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

DYSPNOEA ( 26 FDA reports)
ARRHYTHMIA ( 23 FDA reports)
PNEUMONIA ( 22 FDA reports)
DIZZINESS ( 20 FDA reports)
HYPERTENSION ( 18 FDA reports)
FALL ( 17 FDA reports)
PYREXIA ( 16 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
INSOMNIA ( 14 FDA reports)
MALAISE ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
PAIN ( 13 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
VOMITING ( 12 FDA reports)
CARDIAC DISORDER ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
SWELLING ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
COMA ( 8 FDA reports)
COUGH ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DEATH ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
FEMUR FRACTURE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
SURGERY ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CATARACT ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
APATHY ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BRAIN TUMOUR OPERATION ( 4 FDA reports)
CARDIAC PACEMAKER INSERTION ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
APPLICATION SITE INFLAMMATION ( 3 FDA reports)
APPLICATION SITE WARMTH ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
MEDICAL DEVICE CHANGE ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SLEEP STUDY ABNORMAL ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PHYSICAL EXAMINATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
STARING ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)

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