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Zerit (Stavudine) - Adverse Event Reports - All Cases - Glucose Tolerance Impaired

 



Index of reports > All cases (102) > Cases with Glucose Tolerance Impaired (7)

Below is the selection of adverse event reports related to Zerit (Stavudine) that includes all cases 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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