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Index of reports
> All cases (102)
> Cases with Pregnancy (10)
Below is the selection of adverse event reports related to Zerit (Stavudine) that includes all cases where reactions include pregnancy.
Adverse event in female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-08
Patient: female
Adverse reactions / side effects: Cerebral Disorder, Rhinitis, Neutropenia, Foetal Growth Retardation, Pregnancy, Anaemia Macrocytic
Adverse event resulted in: hospitalization
Suspect drug(s):
Crixivan
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Epivir
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Fortovase
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Lamivudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Retrovir
Dosage: exposure began in week ten of gestation.
Indication: HIV Test Positive
Start date: 1997-07-01
End date: 1998-01-19
Videx
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Zerit
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Zidovudine
Indication: HIV Infection
Start date: 1997-01-01
End date: 1997-01-01
Zidovudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Adverse event in female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-30
Patient: female, weighing 1.0 kg (2.2 pounds)
Adverse reactions / side effects: Ileostomy, Premature Baby, Alanine Aminotransferase Increased, Thrombocythaemia, Necrotising Colitis, Speech Disorder, Colectomy Total, Blood Creatinine Increased, Enterocolitis, Pregnancy
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Invirase
Dosage: exposure during gestation.
Norvir
Dosage: exposure during gestation.
Retrovir
Dosage: exposure during delivery.
Start date: 1999-07-02
End date: 1999-07-02
Retrovir
Dosage: initiated at 8 mg/kg/day, 6 mg/kg/day from 7/6/99, then 1.4 mg/kg twice daily from 7/11/99.
Indication: Prophylaxis
Start date: 1999-07-02
End date: 1999-08-10
Retrovir
Administration route: Oral
Start date: 1999-07-07
End date: 1999-07-18
Videx
Dosage: exposure during gestation.
Zerit
Dosage: exposure during gestation.
Other drugs received by patient: Bactrim; Triflucan; Loxen; Celestene; Salbutamol
Adverse event in female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-30
Patient: female
Adverse reactions / side effects: Cerebral Disorder, Rhinitis, Neutropenia, Foetal Growth Retardation, Pregnancy, Anaemia Macrocytic
Adverse event resulted in: hospitalization
Suspect drug(s):
Crixivan
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Epivir
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Fortovase
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Lamivudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Retrovir
Dosage: exposure began in week ten of gestation.
Indication: HIV Test Positive
Start date: 1997-07-01
End date: 1998-01-19
Videx
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Zerit
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Zidovudine
Indication: HIV Infection
Start date: 1997-01-01
End date: 1997-01-01
Zidovudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Adverse event in 33 year old female receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from Japan on 2007-05-29
Patient: 33 year old female
Adverse reactions / side effects: Normal Newborn, Musculoskeletal Pain, Anaemia, Blood Triglycerides Increased, Pregnancy, Deep Vein Thrombosis
Suspect drug(s):
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-03
Viracept
Dosage: viracept (nfv) 2200-2500 mg/day dosed
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-10
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-03
Other drugs received by patient: Retrovir
Adverse event in 28 month old female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-29
Patient: 28 month old female
Adverse reactions / side effects: Electroencephalogram Abnormal, Drug Exposure During Pregnancy, Nervous System Disorder, Nuclear Magnetic Resonance Imaging Abnormal, Pregnancy
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Dosage: from the 17th week of gestation to the 26th week.
Start date: 1997-11-01
End date: 1998-04-01
Epivir
Dosage: syrup
Administration route: Oral
Start date: 1997-11-01
End date: 1998-01-01
Invirase
Dosage: from the 17th week to the end of pregnancy.
Start date: 1997-11-01
End date: 1998-04-01
Norvir
Dosage: from the 17th week to the end of pregnancy.
Start date: 1997-11-01
End date: 1998-04-01
Retrovir
Dosage: from the 13th week to the 26th week of gestation.
Start date: 1997-10-01
End date: 1998-01-01
Retrovir
Dosage: syrup
Administration route: Oral
Start date: 1997-10-01
End date: 1998-01-01
Videx
Dosage: from the 26th week of gestation.
Start date: 1998-01-14
Zerit
Dosage: from the 26th week of gestation.
Start date: 1998-01-14
Adverse event in 33 year old female receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from Japan on 2007-05-01
Patient: 33 year old female
Adverse reactions / side effects: Anaemia, Musculoskeletal Pain, Blood Triglycerides Increased, Pregnancy, Deep Vein Thrombosis, Infant
Suspect drug(s):
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-03
Viracept
Dosage: viracept (nfv) 2200-2500 mg/day dosed
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-10
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-03
Adverse event in female receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from Botswana on 2007-03-01
Patient: female, weighing 3.0 kg (6.6 pounds)
Adverse reactions / side effects: Drug Exposure During Pregnancy, Vitiligo, Pregnancy, Umbilical Hernia
Suspect drug(s):
Epivir
Start date: 2004-06-01
End date: 2005-04-09
Viramune
Start date: 2004-06-01
End date: 2005-04-09
Zerit
Start date: 2004-06-01
End date: 2005-04-09
Adverse event in male receiving Zerit (Stavudine)
Reported by a physician from United States on 2007-02-15
Patient: male
Adverse reactions / side effects: Nose Deformity, Premature Baby, Talipes, Lower Limb Deformity, Pregnancy
Adverse event resulted in: disablity
Suspect drug(s):
Efavirenz
Indication: HIV Infection
Start date: 2005-02-23
End date: 2005-12-29
Epivir
Start date: 2005-02-23
Retrovir
Start date: 2005-12-29
Viramune
Start date: 2005-12-29
Zerit
Start date: 2005-02-23
End date: 2005-12-29
Other drugs received by patient: Bactrim; Vitamin B Complex CAP
Adverse event in male receiving Zerit (Stavudine)
Reported by a physician from United States on 2007-02-09
Patient: male
Adverse reactions / side effects: Nose Deformity, Premature Baby, Talipes, Lower Limb Deformity, Pregnancy
Adverse event resulted in: disablity
Suspect drug(s):
Efavirenz
Indication: HIV Infection
Start date: 2005-02-23
End date: 2005-12-29
Epivir
Start date: 2005-02-23
Retrovir
Start date: 2005-12-29
Viramune
Start date: 2005-12-29
Zerit
Start date: 2005-02-23
End date: 2005-12-29
Other drugs received by patient: Bactrim; Vitamin B Complex CAP
Adverse event in female receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from United States on 2007-01-12
Patient: female
Adverse reactions / side effects: Anaemia, Thrombocythaemia, Pregnancy, Blood Lactic Acid Increased, Hypertriglyceridaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Administration route: Oral
Start date: 1999-02-19
Retrovir
Indication: HIV Test Positive
Start date: 1999-02-19
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-19
Zerit
Administration route: Oral
Start date: 1999-02-19
Other drugs received by patient: Methadone HCL
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