31 January 2017
Dear Dr Harrison,
REQUEST FOR INFORMATION
Thank you for your request dated 25 November 2016 under the Official Information Act 1982
(OIA) for information relating to the management of Stelazine (trifluoperazine) supply. You
asked for:
information, documentation, costings, advice sought and provided, correspondence
between suppliers, manufacturers, pharmacy wholesalers, regarding the management
of supply of Stelazine (trifluoperazine); and
all documentation and advice received/sought from patients, customers, MPs,
pharmacists/pharmacies, doctors, nurses/all health care professionals regarding the
supply of Stelazine (trifluoperazine) in recent times.
Please find information covered by your request attached. I understand that some of the
enquires were resolved over the phone.
In our response, we have redacted a small amount of information from the documents as we
consider this necessary to:
protect the privacy of natural persons (section 9(2)(a));
protect information which is subject to an obligation of confidence or which any person has
been or could be compelled to provide under the authority of any enactment, where the
making available of the information would be likely to prejudice the supply of similar
information, or information from the same source, and it is in the public interest that such
information should continue to be supplied (section 9(2)(ba)(i));
protect information where the making available of the information would be likely to
unreasonably prejudice the commercial position of the person who supplied or who is the
subject of the information (section 9(2)(b)(ii));
enable PHARMAC to carry out, without prejudice or disadvantage, commercial activities
(section 9(2)(i)); and
enable PHARMAC to carry on, without prejudice or disadvantage, negotiations, including
commercial negotiations (section 9(2)(j)).
As required under the OIA, we also considered whether, in the circumstances, the withholding
of this information was outweighed by other considerations which render it desirable, in the
public interest, to make this information available – and decided it was not. Please note you
have the right, by way of complaint under section 28(3) of the OIA to an Ombudsman, to seek
an investigation and review of our decision.
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PHARMAC takes medicine supply very seriously. Unfortunately, supply issues are a reality of
pharmaceutical markets and an ongoing international issue. We maintain good communication
with suppliers about supply challenges, and have a number of contractual and procedural
mechanisms in place to incentivise secure supply and, when required, professionally manage
supply risks (and, when necessary, introduce alternative supply).
As noted in our extension letter to you in December, trifluoperazine hydrochloride tablets will
be delisted from the Pharmaceutical Schedule from 1 July 2017.
I trust that these documents are what you were after. If you have any further questions please
feel free to contact us again. Thank you for your interest in our work.
Yours sincerely
Peter Alsop
Director, Engagement and Implementation
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