Index of reports
> Hospitalization (306)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Kaletra (Lopinavir / Ritonavir) hospitalization. The selected reports were submitted to the FDA during the sample period of about a year.
Reports 1 - 30 of 306 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:
Invirase
Dosage: divided dose requency u
Administration route: Oral
Indication: HIV Infection
Start date: 2006-10-26
Isentress
Dosage: divided dose frequency unknown
Administration route: Oral
Indication: HIV Infection
Start date: 2008-07-31
End date: 2011-08-07
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
Kaletra
Dosage: divided dose frequency unknown
Administration route: Oral
Indication: HIV Infection
Start date: 2002-09-03
End date: 2004-08-04
Other drugs received by patient: Halcion
Possible Kaletra side effects in male
Reported by a physician from Chile on 2012-08-24
Patient: male, weighing 87.0 kg (191.4 pounds)
Reactions: Asthmatic Crisis
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Lamivudine (Epivir Hbv); Escitalopram; Valproic Acid; Flemar; Clotiazepam; Acyclovir
Possible Kaletra side effects in female
Reported by a physician from France on 2012-08-24
Patient: female
Reactions: Cholestasis of Pregnancy, Maternal Exposure During Pregnancy, Adverse Reaction
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Abacavir Sulfate / Lamivudine
Dosage: 1tab per day
Administration route: Oral
Indication: Antiviral Prophylaxis
Start date: 2012-03-05
End date: 2012-03-19
Combivir
Dosage: 1tab twice per day
Administration route: Oral
Indication: Antiviral Prophylaxis
Start date: 2012-03-19
End date: 2012-05-24
Kaletra
Dosage: 2tab twice per day
Administration route: Oral
Indication: Antiviral Prophylaxis
Start date: 2012-03-19
End date: 2012-05-24
Possible Kaletra side effects in male
Reported by a physician from United States on 2012-08-23
Patient: male, weighing 2.6 kg (5.7 pounds)
Reactions: Foetal Growth Restriction, Premature Baby, Foetal Exposure During Pregnancy
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Indication: Maternal Exposure Timing Unspecified
Norvir
Indication: Maternal Exposure Timing Unspecified
Other drugs received by patient: Combivir; Zidovudine; Darunavir Ethanolate
Possible Kaletra side effects in female
Reported by a physician from Israel on 2012-08-23
Patient: female
Reactions: Caesarean Section
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Combivir
Possible Kaletra side effects in
Reported by a physician from Japan on 2012-08-22
Patient:
Reactions: Diabetes Mellitus, Hypertriglyceridaemia
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Epivir
Dosage: 150 mg, bid
Administration route: Oral
Indication: HIV Infection
Start date: 2003-09-16
End date: 2006-02-28
Epivir
Dosage: 150 mg, bid
Administration route: Oral
Start date: 2008-12-16
Intelence
Dosage: 200 mg, bid
Administration route: Oral
Indication: HIV Infection
Start date: 2009-02-11
Isentress
Dosage: 800 mg divided dose frequency u
Administration route: Oral
Start date: 2008-08-05
Kaletra
Dosage: 4 df
Administration route: Oral
Indication: HIV Infection
Start date: 2007-07-04
End date: 2008-01-08
Prezista
Dosage: 1200 mg
Administration route: Oral
Indication: HIV Infection
Start date: 2008-01-09
End date: 2008-05-01
Truvada
Dosage: 1 df, unk
Administration route: Oral
Start date: 2008-08-05
End date: 2008-12-15
Truvada
Dosage: 1df
Administration route: Oral
Indication: HIV Infection
Start date: 2007-07-04
End date: 2008-05-01
Zerit
Dosage: 60 mg divided dose frequency u
Administration route: Oral
Start date: 2008-12-16
End date: 2009-02-10
Zerit
Dosage: 80 mg
Administration route: Oral
Indication: HIV Infection
Start date: 2003-09-16
End date: 2006-02-28
Other drugs received by patient: Rhythmy
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:
Abacavir
Administration route: Oral
Indication: HIV Infection
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
Isentress
Dosage: 800mg daily
Administration route: Oral
Indication: HIV Infection
Start date: 2011-08-07
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
Kaletra
Administration route: Oral
Start date: 2004-08-31
End date: 2006-09-21
Stavudine
Administration route: Oral
Indication: HIV Infection
Start date: 2002-04-01
End date: 2004-08-04
Tenofovir Disoproxil Fumarate
Administration route: Oral
Indication: HIV Infection
Start date: 2004-08-31
End date: 2006-09-21
Other drugs received by patient: Glycyron; Saquinavir; Allopurinol; Bifidobacterium; Loperamide HCL; Allopurinol
Possible Kaletra side effects in female
Reported by a pharmacist from France on 2012-08-20
Patient: female
Reactions: Cholestasis of Pregnancy, Gestational Diabetes, Adverse Reaction
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-19
End date: 2012-05-24
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2012-03-19
End date: 2012-05-24
Other drugs received by patient: Isentress; Truvada
Possible Kaletra side effects in female
Reported by a physician from Russian Federation on 2012-08-17
Patient: female
Reactions: Umbilical Cord Abnormality, Anaemia, Placental Disorder, PRE-Eclampsia, Enterocolitis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Epivir
Indication: Product Used FOR Unknown Indication
Kaletra
Indication: HIV Infection
Start date: 2012-02-17
Kaletra
Nikavir
Indication: HIV Infection
Other drugs received by patient: Valcit; Elevit; Folic Acid; Kipferon; Erythromycin; Combivir; Wobenzym; Hexicon Suppositories; Trichopol; Acyclovir
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:
Kaletra
Dosage: 4 dosage forms daily
Administration route: Oral
Indication: HIV Infection
Start date: 2007-09-12
End date: 2011-01-14
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
Other drugs received by patient: Zerit; Lamivudine
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:
Acetaminophen
Dosage: df 10mg/ml
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
End date: 2012-07-16
Amikacin
Dosage: 900 mg daily
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
End date: 2012-07-16
Cernevit-12
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
End date: 2012-07-16
Clarithromycin
Dosage: df 50mg/ml
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
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
Myambutol
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
Olanzapine
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-01-01
Perikabiven (Parenteral Nutrition)
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
End date: 2012-07-16
Potassium Chloride
Administration route: Oral
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
Rifabutin
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-11
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
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:
Acetaminophen
Dosage: df 10mg/ml
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
Bactrim
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
Cernevit-12
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
End date: 2012-07-16
Clarithromycin
Dosage: df 50mg/ml
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
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
Myambutol
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
Olanzapine
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-01-01
Perikabiven (Parenteral Nutrition)
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
Potassium Chloride
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-07-10
Prazepam
Administration route: Oral
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
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
Other drugs received by patient: Adavat; Propofol
Possible Kaletra side effects in male
Reported by a consumer/non-health professional from Canada on 2012-08-13
Patient: male
Reactions: Weight Decreased, Pneumonia, Tuberculosis, Pleural Effusion, Brain Neoplasm
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
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:
Kaletra
Indication: HIV Infection
Start date: 2010-06-01
Truvada
Indication: Product Used FOR Unknown Indication
Possible Kaletra side effects in male
Reported by a physician from Germany on 2012-08-09
Patient: male
Reactions: Suicidal Ideation
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Novaminosulfon; Diclofenac; Isentress
Possible Kaletra side effects in male
Reported by a physician from United States on 2012-08-09
Patient: male, weighing 2.6 kg (5.7 pounds)
Reactions: Foetal Growth Restriction, Premature Baby, Foetal Exposure During Pregnancy
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Indication: Maternal Exposure Timing Unspecified
Norvir
Indication: Maternal Exposure Timing Unspecified
Other drugs received by patient: Darunavir Ethanolate; Zidovudine; Combivir
Possible Kaletra side effects in 42 year old male
Reported by a physician from Germany on 2012-08-08
Patient: 42 year old male, weighing 82.0 kg (180.4 pounds)
Reactions: Meniscal Degeneration, Arthralgia, Chondrocalcinosis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Isentress; Cialis; Enalapril Maleate
Possible Kaletra side effects in male
Reported by a physician from United States on 2012-08-08
Patient: male, weighing 2.1 kg (4.6 pounds)
Reactions: Atrial Septal Defect, Congenital Anaemia, Cardiac Murmur, Dysmorphism, Premature Baby, Foetal Exposure During Pregnancy, Jaundice Neonatal, Ascites
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Combivir
Dosage: 2tab per day
Indication: Antiretroviral Therapy
Start date: 2011-09-22
Kaletra
Dosage: 4tab per day
Indication: Antiretroviral Therapy
Start date: 2011-09-22
Other drugs received by patient: Metronidazole
Possible Kaletra side effects in 9 year old female
Reported by a consumer/non-health professional from Ireland on 2012-08-08
Patient: 9 year old female
Reactions: Regurgitation, Aphagia, Malaise, Nausea, Insomnia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Epivir
Indication: Product Used FOR Unknown Indication
Kaletra
Indication: Product Used FOR Unknown Indication
Maxolon
Indication: Product Used FOR Unknown Indication
Motilium
Indication: Product Used FOR Unknown Indication
Retrovir
Indication: Product Used FOR Unknown Indication
Possible Kaletra side effects in male
Reported by a physician from Japan on 2012-08-06
Patient: male
Reactions: Colonic Polyp, Iron Deficiency Anaemia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Allopurinol; Candesartan Cilexetil; Raltegravir; Tenofovir Disoproxil Fumarate
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:
Kaletra
Dosage: 4 dosage forms daily
Administration route: Oral
Indication: HIV Infection
Start date: 2007-09-12
End date: 2011-01-14
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
Other drugs received by patient: Lamivudine; Zerit
Possible Kaletra side effects in 53 year old male
Reported by a physician from Japan on 2012-08-06
Patient: 53 year old male
Reactions: Pyrexia, Mycobacterium Avium Complex Infection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Raltegravir; Fosamprenavir Calcium; Ritonavir; Abacavir Sulfate / Lamivudine
Possible Kaletra side effects in 40 year old female
Reported by a physician from Japan on 2012-08-03
Patient: 40 year old female
Reactions: Abortion Induced
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Raltegravir; Lamivudine + Zidovudine; Emtricitabine / Tenofovir Disoproxil Fumarate
Possible Kaletra side effects in male
Reported by a physician from Japan on 2012-08-02
Patient: male
Reactions: Hyperlipidaemia, Oesophageal Candidiasis, Syphilis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Dosage: 4 dosage forms daily
Administration route: Oral
Indication: HIV Infection
Start date: 2006-11-27
Kaletra
Dosage: 6 dosage form
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-01
End date: 2006-11-26
Truvada
Start date: 2011-08-08
Truvada
Dosage: 1 dosage form daily
Administration route: Oral
Indication: HIV Infection
Start date: 2009-04-29
Zerit
Dosage: 60 mg daily
Administration route: Oral
Indication: HIV Infection
Start date: 2005-04-01
End date: 2008-01-01
Zerit
Dosage: 60 mg daily
Administration route: Oral
Start date: 2009-04-29
End date: 2011-08-07
Other drugs received by patient: Tenofovir Disoproxil Fumarate; Lamivudine; Lamivudine; Tenofovir Disoproxil Fumarate
Possible Kaletra side effects in male
Reported by a physician from Chile on 2012-07-31
Patient: male, weighing 87.0 kg (191.4 pounds)
Reactions: Asthmatic Crisis
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Lamivudine (Epivir Hbv)
Possible Kaletra side effects in male
Reported by a physician from United States on 2012-07-30
Patient: male, weighing 2.1 kg (4.6 pounds)
Reactions: Atrial Septal Defect, Cardiac Murmur, Dysmorphism, Congenital Anaemia, Premature Baby, Foetal Exposure During Pregnancy, Jaundice Neonatal, Ascites
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Combivir
Dosage: 2tab per day
Indication: Antiretroviral Therapy
Start date: 2011-09-22
Kaletra
Dosage: 4tab per day
Indication: Antiretroviral Therapy
Start date: 2011-09-22
Other drugs received by patient: Metronidazole
Possible Kaletra side effects in 9 year old female
Reported by a consumer/non-health professional from Ireland on 2012-07-27
Patient: 9 year old female
Reactions: Poor Quality Sleep, Malaise, Nausea, Hypophagia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
ALL Other Therapeutic Products
Dosage: twice a day
Indication: Product Used FOR Unknown Indication
Epivir
Dosage: twice a day
Indication: Product Used FOR Unknown Indication
Kaletra
Dosage: twice a day
Indication: Product Used FOR Unknown Indication
Maxolon
Dosage: twice a day
Indication: Product Used FOR Unknown Indication
Retrovir
Dosage: twice a day
Indication: Product Used FOR Unknown Indication
Possible Kaletra side effects in 9 year old female
Reported by a consumer/non-health professional from Ireland on 2012-07-27
Patient: 9 year old female
Reactions: Aphagia, Regurgitation, Malaise, Nausea, Insomnia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Epivir
Indication: Product Used FOR Unknown Indication
Kaletra
Indication: Product Used FOR Unknown Indication
Maxolon
Indication: Product Used FOR Unknown Indication
Motilium
Indication: Product Used FOR Unknown Indication
Retrovir
Indication: Product Used FOR Unknown Indication
Possible Kaletra side effects in female
Reported by a physician from Canada on 2012-07-26
Patient: female
Reactions: Immature Respiratory System, Premature Baby, Foetal Exposure During Pregnancy
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Other drugs received by patient: Zidovudine; Septra
Possible Kaletra side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-26
Patient: female
Reactions: Dysphagia, Respiratory Disorder, Foetal Exposure During Pregnancy
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Kaletra
Dosage: 4tab per day
Indication: HIV Infection
Start date: 2009-08-01
Lamivudine + Zidovudine
Dosage: 2tab per day
Indication: HIV Infection
Start date: 2009-08-01
Retrovir
Indication: Antiviral Prophylaxis
Start date: 2010-04-02
End date: 2010-04-02
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