Drug Guide
Mesalamine
Classification
Therapeutic: Aminosalicylate anti-inflammatory
Pharmacological: Drug that reduces inflammation by inhibiting prostaglandin and leukotriene synthesis
FDA Approved Indications
- Ulcerative colitis
- Crohn's disease (certain formulations)
Mechanism of Action
Mesalamine exerts its anti-inflammatory effects locally in the gastrointestinal tract by inhibiting cyclooxygenase (COX) and lipoxygenase pathways, thus reducing the production of inflammatory prostaglandins and leukotrienes.
Dosage and Administration
Adult: Varies based on formulation; typically, 800 mg to 4,000 mg daily divided into doses, taken orally or rectally as prescribed.
Pediatric: Use with caution; dosing depends on age and weight, consult specific formulation guidelines.
Geriatric: Adjust dosing based on renal and hepatic function; monitor for adverse effects.
Renal Impairment: Altered dosing; close monitoring recommended.
Hepatic Impairment: Adjustments may not be necessary, but caution advised.
Pharmacokinetics
Absorption: Limited absorption from the gastrointestinal tract, especially with rectal forms.
Distribution: Primarily local, minimal systemic distribution.
Metabolism: Partially metabolized in the intestinal wall.
Excretion: Excreted primarily in feces; minimal renal excretion.
Half Life: Approximately 7 hours, varies based on formulation.
Contraindications
- Hypersensitivity to mesalamine or salicylates.
- History of hypersensitivity reactions to 5-aminosalicylic acid products.
Precautions
- Monitor renal function; use cautiously in renal impairment.
- Use with caution in hepatic impairment.
- Patients with infections or known TB should be monitored carefully.
Adverse Reactions - Common
- Headache (Common)
- Nausea (Common)
- Abdominal pain (Common)
- Flatulence (Common)
Adverse Reactions - Serious
- Pancreatitis (Uncommon)
- Rectal bleeding (with rectal formulations) (Uncommon)
- Hypersensitivity reactions, including rash and fever (Uncommon)
- Acute intolerance syndrome (fever, eosinophilia, malaise) (Rare)
Drug-Drug Interactions
- Azathioprine or 6-mercaptopurine (may increase risk of pancreatitis)
- Other NSAIDs
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor renal function, complete blood count, and liver function tests periodically.
Diagnoses:
- Risk for renal impairment
- Impaired comfort related to gastrointestinal discomfort
Implementation: Administer as prescribed; educate patient on correct administration, especially for rectal formulations.
Evaluation: Assess symptom improvement and monitor for adverse effects.
Patient/Family Teaching
- Take medication as directed.
- Report any signs of allergic reactions, sore throat, unusual bleeding, or symptoms of pancreatitis.
- Maintain hydration and follow dietary guidance.
- Be aware of possible gastrointestinal side effects.
Special Considerations
Black Box Warnings:
- Potential for increased risk of cardiovascular, renal, and gastrointestinal adverse effects with high-dose or long-term use.
- Rare reports of cardiac hypersensitivity reactions.
Genetic Factors: N/A
Lab Test Interference: May cause elevated serum amylase or lipase during pancreatitis.
Overdose Management
Signs/Symptoms: Nausea, vomiting, abdominal pain, bleeding, tinnitus (rare).
Treatment: Supportive care; activated charcoal if ingestion was recent; hemodialysis in severe cases.
Storage and Handling
Storage: Store at room temperature (20°C to 25°C); protect from moisture.
Stability: Stable under recommended storage conditions.