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

FALL ( 250 FDA reports)
FATIGUE ( 240 FDA reports)
DEPRESSION ( 211 FDA reports)
PAIN ( 200 FDA reports)
DIZZINESS ( 184 FDA reports)
TREMOR ( 180 FDA reports)
ANXIETY ( 179 FDA reports)
ASTHENIA ( 177 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 157 FDA reports)
NAUSEA ( 156 FDA reports)
GAIT DISTURBANCE ( 152 FDA reports)
URINARY TRACT INFECTION ( 150 FDA reports)
CONVULSION ( 146 FDA reports)
DYSPNOEA ( 146 FDA reports)
CONDITION AGGRAVATED ( 143 FDA reports)
HEADACHE ( 138 FDA reports)
PYREXIA ( 133 FDA reports)
CONFUSIONAL STATE ( 132 FDA reports)
DIARRHOEA ( 130 FDA reports)
HALLUCINATION ( 129 FDA reports)
SOMNOLENCE ( 129 FDA reports)
INSOMNIA ( 128 FDA reports)
PATHOLOGICAL GAMBLING ( 128 FDA reports)
MULTIPLE SCLEROSIS ( 127 FDA reports)
PNEUMONIA ( 127 FDA reports)
DYSKINESIA ( 123 FDA reports)
VOMITING ( 121 FDA reports)
DYSPHAGIA ( 120 FDA reports)
HYPOAESTHESIA ( 118 FDA reports)
ANAEMIA ( 109 FDA reports)
OEDEMA PERIPHERAL ( 108 FDA reports)
WEIGHT DECREASED ( 108 FDA reports)
PARKINSON'S DISEASE ( 104 FDA reports)
BACK PAIN ( 100 FDA reports)
CONSTIPATION ( 99 FDA reports)
DEHYDRATION ( 99 FDA reports)
EMOTIONAL DISTRESS ( 99 FDA reports)
MUSCULAR WEAKNESS ( 96 FDA reports)
HYPERTENSION ( 94 FDA reports)
BALANCE DISORDER ( 91 FDA reports)
DRUG INEFFECTIVE ( 90 FDA reports)
MUSCLE SPASMS ( 88 FDA reports)
CHEST PAIN ( 84 FDA reports)
SEPSIS ( 84 FDA reports)
ARTHRALGIA ( 82 FDA reports)
DRUG INTERACTION ( 82 FDA reports)
INJURY ( 82 FDA reports)
HALLUCINATION, VISUAL ( 81 FDA reports)
PAIN IN EXTREMITY ( 80 FDA reports)
LOSS OF CONSCIOUSNESS ( 79 FDA reports)
ABDOMINAL PAIN ( 77 FDA reports)
COGNITIVE DISORDER ( 72 FDA reports)
MITRAL VALVE INCOMPETENCE ( 71 FDA reports)
RENAL FAILURE ( 71 FDA reports)
VERTIGO ( 71 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 70 FDA reports)
ABNORMAL BEHAVIOUR ( 69 FDA reports)
HYPOTENSION ( 68 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 66 FDA reports)
BONE PAIN ( 65 FDA reports)
DELIRIUM ( 65 FDA reports)
MYOCARDIAL INFARCTION ( 65 FDA reports)
DEEP VEIN THROMBOSIS ( 62 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 62 FDA reports)
SPINAL OSTEOARTHRITIS ( 62 FDA reports)
INFLUENZA LIKE ILLNESS ( 61 FDA reports)
OSTEOPOROSIS ( 61 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 60 FDA reports)
AGITATION ( 59 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 58 FDA reports)
CELLULITIS ( 57 FDA reports)
MEMORY IMPAIRMENT ( 57 FDA reports)
HAEMOGLOBIN DECREASED ( 56 FDA reports)
HYPERHIDROSIS ( 56 FDA reports)
INFECTION ( 56 FDA reports)
PULMONARY EMBOLISM ( 56 FDA reports)
CHOLELITHIASIS ( 55 FDA reports)
MALAISE ( 55 FDA reports)
PSYCHOTIC DISORDER ( 55 FDA reports)
SWELLING ( 55 FDA reports)
SYNCOPE ( 55 FDA reports)
WEIGHT INCREASED ( 55 FDA reports)
PLEURAL EFFUSION ( 54 FDA reports)
DECREASED APPETITE ( 53 FDA reports)
AMNESIA ( 52 FDA reports)
ASTHMA ( 52 FDA reports)
DIABETES MELLITUS ( 52 FDA reports)
ECONOMIC PROBLEM ( 52 FDA reports)
SPEECH DISORDER ( 52 FDA reports)
DISTURBANCE IN ATTENTION ( 51 FDA reports)
MIGRAINE ( 51 FDA reports)
DYSARTHRIA ( 50 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 50 FDA reports)
OSTEONECROSIS OF JAW ( 50 FDA reports)
URINARY INCONTINENCE ( 50 FDA reports)
SUICIDAL IDEATION ( 49 FDA reports)
INJECTION SITE PAIN ( 48 FDA reports)
HYPERSEXUALITY ( 47 FDA reports)
VISUAL ACUITY REDUCED ( 47 FDA reports)
CEREBROVASCULAR ACCIDENT ( 46 FDA reports)
RENAL FAILURE ACUTE ( 46 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 46 FDA reports)
BRONCHITIS ( 45 FDA reports)
OSTEOARTHRITIS ( 45 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 45 FDA reports)
FEELING ABNORMAL ( 44 FDA reports)
SINUSITIS ( 44 FDA reports)
POOR DENTAL CONDITION ( 43 FDA reports)
BLOOD PRESSURE DECREASED ( 42 FDA reports)
BLOOD PRESSURE INCREASED ( 42 FDA reports)
VISION BLURRED ( 41 FDA reports)
ABASIA ( 40 FDA reports)
DEATH ( 40 FDA reports)
GRAND MAL CONVULSION ( 40 FDA reports)
VASCULITIS ( 40 FDA reports)
AGGRESSION ( 39 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 39 FDA reports)
DRY MOUTH ( 39 FDA reports)
MOVEMENT DISORDER ( 39 FDA reports)
ORTHOSTATIC HYPOTENSION ( 39 FDA reports)
OSTEOMYELITIS ( 39 FDA reports)
BONE DISORDER ( 38 FDA reports)
CYSTITIS ( 38 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 38 FDA reports)
TOOTH ABSCESS ( 38 FDA reports)
ABDOMINAL PAIN UPPER ( 37 FDA reports)
ATRIAL FIBRILLATION ( 37 FDA reports)
BLOOD GLUCOSE INCREASED ( 37 FDA reports)
COUGH ( 37 FDA reports)
GINGIVAL INFECTION ( 37 FDA reports)
HYPONATRAEMIA ( 37 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 37 FDA reports)
PAIN IN JAW ( 37 FDA reports)
PARAESTHESIA ( 37 FDA reports)
GASTRITIS ( 36 FDA reports)
MUSCLE RIGIDITY ( 36 FDA reports)
STRESS ( 36 FDA reports)
CHEST DISCOMFORT ( 35 FDA reports)
EXOSTOSIS ( 35 FDA reports)
GENERALISED OEDEMA ( 35 FDA reports)
MENTAL DISORDER ( 35 FDA reports)
MOBILITY DECREASED ( 35 FDA reports)
MYALGIA ( 35 FDA reports)
OVERDOSE ( 35 FDA reports)
ANHEDONIA ( 34 FDA reports)
AORTIC VALVE INCOMPETENCE ( 34 FDA reports)
CARDIOMYOPATHY ( 34 FDA reports)
RHABDOMYOLYSIS ( 34 FDA reports)
DELUSION ( 33 FDA reports)
LUNG DISORDER ( 33 FDA reports)
NEUROPATHY PERIPHERAL ( 33 FDA reports)
OSTEITIS ( 33 FDA reports)
ROTATOR CUFF SYNDROME ( 33 FDA reports)
TOOTH DISORDER ( 33 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 32 FDA reports)
CATARACT ( 32 FDA reports)
CHILLS ( 32 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 32 FDA reports)
DYSSTASIA ( 32 FDA reports)
FEAR ( 32 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 32 FDA reports)
PARKINSONISM ( 32 FDA reports)
VISUAL IMPAIRMENT ( 32 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 32 FDA reports)
CORNEAL OEDEMA ( 31 FDA reports)
DISORIENTATION ( 31 FDA reports)
DYSTONIA ( 31 FDA reports)
FOOT FRACTURE ( 31 FDA reports)
HEART RATE INCREASED ( 31 FDA reports)
LACUNAR INFARCTION ( 31 FDA reports)
MYOCLONUS ( 31 FDA reports)
PULMONARY HYPERTENSION ( 31 FDA reports)
SCLERODERMA ( 31 FDA reports)
SWELLING FACE ( 31 FDA reports)
TOOTH EXTRACTION ( 31 FDA reports)
URTICARIA ( 31 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 31 FDA reports)
DENTAL CARIES ( 30 FDA reports)
ENTEROCOCCAL INFECTION ( 30 FDA reports)
INJECTION SITE ERYTHEMA ( 30 FDA reports)
JOINT SWELLING ( 30 FDA reports)
MOUTH ULCERATION ( 30 FDA reports)
RECTAL HAEMORRHAGE ( 30 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 29 FDA reports)
BASAL CELL CARCINOMA ( 29 FDA reports)
BRONCHOPNEUMONIA ( 29 FDA reports)
CONTUSION ( 29 FDA reports)
ENCEPHALOPATHY ( 29 FDA reports)
GINGIVITIS ( 29 FDA reports)
HYPERPHAGIA ( 29 FDA reports)
INFLUENZA ( 29 FDA reports)
MENTAL STATUS CHANGES ( 29 FDA reports)
NASAL CONGESTION ( 29 FDA reports)
PERIODONTAL DISEASE ( 29 FDA reports)
STAPHYLOCOCCAL INFECTION ( 29 FDA reports)
THROMBOSIS ( 29 FDA reports)
BLOOD CREATININE INCREASED ( 28 FDA reports)
CARDIAC FAILURE ( 28 FDA reports)
GINGIVAL PAIN ( 28 FDA reports)
HALLUCINATIONS, MIXED ( 28 FDA reports)
HYPOKALAEMIA ( 28 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 28 FDA reports)
MOTOR DYSFUNCTION ( 28 FDA reports)
NODULE ( 28 FDA reports)
OSTEONECROSIS ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
PLATELET COUNT DECREASED ( 28 FDA reports)
RASH ( 28 FDA reports)
APPENDICITIS ( 27 FDA reports)
APTYALISM ( 27 FDA reports)
BONE EROSION ( 27 FDA reports)
CEREBRAL INFARCTION ( 27 FDA reports)
COLITIS ULCERATIVE ( 27 FDA reports)
DRUG EFFECT DECREASED ( 27 FDA reports)
LETHARGY ( 27 FDA reports)
METASTATIC NEOPLASM ( 27 FDA reports)
STOMATITIS ( 27 FDA reports)
TARDIVE DYSKINESIA ( 27 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 27 FDA reports)
UTERINE LEIOMYOMA ( 27 FDA reports)
DRUG TOXICITY ( 26 FDA reports)
ENDODONTIC PROCEDURE ( 26 FDA reports)
ERECTILE DYSFUNCTION ( 26 FDA reports)
GAMBLING ( 26 FDA reports)
GINGIVAL SWELLING ( 26 FDA reports)
HYPERGLYCAEMIA ( 26 FDA reports)
HYPOPHAGIA ( 26 FDA reports)
MUSCULOSKELETAL PAIN ( 26 FDA reports)
OLIGURIA ( 26 FDA reports)
OSTEOLYSIS ( 26 FDA reports)
PERIODONTITIS ( 26 FDA reports)
RESTLESS LEGS SYNDROME ( 26 FDA reports)
RESTLESSNESS ( 26 FDA reports)
RIB FRACTURE ( 26 FDA reports)
SLEEP DISORDER ( 26 FDA reports)
UNRESPONSIVE TO STIMULI ( 26 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 25 FDA reports)
BLOOD UREA INCREASED ( 25 FDA reports)
BONE FRAGMENTATION ( 25 FDA reports)
CARDIAC ARREST ( 25 FDA reports)
DEPRESSED MOOD ( 25 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 25 FDA reports)
DYSPEPSIA ( 25 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 25 FDA reports)
HAEMATOCRIT DECREASED ( 25 FDA reports)
HYPOMAGNESAEMIA ( 25 FDA reports)
INJECTION SITE HAEMATOMA ( 25 FDA reports)
LUMBAR SPINAL STENOSIS ( 25 FDA reports)
MALOCCLUSION ( 25 FDA reports)
NEPHROLITHIASIS ( 25 FDA reports)
PANCYTOPENIA ( 25 FDA reports)
PLATELET COUNT INCREASED ( 25 FDA reports)
PNEUMONIA ASPIRATION ( 25 FDA reports)
PRURITUS ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
SENSORY LOSS ( 25 FDA reports)
TOOTH INJURY ( 25 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 25 FDA reports)
WOUND DEHISCENCE ( 25 FDA reports)
APHASIA ( 24 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
BLOOD POTASSIUM DECREASED ( 24 FDA reports)
COMPLETED SUICIDE ( 24 FDA reports)
DECUBITUS ULCER ( 24 FDA reports)
DIPLOPIA ( 24 FDA reports)
DYSPHONIA ( 24 FDA reports)
ESCHERICHIA INFECTION ( 24 FDA reports)
HALLUCINATION, AUDITORY ( 24 FDA reports)
IMPAIRED HEALING ( 24 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 24 FDA reports)
PELVIC FRACTURE ( 24 FDA reports)
SCAB ( 24 FDA reports)
SUICIDE ATTEMPT ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
AKINESIA ( 23 FDA reports)
ANGINA PECTORIS ( 23 FDA reports)
CORONARY ARTERY DISEASE ( 23 FDA reports)
DRY EYE ( 23 FDA reports)
HERPES ZOSTER ( 23 FDA reports)
IMPULSE-CONTROL DISORDER ( 23 FDA reports)
IRRITABILITY ( 23 FDA reports)
JOINT DISLOCATION ( 23 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 23 FDA reports)
POLLAKIURIA ( 23 FDA reports)
PULMONARY OEDEMA ( 23 FDA reports)
URINARY RETENTION ( 23 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 22 FDA reports)
ATELECTASIS ( 22 FDA reports)
DECREASED INTEREST ( 22 FDA reports)
DEMENTIA ( 22 FDA reports)
DISEASE PROGRESSION ( 22 FDA reports)
EMOTIONAL DISORDER ( 22 FDA reports)
ENTERITIS ( 22 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 22 FDA reports)
HAEMANGIOMA ( 22 FDA reports)
HYPERSENSITIVITY ( 22 FDA reports)
INCONTINENCE ( 22 FDA reports)
MUSCLE STRAIN ( 22 FDA reports)
NECK PAIN ( 22 FDA reports)
PANCREATITIS ( 22 FDA reports)
PRESYNCOPE ( 22 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
VITREOUS DETACHMENT ( 22 FDA reports)
WEGENER'S GRANULOMATOSIS ( 22 FDA reports)
BONE OPERATION ( 21 FDA reports)
CEREBRAL ATROPHY ( 21 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 21 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
HAEMORRHAGE ( 21 FDA reports)
HAEMORRHOIDS ( 21 FDA reports)
HEPATIC ENZYME INCREASED ( 21 FDA reports)
HIATUS HERNIA ( 21 FDA reports)
HYPOTONIA ( 21 FDA reports)
LIFE EXPECTANCY SHORTENED ( 21 FDA reports)
MUSCLE SPASTICITY ( 21 FDA reports)
NERVOUSNESS ( 21 FDA reports)
PULPITIS DENTAL ( 21 FDA reports)
RESPIRATORY DISTRESS ( 21 FDA reports)
THROMBOCYTOSIS ( 21 FDA reports)
TOOTH INFECTION ( 21 FDA reports)
ARTHRITIS ( 20 FDA reports)
DIVERTICULUM ( 20 FDA reports)
DYSURIA ( 20 FDA reports)
FACIAL NEURALGIA ( 20 FDA reports)
HUMERUS FRACTURE ( 20 FDA reports)
HYPOACUSIS ( 20 FDA reports)
OSTEITIS DEFORMANS ( 20 FDA reports)
PROSTATE CANCER ( 20 FDA reports)
RADICULOPATHY ( 20 FDA reports)
ALOPECIA ( 19 FDA reports)
ARTERIOSCLEROSIS ( 19 FDA reports)
CARDIAC DISORDER ( 19 FDA reports)
CARDIOMEGALY ( 19 FDA reports)
DEMENTIA WITH LEWY BODIES ( 19 FDA reports)
ERYTHEMA ( 19 FDA reports)
GYNAECOMASTIA ( 19 FDA reports)
JAW DISORDER ( 19 FDA reports)
MASS ( 19 FDA reports)
ON AND OFF PHENOMENON ( 19 FDA reports)
SCAR ( 19 FDA reports)
SINUS BRADYCARDIA ( 19 FDA reports)
SPINAL COMPRESSION FRACTURE ( 19 FDA reports)
SUDDEN DEATH ( 19 FDA reports)
TYPE 2 DIABETES MELLITUS ( 19 FDA reports)
WOUND INFECTION ( 19 FDA reports)
ASPIRATION ( 18 FDA reports)
AUTONOMIC NEUROPATHY ( 18 FDA reports)
BRADYKINESIA ( 18 FDA reports)
BREAST HYPERPLASIA ( 18 FDA reports)
BURSITIS ( 18 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 18 FDA reports)
EJECTION FRACTION DECREASED ( 18 FDA reports)
FOOT DEFORMITY ( 18 FDA reports)
HEARING DISABILITY ( 18 FDA reports)
HERNIA ( 18 FDA reports)
HYPOKINESIA ( 18 FDA reports)
HYPOVOLAEMIA ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
INCOHERENT ( 18 FDA reports)
LOOSE TOOTH ( 18 FDA reports)
LYMPHADENOPATHY ( 18 FDA reports)
MAJOR DEPRESSION ( 18 FDA reports)
OLFACTORY NERVE DISORDER ( 18 FDA reports)
OSTEOSCLEROSIS ( 18 FDA reports)
PARALYSIS ( 18 FDA reports)
POST PROCEDURAL COMPLICATION ( 18 FDA reports)
RAYNAUD'S PHENOMENON ( 18 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 18 FDA reports)
TOURETTE'S DISORDER ( 18 FDA reports)
ABNORMAL DREAMS ( 17 FDA reports)
APATHY ( 17 FDA reports)
ARRHYTHMIA ( 17 FDA reports)
ARTHROPATHY ( 17 FDA reports)
BLOOD ALBUMIN DECREASED ( 17 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 17 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
BONE DENSITY DECREASED ( 17 FDA reports)
CAROTID ARTERY STENOSIS ( 17 FDA reports)
COMA ( 17 FDA reports)
DEFORMITY ( 17 FDA reports)
DERMATOPHYTOSIS ( 17 FDA reports)
EATING DISORDER ( 17 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 17 FDA reports)
FIBROMYALGIA ( 17 FDA reports)
LIBIDO INCREASED ( 17 FDA reports)
LIVEDO RETICULARIS ( 17 FDA reports)
NERVOUS SYSTEM DISORDER ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
PANIC ATTACK ( 17 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 17 FDA reports)
ROAD TRAFFIC ACCIDENT ( 17 FDA reports)
SCIATICA ( 17 FDA reports)
TACHYCARDIA ( 17 FDA reports)
VIRAL INFECTION ( 17 FDA reports)
BLINDNESS ( 16 FDA reports)
BLISTER ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
BURNING SENSATION ( 16 FDA reports)
DEVICE FAILURE ( 16 FDA reports)
DRUG HYPERSENSITIVITY ( 16 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 16 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 16 FDA reports)
EPISTAXIS ( 16 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 16 FDA reports)
HEAD INJURY ( 16 FDA reports)
HIP FRACTURE ( 16 FDA reports)
HYPERAESTHESIA ( 16 FDA reports)
HYPOGLYCAEMIA ( 16 FDA reports)
HYPOMANIA ( 16 FDA reports)
INTERSTITIAL LUNG DISEASE ( 16 FDA reports)
LEUKOPENIA ( 16 FDA reports)
NEUROGENIC BLADDER ( 16 FDA reports)
OFF LABEL USE ( 16 FDA reports)
PULMONARY FIBROSIS ( 16 FDA reports)
SENSATION OF HEAVINESS ( 16 FDA reports)
SPINAL COLUMN STENOSIS ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
SUDDEN ONSET OF SLEEP ( 16 FDA reports)
TEMPORAL ARTERITIS ( 16 FDA reports)
TREATMENT NONCOMPLIANCE ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 15 FDA reports)
ANGINA UNSTABLE ( 15 FDA reports)
BONE LESION ( 15 FDA reports)
CRYING ( 15 FDA reports)
DRUG ABUSE ( 15 FDA reports)
DUODENAL ULCER ( 15 FDA reports)
DYSGRAPHIA ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
EPILEPSY ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
HYPOGONADISM ( 15 FDA reports)
ILL-DEFINED DISORDER ( 15 FDA reports)
JAUNDICE ( 15 FDA reports)
JOINT STIFFNESS ( 15 FDA reports)
LUNG INFILTRATION ( 15 FDA reports)
MANIA ( 15 FDA reports)
NASOPHARYNGITIS ( 15 FDA reports)
SCAN BONE MARROW ABNORMAL ( 15 FDA reports)
TRIGEMINAL NEURALGIA ( 15 FDA reports)
ABDOMINAL DISTENSION ( 14 FDA reports)
APPENDICECTOMY ( 14 FDA reports)
ATAXIA ( 14 FDA reports)
BONE DEBRIDEMENT ( 14 FDA reports)
COMPULSIONS ( 14 FDA reports)
DIFFICULTY IN WALKING ( 14 FDA reports)
DRUG DEPENDENCE ( 14 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 14 FDA reports)
HAEMODIALYSIS ( 14 FDA reports)
HYPERCHOLESTEROLAEMIA ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
INCREASED APPETITE ( 14 FDA reports)
INJECTION SITE REACTION ( 14 FDA reports)
MULTIPLE MYELOMA ( 14 FDA reports)
MUSCLE TWITCHING ( 14 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 14 FDA reports)
PROTHROMBIN TIME PROLONGED ( 14 FDA reports)
PULMONARY CONGESTION ( 14 FDA reports)
SEROTONIN SYNDROME ( 14 FDA reports)
THYROID DISORDER ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
ACTINIC KERATOSIS ( 13 FDA reports)
BLEPHARITIS ( 13 FDA reports)
BLOOD GLUCOSE DECREASED ( 13 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 13 FDA reports)
BRADYCARDIA ( 13 FDA reports)
CHOKING ( 13 FDA reports)
COORDINATION ABNORMAL ( 13 FDA reports)
DEAFNESS ( 13 FDA reports)
DRY SKIN ( 13 FDA reports)
EXCORIATION ( 13 FDA reports)
FEBRILE NEUTROPENIA ( 13 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
MICTURITION URGENCY ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
PHYSICAL DISABILITY ( 13 FDA reports)
PRODUCT QUALITY ISSUE ( 13 FDA reports)
RENAL DISORDER ( 13 FDA reports)
RESPIRATORY ARREST ( 13 FDA reports)
RHEUMATOID ARTHRITIS ( 13 FDA reports)
SKIN ULCER ( 13 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
ABDOMINAL DISCOMFORT ( 12 FDA reports)
ACUTE RESPIRATORY FAILURE ( 12 FDA reports)
APPLICATION SITE ERYTHEMA ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 12 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 12 FDA reports)
CORONARY ARTERY OCCLUSION ( 12 FDA reports)
CORONARY ARTERY STENOSIS ( 12 FDA reports)
DENTAL PROSTHESIS USER ( 12 FDA reports)
DISABILITY ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
DISEASE RECURRENCE ( 12 FDA reports)
DRUG DOSE OMISSION ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
EYE LASER SURGERY ( 12 FDA reports)
FLUID RETENTION ( 12 FDA reports)
GASTROENTERITIS ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
HAEMATOCHEZIA ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HALLUCINATION, OLFACTORY ( 12 FDA reports)
HEART RATE DECREASED ( 12 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 12 FDA reports)
IRRITABLE BOWEL SYNDROME ( 12 FDA reports)
LACERATION ( 12 FDA reports)
PERIVASCULAR DERMATITIS ( 12 FDA reports)
POSTURE ABNORMAL ( 12 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 12 FDA reports)
RASH MACULAR ( 12 FDA reports)
SALIVARY HYPERSECRETION ( 12 FDA reports)
SKIN CANCER ( 12 FDA reports)
SKIN DISCOLOURATION ( 12 FDA reports)
SPONDYLOLISTHESIS ( 12 FDA reports)
THYROID NEOPLASM ( 12 FDA reports)
UNEVALUABLE EVENT ( 12 FDA reports)
VENTRICULAR HYPERTROPHY ( 12 FDA reports)
VISUAL DISTURBANCE ( 12 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
ACUTE PSYCHOSIS ( 11 FDA reports)
AMAUROSIS FUGAX ( 11 FDA reports)
ANGER ( 11 FDA reports)
ANGIOLIPOMA ( 11 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 11 FDA reports)
APPLICATION SITE PRURITUS ( 11 FDA reports)
BACTERIAL DISEASE CARRIER ( 11 FDA reports)
BLINDNESS UNILATERAL ( 11 FDA reports)
BLOOD IRON DECREASED ( 11 FDA reports)
BODY TEMPERATURE INCREASED ( 11 FDA reports)
CEREBRAL ARTERY STENOSIS ( 11 FDA reports)
FEELING HOT ( 11 FDA reports)
FRACTURED SACRUM ( 11 FDA reports)
GINGIVAL ABSCESS ( 11 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 11 FDA reports)
HYPERSOMNIA ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
KIDNEY INFECTION ( 11 FDA reports)
LOCALISED INFECTION ( 11 FDA reports)
MALNUTRITION ( 11 FDA reports)
MERALGIA PARAESTHETICA ( 11 FDA reports)
OESOPHAGITIS ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
OROPHARYNGEAL BLISTERING ( 11 FDA reports)
OTITIS EXTERNA ( 11 FDA reports)
OXYGEN SATURATION DECREASED ( 11 FDA reports)
PITUITARY ENLARGEMENT ( 11 FDA reports)
POLYARTERITIS NODOSA ( 11 FDA reports)
PRINZMETAL ANGINA ( 11 FDA reports)
RASH VESICULAR ( 11 FDA reports)
REFLUX OESOPHAGITIS ( 11 FDA reports)
SCOTOMA ( 11 FDA reports)
THROMBOPHLEBITIS ( 11 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 11 FDA reports)
TONGUE BITING ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 11 FDA reports)
APPLICATION SITE REACTION ( 10 FDA reports)
BEDRIDDEN ( 10 FDA reports)
BLADDER DISORDER ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
DRUG INTOLERANCE ( 10 FDA reports)
EYE DISORDER ( 10 FDA reports)
FACIAL PALSY ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
GASTRIC ULCER ( 10 FDA reports)
GASTROENTERITIS VIRAL ( 10 FDA reports)
HEART RATE IRREGULAR ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
INFLAMMATION ( 10 FDA reports)
INJECTION SITE NECROSIS ( 10 FDA reports)
INTENTIONAL DRUG MISUSE ( 10 FDA reports)
INTENTIONAL OVERDOSE ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
LEUKOCYTOSIS ( 10 FDA reports)
LUNG NEOPLASM MALIGNANT ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
MALIGNANT MELANOMA ( 10 FDA reports)
MUSCLE TIGHTNESS ( 10 FDA reports)
NEURALGIA ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
STEM CELL TRANSPLANT ( 10 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 10 FDA reports)
VISUAL FIELD DEFECT ( 10 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BRADYPHRENIA ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
CORNEAL DISORDER ( 9 FDA reports)
DELUSION OF GRANDEUR ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
GASTRIC DISORDER ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
HEPATIC STEATOSIS ( 9 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 9 FDA reports)
IMPULSIVE BEHAVIOUR ( 9 FDA reports)
INCREASED TENDENCY TO BRUISE ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
MENORRHAGIA ( 9 FDA reports)
METASTASES TO BONE ( 9 FDA reports)
MYOCARDIAL ISCHAEMIA ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
NO THERAPEUTIC RESPONSE ( 9 FDA reports)
PATHOGEN RESISTANCE ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
POLYNEUROPATHY ( 9 FDA reports)
PSYCHIATRIC SYMPTOM ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
RECURRENT CANCER ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
SEDATION ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 9 FDA reports)
SUBDURAL HAEMATOMA ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
TINNITUS ( 9 FDA reports)
TOXIC ENCEPHALOPATHY ( 9 FDA reports)
ADVERSE DRUG REACTION ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
BLEPHAROSPASM ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BREAST CANCER FEMALE ( 8 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 8 FDA reports)
CLOSTRIDIAL INFECTION ( 8 FDA reports)
COGWHEEL RIGIDITY ( 8 FDA reports)
COMPULSIVE SHOPPING ( 8 FDA reports)
DENTAL OPERATION ( 8 FDA reports)
DIABETIC NEUROPATHY ( 8 FDA reports)
EXOPHTHALMOS ( 8 FDA reports)
EYE MOVEMENT DISORDER ( 8 FDA reports)
FACIAL PAIN ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
HAEMOLYTIC ANAEMIA ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
INJECTION SITE MASS ( 8 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
IRON DEFICIENCY ANAEMIA ( 8 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 8 FDA reports)
KLEBSIELLA TEST POSITIVE ( 8 FDA reports)
LIBIDO DECREASED ( 8 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 8 FDA reports)
MASKED FACIES ( 8 FDA reports)
MELANOSIS COLI ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 8 FDA reports)
PERSONALITY CHANGE ( 8 FDA reports)
PHLEBOLITH ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
PYELONEPHRITIS ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 8 FDA reports)
STATUS EPILEPTICUS ( 8 FDA reports)
STOMACH DISCOMFORT ( 8 FDA reports)
SURGERY ( 8 FDA reports)
TONGUE INJURY ( 8 FDA reports)
TONGUE ULCERATION ( 8 FDA reports)
TOOTHACHE ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
AKATHISIA ( 7 FDA reports)
ANKLE FRACTURE ( 7 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 7 FDA reports)
BILE DUCT CANCER ( 7 FDA reports)
BLADDER PROLAPSE ( 7 FDA reports)
BLOOD AMYLASE INCREASED ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
BREAST CANCER IN SITU ( 7 FDA reports)
CEREBELLAR SYNDROME ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
COLITIS ( 7 FDA reports)
COLON CANCER ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
COR PULMONALE CHRONIC ( 7 FDA reports)
DEPERSONALISATION ( 7 FDA reports)
DISINHIBITION ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
EAR PAIN ( 7 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
EYE PAIN ( 7 FDA reports)
FAECALOMA ( 7 FDA reports)
FEMUR FRACTURE ( 7 FDA reports)
FISTULA ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GRANULOCYTOPENIA ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HEPATIC CYST ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HYPERKINESIA ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
ILEUS ( 7 FDA reports)
IMMOBILE ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INFECTED SKIN ULCER ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
MONONEUROPATHY MULTIPLEX ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PANCREATIC CYST ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
RETINAL DETACHMENT ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SKIN HYPERTROPHY ( 7 FDA reports)
STEREOTYPY ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
THALASSAEMIA ( 7 FDA reports)
THROMBOSED VARICOSE VEIN ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
UTERINE ENLARGEMENT ( 7 FDA reports)
VENTRICULAR DYSFUNCTION ( 7 FDA reports)
ADHESION ( 6 FDA reports)
ADJUSTMENT DISORDER ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
BRUXISM ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
CYST ( 6 FDA reports)
DEPRESSIVE SYMPTOM ( 6 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 6 FDA reports)
DRUG EFFECT DELAYED ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
ERYTHROMELALGIA ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
FREEZING PHENOMENON ( 6 FDA reports)
GAZE PALSY ( 6 FDA reports)
GOITRE ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HERPES SIMPLEX ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
INJECTION SITE SWELLING ( 6 FDA reports)
JEALOUS DELUSION ( 6 FDA reports)
JOINT INJURY ( 6 FDA reports)
KLEBSIELLA INFECTION ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
METASTASES TO SPINE ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 6 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
OBESITY ( 6 FDA reports)
OCULAR HYPERAEMIA ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PANNICULITIS ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SARCOIDOSIS ( 6 FDA reports)
SELF-MEDICATION ( 6 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
THYROID CYST ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
ULCER ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VOLVULUS ( 6 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
AGORAPHOBIA ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ANAESTHETIC COMPLICATION ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
BREAST CANCER STAGE I ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DILATATION ATRIAL ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DYSAESTHESIA ( 5 FDA reports)
DYSPHEMIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FEELING GUILTY ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HYPERREFLEXIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INGUINAL HERNIA ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE INFLAMMATION ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LYMPHOMA ( 5 FDA reports)
METASTASES TO LUNG ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
OESOPHAGEAL DILATATION ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORAL INTAKE REDUCED ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PIGMENTATION DISORDER ( 5 FDA reports)
PLANTAR FASCIITIS ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
POISONING ( 5 FDA reports)
POLYP ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
REFLEXES ABNORMAL ( 5 FDA reports)
RESUSCITATION ( 5 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SLEEP ATTACKS ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 5 FDA reports)
SPINAL FRACTURE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
TELANGIECTASIA ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THYROID ATROPHY ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TRAUMATIC RENAL INJURY ( 5 FDA reports)
TREATMENT FAILURE ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
WOUND ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
ABSCESS ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
BRUGADA SYNDROME ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CHOREA ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 4 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DYSPHORIA ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
FEELINGS OF WORTHLESSNESS ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 4 FDA reports)
HAEMORRHOID OPERATION ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HELMINTHIC INFECTION ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INJECTION SITE ULCER ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LIPOMA EXCISION ( 4 FDA reports)
LIPOPROTEIN (A) INCREASED ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MALIGNANT MELANOMA IN SITU ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MASS EXCISION ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MICROGRAPHIA ( 4 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
OVARIAN EPITHELIAL CANCER ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PARADOXICAL EMBOLISM ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 4 FDA reports)
PERICARDITIS CONSTRICTIVE ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
PRESBYOPIA ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
REGRESSIVE BEHAVIOUR ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RETCHING ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN NODULE ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SPONTANEOUS PENILE ERECTION ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
TENSION ( 4 FDA reports)
TESTIS CANCER ( 4 FDA reports)
THIRST ( 4 FDA reports)
THIRST DECREASED ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TOOTH REPAIR ( 4 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
AURA ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BAND SENSATION ( 3 FDA reports)
BASAL GANGLION DEGENERATION ( 3 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BINGE EATING ( 3 FDA reports)
BLADDER CYST ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CRYOGLOBULINAEMIA ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HUNTINGTON'S DISEASE ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PUTAMEN HAEMORRHAGE ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
STARING ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
UHTHOFF'S PHENOMENON ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VENOUS OCCLUSION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DECREASED ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AVIAN INFLUENZA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BALLISMUS ( 2 FDA reports)
BASAL GANGLIA STROKE ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUNION ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CRYOGLOBULINS PRESENT ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYCLOTHYMIC DISORDER ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXCESSIVE EXERCISE ( 2 FDA reports)
EXCESSIVE MASTURBATION ( 2 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HUNTINGTON'S CHOREA ( 2 FDA reports)
HYDROPHOBIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC GENERALISED EPILEPSY ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
MYOSCLEROSIS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OROMANDIBULAR DYSTONIA ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARAPHILIA ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RALES ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VIRAL SKIN INFECTION ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALEXIA ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALCOHOL ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CATECHOLAMINES ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICITIS TRICHOMONAL ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL ENDOTHELIITIS ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL CANCER STAGE III ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYSOZYME INCREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT PITUITARY TUMOUR ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
PALATAL DYSPLASIA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHLEBITIS ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
POVERTY ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION NEUROPATHY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DYSKINESIA ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATIVE THERAPY ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEROCONVERSION TEST POSITIVE ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHIGELLA INFECTION ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TIC ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNSTABLE FOETAL LIE ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URINARY BLADDER EXCISION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE SODIUM ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
UROSTOMY COMPLICATION ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VASCULAR FRAGILITY ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISCERAL OEDEMA ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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