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

ABDOMINAL PAIN ( 15 FDA reports)
DYSPNOEA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
VENTRICULAR FIBRILLATION ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
ASTHENIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
VOMITING ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ABDOMINAL X-RAY ( 3 FDA reports)
BARIUM ENEMA ABNORMAL ( 3 FDA reports)
BIOPSY COLON ABNORMAL ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
FALL ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STRESS ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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