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Index of reports
> Cases resulting in hospitalization (288)
> Cases with Vomiting (28)
Below is the selection of adverse event reports related to Kaletra (Lopinavir / Ritonavir) that includes cases resulting in hospitalization where reactions include vomiting.
Reports 1 - 25 of 28 Next >>
Adverse event in 49 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a consumer/non-health professional from France on 2007-07-24
Patient: 49 year old male
Adverse reactions / side effects: Weight Decreased, Pancreatitis Acute, Diabetes Mellitus, Polyuria, Lactic Acidosis, Pyrexia, Ketoacidosis, Constipation, Speech Disorder, Hypovolaemia, Polydipsia, Vomiting, Nausea, Blood Lactic Acid Increased, Ascites, Haemolysis, Cachexia, Haemoglobin Decreased, Renal Failure, Anorexia, Lipase Increased, Haptoglobin Increased, Asthenia, Sinus Tachycardia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Kivexa
Dosage: 4tab per day
Administration route: Oral
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Kaletra
Dosage: 1tab per day
Administration route: Oral
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1997-10-01
End date: 2006-12-09
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Viracept
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Other drugs received by patient: Bactrim; Lipanthyl; Rivotril; Laroxyl
Adverse event in female receiving Kaletra (Lopinavir / Ritonavir)
Reported by a individual with unspecified qualification from Czech Republic on 2007-07-20
Patient: female, weighing 41.0 kg (90.2 pounds)
Adverse reactions / side effects: Bronchopneumonia, Fall, Faeces Discoloured, Oesophageal Candidiasis, Abdominal Discomfort, Iron Deficiency Anaemia, Cardiopulmonary Failure, HIV Infection CDC Category C3, Thrombocytopenia, Vomiting, Dysphagia, Nausea, Urinary Tract Infection, Chromaturia, General Physical Health Deterioration, Cervical Dysplasia, Cachexia, Communication Disorder, Diarrhoea, Leukopenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Trizivir; Furosemide; Ciprofloxacin HCL; Lamivudine + Zidovudine; Lamivudine + Zidovudine; Efavirenz; Bactrim; Parafon; Ambroxol; Lactobacillus AC; Zolpidem Tartrate; Codein; Diazepam; Donagan; Tramadol HCL; Thiethylperazine Maleate; Ranitidine HCL; Phytomenadione; Ferrlecit; Dexamethasone Sodium Phosphate; Aminophylline; Folic Acid; Ferrous Fumarate; Mycomax
Adverse event in 55 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a individual with unspecified qualification from Japan on 2007-07-20
Patient: 55 year old male
Adverse reactions / side effects: Ventricular Extrasystoles, Vomiting, Chest Discomfort, Nausea, Headache, Sick Sinus Syndrome, Malaise, Diarrhoea, Palpitations, Dizziness, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg
Administration route: Oral
Indication: HIV Infection
Stocrin
Dosage: daily dose:600mg
Administration route: Oral
Indication: HIV Infection
Start date: 2001-03-23
End date: 2005-07-14
Ziagen
Dosage: daily dose:600mg
Administration route: Oral
Indication: HIV Infection
Start date: 2001-04-06
End date: 2003-04-08
Kaletra
Dosage: text:6 dosage form
Administration route: Oral
Indication: HIV Infection
Start date: 2002-05-13
End date: 2003-04-09
Viread
Dosage: daily dose:300mg
Administration route: Oral
Other drugs received by patient: Amylase; LAC B; Baktar; Baktar; Epivir; Alotec; Aspirin; Mexitil; Sulfamethoxazole W / Trimethoprim
Adverse event in 49 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-20
Patient: 49 year old male, weighing 52.0 kg (114.4 pounds)
Adverse reactions / side effects: Weight Decreased, Speech Disorder, Pancreatitis Acute, Vomiting, Nausea, Diabetes Mellitus, Lactic Acidosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Zerit
Administration route: Oral
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Kaletra
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Kivexa
Indication: HIV Infection
Start date: 2007-04-15
End date: 2007-06-13
Viracept
Indication: HIV Infection
Start date: 1998-04-01
End date: 2006-12-09
Other drugs received by patient: Bactrim; Lipanthyl; Rivotril; Laroxyl
Adverse event in 56 year old female receiving Kaletra (Lopinavir / Ritonavir)
Reported by a individual with unspecified qualification from Czech Republic on 2007-07-11
Patient: 56 year old female, weighing 41.0 kg (90.2 pounds)
Adverse reactions / side effects: Vomiting, Bronchopneumonia, Nausea, General Physical Health Deterioration, Oesophageal Candidiasis, Cachexia, Communication Disorder, Iron Deficiency Anaemia, HIV Infection CDC Category C3, Cardiopulmonary Failure, Thrombocytopenia, Leukopenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Trizivir
Adverse event in 39 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from Japan on 2007-06-26
Patient: 39 year old male
Adverse reactions / side effects: Vomiting, Neurogenic Bladder, Nasopharyngitis, Nausea, Costovertebral Angle Tenderness, Urinary Tract Infection, Pyrexia, Epilepsy, Eating Disorder, Convulsion, Ascites, Blood Potassium Decreased, Tenderness, Pyuria, Pyelonephritis
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 1996-12-18
End date: 1997-03-13
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Start date: 1998-07-10
End date: 1999-10-31
Epivir
Administration route: Oral
Start date: 1999-11-01
End date: 2003-03-31
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Start date: 2003-04-01
End date: 2003-04-26
Epivir
Dosage: 150mg twice per day
Administration route: Oral
Start date: 2004-07-28
Ziagen
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-04-27
End date: 2003-12-24
Ziagen
Dosage: 300mg twice per day
Administration route: Oral
Start date: 2004-05-28
End date: 2004-06-29
Ziagen
Dosage: 300mg twice per day
Administration route: Oral
Start date: 2004-12-17
Kaletra
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-06-30
End date: 2006-11-23
Other drugs received by patient: Kaletra
Adverse event in female receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-25
Patient: female, weighing 2.2 kg (4.8 pounds)
Adverse reactions / side effects: Accidental Overdose, Electroencephalogram Abnormal, Malaise, Sinoatrial Block, Oxygen Saturation Decreased, Renal Failure Acute, Vomiting, Premature Baby, Nodal Rhythm, Blood Potassium Increased, Staphylococcal Sepsis, Drug Prescribing Error, Cardiogenic Shock, Arrhythmia, Haemoglobin Decreased, Bradycardia, Anion GAP Decreased, Neonatal Respiratory Arrest
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra
Administration route: Oral
Indication: Blood HIV RNA
Start date: 2007-03-29
End date: 2007-03-29
Kaletra
Indication: Drug Exposure During Pregnancy
Other drugs received by patient: Ritonavir; Lamivudine; Abacavir
Adverse event in 60 year old female receiving Kaletra (Lopinavir / Ritonavir)
Reported by a consumer/non-health professional from France on 2007-06-18
Patient: 60 year old female, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Fatigue, Hypersensitivity, Vomiting, Diarrhoea, Headache, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Kivexa
Dosage: 1unit per day
Administration route: Oral
Start date: 2007-01-13
End date: 2007-02-02
Kaletra
Dosage: 2unit twice per day
Administration route: Oral
Start date: 2007-01-13
End date: 2007-02-02
Other drugs received by patient: Mepronizine; Tercian; Athymil; Alprazolam
Adverse event in female receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-15
Patient: female, weighing 2.2 kg (4.8 pounds)
Adverse reactions / side effects: Accidental Overdose, Electroencephalogram Abnormal, Malaise, Sinoatrial Block, Oxygen Saturation Decreased, Renal Failure Acute, Vomiting, Premature Baby, Incorrect Dose Administered, Nodal Rhythm, Blood Potassium Increased, Staphylococcal Sepsis, Cardiogenic Shock, Arrhythmia, Haemoglobin Decreased, Bradycardia, Anion GAP Decreased, Neonatal Respiratory Arrest
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra
Administration route: Oral
Indication: Blood HIV RNA
Start date: 2007-03-29
End date: 2007-03-29
Kaletra
Indication: Drug Exposure During Pregnancy
Other drugs received by patient: Ritonavir; Lamivudine; Abacavir
Adverse event in female receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-04
Patient: female, weighing 2.2 kg (4.8 pounds)
Adverse reactions / side effects: Vomiting, Incorrect Dose Administered, Blood Potassium Increased, Accidental Overdose, Haemoglobin Decreased, Electroencephalogram Abnormal, Malaise, Bradycardia, Sinoatrial Block, Neonatal Respiratory Arrest, Renal Failure Acute, Oxygen Saturation Decreased, Anion GAP Decreased
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Ritonavir; Lamivudine; Abacavir
Adverse event in 50 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a consumer/non-health professional from United Kingdom on 2007-04-30
Patient: 50 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Vomiting, Lactic Acidosis, Renal Failure Acute
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Zidovudine
Dosage: 250mg per day
Start date: 2005-07-01
End date: 2005-12-27
Kaletra
Dosage: 3unit twice per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-16
End date: 2005-12-27
Lopinavir
Dosage: 3unit twice per day
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Videx
Dosage: 400mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-16
End date: 2005-12-27
Viread
Dosage: 245mg per day
Administration route: Oral
Start date: 2004-11-16
End date: 2005-12-27
Diclofenac
Dosage: 50mg three times per day
Administration route: Oral
Indication: Pain
Start date: 2005-12-19
End date: 2005-12-26
Other drugs received by patient: Gabapentin; MS Contin; Acyclovir
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from Mexico on 2007-04-16
Patient: male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Vomiting, Pneumonia, Nausea, Lung Neoplasm, Diplopia, Iiird Nerve Paralysis, Eyelid Ptosis, Escherichia Infection
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Trimetroprim; Fluconazole; Clindamycin; Pirimetamine; Folinic Acid; Metamizol; Sulfamethoxazole
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from France on 2007-04-03
Patient: male, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Back Pain, Vomiting, Nausea, Hyperkalaemia, Lactic Acidosis, Renal Failure, Diarrhoea, Gastrointestinal Disorder
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-24
End date: 2007-02-09
Truvada
Administration route: Oral
End date: 2007-02-18
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-24
End date: 2007-02-09
Other drugs received by patient: Reyataz; Ritonavir; Bactrim DS
Adverse event in 50 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a consumer/non-health professional from United Kingdom on 2007-04-02
Patient: 50 year old male
Adverse reactions / side effects: Vomiting, Lactic Acidosis, Renal Failure Acute
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Zidovudine
Dosage: 250mg per day
Indication: HIV Infection
Start date: 2005-07-01
End date: 2005-12-27
Kaletra
Dosage: 3unit twice per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-01
End date: 2005-12-27
Lopinavir
Dosage: 3unit twice per day
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Videx
Dosage: 400mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-01
Viread
Dosage: 245mg per day
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Other drugs received by patient: Diclofenac Sodium; Gabapentin; MS Contin; Acyclovir
Adverse event in 55 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a individual with unspecified qualification from Japan on 2007-04-02
Patient: 55 year old male
Adverse reactions / side effects: Ventricular Extrasystoles, Chest Discomfort, Vomiting, Nausea, Headache, Sick Sinus Syndrome, Malaise, Palpitations, Diarrhoea, Dizziness, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Viracept
Dosage: daily dose:2500mg
Administration route: Oral
Indication: HIV Infection
Stocrin
Dosage: daily dose:600mg
Administration route: Oral
Indication: HIV Infection
Start date: 2001-03-23
End date: 2005-07-14
Ziagen
Dosage: daily dose:600mg
Administration route: Oral
Indication: HIV Infection
Start date: 2001-04-06
End date: 2003-04-08
Kaletra
Dosage: text:6 dosage form
Administration route: Oral
Indication: HIV Infection
Start date: 2002-05-13
End date: 2003-04-09
Other drugs received by patient: Amylase; LAC B; Baktar; Viread; Epivir
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from Mexico on 2007-03-30
Patient: male, weighing 62.5 kg (137.5 pounds)
Adverse reactions / side effects: Abdominal Pain, Vomiting, Abdominal Distension, Infrequent Bowel Movements
Adverse event resulted in: hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Lamivudine + Zidovudine; Fluconazole
Adverse event in 50 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a pharmacist from United Kingdom on 2007-03-30
Patient: 50 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Vomiting, Therapeutic Agent Toxicity, Post Herpetic Neuralgia, Lactic Acidosis, Renal Failure Acute, Herpes Zoster Multi-Dermatomal
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-01
End date: 2005-12-27
Lopinavir
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Viread
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Zidovudine
Indication: HIV Infection
Start date: 2005-07-01
End date: 2005-12-27
Didanosine
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-01
Kaletra
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-01
End date: 2005-12-27
Lopinavir
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Viread
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Zidovudine
Indication: HIV Infection
Start date: 2005-07-01
End date: 2005-12-27
Didanosine
Indication: Drug USE FOR Unknown Indication
Start date: 2004-11-01
Adverse event in 50 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-28
Patient: 50 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Vomiting, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Blood Bicarbonate Decreased, Lactic Acidosis, Renal Failure Acute
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Zidovudine
Administration route: Oral
Indication: HIV Infection
Start date: 2005-07-01
End date: 2005-12-27
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Lopinavir
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Videx
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Zidovudine
Administration route: Oral
Indication: HIV Infection
Start date: 2005-07-01
End date: 2005-12-27
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Lopinavir
Indication: HIV Infection
Start date: 2004-11-16
End date: 2005-12-27
Other drugs received by patient: Diclofenac Sodium; MS Contin; Gabapentin; Diclofenac Sodium; MS Contin; Gabapentin
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from France on 2007-03-20
Patient: male, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Back Pain, Vomiting, Nausea, Hyperkalaemia, Lactic Acidosis, Renal Failure, Diarrhoea, Gastrointestinal Disorder
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-24
End date: 2007-02-09
Truvada
Administration route: Oral
Start date: 2007-02-14
End date: 2007-02-18
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-24
End date: 2007-02-09
Other drugs received by patient: Reyataz; Ritonavir; Bactrim DS
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from Mexico on 2007-03-09
Patient: male, weighing 62.5 kg (137.5 pounds)
Adverse reactions / side effects: Abdominal Pain, Vomiting, Abdominal Distension, Infrequent Bowel Movements
Adverse event resulted in: hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Lamivudine + Zidovudine; Fluconazole
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from Mexico on 2007-03-09
Patient: male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Vomiting, Pneumonia, Nausea, Lung Neoplasm, Eyelid Ptosis, Escherichia Infection
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kaletra (Lopinavir / Ritonavir)
Other drugs received by patient: Trimetroprim; Fluconazole; Cefotaxime; Clindamycin; Pirimetamine; Folinic Acid; Metamizol
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from Japan on 2007-03-08
Patient: male
Adverse reactions / side effects: Abdominal Pain, Vomiting, Nausea, Subileus, Enterocolitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2005-09-30
End date: 2005-11-02
Kaletra
Administration route: Oral
Start date: 2005-11-07
End date: 2005-12-01
Kaletra
Administration route: Oral
Start date: 2006-01-11
End date: 2006-01-24
Kaletra
Administration route: Oral
Start date: 2006-03-22
Other drugs received by patient: Lamivudine; Lamivudine; Lamivudine; Lamivudine; Stavudine; Stavudine; Stavudine; Stavudine; Bactrim; Flunitrazepam; Flunitrazepam; Clonazepam; Magnesium Oxide
Adverse event in 45 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a physician from United States on 2007-02-22
Patient: 45 year old male
Adverse reactions / side effects: Oral Intake Reduced, Vomiting, Nausea, Blood Creatinine Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Valtrex
Indication: Herpes Simplex
End date: 2006-12-01
Truvada
Indication: HIV Infection
Start date: 2005-12-29
End date: 2006-12-28
Kaletra
Administration route: Oral
Start date: 2005-12-29
End date: 2006-12-28
Prinzide
Start date: 2006-04-24
End date: 2006-12-01
Other drugs received by patient: Paxil; Proscar; Vistaril; Prevacid
Adverse event in 55 year old male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-01-31
Patient: 55 year old male
Adverse reactions / side effects: Ventricular Extrasystoles, Vomiting, Chest Discomfort, Supraventricular Extrasystoles, Nausea, Extrasystoles, Headache, Sick Sinus Syndrome, Malaise, Palpitations, Diarrhoea, Dizziness, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-05-13
End date: 2002-07-15
Kaletra
Administration route: Oral
Start date: 2003-04-09
End date: 2003-04-09
Efavirenz
Administration route: Oral
Indication: HIV Infection
Start date: 2001-03-23
End date: 2002-05-13
Efavirenz
Start date: 2003-04-09
End date: 2003-04-09
Efavirenz
Start date: 2003-04-25
End date: 2003-05-21
Efavirenz
Start date: 2004-10-04
Abacavir Sulfate
Administration route: Oral
Indication: HIV Infection
Start date: 2001-04-06
End date: 2003-04-08
Nelfinavir Mesilate
Administration route: Oral
Indication: HIV Infection
Start date: 2003-04-25
End date: 2004-05-21
Nelfinavir Mesilate
Start date: 2004-10-04
Other drugs received by patient: Aspergillus Oryzae Enzyme Extract; LAC-B; Bactrim; Viread; Lamivudine; Tenofovir; Tenofovir; Aspirin; Aspirin
Adverse event in male receiving Kaletra (Lopinavir / Ritonavir)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-31
Patient: male
Adverse reactions / side effects: Ventricular Extrasystoles, Chest Discomfort, Vomiting, Nausea, Supraventricular Extrasystoles, Extrasystoles, Retinal Vein Occlusion, Headache, Arrhythmia, Sick Sinus Syndrome, Malaise, Anhedonia, Palpitations, Diarrhoea, Dizziness, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-05-13
End date: 2002-07-15
Kaletra
Administration route: Oral
Start date: 2003-04-09
End date: 2003-04-09
Efavirenz
Administration route: Oral
Indication: HIV Infection
Start date: 2001-03-23
End date: 2002-05-13
Efavirenz
Administration route: Oral
Start date: 2003-04-09
End date: 2003-04-09
Efavirenz
Administration route: Oral
Start date: 2003-04-25
End date: 2004-05-21
Efavirenz
Administration route: Oral
Start date: 2004-10-04
End date: 2005-07-14
Abacavir Sulfate
Administration route: Oral
Indication: HIV Infection
Start date: 2001-04-06
End date: 2003-04-08
Nelfinavir Mesilate
Administration route: Oral
Indication: HIV Infection
Start date: 2003-04-25
End date: 2004-05-21
Nelfinavir Mesilate
Administration route: Oral
Start date: 2004-10-04
Other drugs received by patient: Bactrim; Bactrim; Bactrim; Bactrim; Bactrim; Lamivudine; Abacavir Sulfate; Didanosine; Viread; Viread; Viread; Concentrated Glycerin Fructose; Digestive Enzyme Preparations; Digestive Enzyme Preparations; Digestive Enzyme Preparations; Berizym; Acetylsalicylic Acid; Acetylsalicylic Acid; Aspergillus Oryzae Enzyme Extract; Lactobacillus Bifidus, Lyophilized
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