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

MYOCARDIAL INFARCTION ( 27 FDA reports)
CEREBROVASCULAR ACCIDENT ( 26 FDA reports)
CHEST PAIN ( 21 FDA reports)
DYSPNOEA ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
INJURY ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COMA ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FALL ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
ULCER ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GOUT ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
POLYP ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RASH ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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