Share This Link

Celecoxib does not block both COX-1 and COX-2 enzymes, but only COX-2 enzyme. Therefore, it does not have more anti-inflammatory and analgesic effects than nonselective COX inhibitors, but similar effects .

Celecoxib does not inhibit vasodilatory and antiplatelet prostaglandins produced by COX-2 in the endothelium, but rather it inhibits the production of these prostaglandins by COX-2 in the inflammatory sites. Therefore, it does not have less cardiovascular risk than nonselective COX inhibitors, but more risk .

Celecoxib does not block the production of prostaglandins involved in fever and platelet aggregation, but rather it spares the production of these prostaglandins by COX-1. Therefore, it does not have more antipyretic and antiplatelet effects than nonselective COX inhibitors, but none or minimal effects .

It is not a specific indication of aspirin in rheumatoid arthritis, but a general indication of aspirin in cardiovascular prevention. Aspirin can prevent cardiovascular events such as myocardial infarction and stroke by inhibiting platelet aggregation and thromboxane synthesis, but this effect requires low doses of aspirin that are not effective for rheumatoid arthritis .

Option C is wrong because it is not the mechanism of action of aspirin, but of allopurinol, a drug used for gout. Aspirin does not inhibit the enzyme xanthine oxidase and reduce the production of uric acid, but rather it inhibits both COX-1 and COX-2 enzymes and blocks the production of prostaglandins. Aspirin is not used to treat gouty arthritis, but rather it can worsen it by increasing uric acid levels in the blood and decreasing its excretion in the urine.

Option D is wrong because it is not the mechanism of action of aspirin, but of misoprostol, a drug used for labor induction. Aspirin does not stimulate uterine contractions and cervical ripening by blocking the production of prostaglandins, but rather it inhibits both COX-1 and COX-2 enzymes and blocks the production of prostaglandins. Aspirin is not used to induce labor, but rather it is contraindicated in pregnancy because it can cause bleeding complications, premature closure of the ductus arteriosus, and delayed onset of labor.

These are the most common and serious side effects of indomethacin and other NSAIDs . They occur because indomethacin blocks the production of prostaglandins that protect the gastric mucosa from acid and pepsin, maintain the mucosal blood flow, and promote healing of ulcers. The risk of these effects is higher in older adults, those with a history of peptic ulcer disease or gastrointestinal bleeding, those who use alcohol or tobacco, and those who take other drugs that irritate the stomach, such as corticosteroids or anticoagulants . The nurse should advise the client to take indomethacin with food or milk, avoid alcohol and tobacco, report any signs of gastrointestinal bleeding (such as black or tarry stools, abdominal pain, vomiting blood), and use the lowest effective dose for the shortest duration possible .

These are less common but potentially serious side effects of indomethacin and other NSAIDs . They occur because indomethacin blocks the production of prostaglandins that regulate renal blood flow, glomerular filtration rate, sodium excretion, and water balance. The risk of these effects is higher in those with preexisting renal impairment, heart failure, liver cirrhosis, dehydration, or hypovolemia, and those who use diuretics or angiotensin-converting enzyme inhibitors . The nurse should monitor the client's fluid intake and output, body weight, blood pressure, electrolytes, and renal function tests, and report any signs of renal dysfunction (such as oliguria, anuria, edema) or worsening heart failure (such as dyspnea, fatigue) to the doctor .

These are rare but potentially fatal side effects of indomethacin and other NSAIDs . They occur because indomethacin blocks the production of prostaglandins that inhibit platelet aggregation and vasodilation. The risk of these effects is higher in those with a history of cardiovascular disease or risk factors such as hypertension, diabetes mellitus, hyperlipidemia, smoking, or obesity . The nurse should assess the client's cardiovascular status and history before starting indomethacin therapy and advise the client to seek immediate medical attention if they experience any signs of a heart attack (such as chest pain or pressure) or a stroke (such as sudden weakness or numbness on one side of the body) while taking this drug.

Option B is wrong because acetaminophen does not reduce inflammation, pain, and swelling, but only pain and fever. Acetaminophen does not inhibit the synthesis of prostaglandins in the peripheral tissues, where they mediate inflammation and pain, but only in the central nervous system and the hypothalamus, where they modulate pain perception and body temperature.

Option C is wrong because acetaminophen does not reduce the risk of gastrointestinal bleeding and ulceration, but rather it has no effect on it. Acetaminophen does not inhibit the synthesis of prostaglandins in the gastrointestinal mucosa, where they protect the lining from acid and enzymes, but only in the central nervous system and the hypothalamus. Therefore, acetaminophen is safer than nonselective COX inhibitors for patients with peptic ulcer disease or bleeding disorders.

Option D is wrong because acetaminophen does not reduce the risk of hepatotoxicity and liver impairment, but rather it can cause it if taken in high doses or with alcohol or other drugs that affect the liver. Acetaminophen is metabolized by the liver into a toxic intermediate that can deplete glutathione, a substance that protects the liver cells from damage. If the amount of this intermediate exceeds the amount of glutathione, liver injury can occur.

Ketorolac can cause gastrointestinal effects such as nausea, vomiting, ulceration, bleeding, and perforation because it inhibits the synthesis of prostaglandins that protect the gastric mucosa .

Ketorolac can cause hypotension by inhibiting the synthesis of prostaglandins that regulate blood pressure and renal blood flow . It can also cause thrombophlebitis by irritating the vein wall and activating platelets.

Ketorolac can cause renal impairment by reducing the glomerular filtration rate and causing sodium and water retention, edema, hypertension, and acute renal failure . It can also cause gastrointestinal bleeding by inhibiting the synthesis of prostaglandins that maintain mucosal blood flow and integrity .