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Abstract
- Paracetamol is the first-choice
analgesic for joint pain. Nonsteroidal
antiinflammatory drugs (NSAIDs),
especially ibuprofen, are second-line
options. Cox-2 inhibitors are no more
effective than traditional NSAIDs and
have no tangible advantages in terms
of gastrointestinal tolerability. In contrast,
they expose patients to an
increased risk of cardiovascular
adverse effects.
- Etoricoxib is marketed in some
European countries to relieve symptoms
of osteoarthritis, rheumatoid
arthritis, and gout attacks.
- Many clinical trials have tested
etoricoxib in these indications, as well
as in ankylosing spondylitis, low back
pain, and various types of acute pain.
Etoricoxib was no more effective than
other NSAIDs such as ibuprofen,
naproxen or diclofenac in these situations.
- Comparative trials showed a higher
overall mortality rate with etoricoxib
than with naproxen. A combined
analysis of long-term comparative
trials including 5441 patients,
mainly versus naproxen, showed that
etoricoxib does not reduce the risk of
perforation, ulcer or severe gastrointestinal
haemorrhage. Similarly, it
does not reduce the risk of mild gastrointestinal
events in at-risk patients:
those with a history of gastrointestinal
disorders, aspirin use, etc.
- Three trials including a total of
34 701 patients (MEDAL programme)
compared cardiovascular thrombotic
events associated with etoricoxib and
diclofenac. Overall, the cardiovascular
risks appear to be similar but the
thrombotic risk may be slightly higher
with diclofenac than with other conventional
NSAIDs.
- Etoricoxib provoked arterial
hypertension, oedema and heart failure
during clinical trials. Serious skin
reactions were reported both during
clinical trials and after marketing, but
their precise incidence is not known.
Etoricoxib is partly metabolised by
the cytochrome P450 isoenzyme
CYP 3A4 and increases the bioavailability
of ethinylestradiol.