Ortho Pharm Review Flashcards

1
Q

What two NSAIDs are preferred for most patients?

A

Naproxen and ibuprofen

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2
Q

What does the inhibition of COX impair the transformation of?

A

Arachadonic acid → prostaglandins → prostacyclin and thromboxanes

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3
Q

How soon does platelet function normalize after discontinuation of most NSAIDs?

A

within 3 days

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4
Q

Adverse effect of NSAIDs which is why you may want to avoid NSAIDs for up to 90 days post fracture

A

may cause non-union

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5
Q

How is aspirin different from other NSAIDs?

A

irreversible platelet inhibition for the life of the platelet

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6
Q

Name the NSAID with less CV risk compared to others

A

naproxen (aleve)

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7
Q

Good choice for treatment of acute or chronic pain if an NSAID is indicated

A

naproxen (aleve)

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8
Q

What is the maximum dose of ibuprofen per day?

A

2400 mg per day

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9
Q

Name the acetic acid NSAIDs

A
IV Ketorolac (Toradol)
Indomethacin (Indocin)
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10
Q

Treatment of moderate to severe postoperative pain. Risk of gastropathy when used > 5 days

A

ketorolac (toradol)

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11
Q

Used for treatment of acute gout and pericarditis mainly. May be associated with aplastic anemia

A

indomethacin (indocin)

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12
Q

Name the oxicam NSAIDs

A

Meloxicam (Mobic)

Prioxicam (Feldene)

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13
Q

Long duration of effect (Qday dosing). Relatively COX-2 selective at lower total dose of 7.5 mg

A

meloxicam (mobic)

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14
Q

An option for treatment of chronic pain and inflammation poorly responsive to other NSAIDs. Daily doses of ≥ 20 mg increase risk of serious GI complications

A

piroxicam (feldene)

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15
Q

Name the selective cox-2 inhibitor

A

Celecoxib (Celebrex)

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16
Q

No effect on platelet function. Decreased GI toxicity. Dose related renal and CV effects

A

celecoxib (celebrex)

17
Q

Considered a weak opioid. For mild to moderate pain

Schedule III. Metabolized to morphine

A

codeine

18
Q

Schedule III. For moderate to severe pain. Onset of action 10-20 min. In combination with acetaminophen

A

hydrocodone (vicodin)

19
Q

Schedule II. Moderate to moderately severe pain. Onset of action 10-30 minutes. In combination with acetaminophen. Avoid long acting combinations for acute pain

A

oxycodone (percocet)

20
Q

Used to reverse respiratory depression, sedation and analgesia

A

naloxone

21
Q

What are the toxicities of all opioids in general?

A

sedation, constipation, decreased effectiveness of diuretics, QT prolongation

22
Q

Name the extended release and long acting opioid analgesics

A

morphine, buprenorphine, methadone, fentanyl, hydromorphone

23
Q

can increase release and absorption of transdermal opioid analgesics

A

heat exposure

24
Q

Not a controlled substance but high potential for physical and psychological dependence. Works at the mu receptors and also inhibits NE and serotonin. Effective for relief of neuropathic pain

A

tramadol

25
Q

Where is tramadol extensively metabolized?

A

liver

26
Q

Name the skeletal muscle relaxants

A

Cyclobenzaprine (Flexeril)
Tizanadine (Zanaflex)
Metaxalone (Skelaxin)
Diazepam (Valium)

27
Q

Where is most benefit of muscle relaxants observed?

A

first 1-2 weeks of therapy

28
Q

Which two muscle relaxants have a high potential for abuse and should be used for only a few days?

A

Diazepam (Valium) and carisoprodol (Soma)

29
Q

What drug class might muscle relaxants have a synergistic effect when used as treatment for acute low back pain?

A

NSAIDs

30
Q

When used in combination with narcotics offers the best relief

A

NSAIDs or acetaminophen

31
Q

When do you switch from a PCA pump to oral narcotics?

A

once patient is able to tolerate PO intake