Phenazopyridine

Phenazopyridine
Systematic (IUPAC) name
3-phenyldiazenylpyridine-2,6-diamine
Clinical data
Trade names Pyridiumplus
AHFS/Drugs.com monograph
MedlinePlus a682231
Licence data US FDA:link
Pregnancy cat. B
Legal status OTC (US) OTC(Canada)
Routes oral
Identifiers
CAS number 94-78-0 Y
ATC code G04BX06
PubChem CID 4756
DrugBank DB01438
ChemSpider 4592 N
UNII K2J09EMJ52 N
KEGG D08346 Y
ChEMBL CHEMBL1242 N
Chemical data
Formula C11H11N5 
Mol. mass 213.239 g/mol
 N(what is this?)  (verify)

Phenazopyridine is a chemical which, when excreted into the urine, has a local analgesic effect. It is often used to alleviate the pain, irritation, discomfort, or urgency caused by urinary tract infections, surgery, or injury to the urinary tract. Phenazopyridine was discovered by Bernhard Joos, the founder of Cilag.

Contents

Medical uses

Phenazopyridine is prescribed for its local analgesic effects on the urinary tract. It is typically used in conjunction with an antibiotic when treating a urinary tract infection. Phenazopyridine is not an antibiotic, but used in conjunction with an antibiotic can speed the early period of recovery from such an infection. In this combination, phenazopyridine is taken for only a short time, typically two days, while the antibiotic is continued for longer. After two days, there is little evidence of any benefit from continued administration of phenazopyridine versus administration of an antibiotic only.

Phenazopyridine is also prescribed for other cases to relieve irritation or discomfort during urination. For example, it is often prescribed after the use of a catheter or after penile surgery which results in the irritation of the lining of the urinary tract.

The American Urological Association has recommended the use of phenazopyridine as a first stage treatment for interstitial cystitis.

Pharmacokinetics

The drug is administered as a tablet, in either 100 mg or 200 mg doses of phenazopyridine hydrochloride. The tablets have a light red, dark red or dark violet color, and are taken with food.

The full pharmacokinetic properties of phenazopyridine have not been determined. It has mostly been studied in animal models, but they may not be very representative of humans.[1] Rat models have shown its half-life to be 7.35 hours,[2] and that it is excreted 40% hepatically.[2]

Its mode of action is not well known, and only basic information on its interaction with the body is available. It is known that the chemical has a direct topical analgesic effect on the mucosa lining of the urinary tract. It is rapidly excreted by the kidneys directly into the urine.[1] Hydroxylation is the major form of metabolism in humans,[1] and the azo bond is usually not cleaved.[1] On the order of 65% of an oral dose will be excreted directly into the urine chemically unchanged.

Side effects

Phenazopyridine frequently causes a distinct color change in the urine, typically to a dark orange to reddish color. This effect is common and harmless, and indeed a key indicator of the presence of the drug in the body. Users of phenazopyridine are warned not to wear contact lenses, as phenazopyridine has been known to permanently discolor contact lenses and fabrics.

Phenazopyridine can also cause headaches, upset stomach (especially when not taken with food), or dizziness. Less frequently it can cause a pigment change in the skin or eyes, to a noticeable yellowish color. This is due to a depressed excretion via the kidneys causing a build up of the drug in the skin, and normally indicates a need to discontinue usage. Other such side effects include fever, confusion, shortness of breath, skin rash, and swelling of the face, fingers, feet, or legs. Long-term use may cause yellowing of nails.[3]

Phenazopyridine should be avoided by people with glucose-6-phosphate dehydrogenase deficiency,[4][5][6] because it can cause hemolysis (destruction of red blood cells) due to oxidative stress.[7] It has been reported to cause methemoglobinemia after overdose and even normal doses.[8] In at least one case the patient had pre-existing low levels of methemoglobin reductase,[9] which likely predisposed her to the condition. It has also been reported to cause sulfhemoglobinemia.[10][11][12]

Phenazopyridine is a type of azo dye.[13] Other azo dyes, which were previously used in textiles, printing, and plastic manufacturing, have been implicated as carcinogenic agents that can cause bladder cancer.[14] While phenazopyridine has never been shown to cause cancer in humans, evidence from animal models suggests that it is potentially carcinogenic.[15]

Criticism

Because it does not kill the organisms causing a bladder infection, there is a risk that some patients will take phenazopyridine alone to relieve their symptoms instead of seeking a physician first and starting an appropriate antibiotic. The medicine serves to only mask the pain, and does not kill the infection, possibly allowing a simple bladder infection to become a more serious kidney infection if taken alone.

Since phenazopyridine discolors the urine, it interferes with the standard urine dipstick test done in a physician's office, especially the leukocyte esterase parameter.[16] If the physician determines that the patient is taking phenazopyridine, he or she will tell the patient to discontinue the drug and return in 2 or 3 days for a standard urine test to determine whether the pain is caused by a bladder/urinary tract infection.

Use of phenazopyridine is generally more appropriate once a diagnosis of bladder infection has been established by a medical provider and an antibiotic has been started to kill the infection.

Some physicians use phenazopyridine to relieve symptons of catheter discomfort following gynecologic surgery. A recent study investigates this relation and concludes that phenazopyridine does not improve catheter discomfort following gynecologic surgery [17] As of November 2011, no other eviddence was found in Pubmed that supports the use of phenazopyridine in catheter discomfort following gynecologic surgery.

Brand names

In addition to its generic form, phenazopyridine is distributed under the following brand names:

References

  1. ^ a b c d Thomas BH, Whitehouse LW, Solomonraj G, Paul CJ (April 1990). "Excretion of phenazopyridine and its metabolites in the urine of humans, rats, mice, and guinea pigs". Journal of Pharm Sci 79 (4): 321–5. doi:10.1002/jps.2600790410. PMID 2352143. 
  2. ^ a b Jurima-Romet M, Thomas BH, Solomonraj G, Paul CJ, Huang H (March 1993). "Metabolism of phenazopyridine by isolated rat hepatocytes". Biopharm Drug Dispos 14 (2): 171–9. doi:10.1002/bdd.2510140208. PMID 8453026. 
  3. ^ Amit, G; Halkin, A (15 December 1997). "Lemon-yellow nails and long-term phenazopyridine use" (letter). Annals of Internal Medicine 127 (12): 1137. PMID 9412335. 
  4. ^ Tishler, M; Abramov, A (1983). "Phenazopyridine-induced hemolytic anemia in a patient with G6PD deficiency". Acta Haematol 70 (3): 208–9. doi:10.1159/000206727. PMID 6410650. 
  5. ^ Galun E, Oren R, Glikson M, Friedlander M, Heyman A (November 1987). "Phenazopyridine-induced hemolytic anemia in G-6-PD deficiency". Drug Intell Clin Pharm 21 (11): 921–2. PMID 3678069. 
  6. ^ Mercieca JE, Clarke MF, Phillips ME, Curtis JR (4 Sep 1982). "Acute hemolytic anaemia due to phenazopyridine hydrochloride in G-6-PD deficient subject". Lancet 2 (8297): 564. PMID 6125724. 
  7. ^ Frank JE (October 2005). "Diagnosis and management of G6PD deficiency". American Family Physician 72 (7): 1277–82. PMID 16225031. http://www.aafp.org/afp/20051001/1277.html. 
  8. ^ Jeffery WH, Zelicoff AP, Hardy WR. (February 1982). "Acquired methemoglobinemia and hemolytic anemia after usual doses of phenazopyridine". Drug Intell Clin Pharm 16 (2): 57–9. PMID 7075467. 
  9. ^ Daly JS, Hultquist DE, Rucknagel DL (August 1983). "Phenazopyridine induced methaemoglobinaemia associated with decreased activity of erythrocyte cytochrome b5 reductase". Journal of Med Genet 20 (4): 307–9. doi:10.1136/jmg.20.4.307. PMC 1049126. PMID 6620333. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1049126. 
  10. ^ Halvorsen, SM; Dull, WL (September 1991). "Phenazopyridine-induced sulfhemoglobinemia: inadvertent rechallenge". American Journal of Medicine 91 (3): 315–7. doi:10.1016/0002-9343(91)90135-K. PMID 1892154. 
  11. ^ Kermani TA; Pislaru SV; Osborn TG (April 2009). "Acrocyanosis from phenazopyridine-induced sulfhemoglobinemia mistaken for Raynaud phenomenon". Journal of Clinical Rheumatology 15 (3): 127–9. doi:10.1097/RHU.0b013e31819db6db. PMID 19300288. 
  12. ^ Gopalachar AS; Bowie VL; Bharadwaj P (June 2005). "Phenazopyridine-induced sulfhemoglobinemia". Annals of Pharmacotherapy 39 (6): 1128–30. doi:10.1345/aph.1E557. PMID 15886294. 
  13. ^ http://emedicine.medscape.com/article/778670-treatment
  14. ^ http://emedicine.medscape.com/article/381323-overview
  15. ^ http://ntp.niehs.nih.gov/ntp/roc/eleventh/profiles/s144phen.pdf | National Toxicology Program
  16. ^ Kerr JE, Magee-Nolan C, Schuster BL (July 1986). "Interference by phenazopyridine with the leukocyte esterase dipstick". Journal of the American Medical Association 256 (1): 38–9. doi:10.1001/jama.256.1.38. PMID 3712709. 
  17. ^ http://www.ajog.org/article/S0002-9378%2810%2902530-5/abstract

External links