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Zerit (Stavudine) - Adverse Event Reports - Other Serious Reactions - Anaemia

 



Index of reports > Cases resulting in other serious reactions (42) > Cases with Anaemia (5)

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

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 female receiving Zerit (Stavudine)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-25

Patient: female, weighing 3.0 kg (6.6 pounds)

Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Hyperlactacidaemia, Flatulence, Mucous Stools, Platelet Count Increased, Hypercholesterolaemia, Hepatomegaly, Malaise, Obesity, Abdominal Distension, Hypertriglyceridaemia, Oxygen Saturation Decreased, Anaemia, Ventricular Tachycardia, Hypotonia, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Fortovase
    Dosage: received from week 27 of gestation to delivery

Invirase
    Dosage: initiated at 27 weeks of gestation
    Indication: HIV Infection

Norvir
    Dosage: received from week 27 of gestation to delivery

Retrovir
    Dosage: received 6 weeks of antiretroviral therapy after delivery, 200mg/20ml

Retrovir
    Dosage: received from conception to day 3 of gestation and from week 27 of gestation to and at delivery.

Sustiva

Videx
    Dosage: received from conception to day 3 of gestation, then from week 27 of gestation to delivery

Viramune
    Dosage: received one single oral dose, from 27 weeks gestation transplacental exposure
    Administration route: Oral
    Indication: HIV Infection

Viramune
    Dosage: received infusion during delivery,

Zerit

Other drugs received by patient: Cordarone; Speciafoldine; Ferrostrane; Uvesterol D; Fluorex; AZT



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 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 44 year old male receiving Zerit (Stavudine)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-02-26

Patient: 44 year old male

Adverse reactions / side effects: HIV Infection, Anaemia

Adverse event resulted in: death

Suspect drug(s):
Zerit (Stavudine)

Other drugs received by patient: Videx EC; Viracept; Retrovir; Lamivudine

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