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ARCHIVES OF LEPROSY MAILING LIST
Archives of recent messages from Leprosy Mailing List (LML) managed by Dr Salvatore Noto.

Over the past few years, LML moderated by Dr Noto has become one of the most important online resource for promoting discussions about leprosy. For joining this mailing list kindly send an email to Dr. Salvatore Noto: salvatore.notoathsanmartino.it  (substitute at with @ in the email address)

Leprosy mailing list – November 9th, 2005

Ccn:    all.

Ref.:

1.

Moreira de Souza A C, “Thalidomide in Brazil: monitoring with shared responsibility? LML Oct. 28, 2005.

2.

Ganapati R, “Thalidomide freely available in India”, LML Oct.17, 2005.

3.

Ganapati R, “BLP press release on Seminar on Role of Thalidomide in Leprosy”, LML Oct.16, 2005.

From:   C R Revankar, New Jersey, USA.


 

 

 

Dear Members of the forum,

 

Indeed, it is good news that Thalidomide is freely available in India though it is expensive at present. It is equally disturbing that some physicians influenced by pharmaceutical/sale promoters use this drug in leprosy without proper indication (2.)

 

All of us agree (both clinical and public health leprologists) without any doubt that thalidomide is effective in leprosy patients with chronic, recurrent type-II reactions with or without neuritis not responding to steroids and to steroids in combination with clofazimine.  All of us agree that the needy leprosy patients have a right to receive best available treatment with thalidomide.

  

It is the moral responsibility of treating physicians and professional organizations to follow medical ethics and standard guidelines rather than follow sale promoters while using Thalidomide. Thalidomide beneficiaries and their family members also take the responsibilities to prevent improper use of this drug.  It could be a shared responsibility of all in India as followed in Brazil (Moreira de Souza, LML, Oct. 28). Can we achieve this shared monitoring in a vast country like India?

 

Medical professional associations such as Indian Association of Leprologists (IAL), Indian Association of Dermatologists, Venereologists and Leprologists (IADVL), Indian Medical Association (IMA) and other national bodies such as National Leprosy Organization (NLO) and Hind Kushta Nivaran Sangh (HKNS) should write to national government and donor agencies to support the cause.

 

The fourth coming IAL conference in AGRA, India (November, 2005) may be a good opportunity to discuss these issues to draw the attention of the government, donor agencies and treatment providers.

 

Regards,

 

CR Revankar

revankarcr@gmail.com

 

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