Diclofenac

(die-KLOE-fen-ak)

Trade Name(s):
Cataflam
  • Tablets
  • 50 mg (as potassium)

    Solaraze
  • Gel
  • 3% (1 g contains 30 mg diclofenac sodium)

    Voltaren
  • Tablets, delayed-release
  • 25 mg (as sodium)
  • Tablets, delayed-release
  • 50 mg (as sodium)
  • Tablets, delayed-release
  • 75 mg (as sodium)

    Voltaren-XR
  • Tablets, delayed-release
  • 100 mg (as sodium)

    Apo-Diclo
    Apo-Diclo SR
    Novo-Difenac
    Novo-Difenac SR
    Nu-Diclo
    Taro-Diclofenac
    Voltaren Ophtha
    Indicates Canadian trade names.

    Class:  AnalgesicNSAID

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

      Indications:
    Treatment of rheumatoid arthritis, ankylosing spondylitis, osteoarthritis. Potassium salt is approved for management of pain and primary dysmenorrhea, when prompt pain relief is needed.

    Ophthalmic: Treatment of postoperative inflammation after cataract removal.

    Topical: Treatment of actinic keratosis. Unlabeled use(s): Treatment of biliary colic, dysmenorrhea, enuresis, glomerular disease, gout, migraine headache, renal colic.

      Contraindications:
    Sensitivity to aspirin or any NSAID; soft contact lenses (ophthalmic); benzyl alcohol, polyethylene glycol monomethyl ether 350, and hyaluronate sodium (topical).

      Route/Dosage:

    Osteoarthritis
    PO 100 to 150 mg/day in divided doses.

    Rheumatoid Arthritis
    PO 150 to 200 mg/day in divided doses.

    Ankylosing Spondylitis
    PO 100 to 125 mg/day in divided doses; may give additional 25 mg at bedtime.

    Analgesia and Primary Dysmenorrhea (Potassium Salt Only)
    PO 50 mg tid; may give initial dose of 100 mg if needed.

    Ophthalmic 1 drop of 0.1% solution in affected eye qid.

    Actinic Keratosis

    Adult:
    Topical Apply gel to lesions twice daily.

      Interactions:

    Cyclosporine: May increase nephrotoxicity.

    Digoxin: May increase digoxin serum concentrations.

    Diuretics: May inhibit diuretic and antihypertensive effects.

    Lithium: May decrease lithium clearance.

    Methotrexate: May increase methotrexate levels.

    Warfarin: May increase risk of gastric erosion and bleeding.

      Lab Test Interferences:
    May prolong bleeding time.

      Adverse Reactions:

    CV:
    Edema; water retention; hypertension; CHF.
    CNS:
    Headache; vertigo; drowsiness; dizziness.
    DERM:
    Rash; urticaria; fasciitis; photosensitivity; contact dermatitis, exfoliation (topical).
    EENT:
    Transient stinging and burning (ophthalmic); tinnitus.
    GI:
    Diarrhea; vomiting; abdominal pain; dyspepsia; peptic ulcer; GI bleeding.
    GU:
    Acute renal failure; nephrotic syndrome.
    HEMA:
    Fall in hemoglobin; bruising; prolonged bleeding time; thrombocytopenia purpura; anemia.
    RESP:
    Breathing difficulties in aspirin-sensitive individuals.
    OTHER:
    Hypersensitivity reactions. Ophthalmic use may cause bleeding tendencies and other effects associated with systemic use, caused by absorption.

      Precautions:

    Pregnancy: Category B.

    Lactation: Undetermined.

    Children: Safety and efficacy not established.

    Elderly: Increased risk of adverse reactions.

    GI effects: Serious GI toxicity (eg, bleeding, ulceration, perforation) can occur at any time, with or without warning symptoms.

    Renal effects: Acute renal insufficiency; interstitial nephritis; hyperkalemia; hyponatremia; and renal papillary necrosis may occur.


    Patient Care Considerations

      Administration/Storage:

      Assessment/Interventions:


    OVERDOSAGE: SIGNS & SYMPTOMS
    Acute renal failure, nausea, vomiting, drowsiness

      Patient/Family Education:


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