A fixed-dose combination (FDC) of an antifibrinolytic agent (Tranexamic Acid) and a non-steroidal anti-inflammatory drug (NSAID) of the fenamate class (Mefenamic Acid). It is primarily indicated for the management of heavy menstrual bleeding (menorrhagia) associated with pain and inflammation, providing a dual mechanism of action to reduce bleeding and alleviate pain. The combination is widely used in the Indian context for dysmenorrhea and menorrhagia.
Adult: 1 tablet (Tranexamic Acid 500mg + Mefenamic Acid 250mg) three times daily, starting at the onset of menses. Duration typically 3-5 days, not to exceed 5 days per menstrual cycle.
Note: Take with or immediately after food with a full glass of water to minimize gastric irritation. Do not crush or chew. Swallow whole. The tablet should be taken at evenly spaced intervals during the days of menstruation.
The combination works synergistically. Tranexamic Acid competitively inhibits the activation of plasminogen to plasmin, thereby preventing the breakdown of fibrin clots and reducing menstrual blood loss. Mefenamic Acid inhibits the enzymes cyclooxygenase-1 and 2 (COX-1 & COX-2), leading to reduced synthesis of prostaglandins (especially PGE2 and PGF2α) which are mediators of pain, inflammation, and uterine hypercontractility in dysmenorrhea.
Pregnancy: Category C (US FDA). Avoid in first and second trimesters unless clearly needed. Contraindicated in third trimester due to risk of premature closure of ductus arteriosus in the fetus, oligohydramnios, and potential interference with labor. Tranexamic acid crosses placenta; use only if potential benefit justifies potential risk.
Driving: May cause dizziness, vertigo, or visual disturbances. Patients should not drive or operate machinery if affected.
| Anticoagulants (Warfarin, Heparin, DOACs) | Increased risk of bleeding with Tranexamic Acid; increased risk of GI bleed with Mefenamic Acid. Conflicting effects require extreme caution. | Major |
| Anti-platelets (Aspirin, Clopidogrel) | Increased risk of gastrointestinal bleeding and ulceration. | Major |
| Other NSAIDs (Ibuprofen, Diclofenac) | Increased risk of GI toxicity (ulcers, bleeding) and renal impairment. | Major |
| Corticosteroids (Prednisolone) | Increased risk of GI ulceration and bleeding. | Major |
| ACE Inhibitors (Ramipril, Enalapril) / ARBs (Losartan) | Mefenamic Acid may reduce antihypertensive effect and increase risk of renal impairment. | Moderate |
| Diuretics (Furosemide, Hydrochlorothiazide) | Reduced diuretic and antihypertensive efficacy; risk of renal failure. | Moderate |
| Lithium | Mefenamic Acid can increase lithium serum levels, risking toxicity. | Major |
| Methotrexate | Mefenamic Acid may increase methotrexate toxicity. | Major |
| Selective Serotonin Reuptake Inhibitors (SSRIs e.g., Sertraline) | Increased risk of upper gastrointestinal bleeding. | Moderate |
Same composition (Tranexamic Acid (500mg) + Mefenamic Acid (250mg)), different brands: