Product image of Mefenamic Acid Teva (Mefenamic Acid) supplied by GNH India

Mefenamic Acid Teva

Active Ingredient:
Mefenamic Acid
Origin:
EU

Mefenamic Acid Teva (Mefenamic Acid)

Mefenamic Acid, the active ingredient in Mefenamic Acid Teva, is a nonsteroidal anti‑inflammatory drug presented as an oral tablet for oral use. It is employed to relieve mild to moderate pain, dysmenorrhea, and inflammatory musculoskeletal conditions.

GNH India supplies Mefenamic Acid Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance and reliable global logistics. The company maintains stringent manufacturing standards and provides comprehensive documentation to support import and distribution requirements.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

Mefenamic Acid is an NSAID that reduces inflammation and pain in several musculoskeletal and gynecologic conditions.

  • Mild to moderate pain: provides analgesic relief for acute or chronic pain episodes.
  • Dysmenorrhea: alleviates menstrual cramps and associated discomfort.
  • Inflammatory musculoskeletal conditions: reduces swelling and improves mobility in conditions such as arthritis.

How It Works

  • Mefenamic Acid exerts its effect by non‑selectively inhibiting cyclooxygenase enzymes COX‑1 and COX‑2, which blocks the conversion of arachidonic acid to prostaglandins. The resulting decrease in prostaglandin synthesis diminishes inflammation, pain signaling, and fever generation at the site of tissue injury. By limiting prostaglandin‑mediated vasodilation and sensitization of nociceptors, the drug contributes to reduced edema and heightened pain threshold. These actions collectively provide the therapeutic benefit observed in clinical use.

Side Effects

Mefenamic Acid may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Gastrointestinal discomfort: nausea, dyspepsia or abdominal pain.
  • Diarrhea: loose stools occurring intermittently.
  • Headache: mild to moderate intensity.
  • Dizziness: transient sensation of light‑headedness.
  • Skin rash: mild erythema or itching.
  • Mouth ulcers: painful lesions on oral mucosa.

Serious or Rare Side Effects

  • Gastrointestinal ulceration or bleeding: potentially life‑threatening hemorrhage.
  • Renal impairment: reduced kidney function or acute renal failure.
  • Severe hypersensitivity: anaphylaxis, angioedema or Stevens‑Johnson syndrome.
  • Hepatotoxicity: elevated liver enzymes or hepatitis.

Precautions & Warnings

When prescribing Mefenamic Acid, clinicians should consider several precautionary measures to minimize risk.

  • Assess renal function: avoid use in patients with severe renal impairment.
  • Evaluate gastrointestinal risk: use with caution in history of ulcers or bleeding.
  • Monitor cardiovascular status: NSAIDs may increase risk of thrombotic events.
  • Use the lowest effective dose: limit duration to the shortest necessary period.
  • Pregnancy and lactation: avoid in the third trimester and assess benefit‑risk in pregnancy.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture.

Avoid Interactions

Mefenamic Acid can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased bleeding risk.
  • Other NSAIDs or aspirin: heightened gastrointestinal toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): elevated risk of bleeding.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may reduce antihypertensive effect and impair renal function.
  • Diuretics: potential for reduced diuretic efficacy and renal compromise.
  • Lithium: NSAIDs can increase lithium serum concentrations.

Frequently Asked Questions

Mefenamic Acid Teva is prescribed to manage mild to moderate pain, relieve menstrual cramps associated with dysmenorrhea, and treat inflammatory musculoskeletal conditions such as arthritis. It works by reducing inflammation and pain signals in the affected tissues.

The drug non‑selectively blocks the cyclooxygenase enzymes COX‑1 and COX‑2, which are essential for converting arachidonic acid into prostaglandins. By lowering prostaglandin levels, it diminishes inflammation, pain perception, and fever at the site of injury.

The appropriate dose and dosing schedule are determined by the prescribing clinician based on the individual’s medical condition, age, weight, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Mefenamic Acid is classified as Pregnancy Category B, indicating no proven risk in animal studies but limited human data. It should be used only if clearly needed and after consulting a healthcare professional. Breastfeeding mothers should discuss potential risks with their doctor.

To place an order, 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.

Mefenamic Acid belongs to the anthranilic acid class of NSAIDs and shares the COX‑inhibition mechanism with drugs like ibuprofen and naproxen. It may offer comparable analgesic efficacy but has a distinct safety profile, especially regarding gastrointestinal and renal effects, which clinicians weigh when selecting therapy.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and ensure the packaging is tightly closed to maintain product stability.

Mefenamic Acid Teva is taken orally, usually with a full glass of water. It can be taken with or without food, but patients who experience stomach upset may benefit from taking it with meals or an antacid as advised by their physician.

Serious adverse events include gastrointestinal ulceration or bleeding, severe renal impairment, and hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they notice signs of bleeding, sudden kidney problems, or severe skin reactions.

Individuals with a known hypersensitivity to mefenamic acid or other NSAIDs, those with active gastrointestinal ulcers, severe renal or hepatic impairment, and patients in the third trimester of pregnancy should avoid this medication. A healthcare professional should evaluate suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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