMINAL PAIN ( 59 FDA reports)
DIARRHOEA ( 59 FDA reports)
RASH ( 58 FDA reports)
COUGH ( 56 FDA reports)
VOMITING ( 56 FDA reports)
SINUSITIS ( 55 FDA reports)
INSOMNIA ( 53 FDA reports)
OEDEMA PERIPHERAL ( 52 FDA reports)
PAIN IN EXTREMITY ( 52 FDA reports)
CONSTIPATION ( 51 FDA reports)
FALL ( 51 FDA reports)
PNEUMONIA ( 50 FDA reports)
ANAEMIA ( 49 FDA reports)
ATRIAL FIBRILLATION ( 46 FDA reports)
INJURY ( 46 FDA reports)
BRONCHITIS ( 45 FDA reports)
HYPERTENSION ( 45 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 44 FDA reports)
HYPOAESTHESIA ( 44 FDA reports)
SYNCOPE ( 44 FDA reports)
MITRAL VALVE INCOMPETENCE ( 43 FDA reports)
MYALGIA ( 43 FDA reports)
ASTHENIA ( 42 FDA reports)
CELLULITIS ( 41 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 41 FDA reports)
DRUG INTERACTION ( 40 FDA reports)
ERYTHEMA ( 40 FDA reports)
MUSCLE SPASMS ( 39 FDA reports)
PHARYNGITIS ( 39 FDA reports)
PRURITUS ( 39 FDA reports)
SENSATION OF FOREIGN BODY ( 39 FDA reports)
LOSS OF CONSCIOUSNESS ( 38 FDA reports)
BRADYCARDIA ( 37 FDA reports)
DYSPEPSIA ( 37 FDA reports)
FLUSHING ( 37 FDA reports)
RENAL FAILURE ACUTE ( 37 FDA reports)
EMOTIONAL DISTRESS ( 34 FDA reports)
PALPITATIONS ( 34 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 34 FDA reports)
ATRIAL FLUTTER ( 33 FDA reports)
CANDIDIASIS ( 33 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 33 FDA reports)
GAIT DISTURBANCE ( 33 FDA reports)
HYPERHIDROSIS ( 33 FDA reports)
DIABETES MELLITUS ( 32 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 32 FDA reports)
MYOCARDIAL INFARCTION ( 32 FDA reports)
DYSPHAGIA ( 31 FDA reports)
HEART RATE IRREGULAR ( 31 FDA reports)
HYPERSENSITIVITY ( 31 FDA reports)
ABDOMINAL PAIN UPPER ( 30 FDA reports)
GROIN PAIN ( 30 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 30 FDA reports)
CAROTID ARTERY DISEASE ( 29 FDA reports)
DIABETIC RETINOPATHY ( 29 FDA reports)
MUSCLE CRAMP ( 29 FDA reports)
NECK PAIN ( 29 FDA reports)
RHINITIS ALLERGIC ( 29 FDA reports)
TONGUE DISORDER ( 29 FDA reports)
AMNESIA ( 28 FDA reports)
AORTIC VALVE SCLEROSIS ( 28 FDA reports)
HEPATIC STEATOSIS ( 28 FDA reports)
PIGMENTED NAEVUS ( 28 FDA reports)
RHABDOMYOLYSIS ( 28 FDA reports)
SWEAT DISCOLOURATION ( 28 FDA reports)
COLITIS ( 26 FDA reports)
EAR DISORDER ( 26 FDA reports)
ATELECTASIS ( 25 FDA reports)
BLADDER DISORDER ( 25 FDA reports)
PANCREATITIS ( 25 FDA reports)
PELVIC PAIN ( 25 FDA reports)
SWELLING ( 25 FDA reports)
ADENOMA BENIGN ( 24 FDA reports)
ANHEDONIA ( 24 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 24 FDA reports)
HEPATITIS ( 24 FDA reports)
MUSCULOSKELETAL PAIN ( 24 FDA reports)
OTITIS EXTERNA ( 24 FDA reports)
WEIGHT DECREASED ( 24 FDA reports)
NERVOUSNESS ( 23 FDA reports)
PARAESTHESIA ( 23 FDA reports)
SOMNOLENCE ( 23 FDA reports)
SPINAL OSTEOARTHRITIS ( 23 FDA reports)
VISION BLURRED ( 23 FDA reports)
VISUAL ACUITY REDUCED ( 23 FDA reports)
ASTHMA ( 22 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 22 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
CONDITION AGGRAVATED ( 22 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 22 FDA reports)
GASTROENTERITIS ( 22 FDA reports)
IRRITABLE BOWEL SYNDROME ( 22 FDA reports)
RENAL FAILURE ( 22 FDA reports)
ATRIAL SEPTAL DEFECT ( 21 FDA reports)
BLINDNESS ( 21 FDA reports)
CARDIAC MURMUR ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
CORONARY ARTERY DISEASE ( 21 FDA reports)
DRUG DEPENDENCE ( 21 FDA reports)
DRY MOUTH ( 21 FDA reports)
MENTAL DISORDER ( 21 FDA reports)
OSTEOARTHRITIS ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
RENAL IMPAIRMENT ( 21 FDA reports)
CARDIAC DISORDER ( 20 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 20 FDA reports)
HEPATIC ENZYME INCREASED ( 20 FDA reports)
URTICARIA ( 20 FDA reports)
BLOOD GLUCOSE INCREASED ( 19 FDA reports)
HYPERGLYCAEMIA ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
ASCITES ( 18 FDA reports)
BALANCE DISORDER ( 18 FDA reports)
CATARACT ( 18 FDA reports)
CHEST DISCOMFORT ( 18 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 18 FDA reports)
LETHARGY ( 18 FDA reports)
MUSCULAR WEAKNESS ( 18 FDA reports)
NEUTROPENIA ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
TARDIVE DYSKINESIA ( 18 FDA reports)
TINNITUS ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
MACULAR DEGENERATION ( 17 FDA reports)
MALAISE ( 17 FDA reports)
NIGHT SWEATS ( 17 FDA reports)
RADICULOPATHY ( 17 FDA reports)
TYPE 1 DIABETES MELLITUS ( 17 FDA reports)
WHEEZING ( 17 FDA reports)
BENIGN COLONIC POLYP ( 16 FDA reports)
CARDIO-RESPIRATORY ARREST ( 16 FDA reports)
COLITIS ULCERATIVE ( 16 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 16 FDA reports)
DRUG HYPERSENSITIVITY ( 16 FDA reports)
DRY SKIN ( 16 FDA reports)
EAR PAIN ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
INFLUENZA ( 16 FDA reports)
MEDICATION ERROR ( 16 FDA reports)
RADIOTHERAPY ( 16 FDA reports)
RASH MACULO-PAPULAR ( 16 FDA reports)
RENAL ARTERY STENOSIS ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
SUICIDAL IDEATION ( 16 FDA reports)
URINE ODOUR ABNORMAL ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 15 FDA reports)
CARDIOMEGALY ( 15 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
CONVULSION ( 15 FDA reports)
CROHN'S DISEASE ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
DEATH ( 15 FDA reports)
DISTURBANCE IN ATTENTION ( 15 FDA reports)
GASTROINTESTINAL PAIN ( 15 FDA reports)
HEART VALVE CALCIFICATION ( 15 FDA reports)
HEART VALVE INCOMPETENCE ( 15 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 15 FDA reports)
LABILE BLOOD PRESSURE ( 15 FDA reports)
WEIGHT INCREASED ( 15 FDA reports)
ACNE ( 14 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 14 FDA reports)
ANGINA PECTORIS ( 14 FDA reports)
BRONCHOSPASM ( 14 FDA reports)
BURNING SENSATION ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
CHOLECYSTITIS CHRONIC ( 14 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
DYSPNOEA EXERTIONAL ( 14 FDA reports)
EXCORIATION ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
HYPERTENSIVE CRISIS ( 14 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 14 FDA reports)
HYPONATRAEMIA ( 14 FDA reports)
INTESTINAL OBSTRUCTION ( 14 FDA reports)
MEMORY IMPAIRMENT ( 14 FDA reports)
NERVOUS SYSTEM DISORDER ( 14 FDA reports)
ORAL HERPES ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
SKIN EXFOLIATION ( 14 FDA reports)
SWELLING FACE ( 14 FDA reports)
TREATMENT NONCOMPLIANCE ( 14 FDA reports)
VERTIGO ( 14 FDA reports)
VIRAL INFECTION ( 14 FDA reports)
ANOREXIA ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
FEAR ( 13 FDA reports)
IMPAIRED HEALING ( 13 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 13 FDA reports)
OXYGEN SATURATION DECREASED ( 13 FDA reports)
STRESS ( 13 FDA reports)
TOOTHACHE ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
ABDOMINAL DISCOMFORT ( 12 FDA reports)
AGITATION ( 12 FDA reports)
ARRHYTHMIA ( 12 FDA reports)
ARTHRITIS ( 12 FDA reports)
BLOOD BILIRUBIN INCREASED ( 12 FDA reports)
CAROTID ARTERY STENOSIS ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
DYSKINESIA ( 12 FDA reports)
ECONOMIC PROBLEM ( 12 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
HYPERSOMNIA ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
JAUNDICE ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
MULTIPLE INJURIES ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
RESPIRATORY ARREST ( 12 FDA reports)
SLEEP DISORDER ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
TREMOR ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
ANAL ULCER ( 11 FDA reports)
ANAPHYLACTIC REACTION ( 11 FDA reports)
BLAST CELL CRISIS ( 11 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 11 FDA reports)
BONE DISORDER ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CAROTID ARTERY OCCLUSION ( 11 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
DEFORMITY ( 11 FDA reports)
DISABILITY ( 11 FDA reports)
DYSURIA ( 11 FDA reports)
FEELING JITTERY ( 11 FDA reports)
HAEMATOCHEZIA ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
JOINT SWELLING ( 11 FDA reports)
MIGRAINE ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 11 FDA reports)
POSTNASAL DRIP ( 11 FDA reports)
RASH ERYTHEMATOUS ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
RHINALGIA ( 11 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 11 FDA reports)
UNEVALUABLE EVENT ( 11 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
AGGRESSION ( 10 FDA reports)
ARTHROPATHY ( 10 FDA reports)
COLONIC POLYP ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
EAR INFECTION ( 10 FDA reports)
GALLBLADDER DISORDER ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
LARYNGITIS ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
NASAL CONGESTION ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
OSTEOPOROSIS ( 10 FDA reports)
PALLOR ( 10 FDA reports)
POST PROCEDURAL COMPLICATION ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
URINARY INCONTINENCE ( 10 FDA reports)
VIRAL PHARYNGITIS ( 10 FDA reports)
ACUTE SINUSITIS ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
CHILLS ( 9 FDA reports)
CIRCULATORY COLLAPSE ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 9 FDA reports)
DRUG TOLERANCE ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
FEELING COLD ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
OSTEOMYELITIS ( 9 FDA reports)
PRIMARY SEQUESTRUM ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
RHINITIS ( 9 FDA reports)
SEDATION ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
SPINAL COLUMN STENOSIS ( 9 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 9 FDA reports)
TENDERNESS ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
AORTIC STENOSIS ( 8 FDA reports)
ATROPHIC VULVOVAGINITIS ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
BRONCHOPNEUMONIA ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CHAPPED LIPS ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DEVELOPMENTAL DELAY ( 8 FDA reports)
EMPHYSEMA ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
HAEMORRHOIDS ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
MASS ( 8 FDA reports)
MOUTH ULCERATION ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
COORDINATION ABNORMAL ( 7 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 7 FDA reports)
DIGEORGE'S SYNDROME ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EXPOSURE TO TOXIC AGENT ( 7 FDA reports)
FALLOT'S TETRALOGY ( 7 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HEPATITIS C ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
ILEITIS ( 7 FDA reports)
ILEUS ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
LEFT ATRIAL DILATATION ( 7 FDA reports)
LEUKOPLAKIA ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
LUMBAR RADICULOPATHY ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
MICROCEPHALY ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
OBESITY ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PULMONARY ARTERY DILATATION ( 7 FDA reports)
RASH MACULAR ( 7 FDA reports)
SCAR ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SPINAL DISORDER ( 7 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
UNDERWEIGHT ( 7 FDA reports)
VELO-CARDIO-FACIAL SYNDROME ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ADENOIDAL HYPERTROPHY ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ANGIONEUROTIC OEDEMA ( 6 FDA reports)
BACK DISORDER ( 6 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CEREBRAL CALCIFICATION ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRUG SCREEN POSITIVE ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
EXPOSED BONE IN JAW ( 6 FDA reports)
FIBROSIS ( 6 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 6 FDA reports)
GENITAL DISCOMFORT ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GRIMACING ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
INFECTION ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MENINGIOMA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NERVE ROOT LESION ( 6 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
OSTEITIS ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
OVERGROWTH BACTERIAL ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
PROCTITIS ULCERATIVE ( 6 FDA reports)
PRODUCT QUALITY ISSUE ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SOFT TISSUE DISORDER ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STRIDOR ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
AUTISM ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
CERVICAL MYELOPATHY ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
CROUP INFECTIOUS ( 5 FDA reports)
CYST ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEELING HOT AND COLD ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
GOUT ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KLIPPEL-FEIL SYNDROME ( 5 FDA reports)
LABYRINTHITIS ( 5 FDA reports)
LARYNGEAL STENOSIS ( 5 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
METAMORPHOPSIA ( 5 FDA reports)
MORGANELLA INFECTION ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
OESOPHAGEAL ACHALASIA ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
PAIN OF SKIN ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
POLYP ( 5 FDA reports)
POST LAMINECTOMY SYNDROME ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
RETCHING ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN TEST POSITIVE ( 5 FDA reports)
SPONDYLOARTHROPATHY ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
TOOTH INFECTION ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
BALANOPOSTHITIS ( 4 FDA reports)
BILIARY CIRRHOSIS ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CAROTID ARTERY ATHEROMA ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CEREBROVASCULAR DISORDER ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
EPIDIDYMAL CYST ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
ESSENTIAL HYPERTENSION ( 4 FDA reports)
EXTERNAL EAR LESION EXCISION ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FLATBACK SYNDROME ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
FORAMEN MAGNUM STENOSIS ( 4 FDA reports)
FORCEPS DELIVERY ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GENITAL CANDIDIASIS ( 4 FDA reports)
GILBERT'S SYNDROME ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
ODONTOGENIC CYST ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OSTEITIS DEFORMANS ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
OSTEOMYELITIS CHRONIC ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
PARONYCHIA ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RASH SCARLATINIFORM ( 4 FDA reports)
RIB DEFORMITY ( 4 FDA reports)
RIGHT ATRIAL DILATATION ( 4 FDA reports)
SCROTAL ABSCESS ( 4 FDA reports)
SCROTAL INFECTION ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOOTH DEPOSIT ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 4 FDA reports)
VASCULITIC RASH ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APHONIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATELECTASIS NEONATAL ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHORIOAMNIONITIS ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
COXSACKIE VIRAL INFECTION ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EARLY SATIETY ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
EPIPHYSES PREMATURE FUSION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
MINERAL METABOLISM DISORDER ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MURPHY'S SIGN POSITIVE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
OTITIS MEDIA CHRONIC ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHYSICAL DISABILITY ( 3 FDA reports)
PLACENTAL INFARCTION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY OEDEMA NEONATAL ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
ROTAVIRUS TEST POSITIVE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENSION ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
VACCINATION FAILURE ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BILE ACID MALABSORPTION ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COARCTATION OF THE AORTA ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ECTODERMAL DYSPLASIA ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MIXED INCONTINENCE ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SHARED PSYCHOTIC DISORDER ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SNORING ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TOXICOLOGIC TEST ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
AMNIOCENTESIS ABNORMAL ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY HEIGHT ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIPHYSEAL FRACTURE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EWING'S SARCOMA RECURRENT ( 1 FDA reports)
EXANTHEMA SUBITUM ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPHTHALMIA NEONATORUM ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINOBLASTOMA BILATERAL ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
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VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
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WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
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