Meclofenamate Sodium

A to Z Drug Facts

Meclofenamate Sodium

  Action
  Indications
  Contraindications
  Route/Dosage
  Interactions
  Lab Test Interferences
  Adverse Reactions
  Precautions
Patient Care Considerations
  Administration/Storage
  Assessment/Interventions
  Patient/Family Education


(mek-loe-FEN-uh-mate SO-dee-uhm)
Available in generic only
Class: Analgesic/NSAID

 Action Decreases inflammation, pain and fever, probably through inhibition of cyclooxygenase activity and prostaglandin synthesis.

 Indications Treatment of rheumatoid and osteoarthritis; treatment of primary dysmenorrhea; elief of mild to moderate pain; idiopathic heavy menstrual blood loss. Unlabeled use(s): Relief of sunburn; pain; migraine (abort acute attacks).

 Contraindications Patients in whom aspirin, iodides or any NSAID has caused allergic-type reactions.

 Route/Dosage

Osteoarthritis or Rheumatoid Arthritis; Mild to Moderate Pain

ADULTS: PO 200–400 mg/day in 3–4 equally divided doses.

Excessive Menstrual Blood Loss; Primary Dysmenorrhea

ADULTS: PO 100 mg tid for up to 6 days.

 Interactions

Anticoagulants: Increased risk of gastric erosion and bleeding. Cyclosporine: Nephrotoxicity of both agents may be increased. Lithium: Serum lithium levels may be increased. Methotrexate: Increased methotrexate levels. Salicylates: Additive GI toxicity.

 Lab Test Interferences May prolong bleeding time.

 Adverse Reactions

CV: Edema. CNS: Headache; vertigo; drowsiness; dizziness; tinnitus. DERM: Rash; urticaria; fasciitis. EENT: Tinnitus. GI: Diarrhea; vomiting; nausea; abdominal pain; dyspepsia; peptic ulcer; GI bleeding; constipation; flatulence; anorexia; stomatitis; heartburn. GU: Acute renal failure; nephrotic syndrome. HEMA: Fall in hemoglobin; positive Coombs' est; bruising; prolonged bleeding time; thrombocytopenia purpura; anemia. HEPA: Abnormal liver function test results. META: Porphyria; hyponatremia. RESP: Breathing difficulties in aspirin-sensitive individuals.

 Precautions

Pregnancy: Safety not established; avoid use, especially during first and last trimester. Lactation: Undetermined. Children: Not recommended for children < 14 yr. Elderly patients: Increased risk of adverse reactions. Diarrhea: If diarrhea occurs, reduce dosage or temporarily discontinue. GI toxicity: Bleeding, ulceration or perforation can occur at any time, with or without warning symptoms. Heavy menstrual flow: It is recommended that meclofenamate sodium treatment not be prescribed for heavy menstrual flow without establishing its idiopathic nature. Hypersensitivity: May occur; use with caution in aspirin-sensitive individuals due to possible cross-sensitivity. Renal effects: Acute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia and renal papillary necrosis may occur. Renal impairment: Lower doses may be necessary.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

OVERDOSAGE: SIGNS & SYMPTOMS
  Sweating, disorientation, vomiting, convulsions, electrolyte imbalance, metabolic acidosis

 Patient/Family Education

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© 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts