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Rofecoxib (Vioxx) withdrawal: do product monographs adequately inform physicians?

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Clinical Pract ice Pratique clinique

Th erapeutics Letter

P

roduct monographs are legal documents that in eff ect transfer responsibility from drug manufac- turers to prescribing physicians. At issue is whether the product monographs for rofecoxib and other nonsteroidal anti-inflammatory drugs (NSAIDs) marketed as cyclooxygenase-2 (COX-2) selective NSAIDs adequately inform clinicians about the ben- efi ts and drawbacks of these drugs. Th e Th erapeutic Products Directorate at Health Canada has detailed guidelines for preparing product monographs (www.hc-sc.gc.ca/hpfb-dgpsa/tpd-dpt/product_

monograph_e.html).

Conclusions

Product monographs:

• sometimes provide data about drug harm, includ- ing serious adverse events, that is not published elsewhere;

• prove a challenge for finding, extracting, and interpreting the relevant information; and

• inadequately inform clinicians (eg, the rofecoxib monograph gives an incomplete picture of the relative risk of myocardial infarction and total serious adverse events for rofecoxib versus com- parable drugs in all trials).

Celecoxib, meloxicam, and valdecoxib 2004 monographs:

• do not claim to improve arthritis symptoms more than non-selective NSAIDs;

• warn against prescribing to patients with a his- tory of peptic ulcer disease;

• do not claim to reduce complicated ulcers as compared with non-selective NSAIDs; and

• provide insufficient information as to whether these drugs increase risk of myocardial infarction or total cardiovascular thrombotic events.

Source:Th erapeutics Letter 2004;53:1-4. For the complete text of this report, check the Th erapeutics Initiative website http://www.ti.ubc.ca.

T

he Therapeutics Letter presents critically appraised summary evidence primarily from controlled drug trials. Such evidence applies to patients similar to those involved in the trials and might not be generalizable to every patient. The Therapeutics Initiative provides evidence-based advice about drug therapy and is not responsible for formulating or adjudicating provincial drug policies.

Website: www.ti.ubc.ca

212 Canadian Family Physician • Le Médecin de famille canadiendVOL 5: FEBRUARY • FÉVRIER 2005

Rofecoxib (Vioxx) withdrawal

Do product monographs adequately inform physicians?

...

Th erapeutics Letter

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