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Combivir (Lamivudine / Zidovudine) - Heart Disease Congenital - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Heart Disease Congenital (18)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Combivir (Lamivudine / Zidovudine) where reactions include heart disease congenital. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Combivir side effects in

Reported by a physician from United States on 2012-08-15

Patient:

Reactions: Foetal Exposure During Pregnancy, Foetal Death, Nervous System Disorder, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy

Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-15

Patient:

Reactions: Congenital Aortic Stenosis, Dandy-Walker Syndrome, Premature Baby, Foetal Exposure During Pregnancy, Congenital Pulmonary Artery Anomaly, Sepsis, Foetal Heart Rate Abnormal, Heart Disease Congenital, Talipes

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: HIV Infection
    Start date: 2010-08-30

Combivir
    Dosage: 2tab per day
    Indication: HIV Infection
    Start date: 2010-08-30



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-14

Patient:

Reactions: Stillbirth, Congenital Central Nervous System Anomaly, Foetal Exposure During Pregnancy, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10

Patient:

Reactions: Dandy-Walker Syndrome, Congenital Aortic Stenosis, Premature Baby, Foetal Exposure During Pregnancy, Sepsis, Congenital Pulmonary Artery Anomaly, Talipes, Heart Disease Congenital, Foetal Heart Rate Abnormal

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: HIV Infection
    Start date: 2010-08-30

Combivir
    Dosage: 2tab per day
    Indication: HIV Infection
    Start date: 2010-08-30



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10

Patient:

Reactions: Dandy-Walker Syndrome, Aortic Stenosis, Foetal Exposure During Pregnancy, Congenital Cardiovascular Anomaly, Foetal Monitoring Abnormal, Congenital Pulmonary Artery Anomaly, Sepsis, Talipes, Heart Disease Congenital

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir
    Indication: Maternal Exposure Timing Unspecified

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-19

Patient:

Reactions: Dandy-Walker Syndrome, Aortic Stenosis, Foetal Exposure During Pregnancy, Congenital Cardiovascular Anomaly, Foetal Monitoring Abnormal, Congenital Pulmonary Artery Anomaly, Sepsis, Talipes, Heart Disease Congenital

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Indication: Maternal Exposure Timing Unspecified

Combivir
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-15

Patient:

Reactions: Dandy-Walker Syndrome, Aortic Stenosis, Foetal Exposure During Pregnancy, Congenital Cardiovascular Anomaly, Foetal Monitoring Abnormal, Congenital Pulmonary Artery Anomaly, Sepsis, Heart Disease Congenital, Talipes

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir
    Indication: Maternal Exposure Timing Unspecified

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-12

Patient:

Reactions: Congenital Aortic Stenosis, Dandy-Walker Syndrome, Premature Baby, Foetal Exposure During Pregnancy, Sepsis, Congenital Pulmonary Artery Anomaly, Talipes, Heart Disease Congenital, Foetal Heart Rate Abnormal

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: HIV Infection
    Start date: 2010-08-30

Combivir
    Dosage: 2tab per day
    Indication: HIV Infection
    Start date: 2010-08-30



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-08

Patient:

Reactions: Dandy-Walker Syndrome, Foetal Monitoring Abnormal, Sepsis, Foetal Exposure During Pregnancy, Heart Disease Congenital, Talipes

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Indication: Maternal Exposure Timing Unspecified

Combivir
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-25

Patient:

Reactions: Dandy-Walker Syndrome, Premature Baby, Sepsis, Foetal Exposure During Pregnancy, Heart Disease Congenital, Talipes, Foetal Heart Rate Abnormal

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: HIV Infection
    Start date: 2010-08-30

Combivir
    Dosage: 2tab per day
    Indication: HIV Infection
    Start date: 2010-08-30



Possible Combivir side effects in

Reported by a individual with unspecified qualification from United States on 2012-04-24

Patient:

Reactions: Dandy-Walker Syndrome, Foetal Monitoring Abnormal, Foetal Exposure During Pregnancy, Sepsis, Talipes, Heart Disease Congenital

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir
    Indication: Maternal Exposure Timing Unspecified

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-24

Patient:

Reactions: Dandy-Walker Syndrome, Foetal Monitoring Abnormal, Sepsis, Foetal Exposure During Pregnancy, Talipes, Heart Disease Congenital

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Indication: Maternal Exposure Timing Unspecified

Combivir
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-20

Patient:

Reactions: Congenital Central Nervous System Anomaly, Stillbirth, Foetal Exposure During Pregnancy, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-20

Patient:

Reactions: Foetal Exposure During Pregnancy, Foetal Death, Nervous System Disorder, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy

Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-10

Patient:

Reactions: Congenital Central Nervous System Anomaly, Stillbirth, Foetal Exposure During Pregnancy, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Indication: Maternal Exposure Timing Unspecified

Combivir



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-10

Patient:

Reactions: Foetal Exposure During Pregnancy, Stillbirth, Congenital Central Nervous System Anomaly, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Indication: Maternal Exposure Timing Unspecified

Combivir



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-09

Patient:

Reactions: Foetal Exposure During Pregnancy, Foetal Death, Nervous System Disorder, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy

Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy



Possible Combivir side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-02

Patient:

Reactions: Stillbirth, Congenital Central Nervous System Anomaly, Foetal Exposure During Pregnancy, Heart Disease Congenital, Single Umbilical Artery

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir

Kaletra
    Indication: Maternal Exposure Timing Unspecified

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