Product image of Diclac (Diclofenac Sodium) supplied by GNH India

Diclac

Active Ingredient:
Diclofenac Sodium
Origin:
EU

Diclac (Diclofenac Sodium)

Diclac is a prescription medication that contains the non‑steroidal anti‑inflammatory drug (NSAID) diclofenac sodium. It is supplied for intramuscular injection, with the specific strength and dosage form varying by market; in the European Union the product is marketed without a listed strength on the label. Classified under ATC code M01AB05, Diclac is used to manage pain and inflammation associated with musculoskeletal conditions in clinical practice.

Manufacturer / TM Owner

Sandoz Gmbh

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Indications & Clinical Uses

Diclac is prescribed for short‑term relief of pain and inflammation that arise from musculoskeletal injuries, postoperative states, and certain inflammatory joint disorders.

  • Acute musculoskeletal pain, including sprains, strains, bruises, and soft‑tissue injuries.
  • Post‑operative pain management after minor surgical or dental procedures.
  • Inflammatory joint conditions such as osteoarthritis flare‑ups or rheumatoid arthritis exacerbations.
  • Dental pain, including discomfort following tooth extraction or periodontal surgery.
  • Low‑grade fever that accompanies inflammatory pain syndromes.
  • Acute gout attacks where NSAID therapy is appropriate.
  • Chronic low back pain episodes that respond to short courses of NSAIDs.

Side Effects

The safety profile of intramuscular diclofenac (Diclac) includes both frequent, mild reactions and less common, potentially serious events.

Common

  • Nausea, dyspepsia, or abdominal discomfort that may occur shortly after injection.
  • Headache, dizziness, or a feeling of light‑headedness.
  • Local injection‑site reactions such as erythema, swelling, warmth, or mild pain.
  • Transient rise in blood pressure or mild fluid retention.

Serious

  • Gastrointestinal ulceration, perforation, or bleeding that can be life‑threatening.
  • Hepatic injury presenting as elevated transaminases, hepatitis, or jaundice.
  • Renal adverse effects including acute kidney injury, reduced urine output, or worsening of chronic kidney disease.

Precautions & Warnings

When prescribing Diclac, clinicians should evaluate patient history and monitor for conditions that may increase the risk of adverse effects.

  • Known hypersensitivity to diclofenac, other NSAIDs, or any excipients.
  • History of gastrointestinal ulcer disease, bleeding, or chronic gastritis.
  • Cardiovascular disease, hypertension, or risk factors for thrombotic events.
  • Impaired liver function or existing hepatic disease.
  • Reduced renal function, dehydration, or concurrent nephrotoxic drugs.
  • Pregnancy, especially the third trimester, and lactation (use only if clearly needed).
  • Concomitant use of anticoagulants or antiplatelet agents.

Avoid Interactions

Diclofenac can interact with several medicines, altering efficacy or increasing toxicity; some combinations should be avoided, while others require careful monitoring.

Avoid

  • Concurrent use with other NSAIDs or COX‑2 selective inhibitors, which raises the risk of gastrointestinal bleeding.
  • Combination with anticoagulants such as warfarin, direct oral anticoagulants, or antiplatelet agents, increasing bleeding potential.

Use with caution

  • Concurrent administration of antihypertensive agents (e.g., ACE inhibitors, diuretics, beta‑blockers) as diclofenac may reduce their blood‑pressure‑lowering effect.
  • Co‑prescription with lithium or methotrexate, which can raise serum levels of these drugs.
  • Use together with corticosteroids, which may enhance the risk of gastrointestinal ulceration.

Frequently Asked Questions

Diclac is commonly prescribed for short‑term relief of pain and inflammation associated with acute musculoskeletal injuries, postoperative discomfort, inflammatory joint disorders such as osteoarthritis or rheumatoid arthritis flares, dental pain, and low‑grade fever linked to inflammatory processes.

Diclofenac sodium inhibits cyclooxygenase (COX‑1 and COX‑2) enzymes, which decreases the synthesis of prostaglandins—chemical mediators that promote inflammation, pain, and fever.

No. In the EU, Diclac is classified as a prescription‑only medication (Rx) and must be prescribed by a qualified healthcare professional.

Common side effects include nausea, dyspepsia, abdominal discomfort, headache, dizziness, and local reactions at the injection site such as redness, swelling, warmth, or mild pain.

Patients should seek immediate medical care if they experience signs of gastrointestinal bleeding (e.g., black stools, vomiting blood), severe abdominal pain, jaundice, sudden swelling or reduced urine output, or any unexpected severe allergic reaction.

Diclac should be used during pregnancy only when clearly needed, especially avoiding the third trimester. Breastfeeding is not recommended unless the benefit outweighs potential risk to the infant.

Concurrent use of Diclac with warfarin or other anticoagulants can increase the risk of bleeding. Close monitoring of coagulation parameters and dose adjustments may be required.

There are no specific dietary restrictions, but taking Diclac with food or a full glass of water may reduce gastrointestinal irritation.

For prolonged use, clinicians often monitor liver function tests, renal function, blood pressure, and assess for gastrointestinal symptoms or signs of bleeding.

Diclac should be stored at controlled room temperature, away from excess heat, moisture, and direct sunlight. Keep the product out of reach of children.

Diclac is generally not indicated for pediatric use unless specifically prescribed by a pediatric specialist; dosing and safety in children have not been established for the intramuscular formulation.

Because Diclac is administered by injection and typically given as a single dose for acute conditions, a missed dose should be discussed with a healthcare provider rather than self‑administered later.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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