Olfen SR (Sustained Release) is a brand-name nonsteroidal anti-inflammatory drug (NSAID) manufactured by Mepha / Acino. It contains Diclofenac Sodium as its active ingredient in a prolonged-release formulation designed to provide extended pain and inflammation relief over 12 to 24 hours.
Active Ingredient & Mechanism of Action
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Active Ingredient: Diclofenac Sodium (in extended/sustained-release pellets or matrix).
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Mechanism: Inhibits cyclooxygenase (COX-1 and COX-2) enzymes, blocking the biosynthesis of prostaglandins—the primary chemical mediators responsible for localized pain, swelling, fever, and joint inflammation.
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SR Advantage: The sustained-release formulation releases the active drug gradually into the gastrointestinal tract, maintaining steady therapeutic blood levels and allowing once- or twice-daily dosing.
Available Dosage Forms & Strengths
Olfen SR is available in solid oral sustained-release formulations:
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Olfen 75 SR: 75 mg prolonged-release depot tablets or capsules.
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Olfen 100 SR: 100 mg prolonged-release depot capsules (Depocaps).
Clinical Indications
Olfen SR is prescribed for long-term or acute management of painful and inflammatory conditions:
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Arthritic & Joint Disorders: Rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis.
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Musculoskeletal & Soft Tissue Pain: Acute backache, frozen shoulder, bursitis, tendinitis, tenosynovitis, and sprains/strains.
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Gout & Trauma: Acute gout flares, post-traumatic or post-surgical inflammation and swelling, and fractures.
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Dysmenorrhea: Severe menstrual cramps.
Key Pharmacokinetics
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Absorption: Gradually absorbed throughout the digestive tract to provide extended therapeutic coverage. Peak plasma concentrations are reached more slowly compared to immediate-release diclofenac, avoiding sharp drug spikes.
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Distribution: Accumulates and persists in joint synovial fluid at higher concentrations than in blood plasma over extended periods.
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Metabolism & Elimination: Metabolized by the liver (primarily CYP2C9) and excreted predominantly through the kidneys in urine and via bile/feces.
Administration Guidelines
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How to Take:
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Take with or immediately after a meal with a full glass of water to minimize stomach discomfort.
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Swallow whole: Do not chew, crush, split, or open the sustained-release capsules/tablets, as damaging the coating destroys the extended-release mechanism and increases the risk of side effects or overdose.
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Typical Adult Dosing:
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100 mg SR once daily (often taken in the evening to relieve nocturnal pain and morning stiffness).
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Or 75 mg SR 1 to 2 times daily depending on clinical severity.
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Maximum Daily Dose Limit: 150 mg per 24 hours.
Safety Profile & Critical Warnings
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Black Box / Serious Safety Warnings:
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Cardiovascular Risk: Like all NSAIDs, prolonged use or high doses increase the risk of serious cardiovascular thrombotic events, heart attack, and stroke.
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Gastrointestinal Risk: Can cause stomach ulcers, internal bleeding, and intestinal perforation.
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Common Side Effects: Nausea, indigestion, epigastric pain, flatulence, diarrhea, headache, dizziness, and mild skin rash.
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Contraindications:
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Active peptic/gastric ulcers or history of gastrointestinal bleeding.
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Severe heart failure, established ischemic heart disease, or severe liver/kidney failure.
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History of asthma, hives, or acute allergic reactions triggered by aspirin or other NSAIDs.
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Pregnancy: Contraindicated starting at 20 weeks of gestation (risk of premature closure of the fetal ductus arteriosus and low amniotic fluid).
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Key Drug Interactions:
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Blood Thinners (e.g., Warfarin, Aspirin): Significantly increases GI and systemic bleeding risk.
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Antihypertensives & Diuretics: Can diminish blood-pressure-lowering effects and increase risk of kidney injury.
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Other NSAIDs / Steroids: Co-administration increases risk of gastric ulceration without additional benefit.
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Lithium & Methotrexate: Inhibits renal clearance, raising toxic blood levels of these drugs.
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Note: Olfen SR is a prescription-only sustained-release medication. Dosing duration, gastroprotective needs (such as taking a proton pump inhibitor alongside it), and individual cardiovascular or renal risks should be supervised by a healthcare professional.











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