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Index of reports
> All cases (135)
> Cases with Drug Exposure During Pregnancy (37)
Below is the selection of adverse event reports related to Retrovir (Zidovudine) that includes all cases where reactions include drug exposure during pregnancy.
Reports 1 - 25 of 37 Next >>
Adverse event in receiving Retrovir (Zidovudine)
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypospadias
Suspect drug(s):
Viracept
Administration route: Oral
Indication: HIV Infection
Videx
Sustiva
Epivir
Norvir
Retrovir
Indinivir Sulfate
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 male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-24
Patient: male, weighing 3.4 kg (7.4 pounds)
Adverse reactions / side effects: Abdominal Hernia, Cardiac Murmur, Drug Exposure During Pregnancy, Congenital Anomaly, Cryptorchism, Abdominal Distension
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-06-01
Combivir
Dosage: daily dose:600mg
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-06-01
Kaletra
Dosage: daily dose:600mg
Indication: HIV Infection
Retrovir
Dosage: daily dose:600mg
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Viread
Dosage: daily dose:300mg
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Other drugs received by patient: Folic Acid
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 28 year old female receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from France on 2007-06-25
Patient: 28 year old female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Drug Dependence, Treatment Noncompliance
Suspect drug(s):
Epivir
Administration route: Oral
Indication: HIV Infection
Retrovir
Administration route: Oral
Indication: HIV Infection
Viracept
Administration route: Oral
Indication: HIV Infection
Morphine
Administration route: Oral
Adverse event in receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from France on 2007-06-25
Patient:
Adverse reactions / side effects: Agitation, Overdose, Body Temperature Increased, Drug Exposure During Pregnancy, Abdominal Distension, Sneezing, Feeding Disorder Neonatal, Faecaloma
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Indication: HIV Infection
Retrovir
Indication: HIV Infection
Epivir
Administration route: Oral
Indication: Antiviral Prophylaxis
Retrovir
Administration route: Oral
Indication: Antiviral Prophylaxis
Morphine
Viracept
Indication: HIV Infection
Viracept
Administration route: Oral
Indication: Antiviral Prophylaxis
Adverse event in female receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from United States on 2007-06-18
Patient: female, weighing 2.6 kg (5.7 pounds)
Adverse reactions / side effects: Metabolic Acidosis, Drug Exposure During Pregnancy, Atrioventricular Block Complete, Patent Ductus Arteriosus, Heat Rash, Ventricular Septal Defect, Coarctation of THE Aorta
Suspect drug(s):
Retrovir (Zidovudine)
Other drugs received by patient: Kaletra; Didanosine
Adverse event in female receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from United States on 2007-06-14
Patient: female
Adverse reactions / side effects: Electroencephalogram Abnormal, Cerebral Disorder, Drug Exposure During Pregnancy, Rhinitis, Neutropenia, Foetal Growth Retardation, Anaemia Macrocytic
Adverse event resulted in: hospitalization
Suspect drug(s):
Zerit
Dosage: ongoing gestational weeks 2 through 10
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Videx
Dosage: ongoing at gestational weeks 2 through 10
Indication: HIV Infection
Start date: 1997-05-29
End date: 1997-07-01
Fortovase
Dosage: initiated at gestational week 29
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Retrovir
Dosage: initiated at gestational week 10
Indication: HIV Test Positive
Start date: 1997-07-01
End date: 1998-01-19
Retrovir
Dosage: infusion at delivery
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Crixivan
Dosage: ongoing gestational week 2 through 10
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Epivir
Dosage: initiated at gestational week 29
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Epivir
Dosage: 6 week course after birth
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Adverse event in 28 month old female receiving Retrovir (Zidovudine)
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):
Zerit
Dosage: from the 26th week of gestation.
Start date: 1998-01-14
Videx
Dosage: from the 26th week of gestation.
Start date: 1998-01-14
Retrovir
Dosage: from the 13th week to the 26th week of gestation.
Start date: 1997-10-01
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
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
Retrovir
Dosage: syrup
Administration route: Oral
Start date: 1997-10-01
End date: 1998-01-01
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-15
Patient: male, weighing 3.4 kg (7.4 pounds)
Adverse reactions / side effects: Abdominal Hernia, Cardiac Murmur, Drug Exposure During Pregnancy, Congenital Anomaly, Cryptorchism, Abdominal Distension
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-07-20
Combivir
Dosage: daily dose:600mg
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-06-01
Kaletra
Dosage: daily dose:600mg
Indication: HIV Infection
Retrovir
Dosage: daily dose:600mg
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Viread
Dosage: daily dose:300mg
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Other drugs received by patient: Folic Acid
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-08
Patient: male, weighing 3.4 kg (7.4 pounds)
Adverse reactions / side effects: Abdominal Hernia, Cardiac Murmur, Drug Exposure During Pregnancy, Congenital Anomaly, Cryptorchism, Abdominal Distension
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-07-20
Combivir
Dosage: daily dose:600mg
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-06-01
Kaletra
Dosage: daily dose:600mg
Indication: HIV Infection
Retrovir
Dosage: daily dose:600mg
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Viread
Dosage: daily dose:300mg
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Other drugs received by patient: Folic Acid
Adverse event in receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from United States on 2007-05-08
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Coarctation of THE Aorta
Suspect drug(s):
Retrovir (Zidovudine)
Other drugs received by patient: Kaletra; Didanosine
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-04
Patient: male, weighing 3.4 kg (7.4 pounds)
Adverse reactions / side effects: Abdominal Hernia, Cardiac Murmur, Drug Exposure During Pregnancy, Congenital Anomaly, Cryptorchism, Abdominal Distension
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg-freq:unknown
Administration route: Oral
Indication: HIV Test Positive
Start date: 2004-01-30
End date: 2004-06-01
Truvada
Dosage: daily dose:300mg-freq:unknown
Administration route: Oral
Indication: HIV Test Positive
Start date: 2004-06-01
End date: 2004-07-20
Combivir
Dosage: daily dose:600mg-freq:unknown
Administration route: Oral
Indication: HIV Test Positive
Start date: 2004-01-30
End date: 2004-06-01
Kaletra
Dosage: daily dose:600mg-freq:unknown
Administration route: Oral
Indication: HIV Test Positive
Retrovir
Dosage: daily dose:600mg-freq:unknown
Administration route: Oral
Indication: HIV Test Positive
Start date: 2004-06-01
End date: 2004-07-20
Other drugs received by patient: Folic Acid
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from United Kingdom on 2007-05-03
Patient: male
Adverse reactions / side effects: Abdominal Hernia, Cardiac Murmur, Drug Exposure During Pregnancy, Congenital Anomaly, Cryptorchism, Abdominal Distension
Suspect drug(s):
Combivir
Dosage: 600mg per day
Start date: 2004-01-30
End date: 2004-06-01
Truvada
Dosage: 300mg per day
Start date: 2004-06-01
End date: 2004-07-20
Viracept
Dosage: 2500mg per day
Start date: 2004-01-30
End date: 2004-06-01
Kaletra
Dosage: 600mg per day
Start date: 2004-06-01
Retrovir
Dosage: 600mg per day
Start date: 2004-06-01
End date: 2004-07-20
Other drugs received by patient: Folic Acid
Adverse event in 4 year old female receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from France on 2007-04-19
Patient: 4 year old female, weighing 21.6 kg (47.5 pounds)
Adverse reactions / side effects: Abdominal Pain, White Blood Cell Count Decreased, Vomiting, Tachycardia, Pyrexia, Blood Fibrinogen Increased, Pallor, Acute Lymphocytic Leukaemia, Haemoglobin Decreased, Diarrhoea, C-Reactive Protein Increased, Drug Exposure During Pregnancy, Ecchymosis, Blood Sodium Decreased, Asthenia
Adverse event resulted in: disablity
Suspect drug(s):
Combivir
Indication: Antiviral Prophylaxis
Start date: 2002-07-12
End date: 2002-10-01
Retrovir
Dosage: .75ml four times per day
Administration route: Oral
Indication: Antiviral Prophylaxis
Start date: 2002-10-12
End date: 2002-11-26
Adverse event in receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-17
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Stillbirth, Foetal Malformation
Adverse event resulted in: death
Suspect drug(s):
Retrovir
Dosage: 500mg per day
Indication: HIV Infection
Videx
Dosage: 250mg per day
Indication: HIV Infection
Viramune
Indication: HIV Infection
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-11
Patient: male, weighing 2.9 kg (6.4 pounds)
Adverse reactions / side effects: Trisomy 21, Atrial Septal Defect, Drug Exposure During Pregnancy, Patent Ductus Arteriosus
Suspect drug(s):
Combivir
Dosage: 2tab per day
Indication: HIV Infection
Start date: 2006-09-28
End date: 2006-10-04
Trizivir
Dosage: 2tab per day
Indication: HIV Infection
Start date: 2006-09-21
End date: 2006-09-21
Retrovir
Dosage: 476mg per day
Indication: HIV Infection
Start date: 2006-10-04
End date: 2006-10-04
Adverse event in receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-03
Patient:
Adverse reactions / side effects: Caesarean Section, Lymphadenopathy, Drug Exposure During Pregnancy, HIV Infection, Human Immunodeficiency Virus Transmission, Failure TO Thrive, Hepatosplenomegaly
Suspect drug(s):
Retrovir
Indication: Antiviral Prophylaxis
Retrovir
Dosage: transplacentary
Indication: Antiviral Prophylaxis
Nevirapine
Dosage: single dose
Indication: Antiviral Prophylaxis
Didanosine
Indication: Antiviral Prophylaxis
Didanosine
Dosage: transplacentary
Indication: Antiviral Prophylaxis
Nevirapine
Dosage: transplacentary
Indication: Antiviral Prophylaxis
Adverse event in receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-03
Patient:
Adverse reactions / side effects: Vertical Infection Transmission, Drug Exposure During Pregnancy, Human Immunodeficiency Virus Transmission, Maternal Condition Affecting Foetus, Failure TO Thrive, Hepatosplenomegaly
Suspect drug(s):
Retrovir
Dosage: transplacentary
Indication: Antiviral Prophylaxis
Epivir
Dosage: transplacentary
Indication: Antiviral Prophylaxis
Nevirapine
Dosage: transplacentary
Indication: Antiviral Prophylaxis
Quinine Sulfate
Dosage: transplacentary
Indication: Plasmodium Falciparum Infection
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-02
Patient: male, weighing 1.4 kg (3.1 pounds)
Adverse reactions / side effects: Congenital Hydronephrosis, Congenital Musculoskeletal Anomaly, Umbilical Cord Abnormality, Drug Exposure During Pregnancy, Patent Ductus Arteriosus, Arachnoid Cyst, Interruption of Aortic Arch, Atrioventricular Septal Defect
Suspect drug(s):
Trizivir
Dosage: 2tab per day
Indication: HIV Infection
Start date: 2006-03-30
End date: 2006-05-12
Retrovir
Dosage: 423mg per day
Indication: HIV Infection
Start date: 2006-05-10
End date: 2006-05-10
Adverse event in female receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from France on 2007-03-30
Patient: female, weighing 1.0 kg (2.2 pounds)
Adverse reactions / side effects: Drug Exposure During Pregnancy, Necrotising Enterocolitis Neonatal
Adverse event resulted in: life threatening event
Suspect drug(s):
Retrovir
Dosage: 1.6mg twice per day
Indication: Antiviral Prophylaxis
Start date: 2007-01-19
End date: 2007-01-26
Retrovir
Dosage: 2mg twice per day
Administration route: Oral
Start date: 2007-01-26
End date: 2007-02-08
Other drugs received by patient: Antiretroviral Medications
Adverse event in receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from United States on 2007-03-26
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Coarctation of THE Aorta
Suspect drug(s):
Retrovir (Zidovudine)
Other drugs received by patient: Kaletra; Didanosine
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 health professional (non-physician/pharmacist) from France on 2007-02-27
Patient: female
Adverse reactions / side effects: Dysmorphism, Drug Exposure During Pregnancy
Adverse event resulted in: disablity
Suspect drug(s):
Viracept
Administration route: Oral
Indication: HIV Test Positive
Retrovir
Administration route: Oral
Indication: HIV Test Positive
Combivir
Dosage: text:unknown-freq:unknown
Administration route: Oral
Indication: HIV Test Positive
Adverse event in receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from South Africa on 2007-02-21
Patient:
Adverse reactions / side effects: Nose Deformity, Drug Exposure During Pregnancy, Premature Baby, Talipes, Limb Malformation
Suspect drug(s):
Epivir
Dosage: 150mg per day
Indication: HIV Infection
Start date: 2005-02-23
Retrovir
Dosage: 600mg per day
Indication: HIV Infection
Start date: 2005-12-29
Zerit
Dosage: 80mg per day
Indication: HIV Infection
Start date: 2005-02-23
End date: 2005-12-29
Sustiva
Dosage: 600mg per day
Indication: HIV Infection
Start date: 2005-02-23
End date: 2005-12-29
Viramune
Dosage: 400mg per day
Indication: HIV Infection
Start date: 2005-12-29
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