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From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes, said the Institute of Medicine report, released yesterday.
Many Unfavorable Drug Studies Aren’t Published. Nearly a third of antidepressant drug studies are never published in the medical literature, and nearly all of those happen to show that the drug being tests failed to work.
Only Drugs That are Safe Should be put on the Market. Drug developers are just beginning to come to grips with recent FDA oversight reforms and how they will affect drug safety. But, it appears that industry and consumer advocates are not together on how well the overhaul will be able to prevent future drug safety scandals.

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Total Probenecid reports: 7.
Probenecid FDA safety alerts: No.
Reported deaths: 1    Reported hospitalizations: 5.
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FDA Reported Probenecid Side Effects: anaemia, rocky mountain spotted fever, renal failure acute, pneumonitis, hypoxia, renal failure, pain in extremity, nerve injury, epididymitis, cerebrovascular accident, back pain.
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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.

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