PROBENECID Side Effects

6698478-6 | Cholestasis, International Normalised Ratio Abnormal
on Apr 26, 2010 Male patient from UNITED STATES , 73 years of age, weighting 232.8 lb, was diagnosed with gout (What is gout?), hypertension and was treated with Probenecid (View Usage). Patient experienced the following unwanted or unexpected effects: cholestasis, international normalised ratio abnormal. Probenecid dosage: 500 Mg Bid Po. During the same period patient was treated with FUROSEMIDE (40 Mg Every Day Po) (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6390473-X | Thrombocytopenia
Patient was taking Probenecid (View Usage). Patient had the following side effects: thrombocytopenia on Sep 22, 2009 from UNITED STATES Additional patient health information: Female patient , 68 years of age, . Probenecid dosage: . During the same period patient was treated with OSELTAMIVIR (View Oseltamivir Review and Oseltamivir Label ). Patient was hospitalized.

6371299-X | Thrombocytopenia
Adverse event was reported on Sep 21, 2009 by a Female patient taking Probenecid (View Usage) (Dosage: Four Times Daily For 15 Days) . Location: UNITED STATES , 68 years of age, After Probenecid was administered, patient had the following side effects: thrombocytopenia. During the same period patient was treated with OSELTAMIVIR (View Oseltamivir Review and Oseltamivir Label ). Patient was hospitalized.

5421889-3 | Glomerulonephritis Membranous, Nephrotic Syndrome
on Aug 03, 2007 Male patient from FRANCE , 79 years of age, was diagnosed with gout (What is gout?) and was treated with Probenecid (View Usage). Patient experienced the following unwanted or unexpected effects: glomerulonephritis membranous, nephrotic syndrome. Probenecid dosage: 500 Mg; Twice A Day; Oral; 1500 Mg; Daily; Oralq. Patient was hospitalized.


5283923-3 | Atrial Fibrillation, Back Pain, Cerebrovascular Accident, Epididymitis, Iatrogenic Injury, Nerve Injury, Pain In Extremity
on Mar 12, 2007 Male patient from UNITED STATES , 67 years of age, weighting 190.0 lb, was diagnosed with gout (What is gout?) and was treated with Probenecid (View Usage). Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), back pain (What is back pain?), cerebrovascular accident, epididymitis, iatrogenic injury, nerve injury, pain in extremity. Probenecid dosage: See Image. During the same period patient was treated with CORTISONE ACETATE (X1) (View Cortisone Acetate Review and Cortisone Acetate Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

5264428-2 | Atrial Fibrillation, Back Pain, Cerebrovascular Accident, Epididymitis, Mobility Decreased, Nerve Injury, Pain In Extremity, Transient Ischaemic Attack
Patient was taking Probenecid (View Usage). After Probenecid was administered, patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), back pain (What is back pain?), cerebrovascular accident, epididymitis, mobility decreased, nerve injury, pain in extremity, transient ischaemic attack on Feb 27, 2007 from UNITED STATES Additional patient health information: Male patient , 68 years of age, was diagnosed with gout (What is gout?) and. Probenecid dosage: 500 Mg, Daily, Oral, 250 Mg, Daily, Oral. During the same period patient was treated with CORTISONE ACETATE (Single Shot) (View Cortisone Acetate Review and Cortisone Acetate Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

5105941-8 | Anaemia, Hypoxia, Myalgia, Pneumonitis, Renal Failure, Renal Failure Acute, Rocky Mountain Spotted Fever
Adverse event was reported on Aug 28, 2006 by a Female patient taking Probenecid (View Usage) (Dosage: 500 Mg; Bid; Po) was diagnosed with gout (What is gout?) and. Location: UNITED STATES , 57 years of age, weighting 191.0 lb, Patient experienced the following unwanted or unexpected effects: anaemia, hypoxia, myalgia, pneumonitis, renal failure, renal failure acute, rocky mountain spotted fever. During the same period patient was treated with RAMIPRIL (View Ramipril Review and Ramipril Label ), INDOMETHACIN (View Indomethacin Review and Indomethacin Label ). Patient was hospitalized.

5092184-X | Anaemia, Hypoxia, Pneumonitis, Renal Failure Acute, Rocky Mountain Spotted Fever
on Aug 10, 2006 Female patient from UNITED STATES , 57 years of age, weighting 191.0 lb, was diagnosed with gout (What is gout?) and was treated with Probenecid (View Usage). Patient had 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 (View Ramipril Review and Ramipril Label ), INDOMETHACIN (View Indomethacin Review and Indomethacin Label ). Patient was hospitalized.

5081535-8 | Anaemia, Pyrexia, Renal Failure
on Jul 27, 2006 Female patient from UNITED STATES , 57 years of age, was diagnosed with gout (What is gout?) and was treated with Probenecid (View Usage). After Probenecid was administered, patient had the following side effects: anaemia, pyrexia, renal failure. Probenecid dosage: Po. During the same period patient was treated with RAMIPRIL (CON.) (View Ramipril (con.) Review and Ramipril (con.) Label ).

4938837-2 | Anxiety, Chest Pain, Emotional Distress, Fear, Injury, Myocardial Infarction, Neck Pain
Patient was taking Probenecid (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), chest pain (What is chest pain?), emotional distress, fear, injury, myocardial infarction, neck pain on Jul 05, 2005 from UNITED STATES Additional patient health information: Male patient , 62 years of age, weighting 180.8 lb, was diagnosed with arthritis (What is arthritis?) and. Probenecid dosage: . During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), LIPITOR (View Lipitor Review and Lipitor Label ), SKELAXIN (View Skelaxin Review and Skelaxin Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), AMBIEN (View Ambien Review and Ambien Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), ALLEGRA (View Allegra Review and Allegra Label ), VIOXX (View Vioxx Review and Vioxx Label ). Patient was hospitalized and became disabled.

4772136-7 | Blood Lactate Dehydrogenase Increased, Gout, Hyporeflexia, Muscular Weakness, Myopathy, Nerve Conduction Studies Abnormal
Adverse event was reported on Sep 02, 2005 by a Female patient taking Probenecid (View Usage) (Dosage: 1.5-1.0mg Qd) was diagnosed with gout (What is gout?) and. Location: TURKEY , 65 years of age, Patient had the following side effects: blood lactate dehydrogenase increased, gout (What is gout?), hyporeflexia, muscular weakness, myopathy, nerve conduction studies abnormal. During the same period patient was treated with PRAVASTATIN (20mg Qd) (View Pravastatin Review and Pravastatin Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LOSARTAN POTASSIUM (View Losartan Potassium Review and Losartan Potassium Label ). Patient was hospitalized.