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

ATRIAL FIBRILLATION ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
SYNCOPE ( 8 FDA reports)
VOMITING ( 8 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CATARACT ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
FALL ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
BARTTER'S SYNDROME ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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