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

BLOOD CREATININE INCREASED ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
DRUG ABUSE ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
VOMITING ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
RED BLOOD CELL ROULEAUX FORMATION PRESENT ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CATATONIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ANTI-SS-B ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
POISONING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
ANGER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use