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Sulfasalazine

Sulfasalazine is a sulfa drug used primarily in the treatment of inflammatory bowel disease. It is a 5-aminosalicylic acid derivative. It is sold as Azulfidine in the United States. It is also used for rheumatoid arthritis (see Disease-modifying antirheumatic drugs). It is usually not given to children under 2 years of age. more...

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Side effects

  1. diarrhea
  2. headache

Brand Names

  • Azulfidine ®
  • Salazopyrin ®
  • Pyralin ®

MIMS Guide to Sulfasalazine

Section: 1(d) Antidiarrhoeals Pregnancy Category: A

Sport Category: Permitted in sport

Uses/Indications: Ulcerative colitis; Inflammatory Bowel Syndrome; Crohn's disease; rheumatoid arthritis unresponsive to NSAIDs

Contraindications: Haematological, renal or hepatic dysfunction; hypersensitivity to salicylates or sulfonamide derivatives; GI or urinary tract obstruction; porphyria; children < 2 yrs

Precautions: Perform blood counts, urinalysis before and during treatment; maintain fluid intake; G-6-PD deficiency; atopy; slow acetylators; lactation

Adverse Reactions: Hypersensitivity; GI upset; fever; rash; headache; oligospermia; folate deficiency; others, see full PI

Drug Interactions: Oral anticoagulants; methotrexate; sulfonylurea hypoglycaemics; urinary acidifiers; phenylbutazone; indomethacin; sulfinpyrazone; salicylates; antacids, ferrous sulfate (concurrent); penicillins, oxacillin; some local anaesthetics; digoxin

PYRALIN EN (Tablets) Prescription required. S4 Sulfasalazine; yellow e-c tab; Dose: Should be taken with food. GI disease. Initial dosage. Adults: 1-2 g 4 times daily; children: 40-60 mg/kg daily in 3-6 divided doses. Maintenance. Adults: 2 g daily in 4 divided doses; children: 40 mg/kg daily in 4 divided doses. Rheumatoid arthritis. Adults: 1 g 2-3 times daily Pack: 500 mg x2 Brand substitution is permitted. : PBS/RPBS (Rp 5) PBS: $58.15

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Pharmacodynamics.

Sulfasalazine has, among others, an immunosuppressive effect and has shown affinity to connective tissue. It has also been shown to have a wide range of effects in other biological systems. It is, however, difficult to judge the clinical relevance of its various pharmacological actions since the aetiology of rheumatoid arthritis is largely unknown. Moreover, the mode of action of sulfasalazine in the treatment of ulcerative colitis is also not known. A metabolite of the drug may have an inhibitory effect on an antigen-antibody process occurring in the intestinal wall and the salicylate component may act as an anti-inflammatory agent. The drug does not appear to have any long-term antibacterial effect on the stool flora of patients with ulcerative colitis (see Antibacterial effect, below).

The following effects have been found in vitro: inhibition of bacterial growth; inhibition of prostaglandin synthesis; increased intestinal cytoprotection due to inhibition of prostaglandin degradation; reduction of leukotriene formation; modulation of polymorphonuclear leucocyte function; inhibition of proteolytic enzymes; inhibition of DNA synthesis; and impairment of folate absorption and metabolism.

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Rheumatoid arthritis drugs
From OB/GYN News, 4/15/05 by Gerald G. Briggs

The autoimmune disorder rheumatoid arthritis occurs in about 1%-2% of the population. The disease is more prevalent in women than men by about a 3:1 ratio, but in the reproductive years, the ratio may be as high as 6:1. During pregnancy, the incidence is about 1:1,000.

RA is characterized by the production of cytokines, including tumor necrosis factor-[alpha] (TNF-[alpha]) and interleukin-1 in the synovial cavity, and irreversible damage to soft tissues and bones. Drug therapy of RA involves the use of disease-modifying antirheumatic drugs (DMARDs) to prevent or lessen this damage. The therapy can be categorized as biologic DMARDs, synthetic DMARDs, and anti-inflammatory agents.

Biologic DMARDs include three agents that inhibit TNF-[alpha]--adalimumab (Humira), etanercept (Enbrel), and infliximab (Remicade)--and one interleukin-1 receptor antagonist, anakinra (Kineret). Although the human pregnancy data for these four drugs are very limited or completely absent, animal reproduction data suggest they pose a low risk for developmental toxicity (growth retardation, structural defects, functional/behavioral defects, or death).

The safest course is to avoid these agents during the first trimester, but with their long elimination half-lives, inadvertent exposures during organogenesis of unplanned pregnancies is likely.

The synthetic DMARDs include azathioprine (Imuran), cyclosporine (Sandimmune, Neoral), gold compounds, hydroxychloroquine (Plaquenil), leflunomide (Arava), methotrexate, penicillamine, and sulfasalazine (Azulfidine).

The immunosuppressants, azathioprine and cyclosporine, do not appear to cause congenital defects, but may be associated with growth retardation. There is limited human pregnancy experience with the gold compounds--auranofin (Ridaura), aurothioglucose (Solganal), and gold sodium thiomalate (Aurolate)--but the animal data suggest the risk for developmental toxicity is low.

Hydroxychloroquine is probably compatible in pregnancy. However, there is limited pregnancy experience with the high doses commonly used in RA. The drug has a very long elimination half-life from maternal tissues (weeks to months). Thus, stopping the drug when pregnancy is confirmed will not prevent embryo/fetal exposure.

Leflunomide, a pyrimidine synthesis inhibitor, causes dose-related teratogenicity and toxicity in animals at doses much lower than those used in humans. Human pregnancy experience is too limited to determine the risk to the embryo or fetus, and the drug is contraindicated in pregnancy. Exposure of unplanned pregnancies will probably occur because the drug and its active metabolite may take up to 2 years to reach nondetectable plasma levels.

The folic acid antagonist methotrexate is contraindicated during pregnancy. The drug is associated with spontaneous abortions and a spectrum of congenital defects collectively termed methotrexate embryopathy. The critical exposure period for structural defects is 8-10 weeks after the first day of the last menstrual period. Exposure after this period is associated with fetal toxicity and mortality. The critical dose is thought to be 10 mg or more per week.

Another folate antagonist, sulfasalazine, does not appear to cause developmental toxicity, but supplemental folic acid (1 mg/day) should be used if there is a risk of unplanned pregnancy or if pregnancy occurs. The drug has caused bloody diarrhea in a nursing infant, so breast-feeding should be undertaken cautiously. Penicillamine, a chelating agent, is linked with a risk of fetal connective tissue defects (cutis laxa) and should be avoided during pregnancy.

The anti-inflammatory agents include prednisone and the nonsteroidal anti-inflammatory drugs (NSAIDs), which include aspirin. There is considerable potential for embryo/fetal toxicity from NSAIDs: spontaneous abortions when used around the time of conception, fetal renal toxicity, and premature closure of the ductus arteriosus in the third trimester. Aspirin use near term may increase the risk of bleeding in the mother and the infant. The use of prednisone during organogenesis carries a low risk for oral clefts and prolonged use in pregnancy has been associated with growth retardation.

The biologic DMARDs, gold compounds, hydroxychloroquine, NSAIDs (except high-dose aspirin), and prednisone are likely compatible with breast-feeding. The other agents are contraindicated (methotrexate) or should be avoided due to potential toxicity.

The Organization of Teratology Information Services is conducting a study of pregnancy exposure to rheumatoid arthritis drugs. Health care professionals may call toll-free (877-311-8972) for information on enrolling patients in this study.

BY. GERALD G. BRIGGS, B. PHARM.

MR. BRIGGS is pharmacist clinical specialist, Women's Pavilion at Miller Children's Hospital, Long Beach, Calif.; clinical professor of pharmacy, University of California, San Francisco; and adjunct professor, University of Southern California, Los Angeles. He also is coauthor of "Drugs in Pregnancy and Lactation."

COPYRIGHT 2005 International Medical News Group
COPYRIGHT 2005 Gale Group

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