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The route and dosage form decide how much drug reaches the circulation, how fast, and for how long. Choosing or changing a route changes the pharmacokinetics (Topic 1): bioavailability, onset, peak, and duration. A dose that is correct for one route can be dangerous by another, so route is one of the core rights of medication administration, and a route change always needs a prescriber order.
| Route | Absorption | Onset (general) | First-pass | Key advantages | Key risks |
|---|---|---|---|---|---|
| Intravenous (IV) | None needed; bioavailability 100% | Seconds to minutes | Bypassed | Fastest, precise, titratable; for emergencies and irritating drugs | Cannot be recalled; infection, phlebitis, infiltration and extravasation, speed shock, air embolism |
| Intraosseous (IO) | Into marrow → circulation | Similar to IV | Bypassed | Emergency access when IV fails (resuscitation) | Compartment syndrome, osteomyelitis; temporary use only |
| Inhalation | Airway and alveolar surface | Minutes | Bypassed | Local lung effect with lower systemic dose | Technique-dependent; systemic effects still possible (tremor, tachycardia, thrush with corticosteroids) |
| Sublingual / buccal | Oral mucosa → systemic veins | Minutes | Bypassed | Fast; for drugs destroyed by first-pass (nitroglycerin) | Must not be swallowed or chewed |
| Intramuscular (IM) | Muscle blood flow | 10–30 minutes (aqueous) | Bypassed | Moderate volumes; depot forms last weeks | Pain, nerve injury, abscess; poor absorption in shock; avoid with bleeding risk |
| Subcutaneous (SC) | Slower than IM (less blood flow) | Variable | Bypassed | Self-injection (insulin, heparin, enoxaparin) | Lipohypertrophy; small volumes only; poor absorption with edema or poor perfusion |
| Intradermal (ID) | Very slow, local | Local | Not applicable | Skin tests (tuberculin, allergy testing) | Not for systemic drugs |
| Oral (PO) | GI tract → portal vein → liver | 30–60 minutes or more | Yes | Safe, convenient, cheap; partly reversible (activated charcoal for selected ingestions; induced vomiting is no longer recommended) | Variable absorption; food and drug interactions; needs swallowing and a working GI tract |
| Rectal | Rectal mucosa | Variable | Partly bypassed | When oral route is not possible (vomiting, seizure, unconscious) | Erratic absorption; avoid in neutropenia and after rectal surgery |
| Transdermal | Skin → circulation, slow and steady | Hours (delayed onset) | Bypassed | Steady levels for days | Heat increases absorption; skin irritation; continued effect after removal |
| Topical (skin, eye, ear, nose, vaginal) | Mainly local | Local | Mostly bypassed | Local effect | Systemic absorption can occur (timolol eye drops → bradycardia; corticosteroid creams on large areas) |
| Intrathecal / epidural | Cerebrospinal fluid or epidural space | Rapid, central | Bypassed | Anesthesia, analgesia, some chemotherapy | Only specific preservative-free drugs; wrong-route errors can be fatal |
Onset order for a typical drug, from fastest: IV > inhalation > sublingual > IM > SC > oral > transdermal (with exceptions for specific drugs and formulations).
| Form | Purpose | Nursing point |
|---|---|---|
| Tablet, capsule (immediate release) | Standard | Some tablets may be crushed or split — check before altering |
| Enteric-coated (EC) | Protects the stomach or protects an acid-sensitive drug; dissolves in the small intestine | Do not crush or chew; separate from antacids |
| Extended-release (ER, XR, SR, CR, LA) | Releases drug over hours for once- or twice-daily dosing | Do not crush, chew, or open — crushing releases the whole dose at once (dose dumping → overdose, e.g., oxycodone ER, nifedipine ER) |
| Orally disintegrating tablet (ODT) | Dissolves on the tongue | Handle with dry hands; place on the tongue; no water needed |
| Sublingual tablet, spray | Absorbed under the tongue | Do not swallow; e.g., nitroglycerin |
| Solution, syrup, elixir | Liquid; elixirs contain alcohol | Measure with an oral syringe or calibrated cup, never a household spoon |
| Suspension | Particles in liquid | Shake well before each dose — otherwise doses vary |
| Chewable tablet | For children and people who cannot swallow tablets | Must be chewed |
Parenteral forms: solutions, suspensions (never IV unless labeled for IV), emulsions (propofol, lipid emulsion), powders for reconstitution (check diluent, volume, and stability), depot/long-acting injections (medroxyprogesterone every 3 months, long-acting antipsychotics).
Other forms: metered-dose inhaler (MDI), dry-powder inhaler (DPI), nebulizer solution; transdermal patches (fentanyl, nitroglycerin, clonidine, estrogen, nicotine, scopolamine, buprenorphine); suppositories; eye drops and ointments; nasal sprays (including naloxone and intranasal midazolam); vaginal rings.
| Problem | Route | Signs |
|---|---|---|
| Infiltration | IV | Cool, pale, swollen skin; slowed infusion |
| Extravasation of vesicants (vasopressors, some chemotherapy, calcium, concentrated potassium, contrast) | IV | Pain, burning, blistering, tissue necrosis |
| Phlebitis | IV | Redness, warmth, tenderness along the vein, palpable cord |
| Speed shock | IV push given too fast | Flushing, headache, hypotension, dysrhythmias |
| Circulatory overload | IV | Dyspnea, crackles, rising blood pressure, jugular venous distension |
| Nerve injury, abscess | IM | Pain radiating down the leg (sciatic nerve with dorsogluteal site) |
| Lipohypertrophy | Repeated SC in one site | Lumpy tissue, erratic insulin absorption |
| Aspiration | Oral | Coughing, choking in drowsy clients or those with dysphagia |
| Local irritation, thrush | Inhaled corticosteroids | Hoarseness, oral candidiasis |
| Skin reaction, heat-related overdose | Transdermal | Redness; sedation or hypotension with heat |
Listed in priority order.
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