Drug Guide
Sulfapyridine
Classification
Therapeutic: Antibacterial, Sulfonamide antibiotic
Pharmacological: Sulfonamide (antimicrobial)
FDA Approved Indications
- Treatment of bacterial infections caused by susceptible organisms
Mechanism of Action
Inhibits bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid (PABA), leading to inhibition of bacterial growth.
Dosage and Administration
Adult: 250-500 mg orally every 6-8 hours, dose adjusted based on severity and organism susceptibility
Pediatric: Not typically used in pediatric patients due to availability of newer agents
Geriatric: Adjust dose based on renal function; careful monitoring for adverse effects
Renal Impairment: Dose adjustment needed; usually reduced or extended dosing interval
Hepatic Impairment: Use with caution; no specific adjustment detailed
Pharmacokinetics
Absorption: Well absorbed from the gastrointestinal tract
Distribution: Widely distributed including into cerebrospinal fluid and urine
Metabolism: Partially metabolized in the liver
Excretion: Primarily via kidneys in unchanged form
Half Life: Approximately 10-20 hours
Contraindications
- Hypersensitivity to sulfamethoxazole or other sulfonamides
- History of hypersensitivity reactions to sulfonamides
Precautions
- Use with caution in patients with compromised renal or hepatic function, porphyria, or blood dyscrasias; risk of hypersensitivity reactions
Adverse Reactions - Common
- Rash or skin hypersensitivity reactions (Less common)
- Gastrointestinal upset (Common)
Adverse Reactions - Serious
- Stevens-Johnson syndrome (Rare)
- Blood dyscrasias such as agranulocytosis or aplastic anemia (Rare)
- Drug fever, hepatotoxicity (Rare)
Drug-Drug Interactions
- Methotrexate (increased toxicity)
- Warfarin (increased bleeding risk)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for allergic reactions, blood counts, renal and hepatic function
Diagnoses:
- Risk for hypersensitivity reactions
- Risk of blood dyscrasias
Implementation: Administer with adequate hydration to prevent crystalluria; monitor blood counts regularly
Evaluation: Observe for resolution of infection and any adverse reactions
Patient/Family Teaching
- Take medication as prescribed and complete the course
- Report any skin rash, fever, or unusual bleeding immediately
- Maintain adequate hydration
- Avoid exposure to sunlight or tanning beds due to photosensitivity
Special Considerations
Black Box Warnings:
- Hypersensitivity reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis, can be severe and life-threatening
Genetic Factors: None specifically noted for sulfapyridine
Lab Test Interference: May cause false positive results in certain laboratory tests such as urinary ketones
Overdose Management
Signs/Symptoms: Nausea, vomiting, dizziness, headache, bloody dyscrasias, allergic reactions
Treatment: Supportive care; rapid removal of the drug through gastric lavage or activated charcoal if recent ingestion; hemodialysis in severe cases may be considered
Storage and Handling
Storage: Store at room temperature, away from moisture and light
Stability: Stable under recommended storage conditions for the period specified by the manufacturer