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DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
APHASIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
TREMOR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)

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