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Zerit (Stavudine) - Adverse Event Reports - Serious Event - Glucose Tolerance Impaired

 



Index of reports > Cases resulting in a serious event (101) > Cases with Glucose Tolerance Impaired (7)

Below is the selection of adverse event reports related to Zerit (Stavudine) that includes cases resulting in a serious event where reactions include glucose tolerance impaired.

Adverse event in 33 year old male receiving Zerit (Stavudine)

Reported by a consumer/non-health professional from United States on 2007-04-04

Patient: 33 year old male

Adverse reactions / side effects: Glucose Tolerance Impaired

Suspect drug(s):
Efavirenz
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-10-19
    End date: 2005-04-04

Epivir
    Dosage: started 13-sep-04 stopped 18-oct-04. restarted 12-jan-05
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2005-04-04

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-27
    End date: 2004-10-18

Predonine
    Dosage: iv(50 mg/d 23/09/04,60mg/d from 24to26/09/04)po titrated from 30mgx2/d on 30/09/04 to 5mg/d 02/12/04
    Indication: Drug Eruption
    Start date: 2004-09-23
    End date: 2004-09-26

Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Dosage: dosed from 13-sep-04 to 18-oct-04. restarted 09-mar-05, 80 mg on 01-apr-2005
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2005-04-04

Other drugs received by patient: Combivir; Clarithromycin; Allelock; Solu-Medrol; Baktar; Viread; Adriamycin PFS; Clarithromycin; Doxorubicin HCL; Olopatadine HCL; Sulfamethoxazole + Trimethoprim



Adverse event in 33 year old male receiving Zerit (Stavudine)

Reported by a physician from Japan on 2007-04-03

Patient: 33 year old male

Adverse reactions / side effects: Drug Eruption, Anaemia, Glucose Tolerance Impaired

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Combivir
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2004-10-19
    End date: 2005-01-11

Epivir
    Dosage: 300mg per day
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2004-09-13

Kaletra
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2004-09-27
    End date: 2004-10-18

Viramune
    Dosage: 400mg per day
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2004-09-13
    End date: 2004-10-18

Other drugs received by patient: Stocrin; Viread; Clarithromycin; Baktar; Unknown Drug; Ciprofloxacin; Ebutol



Adverse event in male receiving Zerit (Stavudine)

Reported by a individual with unspecified qualification from Japan on 2007-03-30

Patient: male

Adverse reactions / side effects: Drug Eruption, Glucose Tolerance Impaired

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-10-18

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-27
    End date: 2004-10-18

Predonine
    Indication: Drug Eruption
    Start date: 2004-09-23
    End date: 2004-09-26

Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-10-18

Other drugs received by patient: Clarithromycin; Baktar



Adverse event in 33 year old male receiving Zerit (Stavudine)

Reported by a consumer/non-health professional from United States on 2007-03-01

Patient: 33 year old male

Adverse reactions / side effects: Glucose Tolerance Impaired

Suspect drug(s):
Efavirenz
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-10-19
    End date: 2005-04-04

Epivir
    Dosage: started 13-sep-04 stopped 18-oct-04. restarted 12-jan-05
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2005-04-04

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-27
    End date: 2004-10-18

Predonine
    Dosage: iv(50 mg/d 23/09/04,60mg/d from 24to26/09/04)po titrated from 30mgx2/d on 30/09/04 to 5mg/d 02/12/04
    Indication: Drug Eruption
    Start date: 2004-09-23
    End date: 2004-09-26

Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Dosage: dosed from 13-sep-04 to 18-oct-04. restarted 09-mar-05, 80 mg on 01-apr-2005
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2005-04-04

Other drugs received by patient: Combivir; Clarithromycin; Allelock; Solu-Medrol; Baktar; Viread; Adriamycin PFS



Adverse event in male receiving Zerit (Stavudine)

Reported by a individual with unspecified qualification from Japan on 2007-02-16

Patient: male

Adverse reactions / side effects: Drug Eruption, Glucose Tolerance Impaired

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-10-18

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-27
    End date: 2004-10-18

Predonine
    Indication: Drug Eruption
    Start date: 2004-09-23
    End date: 2004-09-26

Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-10-18

Other drugs received by patient: Clarithromycin; Baktar



Adverse event in 33 year old male receiving Zerit (Stavudine)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-01-30

Patient: 33 year old male

Adverse reactions / side effects: Glucose Tolerance Impaired

Suspect drug(s):
Epivir
    Dosage: started 13-sep-04 stopped 18-oct-04. restarted 12-jan-05 to unknown.
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13

Kaletra
    Administration route: Oral
    Start date: 2004-09-27
    End date: 2004-10-18

Predonine
    Dosage: iv(50 mg/d 23/09/04,60mg/d from 24to26/09/04)po titrated from 30mgx2/d on 30/09/04 to 5mg/d 02/12/04
    Indication: Drug Eruption
    Start date: 2004-09-23
    End date: 2004-09-26

Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Dosage: dosed from 13-sep-04 to 18-oct-04. restarted 09-mar-05 to unknown.
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13

Other drugs received by patient: Stocrin; Combivir; Clarithromycin; Allelock; Solu-Medrol; Bactrim; Viread; Adriamycin PFS



Adverse event in male receiving Zerit (Stavudine)

Reported by a individual with unspecified qualification from Japan on 2007-01-22

Patient: male

Adverse reactions / side effects: Drug Eruption, Glucose Tolerance Impaired

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-10-18

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-27
    End date: 2004-10-18

Predonine
    Indication: Drug Eruption
    Start date: 2004-09-23
    End date: 2004-09-26

Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-09-26

Zerit
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-13
    End date: 2004-10-18

Other drugs received by patient: Clarithromycin; Bactrim

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