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

HEADACHE ( 532 FDA reports)
CEREBROVASCULAR ACCIDENT ( 466 FDA reports)
NAUSEA ( 408 FDA reports)
DIZZINESS ( 303 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 267 FDA reports)
VOMITING ( 254 FDA reports)
ASTHENIA ( 240 FDA reports)
DIARRHOEA ( 234 FDA reports)
FATIGUE ( 182 FDA reports)
PAIN ( 176 FDA reports)
FALL ( 170 FDA reports)
PAIN IN EXTREMITY ( 149 FDA reports)
DYSPNOEA ( 144 FDA reports)
ANAEMIA ( 134 FDA reports)
CHEST PAIN ( 130 FDA reports)
RENAL FAILURE ACUTE ( 124 FDA reports)
OEDEMA PERIPHERAL ( 122 FDA reports)
ANXIETY ( 121 FDA reports)
DEPRESSION ( 118 FDA reports)
ABDOMINAL PAIN UPPER ( 113 FDA reports)
HYPOAESTHESIA ( 112 FDA reports)
HYPERTENSION ( 110 FDA reports)
HYPOTENSION ( 105 FDA reports)
MALAISE ( 104 FDA reports)
CONFUSIONAL STATE ( 103 FDA reports)
URINARY TRACT INFECTION ( 99 FDA reports)
BACK PAIN ( 98 FDA reports)
RENAL FAILURE ( 98 FDA reports)
PNEUMONIA ( 96 FDA reports)
WEIGHT DECREASED ( 95 FDA reports)
ARTHRALGIA ( 94 FDA reports)
GAIT DISTURBANCE ( 94 FDA reports)
MYOCARDIAL INFARCTION ( 89 FDA reports)
PYREXIA ( 89 FDA reports)
DEHYDRATION ( 85 FDA reports)
COUGH ( 83 FDA reports)
DRUG INEFFECTIVE ( 83 FDA reports)
ATRIAL FIBRILLATION ( 79 FDA reports)
MYALGIA ( 79 FDA reports)
CONVULSION ( 77 FDA reports)
MUSCULAR WEAKNESS ( 77 FDA reports)
DYSPHAGIA ( 76 FDA reports)
LOSS OF CONSCIOUSNESS ( 76 FDA reports)
PRURITUS ( 73 FDA reports)
CEREBRAL HAEMORRHAGE ( 72 FDA reports)
CONSTIPATION ( 72 FDA reports)
FEELING ABNORMAL ( 72 FDA reports)
SOMNOLENCE ( 72 FDA reports)
INSOMNIA ( 71 FDA reports)
ABDOMINAL PAIN ( 68 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 68 FDA reports)
DECREASED APPETITE ( 67 FDA reports)
RASH ( 67 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 66 FDA reports)
BLOOD PRESSURE INCREASED ( 65 FDA reports)
HAEMORRHAGE ( 65 FDA reports)
DEATH ( 62 FDA reports)
DYSPEPSIA ( 60 FDA reports)
BLOOD GLUCOSE INCREASED ( 59 FDA reports)
INJURY ( 59 FDA reports)
SYNCOPE ( 59 FDA reports)
ABDOMINAL DISCOMFORT ( 58 FDA reports)
CEREBRAL INFARCTION ( 57 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 57 FDA reports)
VISION BLURRED ( 57 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 56 FDA reports)
HEMIPARESIS ( 56 FDA reports)
RESPIRATORY FAILURE ( 55 FDA reports)
CARDIAC DISORDER ( 54 FDA reports)
CONTUSION ( 54 FDA reports)
MEMORY IMPAIRMENT ( 54 FDA reports)
MUSCLE SPASMS ( 54 FDA reports)
NEUROPATHY PERIPHERAL ( 54 FDA reports)
FLUSHING ( 53 FDA reports)
GASTRITIS ( 53 FDA reports)
HAEMOGLOBIN DECREASED ( 53 FDA reports)
PARAESTHESIA ( 53 FDA reports)
PALPITATIONS ( 52 FDA reports)
DYSARTHRIA ( 50 FDA reports)
RENAL FAILURE CHRONIC ( 50 FDA reports)
SINUSITIS ( 50 FDA reports)
EPISTAXIS ( 49 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 48 FDA reports)
HYPERHIDROSIS ( 48 FDA reports)
THROMBOCYTOPENIA ( 46 FDA reports)
TREMOR ( 45 FDA reports)
BALANCE DISORDER ( 44 FDA reports)
DYSGEUSIA ( 44 FDA reports)
CATARACT ( 43 FDA reports)
SEPSIS ( 43 FDA reports)
APHASIA ( 42 FDA reports)
CORONARY ARTERY DISEASE ( 41 FDA reports)
DEMENTIA ( 41 FDA reports)
ABDOMINAL DISTENSION ( 40 FDA reports)
CONDITION AGGRAVATED ( 40 FDA reports)
DIABETES MELLITUS ( 40 FDA reports)
OFF LABEL USE ( 40 FDA reports)
SPEECH DISORDER ( 40 FDA reports)
BLOOD PRESSURE DECREASED ( 39 FDA reports)
NECK PAIN ( 39 FDA reports)
RETCHING ( 39 FDA reports)
ARTERIOSCLEROSIS ( 38 FDA reports)
ATELECTASIS ( 38 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 38 FDA reports)
OSTEONECROSIS OF JAW ( 38 FDA reports)
WEIGHT INCREASED ( 38 FDA reports)
DIVERTICULUM ( 37 FDA reports)
DUODENAL ULCER ( 37 FDA reports)
DYSPNOEA EXERTIONAL ( 37 FDA reports)
EMOTIONAL DISTRESS ( 37 FDA reports)
CHEST DISCOMFORT ( 36 FDA reports)
DEEP VEIN THROMBOSIS ( 36 FDA reports)
OSTEOPENIA ( 36 FDA reports)
RECTAL HAEMORRHAGE ( 36 FDA reports)
RIB FRACTURE ( 36 FDA reports)
ANHEDONIA ( 35 FDA reports)
URINARY INCONTINENCE ( 35 FDA reports)
ABASIA ( 33 FDA reports)
BLOOD CREATININE INCREASED ( 33 FDA reports)
HYPERSENSITIVITY ( 33 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 32 FDA reports)
CARDIAC ARREST ( 32 FDA reports)
HYPERLIPIDAEMIA ( 32 FDA reports)
LUNG NEOPLASM MALIGNANT ( 32 FDA reports)
VERTIGO ( 32 FDA reports)
CAROTID ARTERY STENOSIS ( 31 FDA reports)
COLONIC POLYP ( 31 FDA reports)
DYSPHONIA ( 31 FDA reports)
ERYTHEMA ( 31 FDA reports)
ISCHAEMIC STROKE ( 31 FDA reports)
MENTAL STATUS CHANGES ( 31 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 31 FDA reports)
OVERDOSE ( 31 FDA reports)
TOOTHACHE ( 31 FDA reports)
BLINDNESS ( 30 FDA reports)
NIGHT SWEATS ( 30 FDA reports)
TOOTH DISORDER ( 30 FDA reports)
AGEUSIA ( 29 FDA reports)
BRONCHITIS ( 29 FDA reports)
HAEMORRHOIDS ( 29 FDA reports)
INFECTION ( 29 FDA reports)
LETHARGY ( 29 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 29 FDA reports)
URINARY RETENTION ( 29 FDA reports)
CYST ( 28 FDA reports)
DRY MOUTH ( 28 FDA reports)
HAEMATURIA ( 28 FDA reports)
HALLUCINATION ( 28 FDA reports)
HEAD INJURY ( 28 FDA reports)
HERPES ZOSTER ( 28 FDA reports)
HYPOGLYCAEMIA ( 28 FDA reports)
NEPHROLITHIASIS ( 28 FDA reports)
RENAL CYST ( 28 FDA reports)
AMNESIA ( 27 FDA reports)
ANOREXIA ( 27 FDA reports)
CHILLS ( 27 FDA reports)
DISORIENTATION ( 27 FDA reports)
EMPHYSEMA ( 27 FDA reports)
FOOT FRACTURE ( 27 FDA reports)
GASTRITIS EROSIVE ( 27 FDA reports)
HAEMATOMA ( 27 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 27 FDA reports)
PLATELET COUNT DECREASED ( 27 FDA reports)
THROMBOSIS ( 27 FDA reports)
DRUG INTERACTION ( 26 FDA reports)
HIP FRACTURE ( 26 FDA reports)
ROTATOR CUFF SYNDROME ( 26 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 26 FDA reports)
VISUAL IMPAIRMENT ( 26 FDA reports)
WHEEZING ( 26 FDA reports)
BONE PAIN ( 25 FDA reports)
CARDIO-RESPIRATORY ARREST ( 25 FDA reports)
CARDIOMEGALY ( 25 FDA reports)
CAROTID ARTERY OCCLUSION ( 25 FDA reports)
FAECAL INCONTINENCE ( 25 FDA reports)
HYPOKALAEMIA ( 25 FDA reports)
INCORRECT DOSE ADMINISTERED ( 25 FDA reports)
MITRAL VALVE INCOMPETENCE ( 25 FDA reports)
ORTHOSTATIC HYPOTENSION ( 25 FDA reports)
OSTEOARTHRITIS ( 25 FDA reports)
SUBDURAL HAEMATOMA ( 25 FDA reports)
HEART RATE INCREASED ( 24 FDA reports)
HOT FLUSH ( 24 FDA reports)
HYPERKALAEMIA ( 24 FDA reports)
INFLUENZA LIKE ILLNESS ( 24 FDA reports)
IRRITABLE BOWEL SYNDROME ( 24 FDA reports)
JOINT SWELLING ( 24 FDA reports)
MIGRAINE ( 24 FDA reports)
NOCTURIA ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
PLEURAL EFFUSION ( 24 FDA reports)
PULMONARY FIBROSIS ( 24 FDA reports)
SKIN TIGHTNESS ( 24 FDA reports)
TINNITUS ( 24 FDA reports)
UNRESPONSIVE TO STIMULI ( 24 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
ALOPECIA ( 23 FDA reports)
CEREBRAL ATROPHY ( 23 FDA reports)
COMA ( 23 FDA reports)
HAEMATEMESIS ( 23 FDA reports)
HYPERCALCAEMIA ( 23 FDA reports)
INFLUENZA ( 23 FDA reports)
METABOLIC ACIDOSIS ( 23 FDA reports)
OESOPHAGITIS ( 23 FDA reports)
RASH GENERALISED ( 23 FDA reports)
SINUS BRADYCARDIA ( 23 FDA reports)
SPINAL OSTEOARTHRITIS ( 23 FDA reports)
TACHYCARDIA ( 23 FDA reports)
AGITATION ( 22 FDA reports)
BURNING SENSATION ( 22 FDA reports)
ECONOMIC PROBLEM ( 22 FDA reports)
FOOT DEFORMITY ( 22 FDA reports)
GASTROINTESTINAL DISORDER ( 22 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 22 FDA reports)
HEART RATE IRREGULAR ( 22 FDA reports)
LACERATION ( 22 FDA reports)
PULMONARY OEDEMA ( 22 FDA reports)
TIBIA FRACTURE ( 22 FDA reports)
ADVERSE EVENT ( 21 FDA reports)
ANGINA PECTORIS ( 21 FDA reports)
ANGINA UNSTABLE ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
CEREBELLAR INFARCTION ( 21 FDA reports)
CEREBROVASCULAR DISORDER ( 21 FDA reports)
NASOPHARYNGITIS ( 21 FDA reports)
PANCREATITIS ( 21 FDA reports)
SKIN DISCOLOURATION ( 21 FDA reports)
URTICARIA ( 21 FDA reports)
BLOOD CREATININE DECREASED ( 20 FDA reports)
DRUG INTOLERANCE ( 20 FDA reports)
DYSURIA ( 20 FDA reports)
FLATULENCE ( 20 FDA reports)
GASTRIC ULCER ( 20 FDA reports)
HYPONATRAEMIA ( 20 FDA reports)
HYPOXIA ( 20 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 20 FDA reports)
LIP SWELLING ( 20 FDA reports)
PNEUMOTHORAX ( 20 FDA reports)
RENAL DISORDER ( 20 FDA reports)
RHINORRHOEA ( 20 FDA reports)
TOOTH FRACTURE ( 20 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 20 FDA reports)
ACUTE RESPIRATORY FAILURE ( 19 FDA reports)
HAEMATOCRIT DECREASED ( 19 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 19 FDA reports)
LIVER DISORDER ( 19 FDA reports)
MENOPAUSE ( 19 FDA reports)
PAIN IN JAW ( 19 FDA reports)
SCAR ( 19 FDA reports)
SKIN HYPERTROPHY ( 19 FDA reports)
STOMACH DISCOMFORT ( 19 FDA reports)
ABSCESS ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
B-CELL LYMPHOMA ( 18 FDA reports)
BACTERIAL DISEASE CARRIER ( 18 FDA reports)
BLOOD URINE PRESENT ( 18 FDA reports)
CARDIAC MURMUR ( 18 FDA reports)
DRUG HYPERSENSITIVITY ( 18 FDA reports)
FIBULA FRACTURE ( 18 FDA reports)
GASTRIC DISORDER ( 18 FDA reports)
HYPERGLYCAEMIA ( 18 FDA reports)
JOINT STIFFNESS ( 18 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 18 FDA reports)
LIP DISCOLOURATION ( 18 FDA reports)
MACULAR DEGENERATION ( 18 FDA reports)
NERVOUS SYSTEM DISORDER ( 18 FDA reports)
OCCULT BLOOD POSITIVE ( 18 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
SENSATION OF HEAVINESS ( 18 FDA reports)
TENDERNESS ( 18 FDA reports)
AORTIC VALVE INCOMPETENCE ( 17 FDA reports)
ARTHRITIS ( 17 FDA reports)
BLOOD SODIUM DECREASED ( 17 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
BRONCHOPLEURAL FISTULA ( 17 FDA reports)
EMPYEMA ( 17 FDA reports)
FEBRILE NEUTROPENIA ( 17 FDA reports)
HYDROPNEUMOTHORAX ( 17 FDA reports)
HYPERCHOLESTEROLAEMIA ( 17 FDA reports)
IMPAIRED HEALING ( 17 FDA reports)
NEOPLASM MALIGNANT ( 17 FDA reports)
ONYCHOMYCOSIS ( 17 FDA reports)
PRURITUS GENERALISED ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
SURGERY ( 17 FDA reports)
AORTIC ANEURYSM ( 16 FDA reports)
ATRIAL FLUTTER ( 16 FDA reports)
CELLULITIS ( 16 FDA reports)
CERVICAL SPINAL STENOSIS ( 16 FDA reports)
CYSTITIS ( 16 FDA reports)
EYE DISCHARGE ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
INJECTION SITE PAIN ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 16 FDA reports)
LUNG HYPERINFLATION ( 16 FDA reports)
MASTICATION DISORDER ( 16 FDA reports)
NASAL CONGESTION ( 16 FDA reports)
OSTEORADIONECROSIS ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
PRESYNCOPE ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
SUICIDE ATTEMPT ( 16 FDA reports)
SWELLING FACE ( 16 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 16 FDA reports)
UNEVALUABLE EVENT ( 16 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 16 FDA reports)
BLOOD SODIUM INCREASED ( 15 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 15 FDA reports)
COGNITIVE DISORDER ( 15 FDA reports)
DECREASED INTEREST ( 15 FDA reports)
DRUG DOSE OMISSION ( 15 FDA reports)
HEART RATE DECREASED ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
HYPOKINESIA ( 15 FDA reports)
KYPHOSIS ( 15 FDA reports)
LIVER INJURY ( 15 FDA reports)
LUNG INFECTION ( 15 FDA reports)
MOBILITY DECREASED ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 15 FDA reports)
OSTEONECROSIS ( 15 FDA reports)
RHINITIS ( 15 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 15 FDA reports)
THROAT IRRITATION ( 15 FDA reports)
VISUAL ACUITY REDUCED ( 15 FDA reports)
WALKING AID USER ( 15 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 15 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 14 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 14 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
BEDRIDDEN ( 14 FDA reports)
BLOOD GLUCOSE DECREASED ( 14 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 14 FDA reports)
BRADYCARDIA ( 14 FDA reports)
CHOLELITHIASIS ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 14 FDA reports)
ENCEPHALOPATHY ( 14 FDA reports)
EYE HAEMORRHAGE ( 14 FDA reports)
FEELING COLD ( 14 FDA reports)
LACUNAR INFARCTION ( 14 FDA reports)
LUNG DISORDER ( 14 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 14 FDA reports)
OEDEMA ( 14 FDA reports)
OROPHARYNGEAL PAIN ( 14 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 14 FDA reports)
PLATELET DISORDER ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
SKIN BURNING SENSATION ( 14 FDA reports)
SLEEP DISORDER ( 14 FDA reports)
TOOTH EXTRACTION ( 14 FDA reports)
TOOTH INFECTION ( 14 FDA reports)
ACUTE PULMONARY OEDEMA ( 13 FDA reports)
ADVERSE DRUG REACTION ( 13 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 13 FDA reports)
BACTERIAL INFECTION ( 13 FDA reports)
BLINDNESS UNILATERAL ( 13 FDA reports)
BONE DISORDER ( 13 FDA reports)
BONE LESION ( 13 FDA reports)
CANDIDIASIS ( 13 FDA reports)
COMPRESSION FRACTURE ( 13 FDA reports)
CORONARY ARTERY OCCLUSION ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
DIVERTICULUM INTESTINAL ( 13 FDA reports)
ERECTILE DYSFUNCTION ( 13 FDA reports)
FIBROMYALGIA ( 13 FDA reports)
HAEMATOCHEZIA ( 13 FDA reports)
HAEMODIALYSIS ( 13 FDA reports)
HEMIPLEGIA ( 13 FDA reports)
HYPOAESTHESIA ORAL ( 13 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 13 FDA reports)
LACRIMATION INCREASED ( 13 FDA reports)
LEUKOCYTOSIS ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
PNEUMONIA ASPIRATION ( 13 FDA reports)
POSTOPERATIVE INFECTION ( 13 FDA reports)
PRODUCT QUALITY ISSUE ( 13 FDA reports)
RASH MACULAR ( 13 FDA reports)
RESTLESS LEGS SYNDROME ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
SWOLLEN TONGUE ( 13 FDA reports)
VENTRICULAR HYPERTROPHY ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 12 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 12 FDA reports)
DECUBITUS ULCER ( 12 FDA reports)
EAR INFECTION ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
ERUCTATION ( 12 FDA reports)
HAEMORRHAGIC STROKE ( 12 FDA reports)
IMPAIRED WORK ABILITY ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
MEDICATION ERROR ( 12 FDA reports)
METASTASES TO LYMPH NODES ( 12 FDA reports)
MOVEMENT DISORDER ( 12 FDA reports)
MULTIPLE MYELOMA ( 12 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
ORAL PAIN ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
PARAESTHESIA ORAL ( 12 FDA reports)
PEPTIC ULCER ( 12 FDA reports)
RASH ERYTHEMATOUS ( 12 FDA reports)
SKIN PLAQUE ( 12 FDA reports)
SKIN ULCER ( 12 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 12 FDA reports)
SPLEEN DISORDER ( 12 FDA reports)
TENDON RUPTURE ( 12 FDA reports)
VAGINAL HAEMORRHAGE ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
AGGRESSION ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 11 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 11 FDA reports)
BREAST CALCIFICATIONS ( 11 FDA reports)
CEREBRAL ISCHAEMIA ( 11 FDA reports)
CIRCULATORY COLLAPSE ( 11 FDA reports)
DECREASED ACTIVITY ( 11 FDA reports)
DENTAL CARIES ( 11 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 11 FDA reports)
DRY SKIN ( 11 FDA reports)
DYSSTASIA ( 11 FDA reports)
FACIAL PALSY ( 11 FDA reports)
FAECES DISCOLOURED ( 11 FDA reports)
FEELING HOT ( 11 FDA reports)
FEELING JITTERY ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
HYPOPHAGIA ( 11 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 11 FDA reports)
OSTEITIS ( 11 FDA reports)
PARKINSON'S DISEASE ( 11 FDA reports)
PERIPHERAL COLDNESS ( 11 FDA reports)
PLEURAL FIBROSIS ( 11 FDA reports)
POLLAKIURIA ( 11 FDA reports)
RECTAL POLYP ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
SKIN FIBROSIS ( 11 FDA reports)
SNORING ( 11 FDA reports)
SPINAL COMPRESSION FRACTURE ( 11 FDA reports)
VISUAL FIELD DEFECT ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 10 FDA reports)
ANAPHYLACTIC REACTION ( 10 FDA reports)
APNOEA ( 10 FDA reports)
ASTHMA ( 10 FDA reports)
BLISTER ( 10 FDA reports)
BLOOD CALCIUM DECREASED ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
COORDINATION ABNORMAL ( 10 FDA reports)
DRY THROAT ( 10 FDA reports)
DUODENAL ULCER PERFORATION ( 10 FDA reports)
EARLY SATIETY ( 10 FDA reports)
EATING DISORDER ( 10 FDA reports)
ENDARTERECTOMY ( 10 FDA reports)
GRAND MAL CONVULSION ( 10 FDA reports)
GROIN PAIN ( 10 FDA reports)
HERNIA ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
HYPERTENSIVE CRISIS ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
HYPOCALCAEMIA ( 10 FDA reports)
ILL-DEFINED DISORDER ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 10 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 10 FDA reports)
MANIA ( 10 FDA reports)
MIDDLE INSOMNIA ( 10 FDA reports)
MULTIPLE INJURIES ( 10 FDA reports)
MUSCLE ATROPHY ( 10 FDA reports)
NAIL DISORDER ( 10 FDA reports)
ORAL DISCOMFORT ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
SENSORY LOSS ( 10 FDA reports)
SKIN DISORDER ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
SNEEZING ( 10 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
UROSEPSIS ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
ABDOMINAL PAIN LOWER ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
ANOSMIA ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
AORTIC STENOSIS ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
BLADDER OBSTRUCTION ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 9 FDA reports)
BREAKTHROUGH PAIN ( 9 FDA reports)
CAROTID BRUIT ( 9 FDA reports)
CHOKING ( 9 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
CHROMATURIA ( 9 FDA reports)
COAGULOPATHY ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DEBRIDEMENT ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
DIVERTICULITIS ( 9 FDA reports)
DYSKINESIA ( 9 FDA reports)
EAR PAIN ( 9 FDA reports)
EMBOLIC STROKE ( 9 FDA reports)
EPIGLOTTITIS ( 9 FDA reports)
EYE PAIN ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HIATUS HERNIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
KERATOACANTHOMA ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LOBAR PNEUMONIA ( 9 FDA reports)
MAMMOPLASTY ( 9 FDA reports)
MELANOCYTIC NAEVUS ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
MUSCLE INJURY ( 9 FDA reports)
ONYCHALGIA ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PROSTATOMEGALY ( 9 FDA reports)
RHEUMATOID ARTHRITIS ( 9 FDA reports)
SEBORRHOEIC KERATOSIS ( 9 FDA reports)
SKIN INDURATION ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
STASIS DERMATITIS ( 9 FDA reports)
STRESS ( 9 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
URINARY TRACT OBSTRUCTION ( 9 FDA reports)
URINE COLOUR ABNORMAL ( 9 FDA reports)
URINE FLOW DECREASED ( 9 FDA reports)
VENOOCCLUSIVE DISEASE ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ACUTE PRERENAL FAILURE ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
ATAXIA ( 8 FDA reports)
BASAL CELL CARCINOMA ( 8 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 8 FDA reports)
CHEST TUBE INSERTION ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
DEFORMITY ( 8 FDA reports)
DERMATITIS ALLERGIC ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DRUG DISPENSING ERROR ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
EJECTION FRACTION DECREASED ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
EYE SWELLING ( 8 FDA reports)
EYELID OEDEMA ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
GLOSSODYNIA ( 8 FDA reports)
HALLUCINATION, VISUAL ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 8 FDA reports)
INJECTION SITE HAEMORRHAGE ( 8 FDA reports)
ISCHAEMIA ( 8 FDA reports)
LIMB INJURY ( 8 FDA reports)
LOOSE TOOTH ( 8 FDA reports)
MELAENA ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OESOPHAGITIS ULCERATIVE ( 8 FDA reports)
ORAL HERPES ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
RADICULOPATHY ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
SALIVARY HYPERSECRETION ( 8 FDA reports)
SCLERAL DISCOLOURATION ( 8 FDA reports)
SEASONAL ALLERGY ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
SKIN HYPERPIGMENTATION ( 8 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 8 FDA reports)
SWELLING ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
TOOTH ABSCESS ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
WOUND DEHISCENCE ( 8 FDA reports)
AMBLYOPIA ( 7 FDA reports)
ANIMAL BITE ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
ASCITES ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD MAGNESIUM DECREASED ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
BONE SCAN ABNORMAL ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 7 FDA reports)
CHRONIC SINUSITIS ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DILATATION ATRIAL ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 7 FDA reports)
ENDODONTIC PROCEDURE ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
FACIAL PARESIS ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FIBROSIS ( 7 FDA reports)
FISTULA ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
GOITRE ( 7 FDA reports)
GYNAECOMASTIA ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HELICOBACTER INFECTION ( 7 FDA reports)
HYPERKERATOSIS ( 7 FDA reports)
HYPERPARATHYROIDISM ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
IMMOBILE ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
JOINT CONTRACTURE ( 7 FDA reports)
LABORATORY TEST ABNORMAL ( 7 FDA reports)
LEG AMPUTATION ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LUNG OPERATION ( 7 FDA reports)
LYMPHOEDEMA ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MONOPLEGIA ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
NEURITIS ( 7 FDA reports)
OBSTRUCTIVE UROPATHY ( 7 FDA reports)
OEDEMA MOUTH ( 7 FDA reports)
ORAL DISCHARGE ( 7 FDA reports)
PARATHYROID TUMOUR BENIGN ( 7 FDA reports)
PERIODONTAL DISEASE ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
PITTING OEDEMA ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PROSTATE CANCER ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
PULMONARY GRANULOMA ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RENAL TUBULAR NECROSIS ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
RETINAL ISCHAEMIA ( 7 FDA reports)
ROTATOR CUFF REPAIR ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
THYROID CANCER ( 7 FDA reports)
TOE AMPUTATION ( 7 FDA reports)
TONGUE DISCOLOURATION ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
URINE OUTPUT ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ABSCESS JAW ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DIABETIC NEPHROPATHY ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
EXTRADURAL HAEMATOMA ( 6 FDA reports)
EYE IRRITATION ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 6 FDA reports)
IRON DEFICIENCY ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LABYRINTHITIS ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
MIDDLE EAR EFFUSION ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MYASTHENIA GRAVIS ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PANIC DISORDER ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
PERIORBITAL OEDEMA ( 6 FDA reports)
PHLEBOSCLEROSIS ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
RESUSCITATION ( 6 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SKIN NEOPLASM EXCISION ( 6 FDA reports)
SPINAL CORD HAEMORRHAGE ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
STEAL SYNDROME ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
VITREOUS DETACHMENT ( 6 FDA reports)
ACCIDENT ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
AGRAPHIA ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
BRUXISM ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CAUDA EQUINA SYNDROME ( 5 FDA reports)
CEREBRAL DISORDER ( 5 FDA reports)
CERUMEN IMPACTION ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EXTREMITY CONTRACTURE ( 5 FDA reports)
FEAR ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 5 FDA reports)
HYPOPNOEA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
LEARNING DISORDER ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LIVER OPERATION ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
MULTI-ORGAN DISORDER ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
NASAL SEPTUM DISORDER ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
PURPURA ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SPONTANEOUS HAEMATOMA ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
THROMBOSIS IN DEVICE ( 5 FDA reports)
TOE DEFORMITY ( 5 FDA reports)
TONGUE ULCERATION ( 5 FDA reports)
TONSILLAR DISORDER ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
ULCER ( 5 FDA reports)
VIITH NERVE PARALYSIS ( 5 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANDROGEN DEFICIENCY ( 4 FDA reports)
ANEURYSM RUPTURED ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLINDNESS TRANSIENT ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 4 FDA reports)
CORONARY ARTERY BYPASS ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETIC GASTROPARESIS ( 4 FDA reports)
DIABETIC MICROANGIOPATHY ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EYE ROLLING ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INJECTION SITE PRURITUS ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LOSS OF BLADDER SENSATION ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
LYMPHANGITIS ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 4 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
POST PROCEDURAL HAEMATURIA ( 4 FDA reports)
POSTERIOR TIBIAL NERVE INJURY ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
PRIMARY SEQUESTRUM ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
PUPILLARY DEFORMITY ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
SALIVARY GLAND PAIN ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SPINAL CORD INJURY ( 4 FDA reports)
SPINAL HAEMATOMA ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
SYNOVIAL DISORDER ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
TESTICULAR PAIN ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
TETANY ( 4 FDA reports)
THALAMUS HAEMORRHAGE ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYMUS DISORDER ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TRAUMATIC ULCER ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
UMBILICAL HERNIA ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
URINARY TRACT DISORDER ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACHLORHYDRIA ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPLICATION SITE DISCHARGE ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYSTITIS KLEBSIELLA ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
IRON METABOLISM DISORDER ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MASS ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
POLYP ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROSTATECTOMY ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SCROTAL HAEMATOCOELE ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THIRST ( 3 FDA reports)
TONGUE HAEMATOMA ( 3 FDA reports)
TRACHEAL PAIN ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
UMBILICAL HERNIA REPAIR ( 3 FDA reports)
URINE CALCIUM DECREASED ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ABDOMINAL X-RAY ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APOLIPOPROTEIN A-I INCREASED ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BUNION ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHOLELITHOTOMY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASTOCYTOSIS ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUROPATHIC ULCER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NODULE ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLASMACYTOSIS ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TRACHEAL INJURY ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE ARSENIC ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFERENT LOOP SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMMONIA ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE FREE ABNORMAL ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
COX-MAZE PROCEDURE ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE PHYSICAL PROPERTY ISSUE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNAL CAROTID ARTERY KINKING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
IRIS HAEMORRHAGE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARAESTHESIA MUCOSAL ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENETRATING ABDOMINAL TRAUMA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL NERVE INJURY ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
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POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT EXPIRATION DATE ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN TOTAL ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TESTIS DISCOMFORT ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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