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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