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

MYOCARDIAL INFARCTION ( 653 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 360 FDA reports)
CORONARY ARTERY DISEASE ( 204 FDA reports)
CEREBROVASCULAR ACCIDENT ( 190 FDA reports)
CARDIAC DISORDER ( 154 FDA reports)
MYOCARDIAL ISCHAEMIA ( 129 FDA reports)
BLOOD GLUCOSE INCREASED ( 100 FDA reports)
CARDIOVASCULAR DISORDER ( 92 FDA reports)
DYSPNOEA ( 78 FDA reports)
CHEST PAIN ( 74 FDA reports)
NAUSEA ( 69 FDA reports)
WEIGHT INCREASED ( 67 FDA reports)
DIZZINESS ( 65 FDA reports)
HYPERTENSION ( 64 FDA reports)
ATRIAL FIBRILLATION ( 62 FDA reports)
BLOOD GLUCOSE DECREASED ( 58 FDA reports)
PAIN ( 58 FDA reports)
HEART INJURY ( 55 FDA reports)
FATIGUE ( 54 FDA reports)
DRUG INEFFECTIVE ( 53 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 49 FDA reports)
OEDEMA PERIPHERAL ( 48 FDA reports)
INJURY ( 47 FDA reports)
ASTHENIA ( 42 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 42 FDA reports)
HEADACHE ( 41 FDA reports)
DEATH ( 40 FDA reports)
WEIGHT DECREASED ( 38 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 35 FDA reports)
ARRHYTHMIA ( 35 FDA reports)
HYPOGLYCAEMIA ( 35 FDA reports)
MUSCULAR WEAKNESS ( 34 FDA reports)
RENAL FAILURE ( 33 FDA reports)
OEDEMA ( 32 FDA reports)
DIARRHOEA ( 30 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 28 FDA reports)
PNEUMONIA ( 28 FDA reports)
CORONARY ARTERY BYPASS ( 25 FDA reports)
STENT PLACEMENT ( 25 FDA reports)
VOMITING ( 25 FDA reports)
ANXIETY ( 24 FDA reports)
GAIT DISTURBANCE ( 24 FDA reports)
HYPERLIPIDAEMIA ( 24 FDA reports)
VISION BLURRED ( 24 FDA reports)
ARTERIOSCLEROSIS ( 23 FDA reports)
CARDIAC FAILURE ( 23 FDA reports)
DECREASED APPETITE ( 23 FDA reports)
DEPRESSION ( 23 FDA reports)
SWELLING ( 22 FDA reports)
ECONOMIC PROBLEM ( 21 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
BALANCE DISORDER ( 20 FDA reports)
CARDIAC ARREST ( 20 FDA reports)
PAIN IN EXTREMITY ( 20 FDA reports)
ANGINA PECTORIS ( 19 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 19 FDA reports)
MULTIPLE INJURIES ( 19 FDA reports)
CARDIOMYOPATHY ( 18 FDA reports)
TREMOR ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
MITRAL VALVE INCOMPETENCE ( 17 FDA reports)
RENAL FAILURE CHRONIC ( 17 FDA reports)
ANGINA UNSTABLE ( 16 FDA reports)
ACUTE CORONARY SYNDROME ( 15 FDA reports)
CORONARY ARTERY OCCLUSION ( 15 FDA reports)
DEEP VEIN THROMBOSIS ( 15 FDA reports)
ENCEPHALOPATHY ( 15 FDA reports)
FLUID RETENTION ( 15 FDA reports)
PULMONARY CONGESTION ( 15 FDA reports)
PULMONARY HYPERTENSION ( 15 FDA reports)
RASH ( 15 FDA reports)
VENTRICULAR FIBRILLATION ( 15 FDA reports)
ABDOMINAL DISTENSION ( 14 FDA reports)
ABDOMINAL PAIN UPPER ( 14 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 14 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 14 FDA reports)
FALL ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
MENTAL DISORDER ( 14 FDA reports)
AMNESIA ( 13 FDA reports)
BLOOD PRESSURE INCREASED ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
RENAL DISORDER ( 13 FDA reports)
INSOMNIA ( 12 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
DYSPEPSIA ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
HEART RATE INCREASED ( 11 FDA reports)
MALAISE ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
OPEN WOUND ( 11 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
THROMBOSIS ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
COUGH ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
JOINT SWELLING ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
ADVERSE EVENT ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
MACULAR OEDEMA ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
SICK SINUS SYNDROME ( 9 FDA reports)
ANEURYSM ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CARDIAC ANEURYSM ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DEFORMITY ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MALIGNANT HYPERTENSION ( 8 FDA reports)
SURGERY ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RETCHING ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BLADDER CANCER STAGE IV ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD COPPER DECREASED ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACUTE LUNG INJURY ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
COMA ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
LEFT ATRIAL DILATATION ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEAR DROWNING ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BITE ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
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EYELID OEDEMA ( 1 FDA reports)
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FEAR OF DISEASE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
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GASTROENTERITIS VIRAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
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GESTATIONAL DIABETES ( 1 FDA reports)
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HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
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HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
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HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
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HUNGER ( 1 FDA reports)
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HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
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ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
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OPEN FRACTURE ( 1 FDA reports)
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ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
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PAPILLOEDEMA ( 1 FDA reports)
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PATIENT ISOLATION ( 1 FDA reports)
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PHYSICAL DISABILITY ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
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PRESYNCOPE ( 1 FDA reports)
PREVENTIVE SURGERY ( 1 FDA reports)
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PULSE PRESSURE DECREASED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
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RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
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RESTLESS LEGS SYNDROME ( 1 FDA reports)
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RETINAL VEIN OCCLUSION ( 1 FDA reports)
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RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
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STERNOTOMY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
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TOOTH EXTRACTION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
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VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
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VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
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WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
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