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# Mefenamic Acid
## Overview
Mefenamic acid is a nonsteroidal anti-inflammatory drug (NSAID) of the fenamate class. It acts by inhibiting cyclooxygenase (COX-1 and COX-2) enzymes, reducing prostaglandin synthesis. Its use is limited to short-term therapy (generally ≤7 days).
## Primary Indications
* Treatment of mild to moderate pain.
* Primary dysmenorrhea.
## Adult Dosing
* **Standard dose:** 500 mg initially, followed by 250 mg every 6 hours as needed.
* **Maximum duration:** Not to exceed 7 days of therapy.
## Pediatric Dosing
* **Children 14 years and older:** 500 mg initially, followed by 250 mg every 6 hours as needed.
* **Children under 14 years:** Safety and efficacy have not been established; use is generally avoided.
## Dose Adjustments
* **Renal Impairment:** Avoid in patients with severe renal impairment (CrCl <30 mL/min). Use with caution and monitor closely in mild to moderate impairment.
* **Hepatic Impairment:** Reduce dose in patients with hepatic impairment; monitor for toxicity.
## Contraindications
* History of asthma, urticaria, or allergic-type reactions after taking aspirin or other NSAIDs.
* Perioperative pain in the setting of coronary artery bypass graft (CABG) surgery.
* Active peptic ulcer disease or history of gastrointestinal (GI) bleeding.
* Severe renal or hepatic failure.
* Third trimester of pregnancy.
## Adverse Effects
* **GI:** Diarrhea (common and sometimes severe), nausea, abdominal pain, GI ulceration/bleeding.
* **Renal:** Fluid retention, edema, acute renal failure.
* **CV:** Increased risk of thrombotic events, hypertension.
* **Hematologic:** Anemia, blood dyscrasias (rare).
* **CNS:** Dizziness, headache, drowsiness.
## Key Drug Interactions
* **Anticoagulants (e.g., Warfarin):** Increased risk of bleeding due to antiplatelet effects and gastric mucosal injury.
* **Anti-hypertensives:** NSAIDs may diminish the antihypertensive effect of ACE inhibitors, ARBs, and diuretics.
* **Lithium/Methotrexate:** NSAIDs may decrease renal clearance, increasing risk of toxicity.
* **Other NSAIDs/Corticosteroids:** Increased risk of GI toxicity and ulceration.
## Monitoring
* **Baseline:** Renal function (BUN/SCr) and LFTs if long-term or high-risk.
* **Ongoing:** Monitor for signs of GI bleeding, changes in blood pressure, and peripheral edema. Monitor Hb/Hct if chronic use occurs (not recommended).
## Clinical Pearls
* **Diarrhea:** Mefenamic acid is uniquely associated with diarrhea, which can be severe; discontinue if diarrhea occurs.
* **Duration:** Strict adherence to the 7-day limit is imperative due to the increased risk of GI and renal adverse events with prolonged use.
* **Administration:** Administer with food to minimize GI upset.
* **NSAID Class Effect:** All NSAIDs carry a boxed warning for increased risk of serious cardiovascular thrombotic events and serious gastrointestinal adverse events.
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*Educational Disclaimer: This information is for educational purposes only and does not constitute medical advice. Always consult the latest prescribing information (USPI/SmPC) and institutional clinical protocols before prescribing or administering medication.*