Sulfadiazine (Monograph)

Drug class: Sulfonamides
VA class: AM650
Chemical name: N1-2-pyrimidinylsulfanilamide
Molecular formula: C₁₀H₁₀N₄O₂S
CAS number: 68-35-9

Medically reviewed by Drugs.com on Oct 10, 2024. Written by ASHP.

Introduction

Antibacterial; intermediate-acting sulfonamide.^{a b}

Uses for Sulfadiazine

Prevention of Rheumatic Fever Recurrence

Alternative for prevention of recurrent attacks of rheumatic fever (secondary prophylaxis).^{123 292 375}

IM penicillin G benzathine is drug of choice for secondary prophylaxis of rheumatic fever;^{292 375} alternatives include oral penicillin V, oral sulfadiazine, and oral sulfisoxazole (only available in the US in fixed combination with erythromycin).^{292 375}

AHA and AAP recommend long-term (continuous) secondary prophylaxis in patients who have been treated for documented acute rheumatic fever (even if manifested solely by Sydenham chorea) and in those with evidence of rheumatic heart disease (even after prosthetic valve replacement).^{292 375}

Do not use for treatment of Streptococcus pyogenes (group A β-hemolytic streptococci, GAS) infections (e.g., pharyngitis and tonsillitis).^{123 292 375 580} Sulfadiazine will not eradicate S. pyogenes and, therefore, will not prevent sequelae such as rheumatic fever and glomerulonephritis.^{123 375 580}

Toxoplasmosis

Treatment of toxoplasmosis caused by Toxoplasma gondii;^{123 134 155 156 184 185} usually used in conjunction with pyrimethamine (and leucovorin).^{123 134 155 156 184 185} Designated an orphan drug by FDA for use in conjunction with pyrimethamine for treatment of T. gondii encephalitis in patients with or without HIV infection.¹³⁷

CDC, NIH, IDSA, and AAP recommend sulfadiazine in conjunction with pyrimethamine (and leucovorin) as the regimen of choice for initial treatment of toxoplasmosis in HIV-infected adults and adolescents¹⁵⁵ and for treatment of acquired CNS, ocular, or systemic toxoplasmosis in HIV-infected children.¹⁵⁶

Sulfadiazine in conjunction with atovaquone is recommended by CDC, NIH, and IDSA as one of several alternative regimens for treatment of toxoplasmosis in HIV-infected adults and adolescents who cannot tolerate or do not respond to or relapsed with the regimen of choice;¹⁵⁵ sulfadiazine and atovaquone regimen not adequately studied for treatment of toxoplasmosis in children.¹⁵⁶

Sulfadiazine in conjunction with pyrimethamine (and leucovorin) is the regimen of choice for treatment of congenital toxoplasmosis.¹⁵⁶ Empiric treatment of congenital toxoplasmosis should be strongly considered if the mother had symptomatic or asymptomatic Toxoplasma infection during pregnancy, even if the mother received toxoplasmosis treatment during the pregnancy.¹⁵⁶

Sulfadiazine used in conjunction with pyrimethamine (and leucovorin) is the regimen of choice for chronic maintenance therapy (secondary prophylaxis) to prevent relapse of T. gondii encephalitis^{† [off-label]} in HIV-infected adults, adolescents, and children who have completed initial treatment of the disease.^{155 156}

Acute Otitis Media (AOM)

Has been used in conjunction with penicillin for treatment of AOM caused by susceptible Haemophilus influenzae.^{123 b}

When anti-infective therapy indicated for treatment of AOM, AAP recommends high-dose amoxicillin or fixed combination of amoxicillin and clavulanate as drugs of first choice for initial treatment and certain cephalosporins (cefdinir, cefpodoxime, cefuroxime, ceftriaxone) as alternatives for initial treatment in penicillin-allergic patients who do not have a history of severe and/or recent penicillin-allergic reactions.³²¹ AAP states that sulfonamides should not be used as alternatives in patients who do not respond to amoxicillin.³²¹

Chancroid

Has been used for treatment of chancroid caused by H. ducreyi.^{123 b} CDC recommends azithromycin, ceftriaxone, ciprofloxacin, or erythromycin as the drugs of choice for chancroid;³⁴⁴ sulfadiazine not included in CDC recommendations.³⁴⁴

Chlamydial Infections

Has been used for treatment of infections caused by Chlamydia trachomatis (e.g., inclusion conjunctivitis, trachoma).¹²³ Other anti-infectives (e.g., azithromycin, erythromycin) usually drugs of choice for these infections.²⁹²

Haemophilus influenzae Infections

Has been used for treatment of meningitis caused by H. influenzae as an adjunct to streptomycin.¹²³ Other anti-infectives (e.g., ceftriaxone, cefotaxime, chloramphenicol, cefepime, meropenem, fluoroquinolones) usually recommended.⁵⁰⁶

Malaria

Has been used as an adjunct in the treatment of malaria caused by chloroquine-resistant Plasmodium falciparum.¹²³ Not included in recommendations for treatment of malaria.¹³⁴

Neisseria meningitidis Infections

Has been used for chemoprophylaxis in close contacts of individuals with invasive meningococcal disease caused by sulfonamide-susceptible Neisseria meningitidis serogroup A.¹²³ No longer recommended because of high prevalence of N. meningitidis resistant to sulfonamides.^b CDC and AAP recommend rifampin, ciprofloxacin, or ceftriaxone for such prophylaxis.^{292 376}

Has been used for treatment of infections caused by susceptible N. meningitidis (including meningitis).¹²³ Other anti-infectives (e.g., ceftriaxone, cefotaxime, penicillin G, ampicillin, chloramphenicol, fluoroquinolones, aztreonam) usually recommended.⁵⁰⁶

Nocardia Infections

Has been used for treatment of nocardiosis.^{123 292} Fixed combination of sulfamethoxazole and trimethoprim (co-trimoxazole) usually treatment of choice for Nocardia infections;^{197 292} some experts suggest avoiding sulfonamides that are less urine soluble (e.g., sulfadiazine).²⁹²

Multiple-drug regimens may be necessary in immunocompromised patients or those with severe or disseminated infections.²⁹² Other drugs used alone or in multiple-drug regimens for treatment of nocardiosis include amikacin, tetracyclines, cephalosporins (ceftriaxone), carbapenems (imipenem, meropenem), fixed combination of amoxicillin and clavulanate, clarithromycin, cycloserine, or linezolid.^{197 292} In vitro susceptibility testing, if available, recommended to guide selection of anti-infectives for treatment of severe nocardiosis or for those who cannot tolerate or fail to respond to sulfonamide treatment.²⁹²

Plague

Has been used for treatment of plague^{† [off-label]} caused by Yersinia pestis.⁶⁸⁸ May reduce mortality in patients with bubonic plague, but sulfonamides not generally recommended for pneumonic plague.⁶⁸⁸

Not considered a preferred or alternative agent for treatment of plague;^{197 688} sulfonamides appear to be less effective than other anti-infectives used in the treatment of plague (e.g., streptomycin, tetracycline, doxycycline).⁶⁸⁸

Urinary Tract Infections (UTIs)

Has been used for treatment of UTIs (e.g., pyelonephritis, pyelitis, cystitis) in the absence of obstructive uropathy or foreign bodies.¹²³

Use only when UTIs are caused by susceptible Escherichia coli, Klebsiella, Enterobacter, Staphylococcus aureus, Proteus mirabilis, or P. vulgaris and only when other more soluble sulfonamides have been ineffective.¹²³

Sulfadiazine Dosage and Administration

Administration

Oral Administration

Administer orally with a full glass (250 mL) of water.¹²³

Maintain adequate fluid intake during therapy to minimize risk of crystalluria and stone formation.¹²³

Dosage

Pediatric Patients

General Pediatric Dosage

Oral

Infants and children >2 months of age: Manufacturer recommends 75 mg/kg or 2 g/m² initially, followed by 150 mg/kg or 4 g/m² daily given in 4–6 equally divided doses.¹²³

Children beyond neonatal period: AAP recommends 120–150 mg/kg daily given in 4–6 divided doses for the treatment of mild, moderate, or severe infections.²⁹²

Prevention of Rheumatic Fever Recurrence

Oral

Infants and children >2 months of age: Manufacturer recommends 500 mg once daily in those weighing <30 kg or 1 g once daily in those weighing >30 kg.¹²³

AHA and AAP recommend 500 mg once daily in those weighing ≤27 kg or 1 g once daily in those weighing >27 kg.^{292 375}

Long-term, continuous prophylaxis required.^{292 375} (See Adults under Dosage and Administration.)

Toxoplasmosis

Treatment of Congenital Toxoplasmosis

Oral

50 mg/kg twice daily in conjunction with oral pyrimethamine (2 mg/kg once daily for 2 days, then 1 mg/kg once daily for 2–6 months, then 1 mg/kg 3 times weekly) and oral or IM leucovorin (10 mg with each pyrimethamine dose).¹⁵⁶

Recommended duration in HIV-infected infants is 12 months.¹⁵⁶

Treatment of Toxoplasmosis in HIV-infected Infants and Children

Oral

25–50 mg/kg (up to 1–1.5 g) 4 times daily in conjunction with oral pyrimethamine (2 mg/kg [up to 50 mg] once daily for 3 days, then 1 mg/kg [up to 25 mg] once daily) and oral leucovorin (10–25 mg once daily).¹⁵⁶

Treatment duration at least 6 weeks;¹⁵⁶ longer duration may be appropriate if disease is extensive or response incomplete at 6 weeks.¹⁵⁶

Treatment of Toxoplasmosis in HIV-infected Adolescents

Oral

1 g every 6 hours in those weighing <60 kg or 1.5 g every 6 hours in those weighing ≥60 kg in conjunction with oral pyrimethamine (200-mg loading dose, then 50 mg once daily in those weighing <60 kg or 75 mg once daily in those weighing ≥60 kg) and oral leucovorin (10–25 mg once daily; may be increased to 50 mg once or twice daily).¹⁵⁵

Alternatively, 1 g every 6 hours in those weighing <60 kg or 1.5 g every 6 hours in those weighing ≥60 kg in conjunction with oral atovaquone (1.5 g twice daily).¹⁵⁵

Treatment duration at least 6 weeks;¹⁵⁵ longer duration may be appropriate if clinical or radiologic disease is extensive or response incomplete at 6 weeks.¹⁵⁵

Prevention of Recurrence (Secondary Prophylaxis) of Toxoplasmosis in HIV-infected Infants and Children† [off-label]

Oral

42.5–60 mg/kg twice daily (up to 2–4 g daily) in conjunction with oral pyrimethamine (1 mg/kg or 15 mg/m² [up to 25 mg] once daily) and oral leucovorin (5 mg once every 3 days).¹⁵⁶

Safety of discontinuing secondary prophylaxis against toxoplasmosis in HIV-infected children receiving potent antiretroviral therapy not extensively studied.¹⁵⁶ If child has completed initial toxoplasmosis treatment, is asymptomatic for toxoplasmosis, and has received ≥6 months of antiretroviral therapy, can consider discontinuing secondary prophylaxis in those 1 to <6 years of age if CD4⁺ T-cell percentages remain ≥15% for >6 consecutive months or in those ≥6 years of age if CD4⁺ T-cell counts remain >200/mm³ for >6 consecutive months.¹⁵⁶

Reinitiate secondary toxoplasmosis prophylaxis if CD4⁺ T-cell percentages decrease to <15% in HIV-infected children <6 years of age or if CD4⁺ T-cell counts decrease to <200/mm³ in HIV-infected children ≥6 years of age.¹⁵⁶

Prevention of Recurrence (Secondary Prophylaxis) of Toxoplasmosis in HIV-infected Adolescents† [off-label]

Oral

2–4 g daily in 2–4 divided doses in conjunction with oral pyrimethamine (25–50 mg once daily) and oral leucovorin (10–25 mg once daily).¹⁵⁵

Criteria for initiating or discontinuing secondary prophylaxis against toxoplasmosis in adolescents are the same as those for adults.¹⁵⁵ (See Adults under Dosage and Administration.)

Adults

General Adult Dosage

Oral

2–4 g initially, followed by 2–4 g daily in 3–6 equally divided doses.¹²³

Prevention of Rheumatic Fever Recurrence

Oral

Adults weighing >30 kg: Manufacturer recommends 1 g once daily.¹²³

Adults weighing >27 kg: AHA and AAP recommend 1 g once daily.^{292 375}

AHA and AAP recommend long-term, continuous prophylaxis.^{292 375} (See Table 1.)

Toxoplasmosis

Treatment of Toxoplasmosis in HIV-infected Adults

Oral

1 g every 6 hours in those weighing <60 kg or 1.5 g every 6 hours in those weighing ≥60 kg in conjunction with oral pyrimethamine (200-mg loading dose, then 50 mg once daily in those weighing <60 kg or 75 mg once daily in those weighing ≥60 kg) and oral leucovorin (10–25 mg once daily; may be increased to 50 mg once or twice daily).¹⁵⁵

Alternatively, 1 g every 6 hours in those weighing <60 kg or 1.5 g every 6 hours in those weighing ≥60 kg in conjunction with oral atovaquone (1.5 g twice daily).¹⁵⁵

Treatment duration at least 6 weeks; longer duration may be appropriate if clinical or radiologic disease is extensive or response incomplete at 6 weeks.¹⁵⁵

Prevention of Recurrence (Secondary Prophylaxis) of Toxoplasmosis in HIV-infected Adults† [off-label]

Oral

2–4 g daily in 2–4 divided doses in conjunction with oral pyrimethamine (25–50 mg once daily) and oral leucovorin (10–25 mg once daily).¹⁵⁵

Initiate secondary toxoplasmosis prophylaxis in all HIV-infected adults who have been treated for T. gondii encephalitis.¹⁵⁵

Consider discontinuing secondary toxoplasmosis prophylaxis in adults who completed toxoplasmosis treatment, are asymptomatic with respect to toxoplasmic encephalitis, and have responded to antiretroviral therapy with CD4⁺ T-cell counts that have remained >200/mm³ for >6 months.¹⁵⁵

Reinitiate secondary toxoplasmosis prophylaxis if CD4⁺ T-cell count decreases to <200/mm³.¹⁵⁵

Nocardiosis

Oral

4–8 g daily for a minimum of 6 weeks.^a Continue for several months after apparent cure to prevent relapse.^a

Prescribing Limits

Pediatric Patients

General Pediatric Dosage

Oral

Maximum 6 g daily.¹²³

Toxoplasmosis

Treatment in HIV-infected Infants and Children

Oral

Maximum 1–1.5 g per dose 4 times daily.¹⁵⁶

Prevention of Recurrence (Secondary Prophylaxis) of Toxoplasmosis in HIV-infected Infants and Children†

Oral

Maximum 2–4 g daily.¹⁵⁶

Special Populations

No specific dosage recommendations.¹²³

Cautions for Sulfadiazine

Contraindications

• Hypersensitivity to sulfonamides¹²³ or other chemically related drugs (e.g., sulfonylureas, thiazides).^b

• Infants <2 months of age (except as adjunctive therapy with pyrimethamine for treatment of congenital toxoplasmosis).¹²³ (See Toxoplasmosis under Uses.)

• Pregnancy at term.¹²³

• Nursing women.¹²³

• Porphyria.^b

Warnings/Precautions

Warnings

Severe Reactions

Severe (sometimes fatal) reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias, reported with sulfonamides.^{123 b}

Sore throat, fever, pallor, purpura, or jaundice may be early indications of serious reactions.¹²³

Discontinue sulfadiazine at first appearance of rash or any sign of adverse reactions.^b

Sensitivity Reactions

Hypersensitivity Reactions

Deaths associated with sulfonamide hypersensitivity reactions reported.¹²³

Serum sickness syndrome or serum sickness-like reactions (e.g., fever, chills, rigors, flushing, joint pain, urticarial eruptions, conjunctivitis, bronchospasm, leukopenia) reported with sulfonamides.^b

Various dermatologic reactions, including rash, pruritus, urticaria, erythema nodosum, erythema multiforme (Stevens-Johnson syndrome), Lyell’s syndrome (may be associated with corneal damage), Behcet’s syndrome, toxic epidermal necrolysis, and exfoliative dermatitis, reported in patients receiving sulfonamides.^b

Photosensitivity reported.^b

Incidence of hypersensitivity reactions appears to increase with increased sulfonamide dosage.^b

Use with caution in patients with severe allergy or bronchial asthma.¹²³

If a hypersensitivity reaction occurs during sulfonamide therapy, immediately discontinue the drug.^b

Desensitization

Desensitization to sulfadiazine has been performed when use of the drug for the treatment of toxoplasmosis was considered necessary in HIV-infected patients who had a history of sulfadiazine hypersensitivity.¹⁰⁷

Consult specialized references for specific information on desensitization procedures and dosage.¹⁰⁷

Cross-sensitivity

Although cross-sensitization has been reported to occur between the various anti-infective sulfonamides, some diuretics such as acetazolamide and the thiazides, some goitrogens, and sulfonylurea antidiabetic agents,^{119 123} the association between hypersensitivity to sulfonamide anti-infectives and subsequent sensitivity reactions to non-anti-infective sulfonamides (e.g., thiazides, sulfonylurea antidiabetic agents, furosemide, dapsone, probenecid) appears to result from a predisposition to allergic reactions in general rather than to cross-sensitivity to the sulfa moiety per se.¹¹⁹

General Precautions

Renal Effects

Sulfonamides have been associated with renal toxicity manifested by renal colic, nephritis, urolithiasis, toxic nephrosis with anuria and oliguria, hematuria, proteinuria, crystalluria, kidney stone formation, and elevation of BUN and serum creatinine concentrations.^b Nephritis and hemolytic-uremic syndrome also have been reported.^b

Adverse renal effects usually are the result of crystalluria.^b Risk of crystalluria may be decreased by maintaining an adequate urinary output and by increasing urinary pH.^b Unless the urine is highly acidic and/or the drug is relatively insoluble, alkalinization of the urine usually is not necessary if urinary output is maintained at a minimum of 1.5 L daily.^b

Perform urinalysis and assess kidney function frequently during sulfonamide therapy.^b Maintain adequate fluid intake to minimize risk of crystalluria and stone formation.^{123 b}

If persistent, heavy crystalluria, hematuria, or oliguria occurs, sulfonamide therapy should be discontinued and alkali therapy maintained.^b

Patients with G6PD Deficiency

Hemolysis may occur in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency; this effect may be dose-related.^{123 b}

Laboratory Monitoring

Perform CBCs frequently during sulfadiazine therapy.¹²³

Perform urinalysis (with careful microscopic examination) frequently during sulfadiazine therapy, especially in patients with impaired renal function.¹²³

Considerable interindividual variations in sulfadiazine plasma concentrations occur with a given dosage.¹²³ Measure sulfadiazine blood concentrations in patients being treated for serious infections.¹²³ Free sulfonamide concentrations of 5–15 mg/100 mL may be considered therapeutically effective for most infections; concentrations of 12–15 mg/100 mL may be considered optimal for serious infections.¹²³ Do not exceed total blood concentrations of 20 mg/100 mL since adverse reactions occur more frequently above this level.¹²³

Selection and Use of Anti-infectives

To reduce development of drug-resistant bacteria and maintain effectiveness of sulfadiazine and other antibacterials, use only for treatment or prevention of infections proven or strongly suspected to be caused by susceptible bacteria.^b

When selecting or modifying anti-infective therapy, use results of culture and in vitro susceptibility testing.^{123 b} Consider that in vitro susceptibility tests are not always reliable for sulfonamides.¹²³ If the patient is already taking sulfonamides, ensure that follow-up cultures have aminobenzoic acid added to the culture media.¹²³

Specific Populations

Pregnancy

Category C.¹²³

Contraindicated in pregnant women at term.¹²³ Crosses placenta;¹²³ may increase risk of neonatal hyperbilirubinemia and kernicterus.¹²³

Lactation

Contraindicated in nursing women;¹²³ discontinue drug or nursing.¹²³

Distributed into milk;¹²³ may cause kernicterus in the infant.¹²³

Pediatric Use

Contraindicated in infants <2 months of age (except when considered necessary for adjunctive use with pyrimethamine for treatment of congenital toxoplasmosis).¹²³ (See Toxoplasmosis under Uses.)

Kernicterus, caused by displacement of bilirubin from protein binding sites, has occurred in neonates treated with sulfonamides.^b

Hepatic Impairment

Use with caution.¹²³

Renal Impairment

Use with caution.¹²³ (See Renal Effects under Cautions.)

Common Adverse Effects

GI effects (anorexia, nausea, vomiting, abdominal pain), headache, peripheral neuritis, fever, rash, pancreatitis, stomatitis, depression.¹²³

Drug Interactions

Specific Drugs

Sulfadiazine Pharmacokinetics

Absorption

Bioavailability

Readily absorbed from GI tract.¹²³

Peak plasma concentrations attained within 3–7 hours.^{123 b} Considerable interindividual variations in plasma sulfadiazine concentrations attained with a given dosage.¹²³

Exists in blood as free, conjugated, and protein-bound drug; only the free form is microbiologically active.¹²³

Distribution

Extent

Distributed into most body tissues; appears to freely cross cell membranes.^a

Distributed into CSF.¹²³ Free and total CSF concentrations may reach 32–65 and 40–60% of concurrent blood concentrations, respectively.¹²³ Higher sulfonamide CSF concentrations may be reached if meninges are inflamed.^a

Crosses placenta.¹²³

Distributed into milk.¹²³

Plasma Protein Binding

38–48%.¹²³

Elimination

Metabolism

Liver; undergoes N⁴-acetylation (up to 40%).^b

Elimination Route

Excreted principally in urine in the N⁴-acetylated form (about 15–40%) and unchanged (about 43–60%).^{123 a} Approximately 50% of a single dose is excreted in the urine within 24 hours; 60–85% can be recovered within 72 hours.^{123 a}

Half-life

About 7–17 hours.^b

Stability

Storage

Oral

Tablets

20–25°C in tight, light-resistant container.¹²³

Actions and Spectrum

• Competitively inhibits bacterial synthesis of folic acid (pteroylglutamic acid) from aminobenzoic acid.¹²³

• Bacteriostatic in action.¹²³

• Inhibits only microorganisms that synthesize their own folic acid.^b Animal cells and bacteria capable of utilizing folic acid precursors or preformed folic acid are resistant to sulfonamides.^b

Advice to Patients

• Advise patients to drink a full glass of water (250 mL) with each dose and at frequent intervals throughout the day to prevent crystalluria and stone formation.¹²³

• Importance of reporting the occurrence of sore throat, fever, pallor, purpura, or jaundice to a clinician since this may indicate a serious blood disorder.¹²³

• Advise patients that photosensitivity has been reported with sulfonamides and they should avoid exposure to UV light or prolonged exposure to sunlight.^b

• Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.¹²³

• Importance of women informing clinician if they are or plan to become pregnant or plan to breast-feed.¹²³

• Importance of advising patients of other important precautionary information.¹²³ (See Cautions.)

Preparations

Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.

Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.

* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

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