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Probenecid (Probenecid) - Therapeutic Response Decreased - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Therapeutic Response Decreased (4)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Probenecid where reactions include therapeutic response decreased. The selected reports were submitted to the FDA during the sample period of about a year.

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

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