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Retrovir (Zidovudine) - Congenital Cytomegalovirus Infection - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Congenital Cytomegalovirus Infection (9)

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

Possible Retrovir side effects in male

Reported by a physician from United States on 2012-08-09

Patient: male, weighing 2.1 kg (4.6 pounds)

Reactions: Premature Baby, Foetal Exposure During Pregnancy, Rash, Congenital Cytomegalovirus Infection, Foetal Growth Restriction, Microcephaly, Laboratory Test Abnormal, Hepatomegaly, Hypervitaminosis

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14
    End date: 2011-12-05

Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Retrovir
    Indication: Antiretroviral Therapy
    Start date: 2011-12-05
    End date: 2011-12-05



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-19

Patient: male, weighing 2.1 kg (4.6 pounds)

Reactions: Foetal Growth Restriction, Hepatomegaly, Microcephaly, Laboratory Test Abnormal, Premature Baby, Foetal Exposure During Pregnancy, Rash, Hypervitaminosis, Congenital Cytomegalovirus Infection

Drug(s) suspected as cause:
Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Retrovir
    Indication: Antiretroviral Therapy
    Start date: 2011-12-05
    End date: 2011-12-05

Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Kaletra
    Dosage: 6tab per day
    Start date: 2011-09-22
    End date: 2011-12-05



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-17

Patient: male

Reactions: Full Blood Count Abnormal, Premature Baby, Foetal Exposure During Pregnancy, Rash, Congenital Cytomegalovirus Infection, Foetal Growth Restriction, Hepatomegaly, Microcephaly, Hypervitaminosis

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

Kaletra
    Indication: Maternal Exposure Timing Unspecified

Retrovir
    Indication: Maternal Exposure Timing Unspecified



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-27

Patient: male

Reactions: Foetal Growth Restriction, Microcephaly, Hepatomegaly, Premature Baby, Full Blood Count Abnormal, Foetal Exposure During Pregnancy, Rash, Hypervitaminosis, Congenital Cytomegalovirus Infection

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

Combivir
    Indication: Maternal Exposure Timing Unspecified

Retrovir
    Indication: Maternal Exposure Timing Unspecified



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-23

Patient: male

Reactions: Full Blood Count Abnormal, Premature Baby, Foetal Exposure During Pregnancy, Rash, Congenital Cytomegalovirus Infection, Vitamin D Increased, Foetal Growth Restriction, Hepatomegaly, Microcephaly

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

Retrovir
    Indication: Maternal Exposure Timing Unspecified

Combivir
    Indication: Maternal Exposure Timing Unspecified



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-19

Patient: male, weighing 2.1 kg (4.6 pounds)

Reactions: Foetal Growth Restriction, Hepatomegaly, Laboratory Test Abnormal, Microcephaly, Premature Baby, Foetal Exposure During Pregnancy, Rash, Hypervitaminosis, Congenital Cytomegalovirus Infection

Drug(s) suspected as cause:
Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Kaletra
    Dosage: 6tab per day
    Start date: 2011-09-22
    End date: 2011-12-05

Retrovir
    Indication: Antiretroviral Therapy
    Start date: 2011-12-05
    End date: 2011-12-05



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-12

Patient: male

Reactions: Premature Baby, Foetal Exposure During Pregnancy, Congenital Cytomegalovirus Infection

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

Combivir
    Indication: Maternal Exposure Timing Unspecified

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-23

Patient: male, weighing 2.1 kg (4.7 pounds)

Reactions: Premature Baby, Foetal Exposure During Pregnancy, Congenital Cytomegalovirus Infection

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

Retrovir
    Indication: Maternal Exposure Timing Unspecified

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Retrovir side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-23

Patient: male, weighing 2.1 kg (4.6 pounds)

Reactions: Premature Baby, Foetal Exposure During Pregnancy, Congenital Cytomegalovirus Infection

Drug(s) suspected as cause:
Kaletra
    Dosage: 6tab per day
    Start date: 2011-09-22
    End date: 2011-12-05

Combivir
    Dosage: 2tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Kaletra
    Dosage: 4tab per day
    Indication: Antiretroviral Therapy
    Start date: 2011-07-14

Retrovir
    Indication: Antiretroviral Therapy
    Start date: 2011-12-05
    End date: 2011-12-05

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