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

 
 



Index of reports > Cases with Diarrhoea (38)

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

 Reports 1 - 30 of 38   Next >>

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 male

Reported by a physician from France on 2012-08-16

Patient: male

Reactions: Agitation, Urinary Incontinence, Coma, Coma Scale Abnormal, Pyrexia, Hepatotoxicity, Eye Movement Disorder, Hepatosplenomegaly, Anaemia, Malnutrition, General Physical Health Deterioration, Encephalopathy, Faecal Incontinence, Convulsion, Respiratory Tract Congestion, Apathy, Depressed Level of Consciousness, Nervous System Disorder, Confusional State, Immune Reconstitution Syndrome, Snoring, Hepatitis Cholestatic, Intracranial Pressure Increased, Hepatic Ischaemia, Thrombocytopenia, Oxygen Saturation Decreased, Refusal of Treatment by Patient, Necrotising Granulomatous Lymphadenitis, Hepatic Fibrosis, Mycobacterial Infection, Hyponatraemia, Cerebral Atrophy, White Blood Cell Disorder, Renal Failure, Hypoproteinaemia, Diarrhoea, Brain Abscess, Heart Rate Increased, Encephalitic Infection, Heart Sounds Abnormal

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Bactrim
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Olanzapine
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-01

Clarithromycin
    Dosage: df 50mg/ml
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Nefopam
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Prazepam
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Truvada
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-03-01

Viramune
    Indication: HIV Infection
    Start date: 2012-03-01
    End date: 2012-05-01

Myambutol
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Amikacin
    Dosage: 900 mg daily
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Cernevit-12
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Rifabutin
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Folic Acid
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Kaletra
    Dosage: df 80/20 mg
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-03-01

Perikabiven (Parenteral Nutrition)
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Isentress
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-05-01

Potassium Chloride
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Acetaminophen
    Dosage: df 10mg/ml
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Other drugs received by patient: Propofol; Adavat



Possible Kaletra side effects in male

Reported by a physician from France on 2012-08-15

Patient: male

Reactions: Agitation, Urinary Incontinence, Coma, Pyrexia, Coma Scale Abnormal, Hepatotoxicity, Eye Movement Disorder, Hepatosplenomegaly, Anaemia, Malnutrition, Encephalopathy, Faecal Incontinence, General Physical Health Deterioration, Convulsion, Apathy, Respiratory Tract Congestion, Depressed Level of Consciousness, Nervous System Disorder, Confusional State, Immune Reconstitution Syndrome, Snoring, Hepatitis Cholestatic, Intracranial Pressure Increased, Hepatic Ischaemia, Thrombocytopenia, Oxygen Saturation Decreased, Refusal of Treatment by Patient, Necrotising Granulomatous Lymphadenitis, Hepatic Fibrosis, Mycobacterial Infection, Cerebral Atrophy, Hyponatraemia, Renal Failure, White Blood Cell Disorder, Diarrhoea, Hypoproteinaemia, Heart Rate Increased, Brain Abscess, Encephalitic Infection, Heart Sounds Abnormal

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Olanzapine
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-01

Clarithromycin
    Dosage: df 50mg/ml
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Bactrim
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Amikacin
    Dosage: 900 mg daily
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Acetaminophen
    Dosage: df 10mg/ml
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Perikabiven (Parenteral Nutrition)
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Rifabutin
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Cernevit-12
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Nefopam
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-07-16

Viramune
    Indication: HIV Infection
    Start date: 2012-03-01
    End date: 2012-05-01

Myambutol
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Potassium Chloride
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Folic Acid
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Isentress
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-05-01

Kaletra
    Dosage: df 80/20 mg
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-03-01

Prazepam
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Truvada
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-03-01

Other drugs received by patient: Adavat; Propofol



Possible Kaletra side effects in male

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

Patient: male

Reactions: Confusional State, Agitation, Refusal of Treatment by Patient, Malnutrition, Anaemia, Coma, General Physical Health Deterioration, Pyrexia, Convulsion, Apathy, Hepatotoxicity, Diarrhoea, Thrombocytopenia

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Rifabutin
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Bactrim
    Dosage: 800 mg, qd
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-13

Acetaminophen
    Dosage: unk
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Truvada
    Dosage: unk
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-03-01

Potassium Chloride
    Dosage: unk
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Leucovorin Calcium
    Dosage: unk
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Kaletra
    Dosage: unk
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-03-01

Cernevit / 01027001 /
    Dosage: unk
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10
    End date: 2012-08-02

Perikabiven
    Dosage: unk
    Indication: Parenteral Nutrition
    Start date: 2012-07-10

Isentress
    Dosage: unk
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-05-01

Acupan
    Dosage: 120 mg, unk
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-16
    End date: 2012-07-27

Olanzapine
    Dosage: 1 df, unk
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-01

Amikacin
    Dosage: 900 mg, unk
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Prazepam
    Dosage: 1 df, qd
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-10

Myambutol
    Dosage: 2 df, qd
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11

Clarithromycin
    Dosage: 500 mg, qd
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-11



Possible Kaletra side effects in female

Reported by a consumer/non-health professional from Australia on 2012-08-10

Patient: female

Reactions: Pneumonia Aspiration, Diarrhoea, Intestinal Prolapse, Pneumothorax, Impaired Gastric Emptying, Gastric Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Truvada
    Indication: Product Used FOR Unknown Indication

Kaletra
    Indication: HIV Infection
    Start date: 2010-06-01



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 consumer/non-health professional from Australia on 2012-06-05

Patient: female

Reactions: Pneumonia Aspiration, Intestinal Prolapse, Diarrhoea, Pneumothorax, Impaired Gastric Emptying, Gastric Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra
    Indication: HIV Infection
    Start date: 2010-06-01

Truvada
    Indication: Product Used FOR Unknown Indication



Possible Kaletra side effects in 65 year old male

Reported by a physician from Korea, Republic of on 2012-05-29

Patient: 65 year old male

Reactions: White Blood Cell Count Decreased, Pneumonia, Anaemia, Hepatic Failure, Haemoglobin Decreased, Renal Failure, Diarrhoea, Sepsis, Dizziness, Bone Marrow Failure, Diarrhoea Infectious, Leukopenia, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Azt(zdv); Megace Suspension 40mg / 240ml; CJ 20% Dextrose Water 0.2g / ML 1000ml; ABC; TS TAB; Cebatrim INJ; Dapsone; Ziagen; Norpine; Combivir; Lamivudine (Epivir Hbv)



Possible Kaletra side effects in female

Reported by a physician from France on 2012-05-29

Patient: female

Reactions: Cholelithiasis, Diarrhoea, Clostridium Test Positive, Cytolytic Hepatitis, Hyperuricaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pyrazinamide
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-11-10
    End date: 2012-01-07

Combivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-11-10
    End date: 2012-01-10

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-11-10
    End date: 2012-01-10

Myambutol
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-11-10
    End date: 2012-01-07

Other drugs received by patient: Isoniazid; Rifampicin



Possible Kaletra side effects in female

Reported by a physician from Guinea-Bissau on 2012-05-25

Patient: female

Reactions: Diarrhoea

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Lamivudine; Zidovudine; Folic Acid; Cotrim



Possible Kaletra side effects in female

Reported by a physician from France on 2012-05-22

Patient: female

Reactions: Diarrhoea, Cytolytic Hepatitis, Maternal Exposure During Pregnancy, Hyperuricaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pyrazinamide
    Dosage: 1000mg per day
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-11-10
    End date: 2012-01-07

Myambutol
    Dosage: 800mg per day
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-11-10
    End date: 2012-01-07

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-11-10
    End date: 2012-01-10

Combivir
    Dosage: 2unit per day
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-11-10
    End date: 2012-01-10

Other drugs received by patient: Rifadin; Rimifon



Possible Kaletra side effects in female

Reported by a physician from France on 2012-05-21

Patient: female

Reactions: Cholelithiasis, Diarrhoea, Clostridium Test Positive, Cytolytic Hepatitis, Lymph Node Tuberculosis, Hyperuricaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-11-10
    End date: 2012-01-10

Combivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2011-11-10
    End date: 2012-01-10

Myambutol
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-11-10
    End date: 2012-01-07

Pyrazinamide
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-11-10
    End date: 2012-01-07

Other drugs received by patient: Isoniazid; Rifampicin



Possible Kaletra side effects in 65 year old male

Reported by a physician from Korea, Republic of on 2012-05-18

Patient: 65 year old male, weighing 67.0 kg (147.4 pounds)

Reactions: Nausea, Diarrhoea, Insomnia, General Physical Health Deterioration

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Meckool; Smofilpid; Macperan; Glamin; 3-TC Complex; Spatam; Cefriaxone; Trizel; Cefriaxone; Spatam; Cirok; Flasinyl



Possible Kaletra side effects in female

Reported by a physician from Guinea-Bissau on 2012-05-18

Patient: female

Reactions: Diarrhoea

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Zidovudine; Folic Acid; Cotrim; Lamivudine (Epivir Hbv)



Possible Kaletra side effects in 65 year old male

Reported by a physician from Korea, Republic of on 2012-04-25

Patient: 65 year old male, weighing 67.0 kg (147.4 pounds)

Reactions: Diarrhoea, Nausea, Insomnia, General Physical Health Deterioration

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: 3-TC Complex; Macperan; Meckool; Smofilpid; Flasinyl; Cirok; Glamin; Cefriaxone; Cefriaxone; Spatam; Spatam; Trizel



Possible Kaletra side effects in male

Reported by a physician from Korea, Republic of on 2012-04-12

Patient: male

Reactions: Nausea, Diarrhoea, Insomnia, General Physical Health Deterioration

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Smofilpid; Cefriaxone; Glamin; Flasinyl; 3TC / AZT; Macperan; Meckool; Cefriaxone; Spatam; Cirok; Spatam; Trizel



Possible Kaletra side effects in 54 year old female

Reported by a physician from United Kingdom on 2012-04-12

Patient: 54 year old female

Reactions: Vomiting, Nausea, Diarrhoea, Blood Creatinine Increased, Renal Failure Acute

Drug(s) suspected as cause:
Truvada
    Indication: Prophylaxis Against HIV Infection
    Start date: 2012-03-15
    End date: 2012-03-19

Kaletra
    Administration route: Oral
    Indication: Prophylaxis Against HIV Infection
    Start date: 2012-03-15
    End date: 2012-03-19



Possible Kaletra side effects in 65 year old male

Reported by a physician from Korea, Republic of on 2012-04-09

Patient: 65 year old male

Reactions: White Blood Cell Count Decreased, Pneumonia, Anaemia, Hepatic Failure, Haemoglobin Decreased, Renal Failure, Diarrhoea, Sepsis, Bone Marrow Failure, Diarrhoea Infectious, Leukopenia, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Norpine; TS TAB; ABC; Dapsone; Combivir; Cebatrim INJ; Lamivudine (Epivir Hbv); Megace Suspension 40mg / 240ml; Azt(zdv); CJ 20% Dextrose Water 0.2g / ML 1000ml; Ziagen



Possible Kaletra side effects in 32 year old male

Reported by a physician from Korea, Republic of on 2012-04-06

Patient: 32 year old male

Reactions: Pruritus, Diarrhoea, Herpes Zoster, Cough

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: 3TC / AZT; Combivir; SK Influenza Vaccine



Possible Kaletra side effects in 41 year old male

Reported by a physician from Japan on 2012-03-28

Patient: 41 year old male

Reactions: Pancreatitis Acute, Death, Hyperlipidaemia, Hyperlactacidaemia, Amylase Increased, Neuropathy Peripheral, Diarrhoea, Lactic Acidosis, Renal Failure Acute

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

Drug(s) suspected as cause:
Fosamprenavir Calcium
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-08-04

Combivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-02-13
    End date: 2001-05-10

Epivir
    Dosage: therapy interrupted on 09-jan-2000, discontinued on 06-jul-2001.
    Administration route: Oral
    Start date: 1996-10-01
    End date: 2001-07-06

Saquinavir Mesylate
    Indication: HIV Infection
    Start date: 2001-01-05
    End date: 2001-03-08

Ziagen
    Dosage: therapy interrupted from 08-dec-2000 to 05-jun-2001
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2000-01-24
    End date: 2001-07-06

Somatropin
    Indication: Weight Decreased
    Start date: 2001-03-19
    End date: 2001-11-12

Raltegravir
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2008-09-26

Zerit
    Dosage: ongoing 01-aug-1995 to 01-mar-1996 and 01-apr-1998 to 08-dec-2000.
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 1995-08-01
    End date: 2000-12-08

Efavirenz
    Dosage: therapy interp 12/8/00,restarted 3/9/01,interrupt7/01,+restarted 7/23/01-25sep8(2622 days)
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2000-01-10
    End date: 2008-09-25

Prezista
    Dosage: tabs
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-09-26

Videx
    Dosage: ongoing 01/sept/1993 - 01/aug/1994; 01/mar/1996 - 01/oct/1996; and 10/jan/2000 - 08/dec/2000
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 1993-09-01
    End date: 2000-12-08

Truvada
    Dosage: 1 df = 1 tablet
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-09-26
    End date: 2009-10-01

Kaletra
    Dosage: 8 caps 9mar-6jul01, restarted 23jul01 stopped 4oct6 reduced to 6 tabs from 05oct6-15sep8 (1900 days)
    Indication: HIV Infection
    Start date: 2001-03-09
    End date: 2008-09-25

Norvir
    Dosage: 05jan01 to 04feb01, 05feb01 to 08mar01 and 26sep08 to ongoing.
    Indication: HIV Infection
    Start date: 2001-01-05

Amprenavir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-07-23
    End date: 2005-08-03

Other drugs received by patient: Retrovir; Viracept; Recombinate; Loperamide HCL; Crixivan; Octocog Alpha; Loperamide HCL; OIF



Possible Kaletra side effects in female

Reported by a physician from Spain on 2012-03-23

Patient: female, weighing 44.0 kg (96.8 pounds)

Reactions: Diarrhoea, Purpura

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Methadone HCL; Lorazepam; Gabapentin



Possible Kaletra side effects in 46 year old male

Reported by a physician from Spain on 2012-03-23

Patient: 46 year old male, weighing 66.0 kg (145.2 pounds)

Reactions: Abdominal Discomfort, Abdominal Pain, Diarrhoea

Drug(s) suspected as cause:
Combivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2007-01-01

Kaletra
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2007-01-01
    End date: 2012-03-06



Possible Kaletra side effects in 67 year old female

Reported by a physician from Korea, Republic of on 2012-03-08

Patient: 67 year old female

Reactions: Jaundice, Pneumonia Fungal, Immune Reconstitution Syndrome, Hyperbilirubinaemia, Osteoporosis, Anaemia, Urinary Tract Infection, Hyponatraemia, Delirium, Herpes Zoster, Cytomegalovirus Colitis, AIDS Encephalopathy, Diarrhoea, Pneumothorax, Neutropenia, Depressed Mood, Shock

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Kaletra
    Dosage: 2 tabs, twice a day
    Administration route: Oral
    Start date: 2011-08-19
    End date: 2011-10-07

Kaletra
    Dosage: 2 tabs, twice a day
    Indication: HIV Infection
    Start date: 2011-05-18
    End date: 2011-06-16

Kaletra
    Dosage: 2 tabs, twice a day
    Start date: 2011-07-13
    End date: 2011-07-28

Other drugs received by patient: Raltegravir; Armodafinil; Armodafinil; Daihan Potassuim Choloride; Vincristine Pharmachemie; Megestrol Acetate; Sodium Bicarbonate; Greencross Albumin; Greencross Albumin; Famotidine; Thiamine HCL; Tamipool; CJ Calcium Gluconate; Tridel; Platelets, Concentrated; Dbpharm Pentamide Isethionate; Peniramine; Lasix; Mezagtam; Levofexin; Famotidine; Macperan; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Pheniramine; Cyclophosphamide; Septra; K-Contin Continus; Tamipool; CJ Calcium Gluconate; CJ Calcium Gluconate; CJ Sodium Chloride; Multi-Vitamins; Tridol; Vancomycin Hydrochloride; Peniramine; Famotidine; Zithromax; Bearse; Daihan Potassuim Choloride; Pheniramine; Emend; Nisorone; Jeil Thiamine; K-Contin Continus; Hanil Flasynil; CJ Calcium Gluconate; Masi; Dbpharm Pentamide Isethionate; Peniramine; Lasix; Lamivudine (Epivir Hbv); Famotidine; Armodafinil; Zithromax; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Pheniramine; Pheniramine; Greencross Albumin; Famotidine; Ganciclovir Sodium; Centrum; K-Contin Continus; Actonel; Stogar; JW KCL; Pheniramine; Tridol; Tylenol ER; Pantoprazole Sodium; Phosten; Peniramine; Raltegravir; Armodafinil; Daihan Potassuim Choloride; Pheniramine; Aloxi; Ganciclovir Sodium; MVH; K-Contin Continus; Sinil Thiamine HCL; Sinil Thiamine HCL; Pheniramine; Trodol; CJ Sodium Chloride; Platelets, Concentrated; K-Contin Continus; Abacavir; Daihan Potassuim Choloride; Pheniramine; Septra; Septra; Greencross Albumin; Greencross Albumin; Tamipool; Tamipool; K-Contin Continus; Daewon Megesterol Acetate Suspension; Trodol; CJ Sodium Chloride; Tridel; Platelets, Concentrated; Platelets, Concentrated; Macperan; Peniramine; Peniramine; Peniramine; Lamivudine (Epivir Hbv); Daihan Potassuim Choloride; Daihan Potassuim Choloride; Mabthera; Septra; K-Contin Continus; CJ Sodium Chloride; Packed RED Cell; Platelets, Concentrated; Platelets, Concentrated; Platelets, Concentrated; Platelets, Concentrated; Meropenem; Raltegravir; Bearse; Macperan; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Daihan Potassuim Choloride; Pheniramine; Rabeprazole Sodium; MVH; K-Contin Continus; Peniramine



Possible Kaletra side effects in 67 year old female

Reported by a pharmacist from United States on 2012-03-05

Patient: 67 year old female

Reactions: Hepatotoxicity, Diarrhoea, International Normalised Ratio Increased

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Truvada



Possible Kaletra side effects in male

Reported by a physician from Guinea-Bissau on 2012-02-24

Patient: male, weighing 45.0 kg (99.0 pounds)

Reactions: Death, Diarrhoea, Pyrexia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: AZT + 3TC; Lamivudine; Cotrim; Isoniazid; Zidovudine



Possible Kaletra side effects in 41 year old male

Reported by a physician from Japan on 2012-02-20

Patient: 41 year old male

Reactions: Pancreatitis Acute, Death, Hyperlipidaemia, Hyperlactacidaemia, Amylase Increased, Neuropathy Peripheral, Diarrhoea, Lactic Acidosis, Renal Failure Acute

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

Drug(s) suspected as cause:
Zerit
    Dosage: ongoing 01-aug-1995 to 01-mar-1996 and 01-apr-1998 to 08-dec-2000.
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 1995-08-01
    End date: 2000-12-08

Videx
    Dosage: ongoing 01/sept/1993 - 01/aug/1994; 01/mar/1996 - 01/oct/1996; and 10/jan/2000 - 08/dec/2000
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 1993-09-01
    End date: 2000-12-08

Efavirenz
    Dosage: therapy interp 12/8/00,restarted 3/9/01,interrupt7/01,+restarted 7/23/01-25sep8(2622 days)
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2000-01-10
    End date: 2008-09-25

Ziagen
    Dosage: therapy interrupted from 08-dec-2000 to 05-jun-2001
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2000-01-24
    End date: 2001-07-06

Somatropin Rdna
    Indication: Weight Decreased
    Start date: 2001-03-19
    End date: 2001-11-12

Norvir
    Dosage: 05jan01 to 04feb01, 05feb01 to 08mar01 and 26sep08 to ongoing.
    Indication: HIV Infection
    Start date: 2001-01-05

Kaletra
    Dosage: 8 caps 9mar-6jul01, restarted 23jul01 stopped 4oct6 reduced to 6 tabs from 05oct6-15sep8 (1900 days)
    Indication: HIV Infection
    Start date: 2001-03-09
    End date: 2008-09-25

Fosamprenavir Calcium
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2005-08-04

Prezista
    Dosage: tabs
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-09-26

Raltegravir
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2008-09-26

Amprenavir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-07-23
    End date: 2005-08-03

Combivir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2001-02-13
    End date: 2001-05-10

Epivir
    Dosage: therapy interrupted on 09-jan-2000, discontinued on 06-jul-2001.
    Administration route: Oral
    Start date: 1996-10-01
    End date: 2001-07-06

Truvada
    Dosage: 1 df = 1 tablet
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-09-26
    End date: 2009-10-01

Saquinavir Mesylate
    Indication: HIV Infection
    Start date: 2001-01-05
    End date: 2001-03-08

Other drugs received by patient: OIF; Loperamide HCL; Retrovir; Crixivan; Viracept; Recombinate; Loperamide HCL



Possible Kaletra side effects in 44 year old male

Reported by a physician from Greece on 2012-01-26

Patient: 44 year old male

Reactions: Weight Decreased, Diarrhoea

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra

Kaletra
    Indication: HIV Test Positive

Other drugs received by patient: Combivir; Solu-Medrol; Bactrimel; Cyclophosphamide; Cyclophosphamide; Intratect; Solu-Medrol; Intratect



Possible Kaletra side effects in 44 year old male

Reported by a physician from Greece on 2012-01-23

Patient: 44 year old male

Reactions: Weight Decreased, Diarrhoea

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kaletra
    Indication: HIV Test Positive

Kaletra

Other drugs received by patient: Cyclophosphamide; Bactrimel; Intratect; Combivir; Solu-Medrol



Possible Kaletra side effects in male

Reported by a physician from Guinea-Bissau on 2012-01-20

Patient: male, weighing 45.0 kg (99.0 pounds)

Reactions: Death, Diarrhoea, Pyrexia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: AZT + 3TC; Cotrim; Zidovudine; Lamivudine; Isoniazid



Possible Kaletra side effects in male

Reported by a physician from Mexico on 2012-01-16

Patient: male

Reactions: Weight Decreased, Drug Resistance, Dyslipidaemia, Diarrhoea, Faecal Incontinence, Kaposi's Sarcoma

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Kaletra

Other drugs received by patient: Enterogermina; Truvada; Calcium Carbonate



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