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

MYOCARDIAL INFARCTION ( 120 FDA reports)
CEREBROVASCULAR ACCIDENT ( 99 FDA reports)
HYPERTENSION ( 97 FDA reports)
CHEST PAIN ( 84 FDA reports)
CORONARY ARTERY DISEASE ( 80 FDA reports)
DEPRESSION ( 78 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 45 FDA reports)
URINARY TRACT INFECTION ( 40 FDA reports)
INSOMNIA ( 39 FDA reports)
FALL ( 37 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 37 FDA reports)
DYSPNOEA ( 36 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 36 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 32 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 31 FDA reports)
HYPERLIPIDAEMIA ( 30 FDA reports)
ANXIETY ( 28 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 28 FDA reports)
PAIN IN EXTREMITY ( 26 FDA reports)
ANAEMIA ( 25 FDA reports)
DYSPEPSIA ( 24 FDA reports)
HYPOTENSION ( 24 FDA reports)
BACK PAIN ( 23 FDA reports)
CARDIAC DISORDER ( 23 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
SLEEP APNOEA SYNDROME ( 23 FDA reports)
ARTHROPATHY ( 22 FDA reports)
DIZZINESS ( 22 FDA reports)
ANGINA PECTORIS ( 21 FDA reports)
CONSTIPATION ( 21 FDA reports)
DIABETES MELLITUS ( 21 FDA reports)
MITRAL VALVE INCOMPETENCE ( 21 FDA reports)
HEADACHE ( 20 FDA reports)
ARTERIOSCLEROSIS ( 19 FDA reports)
COLONIC POLYP ( 19 FDA reports)
HYPERCHOLESTEROLAEMIA ( 19 FDA reports)
INJURY ( 19 FDA reports)
SLEEP DISORDER ( 19 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 18 FDA reports)
ISCHAEMIC STROKE ( 18 FDA reports)
CORONARY ARTERY STENOSIS ( 17 FDA reports)
HAEMATOMA ( 17 FDA reports)
HYPOAESTHESIA ( 17 FDA reports)
TENDONITIS ( 17 FDA reports)
GENERALISED ANXIETY DISORDER ( 16 FDA reports)
GOUT ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
ROTATOR CUFF SYNDROME ( 16 FDA reports)
ANGINA UNSTABLE ( 15 FDA reports)
BENIGN NEOPLASM ( 15 FDA reports)
EMOTIONAL DISTRESS ( 15 FDA reports)
GASTRITIS ( 15 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 14 FDA reports)
DIARRHOEA ( 14 FDA reports)
GASTROENTERITIS VIRAL ( 14 FDA reports)
MIGRAINE ( 14 FDA reports)
OSTEOCHONDROSIS ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
COUGH ( 13 FDA reports)
MYOSITIS ( 13 FDA reports)
ASTHMA ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
CORONARY ARTERY RESTENOSIS ( 12 FDA reports)
DEEP VEIN THROMBOSIS ( 12 FDA reports)
EPICONDYLITIS ( 12 FDA reports)
EXOSTOSIS ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
HEART RATE IRREGULAR ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 12 FDA reports)
ARTHRITIS ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 11 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 11 FDA reports)
CEREBRAL INFARCTION ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
LUNG NEOPLASM ( 11 FDA reports)
NECK PAIN ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
SYNCOPE ( 11 FDA reports)
DERMATITIS ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HIATUS HERNIA ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
POSTNASAL DRIP ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
SINUS DISORDER ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
VENTRICULAR DYSFUNCTION ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
AMNESIA ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BLADDER DISORDER ( 9 FDA reports)
CARDIAC MURMUR ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
HEMIPARESIS ( 9 FDA reports)
HERNIA ( 9 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
NERVOUSNESS ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
OSTEOARTHRITIS ( 9 FDA reports)
RASH ( 9 FDA reports)
SPINAL DISORDER ( 9 FDA reports)
SWELLING ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ACUTE CORONARY SYNDROME ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
AZOTAEMIA ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
GASTRITIS EROSIVE ( 8 FDA reports)
HAIR TEXTURE ABNORMAL ( 8 FDA reports)
INCREASED TENDENCY TO BRUISE ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
LABYRINTHITIS ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
RADICULITIS CERVICAL ( 8 FDA reports)
REFLUX OESOPHAGITIS ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SINUSITIS ( 8 FDA reports)
SPINAL COLUMN STENOSIS ( 8 FDA reports)
SPINAL OSTEOARTHRITIS ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ANGER ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
ATHEROSCLEROSIS ( 7 FDA reports)
BIPOLAR I DISORDER ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CHRONIC FATIGUE SYNDROME ( 7 FDA reports)
DRUG INTOLERANCE ( 7 FDA reports)
EARLY MORNING AWAKENING ( 7 FDA reports)
FOOD INTOLERANCE ( 7 FDA reports)
HAEMORRHOIDS ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
INFECTION ( 7 FDA reports)
IRRITABLE BOWEL SYNDROME ( 7 FDA reports)
MITRAL VALVE PROLAPSE ( 7 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 7 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
OESOPHAGITIS ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
STOMACH DISCOMFORT ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
ULCER ( 7 FDA reports)
VASCULAR DEMENTIA ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
BACK INJURY ( 6 FDA reports)
BODY TINEA ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
IMPLANT SITE EFFUSION ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
OBESITY ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
STRESS SYMPTOMS ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
ADRENAL MASS ( 5 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
LOCALISED OSTEOARTHRITIS ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DEATH ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PAIN ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
TINEA CRURIS ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TINEA VERSICOLOUR ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CERVICAL NEURITIS ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FEAR ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
IMPINGEMENT SYNDROME ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLATELET AGGREGATION INCREASED ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STRESS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LIPOPROTEIN (A) ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYP ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VERTIGO CNS ORIGIN ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONJUNCTIVAL ABRASION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
REPERFUSION ARRHYTHMIA ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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