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Index of reports
> Cases resulting in hospitalization (46)
Below is the selection of adverse event reports related to Zerit (Stavudine) that includes cases resulting in hospitalization.
Reports 1 - 25 of 46 Next >>
Adverse event in 71 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-22
Patient: 71 year old male, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Neuropathy, Vitamin D Deficiency
Adverse event resulted in: hospitalization
Suspect drug(s):
Zerit
Videx
Adverse event in male receiving Zerit (Stavudine)
Reported by a individual with unspecified qualification from Japan on 2007-10-08
Patient: male
Adverse reactions / side effects: Nausea, Diabetes Mellitus, Diarrhoea, Hypertriglyceridaemia, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Viramune
Administration route: Oral
Indication: HIV Infection CDC Group IV Subgroup E
Start date: 1998-11-24
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-11-24
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1998-11-24
Other drugs received by patient: Diovan
Adverse event in 65 year old female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-26
Patient: 65 year old female
Adverse reactions / side effects: Dyspnoea, Palpitations, Hypothyroidism, Cardiomegaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Stocrin Caps
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
End date: 2006-04-17
Epivir
Dosage: interrupted on 17-apr-2006 restarted on 18-apr-2006 at 300mg daily
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
End date: 2006-04-17
Other drugs received by patient: Euglucon; Predonine; Rimatil; Evoxac; Azulfidine; Lansoprazole; Pentamidine Isethionate; Abacavir Sulfate
Adverse event in 65 year old female receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-07-24
Patient: 65 year old female
Adverse reactions / side effects: Dyspnoea, Palpitations, Hypothyroidism, Cardiomegaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Zerit
Dosage: 60mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
End date: 2006-04-17
Stocrin
Dosage: 600mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Ziagen
Dosage: 300mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2006-04-18
Other drugs received by patient: Euglucon; Predonine; Rimatil; Evoxac; Azulfidine; Lansoprazole; Pentamidine Isethionate; Simavastatin
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 health professional (non-physician/pharmacist) from France on 2007-07-20
Patient: 49 year old male, weighing 52.0 kg (114.4 pounds)
Adverse reactions / side effects: Weight Decreased, Speech Disorder, Pancreatitis Acute, Vomiting, Nausea, Diabetes Mellitus, Lactic Acidosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Kaletra
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Kivexa
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Viracept
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 17 year old male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from United Kingdom on 2007-07-17
Patient: 17 year old male
Adverse reactions / side effects: Hyperlipidaemia, Pancreatitis Haemorrhagic, Type 1 Diabetes Mellitus
Adverse event resulted in: hospitalization
Suspect drug(s):
Efavirenz
Dosage: stopped 20-sep-2002 restarted 13-mar-2003.
Administration route: Oral
Indication: HIV Infection
Start date: 2000-11-14
Videx
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-10-01
End date: 2000-05-02
Zerit
Dosage: stopped feb 17-1999, restarted 12-sep-1999
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1997-09-11
End date: 2002-09-20
Zerit
Dosage: stopped feb 17-1999, restarted 12-sep-1999
Administration route: Oral
Indication: HIV Infection
Start date: 1997-09-11
End date: 2002-09-20
Invirase
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-09-02
End date: 2000-11-13
Norvir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1999-09-02
End date: 2000-11-13
Lamivudine
Dosage: 01nov98 to unk;unk to 31oct1999 started 26jun2000 to 28jan2000, stopped 20sep2002; 27feb2003on
Administration route: Oral
Indication: HIV Infection
Start date: 1996-11-21
End date: 1999-09-30
Other drugs received by patient: Loxonin; Selbex; Diflucan; Baktar; Factor IX Complex; Zidovudine; Camostat Mesylate
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 50 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-06-26
Patient: 50 year old male
Adverse reactions / side effects: Drug Toxicity, Hepatic Encephalopathy, Hyperammonaemia, Lumbar Vertebral Fracture, Cerebellar Haemorrhage, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2005-02-01
Zerit
Dosage: started on 06-sep-2001 at 80 mg then dosage decreased to 60 mg per day on 05-jul-2004.
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2005-02-01
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 2001-09-06
End date: 2004-12-06
Other drugs received by patient: Recombinate; Monilac; Epivir; Stocrin; Viread
Adverse event in 35 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-26
Patient: 35 year old male
Adverse reactions / side effects: Hyperlipidaemia, Pseudomembranous Colitis, Lymphoma, Herpes Zoster
Adverse event resulted in: hospitalization
Suspect drug(s):
Efavirenz
Dosage: interrupted 11/8/00, restarted 11/16/00.
Administration route: Oral
Indication: HIV Infection
Start date: 1999-10-04
End date: 2000-11-08
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1997-05-01
End date: 1999-10-03
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-10-04
End date: 2000-11-08
Norvir
Dosage: 400 mg/bid 20jan99 to 3oct99, 200 mg/bid 9oct99 to 8nov00 then 400 mg/bid 16nov00 to cont.
Administration route: Oral
Indication: HIV Infection
Start date: 1990-10-09
End date: 2000-11-08
Ziagen
Dosage: therapy interrupted 11/8/00, restarted 11/16/00
Administration route: Oral
Indication: HIV Infection
Start date: 1999-10-04
End date: 2001-11-08
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 1990-01-18
End date: 2001-10-03
Prozei
Dosage: therapy interrupted 11/8/00, restarted 11/16/00
Administration route: Oral
Indication: HIV Infection
Start date: 1999-10-04
End date: 2001-11-08
Other drugs received by patient: Amikacin Sulfate; Ciprofloxacin; Allopurinol; Azithromycin; Ethambutol Hydrochloride; Metronidazole; Sulfamethoxazole and Trimethoprim; Clarithromycin; Polaramine; Crixivan
Adverse event in 39 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-21
Patient: 39 year old male
Adverse reactions / side effects: Hepatic Cirrhosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Efavirenz
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-25
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-12-21
End date: 2005-04-24
Reyataz
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-30
End date: 2005-04-24
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1997-12-29
End date: 2005-04-24
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-07-28
End date: 2005-04-24
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-25
End date: 2005-05-23
Other drugs received by patient: NEO-Minophagen C; Factor Viii; Kogenate
Adverse event in 37 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-06-18
Patient: 37 year old male
Adverse reactions / side effects: Neutropenia, Rash, Cerebral Toxoplasmosis, Herpes Zoster
Adverse event resulted in: hospitalization
Suspect drug(s):
Denosine IV
Dosage: form reported as i.v. infusion.
Indication: Cytomegalovirus Enterocolitis
Start date: 2005-03-11
End date: 2005-03-29
Denosine IV
Dosage: form reported as i.v. infusion.
Start date: 2005-04-19
End date: 2005-04-24
Valixa
Administration route: Oral
Indication: Cytomegalovirus Enterocolitis
Start date: 2005-04-25
End date: 2005-05-17
Valixa
Dosage: maintenance threrapy.
Administration route: Oral
Start date: 2005-05-18
End date: 2005-07-21
Baktar
Administration route: Oral
Start date: 2005-03-12
End date: 2005-04-06
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-29
End date: 2005-05-06
Epivir
Administration route: Oral
Start date: 2005-06-10
Zerit
Dosage: reported as zerit (sanilvudine).
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-29
End date: 2005-05-06
Zerit
Dosage: reported as zerit (sanilvudine).
Administration route: Oral
Start date: 2005-06-10
End date: 2006-03-23
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-29
End date: 2005-05-06
Kaletra
Administration route: Oral
Start date: 2005-06-10
Lectisol
Dosage: reported as lectisol (diaphenylsulfone).
Administration route: Oral
Start date: 2005-06-23
End date: 2005-06-28
Other drugs received by patient: Pentamidine Isethionate; Cortril; Diflucan; Fungizone; Zithromac; Pyrimethamine TAB; Clindamycin Hydrochloride; Calcium Folinate; Lenograstim; Prednisolone
Adverse event in female receiving Zerit (Stavudine)
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 female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-08
Patient: female
Adverse reactions / side effects: Cerebral Disorder, Rhinitis, Neutropenia, Foetal Growth Retardation, Pregnancy, Anaemia Macrocytic
Adverse event resulted in: hospitalization
Suspect drug(s):
Videx
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Zerit
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Crixivan
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Fortovase
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Retrovir
Dosage: exposure began in week ten of gestation.
Indication: HIV Test Positive
Start date: 1997-07-01
End date: 1998-01-19
Epivir
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Zidovudine
Indication: HIV Infection
Start date: 1997-01-01
End date: 1997-01-01
Zidovudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Lamivudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Adverse event in 39 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-07
Patient: 39 year old male
Adverse reactions / side effects: Hepatic Cirrhosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Efavirenz
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-25
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-12-21
End date: 2005-04-24
Reyataz
Administration route: Oral
Indication: HIV Infection
Start date: 2004-01-30
End date: 2005-04-24
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 1997-12-29
End date: 2005-04-24
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-07-28
End date: 2005-04-24
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-25
End date: 2005-05-23
Other drugs received by patient: NEO-Minophagen C; Factor Viii; Kogenate
Adverse event in 33 year old male receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-06-05
Patient: 33 year old male
Adverse reactions / side effects: Immune Reconstitution Syndrome, Rhinitis Allergic, Iron Deficiency Anaemia, Cytomegalovirus Viraemia, Upper Respiratory Tract Inflammation
Adverse event resulted in: hospitalization
Suspect drug(s):
Valixa
Administration route: Oral
Start date: 2005-04-01
End date: 2005-06-13
Valixa
Dosage: indication: cytomegalovirus viraemia. drug maintained as of 31 march 2006.
Administration route: Oral
Start date: 2005-09-21
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-01
End date: 2005-05-18
Epivir
Administration route: Oral
Start date: 2005-08-03
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-01
End date: 2005-05-18
Zerit
Administration route: Oral
Start date: 2005-08-03
Other drugs received by patient: Stocrin; Diflucan; Truvada; Ketotifen
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 female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-30
Patient: female
Adverse reactions / side effects: Cerebral Disorder, Rhinitis, Neutropenia, Foetal Growth Retardation, Pregnancy, Anaemia Macrocytic
Adverse event resulted in: hospitalization
Suspect drug(s):
Videx
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Zerit
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Crixivan
Dosage: exposure began in week two of gestation.
Indication: HIV Test Positive
Start date: 1997-05-29
End date: 1997-07-01
Fortovase
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Retrovir
Dosage: exposure began in week ten of gestation.
Indication: HIV Test Positive
Start date: 1997-07-01
End date: 1998-01-19
Epivir
Dosage: exposure began in week 29 of gestation.
Indication: HIV Test Positive
Start date: 1997-11-12
End date: 1998-01-19
Zidovudine
Indication: HIV Infection
Start date: 1997-01-01
End date: 1997-01-01
Zidovudine
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 1998-01-01
End date: 1998-03-01
Lamivudine
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 Zerit (Stavudine)
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 female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-25
Patient: female, weighing 3.0 kg (6.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Hyperlactacidaemia, Flatulence, Mucous Stools, Platelet Count Increased, Hypercholesterolaemia, Hepatomegaly, Malaise, Obesity, Abdominal Distension, Hypertriglyceridaemia, Oxygen Saturation Decreased, Anaemia, Ventricular Tachycardia, Hypotonia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Videx
Dosage: received from conception to day 3 of gestation, then from week 27 of gestation to delivery
Zerit
Sustiva
Invirase
Dosage: initiated at 27 weeks of gestation
Indication: HIV Infection
Norvir
Dosage: received from week 27 of gestation to delivery
Fortovase
Dosage: received from week 27 of gestation to delivery
Viramune
Dosage: received one single oral dose, from 27 weeks gestation transplacental exposure
Administration route: Oral
Indication: HIV Infection
Viramune
Dosage: received infusion during delivery,
Retrovir
Dosage: received 6 weeks of antiretroviral therapy after delivery, 200mg/20ml
Retrovir
Dosage: received from conception to day 3 of gestation and from week 27 of gestation to and at delivery.
Other drugs received by patient: Cordarone; Speciafoldine; Ferrostrane; Uvesterol D; Fluorex; AZT
Adverse event in 38 year old male receiving Zerit (Stavudine)
Reported by a physician from United States on 2007-05-18
Patient: 38 year old male
Adverse reactions / side effects: Abdominal Pain, Immune Reconstitution Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Prezista
Administration route: Oral
Indication: HIV Infection
Mk0518
Administration route: Oral
Indication: HIV Infection
Ritonavir
Indication: HIV Infection
Ziagen
Indication: HIV Infection
Truvada
Indication: HIV Infection
Zerit
Indication: HIV Infection
Other drugs received by patient: Valcyte; Bactrim DS; Zyvox
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 65 year old female receiving Zerit (Stavudine)
Reported by a physician from Japan on 2007-04-23
Patient: 65 year old female
Adverse reactions / side effects: Dyspnoea, Palpitations, Hypothyroidism, Cardiomegaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Zerit
Dosage: 60mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
End date: 2006-04-17
Stocrin
Dosage: 600mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Ziagen
Dosage: 300mg twice per day
Administration route: Oral
Indication: HIV Infection
Start date: 2006-04-18
Other drugs received by patient: Euglucon; Predonine; Rimatil; Evoxac; Azulfidine; Takepron; Pentamidine Isethionate; Lipovas
Adverse event in 65 year old female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-19
Patient: 65 year old female
Adverse reactions / side effects: Hypothyroidism
Adverse event resulted in: hospitalization
Suspect drug(s):
Stocrin Caps
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
End date: 2006-04-17
Epivir
Dosage: interrupted on 17-apr-2006 restarted on 18-apr-2006
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-30
Abacavir Sulfate
Administration route: Oral
Indication: HIV Infection
Start date: 2006-04-18
Other drugs received by patient: Euglucon; Predonine; Rimatil; Evoxac; Azulfidine; Takepron; Pentamidine Isethionate
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