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Kaletra (Lopinavir / Ritonavir) - Death - Suspected Cause - Side Effect Reports

 
 



Index of reports > Death (178)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Kaletra (Lopinavir / Ritonavir) death. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 178   Next >>

Possible Kaletra side effects in

Reported by a physician from Japan on 2012-08-27

Patient:

Reactions: Hepatic Function Abnormal, Cardiac Failure

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra
    Dosage: divided dose frequency unknown
    Administration route: Oral
    Start date: 2004-08-31
    End date: 2006-09-21

Kaletra
    Dosage: divided dose frequency unknown
    Administration route: Oral
    Start date: 2006-10-26
    End date: 2011-07-07

Invirase
    Dosage: divided dose requency u
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-10-26

Kaletra
    Dosage: divided dose frequency unknown
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2002-09-03
    End date: 2004-08-04

Isentress
    Dosage: divided dose frequency unknown
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-07-31
    End date: 2011-08-07

Other drugs received by patient: Halcion



Possible Kaletra side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-27

Patient:

Reactions: Ultrasound Scan Abnormal, Foetal Exposure During Pregnancy, Abortion Induced, Talipes, Meningomyelocele

Adverse event resulted in: death

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

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Kaletra side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-23

Patient: female

Reactions: Foetal Growth Restriction

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Combivir



Possible Kaletra side effects in male

Reported by a physician from Japan on 2012-08-22

Patient: male

Reactions: Hypophosphataemia, Diarrhoea, Cardiac Failure, Lactic Acidosis, Liver Disorder

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2002-09-03
    End date: 2004-08-04

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2006-10-26
    End date: 2011-08-07

Abacavir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-08-31
    End date: 2006-09-21

Kaletra
    Administration route: Oral
    Start date: 2004-08-31
    End date: 2006-09-21

Didanosine
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2002-09-03
    End date: 2004-08-04

Didanosine
    Administration route: Oral
    Start date: 2004-08-31
    End date: 2006-09-21

Didanosine
    Administration route: Oral
    Start date: 2006-10-26

Tenofovir Disoproxil Fumarate
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-08-31
    End date: 2006-09-21

Isentress
    Dosage: 800mg daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-08-07

Stavudine
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2002-04-01
    End date: 2004-08-04

Other drugs received by patient: Glycyron; Saquinavir; Allopurinol; Bifidobacterium; Loperamide HCL; Allopurinol



Possible Kaletra side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-20

Patient:

Reactions: Ultrasound Scan Abnormal, Foetal Exposure During Pregnancy, Abortion Induced, Talipes, Meningomyelocele

Adverse event resulted in: death

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

Combivir
    Indication: Maternal Exposure Timing Unspecified



Possible Kaletra side effects in male

Reported by a physician from Japan on 2012-08-17

Patient: male

Reactions: Rhabdomyolysis, Dyspnoea, Hepatic Failure, Lactic Acidosis, Acidosis, Fall, Haematemesis, Haematochezia, Multi-Organ Failure, Spinal Compression Fracture, Fractured Ischium, Melaena, Renal Failure Acute, Hepatic Cirrhosis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Sulfamethoxazole and Trimethoprim
    Indication: Prophylaxis

Sulfamethoxazole and Trimethoprim
    Administration route: Oral
    Indication: Pneumocystis Jiroveci Pneumonia
    End date: 2011-01-14

Truvada
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2010-04-27
    End date: 2011-01-14

Kaletra
    Dosage: 4 dosage forms daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2007-09-12
    End date: 2011-01-14

Other drugs received by patient: Zerit; Lamivudine



Possible Kaletra 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 Kaletra 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 Kaletra side effects in

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

Patient:

Reactions: Foetal Exposure During Pregnancy, Nervous System Disorder, Foetal Death

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 Kaletra side effects in

Reported by a physician from Russian Federation on 2012-08-14

Patient:

Reactions: Atelectasis Neonatal, Neonatal Respiratory Distress Syndrome, Premature Baby, Respiratory Failure, Congenital Hydrocephalus, Foetal Exposure During Pregnancy, Cerebral Atrophy, Cerebellar Hypoplasia

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Kaletra



Possible Kaletra 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 Kaletra side effects in

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

Patient:

Reactions: Congenital Central Nervous System Anomaly, Stillbirth, Foetal Exposure During Pregnancy

Adverse event resulted in: death

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

Combivir
    Indication: Maternal Exposure Timing Unspecified



Possible Kaletra side effects in male

Reported by a physician from Canada on 2012-08-13

Patient: male, weighing 104.0 kg (228.8 pounds)

Reactions: Asthma, Hepatic Neoplasm Malignant, Benign Prostatic Hyperplasia

Adverse event resulted in: death

Drug(s) suspected as cause:
Qvar 40
    Dosage: 100/ug/pf 2 pf
    Indication: Product Used FOR Unknown Indication
    Start date: 2008-06-23

Kaletra
    Indication: HIV Infection

Levothyroxine Sodium
    Indication: Product Used FOR Unknown Indication
    Start date: 2006-02-23

Kaletra
    Dosage: 200/50; stopped 4 months prior to death
    Administration route: Oral
    Indication: Antiretroviral Therapy
    Start date: 2007-11-07
    End date: 2010-09-10

Effexor XR
    Indication: Product Used FOR Unknown Indication
    Start date: 2007-05-09

Hydrochlorothiazide
    Dosage: 50 mg 1 qd
    Indication: Product Used FOR Unknown Indication

Crestor
    Indication: Product Used FOR Unknown Indication
    Start date: 2006-02-23

Truvada
    Dosage: 100/ug/pf 2 pf
    Indication: Product Used FOR Unknown Indication
    Start date: 2007-11-08

Altace
    Indication: Product Used FOR Unknown Indication
    Start date: 2006-02-23

Other drugs received by patient: Crestor; Serevent; Valproate Sodium; Ventolin; Norvir; Potassium Chloride; Ranitidine; Intelence; Procar; Lamictal; Rabeprazole Sodium; Prezista



Possible Kaletra side effects in 26 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-13

Patient: 26 year old female

Reactions: Maternal Exposure During Pregnancy, Premature Labour, Congenital Anomaly in Offspring

Adverse event resulted in: death

Drug(s) suspected as cause:
Combivir
    Dosage: unk
    Administration route: Oral
    Indication: Antiretroviral Therapy
    Start date: 2011-04-21
    End date: 2011-09-15

Prezista
    Dosage: 800mg/day
    Administration route: Oral
    Indication: Antiretroviral Therapy
    Start date: 2011-04-28

Kaletra
    Dosage: unk
    Administration route: Oral
    Indication: Antiretroviral Therapy
    Start date: 2011-04-21
    End date: 2011-04-28

Norvir
    Dosage: 200mg/day
    Administration route: Oral
    Indication: Antiretroviral Therapy
    Start date: 2011-04-28
    End date: 2011-05-10

Norvir
    Dosage: 100 mg/day
    Administration route: Oral
    Start date: 2011-05-11

Zidovudine
    Dosage: 2.0 mg/day
    Indication: Antiretroviral Therapy
    Start date: 2011-09-15
    End date: 2011-09-15



Possible Kaletra side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-13

Patient: male, weighing 2.7 kg (5.9 pounds)

Reactions: Foetal Growth Restriction, Premature Baby, Foetal Exposure During Pregnancy

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: unk
    Indication: Maternal Exposure During Pregnancy
    Start date: 2011-04-21
    End date: 2011-04-28

Norvir
    Dosage: 100 mg/day
    Start date: 2011-05-11

Prezista
    Dosage: 800 mg/day
    Indication: Maternal Exposure During Pregnancy
    Start date: 2011-04-28

Zidovudine
    Dosage: 2.0 mg/day
    Indication: Maternal Exposure During Pregnancy
    Start date: 2011-09-15
    End date: 2011-09-15

Norvir
    Dosage: 200 mg/day
    Indication: Maternal Exposure During Pregnancy
    Start date: 2011-04-28
    End date: 2011-05-10

Combivir
    Dosage: unk
    Indication: Maternal Exposure During Pregnancy
    Start date: 2011-04-21
    End date: 2011-09-15



Possible Kaletra side effects in male

Reported by a physician from Canada on 2012-08-10

Patient: male, weighing 104.0 kg (228.8 pounds)

Reactions: Asthma, Hepatic Neoplasm Malignant, Benign Prostatic Hyperplasia

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 200/50; stopped 4 months prior to death
    Administration route: Oral
    Indication: Antiretroviral Therapy
    Start date: 2007-11-07
    End date: 2010-09-10

Truvada
    Dosage: 200/300mg
    Indication: Product Used FOR Unknown Indication
    Start date: 2007-11-08

Hydrochlorothiazide
    Indication: Product Used FOR Unknown Indication

Levothyroxine Sodium
    Indication: Product Used FOR Unknown Indication
    Start date: 2006-02-23

Crestor
    Indication: Product Used FOR Unknown Indication
    Start date: 2006-02-23

Kaletra
    Indication: HIV Infection

Altace
    Indication: Product Used FOR Unknown Indication
    Start date: 2006-02-23

Effexor XR
    Indication: Product Used FOR Unknown Indication
    Start date: 2007-05-09

Qvar 40
    Dosage: 100/ug/pf 2 pf
    Indication: Product Used FOR Unknown Indication
    Start date: 2008-06-23

Other drugs received by patient: Valproate Sodium; Rabeprazole Sodium; Lamictal; Norvir; Crestor; Potassium Chloride; Intelence; Serevent; Ventolin; Procar; Prezista; Ranitidine



Possible Kaletra 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 Kaletra 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 Kaletra side effects in male

Reported by a pharmacist from Canada on 2012-08-09

Patient: male

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Administration route: Oral
    Indication: Antiretroviral Therapy
    End date: 2010-09-15

Kaletra
    Indication: HIV Infection



Possible Kaletra side effects in

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

Patient:

Reactions: Ultrasound Scan Abnormal, Foetal Exposure During Pregnancy, Talipes, Abortion Induced, Meningomyelocele

Adverse event resulted in: death

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

Kaletra
    Indication: Maternal Exposure Timing Unspecified



Possible Kaletra side effects in female

Reported by a health professional (non-physician/pharmacist) from France on 2012-08-06

Patient: female

Reactions: Macrocephaly, Dysmorphism, Holoprosencephaly, Foetal Malformation

Adverse event resulted in: death

Drug(s) suspected as cause:
Truvada
    Dosage: 1 df, unk
    Indication: HIV Infection
    Start date: 2007-01-15

Kaletra
    Indication: HIV Infection
    Start date: 2007-01-15



Possible Kaletra side effects in male

Reported by a physician from Japan on 2012-08-06

Patient: male

Reactions: Rhabdomyolysis, Dyspnoea, Hepatic Failure, Lactic Acidosis, Acidosis, Fall, Haematemesis, Multi-Organ Failure, Haematochezia, Spinal Compression Fracture, Fractured Ischium, Melaena, Hepatic Cirrhosis, Renal Failure Acute

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Sulfamethoxazole and Trimethoprim
    Indication: Prophylaxis

Kaletra
    Dosage: 4 dosage forms daily
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2007-09-12
    End date: 2011-01-14

Truvada
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2010-04-27
    End date: 2011-01-14

Sulfamethoxazole and Trimethoprim
    Administration route: Oral
    Indication: Pneumocystis Jiroveci Pneumonia
    End date: 2011-01-14

Other drugs received by patient: Lamivudine; Zerit



Possible Kaletra side effects in 32 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-03

Patient: 32 year old female

Reactions: Squamous Cell Carcinoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra
    Dosage: 1 course
    Administration route: Oral
    Indication: Antiviral Treatment
    Start date: 2010-12-07

Isentress
    Dosage: 1 course
    Administration route: Oral
    Indication: Antiviral Treatment
    Start date: 2010-12-07



Possible Kaletra side effects in

Reported by a consumer/non-health professional from France on 2012-07-30

Patient:

Reactions: Drug Eruption, Death, Aspartate Aminotransferase Increased, Anaemia, Neutropenia, Leukopenia

Adverse event resulted in: death

Drug(s) suspected as cause:
Viread
    Dosage: 300 mg, qd
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2010-05-30

Rifampin
    Dosage: 600 mg, qd
    Administration route: Oral
    Indication: Tuberculosis
    Start date: 2010-05-22
    End date: 2010-08-10

Isentress
    Dosage: 800 mg, qd
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2010-05-30
    End date: 2010-08-31

Isoniazid
    Dosage: 400 mg, qd
    Administration route: Oral
    Indication: Tuberculosis
    Start date: 2010-05-22
    End date: 2010-08-10

Dapsone
    Dosage: 100 mg, qd
    Indication: Prophylaxis
    Start date: 2011-01-15

Pyrazinamide
    Dosage: 2 g, qd
    Administration route: Oral
    Indication: Tuberculosis
    Start date: 2010-05-22
    End date: 2010-07-26

Epivir
    Dosage: 300 mg, qd
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2010-06-30

Kaletra
    Dosage: 20
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2010-11-22

Other drugs received by patient: Bactrim; Leucovorin Calcium; Leucovorin Calcium; Ivermectin; Acyclovir; Ciproflaxacin; Azithromycin; Pyridoxine HCL; Omeprazole



Possible Kaletra side effects in

Reported by a physician from Australia on 2012-07-27

Patient:

Reactions: Sudden Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Sultepyn; Clopamon; DPH; Ferrous Sulfate TAB; Vitamin B Complex CAP; Rehidrate; Phenazopyridine HCL TAB; Ranceph; Nystacid; Emtricitabine and Tenofovir Disoproxil Fumarate; Ascorbic Acid; Bactrim; Folic Acid



Possible Kaletra side effects in female

Reported by a physician from Argentina on 2012-07-20

Patient: female

Reactions: Diarrhoea, Respiratory Failure, Sepsis, Hypokalaemia

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Trimethoprim + Sulfamethoxazole; Azithromycin; Lamivudine; Azithromycin; Trimethoprim + Sulfamethoxazole



Possible Kaletra side effects in female

Reported by a physician from Argentina on 2012-07-10

Patient: female

Reactions: Respiratory Failure, Hypokalaemia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: TMS / SMX; Azithromycin; Lamivudine



Possible Kaletra side effects in female

Reported by a pharmacist from United States on 2012-07-06

Patient: female, weighing 2.2 kg (4.8 pounds)

Reactions: Foetal Exposure During Pregnancy, Accidental Overdose, Electroencephalogram Abnormal, Malaise, Sinoatrial Block, Oxygen Saturation Decreased, Renal Failure Acute, Vomiting, Premature Baby, Blood Potassium Increased, Nodal Rhythm, Toxicity To Various Agents, Cardiogenic Shock, Drug Prescribing Error, Staphylococcal Sepsis, Arrhythmia, Haemoglobin Decreased, Bradycardia, Anion GAP Decreased, Neonatal Respiratory Arrest

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra
    Administration route: Oral
    Indication: Blood HIV RNA
    Start date: 2007-03-29
    End date: 2007-03-29

Kaletra
    Indication: Maternal Exposure Timing Unspecified

Other drugs received by patient: Lamivudine; Ritonavir; Abacavir



Possible Kaletra side effects in female

Reported by a physician from Guinea-Bissau on 2012-06-29

Patient: female

Reactions: Death

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Zidovudine; Abacavir; Lamivudine



Possible Kaletra side effects in male

Reported by a physician from Germany on 2012-06-29

Patient: male

Reactions: Pancreatic Carcinoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Aspirin; Fluconazole; Invirase; Pantoprazole; Torsemide



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