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Index of reports
> Cases resulting in life threatening events (17)
Below is the selection of adverse event reports related to Zerit (Stavudine) that includes cases resulting in life threatening events.
Adverse event in 37 year old female receiving Zerit (Stavudine)
Reported by a physician from Italy on 2007-10-12
Patient: 37 year old female
Adverse reactions / side effects: Lactic Acidosis
Adverse event resulted in: life threatening event
Suspect drug(s):
Zerit
Administration route: Oral
Start date: 2006-07-04
End date: 2007-05-05
Epivir
Administration route: Oral
Start date: 2006-07-04
End date: 2007-05-05
Adverse event in 49 year old male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from France on 2007-07-24
Patient: 49 year old male
Adverse reactions / side effects: Weight Decreased, Pancreatitis Acute, Diabetes Mellitus, Polyuria, Lactic Acidosis, Pyrexia, Ketoacidosis, Constipation, Speech Disorder, Hypovolaemia, Polydipsia, Vomiting, Nausea, Blood Lactic Acid Increased, Ascites, Haemolysis, Cachexia, Haemoglobin Decreased, Renal Failure, Anorexia, Lipase Increased, Haptoglobin Increased, Asthenia, Sinus Tachycardia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Kivexa
Dosage: 4tab per day
Administration route: Oral
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Kaletra
Dosage: 1tab per day
Administration route: Oral
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1997-10-01
End date: 2006-12-09
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Other drugs received by patient: Bactrim; Lipanthyl; Rivotril; Laroxyl
Adverse event in 49 year old male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from United States on 2007-07-06
Patient: 49 year old male
Adverse reactions / side effects: Hepatic Encephalopathy, Spinal Compression Fracture, Hepatic Failure, Cerebellar Haemorrhage, Hypertension
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zerit
Dosage: 80mg daily (06-sep-2001-04-jul-2004), dose decreased 60mg daily (05-jul-2004-01-feb-2005)
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2005-02-01
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2004-07-04
Stocrin Caps
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-11
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2004-12-06
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-07
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-07
Other drugs received by patient: Monilac; Recombinate; Octocog Alpha; Tenormin; Losartan Potassium; Adalat; Diovan; Nifedipine; Octocog Alpha; Valsartan; Lactulose
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 37 year old female receiving Zerit (Stavudine)
Reported by a physician from Italy on 2007-06-06
Patient: 37 year old female
Adverse reactions / side effects: Abdominal Pain, Vomiting, Nausea, Acidosis
Adverse event resulted in: life threatening event
Suspect drug(s):
Zerit
Administration route: Oral
Start date: 2006-07-04
End date: 2007-05-05
Epivir
Administration route: Oral
Start date: 2006-07-04
End date: 2007-05-05
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 female receiving Zerit (Stavudine)
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):
Zerit
Dosage: exposure during gestation.
Videx
Dosage: exposure during gestation.
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
Other drugs received by patient: Bactrim; Triflucan; Loxen; Celestene; Salbutamol
Adverse event in 40 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-05-10
Patient: 40 year old male
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event
Suspect drug(s):
Zerit
Dosage: therapy dates: 1996 to 2004, then 12-apr-2007 to 17-apr-2007
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-01
End date: 2007-04-17
Epivir
Dosage: therapy dates: 1996 to 2004, jun-2006 to unknown, 12-apr-2007 to 17-apr-2007
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-01
End date: 2007-04-17
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 2007-04-12
End date: 2007-04-17
Other drugs received by patient: Stocrin; Valtrex; Ziagen
Adverse event in 49 year old male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from United States on 2007-05-02
Patient: 49 year old male
Adverse reactions / side effects: Hepatic Encephalopathy, Spinal Compression Fracture, Hepatic Failure, Cerebellar Haemorrhage, Fall, Hypertension
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zerit
Dosage: 80mg daily (06-sep-2001-04-jul-2004), dose decreased 60mg daily (05-jul-2004-01-feb-2005)
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2005-02-01
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2005-02-01
Stocrin Caps
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-11
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2004-12-06
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-07
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-07
Other drugs received by patient: Monilac; Recombinate; Octocog Alpha; Tenormin; Losartan Potassium; Adalat; Diovan; Nifedipine; Octocog Alpha; Valsartan; Lactulose
Adverse event in 37 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-04-26
Patient: 37 year old male
Adverse reactions / side effects: Dysgeusia, Liver Function Test Abnormal, General Physical Health Deterioration, Neutropenia, Infection
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2006-04-06
End date: 2006-04-22
Epzicom
Administration route: Oral
Indication: HIV Infection
Start date: 2006-05-11
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2006-04-06
End date: 2006-04-22
Zerit
Dosage: 30mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2006-04-06
End date: 2006-04-22
Baktar
Administration route: Oral
Indication: Pneumocystis Jiroveci Pneumonia
Start date: 2006-03-23
End date: 2006-04-27
Diflucan
Dosage: 100mg per day
Administration route: Oral
Indication: Oral Candidiasis
Start date: 2006-04-13
End date: 2006-05-10
Other drugs received by patient: Stocrin; Itraconazole; Gaster; Predonine; Myslee; Fungizone; Benambax
Adverse event in 33 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-04-03
Patient: 33 year old male
Adverse reactions / side effects: Drug Eruption, Anaemia, Glucose Tolerance Impaired
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-09-13
Combivir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-10-19
End date: 2005-01-11
Zerit
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-09-13
End date: 2004-10-18
Viramune
Dosage: 400mg per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-09-13
End date: 2004-09-26
Kaletra
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-09-27
End date: 2004-10-18
Other drugs received by patient: Stocrin; Viread; Clarithromycin; Baktar; Unknown Drug; Ciprofloxacin; Ebutol
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 2007-02-16
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 Japan on 2007-01-23
Patient: male, weighing 56.0 kg (123.2 pounds)
Adverse reactions / side effects: Dysarthria, Soliloquy, Leukoencephalomyelitis, Encephalopathy, Depressed Level of Consciousness, Disorientation, Cerebral Haemorrhage
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Ziagen
Dosage: 300mg twice per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Zerit
Dosage: 30mg twice per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Other drugs received by patient: Selbex; Landsen; Unknown Drug; Adona (AC-17); Carnaculin; Juvela Nicotinate; Novoseven; Tienam; Meropen; SOL-Melcort; Predonine; Diflucan
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
Adverse event in male receiving Zerit (Stavudine)
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):
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
Retrovir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-01-11
End date: 1999-02-18
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-01-11
End date: 2005-10-11
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