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Aspirin Uses, Dosage, Side Effects & Benefits | DrugsAtlas

Authoritative Clinical Reference

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Therapeutic Class
Antiplatelet agent / Analgesic / Antipyretic
Subclass
Non-steroidal anti-inflammatory drug (NSAID), Salicylate
Speciality
Cardiology
Schedule (India)
Schedule H
Routes
Oral, Rectal, Intravenous (NOT AVAILABLE in India)
Formulations
  • 75 mg, 81 mg, 100 mg, 150 mg, 300 mg tablets (enteric-coated or plain)
  • 325 mg, 500 mg tablets (analgesic/antipyretic use)
  • 75 mg, 150 mg dispersible/chewable tablets (specialist use)
  • 350 mg, 500 mg rectal suppository (limited availability)
  • NOT AVAILABLE in India: IV formulation
Adult indications

Primary Indications (Approved / Standard in India)

1. Secondary Prevention of Cardiovascular and Cerebrovascular Events
(Post-MI, Post-stroke, TIA, Peripheral Arterial Disease)
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
Clinical Notes:
  • Enteric-coated formulation preferred for long-term use
  • Combine with clopidogrel for first 12 months post-ACS or post-PCI
  • Indefinite therapy unless contraindicated

2. Acute Coronary Syndrome (STEMI / NSTEMI / Unstable Angina)
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)
Clinical Notes:
  • Co-administer with P2Y12 inhibitor (clopidogrel/ticagrelor/prasugrel) as per DAPT protocol
  • Continue anticoagulation per institutional ACS pathway
  • Do NOT use enteric-coated tablets for loading (delayed absorption)

3. Analgesic / Antipyretic (Short-term Use Only)
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
Clinical Notes:
  • Use limited to short-term only due to GI and bleeding risks
  • Paracetamol preferred in most analgesic/antipyretic settings
  • Avoid in patients with peptic ulcer history or concurrent anticoagulation

Secondary Indications – Adults (Off-label)

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
Paediatric indications

PAEDIATRIC DOSING (Specialist Only)

Not recommended in children <16 years except for specific indications below due to risk of Reye's syndrome.

Primary Indication: Kawasaki Disease

Minimum Age: ≥6 months
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)
Clinical Notes:
  • Always use with IVIG in acute Kawasaki disease
  • Continue low-dose aspirin until coronary arteries normalise on imaging
  • Follow IAP Kawasaki Management Guidelines

Secondary Indications – Paediatrics (Off-label)

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
Renal Adjustments
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
Hepatic adjustment
Contraindications
  • Hypersensitivity to aspirin, salicylates, or any excipients
  • Active peptic ulcer disease or gastrointestinal bleeding
  • Haemorrhagic disorders (haemophilia, severe thrombocytopenia)
  • Severe hepatic impairment
  • Severe renal impairment (eGFR <30)
  • Third trimester of pregnancy
  • Children/adolescents with viral illness (varicella, influenza) — Reye's syndrome risk
  • History of aspirin-induced asthma, urticaria, or angioedema
Cautions
  • Asthma or history of bronchospasm (aspirin-exacerbated respiratory disease)
  • Concurrent anticoagulant or antiplatelet therapy
  • History of peptic ulcer disease (healed)
  • G6PD deficiency (risk of haemolysis at high doses)
  • Chronic kidney disease (dose-dependent worsening)
  • Uncontrolled hypertension
  • Perioperative period — discontinue 5–7 days prior to surgery if bleeding risk unacceptable
  • Gout (low-dose aspirin may increase uric acid levels)

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
Preferred Alternative for Analgesia: Paracetamol
Monitoring: Bleeding parameters, amniotic fluid volume (if continued beyond 28 weeks)
Lactation
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)
Elderly
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
Major drug interactions
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
Moderate drug interactions
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
Common Adverse effects
  • Dyspepsia, epigastric discomfort
  • Nausea, heartburn
  • Easy bruising
  • Minor bleeding (gingival, epistaxis)
  • Tinnitus (dose-related; may indicate toxicity

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
Monitoring requirements
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)
Brands in India
  • Ecosprin™ (USV) — 75 mg, 150 mg, 325 mg
  • Loprin™ (Shreya Life Sciences) — 75 mg, 150 mg
  • Cardispan™ — enteric-coated low-dose
  • Aspisol™ — analgesic dose tablets
  • Disprin™ (Reckitt) — dispersible 350 mg
  • Colsprin™ — 100 mg
  • Fixed-Dose Combinations: Ecosprin-AV (with atorvastatin), Ecosprin Gold (with clopidogrel + atorvastatin), Clopitab-A (with clopidogrel)

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
Regulatory: Listed under NLEM 2022; select strengths under NPPA price control
Clinical pearls
  1. Acute ACS: Always use non-enteric coated, chewable aspirin for loading — enteric coating delays absorption by 3–4 hours
  2. Long-term CV prevention: Use enteric-coated formulations to reduce gastric irritation
  3. NSAID interaction: Ibuprofen given before aspirin blocks the antiplatelet binding site — give aspirin at least 30 minutes before ibuprofen if both required
  4. Elderly patients: Co-prescribe PPI (pantoprazole/omeprazole) routinely for GI protection in long-term therapy
  5. Paediatrics: Never prescribe to children <16 years with fever/viral illness — always rule out viral aetiology before considering aspirin
  6. Bleeding counselling: Educate patients to report black stools, blood in vomit, unusual bruising, or prolonged bleeding from cuts
Version
RxIndia v1.1 — 01 May 2025
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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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