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Index of reports
> Cases resulting in other serious reactions (42)
> Cases with Pregnancy (5)
Below is the selection of adverse event reports related to Zerit (Stavudine) that includes cases resulting in other serious reactions where reactions include pregnancy.
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):
Zerit
Dosage: exposure during gestation.
Videx
Dosage: exposure during gestation.
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
Other drugs received by patient: Bactrim; Triflucan; Loxen; Celestene; Salbutamol
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):
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-03
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
Other drugs received by patient: Retrovir
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):
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1999-02-03
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
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
Zerit
Start date: 2005-02-23
End date: 2005-12-29
Epivir
Start date: 2005-02-23
Viramune
Start date: 2005-12-29
Retrovir
Start 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
Zerit
Start date: 2005-02-23
End date: 2005-12-29
Epivir
Start date: 2005-02-23
Viramune
Start date: 2005-12-29
Retrovir
Start date: 2005-12-29
Other drugs received by patient: Bactrim; Vitamin B Complex CAP
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