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Drug Information Table: NSAIDs, Acetaminophen, Opioids, and Glucocorticoids, Study notes of Nursing

notes on various nursing topics

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2022/2023

Uploaded on 04/24/2023

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Drug Information Table
NSAIDs (COX-1 and COX-2 Inhibitors) – aspirin (ASA); ibuprofen (Advil, Motrin)
THERAPEUTIC USE Inflammation suppression
Analgesia for mild to moderate pain
Fever reduction
Dysmenorrhea
Inhibition of platelet aggregation (aspirin)
ADVERSE DRUG
REACTIONS
Gastric upset, heartburn, nausea, gastric ulceration
Bleeding (less with non-aspirin NSAIDs)
Kidney dysfunction
Salicylism (aspirin)
Reye’s syndrome (aspirin)
Thromboembolic events (non-aspirin NSAIDs)
INTERVENTIONS Monitor for signs of gastrointestinal bleeding (black or dark-colored stools, ab-
dominal pain, nausea, hematemesis).
Test for and treat Helicobacter pylori infection prior to long-term therapy.
For clients at high risk for gastric bleeding, recommend a proton pump inhibitor.
Monitor for signs of bleeding (easy bruising, petechiae, excessive bleeding from
minor injuries).
Monitor intake and output; watch for low urine output and fluid retention.
Monitor for rapid rises in BUN and creatinine.
Monitor for tinnitus, diaphoresis, headache, dizziness, and respiratory alkalosis.
Stop aspirin therapy for clients reporting these symptoms.
Recommend acetaminophen (Tylenol) and not aspirin or NSAIDs for children and
adolescents under age 18 who have viral infections, particularly chickenpox and
influenza.
Recommend non-aspirin NSAIDs for short periods and in low doses only.
Recommend low-dose aspirin to prevent these events if prescribed by provider.
Monitor for signs of myocardial infarction and cerebrovascular accident.
ADMINISTRATION Make sure clients swallow enteric-coated or sustained-release forms whole and
do not crush or chew them.
Discontinue 1 week before scheduled surgery.
Monitor for initial and continued therapeutic effects.
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Drug Information Table

NSAIDs (COX-1 and COX-2 Inhibitors) – aspirin (ASA); ibuprofen (Advil, Motrin)

THERAPEUTIC USE •^ Inflammation suppression

  • Analgesia for mild to moderate pain
  • Fever reduction
  • Dysmenorrhea
  • Inhibition of platelet aggregation (aspirin) ADVERSE DRUG REACTIONS
  • Gastric upset, heartburn, nausea, gastric ulceration
  • Bleeding (less with non-aspirin NSAIDs)
  • Kidney dysfunction
  • Salicylism (aspirin)
  • Reye’s syndrome (aspirin)
  • Thromboembolic events (non-aspirin NSAIDs) INTERVENTIONS •^ Monitor for signs of gastrointestinal bleeding (black or dark-colored stools, ab- dominal pain, nausea, hematemesis).
  • Test for and treat Helicobacter pylori infection prior to long-term therapy.
  • For clients at high risk for gastric bleeding, recommend a proton pump inhibitor.
  • Monitor for signs of bleeding (easy bruising, petechiae, excessive bleeding from minor injuries).
  • Monitor intake and output; watch for low urine output and fluid retention.
  • Monitor for rapid rises in BUN and creatinine.
  • Monitor for tinnitus, diaphoresis, headache, dizziness, and respiratory alkalosis. Stop aspirin therapy for clients reporting these symptoms.
  • Recommend acetaminophen (Tylenol) and not aspirin or NSAIDs for children and adolescents under age 18 who have viral infections, particularly chickenpox and influenza.
  • Recommend non-aspirin NSAIDs for short periods and in low doses only.
  • Recommend low-dose aspirin to prevent these events if prescribed by provider.
  • Monitor for signs of myocardial infarction and cerebrovascular accident. ADMINISTRATION •^ Make sure clients swallow enteric-coated or sustained-release forms whole and do not crush or chew them.
  • Discontinue 1 week before scheduled surgery.
  • Monitor for initial and continued therapeutic effects.

CLIENT INSTRUCTIONS •^ Take with food, milk, or 8 oz of water to minimize gastrointestinal effects.

  • Avoid alcohol.
  • Report persistent gastric irritation and signs of bleeding.
  • Report any unusual or prolonged bleeding.
  • Report changes in urine output, weight gain, or signs of fluid retention such as edema or bloating.
  • Report ringing or buzzing in the ears, sweating, headache, and dizziness.
  • Stop taking aspirin if these symptoms develop.
  • Do not give aspirin or NSAIDs to children under age 19 who have viral infections, particularly chickenpox and influenza; use acetaminophen instead.
  • Report chest pain or heaviness, shortness of breath, sudden and severe headache, numbness, weakness, visual disturbances, or confusion.
  • Take low-dose aspirin once daily to reduce the risk of heart attack and stroke if prescribed.

CONTRAINDICATIONS •^ Teratogenic

  • Hypersensitivity to aspirin and other NSAIDS
  • Peptic ulcer disease
  • Bleeding disorders (hemophilia, vitamin K deficiency)
  • Children or adolescents with chickenpox or influenza (especially aspirin)
  • Perioperative use prior to coronary artery bypass grafting (non-aspirin NSAIDs)
  • Within 1 week of any elective surgery (aspirin)

PRECAUTIONS •^ Older adults

  • Cigarette smoking
  • Alcohol use disorder
  • Helicobacter pylori infection
  • Heart failure
  • Hypertension
  • Hypovolemia
  • Asthma
  • Chronic urticaria
  • Advanced kidney dysfunction

INTERACTIONS •^ Anticoagulants, glucocorticoids, and alcohol increase the risk of bleeding.

  • Ibuprofen decreases the antiplatelet effects of low-dose aspirin.
  • ACE inhibitors and angiotensin receptor blockers increase the risk of kidney failure.
  • Antihypertensive effects of ACE inhibitors decrease the risk of lithium carbonate (Lithobid) and methotrexate toxicity increases.

PRECAUTIONS •^ Alcohol use disorder

  • Heart failure
  • Diabetes mellitus
  • Hypertension
  • Asthma
  • History of gastrointestinal bleeding or peptic ulcer disease
  • Cardiovascular disease
  • Mild or moderate liver impairment
  • Renal insufficiency
  • Cerebrovascular accident

INTERACTIONS •^ Diuretic effects of furosemide (Lasix) decrease.

  • Fluconazole (Diflucan) increases celecoxib levels.
  • Anticoagulant effects of warfarin (Coumadin) increase.
  • Glucocorticoids and alcohol increase the risk of bleeding.
  • Antihypertensive effects of ACE inhibitors decrease.
  • Risk of lithium carbonate (Lithobid) toxicity increases.

Drug Information Table

Acetaminophen – acetaminophen (Tylenol)

THERAPEUTIC USE •^ Analgesia for mild to moderate pain

  • Fever reduction ADVERSE DRUG REACTIONS
  • Liver damage (overdose)
  • Hypertension (with daily use, particularly women) INTERVENTIONS •^ Monitor for early symptoms of overdose/poisoning (abdominal discomfort, nau- sea, vomiting, sweating, diarrhea); liver damage results in 48 to 72 hr following overdose.
  • Prepare to administer acetylcysteine (Mucomyst, Acetadote) orally or IV to coun- teract overdose and reduce liver injury.
  • Monitor blood pressure. ADMINISTRATION •^ Administer orally or rectally.
  • Caution clients that the drug is available in many combination products as well as many formulations; clients must read labels carefully to avoid overdose.
  • Do not administer more than 4 g/day (adults).
  • Infants and children should be given the manufacturer’s recommended dose based on their age. CLIENT INSTRUCTIONS •^ Do not exceed 4 g/day (adults).
  • Report any abdominal discomfort, nausea, vomiting, sweating, or diarrhea imme- diately.
  • Have blood pressure checked regularly. CONTRAINDICATIONS •^ Alcohol use disorder PRECAUTIONS •^ Anemia
  • Immunosuppression
  • Hepatic or kidney disease INTERACTIONS •^ Alcohol increases the risk of liver injury (with high doses of acetaminophen).
  • Warfarin (Coumadin) increases the risk of bleeding.
  • Cholestyramine (Questran) reduces absorption.

INTERACTIONS •^ Monoamine oxidase inhibitors (MAOIs) pose a risk for hypertensive crisis.

  • Selective serotonin reuptake inhibitors, serotonin-norepinephrine reuptake inhibitors, tricyclic antidepressants, MAOIs, and triptans pose a risk for serotonin syndrome.
  • Responses to CNS depressants increase.
  • Carbamazepine (Tegretol) decreases levels.
  • St. John’s wort increases sedative effects.

Drug Information Table

Opioid agonists – morphine

THERAPEUTIC USE •^ Analgesia for moderate to severe pain

  • Preoperative sedation and anxiety reduction
  • NOTE: For detailed information about fentanyl (Sublimaze), see the Neurological System 1 module. ADVERSE DRUG REACTIONS
  • Respiratory depression
  • Sedation, dizziness, lightheadedness, drowsiness
  • Constipation
  • Nausea, vomiting
  • Orthostatic hypotension
  • Urinary retention
  • Cough suppression
  • Potential for abuse along with tolerance and cross-tolerance with other opioids (larger doses required for usual effect) INTERVENTIONS •^ Monitor vital signs, pulse oximetry, lung sounds.
  • For respiratory rates below 12/min, withhold the drug and stimulate breathing.
  • Administer an opioid antagonist such as naloxone to restore respiratory rate.
  • Monitor clients when ambulating.
  • Monitor bowel function.
  • Administer fiber supplement and/or stool softeners.
  • Administer an antiemetic.
  • For vomiting, ensure adequate hydration.
  • Monitor blood pressure.
  • Monitor intake and output, watching for signs of urinary retention, such as blad- der distention.
  • Encourage clients to urinate every 4 hr.
  • Prepare to insert a urinary catheter to drain the bladder.
  • Auscultate lung sounds regularly.
  • Encourage clients (especially postoperatively) to cough frequently to prevent a buildup of respiratory secretions.
  • Have suction equipment available.
  • Recommend the lowest possible effective dose and short-term only.
  • Advise clients with physical dependence not to discontinue opioids abruptly; taper the dose over 3 days. ADMINISTRATION •^ Measure baseline vital signs before administration and monitor throughout therapy.
  • Administer orally, IM, IV, SC, rectally, or epidurally.
  • Make sure clients swallow sustained-release forms whole and do not crush or chew them.
  • Administer IV opioids slowly and with recommended dilution over 4 to 5 min; have naloxone and resuscitation equipment available.
  • Monitor PCA use and pump settings carefully.
  • Administer to clients with cancer on a fixed, around-the-clock dosing schedule, not PRN.

Drug Information Table

Opioid agonist-antagonists – butorphanol, pentazocine (Talwin, Talwin NX)

THERAPEUTIC USE •^ Analgesia for moderate to severe pain

  • Anesthesia adjunct ADVERSE DRUG REACTIONS
  • Respiratory depression (limited)
  • Sedation, dizziness, lightheadedness, drowsiness, headache
  • Nausea
  • Increased cardiac workload
  • Abstinence syndrome (hypertension, vomiting, cramping in opioid-dependent clients) INTERVENTIONS •^ Measure baseline vital signs.
  • Monitor respirations.
  • For respiratory rates below 12/min, withhold the drug and stimulate breathing.
  • Monitor clients when ambulating.
  • Consider alternative drug if nausea does not resolve.
  • Do not administer to clients with myocardial infarction or cardiac insufficiency.
  • Ask clients about opioid use before administration. ADMINISTRATION •^ Administer butorphanol IM, IV, or intranasally and pentazocine orally (in combina- tion with acetaminophen or naloxone), subcutaneously, IM, or IV.
  • Measure baseline vital signs before administration and monitor throughout ther- apy. Do not give the drug if the respirations are slower than 12/min.
  • Have naloxone and resuscitation equipment available.
  • For intranasal administration, give one spray and repeat every 60 to 90 min as needed.
  • For preoperative IM administration, give 60 to 90 min before surgery.
  • Monitor therapeutic effects.
  • Do not discontinue the drug abruptly. CLIENT INSTRUCTIONS •^ Use the drug only when needed and short-term.
  • Do not take prior to driving or activities requiring mental alertness.
  • Sit or lie down if feeling lightheaded.
  • Change positions gradually.
  • Lie down when feeling nauseated.
  • Do not use for anginal pain.
  • Do not take opioids while taking butorphanol. CONTRAINDICATIONS •^ Acute myocardial infarction
  • Opioid dependence PRECAUTIONS •^ Schedule IV controlled substance
  • History of substance abuse
  • Cardiac insufficiency
  • Reduced respiratory reserve
  • Head injury, increased intracranial pressure
  • Hypertension
  • Hepatic or kidney disease

INTERACTIONS •^ CNS depressants (barbiturates, phenobarbital, benzodiazepines, and alcohol) increase CNS depression and increase the risk of respiratory depression.

  • Opioid effects decrease.

Drug Information Table

Uricosurics/Antihyperuricemic – allopurinol (Zyloprim)

THERAPEUTIC USE •^ Hyperuricemia due to chronic tophaceous gout, cancer chemotherapy, and some blood dyscrasias ADVERSE DRUG REACTIONS

  • Hypersensitivity syndrome (fever, rash, eosinophilia, liver and kidney dysfunction)
  • Gastrointestinal disturbances (nausea, vomiting, diarrhea)
  • Drowsiness, headache, vertigo
  • Agranulocytosis, aplastic anemia, bone marrow depression
  • Metallic taste in the mouth
  • Cataracts (with drug therapy longer than 3 yr) INTERVENTIONS •^ Monitor for symptoms of hypersensitivity syndrome.
  • Stop drug therapy immediately for signs of hypersensitivity syndrome.
  • For vomiting, ensure adequate hydration.
  • Give after meals.
  • Monitor clients when ambulating.
  • Give mild analgesic for headache.
  • Monitor CBC.
  • Monitor for unusual taste sensations.
  • Recommend regular ophthalmologic examinations. ADMINISTRATION •^ Give orally or IV.
  • Monitor uric acid levels (initially, every 1 to 2 weeks to establish the appropriate dosage).
  • Obtain baseline CBC and test liver and kidney function before therapy and moni- tor periodically thereafter.
  • Allow crushing tablets and mixing them with food or fluid.
  • Administer IV using recommended dilution and infuse over 30 to 60 minutes
  • Make sure clients drink at least 3 L of fluid per day. CLIENT INSTRUCTIONS •^ Report fever, rash, abdominal pain, swelling, or low urine output immediately and stop taking the drug.
  • Take the drug with food.
  • Avoid driving or activities requiring mental alertness if drowsy.
  • Try over-the-counter analgesics as needed to relieve headache.
  • Report bleeding, easy bruising, or sore throat.
  • Suck on hard candy or chew gum to minimize unusual taste sensations.
  • Report blurred vision and/or loss of color acuity.
  • Minimize exposure of eyes to sunlight.
  • Obtain periodic eye examinations. CONTRAINDICATIONS •^ Hypersensitivity to allopurinol PRECAUTIONS •^ Bone marrow depression
  • Liver or kidney dysfunction
  • Peptic ulcer disease
  • Lower gastrointestinal tract disease

INTERACTIONS •^ Warfarin (Coumadin) requires lower dosages.

  • The risk of mercaptopurine (Purinethol), theophylline (Theolair), and azathioprine (Imuran) toxicity increases.
  • Ampicillin (Principen) increases the risk for rash.

CLIENT INSTRUCTIONS •^ Report increased stress, as higher dosages are required at such times.

  • Taper the dose before discontinuing it.
  • Report polyphagia, polydipsia, and polyuria.
  • Report muscle pain or weakness.
  • Avoid taking NSAIDs.
  • Take the drug with food or meals.
  • Report indigestion or bloody vomitus as well as black, tarry stools.
  • Report signs of infection, such as a sore throat.
  • Report weight gain or edema (hypernatremia).
  • Report weakness (hypokalemia).
  • Understand that long-term therapy may cause some changes in fat distribution throughout the body.
  • Take the drug on alternate days for long-term therapy.
  • Perform weight-bearing exercise daily.
  • Consume adequate calcium and vitamin D.
  • Report blurred vision and loss of color acuity.
  • Minimize exposure of eyes to sunlight.
  • Obtain periodic eye examinations.

CONTRAINDICATIONS •^ Recent live virus immunization

  • Systemic fungal infection
  • Cataracts

PRECAUTIONS •^ Heart failure

  • Peptic ulcer disease
  • Diabetes mellitus
  • Hypertension
  • Kidney dysfunction
  • Myasthenia gravis
  • Osteoporosis

INTERACTIONS •^ Potassium-depleting diuretics, such as furosemide (Lasix), increase risk of hypoka- lemia.

  • The risk of digoxin-induced dysrhythmias increases with digoxin.
  • NSAIDs increase risk of gastrointestinal bleeding and ulceration.
  • Effects of insulin and oral hypoglycemics decrease in clients who have diabetes.
  • Prednisone prevents the body from responding to vaccines
  • Live vaccine administration increases risk for decreased antibody response and increased risk of adverse effects