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Authoritative Clinical Reference
| Parameter | Dose |
|---|---|
|
Starting dose
|
75–150 mg once daily |
|
Titration
|
Not applicable |
|
Usual maintenance dose
|
75–150 mg once daily |
|
Maximum dose
|
150 mg once daily |
| Phase | Dose | Notes |
|---|---|---|
|
Loading dose
|
150–325 mg stat | Chew non-enteric coated tablet for rapid absorption |
|
Titration
|
Not applicable | — |
|
Maintenance dose
|
75–150 mg once daily | Start from Day 1 |
|
Maximum dose
|
325 mg (loading); 150 mg (maintenance) | — |
| Parameter | Dose |
|---|---|
|
Starting dose
|
325–500 mg every 4–6 hours as needed |
|
Titration
|
Not applicable |
|
Usual maintenance dose
|
325–500 mg every 4–6 hours |
|
Maximum dose
|
4 g/day |
| Indication | Dose | Duration | Supervision | Evidence Basis |
|---|---|---|---|---|
|
Prevention of Pre-eclampsia (OFF-LABEL)
|
75–150 mg once daily at bedtime | 12–16 weeks gestation until 36 weeks | Specialist only (Obstetrician) | FOGSI consensus; ICMR high-risk pregnancy guidance |
|
Colorectal Cancer Chemoprevention (OFF-LABEL)
|
75–100 mg once daily | Long-term (years) | Specialist only (Oncologist/Gastroenterologist) | International RCTs (CAPP2, ASPREE); not standard Indian public health practice |
| Phase | Dose | Duration | Monitoring |
|---|---|---|---|
|
Acute phase (High-dose)
|
30–50 mg/kg/day in 4 divided doses | Until 2–3 days after fever resolution | Platelet count, LFTs, bleeding signs |
|
Titration
|
Step down to low-dose once afebrile | — | — |
|
Maintenance (Low-dose)
|
3–5 mg/kg once daily | 6–8 weeks minimum; longer if coronary abnormalities persist | Echocardiography, platelet count |
|
Maximum dose
|
4 g/day (acute phase) | — | — |
| Indication | Dose | Duration | Supervision | Evidence Basis |
|---|---|---|---|---|
|
Antiplatelet therapy post cardiac surgery / congenital heart disease (OFF-LABEL)
|
1–5 mg/kg once daily | As directed by cardiologist | Specialist only (Paediatric Cardiologist) | Indian paediatric cardiology practice; limited RCT data |
| eGFR (mL/min/1.73 m²) | Recommendation |
|---|---|
| >60 | No adjustment required |
| 30–60 | Use with caution; monitor renal function regularly |
| <30 |
Avoid — increased bleeding and nephrotoxicity risk
|
| Haemodialysis | Avoid chronic use; not effectively dialysed |
Pregnancy
| Trimester | Safety | Notes |
|---|---|---|
|
1st
|
Use only if essential; avoid high doses | Theoretical risk of fetal loss; limited data |
|
2nd
|
May be used with caution at low doses | Consider for high-risk pre-eclampsia prophylaxis under specialist guidance |
|
3rd
|
Avoid
|
Risk of premature ductus arteriosus closure, oligohydramnios, maternal/fetal bleeding; stop by 36 weeks |
| Parameter | Information |
|---|---|
|
Compatibility
|
Compatible at low doses (≤150 mg/day) |
|
Preferred Alternative
|
Paracetamol (for analgesia) |
|
Expected Drug Level in Milk
|
Low |
|
Infant Monitoring
|
Bruising, feeding difficulties, GI symptoms (rare) |
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
Same as adult; use lower end of range |
|
Titration
|
Slower titration for analgesic use |
|
Increased Risks
|
GI bleeding, renal impairment, tinnitus, falls (via drug interactions) |
|
Additional Measures
|
Co-prescribe PPI for long-term CV prevention use |
| Interacting Drug | Effect | Management |
|---|---|---|
|
Warfarin
|
↑↑ Bleeding risk | Avoid unless compelling indication; close INR and bleeding monitoring |
|
DOACs (apixaban, rivaroxaban, dabigatran)
|
↑↑ Bleeding risk | Avoid unless cardiologist-directed; monitor for bleeding |
|
Ibuprofen and other NSAIDs
|
May antagonise antiplatelet effect of aspirin | Avoid; if essential, give aspirin 30 min before ibuprofen |
|
Methotrexate (high-dose)
|
↓ MTX clearance → ↑ toxicity | Avoid concurrent use with high-dose MTX; monitor closely with low-dose MTX |
|
SSRIs (sertraline, fluoxetine)
|
↑ GI bleeding risk | Consider PPI cover; monitor for bleeding |
|
Probenecid / Sulfinpyrazone
|
Aspirin antagonises uricosuric effect | Avoid combination in gout management |
| Interacting Drug | Effect | Management |
|---|---|---|
|
ACE inhibitors / ARBs
|
Reduced antihypertensive effect | Monitor blood pressure |
|
Diuretics (loop, thiazide)
|
Reduced diuretic efficacy; ↑ nephrotoxicity | Monitor renal function and fluid status |
|
Sulfonylureas
|
Hypoglycaemia (protein binding displacement) | Monitor blood glucose; rare clinical significance |
|
Corticosteroids
|
Additive gastric toxicity | Use PPI cover if concurrent use required |
|
Valproic acid
|
↑ Valproate levels (protein binding displacement) | Monitor valproate levels |
|
Alcohol
|
↑ GI bleeding risk | Counsel patient to limit alcohol |
Serious Adverse effects
| Adverse Effect | Clinical Action |
|---|---|
|
GI haemorrhage / peptic ulceration
|
Discontinue; may require hospitalisation, endoscopy, blood transfusion |
|
Intracranial haemorrhage
|
Discontinue immediately; neurosurgical evaluation |
|
Reye's syndrome (children)
|
Contraindicated in viral illness; supportive care if occurs |
|
Anaphylaxis / Aspirin-induced asthma
|
Discontinue permanently; emergency management |
|
Stevens-Johnson Syndrome / TEN
|
Rare; discontinue permanently |
|
Severe bronchospasm
|
Discontinue; bronchodilator therapy |
| Timing | Parameters |
|---|---|
|
Baseline
|
CBC, renal function (creatinine, eGFR), liver enzymes, bleeding history assessment |
|
During therapy (long-term)
|
CBC periodically, faecal occult blood (if GI symptoms), serum creatinine |
|
Acute CV use
|
Bleeding assessment, blood pressure, symptom control |
|
Paediatric (Kawasaki)
|
Platelet count, LFTs, echocardiography, fever curve |
|
Signs of toxicity
|
Tinnitus, hearing changes, hyperventilation (salicylism) |
Price range (INR)
| Formulation | Price Range | Notes |
|---|---|---|
| 75 mg tablet | ₹0.30–₹1.00 per tablet | Generic/branded |
| 150 mg tablet | ₹0.50–₹1.50 per tablet | — |
| 325 mg tablet | ₹0.80–₹2.00 per tablet | — |
| 500 mg tablet | ₹1.00–₹2.50 per tablet | — |
This platform is designed strictly for healthcare professionals. Data provided is synthesized from authoritative pharmacological sources and clinical registries. Do not use for consumer medical decisions. Always verify critical dosing and contraindications with official institutional protocols and peer-reviewed journals.
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