Drug Guide

Generic Name

Sulfasalazine

Brand Names Azulfidine, Azulfidine En-tabs, S.a.s.-500

Classification

Therapeutic: Anti-inflammatory, Disease-modifying antirheumatic drug (DMARD)

Pharmacological: Immunomodulator, Anti-inflammatory

FDA Approved Indications

Mechanism of Action

Sulfasalazine is metabolized in the colon to sulfapyridine and 5-aminosalicylic acid (5-ASA). The active metabolites exert anti-inflammatory effects by inhibiting prostaglandin synthesis and suppressing inflammatory mediators, leading to decreased inflammation in the colon and joints.

Dosage and Administration

Adult: Typically, 2-4 g/day in divided doses; dosage varies based on condition and response.

Pediatric: Use is based on weight and clinical response; consult specific guidelines.

Geriatric: Start at lower doses due to potential renal or hepatic impairments; monitor closely.

Renal Impairment: Adjust dose based on severity; monitor renal function.

Hepatic Impairment: Use with caution; monitor liver function.

Pharmacokinetics

Absorption: Moderate oral absorption, subject to variability.

Distribution: Widely distributed; crosses placental barrier but minimal into CSF.

Metabolism: Partially metabolized in the liver, with active metabolites.

Excretion: Excreted primarily in urine; some in feces.

Half Life: Approximately 10 hours.

Contraindications

Precautions

Adverse Reactions - Common

Adverse Reactions - Serious

Drug-Drug Interactions

Drug-Food Interactions

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor complete blood counts, liver and renal function tests regularly.

Diagnoses:

  • Risk for gastrointestinal disturbances
  • Risk for hematologic abnormalities

Implementation: Administer with food to decrease GI upset. Educate patients about potential side effects.

Evaluation: Assess for improvement in symptoms and monitor labs for adverse effects.

Patient/Family Teaching

Special Considerations

Black Box Warnings:

Genetic Factors: G6PD deficiency can increase risk of hemolytic anemia. Consider screening before initiation.

Lab Test Interference: May cause false-positive tests for glucose or ketones in urine.

Overdose Management

Signs/Symptoms: Gastrointestinal distress, vomiting, dizziness, and hematologic abnormalities.

Treatment: Supportive care; hemodialysis may be considered in severe cases.

Storage and Handling

Storage: Store at room temperature away from moisture and heat.

Stability: Stable under proper storage conditions.

This guide is for educational purposes only and is not intended for clinical use.