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Probenecid Side Effects summary

Total Probenecid reports: 8.
Probenecid FDA safety alerts: No.
Reported deaths: 1    Reported hospitalizations: 5.
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Probenecid Poll Results

Have you experienced Probenecid side effects?

Yes, Severe	50%
Yes, Mild	50%
Yes, Minor	0%
No	0%

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Probenecid Side Effects reported on Patientsville.com

None reported at this time.

Probenecid FDA reported side effects and reactions

2008

2007

2006

Probenecid Side Effects reported to FDA

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Probenecid Side Effects Report #5264428-2
Health Professional from UNITED STATES reported PROBENECID problem on Feb 27, 2007. Male patient, 68 years of age, was diagnosed with gout  and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation , back pain , cerebrovascular accident, epididymitis, mobility decreased, nerve injury, pain in extremity, transient ischaemic attack. PROBENECID dosage: 500 MG, DAILY, ORAL, 250 MG, DAILY, ORAL. During the same period patient was treated with CORTISONE ACETATE, COUMADIN. Patient was hospitalized. Patient recovered.



Probenecid Side Effects Report #5283923-3
PROBENECID problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2007. Male patient, 67 years of age, weighting 190.0 lb, was diagnosed with gout  and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation , back pain , cerebrovascular accident, epididymitis, iatrogenic injury, nerve injury, pain in extremity. PROBENECID dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, WARFARIN, AMLODIPINE. Patient was hospitalized. Patient recovered.



Probenecid Side Effects Report #5081535-8
Consumer or non-health professional from UNITED STATES reported PROBENECID problem on July 27, 2006. Female patient, 57 years of age, was diagnosed with gout  and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: anaemia, pyrexia, renal failure. PROBENECID dosage: unknown. During the same period patient was treated with RAMIPRIL. Patient recovered.



Probenecid Side Effects Report #5092184-X
PROBENECID problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 10, 2006. Female patient, 57 years of age, weighting 191.0 lb, was diagnosed with gout  and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: anaemia, hypoxia, pneumonitis, renal failure acute, rocky mountain spotted fever. PROBENECID dosage: 500 MG; BID; PO. During the same period patient was treated with RAMIPRIL, INDOMETHACIN. Patient was hospitalized. Patient recovered.




Probenecid Side Effects Report #5105941-8
Consumer or non-health professional from UNITED STATES reported PROBENECID problem on Aug 28, 2006. Female patient, 57 years of age, weighting 191.0 lb, was diagnosed with gout  and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: anaemia, hypoxia, myalgia, pneumonitis, renal failure, renal failure acute, rocky mountain spotted fever. PROBENECID dosage: 500 MG; BID; PO. During the same period patient was treated with RAMIPRIL, INDOMETHACIN. Patient was hospitalized. Patient recovered.



Probenecid Side Effects Report #5421889-3
PROBENECID problem was reported by a Consumer or non-health professional from FRANCE on Aug 03, 2007. Male patient, 79 years of age, was diagnosed with gout  and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: glomerulonephritis membranous, nephrotic syndrome. PROBENECID dosage: 500 MG; TWICE A DAY; ORAL; 1500 MG; DAILY; ORALQ. Patient was hospitalized. Patient recovered.



Probenecid Side Effects Report #5444193-6
Physician from UNITED KINGDOM reported PROBENECID problem on Aug 17, 2007. Male patient was diagnosed with gouty arthritis and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, ascites, azotaemia, bacteria urine identified, blood pressure increased, blood urea increased, blood uric acid increased, cardiomegaly. PROBENECID dosage: 1000 MG; DAILY; ORAL. During the same period patient was treated with COLCHICINE. Patient died on 09/18/1965.



Probenecid Side Effects Report #5788809-3
PROBENECID problem was reported by a Health Professional from JAPAN on June 16, 2008. Male patient, 54 years of age, was diagnosed with prophylaxis, cytomegalovirus chorioretinitis and was treated with PROBENECID. After drug was administered, patient experienced the following problems/side effects: anaemia haemolytic autoimmune, aplasia pure red cell. PROBENECID dosage: unknown. During the same period patient was treated with CIDOFOVIR. Patient recovered.