Product image of Metindol (Indometacin) supplied by GNH India

Metindol

Active Ingredient:
Indometacin
Origin:
EU

Metindol (Indometacin)

Indometacin, the active ingredient in Metindol, is a nonsteroidal anti‑inflammatory drug (NSAID) presented as an oral dosage form for systemic use. It reduces pain, inflammation and swelling associated with rheumatic and musculoskeletal conditions in adult patients and can be prescribed by physicians for short‑term management.

GNH India supplies Metindol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and regulatory requirements across EU and global markets, ensuring product consistency and safety for end‑users.

Manufacturer / TM Owner

Viatris Healthcare Limited

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Indications & Clinical Uses

Indometacin acts on inflammatory pathways to relieve symptoms in several musculoskeletal and crystal‑induced disorders.

  • Rheumatoid arthritis: decreases joint pain, swelling and stiffness, improving functional ability.
  • Osteoarthritis: alleviates chronic knee, hip or hand pain and reduces inflammation.
  • Gout flares: rapidly controls acute gouty arthritis pain and swelling.
  • General musculoskeletal pain: provides analgesia for sprains, strains and postoperative discomfort.
  • Inflammatory conditions: reduces systemic inflammation in various acute inflammatory states.

How It Works

  • Indometacin inhibits cyclooxygenase (COX‑1 and COX‑2) enzymes, blocking the conversion of arachidonic acid to prostaglandins. This reduction in prostaglandin synthesis diminishes inflammation, pain signaling, and fever responses at the site of tissue injury or disease.

Side Effects

Indometacin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Gastrointestinal upset: nausea, dyspepsia or abdominal discomfort.
  • Headache or dizziness: transient central nervous system symptoms.
  • Skin rash: mild erythema or pruritus.

Serious or Rare Side Effects

  • Gastrointestinal ulceration or bleeding: may present as melena or hematemesis.
  • Renal impairment: reduced urine output or increased serum creatinine.
  • Hepatic dysfunction: elevated transaminases or jaundice.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Anaphylaxis: sudden onset of respiratory distress, hypotension or urticaria.

Precautions & Warnings

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

  • Assess renal function: check baseline creatinine and monitor during treatment.
  • Evaluate gastrointestinal risk: consider ulcer prophylaxis in patients with prior GI bleeding.
  • Review cardiovascular history: avoid in uncontrolled hypertension or active cardiovascular disease.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Indometacin can alter the pharmacokinetics or pharmacodynamics of several medicines; careful review is required.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased bleeding risk.
  • Lithium: reduced renal clearance leading to toxicity.
  • Methotrexate: enhanced toxicity, especially renal.
  • ACE inhibitors or ARBs: may worsen renal function.

Moderate Interactions (Monitor Closely)

  • Corticosteroids: additive gastrointestinal ulcer risk.
  • SSRIs or SNRIs: heightened bleeding potential.
  • Diuretics: possible reduction in renal perfusion.
  • Other NSAIDs: increased adverse effect profile.

Frequently Asked Questions

Metindol contains indometacin, an NSAID that is prescribed to manage pain, inflammation and swelling in conditions such as rheumatoid arthritis, osteoarthritis, gout flares and other acute musculoskeletal inflammatory disorders.

Indometacin blocks the cyclooxygenase enzymes COX‑1 and COX‑2, which are essential for converting arachidonic acid into prostaglandins. By reducing prostaglandin production, it diminishes inflammation, pain signaling and fever responses at the affected sites.

The appropriate dose of Metindol is determined by the prescribing clinician based on the patient’s condition, severity, renal and hepatic function, and other individual factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for indometacin in pregnancy and lactation are limited. It should only be used if the potential therapeutic benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Metindol, 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 necessary import documentation.

Indometacin is a potent NSAID with strong anti‑inflammatory activity, often considered more effective for gout and severe rheumatic pain than some other NSAIDs. However, its gastrointestinal and renal risk profile may be higher, so clinicians balance efficacy against safety when selecting therapy.

Metindol should be stored at ambient temperature, below 25 °C, in the original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children.

Metindol is taken orally, usually with a full glass of water. It may be taken with food or milk to lessen gastrointestinal irritation, but patients should follow the specific instructions provided by their healthcare provider.

Serious risks include gastrointestinal ulceration or bleeding, severe renal impairment, hepatic dysfunction, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored for signs of these events and seek immediate medical attention if they occur.

Metindol is contraindicated in patients with known hypersensitivity to indometacin or other NSAIDs, those with active gastrointestinal ulceration or bleeding, severe renal or hepatic impairment, and in late pregnancy. Clinicians should also avoid use in patients with uncontrolled hypertension or certain cardiovascular conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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