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PJ Online homeThe Pharmaceutical Journal
Vol 276 No 7398 p503
29 April 2006

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· Branded prescribing
· Antibiotics
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· The profession
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Letters to the Editor

Branded prescribing

When to prescribe by brand

From Mr N. V. Morley, MRPharmS

I write further to William Horsley’s letter (PJ, 11 March, p293) on the decision by the Practice Committee of the Royal Pharmaceutical Society to allow proprietary prescribing of sustained release opiate medicines. That the committee has come to this decision based on sound clinical and therapeutic conditions is undoubted.

It is a well established fact that: “In many cases the Prescription Pricing Authority is unable to process prescriptions written generically because no true generic approved name exists or the preparation has a number of ingredients, eg, ointments and mixtures, and there is no recognised combination approved name for these products. In addition to the necessity to write by brand to facilitate the processing by the PPA there are many pharmaceuticals where for clinical reasons it is recommended by various medical authorities, including the British National Formulary, that preparations should be prescribed by brand. Such therapeutic areas include nicotine replacement therapy, opiates, anticonvulsants and most sustained release preparations — such as nifedipine, diltiazem and modified release patches, eg, fentanyl, and other therapeutic areas where clinical equivalence cannot be assumed. Prescribers should for these products prescribe them by brand to avoid patients being given the wrong product or prescriptions being returned to a retail pharmacy contractor by the PPA for elucidation.” This advice has been circulated to prescribers by the PPA over many years.

I would also say that, from the point of view of probity, the choice of drug will have no effect on community pharmacy income, since invariably these are zero discount lines.

As regards the public purse, it would be noted that in many cases the list prices of the “me too” brands are identical to those of the original brands or the Drug Tariff listing and, therefore, the cost to the public purse is the same.

Finally, while noting the comment concerning possible restraint to entry of new products, if the new products have merit, whether clinically, operationally in drug delivery, or from the point of view of cost-effective prescribing, then the advice to prescribe by brand is paramount.

Nigel Morley
Managing Director
Surelines Pharmaceutical Services Ltd

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