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

DYSPNOEA ( 203 FDA reports)
ASTHMA ( 166 FDA reports)
NAUSEA ( 146 FDA reports)
PAIN ( 141 FDA reports)
DIZZINESS ( 126 FDA reports)
ANXIETY ( 124 FDA reports)
CHEST PAIN ( 109 FDA reports)
BACK PAIN ( 104 FDA reports)
ASTHENIA ( 103 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 102 FDA reports)
FATIGUE ( 93 FDA reports)
DRUG INEFFECTIVE ( 90 FDA reports)
COUGH ( 88 FDA reports)
DEPRESSION ( 88 FDA reports)
HEADACHE ( 85 FDA reports)
MYOCARDIAL INFARCTION ( 83 FDA reports)
VOMITING ( 81 FDA reports)
INSOMNIA ( 77 FDA reports)
PNEUMONIA ( 74 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 72 FDA reports)
DIARRHOEA ( 71 FDA reports)
FALL ( 71 FDA reports)
INJURY ( 71 FDA reports)
OEDEMA PERIPHERAL ( 69 FDA reports)
PAIN IN EXTREMITY ( 67 FDA reports)
CORONARY ARTERY DISEASE ( 66 FDA reports)
WEIGHT DECREASED ( 65 FDA reports)
ARTHRALGIA ( 64 FDA reports)
CONSTIPATION ( 62 FDA reports)
BRONCHITIS ( 61 FDA reports)
PRURITUS ( 59 FDA reports)
HYPERTENSION ( 57 FDA reports)
CEREBROVASCULAR ACCIDENT ( 56 FDA reports)
WEIGHT INCREASED ( 56 FDA reports)
RENAL FAILURE ( 55 FDA reports)
ATRIAL FIBRILLATION ( 54 FDA reports)
HYPOAESTHESIA ( 53 FDA reports)
CARDIOMEGALY ( 49 FDA reports)
DIABETES MELLITUS ( 48 FDA reports)
SINUSITIS ( 48 FDA reports)
SYNCOPE ( 48 FDA reports)
MUSCLE SPASMS ( 47 FDA reports)
RASH ( 47 FDA reports)
URINARY TRACT INFECTION ( 45 FDA reports)
FEELING ABNORMAL ( 44 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 44 FDA reports)
BLOOD PRESSURE INCREASED ( 43 FDA reports)
PULMONARY EMBOLISM ( 43 FDA reports)
BLOOD GLUCOSE INCREASED ( 42 FDA reports)
PALPITATIONS ( 42 FDA reports)
ANHEDONIA ( 41 FDA reports)
ECONOMIC PROBLEM ( 41 FDA reports)
HYPERHIDROSIS ( 41 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 41 FDA reports)
ABDOMINAL PAIN ( 40 FDA reports)
DYSPEPSIA ( 40 FDA reports)
RENAL FAILURE ACUTE ( 40 FDA reports)
CHEST DISCOMFORT ( 39 FDA reports)
ABDOMINAL PAIN UPPER ( 38 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 38 FDA reports)
EMOTIONAL DISTRESS ( 38 FDA reports)
EPISTAXIS ( 38 FDA reports)
TREMOR ( 38 FDA reports)
CONDITION AGGRAVATED ( 37 FDA reports)
DRY MOUTH ( 37 FDA reports)
MITRAL VALVE INCOMPETENCE ( 36 FDA reports)
NEUROPATHY PERIPHERAL ( 36 FDA reports)
PYREXIA ( 36 FDA reports)
UNDERDOSE ( 36 FDA reports)
ANAEMIA ( 35 FDA reports)
ANOREXIA ( 35 FDA reports)
HEART RATE INCREASED ( 35 FDA reports)
DEATH ( 34 FDA reports)
CARDIAC DISORDER ( 33 FDA reports)
CELLULITIS ( 33 FDA reports)
OSTEOARTHRITIS ( 33 FDA reports)
WHEEZING ( 33 FDA reports)
DYSPHONIA ( 31 FDA reports)
CATARACT ( 30 FDA reports)
ERYTHEMA ( 30 FDA reports)
CARDIAC ARREST ( 29 FDA reports)
DECREASED APPETITE ( 29 FDA reports)
DEEP VEIN THROMBOSIS ( 29 FDA reports)
HYPOTHYROIDISM ( 29 FDA reports)
NECK PAIN ( 29 FDA reports)
SOMNOLENCE ( 29 FDA reports)
TACHYCARDIA ( 29 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 29 FDA reports)
VISION BLURRED ( 29 FDA reports)
ARTHROPATHY ( 28 FDA reports)
GAIT DISTURBANCE ( 28 FDA reports)
ARTHRITIS ( 27 FDA reports)
CONFUSIONAL STATE ( 27 FDA reports)
DEHYDRATION ( 27 FDA reports)
CHOLELITHIASIS ( 26 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 26 FDA reports)
FEMUR FRACTURE ( 26 FDA reports)
MALAISE ( 26 FDA reports)
MYALGIA ( 26 FDA reports)
NERVOUSNESS ( 26 FDA reports)
TINNITUS ( 26 FDA reports)
ANGINA PECTORIS ( 25 FDA reports)
BURSITIS ( 25 FDA reports)
DYSPHAGIA ( 25 FDA reports)
HYPERSENSITIVITY ( 25 FDA reports)
HYPOTENSION ( 25 FDA reports)
BRONCHOSPASM ( 24 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 24 FDA reports)
HYPERCHOLESTEROLAEMIA ( 23 FDA reports)
RESPIRATORY FAILURE ( 23 FDA reports)
UNEVALUABLE EVENT ( 23 FDA reports)
ASCITES ( 22 FDA reports)
CHILLS ( 22 FDA reports)
COMA ( 22 FDA reports)
DRUG HYPERSENSITIVITY ( 22 FDA reports)
HAEMOPTYSIS ( 22 FDA reports)
HEPATIC STEATOSIS ( 22 FDA reports)
LIVER DISORDER ( 22 FDA reports)
LOSS OF CONSCIOUSNESS ( 22 FDA reports)
PANCREATITIS ( 22 FDA reports)
RENAL FAILURE CHRONIC ( 22 FDA reports)
TYPE 2 DIABETES MELLITUS ( 22 FDA reports)
ABDOMINAL DISTENSION ( 21 FDA reports)
BALANCE DISORDER ( 21 FDA reports)
CANDIDIASIS ( 21 FDA reports)
CONTUSION ( 21 FDA reports)
CYANOSIS ( 21 FDA reports)
DILATATION ATRIAL ( 21 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 21 FDA reports)
FLATULENCE ( 21 FDA reports)
GASTROINTESTINAL DISORDER ( 21 FDA reports)
HEPATOMEGALY ( 21 FDA reports)
HYPOKALAEMIA ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 21 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 21 FDA reports)
CONVULSION ( 20 FDA reports)
DENTAL CARIES ( 20 FDA reports)
DRUG DOSE OMISSION ( 20 FDA reports)
HYPERLIPIDAEMIA ( 20 FDA reports)
MEMORY IMPAIRMENT ( 20 FDA reports)
OROPHARYNGEAL PAIN ( 20 FDA reports)
PANCYTOPENIA ( 20 FDA reports)
POLLAKIURIA ( 20 FDA reports)
ABSCESS ( 19 FDA reports)
ACUTE RESPIRATORY FAILURE ( 19 FDA reports)
ARRHYTHMIA ( 19 FDA reports)
ARTERIOSCLEROSIS ( 19 FDA reports)
EMPHYSEMA ( 19 FDA reports)
SEPTIC SHOCK ( 19 FDA reports)
STRESS ( 19 FDA reports)
THYROID DISORDER ( 19 FDA reports)
URTICARIA ( 19 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 18 FDA reports)
CARDIO-RESPIRATORY ARREST ( 18 FDA reports)
DILATATION VENTRICULAR ( 18 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
GROIN PAIN ( 18 FDA reports)
HEPATIC FAILURE ( 18 FDA reports)
HIATUS HERNIA ( 18 FDA reports)
OBESITY ( 18 FDA reports)
OSTEONECROSIS OF JAW ( 18 FDA reports)
OVERDOSE ( 18 FDA reports)
PARAESTHESIA ( 18 FDA reports)
PULMONARY HYPERTENSION ( 18 FDA reports)
ROTATOR CUFF SYNDROME ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
SWELLING ( 18 FDA reports)
TOOTH LOSS ( 18 FDA reports)
ADVERSE DRUG REACTION ( 17 FDA reports)
AGITATION ( 17 FDA reports)
AMNESIA ( 17 FDA reports)
ATRIAL SEPTAL DEFECT ( 17 FDA reports)
CARPAL TUNNEL SYNDROME ( 17 FDA reports)
DYSURIA ( 17 FDA reports)
EAR PAIN ( 17 FDA reports)
FIBROMYALGIA ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
IMPAIRED HEALING ( 17 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 17 FDA reports)
VENTRICULAR TACHYCARDIA ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 16 FDA reports)
DIVERTICULUM INTESTINAL ( 16 FDA reports)
HEAD INJURY ( 16 FDA reports)
HERPES ZOSTER ( 16 FDA reports)
HYPOXIA ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 16 FDA reports)
LARYNGITIS ( 16 FDA reports)
LEUKOCYTOSIS ( 16 FDA reports)
MULTIPLE ALLERGIES ( 16 FDA reports)
OEDEMA ( 16 FDA reports)
OSTEONECROSIS ( 16 FDA reports)
SUICIDAL IDEATION ( 16 FDA reports)
TENDONITIS ( 16 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 16 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 16 FDA reports)
ATELECTASIS ( 15 FDA reports)
BRADYCARDIA ( 15 FDA reports)
CONJUNCTIVITIS ( 15 FDA reports)
DEFORMITY ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
EXCORIATION ( 15 FDA reports)
HAEMORRHAGE ( 15 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
PULMONARY OEDEMA ( 15 FDA reports)
RHINORRHOEA ( 15 FDA reports)
STOMATITIS ( 15 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
CARDIOGENIC SHOCK ( 14 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 14 FDA reports)
DYSARTHRIA ( 14 FDA reports)
DYSGEUSIA ( 14 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 14 FDA reports)
FAECAL INCONTINENCE ( 14 FDA reports)
GALLBLADDER DISORDER ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
INGROWING NAIL ( 14 FDA reports)
JAW FRACTURE ( 14 FDA reports)
MENTAL DISORDER ( 14 FDA reports)
MUSCULAR WEAKNESS ( 14 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 14 FDA reports)
OSTEOMYELITIS ( 14 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 14 FDA reports)
RESPIRATORY DISORDER ( 14 FDA reports)
RESTLESS LEGS SYNDROME ( 14 FDA reports)
ROAD TRAFFIC ACCIDENT ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
STATUS ASTHMATICUS ( 14 FDA reports)
THROAT IRRITATION ( 14 FDA reports)
THROAT TIGHTNESS ( 14 FDA reports)
THROMBOCYTOPENIA ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ALOPECIA ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ATRIAL FLUTTER ( 13 FDA reports)
BIPOLAR DISORDER ( 13 FDA reports)
CARDIOMYOPATHY ( 13 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
EYE DISORDER ( 13 FDA reports)
GASTRIC DISORDER ( 13 FDA reports)
GOUT ( 13 FDA reports)
HEART RATE IRREGULAR ( 13 FDA reports)
HEPATIC ENZYME INCREASED ( 13 FDA reports)
INFECTION ( 13 FDA reports)
IRON DEFICIENCY ANAEMIA ( 13 FDA reports)
LOBAR PNEUMONIA ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
LYMPHOEDEMA ( 13 FDA reports)
NEPHROLITHIASIS ( 13 FDA reports)
ORAL INFECTION ( 13 FDA reports)
ORAL PAIN ( 13 FDA reports)
RESPIRATORY DISTRESS ( 13 FDA reports)
VENTRICULAR HYPERTROPHY ( 13 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 12 FDA reports)
BLOOD POTASSIUM DECREASED ( 12 FDA reports)
BURNING SENSATION ( 12 FDA reports)
CARDIAC MURMUR ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 12 FDA reports)
DERMATOMYOSITIS ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
DRUG DEPENDENCE ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
GLAUCOMA ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 12 FDA reports)
IRRITABILITY ( 12 FDA reports)
JOINT INJURY ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
MAJOR DEPRESSION ( 12 FDA reports)
MIGRAINE ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
NERVE COMPRESSION ( 12 FDA reports)
PERONEAL NERVE PALSY ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
SCHIZOPHRENIA ( 12 FDA reports)
VENTRICULAR FIBRILLATION ( 12 FDA reports)
ACUTE PULMONARY OEDEMA ( 11 FDA reports)
APNOEA ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
BRONCHITIS CHRONIC ( 11 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 11 FDA reports)
CERUMEN IMPACTION ( 11 FDA reports)
FEELING JITTERY ( 11 FDA reports)
FRACTURE NONUNION ( 11 FDA reports)
HAEMATOMA ( 11 FDA reports)
HUNGER ( 11 FDA reports)
HYPERPHAGIA ( 11 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 11 FDA reports)
MEDICATION ERROR ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
NASAL CONGESTION ( 11 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 11 FDA reports)
OSTEOPOROSIS ( 11 FDA reports)
OXYGEN SATURATION DECREASED ( 11 FDA reports)
PARONYCHIA ( 11 FDA reports)
PROSTATE CANCER METASTATIC ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
RENAL DISORDER ( 11 FDA reports)
RENAL INJURY ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
SHOULDER PAIN ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
THROMBOSIS ( 11 FDA reports)
TREATMENT NONCOMPLIANCE ( 11 FDA reports)
UTERINE CANCER ( 11 FDA reports)
VERTIGO ( 11 FDA reports)
ABASIA ( 10 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 10 FDA reports)
AZOTAEMIA ( 10 FDA reports)
BACK DISORDER ( 10 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 10 FDA reports)
BONE EROSION ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
DYSSTASIA ( 10 FDA reports)
EJECTION FRACTION DECREASED ( 10 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 10 FDA reports)
ENCEPHALOPATHY ( 10 FDA reports)
ENDOTRACHEAL INTUBATION ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
MUSCULAR DYSTROPHY ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
MUSCULOSKELETAL PAIN ( 10 FDA reports)
NASAL DRYNESS ( 10 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 10 FDA reports)
PRESYNCOPE ( 10 FDA reports)
PROSTATOMEGALY ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
SKELETAL INJURY ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
TESTICULAR PAIN ( 10 FDA reports)
TRISMUS ( 10 FDA reports)
UPPER LIMB FRACTURE ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
VISUAL ACUITY REDUCED ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
BLOOD GLUCOSE DECREASED ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CARDIAC OUTPUT DECREASED ( 9 FDA reports)
CARDIAC TAMPONADE ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CHOKING ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
CONGENITAL HAIR DISORDER ( 9 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
DEAFNESS NEUROSENSORY ( 9 FDA reports)
DEFORMITY THORAX ( 9 FDA reports)
DIABETIC ULCER ( 9 FDA reports)
DIFFICULTY IN WALKING ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
ESSENTIAL HYPERTENSION ( 9 FDA reports)
EXPOSED BONE IN JAW ( 9 FDA reports)
FOETAL HEART RATE ABNORMAL ( 9 FDA reports)
FOOT DEFORMITY ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
HYDROCELE ( 9 FDA reports)
HYDRONEPHROSIS ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
JAW CYST ( 9 FDA reports)
LACRIMATION INCREASED ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
LOCALISED INFECTION ( 9 FDA reports)
LOW TURNOVER OSTEOPATHY ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
LUNG NEOPLASM MALIGNANT ( 9 FDA reports)
MOOD SWINGS ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
MULTIPLE INJURIES ( 9 FDA reports)
PANIC ATTACK ( 9 FDA reports)
PARANOIA ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
PTERYGIUM COLLI ( 9 FDA reports)
RADICULOPATHY ( 9 FDA reports)
RIB FRACTURE ( 9 FDA reports)
SHOCK ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
SPLEEN DISORDER ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
STOMACH DISCOMFORT ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
TACHYPNOEA ( 9 FDA reports)
TOOTH ABSCESS ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
TOOTH FRACTURE ( 9 FDA reports)
TURNER'S SYNDROME ( 9 FDA reports)
UTERINE DISORDER ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
VOCAL CORD POLYP ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
ANEURYSM ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
BLOOD PROLACTIN INCREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BREAST CANCER ( 8 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COLITIS ( 8 FDA reports)
CYSTITIS INTERSTITIAL ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DIABETIC NEUROPATHY ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
DYSPNOEA EXACERBATED ( 8 FDA reports)
HAND FRACTURE ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MYCOTIC ALLERGY ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
OROPHARYNGITIS FUNGAL ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
RECTAL POLYP ( 8 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
RHINITIS ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SKIN DEGENERATIVE DISORDER ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
SURGERY ( 8 FDA reports)
THYROID NEOPLASM ( 8 FDA reports)
TINEA INFECTION ( 8 FDA reports)
TRIGEMINAL NEURALGIA ( 8 FDA reports)
ULCER ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
VITREOUS FLOATERS ( 8 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
APHONIA ( 7 FDA reports)
ASPERGILLOSIS ( 7 FDA reports)
BLINDNESS ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BONE DISORDER ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 7 FDA reports)
CEREBRAL PALSY ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
DISCOMFORT ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG ADMINISTRATION ERROR ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
EMOTIONAL DISORDER ( 7 FDA reports)
ENURESIS ( 7 FDA reports)
FACE INJURY ( 7 FDA reports)
FEAR ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FEELING DRUNK ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
HYPERREFLEXIA ( 7 FDA reports)
ISCHAEMIA ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
LOWER LIMB FRACTURE ( 7 FDA reports)
MENIERE'S DISEASE ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
ORAL DISCOMFORT ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 7 FDA reports)
PERIODONTITIS ( 7 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
PULMONARY MASS ( 7 FDA reports)
PULSE ABSENT ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
RADICULITIS LUMBOSACRAL ( 7 FDA reports)
SINUS CONGESTION ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
TALIPES ( 7 FDA reports)
TENDINOUS CONTRACTURE ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BREAST MASS ( 6 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
CERVICOBRACHIAL SYNDROME ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
DERMATITIS ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EROSIVE DUODENITIS ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
GINGIVAL INFECTION ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GOITRE ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
LIMB DISCOMFORT ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
MUSCLE TWITCHING ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
RALES ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
SCOLIOSIS ( 6 FDA reports)
SEBORRHOEIC KERATOSIS ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
SPINAL FRACTURE ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ADENOMA BENIGN ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
APPENDIX DISORDER ( 5 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BRONCHIAL INFECTION ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CARTILAGE INJURY ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
DEVICE FAILURE ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 5 FDA reports)
DRUG TOLERANCE ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
DUPUYTREN'S CONTRACTURE ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 5 FDA reports)
ENANTHEMA ( 5 FDA reports)
ERUCTATION ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
GINGIVAL SWELLING ( 5 FDA reports)
HAEMOPHILUS INFECTION ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEART BLOCK CONGENITAL ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
MITRAL VALVE PROLAPSE ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
NODULE ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARAESTHESIA ORAL ( 5 FDA reports)
PARKINSONIAN GAIT ( 5 FDA reports)
PATHOLOGICAL FRACTURE ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RENAL PAIN ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RETCHING ( 5 FDA reports)
RETINAL DETACHMENT ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SACROILIITIS ( 5 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 5 FDA reports)
SEDATION ( 5 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 5 FDA reports)
TENDERNESS ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
TENSION ( 5 FDA reports)
THERAPY REGIMEN CHANGED ( 5 FDA reports)
TOOTH DISORDER ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VERTIGO CNS ORIGIN ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
ACNE ( 4 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ALCOHOL PROBLEM ( 4 FDA reports)
ANAESTHETIC COMPLICATION ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
APATHY ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
ATROPHIC VULVOVAGINITIS ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BONE MARROW TRANSPLANT ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DEVELOPMENTAL DELAY ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FACTOR XI DEFICIENCY ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GANGLION ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
JAW OPERATION ( 4 FDA reports)
LIFE EXPECTANCY SHORTENED ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUCOSAL ULCERATION ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
NON-CARDIAC CHEST PAIN ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
POLYP ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
POST PROCEDURAL NAUSEA ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SPLENIC LESION ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
UNEMPLOYMENT ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHITIS FUNGAL ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOLIPIN ANTIBODY ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MASS ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
RADICULAR PAIN ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UPPER EXTREMITY MASS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL PRESSURE INCREASED ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY LIP ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MASSAGE ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PYELOPLASTY ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SPLENIC CALCIFICATION ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THIRST ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONSILLAR CYST ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AURA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF MONOCYTE COUNT DECREASED ( 1 FDA reports)
CSF OLIGOCLONAL BAND PRESENT ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYST ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VICTIM OF CHILD ABUSE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITAMIN K INCREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
WATER POLLUTION ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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