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Epivir (Lamivudine) - Adverse Event Reports - Hospitalization - Vomiting

 



Index of reports > Cases resulting in hospitalization (92) > Cases with Vomiting (7)

Below is the selection of adverse event reports related to Epivir (Lamivudine) that includes cases resulting in hospitalization where reactions include vomiting.

Adverse event in 39 year old male receiving Epivir (Lamivudine)

Reported by a physician from Japan on 2007-06-26

Patient: 39 year old male

Adverse reactions / side effects: Vomiting, Neurogenic Bladder, Nasopharyngitis, Nausea, Costovertebral Angle Tenderness, Urinary Tract Infection, Pyrexia, Epilepsy, Eating Disorder, Convulsion, Ascites, Blood Potassium Decreased, Tenderness, Pyuria, Pyelonephritis

Adverse event resulted in: hospitalization

Suspect drug(s):
Epivir
    Dosage: 150mg twice per day
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 1996-12-18
    End date: 1997-03-13

Epivir
    Dosage: 150mg twice per day
    Administration route: Oral
    Start date: 1998-07-10
    End date: 1999-10-31

Epivir
    Administration route: Oral
    Start date: 1999-11-01
    End date: 2003-03-31

Epivir
    Dosage: 150mg twice per day
    Administration route: Oral
    Start date: 2003-04-01
    End date: 2003-04-26

Epivir
    Dosage: 150mg twice per day
    Administration route: Oral
    Start date: 2004-07-28

Ziagen
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2003-04-27
    End date: 2003-12-24

Ziagen
    Dosage: 300mg twice per day
    Administration route: Oral
    Start date: 2004-05-28
    End date: 2004-06-29

Ziagen
    Dosage: 300mg twice per day
    Administration route: Oral
    Start date: 2004-12-17

Kaletra
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2004-06-30
    End date: 2006-11-23

Other drugs received by patient: Kaletra



Adverse event in 37 year old male receiving Epivir (Lamivudine)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-04-02

Patient: 37 year old male

Adverse reactions / side effects: Vomiting, Overdose, Depressed Level of Consciousness, Suicide Attempt, Depression, Lipodystrophy Acquired

Adverse event resulted in: hospitalization

Suspect drug(s):
Stocrin Caps
    Dosage: normal dosage 600 mg daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01
    End date: 2005-11-15

Stocrin Caps
    Administration route: Oral
    Start date: 2005-11-16
    End date: 2005-11-16

Zerit
    Dosage: stopped in apr-2005, restarted on an unspecified date
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01
    End date: 2005-11-16

Viread
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-04-01
    End date: 2005-11-15

Viread
    Administration route: Oral
    Start date: 2005-11-16
    End date: 2005-11-16

Epivir
    Dosage: 300 mg daily normal daily dosage stopped in may-2001, restarted on an unspecified date
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01
    End date: 2005-11-15

Epivir
    Administration route: Oral
    Start date: 2005-11-16
    End date: 2005-11-16

Other drugs received by patient: Rhythmy; Valtrex



Adverse event in 36 year old male receiving Epivir (Lamivudine)

Reported by a physician from Japan on 2007-04-02

Patient: 36 year old male

Adverse reactions / side effects: Vomiting, Intentional Overdose, Depressed Level of Consciousness, Suicide Attempt, Depression, Lipodystrophy Acquired

Adverse event resulted in: hospitalization

Suspect drug(s):
Epivir
    Dosage: 300mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01

Stocrin
    Dosage: 600mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01

Viread
    Dosage: 300mg per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-04-01

Zerit
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01
    End date: 2005-03-01



Adverse event in 32 year old male receiving Epivir (Lamivudine)

Reported by a individual with unspecified qualification from France on 2007-03-21

Patient: 32 year old male

Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Metabolic Acidosis, Blood Creatine Phosphokinase Increased, Vomiting, Alanine Aminotransferase Increased, Respiratory Alkalosis, Lactic Acidosis, Myalgia, Heart Rate Increased, Aspartate Aminotransferase Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Epivir
    Indication: HIV Infection

Lopinavir (Formulation Unknown) (Lopinavir)
    Indication: HIV Infection

Stavudine
    Indication: HIV Infection

Other drugs received by patient: CO-Trimoxazole



Adverse event in 46 year old male receiving Epivir (Lamivudine)

Reported by a physician from Japan on 2007-03-05

Patient: 46 year old male

Adverse reactions / side effects: Back Pain, Abdominal Pain, Vomiting, Lymphadenopathy, Nausea, Musculoskeletal Pain, Abasia, Muscular Weakness, Hypoaesthesia, Renal Impairment, Malaise, Fatigue, Diarrhoea, Anorexia, Lipoatrophy, Decreased Appetite

Adverse event resulted in: hospitalization

Suspect drug(s):
Zerit
    Administration route: Oral
    Indication: HIV Infection CDC Group IV Subgroup C1
    Start date: 1997-08-04
    End date: 2006-05-10

Epivir
    Dosage: restarted on 16-feb-2004 to 10-may-2006.
    Administration route: Oral
    Indication: HIV Infection CDC Group IV Subgroup C1
    Start date: 1997-03-31
    End date: 2000-02-17

Crixivan
    Administration route: Oral
    Indication: HIV Infection CDC Group IV Subgroup C1
    Start date: 1997-08-04
    End date: 1997-09-18

Crixivan
    Administration route: Oral
    Start date: 1997-09-21
    End date: 1999-01-28

Other drugs received by patient: Stadol; Prochlorperazine; Voltaren; Buprenorphine HCL; Magnesium Sulfate; Vitamins; Zovirax; Diflucan; Baktar; Videx; Fungizone; Retrovir; Hivid; Solita-T NO. 3; Buscopan; Folic Acid; Resplen; Clarithromycin; Viracept; Invirase; Norvir; Ziagen; Neurotropin; Hyaluronic Acid; Bendrofluazide; CO-Dydramol; Stocrin; Xylocaine; Amicaliq; Viramune



Adverse event in male receiving Epivir (Lamivudine)

Reported by a consumer/non-health professional from France on 2007-01-19

Patient: male

Adverse reactions / side effects: Paresis Cranial Nerve, Vomiting, Visual Acuity Reduced, Neoplasm, Somnolence, Strabismus, Papilloedema, Diplopia, Pinealoblastoma, Fatigue, Drug Exposure During Pregnancy, Hydrocephalus

Adverse event resulted in: hospitalization

Suspect drug(s):
Retrovir
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 1998-04-28
    End date: 1998-06-05

Epivir
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 1998-04-28
    End date: 1998-06-05

Other drugs received by patient: Retrovir; Epivir; Retrovir; Clamoxyl



Adverse event in male receiving Epivir (Lamivudine)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-01-17

Patient: male

Adverse reactions / side effects: Vomiting, Dialysis, Intentional Overdose, Depressed Level of Consciousness, Depression, Lipodystrophy Acquired

Adverse event resulted in: hospitalization

Suspect drug(s):
Viread
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-04-01

Stocrin
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01

Epivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01

Stavudine
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-04-01
    End date: 2005-03-01

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