Advil
Advil
Generic Name
Advil
Mechanism
- Ibuprofen competitively inhibits the cyclo‑oxygenase (COX) enzymes, primarily COX‑1 and COX‑2, which convert arachidonic acid to prostaglandins.
- By reducing prostaglandin production, it diminishes pain signaling, inhibits fever by acting on the hypothalamic thermoregulatory center, and reduces local inflammation and edema.
- The non‑selective inhibition explains both its therapeutic benefits and its gastrointestinal (GI) side‑effects.
Pharmacokinetics
- Absorption: Rapid oral absorption; peak plasma concentration occurs within 1–2 h.
- Bioavailability: ~80 % with food, reduced slightly with high‑fat meals.
- Distribution: Widely distributed; protein binding ~87 % (primarily to albumin).
- Metabolism: Primarily hepatic via CYP2C9 to inactive metabolites; minimal renal excretion of unchanged drug.
- Elimination: Half‑life ~2 – 3 h; clear by the kidneys.
- Drug interactions: Inhibits CYP2C9, can increase levels of warfarin, methotrexate, and other NSAIDs.
Indications
- Analgesia: Mild‑to‑moderate pain (headache, dental pain, musculoskeletal pain).
- Anti‑inflammation: Rheumatoid arthritis, osteoarthritis, gouty arthritis.
- Antipyresis: Febrile illnesses including viral infections.
- Pre‑operative analgesia to reduce opioid requirement.
Contraindications
- Absolute Contraindications: Known hypersensitivity to ibuprofen or other NSAIDs; active peptic ulcer disease or GI bleeding; severe hepatic impairment.
- Relative Contraindications:
- *Pregnancy* – use only in the third trimester for pain control; avoid in first and second trimesters.
- *Cardiovascular disease* – increased risk of hypertension and water‑retention.
- *Renal impairment* – dosage adjustment may be needed.
- Warnings:
- Long‑term use (>10 days) raises GI, renal, and cardiovascular risks.
- Concurrent use with anticoagulants amplifies bleeding risk.
Dosing
| Population | Dose | Frequency | Duration |
| Adults (≥ 18 y) | 200–400 mg PO, every 6–8 h | Max 1200 mg/day | Use ≤ 10 days unless prescribed for chronic arthritis (max 2400 mg/day) |
| Children (6–17 y) | 5 mg/kg PO, every 6–8 h | Max 400 mg/day (10 mg/kg) | ≤ 7 days except for inflammatory arthropathies (max 15 mg/kg/day) |
| < 6 y | Not recommended due to limited safety data. |
• Route: Oral (tablet, capsule, suspension); intravenous is used in hospital settings for severe pain.
Adverse Effects
- Common (≥ 1 %):
- Gastrointestinal upset (nausea, dyspepsia)
- Headache, dizziness
- Rash, pruritus
- Mild elevation of liver enzymes
- Serious (≤ 0.1 %):
- Upper GI bleeding, perforation
- Renal failure/chronic kidney disease exacerbation
- Hypersensitivity reactions (angioedema, anaphylaxis)
- Cardiovascular events (hypertension, edema, MI risk escalation)
Monitoring
- Baseline labs: CBC, renal function tests (serum creatinine, BUN), liver enzymes.
- Periodic assessment:
- Check renal function monthly if used > 2 weeks.
- Monitor blood pressure and edema.
- Assess for GI symptoms or bleeding.
Clinical Pearls
1. IBU → U & B:
• For patients at high GI risk, co‑prescribe *proton‑pump inhibitors* or *misoprostol*.
2. Short‑term only:
• Keep therapy ≤ 10 days for acute pain to minimize GI bleeding risk; for chronic arthritis, prescribe the lowest effective dose.
3. Weilard Effect:
• Use with caution in patients on anticoagulants; consider use of *paracetamol* (acetaminophen) as first‑line alternative if risk high.
4. Pediatric dosing:
• Weight‑based dosing is crucial; avoid exceeding 10 mg/kg/day in children 6–12 y.
5. Pregnancy cautious:
• Use only in third trimester for maternal comfort; avoid otherwise.
This Advil drug card provides essential pharmacology facts—mechanism, PK, indications, contraindications, dosing, side‑effects, and practice pearls—tailored for medical students, clinicians, and pharmacists seeking quick reference.