Probenecid Information
Probenecid () Description
Probenecid () is a uricosuric and renal tubular transport blocking agent.
The chemical name for Probenecid () is 4-[(dipropylamino) sulfonyl] benzoic acid (molecular weight 285.37). It has the following structural formula:
CHNOS
Probenecid () , USP is a white or nearly white, fine, crystalline powder. Probenecid () is soluble in dilute alkali, in alcohol, in chloroform, and in acetone; it is practically insoluble in water and in dilute acids.
Each tablet for oral administration contains 500 mg of Probenecid () and the following inactive ingredients: colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, sodium carbonate, sodium lauryl sulfate, sodium starch glycolate, cornstarch, titanium dioxide, triacetin, FD&C Yellow #6, D&C Yellow #10, and FD&C Blue #2.
Probenecid () Clinical Pharmacology
Probenecid () is a uricosuric and renal tubular blocking agent. It inhibits the tubular reabsorption of urate, thus increasing the urinary excretion of uric acid and decreasing serum urate levels. Effective uricosuria reduces the miscible urate pool, retards urate deposition, and promotes resorption of urate deposits.
Probenecid () inhibits the tubular secretion of penicillin and usually increases penicillin plasma levels by any route the antibiotic is given. A 2-fold to 4-fold elevation has been demonstrated for various penicillins.
Probenecid () also has been reported to inhibit the renal transport of many other compounds including aminohippuric acid (PAH), aminosalicylic acid (PAS), indomethacin, sodium iodomethamate and related iodinated organic acids, 17-ketosteroids, pantothenic acid, phenolsulfonphthalein (PSP), sulfonamides, and sulfonylureas. See also .
Probenecid () decreases both hepatic and renal excretion of sulfobromophthalein (BSP). The tubular reabsorption of phosphorus is inhibited in hypoparathyroid but not in euparathyroid individuals.
Probenecid () does not influence plasma concentrations of salicylates, nor the excretion of streptomycin, chloramphenicol, chlortetracycline, oxytetracycline, or neomycin.
Probenecid () Indications And Usage
Probenecid () tablets are indicated for the treatment of the hyperuricemia associated with gout and gouty arthritis.
As an adjuvant to therapy with penicillin or with ampicillin, methicillin, oxacillin, cloxacillin, or nafcillin, for elevation and prolongation of plasma levels by whatever route the antibiotic is given.
Probenecid () Contraindications
Hypersensitivity to Probenecid () .
Children under 2 years of age.
Not recommended in persons with known blood dyscrasias or uric acid kidney stones.
Therapy with Probenecid () should not be started until an acute gouty attack has subsided.
Probenecid () Warnings
Exacerbation of gout following therapy with Probenecid () may occur; in such cases colchicine or other appropriate therapy is advisable.
Probenecid () increases plasma concentrations of methotrexate in both animals and humans. In animal studies, increased methotrexate toxicity has been reported. If Probenecid () is given with methotrexate, the dosage of methotrexate should be reduced and serum levels may need to be monitored.
In patients on Probenecid () the use of salicylates in either small or large doses is contraindicated because it antagonizes the uricosuric action of Probenecid () . The biphasic action of salicylates in the renal tubules accounts for the so-called "paradoxical effect" of uricosuric agents. In patients on Probenecid () who require a mild analgesic agent the use of acetaminophen rather than small doses of salicylates would be preferred.
Rarely, severe allergic reactions and anaphylaxis have been reported with the use of Probenecid () . Most of these have been reported to occur within several hours after readministration following prior usage of the drug.
The appearance of hypersensitivity reactions requires cessation of therapy with Probenecid () .
Probenecid () Precautions
Hematuria, renal colic, costovertebral pain, and formation of uric acid stones associated with the use of Probenecid () in gouty patients may be prevented by alkalization of the urine and a liberal fluid intake (see ). In these cases when alkali is administered, the acid-base balance of the patient should be watched.
Use with caution in patients with a history of peptic ulcer.
Probenecid () has been used in patients with some renal impairment, but dosage requirements may be increased. Probenecid () may not be effective in chronic renal insufficiency particularly when the glomerular filtration rate is 30 mL/minute or less. Because of its mechanism of action, Probenecid () is not recommended in conjunction with a penicillin in the presence of renal impairment.
A reducing substance may appear in the urine of patients receiving Probenecid () . This disappears with discontinuance of therapy. Suspected glycosuria should be confirmed by using a test specific for glucose.
When Probenecid () is used to elevate plasma concentrations of penicillin or other beta-lactams, or when such drugs are given to patients taking Probenecid () therapeutically, high plasma concentrations of the other drug may increase the incidence of adverse reactions associated with that drug. In the case of penicillin or other beta-lactams, psychic disturbances have been reported.
The use of salicylates antagonizes the uricosuric action of Probenecid () (see ). The uricosuric action of Probenecid () is also antagonized by pyrazinamide.
Probenecid () produces an insignificant increase in free sulfonamide plasma concentrations, but a significant increase in total sulfonamide plasma levels. Since Probenecid () decreases the renal excretion of conjugated sulfonamides, plasma concentrations of the latter should be determined from time to time when a sulfonamide and Probenecid () are coadministered for prolonged periods. Probenecid () may prolong or enhance the action of oral sulfonylureas and thereby increase the risk of hypoglycemia.
It has been reported that patients receiving Probenecid () require significantly less thiopental for induction of anesthesia. In addition, ketamine and thiopental anesthesia were significantly prolonged in rats receiving Probenecid () .
The concomitant administration of Probenecid () increases the mean plasma elimination half-life of a number of drugs which can lead to increased plasma concentrations. These include agents such as indomethacin, acetaminophen, naproxen, ketoprofen, meclofenamate, lorazepam, and rifampin. Although the clinical significance of this observation has not been established, a lower dosage of the drug may be required to produce a therapeutic effect, and increases in dosage of the drug in question should be made cautiously and in small increments when Probenecid () is being coadministrated. Although specific instances of toxicity due to this potential interaction have not been observed to date, physicians should be alert to this possibility.
Probenecid () given concomitantly with sulindac had only a slight effect on plasma sulfide levels, while plasma levels of sulindac and sulfone were increased. Sulindac was shown to produce a modest reduction in the uricosuric action of Probenecid () , which probably is not significant under most circumstances.
In animals and in humans, Probenecid () has been reported to increase plasma concentrations of methotrexate (see ).
Falsely high readings for theophylline have been reported in an study, using the Schack and Waxler technique, when therapeutic concentrations of theophylline and Probenecid () were added to human plasma.
Probenecid () Adverse Reactions
The following adverse reactions have been observed and within each category are listed in order of decreasing severity.
Probenecid () Dosage And Administration
Therapy with Probenecid () should not be until an acute gouty attack has subsided. However, if an acute attack is precipitated therapy, Probenecid () may be continued without changing the dosage, and full therapeutic dosage of colchicine, or other appropriate therapy, should be given to control the acute attack.
The recommended adult dosage is 250 mg (1/2 Probenecid () tablet), twice a day for one week, followed by 500 mg (1 tablet) twice a day thereafter.
Some degree of renal impairment may be present in patients with gout. A daily dosage of 1000 mg may be adequate. However, if necessary, the daily dosage may be increased by 500 mg increments every 4 weeks within tolerance (and usually not above 2000 mg per day) if symptoms of gouty arthritis are not controlled or the 24 hour uric acid excretion is not above 700 mg. As noted, Probenecid () may not be effective in chronic renal insufficiency particularly when the glomerular filtration rate is 30 mL/minute or less.
Gastric intolerance may be indicative of overdosage, and may be corrected by decreasing the dosage.
As uric acid tends to crystallize out of an acid urine, a liberal fluid intake is recommended, as well as sufficient sodium bicarbonate (3 to 7.5 g daily), or potassium citrate (7.5 g daily) to maintain an alkaline urine (see ).
Alkalization of the urine is recommended until the serum urate level returns to normal limits and tophaceous deposits disappear, i.e., during the period when urinary excretion of uric acid is at a high level. Thereafter, alkalization of the urine and the usual restriction of purine-producing foods may be somewhat relaxed.
Probenecid () should be continued at the dosage that will maintain normal serum urate levels. When acute attacks have been absent for 6 months or more and serum urate levels remain within normal limits, the daily dosage may be decreased by 500 mg every 6 months. The maintenance dosage should not be reduced to the point where serum urate levels tend to rise.
In uncomplicated gonococcal infections in men and women (urethral, cervical, rectal), 1 g of Probenecid () should be given orally with 4.8 million units of aqueous procaine penicillin G (given IM), or 3 g of amoxicillin (given orally), or 3.5 g of ampicillin (given orally).
For further guidance, see CDC recommendations for definition of regimens of choice, alternative regimens, treatment of hypersensitive patients, and other aspects of therapy.
*Recommended by the Center for Disease Control, U.S. Department of Health and Human Services, Public Health Service (Morbidity and Mortality Weekly Report Supplement, Volume 34, Number 4S, October 18, 1985).
Probenecid () How Supplied
Probenecid () Tablets, USP are available containing 500 mg of Probenecid () , USP.
The tablets are capsule shaped, film-coated yellow, debossed with on one side, on the other side. They are available as follows:
NDC 0378-0156-01bottles of 100 tablets
Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure.
Mylan Pharmaceuticals Inc.Morgantown, WV 26505
Probenecid ()
100 TABLETS
Each tablet contains:Probenecid () , USP 500 mg
Dispense in a tight, light-resistantcontainer as defined in the USPusing a child-resistant closure.
Keep container tightly closed.
Keep this and all medication outof the reach of children.
