Action-XR
Generic Name
action-xr-665-mg-tablet
Manufacturer
PharmaCorp Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| action xr 665 mg tablet | ৳ 2.00 | ৳ 20.00 |
Description
Overview of the medicine
Action-XR 665 mg Tablet is an extended-release formulation designed to provide prolonged relief from pain and inflammation. It is commonly used for conditions such as osteoarthritis, rheumatoid arthritis, and other musculoskeletal pain.
Uses & Indications
Dosage
Adults
One tablet (665 mg) orally once daily, preferably with food.
Elderly
Lower doses may be considered, starting with one tablet every other day, with careful monitoring due to increased risk of adverse effects.
Renal_impairment
Use with caution; dose adjustment may be necessary. Not recommended in severe renal impairment.
How to Take
Take orally with a full glass of water, preferably with or after food to minimize gastrointestinal upset. Do not crush, chew, or break the extended-release tablet.
Mechanism of Action
It works by inhibiting the activity of cyclooxygenase (COX) enzymes, particularly COX-2, which are responsible for the production of prostaglandins. Prostaglandins are mediators of pain, inflammation, and fever. By reducing prostaglandin synthesis, Action-XR alleviates pain and inflammation.
Pharmacokinetics
Onset
1-2 hours for initial effect, peak effect within 4-6 hours.
Excretion
Mainly renal (urine) as metabolites, with some biliary excretion.
Half life
Approximately 10-12 hours.
Absorption
Slow and sustained absorption over several hours, leading to prolonged plasma concentrations.
Metabolism
Primarily hepatic, often via CYP450 enzymes (e.g., CYP2C9).
Side Effects
Contraindications
- •Hypersensitivity to the active substance or any excipients
- •Active gastrointestinal bleeding or ulceration
- •Severe renal or hepatic impairment
- •Severe heart failure
- •Third trimester of pregnancy
- •History of asthma, urticaria, or allergic-type reactions after taking aspirin or other NSAIDs
Drug Interactions
Lithium
Increased lithium plasma levels.
Warfarin
Increased risk of bleeding.
Methotrexate
Increased methotrexate toxicity.
Diuretics and ACE inhibitors
Reduced antihypertensive effect and increased risk of renal impairment.
Storage
Store below 30°C in a dry place, away from direct sunlight and moisture. Keep out of reach of children.
Overdose
Symptoms may include nausea, vomiting, epigastric pain, lethargy, and drowsiness. Management involves symptomatic and supportive care. Gastric lavage, activated charcoal, and forced diuresis may be considered. There is no specific antidote.
Pregnancy & Lactation
Not recommended during the third trimester of pregnancy due to potential fetal harm (premature closure of ductus arteriosus). Use during the first and second trimesters only if clearly needed and the potential benefit outweighs the potential risk. Excreted in breast milk; avoid during lactation or use with caution after consulting a doctor.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
36 months from manufacturing date.
Availability
Available in all pharmacies nationwide
Approval Status
Approved by Drug Administration
Patent Status
Generic available
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Global Brand Names
International brand names for this medicine
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