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

SEPSIS ( 14 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
JOINT DISLOCATION ( 12 FDA reports)
WOUND INFECTION ( 9 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
NEUTROPENIA ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
MYOPERICARDITIS ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RABBIT SYNDROME ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)

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