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

AMNESIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
RETROGRADE AMNESIA ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
INAPPROPRIATE AFFECT ( 5 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
RESTLESSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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