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Index of reports
> Cases resulting in a serious event (101)
Below is the selection of adverse event reports related to Zerit (Stavudine) that includes cases resulting in a serious event.
Reports 1 - 25 of 101 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, Renal Tubular Disorder, Vitamin D Deficiency, Blood Parathyroid Hormone Increased
Suspect drug(s):
Sustiva
Start date: 2002-03-01
Zerit
Videx
Kaletra
Start date: 2002-03-01
Viread
Start date: 2002-03-01
Plaquenil
Other drugs received by patient: Virlix; Tenormin; Corvasal; Aspegic 325; Omeprazole
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 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 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 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 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 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 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 male receiving Zerit (Stavudine)
Reported by a consumer/non-health professional from United Kingdom on 2007-07-27
Patient: male
Adverse reactions / side effects: Hepatic Cirrhosis
Suspect drug(s):
Sustiva
Videx
Zerit
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 28 year old female receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from Botswana on 2007-07-06
Patient: 28 year old female
Adverse reactions / side effects: Abortion Induced
Suspect drug(s):
Viramune
Administration route: Oral
Indication: HIV Infection
Start date: 2004-03-08
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2004-02-23
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-18
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-18
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 41 year old male receiving Zerit (Stavudine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-05
Patient: 41 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Hyperlipidaemia, Hepatic Function Abnormal, Gamma-Glutamyltransferase Increased, Pancytopenia
Suspect drug(s):
Efavirenz
Administration route: Oral
Indication: HIV Infection
Start date: 2001-12-08
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1992-09-04
End date: 2001-04-16
Videx EC
Administration route: Oral
Indication: HIV Infection
Start date: 2001-04-17
End date: 2001-12-07
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 2001-12-08
End date: 2004-07-02
Epiver
Dosage: 150 mg twice daily 03-jul-2004 to 02-jul-2000; 300 mg daily 03-jul-2004-continue
Administration route: Oral
Indication: HIV Infection
Start date: 2001-12-08
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-01-23
End date: 2001-12-07
PEG-Intron
Indication: Hepatitis C
Start date: 2005-01-19
Rebetol
Dosage: 200 mg in the morning and 400 mg in the afternoon.
Administration route: Oral
Indication: Hepatitis C
Start date: 2005-01-19
End date: 2006-11-16
Other drugs received by patient: Kogenate
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 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 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 male receiving Zerit (Stavudine)
Reported by a physician from United Kingdom on 2007-06-25
Patient: male
Adverse reactions / side effects: Hepatic Fibrosis
Suspect drug(s):
Videx
Administration route: Oral
Zerit
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 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
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