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Index of reports
> Cases with Anaemia (28)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Combivir (Lamivudine / Zidovudine) where reactions include anaemia. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Combivir side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-21
Patient:
Reactions: Atrial Septal Defect, Jaundice, Cardiac Murmur, Dysmorphism, Premature Baby, Foetal Exposure During Pregnancy, Anaemia, Ascites, Hydrops Foetalis, Talipes
Drug(s) suspected as cause:
Combivir
Indication: Maternal Exposure Timing Unspecified
Kaletra
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in 31 year old female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10
Patient: 31 year old female
Reactions: Anaemia
Drug(s) suspected as cause:
Norvir
Administration route: Oral
Indication: Antiretroviral Therapy
Start date: 2012-03-12
Epzicom
Administration route: Oral
Indication: Antiretroviral Therapy
Start date: 2012-05-05
Combivir
Administration route: Oral
Indication: Antiretroviral Therapy
Start date: 2012-03-12
Invirase
Administration route: Oral
Indication: Antiretroviral Therapy
Start date: 2012-03-12
Possible Combivir side effects in female
Reported by a health professional (non-physician/pharmacist) from Russian Federation on 2012-08-08
Patient: female
Reactions: Anaemia, Maternal Exposure During Pregnancy
Drug(s) suspected as cause:
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-12
Ritonavir
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-12
Abacavir Sulfate / Lamivudine
Administration route: Oral
Indication: HIV Infection
Start date: 2012-05-05
Combivir
Dosage: 1u unknown
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-12
Possible Combivir side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-31
Patient:
Reactions: Jaundice, Atrial Septal Defect, Cardiac Murmur, Dysmorphism, Premature Baby, Anaemia, Foetal Exposure During Pregnancy, Limb Malformation, Ascites, Hydrops Foetalis, Talipes
Drug(s) suspected as cause:
Combivir
Indication: Maternal Exposure Timing Unspecified
Kaletra
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in female
Reported by a health professional (non-physician/pharmacist) from Russian Federation on 2012-07-05
Patient: female
Reactions: Maternal Exposure During Pregnancy, Anaemia
Drug(s) suspected as cause:
Invirase
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-12
Ritonavir
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-12
Abacavir Sulfate / Lamivudine
Administration route: Oral
Indication: HIV Infection
Start date: 2012-05-05
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-12
Possible Combivir side effects in male
Reported by a health professional (non-physician/pharmacist) from Brazil on 2012-07-02
Patient: male
Reactions: Tumour Necrosis, Pulmonary Haemorrhage, Immune Reconstitution Syndrome, Cytomegalovirus Chorioretinitis, Anaemia, Kaposi's Sarcoma, Leukopenia
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Etravirine
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2011-01-01
End date: 2012-03-08
Dolutegravir Tablet
Dosage: daily
Indication: HIV Infection
Start date: 2012-02-02
Paclitaxel
Dosage: daily
Indication: Kaposi's Sarcoma
Start date: 2010-09-01
Maraviroc
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2011-01-01
End date: 2012-03-08
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2012-02-02
Ganciclovir
Dosage: daily
Indication: Cytomegalovirus Chorioretinitis
Start date: 2012-02-15
End date: 2012-03-05
Darunavir Hydrate
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2009-02-01
End date: 2012-03-08
Norvir
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-03-01
End date: 2012-03-08
Ganciclovir
Start date: 2012-03-06
End date: 2012-03-06
Possible Combivir side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-28
Patient:
Reactions: Atrial Septal Defect, Jaundice, Cardiac Murmur, Dysmorphism, Premature Baby, Foetal Exposure During Pregnancy, Anaemia, Limb Malformation, Ascites, Hydrops Foetalis, Talipes
Drug(s) suspected as cause:
Kaletra
Indication: Maternal Exposure Timing Unspecified
Combivir
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in male
Reported by a pharmacist from United States on 2012-06-26
Patient: male, weighing 2.1 kg (4.6 pounds)
Reactions: Ventricular Hypokinesia, Premature Baby, Hyperkalaemia, Colitis Ulcerative, Anaemia, Maternal Exposure During Pregnancy, General Physical Health Deterioration, Toxicity To Various Agents, Cardiac Failure, Electrocardiogram Abnormal, Hypotonia, Abdominal Distension, Bradycardia, Sinoatrial Block, Renal Failure Acute
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Indication: Maternal Exposure Timing Unspecified
Combivir
Indication: Maternal Exposure Timing Unspecified
Kaletra
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2007-05-26
End date: 2007-05-30
Saquinavir
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-20
Patient:
Reactions: Jaundice, Atrial Septal Defect, Cardiac Murmur, Dysmorphism, Premature Baby, Foetal Exposure During Pregnancy, Anaemia, Limb Malformation, Ascites, Hydrops Foetalis, Talipes
Drug(s) suspected as cause:
Kaletra
Indication: Maternal Exposure Timing Unspecified
Combivir
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in female
Reported by a physician from Japan on 2012-06-08
Patient: female
Reactions: Caesarean Section, Maternal Exposure During Pregnancy, Anaemia, Delivery
Drug(s) suspected as cause:
Epivir
Dosage: 2iuax per day
Administration route: Oral
Indication: HIV Infection
Start date: 2011-09-29
End date: 2011-11-09
Combivir
Dosage: 2iuax per day
Administration route: Oral
Start date: 2011-11-10
Kaletra
Dosage: 4iuax per day
Administration route: Oral
Indication: HIV Infection
Start date: 2011-09-22
Combivir
Dosage: 2iuax per day
Administration route: Oral
Indication: HIV Infection
Start date: 2011-09-22
End date: 2011-09-28
Retrovir
Dosage: 4iuax per day
Administration route: Oral
Indication: HIV Infection
Start date: 2011-09-29
End date: 2011-11-09
Possible Combivir side effects in male
Reported by a physician from France on 2012-05-22
Patient: male
Reactions: Dyspnoea Exertional, Anaemia, Pallor
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Tipranavir
Administration route: Oral
Indication: HIV Infection CDC Category A3
Start date: 2009-01-16
End date: 2012-01-09
Combivir
Administration route: Oral
Indication: HIV Infection CDC Category A3
Start date: 2011-09-23
End date: 2012-01-02
Other drugs received by patient: Norvir; Intelence
Possible Combivir side effects in male
Reported by a health professional (non-physician/pharmacist) from France on 2012-05-15
Patient: male
Reactions: Dyspnoea Exertional, Anaemia, Pallor
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Aptivus
Administration route: Oral
Indication: HIV Infection CDC Category A3
Start date: 2009-01-16
End date: 2012-01-09
Combivir
Indication: HIV Infection CDC Category A3
Start date: 2011-09-23
End date: 2012-01-02
Other drugs received by patient: Intelence; Norvir
Possible Combivir side effects in male
Reported by a health professional (non-physician/pharmacist) from Brazil on 2012-05-10
Patient: male
Reactions: Tumour Necrosis, Pulmonary Haemorrhage, Immune Reconstitution Syndrome, Cytomegalovirus Chorioretinitis, Anaemia, Kaposi's Sarcoma, Leukopenia
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Paclitaxel
Dosage: daily
Indication: Kaposi's Sarcoma
Start date: 2010-09-01
Darunavir Hydrate
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2009-02-01
End date: 2012-03-08
Ganciclovir
Dosage: daily
Indication: Cytomegalovirus Chorioretinitis
Start date: 2012-02-15
End date: 2012-03-05
Etravirine
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2011-01-01
End date: 2012-03-08
Norvir
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2000-03-01
End date: 2012-03-08
Ganciclovir
Start date: 2012-03-06
End date: 2012-03-06
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2012-02-02
Maraviroc
Dosage: daily
Administration route: Oral
Indication: HIV Infection
Start date: 2011-01-01
End date: 2012-03-08
Dolutegravir Tablet
Dosage: daily
Indication: HIV Infection
Start date: 2012-02-02
Possible Combivir side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-12
Patient:
Reactions: Jaundice, Atrial Septal Defect, Cardiac Murmur, Dysmorphism, Premature Baby, Anaemia, Foetal Exposure During Pregnancy, Limb Malformation, Ascites, Hydrops Foetalis, Talipes
Drug(s) suspected as cause:
Kaletra
Indication: Maternal Exposure Timing Unspecified
Combivir
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in 34 year old male
Reported by a consumer/non-health professional from Russian Federation on 2012-03-29
Patient: 34 year old male
Reactions: Anaemia
Drug(s) suspected as cause:
Combivir
Atazanavir
Possible Combivir side effects in 21 year old female
Reported by a physician from Korea, Republic of on 2012-02-27
Patient: 21 year old female, weighing 56.0 kg (123.2 pounds)
Reactions: Anaemia, Bone Marrow Failure, Neutropenia, Hypertriglyceridaemia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Indication: HIV Infection
Start date: 2010-07-22
End date: 2010-10-08
Kaletra
Dosage: 2 tabs 2x/day
Start date: 2010-11-16
Combivir
Dosage: 2 tablets daily
Indication: Antiretroviral Therapy
Start date: 2010-07-22
End date: 2010-10-08
Other drugs received by patient: Lamivudine (Epivir Hbv); Adacel; ABC
Possible Combivir side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-24
Patient:
Reactions: Atrial Septal Defect, Jaundice, Cardiac Murmur, Dysmorphism, Premature Baby, Anaemia, Foetal Exposure During Pregnancy, Limb Malformation, Ascites, Hydrops Foetalis, Talipes
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 2012-02-16
Patient:
Reactions: Atrial Septal Defect, Jaundice, Dysmorphism, Cardiac Murmur, Premature Baby, Foetal Exposure During Pregnancy, Anaemia, Limb Malformation, Ascites, Hydrops Foetalis, Talipes
Drug(s) suspected as cause:
Combivir
Indication: Maternal Exposure Timing Unspecified
Kaletra
Indication: Maternal Exposure Timing Unspecified
Possible Combivir side effects in 35 year old female
Reported by a health professional (non-physician/pharmacist) from Greece on 2012-01-31
Patient: 35 year old female
Reactions: Caesarean Section, Maternal Exposure During Pregnancy, Anaemia
Drug(s) suspected as cause:
Combivir
Indication: HIV Infection
Nelfinavir Mesylate
Indication: HIV Infection
Possible Combivir side effects in 31 year old male
Reported by a consumer/non-health professional from United States on 2012-01-27
Patient: 31 year old male
Reactions: Anaemia
Drug(s) suspected as cause:
Combivir
Other drugs received by patient: Caltrate; M.v.i.
Possible Combivir side effects in female
Reported by a physician from Japan on 2012-01-26
Patient: female, weighing 2.2 kg (4.8 pounds)
Reactions: Foetal Exposure During Pregnancy, Anaemia
Drug(s) suspected as cause:
Retrovir
Dosage: 16.8mg per day
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Start date: 2009-11-25
End date: 2012-01-05
Retrovir
Dosage: 400mg per day
Start date: 2009-11-25
End date: 2009-11-25
Combivir
Dosage: 2iuax per day
Indication: HIV Infection
Kaletra
Dosage: 4iuax per day
Indication: Prophylaxis Against HIV Infection
Possible Combivir side effects in 37 year old male
Reported by a consumer/non-health professional from United States on 2012-01-05
Patient: 37 year old male, weighing 56.0 kg (123.2 pounds)
Reactions: Anaemia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Efavirenz
Dosage: interrupted on 16sep11:88days.
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
Combivir
Dosage: 1df= 150-300 mg/bid
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
End date: 2011-09-16
Possible Combivir side effects in male
Reported by a physician from Japan on 2011-12-28
Patient: male, weighing 2.0 kg (4.4 pounds)
Reactions: Anaemia, Foetal Exposure During Pregnancy
Drug(s) suspected as cause:
Retrovir
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Combivir
Indication: HIV Infection
Possible Combivir side effects in female
Reported by a physician from Japan on 2011-12-28
Patient: female, weighing 2.0 kg (4.4 pounds)
Reactions: Anaemia, Foetal Exposure During Pregnancy
Drug(s) suspected as cause:
Retrovir
Administration route: Oral
Indication: Prophylaxis Against HIV Infection
Combivir
Indication: HIV Infection
Possible Combivir side effects in 37 year old male
Reported by a consumer/non-health professional from United States on 2011-12-07
Patient: 37 year old male, weighing 56.0 kg (123.2 pounds)
Reactions: Anaemia
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Efavirenz
Dosage: interrupted on 16sep11:88days.
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
Combivir
Dosage: 1df= 150-300 mg/bid
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
End date: 2011-09-16
Possible Combivir side effects in 37 year old male
Reported by a health professional (non-physician/pharmacist) from United States on 2011-12-06
Patient: 37 year old male, weighing 56.0 kg (123.2 pounds)
Reactions: Anaemia
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Combivir
Dosage: 1df= 150-300 mg/bid
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
End date: 2011-09-16
Efavirenz
Dosage: interrupted on 16sep11:88days.
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
Possible Combivir side effects in male
Reported by a health professional (non-physician/pharmacist) from France on 2011-11-28
Patient: male, weighing 90.0 kg (198.0 pounds)
Reactions: Anaemia, Ulcer
Drug(s) suspected as cause:
Combivir
Possible Combivir side effects in 37 year old male
Reported by a consumer/non-health professional from United States on 2011-10-11
Patient: 37 year old male
Reactions: Anaemia
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Efavirenz
Dosage: interrupted on 16sep11:88days.
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
Combivir
Dosage: 1df= 150-300 mg/bid
Administration route: Oral
Indication: HIV Infection
Start date: 2011-06-21
End date: 2011-09-16
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