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Retrovir (Zidovudine) - Adverse Event Reports - All Cases - Anaemia

 



Index of reports > All cases (135) > Cases with Anaemia (22)

Below is the selection of adverse event reports related to Retrovir (Zidovudine) that includes all cases where reactions include anaemia.

Adverse event in female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-07-30

Patient: female, weighing 3.9 kg (8.6 pounds)

Adverse reactions / side effects: Drug Exposure During Pregnancy, Anaemia, Drug Administration Error, Accidental Overdose

Adverse event resulted in: hospitalization

Suspect drug(s):
Retrovir (Zidovudine)

Other drugs received by patient: Zidovudine



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-07-24

Patient: female

Adverse reactions / side effects: Anaemia, Accidental Overdose

Adverse event resulted in: hospitalization

Suspect drug(s):
Retrovir (Zidovudine)



Adverse event in 47 year old female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from United States on 2007-07-13

Patient: 47 year old female

Adverse reactions / side effects: Abdominal Pain Lower, Fatigue, Anaemia, Pharmaceutical Product Complaint, Eructation, Decreased Appetite

Suspect drug(s):
Epivir
    Dosage: 1tab twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2007-05-12
    End date: 2007-05-14

Retrovir
    Dosage: 1tab twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2007-05-12
    End date: 2007-05-14

Combivir
    Dosage: 1tab twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2007-05-14

Other drugs received by patient: Wellbutrin



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-06-29

Patient: male, weighing 2.8 kg (6.2 pounds)

Adverse reactions / side effects: Drug Exposure During Pregnancy, Anaemia, Neutropenia

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Combivir
    Indication: Antiviral Prophylaxis
    Start date: 2005-02-17
    End date: 2005-04-06

Retrovir
    Dosage: 1.1ml twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2005-04-06
    End date: 2005-05-17

Other drugs received by patient: Retrovir; Kaletra



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-06-18

Patient: male, weighing 3.4 kg (7.5 pounds)

Adverse reactions / side effects: Anaemia, Pallor, Blood Lactic Acid Increased

Adverse event resulted in: life threatening event

Suspect drug(s):
Retrovir (Zidovudine)



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-06-08

Patient: female, weighing 3.2 kg (7.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Flatulence, Platelet Count Increased, Blood Ketone Body Present, Hypercholesterolaemia, Malaise, Hepatomegaly, Obesity, Talipes, Hypertriglyceridaemia, Blood Pyruvic Acid Decreased, Oxygen Saturation Decreased, Supraventricular Tachycardia, Anaemia, Polyhydramnios, Tachycardia Foetal, Blood Lactic Acid Increased, Faeces Pale, Hypotonia, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Retrovir
    Administration route: Oral
    Indication: Antiviral Prophylaxis

Nevirapine
    Indication: Antiviral Prophylaxis
    Start date: 1999-09-12
    End date: 1999-09-12

Zidovudine
    Indication: Antiviral Prophylaxis

Zidovudine
    Indication: HIV Infection

Nevirapine
    Administration route: Oral
    Indication: HIV Infection

Other drugs received by patient: Ritonavir; Saquinavir; Efavirenz; Didanosine; Stavudine; Ferrostrane; Fluorex; Folic Acid; Uvesterol



Adverse event in 37 year old male receiving Retrovir (Zidovudine)

Reported by a physician from Japan on 2007-06-05

Patient: 37 year old male

Adverse reactions / side effects: Anaemia

Suspect drug(s):
Epivir
    Dosage: 300mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-10-12

Ziagen
    Dosage: 600mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-10-22
    End date: 2005-06-08

Retrovir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-06-13
    End date: 2005-11-10

Lexiva
    Dosage: 700mg twice per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-02-16
    End date: 2005-06-08

Norvir
    Dosage: 200mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-02-16
    End date: 2005-06-08

Viracept
    Dosage: 1000mg twice per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-10-12
    End date: 2005-11-10

Other drugs received by patient: Videx EC; Zerit; Stocrin; Reyataz; Diflucan; Loxonin; Urinorm; Furosemide; Aldactone



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-05-31

Patient: female, weighing 3.2 kg (7.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Hyperlactacidaemia, Anaemia, Flatulence, Supraventricular Tachycardia, Malaise, Hepatomegaly, Obesity, Hypotonia, Neutropenia, Hypertriglyceridaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Viramune
    Indication: HIV Infection
    Start date: 1999-09-09
    End date: 1999-09-09

Invirase
    Indication: HIV Infection

Videx
    Indication: Drug USE FOR Unknown Indication

Retrovir
    Indication: HIV Infection

Norvir
    Indication: Drug USE FOR Unknown Indication

D4T
    Indication: HIV Infection



Adverse event in female receiving Retrovir (Zidovudine)

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

Zerit

Sustiva

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

Norvir
    Dosage: received from week 27 of gestation to delivery

Fortovase
    Dosage: received 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,

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.

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



Adverse event in 47 year old female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from United States on 2007-05-23

Patient: 47 year old female

Adverse reactions / side effects: Abdominal Pain Lower, Fatigue, Anaemia, Pharmaceutical Product Complaint, Eructation, Decreased Appetite

Suspect drug(s):
Epivir
    Dosage: 1tab twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2007-05-12
    End date: 2007-05-14

Retrovir
    Dosage: 1tab twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2007-05-12
    End date: 2007-05-14

Combivir
    Dosage: 1tab twice per day
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2007-05-14

Other drugs received by patient: Wellbutrin



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a physician from Japan on 2007-05-16

Patient: female

Adverse reactions / side effects: Anaemia

Suspect drug(s):
Crixivan
    Indication: HIV Infection
    Start date: 1998-06-25
    End date: 1998-06-30

Retrovir
    Indication: HIV Infection
    Start date: 1998-06-25
    End date: 1998-06-30

Retrovir
    Start date: 1998-06-30
    End date: 1998-06-30

Retrovir
    Indication: Prophylaxis
    Start date: 1998-06-30
    End date: 1998-08-11

Other drugs received by patient: Epivir



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a physician from United States on 2007-03-30

Patient: male

Adverse reactions / side effects: Anaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Efavirenz
    Administration route: Oral
    Start date: 2006-10-01
    End date: 2007-01-01

Epivir
    Administration route: Oral
    Start date: 2006-10-01
    End date: 2007-01-01

Retrovir
    Administration route: Oral
    Start date: 2006-10-01
    End date: 2007-01-01



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a physician from Japan on 2007-03-05

Patient: female

Adverse reactions / side effects: Cleft LIP and Palate, Drug Exposure During Pregnancy, Anaemia, Drug Exposure VIA Breast Milk

Suspect drug(s):
Epivir
    Dosage: 150mg twice per day
    Indication: HIV Infection
    Start date: 2004-02-13

Retrovir
    Dosage: 400mg per day
    Indication: HIV Infection
    Start date: 2004-02-13

Viracept
    Dosage: 2500mg per day
    Indication: HIV Infection
    Start date: 2004-02-13

Retrovir
    Dosage: .46ml four times per day
    Administration route: Oral
    Start date: 2004-06-22
    End date: 2004-08-03

Other drugs received by patient: Lopemin; Ferrum; Utemerin



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a physician from Japan on 2007-03-05

Patient: female

Adverse reactions / side effects: Cleft LIP and Palate, Anaemia, Drug Exposure VIA Breast Milk

Adverse event resulted in: hospitalization

Suspect drug(s):
Epivir
    Dosage: 150mg twice per day
    Indication: HIV Infection
    Start date: 2004-02-13

Retrovir
    Indication: HIV Infection
    Start date: 2004-02-13

Viracept
    Indication: HIV Infection
    Start date: 2004-02-13

Retrovir
    Dosage: .46ml four times per day
    Administration route: Oral
    Start date: 2004-06-22
    End date: 2004-08-03

Other drugs received by patient: Espo; Espo



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a individual with unspecified qualification from Japan on 2007-02-28

Patient: male

Adverse reactions / side effects: Anaemia, Epilepsy

Adverse event resulted in: hospitalization

Suspect drug(s):
Viramune
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-23

Nevirapine
    Administration route: Oral
    Start date: 2004-09-25
    End date: 2004-09-25

Retrovir
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Zidovudine
    Start date: 2004-09-23
    End date: 2004-11-18

Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Lamivudine
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18

Nelfinavir Mesilate
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18



Adverse event in 19 year old female receiving Retrovir (Zidovudine)

Reported by a health professional (non-physician/pharmacist) on 2007-02-07

Patient: 19 year old female

Adverse reactions / side effects: Anaemia, Premature Labour

Suspect drug(s):
Zidovudine Tablets Usp, 300 MG
    Dosage: 600 mg daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-06-05

Retrovir
    Dosage: 2 mg/kg/hr
    Indication: HIV Infection
    Start date: 2006-10-24
    End date: 2006-10-24

Retrovir
    Dosage: 1 mg/kg/hr
    Start date: 2006-10-24
    End date: 2006-10-24

Kaletra
    Dosage: 10 ml per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-06-27

Epivir
    Dosage: 300 mg daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-06-05

Viracept
    Dosage: 2500 mg daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-06-05
    End date: 2006-06-27



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a individual with unspecified qualification from Japan on 2007-02-01

Patient: male

Adverse reactions / side effects: Anaemia, Epilepsy

Adverse event resulted in: hospitalization

Suspect drug(s):
Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-23

Nevirapine
    Administration route: Oral
    Start date: 2004-09-25
    End date: 2004-09-25

Retrovir
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Zidovudine
    Start date: 2004-09-23
    End date: 2004-11-18

Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Lamivudine
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18

Nelfinavir Mesilate
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18



Adverse event in female receiving Retrovir (Zidovudine)

Reported by a physician from Japan on 2007-01-29

Patient: female

Adverse reactions / side effects: Cleft LIP and Palate, Anaemia, Drug Exposure VIA Breast Milk

Adverse event resulted in: hospitalization

Suspect drug(s):
Epivir
    Dosage: 150mg twice per day
    Start date: 2004-02-13

Retrovir
    Start date: 2004-02-13

Viracept
    Start date: 2004-02-13

Retrovir
    Dosage: .46ml four times per day
    Administration route: Oral
    Start date: 2004-06-22
    End date: 2004-08-03

Other drugs received by patient: Espo; Espo



Adverse event in 6 month old male receiving Retrovir (Zidovudine)

Reported by a physician from Japan on 2007-01-25

Patient: 6 month old male, weighing 2.5 kg (5.5 pounds)

Adverse reactions / side effects: Drug Exposure During Pregnancy, Anaemia, Epilepsy

Adverse event resulted in: hospitalization

Suspect drug(s):
Epivir
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18

Retrovir
    Dosage: .38ml per day
    Start date: 2004-09-23
    End date: 2004-09-24

Retrovir
    Administration route: Oral
    Start date: 2004-09-26
    End date: 2004-11-18

Retrovir
    Dosage: .7ml three times per day
    Administration route: Oral
    Start date: 2004-10-26
    End date: 2004-11-18

Epivir
    Dosage: 400mg per day
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Retrovir
    Dosage: 300mg per day
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Viramune
    Start date: 2004-09-22
    End date: 2004-09-23

Viracept
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18

Viracept
    Dosage: 280mg twice per day
    Administration route: Oral
    Start date: 2004-10-26
    End date: 2004-11-18

Marijuana

Other drugs received by patient: Viramune; Bactrim; Espo; Glucose; Glucose



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a individual with unspecified qualification from Japan on 2007-01-24

Patient: male

Adverse reactions / side effects: Anaemia, Epilepsy

Adverse event resulted in: hospitalization

Suspect drug(s):
Viramune
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-23

Nevirapine
    Administration route: Oral
    Start date: 2004-09-25
    End date: 2004-09-25

Retrovir
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Zidovudine
    Start date: 2004-09-23
    End date: 2004-11-18

Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-09-22
    End date: 2004-09-30

Lamivudine
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18

Nelfinavir Mesilate
    Administration route: Oral
    Start date: 2004-09-28
    End date: 2004-11-18



Adverse event in female receiving Retrovir (Zidovudine)

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):
Zerit
    Administration route: Oral
    Start date: 1999-02-19

Viracept
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1999-02-19

Retrovir
    Indication: HIV Test Positive
    Start date: 1999-02-19

Epivir
    Administration route: Oral
    Start date: 1999-02-19

Other drugs received by patient: Methadone HCL



Adverse event in 19 year old female receiving Retrovir (Zidovudine)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-08

Patient: 19 year old female

Adverse reactions / side effects: Premature Baby, Drug Exposure During Pregnancy, Anaemia

Suspect drug(s):
Epivir
    Dosage: 300mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-06-05

Retrovir
    Dosage: 1mgkh per day
    Indication: HIV Infection
    Start date: 2006-10-24
    End date: 2006-10-24

Zidovudine
    Dosage: 600mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-06-05

Other drugs received by patient: Kaletra; Viracept; Trimethoprim + Sulfamethoxazole; Macrobid; Clotrimazole Troches; Reglan; Promethazine; Cefazolin

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