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Anaphylaxis
Life-threatening systemic allergic reaction: airway swelling, wheezing, hypotension, hives; IM epinephrine is first-line.
Tachyphylaxis
Rapid loss of drug response after repeated doses over a short period.
Agonist vs antagonist
Agonist activates a receptor (e.g., morphine at opioid receptors); antagonist blocks receptor activity (e.g., naloxone).
Synergism
Two drugs together produce a greater effect than expected from adding their individual effects.
Summation/additive effect
Combined effect equals the sum of individual effects (1 + 1 = 2).
Potentiation
One drug increases another drug's effect, even if the first has little/no effect by itself.
Cumulative effect
Drug accumulates when repeat dosing outpaces elimination, raising toxicity risk.
Cross-tolerance
Tolerance to one drug reduces response to another drug with similar action.
Idiosyncratic reaction
Unusual, unpredictable response specific to an individual.
Therapeutic index
Ratio of toxic dose to effective dose; narrow index = small safety margin.
Therapeutic level
Drug concentration in the effective, acceptably safe range.
Onset / peak / duration
Onset = when effect begins; peak = strongest effect; duration = how long effect lasts.
Half-life
Time for blood/plasma drug concentration to decrease by half.
Generic vs brand/trade
Generic is standardized drug name; brand and trade are two names for the marketed product (e.g., acetaminophen = Tylenol).
Why drugs become OTC
Regulators may permit nonprescription sale when a drug has an acceptable safety profile and clear labeling for self-use.
Pill / tablet / caplet / capsule
Pill = informal term; tablet = compressed solid; caplet = capsule-shaped tablet; capsule = medication inside a dissolvable shell.
Storage
Follow manufacturer temperature, light and moisture requirements; check expiration and integrity.
Discarding medication
Follow agency policy and drug-waste rules. Never put loose needles in trash: sharps container.
Opioids toxidrome
Slow/absent respirations, reduced consciousness, often pinpoint pupils; provide airway/ventilation support and naloxone when indicated.
Benzodiazepines toxidrome
Sedation, ataxia, slurred speech; act by enhancing GABA-A inhibitory signaling.
Barbiturates toxidrome
Profound CNS/respiratory depression, hypotension; increase GABA-A chloride channel opening duration.
Amphetamines/stimulants toxidrome
Agitation, tachycardia, hypertension, sweating, dilated pupils, hyperthermia, seizures.
Alcohol toxidrome
Slurred speech, ataxia, altered mental status, possible hypoglycemia and respiratory depression.
Cannabis toxidrome
Anxiety, altered perception, tachycardia; usually supportive care, but assess for co-ingestion or medical emergencies.
Class I - sodium-channel blockers
Slow rapid sodium influx in cardiac cells.
Class II - beta blockers
Reduce heart rate, AV conduction and contractility.
Class III - potassium-channel blockers
Amiodarone (also blocks sodium/calcium channels and beta receptors); prolongs repolarization/refractory period.
Class IV - calcium-channel blockers
Diltiazem (Cardizem) and verapamil slow AV nodal conduction; can lower HR, BP and contractility.
Digoxin/digitalis
Increases contractility and slows AV nodal conduction; narrow therapeutic index, toxicity/arrhythmia risk.
Chronotropic / inotropic / dromotropic
Chronotropy = heart rate; inotropy = strength of contraction; dromotropy = conduction speed, especially through AV node.
Preload / stroke volume / cardiac output
Preload = ventricular filling/stretch; stroke volume = blood pumped per beat; cardiac output = heart rate x stroke volume.
Alpha-1
Vasoconstriction, raising peripheral vascular resistance/BP (e.g., norepinephrine).
Beta-1
Increases heart rate, contractility and AV conduction; beta blockers oppose these effects.
Beta-2
Bronchodilation (e.g., albuterol) and some vascular smooth muscle relaxation.
Sympathomimetic
Mimics fight-or-flight (epinephrine, albuterol); sympatholytic blocks sympathetic effects (metoprolol).
Parasympathomimetic
Mimics rest-and-digest, slows HR and increases secretions (e.g., pilocarpine); parasympatholytic blocks muscarinic effects (atropine, ipratropium).
Analgesic vs anesthetic
Analgesic reduces pain; anesthetic reduces sensation (local or general), sometimes consciousness.
Renin / angiotensin I / ACE / angiotensin II
Renin starts conversion of angiotensinogen to angiotensin I; ACE converts I to II; angiotensin II causes vasoconstriction and stimulates aldosterone, increasing salt/water retention.
ACE inhibitors
Lisinopril, enalapril (often -pril): reduce angiotensin II and BP; adverse effects include cough, hyperkalemia, hypotension and angioedema.
Peptic ulcer treatment
Proton-pump inhibitors (omeprazole, pantoprazole) are commonly used; H2 blockers (famotidine) also reduce acid.
Avoid/caution with ulcers
Aspirin and other NSAIDs (ibuprofen, ketorolac) increase GI irritation and bleeding risk; check specific contraindications.
Bronchoconstriction/asthma
Inhaled beta-2 agonists such as albuterol relax bronchial smooth muscle; ipratropium blocks muscarinic bronchoconstriction; severe anaphylaxis requires IM epinephrine.
CHF/pulmonary edema
Assess oxygenation and ventilation; CPAP may help if appropriate. Nitroglycerin may reduce preload/BP if indicated and not contraindicated.
Erectile dysfunction (ED) medications
Sildenafil (Viagra), tadalafil (Cialis), vardenafil are PDE-5 inhibitors.
Shortest half-life / rapid push
Adenosine has an extremely short half-life (seconds) and is administered as a rapid IV push with flush for appropriate regular SVT.
Digitalis caution
Digoxin has a narrow therapeutic index and can cause dangerous dysrhythmias; not generally administered for acute rate control in the ambulance.
Organophosphate poisoning
Cholinesterase inhibition causes excessive acetylcholine. SLUDGE: Salivation, Lacrimation, Urination, Defecation, GI upset, Emesis.
Treatment for organophosphate poisoning
PPE/decontamination and airway suction/ventilation; atropine to reverse muscarinic effects, pralidoxime (2-PAM) to reactivate cholinesterase when indicated, benzodiazepines for seizures, per protocol.
Tricyclic antidepressant overdose
Amitriptyline, nortriptyline: anticholinergic findings, seizures, hypotension, widened QRS and ventricular dysrhythmias.
Schedule I
Federal category with no currently accepted medical use under federal law and high abuse potential; heroin is an example.
Schedule II
High abuse potential with accepted medical use, e.g., fentanyl, morphine, oxycodone.
Schedule III
Lower abuse potential than I/II, e.g., ketamine, certain codeine combinations.
Schedule IV
Lower abuse potential than III, e.g., diazepam, lorazepam, alprazolam.
NSAIDs
Nonsteroidal anti-inflammatory drugs inhibit COX/prostaglandin production, reducing pain, inflammation and fever. Examples: ibuprofen, naproxen, aspirin, ketorolac.
Medication calculations - drops/minute (gravity)
(Volume in mL x drop factor in gtt/mL) / time in minutes = gtt/min.
Infusion pump
mL/hr = total volume (mL) / time (hours).
Drug concentration
mg/mL = drug amount (mg) / total solution volume (mL). For mcg/mL, multiply mg by 1,000 before dividing by mL.
Weight-based drip (mcg/kg/min)
mL/hr = [ordered mcg/kg/min x weight (kg) x 60] / concentration (mcg/mL).
Safety
Check units, concentration, weight, pump/drip set, clinical appropriateness and local protocol.