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

ABNORMAL BEHAVIOUR ( 7 FDA reports)
RASH ( 6 FDA reports)
DELIRIUM ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
ZINC SULPHATE TURBIDITY INCREASED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
AGITATION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
DYSKINESIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DEATH ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)

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