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|Meclofenamate Sodium |
Drugs search, click the first letter of a drug name: | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 1 | 2 | 3 | 4 | 5 | 6 | 8 | 9 Home Meclofenamate SodiumPronouncation: (mek-loe-FEN-uh-mate SO-dee-uhm)Class: NSAID Trade Names: Mechanism of ActionPharmacologyDecreases inflammation, pain and fever, probably through inhibition of cyclooxygenase activity and prostaglandin synthesis. PharmacokineticsAbsorptionT max is 0.5 to 2 hr and the bioavailability is approximately 100%. DistributionVd is 23 L and the protein binding is greater than 99%. EliminationMeclofenamate is excreted renally (70%) and fecally (30%). The t ½ is 1.3 hr and clearance is 206 mL/min. Indications and UsageTreatment of rheumatoid and osteoarthritis; treatment of primary dysmenorrhea; relief of mild to moderate pain; idiopathic heavy menstrual blood loss. Unlabeled UsesRelief of sunburn; pain; migraine (abort acute attacks). ContraindicationsPatients in whom aspirin, iodides, or any NSAID has caused allergic-type reactions. Dosage and AdministrationOsteoarthritis or Rheumatoid Arthritis; Mild to Moderate PainAdults PO 200 to 400 mg/day in 3 to 4 equally divided doses. Excessive Menstrual Blood Loss; Primary DysmenorrheaAdults PO 100 mg tid for up to 6 days. Storage/StabilityStore at room temperature (59° to 86°F) in tightly closed, light-resistant container. Drug InteractionsAnticoagulantsIncreased risk of gastric erosion and bleeding. CyclosporineNephrotoxicity of both agents may be increased. LithiumSerum lithium levels may be increased. MethotrexateIncreased methotrexate levels. SalicylatesAdditive GI toxicity. Laboratory Test InteractionsMay prolong bleeding time. Adverse ReactionsCardiovascularEdema. CNSHeadache; vertigo; drowsiness; dizziness; tinnitus. DermatologicRash; urticaria; fasciitis. EENTTinnitus. GIDiarrhea; vomiting; nausea; abdominal pain; dyspepsia; peptic ulcer; GI bleeding; constipation; flatulence; anorexia; stomatitis; heartburn. GenitourinaryAcute renal failure; nephrotic syndrome. HematologicFall in hemoglobin; positive Coombs" test; bruising; prolonged bleeding time; thrombocytopenia purpura; anemia. HepaticAbnormal LFT results. MetabolicPorphyria; hyponatremia. RespiratoryBreathing difficulties in aspirin-sensitive individuals. PrecautionsPregnancySafety not established; avoid use, especially during first and last trimester. LactationUndetermined. ChildrenNot recommended for children younger than 14 yr. ElderlyIncreased risk of adverse reactions. HypersensitivityMay occur; use with caution in aspirin-sensitive individuals due to possible cross-sensitivity. Renal FunctionAcute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia and renal papillary necrosis may occur. Lower doses may be necessary in patients with renal impairment. DiarrheaIf diarrhea occurs, reduce dosage or temporarily discontinue. GI toxicityBleeding, ulceration, or perforation can occur at any time, with or without warning symptoms. Heavy menstrual flowIt is recommended that meclofenamate sodium treatment not be prescribed for heavy menstrual flow without establishing its idiopathic nature. OverdosageSymptomsSweating, disorientation, vomiting, convulsions, electrolyte imbalance, metabolic acidosis. Patient Information
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