Medicine Information

Epicet-XR

Name: Epicet-XR
Brand: Epicet-XR

Extended-release Tablet1500 mgAnalgesic, Anti-inflammatoryATC: N02BGXX

Generic Name

epicet-xr-1500-mg-tablet

Manufacturer

Global Pharma Inc.

Country

USA

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Price Details

Current market pricing information

Variant	Unit Price	Strip Price
epicet xr 1500 mg tablet	৳ 50.00	৳ 200.00

Description

Overview of the medicine

Epicet-XR 1500 mg tablet is an extended-release analgesic used for the management of moderate to severe chronic pain and inflammatory conditions. Its extended-release formulation ensures prolonged pain relief.

Uses & Indications

Moderate to severe chronic pain

Osteoarthritis

Rheumatoid arthritis

Dosage

Adults

1500 mg once daily, swallowed whole.

Elderly

Start with a reduced dose; monitor renal and hepatic function.

Renal_impairment

Contraindicated in severe renal impairment; dose reduction may be necessary in mild to moderate impairment.

How to Take

Take orally with or without food. Tablets must be swallowed whole, not crushed, chewed, or divided.

Mechanism of Action

Epicet-XR is thought to exert its analgesic effects by modulating pain pathways in the central nervous system and potentially inhibiting the release of inflammatory mediators, providing sustained pain relief.

Pharmacokinetics

Onset

Onset of action within 1-2 hours, with peak effects observed around 4-6 hours.

Excretion

Mainly excreted via the kidneys in urine.

Half life

Approximately 12-15 hours, suitable for once-daily dosing.

Absorption

Slowly and almost completely absorbed from the gastrointestinal tract due to its extended-release formulation, leading to stable plasma concentrations.

Metabolism

Primarily metabolized in the liver.

Side Effects

Contraindications

Hypersensitivity to the active substance or excipients
Severe hepatic or renal impairment
Active gastrointestinal bleeding

Drug Interactions

Warfarin

May increase the risk of bleeding.

Other Analgesics

Increased risk of adverse effects.

Storage

Store below 30°C. Protect from light and moisture.

Overdose

In case of overdose, seek immediate medical attention. Supportive care and symptomatic treatment should be provided. Gastric lavage may be considered if ingestion was recent.

Pregnancy & Lactation

Pregnancy Category C. Should be used during pregnancy and lactation only if the potential benefit justifies the potential risk to the fetus or infant.

Side Effects

Contraindications

Hypersensitivity to the active substance or excipients
Severe hepatic or renal impairment
Active gastrointestinal bleeding

Drug Interactions

Warfarin

May increase the risk of bleeding.

Other Analgesics

Increased risk of adverse effects.

Storage

Store below 30°C. Protect from light and moisture.

Overdose

In case of overdose, seek immediate medical attention. Supportive care and symptomatic treatment should be provided. Gastric lavage may be considered if ingestion was recent.

Pregnancy & Lactation

Pregnancy Category C. Should be used during pregnancy and lactation only if the potential benefit justifies the potential risk to the fetus or infant.

Frequently Asked Questions

Common questions about this medicine

Pack Sizes

10 tablets per pack30 tablets per pack

Shelf Life

36 months

Availability

Worldwide

Approval Status

Approved

Patent Status

Patented

Clinical Trials

Phase III clinical trials completed successfully. Post-marketing surveillance is ongoing to monitor long-term safety and efficacy.

Lab Monitoring

Renal function tests
Liver function tests
Complete blood count (for long-term use)

Doctor Notes

Patients should be monitored for gastrointestinal and renal adverse events.
Consider for chronic pain management, potentially in conjunction with other therapies.

Patient Guidelines

Do not crush or chew the tablet; swallow it whole.
Report any severe side effects to your doctor immediately.
Complete the full course of treatment as prescribed.

Missed Dose Advice

If a dose is missed, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not double the dose.