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Probenecid (Probenecid) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Probenecid and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (6)

Reports by Reaction Type

Myelodysplastic Syndrome (4)Therapeutic Response Decreased (4)Chills (1)Fatigue (1)Dyspepsia (1)Dizziness (1)Blood Creatinine Increased (1)Decreased Appetite (1)Dyspnoea (1)Nausea (1)Hypoaesthesia (1)Paraesthesia (1)

Possible Probenecid side effects in male

Reported by a physician from Belgium on 2012-08-01

Patient: male

Reactions: Therapeutic Response Decreased, Myelodysplastic Syndrome

Drug(s) suspected as cause:
Aranesp
    Dosage: 500 unknown, q3wk
    Indication: Acute Myeloid Leukaemia
    Start date: 2011-12-01
    End date: 2012-04-01

Probenecid
    Dosage: unk
    Indication: Nephropathy Toxic
    Start date: 2011-11-01
    End date: 2012-04-01

Vistide
    Dosage: unk
    Indication: Cytomegalovirus Infection
    Start date: 2011-11-01
    End date: 2012-04-01

Other drugs received by patient: Mabthera; Solian; Medrol; Omeprazole; Neoral



Possible Probenecid side effects in male

Reported by a physician from Belgium on 2012-07-25

Patient: male

Reactions: Therapeutic Response Decreased, Myelodysplastic Syndrome

Drug(s) suspected as cause:
Aranesp
    Dosage: 500 unknown, q3wk
    Indication: Acute Myeloid Leukaemia
    Start date: 2011-12-01
    End date: 2012-04-01

Probenecid
    Dosage: unk
    Indication: Nephropathy Toxic
    Start date: 2011-11-01
    End date: 2012-04-01

Vistide
    Dosage: unk
    Indication: Cytomegalovirus Infection
    Start date: 2011-11-01
    End date: 2012-04-01

Other drugs received by patient: Medrol; Solian; Mabthera; Omeprazole; Neoral



Possible Probenecid side effects in 37 year old male

Reported by a physician from Belgium on 2012-07-04

Patient: 37 year old male, weighing 58.0 kg (127.6 pounds)

Reactions: Therapeutic Response Decreased, Myelodysplastic Syndrome

Drug(s) suspected as cause:
Aranesp
    Dosage: 500 mug, q3wk
    Indication: Acute Myeloid Leukaemia
    Start date: 2011-12-01

Probenecid
    Dosage: unk
    Indication: Nephropathy Toxic
    Start date: 2011-11-01
    End date: 2012-04-01

Vistide
    Dosage: unk
    Indication: Cytomegalovirus Infection
    Start date: 2011-11-01
    End date: 2012-04-01

Other drugs received by patient: Mabthera; Medrol; Solian; Omeprazole; Neoral; Mabthera



Possible Probenecid side effects in 37 year old male

Reported by a health professional (non-physician/pharmacist) from Belgium on 2012-06-26

Patient: 37 year old male, weighing 58.0 kg (127.6 pounds)

Reactions: Therapeutic Response Decreased, Myelodysplastic Syndrome

Drug(s) suspected as cause:
Aranesp
    Dosage: 500 mug, q3wk
    Indication: Acute Myeloid Leukaemia
    Start date: 2011-12-01

Probenecid
    Dosage: unk
    Indication: Nephropathy Toxic
    Start date: 2011-11-01
    End date: 2012-04-01

Vistide
    Dosage: unk
    Indication: Cytomegalovirus Infection
    Start date: 2011-11-01
    End date: 2012-04-01

Other drugs received by patient: Solian; Medrol; Mabthera; Neoral; Omeprazole; Mabthera



Possible Probenecid side effects in 67 year old male

Reported by a consumer/non-health professional from United States on 2012-02-15

Patient: 67 year old male, weighing 89.8 kg (197.6 pounds)

Reactions: Blood Creatinine Increased

Drug(s) suspected as cause:
Probenecid

Other drugs received by patient: Nadolol; Azathioprine; Cyclosporine



Possible Probenecid side effects in female

Reported by a individual with unspecified qualification from United States on 2011-10-26

Patient: female, weighing 101.7 kg (223.7 pounds)

Reactions: Dyspnoea, Nausea, Chills, Hypoaesthesia, Paraesthesia, Fatigue, Dyspepsia, Dizziness, Decreased Appetite

Drug(s) suspected as cause:
Colcrys
    Administration route: Oral
    Indication: Gout
    Start date: 2011-08-18
    End date: 2011-08-24

Probenecid
    Administration route: Oral
    Indication: Gout
    Start date: 2011-08-18
    End date: 2011-08-24

Other drugs received by patient: Prilosec; Metformin HCL; Theophylline; Alpha Lipoic Acid; Spironolactone; Flovent; Zafirlukast; Budesonide; Albuterol Sulfate 0.83%; Zetalin; Daliresp; Albuterol Sulfate; Advair Diskus 500 / 50

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