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Index of reports
> Cases resulting in disability (23)
Below is the selection of adverse event reports related to Zerit (Stavudine) that includes cases resulting in disability.
Adverse event in 46 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-15
Patient: 46 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Coronary Artery Disease
Adverse event resulted in: disablity
Suspect drug(s):
Zerit
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Invirase
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Combivir
Indication: HIV Infection
Start date: 2005-01-31
End date: 2005-09-21
Kaletra
Indication: HIV Infection
Start date: 2005-01-31
Trizivir
Indication: HIV Infection
Start date: 2005-09-21
Norvir
Indication: HIV Infection
Start date: 2006-01-11
Adverse event in 46 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: 46 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Coronary Artery Disease
Adverse event resulted in: disablity
Suspect drug(s):
Zerit
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Invirase
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Combivir
Indication: HIV Infection
Start date: 2005-01-31
End date: 2005-09-21
Kaletra
Indication: HIV Infection
Start date: 2005-01-31
Trizivir
Indication: HIV Infection
Start date: 2005-09-21
Norvir
Indication: HIV Infection
Start date: 2006-01-11
Adverse event in 46 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: 46 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Coronary Artery Disease
Adverse event resulted in: disablity
Suspect drug(s):
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Trizivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-09-21
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-31
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-31
End date: 2005-09-21
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2006-01-11
Norvir
Administration route: Oral
Start date: 1998-12-30
End date: 2004-10-25
Other drugs received by patient: Zelitrex; Escitalopram; Seresta
Adverse event in 46 year old male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from France on 2007-10-01
Patient: 46 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Cardiac Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Trizivir
Dosage: 1tab twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2005-09-21
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-31
End date: 2005-09-21
Norvir
Dosage: 100mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2006-01-11
Kaletra
Dosage: 4tab twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-31
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-12-30
End date: 2004-10-25
Other drugs received by patient: Zelitrex; Escitalopram; Seresta
Adverse event in 49 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-07-06
Patient: 49 year old male
Adverse reactions / side effects: Renal Failure, Renal Disorder, Diabetes Mellitus, Nephrogenic Anaemia, Hypertension, Nephropathy
Adverse event resulted in: disablity
Suspect drug(s):
Lamivudine
Dosage: 150mg twice per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1997-04-24
End date: 1999-10-31
Lamivudine
Administration route: Oral
Start date: 1999-11-01
End date: 2003-03-31
Lamivudine
Dosage: 150mg twice per day
Administration route: Oral
Start date: 2003-04-01
End date: 2005-11-28
Lamivudine
Administration route: Oral
Start date: 2007-01-11
Zerit
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1998-03-05
End date: 2004-01-26
Crixivan
Dosage: 800mg three times per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1996-07-25
End date: 1998-12-23
Viracept
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1998-12-24
End date: 2000-10-18
Other drugs received by patient: Ziagen; Ziagen; Ziagen; Stocrin; Stocrin; Baktar; Zantac; Urinorm; Urinorm; Novact M; Epzicom
Adverse event in 49 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-05
Patient: 49 year old male
Adverse reactions / side effects: Diabetes Mellitus
Adverse event resulted in: disablity
Suspect drug(s):
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-03-05
End date: 2004-01-26
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1997-11-01
End date: 2005-11-28
Other drugs received by patient: Viracept; Novact M; Baktar; Crixivan; Zantac; Urinorm
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-07-02
Patient: male
Adverse reactions / side effects: Hyperbilirubinaemia, Lipoatrophy, Lipodystrophy Acquired, Hepatic Cirrhosis
Adverse event resulted in: disablity
Suspect drug(s):
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2003-10-17
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-05-16
End date: 2003-10-16
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
End date: 2003-10-16
Zerit
Administration route: Oral
Start date: 1997-10-18
End date: 1999-10-31
Ziagen
Administration route: Oral
Indication: HIV Infection
Start date: 2000-04-03
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-16
Stocrin
Administration route: Oral
Indication: HIV Infection
Start date: 2000-04-03
End date: 2003-10-16
Reyataz
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-16
Other drugs received by patient: Kaletra; Novact M
Adverse event in 24 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-06-22
Patient: 24 year old male
Adverse reactions / side effects: Pulmonary Hypertension
Adverse event resulted in: disablity
Suspect drug(s):
Saquinavir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
End date: 2000-03-18
Saquinavir
Administration route: Oral
Start date: 2000-05-24
End date: 2000-12-24
Crixivan
Administration route: Oral
Indication: HIV Infection
Start date: 2000-03-18
End date: 2000-05-24
Videx
Dosage: dose form: oral formulation (not otherwise specified).
Administration route: Oral
Indication: HIV Infection
Videx
Administration route: Oral
Zerit
Administration route: Oral
Indication: HIV Infection
End date: 1998-11-09
Zerit
Administration route: Oral
Start date: 1998-11-09
End date: 1999-06-19
Zerit
Administration route: Oral
Start date: 2000-12-25
End date: 2001-10-20
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
End date: 2000-12-24
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
Stocrin
Administration route: Oral
Indication: HIV Infection
Start date: 2000-07-24
End date: 2000-07-25
Stocrin
Dosage: the drug was interrupted from 02 oct 2000 to 24 jul 2001
Administration route: Oral
Start date: 2000-09-25
End date: 2000-10-02
Other drugs received by patient: Ziagen; Crosseight M
Adverse event in 24 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-06-11
Patient: 24 year old male
Adverse reactions / side effects: Pulmonary Hypertension, Cardiomegaly
Adverse event resulted in: disablity
Suspect drug(s):
Saquinavir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
End date: 2000-03-18
Saquinavir
Administration route: Oral
Start date: 2000-05-24
End date: 2000-12-24
Crixivan
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2000-03-18
End date: 2000-05-24
Videx
Dosage: dose form: oral formulation (not otherwise specified).
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 1999-11-01
Zerit
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2000-12-25
End date: 2001-10-20
Norvir
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 1999-11-01
End date: 2000-12-24
Kaletra
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2000-12-25
Other drugs received by patient: Stocrin; Ziagen; Crosseight M
Adverse event in 24 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-08
Patient: 24 year old male
Adverse reactions / side effects: Pulmonary Hypertension, Palpitations, Dizziness
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1994-11-19
Efavirenz
Dosage: therapy stopped on 25-jul-2000, restarted on 25-sep-2000.
Administration route: Oral
Indication: HIV Infection
Start date: 2000-07-24
End date: 2000-10-02
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
End date: 2001-10-20
Indinivir Sulfate
Administration route: Oral
Indication: HIV Infection
Start date: 2000-03-08
End date: 2000-05-24
Ziagen
Dosage: therapy stopped on 25-jul-2000, restarted on 20-oct-2001.
Administration route: Oral
Start date: 2000-07-24
End date: 2001-10-27
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
Ritonavir
Dosage: therapy stopped on 24-dec-2000, restarted on 01-apr-2005.
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
End date: 2000-12-24
Lopinavir + Ritonavir
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
End date: 2004-04-24
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-05-15
Other drugs received by patient: Factor Viii
Adverse event in 24 year old male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-06-06
Patient: 24 year old male
Adverse reactions / side effects: Pulmonary Hypertension, Palpitations, Cardiomegaly
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Crixivan
Dosage: 800 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-03-18
End date: 2000-05-24
Efavirenz
Dosage: 600 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-07-24
End date: 2000-07-25
Efavirenz
Dosage: 600 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-09-25
End date: 2000-10-02
Didanosine
Dosage: 300 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
CAP Stavudine
Dosage: 80 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
TAB (Therapy Unspecified)
Dosage: 600 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-07-24
End date: 2000-07-25
CAP Invirase (Saquinavir Mesylate)
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
End date: 2000-03-18
CAP Invirase (Saquinavir Mesylate)
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
End date: 2000-03-18
CAP Invirase (Saquinavir Mesylate)
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 2000-05-24
End date: 2000-12-24
Norvir
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
End date: 1999-10-31
Norvir
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
End date: 2000-12-24
Norvir
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-01
Videx
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1994-12-19
End date: 1997-03-07
Videx
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1997-03-08
End date: 2001-07-21
Videx
Dosage: 400 mg/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2001-07-22
End date: 2004-05-14
Ziagen
Dosage: 600 mg/daily
Administration route: Oral
Start date: 2000-07-24
End date: 2000-07-25
Ziagen
Dosage: 600 mg/daily
Administration route: Oral
Start date: 2001-10-20
End date: 2001-10-27
Kaletra
Dosage: 6 dose/daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
End date: 2004-04-24
Zerit
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1997-08-25
End date: 1998-02-27
Zerit
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1998-02-28
End date: 1998-08-03
Zerit
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1998-08-04
End date: 1998-11-09
Zerit
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 1998-11-10
End date: 1999-06-19
Zerit
Dosage: see image
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
End date: 2001-10-20
Other drugs received by patient: Factor Viii
Adverse event in 23 year old male receiving Zerit (Stavudine)
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):
Ziagen
Dosage: 300mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 1999-03-29
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1995-10-30
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-01-14
Stocrin
Dosage: 600mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 1999-03-29
End date: 2002-03-03
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 1997-08-04
End date: 2002-03-03
Norvir
Dosage: 400mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 1997-11-11
End date: 1998-03-11
Kaletra
Dosage: 6cap per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-04
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1997-02-11
End date: 1998-03-11
Serostim
Indication: Weight Decreased
Start date: 2001-04-23
End date: 2005-06-23
Retrovir
Administration route: Oral
Indication: HIV Infection
Start date: 1993-05-15
End date: 1997-11-11
Other drugs received by patient: Loperamide Hydrochloride; Epivir; Hivid; Prozei; Recombinate; Pegasys; Rebetol
Adverse event in 24 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-06-05
Patient: 24 year old male
Adverse reactions / side effects: Pulmonary Hypertension, Dyspnoea, Palpitations, Asthenia, Pulmonary Artery Dilatation, Cardiomegaly
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2004-05-15
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
End date: 2000-12-24
Norvir
Administration route: Oral
Start date: 2004-04-25
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-07-21
End date: 2004-05-14
Stocrin
Administration route: Oral
Indication: HIV Infection
Start date: 2000-07-24
End date: 2000-07-25
Stocrin
Administration route: Oral
Start date: 2000-09-25
End date: 2000-10-02
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2000-12-25
End date: 2004-04-24
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1994-12-19
End date: 2001-07-21
Zerit
Administration route: Oral
Start date: 1997-08-25
End date: 2001-10-20
Crixivan
Dosage: 800mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2000-03-18
End date: 2000-05-24
Invirase
Dosage: 800mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 1999-06-19
End date: 2000-12-24
Other drugs received by patient: Reyataz; Viread; Anti-Hemophilic Globulin; Ziagen
Adverse event in 49 year old male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from United States on 2007-04-30
Patient: 49 year old male, weighing 87.0 kg (191.4 pounds)
Adverse reactions / side effects: Disorientation, Hepatitis, Amnesia, Somnolence, Neuropathy Peripheral, Fatigue, Visual Disturbance, Balance Disorder, Chest Pain, Pancreatitis, Myocardial Infarction, Hypertension
Adverse event resulted in: disablity
Suspect drug(s):
Zerit
Dosage: therapy start date: 1997 or 1998
Indication: HIV Infection
End date: 2003-08-01
Videx
Dosage: therapy start date: 1997 or 1998
Indication: HIV Infection
Viracept
Dosage: therapy start date: 1997 or 1998
Indication: HIV Infection
Epivir
Indication: HIV Infection
Viread
Indication: HIV Infection
Other drugs received by patient: Centrum
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-03-30
Patient: male
Adverse reactions / side effects: Drug Eruption, Glucose Tolerance Impaired
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-09-26
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-10-18
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-10-18
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-27
End date: 2004-10-18
Predonine
Indication: Drug Eruption
Start date: 2004-09-23
End date: 2004-09-26
Other drugs received by patient: Clarithromycin; Baktar
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-03-22
Patient: male
Adverse reactions / side effects: Nephritis Interstitial, Nephrotic Syndrome
Adverse event resulted in: disablity
Suspect drug(s):
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-28
End date: 2004-01-13
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-28
End date: 2004-09-24
Kaletra
Administration route: Oral
Start date: 2001-10-22
End date: 2002-03-11
Ziagen
Administration route: Oral
Indication: HIV Infection
Start date: 2001-10-22
End date: 2002-03-11
Ziagen
Administration route: Oral
Start date: 2002-03-28
End date: 2004-11-03
Ziagen
Administration route: Oral
Start date: 2005-03-18
Diflucan
Indication: Oral Candidiasis
Start date: 2002-07-24
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 2001-08-06
End date: 2001-10-21
Viracept
Administration route: Oral
Start date: 2004-09-27
End date: 2004-11-03
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2001-08-06
End date: 2001-10-21
Epivir
Administration route: Oral
Start date: 2004-09-27
End date: 2004-11-03
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2001-08-06
End date: 2002-03-11
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 2004-05-10
End date: 2004-09-14
PEG-Intron
Dosage: 100 micro g/kg
Indication: Hepatitis C
Start date: 2004-12-13
End date: 2005-01-17
Ribavirin
Administration route: Oral
Indication: Hepatitis C
Start date: 2004-12-13
End date: 2005-01-14
Ribavirin
Administration route: Oral
Start date: 2005-01-15
End date: 2005-01-17
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-02-16
Stocrin
Administration route: Oral
Indication: HIV Infection
Start date: 2005-02-16
End date: 2005-03-28
Lexiva
Administration route: Oral
Indication: HIV Infection
Start date: 2005-02-16
Epzicom
Indication: HIV Infection
Start date: 2005-02-16
End date: 2005-03-17
Other drugs received by patient: Loxonin
Adverse event in 23 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-20
Patient: 23 year old male, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Cachexia, Hyperlactacidaemia, Osteonecrosis, Platelet Count Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Zerit
Dosage: 22-oct-2002 decreased to 60 mg daily from 80 mg daily.
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1998-01-14
End date: 2004-05-27
Videx
Dosage: 150 mg bid 10/30/95, 100 mg bid 12/25/95, 150 mg bid 3/11/98, 200 mg bid 7/12/99-4/20/01
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1995-10-30
Videx
Dosage: 150 mg bid 10/30/95, 100 mg bid 12/25/95, 150 mg bid 3/11/98, 200 mg bid 7/12/99-4/20/01
Administration route: Oral
Indication: HIV Infection
Start date: 1995-10-30
Videx EC
Start date: 2001-04-21
Stocrin Caps
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-03-29
End date: 2002-03-03
Reyataz
Administration route: Oral
Start date: 2004-10-08
Viracept
Dosage: initiated at 500 mg three times daily to 11-nov-1997, restarted 17-aug-1999
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1997-08-04
End date: 2002-03-03
Ziagen
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-03-29
Kaletra
Dosage: dosage form=dose
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2002-03-04
Somatropin
Indication: Weight Decreased
Start date: 2001-04-23
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-04
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1997-11-11
End date: 1998-03-11
Other drugs received by patient: Lopemin; Recombinate; Amprenavir; Retrovir; Epivir; Hivid; Prozei; Loxonin; Celestone
Adverse event in 23 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-16
Patient: 23 year old male, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Cachexia, Hyperlactacidaemia, Osteonecrosis, Platelet Count Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Zerit
Dosage: 22-oct-2002 decreased to 60 mg daily from 80 mg daily.
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1998-01-14
End date: 2004-05-27
Videx
Dosage: 150 mg bid 10/30/95, 100 mg bid 12/25/95, 150 mg bid 3/11/98, 200 mg bid 7/12/99-4/20/01
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1995-10-30
Videx
Dosage: 150 mg bid 10/30/95, 100 mg bid 12/25/95, 150 mg bid 3/11/98, 200 mg bid 7/12/99-4/20/01
Administration route: Oral
Indication: HIV Infection
Start date: 1995-10-30
Videx EC
Start date: 2001-04-21
Stocrin Caps
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-03-29
End date: 2002-03-03
Reyataz
Administration route: Oral
Start date: 2004-10-08
Viracept
Dosage: initiated at 500 mg three times daily to 11-nov-1997, restarted 17-aug-1999
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1997-08-04
End date: 2002-03-03
Ziagen
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-03-29
Kaletra
Dosage: dosage form=dose
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2002-03-04
Somatropin
Indication: Weight Decreased
Start date: 2001-04-23
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-04
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1997-11-11
End date: 1998-03-11
Other drugs received by patient: Lopemin; Recombinate; Amprenavir; Retrovir; Epivir; Hivid; Prozei; Loxonin; Celestone
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-03-12
Patient: male
Adverse reactions / side effects: Hyperbilirubinaemia, Lipoatrophy, Lipodystrophy Acquired, Hepatic Cirrhosis
Adverse event resulted in: disablity
Suspect drug(s):
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2003-10-17
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-05-16
End date: 2003-10-16
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1999-11-01
End date: 2003-10-16
Zerit
Administration route: Oral
Start date: 1997-10-18
End date: 1999-10-31
Ziagen
Administration route: Oral
Indication: HIV Infection
Start date: 2000-04-03
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-16
Stocrin
Administration route: Oral
Indication: HIV Infection
Start date: 2000-04-03
End date: 2003-10-16
Reyataz
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-16
Other drugs received by patient: Kaletra; Novact M
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-02-16
Patient: male
Adverse reactions / side effects: Drug Eruption, Glucose Tolerance Impaired
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-09-26
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-10-18
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-10-18
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-27
End date: 2004-10-18
Predonine
Indication: Drug Eruption
Start date: 2004-09-23
End date: 2004-09-26
Other drugs received by patient: Clarithromycin; Baktar
Adverse event in male receiving Zerit (Stavudine)
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
Zerit
Start date: 2005-02-23
End date: 2005-12-29
Epivir
Start date: 2005-02-23
Viramune
Start date: 2005-12-29
Retrovir
Start date: 2005-12-29
Other drugs received by patient: Bactrim; Vitamin B Complex CAP
Adverse event in male receiving Zerit (Stavudine)
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
Zerit
Start date: 2005-02-23
End date: 2005-12-29
Epivir
Start date: 2005-02-23
Viramune
Start date: 2005-12-29
Retrovir
Start date: 2005-12-29
Other drugs received by patient: Bactrim; Vitamin B Complex CAP
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-01-22
Patient: male
Adverse reactions / side effects: Drug Eruption, Glucose Tolerance Impaired
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-09-26
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-10-18
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-13
End date: 2004-10-18
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2004-09-27
End date: 2004-10-18
Predonine
Indication: Drug Eruption
Start date: 2004-09-23
End date: 2004-09-26
Other drugs received by patient: Clarithromycin; Bactrim
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