Forest '00 for pdf only 7/6/00 1:08 PM Page 8drug most suitable for particular patients. Although different patients may respond differently to a particular SSRI in general, one SSRI may tend to be sedating andanother may be activating or may cause gastrointestinalproblems or sexual dysfunction. Celexa is usually well tolerated and has minimal side effects. • Celexa has a favorable drug
Chem-t.comGlaxoSmithKline and Dainippon Sumitomo Pharma commence the co-promotion of anti-depressant Paxil® CR Tablets
GlaxoSmithKline K.K. (President: Philippe Fauchet, Head Office: Shibuya-ku, Tokyo,
hereinafter referred to as GSK) and Dainippon Sumitomo Pharma Co, Ltd. (President:
Masayo Tada, Head Office: Chuo-ku, Osaka, hereinafter referred to as DSP) announce
that the companies will commence the co-promotion of GSK’s anti-depressant Paxil®
CR Tablets 12.5mg and Paxil® CR Tablets 25mg (paroxetine hydrochloride hydrate,
hereinafter referred to as Paxil® CR) in Japan from April 1, 2012.
As announced on January 19, 2012, the two companies have already signed a "basic
agreement". This time the two companies signed a "Co-promotion agreement".
Under this agreement, effective April 1, 2012, GSK and DSP will co-promote Paxil® CR
Tablets to medical institutions. GSK will deal with distribution and sales.
Paxil® CR is the controlled-release1 formulation of Paxil® tablets, an SSRI (selective
serotonin reuptake inhibitor) anti-depressant. It received regulatory approval in Japan
from MHLW on 18 January 2012 for the indication of depression and depressive state.
Paxil® CR will be launched soon after insurance price has been decided. Overseas,
development of anti-depressants using new formulation technology are being
conducted actively and with the approval of Paxil® CR Tablets, Japan too has entered
the era of controlled-release formulations. Paxil® CR Tablets was approved in the US
in 1999 and as of June 2011, has been approved and widely used in over 40 countries
Commenting on the co-promotion Philippe Fauchet, president of GSK, said, “GSK
obtained marketing approval on Paxil®CR from the MHLW in addition to the existing
Paxil® IR. By adopting new formulation technology Paxil® CR Tablets is expected to
alleviate gastrointestinal symptoms in the early stages of administration of
anti-depressants and contribute to improving the continuity of long-term treatment.
Through the partnership with DSP, which has expertise and extensive experience in the
psychiatry area, GSK hopes to contribute to the treatment of depression by further
enhancing medical information provision to medical institutions regarding the drug's
safety and efficacy.”
Masayo Tada, President and Chief Executive Officer, Dainippon Sumitomo Pharma Co.,
Ltd. commented, "We are working on the CNS area as one of our focus marketing areas
and have developed promotional activities in this area including antipsychotic drugs.
With this agreement, by adding Paxil® CR Tablets to our product line, we believe our
activities can be expanded in the area of anti-depressants and we can further enhance
our presence in the CNS area. We hope to contribute further to the treatment of
depression by providing proper information to medical institutions in collaboration with
Profile of Paxil® CR
Product name Paxil® CR Tablets 12.5mg, Paxil® CR Tablets 25mg
Generic name paroxetine hydrochloride hydrate Usually for adults, paroxetine is administered orally at 12.5 mg as the initial dose once daily after evening meal, and the dose is subsequently increased to 25 mg a day taking a week or longer. Dosage should be adjusted according to symptoms and age in the dosing range not Administration exceeding 50 mg a day and either of the above dose will be administered once daily after evening meal. When the dose is increased, it should be increased by 12.5 mg as a daily dose at intervals of a week or longer. About Paxil® CR Tablets
anti-depressant in Japan, which has a slow pharmacokinetic profile by using formulation technology. z Using an enteric coating and two layer controlled-release technology 2, it is designed so that the drug is released gradually and continuously after it has left the stomach. Paxil® IR Tablets, blood concentration increases gradually during single dose administration and as change in blood concentration during repeated administration is small, it is expected to reduce the risk of adverse events. z Overseas clinical trial3 、4results have shown that treatment dropout due to adverse events do not differ greatly to placebo making it easy to take and it is expected to contribute to improving the continuity of long-term treatment. 1) Controlled-release formulation: Formulation using CR technology that controls drug release for continuous and gradual release 2）Two layer controlled-release technology. Paxil CR Tablets is made up of 2 layers – an affinity matrix layer that includes active ingredients in the plain tablet (inner core) and an erodent barrier layer that does not include active ingredients, thereby controlling the rate of drug release. 3）Golden RN et al :J Clin Psychiatry,2002；63（7）：577-584 4) Eaddy M, et al: Manage Care Interface,2003; 16(12 ): 22-7
Arzneimittelausgabenentwicklung in Brandenburg Leitfaden für Kostentransparenz Editorial Sehr geehrte Ärztinnen und Ärzte, zum Sicherstellungsauftrag der Vertragsärzte gehört es auch, Patienten mit Arzneimitteln zu versorgen. Entsprechend dem Wirtschaftlichkeitsgebot nach § 12 SGB V ist der Behandlungserfolg auf wirtschaftlichem und zweckmäßigem Weg zu erreichen. Die hierfür ve