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

DEPRESSION ( 413 FDA reports)
ANXIETY ( 390 FDA reports)
CEREBROVASCULAR ACCIDENT ( 358 FDA reports)
NAUSEA ( 330 FDA reports)
HYPERTENSION ( 322 FDA reports)
DIZZINESS ( 318 FDA reports)
DYSPNOEA ( 317 FDA reports)
MYOCARDIAL INFARCTION ( 311 FDA reports)
ARTHRALGIA ( 309 FDA reports)
HEADACHE ( 308 FDA reports)
FATIGUE ( 305 FDA reports)
CHEST PAIN ( 285 FDA reports)
FALL ( 282 FDA reports)
PAIN ( 270 FDA reports)
PAIN IN EXTREMITY ( 214 FDA reports)
ASTHENIA ( 206 FDA reports)
OEDEMA PERIPHERAL ( 206 FDA reports)
ANAEMIA ( 201 FDA reports)
BACK PAIN ( 198 FDA reports)
CORONARY ARTERY DISEASE ( 196 FDA reports)
VOMITING ( 196 FDA reports)
PYREXIA ( 185 FDA reports)
DRUG INEFFECTIVE ( 180 FDA reports)
HYPERLIPIDAEMIA ( 179 FDA reports)
DIARRHOEA ( 177 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 175 FDA reports)
INSOMNIA ( 174 FDA reports)
PNEUMONIA ( 174 FDA reports)
CONVULSION ( 149 FDA reports)
SINUSITIS ( 148 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 144 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 143 FDA reports)
HYPOAESTHESIA ( 140 FDA reports)
OSTEOARTHRITIS ( 139 FDA reports)
CONFUSIONAL STATE ( 136 FDA reports)
CARDIAC DISORDER ( 134 FDA reports)
DRUG INTERACTION ( 133 FDA reports)
SYNCOPE ( 130 FDA reports)
ABDOMINAL PAIN UPPER ( 129 FDA reports)
ABDOMINAL PAIN ( 128 FDA reports)
WEIGHT DECREASED ( 127 FDA reports)
CONSTIPATION ( 126 FDA reports)
COUGH ( 126 FDA reports)
URINARY TRACT INFECTION ( 126 FDA reports)
LOSS OF CONSCIOUSNESS ( 125 FDA reports)
HYPOTENSION ( 122 FDA reports)
RENAL FAILURE ACUTE ( 122 FDA reports)
OSTEONECROSIS ( 121 FDA reports)
MALAISE ( 120 FDA reports)
WEIGHT INCREASED ( 120 FDA reports)
OVERDOSE ( 113 FDA reports)
HYPERHIDROSIS ( 112 FDA reports)
EMOTIONAL DISTRESS ( 111 FDA reports)
PANIC ATTACK ( 111 FDA reports)
BURSITIS ( 110 FDA reports)
ANGINA PECTORIS ( 108 FDA reports)
PARAESTHESIA ( 108 FDA reports)
RENAL FAILURE ( 108 FDA reports)
SOMNOLENCE ( 102 FDA reports)
AGITATION ( 96 FDA reports)
BRONCHITIS ( 95 FDA reports)
RASH ( 95 FDA reports)
CARPAL TUNNEL SYNDROME ( 93 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 93 FDA reports)
MITRAL VALVE INCOMPETENCE ( 92 FDA reports)
VISION BLURRED ( 92 FDA reports)
BLOOD PRESSURE INCREASED ( 89 FDA reports)
DECREASED APPETITE ( 89 FDA reports)
DYSPHAGIA ( 89 FDA reports)
NECK PAIN ( 89 FDA reports)
NEUROPATHY PERIPHERAL ( 89 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 88 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 88 FDA reports)
FIBROMYALGIA ( 86 FDA reports)
CONDITION AGGRAVATED ( 85 FDA reports)
TREMOR ( 85 FDA reports)
OSTEONECROSIS OF JAW ( 84 FDA reports)
DYSPEPSIA ( 83 FDA reports)
HEART RATE INCREASED ( 83 FDA reports)
IRRITABLE BOWEL SYNDROME ( 83 FDA reports)
OSTEOMYELITIS ( 83 FDA reports)
INFECTION ( 82 FDA reports)
MUSCLE SPASMS ( 82 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 81 FDA reports)
MENISCUS LESION ( 79 FDA reports)
DRUG HYPERSENSITIVITY ( 78 FDA reports)
DEHYDRATION ( 77 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 77 FDA reports)
PALPITATIONS ( 77 FDA reports)
LACUNAR INFARCTION ( 76 FDA reports)
DIVERTICULUM ( 75 FDA reports)
MUSCULAR WEAKNESS ( 75 FDA reports)
RHABDOMYOLYSIS ( 74 FDA reports)
CARDIOMEGALY ( 73 FDA reports)
DEATH ( 73 FDA reports)
EMPHYSEMA ( 73 FDA reports)
IMPAIRED HEALING ( 73 FDA reports)
MYALGIA ( 73 FDA reports)
AMNESIA ( 71 FDA reports)
FEELING ABNORMAL ( 71 FDA reports)
HAEMATOCHEZIA ( 71 FDA reports)
FEMUR FRACTURE ( 70 FDA reports)
ARTHROPATHY ( 69 FDA reports)
DEEP VEIN THROMBOSIS ( 69 FDA reports)
INJURY ( 68 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 68 FDA reports)
PULMONARY EMBOLISM ( 67 FDA reports)
CELLULITIS ( 66 FDA reports)
CHEST DISCOMFORT ( 66 FDA reports)
GASTRITIS ( 65 FDA reports)
ASTHMA ( 64 FDA reports)
CONTUSION ( 63 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 63 FDA reports)
ATELECTASIS ( 59 FDA reports)
CATARACT ( 59 FDA reports)
HYPOXIA ( 59 FDA reports)
OEDEMA ( 59 FDA reports)
PLEURAL EFFUSION ( 59 FDA reports)
PRURITUS ( 59 FDA reports)
SLEEP DISORDER ( 59 FDA reports)
SUICIDE ATTEMPT ( 59 FDA reports)
ATRIAL FIBRILLATION ( 58 FDA reports)
DRUG TOXICITY ( 58 FDA reports)
ABDOMINAL DISCOMFORT ( 57 FDA reports)
ARTHRITIS ( 57 FDA reports)
HAEMOGLOBIN DECREASED ( 57 FDA reports)
HALLUCINATION ( 57 FDA reports)
HIATUS HERNIA ( 57 FDA reports)
JOINT SWELLING ( 56 FDA reports)
MENTAL STATUS CHANGES ( 56 FDA reports)
ADVERSE EVENT ( 55 FDA reports)
HYPONATRAEMIA ( 55 FDA reports)
BLOOD GLUCOSE INCREASED ( 54 FDA reports)
CARDIAC ARREST ( 53 FDA reports)
COMPLETED SUICIDE ( 53 FDA reports)
HYPOKALAEMIA ( 53 FDA reports)
OSTEOPOROSIS ( 53 FDA reports)
AGGRESSION ( 52 FDA reports)
CHOLELITHIASIS ( 52 FDA reports)
DISTURBANCE IN ATTENTION ( 52 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 52 FDA reports)
ANGINA UNSTABLE ( 51 FDA reports)
THROMBOCYTOPENIA ( 51 FDA reports)
BACK DISORDER ( 50 FDA reports)
BONE DISORDER ( 50 FDA reports)
OSTEOPENIA ( 50 FDA reports)
RESPIRATORY FAILURE ( 50 FDA reports)
LUMBAR RADICULOPATHY ( 49 FDA reports)
SPINAL OSTEOARTHRITIS ( 49 FDA reports)
SUICIDAL IDEATION ( 49 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 49 FDA reports)
BALANCE DISORDER ( 48 FDA reports)
ERYTHEMA ( 48 FDA reports)
MYOCARDIAL ISCHAEMIA ( 48 FDA reports)
ROAD TRAFFIC ACCIDENT ( 48 FDA reports)
TACHYCARDIA ( 48 FDA reports)
HYPERCHOLESTEROLAEMIA ( 47 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 47 FDA reports)
LETHARGY ( 47 FDA reports)
PAIN IN JAW ( 47 FDA reports)
DENTAL CARIES ( 46 FDA reports)
DIABETES MELLITUS ( 46 FDA reports)
RENAL CYST ( 46 FDA reports)
ABASIA ( 45 FDA reports)
ABDOMINAL DISTENSION ( 45 FDA reports)
BLOOD CREATININE INCREASED ( 45 FDA reports)
CAROTID ARTERY STENOSIS ( 45 FDA reports)
HAEMATURIA ( 45 FDA reports)
NEPHROLITHIASIS ( 45 FDA reports)
RHEUMATOID ARTHRITIS ( 45 FDA reports)
STAPHYLOCOCCAL INFECTION ( 45 FDA reports)
TINNITUS ( 45 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 44 FDA reports)
COMA ( 44 FDA reports)
DELIRIUM ( 44 FDA reports)
MEMORY IMPAIRMENT ( 44 FDA reports)
TREATMENT NONCOMPLIANCE ( 44 FDA reports)
VERTIGO ( 44 FDA reports)
BLOOD PRESSURE DECREASED ( 43 FDA reports)
PULMONARY OEDEMA ( 43 FDA reports)
SEPSIS ( 43 FDA reports)
THROMBOSIS ( 43 FDA reports)
AORTIC VALVE INCOMPETENCE ( 42 FDA reports)
CARDIOVASCULAR DISORDER ( 42 FDA reports)
HYPERSENSITIVITY ( 42 FDA reports)
NASOPHARYNGITIS ( 42 FDA reports)
OESOPHAGITIS ( 42 FDA reports)
SPONDYLOLYSIS ( 42 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 41 FDA reports)
CARDIAC FAILURE ( 41 FDA reports)
DYSPNOEA EXERTIONAL ( 41 FDA reports)
HAEMORRHAGE ( 41 FDA reports)
HOT FLUSH ( 41 FDA reports)
JOINT DISLOCATION ( 41 FDA reports)
MOUTH ULCERATION ( 41 FDA reports)
TOOTH DISORDER ( 41 FDA reports)
VENTRICULAR HYPERTROPHY ( 41 FDA reports)
ATHEROSCLEROSIS ( 40 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 40 FDA reports)
DRY MOUTH ( 40 FDA reports)
HERPES ZOSTER ( 40 FDA reports)
SPINAL COLUMN STENOSIS ( 40 FDA reports)
ABNORMAL BEHAVIOUR ( 39 FDA reports)
ADVERSE DRUG REACTION ( 39 FDA reports)
ARTERIOSCLEROSIS ( 39 FDA reports)
DYSKINESIA ( 39 FDA reports)
HYPERGLYCAEMIA ( 39 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 38 FDA reports)
CEREBRAL INFARCTION ( 38 FDA reports)
DISORIENTATION ( 38 FDA reports)
HYPOGLYCAEMIA ( 38 FDA reports)
IRRITABILITY ( 38 FDA reports)
PNEUMONIA ASPIRATION ( 38 FDA reports)
SEROTONIN SYNDROME ( 38 FDA reports)
GINGIVAL DISORDER ( 37 FDA reports)
INTENTIONAL OVERDOSE ( 37 FDA reports)
OROPHARYNGEAL PAIN ( 37 FDA reports)
URINARY INCONTINENCE ( 37 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 37 FDA reports)
ALOPECIA ( 36 FDA reports)
DRUG DEPENDENCE ( 36 FDA reports)
GAIT DISTURBANCE ( 36 FDA reports)
LUNG NEOPLASM ( 36 FDA reports)
MUSCULOSKELETAL PAIN ( 36 FDA reports)
RECTAL HAEMORRHAGE ( 36 FDA reports)
RENAL DISORDER ( 36 FDA reports)
CRYING ( 35 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 35 FDA reports)
DYSARTHRIA ( 35 FDA reports)
SKIN LESION ( 35 FDA reports)
BLOOD UREA INCREASED ( 34 FDA reports)
BURNING SENSATION ( 34 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 34 FDA reports)
DIABETIC NEUROPATHY ( 34 FDA reports)
HYPOTHYROIDISM ( 34 FDA reports)
PANCYTOPENIA ( 34 FDA reports)
SLEEP APNOEA SYNDROME ( 34 FDA reports)
CORONARY ARTERY OCCLUSION ( 33 FDA reports)
FLUID RETENTION ( 33 FDA reports)
GINGIVITIS ( 33 FDA reports)
HEPATIC STEATOSIS ( 33 FDA reports)
LOBAR PNEUMONIA ( 33 FDA reports)
NEUTROPENIA ( 33 FDA reports)
PANCREATITIS ( 33 FDA reports)
POLLAKIURIA ( 33 FDA reports)
RENAL FAILURE CHRONIC ( 33 FDA reports)
RESTLESSNESS ( 33 FDA reports)
SPEECH DISORDER ( 33 FDA reports)
TOOTH FRACTURE ( 33 FDA reports)
WHEEZING ( 33 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 32 FDA reports)
CORONARY ARTERY STENOSIS ( 32 FDA reports)
GASTROENTERITIS ( 32 FDA reports)
HAEMATEMESIS ( 32 FDA reports)
LUMBAR SPINAL STENOSIS ( 32 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 32 FDA reports)
CHILLS ( 31 FDA reports)
DYSURIA ( 31 FDA reports)
INFLUENZA ( 31 FDA reports)
MIGRAINE ( 31 FDA reports)
RIB FRACTURE ( 31 FDA reports)
SCIATICA ( 31 FDA reports)
SWELLING FACE ( 31 FDA reports)
DYSPHONIA ( 30 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 30 FDA reports)
WRIST FRACTURE ( 30 FDA reports)
BACK INJURY ( 29 FDA reports)
CARDIO-RESPIRATORY ARREST ( 29 FDA reports)
FIBROSIS ( 29 FDA reports)
HYPERKALAEMIA ( 29 FDA reports)
ILEUS ( 29 FDA reports)
LEUKOPENIA ( 29 FDA reports)
LIMB DISCOMFORT ( 29 FDA reports)
NERVOUSNESS ( 29 FDA reports)
PNEUMOTHORAX ( 29 FDA reports)
PULMONARY HYPERTENSION ( 29 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 29 FDA reports)
CHRONIC FATIGUE SYNDROME ( 28 FDA reports)
GINGIVAL PAIN ( 28 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 28 FDA reports)
SPINAL COMPRESSION FRACTURE ( 28 FDA reports)
SWELLING ( 28 FDA reports)
URINARY RETENTION ( 28 FDA reports)
DIPLOPIA ( 27 FDA reports)
GALLBLADDER DISORDER ( 27 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 27 FDA reports)
HEPATITIS C ( 27 FDA reports)
HYPOCALCAEMIA ( 27 FDA reports)
ORTHOSTATIC HYPOTENSION ( 27 FDA reports)
RADICULOPATHY ( 27 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 27 FDA reports)
ACUTE CORONARY SYNDROME ( 26 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 26 FDA reports)
ACUTE SINUSITIS ( 26 FDA reports)
BONE DENSITY DECREASED ( 26 FDA reports)
CANDIDIASIS ( 26 FDA reports)
COMPRESSION FRACTURE ( 26 FDA reports)
DEPRESSED MOOD ( 26 FDA reports)
FOOT FRACTURE ( 26 FDA reports)
IMPAIRED WORK ABILITY ( 26 FDA reports)
OBESITY ( 26 FDA reports)
ROTATOR CUFF SYNDROME ( 26 FDA reports)
SCOLIOSIS ( 26 FDA reports)
SPINAL DISORDER ( 26 FDA reports)
ABDOMINAL PAIN LOWER ( 25 FDA reports)
ANOREXIA ( 25 FDA reports)
BONE PAIN ( 25 FDA reports)
CARDIOMYOPATHY ( 25 FDA reports)
COLITIS ( 25 FDA reports)
DEAFNESS ( 25 FDA reports)
ERECTILE DYSFUNCTION ( 25 FDA reports)
HAEMORRHOIDS ( 25 FDA reports)
INCONTINENCE ( 25 FDA reports)
INFLAMMATION ( 25 FDA reports)
JAW DISORDER ( 25 FDA reports)
JOINT INJURY ( 25 FDA reports)
MOOD SWINGS ( 25 FDA reports)
ORAL PAIN ( 25 FDA reports)
POST PROCEDURAL COMPLICATION ( 25 FDA reports)
SKIN ULCER ( 25 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 25 FDA reports)
TOOTH ABSCESS ( 25 FDA reports)
CERUMEN IMPACTION ( 24 FDA reports)
GASTRIC DISORDER ( 24 FDA reports)
GENERALISED ANXIETY DISORDER ( 24 FDA reports)
JOINT EFFUSION ( 24 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 24 FDA reports)
MULTIPLE DRUG OVERDOSE ( 24 FDA reports)
MUSCLE TWITCHING ( 24 FDA reports)
ORAL INFECTION ( 24 FDA reports)
PHARYNGITIS ( 24 FDA reports)
PRODUCT QUALITY ISSUE ( 24 FDA reports)
REFLEXES ABNORMAL ( 24 FDA reports)
SWOLLEN TONGUE ( 24 FDA reports)
TOOTH EXTRACTION ( 24 FDA reports)
TOOTH LOSS ( 24 FDA reports)
ULCER ( 24 FDA reports)
VISUAL DISTURBANCE ( 24 FDA reports)
ARRHYTHMIA ( 23 FDA reports)
ARTHRITIS BACTERIAL ( 23 FDA reports)
BLISTER ( 23 FDA reports)
BRADYCARDIA ( 23 FDA reports)
CYSTITIS ( 23 FDA reports)
DELUSION ( 23 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 23 FDA reports)
EYE PAIN ( 23 FDA reports)
FEAR ( 23 FDA reports)
FLUSHING ( 23 FDA reports)
GASTROINTESTINAL DISORDER ( 23 FDA reports)
INTENTIONAL DRUG MISUSE ( 23 FDA reports)
LIVER DISORDER ( 23 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 23 FDA reports)
NIGHT SWEATS ( 23 FDA reports)
PRODUCTIVE COUGH ( 23 FDA reports)
RHINORRHOEA ( 23 FDA reports)
SHOCK ( 23 FDA reports)
SINUS TACHYCARDIA ( 23 FDA reports)
URTICARIA ( 23 FDA reports)
ANGIOEDEMA ( 22 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 22 FDA reports)
CYSTOCELE ( 22 FDA reports)
DRUG DOSE OMISSION ( 22 FDA reports)
HYPERCALCAEMIA ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 22 FDA reports)
LEUKOCYTOSIS ( 22 FDA reports)
MUSCLE STRAIN ( 22 FDA reports)
NEURALGIA ( 22 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 22 FDA reports)
PRIMARY SEQUESTRUM ( 22 FDA reports)
PROSTATITIS ( 22 FDA reports)
RASH ERYTHEMATOUS ( 22 FDA reports)
RESPIRATORY DISORDER ( 22 FDA reports)
SQUAMOUS CELL CARCINOMA ( 22 FDA reports)
TOOTHACHE ( 22 FDA reports)
VISUAL IMPAIRMENT ( 22 FDA reports)
ANEURYSM ( 21 FDA reports)
BASAL CELL CARCINOMA ( 21 FDA reports)
CONJUNCTIVITIS ( 21 FDA reports)
EJECTION FRACTION DECREASED ( 21 FDA reports)
HAEMATOMA ( 21 FDA reports)
HYPOMAGNESAEMIA ( 21 FDA reports)
INTESTINAL OBSTRUCTION ( 21 FDA reports)
MEDICATION ERROR ( 21 FDA reports)
MENTAL DISORDER ( 21 FDA reports)
PERICARDIAL EFFUSION ( 21 FDA reports)
RHINITIS ALLERGIC ( 21 FDA reports)
SPINAL FRACTURE ( 21 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 21 FDA reports)
TOOTH INFECTION ( 21 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 21 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 21 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 20 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 20 FDA reports)
BREAST CANCER ( 20 FDA reports)
BRONCHITIS ACUTE ( 20 FDA reports)
BRONCHOPNEUMONIA ( 20 FDA reports)
CIRCULATORY COLLAPSE ( 20 FDA reports)
CLOSTRIDIUM COLITIS ( 20 FDA reports)
COAGULOPATHY ( 20 FDA reports)
DUODENITIS ( 20 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 20 FDA reports)
FACET JOINT SYNDROME ( 20 FDA reports)
HAEMATOCRIT DECREASED ( 20 FDA reports)
HEPATIC FAILURE ( 20 FDA reports)
HIP FRACTURE ( 20 FDA reports)
HYPERKERATOSIS ( 20 FDA reports)
IMPAIRED DRIVING ABILITY ( 20 FDA reports)
MAJOR DEPRESSION ( 20 FDA reports)
MOBILITY DECREASED ( 20 FDA reports)
MUSCLE ATROPHY ( 20 FDA reports)
MUSCLE CRAMP ( 20 FDA reports)
PULMONARY FIBROSIS ( 20 FDA reports)
RESPIRATORY ARREST ( 20 FDA reports)
SPONDYLOLISTHESIS ( 20 FDA reports)
TONGUE ULCERATION ( 20 FDA reports)
TYPE 2 DIABETES MELLITUS ( 20 FDA reports)
VENTRICULAR DYSFUNCTION ( 20 FDA reports)
VENTRICULAR TACHYCARDIA ( 20 FDA reports)
ANGER ( 19 FDA reports)
APHASIA ( 19 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 19 FDA reports)
BLOOD GLUCOSE DECREASED ( 19 FDA reports)
CARDIAC MURMUR ( 19 FDA reports)
COLONIC POLYP ( 19 FDA reports)
DECREASED INTEREST ( 19 FDA reports)
DEVICE RELATED INFECTION ( 19 FDA reports)
DRUG ABUSER ( 19 FDA reports)
DRUG ADMINISTRATION ERROR ( 19 FDA reports)
HEART RATE IRREGULAR ( 19 FDA reports)
INCORRECT DOSE ADMINISTERED ( 19 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 19 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 19 FDA reports)
MALNUTRITION ( 19 FDA reports)
MULTIPLE SCLEROSIS ( 19 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 19 FDA reports)
RADIUS FRACTURE ( 19 FDA reports)
REBOUND HYPERTENSION ( 19 FDA reports)
SHOULDER PAIN ( 19 FDA reports)
SINUS BRADYCARDIA ( 19 FDA reports)
VAGINAL HAEMORRHAGE ( 19 FDA reports)
VERTIGO POSITIONAL ( 19 FDA reports)
ABSCESS ( 18 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 18 FDA reports)
COORDINATION ABNORMAL ( 18 FDA reports)
DRY EYE ( 18 FDA reports)
EAR PAIN ( 18 FDA reports)
EXOSTOSIS ( 18 FDA reports)
FISTULA ( 18 FDA reports)
GRAND MAL CONVULSION ( 18 FDA reports)
HEPATITIS ( 18 FDA reports)
LUNG DISORDER ( 18 FDA reports)
LUNG INFILTRATION ( 18 FDA reports)
MASS ( 18 FDA reports)
MELAENA ( 18 FDA reports)
PSYCHOTIC DISORDER ( 18 FDA reports)
RASH PRURITIC ( 18 FDA reports)
RECTOCELE ( 18 FDA reports)
RESTLESS LEGS SYNDROME ( 18 FDA reports)
STOMATITIS ( 18 FDA reports)
STRESS ( 18 FDA reports)
STRESS FRACTURE ( 18 FDA reports)
STRESS SYMPTOMS ( 18 FDA reports)
THYROID NEOPLASM ( 18 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 18 FDA reports)
BLOOD BILIRUBIN INCREASED ( 17 FDA reports)
BONE LOSS ( 17 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 17 FDA reports)
DEFORMITY ( 17 FDA reports)
DRUG SCREEN POSITIVE ( 17 FDA reports)
DYSSTASIA ( 17 FDA reports)
EXCORIATION ( 17 FDA reports)
FACIAL PALSY ( 17 FDA reports)
FEELING HOT ( 17 FDA reports)
GINGIVAL INFECTION ( 17 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 17 FDA reports)
HALLUCINATION, VISUAL ( 17 FDA reports)
HAND FRACTURE ( 17 FDA reports)
HYPERTENSIVE HEART DISEASE ( 17 FDA reports)
INCREASED APPETITE ( 17 FDA reports)
INJECTION SITE ERYTHEMA ( 17 FDA reports)
JUDGEMENT IMPAIRED ( 17 FDA reports)
LACERATION ( 17 FDA reports)
LARYNGITIS ( 17 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 17 FDA reports)
MULTIPLE MYELOMA ( 17 FDA reports)
NERVOUS SYSTEM DISORDER ( 17 FDA reports)
OFF LABEL USE ( 17 FDA reports)
PERIODONTITIS ( 17 FDA reports)
PLATELET COUNT DECREASED ( 17 FDA reports)
SEBORRHOEIC KERATOSIS ( 17 FDA reports)
UNRESPONSIVE TO STIMULI ( 17 FDA reports)
VIRAL INFECTION ( 17 FDA reports)
ADHESION ( 16 FDA reports)
ANGIOPATHY ( 16 FDA reports)
BLOOD DISORDER ( 16 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 16 FDA reports)
FLATULENCE ( 16 FDA reports)
HYPERSOMNIA ( 16 FDA reports)
NIGHTMARE ( 16 FDA reports)
NON-CARDIAC CHEST PAIN ( 16 FDA reports)
PEPTIC ULCER ( 16 FDA reports)
PERIODONTAL DISEASE ( 16 FDA reports)
PLATELET COUNT INCREASED ( 16 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 16 FDA reports)
SCAR ( 16 FDA reports)
SKIN LACERATION ( 16 FDA reports)
STOMACH DISCOMFORT ( 16 FDA reports)
TENDONITIS ( 16 FDA reports)
VISUAL ACUITY REDUCED ( 16 FDA reports)
ABNORMAL DREAMS ( 15 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 15 FDA reports)
BREAST CANCER FEMALE ( 15 FDA reports)
CEREBRAL ISCHAEMIA ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
COSTOCHONDRITIS ( 15 FDA reports)
CYST ( 15 FDA reports)
DYSGEUSIA ( 15 FDA reports)
EPILEPSY ( 15 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 15 FDA reports)
FOOT DEFORMITY ( 15 FDA reports)
GASTRIC HAEMORRHAGE ( 15 FDA reports)
GASTRIC ULCER ( 15 FDA reports)
HAEMOPTYSIS ( 15 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 15 FDA reports)
HEPATIC ENZYME INCREASED ( 15 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 15 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 15 FDA reports)
HYPERTENSIVE CRISIS ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
INJECTION SITE PAIN ( 15 FDA reports)
LEFT VENTRICULAR FAILURE ( 15 FDA reports)
LYMPHADENOPATHY ( 15 FDA reports)
MENTAL IMPAIRMENT ( 15 FDA reports)
MYOCLONUS ( 15 FDA reports)
NASAL CONGESTION ( 15 FDA reports)
NOCTURIA ( 15 FDA reports)
OESOPHAGEAL DISORDER ( 15 FDA reports)
ORAL CANDIDIASIS ( 15 FDA reports)
PANIC DISORDER ( 15 FDA reports)
POOR QUALITY SLEEP ( 15 FDA reports)
PRESYNCOPE ( 15 FDA reports)
PULMONARY CONGESTION ( 15 FDA reports)
SEDATION ( 15 FDA reports)
SINUS CONGESTION ( 15 FDA reports)
SKIN DISCOLOURATION ( 15 FDA reports)
APHTHOUS STOMATITIS ( 14 FDA reports)
AZOTAEMIA ( 14 FDA reports)
BACTERIAL INFECTION ( 14 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
COLITIS ISCHAEMIC ( 14 FDA reports)
DERMATITIS CONTACT ( 14 FDA reports)
DEVICE FAILURE ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
DISCOMFORT ( 14 FDA reports)
DROOLING ( 14 FDA reports)
EATING DISORDER ( 14 FDA reports)
EPISTAXIS ( 14 FDA reports)
HYPOACUSIS ( 14 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 14 FDA reports)
LOOSE TOOTH ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 14 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
RESPIRATORY DEPRESSION ( 14 FDA reports)
STASIS DERMATITIS ( 14 FDA reports)
STRESS INCONTINENCE ( 14 FDA reports)
SUDDEN DEATH ( 14 FDA reports)
SURGERY ( 14 FDA reports)
ALCOHOLISM ( 13 FDA reports)
BREAST CALCIFICATIONS ( 13 FDA reports)
BUNION ( 13 FDA reports)
CARDIAC VALVE DISEASE ( 13 FDA reports)
CHOLESTASIS ( 13 FDA reports)
COLON CANCER ( 13 FDA reports)
DEMENTIA ( 13 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
ESSENTIAL HYPERTENSION ( 13 FDA reports)
EYE SWELLING ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FIBROADENOMA OF BREAST ( 13 FDA reports)
GOITRE ( 13 FDA reports)
HEAD INJURY ( 13 FDA reports)
HEARING IMPAIRED ( 13 FDA reports)
HEART INJURY ( 13 FDA reports)
HEMIPARESIS ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 13 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 13 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 13 FDA reports)
JOINT SPRAIN ( 13 FDA reports)
KYPHOSIS ( 13 FDA reports)
LABILE HYPERTENSION ( 13 FDA reports)
LIMB INJURY ( 13 FDA reports)
LIPIDS INCREASED ( 13 FDA reports)
METASTASES TO BONE ( 13 FDA reports)
MICTURITION URGENCY ( 13 FDA reports)
MUSCLE RIGIDITY ( 13 FDA reports)
MUSCULOSKELETAL DISORDER ( 13 FDA reports)
OESOPHAGEAL STENOSIS ( 13 FDA reports)
OSTEOSCLEROSIS ( 13 FDA reports)
PANCREATITIS ACUTE ( 13 FDA reports)
PARALYSIS ( 13 FDA reports)
PHLEBITIS ( 13 FDA reports)
POLYNEUROPATHY ( 13 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 13 FDA reports)
PROSTATE CANCER ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
RESPIRATORY TRACT INFECTION ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
UNEVALUABLE EVENT ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
ACCIDENT AT WORK ( 12 FDA reports)
ACUTE PULMONARY OEDEMA ( 12 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 12 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 12 FDA reports)
AORTIC ANEURYSM ( 12 FDA reports)
AORTIC STENOSIS ( 12 FDA reports)
ATAXIA ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 12 FDA reports)
BILIARY NEOPLASM ( 12 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 12 FDA reports)
BLOOD SODIUM DECREASED ( 12 FDA reports)
BODY TEMPERATURE DECREASED ( 12 FDA reports)
BRAIN OEDEMA ( 12 FDA reports)
BRONCHIECTASIS ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
DECUBITUS ULCER ( 12 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 12 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 12 FDA reports)
FEBRILE NEUTROPENIA ( 12 FDA reports)
FRACTURE NONUNION ( 12 FDA reports)
INFLUENZA LIKE ILLNESS ( 12 FDA reports)
INTENTIONAL SELF-INJURY ( 12 FDA reports)
LOCALISED INFECTION ( 12 FDA reports)
MASTICATION DISORDER ( 12 FDA reports)
MUCOSAL INFLAMMATION ( 12 FDA reports)
PARAESTHESIA ORAL ( 12 FDA reports)
PLEURITIC PAIN ( 12 FDA reports)
POLYTRAUMATISM ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
RESPIRATORY DISTRESS ( 12 FDA reports)
SEASONAL ALLERGY ( 12 FDA reports)
SKIN PAPILLOMA ( 12 FDA reports)
SUBCUTANEOUS ABSCESS ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
VAGINITIS BACTERIAL ( 12 FDA reports)
WITHDRAWAL SYNDROME ( 12 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 11 FDA reports)
ADJUSTMENT DISORDER ( 11 FDA reports)
ASPIRATION ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 11 FDA reports)
BREAST HAEMATOMA ( 11 FDA reports)
CEREBRAL ATROPHY ( 11 FDA reports)
CEREBROVASCULAR DISORDER ( 11 FDA reports)
CERVICAL SPINAL STENOSIS ( 11 FDA reports)
CHOKING SENSATION ( 11 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 11 FDA reports)
DENTAL FISTULA ( 11 FDA reports)
DERMATITIS ( 11 FDA reports)
DIABETIC COMPLICATION ( 11 FDA reports)
DIFFICULTY IN WALKING ( 11 FDA reports)
DIVERTICULUM INTESTINAL ( 11 FDA reports)
DRUG EFFECT DECREASED ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
FAECES DISCOLOURED ( 11 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 11 FDA reports)
FUNGAL INFECTION ( 11 FDA reports)
HERNIA ( 11 FDA reports)
HYPERCOAGULATION ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 11 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
LYMPHOEDEMA ( 11 FDA reports)
MOVEMENT DISORDER ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
ORAL DISORDER ( 11 FDA reports)
OSTEITIS DEFORMANS ( 11 FDA reports)
PERIPHERAL ISCHAEMIA ( 11 FDA reports)
PIGMENTATION LIP ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
RESPIRATORY RATE INCREASED ( 11 FDA reports)
RHINITIS ( 11 FDA reports)
SKIN DISORDER ( 11 FDA reports)
TOOTH INJURY ( 11 FDA reports)
VENTRICULAR HYPOKINESIA ( 11 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 11 FDA reports)
ACCIDENTAL DEATH ( 10 FDA reports)
ACNE ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 10 FDA reports)
ADRENAL ADENOMA ( 10 FDA reports)
AGEUSIA ( 10 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
ANHEDONIA ( 10 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 10 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 10 FDA reports)
BONE LESION ( 10 FDA reports)
BRUXISM ( 10 FDA reports)
CHRONIC SINUSITIS ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 10 FDA reports)
DISEASE RECURRENCE ( 10 FDA reports)
DIVERTICULITIS ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
ECONOMIC PROBLEM ( 10 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
FLANK PAIN ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INCREASED TENDENCY TO BRUISE ( 10 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 10 FDA reports)
INFUSION RELATED REACTION ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
JAW FRACTURE ( 10 FDA reports)
LEFT ATRIAL DILATATION ( 10 FDA reports)
LIGAMENT SPRAIN ( 10 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 10 FDA reports)
LOW TURNOVER OSTEOPATHY ( 10 FDA reports)
METASTASES TO LUNG ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 10 FDA reports)
MUSCLE TIGHTNESS ( 10 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 10 FDA reports)
MYELODYSPLASTIC SYNDROME ( 10 FDA reports)
NEUROGENIC BLADDER ( 10 FDA reports)
NEUROPATHY ( 10 FDA reports)
OCCULT BLOOD POSITIVE ( 10 FDA reports)
ORAL TORUS ( 10 FDA reports)
OSTEITIS ( 10 FDA reports)
OTITIS EXTERNA ( 10 FDA reports)
PARANOIA ( 10 FDA reports)
PATHOLOGICAL FRACTURE ( 10 FDA reports)
POLYP ( 10 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 10 FDA reports)
PULMONARY GRANULOMA ( 10 FDA reports)
PYELONEPHRITIS ( 10 FDA reports)
SENSORY DISTURBANCE ( 10 FDA reports)
SINUS DISORDER ( 10 FDA reports)
SKIN CANCER ( 10 FDA reports)
SKIN EXFOLIATION ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
SNORING ( 10 FDA reports)
THROAT TIGHTNESS ( 10 FDA reports)
TOE AMPUTATION ( 10 FDA reports)
UMBILICAL HERNIA ( 10 FDA reports)
WOUND ( 10 FDA reports)
WOUND DEHISCENCE ( 10 FDA reports)
ALCOHOL USE ( 9 FDA reports)
ANAEMIA POSTOPERATIVE ( 9 FDA reports)
APNOEA ( 9 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
ARTERIAL THROMBOSIS ( 9 FDA reports)
ASCITES ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
BONE DEBRIDEMENT ( 9 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 9 FDA reports)
CAROTID BRUIT ( 9 FDA reports)
CATATONIA ( 9 FDA reports)
CHOLECYSTITIS CHRONIC ( 9 FDA reports)
CYSTITIS INTERSTITIAL ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DIABETIC RETINOPATHY ( 9 FDA reports)
DILATATION ATRIAL ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
EMBOLISM ( 9 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 9 FDA reports)
FEEDING DISORDER ( 9 FDA reports)
FINGER DEFORMITY ( 9 FDA reports)
FRACTURE DELAYED UNION ( 9 FDA reports)
GENERALISED OEDEMA ( 9 FDA reports)
GINGIVAL BLEEDING ( 9 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 9 FDA reports)
HELICOBACTER INFECTION ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HYPERTONIC BLADDER ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
INJECTION SITE PRURITUS ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
LUNG CONSOLIDATION ( 9 FDA reports)
MELANOCYTIC NAEVUS ( 9 FDA reports)
METRORRHAGIA ( 9 FDA reports)
MITRAL VALVE PROLAPSE ( 9 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 9 FDA reports)
PERFORMANCE STATUS DECREASED ( 9 FDA reports)
PERONEAL NERVE PALSY ( 9 FDA reports)
PROTEINURIA ( 9 FDA reports)
PRURITUS GENERALISED ( 9 FDA reports)
SPLENOMEGALY ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
TENDERNESS ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
VARICOSE VEIN ( 9 FDA reports)
ABORTION SPONTANEOUS ( 8 FDA reports)
ABSCESS DRAINAGE ( 8 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 8 FDA reports)
ACUTE PRERENAL FAILURE ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
AMAUROSIS FUGAX ( 8 FDA reports)
ANKLE FRACTURE ( 8 FDA reports)
ATROPHY ( 8 FDA reports)
BONE MARROW FAILURE ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
DERMATITIS ALLERGIC ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIABETES INSIPIDUS ( 8 FDA reports)
DIABETIC NEPHROPATHY ( 8 FDA reports)
DIABETIC RETINAL OEDEMA ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
EMOTIONAL DISORDER ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
EOSINOPHILIA ( 8 FDA reports)
EPICONDYLITIS ( 8 FDA reports)
EYE INJURY ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
GINGIVAL SWELLING ( 8 FDA reports)
GLOSSODYNIA ( 8 FDA reports)
GRIEF REACTION ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
HELICOBACTER GASTRITIS ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HYPOPARATHYROIDISM ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
HYSTERECTOMY ( 8 FDA reports)
INNER EAR DISORDER ( 8 FDA reports)
LARYNGITIS ALLERGIC ( 8 FDA reports)
LIVER TENDERNESS ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
MALIGNANT MELANOMA ( 8 FDA reports)
MAMMOGRAM ABNORMAL ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
MITRAL VALVE DISEASE ( 8 FDA reports)
MOOD ALTERED ( 8 FDA reports)
NERVE INJURY ( 8 FDA reports)
ORTHOPNOEA ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
PNEUMONIA VIRAL ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 8 FDA reports)
RESORPTION BONE INCREASED ( 8 FDA reports)
SECRETION DISCHARGE ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
SICK SINUS SYNDROME ( 8 FDA reports)
TEARFULNESS ( 8 FDA reports)
THIRST ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 8 FDA reports)
TOE DEFORMITY ( 8 FDA reports)
TRIGONITIS ( 8 FDA reports)
TROPONIN INCREASED ( 8 FDA reports)
VASCULITIS ( 8 FDA reports)
ABDOMINAL HERNIA ( 7 FDA reports)
ABSCESS JAW ( 7 FDA reports)
ADRENAL INSUFFICIENCY ( 7 FDA reports)
ADRENAL MASS ( 7 FDA reports)
BACTERIURIA ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CALCULUS URETERIC ( 7 FDA reports)
CAROTID ARTERY DISEASE ( 7 FDA reports)
CEREBELLAR INFARCTION ( 7 FDA reports)
CERVICOBRACHIAL SYNDROME ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
CHEST X-RAY ABNORMAL ( 7 FDA reports)
CHOLECYSTECTOMY ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
CUBITAL TUNNEL SYNDROME ( 7 FDA reports)
DENTURE WEARER ( 7 FDA reports)
DERMAL CYST ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
DYSLIPIDAEMIA ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ENDODONTIC PROCEDURE ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
EXERCISE LACK OF ( 7 FDA reports)
FIBROMA ( 7 FDA reports)
GALLBLADDER POLYP ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GASTROINTESTINAL PAIN ( 7 FDA reports)
GOUT ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
GYNAECOMASTIA ( 7 FDA reports)
HAEMORRHAGIC ANAEMIA ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HIP ARTHROPLASTY ( 7 FDA reports)
HYPOAESTHESIA ORAL ( 7 FDA reports)
HYPOKINESIA ( 7 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 7 FDA reports)
INFARCTION ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 7 FDA reports)
INTESTINAL POLYP ( 7 FDA reports)
INTRACRANIAL ANEURYSM ( 7 FDA reports)
JOINT STIFFNESS ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LARGE INTESTINAL ULCER ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LEG AMPUTATION ( 7 FDA reports)
MENOPAUSAL SYMPTOMS ( 7 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 7 FDA reports)
METASTASES TO LIVER ( 7 FDA reports)
MUSCLE SPASTICITY ( 7 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 7 FDA reports)
MYOPATHY ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
NEURITIS ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
OEDEMA MOUTH ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 7 FDA reports)
PERICARDITIS ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 7 FDA reports)
RESPIRATORY ACIDOSIS ( 7 FDA reports)
RESPIRATORY RATE DECREASED ( 7 FDA reports)
SARCOIDOSIS ( 7 FDA reports)
SENSORY LOSS ( 7 FDA reports)
SKIN IRRITATION ( 7 FDA reports)
SPONDYLOSIS ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
TENSION ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
THROMBOPHLEBITIS ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TONSILLAR DISORDER ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
VASCULAR PSEUDOANEURYSM ( 7 FDA reports)
VULVAL DISORDER ( 7 FDA reports)
ABDOMINAL BRUIT ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ALVEOLAR OSTEITIS ( 6 FDA reports)
ALVEOLOPLASTY ( 6 FDA reports)
AMYOTROPHY ( 6 FDA reports)
APPENDIX DISORDER ( 6 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 6 FDA reports)
ATRIAL TACHYCARDIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BREAST RECONSTRUCTION ( 6 FDA reports)
CALCINOSIS ( 6 FDA reports)
CARDIAC FLUTTER ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
COLITIS ULCERATIVE ( 6 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
CONVERSION DISORDER ( 6 FDA reports)
CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
DENTAL NECROSIS ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DRESSLER'S SYNDROME ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FAILURE OF IMPLANT ( 6 FDA reports)
FAMILY STRESS ( 6 FDA reports)
FEEDING TUBE COMPLICATION ( 6 FDA reports)
FEMORAL NECK FRACTURE ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
GLOMUS TUMOUR ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
HAEMOPHILUS INFECTION ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOVOLAEMIA ( 6 FDA reports)
ILIAC ARTERY THROMBOSIS ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INJECTION SITE SWELLING ( 6 FDA reports)
KIDNEY MALROTATION ( 6 FDA reports)
KLEBSIELLA TEST POSITIVE ( 6 FDA reports)
LERICHE SYNDROME ( 6 FDA reports)
LIBIDO DECREASED ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 6 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
MONOCYTOSIS ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PAPILLOMA ( 6 FDA reports)
PCO2 DECREASED ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POISONING DELIBERATE ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POSTOPERATIVE INFECTION ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 6 FDA reports)
PROTEIN S DEFICIENCY ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PULMONARY MASS ( 6 FDA reports)
PULSE ABNORMAL ( 6 FDA reports)
QUADRIPLEGIA ( 6 FDA reports)
RADICULITIS ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
RETCHING ( 6 FDA reports)
RETROGRADE EJACULATION ( 6 FDA reports)
SEBORRHOEA ( 6 FDA reports)
SEXUAL DYSFUNCTION ( 6 FDA reports)
SICCA SYNDROME ( 6 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
SPINAL CORD COMPRESSION ( 6 FDA reports)
SPLENIC RUPTURE ( 6 FDA reports)
SPONDYLITIC MYELOPATHY ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
SWEAT GLAND INFECTION ( 6 FDA reports)
SYNOVIAL CYST ( 6 FDA reports)
TONGUE PARALYSIS ( 6 FDA reports)
TRISMUS ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
URETERIC OBSTRUCTION ( 6 FDA reports)
URETHRAL PROLAPSE ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
UTERINE DISORDER ( 6 FDA reports)
UTERINE POLYP ( 6 FDA reports)
VAGINAL LEUKOPLAKIA ( 6 FDA reports)
VAGINAL ULCERATION ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
WOUND INFECTION ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AKINESIA ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BONE OPERATION ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COCCYDYNIA ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DERMATOMYOSITIS ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DRUG ABUSE ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ESSENTIAL TREMOR ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEMORAL ARTERY OCCLUSION ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GANGRENE ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GINGIVAL RECESSION ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMORRHAGIC STROKE ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
ILEAL STENOSIS ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MENSTRUAL DISORDER ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NARCOTIC INTOXICATION ( 5 FDA reports)
NASAL ULCER ( 5 FDA reports)
NEOPLASM ( 5 FDA reports)
ORAL CAVITY FISTULA ( 5 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 5 FDA reports)
PERIARTHRITIS ( 5 FDA reports)
POISONING ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
RALES ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STEM CELL TRANSPLANT ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
SYNOVITIS ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
THALAMIC SYNDROME ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TONGUE INJURY ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TRIGGER FINGER ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
VAGINAL INFECTION ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 5 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANAL STENOSIS ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANURIA ( 4 FDA reports)
APHONIA ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARACHNOID CYST ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BASE EXCESS NEGATIVE ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BODY MASS INDEX DECREASED ( 4 FDA reports)
BONE MARROW NECROSIS ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CERVICAL SPINE FLATTENING ( 4 FDA reports)
COCCIDIOIDOMYCOSIS ( 4 FDA reports)
COLLAPSE OF LUNG ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
DYSTROPHIC CALCIFICATION ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
FROSTBITE ( 4 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT DYSFUNCTION ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 4 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFECTED VARICOSE VEIN ( 4 FDA reports)
INGROWN HAIR ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
JAW CYST ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LIP PAIN ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPH GLAND INFECTION ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MANIA ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MENOPAUSE ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MERALGIA PARAESTHETICA ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NIGHT CRAMPS ( 4 FDA reports)
NODULE ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
ORAL NEOPLASM ( 4 FDA reports)
OSTEOCHONDROSIS ( 4 FDA reports)
OSTEORADIONECROSIS ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PAPILLARY THYROID CANCER ( 4 FDA reports)
PARAGANGLION NEOPLASM ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 4 FDA reports)
PERONEAL NERVE INJURY ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PRESBYOPIA ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PSEUDOPOLYP ( 4 FDA reports)
PULMONARY CALCIFICATION ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
RADICULITIS LUMBOSACRAL ( 4 FDA reports)
RADIOTHERAPY ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RENAL HAEMATOMA ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
SCAB ( 4 FDA reports)
SCRATCH ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SENSATION OF HEAVINESS ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SKIN TIGHTNESS ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPUTUM PURULENT ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STATUS ASTHMATICUS ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TENOSYNOVITIS STENOSANS ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
VAGINITIS ( 4 FDA reports)
VENTRICULAR FLUTTER ( 4 FDA reports)
VITREOUS FLOATERS ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BILIARY CYST ( 3 FDA reports)
BLADDER CONSTRICTION ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 3 FDA reports)
BONE FORMATION DECREASED ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRAIN OPERATION ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
BREAST DISORDER ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST OPERATION ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRONCHIAL HYPERACTIVITY ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CAROTID SINUS SYNDROME ( 3 FDA reports)
CARTILAGE INJURY ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EXTRAVASATION ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GENERAL SYMPTOM ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HAND DEFORMITY ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HILAR LYMPHADENOPATHY ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERSPLENISM ACQUIRED ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
ILEOSTOMY ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 3 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 3 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MYELITIS TRANSVERSE ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEUROPATHIC PAIN ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PELVIC ADHESIONS ( 3 FDA reports)
PERICARDIAL DISEASE ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLEURAL ADHESION ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTMENOPAUSE ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PSEUDOPOLYPOSIS ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SALPINGITIS ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSATION OF PRESSURE IN EAR ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SOPOR ( 3 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
TABLET ISSUE ( 3 FDA reports)
TEETH BRITTLE ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
URETHRAL CARUNCLE ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VOCAL CORD PARESIS ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ZINC DEFICIENCY ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADMINISTRATION SITE PAIN ( 2 FDA reports)
ADRENALITIS ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
CALCIUM DEFICIENCY ( 2 FDA reports)
CALCIUM METABOLISM DISORDER ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL NEURITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FALLOPIAN TUBE DISORDER ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
GROWTH HORMONE DEFICIENCY ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HELMINTHIC INFECTION ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
IDIOPATHIC URTICARIA ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIFE EXPECTANCY SHORTENED ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOARTHROPATHY ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PAPILLARY TUMOUR OF RENAL PELVIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ADVANCED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDOANGINA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SHARED PSYCHOTIC DISORDER ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOCIAL FEAR ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TOOTH IMPACTED ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRIGEMINAL NERVE DISORDER ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERBAL ABUSE ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPYRESIS ( 1 FDA reports)
ANXIOUS PARENT ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BABINSKI REFLEX TEST ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY BLADDER ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL VERTEBRA INJURY ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX INFLAMMATION ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL TRACHEOMALACIA ( 1 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVAL VASCULAR DISORDER ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEXTROCARDIA ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIHYDROTESTOSTERONE LEVEL ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSKINESIA NEONATAL ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPIGLOTTIS ULCER ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FIBRIN D DIMER NORMAL ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL MALNUTRITION ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HETEROTAXIA ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA TEETH ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHYROIDISM POSTOPERATIVE ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL PICKING ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OVARIAN HAEMATOMA ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SEROCONVERSION TEST POSITIVE ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS TARSI SYNDROME ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUNCT SYNDROME ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBIN TIME ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYMOL TURBIDITY TEST INCREASED ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VICTIM OF CHILD ABUSE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOCAL CORD POLYPECTOMY ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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