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 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
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 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 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 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 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 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 2012-08-13
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
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 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 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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