Medical studies have demonstrated that a pain-relieving drug – such as
an NSAID (non-steroidal, anti-inflammatory drug) or a COX-2 – can help
enormously, especially in cases of acute pain.
However, it’s important to remember that the drug is only masking
the pain, and the underlying problem cause hasn’t gone away. Seen in
this context, they are useful, and sometimes vital, allies in the
short-term fight against pain, but they shouldn’t be seen as the
solution, or taken long-term without investigating the real cause of
the pain.
The NSAIDs
The NSAID (nonsteroidal, anti-inflammatory drug) is the most common
drug for pain relief. As its name suggests, it is a painkiller that
also reduces swelling, and so is commonly prescribed if your pain
relates to some swelling or inflammation, such as with arthritis.
The best-known NSAID is aspirin. However, it and its derivatives, known
as salicylates, can cause gastrointestinal problems, such as stomach
bleeding and ulcers, a reaction common among all the NSAIDs.
A study of 204 patients found that large (2400 mg) and small (1200 mg)
daily doses of the NSAID ibuprofen worked about the same as high daily
doses (4000 mg) of acetaminophen—a non-aspirin, pain-relieving drug
used in many over-the-counter-preparations—in controlling pain and
inflammation.
According to Drs Peter M. Brooks and Richard O. Day, two Australian
rheumatologists: “The gastrointestinal effects of NSAIDs include
gastric erosion, peptic ulcer formation and perforation, major upper
gastrointestinal haemorrhage, and inflammation and change in the
permeability of the intestine and lower bowel.”
In case your doctor says that these risks are remote, Brooks and Day
quote another study showing that the risks of being hospitalised due to
gastrointestinal adverse effects are “seven times” that of patients not
given the NSAIDs. “These results led these investigators to suggest
that, in the United States, the syndrome of NSAID-associated
gastropathy accounts for at least 2,600 deaths and 20,000
hospitalizations each year in patients with rheumatoid arthritis
alone.”
In the UK, some 4,000 people die each year from taking NSAIDs—double
the number of deaths from asthma, while, in the USA, over 10,000 people
die every year from some gut-related problem caused by an NSAID.
Brooks and Day say that the elderly or those with a history of
peptic ulcers are at particular risk of gastrointestinal complications,
“including death”. They go on to conclude that NSAIDs are the direct
cause of 20 to 30 per cent of all cases of complications following
peptic ulcers.
The FDA now places a warning in with each NSAID prescription: “Serious
gastrointestinal toxicity such as bleeding, ulceration and perforation
can occur at any time, with or without warning symptoms, in patients
treated chronically with NSAID therapy.”
Besides ulcers, other studies have shown that ibuprofen can cause
colitis; and indomethacin, naproxen and a sustained release preparation
of ketoprofen may cause perforations of the colon. Ibuprofen has also
been linked to deaths among asthmatics, and has caused severe stomach
bleeding which has also been fatal, according to the Physicians’ Desk
Reference, the US’s drugs reference bible.
NSAIDs have also been known to cause Parkinson’s disease, hair and
fingernail loss, and damage to the liver and kidneys. Doctors from Beth
Israel, Harvard Medical School and elsewhere reported seven cases of
“significant hepatitis” and one death from using diclofenac sodium, an
NSAID marketed as Voltaren. Hepatitis can develop several weeks after
initiation of the drug and last four to six weeks after
discontinuation. One death has been reported even after early
withdrawal and three other deaths have been associated with this drug.
It is not known whether this particular drug is more likely to cause
hepatitis than any of the other NSAIDs.
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