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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Epivir (Lamivudine). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (204)
Cases resulting in a serious event (203)
Cases resulting in death (20)
Cases resulting in life threatening events (27)
Cases resulting in hospitalization (92)
Cases resulting in disability (19)
Cases resulting in other serious reactions (80)
Below is a sample of reports where side effects / adverse reactions may be related to Epivir (Lamivudine). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in female receiving Epivir (Lamivudine)
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: female, weighing 9.2 kg (20.2 pounds)
Adverse reactions / side effects: Breech Delivery, Premature Baby, Congenital Anomaly, Patent Ductus Arteriosus, Joint Dislocation
Adverse event resulted in: hospitalization
Suspect drug(s):
Saquinavir
Indication: HIV Infection
Nelfinavir
Indication: HIV Infection
Start date: 2003-03-12
Nelfinavir
Abacavir Sulfate
Indication: HIV Infection
3TC
Indication: HIV Infection
Nevirapine
Indication: HIV Infection
Start date: 2003-03-12
AZT
Indication: HIV Infection
Epivir
Indication: HIV Infection
Zidovudine
Indication: HIV Infection
Start date: 2003-03-12
Dexamethasone 0.5mg TAB
Indication: Drug USE FOR Unknown Indication
Indomethacin
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Didanosine
Adverse event in male receiving Epivir (Lamivudine)
Reported by a physician on 2007-10-23
Patient: male, weighing 89.0 kg (195.8 pounds)
Adverse reactions / side effects: Drug Resistance
Suspect drug(s):
Viramune
Dosage: 200mg during 14 days, thereafter 400mg
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-21
End date: 2007-07-30
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-21
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-21
End date: 2007-07-30
Other drugs received by patient: Glucovance; Eusaprim; Eusaprim
Adverse event in 39 year old female receiving Epivir (Lamivudine)
Reported by a pharmacist from United Kingdom on 2007-10-22
Patient: 39 year old female
Adverse reactions / side effects: Mitochondrial Cytopathy, Portal Vein Thrombosis, Hepatic Failure, Lactic Acidosis, Constipation
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2001-12-01
Indinivir Sulfate
Indication: Drug USE FOR Unknown Indication
Nevirapine
Dosage: 200mg twice per day
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Septrin
Adverse event in male receiving Epivir (Lamivudine)
Reported by a individual with unspecified qualification from Australia on 2007-10-22
Patient: male
Adverse reactions / side effects: Hepatitis
Adverse event resulted in: death
Suspect drug(s):
Hepsera
Administration route: Oral
Indication: Hepatitis B
Epivir
Administration route: Oral
Indication: Hepatitis B
Adverse event in female receiving Epivir (Lamivudine)
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient: female, weighing 0.9 kg (2.0 pounds)
Adverse reactions / side effects: Breech Delivery, Premature Baby, Congenital Anomaly, Patent Ductus Arteriosus, Joint Dislocation
Adverse event resulted in: hospitalization
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg-freq:daily
Administration route: Oral
Indication: HIV Infection
Ziagen
Dosage: daily dose:600mg-freq:daily
Administration route: Oral
Indication: HIV Infection
3TC
Indication: HIV Infection
Viramune
Dosage: daily dose:400mg-freq:daily
Indication: HIV Infection
Fortovase
Dosage: daily dose:2400mg
Administration route: Oral
Indication: HIV Infection
AZT
Indication: HIV Infection
Epivir
Dosage: daily dose:300mg-freq:daily
Indication: HIV Infection
Retrovir
Dosage: daily dose:600mg-freq:daily
Administration route: Oral
Indication: HIV Infection
End date: 2003-03-12
Dexamethasone 0.5mg TAB
Indocin
Other drugs received by patient: Videx
Adverse event in receiving Epivir (Lamivudine)
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypospadias
Suspect drug(s):
Viracept
Administration route: Oral
Indication: HIV Infection
Videx
Sustiva
Epivir
Norvir
Retrovir
Indinivir Sulfate
Adverse event in receiving Epivir (Lamivudine)
Reported by a individual with unspecified qualification from Australia on 2007-10-15
Patient:
Adverse reactions / side effects: Hepatitis
Adverse event resulted in: death
Suspect drug(s):
Hepsera
Administration route: Oral
Indication: Hepatitis B
Epivir
Administration route: Oral
Indication: Hepatitis B
Adverse event in 53 year old male receiving Epivir (Lamivudine)
Reported by a physician from United States on 2007-10-12
Patient: 53 year old male
Adverse reactions / side effects: Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased
Suspect drug(s):
Letairis
Dosage: 5mg per day
Administration route: Oral
Start date: 2007-08-09
End date: 2007-09-12
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: HIV Infection
Spiriva
Viread
Dosage: 300mg per day
Indication: HIV Infection
Sustiva
Dosage: 600mg per day
Administration route: Oral
Indication: HIV Infection
Other drugs received by patient: Lasix; Sildenafil Citrate; Warfarin Sodium; Advair Diskus 100 / 50; Singulair; Metformin HCL; Flomax; Wellbutrin
Adverse event in 37 year old female receiving Epivir (Lamivudine)
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 44 year old male receiving Epivir (Lamivudine)
Reported by a consumer/non-health professional from France on 2007-10-11
Patient: 44 year old male
Adverse reactions / side effects: Optic Atrophy, Glaucoma, Optic Nerve Disorder, Drug Ineffective, Tooth Abscess, Trigeminal Neuralgia, Sciatica, Tooth Extraction, Visual Acuity Reduced, Treatment Noncompliance, Balance Disorder, Leukoencephalopathy, Depression, Optic Neuritis Retrobulbar, Facial Pain, Mononeuropathy Multiplex, Visual Disturbance, Gastrointestinal Disorder, Memory Impairment, Neuralgia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Retrovir
Indication: HIV Infection
Start date: 2006-06-23
Telzir
Indication: HIV Infection
Start date: 2005-03-29
End date: 2006-06-23
Combivir
Indication: HIV Infection
Start date: 2005-09-28
End date: 2006-06-23
Epivir
Indication: HIV Infection
Start date: 1998-04-01
Viread
Indication: HIV Infection
Start date: 2006-06-23
Invirase
Indication: HIV Infection
Start date: 2006-06-23
Lyrica
Indication: Trigeminal Neuralgia
Start date: 2006-06-23
End date: 2006-07-01
Neurontin
Indication: Trigeminal Neuralgia
Start date: 2006-01-01
End date: 2006-01-01
Bactrim
Start date: 1998-09-01
Norvir
Indication: HIV Infection
Start date: 2004-04-17
Other drugs received by patient: Viracept; Zerit
Adverse event in 44 year old female receiving Epivir (Lamivudine)
Reported by a physician from Japan on 2007-10-11
Patient: 44 year old female
Adverse reactions / side effects: Jaundice, Liver Disorder
Suspect drug(s):
Epivir
Dosage: 4tab per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
End date: 2007-01-01
Retrovir
Dosage: 600mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
End date: 2007-01-01
Other drugs received by patient: Viracept
Adverse event in 45 year old male receiving Epivir (Lamivudine)
Reported by a physician from France on 2007-10-09
Patient: 45 year old male
Adverse reactions / side effects: Hypovitaminosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Epivir
Tenofovir
Adverse event in 45 year old male receiving Epivir (Lamivudine)
Reported by a physician from France on 2007-10-09
Patient: 45 year old male
Adverse reactions / side effects: Hypovitaminosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Epivir
Tenofovir
Adverse event in male receiving Epivir (Lamivudine)
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 44 year old female receiving Epivir (Lamivudine)
Reported by a physician from Japan on 2007-10-03
Patient: 44 year old female
Adverse reactions / side effects: Jaundice, Liver Disorder
Suspect drug(s):
Epivir
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Retrovir
Dosage: 600mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Viracept
Adverse event in 36 year old male receiving Epivir (Lamivudine)
Reported by a physician from Japan on 2007-10-01
Patient: 36 year old male
Adverse reactions / side effects: Blood Urea Increased, AIDS Encephalopathy, Altered State of Consciousness, Blood Creatinine Increased, Renal Failure Chronic, Convulsion, Nephropathy
Adverse event resulted in: life threatening event
Suspect drug(s):
Ziagen
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2002-11-26
End date: 2007-03-17
Viread
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-05-20
End date: 2006-11-14
Epivir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2000-09-19
End date: 2007-03-17
Retrovir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2000-09-19
End date: 2006-12-11
Norvir
Dosage: 100mg as directed
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-04-07
End date: 2007-03-17
Norvir
Dosage: 200mg unknown
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-05-20
End date: 2003-11-10
Zithromax
Administration route: Oral
Indication: Opportunistic Infection Prophylaxis
Start date: 2002-04-09
Baktar
Administration route: Oral
Indication: Antifungal Prophylaxis
Start date: 2006-04-01
Tipranavir
Indication: Drug USE FOR Unknown Indication
Darunavir
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Unknown Drug; Unknown Drug
Adverse event in 61 year old male receiving Epivir (Lamivudine)
Reported by a consumer/non-health professional from France on 2007-07-30
Patient: 61 year old male, weighing 62.0 kg (136.4 pounds)
Adverse reactions / side effects: Renal Tubular Disorder, Blood Creatine Phosphokinase Increased, Hyperkalaemia, Parkinsonism, Muscle Rigidity, Hyperuricaemia, Neuropathy Peripheral, Mitochondrial Cytopathy, Proteinuria, Blood Creatinine Increased, Acid Base Balance Abnormal, Pain in Extremity, Folate Deficiency, Akinesia, General Physical Health Deterioration, Paraesthesia, Anaemia Macrocytic, Renal Failure, Areflexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-15
Videx
Dosage: 250mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-15
Zyprexa
Dosage: 7.5mg per day
Indication: Neuropathy
Other drugs received by patient: Reyataz; Norvir
Adverse event in 40 year old female receiving Epivir (Lamivudine)
Reported by a physician from France on 2007-07-30
Patient: 40 year old female
Adverse reactions / side effects: Hepatitis Cholestatic, Portal Hypertension, Hepatic Fibrosis, Lymphopenia, Varices Oesophageal, Lipodystrophy Acquired
Suspect drug(s):
Aprovel Tabs
Administration route: Oral
Indication: Hypertension
End date: 2006-04-18
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 2001-10-01
End date: 2005-05-16
Epivir
Indication: HIV Infection
Start date: 2001-10-01
Viramune
Indication: HIV Infection
Start date: 2001-01-01
Viread
Start date: 2005-03-16
Adverse event in 65 year old female receiving Epivir (Lamivudine)
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 Epivir (Lamivudine)
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 36 year old male receiving Epivir (Lamivudine)
Reported by a individual with unspecified qualification from United States on 2007-07-23
Patient: 36 year old male
Adverse reactions / side effects: Immune Reconstitution Syndrome, Body Temperature Increased, Pleuritic Pain, Wheezing, Kaposi's Sarcoma, Pyrexia, Chest X-RAY Abnormal, Mycobacterium Avium Complex Infection, Acid Fast Bacilli Infection, Acute Respiratory Distress Syndrome, Crepitations, Sputum Culture Positive, Cough, Respiratory Rate Increased, Dyspnoea, Necrotising Granulomatous Lymphadenitis, Granuloma, Computerised Tomogram Abnormal, Human Herpesvirus 8 Infection, Bronchoalveolar Lavage Abnormal, Respiratory Failure, Inflammation
Adverse event resulted in: death
Suspect drug(s):
Epivir
Indication: Kaposi's Sarcoma
Tenofovir Disoproxil Fumarate
Indication: Kaposi's Sarcoma
Ritonavir (Formulation Unknown) (Ritonavir)
Indication: Kaposi's Sarcoma
Atazanavir (Formulation Unknown) (Atazanavir)
Indication: Kaposi's Sarcoma
Stealth Lip.doxorubicin (Formulation Unknown) (Stealth Lip.doxorubicin
Indication: Kaposi's Sarcoma
Adverse event in 31 year old female receiving Epivir (Lamivudine)
Reported by a pharmacist from United Kingdom on 2007-07-19
Patient: 31 year old female, weighing 60.5 kg (133.1 pounds)
Adverse reactions / side effects: Umbilical Cord Abnormality, Intra-Uterine Death, Placental Infarction, Abortion Spontaneous
Suspect drug(s):
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: Retroviral Infection
Didanosine
Dosage: 250mg per day
Administration route: Oral
Indication: Retroviral Infection
Start date: 2004-09-01
Norvir
Dosage: 100mg per day
Administration route: Oral
Indication: Retroviral Infection
Fuzeon
Dosage: 180mg per day
Indication: Retroviral Infection
Reyataz
Dosage: 300mg per day
Administration route: Oral
Indication: Retroviral Infection
Valgancyclovir
Indication: Cytomegalovirus Infection
Start date: 2004-09-01
Other drugs received by patient: Cotrim
Adverse event in 27 year old female receiving Epivir (Lamivudine)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-07-18
Patient: 27 year old female
Adverse reactions / side effects: Cholestasis of Pregnancy, Drug Exposure During Pregnancy, Proteus Infection, Anogenital Warts, Genital Infection
Suspect drug(s):
Combivir
Dosage: 900mg per day
Administration route: Oral
Start date: 2005-02-16
Epivir
Dosage: 300mg per day
Administration route: Oral
Start date: 2004-07-29
End date: 2005-02-16
Viread
Dosage: 300mg per day
Start date: 2004-07-29
Norvir
Dosage: 400mg per day
Start date: 2004-07-29
End date: 2005-02-16
Fuzeon
Dosage: 180mg per day
Start date: 2005-03-22
End date: 2005-03-31
Invirase
Dosage: 2000mg per day
Start date: 2004-09-29
End date: 2005-02-16
Adverse event in male receiving Epivir (Lamivudine)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-07-18
Patient: male, weighing 2.8 kg (6.2 pounds)
Adverse reactions / side effects: Diaphragmatic Hernia
Suspect drug(s):
Combivir
Dosage: 900mg per day
Start date: 2005-02-16
Epivir
Dosage: 300mg per day
Start date: 2004-07-29
End date: 2005-02-16
Viread
Dosage: 300mg per day
Start date: 2004-07-29
Norvir
Dosage: 400mg per day
Start date: 2004-07-29
End date: 2005-02-16
Fuzeon
Dosage: 180mg per day
Start date: 2005-03-22
End date: 2005-03-31
Invirase
Dosage: 2000mg per day
Start date: 2004-09-29
End date: 2005-02-16
Adverse event in 2 month old male receiving Epivir (Lamivudine)
Reported by a physician from France on 2007-07-16
Patient: 2 month old male
Adverse reactions / side effects: Gastrointestinal Malformation, Heart Disease Congenital, Pregnancy
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Videx
Start date: 2001-06-12
End date: 2001-08-11
Retrovir
Start date: 2001-03-27
End date: 2001-08-11
Epivir
Start date: 2001-03-27
End date: 2001-08-11
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