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

PAIN ( 56 FDA reports)
NAUSEA ( 51 FDA reports)
HEADACHE ( 48 FDA reports)
ANXIETY ( 46 FDA reports)
VOMITING ( 44 FDA reports)
DYSPNOEA ( 42 FDA reports)
FALL ( 37 FDA reports)
DIARRHOEA ( 36 FDA reports)
FATIGUE ( 34 FDA reports)
DEPRESSION ( 33 FDA reports)
BACK PAIN ( 32 FDA reports)
INSOMNIA ( 31 FDA reports)
ASTHENIA ( 30 FDA reports)
WEIGHT DECREASED ( 29 FDA reports)
ANAEMIA ( 28 FDA reports)
DIZZINESS ( 28 FDA reports)
CONSTIPATION ( 27 FDA reports)
ARTHRALGIA ( 26 FDA reports)
DRUG INEFFECTIVE ( 25 FDA reports)
HYPERTENSION ( 25 FDA reports)
PNEUMONIA ( 25 FDA reports)
TREMOR ( 25 FDA reports)
DRUG INTERACTION ( 24 FDA reports)
CHEST PAIN ( 23 FDA reports)
GAIT DISTURBANCE ( 21 FDA reports)
PAIN IN EXTREMITY ( 21 FDA reports)
PYREXIA ( 21 FDA reports)
COUGH ( 20 FDA reports)
ABDOMINAL PAIN ( 19 FDA reports)
MUSCLE SPASMS ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
DIABETES MELLITUS ( 18 FDA reports)
NEUROPATHY PERIPHERAL ( 18 FDA reports)
OEDEMA PERIPHERAL ( 18 FDA reports)
PALPITATIONS ( 17 FDA reports)
VISION BLURRED ( 17 FDA reports)
EMOTIONAL DISTRESS ( 16 FDA reports)
SYNCOPE ( 16 FDA reports)
AMNESIA ( 15 FDA reports)
DYSPHAGIA ( 15 FDA reports)
URINARY TRACT INFECTION ( 15 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
CONFUSIONAL STATE ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
MALAISE ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
PARAESTHESIA ( 14 FDA reports)
SEDATION ( 14 FDA reports)
BONE DISORDER ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
DEHYDRATION ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
OSTEOARTHRITIS ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
UNRESPONSIVE TO STIMULI ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
INJURY ( 12 FDA reports)
MEMORY IMPAIRMENT ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
BALANCE DISORDER ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
CHILLS ( 11 FDA reports)
COLITIS ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
MUSCULOSKELETAL PAIN ( 11 FDA reports)
OSTEONECROSIS ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
HALLUCINATION ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 10 FDA reports)
IRRITABILITY ( 10 FDA reports)
MIGRAINE ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
SEROTONIN SYNDROME ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
AGITATION ( 9 FDA reports)
ANGER ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DEATH ( 9 FDA reports)
DRUG DOSE OMISSION ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
MENTAL STATUS CHANGES ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
SWELLING ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
ARTHRITIS ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
RASH ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SPINAL OSTEOARTHRITIS ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
ABASIA ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
COMPLETED SUICIDE ( 7 FDA reports)
DELUSION ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
DISCOMFORT ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
NEURALGIA ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ARTHROPATHY ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DEFORMITY ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
FEAR ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERSOMNIA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPINAL OPERATION ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LUMBAR SPINAL STENOSIS ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
STRESS ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
THYROID CANCER ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ASPERGER'S DISORDER ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GOITRE ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TENSION ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CRYING ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT PALATE NEOPLASM ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
SCAR ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY BONE MARROW ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENZYME LEVEL INCREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHANGIOMA ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS CHEMICAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PARACHUTE MITRAL VALVE ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHRINKING LUNG SYNDROME ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUS TARSI SYNDROME ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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