Benemid Side Effects
Generic Name: probenecid
Note: This page contains information about the side effects of probenecid. Some of the dosage forms included on this document may not apply to the brand name Benemid.
Not all side effects for Benemid may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here.
For the Consumer
Applies to probenecid: oral tablet
In addition to its needed effects, some unwanted effects may be caused by probenecid (the active ingredient contained in Benemid). In the event that any of these side effects do occur, they may require medical attention.
You should check with your doctor immediately if any of these side effects occur when taking probenecid:Rare
- Fast or irregular breathing
- puffiness or swellings of the eyelids or around the eyes
- shortness of breath, troubled breathing, tightness in chest, or wheezing
- changes in the skin color of the face occurring together with any of the other side effects listed here
- or skin rash, hives, or itching occurring together with any of the other side effects listed here
If any of the following side effects occur while taking probenecid, check with your doctor or nurse as soon as possible:Less common
- Bloody urine
- difficult or painful urination
- lower back or side pain (especially if severe or sharp)
- skin rash, hives, or itching (occurring without other signs of an allergic reaction)
- Cloudy urine
- cough or hoarseness
- fast or irregular breathing
- pain in back and/or ribs
- sores, ulcers, or white spots on lips or in mouth
- sore throat and fever with or without chills
- sudden decrease in the amount of urine
- swelling of face, fingers, feet, and/or lower legs
- swollen and/or painful glands
- unusual bleeding or bruising
- unusual tiredness or weakness
- yellow eyes or skin
- weight gain
Some of the side effects that can occur with probenecid may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:More common
- joint pain, redness, or swelling
- loss of appetite
- nausea or vomiting (mild)
- flushing or redness of face (occurring without any signs of an allergic reaction)
- frequent urge to urinate
- sore gums
For Healthcare Professionals
Applies to probenecid: oral tablet
In therapeutic doses, probenecid (the active ingredient contained in Benemid) is generally well tolerated and has a low incidence of side effects.
An increase in acute attacks of gout may occur on initiation of probenecid therapy. The concomitant administration of colchicine or a nonsteroidal anti-inflammatory agent, where appropriate, may decrease the risk of this complication.
Renal side effects have included renal colic, nephrotic syndrome, with or without renal failure, and urinary frequency. In addition, increased concentrations of uric acid in the renal tubules, due to probenecid (the active ingredient contained in Benemid) therapy, may promote development of uric acid stones.
Adequate hydration, to result in urine output of 2 liters per day, if possible, and alkalinization of the urine may reduce the risk of stone formation.
Hypersensitivity side effects have included rash, pruritus, fever, urticaria, and anaphylaxis.
Hypersensitivity reactions may be severe. It has been reported that the risk of severe allergic reactions may be increased in patients previously treated with probenecid. In these cases, onset of hypersensitivity reactions is within several hours after reintroduction of probenecid therapy.
Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency may increase the risk of probenecid-induced hemolytic anemia in some patients. However, probenecid (the active ingredient contained in Benemid) has also been implicated in at least two cases of immune-mediated hemolytic anemia. In both cases, serum antibodies reacted with red blood cells only in the presence of probenecid. In one patient, a generalized rash, fever, malaise, and anorexia were also present.
Hematologic side effects have rarely included hemolytic anemia, aplastic anemia, leukopenia, and anemia.
Hepatic side effects have included hepatic necrosis.
Gastrointestinal side effects have included anorexia, nausea, sore gums, and vomiting.
Nervous system side effects have included headache and dizziness.
Dermatologic side effects including dermatitis, alopecia, and flushing have been reported.
Genitourinary side effects including costovertebral pain have been reported.
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