Posts Tagged ‘Anti Inflammatory Drugs’

Common Medications for Dental Pain (Part 1)

January 29th, 2010

The pathophysiology of dental pain is a complex central and peripheral nervous system process, and the use of combination analgesics that act at multiple pain sites can improve dental pain relief. In general, for the treatment of mild to moderate dental pain, the most appropriate options are:

• Acetaminophen (Tylenol), 650mg every 4-6 hour as needed for dental pain; • Non-steroidal anti-inflammatory drugs, or NSAIDs (Advil, Motrin, Aleve), 400mg every 4-6 hours as needed for dental pain; and • COX-2-selective inhibitors, celecoxib (Celebrex) and rofecoxib (Vioxx), 25-50mg per day as needed for dental pain.

Acetaminophen: Acetic acid and p-aminophenol, or APAP—commonly known as acetaminophen—is classified as a nonnarcotic pain reliever. Dentists generally use it for mild to moderate dental pain. It acts as both anti-pain and anti-fever. It has rapid painkiller action. Acetaminophen, unlike nonsteroidal anti-inflammatory drugs, or NSAIDs, has little anti-inflammatory action. It generally is safe for acute dental pain. At very high single doses it causes liver damages.

Acetaminophen’s dose of 500-650 milligrams is good dental pain-reliever. However, such relief is brief, peaking one hour after administration. Significantly more dental pain relief can be provided by acetaminophen’s dose of 1,000 mg. At this dosage, the maximal efficacy of acetaminophen is achieved and last up to four hours after administration. There is no more oral pain relief in dose higher than 1000 mg. Because of this “ceiling-dose” effect, acetaminophen is good shot-term reliever for mild dental pain.

NSAIDs: NSAIDs have been the traditional treatment for moderate dental pain and inflammation. NSAIDs such as ibuprofen, ketorolac, flurbiprofen, ketoprofen, diclofenac, aspirin and aspirin derivatives diminish local dental pain. Long-term use of NSAIDs, however, can gastrointestinal distress, bleeding, kidney damages, and cardiovascular problems. Also, NSAIDs have been shown to interact with several high blood pressure drugs, which may compromise blood pressure control. The most common short-term side effects of NSAID usage are upset stomach, diarrhea and abdominal pain.

NSAIDs generally require a higher dose to achieve maximum anti-inflammatory and anti-pain effect. Dosage of 800 mg three times per day may be needed for dental pain. The FDA-recommended daily dose is 2,400 mg. Studies has indicated that no more dental pain reliever is achieved with higher-than-the-recommended dosage. Comparing to acetaminophen, NSAID’s are better pain killer, but they act slower and last about the same time (about 4 hours).

COX-2 NSAIDs: COX-2 NSAIDs were developed to limit NSAID’s adverse effects. The two COX-2-selective inhibitors, celecoxib (Celebrex) and rofecoxib (Vioxx) are characterized by the following:

• less risk of GI ulceration than nonselective NSAIDs; • similar types of other GI side effects, such as abdominal pain, dyspepsia, diarrhea and nausea; • lack of effect on platelet function, unlike nonselective NSAIDs; • renal toxicity similar to that of other NSAIDS; • generally long duration of action, with once-daily administration for rofecoxib and once- or twice-daily administration for celecoxib.

However, while COX-2 therapy may reduce the risk of GI ulcerations, recent evidence indicates that COX-2 therapy may not reduce the risk of cardiovascular complications (heart attacks). This is the reason why Vioxx is currently taken off the US market.



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Doctor. Do Rubs Work For Arthritis?

January 18th, 2010

Treatments for arthritis pain vary in terms of type, effectiveness, and mode of administration. Types of therapies include oral analgesics, topical analgesics, oral non-steroidal anti-inflammatory drugs (NSAIDS), topical NSAIDS, oral narcotics, and parenteral (meaning intramuscular or intravenous) narcotics.

As a general rule, for mild to moderate pain, narcotics should not be used. What this means is that the non-narcotic analgesics or NSAIDS are the drugs of choice.

The next decision to be made is, “Do I use an oral drug or will a topical agent, a rub, work just as well?”

So how does a patient choose?

One significant measure is efficacy. Does the agent really work?

The perception among many patients as well as physicians is that topical agents may not be as effective as oral drugs.

A recent study looked at this issue of effectiveness and patient preference in regards to oral versus topical NSAIDS.

Their conclusion? “In older patients with knee osteoarthritis, treatment with either oral or topical non-steroidal anti-inflammatory drugs (NSAIDs) had an equal effect on knee pain after one year,” according to the results of this randomized controlled trial reported in the British Medical Journal.

The study was conducted among patients from 26 general practices in the United Kingdom.

Patients eligible for study participation were over the age of 50 and had a history of knee pain on most days of the month for at least 3 months. All participants had been treated for knee pain in the 3 years before study enrollment. Patients with a history of peptic ulcer, significant indigestion, or kidney problems were excluded from study participation.

There were 2 treatment groups. In 1 group, patients were randomized to receive a recommendation for either topical or oral ibuprofen, at a dose determined by the patient. In the other intervention group, patient volunteers were left to decide for themselves whether they used topical or oral ibuprofen.

The volunteers were observed for 24 months. The primary outcome measure was the WOMAC Osteoarthritis Index questionnaire, which was used to assess knee pain and stiffness at 1 year. The WOMAC (Western Ontario McMaster) scale is typically used in arthritis studies to assess quality of life issues.

282 patients were included in the randomized trial and 303 patients participated in the patient preference study. The average age of the volunteers was 64 years, and baseline characteristics were similar regardless of study treatment. The mean global score on the WOMAC at baseline was 40 of a possible 100.

224 subjects in the preference study opted for topical treatment, whereas 79 chose oral ibuprofen. Patients with more severe or widespread pain generally selected oral therapy.

There was a modest change in WOMAC scores at 1 year, regardless of study therapy. WOMAC pain scores at 24 months slightly favored oral therapy, but this difference was not considered significant.

More patients in the topical ibuprofen group experienced significant pain at 3 months, which prompted 11% of the volunteers receiving topical treatment to change to oral ibuprofen.

Quality-of-life scores were similar between the oral and topical ibuprofen groups.

There were no differences in the rate of major side effects in the topical and oral ibuprofen groups. However, oral ibuprofen was associated with side effects involving the respiratory tract in 17% of participants compared to only 7% of subjects receiving topical ibuprofen. In addition, signs of kidney malfunction occurred more frequently in the oral ibuprofen treated patients.

Rates of changing treatment because of adverse effects were 1% and 16% in the topical and oral ibuprofen groups, respectively.

The conclusions were:

Patients with knee pain consider topical NSAIDs effective for mild pain but reserve oral NSAIDs for more severe or persistent pain. Patients generally believe that topical NSAIDs do not have adverse effects, but they will tolerate mild adverse effects associated with oral NSAIDs.

The current study suggests that topical NSAIDs are similarly effective to oral NSAIDs for knee pain for 1 year, and oral NSAIDs are associated with a higher rate of adverse effects.

Dr. Martin Underwood, who was the spokesperson for the research group conducting the study stated, “If topical NSAIDs are as effective as oral NSAIDs for reducing knee pain but produce fewer adverse effects, then topical treatment might be preferred.”

In our practice, we have found that topical agents are generally useful for patients with mild to moderate localized pain. However, if a patient has generalized pain, it makes no sense for them to slather a goo all over themselves.

A big bugaboo though with oral NSAIDS are the potential side effects, particularly in older patients.

One area not explored in the study was the use of pain patches. Lidoderm, which is a patch containing lidocaine, has been found to be helpful for some patients with arthritis, although an FDA approval has not yet been secured for this indication.

Newer NSAID patches containing diclofenac will also be available soon and these look very promising for local arthritis-related pain.

As far as topical agents that don’t contain NSAID, my favorite is Myorx which contains Omega-3 fatty acids. This helps provide anti-inflammatory effect without the potential problems associated with NSAIDS. For more information about Myorx, you can visit http://www.aocm.org or call the Arthritis and Osteoporosis Center of Maryland at (301) 694-5800.



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Journal Reports Dangers Of Nsaids

January 15th, 2010

issue of the Archives of Internal Medicine found that heart failure patients consuming nonsteroidal anti-inflammatory drugs (NSAIDs) may be at an increased risk for NSAIDs side effects and dangers. The article, from January 26, reported that, “nonsteroidal anti-inflammatory drugs are harmful to heart-failure patients.” The study reported that individuals who received the medications were subject to “dose-related increases in risk of death and re-hospitalization for heart failure.? According to the U.S. Food and Drug Administration (FDA), NSAIDs are drugs that are used “to treat pain and redness, swelling, and heart (inflammation) from medical conditions such as different types of arthritis, menstrual cramps and other types of short-term pains.? However, the NSAIDs have recently been associated with an increased risk of developing a heart attack/heart failure or stroke among patients who: * use NSAID medications for longer periods of time * people with heart disease * those who have or will undergo a coronary artery bypass graft Although these drugs are considered to have dangerous side effects, the study notes that their use is still widespread among a heart-diseased population, which could potentially lead to increased risks of heart failure among patients eventually causing death or coma. Heart Failure Causes In addition to the use of NSAIDs, there are several other causes of heart failure among many Americans which are enhanced by the consumption of NSAIDs, including the following, which were reported by the National Heart Lung and Blood Institute, as part of the U.S. Department of Health and Human Services: * coronary artery disease * high blood pressure * diabetes * heart muscle diseases * heart valve disorders * arrhythmias, also irregular heartbeats * congenital heart defects * treatments for cancer, radiation and chemotherapy * thyroid disorders * alcohol abuse * HIV/AIDS * cocaine and other illegal drugs * consumption of too much vitamin E NSAIDs Uses As the study noted, the popularity of NSAIDs continues to grow and many individuals use some form of NSAIDs on a daily or weekly basis for the following conditions: * acute gout * menstrual pain * renal colic * fever * tissue injury pain * rheumatoid arthritis * osteoarthritis * Reiter?s syndrome and other inflammatory arthropathies * metastatic bone pain * headache and migraine * post-operative pain Many NSAIDs are overlooked for their severe side effects, which cannot only cause heart failure, but can also cause the following side effects, according to the online medical resource for doctors, MedicineNet: * upset stomach * nausea * vomiting * heartburn * headache * diarrhea * constipation * drowsiness * unusual fatigue * stomach pain * swelling of feet or ankles * ringing in ears * vision changes * joint pain * muscle pain and weakness * easy bruising, bleeding * persistent sore throat * fever Additionally, MedicineNet reports that the following NSAID side effects must be reported immediately to a medical professional as they often signal a much more serious condition or allergic reaction. * changes in urine color * yellowing of eyes/skin * black stools * persistent stomach and abdominal pain * coffee ground appearing vomit * rash * itching * swelling * dizziness * difficulty breathing Prescription Drug Dangers There are several NSAIDs currently available on the market that are accompanied by severe side effects, one of which is Celebrex. Celebrex (celecoxib) is one of the NSAIDs drugs released from Pfizer in 1998 as a prescription only anti-inflammatory drug. Popular among arthritis patients, this NSAIDs is part of the COX-2 group of drugs. However, in late 2004, the drug came under scrutiny as the U.S. Food and Drug Administration (FDA) learned of additional Celebrex side effects, which might be damaging to patients. The FDA required the drug?s makers to increase the drug?s warning labels to include the newly discovered side effects. Many have insisted the drug be recalled believing that increased warning labels are not a sufficient method of avoiding damage to patients. An additional NSAID, which was recently removed from shelves because of risks including heart attack, stroke and Steven’s Johnson Syndrome (SJS), is known as Bextra from Pfizer. The syndrome, SJS, has a range of side effects including the development of skin rashes ranging up to blindness, depending on the severity of the condition. If an individual has previously or currently suffers from any of the Bextra side effects they may be eligible for the creation of a Bextra class action lawsuit, which could result in being awarded monetary compensation for damages endured by a victim. To learn more about developing litigation involving the use of NSAIDs, it is advisable for a victim to locate a pharmaceutical attorney. Frequently, a law firm specializing in pharmaceuticals will provide a free legal consultation to victims of the NSAIDs side effects including those who have consumed Celebrex or Bextra.

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