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

OEDEMA PERIPHERAL ( 25 FDA reports)
ARTHRALGIA ( 19 FDA reports)
CORONARY ARTERY DISEASE ( 19 FDA reports)
HYPERTENSION ( 19 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 19 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
ARTERIOSCLEROSIS ( 15 FDA reports)
HEADACHE ( 15 FDA reports)
SLEEP APNOEA SYNDROME ( 14 FDA reports)
CORNEAL DEPOSITS ( 13 FDA reports)
HYPERTENSIVE CRISIS ( 13 FDA reports)
MUSCULOSKELETAL DISORDER ( 13 FDA reports)
RENAL CYST ( 13 FDA reports)
ANXIETY ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
OSTEONECROSIS ( 12 FDA reports)
ARTHRITIS ( 11 FDA reports)
FALL ( 11 FDA reports)
JAW DISORDER ( 11 FDA reports)
LYMPHADENOPATHY ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
CORONARY ARTERY STENOSIS ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
ARTHROPATHY ( 9 FDA reports)
CARDIAC ANEURYSM ( 9 FDA reports)
CATARACT ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
FEMUR FRACTURE ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HEPATIC STEATOSIS ( 9 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
PAIN ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ABSCESS JAW ( 8 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
FASCIITIS ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
ORAL CAVITY FISTULA ( 8 FDA reports)
OSTEOMYELITIS ( 8 FDA reports)
OSTEONECROSIS OF JAW ( 8 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 8 FDA reports)
TOOTH DISORDER ( 8 FDA reports)
TOOTHACHE ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
INJURY ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
POST PROCEDURAL OEDEMA ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
GINGIVAL SWELLING ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
MYOCARDIAL RUPTURE ( 5 FDA reports)
NEPHROSCLEROSIS ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
POLYCYSTIC OVARIES ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
SPLEEN CONGESTION ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
TOOTH LOSS ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BONE METABOLISM DISORDER ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIRSUTISM ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INTERTRIGO ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEVATOR SYNDROME ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RASH ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN DEPIGMENTATION ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOSIS PROPHYLAXIS ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOE DEFORMITY ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ENCHONDROMA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RALES ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE WAVEFORM ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use