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Retrovir (Zidovudine) - Adverse Event Reports - Disability

 



Index of reports > Cases resulting in disability (15)

     Drug Exposure During Pregnancy (4)Premature Baby (3)Optic Neuritis Retrobulbar (3)Nose Deformity (3)Talipes (3)White Blood Cell Count Decreased (2)Pregnancy (2)Lipodystrophy Acquired (2)Blood Sodium Decreased (2)Asthenia (2)

Below is the selection of adverse event reports related to Retrovir (Zidovudine) that includes cases resulting in disability.

Adverse event in receiving Retrovir (Zidovudine)

Reported by a physician from United Kingdom on 2007-10-19

Patient:

Adverse reactions / side effects: Stillbirth, Foetal Malformation

Adverse event resulted in: death, disablity

Suspect drug(s):
Retrovir
    Indication: HIV Infection

Videx
    Indication: HIV Infection

Viramune
    Indication: HIV Infection



Adverse event in 52 year old male receiving Retrovir (Zidovudine)

Reported by a physician from France on 2007-10-15

Patient: 52 year old male

Adverse reactions / side effects: Optic Neuritis Retrobulbar

Adverse event resulted in: disablity

Suspect drug(s):
Bactrim DS
    Dosage: also received on 28 september 2005 and 23 june 2006.
    Indication: Drug USE FOR Unknown Indication
    Start date: 1998-10-27

Combivir
    Dosage: reported dosing amount: 2 doses daily.
    Start date: 2005-09-28
    End date: 2006-06-23

Combivir
    Start date: 1999-05-11
    End date: 1999-08-01

Combivir
    Start date: 2001-03-23

Invirase
    Dosage: reported dosing amount: 4 doses daily.
    Start date: 2006-06-23

Invirase
    Start date: 2002-03-18

Lyrica
    Indication: Trigeminal Neuralgia
    Start date: 2006-06-23

Neurontin
    Indication: Trigeminal Neuralgia
    Start date: 2006-01-01

Norvir
    Dosage: also received on 15 october 2004, 29 march 2005, 28 september 2005, 17 june 2005 and 23 june 2006.
    Start date: 2004-04-17

Norvir
    Start date: 1999-09-21

Norvir
    Start date: 2000-06-06

Norvir
    Start date: 2001-03-23

Norvir
    Start date: 2002-03-18

Retrovir
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-06-23

Retrovir
    Start date: 2005-06-17

Telzir
    Dosage: reported dosing amount: 2 doses daily. also received on 17 june 2005.
    Start date: 2005-03-29
    End date: 2006-06-23

Viread
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-06-23

Viread
    Start date: 2003-01-03

Viread
    Start date: 2003-09-12

Viread
    Start date: 2004-04-17

Viread
    Start date: 2004-10-15

Viread
    Start date: 2005-03-29

Viread
    Start date: 2005-06-17

Other drugs received by patient: Sustiva; Videx; Videx; Videx; Zerit; Zerit; Zerit; Zerit; Hivid; Hivid; Crixivan; Crixivan; 1 Concomitant Drug; Epivir; Agenerase; Kaletra; Kaletra; Fuzeon; Fuzeon; 1 Concomitant Drug; 1 Concomitant Drug; Ziagen; Tercian; Laroxyl; Tenofovir



Adverse event in 44 year old male receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-10-11

Patient: 44 year old male

Adverse reactions / side effects: Optic Atrophy, Glaucoma, Optic Nerve Disorder, Drug Ineffective, Tooth Abscess, Trigeminal Neuralgia, Sciatica, Tooth Extraction, Visual Acuity Reduced, Treatment Noncompliance, Balance Disorder, Leukoencephalopathy, Depression, Optic Neuritis Retrobulbar, Facial Pain, Mononeuropathy Multiplex, Visual Disturbance, Gastrointestinal Disorder, Memory Impairment, Neuralgia

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Bactrim
    Start date: 1998-09-01

Combivir
    Indication: HIV Infection
    Start date: 2005-09-28
    End date: 2006-06-23

Epivir
    Indication: HIV Infection
    Start date: 1998-04-01

Invirase
    Indication: HIV Infection
    Start date: 2006-06-23

Lyrica
    Indication: Trigeminal Neuralgia
    Start date: 2006-06-23
    End date: 2006-07-01

Neurontin
    Indication: Trigeminal Neuralgia
    Start date: 2006-01-01
    End date: 2006-01-01

Norvir
    Indication: HIV Infection
    Start date: 2004-04-17

Retrovir
    Indication: HIV Infection
    Start date: 2006-06-23

Telzir
    Indication: HIV Infection
    Start date: 2005-03-29
    End date: 2006-06-23

Viread
    Indication: HIV Infection
    Start date: 2006-06-23

Other drugs received by patient: Viracept; Zerit



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a physician from France on 2007-10-09

Patient: male

Adverse reactions / side effects: Mononeuropathy Multiplex, Glaucoma, Optic Neuropathy, Trigeminal Neuralgia, Optic Neuritis Retrobulbar, Encephalopathy

Adverse event resulted in: disablity

Suspect drug(s):
Bactrim
    Start date: 1998-10-27

Bactrim DS
    Start date: 2002-03-18

Combivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2000-09-01
    End date: 2006-06-23

Lyrica
    Indication: Trigeminal Neuralgia
    Start date: 2006-06-01
    End date: 2006-07-20

Neurontin
    Indication: Trigeminal Neuralgia
    Start date: 2006-01-01
    End date: 2006-07-20

Norvir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1999-09-21

Norvir
    Administration route: Oral
    Start date: 2004-04-17

Retrovir
    Start date: 1992-01-01
    End date: 1997-01-01

Retrovir
    Start date: 2005-06-17

Telzir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-03-29
    End date: 2006-06-23

Viread
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2002-03-18

Viread
    Start date: 2006-06-23

Other drugs received by patient: Invirase; Invirase; Kaletra; Fuzeon; Reyataz; Ziagen; Tercian; Laroxyl



Adverse event in 42 year old male receiving Retrovir (Zidovudine)

Reported by a physician from Germany on 2007-06-19

Patient: 42 year old male, weighing 75.7 kg (166.5 pounds)

Adverse reactions / side effects: Pruritus, Urticaria, Hepatic Steatosis, Lipohypertrophy, Lipomatosis, Lipodystrophy Acquired, FAT Redistribution, Hepatosplenomegaly

Adverse event resulted in: disablity

Suspect drug(s):
Combivir
    Dosage: 450mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-04-11
    End date: 2005-10-24

Epivir
    Dosage: 150mg twice per day
    Administration route: Oral

Retrovir
    Dosage: 250mg twice per day
    Administration route: Oral

Ziagen
    Dosage: 300mg twice per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1999-07-15
    End date: 2005-10-24

Other drugs received by patient: Multiple Medication; Crixivan; Efavirenz; Tenofovir; Peginterferon Alfa-2A; Ribavirin



Adverse event in 42 year old male receiving Retrovir (Zidovudine)

Reported by a physician from Germany on 2007-06-18

Patient: 42 year old male, weighing 75.7 kg (166.5 pounds)

Adverse reactions / side effects: Pruritus, Urticaria, Hepatic Steatosis, Lipohypertrophy, Lipomatosis, Lipodystrophy Acquired, FAT Redistribution, Hepatosplenomegaly

Adverse event resulted in: disablity

Suspect drug(s):
Combivir
    Dosage: 450mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-04-11
    End date: 2005-10-24

Epivir
    Dosage: 150mg twice per day
    Administration route: Oral

Retrovir
    Dosage: 250mg twice per day
    Administration route: Oral

Ziagen
    Dosage: 300mg twice per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1999-07-15
    End date: 2005-10-24

Other drugs received by patient: Multiple Medication; Crixivan; Efavirenz; Tenofovir; Peginterferon Alfa-2A; Ribavirin



Adverse event in 23 year old male receiving Retrovir (Zidovudine)

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

Patient: 23 year old male

Adverse reactions / side effects: Hyperlactacidaemia, Osteonecrosis, Arthralgia, Joint Dislocation, Gait Disturbance

Adverse event resulted in: disablity

Suspect drug(s):
Invirase
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-02-11
    End date: 1998-03-11

Kaletra
    Dosage: 6cap per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2002-03-04

Norvir
    Dosage: 400mg twice per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-11-11
    End date: 1998-03-11

Retrovir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1993-05-15
    End date: 1997-11-11

Serostim
    Indication: Weight Decreased
    Start date: 2001-04-23
    End date: 2005-06-23

Stocrin
    Dosage: 600mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1999-03-29
    End date: 2002-03-03

Videx
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1995-10-30

Viracept
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-08-04
    End date: 2002-03-03

Zerit
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1998-01-14

Ziagen
    Dosage: 300mg twice per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1999-03-29

Other drugs received by patient: Loperamide Hydrochloride; Epivir; Hivid; Prozei; Recombinate; Pegasys; Rebetol



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 31 year old male receiving Retrovir (Zidovudine)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-28

Patient: 31 year old male

Adverse reactions / side effects: Renal Impairment, Schizophrenia

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Efavirenz
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2003-03-28
    End date: 2004-05-27

Epivir
    Dosage: dosing began 20-apr-05. interrupted 27-may-2004. restarted 20-apr-2005. discontinued 13-jun-2005.
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2003-03-28
    End date: 2005-06-13

Retrovir
    Dosage: decreased to 400 mg od, from 06-may-03 to 27-may-04.
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2003-03-28
    End date: 2004-05-27

Other drugs received by patient: Penfill



Adverse event in 57 year old male receiving Retrovir (Zidovudine)

Reported by a individual with unspecified qualification from Japan on 2007-03-16

Patient: 57 year old male

Adverse reactions / side effects: Muscle Atrophy, Blood Triglycerides Increased, Muscular Weakness

Adverse event resulted in: disablity

Suspect drug(s):
Crixivan
    Dosage: see image
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-03-04
    End date: 2001-06-16

Crixivan
    Dosage: see image
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-06-21
    End date: 2005-01-20

Crixivan
    Dosage: see image
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-07-15

Retrovir
    Dosage: see image
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1996-08-01
    End date: 1997-12-25

Retrovir
    Dosage: see image
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-06-21
    End date: 2004-02-06

Retrovir
    Dosage: see image
    Administration route: Oral
    Indication: HIV Infection
    Start date: 1997-12-26
    End date: 2004-06-16

Other drugs received by patient: Epivir



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):
Combivir
    Dosage: text:unknown-freq:unknown
    Administration route: Oral
    Indication: HIV Test Positive

Retrovir
    Administration route: Oral
    Indication: HIV Test Positive

Viracept
    Administration route: Oral
    Indication: HIV Test Positive



Adverse event in male receiving Retrovir (Zidovudine)

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

Epivir
    Start date: 2005-02-23

Retrovir
    Start date: 2005-12-29

Viramune
    Start date: 2005-12-29

Zerit
    Start date: 2005-02-23
    End date: 2005-12-29

Other drugs received by patient: Bactrim; Vitamin B Complex CAP



Adverse event in male receiving Retrovir (Zidovudine)

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

Epivir
    Start date: 2005-02-23

Retrovir
    Start date: 2005-12-29

Viramune
    Start date: 2005-12-29

Zerit
    Start date: 2005-02-23
    End date: 2005-12-29

Other drugs received by patient: Bactrim; Vitamin B Complex CAP



Adverse event in male receiving Retrovir (Zidovudine)

Reported by a physician from United States on 2007-02-08

Patient: male

Adverse reactions / side effects: Nose Deformity, Drug Exposure During Pregnancy, Premature Baby, Congenital Anomaly, Talipes

Adverse event resulted in: disablity

Suspect drug(s):
Efavirenz
    Indication: HIV Infection
    Start date: 2005-02-23
    End date: 2005-12-29

Retrovir
    Start date: 2005-12-29

Viramune
    Start date: 2005-12-29

Other drugs received by patient: Epivir; Zerit; Bactrim; Vitamin B Complex CAP



Adverse event in 4 year old female receiving Retrovir (Zidovudine)

Reported by a consumer/non-health professional from France on 2007-01-26

Patient: 4 year old female

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

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