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

PAIN ( 259 FDA reports)
ANXIETY ( 217 FDA reports)
ANAEMIA ( 202 FDA reports)
BACK PAIN ( 193 FDA reports)
PYREXIA ( 192 FDA reports)
DYSPNOEA ( 166 FDA reports)
DEPRESSION ( 165 FDA reports)
NAUSEA ( 161 FDA reports)
INJURY ( 157 FDA reports)
VOMITING ( 153 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 142 FDA reports)
FATIGUE ( 141 FDA reports)
PNEUMONIA ( 139 FDA reports)
ARTHRALGIA ( 129 FDA reports)
HYPOTENSION ( 129 FDA reports)
HEADACHE ( 125 FDA reports)
ABDOMINAL PAIN ( 123 FDA reports)
OSTEONECROSIS OF JAW ( 123 FDA reports)
ANHEDONIA ( 120 FDA reports)
DIARRHOEA ( 116 FDA reports)
CARDIOMEGALY ( 113 FDA reports)
PAIN IN JAW ( 112 FDA reports)
PLEURAL EFFUSION ( 112 FDA reports)
OSTEOARTHRITIS ( 109 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 108 FDA reports)
GAIT DISTURBANCE ( 107 FDA reports)
EMOTIONAL DISTRESS ( 106 FDA reports)
BONE DISORDER ( 103 FDA reports)
URINARY TRACT INFECTION ( 103 FDA reports)
CONSTIPATION ( 101 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 100 FDA reports)
FALL ( 99 FDA reports)
OSTEOMYELITIS ( 95 FDA reports)
DIZZINESS ( 94 FDA reports)
PAIN IN EXTREMITY ( 94 FDA reports)
HYPERTENSION ( 93 FDA reports)
TOOTH EXTRACTION ( 93 FDA reports)
OEDEMA PERIPHERAL ( 90 FDA reports)
RASH ( 90 FDA reports)
RENAL FAILURE ACUTE ( 90 FDA reports)
RESPIRATORY FAILURE ( 88 FDA reports)
ASTHENIA ( 87 FDA reports)
INSOMNIA ( 85 FDA reports)
RENAL FAILURE ( 85 FDA reports)
SEPSIS ( 82 FDA reports)
INFECTION ( 81 FDA reports)
ATELECTASIS ( 80 FDA reports)
WEIGHT DECREASED ( 80 FDA reports)
ATRIAL SEPTAL DEFECT ( 79 FDA reports)
SPINAL OSTEOARTHRITIS ( 79 FDA reports)
MITRAL VALVE INCOMPETENCE ( 76 FDA reports)
DEHYDRATION ( 75 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 75 FDA reports)
OSTEOPENIA ( 74 FDA reports)
ERYTHEMA ( 73 FDA reports)
THROMBOCYTOPENIA ( 72 FDA reports)
CHEST PAIN ( 71 FDA reports)
NEONATAL DISORDER ( 71 FDA reports)
WEIGHT INCREASED ( 71 FDA reports)
CARDIAC MURMUR ( 70 FDA reports)
STRESS ( 70 FDA reports)
HAEMORRHOIDS ( 69 FDA reports)
TOOTHACHE ( 68 FDA reports)
HYPOKALAEMIA ( 67 FDA reports)
OSTEONECROSIS ( 67 FDA reports)
BRADYCARDIA ( 66 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 66 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 65 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 63 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 63 FDA reports)
EXOSTOSIS ( 62 FDA reports)
ATRIAL FIBRILLATION ( 61 FDA reports)
DEEP VEIN THROMBOSIS ( 61 FDA reports)
DEFORMITY ( 61 FDA reports)
SWELLING ( 60 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 60 FDA reports)
LYMPHADENOPATHY ( 59 FDA reports)
METASTASES TO BONE ( 59 FDA reports)
TOOTH DISORDER ( 59 FDA reports)
CONTUSION ( 58 FDA reports)
COUGH ( 58 FDA reports)
NEUROPATHY PERIPHERAL ( 58 FDA reports)
PREMATURE BABY ( 58 FDA reports)
BLOOD CREATININE INCREASED ( 57 FDA reports)
PNEUMOTHORAX ( 57 FDA reports)
CONFUSIONAL STATE ( 56 FDA reports)
CONVULSION ( 56 FDA reports)
HAEMATURIA ( 56 FDA reports)
MULTI-ORGAN FAILURE ( 56 FDA reports)
IMPAIRED HEALING ( 55 FDA reports)
DRUG INEFFECTIVE ( 54 FDA reports)
MUSCULAR WEAKNESS ( 53 FDA reports)
OBESITY ( 53 FDA reports)
HAEMOGLOBIN DECREASED ( 52 FDA reports)
HYPOGLYCAEMIA ( 52 FDA reports)
HYPOPHAGIA ( 52 FDA reports)
HYPERLIPIDAEMIA ( 51 FDA reports)
HYPOAESTHESIA ( 51 FDA reports)
SCOLIOSIS ( 51 FDA reports)
MUSCLE SPASMS ( 50 FDA reports)
PRIMARY SEQUESTRUM ( 50 FDA reports)
RESPIRATORY DISTRESS ( 50 FDA reports)
SWELLING FACE ( 50 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 48 FDA reports)
DEATH ( 48 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 48 FDA reports)
NEUTROPENIA ( 48 FDA reports)
SINUSITIS ( 48 FDA reports)
SLEEP APNOEA SYNDROME ( 48 FDA reports)
BRONCHITIS ( 47 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 47 FDA reports)
PULMONARY OEDEMA ( 47 FDA reports)
CEREBROVASCULAR ACCIDENT ( 46 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 46 FDA reports)
JOINT SWELLING ( 46 FDA reports)
TACHYCARDIA ( 46 FDA reports)
TOOTH LOSS ( 46 FDA reports)
LIFE EXPECTANCY SHORTENED ( 45 FDA reports)
PANCYTOPENIA ( 45 FDA reports)
RENAL IMPAIRMENT ( 45 FDA reports)
ARRHYTHMIA ( 44 FDA reports)
DYSPHAGIA ( 44 FDA reports)
FISTULA ( 44 FDA reports)
METABOLIC ACIDOSIS ( 44 FDA reports)
SINUS TACHYCARDIA ( 44 FDA reports)
CATARACT ( 43 FDA reports)
LOOSE TOOTH ( 43 FDA reports)
PARAESTHESIA ( 43 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 43 FDA reports)
ARTHRITIS ( 42 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 42 FDA reports)
ASTHMA ( 41 FDA reports)
BONE LESION ( 41 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 41 FDA reports)
MUSCULOSKELETAL PAIN ( 41 FDA reports)
ABDOMINAL DISTENSION ( 39 FDA reports)
CANDIDIASIS ( 39 FDA reports)
CONDITION AGGRAVATED ( 39 FDA reports)
DIVERTICULUM ( 39 FDA reports)
GINGIVITIS ( 39 FDA reports)
MASTICATION DISORDER ( 39 FDA reports)
MENTAL STATUS CHANGES ( 39 FDA reports)
OEDEMA ( 39 FDA reports)
PRURITUS ( 39 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 38 FDA reports)
AORTIC VALVE INCOMPETENCE ( 38 FDA reports)
BONE PAIN ( 38 FDA reports)
CHOLELITHIASIS ( 38 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 38 FDA reports)
RHINORRHOEA ( 38 FDA reports)
HYPOXIA ( 37 FDA reports)
LEUKOCYTOSIS ( 37 FDA reports)
LUNG DISORDER ( 37 FDA reports)
METASTASES TO SPINE ( 37 FDA reports)
PERICARDIAL EFFUSION ( 37 FDA reports)
PHYSICAL DISABILITY ( 37 FDA reports)
PULMONARY HAEMORRHAGE ( 37 FDA reports)
ACNE ( 36 FDA reports)
CARDIAC DISORDER ( 36 FDA reports)
DECREASED APPETITE ( 36 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 36 FDA reports)
EAR PAIN ( 36 FDA reports)
DEBRIDEMENT ( 35 FDA reports)
DENTAL CARIES ( 35 FDA reports)
SOMNOLENCE ( 35 FDA reports)
VENTRICULAR HYPERTROPHY ( 35 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 34 FDA reports)
CELLULITIS ( 34 FDA reports)
DYSURIA ( 34 FDA reports)
GASTRITIS ( 34 FDA reports)
HYPERSENSITIVITY ( 34 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 34 FDA reports)
AGITATION ( 33 FDA reports)
BLOOD UREA INCREASED ( 33 FDA reports)
CARDIAC ARREST ( 33 FDA reports)
CYANOSIS ( 33 FDA reports)
FEBRILE NEUTROPENIA ( 33 FDA reports)
GINGIVAL DISORDER ( 33 FDA reports)
MOUTH ULCERATION ( 33 FDA reports)
MULTIPLE MYELOMA ( 33 FDA reports)
NEPHROLITHIASIS ( 33 FDA reports)
OXYGEN SATURATION DECREASED ( 33 FDA reports)
PULMONARY EMBOLISM ( 33 FDA reports)
RASH MACULO-PAPULAR ( 33 FDA reports)
RHINITIS ( 33 FDA reports)
SEPSIS NEONATAL ( 33 FDA reports)
SINUS BRADYCARDIA ( 33 FDA reports)
SLEEP DISORDER ( 33 FDA reports)
TENDONITIS ( 33 FDA reports)
UNEVALUABLE EVENT ( 33 FDA reports)
VISUAL IMPAIRMENT ( 33 FDA reports)
BURSITIS ( 32 FDA reports)
DIABETES MELLITUS ( 32 FDA reports)
DRUG HYPERSENSITIVITY ( 32 FDA reports)
EYE PAIN ( 32 FDA reports)
HYPERKALAEMIA ( 32 FDA reports)
POLLAKIURIA ( 32 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 32 FDA reports)
ARTHROPATHY ( 31 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 31 FDA reports)
INFLAMMATION ( 31 FDA reports)
MYALGIA ( 31 FDA reports)
MYOCARDIAL INFARCTION ( 31 FDA reports)
NECK PAIN ( 31 FDA reports)
SYNCOPE ( 31 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
BLOOD BILIRUBIN INCREASED ( 30 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 30 FDA reports)
DISCOMFORT ( 30 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 30 FDA reports)
MUCOSAL INFLAMMATION ( 30 FDA reports)
NEOPLASM MALIGNANT ( 30 FDA reports)
OSTEOPOROSIS ( 30 FDA reports)
RENAL CYST ( 30 FDA reports)
STAPHYLOCOCCAL INFECTION ( 30 FDA reports)
TOOTH ABSCESS ( 30 FDA reports)
TOOTH INFECTION ( 30 FDA reports)
BONE DEBRIDEMENT ( 29 FDA reports)
CARPAL TUNNEL SYNDROME ( 29 FDA reports)
CORONARY ARTERY DISEASE ( 29 FDA reports)
GINGIVAL BLEEDING ( 29 FDA reports)
HYPOTHYROIDISM ( 29 FDA reports)
INGUINAL HERNIA ( 29 FDA reports)
LOSS OF CONSCIOUSNESS ( 29 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 29 FDA reports)
METASTASES TO LUNG ( 29 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 29 FDA reports)
PRESYNCOPE ( 29 FDA reports)
URTICARIA ( 29 FDA reports)
VISION BLURRED ( 29 FDA reports)
CHILLS ( 28 FDA reports)
MUSCLE TWITCHING ( 28 FDA reports)
ORAL INFECTION ( 28 FDA reports)
TACHYPNOEA ( 28 FDA reports)
TINNITUS ( 28 FDA reports)
FLANK PAIN ( 27 FDA reports)
HEPATOMEGALY ( 27 FDA reports)
HIATUS HERNIA ( 27 FDA reports)
HYPONATRAEMIA ( 27 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 27 FDA reports)
ORAL PAIN ( 27 FDA reports)
PLATELET COUNT DECREASED ( 27 FDA reports)
RENAL FAILURE CHRONIC ( 27 FDA reports)
AORTIC ANEURYSM ( 26 FDA reports)
BASAL CELL CARCINOMA ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 26 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 26 FDA reports)
CHRONIC SINUSITIS ( 26 FDA reports)
HYPERCALCAEMIA ( 26 FDA reports)
SEPTIC SHOCK ( 26 FDA reports)
BACTERAEMIA ( 25 FDA reports)
DECREASED INTEREST ( 25 FDA reports)
ECZEMA ( 25 FDA reports)
HYPOCALCAEMIA ( 25 FDA reports)
MEMORY IMPAIRMENT ( 25 FDA reports)
PULMONARY HYPERTENSION ( 25 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 25 FDA reports)
SINUS ARRHYTHMIA ( 25 FDA reports)
SKIN ULCER ( 25 FDA reports)
VIRAL INFECTION ( 25 FDA reports)
WHEEZING ( 25 FDA reports)
ANOREXIA ( 24 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 24 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
COLITIS ( 24 FDA reports)
DEVELOPMENTAL DELAY ( 24 FDA reports)
HAEMATOMA ( 24 FDA reports)
HYPERHIDROSIS ( 24 FDA reports)
INTESTINAL PERFORATION ( 24 FDA reports)
IRRITABLE BOWEL SYNDROME ( 24 FDA reports)
LEFT ATRIAL DILATATION ( 24 FDA reports)
PHARYNGITIS ( 24 FDA reports)
PURULENCE ( 24 FDA reports)
RECTAL HAEMORRHAGE ( 24 FDA reports)
SINUS DISORDER ( 24 FDA reports)
CARDIOMYOPATHY ( 23 FDA reports)
DYSKINESIA ( 23 FDA reports)
DYSPNOEA EXERTIONAL ( 23 FDA reports)
FEAR ( 23 FDA reports)
GINGIVAL PAIN ( 23 FDA reports)
GINGIVAL ULCERATION ( 23 FDA reports)
GLAUCOMA ( 23 FDA reports)
HEART RATE INCREASED ( 23 FDA reports)
HYDRONEPHROSIS ( 23 FDA reports)
HYPERGLYCAEMIA ( 23 FDA reports)
JAUNDICE ( 23 FDA reports)
MALAISE ( 23 FDA reports)
NEURALGIA ( 23 FDA reports)
PHARYNGEAL OEDEMA ( 23 FDA reports)
STOMATITIS ( 23 FDA reports)
SUICIDAL IDEATION ( 23 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
WALKING AID USER ( 23 FDA reports)
APHTHOUS STOMATITIS ( 22 FDA reports)
BLOOD PRESSURE DECREASED ( 22 FDA reports)
DISEASE PROGRESSION ( 22 FDA reports)
ENCEPHALOPATHY ( 22 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 22 FDA reports)
LUNG INFILTRATION ( 22 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 22 FDA reports)
OTITIS MEDIA ( 22 FDA reports)
PULMONARY VALVE STENOSIS ( 22 FDA reports)
RENAL DISORDER ( 22 FDA reports)
SCAR ( 22 FDA reports)
SKIN DISCOLOURATION ( 22 FDA reports)
SPINAL COMPRESSION FRACTURE ( 22 FDA reports)
URINARY INCONTINENCE ( 22 FDA reports)
ABDOMINAL PAIN UPPER ( 21 FDA reports)
BLOOD PRESSURE INCREASED ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
EPISTAXIS ( 21 FDA reports)
GENERALISED OEDEMA ( 21 FDA reports)
HERPES SIMPLEX ( 21 FDA reports)
LARYNGITIS ( 21 FDA reports)
MEDICATION ERROR ( 21 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 21 FDA reports)
ORAL SURGERY ( 21 FDA reports)
SPONDYLOLISTHESIS ( 21 FDA reports)
STEVENS-JOHNSON SYNDROME ( 21 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 20 FDA reports)
ATAXIA ( 20 FDA reports)
BALANCE DISORDER ( 20 FDA reports)
BLISTER ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 20 FDA reports)
BODY TEMPERATURE INCREASED ( 20 FDA reports)
CYSTITIS ( 20 FDA reports)
ECONOMIC PROBLEM ( 20 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
JAW OPERATION ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
RASH ERYTHEMATOUS ( 20 FDA reports)
SKIN LESION ( 20 FDA reports)
TORSADE DE POINTES ( 20 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
AORTIC STENOSIS ( 19 FDA reports)
ASCITES ( 19 FDA reports)
BLOOD POTASSIUM DECREASED ( 19 FDA reports)
CARDIO-RESPIRATORY ARREST ( 19 FDA reports)
CEREBRAL INFARCTION ( 19 FDA reports)
COMPRESSION FRACTURE ( 19 FDA reports)
COORDINATION ABNORMAL ( 19 FDA reports)
DERMATITIS ALLERGIC ( 19 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
DRY EYE ( 19 FDA reports)
EXPOSED BONE IN JAW ( 19 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 19 FDA reports)
HAEMOPTYSIS ( 19 FDA reports)
HYPOAESTHESIA ORAL ( 19 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 19 FDA reports)
METASTASES TO LIVER ( 19 FDA reports)
PERIODONTITIS ( 19 FDA reports)
PURULENT DISCHARGE ( 19 FDA reports)
TACHYARRHYTHMIA ( 19 FDA reports)
TREATMENT NONCOMPLIANCE ( 19 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 18 FDA reports)
ALOPECIA ( 18 FDA reports)
BLADDER CANCER ( 18 FDA reports)
BLOOD CALCIUM DECREASED ( 18 FDA reports)
BLOOD URINE PRESENT ( 18 FDA reports)
CAESAREAN SECTION ( 18 FDA reports)
COMA ( 18 FDA reports)
DILATATION ATRIAL ( 18 FDA reports)
DYSLIPIDAEMIA ( 18 FDA reports)
GRAND MAL CONVULSION ( 18 FDA reports)
HEART DISEASE CONGENITAL ( 18 FDA reports)
HYPERNATRAEMIA ( 18 FDA reports)
MOVEMENT DISORDER ( 18 FDA reports)
OROPHARYNGEAL PAIN ( 18 FDA reports)
PRESBYOPIA ( 18 FDA reports)
RENAL INJURY ( 18 FDA reports)
STEM CELL TRANSPLANT ( 18 FDA reports)
TIBIA FRACTURE ( 18 FDA reports)
TREMOR ( 18 FDA reports)
UNRESPONSIVE TO STIMULI ( 18 FDA reports)
ACIDOSIS ( 17 FDA reports)
CARDIOVASCULAR DISORDER ( 17 FDA reports)
CATHETER PLACEMENT ( 17 FDA reports)
COARCTATION OF THE AORTA ( 17 FDA reports)
CONJUNCTIVITIS ( 17 FDA reports)
DIALYSIS ( 17 FDA reports)
DILATATION VENTRICULAR ( 17 FDA reports)
DUODENITIS ( 17 FDA reports)
ENTEROCOCCAL INFECTION ( 17 FDA reports)
ESCHERICHIA INFECTION ( 17 FDA reports)
FALLOT'S TETRALOGY ( 17 FDA reports)
GOITRE ( 17 FDA reports)
HAEMATOCRIT DECREASED ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
HAEMORRHAGE ( 17 FDA reports)
HEPATIC STEATOSIS ( 17 FDA reports)
MITRAL VALVE PROLAPSE ( 17 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 17 FDA reports)
MYCOSIS FUNGOIDES ( 17 FDA reports)
NASAL CONGESTION ( 17 FDA reports)
OPEN WOUND ( 17 FDA reports)
OSTEOSCLEROSIS ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
POST PROCEDURAL COMPLICATION ( 17 FDA reports)
SHOCK ( 17 FDA reports)
SOFT TISSUE DISORDER ( 17 FDA reports)
TOOTH REPAIR ( 17 FDA reports)
VENTRICULAR TACHYCARDIA ( 17 FDA reports)
VERTEBROPLASTY ( 17 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 17 FDA reports)
ADHESION ( 16 FDA reports)
ANAPHYLACTIC REACTION ( 16 FDA reports)
BIPOLAR DISORDER ( 16 FDA reports)
BONE DENSITY DECREASED ( 16 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 16 FDA reports)
CYST ( 16 FDA reports)
DEAFNESS ( 16 FDA reports)
DEAFNESS NEUROSENSORY ( 16 FDA reports)
DENTAL CARE ( 16 FDA reports)
DERMATITIS ( 16 FDA reports)
DISTURBANCE IN ATTENTION ( 16 FDA reports)
DYSAESTHESIA ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 16 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 16 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 16 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 16 FDA reports)
LETHARGY ( 16 FDA reports)
LUNG NEOPLASM ( 16 FDA reports)
OSTEOCHONDROSIS ( 16 FDA reports)
OSTEOLYSIS ( 16 FDA reports)
OVERDOSE ( 16 FDA reports)
PHOTOPHERESIS ( 16 FDA reports)
PRODUCTIVE COUGH ( 16 FDA reports)
SKIN EXFOLIATION ( 16 FDA reports)
SURGERY ( 16 FDA reports)
ANAL FISSURE ( 15 FDA reports)
BLINDNESS ( 15 FDA reports)
BLOOD MAGNESIUM DECREASED ( 15 FDA reports)
BRADYCARDIA NEONATAL ( 15 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 15 FDA reports)
CHOLESTASIS ( 15 FDA reports)
COAGULOPATHY ( 15 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 15 FDA reports)
DYSPEPSIA ( 15 FDA reports)
ENDOCARDITIS ( 15 FDA reports)
FACIAL PAIN ( 15 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
HYPERBILIRUBINAEMIA ( 15 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 15 FDA reports)
JARISCH-HERXHEIMER REACTION ( 15 FDA reports)
JAUNDICE NEONATAL ( 15 FDA reports)
JOINT STIFFNESS ( 15 FDA reports)
MENTAL DISORDER ( 15 FDA reports)
NIGHT SWEATS ( 15 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 15 FDA reports)
ORTHOSTATIC HYPOTENSION ( 15 FDA reports)
OSTEITIS ( 15 FDA reports)
PATHOLOGICAL FRACTURE ( 15 FDA reports)
PREMATURE LABOUR ( 15 FDA reports)
PYELONEPHRITIS ( 15 FDA reports)
RESPIRATORY ACIDOSIS ( 15 FDA reports)
RHINITIS ALLERGIC ( 15 FDA reports)
SICK SINUS SYNDROME ( 15 FDA reports)
SPEECH DISORDER ( 15 FDA reports)
SPINAL COLUMN STENOSIS ( 15 FDA reports)
URINE OUTPUT DECREASED ( 15 FDA reports)
ABSCESS ( 14 FDA reports)
ACTINOMYCOSIS ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 14 FDA reports)
AMNESIA ( 14 FDA reports)
ARTERIOSCLEROSIS ( 14 FDA reports)
BACK INJURY ( 14 FDA reports)
BREAST CANCER METASTATIC ( 14 FDA reports)
CHOLECYSTITIS INFECTIVE ( 14 FDA reports)
CONGENITAL ANOMALY ( 14 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 14 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 14 FDA reports)
DIVERTICULUM INTESTINAL ( 14 FDA reports)
DYSARTHRIA ( 14 FDA reports)
DYSGEUSIA ( 14 FDA reports)
GYNAECOMASTIA ( 14 FDA reports)
HYPERMETABOLISM ( 14 FDA reports)
HYPOMAGNESAEMIA ( 14 FDA reports)
INTESTINAL OBSTRUCTION ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
LUMBAR SPINE FLATTENING ( 14 FDA reports)
MASS ( 14 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 14 FDA reports)
MULTIPLE ALLERGIES ( 14 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 14 FDA reports)
PULMONARY GRANULOMA ( 14 FDA reports)
RHONCHI ( 14 FDA reports)
SERRATIA INFECTION ( 14 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 14 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 14 FDA reports)
VERTIGO ( 14 FDA reports)
ABASIA ( 13 FDA reports)
AGRANULOCYTOSIS ( 13 FDA reports)
APNOEA ( 13 FDA reports)
BACTERIAL INFECTION ( 13 FDA reports)
BLOOD ALBUMIN DECREASED ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
BREATH ODOUR ( 13 FDA reports)
CATHETER REMOVAL ( 13 FDA reports)
CHEST X-RAY ABNORMAL ( 13 FDA reports)
CHOLECYSTITIS ( 13 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 13 FDA reports)
DRY SKIN ( 13 FDA reports)
DYSPHEMIA ( 13 FDA reports)
EAR DISORDER ( 13 FDA reports)
EATING DISORDER ( 13 FDA reports)
EMPHYSEMA ( 13 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 13 FDA reports)
FOETAL GROWTH RETARDATION ( 13 FDA reports)
HAEMATOCHEZIA ( 13 FDA reports)
HOT FLUSH ( 13 FDA reports)
IMPAIRED WORK ABILITY ( 13 FDA reports)
INCISIONAL DRAINAGE ( 13 FDA reports)
MAMMOGRAM ABNORMAL ( 13 FDA reports)
METABOLIC ALKALOSIS ( 13 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 13 FDA reports)
NERVOUS SYSTEM DISORDER ( 13 FDA reports)
ONYCHOMYCOSIS ( 13 FDA reports)
ORTHOPNOEA ( 13 FDA reports)
PERITONITIS ( 13 FDA reports)
PHLEBITIS ( 13 FDA reports)
POLYURIA ( 13 FDA reports)
PROCTALGIA ( 13 FDA reports)
PROCTITIS ( 13 FDA reports)
PSEUDOMONAS INFECTION ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
RENAL ISCHAEMIA ( 13 FDA reports)
SKELETAL INJURY ( 13 FDA reports)
SMEAR CERVIX ABNORMAL ( 13 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 13 FDA reports)
URINARY RETENTION ( 13 FDA reports)
VAGINAL INFECTION ( 13 FDA reports)
ANORECTAL DISCOMFORT ( 12 FDA reports)
ASPIRATION ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
BIOPSY GINGIVAL ( 12 FDA reports)
CIRCULATORY COLLAPSE ( 12 FDA reports)
COLITIS ULCERATIVE ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
DEVICE BREAKAGE ( 12 FDA reports)
DISEASE RECURRENCE ( 12 FDA reports)
DRUG TOXICITY ( 12 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
GALLBLADDER DISORDER ( 12 FDA reports)
GESTATIONAL DIABETES ( 12 FDA reports)
GINGIVAL OEDEMA ( 12 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 12 FDA reports)
GRIP STRENGTH DECREASED ( 12 FDA reports)
HEARING AID USER ( 12 FDA reports)
HERPES ZOSTER ( 12 FDA reports)
INDURATION ( 12 FDA reports)
INTESTINAL ISCHAEMIA ( 12 FDA reports)
INTESTINAL STENOSIS ( 12 FDA reports)
JOINT EFFUSION ( 12 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
LYMPHOMA ( 12 FDA reports)
MENINGITIS ( 12 FDA reports)
MENINGITIS ASEPTIC ( 12 FDA reports)
MULTI-ORGAN DISORDER ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
PERICARDITIS ( 12 FDA reports)
PLASMACYTOMA ( 12 FDA reports)
PLASMACYTOSIS ( 12 FDA reports)
PLATELET COUNT INCREASED ( 12 FDA reports)
PLEURITIC PAIN ( 12 FDA reports)
POST-TRAUMATIC PAIN ( 12 FDA reports)
PULMONARY RADIATION INJURY ( 12 FDA reports)
RESTLESS LEGS SYNDROME ( 12 FDA reports)
SEASONAL ALLERGY ( 12 FDA reports)
SKIN DISORDER ( 12 FDA reports)
SKIN ODOUR ABNORMAL ( 12 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 12 FDA reports)
TELANGIECTASIA ( 12 FDA reports)
THROAT IRRITATION ( 12 FDA reports)
VENTRICULAR ARRHYTHMIA ( 12 FDA reports)
ABSCESS JAW ( 11 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
ACUTE SINUSITIS ( 11 FDA reports)
ANEURYSM ( 11 FDA reports)
ANOGENITAL WARTS ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
BONE MARROW FAILURE ( 11 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 11 FDA reports)
CARDIAC VALVE ABSCESS ( 11 FDA reports)
CARDIOPULMONARY FAILURE ( 11 FDA reports)
COGNITIVE DISORDER ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
DRY MOUTH ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
EPIDIDYMITIS ( 11 FDA reports)
ERECTILE DYSFUNCTION ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
GASTROENTERITIS ( 11 FDA reports)
GENITAL HERPES ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
LIP DRY ( 11 FDA reports)
MULTIPLE INJURIES ( 11 FDA reports)
NEOPLASM PROGRESSION ( 11 FDA reports)
OFF LABEL USE ( 11 FDA reports)
PREGNANCY ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
PULPITIS DENTAL ( 11 FDA reports)
SKIN NEOPLASM EXCISION ( 11 FDA reports)
STRIDOR ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
APGAR SCORE LOW ( 10 FDA reports)
APHASIA ( 10 FDA reports)
BICUSPID AORTIC VALVE ( 10 FDA reports)
BLEPHARITIS ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
CATHETER SEPSIS ( 10 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 10 FDA reports)
CEREBRAL HAEMORRHAGE ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
COLON ADENOMA ( 10 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 10 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
DERMATITIS CONTACT ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DROP ATTACKS ( 10 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 10 FDA reports)
EAR INFECTION ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
FOETAL HEART RATE ABNORMAL ( 10 FDA reports)
GASTROINTESTINAL PERFORATION ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HYPERTENSIVE HEART DISEASE ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
JOINT SPRAIN ( 10 FDA reports)
LASER THERAPY ( 10 FDA reports)
MALNUTRITION ( 10 FDA reports)
MELAENA ( 10 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 10 FDA reports)
NASAL DISORDER ( 10 FDA reports)
NEONATAL HYPOTENSION ( 10 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 10 FDA reports)
PERIPHERAL EMBOLISM ( 10 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
PIGMENTATION DISORDER ( 10 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 10 FDA reports)
PULMONARY CONGESTION ( 10 FDA reports)
RASH GENERALISED ( 10 FDA reports)
RECTAL POLYP ( 10 FDA reports)
RESPIRATORY DISORDER ( 10 FDA reports)
RIB FRACTURE ( 10 FDA reports)
RIGHT ATRIAL DILATATION ( 10 FDA reports)
ROTATOR CUFF SYNDROME ( 10 FDA reports)
SKIN CANDIDA ( 10 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 10 FDA reports)
THYROID NEOPLASM ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
VENTRICULAR FIBRILLATION ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
WOUND DEHISCENCE ( 10 FDA reports)
XEROSIS ( 10 FDA reports)
ACANTHOLYSIS ( 9 FDA reports)
ACETABULUM FRACTURE ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 9 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
BONE SWELLING ( 9 FDA reports)
CACHEXIA ( 9 FDA reports)
CARDIAC ANEURYSM ( 9 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
COLITIS ISCHAEMIC ( 9 FDA reports)
CULTURE URINE POSITIVE ( 9 FDA reports)
CYCLOTHYMIC DISORDER ( 9 FDA reports)
DEPRESSED MOOD ( 9 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 9 FDA reports)
ECZEMA INFECTED ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
ENTEROCOCCAL SEPSIS ( 9 FDA reports)
FACET JOINT SYNDROME ( 9 FDA reports)
FAILURE TO THRIVE ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
FOOD ALLERGY ( 9 FDA reports)
GINGIVAL ERYTHEMA ( 9 FDA reports)
GLOMERULOSCLEROSIS ( 9 FDA reports)
GRAM STAIN POSITIVE ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HAEMATEMESIS ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HYPOACUSIS ( 9 FDA reports)
HYPOVOLAEMIA ( 9 FDA reports)
INFLUENZA ( 9 FDA reports)
INTERCOSTAL RETRACTION ( 9 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 9 FDA reports)
IRON DEFICIENCY ( 9 FDA reports)
KIDNEY FIBROSIS ( 9 FDA reports)
KIDNEY INFECTION ( 9 FDA reports)
LIGAMENT INJURY ( 9 FDA reports)
LIGAMENT SPRAIN ( 9 FDA reports)
LIP EROSION ( 9 FDA reports)
LYMPHOEDEMA ( 9 FDA reports)
MEDICAL DEVICE COMPLICATION ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
MICTURITION URGENCY ( 9 FDA reports)
MITRAL VALVE DISEASE ( 9 FDA reports)
MUMPS ( 9 FDA reports)
NECK INJURY ( 9 FDA reports)
NEONATAL TACHYPNOEA ( 9 FDA reports)
NODULE ( 9 FDA reports)
ORAL CAVITY FISTULA ( 9 FDA reports)
ORAL HERPES ( 9 FDA reports)
ORCHITIS ( 9 FDA reports)
PELVIC PAIN ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
PROTEIN URINE PRESENT ( 9 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 9 FDA reports)
PULMONARY ARTERY STENOSIS ( 9 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
RUBELLA ( 9 FDA reports)
SCARLET FEVER ( 9 FDA reports)
SINUS CONGESTION ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
SUBDURAL HAEMATOMA ( 9 FDA reports)
TENOSYNOVITIS STENOSANS ( 9 FDA reports)
TONGUE DISCOLOURATION ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 9 FDA reports)
UTERINE LEIOMYOMA ( 9 FDA reports)
VITAMIN D DECREASED ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
AMYLOIDOSIS ( 8 FDA reports)
ANAEMIA NEONATAL ( 8 FDA reports)
ANURIA ( 8 FDA reports)
ASTHMA EXERCISE INDUCED ( 8 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 8 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 8 FDA reports)
BLADDER OPERATION ( 8 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 8 FDA reports)
CARDIAC ABLATION ( 8 FDA reports)
CEREBRAL DISORDER ( 8 FDA reports)
CERVICOBRACHIAL SYNDROME ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CHORIOAMNIONITIS ( 8 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 8 FDA reports)
CONGENITAL KNEE DEFORMITY ( 8 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 8 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 8 FDA reports)
DENTAL OPERATION ( 8 FDA reports)
DEVICE OCCLUSION ( 8 FDA reports)
DYSMENORRHOEA ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
FURUNCLE ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
HAEMANGIOMA ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HEARING IMPAIRED ( 8 FDA reports)
HEART INJURY ( 8 FDA reports)
HEPATITIS B ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HYPERCHOLESTEROLAEMIA ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INFANTILE APNOEIC ATTACK ( 8 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 8 FDA reports)
ISCHAEMIC STROKE ( 8 FDA reports)
LARYNGOSPASM ( 8 FDA reports)
LIBIDO DECREASED ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
LYMPHOCYTIC INFILTRATION ( 8 FDA reports)
MACROGLOSSIA ( 8 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 8 FDA reports)
NOCTURIA ( 8 FDA reports)
ORAL CANDIDIASIS ( 8 FDA reports)
PAPILLOMA VIRAL INFECTION ( 8 FDA reports)
PARAPARESIS ( 8 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 8 FDA reports)
PERIODONTAL DISEASE ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
PLEURAL FIBROSIS ( 8 FDA reports)
POSTERIOR CAPSULOTOMY ( 8 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 8 FDA reports)
PULMONARY CALCIFICATION ( 8 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 8 FDA reports)
PYOGENIC GRANULOMA ( 8 FDA reports)
QRS AXIS ABNORMAL ( 8 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 8 FDA reports)
RETINOPATHY OF PREMATURITY ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 8 FDA reports)
STILLBIRTH ( 8 FDA reports)
STRABISMUS ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
WOUND DRAINAGE ( 8 FDA reports)
ALKALOSIS ( 7 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
APPENDICITIS ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BONE LOSS ( 7 FDA reports)
BREAST OPERATION ( 7 FDA reports)
BREECH PRESENTATION ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CAPILLARY LEAK SYNDROME ( 7 FDA reports)
CARDIAC TAMPONADE ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 7 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 7 FDA reports)
DENTURE WEARER ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 7 FDA reports)
EXANTHEM ( 7 FDA reports)
FACE OEDEMA ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
GAMMOPATHY ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HEPATIC NECROSIS ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HICCUPS ( 7 FDA reports)
HIGH FREQUENCY ABLATION ( 7 FDA reports)
HIP ARTHROPLASTY ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
IMPETIGO ( 7 FDA reports)
INFUSION RELATED REACTION ( 7 FDA reports)
INGUINAL HERNIA REPAIR ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
JAW DISORDER ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LIPOMA EXCISION ( 7 FDA reports)
LITHOTRIPSY ( 7 FDA reports)
LIVER TRANSPLANT REJECTION ( 7 FDA reports)
LOSS OF LIBIDO ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
MASTITIS ( 7 FDA reports)
MAXILLOFACIAL OPERATION ( 7 FDA reports)
METASTASES TO MENINGES ( 7 FDA reports)
NEONATAL ASPIRATION ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
NODAL OSTEOARTHRITIS ( 7 FDA reports)
OVARIAN CYST ( 7 FDA reports)
PAPILLOMA ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 7 FDA reports)
PNEUMOCONIOSIS ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
PROSTATIC OBSTRUCTION ( 7 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
QUALITY OF LIFE DECREASED ( 7 FDA reports)
RASH PUSTULAR ( 7 FDA reports)
RENAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
SKIN HYPERPIGMENTATION ( 7 FDA reports)
SMALL FOR DATES BABY ( 7 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TUMOUR INVASION ( 7 FDA reports)
ULCER ( 7 FDA reports)
URETERAL STENT INSERTION ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
UTERINE HAEMORRHAGE ( 7 FDA reports)
VAGINITIS BACTERIAL ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ADRENOGENITAL SYNDROME ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
AORTIC DISORDER ( 6 FDA reports)
APPENDICITIS PERFORATED ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
BLOOD CHLORIDE DECREASED ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
BREAST PROSTHESIS USER ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CONGENITAL GENITAL MALFORMATION FEMALE ( 6 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 6 FDA reports)
CORNEAL ABRASION ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
EBSTEIN'S ANOMALY ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
FIBROUS HISTIOCYTOMA ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HIV INFECTION ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 6 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 6 FDA reports)
HYPOPNOEA ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
HYPOTONIA NEONATAL ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
INTESTINAL POLYP ( 6 FDA reports)
INTUSSUSCEPTION ( 6 FDA reports)
KYPHOSIS ( 6 FDA reports)
LARGE FOR DATES BABY ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 6 FDA reports)
METASTASES TO CHEST WALL ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MUCOSAL EROSION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
MYOPIA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 6 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 6 FDA reports)
ORAL DISORDER ( 6 FDA reports)
ORAL PRURITUS ( 6 FDA reports)
OTITIS EXTERNA ( 6 FDA reports)
OVERWEIGHT ( 6 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 6 FDA reports)
PEPTIC ULCER ( 6 FDA reports)
PERICARDIAL DRAINAGE ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 6 FDA reports)
PULMONARY MASS ( 6 FDA reports)
PUPILS UNEQUAL ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 6 FDA reports)
SCAPULA FRACTURE ( 6 FDA reports)
SKIN BURNING SENSATION ( 6 FDA reports)
SNORING ( 6 FDA reports)
SPINAL FRACTURE ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
TENDON DISORDER ( 6 FDA reports)
TESTICULAR PAIN ( 6 FDA reports)
TESTICULAR SWELLING ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
THYROXINE DECREASED ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TRICUSPID VALVE PROLAPSE ( 6 FDA reports)
URETERAL DISORDER ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
WOUND ( 6 FDA reports)
ACNE CYSTIC ( 5 FDA reports)
ADENOIDECTOMY ( 5 FDA reports)
AMBLYOPIA ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
AORTA HYPOPLASIA ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ATELECTASIS NEONATAL ( 5 FDA reports)
ATROPHY ( 5 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BONE OPERATION ( 5 FDA reports)
BRAIN ABSCESS ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BURN DRESSING ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CATARACT CONGENITAL ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
COLONOSCOPY ( 5 FDA reports)
COMPLEX PARTIAL SEIZURES ( 5 FDA reports)
CONGENITAL EYE DISORDER ( 5 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
CRYPTORCHISM ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DUODENAL PERFORATION ( 5 FDA reports)
DYSPLASIA ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEEDING DISORDER NEONATAL ( 5 FDA reports)
FINE MOTOR DELAY ( 5 FDA reports)
FUNGAEMIA ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
GROWTH RETARDATION ( 5 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPERKINETIC HEART SYNDROME ( 5 FDA reports)
HYPERPLASIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
MERALGIA PARAESTHETICA ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NECROTISING COLITIS ( 5 FDA reports)
NEONATAL ANURIA ( 5 FDA reports)
NEONATAL CARDIAC FAILURE ( 5 FDA reports)
NEONATAL HYPONATRAEMIA ( 5 FDA reports)
NEONATAL HYPOXIA ( 5 FDA reports)
NEPHRITIS INTERSTITIAL ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
ORAL NEOPLASM ( 5 FDA reports)
OSTEOCHONDROMA ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PERICARDIAL EXCISION ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
PREMATURE DELIVERY ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PROCTITIS ULCERATIVE ( 5 FDA reports)
PROSTATE CANCER METASTATIC ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 5 FDA reports)
RENAL FAILURE NEONATAL ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SEBORRHOEIC DERMATITIS ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN CANCER ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SKIN PAPILLOMA ( 5 FDA reports)
SKIN TEST POSITIVE ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SLUGGISHNESS ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
SYNOVIAL DISORDER ( 5 FDA reports)
THALASSAEMIA ALPHA ( 5 FDA reports)
TONSILLECTOMY ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VITILIGO ( 5 FDA reports)
WEIGHT GAIN POOR ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ADRENAL SUPPRESSION ( 4 FDA reports)
AIR EMBOLISM ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
APHONIA ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
AUTISM ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BONE DEFORMITY ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CARDIAC ARREST NEONATAL ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 4 FDA reports)
CAROTID ARTERY DISEASE ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 4 FDA reports)
CLEFT LIP AND PALATE ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CONGENITAL ANAEMIA ( 4 FDA reports)
CONGENITAL AORTIC STENOSIS ( 4 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 4 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 4 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 4 FDA reports)
CONVULSION NEONATAL ( 4 FDA reports)
CROUP INFECTIOUS ( 4 FDA reports)
CRYING ( 4 FDA reports)
CYTOGENETIC ABNORMALITY ( 4 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 4 FDA reports)
DEATH NEONATAL ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DIVERTICULAR HERNIA ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
DYSPLASTIC NAEVUS ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
ENLARGED CLITORIS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 4 FDA reports)
FISTULA DISCHARGE ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GENITAL INFECTION FUNGAL ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HEART VALVE INCOMPETENCE ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOSPADIAS ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INFECTIOUS DISEASE CARRIER ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KIDNEY MALFORMATION ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEARNING DISORDER ( 4 FDA reports)
LICHENOID KERATOSIS ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LIMB REDUCTION DEFECT ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LOW BIRTH WEIGHT BABY ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MALOCCLUSION ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MITRAL VALVE HYPOPLASIA ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
NASAL SEPTUM DEVIATION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 4 FDA reports)
PALMAR ERYTHEMA ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
RADIATION INJURY ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RESPIRATORY MONILIASIS ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 4 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TAENIASIS ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
UNINTENDED PREGNANCY ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 4 FDA reports)
VIRAL TONSILLITIS ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ACUTE POLYNEUROPATHY ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADENOIDAL HYPERTROPHY ( 3 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 3 FDA reports)
ADRENAL INSUFFICIENCY NEONATAL ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
AORTIC ANEURYSM REPAIR ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 3 FDA reports)
BONE ABSCESS ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONGENITAL TORTICOLLIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DYSPRAXIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOETAL HEART RATE DECREASED ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FORCEPS DELIVERY ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 3 FDA reports)
GINGIVAL RECESSION ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
GROUP B STREPTOCOCCUS NEONATAL SEPSIS ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERTENSION NEONATAL ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LABOUR COMPLICATION ( 3 FDA reports)
LAEVOCARDIA ( 3 FDA reports)
LARYNGEAL STENOSIS ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
MANIA ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MORTON'S NEUROMA ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEONATAL INFECTION ( 3 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEURITIS ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OSTEITIS DEFORMANS ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PORENCEPHALY ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PULMONARY HYPOPLASIA ( 3 FDA reports)
PULMONARY OEDEMA NEONATAL ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SINGLE UMBILICAL ARTERY ( 3 FDA reports)
SINUS TARSI SYNDROME ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
STRONGYLOIDIASIS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRACHEAL HAEMORRHAGE ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 3 FDA reports)
TRANSPLANT ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
URETHRAL OBSTRUCTION ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE ATRESIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AVERSION ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC MYXOMA ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 2 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC TONSILLITIS ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
CONJUNCTIVAL ABRASION ( 2 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC ENTEROPATHY ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
EAR MALFORMATION ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENTERITIS NECROTICANS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EPISPADIAS ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE INFECTION SYPHILITIC ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FUNISITIS ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE NEONATAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERMAPHRODITISM ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYDROPS FOETALIS ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 2 FDA reports)
LEARNING DISABILITY ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LOW SET EARS ( 2 FDA reports)
LUNG HERNIA ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
MACROCEPHALY ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGITIS NEONATAL ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NAEVUS FLAMMEUS ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEONATAL CHOLESTASIS ( 2 FDA reports)
NEONATAL PNEUMONIA ( 2 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPENIA NEONATAL ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERINEAL LACERATION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PRESBYACUSIS ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY DEFORMITY ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYURIA ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL DYSPLASIA ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
REPRODUCTIVE TRACT HYPOPLASIA, MALE ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SECONDARY SYPHILIS ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYMBOLIC DYSFUNCTION ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THIRST ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
URINOMA ( 2 FDA reports)
UROGENITAL FISTULA ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UROSTOMY COMPLICATION ( 2 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS DEGENERATION ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT CONTROL ( 2 FDA reports)
WEST NILE VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
XANTHOMA ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FUNGAL INFECTION ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARRHYTHMIA NEONATAL ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTEATOSIS ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NECROSIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOMYOPATHY NEONATAL ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGENITAL BRAIN DAMAGE ( 1 FDA reports)
CONGENITAL CYST ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 1 FDA reports)
CONGENITAL SYPHILIS ( 1 FDA reports)
CONGENITAL TERATOMA ( 1 FDA reports)
CONGENITAL TOXOPLASMOSIS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION IN NEWBORN ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL ATRESIA ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEVER NEONATAL ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 1 FDA reports)
HETEROTAXIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNE AGGLUTININS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED LYMPHOCELE ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARYNGOTRACHEITIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MECONIUM INCREASED ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOANING ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOSAL HYPERAEMIA ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL CANDIDA INFECTION ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEONATAL RESPIRATORY ARREST ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OEDEMA NEONATAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC CARCINOMA RESECTABLE ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PITYRIASIS RUBRA PILARIS ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURAL FISTULA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDO-BARTTER SYNDROME ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RALES ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND SKULL ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE HYPERTONUS ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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