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A high-yield walkthrough of the medication classes, mechanisms, safety rules, and priority actions that show up again and again in nursing pharmacology.
How to Use This Guide
- Each tab groups related drug classes so you can compare them side-by-side (e.g., H2 blockers vs. PPIs).
- Tap any flip card to reveal its meaning; tap any scenario to reveal the answer; tap accordion headers to expand.
- Quick Checks (green boxes) let you self-test inline; the Mastery Quiz tab is a full run-through.
- Track your progress with the checklist below — it saves automatically in your browser.
In pharmacology, the most-tested question is not "what drug?" but "what do I do first?" When a patient is unstable — respiratory depression, anaphylaxis, severe hypotension, uterine rupture, QT prolongation — the answer is almost always stop the drug / reverse it, then call for help.
Three-Day Study Plan
- Day 1: Analgesics & Opioids → Anti-Infectives. Focus on the MOA × safety pairs (e.g., opioid ↔ naloxone, warfarin ↔ metronidazole).
- Day 2: GI & Antiemetics → Respiratory → Neuro & Psych. Drill the "never stop abruptly" list and the narrow-window drugs.
- Day 3: Hormones → Fluids & TPN → Med Safety (pharmacokinetics + administration). Finish with the Mastery Quiz; target 90%+.
Mastery Checklist
Check off each objective as you master it. Progress saves automatically in this browser.
- NSAIDs — COX inhibition, GI/renal risks, acetaminophen as the safer alternative
- Acetaminophen — hepatotoxicity, max dose, acetylcysteine antidote
- Opioids — RR check, constipation, taper, toxicity triad + naloxone
- Gout — allopurinol for prevention vs. NSAIDs/colchicine for acute attacks
- Antibiotic principles — C. diff, birth-control interaction, anaphylaxis, side effect vs. allergy
- Bactericidal vs. bacteriostatic + class examples
- Sulfonamides (TMP-SMX) — UTI use, pregnancy avoidance
- Macrolides / fluoroquinolones / aminoglycosides / glycopeptides — key risks
- Metronidazole (metallic taste, warfarin), antiretrovirals (adherence), nystatin (swish & swallow)
- H2 blockers vs. PPIs vs. sucralfate; loperamide contraindications
- Antiemetics — metoclopramide (tardive dyskinesia) & ondansetron (QT)
- Bulk-forming laxatives (psyllium) — must be taken with water
- Albuterol (rescue) vs. fluticasone (controller) + correct inhaler technique
- Ipratropium (soy allergy), montelukast (black box), theophylline (narrow window)
- Lithium — narrow therapeutic window, kidney excretion, toxicity triggers
- Antipsychotics (EPS), TCAs (2nd line), benzodiazepines (flumazenil), diphenhydramine (anticholinergic)
- Corticosteroids — taper (adrenal crisis), long-term effects
- Oxytocin, testosterone, estradiol, finasteride, sildenafil safety points
- IV potassium (never push), IV fluid tonicity, TPN hyperglycemia & infection
- ADME, first-pass effect, loading doses, routes, crush rules, 6 rights
- Antidote pairs + drugs you must never stop abruptly
Analgesics & Opioids
NSAIDs, acetaminophen, opioids, their antidotes, and gout therapy — the pain-management cornerstones and their biggest dangers.
NSAIDs (ibuprofen, naproxen, ketorolac)
- MOA: inhibit the COX-1 and COX-2 enzymes, reducing prostaglandin synthesis → less pain, fever, and inflammation.
- Contraindications: peptic ulcer disease (PUD) and chronic kidney disease — NSAIDs irritate the GI lining and reduce renal perfusion.
- Adverse effects: gastric ulcers, GI bleeding (watch for positive fecal occult blood), and kidney injury.
- Key teaching: for a patient with gastric or renal problems, acetaminophen is the safer analgesic because it does not disrupt the stomach lining or kidneys.
Think "COX blocks the aches": NSAIDs block CycloOXygenase → fewer prostaglandins → less pain & swelling. Same enzyme that protects the stomach (COX-1), which is why ulcers are the trade-off.
Ketorolac is an NSAID — it is not a "gentle" option. Avoid in CKD and PUD just like any other NSAID. Question the order rather than "giving a smaller dose."
Acetaminophen (Tylenol)
- Mechanism: central analgesic/antipyretic — no GI or renal effects, making it first choice in PUD and kidney disease.
- Toxic metabolite: overdose depletes glutathione, allowing NAPQI to damage the liver → hepatotoxicity.
- Antidote: acetylcysteine (replenishes glutathione, neutralizes NAPQI).
- Dosing limits: 4 g/day in healthy adults; 2 g/day in at-risk patients (liver disease, chronic alcohol use, malnutrition).
High-Yield: acetaminophen is hidden in many combination products (cold remedies, opioid-combo pills). Teach patients to read every label to avoid accidental overdose.
Opioids (morphine, codeine, hydromorphone)
- Priority assessment: respiratory rate before, during, and after administration. Hold if RR < 12/min and notify the provider.
- Most common side effect: constipation — it does not diminish with time. Manage with fluids, fiber, and a stool softener/laxative.
- Other effects: orthostatic hypotension (change positions slowly), sedation (avoid driving), and suppression of the cough reflex.
- Discontinuation: never stop abruptly — taper gradually to avoid withdrawal (muscle aches, sweating, insomnia, GI upset).
- COPD caution: opioids further depress an already-compromised respiratory drive — assess carefully and question the order if needed.
- Never combine: two opioids (or any CNS depressants) cause additive respiratory depression and overdose risk.
Overdose = respiratory depression + pinpoint pupils (miosis) + decreased LOC. Give naloxone immediately. Naloxone is shorter-acting than most opioids — the patient may need repeat doses.
Gout: Allopurinol
- MOA: inhibits xanthine oxidase, lowering uric acid production.
- Role: long-term prevention, NOT acute attack treatment (acute flares use NSAIDs or colchicine). Continue even when asymptomatic.
- Teaching: drink plenty of water (prevents kidney stones); avoid purine-rich foods (shellfish, red meat, organ meats, alcohol).
- Report immediately: fever, sore throat, or rash — possible Stevens-Johnson Syndrome, a life-threatening hypersensitivity reaction.
Allopurinol prevents gout by lowering uric acid; it does not relieve the pain of an active flare. A patient mid-flare needs an anti-inflammatory (NSAID/colchicine), not just their allopurinol.
A patient who received IV morphine is found somnolent with a respiratory rate of 7 and pinpoint pupils.
Anti-Infectives
General antibiotic principles plus the major classes — their mechanisms, side effects, and the safety flags each one is famous for.
Antibiotic Principles (Apply to Every Class)
- C. difficile: antibiotics wipe out normal gut flora, allowing C. diff to overgrow → severe watery diarrhea. Report new diarrhea during therapy.
- Contraception interaction: antibiotics can reduce hormonal-contraceptive effectiveness — teach a backup method (e.g., condoms) during treatment.
- Anaphylaxis: wheezing, hives, hypotension → stop the infusion, call the provider, give epinephrine.
- Side effect vs. allergy: side effects are expected and predictable; allergic reactions are immune-mediated, unexpected, and potentially life-threatening.
- Finish the full course — stopping early breeds resistance.
Bactericidal vs. Bacteriostatic
| Action | Meaning | Examples |
|---|---|---|
| Bactericidal | Kills bacteria directly | Penicillins, vancomycin, fluoroquinolones, gentamicin |
| Bacteriostatic | Stops growth; immune system clears the rest | Macrolides, tetracyclines, sulfonamides |
"CIDAL = kill" (think homi-CIDAL). Bacteriostatic drugs stall the bacteria so your own immune system can finish the job.
Sulfonamides — Sulfamethoxazole / TMP-SMX (Bactrim)
- Use: most commonly prescribed for urinary tract infections (also respiratory infections and PCP prophylaxis).
- Safety: avoid in the first trimester of pregnancy (birth-defect risk); use caution in kidney disease (higher toxicity risk).
Macrolides (azithromycin, erythromycin, clarithromycin)
- Recognition: end in "-mycin".
- MOA: bacteriostatic — bind the 50S ribosomal subunit to block bacterial protein synthesis.
- Use: respiratory infections; a common penicillin alternative.
Careful: gentamicin is an aminoglycoside (also ends in "-mycin") but is bactericidal at the 30S subunit — don't lump all "-mycin" drugs as macrolides.
Fluoroquinolones (ciprofloxacin, levofloxacin, moxifloxacin)
- Recognition: end in "-oxacin"; bactericidal (inhibit DNA replication).
- Absorption trap: antacids with calcium/magnesium/aluminum, and iron, chelate the drug. Space doses — take the antibiotic 2 hours before or 6 hours after antacids/iron. Avoid dairy close to the dose.
- Adverse effect: tendonitis and tendon rupture (especially the Achilles) — higher risk in older adults and those on corticosteroids.
Aminoglycosides — Gentamicin
- MOA: bactericidal — binds the 30S ribosomal subunit.
- Two critical toxicities: nephrotoxicity (rising BUN/creatinine, falling urine output) and ototoxicity (tinnitus, hearing loss, vertigo).
- Monitoring: peak and trough drug levels.
Vancomycin (glycopeptide)
- Red Man Syndrome: rapid infusion → histamine release → red flushing of face/neck/chest + itching. Not a true allergy. Slow or stop the infusion; give diphenhydramine if ordered.
- Prevention: infuse over at least 60 minutes.
- Toxicities: nephrotoxicity (oliguria, rising creatinine) and ototoxicity — monitor peak/trough levels and renal function.
Metronidazole (antiprotozoal / anaerobic)
- Expected side effects: GI upset, metallic taste, and dry mouth — reassure the patient these are normal and resolve after treatment.
- Key interaction: metronidazole increases warfarin's effect → higher bleeding risk — monitor INR and expect a warfarin dose adjustment.
Antiretrovirals (ART for HIV) & Nystatin
- ART #1 priority: adherence. Regimens use 2–3 medications; missed doses → viral resistance → treatment failure. Take with food to improve absorption; monitor liver enzymes and CD4 count.
- Nystatin (antifungal): binds ergosterol in the fungal membrane → cell death. For oral thrush: swish and swallow, then nothing by mouth for 30 minutes. Never given IV (too toxic).
Ten minutes into a rapid IV vancomycin infusion, the patient's face, neck, and upper chest turn red and blotchy, and they report itching.
GI & Antiemetics
Acid control, mucosal protection, diarrhea management, nausea drugs, and laxatives — plus the toxicities each is known for.
Acid Control: H2 Blockers vs. PPIs vs. Sucralfate
| Drug | Class | MOA | Notes |
|---|---|---|---|
| Famotidine (-tidine) | H2 receptor antagonist | Blocks H2 receptors on parietal cells → less acid | Milder GERD; less potent than PPIs |
| Omeprazole (-prazole) | Proton pump inhibitor | Irreversibly blocks the H+/K+ ATPase proton pump | More potent; GERD, ulcers, Zollinger-Ellison |
| Sucralfate | Mucosal protectant | Coats the ulcer against acid/pepsin | Does NOT lower acid; empty stomach (1 hr before meals) |
Endings tell the class: -tidine = H2 blocker · -prazole = PPI. A PPI shuts down the "pump" itself, which is why it is the stronger acid suppressant.
Sucralfate does not neutralize or reduce acid — it only protects the ulcer surface. It needs an empty stomach so the coating can adhere where the ulcer is.
Antidiarrheals — Loperamide
- MOA: slows bowel motility.
- Contraindicated in: infectious diarrhea, bloody stools, and C. diff — slowing motility traps the pathogen longer and prevents the body from clearing it.
- Concept: with an infection, diarrhea is the body's defense — don't shut it off.
Antiemetics — Metoclopramide & Ondansetron
- Metoclopramide (prokinetic/dopamine blocker): the most serious adverse effect is tardive dyskinesia — repetitive involuntary lip-smacking and tongue movements that can be irreversible. Report immediately.
- Ondansetron (5-HT3 antagonist): used for chemotherapy-induced, post-op, and pregnancy-related nausea. IV use can cause QT prolongation → life-threatening arrhythmias — stop the infusion if QT lengthens.
If a patient on IV ondansetron develops QT prolongation with lightheadedness/dizziness, stop the infusion immediately and notify the provider. Never continue an infusion through a serious cardiac adverse effect.
Bulk-Forming Laxatives — Psyllium
- Critical teaching: take with at least 8 oz of water per dose. Without enough fluid, psyllium swells in the GI tract and can worsen constipation or cause obstruction.
- IBS caution: reintroduce gradually to limit gas and bloating.
Respiratory
Rescue vs. controller inhalers, bronchodilators, and the asthma/COPD medications — plus proper inhaler technique.
Albuterol — Short-Acting Beta-2 Agonist (SABA)
- MOA: stimulates beta-2 receptors in bronchial smooth muscle → bronchodilation. Onset 5–15 minutes.
- Use: acute asthma attacks and exercise-induced bronchospasm (take 15–30 minutes before exercise). PRN only — not a scheduled daily med.
- Expected side effects: tachycardia, palpitations, tremors (beta-2 receptors also live in the heart).
- Red flag: needing it more than 2×/week → poorly controlled asthma → notify provider.
Fluticasone — Inhaled Corticosteroid (ICS)
- Role: controller — daily prevention, not for acute attacks. (Use albuterol for acute bronchospasm.)
- Side effect: oral candidiasis (thrush) — white patches in the mouth. Prevent by rinsing the mouth with water after every use.
- Order matters: when using both, take the bronchodilator (albuterol) first to open airways, then the steroid so it penetrates deeper.
Albuterol = fire extinguisher (fast, for the emergency). Fluticasone = smoke detector battery (daily, prevents the emergency). Know which is which — it is one of the most-tested distinctions.
Ipratropium — Anticholinergic Bronchodilator
- MOA: blocks muscarinic receptors in the airways → reduces bronchospasm and mucus secretion. Primarily for COPD.
- High-yield safety: inhaler formulations contain soy lecithin — ask about soy or peanut allergy before giving.
Montelukast — Leukotriene Receptor Antagonist
- MOA: blocks leukotrienes → less bronchoconstriction and airway inflammation. Used for prevention (asthma, allergic rhinitis) — not for acute attacks.
- Black box warning: serious psychiatric effects — mood changes, agitation, depression, suicidal thoughts. Report any mood change to the provider immediately.
Theophylline — Methylxanthine Bronchodilator
- Narrow therapeutic window — requires blood-level monitoring.
- Expected side effects: tachycardia, palpitations, arrhythmias.
- Toxicity: nausea, vomiting, restlessness, irritability, tremors, and seizures (resembles caffeine overdose).
Methylxanthine = "liquid caffeine." Picture the toxicity as a caffeine OD: jittery, tachycardic, and (at the extreme) seizing.
Inhaler Technique (Metered-Dose Inhaler)
- Shake the canister; remain upright.
- Exhale gently, then inhale slowly and deeply.
- Hold your breath 5–10 seconds.
- Wait 1–2 minutes before a second puff.
A spacer holds the aerosol so particles slow down — giving the patient more time to inhale and getting more medication into the lungs (less in the mouth/throat). Great for kids, older adults, and anyone with poor technique.
Neuro & Psych
Mood stabilizers, antipsychotics, antidepressants, antihistamines, and benzodiazepines — the CNS drugs and their monitoring.
Lithium — Mood Stabilizer
- Therapeutic range: 0.6–1.2 mEq/L (narrow window — needs monitoring).
- Excretion: by the kidneys. Rising creatinine → reduced clearance → accumulation and toxicity → hold and notify the provider.
- Toxicity triggers: dehydration, low-sodium diet, and NSAIDs all raise lithium levels. Encourage consistent fluid and sodium intake.
- Onset: takes days to weeks for full effect — stay consistent.
Antipsychotics — Risperidone (2nd-gen / atypical)
- EPS symptoms to report: abnormal face/arm/leg movements, muscle stiffness, tremors, restlessness (akathisia), and spasms (dystonia).
- Discontinuation: never stop abruptly → withdrawal symptoms and rebound psychosis.
- Side effect: weight gain and metabolic changes — address concerns with the provider rather than stopping on their own.
Tricyclic Antidepressants (TCAs) — amitriptyline, nortriptyline
- Place in therapy: second-line — used when SSRIs (first-line) fail or aren't tolerated.
- Profile: more anticholinergic effects and sedation than SSRIs; dangerous in overdose (cardiac arrhythmias).
- Off-label: chronic pain, neuropathy, migraine prevention.
Diphenhydramine — First-Generation Antihistamine
- Dual action: blocks H1 histamine receptors (allergy) and has anticholinergic effects.
- Anticholinergic side effects: urinary retention, dry mouth, constipation, tachycardia, blurred vision.
- Caution: worsening asthma; glaucoma (raises intraocular pressure); high fall/confusion risk in older adults (Beers Criteria).
- Bonus use: its anticholinergic action can reduce Parkinson's tremors by countering the acetylcholine excess from dopamine loss.
Benzodiazepines — Diazepam
- Overdose antidote: flumazenil — competitively blocks benzodiazepine receptors and reverses CNS depression.
Antidote pairs (know cold): opioids → naloxone · acetaminophen → acetylcysteine · benzodiazepines → flumazenil.
Hormones
Corticosteroids, reproductive hormones, and the smooth-muscle and prostate drugs — each with a signature safety point.
Corticosteroids — Prednisone (systemic)
- Never stop abruptly: long-term use suppresses the adrenal glands → abrupt stop = adrenal crisis (severe hypotension, cardiovascular collapse). Taper gradually.
- Long-term effects: hyperglycemia, weight gain, moon face, osteoporosis (supplement calcium/vitamin D), GI irritation (take with food), and increased infection risk (immunosuppression).
- Mindset: steroids manage symptoms — they don't cure the underlying disease.
Oxytocin — Labor & Delivery
- Effect: stimulates uterine smooth muscle → strong, regular contractions (also used postpartum for hemorrhage control).
- Emergency: severe, constant abdominal pain + rigid abdomen during infusion = possible uterine rupture → stop the infusion immediately and notify the provider.
During oxytocin, severe abdominal pain is never "normal labor pain." Stop the drip, call for help, and assess maternal vitals and fetal status. Do not increase the rate.
Testosterone & Estradiol
- Testosterone (androgen): in female patients, watch for virilization — deepening voice, increased body hair, clitoral enlargement, menstrual changes. Report to the provider (dose may need adjusting).
- Estradiol (estrogen): contraindicated with a history of thromboembolic events (DVT, PE, stroke). No smoking — smoking sharply raises clot, stroke, and MI risk on estrogen.
Finasteride — 5-Alpha Reductase Inhibitor (BPH)
- MOA: reduces DHT → shrinks the prostate. Takes weeks to months for full effect.
- If unable to empty the bladder: refer to the provider for lab work and a prostate exam — don't just reassure or double the dose.
- Teratogenic — no handling by pregnant people; no blood donation while taking it.
Sildenafil — PDE-5 Inhibitor (erectile dysfunction)
- Absolute contraindication: nitrates (nitroglycerin, isosorbide). Both cause vasodilation; together → severe, life-threatening hypotension. No dose adjustment makes it safe.
Sildenafil + nitroglycerin is a "never" combination. Always ask about nitrate use before giving a PDE-5 inhibitor, and hold + notify the provider if there is any overlap.
A patient on long-term prednisone tells you they stopped taking it three days ago "because they feel fine now."
Fluids & TPN
Electrolyte safety, IV fluid tonicity, and total parenteral nutrition — the "small mistakes, big consequences" corner of nursing.
IV Potassium — The Safety Classic
- Rule: never IV push or bolus. Infuse slowly (about 10–20 mEq/hour) and always diluted.
- Why: rapid potassium → cardiac arrest and fatal arrhythmias. Monitor with continuous cardiac monitoring.
Potassium chloride given IV push = cardiac arrest. This is one of the single most-tested medication-safety rules in nursing. Also question potassium in anyone with renal failure.
IV Fluid Tonicity
| Type | Example | Purpose |
|---|---|---|
| Isotonic | 0.9% NaCl, Lactated Ringer's | Fluid resuscitation without shifting compartments |
| Hypotonic | 0.45% NaCl | Lowers elevated sodium (hypernatremia) by shifting water into cells |
| Hypertonic | 3% NaCl | Treats severe hyponatremia / cerebral edema (pulls water out of cells) |
Hypotonic = "hypo" pulls water INTO cells (treats hypernatremia). Hypertonic = pulls water OUT of cells (treats cerebral edema). Isotonic = stays put (resuscitation).
Total Parenteral Nutrition (TPN)
- Most frequent complication: hyperglycemia — TPN's high dextrose content. Monitor glucose frequently; sliding-scale insulin may be needed.
- Infection risk: the high glucose is an ideal medium for bacteria/fungi. Fever, chills, or redness at the line site = line infection → strict aseptic technique for all line care.
Med Safety: Pharmacokinetics & Administration
How drugs move through the body (ADME) and how to give them safely — the fundamentals behind every other tab.
Pharmacokinetics — ADME
- Absorption: drug enters the bloodstream from the administration site (first step).
- Distribution: drug travels via blood to target tissues.
- Metabolism: breakdown, primarily in the liver.
- Excretion: elimination, primarily by the kidneys (urine).
First-Pass Effect
- Definition: an oral drug is absorbed from the gut → travels to the liver via the portal vein → the liver metabolizes part of it before it reaches the systemic circulation → reduced bioavailability.
- Liver disease: less metabolism → more drug reaches the blood → higher toxicity risk.
- IV route: bypasses first-pass metabolism (100% bioavailability). Sublingual also largely bypasses it (e.g., nitroglycerin for chest pain).
Routes, Loading Doses, and Names
- Speed of onset (fastest → slowest): IV > IM > subcutaneous > oral. IV = immediate, 100% bioavailability.
- Loading dose: a high initial dose to rapidly reach therapeutic levels (for long-half-life drugs or when speed is critical); maintenance doses follow.
- Generic vs. trade name: the generic name is the same active ingredient regardless of manufacturer; a trade name belongs to one maker. Both are FDA-approved and equally effective.
Safe Administration Rules
- 6 Rights: right patient (2 identifiers), drug, dose, route, time, documentation — verify against the MAR and check allergies/contraindications first.
- Never crush: enteric-coated (EC), sustained-release (SR), and extended-release (ER/XR) forms — crushing causes dose dumping (entire dose released at once).
- Pediatric liquids: use an oral syringe for accuracy — never a kitchen spoon.
- Sublingual: bypasses first-pass metabolism for fast action (nitroglycerin under the tongue).
Antidotes & "Never Stop Abruptly"
Never stop abruptly: corticosteroids (adrenal crisis) · opioids (withdrawal) · antipsychotics (rebound psychosis). Always taper under supervision.
Mastery Quiz
A concept-based check across every tab. Aim for 90%+ before you call it mastered.