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Index of reports
> Cases resulting in life threatening events (13)
Below is the selection of adverse event reports related to Retrovir (Zidovudine) that includes cases resulting in life threatening events.
Adverse event in 36 year old male receiving Retrovir (Zidovudine)
Reported by a physician from Japan on 2007-10-01
Patient: 36 year old male
Adverse reactions / side effects: Blood Urea Increased, AIDS Encephalopathy, Altered State of Consciousness, Blood Creatinine Increased, Renal Failure Chronic, Convulsion, Nephropathy
Adverse event resulted in: life threatening event
Suspect drug(s):
Baktar
Administration route: Oral
Indication: Antifungal Prophylaxis
Start date: 2006-04-01
Darunavir
Indication: Drug USE FOR Unknown Indication
Epivir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2000-09-19
End date: 2007-03-17
Norvir
Dosage: 100mg as directed
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-04-07
End date: 2007-03-17
Norvir
Dosage: 200mg unknown
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-05-20
End date: 2003-11-10
Retrovir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2000-09-19
End date: 2006-12-11
Tipranavir
Indication: Drug USE FOR Unknown Indication
Viread
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-05-20
End date: 2006-11-14
Ziagen
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2002-11-26
End date: 2007-03-17
Zithromax
Administration route: Oral
Indication: Opportunistic Infection Prophylaxis
Start date: 2002-04-09
Other drugs received by patient: Unknown Drug; Unknown Drug
Adverse event in 45 year old male receiving Retrovir (Zidovudine)
Reported by a physician from Japan on 2007-07-31
Patient: 45 year old male, weighing 56.0 kg (123.2 pounds)
Adverse reactions / side effects: Pneumonia, Acute Respiratory Distress Syndrome, Pancytopenia, Histoplasmosis Disseminated, Pyrexia, Renal Failure Acute
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Crixivan
Administration route: Oral
Indication: HIV Infection
Start date: 2001-08-27
End date: 2001-09-04
Daraprim
Administration route: Oral
Indication: Cerebral Toxoplasmosis
Start date: 2001-08-25
End date: 2001-08-31
Daraprim
Administration route: Oral
Start date: 2001-09-01
End date: 2001-09-06
Retrovir
Administration route: Oral
Indication: HIV Infection
Start date: 2001-08-27
End date: 2001-09-04
Other drugs received by patient: Epivir; Clindamycin Hydrochloride; Dalacin S; Hydrocortone; Prednisolone; Prednisolone; Prednisolone; Prednisolone; Glyceol; Glyceol; Glyceol
Adverse event in 2 month old male receiving Retrovir (Zidovudine)
Reported by a physician from France on 2007-07-16
Patient: 2 month old male
Adverse reactions / side effects: Gastrointestinal Malformation, Heart Disease Congenital, Pregnancy
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Epivir
Start date: 2001-03-27
End date: 2001-08-11
Retrovir
Start date: 2001-03-27
End date: 2001-08-11
Videx
Start date: 2001-06-12
End date: 2001-08-11
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-13
Patient: male
Adverse reactions / side effects: Heart Disease Congenital, Duodenal Atresia
Adverse event resulted in: life threatening event
Suspect drug(s):
Epivir
Start date: 2001-03-27
End date: 2001-11-08
Retrovir
Start date: 2001-03-27
End date: 2001-11-08
Videx
Start date: 2001-06-12
End date: 2001-11-08
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 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 4 year old male receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from Denmark on 2007-03-30
Patient: 4 year old male, weighing 17.0 kg (37.4 pounds)
Adverse reactions / side effects: Haemoglobin Decreased, Bone Marrow Failure, Neutropenia, Thrombocytopenia, Reticulocytopenia, Pneumococcal Sepsis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Retrovir (Zidovudine)
Other drugs received by patient: Epivir; Viramune; Bactrim
Adverse event in 59 year old male receiving Retrovir (Zidovudine)
Reported by a pharmacist from United States on 2007-03-30
Patient: 59 year old male
Adverse reactions / side effects: Incorrect Dose Administered, Bone Marrow Failure
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Retrovir
Dosage: 300 mg every 12 hours oral
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2006-11-21
End date: 2007-01-31
Retrovir
Dosage: 300 mg every 12 hours oral
Administration route: Oral
Indication: HIV Infection
Start date: 2006-11-21
End date: 2007-01-31
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 male receiving Retrovir (Zidovudine)
Reported by a health professional (non-physician/pharmacist) from Malaysia on 2007-02-12
Patient: male
Adverse reactions / side effects: Diarrhoea Neonatal, Hyperlactacidaemia, Anion GAP Increased, Coagulopathy, Dyskinesia, Blood Albumin Decreased, Prothrombin Time Prolonged, Neonatal Disorder, Activated Partial Thromboplastin Time Prolonged, Caesarean Section, Hepatic Encephalopathy, Vertical Infection Transmission, Gamma-Glutamyltransferase Increased, Developmental Delay, HIV Infection, Fever Neonatal, Abdominal Distension, Alanine Aminotransferase Increased, Vomiting Neonatal, Convulsion, Drug Exposure During Pregnancy, Dehydration, Aspartate Aminotransferase Increased, Maternal Condition Affecting Foetus, Ammonia Increased, Feeding Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Epivir
Dosage: transplacentary
Indication: HIV Infection
Nevirapine
Dosage: transplacentary
Indication: HIV Infection
Retrovir
Dosage: oral
Administration route: Oral
Retrovir
Dosage: transplacentary
Indication: HIV Infection
Stavudine
Dosage: transplacentary
Indication: HIV Infection
Adverse event in 1 year old male receiving Retrovir (Zidovudine)
Reported by a consumer/non-health professional from France on 2007-01-19
Patient: 1 year old male
Adverse reactions / side effects: Malaise, Drug Exposure During Pregnancy, Pregnancy
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Bactrim
Combivir
Kaletra
Retrovir
Adverse event in male receiving Retrovir (Zidovudine)
Reported by a individual with unspecified qualification from Japan on 2007-01-12
Patient: male
Adverse reactions / side effects: Agranulocytosis, Hepatic Function Abnormal, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-01-11
End date: 2005-10-11
Retrovir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-01-11
End date: 1999-02-18
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 1999-01-11
End date: 2005-10-04
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1996-06-22
End date: 2004-08-19
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