Probenecid Side Effects
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Recent Probenecid Side Effect Reports
Probenecid Side Effects Report #5264428-2
Health Professional from UNITED STATES reported Probenecid side effect 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 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.
Probenecid Side Effects Report #5283923-3
Probenecid side effect 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 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.
Health Professional from UNITED STATES reported Probenecid side effect 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 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. 
Probenecid Side Effects Report #5283923-3
Probenecid side effect 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 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. View More
View All Probenecid FDA Adverse Reports
Probenecid Side Effects
Abdominal pain Abdominal pain upper Acidosis Activities of daily living impaired Alopecia Anaemia Anaemia haemolytic autoimmune Anorexia Anxiety Aplasia pure red cell Arthralgia Ascites Asthenia Atrial fibrillation Azotaemia Back pain Bacteria urine identified Blood creatine phosphokinase increased Blood creatinine increased Blood lactate dehydrogenase increased Blood pressure increased Blood urea increased Blood uric acid increased Buttock pain C-reactive protein increased Cardiac failure congestive Cardiomegaly Cerebrovascular accident Chest pain Cholestasis Csf protein increased Dehydration Diarrhoea Diarrhoea haemorrhagic Emotional distress Eosinophilia Epididymitis Fall Fear Fibromyalgia Gastric ulcer Gastritis erosive Gastrointestinal disorder Glomerulonephritis membranous Gout Guillain-barre syndrome Hepatitis Hyporeflexia Hypoxia Iatrogenic injury Immobile Inflammation Injury Joint swelling Lower motor neurone lesion Lymphadenopathy Mobility decreased Muscular weakness Myalgia Myocardial infarction Myopathy Nausea Neck pain Nephrotic syndrome Nerve conduction studies abnormal Nerve injury Neuromyopathy Pain Pain in extremity Paresis Pneumonitis Pyrexia Rash Renal failure Renal failure acute Rhabdomyolysis Rib fracture Rocky mountain spotted fever Stress Transaminases increased Transient ischaemic attack
Abdominal pain upper Acidosis Activities of daily living impaired Alopecia Anaemia Anaemia haemolytic autoimmune Anorexia Anxiety Aplasia pure red cell Arthralgia Ascites Asthenia Atrial fibrillation Azotaemia Back pain Bacteria urine identified Blood creatine phosphokinase increased Blood creatinine increased Blood lactate dehydrogenase increased Blood pressure increased Blood urea increased Blood uric acid increased Buttock pain C-reactive protein increased Cardiac failure congestive Cardiomegaly Cerebrovascular accident Chest pain Cholestasis Csf protein increased Dehydration Diarrhoea Diarrhoea haemorrhagic Emotional distress Eosinophilia Epididymitis Fall Fear Fibromyalgia Gastric ulcer Gastritis erosive Gastrointestinal disorder Glomerulonephritis membranous Gout Guillain-barre syndrome Hepatitis Hyporeflexia Hypoxia Iatrogenic injury Immobile Inflammation Injury Joint swelling Lower motor neurone lesion Lymphadenopathy Mobility decreased Muscular weakness Myalgia Myocardial infarction Myopathy Nausea Neck pain Nephrotic syndrome Nerve conduction studies abnormal Nerve injury Neuromyopathy Pain Pain in extremity Paresis Pneumonitis Pyrexia Rash Renal failure Renal failure acute Rhabdomyolysis Rib fracture Rocky mountain spotted fever Stress Transaminases increased Transient ischaemic attack
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Dejan Celic Novi Sad | 7:18am on Tuesday, July 28th, 2009 |
Probenecid Adverse Effect Reports (FDA)
Consumer or non-health professional from UNITED STATES reported Probenecid side effect 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 side effects: anaemia, pyrexia, renal failure. Probenecid dosage: unknown. During the same period patient was treated with RAMIPRIL.
Probenecid Side Effects Report #5092184-X
Probenecid side effect 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 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.
Probenecid Side Effects Report #5105941-8
Consumer or non-health professional from UNITED STATES reported Probenecid side effect 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 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.
Probenecid Side Effects Report #5421889-3
Probenecid side effect 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 side effects: glomerulonephritis membranous, nephrotic syndrome. Probenecid dosage: 500 MG; TWICE A DAY; ORAL; 1500 MG; DAILY; ORALQ. Patient was hospitalized.
Probenecid Side Effects Report #5444193-6
Physician from UNITED KINGDOM reported Probenecid side effect on Aug 17, 2007. Male patient was diagnosed with gouty arthritis and was treated with Probenecid. After drug was administered, patient experienced the following 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 side effect 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 side effects: anaemia haemolytic autoimmune, aplasia pure red cell. Probenecid dosage: unknown. During the same period patient was treated with CIDOFOVIR.
Probenecid Side Effects Report #4607116-5
Consumer or non-health professional from reported Probenecid side effect on Mar 02, 2005. Female patient, 61 years of age, weighting 235.9 lb, was diagnosed with gouty arthritis and was treated with Probenecid. After drug was administered, patient experienced the following side effects: back pain, fibromyalgia, gastric ulcer, gastrointestinal disorder, inflammation, stress . Probenecid dosage: unknown. During the same period patient was treated with AVAPRO, MAGNESIUM, VITAMIN E, SOY SUPPLEMENT, VITAMIN B. Patient was hospitalized.
Probenecid Side Effects Report #4632527-1
Probenecid side effect was reported by a Physician from on Mar 29, 2005. Female patient, 83 years of age, was diagnosed with gout and was treated with Probenecid. After drug was administered, patient experienced the following side effects: activities of daily living impaired, anorexia, asthenia, diarrhoea, myalgia, myopathy. Probenecid dosage: 0.6MG; QD. During the same period patient was treated with ASPIRIN, BUMETANIDE, METOPROLOL TARTRATE, LOSARTAN POTASSIUM, AMLODIPINE, REPAGLINIDE, PREDNISONE. Patient was hospitalized.
Probenecid Side Effects Report #4632528-3
Pharmacist from reported Probenecid side effect on Mar 29, 2005. Female patient, 54 years of age, was diagnosed with gout and was treated with Probenecid. After drug was administered, patient experienced the following side effects: abdominal pain upper, activities of daily living impaired, arthralgia, asthenia, buttock pain, hepatitis , joint swelling, myopathy. Probenecid dosage: 0.6 MG, TID. During the same period patient was treated with GABAPENTIN, CALCIUM ACETATE, SEVELAMER, EPOGEN, VITAMINS W, METOCLOPRAMIDE, FERROUS SULPHATE. Patient was hospitalized.
Probenecid Side Effects Report #4663679-5
Probenecid side effect was reported by a Physician from on May 10, 2005. Male patient, 76 years of age, was diagnosed with familial mediterranean fever, helicobacter infection and was treated with Probenecid. After drug was administered, patient experienced the following side effects: abdominal pain, alopecia, blood creatinine increased, blood urea increased, c-reactive protein increased, cholestasis, dehydration, diarrhoea haemorrhagic, gastritis erosive. Probenecid dosage: 1.5-0.5MG QD. During the same period patient was treated with CLARITHROMYCIN, ACEBUTOLOL, RAMIPRIL, SPIRONOLACTONE, MOLSIDOMINE, ACETYLSALICYLATE, AMOXICILLIN, OMEPRAZOLE. Patient was hospitalized.
Probenecid Side Effects Report #4710842-0
Physician from UNITED STATES reported Probenecid side effect on June 29, 2005. Female patient, 48 years of age, was diagnosed with gout and was treated with Probenecid. After drug was administered, patient experienced the following side effects: eosinophilia, lymphadenopathy, pyrexia, rash , renal failure acute, transaminases increased. Probenecid dosage: unknown. During the same period patient was treated with ALLOPURINOL.
Probenecid Side Effects Report #4772136-7
Probenecid side effect was reported by a Physician from TURKEY on Sept 02, 2005. Female patient, 65 years of age, was diagnosed with gout and was treated with Probenecid. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, gout , hyporeflexia, muscular weakness, myopathy, nerve conduction studies abnormal. Probenecid dosage: 1.5-1.0MG QD. During the same period patient was treated with PRAVASTATIN, SPIRONOLACTONE, FUROSEMIDE, ASPIRIN, LOSARTAN POTASSIUM. Patient was hospitalized.
Probenecid Side Effects Report #4787525-4
Physician from TURKEY reported Probenecid side effect on Sept 16, 2005. Male patient, 70 years of age, was diagnosed with gout and was treated with Probenecid. After drug was administered, patient experienced the following side effects: abdominal pain upper, dehydration, nausea , renal failure acute, rhabdomyolysis. Probenecid dosage: unknown. During the same period patient was treated with FLUVASTATIN. Patient was hospitalized.
Probenecid Side Effects Report #4831949-3
Probenecid side effect was reported by a Pharmacist from GERMANY on Nov 03, 2005. Male patient, 83 years of age, was diagnosed with gout, tachyarrhythmia and was treated with Probenecid. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, csf protein increased, guillain-barre syndrome , immobile, lower motor neurone lesion, neuromyopathy, paresis. Probenecid dosage: 2 MG, IN 2 DAYS. During the same period patient was treated with VERAPAMIL, FUROSEMIDE, ACETYLSALICYLIC ACID, AMBROXOL, THEOPHYLLINE. Patient was hospitalized.
Probenecid Side Effects Report #4938837-2
Physician from UNITED STATES reported Probenecid side effect on July 05, 2005. Male patient, 62 years of age, weighting 180.8 lb, was diagnosed with arthritis and was treated with Probenecid. After drug was administered, patient experienced the following side effects: anxiety , chest pain , emotional distress, fear, injury, myocardial infarction, neck pain. Probenecid dosage: unknown. During the same period patient was treated with NORVASC, LIPITOR, SKELAXIN, PRILOSEC, AMBIEN, DIAZEPAM, ALLEGRA, VIOXX. Patient was hospitalized and became disabled.
Probenecid Side Effects Report #4997083-7
Probenecid side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2006. Female patient, 77 years of age, was diagnosed with gout, pain , hypertension and was treated with Probenecid. After drug was administered, patient experienced the following side effects: alopecia, cardiac failure congestive, fall , rib fracture. Probenecid dosage: unknown. During the same period patient was treated with INDOMETHACIN, CLONIDINE, FUROSEMIDE, FOSAMAX, VITAMINS. Patient was hospitalized.
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Probenecid Side Effects Report #5081535-8
Consumer or non-health professional from UNITED STATES reported Probenecid side effect 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 side effects: anaemia, pyrexia, renal failure. Probenecid dosage: unknown. During the same period patient was treated with RAMIPRIL. Probenecid Side Effects Report #5092184-X
Probenecid side effect 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 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. Probenecid Side Effects Report #5105941-8
Consumer or non-health professional from UNITED STATES reported Probenecid side effect 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 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. Probenecid Side Effects Report #5421889-3
Probenecid side effect 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 side effects: glomerulonephritis membranous, nephrotic syndrome. Probenecid dosage: 500 MG; TWICE A DAY; ORAL; 1500 MG; DAILY; ORALQ. Patient was hospitalized. Probenecid Side Effects Report #5444193-6
Physician from UNITED KINGDOM reported Probenecid side effect on Aug 17, 2007. Male patient was diagnosed with gouty arthritis and was treated with Probenecid. After drug was administered, patient experienced the following 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 side effect 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 side effects: anaemia haemolytic autoimmune, aplasia pure red cell. Probenecid dosage: unknown. During the same period patient was treated with CIDOFOVIR.
Probenecid Side Effects Report #4607116-5
Consumer or non-health professional from reported Probenecid side effect on Mar 02, 2005. Female patient, 61 years of age, weighting 235.9 lb, was diagnosed with gouty arthritis and was treated with Probenecid. After drug was administered, patient experienced the following side effects: back pain
, fibromyalgia, gastric ulcer, gastrointestinal disorder, inflammation, stress . Probenecid dosage: unknown. During the same period patient was treated with AVAPRO, MAGNESIUM, VITAMIN E, SOY SUPPLEMENT, VITAMIN B. Patient was hospitalized. Probenecid Side Effects Report #4632527-1
Probenecid side effect was reported by a Physician from on Mar 29, 2005. Female patient, 83 years of age, was diagnosed with gout
and was treated with Probenecid. After drug was administered, patient experienced the following side effects: activities of daily living impaired, anorexia, asthenia, diarrhoea, myalgia, myopathy. Probenecid dosage: 0.6MG; QD. During the same period patient was treated with ASPIRIN, BUMETANIDE, METOPROLOL TARTRATE, LOSARTAN POTASSIUM, AMLODIPINE, REPAGLINIDE, PREDNISONE. Patient was hospitalized. Probenecid Side Effects Report #4632528-3
Pharmacist from reported Probenecid side effect on Mar 29, 2005. Female patient, 54 years of age, was diagnosed with gout
and was treated with Probenecid. After drug was administered, patient experienced the following side effects: abdominal pain upper, activities of daily living impaired, arthralgia, asthenia, buttock pain, hepatitis , joint swelling, myopathy. Probenecid dosage: 0.6 MG, TID. During the same period patient was treated with GABAPENTIN, CALCIUM ACETATE, SEVELAMER, EPOGEN, VITAMINS W, METOCLOPRAMIDE, FERROUS SULPHATE. Patient was hospitalized. Probenecid Side Effects Report #4663679-5
Probenecid side effect was reported by a Physician from on May 10, 2005. Male patient, 76 years of age, was diagnosed with familial mediterranean fever, helicobacter infection and was treated with Probenecid. After drug was administered, patient experienced the following side effects: abdominal pain
, alopecia, blood creatinine increased, blood urea increased, c-reactive protein increased, cholestasis, dehydration, diarrhoea haemorrhagic, gastritis erosive. Probenecid dosage: 1.5-0.5MG QD. During the same period patient was treated with CLARITHROMYCIN, ACEBUTOLOL, RAMIPRIL, SPIRONOLACTONE, MOLSIDOMINE, ACETYLSALICYLATE, AMOXICILLIN, OMEPRAZOLE. Patient was hospitalized. Probenecid Side Effects Report #4710842-0
Physician from UNITED STATES reported Probenecid side effect on June 29, 2005. Female patient, 48 years of age, was diagnosed with gout
and was treated with Probenecid. After drug was administered, patient experienced the following side effects: eosinophilia, lymphadenopathy, pyrexia, rash , renal failure acute, transaminases increased. Probenecid dosage: unknown. During the same period patient was treated with ALLOPURINOL. Probenecid Side Effects Report #4772136-7
Probenecid side effect was reported by a Physician from TURKEY on Sept 02, 2005. Female patient, 65 years of age, was diagnosed with gout
and was treated with Probenecid. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, gout , hyporeflexia, muscular weakness, myopathy, nerve conduction studies abnormal. Probenecid dosage: 1.5-1.0MG QD. During the same period patient was treated with PRAVASTATIN, SPIRONOLACTONE, FUROSEMIDE, ASPIRIN, LOSARTAN POTASSIUM. Patient was hospitalized. Probenecid Side Effects Report #4787525-4
Physician from TURKEY reported Probenecid side effect on Sept 16, 2005. Male patient, 70 years of age, was diagnosed with gout
and was treated with Probenecid. After drug was administered, patient experienced the following side effects: abdominal pain upper, dehydration, nausea , renal failure acute, rhabdomyolysis. Probenecid dosage: unknown. During the same period patient was treated with FLUVASTATIN. Patient was hospitalized. Probenecid Side Effects Report #4831949-3
Probenecid side effect was reported by a Pharmacist from GERMANY on Nov 03, 2005. Male patient, 83 years of age, was diagnosed with gout
, tachyarrhythmia and was treated with Probenecid. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, csf protein increased, guillain-barre syndrome , immobile, lower motor neurone lesion, neuromyopathy, paresis. Probenecid dosage: 2 MG, IN 2 DAYS. During the same period patient was treated with VERAPAMIL, FUROSEMIDE, ACETYLSALICYLIC ACID, AMBROXOL, THEOPHYLLINE. Patient was hospitalized. Probenecid Side Effects Report #4938837-2
Physician from UNITED STATES reported Probenecid side effect on July 05, 2005. Male patient, 62 years of age, weighting 180.8 lb, was diagnosed with arthritis
and was treated with Probenecid. After drug was administered, patient experienced the following side effects: anxiety , chest pain , emotional distress, fear, injury, myocardial infarction, neck pain. Probenecid dosage: unknown. During the same period patient was treated with NORVASC, LIPITOR, SKELAXIN, PRILOSEC, AMBIEN, DIAZEPAM, ALLEGRA, VIOXX. Patient was hospitalized and became disabled. Probenecid Side Effects Report #4997083-7
Probenecid side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2006. Female patient, 77 years of age, was diagnosed with gout
, pain , hypertension and was treated with Probenecid. After drug was administered, patient experienced the following side effects: alopecia, cardiac failure congestive, fall , rib fracture. Probenecid dosage: unknown. During the same period patient was treated with INDOMETHACIN, CLONIDINE, FUROSEMIDE, FOSAMAX, VITAMINS. Patient was hospitalized.
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