Drug Guide
Sulfasalazine
Classification
Therapeutic: Anti-inflammatory, Disease-modifying antirheumatic drug (DMARD)
Pharmacological: Immunomodulator, Anti-inflammatory
FDA Approved Indications
- Ulcerative colitis
- Rheumatoid arthritis
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
- Hypersensitivity to sulfonamides or salicylates
- History of sulfa allergies
- Intestinal or urinary tract obstruction
Precautions
- Use with caution in patients with hepatic or renal impairment, blood dyscrasias, G6PD deficiency, or pregnancy/lactation. Regular blood counts and liver function tests are recommended.
Adverse Reactions - Common
- Nausea, vomiting (Common)
- Headache (Common)
- Rash (Common)
Adverse Reactions - Serious
- Hematologic reactions (e.g., agranulocytosis, aplastic anemia) (Rare)
- Liver toxicity, hepatitis (Rare)
- Uveitis, peripheral neuropathy (Rare)
Drug-Drug Interactions
- Methotrexate (risk of hematologic toxicity)
- Warfarin (increased anticoagulant effects)
Drug-Food Interactions
- Avoid Alcohol (may increase hepatotoxicity)
Drug-Herb Interactions
N/ANursing 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
- Take medication with food to minimize GI discomfort.
- Report signs of allergic reactions, unusual bleeding, fatigue, or jaundice.
- Maintain regular lab monitoring appointments.
Special Considerations
Black Box Warnings:
- Hematologic reactions including agranulocytosis and aplastic anemia, which can be fatal.
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.