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

DRUG INTERACTION ( 19 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
ACUTE PSYCHOSIS ( 6 FDA reports)
CHOREA ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 5 FDA reports)
DEATH ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
CONSTIPATION ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PIGMENT DISPERSION SYNDROME ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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