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

MALAISE ( 7 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
DEHYDRATION ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COMA ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FALL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERINEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use