TITLE

CLINICAL EXPERIENCE WITH THE ANTICOAGULANT PANWARFIN (WARFARIN SODIUM)

AUTHOR(S)
Aravanis, Christ; Evangelou, I.
PUB. DATE
June 1963
SOURCE
Angiology;Jun1963, Vol. 14 Issue 6, p325
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
This report describes our experience with 75 patients given Panwarfin (warfarin sodium, Abbott Laboratories). Our findings are basically in complete agreement with the previously reported facts of others, only our experience with maintenance dosage differs. It was found that an initial dose of 50 mg and a subsequent one of 2.5 to 5.0 mg were sufficient for producing very satisfactory levels of hypoprothroinbinemia in 90 per cent of the patients. Very few �escape periods� from the therapeutic range were observed. Minor hemorrhagic phenomena occurred in only four patients without any serious consequences. Two deaths occurred during the treatment, the one probably related to anticoagulant treatment. No other toxic phenomena were noticed. Vitamin K1 was proved very efficient in counteracting prothrombin depression. No differences were found between the oral and the intravenous use concerning dosage, induction and level of hyporothrombinemia, recovery or toxicity. Our experience with Panwarfin in conjunction with the reports that have been published is that warfarin sodium is a rapidly effective anticoagulant, producing a smooth curve of hyporothrombinemia, presenting no toxic reactions and easily counteracted by vitamin K1. All of these properties make Panwarfin a nearly ideal anticoagulant.
ACCESSION #
16384867

 

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