Product Overview
Calpol is a paracetamol-based medication that serves as a widely trusted over-the-counter pain reliever and fever reducer. Available in multiple formulations including tablets, capsules, and syrup, it provides flexible dosing options for patients of all ages. Clinically proven and healthcare professional-recommended, Calpol effectively manages discomfort from various pain conditions while safely reducing elevated body temperature.
Therapeutic Applications
This medication is indicated for the relief of mild to moderate pain symptoms including cephalalgia (headaches), odontalgia (tooth pain), myalgia (muscle pain), and dysmenorrhea (menstrual cramps). It also demonstrates efficacy in pyrexia (fever) reduction associated with infectious processes including upper respiratory infections, influenza, and other febrile illnesses. The formulation is pediatrician-approved for use in children when dosed appropriately.
Administration Guidelines
For optimal therapeutic outcomes, adhere strictly to the prescribed dosing regimen or package instructions. Tablets/capsules should be ingested intact with adequate hydration. The oral suspension formulation includes a calibrated measuring device for precise pediatric dosing. Important precautions include:
• Maintaining minimum 4-hour intervals between doses
• Strictly observing maximum daily dosage limits
• Avoiding concurrent use with other paracetamol-containing products
Consult healthcare providers for dosing adjustments in special populations.
Mechanism of Action
The active pharmaceutical ingredient, paracetamol (N-acetyl-p-aminophenol), exerts its pharmacologic effects through central inhibition of cyclooxygenase enzymes, particularly COX-3 in the central nervous system. This action:
• Attenuates prostaglandin synthesis in the hypothalamus (mediating antipyretic effects)
• Elevates pain threshold by affecting endogenous cannabinoid systems
• Demonstrates selective COX-2 inhibition with minimal gastrointestinal effects compared to traditional NSAIDs
Dosing Protocol
Standard posology recommendations:
Population | Single Dose | Maximum Daily Dose | Dosing Interval |
---|---|---|---|
Adults (>50kg) | 500-1000mg | 4000mg | 4-6 hours |
Children (6-12y) | 250-500mg | 2000mg | 4-6 hours |
Pediatric Suspension | 15mg/kg | 75mg/kg/day | 4-6 hours |
Note: Renal/hepatic impairment requires dose adjustment – consult prescribing information.
Therapeutic Advantages
Calpol offers distinct clinical benefits:
• Rapid onset of action (30-60 minutes)
• Favorable safety profile for short-term use
• Minimal drug-drug interactions
• Well-tolerated gastric profile
• Flexible pediatric formulations
• Cost-effective analgesic option
Adverse Effects
While generally well-tolerated, potential adverse reactions may include:
• Gastrointestinal: Epigastric discomfort, nausea (incidence <5%)
• Dermatological: Urticaria, pruritus (rare)
• Hematological: Thrombocytopenia (very rare)
• Hepatic: Transaminase elevation (with overdose)
Discontinue immediately and seek medical attention for any hypersensitivity reactions.
Important Precautions
Critical safety considerations:
• Hepatotoxicity risk increases with:
– Chronic alcohol use
– Pre-existing liver impairment
– Concomitant hepatotoxic drugs
• Contraindicated in:
– Known hypersensitivity reactions
– Severe hepatic insufficiency
– G6PD deficiency (theoretical risk)
• Special populations:
– Pregnancy Category B
– Caution in breastfeeding
– Geriatric dose adjustment may be required
Storage Requirements
Proper storage conditions:
• Maintain at controlled room temperature (15-30°C)
• Protect from moisture and light
• Keep oral suspension tightly capped
• Store in original packaging
• Dispose expired products properly
• Implement child-resistant storage measures
Medical Disclaimer
The information provided herein represents carefully curated, evidence-based data reviewed by healthcare professionals. However, this content:
• Does not constitute medical advice
• Cannot replace professional clinical judgment
• May not include all potential contraindications
• Should be verified with current prescribing information
Patients are strongly advised to consult qualified healthcare providers for personalized medical recommendations and to report any adverse events to their national pharmacovigilance program.
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