Product image of Metindol Retard (Indometacin) supplied by GNH India

Metindol Retard

Active Ingredient:
Indometacin
Origin:
EU

Metindol Retard (Indometacin)

Indometacin, the active ingredient in Metindol Retard, is a nonsteroidal anti‑inflammatory drug (NSAID) presented as an oral formulation for systemic use. It is used to relieve pain and inflammation associated with conditions such as rheumatoid arthritis, osteoarthritis and gout.

GNH India supplies Metindol Retard as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bausch Health Ireland Limited

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Indications & Clinical Uses

Indometacin is an NSAID that reduces inflammation and pain in several musculoskeletal and crystal‑induced disorders.

  • Rheumatoid arthritis: decreases joint swelling, pain and stiffness.
  • Osteoarthritis: alleviates chronic joint pain and improves mobility.
  • Gout: reduces acute inflammatory attacks and associated discomfort.
  • Ankylosing spondylitis: lessens spinal inflammation and pain.
  • Acute pain: provides short‑term relief for severe pain episodes.

How It Works

  • Indometacin exerts its anti‑inflammatory and analgesic effects by non‑selectively inhibiting cyclooxygenase enzymes COX‑1 and COX‑2. This inhibition blocks the conversion of arachidonic acid to prostaglandins, thereby reducing prostaglandin-mediated inflammation, pain signaling, and fever generation throughout the body.

Side Effects

Indometacin may cause a range of adverse reactions, from mild to severe, depending on individual susceptibility and duration of therapy.

Common Side Effects

  • Gastrointestinal upset: nausea, dyspepsia, abdominal pain.
  • Headache or dizziness.
  • Skin rash or pruritus.
  • Elevated liver enzymes.
  • Mild renal function changes.

Serious or Rare Side Effects

  • Gastrointestinal ulceration or bleeding.
  • Severe renal impairment or failure.
  • Hepatotoxicity with jaundice.
  • Anaphylactic or severe hypersensitivity reactions.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiovascular events such as myocardial infarction or stroke.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for potential complications.

  • Assess gastrointestinal risk: avoid in patients with active ulcers or history of GI bleeding.
  • Monitor renal function: check serum creatinine and electrolytes regularly.
  • Use lowest effective dose: limit duration to the shortest period needed for symptom control.
  • Avoid in known hypersensitivity to indometacin or other NSAIDs.
  • Caution in cardiovascular disease: consider alternative therapy if high risk.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Indometacin can alter the pharmacokinetics or pharmacodynamics of several medicines, requiring careful management.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • Lithium: reduced renal clearance leading to toxicity.
  • Methotrexate: enhanced toxicity, especially at high doses.
  • Other NSAIDs or aspirin: additive gastrointestinal and renal adverse effects.

Moderate Interactions (Monitor Closely)

  • Diuretics: possible reduction in renal perfusion, monitor kidney function.
  • Corticosteroids: heightened risk of GI ulceration.
  • ACE inhibitors or ARBs: may diminish antihypertensive effect and affect renal function.
  • SSRIs or SNRIs: increased bleeding tendency, monitor for signs of hemorrhage.

Frequently Asked Questions

Metindol Retard contains indometacin, an NSAID indicated for the treatment of inflammatory conditions such as rheumatoid arthritis, osteoarthritis, gout attacks, ankylosing spondylitis, and for short‑term relief of moderate to severe acute pain.

Indometacin blocks the activity of cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which are essential for converting arachidonic acid into prostaglandins. By lowering prostaglandin production, it diminishes inflammation, pain signaling, and fever responses in the affected tissues.

The exact dosage of Metindol Retard is determined by the prescribing clinician based on the specific indication, severity of symptoms, patient age, renal and hepatic function, and other individual factors. Patients should follow the prescriber’s instructions precisely.

Safety data for indometacin in pregnancy and lactation are limited. It is generally avoided during the third trimester because of potential fetal cardiovascular effects, and caution is advised while breastfeeding. The prescriber should weigh benefits against risks before use.

To request Metindol Retard, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Indometacin is a potent NSAID with strong anti‑inflammatory activity, often considered more effective for gout flares than some other NSAIDs. However, it may have a higher incidence of gastrointestinal and renal side effects, so clinicians balance efficacy with safety when selecting an alternative.

Metindol Retard should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat and direct sunlight to maintain its stability and potency.

Metindol Retard is taken orally, usually with a full glass of water. It can be taken with or without food, but taking it with meals may reduce gastrointestinal discomfort. The exact administration schedule is set by the prescriber.

Serious risks include gastrointestinal bleeding or ulceration, severe renal impairment, hepatotoxicity, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be educated to report any signs of bleeding, sudden kidney problems, or severe skin changes immediately.

Metindol Retard is contraindicated in individuals with known hypersensitivity to indometacin or other NSAIDs, active gastrointestinal ulceration or bleeding, severe renal or hepatic impairment, and in the third trimester of pregnancy. Caution is also advised for patients with cardiovascular disease or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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